Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116254 |
| ensemblid | ENSG00000055211.14 |
| hgncid | 21074 |
| symbol | GINM1 |
| name | glycosylated integral membrane protein 1 |
| refseq_nuc | NM_138785.5 |
| refseq_prot | NP_620140.1 |
| ensembl_nuc | ENST00000367419.10 |
| ensembl_prot | ENSP00000356389.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 149566375 |
| end | 149591748 |
| strand | + |
| ver | v1.2 |
| region | chr6:149566375-149591748 |
| region5000 | chr6:149561375-149596748 |
| regionname0 | GINM1_chr6_149566375_149591748 |
| regionname5000 | GINM1_chr6_149561375_149596748 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 330 | 368 | 86 | 73 | 152 | 13 | 42 | 114 | GINM1_chr6_149561375_149596748 | GINM1 | MEGAP others(325): Show |
chr6 | 149561375 | 149596748 |
| a0002 | 0/0 | 330 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | MEGAP others(325): Show |
chr6 | 149561375 | 149596748 |
| a0003 | 0/0 | 330 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | MEGAP others(325): Show |
chr6 | 149561375 | 149596748 |
| a0004 | 0/0 | 330 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | MEGAP others(325): Show |
chr6 | 149561375 | 149596748 |
| a0005 | 0/0 | 330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | MEGAP others(325): Show |
chr6 | 149561375 | 149596748 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 990 | 346 | 72 | 71 | 146 | 13 | 42 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0001c0002 | 0/0 | 990 | 15 | 13 | 2 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0001c0004 | 0/0 | 990 | 5 | 0 | 0 | 5 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0001c0006 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0001c0009 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0002c0003 | 0/0 | 990 | 7 | 7 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0003c0005 | 0/0 | 990 | 3 | 0 | 2 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0004c0007 | 0/0 | 990 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 | ||
| a0005c0008 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ATGGA others(985): Show |
chr6 | 149561375 | 149596748 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1943 | 111 | 29 | 24 | 33 | 8 | 16 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0002 | 0/0 | 1945 | 66 | 1 | 8 | 49 | 0 | 8 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0003 | 0/1 | 1944 | 68 | 16 | 18 | 13 | 5 | 15 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0004 | 0/0 | 1944 | 60 | 9 | 14 | 37 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0005 | 0/0 | 1943 | 12 | 8 | 0 | 4 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0006 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0007 | 0/0 | 1946 | 11 | 2 | 7 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1941): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0008 | 0/0 | 1944 | 6 | 0 | 0 | 6 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0010 | 0/0 | 1943 | 3 | 3 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0011 | 0/0 | 1944 | 2 | 0 | 0 | 0 | 0 | 2 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0012 | 0/0 | 1945 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0013 | 0/0 | 1944 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0015 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0016 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0018 | 0/0 | 1941 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1936): Show |
chr6 | 149561375 | 149596748 |
| a0001c0001t0021 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0001 | 0/0 | 1943 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0004 | 0/0 | 1944 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0006 | 0/0 | 1943 | 4 | 4 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0009 | 0/0 | 1942 | 5 | 5 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1937): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0012 | 0/0 | 1945 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0017 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0020 | 0/0 | 1945 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0002t0022 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0001c0004t0002 | 0/0 | 1945 | 4 | 0 | 0 | 4 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0001c0004t0003 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0006t0013 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0001c0009t0004 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1939): Show |
chr6 | 149561375 | 149596748 |
| a0002c0003t0006 | 0/0 | 1943 | 6 | 6 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0002c0003t0019 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0003c0005t0001 | 0/0 | 1943 | 3 | 0 | 2 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| a0004c0007t0002 | 0/0 | 1945 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1940): Show |
chr6 | 149561375 | 149596748 |
| a0005c0008t0014 | 0/0 | 1943 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | ACCTC others(1938): Show |
chr6 | 149561375 | 149596748 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 19 | 1 | 5 | 11 | 0 | 2 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0006 | 1/0 | 6 | 1 | 3 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0031 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0001 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0007 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0008g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0016g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0018g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0017g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0020g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0002t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0004t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0004t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0006t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0001c0009t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0002c0003t0006g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0002c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0002c0003t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0002c0003t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0003c0005t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0003c0005t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0004c0007t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| a0005c0008t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0093 | EUR | GBR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0122 | EUR | GBR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00609 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | CHS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00741 | hp1 | a0004 | c0007 | t0002 | g0021 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0058 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01168 | hp1 | a0003 | c0005 | t0001 | g0047 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01169 | hp2 | a0003 | c0005 | t0001 | g0006 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0131 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0139 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0034 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02056 | hp1 | a0001 | c0009 | t0004 | g0179 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | CDX | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0159 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02572 | hp1 | a0002 | c0003 | t0006 | g0073 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02615 | hp1 | a0001 | c0002 | t0022 | g0071 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02615 | hp2 | a0001 | c0002 | t0020 | g0050 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02630 | hp2 | a0001 | c0002 | t0012 | g0049 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0080 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02717 | hp2 | a0001 | c0002 | t0006 | g0076 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02723 | hp2 | a0002 | c0003 | t0019 | g0062 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02809 | hp1 | a0001 | c0002 | t0009 | g0034 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02809 | hp2 | a0001 | c0002 | t0009 | g0077 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0068 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0069 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0051 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02970 | hp2 | a0001 | c0002 | t0017 | g0074 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03130 | hp2 | a0002 | c0003 | t0006 | g0012 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03139 | hp1 | a0002 | c0003 | t0006 | g0012 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0072 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0065 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0075 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03491 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03579 | hp2 | a0001 | c0002 | t0009 | g0079 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0025 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | BEB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0078 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | CHB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18906 | hp2 | a0002 | c0003 | t0006 | g0012 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0157 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18975 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19000 | hp2 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19090 | hp1 | a0001 | c0001 | t0021 | g0040 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | YRI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ASW | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20752 | hp1 | a0003 | c0005 | t0001 | g0006 | EUR | TSI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | TSI | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02109 | hp2 | a0002 | c0003 | t0006 | g0012 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02559 | hp1 | a0002 | c0003 | t0006 | g0061 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03471 | hp1 | a0001 | c0006 | t0013 | g0056 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0070 | AFR | MSL | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| HG06807 | hp2 | a0005 | c0008 | t0014 | g0060 | AFR | USA | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | USA | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA20300 | hp2 | a0001 | c0001 | t0012 | g0001 | AFR | USA | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | LWK | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0123 | REF | REF | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | GINM1_chr6_149561375_149596748 | GINM1 | chr6 | 149561375 | 149596748 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149579870 | G | A | 1 | a0002 | 7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.466G>A | p.Val156Ile | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/8 | 506/1943 | 466/993 | 156/330 | chr6 | 149579870 | |||
| chr6:149579880 | G | A | 1 | a0004 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.476G>A | p.Arg159Gln | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/8 | 516/1943 | 476/993 | 159/330 | chr6 | 149579880 | |||
| chr6:149582461 | A | G | 1 | a0003 | 3 | HG01168.hp1 HG01169.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.739A>G | p.Lys247Glu | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/8 | 779/1943 | 739/993 | 247/330 | chr6 | 149582461 | |||
| chr6:149590762 | C | G | 1 | a0005 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.917C>G | p.Pro306Arg | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 957/1943 | 917/993 | 306/330 | chr6 | 149590762 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149566450 | G | A | 3 | a0001c0002 a0001c0006 a0002c0003 |
23 | HG00733.hp1 HG01109.hp2 HG02055.hp2 others(20): Show |
synonymous_variant | LOW | c.36G>A | p.Arg12Arg | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/8 | 76/1943 | 36/993 | 12/330 | chr6 | 149566450 | |||
| chr6:149566495 | G | T | 1 | a0001c0009 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.81G>T | p.Thr27Thr | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/8 | 121/1943 | 81/993 | 27/330 | chr6 | 149566495 | |||
| chr6:149578845 | T | C | 1 | a0001c0004 | 5 | HG00609.hp2 HG00621.hp2 HG02155.hp1 others(2): Show |
synonymous_variant | LOW | c.301T>C | p.Leu101Leu | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/8 | 341/1943 | 301/993 | 101/330 | chr6 | 149578845 | |||
| chr6:149582568 | C | T | 1 | a0001c0006 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.846C>T | p.Thr282Thr | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/8 | 886/1943 | 846/993 | 282/330 | chr6 | 149582568 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149591032 | T | C | 3 | a0001c0001t0011 a0001c0001t0015 a0005c0008t0014 |
4 | HG03195.hp2 HG03491.hp2 HG04184.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*194T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 194 | chr6 | 149591032 | ||||||
| chr6:149591063 | T | G | 16 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(13): Show |
97 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*225T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 225 | chr6 | 149591063 | ||||||
| chr6:149591106 | T | C | 5 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0009 others(2): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*268T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 268 | chr6 | 149591106 | ||||||
| chr6:149591115 | CCT | C | 8 | a0001c0001t0006 a0001c0001t0018 a0001c0002t0006 others(5): Show |
20 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*278_*279delCT | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 278 | chr6 | 149591115 | ||||||
| chr6:149591117 | T | C | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(2): Show |
5 | HG01109.hp2 HG02257.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*279T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 279 | chr6 | 149591117 | ||||||
| chr6:149591126 | TA | T | 1 | a0001c0002t0009 | 5 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*296delA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 296 | INFO_REALIGN_3_PRIME | chr6 | 149591126 | |||||
| chr6:149591135 | T | TA | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(3): Show |
89 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*304dupA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 305 | INFO_REALIGN_3_PRIME | chr6 | 149591135 | |||||
| chr6:149591136 | A | T | 1 | a0001c0001t0021 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 298 | chr6 | 149591136 | ||||||
| chr6:149591291 | C | CA | 12 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(9): Show |
24 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*465dupA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 466 | INFO_REALIGN_3_PRIME | chr6 | 149591291 | |||||
| chr6:149591491 | C | G | 2 | a0001c0001t0010 a0001c0001t0015 |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*653C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 653 | chr6 | 149591491 | ||||||
| chr6:149591721 | C | CT | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*900dupT | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 901 | INFO_REALIGN_3_PRIME | chr6 | 149591721 | |||||
| chr6:149591721 | C | CTT | 2 | a0001c0001t0007 a0001c0001t0021 |
12 | HG01928.hp1 HG01934.hp1 HG01952.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*899_*900dupTT | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 8/8 | 901 | INFO_REALIGN_3_PRIME | chr6 | 149591721 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149566577 | T | C | 36 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0004g0057 others(33): Show |
43 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.120+43T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149566577 | |||||||
| chr6:149566749 | T | C | 40 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(37): Show |
46 | HG00099.hp2 HG01192.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.120+215T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149566749 | |||||||
| chr6:149567116 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | NA19000.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.120+582G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149567116 | |||||||
| chr6:149567128 | G | A | 193 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(190): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.120+594G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149567128 | |||||||
| chr6:149567135 | C | T | 1 | a0001c0001t0007g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.120+601C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149567135 | |||||||
| chr6:149567576 | G | A | 2 | a0001c0002t0012g0049 a0001c0002t0020g0050 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.120+1042G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149567576 | |||||||
| chr6:149568068 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+1534C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568068 | |||||||
| chr6:149568130 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.120+1596T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568130 | |||||||
| chr6:149568493 | C | A | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+1959C>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568493 | |||||||
| chr6:149568629 | A | T | 1 | a0001c0001t0004g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.120+2095A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568629 | |||||||
| chr6:149568729 | G | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0118 a0001c0001t0002g0187 others(1): Show |
5 | HG01975.hp1 HG01978.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2195G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568729 | |||||||
| chr6:149568777 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.120+2243G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568777 | |||||||
| chr6:149568917 | T | C | 203 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0025 others(200): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.120+2383T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149568917 | |||||||
| chr6:149569193 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+2659C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569193 | |||||||
| chr6:149569203 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.120+2669T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569203 | |||||||
| chr6:149569209 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.120+2675T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569209 | |||||||
| chr6:149569313 | G | A | 1 | a0001c0006t0013g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120+2779G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569313 | |||||||
| chr6:149569337 | C | CT | 20 | a0001c0001t0001g0048 a0001c0001t0001g0220 a0001c0001t0001g0221 others(17): Show |
22 | HG00140.hp1 HG00642.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.120+2820dupT | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149569337 | ||||||
| chr6:149569337 | C | CTT | 112 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0151 others(109): Show |
185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.120+2819_120+2820d others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149569337 | ||||||
| chr6:149569337 | C | CTTT | 6 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(3): Show |
7 | HG00544.hp1 HG01175.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2818_120+2820d others(5): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149569337 | ||||||
| chr6:149569363 | G | A | 3 | a0001c0001t0005g0033 a0001c0001t0005g0052 a0001c0001t0018g0051 |
4 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2829G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569363 | |||||||
| chr6:149569432 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0002g0195 a0002c0003t0006g0012 |
8 | HG00558.hp1 HG02109.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-2853G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569432 | |||||||
| chr6:149569527 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-2758C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569527 | |||||||
| chr6:149569549 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121-2736G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569549 | |||||||
| chr6:149569665 | C | A | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.121-2620C>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569665 | |||||||
| chr6:149569706 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.121-2579C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569706 | |||||||
| chr6:149569776 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.121-2509T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569776 | |||||||
| chr6:149569822 | A | T | 1 | a0001c0001t0004g0178 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.121-2463A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569822 | |||||||
| chr6:149569852 | T | C | 1 | a0001c0001t0004g0009 | 5 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2433T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569852 | |||||||
| chr6:149569863 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.121-2422A>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569863 | |||||||
| chr6:149569990 | G | A | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.121-2295G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149569990 | |||||||
| chr6:149570115 | T | C | 1 | a0001c0002t0004g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121-2170T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570115 | |||||||
| chr6:149570134 | TTTTATAT others(1): Show |
T | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0197 others(3): Show |
7 | HG02647.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.121-2149_121-2142d others(10): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(3): Show |
T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
5 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2149_121-2140d others(12): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(5): Show |
T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
5 | HG02602.hp1 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2149_121-2138d others(14): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(7): Show |
T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0196 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2149_121-2136d others(16): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(9): Show |
T | 1 | a0001c0001t0003g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121-2149_121-2134d others(18): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(11): Show |
T | 2 | a0001c0001t0001g0096 a0001c0001t0003g0082 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121-2149_121-2132d others(20): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(13): Show |
T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02080.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.121-2149_121-2130d others(22): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(15): Show |
T | 1 | a0001c0001t0003g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.121-2149_121-2128d others(24): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(19): Show |
T | 1 | a0001c0001t0003g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.121-2149_121-2124d others(28): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(23): Show |
T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0091 a0001c0001t0003g0090 |
4 | HG03041.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2149_121-2120d others(32): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(29): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.121-2149_121-2114d others(38): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(31): Show |
T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0003g0085 others(1): Show |
4 | HG03453.hp1 NA18949.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-2149_121-2112d others(40): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570134 | TTTTATAT others(33): Show |
T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0083 a0001c0001t0003g0084 |
5 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2149_121-2110d others(42): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570134 | ||||||
| chr6:149570135 | TTTA | T | 5 | a0001c0001t0001g0002 a0001c0001t0002g0022 a0001c0001t0002g0175 others(2): Show |
5 | HG03017.hp1 HG03017.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-2148_121-2146d others(5): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570135 | ||||||
| chr6:149570135 | TTTATATA others(14): Show |
T | 2 | a0001c0001t0002g0020 a0001c0001t0003g0142 |
2 | HG03669.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.121-2148_121-2128d others(23): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570135 | ||||||
| chr6:149570135 | TTTATATA others(18): Show |
T | 1 | a0002c0003t0019g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.121-2148_121-2124d others(27): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570135 | ||||||
| chr6:149570136 | T | A | 1 | a0001c0001t0003g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.121-2149T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570136 | |||||||
| chr6:149570136 | T | TTA | 13 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0031 others(10): Show |
15 | HG00558.hp2 HG02004.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-2088_121-2087d others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | T | TTATA | 3 | a0001c0001t0001g0004 a0001c0001t0004g0019 a0001c0004t0002g0157 |
3 | HG02071.hp1 NA18954.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.121-2090_121-2087d others(6): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTA | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(20): Show |
26 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-2088_121-2087d others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATA | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0029 others(23): Show |
32 | HG00558.hp1 HG00609.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.121-2090_121-2087d others(6): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATA | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0038 others(21): Show |
27 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.121-2092_121-2087d others(8): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(1): Show |
T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
41 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.121-2094_121-2087d others(10): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(3): Show |
T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0025 others(29): Show |
38 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.121-2096_121-2087d others(12): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(5): Show |
T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(18): Show |
26 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.121-2098_121-2087d others(14): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(7): Show |
T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0003g0122 others(5): Show |
8 | HG00140.hp1 HG00323.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-2100_121-2087d others(16): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(9): Show |
T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0039 a0001c0001t0003g0001 others(6): Show |
12 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-2102_121-2087d others(18): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(11): Show |
T | 11 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0003g0002 others(8): Show |
15 | HG00738.hp1 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.121-2104_121-2087d others(20): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(13): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0206 others(4): Show |
8 | HG02257.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-2106_121-2087d others(22): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(15): Show |
T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0002g0169 others(3): Show |
11 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-2108_121-2087d others(24): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(17): Show |
T | 6 | a0001c0001t0001g0223 a0001c0001t0003g0170 a0001c0001t0004g0019 others(3): Show |
6 | HG01069.hp1 HG01978.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-2110_121-2087d others(26): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0004 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.121-2114_121-2087d others(30): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(25): Show |
T | 1 | a0001c0002t0017g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121-2118_121-2087d others(34): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(29): Show |
T | 2 | a0001c0001t0002g0161 a0001c0001t0006g0066 |
2 | HG01884.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.121-2122_121-2087d others(38): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(33): Show |
T | 6 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0022 others(3): Show |
7 | HG00544.hp2 HG00741.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-2126_121-2087d others(42): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(35): Show |
T | 6 | a0001c0001t0003g0136 a0001c0001t0003g0138 a0001c0001t0003g0172 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-2128_121-2087d others(44): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570136 | TTATATAT others(37): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121-2130_121-2087d others(46): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570136 | ||||||
| chr6:149570152 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.121-2124_121-2123i others(12): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570152 | ||||||
| chr6:149570156 | A | T | 1 | a0001c0002t0020g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.121-2129A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570156 | |||||||
| chr6:149570158 | A | T | 3 | a0001c0001t0005g0033 a0001c0001t0005g0055 a0001c0002t0012g0049 |
4 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-2127A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570158 | |||||||
| chr6:149570160 | A | T | 6 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(3): Show |
9 | HG02886.hp1 HG02886.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.121-2125A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570160 | |||||||
| chr6:149570162 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.121-2123A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570162 | |||||||
| chr6:149570162 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0005g0052 a0001c0001t0005g0053 others(2): Show |
7 | HG02257.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.121-2123A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570162 | |||||||
| chr6:149570164 | A | T | 1 | a0001c0001t0005g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.121-2121A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570164 | |||||||
| chr6:149570187 | TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0198 a0001c0001t0003g0110 |
2 | HG01123.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.121-2096_121-2086d others(13): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570187 | ||||||
| chr6:149570193 | TATATA | T | 3 | a0001c0001t0001g0201 a0001c0001t0003g0041 a0001c0001t0004g0144 |
3 | HG01167.hp1 HG01167.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.121-2090_121-2086d others(7): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570193 | ||||||
| chr6:149570194 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.121-2091A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570194 | |||||||
| chr6:149570197 | T | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0160 |
3 | HG00639.hp1 HG01258.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.121-2088T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570197 | |||||||
| chr6:149570197 | TA | T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0045 a0001c0001t0004g0020 others(1): Show |
4 | HG02135.hp2 HG02717.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2085delA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570197 | ||||||
| chr6:149570199 | A | G | 1 | a0001c0001t0004g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.121-2086A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570199 | |||||||
| chr6:149570199 | A | T | 2 | a0001c0001t0001g0217 a0001c0001t0004g0177 |
2 | NA18954.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.121-2086A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570199 | |||||||
| chr6:149570200 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.121-2085A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570200 | |||||||
| chr6:149570336 | T | C | 28 | a0001c0001t0001g0063 a0001c0001t0005g0059 a0001c0001t0005g0067 others(25): Show |
32 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.121-1949T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570336 | |||||||
| chr6:149570459 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-1826A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570459 | |||||||
| chr6:149570534 | CAA | C | 120 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0151 others(117): Show |
194 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.121-1749_121-1748d others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149570534 | ||||||
| chr6:149570611 | G | A | 1 | a0001c0002t0006g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.121-1674G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570611 | |||||||
| chr6:149570652 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-1633G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570652 | |||||||
| chr6:149570655 | A | G | 1 | a0001c0001t0004g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.121-1630A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149570655 | |||||||
| chr6:149571129 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.121-1156C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571129 | |||||||
| chr6:149571238 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.121-1047C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571238 | |||||||
| chr6:149571312 | CA | C | 32 | a0001c0001t0001g0063 a0001c0001t0001g0216 a0001c0001t0003g0170 others(29): Show |
36 | HG00733.hp1 HG01069.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-955delA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149571312 | ||||||
| chr6:149571312 | CAAA | C | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-957_121-955del others(3): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149571312 | ||||||
| chr6:149571385 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.121-900G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571385 | |||||||
| chr6:149571608 | T | C | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.121-677T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571608 | |||||||
| chr6:149571639 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.121-646G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571639 | |||||||
| chr6:149571646 | C | G | 1 | a0001c0001t0002g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.121-639C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571646 | |||||||
| chr6:149571834 | G | C | 1 | a0001c0001t0002g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.121-451G>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571834 | |||||||
| chr6:149571864 | C | T | 8 | a0001c0002t0006g0072 a0001c0002t0006g0075 a0001c0002t0006g0076 others(5): Show |
9 | HG02055.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.121-421C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149571864 | |||||||
| chr6:149572049 | C | G | 1 | a0001c0002t0022g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.121-236C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149572049 | |||||||
| chr6:149572078 | A | AAAAT | 153 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0035 others(150): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.121-184_121-181dup others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149572078 | ||||||
| chr6:149572078 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0096 a0001c0001t0001g0098 others(1): Show |
5 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-188_121-181dup others(8): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 149572078 | ||||||
| chr6:149572126 | G | A | 6 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0104 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-159G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149572126 | |||||||
| chr6:149572196 | T | C | 1 | a0001c0001t0003g0125 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.121-89T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149572196 | |||||||
| chr6:149572228 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.121-57G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 1/7 | chr6 | 149572228 | |||||||
| chr6:149572888 | A | G | 1 | a0001c0002t0004g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.277+285A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149572888 | |||||||
| chr6:149572935 | G | A | 26 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0104 others(23): Show |
29 | HG00099.hp2 HG01192.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.277+332G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149572935 | |||||||
| chr6:149572944 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.277+341A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149572944 | |||||||
| chr6:149573012 | T | A | 3 | a0001c0001t0004g0121 a0001c0001t0004g0127 a0001c0001t0004g0128 |
3 | NA18997.hp1 NA19058.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.277+409T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149573012 | |||||||
| chr6:149573032 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.277+429G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149573032 | |||||||
| chr6:149573347 | A | AGAGGATC others(4): Show |
158 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(155): Show |
239 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.277+746_277+747ins others(11): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149573347 | ||||||
| chr6:149573387 | C | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0040 a0001c0001t0004g0129 others(2): Show |
7 | HG02040.hp2 HG02056.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.277+784C>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149573387 | |||||||
| chr6:149573838 | T | A | 4 | a0002c0003t0006g0012 a0002c0003t0006g0061 a0002c0003t0006g0073 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+1235T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149573838 | |||||||
| chr6:149574047 | AT | A | 54 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0047 others(51): Show |
64 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.277+1463delT | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574047 | ||||||
| chr6:149574047 | ATT | A | 107 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0001g0151 others(104): Show |
173 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.277+1462_277+1463d others(4): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574047 | ||||||
| chr6:149574047 | ATTT | A | 10 | a0001c0001t0001g0201 a0001c0001t0003g0007 a0001c0001t0003g0122 others(7): Show |
14 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.277+1461_277+1463d others(5): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574047 | ||||||
| chr6:149574111 | C | T | 37 | a0001c0001t0001g0151 a0001c0001t0002g0003 a0001c0001t0002g0008 others(34): Show |
58 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.277+1508C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574111 | |||||||
| chr6:149574119 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.277+1516C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574119 | |||||||
| chr6:149574120 | G | A | 2 | a0001c0001t0004g0010 a0001c0001t0004g0132 |
6 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+1517G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574120 | |||||||
| chr6:149574168 | A | AGCCTCCC others(129): Show |
24 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0039 others(21): Show |
42 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.277+1573_277+1708d others(138): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574168 | ||||||
| chr6:149574168 | A | AGCCTCCC others(265): Show |
2 | a0001c0001t0002g0181 a0001c0001t0002g0189 |
2 | HG02074.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.277+1708_277+1709i others(274): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574168 | ||||||
| chr6:149574168 | A | AGCCTCCC others(129): Show |
1 | a0001c0001t0007g0159 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.277+1595_277+1596i others(138): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149574168 | ||||||
| chr6:149574168 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0004g0148 |
2 | HG01934.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.277+1565A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574168 | |||||||
| chr6:149574186 | G | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0032 others(6): Show |
21 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.277+1583G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574186 | |||||||
| chr6:149574199 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.277+1596C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574199 | |||||||
| chr6:149574207 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0004g0133 |
3 | HG02129.hp1 NA18957.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.277+1604T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574207 | |||||||
| chr6:149574239 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.277+1636T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574239 | |||||||
| chr6:149574242 | G | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG01243.hp1 HG03453.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+1639G>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574242 | |||||||
| chr6:149574246 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.277+1643T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574246 | |||||||
| chr6:149574260 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.277+1657A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574260 | |||||||
| chr6:149574294 | C | T | 2 | a0001c0001t0005g0059 a0005c0008t0014g0060 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.277+1691C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574294 | |||||||
| chr6:149574303 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0004g0024 |
4 | HG02523.hp2 HG02976.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+1700C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574303 | |||||||
| chr6:149574304 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0081 a0001c0001t0001g0096 others(2): Show |
6 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+1701G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574304 | |||||||
| chr6:149574331 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.277+1728C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574331 | |||||||
| chr6:149574347 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.277+1744C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574347 | |||||||
| chr6:149574372 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.277+1769C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574372 | |||||||
| chr6:149574490 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.277+1887C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574490 | |||||||
| chr6:149574491 | C | G | 25 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0081 others(22): Show |
33 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.277+1888C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574491 | |||||||
| chr6:149574497 | C | A | 2 | a0001c0001t0003g0090 a0001c0002t0001g0064 |
2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.277+1894C>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574497 | |||||||
| chr6:149574952 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.277+2349T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149574952 | |||||||
| chr6:149575080 | C | A | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277+2477C>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575080 | |||||||
| chr6:149575124 | A | G | 1 | a0001c0006t0013g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277+2521A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575124 | |||||||
| chr6:149575182 | T | C | 122 | a0001c0001t0001g0025 a0001c0001t0001g0202 a0001c0001t0002g0001 others(119): Show |
197 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.277+2579T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575182 | |||||||
| chr6:149575247 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.277+2644G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575247 | |||||||
| chr6:149575278 | A | G | 3 | a0001c0001t0003g0023 a0001c0001t0004g0023 a0001c0001t0004g0146 |
4 | HG03927.hp2 NA18747.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2675A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575278 | |||||||
| chr6:149575540 | C | G | 153 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0063 others(150): Show |
232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.277+2937C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575540 | |||||||
| chr6:149575595 | C | T | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277+2992C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575595 | |||||||
| chr6:149575720 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.278-3102G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575720 | |||||||
| chr6:149575919 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.278-2903T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575919 | |||||||
| chr6:149575928 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.278-2894A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149575928 | |||||||
| chr6:149576148 | C | T | 4 | a0001c0001t0010g0068 a0001c0001t0010g0069 a0001c0001t0010g0070 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-2674C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576148 | |||||||
| chr6:149576216 | C | T | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-2606C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576216 | |||||||
| chr6:149576319 | A | G | 198 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0035 others(195): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.278-2503A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576319 | |||||||
| chr6:149576450 | T | A | 1 | a0001c0001t0004g0146 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.278-2372T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576450 | |||||||
| chr6:149576586 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0005g0067 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.278-2236C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576586 | |||||||
| chr6:149576602 | G | GA | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.278-2211dupA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149576602 | ||||||
| chr6:149576618 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(5): Show |
11 | HG02257.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2204A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576618 | |||||||
| chr6:149576634 | A | G | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-2188A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576634 | |||||||
| chr6:149576742 | G | A | 1 | a0001c0001t0003g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-2080G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576742 | |||||||
| chr6:149576773 | G | C | 1 | a0001c0001t0001g0032 | 3 | HG01515.hp1 HG01517.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.278-2049G>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576773 | |||||||
| chr6:149576932 | C | G | 1 | a0001c0001t0004g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.278-1890C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149576932 | |||||||
| chr6:149577053 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278-1769C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577053 | |||||||
| chr6:149577111 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0003g0113 |
3 | HG03209.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.278-1711C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577111 | |||||||
| chr6:149577233 | C | G | 6 | a0001c0001t0003g0092 a0001c0001t0004g0057 a0001c0001t0010g0068 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1589C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577233 | |||||||
| chr6:149577299 | T | A | 1 | a0001c0001t0003g0150 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.278-1523T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577299 | |||||||
| chr6:149577398 | T | C | 1 | a0001c0001t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.278-1424T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577398 | |||||||
| chr6:149577473 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.278-1349C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577473 | |||||||
| chr6:149577689 | G | A | 1 | a0001c0001t0004g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.278-1133G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577689 | |||||||
| chr6:149577800 | G | A | 3 | a0001c0001t0003g0136 a0001c0001t0003g0172 a0001c0001t0004g0135 |
3 | HG01081.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.278-1022G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577800 | |||||||
| chr6:149577830 | C | T | 1 | a0001c0004t0002g0157 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.278-992C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577830 | |||||||
| chr6:149577888 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.278-934T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149577888 | |||||||
| chr6:149578232 | G | A | 1 | a0001c0001t0018g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.278-590G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578232 | |||||||
| chr6:149578355 | T | A | 1 | a0001c0001t0002g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.278-467T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578355 | |||||||
| chr6:149578359 | T | C | 1 | a0001c0001t0005g0033 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.278-463T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578359 | |||||||
| chr6:149578410 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.278-412C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578410 | |||||||
| chr6:149578480 | G | A | 1 | a0001c0001t0004g0146 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.278-342G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578480 | |||||||
| chr6:149578505 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.278-317G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578505 | |||||||
| chr6:149578525 | C | CA | 6 | a0001c0001t0001g0038 a0001c0001t0001g0087 a0001c0001t0001g0190 others(3): Show |
8 | HG00639.hp1 HG01258.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-275dupA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149578525 | ||||||
| chr6:149578525 | CA | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0035 others(163): Show |
244 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.278-275delA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149578525 | ||||||
| chr6:149578525 | CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0012g0049 a0001c0002t0020g0050 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.278-285_278-275del others(11): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 149578525 | ||||||
| chr6:149578698 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.278-124A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578698 | |||||||
| chr6:149578742 | A | G | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.278-80A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578742 | |||||||
| chr6:149578769 | A | G | 1 | a0001c0001t0010g0070 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.278-53A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 3/7 | chr6 | 149578769 | |||||||
| chr6:149579095 | A | G | 1 | a0001c0001t0001g0029 | 3 | NA18951.hp2 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.429+122A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579095 | |||||||
| chr6:149579222 | A | G | 1 | a0001c0006t0013g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.429+249A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579222 | |||||||
| chr6:149579278 | C | G | 1 | a0001c0001t0005g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.429+305C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579278 | |||||||
| chr6:149579295 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.429+322G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579295 | |||||||
| chr6:149579386 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.429+413C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579386 | |||||||
| chr6:149579515 | ACT | A | 152 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0002g0001 others(149): Show |
230 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.430-317_430-316del others(2): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 149579515 | ||||||
| chr6:149579606 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.430-228C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579606 | |||||||
| chr6:149579633 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.430-201G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579633 | |||||||
| chr6:149579719 | G | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0118 a0001c0001t0002g0187 |
4 | HG01975.hp1 HG02293.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-115G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 4/7 | chr6 | 149579719 | |||||||
| chr6:149580005 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.586+15C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/7 | chr6 | 149580005 | |||||||
| chr6:149580006 | A | G | 5 | a0001c0001t0004g0057 a0001c0001t0010g0068 a0001c0001t0010g0069 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+16A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/7 | chr6 | 149580006 | |||||||
| chr6:149580083 | A | G | 1 | a0001c0002t0022g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.586+93A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/7 | chr6 | 149580083 | |||||||
| chr6:149580159 | A | G | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586+169A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/7 | chr6 | 149580159 | |||||||
| chr6:149580435 | T | C | 1 | a0001c0002t0009g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.587-158T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 5/7 | chr6 | 149580435 | |||||||
| chr6:149580779 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.717+56G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149580779 | |||||||
| chr6:149580823 | T | C | 1 | a0001c0001t0002g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.717+100T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149580823 | |||||||
| chr6:149581025 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.717+302G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581025 | |||||||
| chr6:149581163 | A | C | 1 | a0001c0001t0004g0135 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.717+440A>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581163 | |||||||
| chr6:149581507 | T | G | 1 | a0001c0001t0003g0084 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.717+784T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581507 | |||||||
| chr6:149581559 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.717+836T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581559 | |||||||
| chr6:149581612 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0004g0019 |
3 | NA18960.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.718-828G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581612 | |||||||
| chr6:149581653 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.718-787G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581653 | |||||||
| chr6:149581789 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.718-651A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581789 | |||||||
| chr6:149581871 | G | C | 1 | a0001c0002t0006g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718-569G>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149581871 | |||||||
| chr6:149582112 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.718-328C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149582112 | |||||||
| chr6:149582158 | G | A | 1 | a0001c0001t0015g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-282G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149582158 | |||||||
| chr6:149582168 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.718-272T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149582168 | |||||||
| chr6:149582213 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.718-227G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149582213 | |||||||
| chr6:149582378 | A | G | 2 | a0001c0001t0003g0143 a0001c0001t0004g0129 |
2 | HG02040.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.718-62A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 6/7 | chr6 | 149582378 | |||||||
| chr6:149582680 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.881+77A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149582680 | |||||||
| chr6:149582681 | G | T | 1 | a0001c0001t0003g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.881+78G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149582681 | |||||||
| chr6:149582799 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.881+196A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149582799 | |||||||
| chr6:149582978 | T | A | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.881+375T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149582978 | |||||||
| chr6:149582978 | T | TGTA | 201 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(198): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.881+377_881+378ins others(3): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149582978 | ||||||
| chr6:149583158 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.881+555C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583158 | |||||||
| chr6:149583267 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.881+664A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583267 | |||||||
| chr6:149583326 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.881+723G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583326 | |||||||
| chr6:149583336 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.881+733G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583336 | |||||||
| chr6:149583340 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG03579.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+737G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583340 | |||||||
| chr6:149583474 | A | T | 2 | a0001c0001t0006g0066 a0001c0006t0013g0056 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.881+871A>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583474 | |||||||
| chr6:149583541 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.881+938A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583541 | |||||||
| chr6:149583546 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.881+943T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583546 | |||||||
| chr6:149583560 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.881+957C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583560 | |||||||
| chr6:149583575 | G | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0125 a0001c0001t0004g0005 others(2): Show |
11 | HG00558.hp2 HG02056.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+972G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583575 | |||||||
| chr6:149583586 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.881+983G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583586 | |||||||
| chr6:149583610 | C | T | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.881+1007C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583610 | |||||||
| chr6:149583628 | G | GA | 10 | a0001c0001t0001g0191 a0001c0002t0006g0072 a0001c0002t0006g0075 others(7): Show |
11 | HG01433.hp1 HG02055.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+1041dupA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149583628 | ||||||
| chr6:149583628 | GA | G | 7 | a0001c0001t0002g0022 a0001c0001t0004g0022 a0001c0001t0004g0144 others(4): Show |
11 | HG01167.hp2 HG01358.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+1041delA | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149583628 | ||||||
| chr6:149583716 | G | A | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.881+1113G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583716 | |||||||
| chr6:149583727 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.881+1124A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583727 | |||||||
| chr6:149583891 | G | A | 10 | a0001c0002t0006g0072 a0001c0002t0006g0075 a0001c0002t0006g0076 others(7): Show |
11 | HG02055.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+1288G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149583891 | |||||||
| chr6:149584046 | G | A | 1 | a0001c0001t0003g0041 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.881+1443G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584046 | |||||||
| chr6:149584214 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.881+1611G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584214 | |||||||
| chr6:149584597 | T | C | 1 | a0001c0001t0005g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.881+1994T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584597 | |||||||
| chr6:149584675 | G | C | 1 | a0001c0002t0006g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.881+2072G>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584675 | |||||||
| chr6:149584826 | T | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0001g0207 others(11): Show |
18 | HG00544.hp2 HG01361.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+2223T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584826 | |||||||
| chr6:149584828 | G | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0031 others(69): Show |
106 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.881+2225G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584828 | |||||||
| chr6:149584830 | G | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0151 others(13): Show |
20 | HG00140.hp2 HG00323.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.881+2227G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149584830 | |||||||
| chr6:149585089 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.881+2486G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585089 | |||||||
| chr6:149585304 | T | C | 1 | a0001c0002t0022g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+2701T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585304 | |||||||
| chr6:149585576 | T | G | 138 | a0001c0001t0001g0025 a0001c0001t0001g0151 a0001c0001t0002g0001 others(135): Show |
214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.881+2973T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585576 | |||||||
| chr6:149585590 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.881+2987T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585590 | |||||||
| chr6:149585718 | G | A | 3 | a0001c0001t0003g0136 a0001c0001t0003g0172 a0001c0001t0004g0135 |
3 | HG01081.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.881+3115G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585718 | |||||||
| chr6:149585988 | A | G | 4 | a0002c0003t0006g0012 a0002c0003t0006g0061 a0002c0003t0006g0073 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+3385A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149585988 | |||||||
| chr6:149586236 | C | T | 1 | a0001c0001t0005g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881+3633C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586236 | |||||||
| chr6:149586309 | C | G | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02080.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.881+3706C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586309 | |||||||
| chr6:149586319 | A | G | 1 | a0001c0001t0005g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881+3716A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586319 | |||||||
| chr6:149586588 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.881+3985C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586588 | |||||||
| chr6:149586781 | C | T | 1 | a0001c0002t0009g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882-3946C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586781 | |||||||
| chr6:149586796 | G | A | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882-3931G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586796 | |||||||
| chr6:149586831 | GCCTCAAT others(26): Show |
G | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882-3857_882-3825d others(35): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149586831 | ||||||
| chr6:149586870 | A | C | 1 | a0001c0001t0002g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.882-3857A>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149586870 | |||||||
| chr6:149587143 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG01243.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.882-3584G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587143 | |||||||
| chr6:149587187 | T | A | 4 | a0001c0001t0010g0068 a0001c0001t0010g0069 a0001c0001t0010g0070 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-3540T>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587187 | |||||||
| chr6:149587447 | A | G | 5 | a0001c0001t0004g0057 a0001c0001t0010g0068 a0001c0001t0010g0069 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-3280A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587447 | |||||||
| chr6:149587532 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.882-3195A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587532 | |||||||
| chr6:149587710 | C | T | 1 | a0001c0002t0006g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882-3017C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587710 | |||||||
| chr6:149587722 | T | C | 4 | a0002c0003t0006g0012 a0002c0003t0006g0061 a0002c0003t0006g0073 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-3005T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587722 | |||||||
| chr6:149587750 | T | C | 1 | a0001c0001t0006g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882-2977T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149587750 | |||||||
| chr6:149588241 | T | G | 122 | a0001c0001t0001g0025 a0001c0001t0002g0001 a0001c0001t0002g0003 others(119): Show |
194 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.882-2486T>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588241 | |||||||
| chr6:149588314 | G | T | 3 | a0001c0002t0004g0058 a0001c0002t0017g0074 a0001c0002t0022g0071 |
3 | HG01109.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.882-2413G>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588314 | |||||||
| chr6:149588345 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882-2382C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588345 | |||||||
| chr6:149588355 | C | T | 156 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0063 others(153): Show |
235 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.882-2372C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588355 | |||||||
| chr6:149588442 | A | C | 1 | a0001c0001t0005g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882-2285A>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588442 | |||||||
| chr6:149588501 | A | G | 4 | a0002c0003t0006g0012 a0002c0003t0006g0061 a0002c0003t0006g0073 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-2226A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588501 | |||||||
| chr6:149588522 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0005g0059 a0001c0001t0005g0067 |
3 | HG02258.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.882-2205G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588522 | |||||||
| chr6:149588598 | A | G | 1 | a0001c0001t0004g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882-2129A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588598 | |||||||
| chr6:149588795 | T | TTCGTTG | 7 | a0001c0001t0001g0016 a0001c0001t0005g0033 a0001c0001t0005g0052 others(4): Show |
10 | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-1931_882-1930i others(8): Show |
GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 149588795 | ||||||
| chr6:149588797 | T | C | 150 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0002g0001 others(147): Show |
226 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.882-1930T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588797 | |||||||
| chr6:149588897 | G | A | 1 | a0001c0002t0004g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882-1830G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588897 | |||||||
| chr6:149588953 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.882-1774C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149588953 | |||||||
| chr6:149589051 | G | A | 129 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(126): Show |
201 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.882-1676G>A | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589051 | |||||||
| chr6:149589337 | A | G | 1 | a0001c0001t0006g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882-1390A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589337 | |||||||
| chr6:149589392 | C | G | 1 | a0001c0002t0004g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882-1335C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589392 | |||||||
| chr6:149589443 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.882-1284A>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589443 | |||||||
| chr6:149589492 | C | T | 1 | a0001c0002t0020g0050 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882-1235C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589492 | |||||||
| chr6:149589561 | C | G | 1 | a0005c0008t0014g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882-1166C>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589561 | |||||||
| chr6:149589711 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.882-1016T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589711 | |||||||
| chr6:149589796 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0152 a0001c0001t0002g0192 others(4): Show |
11 | HG01433.hp2 HG01928.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.882-931T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589796 | |||||||
| chr6:149589815 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.882-912T>C | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589815 | |||||||
| chr6:149589880 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.882-847C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589880 | |||||||
| chr6:149589913 | C | T | 2 | a0001c0001t0006g0066 a0001c0006t0013g0056 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.882-814C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149589913 | |||||||
| chr6:149590028 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0132 |
6 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-699C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149590028 | |||||||
| chr6:149590096 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.882-631C>T | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149590096 | |||||||
| chr6:149590199 | A | G | 3 | a0001c0001t0005g0053 a0001c0001t0005g0054 a0001c0001t0005g0055 |
3 | HG02257.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882-528A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149590199 | |||||||
| chr6:149590239 | A | G | 1 | a0001c0001t0003g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.882-488A>G | GINM1 | ENSG00000055211.14 | transcript | ENST00000367419.10 | protein_coding | 7/7 | chr6 | 149590239 |