Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 865 |
| ensemblid | ENSG00000067955.15 |
| hgncid | 1539 |
| symbol | CBFB |
| name | core-binding factor subunit beta |
| refseq_nuc | NM_022845.3 |
| refseq_prot | NP_074036.1 |
| ensembl_nuc | ENST00000412916.7 |
| ensembl_prot | ENSP00000415151.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67029149 |
| end | 67101058 |
| strand | + |
| ver | v1.2 |
| region | chr16:67029149-67101058 |
| region5000 | chr16:67024149-67106058 |
| regionname0 | CBFB_chr16_67029149_67101058 |
| regionname5000 | CBFB_chr16_67024149_67106058 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 561 | 191 | 78 | 35 | 50 | 6 | 20 | CBFB_chr16_67024149_67106058 | CBFB | ATGCC others(556): Show |
chr16 | 67024149 | 67106058 | ||
| a0001c0002 | 0/0 | 561 | 21 | 12 | 1 | 6 | 0 | 2 | CBFB_chr16_67024149_67106058 | CBFB | ATGCC others(556): Show |
chr16 | 67024149 | 67106058 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3103 | 132 | 30 | 31 | 49 | 5 | 15 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0002 | 0/0 | 3103 | 23 | 23 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0004 | 0/0 | 3097 | 13 | 13 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3092): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0005 | 0/0 | 3096 | 10 | 4 | 1 | 0 | 1 | 4 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3091): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0007 | 0/0 | 3103 | 3 | 1 | 2 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0008 | 0/0 | 3103 | 3 | 3 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0009 | 0/0 | 3097 | 3 | 3 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3092): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0010 | 0/0 | 3103 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0011 | 0/0 | 3103 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0012 | 0/0 | 3103 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0001t0013 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0002t0003 | 0/0 | 3103 | 14 | 7 | 0 | 6 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0002t0006 | 0/0 | 3103 | 6 | 5 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| a0001c0002t0014 | 0/0 | 3103 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | GGTGA others(3098): Show |
chr16 | 67024149 | 67106058 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0001t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| a0001c0002t0014g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0194 | EUR | GBR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0095 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0050 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0071 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0190 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0211 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0044 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0039 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0187 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0195 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0048 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0049 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0185 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0193 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0043 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0191 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04199 | hp1 | a0001 | c0002 | t0014 | g0032 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0160 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18906 | hp2 | a0001 | c0002 | t0006 | g0036 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | LWK | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0041 | AFR | LWK | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | LWK | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | ASW | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | ACB | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03471 | hp1 | a0001 | c0002 | t0006 | g0046 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | MSL | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | USA | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | USA | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0177 | AFR | USA | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0096 | REF | REF | CBFB_chr16_67024149_67106058 | CBFB | chr16 | 67024149 | 67106058 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67082266 | C | T | 1 | a0001c0002 | 21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
synonymous_variant | LOW | c.453C>T | p.Arg151Arg | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/6 | 712/3103 | 453/564 | 151/187 | chr16 | 67082266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67029154 | G | A | 1 | a0001c0001t0007 | 3 | HG01099.hp1 HG01952.hp2 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-254G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/6 | 254 | chr16 | 67029154 | ||||||
| chr16:67029174 | G | A | 1 | a0001c0001t0005 | 10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-234G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/6 | 234 | chr16 | 67029174 | ||||||
| chr16:67029188 | AGGCGGC | A | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-200_-195delGCGGCG | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/6 | 195 | INFO_REALIGN_3_PRIME | chr16 | 67029188 | |||||
| chr16:67029198 | G | A | 1 | a0001c0001t0004 | 13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-210G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/6 | 210 | chr16 | 67029198 | ||||||
| chr16:67029207 | G | A | 1 | a0001c0002t0006 | 6 | HG00738.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-201G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/6 | 201 | chr16 | 67029207 | ||||||
| chr16:67098900 | C | G | 1 | a0001c0002t0014 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 122 | chr16 | 67098900 | ||||||
| chr16:67098918 | A | G | 1 | a0001c0002t0014 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 140 | chr16 | 67098918 | ||||||
| chr16:67098990 | A | G | 1 | a0001c0001t0013 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 212 | chr16 | 67098990 | ||||||
| chr16:67099273 | A | G | 3 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0014 |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*495A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 495 | chr16 | 67099273 | ||||||
| chr16:67099837 | T | C | 1 | a0001c0001t0010 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1059 | chr16 | 67099837 | ||||||
| chr16:67100016 | A | G | 1 | a0001c0001t0008 | 3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1238A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1238 | chr16 | 67100016 | ||||||
| chr16:67100067 | T | C | 1 | a0001c0001t0011 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1289 | chr16 | 67100067 | ||||||
| chr16:67100133 | A | T | 1 | a0001c0001t0004 | 13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1355A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1355 | chr16 | 67100133 | ||||||
| chr16:67100199 | G | A | 2 | a0001c0001t0002 a0001c0001t0013 |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1421G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1421 | chr16 | 67100199 | ||||||
| chr16:67100637 | AT | A | 1 | a0001c0001t0005 | 10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1866delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 1866 | INFO_REALIGN_3_PRIME | chr16 | 67100637 | |||||
| chr16:67100898 | A | G | 3 | a0001c0002t0003 a0001c0002t0006 a0001c0002t0014 |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2120A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 2120 | chr16 | 67100898 | ||||||
| chr16:67100983 | G | A | 1 | a0001c0001t0012 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 6/6 | 2205 | chr16 | 67100983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67029529 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.78+44G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/5 | chr16 | 67029529 | |||||||
| chr16:67029590 | C | T | 1 | a0001c0001t0007g0211 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.78+105C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/5 | chr16 | 67029590 | |||||||
| chr16:67029596 | G | A | 25 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(22): Show |
25 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.78+111G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/5 | chr16 | 67029596 | |||||||
| chr16:67029599 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.78+114G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/5 | chr16 | 67029599 | |||||||
| chr16:67029709 | G | T | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.79-18G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 1/5 | chr16 | 67029709 | |||||||
| chr16:67030220 | TTC | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+411_165+412del others(2): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67030220 | ||||||
| chr16:67030299 | AG | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(74): Show |
77 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+494delG | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67030299 | ||||||
| chr16:67030307 | GA | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+498delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67030307 | ||||||
| chr16:67030315 | C | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+502C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67030315 | |||||||
| chr16:67030603 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+790T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67030603 | |||||||
| chr16:67030712 | G | T | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+899G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67030712 | |||||||
| chr16:67031102 | T | G | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+1289T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67031102 | |||||||
| chr16:67031179 | G | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+1366G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67031179 | |||||||
| chr16:67031603 | T | C | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+1790T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67031603 | |||||||
| chr16:67031637 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.165+1824A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67031637 | |||||||
| chr16:67031873 | T | C | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+2060T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67031873 | |||||||
| chr16:67032187 | C | G | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2374C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032187 | |||||||
| chr16:67032261 | G | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+2448G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032261 | |||||||
| chr16:67032319 | G | T | 16 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.165+2506G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032319 | |||||||
| chr16:67032576 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.165+2763A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032576 | |||||||
| chr16:67032592 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.165+2779A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032592 | |||||||
| chr16:67032862 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+3049G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67032862 | |||||||
| chr16:67033063 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.165+3250C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033063 | |||||||
| chr16:67033240 | C | T | 2 | a0001c0001t0005g0196 a0001c0001t0005g0197 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.166-3399C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033240 | |||||||
| chr16:67033572 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.166-3067A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033572 | |||||||
| chr16:67033613 | CT | C | 26 | a0001c0001t0001g0069 a0001c0001t0004g0198 a0001c0001t0004g0199 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.166-3010delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67033613 | ||||||
| chr16:67033671 | G | A | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-2968G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033671 | |||||||
| chr16:67033720 | TC | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2916delC | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67033720 | ||||||
| chr16:67033772 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.166-2867C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033772 | |||||||
| chr16:67033819 | G | GT | 53 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0063 others(50): Show |
53 | HG00609.hp1 HG00738.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.166-2800dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67033819 | ||||||
| chr16:67033823 | T | G | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.166-2816T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033823 | |||||||
| chr16:67033856 | C | T | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG00140.hp2 HG02602.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-2783C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033856 | |||||||
| chr16:67033860 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2779C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033860 | |||||||
| chr16:67033861 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.166-2778G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033861 | |||||||
| chr16:67033931 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.166-2708C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67033931 | |||||||
| chr16:67034074 | T | C | 85 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.166-2565T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034074 | |||||||
| chr16:67034089 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.166-2550A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034089 | |||||||
| chr16:67034402 | TTTTG | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0010g0071 |
3 | HG00741.hp2 HG01192.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.166-2233_166-2230d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67034402 | ||||||
| chr16:67034437 | T | C | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.166-2202T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034437 | |||||||
| chr16:67034602 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.166-2037G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034602 | |||||||
| chr16:67034937 | A | G | 1 | a0001c0001t0012g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.166-1702A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034937 | |||||||
| chr16:67034947 | G | A | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.166-1692G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034947 | |||||||
| chr16:67034968 | A | T | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.166-1671A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67034968 | |||||||
| chr16:67035135 | A | G | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-1504A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67035135 | |||||||
| chr16:67035849 | G | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-790G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67035849 | |||||||
| chr16:67036059 | CA | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-577delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 67036059 | ||||||
| chr16:67036237 | T | C | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.166-402T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 2/5 | chr16 | 67036237 | |||||||
| chr16:67036893 | G | A | 1 | a0001c0002t0006g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.282+138G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67036893 | |||||||
| chr16:67036959 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0070 others(44): Show |
48 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.282+204C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67036959 | |||||||
| chr16:67037002 | G | C | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.282+247G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67037002 | |||||||
| chr16:67037666 | A | AT | 18 | a0001c0001t0001g0034 a0001c0001t0001g0121 a0001c0001t0001g0122 others(15): Show |
18 | HG00423.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.282+930dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67037666 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0210 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.282+920_282+930dup others(11): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67037666 | A | ATTTTTTT others(5): Show |
9 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+919_282+930dup others(12): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67037666 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0004g0205 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.282+918_282+930dup others(13): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67037666 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0004g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+917_282+930dup others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67037666 | AT | A | 63 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(60): Show |
63 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.282+930delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67037666 | ||||||
| chr16:67038284 | G | GTA | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(6): Show |
9 | HG00140.hp2 HG01361.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+1542_282+1543d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67038284 | ||||||
| chr16:67038284 | G | GTATA | 2 | a0001c0001t0005g0188 a0001c0001t0005g0190 |
2 | HG01109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.282+1540_282+1543d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67038284 | ||||||
| chr16:67038284 | GTA | G | 16 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+1542_282+1543d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67038284 | ||||||
| chr16:67038321 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.282+1566C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67038321 | |||||||
| chr16:67038372 | G | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+1617G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67038372 | |||||||
| chr16:67038431 | G | A | 85 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.282+1676G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67038431 | |||||||
| chr16:67038694 | TGAA | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+1943_282+1945d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67038694 | ||||||
| chr16:67038716 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.282+1961G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67038716 | |||||||
| chr16:67038865 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.282+2110C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67038865 | |||||||
| chr16:67039128 | A | T | 2 | a0001c0002t0003g0052 a0001c0002t0003g0053 |
2 | NA19056.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.282+2373A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039128 | |||||||
| chr16:67039461 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.282+2706C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039461 | |||||||
| chr16:67039615 | C | A | 2 | a0001c0001t0004g0198 a0001c0001t0004g0209 |
2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.282+2860C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039615 | |||||||
| chr16:67039643 | AATTCT | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+2892_282+2896d others(7): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67039643 | ||||||
| chr16:67039649 | A | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0009 others(2): Show |
5 | HG01884.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+2894A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039649 | |||||||
| chr16:67039649 | A | G | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG00140.hp1 HG01433.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+2894A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039649 | |||||||
| chr16:67039795 | C | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+3040C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039795 | |||||||
| chr16:67039946 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.282+3191C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67039946 | |||||||
| chr16:67040110 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.282+3355C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67040110 | |||||||
| chr16:67040242 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282+3487A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67040242 | |||||||
| chr16:67040347 | G | A | 1 | a0001c0002t0006g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.282+3592G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67040347 | |||||||
| chr16:67040418 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.282+3663C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67040418 | |||||||
| chr16:67040458 | A | G | 1 | a0001c0001t0005g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.282+3703A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67040458 | |||||||
| chr16:67041286 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.282+4531A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041286 | |||||||
| chr16:67041410 | G | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+4655G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041410 | |||||||
| chr16:67041437 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.282+4682A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041437 | |||||||
| chr16:67041557 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.282+4802G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041557 | |||||||
| chr16:67041703 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.282+4948A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041703 | |||||||
| chr16:67041768 | C | CT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(80): Show |
83 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.282+5035dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67041768 | ||||||
| chr16:67041768 | C | CTT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0002g0010 others(3): Show |
6 | HG02055.hp2 HG03209.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+5034_282+5035d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67041768 | ||||||
| chr16:67041768 | CT | C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0110 a0001c0001t0001g0126 others(2): Show |
5 | HG02896.hp2 NA18962.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+5035delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67041768 | ||||||
| chr16:67041790 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.282+5035T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67041790 | |||||||
| chr16:67041900 | C | CT | 5 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0067 others(2): Show |
5 | HG00741.hp1 HG02074.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+5162dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67041900 | ||||||
| chr16:67042143 | C | T | 1 | a0001c0001t0009g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282+5388C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042143 | |||||||
| chr16:67042536 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.282+5781C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042536 | |||||||
| chr16:67042561 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+5806C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042561 | |||||||
| chr16:67042763 | G | A | 16 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+6008G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042763 | |||||||
| chr16:67042789 | G | A | 1 | a0001c0002t0006g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.282+6034G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042789 | |||||||
| chr16:67042859 | T | C | 85 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.282+6104T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67042859 | |||||||
| chr16:67043069 | C | G | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+6314C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043069 | |||||||
| chr16:67043245 | C | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0009 |
3 | HG01884.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.282+6490C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043245 | |||||||
| chr16:67043380 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.282+6625C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043380 | |||||||
| chr16:67043577 | C | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+6822C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043577 | |||||||
| chr16:67043608 | T | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.282+6853T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043608 | |||||||
| chr16:67043821 | G | C | 1 | a0001c0002t0006g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.282+7066G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67043821 | |||||||
| chr16:67044082 | A | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+7327A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67044082 | |||||||
| chr16:67044136 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0065 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.282+7381T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67044136 | |||||||
| chr16:67044575 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.282+7820T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67044575 | |||||||
| chr16:67044580 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+7825A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67044580 | |||||||
| chr16:67044974 | A | G | 1 | a0001c0001t0002g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282+8219A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67044974 | |||||||
| chr16:67045032 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.282+8277T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045032 | |||||||
| chr16:67045095 | T | TTA | 2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.282+8356_282+8357d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045095 | ||||||
| chr16:67045095 | TTA | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+8356_282+8357d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045095 | ||||||
| chr16:67045166 | T | G | 11 | a0001c0002t0003g0038 a0001c0002t0003g0039 a0001c0002t0003g0040 others(8): Show |
11 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.282+8411T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045166 | |||||||
| chr16:67045444 | G | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+8689G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045444 | |||||||
| chr16:67045498 | CAG | C | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.282+8746_282+8747d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045498 | ||||||
| chr16:67045516 | G | GA | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+8773dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045516 | ||||||
| chr16:67045685 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+8930A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045685 | |||||||
| chr16:67045777 | C | T | 88 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.282+9022C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045777 | |||||||
| chr16:67045796 | A | AT | 46 | a0001c0001t0001g0063 a0001c0001t0001g0108 a0001c0001t0001g0150 others(43): Show |
46 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.282+9058dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045796 | ||||||
| chr16:67045796 | A | ATT | 6 | a0001c0001t0004g0205 a0001c0001t0009g0185 a0001c0001t0009g0186 others(3): Show |
6 | HG02074.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+9057_282+9058d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045796 | ||||||
| chr16:67045796 | AT | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0153 others(2): Show |
5 | HG01361.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+9058delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67045796 | ||||||
| chr16:67045867 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG01943.hp2 HG01978.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+9112C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045867 | |||||||
| chr16:67045881 | C | T | 3 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0204 |
3 | HG02109.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.282+9126C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67045881 | |||||||
| chr16:67046254 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.282+9499G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046254 | |||||||
| chr16:67046347 | C | T | 1 | a0001c0001t0004g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.282+9592C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046347 | |||||||
| chr16:67046350 | C | T | 1 | a0001c0002t0006g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.282+9595C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046350 | |||||||
| chr16:67046527 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+9772A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046527 | |||||||
| chr16:67046743 | T | TTGTAATT others(332): Show |
1 | a0001c0001t0001g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282+10002_282+1000 others(343): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67046743 | ||||||
| chr16:67046885 | A | G | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.282+10130A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046885 | |||||||
| chr16:67046946 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.282+10191T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046946 | |||||||
| chr16:67046989 | A | C | 1 | a0001c0002t0006g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.282+10234A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67046989 | |||||||
| chr16:67047113 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.282+10358C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047113 | |||||||
| chr16:67047199 | G | C | 85 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(82): Show |
85 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.282+10444G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047199 | |||||||
| chr16:67047230 | C | A | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+10475C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047230 | |||||||
| chr16:67047469 | A | G | 47 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(44): Show |
47 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.282+10714A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047469 | |||||||
| chr16:67047601 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.282+10846A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047601 | |||||||
| chr16:67047767 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+11012T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047767 | |||||||
| chr16:67047789 | T | C | 88 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(85): Show |
88 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.282+11034T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047789 | |||||||
| chr16:67047860 | G | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+11105G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67047860 | |||||||
| chr16:67048266 | C | A | 1 | a0001c0001t0004g0202 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282+11511C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048266 | |||||||
| chr16:67048390 | G | A | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+11635G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048390 | |||||||
| chr16:67048582 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0065 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.282+11827G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048582 | |||||||
| chr16:67048585 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.282+11830C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048585 | |||||||
| chr16:67048676 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.282+11921G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048676 | |||||||
| chr16:67048707 | C | T | 9 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(6): Show |
9 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+11952C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048707 | |||||||
| chr16:67048808 | CT | C | 13 | a0001c0001t0001g0033 a0001c0001t0004g0198 a0001c0001t0004g0199 others(10): Show |
13 | HG01361.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.282+12067delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67048808 | ||||||
| chr16:67048814 | TTTTTTTT others(2): Show |
T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG00438.hp2 HG01993.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+12068_282+1207 others(13): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67048814 | ||||||
| chr16:67048823 | C | CT | 11 | a0001c0001t0001g0102 a0001c0001t0005g0188 a0001c0001t0005g0189 others(8): Show |
11 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.282+12082dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67048823 | ||||||
| chr16:67048925 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+12170A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67048925 | |||||||
| chr16:67049289 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+12534C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67049289 | |||||||
| chr16:67049363 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+12608C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67049363 | |||||||
| chr16:67049840 | T | G | 1 | a0001c0002t0014g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.282+13085T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67049840 | |||||||
| chr16:67049936 | C | T | 1 | a0001c0001t0008g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+13181C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67049936 | |||||||
| chr16:67049941 | G | A | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+13186G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67049941 | |||||||
| chr16:67050079 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0166 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.282+13324A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67050079 | |||||||
| chr16:67050089 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.282+13334A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67050089 | |||||||
| chr16:67050226 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+13471A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67050226 | |||||||
| chr16:67050453 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.282+13698A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67050453 | |||||||
| chr16:67050744 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.282+13989G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67050744 | |||||||
| chr16:67051384 | G | A | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+14629G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67051384 | |||||||
| chr16:67051596 | G | C | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.282+14841G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67051596 | |||||||
| chr16:67051753 | G | GT | 21 | a0001c0001t0001g0034 a0001c0002t0003g0007 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-14918dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051753 | ||||||
| chr16:67051859 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-14823C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67051859 | |||||||
| chr16:67051905 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.283-14777A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67051905 | |||||||
| chr16:67051912 | T | TAC | 12 | a0001c0001t0001g0033 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG01099.hp2 HG01361.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-14739_283-1473 others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051912 | T | TACAC | 3 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0121 |
4 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-14741_283-1473 others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051912 | TAC | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0057 others(29): Show |
32 | HG00741.hp1 HG00741.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.283-14739_283-1473 others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051912 | TACAC | T | 47 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0059 others(44): Show |
47 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.283-14741_283-1473 others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051912 | TACACAC | T | 11 | a0001c0001t0002g0023 a0001c0001t0005g0188 a0001c0001t0005g0189 others(8): Show |
11 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-14743_283-1473 others(10): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051912 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283-14751_283-1473 others(18): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67051912 | ||||||
| chr16:67051913 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.283-14769A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67051913 | |||||||
| chr16:67052023 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.283-14659C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67052023 | |||||||
| chr16:67052031 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0159 |
2 | NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.283-14651G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67052031 | |||||||
| chr16:67052371 | A | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0164 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.283-14311A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67052371 | |||||||
| chr16:67052379 | G | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-14303G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67052379 | |||||||
| chr16:67052487 | G | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-14195G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67052487 | |||||||
| chr16:67053008 | C | CAA | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-13661_283-1366 others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053008 | ||||||
| chr16:67053140 | T | A | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-13542T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053140 | |||||||
| chr16:67053178 | A | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-13504A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053178 | |||||||
| chr16:67053242 | TTCTC | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.283-13436_283-1343 others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053242 | ||||||
| chr16:67053248 | C | CT | 26 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0064 others(23): Show |
26 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.283-13413dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053248 | ||||||
| chr16:67053248 | CT | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0088 others(9): Show |
12 | HG00423.hp1 HG01361.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-13413delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053248 | ||||||
| chr16:67053504 | T | C | 58 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(55): Show |
58 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.283-13178T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053504 | |||||||
| chr16:67053506 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.283-13176C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053506 | |||||||
| chr16:67053742 | T | C | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-12940T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053742 | |||||||
| chr16:67053742 | T | G | 1 | a0001c0002t0006g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283-12940T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053742 | |||||||
| chr16:67053844 | C | CT | 28 | a0001c0001t0001g0151 a0001c0001t0008g0030 a0001c0001t0008g0031 others(25): Show |
28 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.283-12823dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053844 | ||||||
| chr16:67053844 | CT | C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0061 others(13): Show |
16 | HG00558.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-12823delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67053844 | ||||||
| chr16:67053859 | T | A | 1 | a0001c0001t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283-12823T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67053859 | |||||||
| chr16:67054659 | G | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-12023G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054659 | |||||||
| chr16:67054688 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-11994C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054688 | |||||||
| chr16:67054734 | A | G | 1 | a0001c0002t0003g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283-11948A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054734 | |||||||
| chr16:67054750 | TTTTG | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-11916_283-1191 others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67054750 | ||||||
| chr16:67054854 | G | T | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-11828G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054854 | |||||||
| chr16:67054862 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283-11820C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054862 | |||||||
| chr16:67054930 | A | AT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
66 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.283-11735dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67054930 | ||||||
| chr16:67054964 | C | T | 1 | a0001c0002t0003g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-11718C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054964 | |||||||
| chr16:67054973 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG00558.hp1 HG02071.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-11709C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67054973 | |||||||
| chr16:67055079 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.283-11603C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055079 | |||||||
| chr16:67055352 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283-11330A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055352 | |||||||
| chr16:67055357 | C | CT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0087 others(10): Show |
13 | HG00438.hp1 HG01099.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-11298dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTT | 13 | a0001c0002t0003g0008 a0001c0002t0003g0038 a0001c0002t0003g0039 others(10): Show |
13 | HG00609.hp1 HG02080.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-11300_283-1129 others(7): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTCTTT others(9): Show |
1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283-11322_283-1132 others(20): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTT | 8 | a0001c0002t0003g0007 a0001c0002t0003g0042 a0001c0002t0003g0043 others(5): Show |
8 | HG00738.hp1 HG02074.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-11301_283-1129 others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0005g0197 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283-11307_283-1129 others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283-11308_283-1129 others(15): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0059 |
2 | HG00438.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.283-11309_283-1129 others(16): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283-11311_283-1129 others(18): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0009g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.283-11312_283-1129 others(19): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.283-11315_283-1129 others(22): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0009g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.283-11316_283-1129 others(23): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | CT | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0008g0030 others(2): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-11298delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | CTTT | C | 21 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0002g0009 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.283-11300_283-1129 others(7): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | CTTTTT | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-11302_283-1129 others(9): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055357 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0006 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283-11307_283-1129 others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67055357 | ||||||
| chr16:67055458 | C | T | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-11224C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055458 | |||||||
| chr16:67055591 | C | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-11091C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055591 | |||||||
| chr16:67055617 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-11065A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055617 | |||||||
| chr16:67055648 | A | G | 1 | a0001c0002t0003g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-11034A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055648 | |||||||
| chr16:67055651 | C | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-11031C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055651 | |||||||
| chr16:67055703 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0182 a0001c0001t0007g0177 others(2): Show |
5 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-10979T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055703 | |||||||
| chr16:67055714 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.283-10968C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67055714 | |||||||
| chr16:67056684 | C | CT | 14 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
14 | HG00438.hp1 HG01952.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.283-9982dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67056684 | ||||||
| chr16:67056684 | CT | C | 11 | a0001c0001t0001g0161 a0001c0001t0005g0188 a0001c0001t0005g0189 others(8): Show |
11 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-9982delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67056684 | ||||||
| chr16:67056703 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283-9979G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67056703 | |||||||
| chr16:67056960 | G | A | 1 | a0001c0001t0005g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.283-9722G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67056960 | |||||||
| chr16:67056975 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.283-9707C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67056975 | |||||||
| chr16:67057192 | A | T | 1 | a0001c0001t0002g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283-9490A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67057192 | |||||||
| chr16:67057436 | TTTGA | T | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.283-9243_283-9240d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67057436 | ||||||
| chr16:67057778 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.283-8904T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67057778 | |||||||
| chr16:67057990 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283-8692A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67057990 | |||||||
| chr16:67058128 | G | GGTT | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0055 others(10): Show |
13 | HG00438.hp2 HG01099.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-8525_283-8523d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67058128 | ||||||
| chr16:67058128 | G | GGTTGTTG others(2): Show |
6 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(3): Show |
6 | HG01109.hp1 HG02145.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-8531_283-8523d others(11): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67058128 | ||||||
| chr16:67058128 | G | GGTTGTTG others(5): Show |
1 | a0001c0001t0005g0197 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283-8534_283-8523d others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67058128 | ||||||
| chr16:67058128 | G | GGTTGTTG others(8): Show |
2 | a0001c0001t0005g0191 a0001c0001t0005g0194 |
2 | HG00140.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.283-8537_283-8523d others(17): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67058128 | ||||||
| chr16:67058436 | C | T | 1 | a0001c0002t0003g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-8246C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058436 | |||||||
| chr16:67058445 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.283-8237G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058445 | |||||||
| chr16:67058451 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-8231T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058451 | |||||||
| chr16:67058486 | T | C | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-8196T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058486 | |||||||
| chr16:67058576 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0154 a0001c0001t0001g0157 others(2): Show |
5 | HG00423.hp1 NA18948.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-8106C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058576 | |||||||
| chr16:67058687 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283-7995T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058687 | |||||||
| chr16:67058843 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.283-7839C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67058843 | |||||||
| chr16:67059050 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.283-7632G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059050 | |||||||
| chr16:67059054 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.283-7628T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059054 | |||||||
| chr16:67059077 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283-7605T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059077 | |||||||
| chr16:67059415 | A | T | 1 | a0001c0001t0005g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-7267A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059415 | |||||||
| chr16:67059516 | G | C | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283-7166G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059516 | |||||||
| chr16:67059957 | ATTCT | A | 33 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(30): Show |
33 | HG01081.hp1 HG01361.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.283-6706_283-6703d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67059957 | ||||||
| chr16:67059976 | CT | C | 34 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(31): Show |
34 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.283-6693delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67059976 | ||||||
| chr16:67059979 | T | TC | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.283-6703_283-6702i others(3): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059979 | |||||||
| chr16:67059980 | T | C | 12 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0005g0188 others(9): Show |
12 | HG00140.hp2 HG00741.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-6702T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67059980 | |||||||
| chr16:67060110 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.283-6572G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060110 | |||||||
| chr16:67060166 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG02071.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.283-6516A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060166 | |||||||
| chr16:67060197 | T | A | 26 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0002g0004 others(23): Show |
26 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.283-6485T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060197 | |||||||
| chr16:67060416 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.283-6266A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060416 | |||||||
| chr16:67060543 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0065 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.283-6139T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060543 | |||||||
| chr16:67060566 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283-6116T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060566 | |||||||
| chr16:67060587 | G | T | 23 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(20): Show |
23 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.283-6095G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060587 | |||||||
| chr16:67060712 | C | T | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.283-5970C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060712 | |||||||
| chr16:67060743 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.283-5939C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67060743 | |||||||
| chr16:67061360 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.283-5322A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061360 | |||||||
| chr16:67061543 | T | C | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.283-5139T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061543 | |||||||
| chr16:67061569 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.283-5113A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061569 | |||||||
| chr16:67061892 | T | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(87): Show |
90 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.283-4790T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061892 | |||||||
| chr16:67061956 | T | C | 87 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(84): Show |
87 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.283-4726T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061956 | |||||||
| chr16:67061980 | C | T | 34 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(31): Show |
34 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.283-4702C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67061980 | |||||||
| chr16:67062130 | G | A | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-4552G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67062130 | |||||||
| chr16:67062325 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.283-4357C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67062325 | |||||||
| chr16:67062563 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.283-4119G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67062563 | |||||||
| chr16:67063143 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.283-3539C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063143 | |||||||
| chr16:67063276 | C | T | 3 | a0001c0001t0007g0177 a0001c0001t0007g0180 a0001c0001t0007g0211 |
3 | HG01099.hp1 HG01952.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.283-3406C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063276 | |||||||
| chr16:67063452 | A | ATTTTTTT others(35): Show |
1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3223_283-3222i others(44): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67063452 | ||||||
| chr16:67063465 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3217A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063465 | |||||||
| chr16:67063472 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3210T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063472 | |||||||
| chr16:67063477 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3205A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063477 | |||||||
| chr16:67063481 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3201T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063481 | |||||||
| chr16:67063482 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3200A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063482 | |||||||
| chr16:67063490 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3192A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063490 | |||||||
| chr16:67063496 | C | CA | 26 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0002g0004 others(23): Show |
26 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.283-3185dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67063496 | ||||||
| chr16:67063502 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3180T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063502 | |||||||
| chr16:67063504 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3178C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063504 | |||||||
| chr16:67063507 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3175C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063507 | |||||||
| chr16:67063511 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3171A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063511 | |||||||
| chr16:67063523 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3159C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063523 | |||||||
| chr16:67063527 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3155T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063527 | |||||||
| chr16:67063535 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3147A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063535 | |||||||
| chr16:67063542 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3140A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063542 | |||||||
| chr16:67063545 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3137G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063545 | |||||||
| chr16:67063549 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3133A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063549 | |||||||
| chr16:67063551 | C | T | 1 | a0001c0001t0012g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.283-3131C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063551 | |||||||
| chr16:67063556 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3126A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063556 | |||||||
| chr16:67063570 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3112G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063570 | |||||||
| chr16:67063576 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283-3106A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063576 | |||||||
| chr16:67063599 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.283-3083G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063599 | |||||||
| chr16:67063660 | C | G | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-3022C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063660 | |||||||
| chr16:67063897 | C | A | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-2785C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063897 | |||||||
| chr16:67063994 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.283-2688G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67063994 | |||||||
| chr16:67064364 | G | A | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.283-2318G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67064364 | |||||||
| chr16:67064494 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-2188C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67064494 | |||||||
| chr16:67064822 | TTTG | T | 12 | a0001c0001t0002g0005 a0001c0001t0004g0198 a0001c0001t0004g0199 others(9): Show |
12 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-1851_283-1849d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67064822 | ||||||
| chr16:67064828 | GTTGTTT | G | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.283-1851_283-1846d others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67064828 | ||||||
| chr16:67064838 | A | T | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.283-1844A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67064838 | |||||||
| chr16:67064897 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.283-1785T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67064897 | |||||||
| chr16:67064999 | G | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-1683G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67064999 | |||||||
| chr16:67065160 | A | G | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.283-1522A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065160 | |||||||
| chr16:67065447 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0147 others(4): Show |
7 | HG00438.hp1 HG01496.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-1235A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065447 | |||||||
| chr16:67065544 | T | C | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-1138T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065544 | |||||||
| chr16:67065546 | A | G | 1 | a0001c0001t0005g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-1136A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065546 | |||||||
| chr16:67065640 | A | G | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0147 others(3): Show |
6 | HG00438.hp1 HG01496.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-1042A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065640 | |||||||
| chr16:67065821 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-861A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67065821 | |||||||
| chr16:67066035 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.283-647T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67066035 | |||||||
| chr16:67066157 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-525C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67066157 | |||||||
| chr16:67066393 | C | CA | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0099 others(6): Show |
9 | HG00423.hp2 HG01081.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-272dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(9): Show |
12 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-279_283-272dup others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0072 a0001c0001t0001g0144 a0001c0001t0001g0149 others(7): Show |
10 | HG00558.hp1 HG01192.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-280_283-272dup others(9): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(3): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
73 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.283-281_283-272dup others(10): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0161 a0001c0001t0001g0167 others(4): Show |
7 | HG01109.hp1 HG02080.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-282_283-272dup others(11): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(5): Show |
9 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0080 others(6): Show |
9 | HG02071.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-283_283-272dup others(12): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
9 | HG01993.hp2 HG03225.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-284_283-272dup others(13): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0082 |
2 | HG00438.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.283-285_283-272dup others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0006g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.283-286_283-272dup others(15): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0003g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.283-287_283-272dup others(16): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(10): Show |
7 | a0001c0002t0003g0040 a0001c0002t0003g0041 a0001c0002t0003g0042 others(4): Show |
7 | HG00738.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-288_283-272dup others(17): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(11): Show |
5 | a0001c0001t0001g0058 a0001c0002t0003g0008 a0001c0002t0003g0045 others(2): Show |
5 | HG03041.hp1 HG03130.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-272_283-271ins others(18): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0064 a0001c0002t0003g0038 a0001c0002t0003g0039 others(4): Show |
7 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-272_283-271ins others(19): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(14): Show |
1 | a0001c0002t0003g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283-272_283-271ins others(21): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066393 | C | CAAAAAAA others(15): Show |
1 | a0001c0002t0006g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283-272_283-271ins others(22): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066393 | ||||||
| chr16:67066546 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.283-136C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | chr16 | 67066546 | |||||||
| chr16:67066557 | CTCAA | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-117_283-114del others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 67066557 | ||||||
| chr16:67067212 | TA | T | 5 | a0001c0001t0001g0161 a0001c0001t0005g0188 a0001c0001t0005g0190 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+431delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67067212 | ||||||
| chr16:67067213 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.399+415A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067213 | |||||||
| chr16:67067286 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.399+488G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067286 | |||||||
| chr16:67067353 | G | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+555G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067353 | |||||||
| chr16:67067421 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0081 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.399+623G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067421 | |||||||
| chr16:67067602 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.399+804C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067602 | |||||||
| chr16:67067622 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0124 |
2 | NA18992.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.399+824C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67067622 | |||||||
| chr16:67068519 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | HG03927.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.399+1721G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068519 | |||||||
| chr16:67068567 | C | T | 5 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+1769C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068567 | |||||||
| chr16:67068634 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+1836G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068634 | |||||||
| chr16:67068889 | G | T | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.399+2091G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068889 | |||||||
| chr16:67068916 | G | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.399+2118G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068916 | |||||||
| chr16:67068922 | C | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+2124C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67068922 | |||||||
| chr16:67069082 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.399+2284C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069082 | |||||||
| chr16:67069214 | C | CA | 5 | a0001c0001t0001g0113 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG00140.hp1 HG03195.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+2424dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67069214 | ||||||
| chr16:67069217 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+2419A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069217 | |||||||
| chr16:67069244 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | HG03927.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.399+2446C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069244 | |||||||
| chr16:67069324 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.399+2526C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069324 | |||||||
| chr16:67069369 | C | CA | 12 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+2584dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67069369 | ||||||
| chr16:67069369 | CA | C | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+2584delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67069369 | ||||||
| chr16:67069440 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.399+2642A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069440 | |||||||
| chr16:67069507 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.399+2709T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069507 | |||||||
| chr16:67069773 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0054 |
3 | HG01433.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.399+2975C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069773 | |||||||
| chr16:67069776 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.399+2978G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069776 | |||||||
| chr16:67069847 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 |
3 | HG01361.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.399+3049G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069847 | |||||||
| chr16:67069981 | C | G | 5 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+3183C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67069981 | |||||||
| chr16:67070286 | C | T | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.399+3488C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070286 | |||||||
| chr16:67070475 | A | G | 42 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(39): Show |
42 | HG00609.hp1 HG00738.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.399+3677A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070475 | |||||||
| chr16:67070686 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.399+3888C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070686 | |||||||
| chr16:67070687 | C | CA | 5 | a0001c0001t0001g0086 a0001c0001t0002g0019 a0001c0001t0002g0020 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+3903dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67070687 | ||||||
| chr16:67070753 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.399+3955A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070753 | |||||||
| chr16:67070762 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.399+3964G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070762 | |||||||
| chr16:67070927 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.399+4129G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67070927 | |||||||
| chr16:67071064 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.399+4266A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071064 | |||||||
| chr16:67071189 | G | C | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.399+4391G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071189 | |||||||
| chr16:67071246 | C | T | 90 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(87): Show |
90 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.399+4448C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071246 | |||||||
| chr16:67071384 | G | A | 5 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+4586G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071384 | |||||||
| chr16:67071532 | A | G | 1 | a0001c0002t0003g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.399+4734A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071532 | |||||||
| chr16:67071753 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.399+4955C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071753 | |||||||
| chr16:67071945 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.399+5147G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071945 | |||||||
| chr16:67071980 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.399+5182C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67071980 | |||||||
| chr16:67072064 | T | C | 1 | a0001c0002t0003g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.399+5266T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072064 | |||||||
| chr16:67072531 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+5733A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072531 | |||||||
| chr16:67072570 | G | A | 17 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(14): Show |
17 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.399+5772G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072570 | |||||||
| chr16:67072628 | G | A | 39 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(36): Show |
39 | HG00609.hp1 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.399+5830G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072628 | |||||||
| chr16:67072646 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+5848A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072646 | |||||||
| chr16:67072745 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.399+5947C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072745 | |||||||
| chr16:67072774 | CT | C | 18 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(15): Show |
18 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.399+5989delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67072774 | ||||||
| chr16:67072810 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+6012G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072810 | |||||||
| chr16:67072837 | G | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+6039G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072837 | |||||||
| chr16:67072931 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0061 |
2 | NA18992.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.399+6133T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67072931 | |||||||
| chr16:67073013 | C | G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+6215C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073013 | |||||||
| chr16:67073697 | G | A | 1 | a0001c0002t0006g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.399+6899G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073697 | |||||||
| chr16:67073708 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+6910C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073708 | |||||||
| chr16:67073743 | A | G | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.399+6945A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073743 | |||||||
| chr16:67073752 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.399+6954G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073752 | |||||||
| chr16:67073769 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.399+6971C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073769 | |||||||
| chr16:67073842 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.399+7044C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073842 | |||||||
| chr16:67073851 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.399+7053C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073851 | |||||||
| chr16:67073878 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.399+7080T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073878 | |||||||
| chr16:67073958 | G | A | 1 | a0001c0002t0014g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.399+7160G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67073958 | |||||||
| chr16:67074081 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.399+7283G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074081 | |||||||
| chr16:67074144 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+7346G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074144 | |||||||
| chr16:67074386 | C | CT | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0147 others(7): Show |
10 | HG00438.hp1 HG00621.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.399+7603dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67074386 | ||||||
| chr16:67074386 | CT | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(87): Show |
90 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.399+7603delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67074386 | ||||||
| chr16:67074451 | C | CAGCTCAC others(11): Show |
1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.399+7654_399+7671d others(20): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67074451 | ||||||
| chr16:67074599 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.400-7614T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074599 | |||||||
| chr16:67074890 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.400-7323G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074890 | |||||||
| chr16:67074962 | G | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.400-7251G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074962 | |||||||
| chr16:67074980 | G | A | 2 | a0001c0002t0003g0038 a0001c0002t0003g0039 |
2 | HG00609.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.400-7233G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67074980 | |||||||
| chr16:67075019 | T | C | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-7194T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075019 | |||||||
| chr16:67075194 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.400-7019A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075194 | |||||||
| chr16:67075196 | A | AAT | 13 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0090 others(10): Show |
13 | HG01081.hp2 HG01943.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-7016_400-7015d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075196 | ||||||
| chr16:67075197 | A | ATACG | 3 | a0001c0001t0001g0063 a0001c0001t0005g0195 a0001c0002t0006g0050 |
3 | HG00738.hp1 HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.400-7015_400-7014i others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATACGTG | 2 | a0001c0001t0005g0192 a0001c0001t0005g0193 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.400-7015_400-7014i others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATACGTGT others(1): Show |
4 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0194 others(1): Show |
4 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-7015_400-7014i others(10): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATACGTGT others(3): Show |
2 | a0001c0001t0001g0103 a0001c0001t0005g0197 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.400-7015_400-7014i others(12): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATACGTGT others(5): Show |
1 | a0001c0001t0005g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.400-7015_400-7014i others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATG | 45 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0074 others(42): Show |
46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.400-7015_400-7014i others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATGTG | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(18): Show |
21 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.400-7015_400-7014i others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATGTGT others(1): Show |
15 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0001g0106 others(12): Show |
15 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.400-7015_400-7014i others(10): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATGTGT others(3): Show |
2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.400-7015_400-7014i others(12): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATGTGT others(5): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0121 |
2 | HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.400-7015_400-7014i others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | A | ATATGTGT others(7): Show |
1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-7015_400-7014i others(16): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | ATG | A | 35 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0123 others(32): Show |
35 | HG00423.hp1 HG00609.hp1 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.400-6980_400-6979d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | ATGTG | A | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.400-6982_400-6979d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | ATGTGTGT others(11): Show |
A | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400-6996_400-6979d others(20): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075197 | ATGTGTGT others(13): Show |
A | 25 | a0001c0001t0001g0112 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
25 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.400-6998_400-6979d others(22): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67075197 | ||||||
| chr16:67075198 | T | TAC | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0056 others(14): Show |
17 | HG01361.hp1 HG01884.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-7015_400-7014i others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075198 | |||||||
| chr16:67075199 | G | A | 17 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0057 others(14): Show |
17 | HG00438.hp2 HG01993.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-7014G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075199 | |||||||
| chr16:67075200 | T | C | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG00438.hp2 HG01993.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-7013T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075200 | |||||||
| chr16:67075201 | G | A | 35 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0123 others(32): Show |
35 | HG00423.hp1 HG00609.hp1 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.400-7012G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075201 | |||||||
| chr16:67075202 | T | C | 27 | a0001c0001t0001g0065 a0001c0001t0004g0198 a0001c0001t0004g0199 others(24): Show |
27 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.400-7011T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075202 | |||||||
| chr16:67075203 | G | A | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.400-7010G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075203 | |||||||
| chr16:67075204 | T | C | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.400-7009T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075204 | |||||||
| chr16:67075205 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.400-7008G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075205 | |||||||
| chr16:67075217 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400-6996G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075217 | |||||||
| chr16:67075219 | G | A | 25 | a0001c0001t0001g0112 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
25 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.400-6994G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075219 | |||||||
| chr16:67075220 | T | C | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.400-6993T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075220 | |||||||
| chr16:67075250 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.400-6963T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075250 | |||||||
| chr16:67075566 | G | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-6647G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075566 | |||||||
| chr16:67075864 | G | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400-6349G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67075864 | |||||||
| chr16:67076205 | G | GA | 68 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(65): Show |
68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.400-6008_400-6007i others(3): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076205 | |||||||
| chr16:67076271 | G | A | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-5942G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076271 | |||||||
| chr16:67076323 | G | C | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400-5890G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076323 | |||||||
| chr16:67076421 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.400-5792T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076421 | |||||||
| chr16:67076592 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.400-5621C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076592 | |||||||
| chr16:67076631 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400-5582A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67076631 | |||||||
| chr16:67077079 | T | C | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.400-5134T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077079 | |||||||
| chr16:67077131 | A | G | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.400-5082A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077131 | |||||||
| chr16:67077145 | C | T | 98 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(95): Show |
98 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.400-5068C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077145 | |||||||
| chr16:67077282 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.400-4931A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077282 | |||||||
| chr16:67077320 | TTGA | T | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0035 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.400-4889_400-4887d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67077320 | ||||||
| chr16:67077834 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-4379A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077834 | |||||||
| chr16:67077947 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.400-4266G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67077947 | |||||||
| chr16:67078050 | T | C | 33 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(30): Show |
33 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.400-4163T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67078050 | |||||||
| chr16:67078270 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.400-3943G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67078270 | |||||||
| chr16:67078504 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.400-3709C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67078504 | |||||||
| chr16:67078705 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-3508A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67078705 | |||||||
| chr16:67078899 | C | T | 98 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(95): Show |
98 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.400-3314C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67078899 | |||||||
| chr16:67079005 | A | T | 1 | a0001c0001t0004g0202 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.400-3208A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079005 | |||||||
| chr16:67079044 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.400-3169T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079044 | |||||||
| chr16:67079063 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0064 |
2 | NA19060.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.400-3150T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079063 | |||||||
| chr16:67079251 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.400-2962A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079251 | |||||||
| chr16:67079275 | A | G | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-2938A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079275 | |||||||
| chr16:67079515 | C | CT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0055 others(58): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.400-2675dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67079515 | ||||||
| chr16:67079515 | C | CTT | 22 | a0001c0001t0001g0156 a0001c0001t0004g0198 a0001c0001t0004g0199 others(19): Show |
22 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.400-2676_400-2675d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67079515 | ||||||
| chr16:67079515 | CT | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(10): Show |
13 | HG00140.hp2 HG00558.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-2675delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67079515 | ||||||
| chr16:67079515 | CTT | C | 22 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0009 others(19): Show |
22 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.400-2676_400-2675d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67079515 | ||||||
| chr16:67079952 | G | C | 17 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(14): Show |
17 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-2261G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079952 | |||||||
| chr16:67079962 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-2251A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67079962 | |||||||
| chr16:67080069 | G | T | 1 | a0001c0001t0002g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.400-2144G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080069 | |||||||
| chr16:67080228 | C | CGATGGCT others(17): Show |
1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-1982_400-1959d others(26): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67080228 | ||||||
| chr16:67080241 | G | T | 1 | a0001c0001t0004g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-1972G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080241 | |||||||
| chr16:67080267 | T | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-1946T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080267 | |||||||
| chr16:67080287 | T | TGAGGAGA others(28): Show |
1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.400-1924_400-1890d others(37): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67080287 | ||||||
| chr16:67080427 | G | A | 23 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(20): Show |
23 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.400-1786G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080427 | |||||||
| chr16:67080480 | G | GA | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-1724dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67080480 | ||||||
| chr16:67080554 | T | C | 44 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(41): Show |
44 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.400-1659T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080554 | |||||||
| chr16:67080963 | A | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG02071.hp1 HG02074.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-1250A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080963 | |||||||
| chr16:67080990 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.400-1223A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67080990 | |||||||
| chr16:67081024 | T | C | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.400-1189T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081024 | |||||||
| chr16:67081249 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.400-964A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081249 | |||||||
| chr16:67081572 | C | T | 1 | a0001c0001t0009g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-641C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081572 | |||||||
| chr16:67081731 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | HG03927.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.400-482G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081731 | |||||||
| chr16:67081800 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.400-413T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081800 | |||||||
| chr16:67081803 | CAG | C | 2 | a0001c0002t0003g0007 a0001c0002t0003g0008 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.400-407_400-406del others(2): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67081803 | ||||||
| chr16:67081821 | C | CT | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-381dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67081821 | ||||||
| chr16:67081833 | C | CT | 9 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0191 others(6): Show |
9 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-371dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67081833 | ||||||
| chr16:67081837 | T | C | 1 | a0001c0001t0008g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400-376T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081837 | |||||||
| chr16:67081869 | G | A | 1 | a0001c0001t0005g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.400-344G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67081869 | |||||||
| chr16:67082007 | T | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG01074.hp2 HG01192.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-206T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67082007 | |||||||
| chr16:67082071 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.400-142G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67082071 | |||||||
| chr16:67082114 | C | T | 3 | a0001c0002t0003g0040 a0001c0002t0003g0041 a0001c0002t0003g0042 |
3 | HG02451.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400-99C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67082114 | |||||||
| chr16:67082129 | G | GA | 24 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0067 others(21): Show |
24 | HG00741.hp1 HG01884.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.400-68dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67082129 | ||||||
| chr16:67082129 | GA | G | 22 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0159 others(19): Show |
22 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.400-68delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 67082129 | ||||||
| chr16:67082140 | A | C | 2 | a0001c0001t0004g0198 a0001c0001t0004g0209 |
2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.400-73A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67082140 | |||||||
| chr16:67082141 | A | C | 2 | a0001c0001t0001g0084 a0001c0001t0005g0190 |
2 | HG01109.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.400-72A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 4/5 | chr16 | 67082141 | |||||||
| chr16:67082452 | G | A | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.495+144G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67082452 | |||||||
| chr16:67082521 | T | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+213T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67082521 | |||||||
| chr16:67082864 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.495+556A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67082864 | |||||||
| chr16:67083110 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.495+802T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083110 | |||||||
| chr16:67083186 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.495+878T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083186 | |||||||
| chr16:67083205 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.495+897T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083205 | |||||||
| chr16:67083298 | A | AT | 11 | a0001c0001t0001g0119 a0001c0001t0001g0183 a0001c0001t0002g0006 others(8): Show |
11 | HG00738.hp2 HG01109.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1005dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67083298 | ||||||
| chr16:67083577 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.495+1269C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083577 | |||||||
| chr16:67083632 | G | T | 1 | a0001c0001t0002g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.495+1324G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083632 | |||||||
| chr16:67083698 | C | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+1390C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083698 | |||||||
| chr16:67083923 | C | CT | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1618dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67083923 | ||||||
| chr16:67083959 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.495+1651G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67083959 | |||||||
| chr16:67084165 | C | CA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0029 others(102): Show |
105 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.495+1881dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | C | CAA | 16 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0067 others(13): Show |
16 | HG00140.hp1 HG00621.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1880_495+1881d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | C | CAAA | 14 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0004g0198 others(11): Show |
14 | HG01433.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+1879_495+1881d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | C | CAAAAAAA | 13 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(10): Show |
13 | HG02257.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+1875_495+1881d others(9): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0011 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1874_495+1881d others(10): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.495+1872_495+1881d others(12): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | CAAAA | C | 15 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0040 others(12): Show |
15 | HG00738.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.495+1878_495+1881d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084165 | CAAAAA | C | 6 | a0001c0002t0003g0038 a0001c0002t0003g0039 a0001c0002t0003g0044 others(3): Show |
6 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1877_495+1881d others(7): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67084165 | ||||||
| chr16:67084301 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+1993C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084301 | |||||||
| chr16:67084423 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.495+2115G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084423 | |||||||
| chr16:67084650 | C | T | 16 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+2342C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084650 | |||||||
| chr16:67084780 | C | T | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.495+2472C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084780 | |||||||
| chr16:67084986 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.495+2678A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084986 | |||||||
| chr16:67084995 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.495+2687G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67084995 | |||||||
| chr16:67085040 | ATTAT | A | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.495+2736_495+2739d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085040 | ||||||
| chr16:67085142 | T | TTGTG | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.495+2850_495+2853d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085142 | ||||||
| chr16:67085152 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+2866_495+2877d others(14): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085152 | ||||||
| chr16:67085356 | C | G | 26 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(23): Show |
26 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.495+3048C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085356 | |||||||
| chr16:67085501 | T | TG | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.495+3198dupG | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085501 | ||||||
| chr16:67085504 | G | GA | 3 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0148 |
3 | HG02809.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.495+3196_495+3197i others(3): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085504 | |||||||
| chr16:67085514 | A | G | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.495+3206A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085514 | |||||||
| chr16:67085616 | T | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+3308T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085616 | |||||||
| chr16:67085628 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.495+3320G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085628 | |||||||
| chr16:67085634 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.495+3326A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085634 | |||||||
| chr16:67085659 | C | T | 2 | a0001c0001t0009g0185 a0001c0001t0009g0187 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.495+3351C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085659 | |||||||
| chr16:67085673 | C | CT | 22 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0001g0070 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.495+3387dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085673 | ||||||
| chr16:67085673 | C | CTTTT | 10 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+3384_495+3387d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085673 | ||||||
| chr16:67085673 | CT | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0087 a0001c0001t0001g0106 others(4): Show |
7 | HG01993.hp1 HG01993.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+3387delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085673 | ||||||
| chr16:67085740 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+3432C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085740 | |||||||
| chr16:67085823 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.495+3515G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085823 | |||||||
| chr16:67085853 | AT | A | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG00140.hp1 HG00140.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.495+3551delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67085853 | ||||||
| chr16:67085880 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.495+3572G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085880 | |||||||
| chr16:67085889 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.495+3581A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67085889 | |||||||
| chr16:67086055 | A | C | 1 | a0001c0001t0004g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495+3747A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67086055 | |||||||
| chr16:67086057 | G | A | 1 | a0001c0002t0003g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+3749G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67086057 | |||||||
| chr16:67086450 | T | TTTGTGCC others(4): Show |
1 | a0001c0001t0001g0176 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.495+4143_495+4153d others(13): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67086450 | ||||||
| chr16:67086812 | T | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(100): Show |
103 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.495+4504T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67086812 | |||||||
| chr16:67087001 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.495+4693A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087001 | |||||||
| chr16:67087027 | A | G | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+4719A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087027 | |||||||
| chr16:67087154 | G | C | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+4846G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087154 | |||||||
| chr16:67087272 | T | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+4964T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087272 | |||||||
| chr16:67087274 | T | G | 1 | a0001c0001t0002g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495+4966T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087274 | |||||||
| chr16:67087275 | A | T | 1 | a0001c0001t0002g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495+4967A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087275 | |||||||
| chr16:67087409 | A | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+5101A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087409 | |||||||
| chr16:67087745 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0010g0071 |
3 | HG00741.hp2 HG01192.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.495+5437T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087745 | |||||||
| chr16:67087919 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG02071.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.495+5611A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087919 | |||||||
| chr16:67087943 | G | T | 1 | a0001c0001t0008g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.495+5635G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67087943 | |||||||
| chr16:67088028 | C | G | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+5720C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088028 | |||||||
| chr16:67088162 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.495+5854C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088162 | |||||||
| chr16:67088174 | A | G | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.495+5866A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088174 | |||||||
| chr16:67088196 | TTG | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0171 |
3 | NA18992.hp2 NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.495+5894_495+5895d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67088196 | ||||||
| chr16:67088319 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.495+6011A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088319 | |||||||
| chr16:67088529 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.495+6221C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088529 | |||||||
| chr16:67088571 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0005g0197 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+6263G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088571 | |||||||
| chr16:67088640 | A | G | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+6332A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088640 | |||||||
| chr16:67088777 | A | G | 1 | a0001c0001t0011g0095 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.495+6469A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088777 | |||||||
| chr16:67088880 | A | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+6572A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088880 | |||||||
| chr16:67088891 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.495+6583G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67088891 | |||||||
| chr16:67089338 | C | G | 95 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0055 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.495+7030C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67089338 | |||||||
| chr16:67089938 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.495+7630A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67089938 | |||||||
| chr16:67089993 | A | G | 1 | a0001c0001t0009g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.495+7685A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67089993 | |||||||
| chr16:67090023 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(98): Show |
101 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.495+7715C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67090023 | |||||||
| chr16:67090228 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.495+7920C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67090228 | |||||||
| chr16:67090281 | C | A | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.495+7973C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67090281 | |||||||
| chr16:67090928 | G | A | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.496-7782G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67090928 | |||||||
| chr16:67091117 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.496-7593G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091117 | |||||||
| chr16:67091161 | C | T | 11 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-7549C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091161 | |||||||
| chr16:67091453 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.496-7257A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091453 | |||||||
| chr16:67091615 | A | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0009 |
3 | HG01884.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.496-7095A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091615 | |||||||
| chr16:67091654 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.496-7056C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091654 | |||||||
| chr16:67091734 | T | A | 47 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(44): Show |
47 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.496-6976T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091734 | |||||||
| chr16:67091742 | T | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-6968T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091742 | |||||||
| chr16:67091796 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.496-6914A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091796 | |||||||
| chr16:67091823 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.496-6887T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67091823 | |||||||
| chr16:67091861 | G | GTTGT | 2 | a0001c0001t0001g0127 a0001c0001t0005g0190 |
2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.496-6826_496-6823d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67091861 | ||||||
| chr16:67091861 | GT | G | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-6847delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67091861 | ||||||
| chr16:67091861 | GTTGT | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0065 |
3 | HG01433.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.496-6826_496-6823d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67091861 | ||||||
| chr16:67092048 | TCTCC | T | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496-6656_496-6653d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092048 | ||||||
| chr16:67092054 | T | G | 1 | a0001c0001t0005g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.496-6656T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092054 | |||||||
| chr16:67092221 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.496-6489G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092221 | |||||||
| chr16:67092416 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0009 |
3 | HG01884.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.496-6294C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092416 | |||||||
| chr16:67092453 | T | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0010 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496-6257T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092453 | |||||||
| chr16:67092524 | T | C | 1 | a0001c0001t0004g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.496-6186T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092524 | |||||||
| chr16:67092696 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0005g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.496-6013_496-6012i others(15): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092696 | ||||||
| chr16:67092696 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0005g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.496-6013_496-6012i others(21): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092696 | ||||||
| chr16:67092698 | C | CT | 6 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
6 | HG00438.hp1 HG00438.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-5980dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.496-5996_496-5980d others(19): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0013g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.496-5997_496-5980d others(20): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.496-6003_496-5980d others(26): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.496-6006_496-5980d others(29): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.496-6007_496-5980d others(30): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0014 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.496-6009_496-5980d others(32): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0002g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.496-6010_496-5980d others(33): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0002g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.496-5980_496-5979i others(38): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0001g0033 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.496-5980_496-5979i others(44): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | C | T | 9 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(6): Show |
9 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-6012C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092698 | |||||||
| chr16:67092698 | CT | C | 35 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0068 others(32): Show |
35 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.496-5980delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | CTT | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(65): Show |
69 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.496-5981_496-5980d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | CTTT | C | 7 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0106 others(4): Show |
7 | HG01069.hp2 HG01433.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-5982_496-5980d others(5): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | CTTTTT | C | 11 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG01884.hp1 HG02074.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-5984_496-5980d others(7): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | CTTTTTT | C | 21 | a0001c0001t0001g0101 a0001c0001t0002g0010 a0001c0001t0004g0207 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.496-5985_496-5980d others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092698 | CTTTTTTT | C | 14 | a0001c0001t0001g0158 a0001c0001t0002g0006 a0001c0001t0004g0198 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.496-5986_496-5980d others(9): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67092698 | ||||||
| chr16:67092781 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-5929C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092781 | |||||||
| chr16:67092837 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.496-5873C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67092837 | |||||||
| chr16:67093126 | T | G | 1 | a0001c0001t0009g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-5584T>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67093126 | |||||||
| chr16:67093201 | C | T | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-5509C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67093201 | |||||||
| chr16:67093368 | G | GT | 27 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0061 others(24): Show |
27 | HG00438.hp1 HG01074.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.496-5316dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67093368 | ||||||
| chr16:67093368 | G | GTT | 8 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
8 | HG00438.hp2 HG02071.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-5317_496-5316d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67093368 | ||||||
| chr16:67093368 | GT | G | 26 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0087 others(23): Show |
26 | HG00741.hp2 HG01069.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.496-5316delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67093368 | ||||||
| chr16:67093368 | GTT | G | 19 | a0001c0001t0004g0198 a0001c0001t0004g0200 a0001c0001t0004g0201 others(16): Show |
19 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.496-5317_496-5316d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67093368 | ||||||
| chr16:67093368 | GTTTT | G | 21 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0038 others(18): Show |
21 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.496-5319_496-5316d others(6): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67093368 | ||||||
| chr16:67093455 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.496-5255C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67093455 | |||||||
| chr16:67093458 | C | T | 1 | a0001c0002t0003g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.496-5252C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67093458 | |||||||
| chr16:67093726 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.496-4984C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67093726 | |||||||
| chr16:67094117 | C | CT | 5 | a0001c0001t0005g0188 a0001c0001t0005g0190 a0001c0001t0005g0193 others(2): Show |
5 | HG01109.hp1 HG01952.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-4572dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67094117 | ||||||
| chr16:67094117 | CT | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(63): Show |
66 | HG00140.hp1 HG01361.hp1 HG01433.hp1 others(63): Show |
intron_variant | MODIFIER | c.496-4572delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67094117 | ||||||
| chr16:67094178 | G | T | 64 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(61): Show |
64 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.496-4532G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67094178 | |||||||
| chr16:67094245 | A | G | 34 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(31): Show |
34 | HG00438.hp2 HG01884.hp1 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.496-4465A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67094245 | |||||||
| chr16:67094400 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.496-4310A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67094400 | |||||||
| chr16:67094446 | G | C | 10 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0190 others(7): Show |
10 | HG00140.hp2 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-4264G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67094446 | |||||||
| chr16:67095014 | T | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3696T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095014 | |||||||
| chr16:67095022 | C | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-3688C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095022 | |||||||
| chr16:67095053 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.496-3657A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095053 | |||||||
| chr16:67095206 | G | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3504G>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095206 | |||||||
| chr16:67095208 | C | CA | 2 | a0001c0001t0004g0205 a0001c0001t0004g0207 |
2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.496-3502_496-3501i others(3): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095208 | |||||||
| chr16:67095209 | T | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3501T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095209 | |||||||
| chr16:67095210 | C | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3500C>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095210 | |||||||
| chr16:67095210 | C | CA | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0054 others(77): Show |
80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.496-3474dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67095210 | ||||||
| chr16:67095210 | C | CAA | 9 | a0001c0001t0001g0083 a0001c0001t0001g0116 a0001c0001t0001g0148 others(6): Show |
9 | HG02080.hp1 HG02602.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-3475_496-3474d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67095210 | ||||||
| chr16:67095210 | CA | C | 15 | a0001c0001t0001g0155 a0001c0001t0002g0004 a0001c0001t0002g0005 others(12): Show |
15 | HG01884.hp2 HG01943.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.496-3474delA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67095210 | ||||||
| chr16:67095384 | C | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.496-3326C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095384 | |||||||
| chr16:67095497 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.496-3213C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095497 | |||||||
| chr16:67095629 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.496-3081A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095629 | |||||||
| chr16:67095690 | G | GT | 23 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0075 others(20): Show |
23 | HG00438.hp1 HG00609.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.496-3002dupT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67095690 | ||||||
| chr16:67095690 | GT | G | 13 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
13 | HG01071.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3002delT | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67095690 | ||||||
| chr16:67095754 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.496-2956A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095754 | |||||||
| chr16:67095799 | C | T | 23 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(20): Show |
23 | HG00140.hp2 HG01109.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.496-2911C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095799 | |||||||
| chr16:67095912 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.496-2798G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095912 | |||||||
| chr16:67095922 | C | T | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-2788C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095922 | |||||||
| chr16:67095993 | G | A | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-2717G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67095993 | |||||||
| chr16:67096050 | T | C | 13 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(10): Show |
13 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-2660T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096050 | |||||||
| chr16:67096078 | G | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-2632G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096078 | |||||||
| chr16:67096266 | G | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(8): Show |
11 | HG00438.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2444G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096266 | |||||||
| chr16:67096320 | A | T | 16 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(13): Show |
16 | HG00140.hp2 HG01109.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.496-2390A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096320 | |||||||
| chr16:67096330 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.496-2380A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096330 | |||||||
| chr16:67096378 | C | T | 1 | a0001c0001t0011g0095 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.496-2332C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096378 | |||||||
| chr16:67096466 | C | CAT | 10 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01884.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-2233_496-2232d others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67096466 | ||||||
| chr16:67096679 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.496-2031T>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096679 | |||||||
| chr16:67096866 | C | T | 1 | a0001c0001t0007g0211 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.496-1844C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096866 | |||||||
| chr16:67096883 | G | A | 32 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(29): Show |
32 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.496-1827G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096883 | |||||||
| chr16:67096925 | C | CA | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0139 others(6): Show |
9 | HG00621.hp1 HG00621.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-1767dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67096925 | ||||||
| chr16:67096947 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496-1763A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096947 | |||||||
| chr16:67096951 | G | T | 1 | a0001c0001t0005g0188 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.496-1759G>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67096951 | |||||||
| chr16:67097022 | C | G | 15 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(12): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.496-1688C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67097022 | |||||||
| chr16:67097271 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.496-1439C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67097271 | |||||||
| chr16:67097535 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.496-1175A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67097535 | |||||||
| chr16:67097545 | C | CA | 8 | a0001c0001t0001g0062 a0001c0001t0001g0084 a0001c0001t0001g0092 others(5): Show |
8 | HG02055.hp2 HG02809.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-1147dupA | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67097545 | ||||||
| chr16:67097698 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0033 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.496-1012T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67097698 | |||||||
| chr16:67097738 | C | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.496-972C>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67097738 | |||||||
| chr16:67098021 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.496-689A>G | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098021 | |||||||
| chr16:67098038 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.496-672T>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098038 | |||||||
| chr16:67098055 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.496-655A>C | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098055 | |||||||
| chr16:67098114 | TTTTG | T | 26 | a0001c0001t0001g0062 a0001c0001t0002g0019 a0001c0001t0002g0020 others(23): Show |
26 | HG00609.hp1 HG00738.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.496-564_496-561del others(4): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67098114 | ||||||
| chr16:67098114 | TTTTGTTT others(1): Show |
T | 33 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(30): Show |
33 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.496-568_496-561del others(8): Show |
CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr16 | 67098114 | ||||||
| chr16:67098218 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.496-492C>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098218 | |||||||
| chr16:67098421 | G | A | 3 | a0001c0001t0009g0185 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02257.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496-289G>A | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098421 | |||||||
| chr16:67098545 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.496-165A>T | CBFB | ENSG00000067955.15 | transcript | ENST00000412916.7 | protein_coding | 5/5 | chr16 | 67098545 |