Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1875 |
| ensemblid | ENSG00000133740.11 |
| hgncid | 3119 |
| symbol | E2F5 |
| name | E2F transcription factor 5 |
| refseq_nuc | NM_001951.4 |
| refseq_prot | NP_001942.2 |
| ensembl_nuc | ENST00000416274.7 |
| ensembl_prot | ENSP00000398124.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 85177154 |
| end | 85214518 |
| strand | + |
| ver | v1.2 |
| region | chr8:85177154-85214518 |
| region5000 | chr8:85172154-85219518 |
| regionname0 | E2F5_chr8_85177154_85214518 |
| regionname5000 | E2F5_chr8_85172154_85219518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 346 | 320 | 76 | 51 | 143 | 11 | 37 | 105 | E2F5_chr8_85172154_85219518 | E2F5 | MAAAE others(341): Show |
chr8 | 85172154 | 85219518 |
| a0002 | 0/0 | 346 | 13 | 6 | 5 | 0 | 1 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | MAAAE others(341): Show |
chr8 | 85172154 | 85219518 |
| a0003 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | MAAAE others(341): Show |
chr8 | 85172154 | 85219518 |
| a0004 | 0/0 | 120 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | MAAAE others(115): Show |
chr8 | 85172154 | 85219518 |
| a0005 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | MAAAE others(341): Show |
chr8 | 85172154 | 85219518 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1038 | 171 | 42 | 31 | 68 | 8 | 21 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0001c0002 | 1/0 | 1038 | 149 | 34 | 20 | 75 | 3 | 16 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0002c0003 | 0/0 | 1038 | 12 | 5 | 5 | 0 | 1 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0002c0004 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0003c0005 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0004c0006 | 0/0 | 1038 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 | ||
| a0005c0007 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | ATGGC others(1033): Show |
chr8 | 85172154 | 85219518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1964 | 164 | 38 | 30 | 66 | 8 | 21 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0001c0001t0002 | 0/0 | 1960 | 5 | 4 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1955): Show |
chr8 | 85172154 | 85219518 |
| a0001c0001t0003 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0001c0001t0004 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0001c0002t0001 | 1/0 | 1964 | 147 | 34 | 20 | 73 | 3 | 16 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0001c0002t0003 | 0/0 | 1964 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0002c0003t0001 | 0/0 | 1964 | 12 | 5 | 5 | 0 | 1 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0002c0004t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0003c0005t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0004c0006t0001 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| a0005c0007t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | CTTCT others(1959): Show |
chr8 | 85172154 | 85219518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 5 | 7 | 2 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0002 | 0/0 | 13 | 0 | 5 | 8 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0004 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0007 | 1/0 | 6 | 0 | 0 | 2 | 1 | 2 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0008 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0002c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0003c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0004c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| a0005c0007t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | GBR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0008 | EUR | GBR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0035 | EUR | FIN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CDX | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02630 | hp2 | a0003 | c0005 | t0001 | g0155 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0042 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0046 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | ESN | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CHB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18985 | hp2 | a0004 | c0006 | t0001 | g0064 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ASW | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | GIH | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | USA | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | USA | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20300 | hp1 | a0005 | c0007 | t0001 | g0003 | AFR | USA | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0044 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0145 | REF | REF | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0007 | REF | REF | E2F5_chr8_85172154_85219518 | E2F5 | chr8 | 85172154 | 85219518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85177473 | G | C | 1 | a0002 | 13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
missense_variant | MODERATE | c.53G>C | p.Gly18Ala | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/8 | 320/1964 | 53/1041 | 18/346 | chr8 | 85177473 | |||
| chr8:85203112 | T | A | 1 | a0004 | 1 | NA18985.hp2 | stop_gained | HIGH | c.363T>A | p.Cys121* | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/8 | 630/1964 | 363/1041 | 121/346 | chr8 | 85203112 | |||
| chr8:85206219 | T | A | 1 | a0005 | 1 | NA20300.hp1 | missense_variant&splice_region_variant | MODERATE | c.549T>A | p.Asn183Lys | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 4/8 | 816/1964 | 549/1041 | 183/346 | chr8 | 85206219 | |||
| chr8:85209198 | C | G | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.672C>G | p.Ile224Met | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/8 | 939/1964 | 672/1041 | 224/346 | chr8 | 85209198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85177552 | C | G | 3 | a0001c0001 a0004c0006 a0005c0007 |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
synonymous_variant | LOW | c.132C>G | p.Ala44Ala | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/8 | 399/1964 | 132/1041 | 44/346 | chr8 | 85177552 | |||
| chr8:85203238 | C | T | 1 | a0002c0004 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.489C>T | p.Asp163Asp | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/8 | 756/1964 | 489/1041 | 163/346 | chr8 | 85203238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85177356 | TGGCC | T | 1 | a0001c0001t0002 | 5 | HG01167.hp1 HG01884.hp2 HG02976.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-63_-60delGCCG | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/8 | 60 | INFO_REALIGN_3_PRIME | chr8 | 85177356 | |||||
| chr8:85214107 | C | T | 1 | a0001c0001t0004 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 8/8 | 245 | chr8 | 85214107 | ||||||
| chr8:85214242 | A | C | 2 | a0001c0001t0003 a0001c0002t0003 |
3 | NA18978.hp2 NA18980.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 8/8 | 380 | chr8 | 85214242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85177663 | C | T | 2 | a0001c0002t0001g0233 a0001c0002t0001g0234 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.234+9C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85177663 | |||||||
| chr8:85177679 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.234+25G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85177679 | |||||||
| chr8:85177821 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.234+167G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85177821 | |||||||
| chr8:85177866 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.234+212G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85177866 | |||||||
| chr8:85177921 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234+267G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85177921 | |||||||
| chr8:85178016 | G | C | 8 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(5): Show |
13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+362G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178016 | |||||||
| chr8:85178132 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234+478A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178132 | |||||||
| chr8:85178256 | ATAGT | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0002t0001g0050 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+606_234+609del others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85178256 | ||||||
| chr8:85178452 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG00609.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.234+798G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178452 | |||||||
| chr8:85178673 | G | T | 1 | a0001c0002t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.234+1019G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178673 | |||||||
| chr8:85178693 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234+1039C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178693 | |||||||
| chr8:85178767 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.234+1113G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178767 | |||||||
| chr8:85178817 | GAAGTAGA others(12): Show |
G | 1 | a0001c0001t0001g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.234+1164_234+1182d others(21): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85178817 | |||||||
| chr8:85179034 | ACCACAGC others(4): Show |
A | 1 | a0001c0002t0001g0228 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.234+1381_234+1391d others(13): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179034 | |||||||
| chr8:85179576 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+1922T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179576 | |||||||
| chr8:85179582 | A | G | 1 | a0001c0002t0001g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.234+1928A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179582 | |||||||
| chr8:85179596 | CAT | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0219 others(7): Show |
13 | HG01081.hp1 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+1945_234+1946d others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85179596 | ||||||
| chr8:85179602 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234+1948T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179602 | |||||||
| chr8:85179728 | G | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(158): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.234+2074G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179728 | |||||||
| chr8:85179870 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.234+2216T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179870 | |||||||
| chr8:85179984 | C | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.234+2330C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85179984 | |||||||
| chr8:85180029 | C | CT | 9 | a0001c0002t0001g0218 a0002c0003t0001g0008 a0002c0003t0001g0018 others(6): Show |
14 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+2385dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180029 | ||||||
| chr8:85180098 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.234+2444G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180098 | |||||||
| chr8:85180229 | C | G | 1 | a0001c0002t0001g0172 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234+2575C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180229 | |||||||
| chr8:85180298 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.234+2644G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180298 | |||||||
| chr8:85180300 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.234+2646C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180300 | |||||||
| chr8:85180374 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.234+2720T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180374 | |||||||
| chr8:85180382 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.234+2728C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180382 | |||||||
| chr8:85180471 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.234+2817G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180471 | |||||||
| chr8:85180506 | CTATACAT others(9): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.234+2857_234+2872d others(18): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180506 | ||||||
| chr8:85180511 | C | CAT | 11 | a0001c0001t0004g0188 a0001c0002t0001g0004 a0001c0002t0001g0007 others(8): Show |
11 | HG01243.hp1 HG02056.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+2900_234+2901d others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATAT | 8 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0005 others(5): Show |
9 | HG00733.hp2 HG01168.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+2898_234+2901d others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATAT | 12 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0007 others(9): Show |
16 | HG00408.hp2 HG01106.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+2896_234+2901d others(8): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(1): Show |
6 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0016 others(3): Show |
10 | HG01243.hp2 HG01975.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+2894_234+2901d others(10): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(3): Show |
13 | a0001c0002t0001g0002 a0001c0002t0001g0031 a0001c0002t0001g0035 others(10): Show |
16 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+2892_234+2901d others(12): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(5): Show |
10 | a0001c0002t0001g0005 a0001c0002t0001g0031 a0001c0002t0001g0033 others(7): Show |
10 | HG00423.hp2 HG01433.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+2890_234+2901d others(14): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(7): Show |
4 | a0001c0002t0001g0002 a0001c0002t0001g0213 a0001c0002t0001g0216 others(1): Show |
6 | HG00140.hp1 HG00544.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+2888_234+2901d others(16): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(9): Show |
4 | a0001c0002t0001g0004 a0001c0002t0001g0050 a0001c0002t0001g0228 others(1): Show |
4 | HG02809.hp2 HG02895.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+2886_234+2901d others(18): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(11): Show |
3 | a0001c0002t0001g0004 a0001c0002t0001g0054 a0002c0003t0001g0008 |
4 | HG01257.hp1 HG02083.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+2884_234+2901d others(20): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(13): Show |
5 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0032 others(2): Show |
6 | HG00544.hp2 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+2882_234+2901d others(22): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(15): Show |
2 | a0001c0002t0001g0015 a0001c0002t0001g0212 |
2 | NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.234+2880_234+2901d others(24): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(17): Show |
1 | a0001c0002t0001g0004 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.234+2878_234+2901d others(26): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(19): Show |
2 | a0001c0002t0001g0004 a0002c0003t0001g0042 |
2 | HG02735.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.234+2876_234+2901d others(28): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | C | CATATATA others(23): Show |
1 | a0001c0002t0001g0196 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.234+2872_234+2901d others(32): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATAT | C | 7 | a0001c0002t0001g0004 a0001c0002t0001g0028 a0001c0002t0001g0148 others(4): Show |
8 | HG00597.hp2 HG02083.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+2898_234+2901d others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATAT | C | 4 | a0001c0002t0001g0007 a0001c0002t0001g0154 a0001c0002t0001g0156 others(1): Show |
4 | HG01261.hp2 HG02572.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+2896_234+2901d others(8): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0002t0001g0007 others(1): Show |
5 | HG01071.hp2 HG02717.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+2892_234+2901d others(12): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(5): Show |
C | 18 | a0001c0001t0001g0104 a0001c0001t0001g0115 a0001c0001t0002g0021 others(15): Show |
20 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+2890_234+2901d others(14): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(7): Show |
C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0098 others(12): Show |
17 | HG00438.hp2 HG01099.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.234+2888_234+2901d others(16): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(9): Show |
C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(18): Show |
28 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.234+2886_234+2901d others(18): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(11): Show |
C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(35): Show |
45 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.234+2884_234+2901d others(20): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(13): Show |
C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(73): Show |
98 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.234+2882_234+2901d others(22): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180511 | CATATATA others(17): Show |
C | 1 | a0001c0002t0001g0180 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.234+2878_234+2901d others(26): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180511 | ||||||
| chr8:85180574 | G | GT | 44 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0026 others(41): Show |
46 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.234+2941dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180574 | ||||||
| chr8:85180574 | G | GTT | 8 | a0001c0002t0001g0030 a0001c0002t0001g0055 a0001c0002t0001g0149 others(5): Show |
8 | HG00438.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+2940_234+2941d others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85180574 | ||||||
| chr8:85180608 | C | T | 1 | a0001c0002t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.234+2954C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180608 | |||||||
| chr8:85180670 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.234+3016C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180670 | |||||||
| chr8:85180693 | T | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0060 others(5): Show |
14 | HG00673.hp1 HG00673.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+3039T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180693 | |||||||
| chr8:85180702 | C | T | 1 | a0001c0002t0001g0171 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.234+3048C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180702 | |||||||
| chr8:85180756 | T | G | 3 | a0001c0002t0001g0011 a0001c0002t0003g0011 a0001c0002t0003g0175 |
5 | NA18978.hp2 NA18980.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+3102T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180756 | |||||||
| chr8:85180878 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0146 |
3 | HG01978.hp1 HG02273.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.234+3224C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180878 | |||||||
| chr8:85180908 | T | G | 1 | a0001c0002t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.234+3254T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85180908 | |||||||
| chr8:85181044 | A | C | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+3390A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181044 | |||||||
| chr8:85181100 | A | C | 1 | a0001c0002t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.234+3446A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181100 | |||||||
| chr8:85181191 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.234+3537A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181191 | |||||||
| chr8:85181278 | T | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0066 a0001c0001t0002g0067 others(1): Show |
5 | HG01167.hp1 HG01884.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+3624T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181278 | |||||||
| chr8:85181282 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+3628A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181282 | |||||||
| chr8:85181346 | T | C | 4 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(1): Show |
9 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+3692T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181346 | |||||||
| chr8:85181487 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
5 | HG01074.hp2 HG01261.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+3833C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181487 | |||||||
| chr8:85181502 | G | GT | 19 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0132 others(16): Show |
20 | HG01261.hp2 HG01346.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+3862dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85181502 | ||||||
| chr8:85181510 | T | TTTTTTTG others(177): Show |
1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3870_234+3871i others(186): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85181510 | ||||||
| chr8:85181532 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3878G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181532 | |||||||
| chr8:85181533 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3879T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181533 | |||||||
| chr8:85181544 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0166 a0001c0002t0001g0167 |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+3890C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181544 | |||||||
| chr8:85181552 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3898A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181552 | |||||||
| chr8:85181566 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3912T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181566 | |||||||
| chr8:85181582 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3928T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181582 | |||||||
| chr8:85181586 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+3932A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181586 | |||||||
| chr8:85181672 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+4018T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181672 | |||||||
| chr8:85181757 | C | G | 1 | a0001c0002t0001g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234+4103C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181757 | |||||||
| chr8:85181867 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.234+4213A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85181867 | |||||||
| chr8:85181961 | CA | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.234+4319delA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85181961 | ||||||
| chr8:85182094 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.234+4440T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85182094 | |||||||
| chr8:85182443 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+4789C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85182443 | |||||||
| chr8:85182598 | T | A | 1 | a0001c0002t0001g0178 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.234+4944T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85182598 | |||||||
| chr8:85182979 | C | T | 2 | a0001c0001t0001g0224 a0001c0002t0001g0037 |
3 | HG01884.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.234+5325C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85182979 | |||||||
| chr8:85183023 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.234+5369G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85183023 | |||||||
| chr8:85183108 | C | G | 1 | a0001c0002t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.234+5454C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85183108 | |||||||
| chr8:85183208 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.234+5554C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85183208 | |||||||
| chr8:85183247 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0219 a0001c0001t0001g0225 |
5 | HG01081.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+5593G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85183247 | |||||||
| chr8:85183700 | A | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0219 others(7): Show |
13 | HG01081.hp1 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+6046A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85183700 | |||||||
| chr8:85184071 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234+6417A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184071 | |||||||
| chr8:85184170 | C | A | 3 | a0001c0002t0001g0030 a0001c0002t0001g0166 a0001c0002t0001g0167 |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+6516C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184170 | |||||||
| chr8:85184291 | A | C | 7 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+6637A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184291 | |||||||
| chr8:85184354 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.234+6700G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184354 | |||||||
| chr8:85184367 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.234+6713C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184367 | |||||||
| chr8:85184379 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.234+6725G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184379 | |||||||
| chr8:85184420 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.234+6766A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184420 | |||||||
| chr8:85184452 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG01074.hp2 HG01261.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+6798G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184452 | |||||||
| chr8:85184614 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+6960A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184614 | |||||||
| chr8:85184616 | C | T | 12 | a0001c0002t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0158 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+6962C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184616 | |||||||
| chr8:85184622 | G | A | 12 | a0001c0002t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0158 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+6968G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184622 | |||||||
| chr8:85184824 | C | CAAGGAGA others(8): Show |
1 | a0001c0002t0001g0179 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.234+7171_234+7185d others(17): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85184824 | ||||||
| chr8:85184873 | A | C | 1 | a0001c0002t0001g0156 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234+7219A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184873 | |||||||
| chr8:85184888 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.234+7234C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184888 | |||||||
| chr8:85184958 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.234+7304A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184958 | |||||||
| chr8:85184981 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.234+7327A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85184981 | |||||||
| chr8:85185060 | T | C | 1 | a0001c0002t0001g0031 | 2 | HG00099.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.234+7406T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185060 | |||||||
| chr8:85185127 | A | T | 1 | a0001c0002t0001g0208 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+7473A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185127 | |||||||
| chr8:85185130 | AACCAAAA others(15): Show |
A | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.234+7487_234+7508d others(24): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85185130 | ||||||
| chr8:85185144 | G | A | 12 | a0001c0002t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0158 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+7490G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185144 | |||||||
| chr8:85185386 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.234+7732G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185386 | |||||||
| chr8:85185574 | C | G | 1 | a0001c0002t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.234+7920C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185574 | |||||||
| chr8:85185763 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0166 a0001c0002t0001g0167 |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+8109C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185763 | |||||||
| chr8:85185783 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(139): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.234+8129A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85185783 | |||||||
| chr8:85186014 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(166): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.234+8360C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186014 | |||||||
| chr8:85186039 | A | G | 1 | a0001c0002t0001g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.234+8385A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186039 | |||||||
| chr8:85186087 | T | G | 2 | a0001c0002t0001g0057 a0001c0002t0001g0147 |
2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.234+8433T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186087 | |||||||
| chr8:85186169 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.234+8515C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186169 | |||||||
| chr8:85186179 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+8525G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186179 | |||||||
| chr8:85186352 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+8698G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186352 | |||||||
| chr8:85186554 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(158): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.234+8900C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186554 | |||||||
| chr8:85186630 | TGGTATAT others(6): Show |
T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0166 a0001c0002t0001g0167 |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+8987_234+8999d others(15): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85186630 | ||||||
| chr8:85186707 | G | A | 8 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(5): Show |
13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+9053G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186707 | |||||||
| chr8:85186753 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.234+9099A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186753 | |||||||
| chr8:85186808 | T | A | 1 | a0001c0002t0001g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.234+9154T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85186808 | |||||||
| chr8:85186960 | T | TA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(132): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.234+9315dupA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85186960 | ||||||
| chr8:85187205 | A | G | 2 | a0001c0002t0001g0019 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.234+9551A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187205 | |||||||
| chr8:85187307 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.234+9653A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187307 | |||||||
| chr8:85187360 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234+9706G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187360 | |||||||
| chr8:85187399 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.234+9745A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187399 | |||||||
| chr8:85187424 | C | G | 2 | a0001c0002t0001g0019 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.234+9770C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187424 | |||||||
| chr8:85187466 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.234+9812C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187466 | |||||||
| chr8:85187552 | A | G | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.234+9898A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187552 | |||||||
| chr8:85187569 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.234+9915G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187569 | |||||||
| chr8:85187571 | CT | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0219 a0001c0001t0001g0225 |
5 | HG01081.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+9919delT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85187571 | ||||||
| chr8:85187707 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0125 others(9): Show |
15 | HG01081.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+10053A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187707 | |||||||
| chr8:85187708 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.234+10054T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187708 | |||||||
| chr8:85187938 | A | G | 12 | a0001c0002t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0158 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+10284A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187938 | |||||||
| chr8:85187980 | T | A | 15 | a0001c0001t0004g0188 a0001c0002t0001g0005 a0001c0002t0001g0032 others(12): Show |
23 | HG00408.hp2 HG00423.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.234+10326T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85187980 | |||||||
| chr8:85188056 | C | A | 1 | a0001c0002t0001g0148 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.234+10402C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188056 | |||||||
| chr8:85188147 | A | G | 2 | a0001c0002t0001g0233 a0001c0002t0001g0234 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.234+10493A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188147 | |||||||
| chr8:85188316 | CT | C | 20 | a0001c0001t0001g0071 a0001c0001t0001g0120 a0001c0001t0001g0121 others(17): Show |
26 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.234+10681delT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85188316 | ||||||
| chr8:85188316 | CTT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(152): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.234+10680_234+1068 others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85188316 | ||||||
| chr8:85188351 | C | T | 2 | a0001c0002t0001g0164 a0001c0002t0001g0165 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.234+10697C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188351 | |||||||
| chr8:85188654 | T | C | 6 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0156 others(3): Show |
6 | HG01261.hp2 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+11000T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188654 | |||||||
| chr8:85188682 | C | T | 3 | a0001c0001t0004g0188 a0001c0002t0001g0189 a0001c0002t0001g0228 |
3 | HG02056.hp1 HG02074.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.234+11028C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188682 | |||||||
| chr8:85188735 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.234+11081C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188735 | |||||||
| chr8:85188920 | T | G | 12 | a0001c0002t0001g0029 a0001c0002t0001g0157 a0001c0002t0001g0158 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.234+11266T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85188920 | |||||||
| chr8:85189076 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.234+11422A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189076 | |||||||
| chr8:85189201 | A | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0058 |
3 | HG02055.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.234+11547A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189201 | |||||||
| chr8:85189216 | T | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(183): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.234+11562T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189216 | |||||||
| chr8:85189267 | A | G | 3 | a0001c0002t0001g0030 a0001c0002t0001g0166 a0001c0002t0001g0167 |
4 | HG02486.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+11613A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189267 | |||||||
| chr8:85189372 | ATATTAT | A | 13 | a0001c0002t0001g0028 a0001c0002t0001g0039 a0001c0002t0001g0057 others(10): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.234+11729_234+1173 others(10): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85189372 | ||||||
| chr8:85189423 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.234+11769G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189423 | |||||||
| chr8:85189544 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(102): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.234+11890G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189544 | |||||||
| chr8:85189594 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0041 others(13): Show |
23 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.234+11940C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189594 | |||||||
| chr8:85189616 | G | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0125 others(9): Show |
15 | HG01081.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+11962G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189616 | |||||||
| chr8:85189975 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.235-12172C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189975 | |||||||
| chr8:85189988 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(166): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.235-12159C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85189988 | |||||||
| chr8:85190078 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0106 others(5): Show |
9 | NA18953.hp2 NA18954.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.235-12069C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190078 | |||||||
| chr8:85190121 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.235-12026C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190121 | |||||||
| chr8:85190250 | A | C | 13 | a0001c0002t0001g0028 a0001c0002t0001g0039 a0001c0002t0001g0057 others(10): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.235-11897A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190250 | |||||||
| chr8:85190303 | T | C | 4 | a0001c0002t0001g0029 a0001c0002t0001g0158 a0001c0002t0001g0159 others(1): Show |
5 | HG02145.hp1 HG02280.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-11844T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190303 | |||||||
| chr8:85190362 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.235-11785T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190362 | |||||||
| chr8:85190421 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.235-11726T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190421 | |||||||
| chr8:85190497 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(119): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.235-11626dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85190497 | ||||||
| chr8:85190497 | C | CTT | 29 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(26): Show |
38 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.235-11627_235-1162 others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85190497 | ||||||
| chr8:85190535 | G | T | 1 | a0001c0002t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.235-11612G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190535 | |||||||
| chr8:85190611 | C | G | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.235-11536C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85190611 | |||||||
| chr8:85191157 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.235-10990G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85191157 | |||||||
| chr8:85191499 | C | A | 1 | a0001c0002t0001g0156 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.235-10648C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85191499 | |||||||
| chr8:85191692 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.235-10455A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85191692 | |||||||
| chr8:85191970 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.235-10177A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85191970 | |||||||
| chr8:85192468 | G | A | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0028 others(11): Show |
15 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.235-9679G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192468 | |||||||
| chr8:85192475 | A | T | 1 | a0001c0002t0001g0206 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.235-9672A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192475 | |||||||
| chr8:85192519 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-9628T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192519 | |||||||
| chr8:85192579 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0113 |
5 | HG01109.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-9568G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192579 | |||||||
| chr8:85192600 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.235-9547G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192600 | |||||||
| chr8:85192633 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0052 others(17): Show |
26 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.235-9514G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192633 | |||||||
| chr8:85192806 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0131 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.235-9341C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85192806 | |||||||
| chr8:85193000 | C | A | 8 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(5): Show |
13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-9147C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193000 | |||||||
| chr8:85193026 | T | C | 8 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(5): Show |
13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-9121T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193026 | |||||||
| chr8:85193033 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-9114G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193033 | |||||||
| chr8:85193131 | T | C | 2 | a0001c0002t0001g0176 a0001c0002t0001g0193 |
2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.235-9016T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193131 | |||||||
| chr8:85193186 | T | C | 1 | a0001c0001t0001g0012 | 3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.235-8961T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193186 | |||||||
| chr8:85193263 | C | A | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0028 others(11): Show |
15 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.235-8884C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193263 | |||||||
| chr8:85193693 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0066 a0001c0001t0002g0067 others(1): Show |
5 | HG01167.hp1 HG01884.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-8454G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193693 | |||||||
| chr8:85193734 | G | A | 2 | a0002c0003t0001g0018 a0002c0003t0001g0043 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.235-8413G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193734 | |||||||
| chr8:85193787 | A | G | 1 | a0002c0003t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235-8360A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193787 | |||||||
| chr8:85193821 | A | G | 1 | a0001c0001t0001g0012 | 3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.235-8326A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193821 | |||||||
| chr8:85193917 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0166 |
3 | HG02486.hp1 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.235-8230G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85193917 | |||||||
| chr8:85194001 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.235-8146C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194001 | |||||||
| chr8:85194004 | A | C | 2 | a0001c0001t0001g0049 a0001c0002t0001g0167 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.235-8143A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194004 | |||||||
| chr8:85194013 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18948.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.235-8134T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194013 | |||||||
| chr8:85194034 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235-8113G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194034 | |||||||
| chr8:85194112 | A | T | 2 | a0001c0001t0001g0049 a0001c0002t0001g0167 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.235-8035A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194112 | |||||||
| chr8:85194121 | G | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0067 a0001c0001t0002g0068 |
4 | HG01167.hp1 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-8026G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194121 | |||||||
| chr8:85194517 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.235-7630T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194517 | |||||||
| chr8:85194531 | C | A | 1 | a0001c0002t0001g0015 | 3 | NA18955.hp2 NA18962.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.235-7616C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194531 | |||||||
| chr8:85194533 | C | CT | 19 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0097 others(16): Show |
25 | HG00597.hp2 HG01081.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.235-7595dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85194533 | ||||||
| chr8:85194533 | CT | C | 9 | a0001c0001t0001g0049 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
10 | HG01074.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-7595delT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85194533 | ||||||
| chr8:85194558 | A | G | 1 | a0001c0002t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.235-7589A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194558 | |||||||
| chr8:85194653 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235-7494G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194653 | |||||||
| chr8:85194679 | C | T | 1 | a0001c0002t0001g0205 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.235-7468C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194679 | |||||||
| chr8:85194694 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.235-7453A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194694 | |||||||
| chr8:85194760 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.235-7387C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194760 | |||||||
| chr8:85194772 | A | G | 2 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
2 | HG01928.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.235-7375A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85194772 | |||||||
| chr8:85195190 | T | C | 1 | a0001c0002t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.235-6957T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85195190 | |||||||
| chr8:85195369 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0121 |
2 | NA18984.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.235-6778C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85195369 | |||||||
| chr8:85195601 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
128 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.235-6546G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85195601 | |||||||
| chr8:85195914 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.235-6233C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85195914 | |||||||
| chr8:85196008 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235-6139A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196008 | |||||||
| chr8:85196017 | T | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0127 a0001c0002t0001g0156 |
3 | HG00733.hp1 HG01517.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.235-6130T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196017 | |||||||
| chr8:85196174 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.235-5973C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196174 | |||||||
| chr8:85196235 | T | A | 1 | a0002c0003t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235-5912T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196235 | |||||||
| chr8:85196301 | G | C | 3 | a0001c0001t0001g0116 a0001c0002t0001g0019 a0001c0002t0001g0058 |
4 | HG02055.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-5846G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196301 | |||||||
| chr8:85196319 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.235-5828A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196319 | |||||||
| chr8:85196352 | A | G | 1 | a0001c0002t0001g0214 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.235-5795A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196352 | |||||||
| chr8:85196368 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0128 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.235-5779C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85196368 | |||||||
| chr8:85197145 | G | A | 5 | a0001c0002t0001g0035 a0001c0002t0001g0191 a0001c0002t0001g0199 others(2): Show |
6 | HG00280.hp2 HG01081.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-5002G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85197145 | |||||||
| chr8:85197424 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.235-4723G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85197424 | |||||||
| chr8:85197461 | T | C | 4 | a0001c0002t0001g0028 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
5 | HG00597.hp2 HG02083.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-4686T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85197461 | |||||||
| chr8:85197971 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0115 |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-4176G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85197971 | |||||||
| chr8:85198041 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235-4106C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198041 | |||||||
| chr8:85198124 | A | G | 1 | a0001c0002t0001g0204 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.235-4023A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198124 | |||||||
| chr8:85198169 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.235-3978C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198169 | |||||||
| chr8:85198379 | C | T | 8 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0042 others(5): Show |
13 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-3768C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198379 | |||||||
| chr8:85198473 | T | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.235-3674T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198473 | |||||||
| chr8:85198525 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.235-3622G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198525 | |||||||
| chr8:85198795 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.235-3352C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85198795 | |||||||
| chr8:85199054 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.235-3093T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199054 | |||||||
| chr8:85199113 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.235-3034A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199113 | |||||||
| chr8:85199165 | A | C | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235-2982A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199165 | |||||||
| chr8:85199247 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-2900C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199247 | |||||||
| chr8:85199543 | AGTGGTGG others(2): Show |
A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-2590_235-2582d others(11): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85199543 | ||||||
| chr8:85199786 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235-2361G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199786 | |||||||
| chr8:85199859 | G | C | 1 | a0001c0002t0001g0180 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.235-2288G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199859 | |||||||
| chr8:85199867 | G | C | 1 | a0001c0002t0001g0180 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.235-2280G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85199867 | |||||||
| chr8:85200007 | G | A | 3 | a0001c0001t0001g0116 a0001c0002t0001g0019 a0001c0002t0001g0058 |
4 | HG02055.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-2140G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200007 | |||||||
| chr8:85200121 | C | A | 1 | a0001c0002t0001g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.235-2026C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200121 | |||||||
| chr8:85200126 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.235-2021A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200126 | |||||||
| chr8:85200177 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0096 others(5): Show |
11 | HG00099.hp1 HG00438.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.235-1970G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200177 | |||||||
| chr8:85200183 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0221 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-1964G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200183 | |||||||
| chr8:85200246 | C | CA | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0144 others(16): Show |
20 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.235-1889dupA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85200246 | ||||||
| chr8:85200366 | GAAAT | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-1778_235-1775d others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 85200366 | ||||||
| chr8:85200925 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-1222T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200925 | |||||||
| chr8:85200969 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-1178C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85200969 | |||||||
| chr8:85201083 | T | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0223 others(7): Show |
11 | HG01070.hp2 HG01261.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.235-1064T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201083 | |||||||
| chr8:85201363 | G | T | 1 | a0001c0002t0001g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.235-784G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201363 | |||||||
| chr8:85201421 | C | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0218 |
2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.235-726C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201421 | |||||||
| chr8:85201500 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0221 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-647T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201500 | |||||||
| chr8:85201543 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.235-604A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201543 | |||||||
| chr8:85201569 | T | C | 2 | a0001c0002t0001g0055 a0001c0002t0001g0157 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.235-578T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201569 | |||||||
| chr8:85201821 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235-326T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85201821 | |||||||
| chr8:85202033 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0074 others(7): Show |
17 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-114C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85202033 | |||||||
| chr8:85202129 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0092 |
3 | NA18948.hp1 NA18959.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.235-18G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 1/7 | chr8 | 85202129 | |||||||
| chr8:85202290 | T | TTTA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(158): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.344+36_344+37insAT others(1): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 85202290 | ||||||
| chr8:85202416 | G | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0223 others(7): Show |
11 | HG01070.hp2 HG01261.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+160G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | chr8 | 85202416 | |||||||
| chr8:85202443 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(158): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.344+187A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | chr8 | 85202443 | |||||||
| chr8:85202454 | G | A | 5 | a0001c0001t0001g0110 a0001c0002t0001g0029 a0001c0002t0001g0158 others(2): Show |
6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+198G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | chr8 | 85202454 | |||||||
| chr8:85202824 | C | T | 3 | a0001c0001t0001g0116 a0001c0002t0001g0019 a0001c0002t0001g0058 |
4 | HG02055.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-270C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | chr8 | 85202824 | |||||||
| chr8:85202961 | G | A | 4 | a0001c0002t0001g0016 a0001c0002t0001g0192 a0001c0002t0001g0204 others(1): Show |
6 | NA18959.hp2 NA19003.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-133G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 2/7 | chr8 | 85202961 | |||||||
| chr8:85203442 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.506+187T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203442 | |||||||
| chr8:85203451 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.506+196G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203451 | |||||||
| chr8:85203586 | TTTGTATT others(14): Show |
T | 1 | a0001c0001t0001g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.506+334_506+354del others(21): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 85203586 | ||||||
| chr8:85203616 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.506+361T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203616 | |||||||
| chr8:85203662 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.506+407G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203662 | |||||||
| chr8:85203662 | G | T | 1 | a0004c0006t0001g0064 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.506+407G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203662 | |||||||
| chr8:85203710 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.506+455T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203710 | |||||||
| chr8:85203807 | A | G | 2 | a0001c0001t0001g0049 a0001c0002t0001g0167 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.506+552A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85203807 | |||||||
| chr8:85204017 | G | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0223 others(1): Show |
5 | HG01070.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+762G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204017 | |||||||
| chr8:85204024 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.506+769G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204024 | |||||||
| chr8:85204206 | C | T | 16 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0100 others(13): Show |
17 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.506+951C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204206 | |||||||
| chr8:85204239 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.506+984C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204239 | |||||||
| chr8:85204292 | G | C | 1 | a0001c0002t0001g0207 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.506+1037G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204292 | |||||||
| chr8:85204404 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.506+1149C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204404 | |||||||
| chr8:85204587 | A | G | 1 | a0001c0002t0001g0032 | 2 | HG02165.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.506+1332A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204587 | |||||||
| chr8:85204605 | T | A | 1 | a0001c0002t0001g0032 | 2 | HG02165.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.506+1350T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204605 | |||||||
| chr8:85204614 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.506+1359G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204614 | |||||||
| chr8:85204685 | A | C | 10 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0223 others(7): Show |
11 | HG01070.hp2 HG01261.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+1430A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204685 | |||||||
| chr8:85204731 | G | T | 1 | a0001c0002t0001g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507-1446G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204731 | |||||||
| chr8:85204842 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.507-1335A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204842 | |||||||
| chr8:85204861 | G | T | 1 | a0002c0004t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.507-1316G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204861 | |||||||
| chr8:85204862 | A | T | 1 | a0002c0004t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.507-1315A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204862 | |||||||
| chr8:85204904 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.507-1273G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204904 | |||||||
| chr8:85204908 | A | G | 16 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0177 others(13): Show |
30 | HG00544.hp1 HG00609.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.507-1269A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85204908 | |||||||
| chr8:85205162 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507-1015G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205162 | |||||||
| chr8:85205163 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.507-1014A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205163 | |||||||
| chr8:85205226 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.507-951T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205226 | |||||||
| chr8:85205539 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.507-638C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205539 | |||||||
| chr8:85205640 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.507-537C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205640 | |||||||
| chr8:85205797 | C | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0229 |
2 | NA19059.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.507-380C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205797 | |||||||
| chr8:85205828 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.507-349A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85205828 | |||||||
| chr8:85205885 | CCATT | C | 3 | a0002c0003t0001g0008 a0002c0003t0001g0018 a0002c0003t0001g0043 |
8 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-290_507-287del others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 85205885 | ||||||
| chr8:85206101 | A | T | 3 | a0001c0001t0001g0116 a0001c0002t0001g0019 a0001c0002t0001g0058 |
4 | HG02055.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.507-76A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 3/7 | chr8 | 85206101 | |||||||
| chr8:85206542 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.550+322A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 4/7 | chr8 | 85206542 | |||||||
| chr8:85206805 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0128 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.550+585G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 4/7 | chr8 | 85206805 | |||||||
| chr8:85207143 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.551-282G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 4/7 | chr8 | 85207143 | |||||||
| chr8:85207739 | C | CAAAT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.615+253_615+254ins others(4): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 85207739 | ||||||
| chr8:85207796 | C | T | 1 | a0001c0002t0001g0201 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.615+307C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85207796 | |||||||
| chr8:85207886 | C | A | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.615+397C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85207886 | |||||||
| chr8:85207986 | T | A | 3 | a0001c0001t0001g0116 a0001c0002t0001g0019 a0001c0002t0001g0058 |
4 | HG02055.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+497T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85207986 | |||||||
| chr8:85208177 | AATTAGCC others(3): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.615+689_615+698del others(10): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85208177 | |||||||
| chr8:85208306 | C | A | 1 | a0001c0002t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.615+817C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85208306 | |||||||
| chr8:85208540 | A | C | 1 | a0001c0002t0001g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.616-602A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85208540 | |||||||
| chr8:85209076 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.616-66G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 5/7 | chr8 | 85209076 | |||||||
| chr8:85209776 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883+367A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85209776 | |||||||
| chr8:85209965 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883+556G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85209965 | |||||||
| chr8:85209999 | A | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
5 | NA18954.hp2 NA18984.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+590A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85209999 | |||||||
| chr8:85210186 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.883+777A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210186 | |||||||
| chr8:85210281 | T | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0028 others(8): Show |
12 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.883+872T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210281 | |||||||
| chr8:85210290 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.883+881A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210290 | |||||||
| chr8:85210338 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0166 |
3 | HG02486.hp1 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.883+929C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210338 | |||||||
| chr8:85210602 | A | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0115 others(4): Show |
11 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.883+1193A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210602 | |||||||
| chr8:85210675 | T | TA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0131 others(8): Show |
16 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.883+1281dupA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85210675 | ||||||
| chr8:85210676 | A | T | 1 | a0001c0002t0001g0183 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883+1267A>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210676 | |||||||
| chr8:85210712 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.883+1303C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210712 | |||||||
| chr8:85210734 | A | G | 4 | a0001c0001t0001g0048 a0001c0002t0001g0037 a0001c0002t0001g0050 others(1): Show |
5 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+1325A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210734 | |||||||
| chr8:85210963 | A | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0066 a0001c0001t0002g0067 others(1): Show |
5 | HG01167.hp1 HG01884.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-1194A>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85210963 | |||||||
| chr8:85211043 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0121 |
2 | NA18984.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.884-1114G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211043 | |||||||
| chr8:85211220 | T | TA | 13 | a0001c0002t0001g0036 a0001c0002t0001g0051 a0001c0002t0001g0058 others(10): Show |
14 | HG01106.hp1 HG01978.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.884-914dupA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85211220 | ||||||
| chr8:85211220 | TA | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.884-914delA | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85211220 | ||||||
| chr8:85211286 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0222 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.884-871G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211286 | |||||||
| chr8:85211486 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.884-671T>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211486 | |||||||
| chr8:85211643 | G | GT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(70): Show |
90 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.884-486dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85211643 | ||||||
| chr8:85211643 | G | GTT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0110 others(18): Show |
26 | HG00438.hp2 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.884-487_884-486dup others(2): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85211643 | ||||||
| chr8:85211643 | G | T | 1 | a0001c0001t0001g0013 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.884-514G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211643 | |||||||
| chr8:85211643 | GT | G | 10 | a0001c0001t0001g0041 a0001c0001t0001g0131 a0001c0002t0001g0019 others(7): Show |
10 | HG01070.hp2 HG01257.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.884-486delT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 85211643 | ||||||
| chr8:85211645 | T | TG | 9 | a0001c0001t0001g0077 a0001c0002t0001g0028 a0001c0002t0001g0150 others(6): Show |
10 | HG00597.hp2 HG01099.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.884-512_884-511ins others(1): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211645 | |||||||
| chr8:85211646 | T | G | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.884-511T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211646 | |||||||
| chr8:85211648 | T | G | 1 | a0001c0002t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.884-509T>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85211648 | |||||||
| chr8:85212005 | G | A | 2 | a0001c0001t0001g0049 a0001c0002t0001g0167 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.884-152G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 6/7 | chr8 | 85212005 | |||||||
| chr8:85212427 | C | G | 2 | a0001c0002t0001g0030 a0001c0002t0001g0166 |
3 | HG02486.hp1 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.931+223C>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85212427 | |||||||
| chr8:85212773 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(119): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.931+570dupT | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85212773 | ||||||
| chr8:85212835 | C | A | 1 | a0001c0002t0001g0209 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.931+631C>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85212835 | |||||||
| chr8:85212836 | A | G | 1 | a0001c0002t0001g0209 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.931+632A>G | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85212836 | |||||||
| chr8:85212837 | G | T | 1 | a0001c0002t0001g0209 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.931+633G>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85212837 | |||||||
| chr8:85212847 | CTGTTTGC others(13): Show |
C | 1 | a0001c0001t0001g0229 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.931+644_931+663del others(20): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85212847 | |||||||
| chr8:85212918 | C | CTGTCATC others(10): Show |
162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(159): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.931+734_931+750dup others(17): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85212918 | ||||||
| chr8:85212918 | C | CTGTCATC others(27): Show |
1 | a0001c0002t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.931+717_931+750dup others(34): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85212918 | ||||||
| chr8:85212921 | T | TCATCCAG others(10): Show |
3 | a0001c0001t0002g0021 a0001c0001t0002g0067 a0001c0001t0002g0068 |
4 | HG01167.hp1 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+733_931+734ins others(17): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85212921 | ||||||
| chr8:85213047 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.932-706G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85213047 | |||||||
| chr8:85213070 | G | C | 10 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0002c0003t0001g0008 others(7): Show |
15 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.932-683G>C | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85213070 | |||||||
| chr8:85213316 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.932-437G>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85213316 | |||||||
| chr8:85213326 | C | T | 1 | a0001c0002t0001g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.932-427C>T | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85213326 | |||||||
| chr8:85213542 | T | TAAAAA | 18 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0082 others(15): Show |
24 | HG00673.hp2 HG01099.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.932-196_932-192dup others(5): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85213542 | ||||||
| chr8:85213542 | T | TAAAAAA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(123): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.932-197_932-192dup others(6): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85213542 | ||||||
| chr8:85213542 | T | TAAAAAAA | 23 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0085 others(20): Show |
25 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-198_932-192dup others(7): Show |
E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 85213542 | ||||||
| chr8:85213624 | T | A | 1 | a0001c0002t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.932-129T>A | E2F5 | ENSG00000133740.11 | transcript | ENST00000416274.7 | protein_coding | 7/7 | chr8 | 85213624 |