Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4603 |
| ensemblid | ENSG00000185697.17 |
| hgncid | 7547 |
| symbol | MYBL1 |
| name | MYB proto-oncogene like 1 |
| refseq_nuc | NM_001080416.4 |
| refseq_prot | NP_001073885.1 |
| ensembl_nuc | ENST00000522677.8 |
| ensembl_prot | ENSP00000429633.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 66562175 |
| end | 66613218 |
| strand | - |
| ver | v1.2 |
| region | chr8:66562175-66613218 |
| region5000 | chr8:66557175-66618218 |
| regionname0 | MYBL1_chr8_66562175_66613218 |
| regionname5000 | MYBL1_chr8_66557175_66618218 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 752 | 234 | 77 | 23 | 83 | 14 | 35 | 60 | MYBL1_chr8_66557175_66618218 | MYBL1 | MAKRS others(747): Show |
chr8 | 66557175 | 66618218 |
| a0002 | 0/0 | 752 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | MAKRS others(747): Show |
chr8 | 66557175 | 66618218 |
| a0003 | 0/0 | 752 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | MAKRS others(747): Show |
chr8 | 66557175 | 66618218 |
| a0004 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | MAKRS others(747): Show |
chr8 | 66557175 | 66618218 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2256 | 231 | 74 | 23 | 83 | 14 | 35 | MYBL1_chr8_66557175_66618218 | MYBL1 | ATGGC others(2251): Show |
chr8 | 66557175 | 66618218 | ||
| a0001c0002 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | ATGGC others(2251): Show |
chr8 | 66557175 | 66618218 | ||
| a0002c0003 | 0/0 | 2256 | 2 | 0 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | ATGGC others(2251): Show |
chr8 | 66557175 | 66618218 | ||
| a0003c0005 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | ATGGC others(2251): Show |
chr8 | 66557175 | 66618218 | ||
| a0004c0004 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | ATGGC others(2251): Show |
chr8 | 66557175 | 66618218 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5161 | 158 | 33 | 22 | 62 | 13 | 26 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0002 | 0/0 | 5161 | 24 | 4 | 0 | 14 | 0 | 6 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0003 | 0/0 | 5161 | 16 | 16 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0004 | 0/0 | 5157 | 6 | 6 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5152): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0005 | 0/0 | 5161 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0006 | 0/0 | 5161 | 5 | 5 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0007 | 0/0 | 5161 | 4 | 0 | 1 | 0 | 1 | 2 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0008 | 0/0 | 5161 | 4 | 0 | 0 | 4 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0009 | 0/0 | 5161 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0010 | 0/0 | 5161 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0011 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0012 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0013 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0014 | 0/0 | 5161 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0001t0015 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0001c0002t0003 | 0/0 | 5161 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0002c0003t0003 | 0/0 | 5161 | 2 | 0 | 0 | 1 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0003c0005t0001 | 0/0 | 5161 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| a0004c0004t0003 | 0/0 | 5161 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | GCAGA others(5156): Show |
chr8 | 66557175 | 66618218 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0010g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0014g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0001t0015g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0003c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| a0004c0004t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0095 | EUR | FIN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01081 | hp1 | a0003 | c0005 | t0001 | g0129 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0080 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0076 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02132 | hp1 | a0001 | c0001 | t0012 | g0019 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02165 | hp2 | a0001 | c0001 | t0009 | g0099 | EAS | CDX | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02523 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | KHV | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02683 | hp1 | a0002 | c0003 | t0003 | g0032 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02809 | hp1 | a0004 | c0004 | t0003 | g0042 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0218 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0086 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0081 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03492 | hp2 | a0001 | c0001 | t0014 | g0139 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0209 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0087 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19011 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ASW | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | GIH | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0217 | AFR | MSL | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | USA | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0187 | REF | REF | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0195 | REF | REF | MYBL1_chr8_66557175_66618218 | MYBL1 | chr8 | 66557175 | 66618218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66566196 | T | G | 1 | a0002 | 2 | HG02523.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.1998A>C | p.Glu666Asp | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/16 | 2378/5161 | 1998/2259 | 666/752 | chr8 | 66566196 | |||
| chr8:66573455 | A | G | 1 | a0003 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1522T>C | p.Phe508Leu | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/16 | 1902/5161 | 1522/2259 | 508/752 | chr8 | 66573455 | |||
| chr8:66593128 | A | T | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.754T>A | p.Phe252Ile | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 7/16 | 1134/5161 | 754/2259 | 252/752 | chr8 | 66593128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66592542 | T | C | 2 | a0001c0002 a0004c0004 |
4 | HG02109.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.765A>G | p.Gln255Gln | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/16 | 1145/5161 | 765/2259 | 255/752 | chr8 | 66592542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66562694 | C | A | 1 | a0001c0001t0014 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 2003 | chr8 | 66562694 | ||||||
| chr8:66562741 | G | C | 1 | a0001c0001t0006 | 5 | HG02615.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1956C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1956 | chr8 | 66562741 | ||||||
| chr8:66562854 | CTATT | C | 1 | a0001c0001t0004 | 6 | HG02622.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1839_*1842delAATA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1839 | chr8 | 66562854 | ||||||
| chr8:66562937 | A | T | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1760 | chr8 | 66562937 | ||||||
| chr8:66562968 | T | C | 1 | a0001c0001t0015 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1729 | chr8 | 66562968 | ||||||
| chr8:66563066 | A | G | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(4): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1631T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1631 | chr8 | 66563066 | ||||||
| chr8:66563097 | T | C | 1 | a0001c0001t0008 | 4 | HG00408.hp1 HG02015.hp2 NA18970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1600A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 1600 | chr8 | 66563097 | ||||||
| chr8:66563815 | T | C | 1 | a0001c0001t0002 | 24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*882A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 882 | chr8 | 66563815 | ||||||
| chr8:66563836 | T | C | 1 | a0001c0001t0009 | 2 | HG02165.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*861A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 861 | chr8 | 66563836 | ||||||
| chr8:66564048 | G | T | 1 | a0001c0001t0007 | 4 | HG00323.hp2 HG01433.hp1 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*649C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 16/16 | 649 | chr8 | 66564048 | ||||||
| chr8:66612993 | C | T | 1 | a0001c0001t0012 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-155G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 155 | chr8 | 66612993 | ||||||
| chr8:66613163 | C | T | 1 | a0001c0001t0011 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-325G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 325 | chr8 | 66613163 | ||||||
| chr8:66613179 | G | A | 1 | a0001c0001t0010 | 2 | HG03453.hp2 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-341C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 341 | chr8 | 66613179 | ||||||
| chr8:66613198 | C | T | 1 | a0001c0001t0005 | 5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-360G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/16 | 360 | chr8 | 66613198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:66565413 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2131-588C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565413 | |||||||
| chr8:66565451 | TTGCCAAA others(15): Show |
T | 1 | a0001c0001t0001g0202 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2130+591_2130+612d others(24): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565451 | |||||||
| chr8:66565550 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2130+514T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565550 | |||||||
| chr8:66565630 | GA | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2130+433delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 15/15 | chr8 | 66565630 | |||||||
| chr8:66566323 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0210 |
2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1951-80C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566323 | |||||||
| chr8:66566501 | A | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1950+183T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566501 | |||||||
| chr8:66566663 | C | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1950+21G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 14/15 | chr8 | 66566663 | |||||||
| chr8:66566863 | A | G | 1 | a0003c0005t0001g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1845+13T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 13/15 | chr8 | 66566863 | |||||||
| chr8:66567133 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1729-141T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567133 | |||||||
| chr8:66567410 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1729-418G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567410 | |||||||
| chr8:66567526 | A | AGAGT | 3 | a0001c0001t0006g0007 a0001c0001t0006g0063 a0001c0001t0006g0064 |
4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729-535_1729-534i others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | |||||||
| chr8:66567526 | A | AGT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
23 | HG01070.hp1 HG01071.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1729-536_1729-535d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | |||||||
| chr8:66567526 | A | AGTGT | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1729-538_1729-535d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | |||||||
| chr8:66567526 | AGT | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-536_1729-535d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567526 | |||||||
| chr8:66567528 | T | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(27): Show |
36 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1729-536A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567528 | |||||||
| chr8:66567530 | T | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-538A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567530 | |||||||
| chr8:66567565 | T | C | 2 | a0001c0001t0002g0052 a0001c0001t0002g0054 |
2 | NA18961.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1729-573A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567565 | |||||||
| chr8:66567576 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0135 |
2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1729-584C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567576 | |||||||
| chr8:66567907 | C | A | 1 | a0001c0001t0003g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1729-915G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66567907 | |||||||
| chr8:66568042 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1729-1050C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568042 | |||||||
| chr8:66568046 | C | CA | 14 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG00423.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1729-1055dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568046 | |||||||
| chr8:66568060 | A | C | 1 | a0001c0001t0015g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1729-1068T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568060 | |||||||
| chr8:66568063 | C | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-1071G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568063 | |||||||
| chr8:66568748 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1729-1756G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568748 | |||||||
| chr8:66568791 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1729-1799G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568791 | |||||||
| chr8:66568808 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1729-1816G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568808 | |||||||
| chr8:66568854 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1729-1862C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66568854 | |||||||
| chr8:66569322 | C | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1729-2330G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569322 | |||||||
| chr8:66569339 | C | CT | 13 | a0001c0001t0002g0051 a0001c0001t0003g0034 a0001c0001t0003g0036 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1729-2348dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569339 | |||||||
| chr8:66569339 | CT | C | 6 | a0001c0001t0001g0029 a0001c0001t0003g0044 a0001c0001t0003g0045 others(3): Show |
6 | HG01884.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-2348delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569339 | |||||||
| chr8:66569582 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1729-2590G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569582 | |||||||
| chr8:66569726 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1729-2734T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569726 | |||||||
| chr8:66569781 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1728+2701C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66569781 | |||||||
| chr8:66570065 | G | A | 1 | a0001c0001t0006g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1728+2417C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570065 | |||||||
| chr8:66570111 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1728+2371A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570111 | |||||||
| chr8:66570312 | CT | C | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1728+2169delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570312 | |||||||
| chr8:66570490 | C | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1728+1992G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570490 | |||||||
| chr8:66570769 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1728+1713C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570769 | |||||||
| chr8:66570869 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1728+1613G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66570869 | |||||||
| chr8:66571013 | G | C | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1728+1469C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571013 | |||||||
| chr8:66571201 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1728+1281A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571201 | |||||||
| chr8:66571489 | T | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1728+993A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571489 | |||||||
| chr8:66571665 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1728+817C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571665 | |||||||
| chr8:66571719 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1728+763T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571719 | |||||||
| chr8:66571729 | A | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0058 |
2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1728+753T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571729 | |||||||
| chr8:66571750 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1728+732C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571750 | |||||||
| chr8:66571813 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0005g0013 a0001c0001t0005g0015 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+669C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571813 | |||||||
| chr8:66571892 | GAA | G | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1728+588_1728+589d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66571892 | |||||||
| chr8:66572080 | G | T | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1728+402C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572080 | |||||||
| chr8:66572094 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1728+388A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572094 | |||||||
| chr8:66572147 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1728+335G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572147 | |||||||
| chr8:66572340 | A | C | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1728+142T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572340 | |||||||
| chr8:66572382 | A | C | 3 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0001c0001t0004g0205 |
3 | HG02622.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1728+100T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 12/15 | chr8 | 66572382 | |||||||
| chr8:66572864 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1614-268T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66572864 | |||||||
| chr8:66573060 | C | A | 1 | a0002c0003t0003g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1613+304G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573060 | |||||||
| chr8:66573060 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0182 |
3 | NA18957.hp2 NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1613+304G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573060 | |||||||
| chr8:66573151 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1613+213A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 11/15 | chr8 | 66573151 | |||||||
| chr8:66573957 | T | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1471-451A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573957 | |||||||
| chr8:66573970 | C | CTGGCAAA others(5): Show |
7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-465_1471-464i others(14): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573970 | |||||||
| chr8:66573976 | T | C | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-470A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573976 | |||||||
| chr8:66573977 | G | A | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-471C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573977 | |||||||
| chr8:66573978 | A | G | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-472T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573978 | |||||||
| chr8:66573979 | T | A | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-473A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573979 | |||||||
| chr8:66573980 | A | C | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-474T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66573980 | |||||||
| chr8:66574077 | T | C | 1 | a0001c0001t0006g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1471-571A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574077 | |||||||
| chr8:66574101 | A | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1471-595T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574101 | |||||||
| chr8:66574149 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
7 | NA18952.hp1 NA18957.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1471-643C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574149 | |||||||
| chr8:66574261 | C | T | 1 | a0001c0001t0015g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1471-755G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574261 | |||||||
| chr8:66574662 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1471-1156A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574662 | |||||||
| chr8:66574680 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0072 others(37): Show |
43 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1471-1174A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574680 | |||||||
| chr8:66574821 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1470+1186C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574821 | |||||||
| chr8:66574826 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1470+1181C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66574826 | |||||||
| chr8:66575072 | C | A | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1470+935G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575072 | |||||||
| chr8:66575267 | AC | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1470+739delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575267 | |||||||
| chr8:66575319 | T | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1470+688A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575319 | |||||||
| chr8:66575362 | C | T | 3 | a0001c0001t0006g0007 a0001c0001t0006g0063 a0001c0001t0006g0064 |
4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1470+645G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575362 | |||||||
| chr8:66575363 | G | A | 1 | a0001c0001t0008g0076 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1470+644C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575363 | |||||||
| chr8:66575407 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1470+600T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575407 | |||||||
| chr8:66575473 | A | C | 3 | a0001c0001t0006g0007 a0001c0001t0006g0063 a0001c0001t0006g0064 |
4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1470+534T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575473 | |||||||
| chr8:66575704 | C | CA | 2 | a0001c0001t0001g0101 a0001c0001t0001g0107 |
2 | NA18982.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1470+302dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575704 | |||||||
| chr8:66575741 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1470+266C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575741 | |||||||
| chr8:66575766 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1470+241C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575766 | |||||||
| chr8:66575816 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1470+191T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575816 | |||||||
| chr8:66575961 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1470+46C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 10/15 | chr8 | 66575961 | |||||||
| chr8:66576575 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1102-200A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576575 | |||||||
| chr8:66576687 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1102-312G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576687 | |||||||
| chr8:66576689 | T | G | 20 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
26 | HG02523.hp2 HG02683.hp1 HG02738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1102-314A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576689 | |||||||
| chr8:66576833 | T | C | 1 | a0002c0003t0003g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1102-458A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576833 | |||||||
| chr8:66576926 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0168 |
2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1102-551G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66576926 | |||||||
| chr8:66577134 | G | A | 1 | a0002c0003t0003g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1102-759C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577134 | |||||||
| chr8:66577238 | CAGG | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0151 |
3 | HG00099.hp2 HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1102-866_1102-864d others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577238 | |||||||
| chr8:66577525 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0174 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1102-1150G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577525 | |||||||
| chr8:66577582 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0109 |
2 | NA18992.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1102-1207A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577582 | |||||||
| chr8:66577603 | TC | T | 18 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.1102-1229delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577603 | |||||||
| chr8:66577634 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1102-1259C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577634 | |||||||
| chr8:66577995 | A | G | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1102-1620T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66577995 | |||||||
| chr8:66578024 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1102-1649G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578024 | |||||||
| chr8:66578128 | G | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1102-1753C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578128 | |||||||
| chr8:66578130 | G | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1102-1755C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578130 | |||||||
| chr8:66578170 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1102-1795T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578170 | |||||||
| chr8:66578523 | A | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0207 |
2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1101+1610T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578523 | |||||||
| chr8:66578530 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.1101+1603C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578530 | |||||||
| chr8:66578663 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1101+1470C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578663 | |||||||
| chr8:66578781 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101+1352T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66578781 | |||||||
| chr8:66579010 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1101+1123G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579010 | |||||||
| chr8:66579014 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1101+1119T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579014 | |||||||
| chr8:66579119 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0010g0217 a0001c0001t0010g0218 |
3 | HG03130.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1101+1014A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579119 | |||||||
| chr8:66579239 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1101+894T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579239 | |||||||
| chr8:66579246 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1101+887T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579246 | |||||||
| chr8:66579259 | T | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1101+874A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579259 | |||||||
| chr8:66579262 | TA | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0186 a0001c0001t0004g0125 |
3 | HG02895.hp2 NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1101+870delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579262 | |||||||
| chr8:66579263 | A | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1101+870T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579263 | |||||||
| chr8:66579264 | A | T | 53 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(50): Show |
60 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.1101+869T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579264 | |||||||
| chr8:66579265 | A | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1101+868T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579265 | |||||||
| chr8:66579266 | A | T | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1101+867T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579266 | |||||||
| chr8:66579410 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0197 |
2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1101+723T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579410 | |||||||
| chr8:66579635 | C | T | 1 | a0001c0001t0015g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1101+498G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579635 | |||||||
| chr8:66579648 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1101+485A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579648 | |||||||
| chr8:66579656 | T | TA | 46 | a0001c0001t0001g0172 a0001c0001t0002g0001 a0001c0001t0002g0005 others(43): Show |
53 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1101+476dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579656 | |||||||
| chr8:66579771 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1101+362A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579771 | |||||||
| chr8:66579979 | AC | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101+153delG | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66579979 | |||||||
| chr8:66580048 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1101+85A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66580048 | |||||||
| chr8:66580106 | T | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.1101+27A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 9/15 | chr8 | 66580106 | |||||||
| chr8:66580456 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-90G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580456 | |||||||
| chr8:66580702 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.868-336T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580702 | |||||||
| chr8:66580853 | CTCT | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0167 others(3): Show |
6 | HG01952.hp1 HG02155.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-490_868-488del others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66580853 | |||||||
| chr8:66581270 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-904C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581270 | |||||||
| chr8:66581301 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.868-935T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581301 | |||||||
| chr8:66581414 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-1048G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581414 | |||||||
| chr8:66581550 | G | A | 1 | a0001c0001t0010g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.868-1184C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581550 | |||||||
| chr8:66581566 | C | T | 18 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.868-1200G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66581566 | |||||||
| chr8:66582139 | C | T | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868-1773G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582139 | |||||||
| chr8:66582141 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.868-1775T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582141 | |||||||
| chr8:66582222 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-1856A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582222 | |||||||
| chr8:66582345 | G | T | 10 | a0001c0001t0003g0033 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-1979C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582345 | |||||||
| chr8:66582354 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.868-1988A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582354 | |||||||
| chr8:66582438 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.868-2072G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582438 | |||||||
| chr8:66582514 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0072 others(37): Show |
43 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.868-2148G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582514 | |||||||
| chr8:66582541 | C | CA | 31 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0091 others(28): Show |
36 | HG01433.hp1 HG01433.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.868-2176dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | |||||||
| chr8:66582541 | C | CAA | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0046 others(14): Show |
19 | HG00408.hp1 HG01884.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.868-2177_868-2176d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | |||||||
| chr8:66582541 | C | CAAA | 9 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-2178_868-2176d others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | |||||||
| chr8:66582541 | C | CAAAA | 5 | a0001c0001t0003g0039 a0001c0001t0013g0041 a0001c0002t0003g0068 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-2179_868-2176d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | |||||||
| chr8:66582541 | CA | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(69): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.868-2176delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582541 | |||||||
| chr8:66582648 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.868-2282C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582648 | |||||||
| chr8:66582650 | C | T | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.868-2284G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582650 | |||||||
| chr8:66582692 | TG | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-2327delC | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582692 | |||||||
| chr8:66582693 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-2327C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582693 | |||||||
| chr8:66582698 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-2332C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582698 | |||||||
| chr8:66582718 | C | CA | 14 | a0001c0001t0001g0073 a0001c0001t0001g0172 a0001c0001t0001g0174 others(11): Show |
14 | HG01884.hp2 HG02135.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-2353dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582718 | |||||||
| chr8:66582912 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.868-2546G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66582912 | |||||||
| chr8:66583398 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.868-3032G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583398 | |||||||
| chr8:66583500 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG01070.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.868-3134T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583500 | |||||||
| chr8:66583504 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG00099.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-3138T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583504 | |||||||
| chr8:66583535 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.868-3169T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583535 | |||||||
| chr8:66583554 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.868-3188C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583554 | |||||||
| chr8:66583599 | C | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.868-3233G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583599 | |||||||
| chr8:66583763 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.868-3397C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66583763 | |||||||
| chr8:66584070 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.868-3704G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584070 | |||||||
| chr8:66584404 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0140 others(1): Show |
4 | HG02572.hp1 HG02630.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-4038G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584404 | |||||||
| chr8:66584414 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.868-4048T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584414 | |||||||
| chr8:66584661 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.868-4295G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584661 | |||||||
| chr8:66584867 | C | T | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.868-4501G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584867 | |||||||
| chr8:66584954 | C | T | 3 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0016 |
3 | HG02451.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868-4588G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584954 | |||||||
| chr8:66584976 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-4610G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66584976 | |||||||
| chr8:66585088 | AAAAC | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.868-4726_868-4723d others(6): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585088 | |||||||
| chr8:66585139 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.868-4773G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585139 | |||||||
| chr8:66585158 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.868-4792A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585158 | |||||||
| chr8:66585264 | G | T | 5 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0059 others(2): Show |
5 | HG01884.hp2 HG03225.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-4898C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585264 | |||||||
| chr8:66585356 | T | TA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.868-4991dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585356 | |||||||
| chr8:66585490 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.868-5124G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585490 | |||||||
| chr8:66585496 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.868-5130A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585496 | |||||||
| chr8:66585528 | G | A | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868-5162C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585528 | |||||||
| chr8:66585684 | C | T | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0005g0015 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-5318G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585684 | |||||||
| chr8:66585690 | C | T | 1 | a0001c0001t0008g0076 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.868-5324G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585690 | |||||||
| chr8:66585783 | T | G | 1 | a0004c0004t0003g0042 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.868-5417A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66585783 | |||||||
| chr8:66586042 | G | GT | 48 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0115 others(45): Show |
55 | HG00423.hp2 HG01070.hp2 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.868-5677dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586042 | |||||||
| chr8:66586042 | G | GTT | 10 | a0001c0001t0002g0047 a0001c0001t0002g0058 a0001c0001t0003g0038 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.868-5678_868-5677d others(4): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586042 | |||||||
| chr8:66586053 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.868-5687A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586053 | |||||||
| chr8:66586507 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.867+5933T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586507 | |||||||
| chr8:66586672 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00140.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.867+5768G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586672 | |||||||
| chr8:66586894 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.867+5546G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586894 | |||||||
| chr8:66586954 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.867+5486A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586954 | |||||||
| chr8:66586989 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.867+5451A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66586989 | |||||||
| chr8:66587090 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0126 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+5350T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587090 | |||||||
| chr8:66587105 | C | A | 1 | a0001c0001t0004g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.867+5335G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587105 | |||||||
| chr8:66587399 | C | CA | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+5040dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587399 | |||||||
| chr8:66587520 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.867+4920G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587520 | |||||||
| chr8:66587691 | G | C | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+4749C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587691 | |||||||
| chr8:66587725 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.867+4715C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587725 | |||||||
| chr8:66587877 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867+4563A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587877 | |||||||
| chr8:66587996 | A | G | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+4444T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66587996 | |||||||
| chr8:66588145 | G | A | 8 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0166 others(5): Show |
8 | HG00423.hp2 HG00438.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.867+4295C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588145 | |||||||
| chr8:66588277 | C | CT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0157 a0001c0001t0001g0185 others(5): Show |
8 | HG00323.hp1 HG01071.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.867+4162dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588277 | |||||||
| chr8:66588277 | CT | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0093 others(12): Show |
15 | HG01433.hp1 HG01433.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+4162delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588277 | |||||||
| chr8:66588560 | G | A | 5 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0059 others(2): Show |
5 | HG01884.hp2 HG03225.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+3880C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588560 | |||||||
| chr8:66588715 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.867+3725A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588715 | |||||||
| chr8:66588791 | G | A | 8 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0043 others(5): Show |
13 | NA18946.hp1 NA18952.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.867+3649C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588791 | |||||||
| chr8:66588886 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0130 |
3 | HG02451.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.867+3554C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588886 | |||||||
| chr8:66588912 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.867+3528G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66588912 | |||||||
| chr8:66589026 | A | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.867+3414T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589026 | |||||||
| chr8:66589049 | G | T | 1 | a0001c0001t0003g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+3391C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589049 | |||||||
| chr8:66589067 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.867+3373A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589067 | |||||||
| chr8:66589172 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+3268A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589172 | |||||||
| chr8:66589401 | C | A | 1 | a0001c0001t0010g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.867+3039G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589401 | |||||||
| chr8:66589518 | T | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.867+2922A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589518 | |||||||
| chr8:66589617 | G | A | 48 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0001 others(45): Show |
55 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(52): Show |
intron_variant | MODIFIER | c.867+2823C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589617 | |||||||
| chr8:66589674 | G | A | 14 | a0001c0001t0003g0033 a0001c0001t0003g0044 a0001c0001t0003g0045 others(11): Show |
15 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.867+2766C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589674 | |||||||
| chr8:66589864 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.867+2576C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589864 | |||||||
| chr8:66589898 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.867+2542G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66589898 | |||||||
| chr8:66590018 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.867+2422C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590018 | |||||||
| chr8:66590082 | CCAAAA | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+2353_867+2357d others(7): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590082 | |||||||
| chr8:66590327 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.867+2113A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590327 | |||||||
| chr8:66590387 | G | A | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+2053C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590387 | |||||||
| chr8:66590601 | C | CA | 24 | a0001c0001t0001g0029 a0001c0001t0001g0142 a0001c0001t0001g0173 others(21): Show |
30 | HG00438.hp2 HG02738.hp1 HG02895.hp1 others(27): Show |
intron_variant | MODIFIER | c.867+1838dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66590601 | |||||||
| chr8:66591135 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.867+1305A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591135 | |||||||
| chr8:66591145 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
6 | NA18957.hp2 NA18983.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1295C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591145 | |||||||
| chr8:66591221 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+1219C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591221 | |||||||
| chr8:66591272 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.867+1168T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591272 | |||||||
| chr8:66591279 | G | A | 20 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
26 | HG02523.hp2 HG02683.hp1 HG02738.hp1 others(23): Show |
intron_variant | MODIFIER | c.867+1161C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591279 | |||||||
| chr8:66591359 | AT | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0142 a0001c0001t0001g0173 others(1): Show |
4 | HG00438.hp2 NA18961.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1080delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591359 | |||||||
| chr8:66591553 | A | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.867+887T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591553 | |||||||
| chr8:66591722 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.867+718A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591722 | |||||||
| chr8:66591818 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.867+622T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591818 | |||||||
| chr8:66591861 | A | T | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.867+579T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591861 | |||||||
| chr8:66591922 | T | C | 3 | a0001c0001t0006g0007 a0001c0001t0006g0063 a0001c0001t0006g0064 |
4 | HG02818.hp1 HG03041.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+518A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66591922 | |||||||
| chr8:66592097 | C | A | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.867+343G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 8/15 | chr8 | 66592097 | |||||||
| chr8:66593206 | T | A | 1 | a0001c0001t0014g0139 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.688-12A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593206 | |||||||
| chr8:66593342 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.688-148G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593342 | |||||||
| chr8:66593398 | G | A | 2 | a0001c0002t0003g0068 a0001c0002t0003g0069 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.688-204C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593398 | |||||||
| chr8:66593569 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.688-375T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593569 | |||||||
| chr8:66593858 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.688-664C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593858 | |||||||
| chr8:66593885 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.688-691G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593885 | |||||||
| chr8:66593907 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.688-713C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66593907 | |||||||
| chr8:66594292 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.688-1098A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594292 | |||||||
| chr8:66594437 | A | G | 2 | a0001c0002t0003g0068 a0001c0002t0003g0069 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.687+1146T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594437 | |||||||
| chr8:66594465 | C | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.687+1118G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594465 | |||||||
| chr8:66594558 | C | T | 18 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.687+1025G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66594558 | |||||||
| chr8:66595069 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.687+514A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595069 | |||||||
| chr8:66595123 | T | C | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.687+460A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595123 | |||||||
| chr8:66595420 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.687+163T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 6/15 | chr8 | 66595420 | |||||||
| chr8:66596140 | G | A | 10 | a0001c0001t0003g0033 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-383C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596140 | |||||||
| chr8:66596178 | G | A | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.513-421C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596178 | |||||||
| chr8:66596251 | C | T | 1 | a0002c0003t0003g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.513-494G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596251 | |||||||
| chr8:66596532 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513-775A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596532 | |||||||
| chr8:66596907 | A | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+423T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596907 | |||||||
| chr8:66596931 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.512+399A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596931 | |||||||
| chr8:66596967 | C | T | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.512+363G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 5/15 | chr8 | 66596967 | |||||||
| chr8:66597752 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.292-202T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597752 | |||||||
| chr8:66597847 | T | TA | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(34): Show |
39 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-298dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | |||||||
| chr8:66597847 | TA | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.292-298delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | |||||||
| chr8:66597847 | TAA | T | 25 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(22): Show |
32 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-299_292-298del others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | |||||||
| chr8:66597847 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0009g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.292-311_292-298del others(14): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66597847 | |||||||
| chr8:66598384 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.291+666G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598384 | |||||||
| chr8:66598422 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.291+628A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598422 | |||||||
| chr8:66598674 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.291+376A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598674 | |||||||
| chr8:66598857 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.291+193A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598857 | |||||||
| chr8:66598885 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+165G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 4/15 | chr8 | 66598885 | |||||||
| chr8:66599165 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.199-23C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599165 | |||||||
| chr8:66599243 | T | C | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.199-101A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599243 | |||||||
| chr8:66599393 | C | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.199-251G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599393 | |||||||
| chr8:66599509 | A | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-367T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599509 | |||||||
| chr8:66599639 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-497T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599639 | |||||||
| chr8:66599731 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.199-589A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599731 | |||||||
| chr8:66599761 | T | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0143 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-619A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599761 | |||||||
| chr8:66599850 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.199-708G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599850 | |||||||
| chr8:66599851 | G | A | 18 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(15): Show |
24 | HG02738.hp1 HG02895.hp1 HG02897.hp2 others(21): Show |
intron_variant | MODIFIER | c.199-709C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66599851 | |||||||
| chr8:66600108 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00408.hp2 NA18992.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.199-966C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600108 | |||||||
| chr8:66600376 | T | C | 10 | a0001c0001t0003g0033 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-1234A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600376 | |||||||
| chr8:66600396 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.199-1254G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600396 | |||||||
| chr8:66600644 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+1054G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600644 | |||||||
| chr8:66600660 | C | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+1038G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600660 | |||||||
| chr8:66600760 | T | C | 1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.198+938A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600760 | |||||||
| chr8:66600831 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.198+867C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600831 | |||||||
| chr8:66600973 | C | T | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.198+725G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66600973 | |||||||
| chr8:66601034 | G | A | 10 | a0001c0001t0003g0033 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+664C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601034 | |||||||
| chr8:66601055 | T | C | 2 | a0001c0002t0003g0068 a0001c0002t0003g0069 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+643A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601055 | |||||||
| chr8:66601110 | G | A | 5 | a0001c0001t0003g0033 a0001c0001t0003g0062 a0001c0001t0003g0065 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+588C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601110 | |||||||
| chr8:66601177 | C | CA | 37 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
37 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.198+520dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601177 | |||||||
| chr8:66601177 | CA | C | 23 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0001t0001g0166 others(20): Show |
23 | HG01070.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+520delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601177 | |||||||
| chr8:66601362 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.198+336A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 3/15 | chr8 | 66601362 | |||||||
| chr8:66601785 | A | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.127-16T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66601785 | |||||||
| chr8:66602029 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-260T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602029 | |||||||
| chr8:66602294 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
7 | NA18952.hp1 NA18957.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+124C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602294 | |||||||
| chr8:66602333 | G | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+85C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602333 | |||||||
| chr8:66602351 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.126+67C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 2/15 | chr8 | 66602351 | |||||||
| chr8:66602699 | C | CTA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02738.hp2 HG04115.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-178_21-177dupTA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | |||||||
| chr8:66602699 | CTA | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
12 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.21-178_21-177delTA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | |||||||
| chr8:66602699 | CTATA | C | 19 | a0001c0001t0001g0078 a0001c0001t0001g0120 a0001c0001t0001g0121 others(16): Show |
19 | HG00099.hp2 HG00408.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.21-180_21-177delTA others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | |||||||
| chr8:66602699 | CTATATAT others(3): Show |
C | 1 | a0002c0003t0003g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.21-186_21-177delTA others(8): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | |||||||
| chr8:66602699 | CTATATAT others(11): Show |
C | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.21-194_21-177delTA others(16): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602699 | |||||||
| chr8:66602713 | ATATATAT others(16): Show |
A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG01071.hp1 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.21-213_21-191delAA others(21): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602713 | |||||||
| chr8:66602713 | ATATATAT others(17): Show |
A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0027 |
2 | HG01070.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.21-214_21-191delAA others(22): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602713 | |||||||
| chr8:66602714 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.21-191A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602714 | |||||||
| chr8:66602717 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.21-212_21-195delAA others(16): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602717 | |||||||
| chr8:66602728 | TA | T | 3 | a0001c0001t0001g0140 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02630.hp1 HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.21-206delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | |||||||
| chr8:66602728 | TATA | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0207 a0001c0001t0002g0055 |
3 | HG02109.hp2 HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-208_21-206delTA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | |||||||
| chr8:66602728 | TATATA | T | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0003g0062 others(3): Show |
6 | HG01081.hp2 HG01433.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-210_21-206delTA others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602728 | |||||||
| chr8:66602729 | A | T | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
8 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.21-206T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602729 | |||||||
| chr8:66602730 | TA | T | 10 | a0001c0001t0001g0132 a0001c0001t0002g0001 a0001c0001t0002g0005 others(7): Show |
12 | HG02895.hp1 HG02922.hp2 HG03516.hp1 others(9): Show |
intron_variant | MODIFIER | c.21-208delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602730 | |||||||
| chr8:66602730 | TATA | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0147 a0001c0001t0001g0172 others(7): Show |
10 | HG00323.hp2 HG02135.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-210_21-208delTA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602730 | |||||||
| chr8:66602731 | A | ATT | 3 | a0001c0001t0001g0004 a0001c0001t0008g0076 a0001c0001t0012g0019 |
3 | HG00140.hp1 HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.21-209_21-208insAA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | |||||||
| chr8:66602731 | A | T | 15 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(12): Show |
15 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-208T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | |||||||
| chr8:66602731 | ATAT | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0134 others(6): Show |
9 | HG00423.hp1 HG02602.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-211_21-209delAT others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | |||||||
| chr8:66602731 | ATATT | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0135 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-212_21-209delAA others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | |||||||
| chr8:66602731 | ATATTT | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0130 a0001c0001t0001g0175 others(3): Show |
6 | HG02523.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-213_21-209delAA others(3): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602731 | |||||||
| chr8:66602732 | TA | T | 14 | a0001c0001t0001g0097 a0001c0001t0001g0113 a0001c0001t0001g0133 others(11): Show |
15 | HG01074.hp1 HG01261.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-210delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602732 | |||||||
| chr8:66602733 | A | AT | 5 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0002g0001 others(2): Show |
5 | HG01891.hp2 NA18961.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-211dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | A | ATATATAT others(6): Show |
1 | a0001c0001t0011g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.21-211_21-210insAA others(11): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.21-211_21-210insAA others(13): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | A | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0071 others(49): Show |
56 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.21-210T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | AT | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0104 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-211delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | ATT | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0085 others(18): Show |
21 | HG00423.hp2 HG00558.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.21-212_21-211delAA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602733 | ATTT | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0117 others(7): Show |
11 | HG00323.hp1 HG01515.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-213_21-211delAA others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602733 | |||||||
| chr8:66602734 | T | TA | 4 | a0001c0001t0001g0012 a0001c0001t0001g0094 a0001c0001t0001g0101 others(1): Show |
4 | HG02897.hp1 HG03688.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-212_21-211insT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | |||||||
| chr8:66602734 | T | TATATATA | 2 | a0001c0001t0010g0217 a0001c0001t0010g0218 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.21-212_21-211insTA others(5): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | |||||||
| chr8:66602734 | T | TATATATA others(6): Show |
3 | a0001c0001t0001g0028 a0001c0002t0003g0035 a0004c0004t0003g0042 |
3 | HG02109.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.21-212_21-211insTA others(11): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602734 | |||||||
| chr8:66602735 | T | A | 16 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(13): Show |
16 | HG00741.hp1 HG02165.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.21-212A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602735 | |||||||
| chr8:66602736 | T | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0070 others(7): Show |
10 | HG00140.hp2 HG01070.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-213A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602736 | |||||||
| chr8:66602737 | T | A | 11 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG01071.hp2 HG02486.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-214A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602737 | |||||||
| chr8:66602738 | T | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0110 others(6): Show |
9 | HG00140.hp2 HG00323.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-215A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602738 | |||||||
| chr8:66602739 | T | A | 3 | a0001c0001t0001g0196 a0001c0002t0003g0068 a0001c0002t0003g0069 |
3 | HG02486.hp2 HG03139.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.21-216A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602739 | |||||||
| chr8:66602740 | T | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0004c0004t0003g0042 |
3 | HG02809.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-217A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602740 | |||||||
| chr8:66602741 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21-218A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602741 | |||||||
| chr8:66602742 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-219A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602742 | |||||||
| chr8:66602744 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-221A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602744 | |||||||
| chr8:66602746 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.21-223A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602746 | |||||||
| chr8:66602751 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.21-228A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602751 | |||||||
| chr8:66602761 | T | C | 13 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0059 others(10): Show |
14 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-238A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602761 | |||||||
| chr8:66602847 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.21-324C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602847 | |||||||
| chr8:66602997 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.21-474C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66602997 | |||||||
| chr8:66603018 | T | A | 1 | a0001c0001t0006g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.21-495A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603018 | |||||||
| chr8:66603049 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-526T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603049 | |||||||
| chr8:66603177 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.21-654T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603177 | |||||||
| chr8:66603295 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.21-772C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603295 | |||||||
| chr8:66603310 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.21-787C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603310 | |||||||
| chr8:66603444 | G | A | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-921C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603444 | |||||||
| chr8:66603607 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-1084G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603607 | |||||||
| chr8:66603672 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG01070.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.21-1149A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603672 | |||||||
| chr8:66603706 | G | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.21-1183C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603706 | |||||||
| chr8:66603747 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.21-1224C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603747 | |||||||
| chr8:66603812 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.21-1289G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603812 | |||||||
| chr8:66603896 | A | G | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1373T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603896 | |||||||
| chr8:66603965 | GA | G | 50 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(47): Show |
57 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.21-1443delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603965 | |||||||
| chr8:66603965 | GAA | G | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1444_21-1443del others(2): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66603965 | |||||||
| chr8:66604008 | A | G | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-1485T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604008 | |||||||
| chr8:66604052 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.21-1529A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604052 | |||||||
| chr8:66604294 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.21-1771C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604294 | |||||||
| chr8:66604551 | T | G | 1 | a0001c0002t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.21-2028A>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604551 | |||||||
| chr8:66604794 | T | A | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.21-2271A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604794 | |||||||
| chr8:66604979 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.21-2456A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66604979 | |||||||
| chr8:66605019 | T | C | 3 | a0001c0002t0003g0068 a0001c0002t0003g0069 a0004c0004t0003g0042 |
3 | HG02486.hp2 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.21-2496A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605019 | |||||||
| chr8:66605439 | G | A | 1 | a0001c0001t0009g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.21-2916C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605439 | |||||||
| chr8:66605632 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.21-3109G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605632 | |||||||
| chr8:66605672 | G | A | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.21-3149C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605672 | |||||||
| chr8:66605991 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.21-3468A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66605991 | |||||||
| chr8:66606314 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.21-3791A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606314 | |||||||
| chr8:66606351 | A | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
52 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.21-3828T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606351 | |||||||
| chr8:66606593 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-4070C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606593 | |||||||
| chr8:66606712 | T | C | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-4189A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606712 | |||||||
| chr8:66606774 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.21-4251G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606774 | |||||||
| chr8:66606786 | G | T | 1 | a0001c0001t0001g0008 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.21-4263C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606786 | |||||||
| chr8:66606789 | GT | G | 7 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-4267delA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606789 | |||||||
| chr8:66606936 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.21-4413C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66606936 | |||||||
| chr8:66607051 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.21-4528G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607051 | |||||||
| chr8:66607129 | CA | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0194 others(12): Show |
15 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.21-4607delT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607129 | |||||||
| chr8:66607131 | A | AC | 3 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0207 |
3 | HG02738.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-4609_21-4608ins others(1): Show |
MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607131 | |||||||
| chr8:66607132 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.21-4609T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607132 | |||||||
| chr8:66607133 | A | C | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0199 others(11): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-4610T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607133 | |||||||
| chr8:66607134 | A | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0207 |
3 | HG02738.hp2 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.21-4611T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607134 | |||||||
| chr8:66607135 | A | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.21-4612T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607135 | |||||||
| chr8:66607136 | A | C | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0199 others(11): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.21-4613T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607136 | |||||||
| chr8:66607138 | A | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(139): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.21-4615T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607138 | |||||||
| chr8:66607139 | A | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0199 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.21-4616T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607139 | |||||||
| chr8:66607141 | A | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(50): Show |
56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.21-4618T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607141 | |||||||
| chr8:66607144 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0008g0076 |
2 | HG02015.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.21-4621T>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607144 | |||||||
| chr8:66607211 | C | A | 2 | a0001c0002t0003g0068 a0001c0002t0003g0069 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.21-4688G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607211 | |||||||
| chr8:66607470 | C | A | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.21-4947G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607470 | |||||||
| chr8:66607518 | C | T | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-4995G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607518 | |||||||
| chr8:66607699 | C | CA | 59 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(56): Show |
66 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.20+5119dupT | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607699 | |||||||
| chr8:66607825 | T | C | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+4994A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607825 | |||||||
| chr8:66607837 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.20+4982G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607837 | |||||||
| chr8:66607979 | C | A | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+4840G>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66607979 | |||||||
| chr8:66608107 | C | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
41 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(38): Show |
intron_variant | MODIFIER | c.20+4712G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608107 | |||||||
| chr8:66608272 | A | G | 11 | a0001c0001t0003g0034 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.20+4547T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608272 | |||||||
| chr8:66608551 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+4268C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608551 | |||||||
| chr8:66608564 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+4255T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608564 | |||||||
| chr8:66608964 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.20+3855A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66608964 | |||||||
| chr8:66609124 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.20+3695A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609124 | |||||||
| chr8:66609258 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.20+3561G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609258 | |||||||
| chr8:66609376 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0015g0209 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.20+3443C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609376 | |||||||
| chr8:66609394 | A | G | 1 | a0001c0001t0003g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20+3425T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609394 | |||||||
| chr8:66609784 | C | T | 2 | a0002c0003t0003g0031 a0002c0003t0003g0032 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.20+3035G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66609784 | |||||||
| chr8:66610484 | A | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02135.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.20+2335T>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610484 | |||||||
| chr8:66610509 | G | A | 2 | a0001c0002t0003g0068 a0001c0002t0003g0069 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.20+2310C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610509 | |||||||
| chr8:66610522 | T | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+2297A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610522 | |||||||
| chr8:66610547 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+2272A>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610547 | |||||||
| chr8:66610595 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20+2224G>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610595 | |||||||
| chr8:66610610 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20+2209T>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610610 | |||||||
| chr8:66610615 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20+2204C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66610615 | |||||||
| chr8:66611459 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.20+1360G>C | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611459 | |||||||
| chr8:66611633 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.20+1186C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611633 | |||||||
| chr8:66611993 | A | AT | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+825dupA | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66611993 | |||||||
| chr8:66612229 | G | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(54): Show |
64 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.20+590C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612229 | |||||||
| chr8:66612332 | T | A | 1 | a0001c0001t0003g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20+487A>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612332 | |||||||
| chr8:66612674 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.20+145C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612674 | |||||||
| chr8:66612714 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20+105C>A | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612714 | |||||||
| chr8:66612737 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.20+82C>T | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612737 | |||||||
| chr8:66612777 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20+42C>G | MYBL1 | ENSG00000185697.17 | transcript | ENST00000522677.8 | protein_coding | 1/15 | chr8 | 66612777 |