Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51108 |
| ensemblid | ENSG00000197006.15 |
| hgncid | 24586 |
| symbol | METTL9 |
| name | methyltransferase 9, His-X-His N1(pi)-histidine |
| refseq_nuc | NM_016025.5 |
| refseq_prot | NP_057109.3 |
| ensembl_nuc | ENST00000358154.8 |
| ensembl_prot | ENSP00000350874.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 21599577 |
| end | 21657471 |
| strand | + |
| ver | v1.2 |
| region | chr16:21599577-21657471 |
| region5000 | chr16:21594577-21662471 |
| regionname0 | METTL9_chr16_21599577_21657471 |
| regionname5000 | METTL9_chr16_21594577_21662471 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 954 | 337 | 68 | 66 | 155 | 10 | 36 | METTL9_chr16_21594577_21662471 | METTL9 | ATGAG others(949): Show |
chr16 | 21594577 | 21662471 | ||
| a0001c0002 | 0/0 | 954 | 21 | 0 | 0 | 19 | 0 | 2 | METTL9_chr16_21594577_21662471 | METTL9 | ATGAG others(949): Show |
chr16 | 21594577 | 21662471 | ||
| a0001c0003 | 0/0 | 954 | 4 | 0 | 0 | 4 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | ATGAG others(949): Show |
chr16 | 21594577 | 21662471 | ||
| a0001c0004 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | ATGAG others(949): Show |
chr16 | 21594577 | 21662471 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3153 | 315 | 65 | 63 | 143 | 9 | 34 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0003 | 0/0 | 3152 | 3 | 0 | 0 | 3 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3147): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0004 | 0/0 | 3153 | 2 | 0 | 0 | 2 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0005 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0006 | 0/0 | 3153 | 2 | 0 | 0 | 0 | 0 | 2 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0007 | 0/0 | 3153 | 2 | 0 | 0 | 2 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0008 | 0/1 | 3153 | 2 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0009 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0010 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0011 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0012 | 0/0 | 3153 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0013 | 0/0 | 3153 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0014 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0015 | 0/0 | 3153 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0016 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0001t0017 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0002t0002 | 0/0 | 3153 | 21 | 0 | 0 | 19 | 0 | 2 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0003t0001 | 0/0 | 3153 | 4 | 0 | 0 | 4 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| a0001c0004t0001 | 0/0 | 3153 | 2 | 2 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | CTCCC others(3148): Show |
chr16 | 21594577 | 21662471 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0008g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0011g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0016g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0001t0017g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | GBR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | FIN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0250 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0097 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01346 | hp2 | a0001 | c0001 | t0012 | g0089 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CDX | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0169 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0230 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0341 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0342 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | BEB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0326 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18977 | hp1 | a0001 | c0001 | t0011 | g0174 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18981 | hp2 | a0001 | c0001 | t0014 | g0100 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0327 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19060 | hp2 | a0001 | c0001 | t0007 | g0271 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0302 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19066 | hp1 | a0001 | c0001 | t0009 | g0069 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0328 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19084 | hp2 | a0001 | c0001 | t0017 | g0064 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20805 | hp1 | a0001 | c0001 | t0015 | g0157 | EUR | TSI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | GIH | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | USA | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | USA | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | USA | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0257 | REF | REF | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0218 | REF | REF | METTL9_chr16_21594577_21662471 | METTL9 | chr16 | 21594577 | 21662471 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21612824 | A | G | 1 | a0001c0004 | 2 | HG02723.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.345A>G | p.Thr115Thr | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/5 | 502/3153 | 345/957 | 115/318 | chr16 | 21612824 | |||
| chr16:21624973 | T | C | 1 | a0001c0003 | 4 | NA18954.hp2 NA19058.hp2 NA19070.hp1 others(1): Show |
synonymous_variant | LOW | c.609T>C | p.Tyr203Tyr | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/5 | 766/3153 | 609/957 | 203/318 | chr16 | 21624973 | |||
| chr16:21655393 | C | T | 1 | a0001c0002 | 21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
synonymous_variant | LOW | c.918C>T | p.Tyr306Tyr | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1075/3153 | 918/957 | 306/318 | chr16 | 21655393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21599629 | C | G | 1 | a0001c0001t0008 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/5 | 105 | chr16 | 21599629 | ||||||
| chr16:21599678 | C | T | 1 | a0001c0001t0017 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/5 | 56 | chr16 | 21599678 | ||||||
| chr16:21599691 | C | T | 1 | a0001c0001t0016 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/5 | 43 | chr16 | 21599691 | ||||||
| chr16:21655433 | A | G | 1 | a0001c0001t0007 | 2 | NA18988.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1 | chr16 | 21655433 | ||||||
| chr16:21655534 | G | A | 1 | a0001c0001t0009 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 102 | chr16 | 21655534 | ||||||
| chr16:21655680 | G | T | 1 | a0001c0001t0006 | 2 | HG03491.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*248G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 248 | chr16 | 21655680 | ||||||
| chr16:21655706 | AT | A | 1 | a0001c0001t0003 | 3 | NA18979.hp2 NA19012.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*280delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 280 | INFO_REALIGN_3_PRIME | chr16 | 21655706 | |||||
| chr16:21655870 | A | G | 1 | a0001c0001t0015 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 438 | chr16 | 21655870 | ||||||
| chr16:21655988 | G | T | 1 | a0001c0002t0002 | 21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*556G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 556 | chr16 | 21655988 | ||||||
| chr16:21656235 | C | T | 1 | a0001c0001t0014 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 803 | chr16 | 21656235 | ||||||
| chr16:21656536 | T | A | 1 | a0001c0001t0010 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1104T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1104 | chr16 | 21656536 | ||||||
| chr16:21656766 | C | T | 1 | a0001c0001t0013 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1334 | chr16 | 21656766 | ||||||
| chr16:21656777 | C | T | 1 | a0001c0001t0012 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1345 | chr16 | 21656777 | ||||||
| chr16:21656779 | G | C | 1 | a0001c0001t0004 | 2 | HG00621.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1347G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1347 | chr16 | 21656779 | ||||||
| chr16:21657098 | G | C | 1 | a0001c0001t0011 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1666 | chr16 | 21657098 | ||||||
| chr16:21657106 | T | G | 1 | a0001c0001t0005 | 2 | HG02615.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1674T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 5/5 | 1674 | chr16 | 21657106 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:21600178 | C | T | 33 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(30): Show |
33 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.165+280C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21600178 | |||||||
| chr16:21600440 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+542C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21600440 | |||||||
| chr16:21600472 | T | A | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+574T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21600472 | |||||||
| chr16:21600795 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+897G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21600795 | |||||||
| chr16:21600888 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.165+990C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21600888 | |||||||
| chr16:21601241 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+1343G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21601241 | |||||||
| chr16:21601685 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.165+1787A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21601685 | |||||||
| chr16:21601729 | C | CTG | 118 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.165+1863_165+1864d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601729 | C | CTGTG | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG00558.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1861_165+1864d others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601729 | C | CTGTGTG | 4 | a0001c0001t0001g0017 a0001c0001t0001g0309 a0001c0001t0001g0344 others(1): Show |
4 | HG00408.hp1 HG04199.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1859_165+1864d others(8): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601729 | CTG | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0312 others(1): Show |
4 | HG00544.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1863_165+1864d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601729 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG00140.hp2 HG01952.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.165+1855_165+1864d others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601729 | CTGTGTGT others(5): Show |
C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(81): Show |
88 | HG00642.hp1 HG00673.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+1853_165+1864d others(14): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601729 | ||||||
| chr16:21601780 | TCAG | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.165+1886_165+1888d others(5): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21601780 | ||||||
| chr16:21601850 | C | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+1952C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21601850 | |||||||
| chr16:21601947 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.165+2049G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21601947 | |||||||
| chr16:21602180 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+2282C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21602180 | |||||||
| chr16:21602665 | G | GT | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(221): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.165+2777dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21602665 | ||||||
| chr16:21602688 | C | T | 70 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.165+2790C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21602688 | |||||||
| chr16:21602778 | C | T | 10 | a0001c0001t0001g0117 a0001c0001t0001g0158 a0001c0001t0001g0159 others(7): Show |
10 | HG00733.hp1 HG01515.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2880C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21602778 | |||||||
| chr16:21603119 | T | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+3221T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603119 | |||||||
| chr16:21603142 | C | CT | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0156 others(4): Show |
7 | HG02615.hp1 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+3258dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21603142 | ||||||
| chr16:21603142 | CT | C | 15 | a0001c0001t0001g0012 a0001c0002t0002g0001 a0001c0002t0002g0003 others(12): Show |
22 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+3258delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21603142 | ||||||
| chr16:21603150 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
67 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.165+3252T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603150 | |||||||
| chr16:21603337 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.165+3439C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603337 | |||||||
| chr16:21603417 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.165+3519G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603417 | |||||||
| chr16:21603501 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.165+3603A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603501 | |||||||
| chr16:21603574 | C | G | 2 | a0001c0001t0006g0341 a0001c0001t0006g0342 |
2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.165+3676C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603574 | |||||||
| chr16:21603825 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+3927T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603825 | |||||||
| chr16:21603965 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+4067T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21603965 | |||||||
| chr16:21604168 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.165+4270G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21604168 | |||||||
| chr16:21604318 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.165+4420T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21604318 | |||||||
| chr16:21604327 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+4429T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21604327 | |||||||
| chr16:21604619 | G | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0318 |
3 | NA18985.hp2 NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.165+4721G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21604619 | |||||||
| chr16:21605257 | C | CT | 10 | a0001c0001t0001g0130 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+5398dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTT | 15 | a0001c0001t0001g0013 a0001c0001t0001g0101 a0001c0001t0001g0102 others(12): Show |
15 | HG00099.hp1 HG01258.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.165+5397_165+5398d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTT | 7 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0217 others(4): Show |
7 | HG00408.hp2 HG00438.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+5396_165+5398d others(5): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTT | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG00140.hp1 HG02071.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5395_165+5398d others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0317 a0001c0001t0001g0331 others(3): Show |
6 | HG00323.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5393_165+5398d others(8): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0167 others(5): Show |
8 | HG00558.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+5390_165+5398d others(11): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG01167.hp2 HG02698.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5389_165+5398d others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0143 a0001c0001t0001g0253 others(1): Show |
4 | HG01106.hp1 HG01167.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5388_165+5398d others(13): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0164 a0001c0001t0001g0255 others(5): Show |
8 | HG01169.hp2 HG01192.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+5387_165+5398d others(14): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(6): Show |
9 | a0001c0001t0001g0104 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | HG01109.hp1 HG01123.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+5386_165+5398d others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0314 a0001c0001t0001g0335 |
2 | NA19009.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.165+5385_165+5398d others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0260 a0001c0001t0001g0318 |
3 | HG01361.hp1 HG02559.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.165+5384_165+5398d others(17): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0148 a0001c0003t0001g0336 |
3 | HG01175.hp2 HG01934.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.165+5383_165+5398d others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0149 a0001c0001t0001g0232 a0001c0001t0001g0261 others(3): Show |
6 | HG02809.hp1 HG03130.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5382_165+5398d others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0001g0262 a0001c0001t0001g0298 a0001c0001t0001g0337 others(1): Show |
4 | HG04199.hp1 NA18986.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5381_165+5398d others(20): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0150 |
2 | HG02040.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.165+5380_165+5398d others(21): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0001g0151 a0001c0001t0001g0263 a0001c0001t0001g0339 |
3 | HG00639.hp1 HG02965.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.165+5379_165+5398d others(22): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0340 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.165+5378_165+5398d others(23): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0152 a0001c0001t0001g0264 others(1): Show |
4 | HG01081.hp1 HG03195.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5377_165+5398d others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.165+5376_165+5398d others(25): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0300 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+5375_165+5398d others(26): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0301 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.165+5373_165+5398d others(28): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0303 a0001c0001t0010g0302 |
2 | NA18944.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.165+5372_165+5398d others(29): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+5371_165+5398d others(30): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0265 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.165+5369_165+5398d others(32): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CT | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0211 others(3): Show |
6 | HG00323.hp1 HG02622.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+5398delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTT | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+5397_165+5398d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0124 others(4): Show |
7 | HG01346.hp1 HG01346.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+5392_165+5398d others(9): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(17): Show |
20 | HG00735.hp1 HG01175.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+5389_165+5398d others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(4): Show |
C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
125 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.165+5388_165+5398d others(13): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0039 others(12): Show |
15 | HG01515.hp2 HG02723.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+5387_165+5398d others(14): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0118 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5386_165+5398d others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0313 |
3 | HG02015.hp1 NA18969.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.165+5385_165+5398d others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | HG00099.hp2 HG01884.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+5384_165+5398d others(17): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | NA18960.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.165+5383_165+5398d others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0153 |
2 | HG02273.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.165+5382_165+5398d others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165+5380_165+5398d others(21): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.165+5378_165+5398d others(23): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(15): Show |
C | 3 | a0001c0001t0001g0269 a0001c0004t0001g0168 a0001c0004t0001g0169 |
3 | HG00738.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.165+5377_165+5398d others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0004g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.165+5374_165+5398d others(27): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605257 | CTTTTTTT others(19): Show |
C | 3 | a0001c0001t0001g0156 a0001c0001t0005g0154 a0001c0001t0005g0155 |
3 | HG02615.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.165+5373_165+5398d others(28): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21605257 | ||||||
| chr16:21605370 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.165+5472T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21605370 | |||||||
| chr16:21605702 | G | C | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.165+5804G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21605702 | |||||||
| chr16:21605919 | G | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+6021G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21605919 | |||||||
| chr16:21606100 | G | A | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+6202G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21606100 | |||||||
| chr16:21606251 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.165+6353C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21606251 | |||||||
| chr16:21606293 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.166-6352C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21606293 | |||||||
| chr16:21606546 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG01346.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-6099A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21606546 | |||||||
| chr16:21606864 | T | TTTGTATT others(9): Show |
14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-5769_166-5754d others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21606864 | ||||||
| chr16:21607080 | A | AT | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0205 others(3): Show |
6 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-5549dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21607080 | ||||||
| chr16:21607080 | AT | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
6 | HG00323.hp2 HG01074.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-5549delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21607080 | ||||||
| chr16:21607135 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-5510C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607135 | |||||||
| chr16:21607231 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | NA18944.hp1 NA19057.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.166-5414C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607231 | |||||||
| chr16:21607363 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166-5282C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607363 | |||||||
| chr16:21607493 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.166-5152A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607493 | |||||||
| chr16:21607568 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.166-5077T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607568 | |||||||
| chr16:21607754 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.166-4891T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607754 | |||||||
| chr16:21607775 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0171 |
3 | NA19005.hp2 NA19011.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.166-4870G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607775 | |||||||
| chr16:21607838 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-4807A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607838 | |||||||
| chr16:21607943 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-4702G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607943 | |||||||
| chr16:21607960 | C | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-4685C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21607960 | |||||||
| chr16:21608073 | C | G | 1 | a0001c0002t0002g0024 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-4572C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608073 | |||||||
| chr16:21608121 | C | G | 1 | a0001c0001t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.166-4524C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608121 | |||||||
| chr16:21608148 | C | CAAAAAAA others(6): Show |
12 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(9): Show |
19 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.166-4489_166-4488i others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21608148 | ||||||
| chr16:21608148 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0002g0019 a0001c0002t0002g0026 |
2 | NA18991.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.166-4489_166-4488i others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21608148 | ||||||
| chr16:21608224 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0028 |
2 | NA18941.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.166-4421C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608224 | |||||||
| chr16:21608278 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-4367C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608278 | |||||||
| chr16:21608357 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.166-4288T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608357 | |||||||
| chr16:21608410 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-4235C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608410 | |||||||
| chr16:21608890 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0216 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.166-3755C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608890 | |||||||
| chr16:21608949 | G | A | 14 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0126 others(11): Show |
14 | HG00733.hp1 HG01515.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-3696G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21608949 | |||||||
| chr16:21609126 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-3519A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609126 | |||||||
| chr16:21609226 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.166-3419A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609226 | |||||||
| chr16:21609305 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.166-3340A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609305 | |||||||
| chr16:21609352 | T | C | 11 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
11 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-3293T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609352 | |||||||
| chr16:21609392 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.166-3253G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609392 | |||||||
| chr16:21609406 | G | A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.166-3239G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609406 | |||||||
| chr16:21609428 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.166-3217C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609428 | |||||||
| chr16:21609460 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.166-3185G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609460 | |||||||
| chr16:21609547 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-3098A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609547 | |||||||
| chr16:21609685 | T | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-2960T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609685 | |||||||
| chr16:21609707 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-2938G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609707 | |||||||
| chr16:21609888 | G | T | 2 | a0001c0001t0005g0154 a0001c0001t0005g0155 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-2757G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609888 | |||||||
| chr16:21609908 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-2737A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21609908 | |||||||
| chr16:21609956 | G | GGT | 8 | a0001c0001t0001g0274 a0001c0001t0001g0286 a0001c0001t0001g0290 others(5): Show |
8 | HG00609.hp1 HG00621.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-2676_166-2675d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21609956 | ||||||
| chr16:21610171 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0078 |
2 | NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.166-2474C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610171 | |||||||
| chr16:21610291 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-2354G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610291 | |||||||
| chr16:21610292 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-2353T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610292 | |||||||
| chr16:21610293 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-2352C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610293 | |||||||
| chr16:21610508 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.166-2137A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610508 | |||||||
| chr16:21610531 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.166-2114T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610531 | |||||||
| chr16:21610585 | C | T | 3 | a0001c0001t0003g0296 a0001c0001t0003g0297 a0001c0001t0003g0299 |
3 | NA18979.hp2 NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.166-2060C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610585 | |||||||
| chr16:21610635 | T | C | 1 | a0001c0002t0002g0024 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-2010T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610635 | |||||||
| chr16:21610646 | T | G | 2 | a0001c0001t0006g0341 a0001c0001t0006g0342 |
2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.166-1999T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610646 | |||||||
| chr16:21610726 | ATTG | A | 3 | a0001c0001t0001g0156 a0001c0001t0005g0154 a0001c0001t0005g0155 |
3 | HG02615.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.166-1913_166-1911d others(5): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21610726 | ||||||
| chr16:21610759 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.166-1886A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610759 | |||||||
| chr16:21610896 | G | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.166-1749G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610896 | |||||||
| chr16:21610925 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0269 others(11): Show |
16 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.166-1720C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21610925 | |||||||
| chr16:21611048 | G | GA | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-1591dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21611048 | ||||||
| chr16:21611103 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.166-1542A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611103 | |||||||
| chr16:21611233 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.166-1412A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611233 | |||||||
| chr16:21611238 | T | A | 1 | a0001c0002t0002g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.166-1407T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611238 | |||||||
| chr16:21611255 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-1390C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611255 | |||||||
| chr16:21611298 | C | T | 1 | a0001c0001t0014g0100 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.166-1347C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611298 | |||||||
| chr16:21611578 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-1067C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611578 | |||||||
| chr16:21611687 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.166-958A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611687 | |||||||
| chr16:21611708 | A | G | 2 | a0001c0001t0001g0303 a0001c0001t0010g0302 |
2 | NA18944.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.166-937A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611708 | |||||||
| chr16:21611726 | AT | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-916delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21611726 | ||||||
| chr16:21611916 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-729A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611916 | |||||||
| chr16:21611954 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-691T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21611954 | |||||||
| chr16:21612391 | C | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-254C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21612391 | |||||||
| chr16:21612474 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0145 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.166-171T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | chr16 | 21612474 | |||||||
| chr16:21612623 | C | CT | 28 | a0001c0001t0001g0077 a0001c0001t0001g0126 a0001c0001t0001g0139 others(25): Show |
35 | HG00544.hp1 HG00609.hp2 HG00738.hp1 others(32): Show |
splice_acceptor_variant&intron_variant | HIGH | c.166-3dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21612623 | ||||||
| chr16:21612623 | CT | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0092 others(5): Show |
8 | HG01070.hp2 HG01074.hp1 HG03927.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.166-3delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 21612623 | ||||||
| chr16:21612918 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG02135.hp1 NA18747.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.356+83C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21612918 | |||||||
| chr16:21613054 | C | T | 1 | a0001c0002t0002g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.356+219C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613054 | |||||||
| chr16:21613068 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.356+233G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613068 | |||||||
| chr16:21613108 | G | T | 1 | a0001c0003t0001g0327 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.356+273G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613108 | |||||||
| chr16:21613168 | C | CT | 24 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0047 others(21): Show |
25 | HG00408.hp2 HG00733.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.356+369dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTT | 20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(17): Show |
21 | HG00621.hp2 HG00642.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.356+368_356+369dup others(2): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTT | 9 | a0001c0001t0001g0138 a0001c0001t0001g0215 a0001c0001t0001g0274 others(6): Show |
9 | HG00609.hp1 HG02027.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.356+367_356+369dup others(3): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTT | 6 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0001g0210 others(3): Show |
6 | HG02080.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+366_356+369dup others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0207 others(2): Show |
7 | HG00438.hp1 HG01070.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.356+361_356+369dup others(9): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.356+360_356+369dup others(10): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.356+359_356+369dup others(11): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0186 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.356+358_356+369dup others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.356+357_356+369dup others(13): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0170 |
3 | HG02735.hp2 NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.356+356_356+369dup others(14): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(8): Show |
12 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0150 others(9): Show |
13 | HG01891.hp2 HG02630.hp2 HG03540.hp2 others(10): Show |
intron_variant | MODIFIER | c.356+355_356+369dup others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0171 a0001c0001t0001g0195 a0001c0001t0001g0205 others(2): Show |
5 | HG00544.hp2 HG02083.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+354_356+369dup others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0196 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.356+353_356+369dup others(17): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0223 |
2 | HG03130.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.356+352_356+369dup others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0224 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.356+351_356+369dup others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0198 a0001c0001t0001g0266 |
3 | HG02896.hp2 NA18970.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.356+350_356+369dup others(20): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0199 |
3 | HG01934.hp2 HG03195.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.356+349_356+369dup others(21): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.356+348_356+369dup others(22): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0202 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.356+346_356+369dup others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0016g0230 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.356+344_356+369dup others(26): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.356+341_356+369dup others(29): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0001g0203 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.356+369_356+370ins others(42): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG02559.hp2 HG02647.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+362_356+369del others(8): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.356+358_356+369del others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0249 others(2): Show |
5 | HG02615.hp1 HG03834.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+355_356+369del others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(9): Show |
C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(173): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.356+354_356+369del others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(10): Show |
C | 23 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0079 others(20): Show |
30 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.356+353_356+369del others(17): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.356+352_356+369del others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613168 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.356+351_356+369del others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613168 | ||||||
| chr16:21613202 | T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0182 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.356+369_356+370ins others(10): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613202 | ||||||
| chr16:21613270 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.356+435G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613270 | |||||||
| chr16:21613276 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0144 others(5): Show |
8 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+441C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613276 | |||||||
| chr16:21613356 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.356+521G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613356 | |||||||
| chr16:21613376 | G | T | 8 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
8 | HG01167.hp2 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.356+541G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613376 | |||||||
| chr16:21613422 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.356+587A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613422 | |||||||
| chr16:21613612 | G | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.356+777G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613612 | |||||||
| chr16:21613699 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0253 a0001c0001t0001g0255 others(1): Show |
4 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.356+864G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613699 | |||||||
| chr16:21613743 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.356+908C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21613743 | |||||||
| chr16:21613833 | GT | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.356+1012delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21613833 | ||||||
| chr16:21614028 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.356+1193G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21614028 | |||||||
| chr16:21614185 | C | T | 6 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0329 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+1350C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21614185 | |||||||
| chr16:21615265 | G | C | 3 | a0001c0001t0001g0217 a0001c0004t0001g0168 a0001c0004t0001g0169 |
3 | HG02280.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.356+2430G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21615265 | |||||||
| chr16:21615508 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.357-2357C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21615508 | |||||||
| chr16:21615528 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.357-2337C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21615528 | |||||||
| chr16:21615691 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.357-2174T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21615691 | |||||||
| chr16:21615936 | G | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.357-1929G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21615936 | |||||||
| chr16:21616213 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.357-1652C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21616213 | |||||||
| chr16:21616264 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.357-1601C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21616264 | |||||||
| chr16:21616338 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.357-1527G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21616338 | |||||||
| chr16:21616361 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.357-1504T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21616361 | |||||||
| chr16:21616502 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.357-1363G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21616502 | |||||||
| chr16:21616946 | T | TCACATTC others(1215): Show |
1 | a0001c0001t0001g0034 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.357-905_357-904ins others(1222): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21616946 | ||||||
| chr16:21617014 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0213 |
3 | HG02630.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.357-851C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617014 | |||||||
| chr16:21617282 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0211 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.357-583G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617282 | |||||||
| chr16:21617287 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0130 others(3): Show |
6 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.357-578G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617287 | |||||||
| chr16:21617401 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.357-464G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617401 | |||||||
| chr16:21617420 | CA | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.357-434delA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21617420 | ||||||
| chr16:21617432 | G | GA | 211 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0031 others(208): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.357-423dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 21617432 | ||||||
| chr16:21617432 | G | GGA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | NA18985.hp2 NA19009.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.357-433_357-432ins others(2): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617432 | |||||||
| chr16:21617437 | A | AC | 8 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.357-428_357-427ins others(1): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 2/4 | chr16 | 21617437 | |||||||
| chr16:21618128 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566+54G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21618128 | |||||||
| chr16:21618275 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.566+201C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21618275 | |||||||
| chr16:21618649 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566+575G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21618649 | |||||||
| chr16:21618876 | G | T | 3 | a0001c0001t0001g0156 a0001c0001t0005g0154 a0001c0001t0005g0155 |
3 | HG02615.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.566+802G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21618876 | |||||||
| chr16:21618985 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566+911A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21618985 | |||||||
| chr16:21619006 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0259 |
2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.566+932T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619006 | |||||||
| chr16:21619036 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.566+962G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619036 | |||||||
| chr16:21619083 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+1009G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619083 | |||||||
| chr16:21619347 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.566+1273G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619347 | |||||||
| chr16:21619377 | T | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(186): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.566+1303T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619377 | |||||||
| chr16:21619427 | CT | C | 338 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(335): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.566+1365delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21619427 | ||||||
| chr16:21619587 | A | AT | 61 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.566+1535dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21619587 | ||||||
| chr16:21619587 | A | ATT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0040 others(52): Show |
59 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.566+1534_566+1535d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21619587 | ||||||
| chr16:21619765 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+1691T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619765 | |||||||
| chr16:21619912 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566+1838C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619912 | |||||||
| chr16:21619992 | T | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
55 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.566+1918T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21619992 | |||||||
| chr16:21620280 | G | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.566+2206G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21620280 | |||||||
| chr16:21620299 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.566+2225T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21620299 | |||||||
| chr16:21620844 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.566+2770T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21620844 | |||||||
| chr16:21620953 | A | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.566+2879A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21620953 | |||||||
| chr16:21621020 | G | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.566+2946G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621020 | |||||||
| chr16:21621149 | A | AGAGT | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.566+3076_566+3077i others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21621149 | ||||||
| chr16:21621149 | A | AGT | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0251 others(3): Show |
6 | HG00741.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+3100_566+3101d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21621149 | ||||||
| chr16:21621151 | T | A | 4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+3077T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621151 | |||||||
| chr16:21621174 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.566+3100G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621174 | |||||||
| chr16:21621176 | T | G | 17 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 others(14): Show |
24 | HG00544.hp1 HG00609.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.566+3102T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621176 | |||||||
| chr16:21621205 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566+3131G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621205 | |||||||
| chr16:21621328 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.566+3254T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621328 | |||||||
| chr16:21621566 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.567-3365A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621566 | |||||||
| chr16:21621857 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0144 others(5): Show |
8 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.567-3074C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621857 | |||||||
| chr16:21621889 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0312 |
2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.567-3042C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21621889 | |||||||
| chr16:21622068 | C | T | 1 | a0001c0001t0012g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.567-2863C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21622068 | |||||||
| chr16:21622141 | C | CT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0120 others(6): Show |
9 | HG00621.hp2 HG00642.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.567-2769dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTT | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
50 | HG00621.hp1 HG00673.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.567-2774_567-2769d others(8): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT | 12 | a0001c0001t0001g0143 a0001c0001t0001g0180 a0001c0001t0001g0183 others(9): Show |
12 | HG00438.hp1 HG00544.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.567-2775_567-2769d others(9): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.567-2778_567-2769d others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0015g0157 |
3 | HG01515.hp2 HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.567-2779_567-2769d others(13): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0161 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-2781_567-2769d others(15): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.567-2782_567-2769d others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0156 a0001c0001t0005g0154 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.567-2783_567-2769d others(17): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(9): Show |
22 | a0001c0001t0001g0082 a0001c0001t0001g0128 a0001c0001t0001g0130 others(19): Show |
22 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.567-2784_567-2769d others(18): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(10): Show |
44 | a0001c0001t0001g0030 a0001c0001t0001g0121 a0001c0001t0001g0122 others(41): Show |
44 | HG00558.hp1 HG01099.hp2 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.567-2785_567-2769d others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(11): Show |
29 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0104 others(26): Show |
29 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.567-2786_567-2769d others(20): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(12): Show |
14 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0073 others(11): Show |
14 | HG00741.hp2 HG01109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.567-2787_567-2769d others(21): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(13): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(21): Show |
25 | HG00673.hp1 HG00735.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.567-2788_567-2769d others(22): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(14): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0042 others(21): Show |
27 | HG00140.hp2 HG00741.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.567-2789_567-2769d others(23): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(15): Show |
9 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0063 others(6): Show |
9 | HG01175.hp1 HG01981.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.567-2769_567-2768i others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02602.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(25): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0329 a0001c0001t0001g0343 |
3 | HG00438.hp2 HG00558.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(26): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0099 a0001c0001t0001g0312 a0001c0001t0001g0335 |
3 | HG06807.hp2 NA18951.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(27): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0066 others(1): Show |
4 | HG02015.hp1 HG03453.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-2769_567-2768i others(28): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0114 |
2 | HG01952.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(29): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(21): Show |
4 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG03704.hp1 HG03704.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-2769_567-2768i others(30): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(31): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0126 |
2 | NA18522.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(32): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(35): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(27): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0319 |
2 | HG02155.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(36): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0068 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.567-2769_567-2768i others(38): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0001g0344 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(39): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(31): Show |
1 | a0001c0001t0009g0069 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(40): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(32): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0070 |
2 | NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(41): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(34): Show |
1 | a0001c0001t0001g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.567-2769_567-2768i others(43): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(38): Show |
1 | a0001c0001t0001g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(47): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(40): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0160 |
2 | NA18939.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.567-2769_567-2768i others(49): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | C | CTTTTTTT others(41): Show |
1 | a0001c0001t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.567-2769_567-2768i others(50): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622141 | CT | C | 15 | a0001c0001t0001g0044 a0001c0002t0002g0001 a0001c0002t0002g0003 others(12): Show |
22 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.567-2769delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21622141 | ||||||
| chr16:21622367 | C | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.567-2564C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21622367 | |||||||
| chr16:21622560 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.567-2371A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21622560 | |||||||
| chr16:21622807 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.567-2124T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21622807 | |||||||
| chr16:21623040 | A | T | 2 | a0001c0001t0001g0105 a0001c0001t0013g0097 |
2 | HG01175.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.567-1891A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623040 | |||||||
| chr16:21623317 | T | C | 6 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0329 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-1614T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623317 | |||||||
| chr16:21623606 | C | G | 1 | a0001c0002t0002g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.567-1325C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623606 | |||||||
| chr16:21623665 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.567-1266G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623665 | |||||||
| chr16:21623693 | C | A | 1 | a0001c0001t0001g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.567-1238C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623693 | |||||||
| chr16:21623795 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.567-1136G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623795 | |||||||
| chr16:21623919 | C | T | 3 | a0001c0001t0001g0217 a0001c0004t0001g0168 a0001c0004t0001g0169 |
3 | HG02280.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.567-1012C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21623919 | |||||||
| chr16:21624004 | C | T | 8 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
8 | HG01167.hp2 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.567-927C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624004 | |||||||
| chr16:21624058 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.567-873C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624058 | |||||||
| chr16:21624064 | C | T | 7 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0213 others(4): Show |
7 | HG02630.hp1 HG02647.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.567-867C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624064 | |||||||
| chr16:21624242 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.567-689G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624242 | |||||||
| chr16:21624688 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.567-243C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624688 | |||||||
| chr16:21624739 | A | AT | 3 | a0001c0001t0001g0040 a0001c0001t0001g0318 a0001c0001t0001g0337 |
3 | NA18985.hp2 NA18997.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.567-190dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21624739 | ||||||
| chr16:21624741 | TA | T | 20 | a0001c0001t0001g0051 a0001c0001t0001g0087 a0001c0001t0001g0179 others(17): Show |
27 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.567-175delA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 21624741 | ||||||
| chr16:21624742 | A | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(207): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.567-189A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624742 | |||||||
| chr16:21624743 | A | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0087 others(4): Show |
7 | HG00323.hp2 HG02040.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.567-188A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 3/4 | chr16 | 21624743 | |||||||
| chr16:21625179 | G | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
55 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.751+64G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21625179 | |||||||
| chr16:21625440 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.751+325C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21625440 | |||||||
| chr16:21625509 | G | A | 9 | a0001c0001t0001g0119 a0001c0001t0001g0130 a0001c0001t0001g0134 others(6): Show |
9 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+394G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21625509 | |||||||
| chr16:21625563 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.751+448T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21625563 | |||||||
| chr16:21625584 | GTGT | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+475_751+477del others(3): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21625584 | ||||||
| chr16:21625988 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.751+873C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21625988 | |||||||
| chr16:21626007 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
65 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.751+892C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626007 | |||||||
| chr16:21626185 | C | G | 30 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(27): Show |
30 | HG01167.hp2 HG01243.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.751+1070C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626185 | |||||||
| chr16:21626269 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.751+1154T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626269 | |||||||
| chr16:21626669 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.751+1554C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626669 | |||||||
| chr16:21626722 | G | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.751+1607G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626722 | |||||||
| chr16:21626803 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.751+1688G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626803 | |||||||
| chr16:21626921 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.751+1806G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21626921 | |||||||
| chr16:21627067 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.751+1952G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627067 | |||||||
| chr16:21627147 | T | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+2032T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627147 | |||||||
| chr16:21627226 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.751+2111G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627226 | |||||||
| chr16:21627369 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.751+2254T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627369 | |||||||
| chr16:21627376 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+2261C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627376 | |||||||
| chr16:21627741 | G | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+2626G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627741 | |||||||
| chr16:21627786 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+2671A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627786 | |||||||
| chr16:21627825 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.751+2710C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627825 | |||||||
| chr16:21627866 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.751+2751C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627866 | |||||||
| chr16:21627948 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+2833A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21627948 | |||||||
| chr16:21628001 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(184): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.751+2886A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628001 | |||||||
| chr16:21628030 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.751+2915A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628030 | |||||||
| chr16:21628389 | A | C | 70 | a0001c0001t0001g0082 a0001c0001t0001g0165 a0001c0001t0001g0166 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.751+3274A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628389 | |||||||
| chr16:21628456 | AAC | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+3344_751+3345d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21628456 | ||||||
| chr16:21628601 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | NA18944.hp1 NA19057.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.751+3486C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628601 | |||||||
| chr16:21628695 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.751+3580G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628695 | |||||||
| chr16:21628748 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0259 |
2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.751+3633C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628748 | |||||||
| chr16:21628774 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(235): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.751+3659A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628774 | |||||||
| chr16:21628892 | CT | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(98): Show |
112 | HG00140.hp2 HG00544.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.751+3791delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21628892 | ||||||
| chr16:21628956 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+3841C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628956 | |||||||
| chr16:21628959 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.751+3844G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21628959 | |||||||
| chr16:21629039 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.751+3924G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629039 | |||||||
| chr16:21629246 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0283 a0001c0001t0001g0292 |
3 | HG01074.hp1 HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.751+4131C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629246 | |||||||
| chr16:21629255 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0283 a0001c0001t0001g0292 |
3 | HG01074.hp1 HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.751+4140T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629255 | |||||||
| chr16:21629310 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+4195C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629310 | |||||||
| chr16:21629372 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+4257A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629372 | |||||||
| chr16:21629549 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0072 |
2 | NA19003.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.751+4434G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629549 | |||||||
| chr16:21629673 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.751+4558C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629673 | |||||||
| chr16:21629710 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.751+4595G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629710 | |||||||
| chr16:21629722 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+4607T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629722 | |||||||
| chr16:21629751 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.751+4636T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21629751 | |||||||
| chr16:21629800 | TGCTGATT others(17): Show |
T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0092 others(1): Show |
4 | NA18953.hp1 NA18960.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+4722_751+4745d others(26): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21629800 | ||||||
| chr16:21630149 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+5034T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630149 | |||||||
| chr16:21630150 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+5035G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630150 | |||||||
| chr16:21630209 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0134 |
2 | HG00639.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.751+5094G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630209 | |||||||
| chr16:21630325 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+5210A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630325 | |||||||
| chr16:21630454 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.751+5339G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630454 | |||||||
| chr16:21630454 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0086 |
2 | NA18747.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.751+5339G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630454 | |||||||
| chr16:21630456 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0086 |
2 | NA18747.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.751+5341C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630456 | |||||||
| chr16:21630457 | C | T | 30 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(27): Show |
30 | HG01167.hp2 HG01243.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.751+5342C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630457 | |||||||
| chr16:21630606 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+5491G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630606 | |||||||
| chr16:21630693 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+5578G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630693 | |||||||
| chr16:21630809 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02145.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.751+5694C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630809 | |||||||
| chr16:21630875 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0099 |
2 | NA18942.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.751+5760A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630875 | |||||||
| chr16:21630906 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+5791G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21630906 | |||||||
| chr16:21631133 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
70 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.751+6018T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631133 | |||||||
| chr16:21631210 | A | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+6095A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631210 | |||||||
| chr16:21631386 | T | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0213 |
3 | HG02630.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.751+6271T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631386 | |||||||
| chr16:21631401 | G | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+6286G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631401 | |||||||
| chr16:21631612 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.751+6497C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631612 | |||||||
| chr16:21631648 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+6533T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631648 | |||||||
| chr16:21631697 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0213 |
2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.751+6582C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631697 | |||||||
| chr16:21631754 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.751+6639G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631754 | |||||||
| chr16:21631914 | T | G | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.751+6799T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21631914 | |||||||
| chr16:21632156 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0030 others(188): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.751+7041A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632156 | |||||||
| chr16:21632374 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.751+7259C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632374 | |||||||
| chr16:21632462 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.751+7347A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632462 | |||||||
| chr16:21632514 | A | G | 11 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
11 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.751+7399A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632514 | |||||||
| chr16:21632599 | G | A | 1 | a0001c0002t0002g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.751+7484G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632599 | |||||||
| chr16:21632664 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.751+7549C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632664 | |||||||
| chr16:21632810 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0233 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.751+7695A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632810 | |||||||
| chr16:21632898 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+7783T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21632898 | |||||||
| chr16:21633100 | G | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.751+7985G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633100 | |||||||
| chr16:21633117 | G | A | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.751+8002G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633117 | |||||||
| chr16:21633391 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+8276T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633391 | |||||||
| chr16:21633481 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0077 |
2 | NA19054.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.751+8366G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633481 | |||||||
| chr16:21633491 | AT | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+8377delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633491 | |||||||
| chr16:21633502 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+8387G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633502 | |||||||
| chr16:21633638 | C | CA | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+8525dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21633638 | ||||||
| chr16:21633863 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.751+8748T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633863 | |||||||
| chr16:21633896 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | HG01071.hp1 HG01192.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+8781G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633896 | |||||||
| chr16:21633935 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.751+8820C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633935 | |||||||
| chr16:21633971 | A | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0144 others(5): Show |
8 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.751+8856A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21633971 | |||||||
| chr16:21634061 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0153 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.751+8946A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634061 | |||||||
| chr16:21634063 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.751+8948A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634063 | |||||||
| chr16:21634096 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.751+8981C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634096 | |||||||
| chr16:21634113 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0213 |
3 | HG02630.hp1 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.751+8998G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634113 | |||||||
| chr16:21634259 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.751+9144G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634259 | |||||||
| chr16:21634724 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.751+9609C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634724 | |||||||
| chr16:21634972 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+9857C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21634972 | |||||||
| chr16:21635008 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.751+9893C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635008 | |||||||
| chr16:21635199 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.751+10084C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635199 | |||||||
| chr16:21635474 | TGTGTATT others(3): Show |
T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+10370_751+1037 others(14): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21635474 | ||||||
| chr16:21635574 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.751+10459A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635574 | |||||||
| chr16:21635599 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.751+10484C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635599 | |||||||
| chr16:21635602 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.751+10487G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635602 | |||||||
| chr16:21635616 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.751+10501C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635616 | |||||||
| chr16:21635671 | T | G | 1 | a0001c0001t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.751+10556T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635671 | |||||||
| chr16:21635686 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.751+10571G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635686 | |||||||
| chr16:21635828 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+10713G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635828 | |||||||
| chr16:21635852 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.751+10737C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635852 | |||||||
| chr16:21635853 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.751+10738G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635853 | |||||||
| chr16:21635914 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.751+10799A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635914 | |||||||
| chr16:21635948 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.751+10833C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635948 | |||||||
| chr16:21635975 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.751+10860G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21635975 | |||||||
| chr16:21636022 | T | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.751+10907T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636022 | |||||||
| chr16:21636393 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0015g0157 |
2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.751+11278C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636393 | |||||||
| chr16:21636448 | T | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
171 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.751+11333T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636448 | |||||||
| chr16:21636574 | C | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG03098.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.751+11459C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636574 | |||||||
| chr16:21636642 | C | T | 11 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0141 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.751+11527C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636642 | |||||||
| chr16:21636721 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0071 |
2 | HG01243.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.751+11606C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636721 | |||||||
| chr16:21636859 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+11744G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636859 | |||||||
| chr16:21636892 | G | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+11777G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21636892 | |||||||
| chr16:21637132 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+12017T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637132 | |||||||
| chr16:21637243 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.751+12128C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637243 | |||||||
| chr16:21637244 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.751+12129G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637244 | |||||||
| chr16:21637260 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.751+12145C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637260 | |||||||
| chr16:21637310 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.751+12195G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637310 | |||||||
| chr16:21637337 | C | CAG | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+12223_751+1222 others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21637337 | ||||||
| chr16:21637340 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.751+12225G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637340 | |||||||
| chr16:21637536 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+12421C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637536 | |||||||
| chr16:21637551 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.751+12436A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637551 | |||||||
| chr16:21637654 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.751+12539C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637654 | |||||||
| chr16:21637677 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+12562G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637677 | |||||||
| chr16:21637687 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.751+12572G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637687 | |||||||
| chr16:21637710 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.751+12595G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637710 | |||||||
| chr16:21637777 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.751+12662C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637777 | |||||||
| chr16:21637778 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+12663G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637778 | |||||||
| chr16:21637955 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0211 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+12840G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21637955 | |||||||
| chr16:21638132 | A | G | 7 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
7 | HG00738.hp1 HG01081.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.751+13017A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638132 | |||||||
| chr16:21638135 | G | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+13020G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638135 | |||||||
| chr16:21638191 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.751+13076G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638191 | |||||||
| chr16:21638297 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+13182G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638297 | |||||||
| chr16:21638324 | G | GA | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+13212dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21638324 | ||||||
| chr16:21638328 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+13213G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638328 | |||||||
| chr16:21638540 | G | A | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.751+13425G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638540 | |||||||
| chr16:21638683 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.751+13568G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638683 | |||||||
| chr16:21638724 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.751+13609A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638724 | |||||||
| chr16:21638916 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.751+13801T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21638916 | |||||||
| chr16:21639244 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.751+14129A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639244 | |||||||
| chr16:21639270 | TGC | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0213 others(2): Show |
5 | HG02630.hp1 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.751+14156_751+1415 others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639270 | |||||||
| chr16:21639312 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.751+14197A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639312 | |||||||
| chr16:21639440 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.751+14325G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639440 | |||||||
| chr16:21639474 | G | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0129 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+14359G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639474 | |||||||
| chr16:21639488 | T | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.751+14373T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639488 | |||||||
| chr16:21639544 | A | T | 1 | a0001c0001t0004g0295 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.751+14429A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639544 | |||||||
| chr16:21639666 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.751+14551G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639666 | |||||||
| chr16:21639712 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.751+14597C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639712 | |||||||
| chr16:21639794 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.751+14679A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639794 | |||||||
| chr16:21639925 | T | TTTTA | 3 | a0001c0001t0001g0231 a0001c0001t0001g0335 a0001c0001t0014g0100 |
3 | HG03453.hp2 NA18981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.751+14838_751+1484 others(8): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21639925 | ||||||
| chr16:21639925 | T | TTTTATTT others(1): Show |
53 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
59 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.751+14834_751+1484 others(12): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21639925 | ||||||
| chr16:21639925 | T | TTTTATTT others(5): Show |
6 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0002t0002g0021 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+14830_751+1484 others(16): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21639925 | ||||||
| chr16:21639925 | T | TTTTATTT others(9): Show |
8 | a0001c0002t0002g0001 a0001c0002t0002g0018 a0001c0002t0002g0019 others(5): Show |
13 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.751+14826_751+1484 others(20): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21639925 | ||||||
| chr16:21639925 | T | TTTTATTT others(13): Show |
2 | a0001c0002t0002g0003 a0001c0002t0002g0024 |
4 | NA18971.hp2 NA18973.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+14822_751+1484 others(24): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21639925 | ||||||
| chr16:21639994 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.751+14879A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21639994 | |||||||
| chr16:21640204 | T | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
171 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.752-15023T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21640204 | |||||||
| chr16:21640531 | A | C | 6 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG01071.hp1 HG01099.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-14696A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21640531 | |||||||
| chr16:21640571 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-14656T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21640571 | |||||||
| chr16:21640580 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.752-14647G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21640580 | |||||||
| chr16:21640596 | C | CA | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
46 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.752-14610dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21640596 | ||||||
| chr16:21640596 | CA | C | 31 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0120 others(28): Show |
31 | HG01123.hp1 HG01167.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.752-14610delA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21640596 | ||||||
| chr16:21640639 | T | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(331): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.752-14588T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21640639 | |||||||
| chr16:21640766 | C | CA | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
103 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.752-14445dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21640766 | ||||||
| chr16:21640790 | A | AAAG | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-14435_752-1443 others(7): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21640790 | ||||||
| chr16:21640854 | GT | G | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-14371delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21640854 | ||||||
| chr16:21641014 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.752-14213A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641014 | |||||||
| chr16:21641043 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG01099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.752-14184G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641043 | |||||||
| chr16:21641170 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.752-14057C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641170 | |||||||
| chr16:21641399 | A | G | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.752-13828A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641399 | |||||||
| chr16:21641440 | A | AT | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-13778dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21641440 | ||||||
| chr16:21641707 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.752-13520A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641707 | |||||||
| chr16:21641871 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0160 a0001c0001t0001g0163 others(1): Show |
4 | HG00733.hp1 HG01515.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-13356C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641871 | |||||||
| chr16:21641920 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-13307G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21641920 | |||||||
| chr16:21642140 | C | T | 1 | a0001c0002t0002g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.752-13087C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21642140 | |||||||
| chr16:21642692 | AT | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-12527delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21642692 | ||||||
| chr16:21642834 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.752-12393T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21642834 | |||||||
| chr16:21642944 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.752-12283A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21642944 | |||||||
| chr16:21643048 | A | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.752-12179A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643048 | |||||||
| chr16:21643213 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-12014C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643213 | |||||||
| chr16:21643385 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.752-11842T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643385 | |||||||
| chr16:21643466 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.752-11761T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643466 | |||||||
| chr16:21643759 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.752-11468A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643759 | |||||||
| chr16:21643807 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.752-11420A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21643807 | |||||||
| chr16:21643827 | CCTT | C | 33 | a0001c0001t0001g0082 a0001c0001t0001g0313 a0001c0001t0001g0314 others(30): Show |
33 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.752-11396_752-1139 others(7): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21643827 | ||||||
| chr16:21644231 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.752-10996T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21644231 | |||||||
| chr16:21644441 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.752-10786A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21644441 | |||||||
| chr16:21645050 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.752-10177G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645050 | |||||||
| chr16:21645314 | G | A | 1 | a0001c0001t0011g0174 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.752-9913G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645314 | |||||||
| chr16:21645367 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.752-9860C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645367 | |||||||
| chr16:21645432 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.752-9795G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645432 | |||||||
| chr16:21645641 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.752-9586C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645641 | |||||||
| chr16:21645733 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.752-9494A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21645733 | |||||||
| chr16:21646158 | C | CT | 234 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.752-9060dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21646158 | ||||||
| chr16:21646450 | T | A | 1 | a0001c0001t0001g0325 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.752-8777T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21646450 | |||||||
| chr16:21646945 | C | T | 70 | a0001c0001t0001g0082 a0001c0001t0001g0165 a0001c0001t0001g0166 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.752-8282C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21646945 | |||||||
| chr16:21647068 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
62 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.752-8159G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647068 | |||||||
| chr16:21647183 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.752-8044G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647183 | |||||||
| chr16:21647247 | C | T | 1 | a0001c0002t0002g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.752-7980C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647247 | |||||||
| chr16:21647317 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01884.hp2 HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.752-7910G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647317 | |||||||
| chr16:21647455 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.752-7772C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647455 | |||||||
| chr16:21647481 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.752-7746C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647481 | |||||||
| chr16:21647968 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.752-7259G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21647968 | |||||||
| chr16:21648036 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.752-7191G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648036 | |||||||
| chr16:21648434 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.752-6793G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648434 | |||||||
| chr16:21648475 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.752-6752C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648475 | |||||||
| chr16:21648527 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.752-6700G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648527 | |||||||
| chr16:21648603 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.752-6624C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648603 | |||||||
| chr16:21648649 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02723.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.752-6578G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648649 | |||||||
| chr16:21648815 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.752-6412C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21648815 | |||||||
| chr16:21649189 | C | T | 70 | a0001c0001t0001g0082 a0001c0001t0001g0165 a0001c0001t0001g0166 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.752-6038C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21649189 | |||||||
| chr16:21649820 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0088 |
3 | HG00735.hp1 HG01243.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.752-5407C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21649820 | |||||||
| chr16:21649956 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.752-5271G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21649956 | |||||||
| chr16:21650109 | CTGCACTC others(55): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.752-5089_752-5028d others(64): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650109 | ||||||
| chr16:21650114 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5113C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650114 | |||||||
| chr16:21650116 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5111C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650116 | |||||||
| chr16:21650117 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5110C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650117 | |||||||
| chr16:21650118 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5109A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650118 | |||||||
| chr16:21650122 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5105T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650122 | |||||||
| chr16:21650123 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5104G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650123 | |||||||
| chr16:21650124 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5103G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650124 | |||||||
| chr16:21650125 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5102G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650125 | |||||||
| chr16:21650140 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5087C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650140 | |||||||
| chr16:21650143 | GTCTCTAT others(10): Show |
G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5083_752-5067d others(19): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650143 | |||||||
| chr16:21650161 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5066G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650161 | |||||||
| chr16:21650164 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5063T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650164 | |||||||
| chr16:21650171 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.752-5056G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650171 | |||||||
| chr16:21650171 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5056G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650171 | |||||||
| chr16:21650174 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5053C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650174 | |||||||
| chr16:21650175 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5052A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650175 | |||||||
| chr16:21650185 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5042G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650185 | |||||||
| chr16:21650186 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5041G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650186 | |||||||
| chr16:21650192 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5035A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650192 | |||||||
| chr16:21650194 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5033T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650194 | |||||||
| chr16:21650195 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5032G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650195 | |||||||
| chr16:21650200 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5027A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650200 | |||||||
| chr16:21650201 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5026T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650201 | |||||||
| chr16:21650202 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5025C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650202 | |||||||
| chr16:21650207 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5020C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650207 | |||||||
| chr16:21650208 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5019T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650208 | |||||||
| chr16:21650215 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5012A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650215 | |||||||
| chr16:21650216 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5011A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650216 | |||||||
| chr16:21650218 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5009G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650218 | |||||||
| chr16:21650219 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5008A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650219 | |||||||
| chr16:21650221 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5006T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650221 | |||||||
| chr16:21650223 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5004G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650223 | |||||||
| chr16:21650225 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-5002G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650225 | |||||||
| chr16:21650228 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4999T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650228 | |||||||
| chr16:21650229 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4998G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650229 | |||||||
| chr16:21650233 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4994A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650233 | |||||||
| chr16:21650234 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4993T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650234 | |||||||
| chr16:21650235 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4992G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650235 | |||||||
| chr16:21650236 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4991G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650236 | |||||||
| chr16:21650243 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4984A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650243 | |||||||
| chr16:21650245 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4982G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650245 | |||||||
| chr16:21650246 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4981C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650246 | |||||||
| chr16:21650249 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4978G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650249 | |||||||
| chr16:21650250 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4977T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650250 | |||||||
| chr16:21650253 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4974T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650253 | |||||||
| chr16:21650254 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4973C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650254 | |||||||
| chr16:21650258 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4969G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650258 | |||||||
| chr16:21650269 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4958T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650269 | |||||||
| chr16:21650272 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4955C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650272 | |||||||
| chr16:21650279 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4948G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650279 | |||||||
| chr16:21650281 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4946C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650281 | |||||||
| chr16:21650282 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4945A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650282 | |||||||
| chr16:21650286 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4941C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650286 | |||||||
| chr16:21650287 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4940A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650287 | |||||||
| chr16:21650294 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4933G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650294 | |||||||
| chr16:21650295 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4932T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650295 | |||||||
| chr16:21650305 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4922G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650305 | |||||||
| chr16:21650327 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4900T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650327 | |||||||
| chr16:21650427 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-4800G>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650427 | |||||||
| chr16:21650430 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0096 |
2 | NA18999.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.752-4797C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650430 | |||||||
| chr16:21650508 | C | CA | 26 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0055 others(23): Show |
26 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.752-4699dupA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650508 | ||||||
| chr16:21650508 | C | CAA | 78 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.752-4700_752-4699d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650508 | ||||||
| chr16:21650508 | C | CAAA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
28 | HG00544.hp2 HG00673.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.752-4701_752-4699d others(5): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650508 | ||||||
| chr16:21650508 | CA | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0072 others(3): Show |
6 | HG00735.hp2 HG01256.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-4699delA | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650508 | ||||||
| chr16:21650508 | CAA | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-4700_752-4699d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21650508 | ||||||
| chr16:21650544 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-4683C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650544 | |||||||
| chr16:21650959 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.752-4268C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21650959 | |||||||
| chr16:21651080 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0213 a0001c0001t0001g0310 others(1): Show |
4 | HG02647.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-4147G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651080 | |||||||
| chr16:21651148 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.752-4079G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651148 | |||||||
| chr16:21651201 | T | C | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-4026T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651201 | |||||||
| chr16:21651331 | G | A | 1 | a0001c0003t0001g0326 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.752-3896G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651331 | |||||||
| chr16:21651634 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.752-3593A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651634 | |||||||
| chr16:21651638 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0262 |
2 | HG01358.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.752-3589A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651638 | |||||||
| chr16:21651841 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.752-3386A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651841 | |||||||
| chr16:21651956 | T | A | 1 | a0001c0001t0007g0271 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.752-3271T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651956 | |||||||
| chr16:21651979 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-3248C>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21651979 | |||||||
| chr16:21652112 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00099.hp1 HG01081.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-3115C>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652112 | |||||||
| chr16:21652285 | C | CTTTG | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-2941_752-2938d others(6): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21652285 | ||||||
| chr16:21652341 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.752-2886A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652341 | |||||||
| chr16:21652474 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
68 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.752-2753G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652474 | |||||||
| chr16:21652588 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.752-2639G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652588 | |||||||
| chr16:21652643 | A | G | 1 | a0001c0002t0002g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.752-2584A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652643 | |||||||
| chr16:21652792 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-2435A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21652792 | |||||||
| chr16:21653118 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.752-2109A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653118 | |||||||
| chr16:21653133 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-2094C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653133 | |||||||
| chr16:21653156 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02723.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.752-2071A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653156 | |||||||
| chr16:21653223 | G | A | 1 | a0001c0001t0017g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.752-2004G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653223 | |||||||
| chr16:21653254 | A | AT | 7 | a0001c0001t0001g0177 a0001c0001t0001g0189 a0001c0001t0001g0210 others(4): Show |
7 | HG02630.hp1 NA18941.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.752-1958dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21653254 | ||||||
| chr16:21653356 | C | T | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0330 others(1): Show |
4 | HG00140.hp1 HG00323.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-1871C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653356 | |||||||
| chr16:21653369 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-1858C>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653369 | |||||||
| chr16:21653401 | A | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0144 others(5): Show |
8 | HG01934.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.752-1826A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653401 | |||||||
| chr16:21653790 | A | G | 334 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(331): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.752-1437A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653790 | |||||||
| chr16:21653839 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.752-1388G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21653839 | |||||||
| chr16:21654029 | CTGTTT | C | 13 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(10): Show |
20 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.752-1191_752-1187d others(7): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21654029 | ||||||
| chr16:21654036 | G | GT | 59 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0040 others(56): Show |
59 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.752-1168dupT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21654036 | ||||||
| chr16:21654036 | G | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0116 a0001c0001t0001g0211 |
3 | HG01891.hp1 HG02622.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.752-1191G>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654036 | |||||||
| chr16:21654036 | GT | G | 14 | a0001c0001t0001g0039 a0001c0001t0001g0058 a0001c0001t0001g0067 others(11): Show |
14 | HG01952.hp2 HG02630.hp1 HG03516.hp1 others(11): Show |
intron_variant | MODIFIER | c.752-1168delT | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21654036 | ||||||
| chr16:21654036 | GTT | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
54 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.752-1169_752-1168d others(4): Show |
METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 21654036 | ||||||
| chr16:21654042 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0084 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.752-1185T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654042 | |||||||
| chr16:21654045 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.752-1182T>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654045 | |||||||
| chr16:21654073 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0253 a0001c0001t0001g0255 others(1): Show |
4 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.752-1154G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654073 | |||||||
| chr16:21654159 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.752-1068A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654159 | |||||||
| chr16:21654232 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.752-995A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654232 | |||||||
| chr16:21654529 | G | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0018 others(11): Show |
21 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.752-698G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654529 | |||||||
| chr16:21654543 | T | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0047 others(38): Show |
43 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.752-684T>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654543 | |||||||
| chr16:21654572 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.752-655A>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654572 | |||||||
| chr16:21654576 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.752-651T>C | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654576 | |||||||
| chr16:21654667 | A | G | 1 | a0001c0002t0002g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.752-560A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654667 | |||||||
| chr16:21654995 | A | G | 236 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.752-232A>G | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21654995 | |||||||
| chr16:21655022 | G | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
67 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.752-205G>A | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21655022 | |||||||
| chr16:21655083 | A | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0195 |
2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.752-144A>T | METTL9 | ENSG00000197006.15 | transcript | ENST00000358154.8 | protein_coding | 4/4 | chr16 | 21655083 |