Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79760 |
| ensemblid | ENSG00000142252.11 |
| hgncid | 20045 |
| symbol | GEMIN7 |
| name | gem nuclear organelle associated protein 7 |
| refseq_nuc | NM_024707.3 |
| refseq_prot | NP_078983.1 |
| ensembl_nuc | ENST00000270257.9 |
| ensembl_prot | ENSP00000270257.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 45079260 |
| end | 45091518 |
| strand | + |
| ver | v1.2 |
| region | chr19:45079260-45091518 |
| region5000 | chr19:45074260-45096518 |
| regionname0 | GEMIN7_chr19_45079260_45091518 |
| regionname5000 | GEMIN7_chr19_45074260_45096518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 131 | 418 | 100 | 84 | 173 | 14 | 46 | 135 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | MQTPV others(126): Show |
chr19 | 45074260 | 45096518 |
| a0002 | 0/0 | 126 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | MQTPV others(121): Show |
chr19 | 45074260 | 45096518 |
| a0003 | 0/1 | 131 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | MQTPV others(126): Show |
chr19 | 45074260 | 45096518 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 393 | 418 | 100 | 84 | 173 | 14 | 46 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ATGCA others(388): Show |
chr19 | 45074260 | 45096518 | ||
| a0002c0003 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ATGCA others(404): Show |
chr19 | 45074260 | 45096518 | ||
| a0003c0002 | 0/1 | 393 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ATGCA others(388): Show |
chr19 | 45074260 | 45096518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1653 | 302 | 62 | 52 | 147 | 8 | 32 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0002 | 0/0 | 1653 | 63 | 5 | 21 | 22 | 5 | 10 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0003 | 0/0 | 1653 | 18 | 13 | 3 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0004 | 0/0 | 1653 | 14 | 14 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0005 | 0/0 | 1653 | 14 | 1 | 8 | 0 | 1 | 4 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0006 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0007 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0008 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0001c0001t0009 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| a0002c0003t0001 | 0/0 | 1669 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1664): Show |
chr19 | 45074260 | 45096518 |
| a0003c0002t0001 | 0/1 | 1653 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | ACCAG others(1648): Show |
chr19 | 45074260 | 45096518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 97 | 0 | 18 | 66 | 5 | 7 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 4 | 7 | 1 | 3 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 3 | 3 | 1 | 3 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0007 | 0/0 | 9 | 2 | 1 | 2 | 0 | 4 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0008 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0011 | 0/0 | 5 | 3 | 1 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0002 | 0/0 | 16 | 2 | 6 | 2 | 4 | 2 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0005 | 0/0 | 14 | 2 | 0 | 10 | 0 | 2 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0010 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0021 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0004 | 0/0 | 8 | 5 | 2 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0002c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| a0003c0002t0001g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0035 | EUR | IBS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0121 | SAS | BEB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18963 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ASW | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | USA | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0103 | AFR | USA | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| homoSapiens | chm13v2 | a0003 | c0002 | t0001 | g0001 | REF | REF | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | GEMIN7_chr19_45074260_45096518 | GEMIN7 | chr19 | 45074260 | 45096518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45090407 | A | ATGTGGCC others(9): Show |
1 | a0002 | 1 | NA18963.hp2 | frameshift_variant | HIGH | c.294_309dupTGTGGCCA others(8): Show |
p.Val104fs | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 559/1653 | 310/396 | 104/131 | INFO_REALIGN_3_PRIME | chr19 | 45090407 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45080013 | G | A | 2 | a0001c0001t0003 a0001c0001t0009 |
19 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/3 | 10102 | chr19 | 45080013 | ||||||
| chr19:45090912 | A | G | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*402A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 402 | chr19 | 45090912 | ||||||
| chr19:45091141 | G | A | 1 | a0001c0001t0006 | 2 | NA18955.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*631G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 631 | chr19 | 45091141 | ||||||
| chr19:45091246 | C | G | 2 | a0001c0001t0004 a0001c0001t0005 |
28 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 736 | chr19 | 45091246 | ||||||
| chr19:45091314 | G | C | 1 | a0001c0001t0007 | 2 | HG02486.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*804G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 804 | chr19 | 45091314 | ||||||
| chr19:45091337 | T | C | 2 | a0001c0001t0002 a0001c0001t0004 |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*827T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 827 | chr19 | 45091337 | ||||||
| chr19:45091393 | A | G | 1 | a0001c0001t0007 | 2 | HG02486.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*883A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 883 | chr19 | 45091393 | ||||||
| chr19:45091400 | G | C | 2 | a0001c0001t0008 a0001c0001t0009 |
3 | HG02451.hp2 HG03516.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*890G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 3/3 | 890 | chr19 | 45091400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45079385 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.-132+8C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 1/2 | chr19 | 45079385 | |||||||
| chr19:45079656 | G | T | 1 | a0001c0001t0001g0020 | 4 | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-131-251G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 1/2 | chr19 | 45079656 | |||||||
| chr19:45079834 | G | A | 3 | a0001c0001t0005g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 |
3 | HG01074.hp1 HG01261.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-131-73G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 1/2 | chr19 | 45079834 | |||||||
| chr19:45080043 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9+14C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080043 | |||||||
| chr19:45080113 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-9+84G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080113 | |||||||
| chr19:45080196 | AG | A | 2 | a0001c0001t0008g0029 a0001c0001t0009g0053 |
3 | HG02451.hp2 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9+170delG | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080196 | ||||||
| chr19:45080326 | A | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(57): Show |
114 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.-9+297A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080326 | |||||||
| chr19:45080361 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-9+332C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080361 | |||||||
| chr19:45080372 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG00609.hp1 HG02165.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+343T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080372 | |||||||
| chr19:45080374 | A | AT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0028 others(25): Show |
58 | HG00597.hp1 HG01106.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9+364dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080374 | ||||||
| chr19:45080374 | AT | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(30): Show |
57 | HG00438.hp2 HG00733.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.-9+364delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080374 | ||||||
| chr19:45080374 | ATT | A | 3 | a0001c0001t0005g0016 a0001c0001t0005g0121 a0001c0001t0005g0122 |
6 | HG00639.hp2 HG01496.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+363_-9+364delTT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080374 | ||||||
| chr19:45080523 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0052 |
3 | HG01884.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-9+494G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080523 | |||||||
| chr19:45080532 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9+503C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080532 | |||||||
| chr19:45080591 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-9+562C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080591 | |||||||
| chr19:45080758 | G | GT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(37): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-9+735dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080758 | ||||||
| chr19:45080758 | G | GTT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0018 others(33): Show |
66 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-9+734_-9+735dupTT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080758 | ||||||
| chr19:45080758 | G | GTTT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
9 | HG01175.hp1 HG01361.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+733_-9+735dupTT others(1): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080758 | ||||||
| chr19:45080758 | GTTTTTTG others(4): Show |
G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+736_-9+746delGT others(9): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080758 | ||||||
| chr19:45080765 | G | GT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(18): Show |
54 | HG00280.hp2 HG00621.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-9+753dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080765 | ||||||
| chr19:45080765 | G | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-9+736G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080765 | |||||||
| chr19:45080765 | GT | G | 4 | a0001c0001t0001g0001 a0001c0001t0005g0016 a0001c0001t0005g0025 others(1): Show |
9 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+753delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080765 | ||||||
| chr19:45080771 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9+742T>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080771 | |||||||
| chr19:45080782 | T | TC | 1 | a0001c0001t0002g0021 | 3 | HG02559.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-9+755dupC | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45080782 | ||||||
| chr19:45080783 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-9+754C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080783 | |||||||
| chr19:45080964 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-9+935G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45080964 | |||||||
| chr19:45081006 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+977A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081006 | |||||||
| chr19:45081053 | G | C | 1 | a0001c0001t0001g0030 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+1024G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081053 | |||||||
| chr19:45081127 | C | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(83): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-9+1098C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081127 | |||||||
| chr19:45081159 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9+1130G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081159 | |||||||
| chr19:45081284 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-9+1255G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081284 | |||||||
| chr19:45081304 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+1275A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081304 | |||||||
| chr19:45081388 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0052 others(2): Show |
7 | HG01261.hp2 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+1359G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081388 | |||||||
| chr19:45081434 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(37): Show |
87 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.-9+1405C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081434 | |||||||
| chr19:45081456 | T | TA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0045 others(6): Show |
25 | HG00738.hp2 HG01074.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+1443dupA | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45081456 | ||||||
| chr19:45081456 | TA | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0059 others(10): Show |
16 | HG01169.hp1 HG01257.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+1443delA | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45081456 | ||||||
| chr19:45081524 | GA | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+1509delA | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45081524 | ||||||
| chr19:45081584 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9+1555C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081584 | |||||||
| chr19:45081627 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-9+1598G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081627 | |||||||
| chr19:45081719 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+1690C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081719 | |||||||
| chr19:45081741 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0112 |
2 | NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-9+1712C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081741 | |||||||
| chr19:45081774 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-9+1745G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081774 | |||||||
| chr19:45081777 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0095 |
2 | HG00621.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-9+1748C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081777 | |||||||
| chr19:45081817 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0129 |
3 | HG00438.hp2 HG02074.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.-9+1788G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081817 | |||||||
| chr19:45081903 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+1874G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081903 | |||||||
| chr19:45081909 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9+1880T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081909 | |||||||
| chr19:45081916 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-9+1887C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081916 | |||||||
| chr19:45081991 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-9+1962C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081991 | |||||||
| chr19:45081992 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-9+1963G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081992 | |||||||
| chr19:45081994 | C | T | 2 | a0001c0001t0004g0147 a0001c0001t0004g0151 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-9+1965C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45081994 | |||||||
| chr19:45082060 | C | T | 1 | a0001c0001t0001g0034 | 2 | NA18951.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-9+2031C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082060 | |||||||
| chr19:45082334 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-9+2305C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082334 | |||||||
| chr19:45082448 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+2419T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082448 | |||||||
| chr19:45082534 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-9+2505G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082534 | |||||||
| chr19:45082574 | G | GGCACTCA others(16): Show |
1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-9+2546_-9+2568dup others(23): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45082574 | ||||||
| chr19:45082596 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+2567A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082596 | |||||||
| chr19:45082649 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+2620T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082649 | |||||||
| chr19:45082786 | A | ATT | 5 | a0001c0001t0001g0038 a0001c0001t0001g0106 a0001c0001t0001g0130 others(2): Show |
6 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2771_-9+2772dup others(2): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45082786 | ||||||
| chr19:45082786 | A | ATTT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(79): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-9+2770_-9+2772dup others(3): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45082786 | ||||||
| chr19:45082828 | T | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+2799T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082828 | |||||||
| chr19:45082850 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0045 others(8): Show |
27 | HG00738.hp2 HG01074.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9+2821C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45082850 | |||||||
| chr19:45083001 | A | G | 2 | a0001c0001t0006g0078 a0001c0001t0006g0111 |
2 | NA18955.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-9+2972A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083001 | |||||||
| chr19:45083031 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+3002T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083031 | |||||||
| chr19:45083119 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+3090C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083119 | |||||||
| chr19:45083214 | A | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-9+3185A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083214 | |||||||
| chr19:45083240 | G | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(9): Show |
29 | HG01109.hp2 HG01346.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.-9+3211G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083240 | |||||||
| chr19:45083283 | A | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+3254A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083283 | |||||||
| chr19:45083315 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9+3286C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083315 | |||||||
| chr19:45083355 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9+3326G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083355 | |||||||
| chr19:45083444 | C | A | 1 | a0001c0001t0003g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+3415C>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083444 | |||||||
| chr19:45083473 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+3444T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083473 | |||||||
| chr19:45083519 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9+3490T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083519 | |||||||
| chr19:45083597 | TTC | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0117 a0001c0001t0002g0063 others(3): Show |
7 | HG01257.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3570_-9+3571del others(2): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45083597 | ||||||
| chr19:45083598 | TC | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-9+3570delC | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083598 | |||||||
| chr19:45083599 | C | CT | 2 | a0001c0001t0001g0001 a0001c0001t0001g0007 |
6 | HG01952.hp2 HG02738.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3587dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45083599 | ||||||
| chr19:45083599 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0020 others(14): Show |
25 | HG00735.hp1 HG01074.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+3570C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083599 | |||||||
| chr19:45083599 | CT | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0081 others(10): Show |
20 | HG01169.hp1 HG01433.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3587delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45083599 | ||||||
| chr19:45083616 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-9+3587T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083616 | |||||||
| chr19:45083747 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+3718C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083747 | |||||||
| chr19:45083782 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-9+3753G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083782 | |||||||
| chr19:45083788 | G | C | 4 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0121 others(1): Show |
9 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+3759G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083788 | |||||||
| chr19:45083789 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9+3760A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083789 | |||||||
| chr19:45083883 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA18944.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.-9+3854G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083883 | |||||||
| chr19:45083938 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-9+3909C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083938 | |||||||
| chr19:45083958 | A | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+3929A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083958 | |||||||
| chr19:45083977 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+3948A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45083977 | |||||||
| chr19:45084009 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-9+3980A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084009 | |||||||
| chr19:45084072 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0155 |
7 | HG02109.hp2 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+4043G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084072 | |||||||
| chr19:45084084 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4055A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084084 | |||||||
| chr19:45084099 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-9+4070T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084099 | |||||||
| chr19:45084119 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-9+4090G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084119 | |||||||
| chr19:45084147 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4118G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084147 | |||||||
| chr19:45084148 | T | C | 4 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0121 others(1): Show |
9 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+4119T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084148 | |||||||
| chr19:45084149 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4120T>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084149 | |||||||
| chr19:45084213 | C | CA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-9+4204dupA | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45084213 | ||||||
| chr19:45084213 | C | CAA | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(11): Show |
15 | HG00733.hp2 HG00741.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+4203_-9+4204dup others(2): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45084213 | ||||||
| chr19:45084259 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9+4230T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084259 | |||||||
| chr19:45084377 | AAAATT | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4351_-9+4355del others(5): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45084377 | ||||||
| chr19:45084389 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4360T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084389 | |||||||
| chr19:45084395 | A | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4366A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084395 | |||||||
| chr19:45084402 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4373T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084402 | |||||||
| chr19:45084496 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0052 others(2): Show |
7 | HG01261.hp2 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+4467G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084496 | |||||||
| chr19:45084547 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4518T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084547 | |||||||
| chr19:45084582 | T | C | 3 | a0001c0001t0003g0041 a0001c0001t0003g0126 a0001c0001t0003g0141 |
4 | HG00733.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+4553T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084582 | |||||||
| chr19:45084647 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-9+4618A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084647 | |||||||
| chr19:45084670 | C | T | 1 | a0001c0001t0005g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-9+4641C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084670 | |||||||
| chr19:45084787 | C | T | 2 | a0001c0001t0005g0025 a0001c0001t0005g0121 |
4 | HG01070.hp1 HG01071.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+4758C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084787 | |||||||
| chr19:45084789 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+4760C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084789 | |||||||
| chr19:45084833 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-9+4804A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084833 | |||||||
| chr19:45084863 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4834C>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084863 | |||||||
| chr19:45084864 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4835T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084864 | |||||||
| chr19:45084869 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-9+4840C>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084869 | |||||||
| chr19:45084881 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4852A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084881 | |||||||
| chr19:45084908 | A | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4879A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084908 | |||||||
| chr19:45084960 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9+4931G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45084960 | |||||||
| chr19:45085140 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-4967A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085140 | |||||||
| chr19:45085204 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(94): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-8-4903G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085204 | |||||||
| chr19:45085313 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0096 others(29): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-4794C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085313 | |||||||
| chr19:45085319 | G | A | 2 | a0001c0001t0004g0147 a0001c0001t0004g0151 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-8-4788G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085319 | |||||||
| chr19:45085347 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-4760T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085347 | |||||||
| chr19:45085484 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-8-4623C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085484 | |||||||
| chr19:45085511 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-8-4596T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085511 | |||||||
| chr19:45085624 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG00544.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-8-4483G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085624 | |||||||
| chr19:45085715 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-4392A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085715 | |||||||
| chr19:45085718 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8-4389G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085718 | |||||||
| chr19:45085750 | C | T | 1 | a0001c0001t0001g0045 | 2 | NA19060.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-4357C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085750 | |||||||
| chr19:45085755 | T | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-4352T>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085755 | |||||||
| chr19:45085820 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-4287G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085820 | |||||||
| chr19:45085821 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(77): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-8-4286T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085821 | |||||||
| chr19:45085863 | C | CTTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(10): Show |
16 | HG02280.hp1 HG02559.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-4224_-8-4222dup others(3): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45085863 | ||||||
| chr19:45085863 | C | CTTTT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(64): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-8-4225_-8-4222dup others(4): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45085863 | ||||||
| chr19:45085863 | C | CTTTTT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0046 others(17): Show |
21 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-4226_-8-4222dup others(5): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45085863 | ||||||
| chr19:45085863 | CT | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0065 others(1): Show |
6 | HG01433.hp1 HG02273.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-4222delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45085863 | ||||||
| chr19:45085863 | CTTTTTTT | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(22): Show |
82 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8-4228_-8-4222del others(7): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45085863 | ||||||
| chr19:45085993 | G | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00609.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-8-4114G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45085993 | |||||||
| chr19:45086001 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
15 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8-4106G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086001 | |||||||
| chr19:45086157 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-3950A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086157 | |||||||
| chr19:45086158 | C | T | 3 | a0001c0001t0003g0041 a0001c0001t0003g0126 a0001c0001t0003g0141 |
4 | HG00733.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3949C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086158 | |||||||
| chr19:45086177 | C | G | 3 | a0001c0001t0004g0019 a0001c0001t0004g0127 a0001c0001t0004g0156 |
6 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3930C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086177 | |||||||
| chr19:45086281 | A | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(20): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-8-3826A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086281 | |||||||
| chr19:45086281 | A | G | 2 | a0001c0001t0004g0147 a0001c0001t0004g0151 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-8-3826A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086281 | |||||||
| chr19:45086337 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-3770C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086337 | |||||||
| chr19:45086407 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-8-3700G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086407 | |||||||
| chr19:45086589 | C | T | 3 | a0001c0001t0003g0041 a0001c0001t0003g0126 a0001c0001t0003g0141 |
4 | HG00733.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3518C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086589 | |||||||
| chr19:45086603 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-8-3504G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086603 | |||||||
| chr19:45086762 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8-3345C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086762 | |||||||
| chr19:45086790 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8-3317A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086790 | |||||||
| chr19:45086845 | T | TTTTG | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(54): Show |
116 | HG00438.hp2 HG00733.hp2 HG01069.hp1 others(113): Show |
intron_variant | MODIFIER | c.-8-3250_-8-3247dup others(4): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45086845 | ||||||
| chr19:45086926 | A | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(77): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-8-3181A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086926 | |||||||
| chr19:45086944 | G | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(77): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-8-3163G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086944 | |||||||
| chr19:45086979 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-3128T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45086979 | |||||||
| chr19:45087151 | T | A | 1 | a0001c0001t0001g0022 | 3 | HG00642.hp1 HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-8-2956T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087151 | |||||||
| chr19:45087166 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-8-2941T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087166 | |||||||
| chr19:45087292 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0080 |
4 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2815G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087292 | |||||||
| chr19:45087299 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-2808C>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087299 | |||||||
| chr19:45087300 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-2807A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087300 | |||||||
| chr19:45087332 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-8-2775C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087332 | |||||||
| chr19:45087347 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0136 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-8-2760T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087347 | |||||||
| chr19:45087352 | C | T | 1 | a0001c0001t0003g0044 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-8-2755C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087352 | |||||||
| chr19:45087478 | G | GT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2626dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087478 | ||||||
| chr19:45087537 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-8-2570G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087537 | |||||||
| chr19:45087672 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-8-2435C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087672 | |||||||
| chr19:45087686 | G | A | 1 | a0001c0001t0001g0015 | 4 | HG02280.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2421G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087686 | |||||||
| chr19:45087690 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8-2417C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087690 | |||||||
| chr19:45087730 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2377G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087730 | |||||||
| chr19:45087778 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-2329C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087778 | |||||||
| chr19:45087826 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0002g0005 others(11): Show |
28 | HG00597.hp2 HG00621.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-2281C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087826 | |||||||
| chr19:45087941 | AATTT | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0126 a0001c0001t0003g0141 |
4 | HG00733.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-2165_-8-2162del others(4): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087941 | |||||||
| chr19:45087942 | A | AT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0080 others(5): Show |
12 | HG00639.hp2 HG01071.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-2144dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087942 | ||||||
| chr19:45087942 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-8-2165A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087942 | |||||||
| chr19:45087942 | AT | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
13 | HG01256.hp1 HG01433.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-2144delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087942 | ||||||
| chr19:45087942 | ATT | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0027 others(5): Show |
11 | HG00597.hp2 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-2145_-8-2144del others(2): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087942 | ||||||
| chr19:45087942 | ATTT | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-8-2146_-8-2144del others(3): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087942 | ||||||
| chr19:45087942 | ATTTT | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(5): Show |
13 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-2147_-8-2144del others(4): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45087942 | ||||||
| chr19:45087969 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2138A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087969 | |||||||
| chr19:45087975 | TTG | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2131_-8-2130del others(2): Show |
GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087975 | |||||||
| chr19:45087979 | T | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2128T>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087979 | |||||||
| chr19:45087988 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2119C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087988 | |||||||
| chr19:45087999 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2108A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45087999 | |||||||
| chr19:45088001 | T | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2106T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088001 | |||||||
| chr19:45088007 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2100A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088007 | |||||||
| chr19:45088015 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-8-2092G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088015 | |||||||
| chr19:45088086 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2021C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088086 | |||||||
| chr19:45088095 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-2012G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088095 | |||||||
| chr19:45088218 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0081 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8-1889T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088218 | |||||||
| chr19:45088231 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0124 others(4): Show |
16 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-1876C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088231 | |||||||
| chr19:45088235 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0136 |
2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-8-1872T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088235 | |||||||
| chr19:45088314 | G | C | 1 | a0001c0001t0002g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-8-1793G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088314 | |||||||
| chr19:45088385 | G | A | 2 | a0001c0001t0007g0103 a0001c0001t0007g0119 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8-1722G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088385 | |||||||
| chr19:45088420 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-8-1687G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088420 | |||||||
| chr19:45088482 | A | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8-1625A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088482 | |||||||
| chr19:45088513 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0096 others(29): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-8-1594G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088513 | |||||||
| chr19:45088601 | A | G | 4 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0121 others(1): Show |
9 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-1506A>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088601 | |||||||
| chr19:45088615 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0004g0147 a0001c0001t0004g0151 |
6 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-1492C>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088615 | |||||||
| chr19:45088622 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-8-1485T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088622 | |||||||
| chr19:45088670 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-8-1437C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088670 | |||||||
| chr19:45088725 | T | A | 7 | a0001c0001t0001g0123 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
12 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-1382T>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088725 | |||||||
| chr19:45088762 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-1345C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088762 | |||||||
| chr19:45088811 | G | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0001c0001t0001g0150 others(10): Show |
24 | HG00733.hp2 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8-1296G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088811 | |||||||
| chr19:45088882 | T | G | 2 | a0001c0001t0004g0017 a0001c0001t0004g0137 |
5 | HG01884.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1225T>G | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088882 | |||||||
| chr19:45088936 | C | CT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-1157dupT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45088936 | ||||||
| chr19:45088936 | CT | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0123 a0001c0001t0005g0016 others(3): Show |
11 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-1157delT | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr19 | 45088936 | ||||||
| chr19:45088980 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(14): Show |
34 | HG01109.hp2 HG01346.hp2 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.-8-1127C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45088980 | |||||||
| chr19:45089005 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-8-1102G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089005 | |||||||
| chr19:45089041 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0139 |
3 | HG02486.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-1066A>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089041 | |||||||
| chr19:45089217 | C | T | 6 | a0001c0001t0004g0019 a0001c0001t0004g0127 a0001c0001t0004g0156 others(3): Show |
14 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-890C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089217 | |||||||
| chr19:45089238 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-8-869G>A | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089238 | |||||||
| chr19:45089415 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-8-692T>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089415 | |||||||
| chr19:45089695 | A | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0036 a0001c0001t0002g0063 |
10 | HG00140.hp1 HG01070.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-412A>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089695 | |||||||
| chr19:45089953 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-8-154G>C | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45089953 | |||||||
| chr19:45090031 | G | T | 8 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0035 others(5): Show |
14 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-76G>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45090031 | |||||||
| chr19:45090082 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8-25C>T | GEMIN7 | ENSG00000142252.11 | transcript | ENST00000270257.9 | protein_coding | 2/2 | chr19 | 45090082 |