Search by Gene
| Item | Value |
|---|---|
| geneid | 6059 |
| ensemblid | ENSG00000164163.11 |
| hgncid | 69 |
| symbol | ABCE1 |
| name | ATP binding cassette subfamily E member 1 |
| refseq_nuc | NM_002940.3 |
| refseq_prot | NP_002931.2 |
| ensembl_nuc | ENST00000296577.9 |
| ensembl_prot | ENSP00000296577.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 145098311 |
| end | 145129524 |
| strand | + |
| ver | v1.2 |
| region | chr4:145098311-145129524 |
| region5000 | chr4:145093311-145134524 |
| regionname0 | ABCE1_chr4_145098311_145129524 |
| regionname5000 | ABCE1_chr4_145093311_145134524 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 599 | 259 | 88 | 56 | 77 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | MADKL others(594): Show |
chr4 | 145093311 | 145134524 |
| a0002 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | MADKL others(594): Show |
chr4 | 145093311 | 145134524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1797 | 251 | 81 | 55 | 77 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | ATGGC others(1792): Show |
chr4 | 145093311 | 145134524 | ||
| a0001c0002 | 0/0 | 1797 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ATGGC others(1792): Show |
chr4 | 145093311 | 145134524 | ||
| a0001c0003 | 0/0 | 1797 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ATGGC others(1792): Show |
chr4 | 145093311 | 145134524 | ||
| a0001c0004 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ATGGC others(1792): Show |
chr4 | 145093311 | 145134524 | ||
| a0002c0005 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ATGGC others(1792): Show |
chr4 | 145093311 | 145134524 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3887 | 242 | 75 | 54 | 75 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0001t0002 | 0/0 | 3887 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0001t0005 | 0/0 | 3887 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0001t0007 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0001t0008 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0001t0009 | 0/0 | 3887 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0002t0003 | 0/0 | 3887 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0003t0006 | 0/0 | 3887 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0001c0004t0004 | 0/0 | 3887 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| a0002c0005t0001 | 0/0 | 3887 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | ACCGC others(3882): Show |
chr4 | 145093311 | 145134524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 3 | 8 | 6 | 1 | 5 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0002 | 0/0 | 23 | 2 | 8 | 12 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 9 | 5 | 2 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0004 | 0/0 | 8 | 2 | 2 | 3 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0005 | 0/0 | 8 | 2 | 1 | 2 | 1 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0028 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0003t0006g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0004t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| a0002c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01243 | hp1 | a0001 | c0003 | t0006 | g0022 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02723 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02818 | hp1 | a0001 | c0004 | t0004 | g0130 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18982 | hp1 | a0002 | c0005 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19070 | hp2 | a0001 | c0001 | t0008 | g0127 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0123 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0131 | AFR | USA | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0028 | REF | REF | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | ABCE1_chr4_145093311_145134524 | ABCE1 | chr4 | 145093311 | 145134524 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145123031 | G | A | 1 | a0002 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1274G>A | p.Arg425His | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 14/18 | 1410/3887 | 1274/1800 | 425/599 | chr4 | 145123031 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145109174 | A | T | 1 | a0001c0004 | 2 | HG02818.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.330A>T | p.Gly110Gly | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/18 | 466/3887 | 330/1800 | 110/599 | chr4 | 145109174 | |||
| chr4:145112254 | G | A | 1 | a0001c0002 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.726G>A | p.Glu242Glu | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/18 | 862/3887 | 726/1800 | 242/599 | chr4 | 145112254 | |||
| chr4:145123265 | C | T | 2 | a0001c0003a0001c0004 | 4 | HG01243.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1425C>T | p.Cys475Cys | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/18 | 1561/3887 | 1425/1800 | 475/599 | chr4 | 145123265 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145127583 | G | C | 1 | a0001c0001t0007 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 10 | chr4 | 145127583 | ||||||
| chr4:145127688 | A | G | 1 | a0001c0003t0006 | 2 | HG01243.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 115 | chr4 | 145127688 | ||||||
| chr4:145127757 | C | T | 1 | a0001c0001t0005 | 2 | HG01884.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 184 | chr4 | 145127757 | ||||||
| chr4:145128169 | G | A | 1 | a0001c0004t0004 | 2 | HG02818.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*596G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 596 | chr4 | 145128169 | ||||||
| chr4:145128631 | C | G | 1 | a0001c0002t0003 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1058C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1058 | chr4 | 145128631 | ||||||
| chr4:145128770 | G | A | 1 | a0001c0004t0004 | 2 | HG02818.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1197 | chr4 | 145128770 | ||||||
| chr4:145129022 | T | A | 1 | a0001c0001t0008 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1449T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1449 | chr4 | 145129022 | ||||||
| chr4:145129307 | G | A | 1 | a0001c0001t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1734 | chr4 | 145129307 | ||||||
| chr4:145129350 | T | C | 1 | a0001c0001t0002 | 4 | HG01243.hp2 HG02615.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1777T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1777 | chr4 | 145129350 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145098543 | G | T | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+124G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098543 | |||||||
| chr4:145098544 | C | T | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+125C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098544 | |||||||
| chr4:145098549 | G | A | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+130G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098549 | |||||||
| chr4:145098735 | AAACCTGC others(8): Show |
A | 4 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 8 | HG01261.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+319_-28+333del others(15): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145098735 | ||||||
| chr4:145099019 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-28+600C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099019 | |||||||
| chr4:145099159 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-28+740C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099159 | |||||||
| chr4:145099698 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-28+1279T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099698 | |||||||
| chr4:145100049 | T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-28+1630T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100049 | |||||||
| chr4:145100246 | C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-28+1827C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100246 | |||||||
| chr4:145100298 | G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-28+1879G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100298 | |||||||
| chr4:145100446 | C | T | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+2027C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100446 | |||||||
| chr4:145100538 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-28+2119G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100538 | |||||||
| chr4:145100580 | AAGTTGTC others(14): Show |
A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-28+2164_-28+2184d others(23): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145100580 | ||||||
| chr4:145100630 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-28+2211A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100630 | |||||||
| chr4:145100646 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28+2227A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100646 | |||||||
| chr4:145101061 | A | T | 1 | a0001c0001t0008g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-28+2642A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101061 | |||||||
| chr4:145101073 | A | AT | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0032others(4): Show | 13 | HG01261.hp1 HG01261.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28+2654_-28+2655i others(3): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101073 | |||||||
| chr4:145101073 | A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0057 | 5 | HG01358.hp1 HG02257.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+2654A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101073 | |||||||
| chr4:145101225 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+2806T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101225 | |||||||
| chr4:145101498 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-27-2888G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101498 | |||||||
| chr4:145101669 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-27-2717G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101669 | |||||||
| chr4:145101739 | T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(16): Show | 35 | HG00621.hp2 HG00741.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.-27-2647T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101739 | |||||||
| chr4:145102075 | T | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2311T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102075 | |||||||
| chr4:145102110 | C | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2276C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102110 | |||||||
| chr4:145102213 | G | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2173G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102213 | |||||||
| chr4:145102493 | A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-27-1893A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102493 | |||||||
| chr4:145102696 | A | G | 1 | a0001c0001t0001g0021 | 2 | NA18969.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-27-1690A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102696 | |||||||
| chr4:145102748 | G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-1638G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102748 | |||||||
| chr4:145102772 | T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0032others(3): Show | 12 | HG01261.hp2 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-1614T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102772 | |||||||
| chr4:145102808 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-27-1578G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102808 | |||||||
| chr4:145103029 | CAG | C | 3 | a0001c0001t0001g0125a0001c0004t0004g0130a0001c0004t0004g0131 | 3 | HG02630.hp2 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-1356_-27-1355d others(4): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103029 | |||||||
| chr4:145103123 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-27-1263A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103123 | |||||||
| chr4:145103208 | A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-27-1178A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103208 | |||||||
| chr4:145103620 | G | A | 1 | a0001c0001t0008g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-27-766G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103620 | |||||||
| chr4:145103628 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-27-758C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103628 | |||||||
| chr4:145103766 | G | GT | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 97 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.-27-605dupT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145103766 | ||||||
| chr4:145103766 | GT | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 8 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-605delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145103766 | ||||||
| chr4:145103806 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-27-580G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103806 | |||||||
| chr4:145104201 | A | G | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-185A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145104201 | |||||||
| chr4:145104262 | AT | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0004t0004g0130others(1): Show | 5 | HG02559.hp1 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-114delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145104262 | ||||||
| chr4:145104331 | T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0005g0135others(1): Show | 5 | HG01884.hp1 HG02572.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-55T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145104331 | |||||||
| chr4:145105041 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.103+526G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105041 | |||||||
| chr4:145105046 | ATAGAATT others(9): Show |
A | 1 | a0001c0001t0001g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.103+544_104-531del others(16): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 145105046 | ||||||
| chr4:145105059 | C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.103+544C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105059 | |||||||
| chr4:145105309 | A | T | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.104-296A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105309 | |||||||
| chr4:145105496 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.104-109G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105496 | |||||||
| chr4:145105908 | C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0025 | 5 | HG01192.hp2 HG02055.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+218C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105908 | |||||||
| chr4:145105939 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.189+249C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105939 | |||||||
| chr4:145105955 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189+265A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105955 | |||||||
| chr4:145106153 | C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0134 | 5 | HG01261.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+463C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106153 | |||||||
| chr4:145106225 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189+535G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106225 | |||||||
| chr4:145106282 | G | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0035others(4): Show | 15 | HG00280.hp1 HG01081.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+592G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106282 | |||||||
| chr4:145106409 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.189+719G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106409 | |||||||
| chr4:145106634 | G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.189+944G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106634 | |||||||
| chr4:145106648 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.189+958T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106648 | |||||||
| chr4:145106690 | T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0100 | 2 | NA18942.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+1000T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106690 | |||||||
| chr4:145107164 | A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.190-851A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107164 | |||||||
| chr4:145107192 | G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01074.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.190-823G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107192 | |||||||
| chr4:145107290 | G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.190-725G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107290 | |||||||
| chr4:145107326 | A | G | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.190-689A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107326 | |||||||
| chr4:145107622 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-393A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107622 | |||||||
| chr4:145107636 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.190-379G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107636 | |||||||
| chr4:145107671 | A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18952.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.190-344A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107671 | |||||||
| chr4:145107934 | A | C | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.190-81A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107934 | |||||||
| chr4:145108137 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287+25C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108137 | |||||||
| chr4:145108260 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287+148T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108260 | |||||||
| chr4:145108449 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.287+337C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108449 | |||||||
| chr4:145108555 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.287+443A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108555 | |||||||
| chr4:145108751 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.288-381A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108751 | |||||||
| chr4:145108932 | A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18968.hp2 NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.288-200A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108932 | |||||||
| chr4:145109313 | G | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.405+64G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109313 | |||||||
| chr4:145109396 | T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 3 | NA18947.hp2 NA19010.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.405+147T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109396 | |||||||
| chr4:145109459 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405+210T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109459 | |||||||
| chr4:145109539 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.405+290A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109539 | |||||||
| chr4:145109551 | T | G | 1 | a0001c0001t0001g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.405+302T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109551 | |||||||
| chr4:145109601 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.405+352A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109601 | |||||||
| chr4:145109672 | T | C | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.405+423T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109672 | |||||||
| chr4:145110084 | AT | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0037others(6): Show | 9 | HG00558.hp1 HG00558.hp2 HG02451.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.406-3delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 145110084 | ||||||
| chr4:145110244 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp1 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.543+4G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110244 | |||||||
| chr4:145110275 | A | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+35A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110275 | |||||||
| chr4:145110299 | A | C | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.543+59A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110299 | |||||||
| chr4:145110350 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.544-25A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110350 | |||||||
| chr4:145110451 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.613+7G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110451 | |||||||
| chr4:145110568 | C | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.613+124C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110568 | |||||||
| chr4:145110578 | C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.613+134C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110578 | |||||||
| chr4:145111086 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.710+22G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111086 | |||||||
| chr4:145111123 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.710+59A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111123 | |||||||
| chr4:145111424 | C | T | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.710+360C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111424 | |||||||
| chr4:145111530 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.710+466G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111530 | |||||||
| chr4:145111580 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.710+516G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111580 | |||||||
| chr4:145111779 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.711-460T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111779 | |||||||
| chr4:145111790 | C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.711-449C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111790 | |||||||
| chr4:145111803 | T | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.711-436T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111803 | |||||||
| chr4:145112216 | CT | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0030others(22): Show | 32 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.711-6delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 145112216 | ||||||
| chr4:145112216 | CTT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(35): Show | 73 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(70): Show |
splice_region_variant&intron_variant | LOW | c.711-7_711-6delTT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 145112216 | ||||||
| chr4:145112221 | T | C | 1 | a0001c0004t0004g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711-18T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145112221 | |||||||
| chr4:145112468 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.800+140T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112468 | |||||||
| chr4:145112562 | T | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0063others(4): Show | 10 | HG01496.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.800+234T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112562 | |||||||
| chr4:145112655 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.800+327G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112655 | |||||||
| chr4:145112660 | C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(3): Show | 15 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.800+332C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112660 | |||||||
| chr4:145112727 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.800+399G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112727 | |||||||
| chr4:145112956 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.800+628T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112956 | |||||||
| chr4:145113023 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.800+695T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113023 | |||||||
| chr4:145113047 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.800+719A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113047 | |||||||
| chr4:145113109 | G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.800+781G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113109 | |||||||
| chr4:145113111 | A | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 63 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.800+783A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113111 | |||||||
| chr4:145113177 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.800+849G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113177 | |||||||
| chr4:145113211 | G | C | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.800+883G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113211 | |||||||
| chr4:145113244 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.800+916C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113244 | |||||||
| chr4:145113252 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.800+924A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113252 | |||||||
| chr4:145113462 | T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(3): Show | 15 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.800+1134T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113462 | |||||||
| chr4:145113879 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.800+1551C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113879 | |||||||
| chr4:145114215 | G | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.800+1887G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114215 | |||||||
| chr4:145114522 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800+2194A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114522 | |||||||
| chr4:145114615 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.800+2287G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114615 | |||||||
| chr4:145114885 | A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.801-2408A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114885 | |||||||
| chr4:145114994 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.801-2299G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114994 | |||||||
| chr4:145115012 | G | A | 1 | a0001c0001t0005g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.801-2281G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115012 | |||||||
| chr4:145115210 | G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0107 | 2 | HG02148.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.801-2083G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115210 | |||||||
| chr4:145115236 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.801-2057G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115236 | |||||||
| chr4:145115690 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.801-1603T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115690 | |||||||
| chr4:145116168 | G | A | 1 | a0001c0001t0001g0007 | 5 | HG00099.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1125G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116168 | |||||||
| chr4:145116282 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.801-1011T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116282 | |||||||
| chr4:145116297 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.801-996C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116297 | |||||||
| chr4:145116483 | C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0053others(1): Show | 4 | HG01934.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-810C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116483 | |||||||
| chr4:145116531 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.801-762T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116531 | |||||||
| chr4:145116686 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.801-607T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116686 | |||||||
| chr4:145116795 | T | C | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-498T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116795 | |||||||
| chr4:145116838 | T | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.801-455T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116838 | |||||||
| chr4:145116913 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.801-380C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116913 | |||||||
| chr4:145117252 | G | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.801-41G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145117252 | |||||||
| chr4:145117570 | A | G | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.922+156A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145117570 | |||||||
| chr4:145117639 | A | G | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.922+225A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145117639 | |||||||
| chr4:145117696 | CTGCAGTA others(9): Show |
C | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 64 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.922+284_922+299del others(16): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145117696 | ||||||
| chr4:145118253 | C | CT | 2 | a0001c0001t0001g0011a0001c0003t0006g0022 | 5 | HG01192.hp2 HG01243.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.922+853dupT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145118253 | ||||||
| chr4:145118253 | CT | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0066others(2): Show | 6 | HG01070.hp2 HG01515.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.922+853delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145118253 | ||||||
| chr4:145118582 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.922+1168A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118582 | |||||||
| chr4:145118634 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.922+1220T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118634 | |||||||
| chr4:145118692 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.923-1240C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118692 | |||||||
| chr4:145118729 | G | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.923-1203G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118729 | |||||||
| chr4:145118923 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.923-1009C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118923 | |||||||
| chr4:145119163 | G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0067 | 3 | HG00741.hp2 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.923-769G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119163 | |||||||
| chr4:145119225 | C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.923-707C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119225 | |||||||
| chr4:145119238 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.923-694T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119238 | |||||||
| chr4:145119265 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923-667A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119265 | |||||||
| chr4:145119451 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.923-481A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119451 | |||||||
| chr4:145119589 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.923-343A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119589 | |||||||
| chr4:145119706 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923-226A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119706 | |||||||
| chr4:145119771 | TTAAA | T | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-158_923-155del others(4): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145119771 | ||||||
| chr4:145120200 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1144+47G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120200 | |||||||
| chr4:145120318 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1144+165G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120318 | |||||||
| chr4:145120357 | C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0065others(1): Show | 10 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144+204C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120357 | |||||||
| chr4:145120559 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144+406A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120559 | |||||||
| chr4:145120648 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1144+495A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120648 | |||||||
| chr4:145120989 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1145-185T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120989 | |||||||
| chr4:145121293 | G | C | 1 | a0001c0001t0001g0007 | 5 | HG00099.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1205-40G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 12/17 | chr4 | 145121293 | |||||||
| chr4:145122415 | C | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1264-606C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122415 | |||||||
| chr4:145122656 | T | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1264-365T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122656 | |||||||
| chr4:145122774 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1264-247G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122774 | |||||||
| chr4:145123373 | C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1517+16C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/17 | chr4 | 145123373 | |||||||
| chr4:145123387 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1517+30A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/17 | chr4 | 145123387 | |||||||
| chr4:145123783 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1640+183A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123783 | |||||||
| chr4:145123828 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1640+228C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123828 | |||||||
| chr4:145123841 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1640+241G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123841 | |||||||
| chr4:145124025 | A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0097 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1640+425A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124025 | |||||||
| chr4:145124338 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1641-652T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124338 | |||||||
| chr4:145124533 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1641-457G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124533 | |||||||
| chr4:145124616 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1641-374T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124616 | |||||||
| chr4:145124645 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1641-345C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124645 | |||||||
| chr4:145124986 | T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
splice_region_variant&intron_variant | LOW | c.1641-4T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124986 | |||||||
| chr4:145125237 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1752+136G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125237 | |||||||
| chr4:145125476 | A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025 | 7 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+375A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125476 | |||||||
| chr4:145125857 | C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0005g0135others(1): Show | 5 | HG01884.hp1 HG02572.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1752+756C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125857 | |||||||
| chr4:145125913 | C | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1752+812C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125913 | |||||||
| chr4:145125935 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1752+834G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125935 | |||||||
| chr4:145126155 | T | G | 1 | a0001c0001t0001g0043 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1752+1054T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126155 | |||||||
| chr4:145126247 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1752+1146G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126247 | |||||||
| chr4:145126326 | A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0126 | 4 | HG02630.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1200A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126326 | |||||||
| chr4:145126363 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1753-1163C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126363 | |||||||
| chr4:145126429 | G | A | 1 | a0001c0002t0003g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1753-1097G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126429 | |||||||
| chr4:145126835 | T | C | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1753-691T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126835 | |||||||
| chr4:145126971 | G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(14): Show | 33 | HG00621.hp2 HG01175.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1753-555G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126971 | |||||||
| chr4:145127086 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1753-440A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127086 | |||||||
| chr4:145127402 | T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 64 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1753-124T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127402 | |||||||
| chr4:145127431 | T | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1753-95T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127431 | |||||||
| chr4:145127457 | G | A | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753-69G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127457 |