Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11154 |
| ensemblid | ENSG00000100478.16 |
| hgncid | 575 |
| symbol | AP4S1 |
| name | adaptor related protein complex 4 subunit sigma 1 |
| refseq_nuc | NM_001128126.3 |
| refseq_prot | NP_001121598.1 |
| ensembl_nuc | ENST00000542754.7 |
| ensembl_prot | ENSP00000438170.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 31025649 |
| end | 31096450 |
| strand | + |
| ver | v1.2 |
| region | chr14:31025649-31096450 |
| region5000 | chr14:31020649-31101450 |
| regionname0 | AP4S1_chr14_31025649_31096450 |
| regionname5000 | AP4S1_chr14_31020649_31101450 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 432 | 346 | 82 | 56 | 152 | 12 | 42 | AP4S1_chr14_31020649_31101450 | AP4S1 | ATGAT others(427): Show |
chr14 | 31020649 | 31101450 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4060 | 179 | 30 | 24 | 95 | 7 | 22 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0002 | 0/0 | 4060 | 30 | 1 | 2 | 24 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0003 | 0/1 | 4062 | 23 | 4 | 12 | 0 | 3 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0004 | 0/0 | 4063 | 15 | 2 | 5 | 3 | 1 | 4 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4058): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0005 | 0/0 | 4061 | 13 | 4 | 3 | 3 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0006 | 0/0 | 4061 | 9 | 9 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0007 | 0/0 | 4062 | 8 | 2 | 1 | 0 | 0 | 5 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0008 | 0/0 | 4059 | 5 | 1 | 3 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4054): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0009 | 0/0 | 4062 | 5 | 1 | 4 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0010 | 0/0 | 4062 | 5 | 0 | 0 | 5 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0011 | 0/0 | 4062 | 4 | 0 | 0 | 4 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0012 | 0/0 | 4062 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0013 | 0/0 | 4060 | 3 | 0 | 0 | 3 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0014 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4058): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0015 | 0/0 | 4061 | 3 | 1 | 1 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0016 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0017 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0018 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0019 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0020 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0021 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0022 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0023 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0024 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0025 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0026 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0027 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0028 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0029 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0030 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0031 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0032 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0033 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0034 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0035 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4054): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0036 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0037 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4054): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0038 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0039 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0040 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4055): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0041 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0042 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0043 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0044 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0045 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0046 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0047 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4056): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0048 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4058): Show |
chr14 | 31020649 | 31101450 |
| a0001c0001t0049 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | ACTAA others(4057): Show |
chr14 | 31020649 | 31101450 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0011g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0013g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0013g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0015g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0015g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0017g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0018g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0018g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0020g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0022g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0023g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0024g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0025g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0026g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0027g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0028g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0030g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0031g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0032g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0033g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0035g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0036g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0037g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0038g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0039g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0040g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0041g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0042g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0043g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0044g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0045g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0046g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0047g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0048g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| a0001c0001t0049g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00140 | hp1 | a0001 | c0001 | t0015 | g0211 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0042 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00558 | hp1 | a0001 | c0001 | t0011 | g0088 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0082 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0262 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0244 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01255 | hp2 | a0001 | c0001 | t0044 | g0131 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0070 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01257 | hp2 | a0001 | c0001 | t0015 | g0143 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0062 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01884 | hp1 | a0001 | c0001 | t0031 | g0326 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0200 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0038 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02056 | hp2 | a0001 | c0001 | t0040 | g0324 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0090 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0273 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02135 | hp1 | a0001 | c0001 | t0022 | g0167 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02145 | hp1 | a0001 | c0001 | t0032 | g0250 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02145 | hp2 | a0001 | c0001 | t0039 | g0133 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02155 | hp1 | a0001 | c0001 | t0048 | g0129 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02155 | hp2 | a0001 | c0001 | t0045 | g0086 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0101 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02280 | hp2 | a0001 | c0001 | t0027 | g0164 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02630 | hp1 | a0001 | c0001 | t0042 | g0013 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02630 | hp2 | a0001 | c0001 | t0041 | g0227 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0268 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02723 | hp1 | a0001 | c0001 | t0036 | g0091 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02809 | hp1 | a0001 | c0001 | t0037 | g0041 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02886 | hp2 | a0001 | c0001 | t0020 | g0202 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0198 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0197 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02970 | hp1 | a0001 | c0001 | t0043 | g0204 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03017 | hp1 | a0001 | c0001 | t0030 | g0069 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0328 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0205 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0158 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0263 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0008 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03540 | hp2 | a0001 | c0001 | t0028 | g0194 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0254 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0266 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0226 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0269 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG03942 | hp2 | a0001 | c0001 | t0049 | g0229 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0208 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0279 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0267 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18747 | hp2 | a0001 | c0001 | t0038 | g0089 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18906 | hp1 | a0001 | c0001 | t0026 | g0192 | AFR | YRI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18944 | hp1 | a0001 | c0001 | t0013 | g0301 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18945 | hp1 | a0001 | c0001 | t0024 | g0190 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18950 | hp1 | a0001 | c0001 | t0033 | g0117 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18951 | hp1 | a0001 | c0001 | t0013 | g0317 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18957 | hp1 | a0001 | c0001 | t0017 | g0078 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18971 | hp2 | a0001 | c0001 | t0010 | g0272 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18972 | hp1 | a0001 | c0001 | t0023 | g0176 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0085 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18985 | hp1 | a0001 | c0001 | t0046 | g0087 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18989 | hp2 | a0001 | c0001 | t0010 | g0275 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA18999 | hp2 | a0001 | c0001 | t0017 | g0075 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19011 | hp2 | a0001 | c0001 | t0025 | g0186 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19067 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19075 | hp2 | a0001 | c0001 | t0010 | g0274 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19078 | hp2 | a0001 | c0001 | t0013 | g0276 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19082 | hp1 | a0001 | c0001 | t0035 | g0034 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0130 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0066 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02109 | hp1 | a0001 | c0001 | t0047 | g0264 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0201 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0007 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0199 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG06807 | hp1 | a0001 | c0001 | t0034 | g0010 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0072 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA21309 | hp1 | a0001 | c0001 | t0029 | g0243 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0077 | REF | REF | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31025703 | G | A | 3 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0020 |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-156G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40494 | chr14 | 31025703 | ||||||
| chr14:31025758 | G | A | 1 | a0001c0001t0020 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40439 | chr14 | 31025758 | ||||||
| chr14:31025782 | G | A | 9 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0022 others(6): Show |
38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40415 | chr14 | 31025782 | ||||||
| chr14:31093218 | T | C | 1 | a0001c0001t0029 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 183 | chr14 | 31093218 | ||||||
| chr14:31093352 | A | G | 2 | a0001c0001t0010 a0001c0001t0049 |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*317A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 317 | chr14 | 31093352 | ||||||
| chr14:31093465 | A | AT | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(11): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*443dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 444 | INFO_REALIGN_3_PRIME | chr14 | 31093465 | |||||
| chr14:31093465 | A | ATT | 4 | a0001c0001t0012 a0001c0001t0020 a0001c0001t0028 others(1): Show |
6 | HG01891.hp1 HG02109.hp2 HG02155.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*442_*443dupTT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 444 | INFO_REALIGN_3_PRIME | chr14 | 31093465 | |||||
| chr14:31093635 | C | T | 5 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0020 others(2): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*600C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 600 | chr14 | 31093635 | ||||||
| chr14:31093787 | C | T | 1 | a0001c0001t0040 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 752 | chr14 | 31093787 | ||||||
| chr14:31094332 | C | T | 1 | a0001c0001t0047 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1297C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1297 | chr14 | 31094332 | ||||||
| chr14:31094380 | G | A | 1 | a0001c0001t0006 | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1345G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1345 | chr14 | 31094380 | ||||||
| chr14:31094453 | G | A | 1 | a0001c0001t0049 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1418 | chr14 | 31094453 | ||||||
| chr14:31094467 | A | G | 4 | a0001c0001t0011 a0001c0001t0045 a0001c0001t0046 others(1): Show |
7 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1432 | chr14 | 31094467 | ||||||
| chr14:31094611 | G | A | 1 | a0001c0001t0030 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1576 | chr14 | 31094611 | ||||||
| chr14:31094627 | G | A | 1 | a0001c0001t0029 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1592 | chr14 | 31094627 | ||||||
| chr14:31094641 | C | T | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(15): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1606C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1606 | chr14 | 31094641 | ||||||
| chr14:31094742 | T | C | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(25): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1707T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1707 | chr14 | 31094742 | ||||||
| chr14:31095061 | G | A | 5 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0020 others(2): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2026G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2026 | chr14 | 31095061 | ||||||
| chr14:31095081 | C | G | 1 | a0001c0001t0014 | 3 | HG02572.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2046C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2046 | chr14 | 31095081 | ||||||
| chr14:31095086 | C | G | 1 | a0001c0001t0038 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2051 | chr14 | 31095086 | ||||||
| chr14:31095119 | A | G | 1 | a0001c0001t0017 | 2 | NA18957.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2084 | chr14 | 31095119 | ||||||
| chr14:31095410 | C | T | 2 | a0001c0001t0019 a0001c0001t0039 |
3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2375C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2375 | chr14 | 31095410 | ||||||
| chr14:31095638 | C | T | 1 | a0001c0001t0006 | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2603C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2603 | chr14 | 31095638 | ||||||
| chr14:31095671 | C | T | 2 | a0001c0001t0036 a0001c0001t0037 |
2 | HG02723.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2636 | chr14 | 31095671 | ||||||
| chr14:31095753 | A | G | 1 | a0001c0001t0024 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2718A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2718 | chr14 | 31095753 | ||||||
| chr14:31095768 | A | T | 2 | a0001c0001t0010 a0001c0001t0049 |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2733A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2733 | chr14 | 31095768 | ||||||
| chr14:31095817 | C | T | 3 | a0001c0001t0013 a0001c0001t0023 a0001c0001t0035 |
5 | NA18944.hp1 NA18951.hp1 NA18972.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2782 | chr14 | 31095817 | ||||||
| chr14:31095821 | C | T | 1 | a0001c0001t0034 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2786 | chr14 | 31095821 | ||||||
| chr14:31095822 | G | A | 1 | a0001c0001t0009 | 5 | HG01069.hp2 HG01123.hp1 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2787G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2787 | chr14 | 31095822 | ||||||
| chr14:31095846 | C | T | 1 | a0001c0001t0044 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2811C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2811 | chr14 | 31095846 | ||||||
| chr14:31095929 | C | T | 1 | a0001c0001t0022 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2894 | chr14 | 31095929 | ||||||
| chr14:31096089 | C | CA | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(13): Show |
70 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*3076dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3077 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | |||||
| chr14:31096089 | C | CAA | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(2): Show |
28 | HG00280.hp1 HG00733.hp1 HG01106.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3075_*3076dupAA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3077 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | |||||
| chr14:31096089 | CA | C | 3 | a0001c0001t0008 a0001c0001t0035 a0001c0001t0037 |
7 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3076delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3076 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | |||||
| chr14:31096139 | A | G | 1 | a0001c0001t0049 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3104A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3104 | chr14 | 31096139 | ||||||
| chr14:31096173 | C | T | 8 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0012 others(5): Show |
23 | HG01891.hp1 HG02055.hp2 HG02074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3138 | chr14 | 31096173 | ||||||
| chr14:31096215 | A | AT | 2 | a0001c0001t0010 a0001c0001t0049 |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3182dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3183 | INFO_REALIGN_3_PRIME | chr14 | 31096215 | |||||
| chr14:31096254 | C | CA | 1 | a0001c0001t0014 | 3 | HG02572.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3223dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3224 | INFO_REALIGN_3_PRIME | chr14 | 31096254 | |||||
| chr14:31096284 | G | A | 1 | a0001c0001t0043 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3249G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3249 | chr14 | 31096284 | ||||||
| chr14:31096356 | G | A | 5 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0020 others(2): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3321G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3321 | chr14 | 31096356 | ||||||
| chr14:31096386 | A | G | 1 | a0001c0001t0033 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3351A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3351 | chr14 | 31096386 | ||||||
| chr14:31096408 | C | T | 5 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0020 others(2): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3373C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3373 | chr14 | 31096408 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:31025823 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-72+36G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31025823 | |||||||
| chr14:31025916 | C | T | 1 | a0001c0001t0001g0342 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-72+129C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31025916 | |||||||
| chr14:31026108 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+321C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026108 | |||||||
| chr14:31026140 | C | T | 63 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(60): Show |
63 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-72+353C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026140 | |||||||
| chr14:31026299 | G | A | 1 | a0001c0001t0002g0006 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-72+512G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026299 | |||||||
| chr14:31026341 | G | T | 1 | a0001c0001t0004g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-72+554G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026341 | |||||||
| chr14:31026386 | C | G | 1 | a0001c0001t0002g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-72+599C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026386 | |||||||
| chr14:31026419 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-72+632C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026419 | |||||||
| chr14:31026507 | A | C | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+720A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026507 | |||||||
| chr14:31026568 | G | T | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+781G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026568 | |||||||
| chr14:31026633 | C | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0193 a0001c0001t0001g0195 others(37): Show |
41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-72+846C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026633 | |||||||
| chr14:31026665 | G | A | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+878G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026665 | |||||||
| chr14:31026722 | C | G | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+935C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026722 | |||||||
| chr14:31026722 | C | T | 4 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+935C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026722 | |||||||
| chr14:31026773 | C | G | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+986C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026773 | |||||||
| chr14:31026813 | C | T | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+1026C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026813 | |||||||
| chr14:31026826 | C | T | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+1039C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026826 | |||||||
| chr14:31026869 | AG | A | 28 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(25): Show |
29 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-72+1083delG | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026869 | |||||||
| chr14:31026905 | C | T | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+1118C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026905 | |||||||
| chr14:31027006 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-72+1219T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027006 | |||||||
| chr14:31027162 | G | C | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-72+1375G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027162 | |||||||
| chr14:31027459 | C | T | 1 | a0001c0001t0048g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-72+1672C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027459 | |||||||
| chr14:31027535 | ACCTGTAG others(2): Show |
A | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+1751_-72+1759d others(11): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31027535 | ||||||
| chr14:31027574 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-72+1787A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027574 | |||||||
| chr14:31027928 | T | A | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+2141T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027928 | |||||||
| chr14:31028037 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-72+2250A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028037 | |||||||
| chr14:31028183 | AT | A | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-72+2408delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028183 | ||||||
| chr14:31028394 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-72+2607T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028394 | |||||||
| chr14:31028539 | G | A | 1 | a0001c0001t0002g0163 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-72+2752G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028539 | |||||||
| chr14:31028596 | T | TAC | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(69): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.-72+2831_-72+2832d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | ||||||
| chr14:31028596 | T | TACAC | 57 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(54): Show |
57 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-72+2829_-72+2832d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | ||||||
| chr14:31028596 | T | TACACAC | 17 | a0001c0001t0001g0003 a0001c0001t0001g0280 a0001c0001t0001g0281 others(14): Show |
17 | HG00323.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+2827_-72+2832d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | ||||||
| chr14:31028596 | T | TACACACA others(1): Show |
3 | a0001c0001t0012g0199 a0001c0001t0016g0197 a0001c0001t0016g0198 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-72+2825_-72+2832d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | ||||||
| chr14:31028596 | TAC | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00741.hp2 HG02015.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+2831_-72+2832d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | ||||||
| chr14:31028667 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-72+2880C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028667 | |||||||
| chr14:31028798 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0018g0205 a0001c0001t0043g0204 |
3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+3011C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028798 | |||||||
| chr14:31028850 | G | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(313): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-72+3063G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028850 | |||||||
| chr14:31028851 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+3064T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028851 | |||||||
| chr14:31028879 | C | A | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+3092C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028879 | |||||||
| chr14:31028921 | A | G | 10 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 others(7): Show |
10 | NA18939.hp1 NA18947.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+3134A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028921 | |||||||
| chr14:31029025 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0026g0192 a0001c0001t0027g0164 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+3238A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029025 | |||||||
| chr14:31029096 | T | A | 1 | a0001c0001t0008g0022 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-72+3309T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029096 | |||||||
| chr14:31029112 | A | C | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+3325A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029112 | |||||||
| chr14:31029129 | TC | T | 3 | a0001c0001t0001g0206 a0001c0001t0018g0205 a0001c0001t0043g0204 |
3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+3343delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029129 | |||||||
| chr14:31029204 | T | A | 23 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0212 others(20): Show |
23 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-72+3417T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029204 | |||||||
| chr14:31029341 | A | G | 5 | a0001c0001t0001g0240 a0001c0001t0005g0241 a0001c0001t0005g0242 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+3554A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029341 | |||||||
| chr14:31029357 | A | G | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+3570A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029357 | |||||||
| chr14:31029518 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG02074.hp1 NA18977.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+3731T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029518 | |||||||
| chr14:31029558 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72+3771C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029558 | |||||||
| chr14:31029576 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | NA18995.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-72+3789C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029576 | |||||||
| chr14:31029675 | A | G | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+3888A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029675 | |||||||
| chr14:31029849 | C | CA | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+4074dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31029849 | ||||||
| chr14:31029851 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+4064A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029851 | |||||||
| chr14:31029876 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0193 a0001c0001t0001g0195 others(37): Show |
41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-72+4089C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029876 | |||||||
| chr14:31030007 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG00544.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-72+4220A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030007 | |||||||
| chr14:31030076 | G | A | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+4289G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030076 | |||||||
| chr14:31030185 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+4398G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030185 | |||||||
| chr14:31030223 | T | C | 2 | a0001c0001t0012g0200 a0001c0001t0012g0201 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-72+4436T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030223 | |||||||
| chr14:31030307 | G | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+4520G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030307 | |||||||
| chr14:31030342 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0193 others(67): Show |
71 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-72+4555T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030342 | |||||||
| chr14:31030553 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0035g0034 |
2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-72+4766T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030553 | |||||||
| chr14:31030571 | A | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0246 a0001c0001t0001g0251 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-72+4784A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030571 | |||||||
| chr14:31030578 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0007g0208 |
2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-72+4791G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030578 | |||||||
| chr14:31030628 | C | T | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+4841C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030628 | |||||||
| chr14:31030650 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-72+4863G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030650 | |||||||
| chr14:31030754 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+4967A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030754 | |||||||
| chr14:31030779 | A | G | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-72+4992A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030779 | |||||||
| chr14:31030869 | A | G | 10 | a0001c0001t0001g0206 a0001c0001t0001g0270 a0001c0001t0010g0271 others(7): Show |
10 | HG02074.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+5082A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030869 | |||||||
| chr14:31031102 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-72+5315C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031102 | |||||||
| chr14:31031197 | T | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+5410T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031197 | |||||||
| chr14:31031224 | T | C | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+5437T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031224 | |||||||
| chr14:31031331 | T | A | 64 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(61): Show |
64 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-72+5544T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031331 | |||||||
| chr14:31031440 | C | G | 3 | a0001c0001t0001g0206 a0001c0001t0018g0205 a0001c0001t0043g0204 |
3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+5653C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031440 | |||||||
| chr14:31031478 | C | T | 1 | a0001c0001t0019g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-72+5691C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031478 | |||||||
| chr14:31031553 | A | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-72+5766A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031553 | |||||||
| chr14:31031745 | C | G | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+5958C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031745 | |||||||
| chr14:31031828 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+6041A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031828 | |||||||
| chr14:31031842 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+6055C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031842 | |||||||
| chr14:31031906 | A | G | 3 | a0001c0001t0006g0327 a0001c0001t0006g0328 a0001c0001t0031g0326 |
3 | HG01884.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-72+6119A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031906 | |||||||
| chr14:31031914 | TG | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+6131delG | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31031914 | ||||||
| chr14:31031947 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-72+6160A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031947 | |||||||
| chr14:31031958 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-72+6171G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031958 | |||||||
| chr14:31032071 | C | CA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG00738.hp2 HG01928.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72+6304dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | ||||||
| chr14:31032071 | CAAAAA | C | 24 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0212 others(21): Show |
24 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-72+6300_-72+6304d others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | ||||||
| chr14:31032071 | CAAAAAA | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
153 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-72+6299_-72+6304d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | ||||||
| chr14:31032071 | CAAAAAAA | C | 10 | a0001c0001t0001g0206 a0001c0001t0001g0270 a0001c0001t0010g0271 others(7): Show |
10 | HG02074.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+6298_-72+6304d others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | ||||||
| chr14:31032087 | A | G | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+6300A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032087 | |||||||
| chr14:31032255 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0018g0205 a0001c0001t0043g0204 |
3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+6468G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032255 | |||||||
| chr14:31032274 | A | G | 2 | a0001c0001t0006g0327 a0001c0001t0006g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-72+6487A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032274 | |||||||
| chr14:31032299 | C | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-72+6512C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032299 | |||||||
| chr14:31032403 | C | T | 3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 |
3 | HG02559.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-72+6616C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032403 | |||||||
| chr14:31032523 | A | ATT | 65 | a0001c0001t0001g0270 a0001c0001t0001g0280 a0001c0001t0001g0281 others(62): Show |
65 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-72+6750_-72+6751d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | ||||||
| chr14:31032523 | A | ATTT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0206 a0001c0001t0001g0207 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-72+6749_-72+6751d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | ||||||
| chr14:31032523 | A | ATTTT | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0193 others(44): Show |
48 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-72+6748_-72+6751d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | ||||||
| chr14:31032523 | AT | A | 6 | a0001c0001t0001g0040 a0001c0001t0007g0157 a0001c0001t0007g0161 others(3): Show |
6 | HG00621.hp2 HG01106.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-72+6751delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | ||||||
| chr14:31032587 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-72+6800G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032587 | |||||||
| chr14:31032689 | C | A | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+6902C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032689 | |||||||
| chr14:31032697 | G | A | 23 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0212 others(20): Show |
23 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-72+6910G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032697 | |||||||
| chr14:31032727 | G | A | 9 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(6): Show |
9 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72+6940G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032727 | |||||||
| chr14:31032760 | T | C | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+6973T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032760 | |||||||
| chr14:31032762 | C | T | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+6975C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032762 | |||||||
| chr14:31032771 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-72+6984T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032771 | |||||||
| chr14:31032776 | C | T | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+6989C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032776 | |||||||
| chr14:31033220 | A | AT | 7 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+7444dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31033220 | ||||||
| chr14:31033253 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+7466A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033253 | |||||||
| chr14:31033275 | G | A | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-72+7488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033275 | |||||||
| chr14:31033430 | C | T | 64 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(61): Show |
64 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-72+7643C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033430 | |||||||
| chr14:31033431 | C | T | 1 | a0001c0001t0007g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72+7644C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033431 | |||||||
| chr14:31033440 | C | T | 4 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(1): Show |
4 | HG02257.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+7653C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033440 | |||||||
| chr14:31033606 | G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+7819G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033606 | |||||||
| chr14:31034068 | A | G | 3 | a0001c0001t0001g0206 a0001c0001t0018g0205 a0001c0001t0043g0204 |
3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+8281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034068 | |||||||
| chr14:31034108 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-72+8321G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034108 | |||||||
| chr14:31034255 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-72+8468C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034255 | |||||||
| chr14:31034277 | C | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-72+8490C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034277 | |||||||
| chr14:31034392 | G | A | 2 | a0001c0001t0007g0157 a0001c0001t0007g0161 |
2 | HG01106.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-72+8605G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034392 | |||||||
| chr14:31034413 | C | T | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+8626C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034413 | |||||||
| chr14:31034468 | T | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-72+8681T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034468 | |||||||
| chr14:31034570 | C | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+8783C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034570 | |||||||
| chr14:31034609 | A | AT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0029 others(79): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-72+8847dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | ||||||
| chr14:31034609 | A | ATT | 11 | a0001c0001t0001g0239 a0001c0001t0002g0163 a0001c0001t0002g0165 others(8): Show |
11 | HG00438.hp1 HG02572.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-72+8846_-72+8847d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | ||||||
| chr14:31034609 | AT | A | 73 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0144 others(70): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-72+8847delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | ||||||
| chr14:31034687 | G | A | 67 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(64): Show |
67 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-72+8900G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034687 | |||||||
| chr14:31034703 | C | T | 2 | a0001c0001t0003g0152 a0001c0001t0003g0153 |
2 | HG00099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-72+8916C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034703 | |||||||
| chr14:31034766 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0231 others(32): Show |
35 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-72+8979C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034766 | |||||||
| chr14:31034839 | C | A | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+9052C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034839 | |||||||
| chr14:31034880 | G | T | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+9093G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034880 | |||||||
| chr14:31034910 | A | T | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+9123A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034910 | |||||||
| chr14:31034970 | A | T | 1 | a0001c0001t0024g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-72+9183A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034970 | |||||||
| chr14:31035036 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-72+9249T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035036 | |||||||
| chr14:31035122 | T | G | 11 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72+9335T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035122 | |||||||
| chr14:31035138 | T | C | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+9351T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035138 | |||||||
| chr14:31035193 | C | CT | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-72+9426dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035193 | ||||||
| chr14:31035193 | C | CTT | 47 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(44): Show |
47 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-72+9425_-72+9426d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035193 | ||||||
| chr14:31035232 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-72+9445A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035232 | |||||||
| chr14:31035332 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-72+9545T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035332 | |||||||
| chr14:31035395 | A | ATG | 224 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-72+9609_-72+9610i others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035395 | ||||||
| chr14:31035405 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+9618A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035405 | |||||||
| chr14:31035562 | T | TAAAAAAA others(317): Show |
2 | a0001c0001t0005g0242 a0001c0001t0029g0243 |
2 | HG00639.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+9789_-72+9790i others(326): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035562 | ||||||
| chr14:31035562 | T | TAAAAAAA others(339): Show |
1 | a0001c0001t0005g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-72+9789_-72+9790i others(348): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035562 | ||||||
| chr14:31035563 | A | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0093 others(53): Show |
56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-72+9776A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035563 | |||||||
| chr14:31035627 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-72+9840C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035627 | |||||||
| chr14:31035638 | C | CT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(71): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-72+9866dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035638 | ||||||
| chr14:31035770 | C | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+9983C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035770 | |||||||
| chr14:31035790 | T | C | 8 | a0001c0001t0001g0206 a0001c0001t0012g0199 a0001c0001t0012g0200 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-72+10003T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035790 | |||||||
| chr14:31035831 | T | G | 1 | a0001c0001t0006g0328 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72+10044T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035831 | |||||||
| chr14:31035842 | G | A | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-72+10055G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035842 | |||||||
| chr14:31035843 | C | T | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+10056C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035843 | |||||||
| chr14:31035850 | CT | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-72+10065delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035850 | ||||||
| chr14:31035883 | A | G | 24 | a0001c0001t0001g0035 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-72+10096A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035883 | |||||||
| chr14:31035912 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72+10125G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035912 | |||||||
| chr14:31035920 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0013g0317 |
2 | NA18951.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-72+10133C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035920 | |||||||
| chr14:31035931 | C | T | 2 | a0001c0001t0003g0130 a0001c0001t0044g0131 |
2 | HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-72+10144C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035931 | |||||||
| chr14:31035932 | A | G | 2 | a0001c0001t0003g0130 a0001c0001t0044g0131 |
2 | HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-72+10145A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035932 | |||||||
| chr14:31035955 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0098 |
2 | HG00733.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-72+10168A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035955 | |||||||
| chr14:31035972 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0010g0271 a0001c0001t0010g0272 others(4): Show |
7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+10185C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035972 | |||||||
| chr14:31035981 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-72+10194T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035981 | |||||||
| chr14:31035982 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-72+10195G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035982 | |||||||
| chr14:31036021 | T | C | 5 | a0001c0001t0001g0106 a0001c0001t0001g0121 a0001c0001t0002g0187 others(2): Show |
5 | HG02135.hp1 HG02970.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+10234T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036021 | |||||||
| chr14:31036025 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-72+10238T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036025 | |||||||
| chr14:31036133 | TTA | T | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(19): Show |
22 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+10347_-72+1034 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036133 | |||||||
| chr14:31036134 | T | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0206 a0001c0001t0007g0157 others(6): Show |
9 | HG01106.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-72+10347T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036134 | |||||||
| chr14:31036142 | T | A | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(19): Show |
22 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+10355T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036142 | |||||||
| chr14:31036190 | AT | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0093 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-72+10404delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036190 | |||||||
| chr14:31036201 | A | G | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+10414A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036201 | |||||||
| chr14:31036572 | C | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+10785C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036572 | |||||||
| chr14:31036589 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(26): Show |
29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-72+10802A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036589 | |||||||
| chr14:31036969 | T | TGCCCGGC others(186): Show |
1 | a0001c0001t0005g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(197): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | ||||||
| chr14:31036969 | T | TGCCCGGC others(187): Show |
1 | a0001c0001t0005g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(198): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | ||||||
| chr14:31036969 | T | TGCCCGGC others(190): Show |
1 | a0001c0001t0032g0250 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(201): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | ||||||
| chr14:31037003 | A | G | 3 | a0001c0001t0005g0248 a0001c0001t0005g0249 a0001c0001t0032g0250 |
3 | HG02145.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-72+11216A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037003 | |||||||
| chr14:31037070 | C | T | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-72+11283C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037070 | |||||||
| chr14:31037143 | A | G | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11356A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037143 | |||||||
| chr14:31037181 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-72+11394C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037181 | |||||||
| chr14:31037203 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-72+11416A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037203 | |||||||
| chr14:31037205 | C | G | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11418C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037205 | |||||||
| chr14:31037299 | T | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(284): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.-72+11512T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037299 | |||||||
| chr14:31037339 | A | C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+11552A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037339 | |||||||
| chr14:31037376 | T | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11589T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037376 | |||||||
| chr14:31037410 | T | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+11623T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037410 | |||||||
| chr14:31037427 | C | CT | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11643dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31037427 | ||||||
| chr14:31037439 | C | T | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+11652C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037439 | |||||||
| chr14:31037926 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0109 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+12139T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037926 | |||||||
| chr14:31037943 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0047g0264 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-72+12156C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037943 | |||||||
| chr14:31037953 | A | T | 50 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+12166A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037953 | |||||||
| chr14:31037973 | C | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+12186C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037973 | |||||||
| chr14:31038014 | T | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+12227T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038014 | |||||||
| chr14:31038193 | A | G | 1 | a0001c0001t0010g0275 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-72+12406A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038193 | |||||||
| chr14:31038653 | TC | T | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(19): Show |
22 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+12868delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31038653 | ||||||
| chr14:31038753 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-72+12966T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038753 | |||||||
| chr14:31038788 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-72+13001C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038788 | |||||||
| chr14:31038820 | A | G | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-72+13033A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038820 | |||||||
| chr14:31038870 | A | G | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+13083A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038870 | |||||||
| chr14:31038992 | GT | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(210): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-72+13219delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31038992 | ||||||
| chr14:31039118 | G | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(282): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-72+13331G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039118 | |||||||
| chr14:31039216 | C | T | 1 | a0001c0001t0004g0095 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-72+13429C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039216 | |||||||
| chr14:31039220 | C | G | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+13433C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039220 | |||||||
| chr14:31039225 | G | A | 35 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(32): Show |
35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+13438G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039225 | |||||||
| chr14:31039567 | G | GTT | 18 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0001g0332 others(15): Show |
19 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-72+13783_-72+1378 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039567 | ||||||
| chr14:31039570 | T | TTTTG | 5 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0001c0001t0001g0322 others(2): Show |
5 | HG00544.hp2 HG01192.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+13784_-72+1378 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039570 | ||||||
| chr14:31039571 | T | TTTG | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.-72+13784_-72+1378 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039571 | |||||||
| chr14:31039572 | G | GT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0142 others(7): Show |
10 | HG01981.hp1 HG02109.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+13803dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039572 | ||||||
| chr14:31039572 | G | T | 68 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-72+13785G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039572 | |||||||
| chr14:31039577 | T | G | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-72+13790T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039577 | |||||||
| chr14:31039578 | T | TG | 16 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+13791_-72+1379 others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039578 | |||||||
| chr14:31039579 | T | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(118): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-72+13792T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039579 | |||||||
| chr14:31039588 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG00639.hp1 HG01106.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+13801T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039588 | |||||||
| chr14:31039663 | CCCGGGTT others(11): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-72+13897_-72+1391 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039663 | ||||||
| chr14:31039840 | C | T | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+14053C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039840 | |||||||
| chr14:31039868 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-72+14081C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039868 | |||||||
| chr14:31039878 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+14091C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039878 | |||||||
| chr14:31039881 | G | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+14094G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039881 | |||||||
| chr14:31039884 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+14097C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039884 | |||||||
| chr14:31040041 | T | G | 1 | a0001c0001t0011g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-72+14254T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040041 | |||||||
| chr14:31040089 | A | G | 1 | a0001c0001t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-72+14302A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040089 | |||||||
| chr14:31040148 | C | CT | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(240): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-72+14379dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31040148 | ||||||
| chr14:31040148 | C | CTT | 9 | a0001c0001t0001g0039 a0001c0001t0001g0079 a0001c0001t0001g0080 others(6): Show |
9 | HG00280.hp2 HG02071.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72+14378_-72+1437 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31040148 | ||||||
| chr14:31040165 | T | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+14378T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040165 | |||||||
| chr14:31040244 | C | G | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+14457C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040244 | |||||||
| chr14:31040292 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18988.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-72+14505G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040292 | |||||||
| chr14:31040456 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+14669A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040456 | |||||||
| chr14:31040822 | G | T | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+15035G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040822 | |||||||
| chr14:31040827 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0050 |
2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-72+15040G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040827 | |||||||
| chr14:31040902 | G | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+15115G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040902 | |||||||
| chr14:31041075 | C | CA | 131 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(128): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-72+15303dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041075 | ||||||
| chr14:31041075 | CA | C | 36 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(33): Show |
36 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-72+15303delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041075 | ||||||
| chr14:31041131 | T | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(117): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-72+15344T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041131 | |||||||
| chr14:31041211 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+15424G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041211 | |||||||
| chr14:31041228 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-72+15441C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041228 | |||||||
| chr14:31041338 | G | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-72+15551G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041338 | |||||||
| chr14:31041613 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+15826C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041613 | |||||||
| chr14:31041673 | A | C | 53 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(50): Show |
53 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-72+15886A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041673 | |||||||
| chr14:31041687 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+15900A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041687 | |||||||
| chr14:31041747 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-72+15960G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041747 | |||||||
| chr14:31041807 | T | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+16020T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041807 | |||||||
| chr14:31041853 | A | AT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(10): Show |
13 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-72+16072dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041853 | ||||||
| chr14:31041913 | C | T | 1 | a0001c0001t0005g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-72+16126C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041913 | |||||||
| chr14:31041915 | G | A | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+16128G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041915 | |||||||
| chr14:31041953 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-72+16166G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041953 | |||||||
| chr14:31042145 | T | C | 50 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+16358T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042145 | |||||||
| chr14:31042170 | T | C | 53 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(50): Show |
53 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-72+16383T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042170 | |||||||
| chr14:31042282 | C | G | 35 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(32): Show |
35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+16495C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042282 | |||||||
| chr14:31042376 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | NA18946.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-72+16589A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042376 | |||||||
| chr14:31042537 | G | A | 50 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+16750G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042537 | |||||||
| chr14:31042557 | G | A | 1 | a0001c0001t0005g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+16770G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042557 | |||||||
| chr14:31042707 | A | G | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+16920A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042707 | |||||||
| chr14:31042848 | G | T | 1 | a0001c0001t0002g0168 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+17061G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042848 | |||||||
| chr14:31042992 | G | A | 2 | a0001c0001t0005g0083 a0001c0001t0005g0084 |
2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72+17205G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042992 | |||||||
| chr14:31043034 | G | A | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-72+17247G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043034 | |||||||
| chr14:31043094 | G | T | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72+17307G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043094 | |||||||
| chr14:31043146 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(114): Show |
118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-72+17359G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043146 | |||||||
| chr14:31043182 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-72+17395C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043182 | |||||||
| chr14:31043225 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-72+17438G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043225 | |||||||
| chr14:31043225 | G | GAA | 84 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
85 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-72+17449_-72+1745 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31043225 | ||||||
| chr14:31043283 | T | G | 1 | a0001c0001t0005g0305 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-72+17496T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043283 | |||||||
| chr14:31043310 | C | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+17523C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043310 | |||||||
| chr14:31043405 | G | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-72+17618G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043405 | |||||||
| chr14:31043525 | C | T | 35 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(32): Show |
35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+17738C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043525 | |||||||
| chr14:31043710 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0109 |
2 | HG02135.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-72+17923T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043710 | |||||||
| chr14:31043893 | A | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+18106A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043893 | |||||||
| chr14:31044100 | G | C | 129 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(126): Show |
130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-72+18313G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044100 | |||||||
| chr14:31044106 | A | G | 29 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
30 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.-72+18319A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044106 | |||||||
| chr14:31044219 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+18432C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044219 | |||||||
| chr14:31044260 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0112 others(3): Show |
6 | NA18971.hp1 NA19007.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+18473G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044260 | |||||||
| chr14:31044289 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-72+18502T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044289 | |||||||
| chr14:31044408 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+18621C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044408 | |||||||
| chr14:31044413 | A | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+18626A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044413 | |||||||
| chr14:31044527 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+18740T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044527 | |||||||
| chr14:31044637 | C | T | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0314 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+18850C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044637 | |||||||
| chr14:31044719 | C | G | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+18932C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044719 | |||||||
| chr14:31044811 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-72+19024C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044811 | |||||||
| chr14:31044836 | T | C | 1 | a0001c0001t0020g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-72+19049T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044836 | |||||||
| chr14:31044851 | G | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(117): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-72+19064G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044851 | |||||||
| chr14:31044875 | A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+19088A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044875 | |||||||
| chr14:31044906 | A | AT | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0213 others(3): Show |
6 | HG02280.hp2 HG02622.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+19133dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31044906 | ||||||
| chr14:31044994 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(23): Show |
26 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-72+19207C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044994 | |||||||
| chr14:31045032 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0185 |
2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-72+19245G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045032 | |||||||
| chr14:31045050 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-72+19263C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045050 | |||||||
| chr14:31045167 | G | T | 3 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 |
3 | HG01891.hp1 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-72+19380G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045167 | |||||||
| chr14:31045283 | G | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
30 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.-72+19496G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045283 | |||||||
| chr14:31045392 | G | A | 82 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-72+19605G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045392 | |||||||
| chr14:31045493 | G | A | 12 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0011g0082 others(9): Show |
12 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-72+19706G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045493 | |||||||
| chr14:31045626 | C | T | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+19839C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045626 | |||||||
| chr14:31045627 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-72+19840G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045627 | |||||||
| chr14:31045663 | A | C | 82 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-72+19876A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045663 | |||||||
| chr14:31045753 | G | A | 1 | a0001c0001t0012g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-72+19966G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045753 | |||||||
| chr14:31045790 | A | G | 56 | a0001c0001t0001g0092 a0001c0001t0001g0118 a0001c0001t0001g0251 others(53): Show |
56 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.-72+20003A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045790 | |||||||
| chr14:31045866 | T | G | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-72+20079T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045866 | |||||||
| chr14:31045910 | T | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(27): Show |
30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-72+20123T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045910 | |||||||
| chr14:31045964 | A | AT | 15 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
15 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-20143dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31045964 | ||||||
| chr14:31045964 | AT | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(168): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-71-20143delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31045964 | ||||||
| chr14:31045988 | C | T | 1 | a0001c0001t0009g0038 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-71-20138C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045988 | |||||||
| chr14:31046057 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-71-20069C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046057 | |||||||
| chr14:31046257 | A | G | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-19869A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046257 | |||||||
| chr14:31046567 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-71-19559C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046567 | |||||||
| chr14:31046573 | C | T | 1 | a0001c0001t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-71-19553C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046573 | |||||||
| chr14:31046703 | G | A | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-19423G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046703 | |||||||
| chr14:31046795 | G | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-19331G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046795 | |||||||
| chr14:31046845 | C | CA | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
33 | HG01361.hp1 HG01891.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-71-19262dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046845 | ||||||
| chr14:31046845 | C | CAA | 7 | a0001c0001t0006g0015 a0001c0001t0006g0017 a0001c0001t0010g0271 others(4): Show |
7 | HG02055.hp2 HG02074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-19263_-71-1926 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046845 | ||||||
| chr14:31046862 | AAAG | A | 7 | a0001c0001t0001g0003 a0001c0001t0004g0094 a0001c0001t0004g0095 others(4): Show |
7 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-19257_-71-1925 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046862 | ||||||
| chr14:31046884 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-71-19242A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046884 | |||||||
| chr14:31047178 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-71-18948C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047178 | |||||||
| chr14:31047385 | C | CT | 12 | a0001c0001t0001g0076 a0001c0001t0001g0195 a0001c0001t0001g0232 others(9): Show |
12 | HG00741.hp2 HG01175.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-18721dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047385 | ||||||
| chr14:31047385 | CT | C | 7 | a0001c0001t0001g0206 a0001c0001t0001g0240 a0001c0001t0001g0337 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-18721delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047385 | ||||||
| chr14:31047411 | G | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-18715G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047411 | |||||||
| chr14:31047537 | G | A | 1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-71-18589G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047537 | |||||||
| chr14:31047564 | T | G | 1 | a0001c0001t0007g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-71-18562T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047564 | |||||||
| chr14:31047630 | T | G | 8 | a0001c0001t0011g0082 a0001c0001t0011g0085 a0001c0001t0011g0088 others(5): Show |
8 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-18496T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047630 | |||||||
| chr14:31047631 | G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-18495G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047631 | |||||||
| chr14:31047789 | A | AT | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-18336dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047789 | ||||||
| chr14:31047850 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-18276A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047850 | |||||||
| chr14:31048093 | A | AT | 10 | a0001c0001t0001g0039 a0001c0001t0002g0169 a0001c0001t0002g0183 others(7): Show |
10 | HG00673.hp1 HG02071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-18016dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31048093 | ||||||
| chr14:31048093 | AT | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0228 others(6): Show |
9 | HG01069.hp1 HG01074.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-71-18016delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31048093 | ||||||
| chr14:31048239 | G | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-17887G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048239 | |||||||
| chr14:31048266 | T | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-17860T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048266 | |||||||
| chr14:31048600 | G | T | 2 | a0001c0001t0019g0007 a0001c0001t0019g0008 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-17526G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048600 | |||||||
| chr14:31048799 | G | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-71-17327G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048799 | |||||||
| chr14:31048870 | C | T | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-71-17256C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048870 | |||||||
| chr14:31049025 | G | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-71-17101G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049025 | |||||||
| chr14:31049180 | G | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16946G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049180 | |||||||
| chr14:31049184 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16942C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049184 | |||||||
| chr14:31049188 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-16938T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049188 | |||||||
| chr14:31049199 | G | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16927G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049199 | |||||||
| chr14:31049210 | G | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-16916G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049210 | |||||||
| chr14:31049413 | C | CA | 8 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0110 others(5): Show |
8 | HG01257.hp1 HG01258.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71-16697dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049413 | ||||||
| chr14:31049426 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-71-16700A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049426 | |||||||
| chr14:31049426 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0010g0275 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-71-16698_-71-1668 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049426 | ||||||
| chr14:31049426 | AAAATATA others(9): Show |
A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-16698_-71-1668 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049426 | ||||||
| chr14:31049427 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-71-16699A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049427 | |||||||
| chr14:31049427 | AAATATAT others(2): Show |
A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-16697_-71-1668 others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049427 | ||||||
| chr14:31049428 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0147 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(29): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-71-16697_-71-1669 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(28): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(23): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0003g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(27): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0003g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0152 a0001c0001t0044g0131 |
2 | HG00099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-71-16697_-71-1669 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAAAAATA others(9): Show |
1 | a0001c0001t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAATATAT others(8): Show |
1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AAT | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0116 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16665_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0028 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-71-16673_-71-1666 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AATATATA others(5): Show |
1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-71-16675_-71-1666 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | A | AT | 10 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0234 others(7): Show |
10 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16698_-71-1669 others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | |||||||
| chr14:31049428 | A | ATAT | 8 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0113 others(5): Show |
8 | HG01099.hp1 HG03516.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71-16698_-71-1669 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | |||||||
| chr14:31049428 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-71-16698_-71-1669 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | |||||||
| chr14:31049428 | A | ATATATAT others(8): Show |
1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-71-16698_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | |||||||
| chr14:31049428 | A | T | 11 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0064 others(8): Show |
11 | HG01192.hp2 HG02055.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-71-16698A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | |||||||
| chr14:31049428 | AAT | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0302 a0001c0001t0001g0308 others(9): Show |
12 | HG00558.hp1 HG02056.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-16665_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | AATAT | A | 40 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0120 others(37): Show |
40 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-71-16667_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | AATATAT | A | 32 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(29): Show |
32 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-71-16669_-71-1666 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | AATATATA others(3): Show |
A | 5 | a0001c0001t0003g0145 a0001c0001t0007g0208 a0001c0001t0007g0266 others(2): Show |
5 | HG01099.hp2 HG02886.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16673_-71-1666 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | AATATATA others(5): Show |
A | 4 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(1): Show |
4 | HG02074.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-16675_-71-1666 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049428 | AATATATA others(9): Show |
A | 2 | a0001c0001t0001g0206 a0001c0001t0047g0264 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-16679_-71-1666 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | ||||||
| chr14:31049429 | AT | A | 7 | a0001c0001t0001g0092 a0001c0001t0001g0246 a0001c0001t0001g0303 others(4): Show |
7 | HG01256.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-16696delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | |||||||
| chr14:31049429 | ATAT | A | 3 | a0001c0001t0001g0306 a0001c0001t0001g0315 a0001c0001t0001g0335 |
3 | HG01346.hp2 HG02602.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-71-16696_-71-1669 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | |||||||
| chr14:31049429 | ATATATAT others(2): Show |
A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0337 others(16): Show |
19 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-71-16696_-71-1668 others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | |||||||
| chr14:31049429 | ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0003 a0001c0001t0008g0003 a0001c0001t0012g0199 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-16696_-71-1668 others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | |||||||
| chr14:31049429 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-16696_-71-1668 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | |||||||
| chr14:31049430 | T | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0049 others(28): Show |
31 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-16696T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049430 | |||||||
| chr14:31049432 | T | A | 20 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0246 others(17): Show |
20 | HG01109.hp1 HG01257.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.-71-16694T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049432 | |||||||
| chr14:31049434 | T | A | 42 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0118 others(39): Show |
42 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-71-16692T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049434 | |||||||
| chr14:31049436 | T | A | 6 | a0001c0001t0001g0285 a0001c0001t0001g0311 a0001c0001t0001g0316 others(3): Show |
6 | HG02080.hp1 HG02280.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16690T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049436 | |||||||
| chr14:31049438 | T | A | 1 | a0001c0001t0004g0261 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-71-16688T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049438 | |||||||
| chr14:31049440 | T | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0003g0145 others(17): Show |
20 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-71-16686T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049440 | |||||||
| chr14:31049442 | T | A | 6 | a0001c0001t0001g0003 a0001c0001t0003g0145 a0001c0001t0004g0255 others(3): Show |
6 | HG00733.hp1 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16684T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049442 | |||||||
| chr14:31049442 | T | C | 7 | a0001c0001t0011g0082 a0001c0001t0011g0085 a0001c0001t0011g0090 others(4): Show |
7 | HG00609.hp1 HG02071.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-16684T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049442 | |||||||
| chr14:31049444 | T | A | 1 | a0001c0001t0003g0145 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-71-16682T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049444 | |||||||
| chr14:31049444 | T | C | 1 | a0001c0001t0011g0088 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-71-16682T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049444 | |||||||
| chr14:31049446 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0003g0145 |
2 | HG01099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-16680T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049446 | |||||||
| chr14:31049447 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0014g0158 a0001c0001t0015g0211 |
3 | HG00140.hp1 HG03209.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-71-16679A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049447 | |||||||
| chr14:31049453 | A | ATG | 8 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0001t0002g0166 others(5): Show |
8 | HG00438.hp1 HG02040.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-16672_-71-1667 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049453 | ||||||
| chr14:31049453 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(136): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-71-16673A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049453 | |||||||
| chr14:31049455 | A | G | 13 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0099 others(10): Show |
13 | HG02055.hp1 HG02083.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-71-16671A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049455 | |||||||
| chr14:31049457 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0014g0158 a0001c0001t0015g0211 |
3 | HG00140.hp1 HG03209.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-71-16669A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049457 | |||||||
| chr14:31049459 | ATATG | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0225 a0001c0001t0002g0189 |
3 | NA18612.hp2 NA18957.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-16663_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049459 | ||||||
| chr14:31049459 | ATATGTAT others(7): Show |
A | 1 | a0001c0001t0014g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-71-16664_-71-1665 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049459 | ||||||
| chr14:31049460 | T | C | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-71-16666T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049460 | |||||||
| chr14:31049461 | ATGTATAT others(5): Show |
A | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-71-16663_-71-1665 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049461 | ||||||
| chr14:31049463 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0032 others(21): Show |
24 | HG02055.hp1 HG02055.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-16663G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049463 | |||||||
| chr14:31049464 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71-16662T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049464 | |||||||
| chr14:31049464 | T | TAC | 12 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0055 others(9): Show |
12 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-16661_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | ||||||
| chr14:31049464 | T | TACAC | 3 | a0001c0001t0001g0057 a0001c0001t0008g0022 a0001c0001t0017g0075 |
3 | NA18987.hp2 NA18999.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-71-16661_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | ||||||
| chr14:31049464 | TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-71-16660_-71-1664 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | ||||||
| chr14:31049465 | A | G | 10 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0099 others(7): Show |
10 | HG02055.hp1 HG02083.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16661A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049465 | |||||||
| chr14:31049465 | ATATATAT others(1): Show |
A | 3 | a0001c0001t0001g0093 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG02683.hp1 HG03540.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-71-16658_-71-1665 others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049465 | ||||||
| chr14:31049466 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-71-16660T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049466 | |||||||
| chr14:31049467 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-71-16659A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049467 | |||||||
| chr14:31049467 | ATATATG | A | 10 | a0001c0001t0001g0320 a0001c0001t0002g0001 a0001c0001t0002g0163 others(7): Show |
11 | HG01257.hp1 HG01258.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-71-16656_-71-1665 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049467 | ||||||
| chr14:31049468 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(141): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-71-16658T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049468 | |||||||
| chr14:31049469 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0002g0189 |
2 | NA18612.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-16657A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049469 | |||||||
| chr14:31049469 | ATATG | A | 17 | a0001c0001t0001g0215 a0001c0001t0001g0223 a0001c0001t0001g0228 others(14): Show |
17 | HG01074.hp2 HG01106.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-16654_-71-1665 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049469 | ||||||
| chr14:31049470 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(125): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-71-16656T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049470 | |||||||
| chr14:31049471 | ATG | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(47): Show |
50 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-71-16653_-71-1665 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049471 | ||||||
| chr14:31049472 | T | C | 80 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(77): Show |
80 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-71-16654T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049472 | |||||||
| chr14:31049473 | G | A | 81 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(78): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-71-16653G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049473 | |||||||
| chr14:31049474 | T | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(159): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-71-16652T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049474 | |||||||
| chr14:31049474 | T | TAC | 31 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0119 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-16618_-71-1661 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACAC | 5 | a0001c0001t0001g0098 a0001c0001t0003g0002 a0001c0001t0003g0245 others(2): Show |
6 | HG00323.hp2 HG00733.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-16620_-71-1661 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(3): Show |
3 | a0001c0001t0001g0292 a0001c0001t0006g0327 a0001c0001t0006g0328 |
3 | HG02129.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-16626_-71-1661 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0252 a0001c0001t0001g0285 |
2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-71-16628_-71-1661 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(7): Show |
10 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(7): Show |
10 | HG01081.hp1 HG01243.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16630_-71-1661 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(9): Show |
9 | a0001c0001t0001g0118 a0001c0001t0001g0302 a0001c0001t0001g0303 others(6): Show |
9 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-16632_-71-1661 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(11): Show |
17 | a0001c0001t0001g0251 a0001c0001t0001g0288 a0001c0001t0001g0291 others(14): Show |
17 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.-71-16634_-71-1661 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(13): Show |
7 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0286 others(4): Show |
7 | HG00544.hp2 HG02602.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-16636_-71-1661 others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | T | TACACACA others(15): Show |
3 | a0001c0001t0001g0306 a0001c0001t0001g0332 a0001c0001t0001g0333 |
3 | HG01346.hp2 NA18947.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-71-16638_-71-1661 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | TAC | T | 6 | a0001c0001t0005g0241 a0001c0001t0012g0199 a0001c0001t0012g0200 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16618_-71-1661 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | TACAC | T | 4 | a0001c0001t0001g0012 a0001c0001t0006g0015 a0001c0001t0016g0197 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-16620_-71-1661 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049474 | TACACAC | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16622_-71-1661 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | ||||||
| chr14:31049476 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0092 others(10): Show |
13 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-71-16650C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049476 | |||||||
| chr14:31049477 | A | ATATATG | 6 | a0001c0001t0001g0011 a0001c0001t0006g0016 a0001c0001t0006g0018 others(3): Show |
6 | HG02257.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16649_-71-1664 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049477 | |||||||
| chr14:31049477 | A | G | 1 | a0001c0001t0008g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-71-16649A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049477 | |||||||
| chr14:31049478 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0092 others(9): Show |
12 | HG02257.hp1 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-16648C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049478 | |||||||
| chr14:31049480 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0006g0019 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-16646C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049480 | |||||||
| chr14:31049481 | A | ATG | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-16645_-71-1664 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049481 | |||||||
| chr14:31049482 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-16644C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049482 | |||||||
| chr14:31049510 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-71-16616T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049510 | |||||||
| chr14:31049547 | G | C | 35 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(32): Show |
35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71-16579G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049547 | |||||||
| chr14:31049761 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0096 others(63): Show |
66 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-71-16365G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049761 | |||||||
| chr14:31049821 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-71-16305C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049821 | |||||||
| chr14:31049866 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-16260T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049866 | |||||||
| chr14:31050141 | C | T | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-15985C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050141 | |||||||
| chr14:31050152 | C | T | 50 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-71-15974C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050152 | |||||||
| chr14:31050213 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0004g0042 a0001c0001t0004g0043 others(12): Show |
15 | HG00280.hp1 HG01081.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-15913C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050213 | |||||||
| chr14:31050222 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-71-15904T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050222 | |||||||
| chr14:31050350 | G | A | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-15776G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050350 | |||||||
| chr14:31050382 | G | A | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-71-15744G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050382 | |||||||
| chr14:31050450 | A | T | 1 | a0001c0001t0002g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-71-15676A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050450 | |||||||
| chr14:31050525 | G | C | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-71-15601G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050525 | |||||||
| chr14:31050562 | A | G | 1 | a0001c0001t0017g0075 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-71-15564A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050562 | |||||||
| chr14:31050573 | T | C | 1 | a0001c0001t0005g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-71-15553T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050573 | |||||||
| chr14:31050802 | C | T | 6 | a0001c0001t0006g0021 a0001c0001t0010g0271 a0001c0001t0010g0272 others(3): Show |
6 | HG02074.hp2 HG02965.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-15324C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050802 | |||||||
| chr14:31050806 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-15320C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050806 | |||||||
| chr14:31050813 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-15313C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050813 | |||||||
| chr14:31050823 | A | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-15303A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050823 | |||||||
| chr14:31050932 | T | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-71-15194T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050932 | |||||||
| chr14:31051255 | C | CA | 12 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0074 others(9): Show |
12 | HG01346.hp1 HG01981.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-14855dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31051255 | ||||||
| chr14:31051274 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-71-14852C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051274 | |||||||
| chr14:31051313 | A | G | 2 | a0001c0001t0005g0242 a0001c0001t0029g0243 |
2 | HG00639.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-14813A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051313 | |||||||
| chr14:31051370 | G | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-14756G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051370 | |||||||
| chr14:31051476 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14650G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051476 | |||||||
| chr14:31051477 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14649C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051477 | |||||||
| chr14:31051516 | C | CA | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-14603dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31051516 | ||||||
| chr14:31051605 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-71-14521C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051605 | |||||||
| chr14:31051747 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0322 |
2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-71-14379C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051747 | |||||||
| chr14:31051754 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-71-14372G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051754 | |||||||
| chr14:31051945 | G | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-14181G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051945 | |||||||
| chr14:31051962 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14164A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051962 | |||||||
| chr14:31051963 | T | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14163T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051963 | |||||||
| chr14:31051964 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14162A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051964 | |||||||
| chr14:31051992 | C | T | 2 | a0001c0001t0016g0197 a0001c0001t0016g0198 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-71-14134C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051992 | |||||||
| chr14:31051993 | G | A | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-14133G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051993 | |||||||
| chr14:31052039 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01243.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-71-14087C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052039 | |||||||
| chr14:31052257 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-13869G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052257 | |||||||
| chr14:31052426 | T | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-13700T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052426 | |||||||
| chr14:31052544 | G | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
32 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-71-13582G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052544 | |||||||
| chr14:31052670 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-71-13456C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052670 | |||||||
| chr14:31052728 | C | CA | 21 | a0001c0001t0001g0033 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG00741.hp2 HG01175.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-71-13379dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052728 | ||||||
| chr14:31052728 | CA | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0280 others(9): Show |
12 | HG01496.hp1 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-13379delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052728 | ||||||
| chr14:31052730 | A | G | 1 | a0001c0001t0005g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-71-13396A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052730 | |||||||
| chr14:31052760 | C | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-13366C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052760 | |||||||
| chr14:31052801 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-13325C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052801 | |||||||
| chr14:31052862 | C | T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-13264C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052862 | |||||||
| chr14:31052934 | A | AT | 138 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-71-13169dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052934 | ||||||
| chr14:31052934 | A | ATT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0039 others(10): Show |
13 | HG00280.hp2 HG00741.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-71-13170_-71-1316 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052934 | ||||||
| chr14:31053024 | T | C | 51 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(48): Show |
51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-71-13102T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053024 | |||||||
| chr14:31053067 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71-13059A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053067 | |||||||
| chr14:31053069 | T | A | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-13057T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053069 | |||||||
| chr14:31053078 | T | A | 5 | a0001c0001t0007g0208 a0001c0001t0007g0266 a0001c0001t0007g0267 others(2): Show |
5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-13048T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053078 | |||||||
| chr14:31053258 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-71-12868A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053258 | |||||||
| chr14:31053268 | T | G | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-71-12858T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053268 | |||||||
| chr14:31053420 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-71-12706C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053420 | |||||||
| chr14:31053473 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-71-12653G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053473 | |||||||
| chr14:31053502 | G | C | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-12624G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053502 | |||||||
| chr14:31053543 | T | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-12583T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053543 | |||||||
| chr14:31053589 | C | CT | 25 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(22): Show |
25 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-71-12508dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CT | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(164): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-71-12508delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CTT | C | 25 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0093 others(22): Show |
25 | HG00609.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-71-12509_-71-1250 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CTTT | C | 22 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0207 others(19): Show |
22 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-71-12510_-71-1250 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CTTTTT | C | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
7 | HG00099.hp2 HG00642.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-12512_-71-1250 others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CTTTTTTT | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0337 a0001c0001t0001g0340 others(14): Show |
17 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-12514_-71-1250 others(11): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053589 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0035g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-71-12518_-71-1250 others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | ||||||
| chr14:31053950 | A | G | 2 | a0001c0001t0045g0086 a0001c0001t0046g0087 |
2 | HG02155.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-71-12176A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053950 | |||||||
| chr14:31054377 | A | T | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-11749A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054377 | |||||||
| chr14:31054378 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0050 |
2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-71-11748T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054378 | |||||||
| chr14:31054573 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-71-11553T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054573 | |||||||
| chr14:31054738 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-71-11388C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054738 | |||||||
| chr14:31054859 | C | T | 1 | a0001c0001t0048g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-71-11267C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054859 | |||||||
| chr14:31054867 | C | CA | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
33 | HG00642.hp2 HG01106.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.-71-11230dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | C | CAA | 37 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0280 others(34): Show |
37 | HG00140.hp2 HG00423.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-71-11231_-71-1123 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | C | CAAA | 16 | a0001c0001t0001g0118 a0001c0001t0001g0283 a0001c0001t0001g0285 others(13): Show |
16 | HG00544.hp2 HG00673.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-71-11232_-71-1123 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CA | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(48): Show |
52 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-71-11230delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CAA | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(98): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-71-11231_-71-1123 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CAAA | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0132 others(21): Show |
24 | HG00733.hp1 HG01069.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-11232_-71-1123 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0011g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-71-11241_-71-1123 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-71-11243_-71-1123 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054867 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0073 |
2 | HG01496.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-71-11248_-71-1123 others(23): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | ||||||
| chr14:31054870 | A | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11256A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054870 | |||||||
| chr14:31054904 | A | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11222A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054904 | |||||||
| chr14:31054930 | G | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11196G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054930 | |||||||
| chr14:31055131 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0315 |
2 | HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-71-10995A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055131 | |||||||
| chr14:31055229 | T | G | 51 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(48): Show |
51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-71-10897T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055229 | |||||||
| chr14:31055293 | C | G | 31 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
32 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-71-10833C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055293 | |||||||
| chr14:31055554 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-10572A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055554 | |||||||
| chr14:31055728 | T | TTG | 283 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.-71-10390_-71-1038 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31055728 | ||||||
| chr14:31055856 | T | G | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71-10270T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055856 | |||||||
| chr14:31055957 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-10169C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055957 | |||||||
| chr14:31055989 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-71-10137G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055989 | |||||||
| chr14:31056209 | G | T | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-9917G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056209 | |||||||
| chr14:31056446 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-9680C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056446 | |||||||
| chr14:31056458 | G | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.-71-9668G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056458 | |||||||
| chr14:31056548 | G | A | 2 | a0001c0001t0006g0327 a0001c0001t0006g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-9578G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056548 | |||||||
| chr14:31056601 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0050 |
2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-71-9525C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056601 | |||||||
| chr14:31056660 | A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-9466A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056660 | |||||||
| chr14:31056881 | A | G | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-71-9245A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056881 | |||||||
| chr14:31056982 | G | A | 2 | a0001c0001t0004g0094 a0001c0001t0004g0095 |
2 | HG01928.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-71-9144G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056982 | |||||||
| chr14:31057044 | A | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-71-9082A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057044 | |||||||
| chr14:31057189 | G | A | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-71-8937G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057189 | |||||||
| chr14:31057234 | A | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-8892A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057234 | |||||||
| chr14:31057540 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-8586G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057540 | |||||||
| chr14:31057556 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-8570A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057556 | |||||||
| chr14:31057598 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-71-8528T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057598 | |||||||
| chr14:31057637 | T | C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-8489T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057637 | |||||||
| chr14:31057648 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(114): Show |
118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-71-8478C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057648 | |||||||
| chr14:31057740 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(18): Show |
21 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-71-8386C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057740 | |||||||
| chr14:31057782 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-8344C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057782 | |||||||
| chr14:31057932 | G | T | 2 | a0001c0001t0001g0071 a0001c0001t0008g0070 |
2 | HG01256.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-71-8194G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057932 | |||||||
| chr14:31057935 | T | G | 1 | a0001c0001t0004g0095 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-71-8191T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057935 | |||||||
| chr14:31057958 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-8168C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057958 | |||||||
| chr14:31058086 | GT | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-71-8034delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058086 | ||||||
| chr14:31058173 | G | A | 4 | a0001c0001t0003g0247 a0001c0001t0003g0258 a0001c0001t0003g0259 others(1): Show |
4 | HG00738.hp1 HG01069.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-7953G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058173 | |||||||
| chr14:31058285 | A | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-7841A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058285 | |||||||
| chr14:31058363 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-7763C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058363 | |||||||
| chr14:31058517 | C | CTG | 6 | a0001c0001t0001g0100 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01243.hp1 NA18944.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-7601_-71-7600d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | C | CTGTG | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0004g0042 others(3): Show |
6 | HG00140.hp1 HG00280.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-7603_-71-7600d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0340 a0001c0001t0004g0044 |
2 | HG04204.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-71-7600_-71-7599i others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0004g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-71-7600_-71-7599i others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0007g0157 a0001c0001t0007g0161 |
2 | HG01106.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71-7599_-71-7590d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0006g0327 a0001c0001t0006g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-7599_-71-7588d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7599_-71-7586d others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | CTGTGTGT others(11): Show |
C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0003g0147 others(11): Show |
14 | HG00741.hp1 HG01074.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7582d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058517 | CTGTGTGT others(13): Show |
C | 14 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(11): Show |
15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7580d others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | ||||||
| chr14:31058519 | GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0001g0005 a0001c0001t0007g0268 a0001c0001t0014g0158 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7592d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058519 | ||||||
| chr14:31058523 | GTGTA | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0215 a0001c0001t0001g0224 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7596d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058523 | ||||||
| chr14:31058525 | GTA | G | 10 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0217 others(7): Show |
10 | HG00621.hp1 HG01081.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7598d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058525 | ||||||
| chr14:31058527 | A | ATG | 12 | a0001c0001t0001g0029 a0001c0001t0001g0110 a0001c0001t0001g0113 others(9): Show |
12 | HG01891.hp2 HG02056.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-7551_-71-7550d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | A | ATGTG | 5 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0155 others(2): Show |
5 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-7553_-71-7550d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | A | ATGTGTG | 4 | a0001c0001t0001g0140 a0001c0001t0003g0024 a0001c0001t0019g0007 others(1): Show |
4 | HG00099.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-7555_-71-7550d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0142 a0001c0001t0001g0206 a0001c0001t0003g0247 others(4): Show |
7 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-7557_-71-7550d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-71-7561_-71-7550d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | A | G | 31 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(28): Show |
31 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.-71-7599A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058527 | |||||||
| chr14:31058527 | ATG | A | 11 | a0001c0001t0001g0103 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG00544.hp1 HG02083.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-71-7551_-71-7550d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTG | A | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0289 others(6): Show |
9 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-71-7555_-71-7550d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTGT others(1): Show |
A | 46 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0251 others(43): Show |
46 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71-7557_-71-7550d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-71-7565_-71-7550d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0001g0320 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-71-7569_-71-7550d others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTGT others(17): Show |
A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(123): Show |
127 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-71-7573_-71-7550d others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058527 | ATGTGTGT others(21): Show |
A | 1 | a0001c0001t0009g0262 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-71-7577_-71-7550d others(30): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | ||||||
| chr14:31058531 | G | C | 2 | a0001c0001t0006g0327 a0001c0001t0006g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-7595G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058531 | |||||||
| chr14:31058533 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7593G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058533 | |||||||
| chr14:31058537 | G | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0003g0147 others(11): Show |
14 | HG00741.hp1 HG01074.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71-7589G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058537 | |||||||
| chr14:31058539 | G | C | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-7587G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058539 | |||||||
| chr14:31058541 | G | C | 14 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(11): Show |
15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-7585G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058541 | |||||||
| chr14:31058584 | T | C | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-7542T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058584 | |||||||
| chr14:31058718 | C | G | 1 | a0001c0001t0043g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-71-7408C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058718 | |||||||
| chr14:31058720 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-7406G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058720 | |||||||
| chr14:31058731 | C | CT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0289 a0001c0001t0002g0172 others(3): Show |
6 | HG02080.hp2 HG02280.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-7382dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058731 | ||||||
| chr14:31058752 | TTTTAGTA others(3): Show |
T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-7373_-71-7364d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058752 | |||||||
| chr14:31058756 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG00639.hp1 HG01106.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-7370A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058756 | |||||||
| chr14:31058912 | G | A | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(19): Show |
22 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-71-7214G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058912 | |||||||
| chr14:31059121 | T | C | 2 | a0001c0001t0036g0091 a0001c0001t0037g0041 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-71-7005T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059121 | |||||||
| chr14:31059613 | G | A | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-6513G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059613 | |||||||
| chr14:31059758 | A | G | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-6368A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059758 | |||||||
| chr14:31059866 | G | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(26): Show |
29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-71-6260G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059866 | |||||||
| chr14:31059930 | A | AAT | 7 | a0001c0001t0001g0005 a0001c0001t0002g0184 a0001c0001t0010g0271 others(4): Show |
7 | HG02074.hp2 HG03041.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-6181_-71-6180d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059930 | ||||||
| chr14:31059930 | A | T | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-6196A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059930 | |||||||
| chr14:31059932 | T | A | 23 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0098 others(20): Show |
24 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-6194T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059932 | |||||||
| chr14:31059943 | A | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0206 a0001c0001t0015g0263 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-6183A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059943 | |||||||
| chr14:31059963 | ATATATGT others(25): Show |
A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-71-6127_-71-6096d others(34): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059963 | ||||||
| chr14:31059995 | TTATATGT others(11): Show |
T | 2 | a0001c0001t0001g0206 a0001c0001t0047g0264 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-6127_-71-6110d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059995 | ||||||
| chr14:31060032 | T | A | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-71-6094T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060032 | |||||||
| chr14:31060058 | T | C | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | NA18953.hp2 NA18987.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-71-6068T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060058 | |||||||
| chr14:31060210 | A | G | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-5916A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060210 | |||||||
| chr14:31060275 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-71-5851T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060275 | |||||||
| chr14:31060347 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-71-5779G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060347 | |||||||
| chr14:31060354 | A | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-5772A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060354 | |||||||
| chr14:31060456 | A | G | 2 | a0001c0001t0006g0327 a0001c0001t0006g0328 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-5670A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060456 | |||||||
| chr14:31060703 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-71-5423A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060703 | |||||||
| chr14:31060724 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-71-5402T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060724 | |||||||
| chr14:31060829 | A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-5297A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060829 | |||||||
| chr14:31060958 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-5168C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060958 | |||||||
| chr14:31060961 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-5165T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060961 | |||||||
| chr14:31060976 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-71-5150G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060976 | |||||||
| chr14:31061065 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-5061T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061065 | |||||||
| chr14:31061287 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-4839G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061287 | |||||||
| chr14:31061446 | G | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-4680G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061446 | |||||||
| chr14:31061493 | T | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(113): Show |
117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-71-4633T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061493 | |||||||
| chr14:31061499 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(90): Show |
94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-71-4627C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061499 | |||||||
| chr14:31061647 | A | AT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(27): Show |
30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-71-4465dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31061647 | ||||||
| chr14:31061852 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-71-4274G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061852 | |||||||
| chr14:31061881 | C | G | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-4245C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061881 | |||||||
| chr14:31061914 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0039g0133 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-71-4212G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061914 | |||||||
| chr14:31061941 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-71-4185G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061941 | |||||||
| chr14:31061987 | CCACATTT others(9): Show |
C | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-4136_-71-4121d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31061987 | ||||||
| chr14:31062127 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0337 a0001c0001t0001g0340 others(18): Show |
21 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-71-3999T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062127 | |||||||
| chr14:31062271 | G | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-71-3855G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062271 | |||||||
| chr14:31062274 | T | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3852T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062274 | |||||||
| chr14:31062315 | T | C | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-3811T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062315 | |||||||
| chr14:31062355 | T | G | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-71-3771T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062355 | |||||||
| chr14:31062649 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-71-3477T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062649 | |||||||
| chr14:31062727 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-3399G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062727 | |||||||
| chr14:31062745 | A | G | 1 | a0001c0001t0017g0075 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-71-3381A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062745 | |||||||
| chr14:31062872 | T | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3254T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062872 | |||||||
| chr14:31062926 | C | T | 35 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(32): Show |
35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71-3200C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062926 | |||||||
| chr14:31062927 | A | G | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(67): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-71-3199A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062927 | |||||||
| chr14:31062963 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(113): Show |
117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-71-3163C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062963 | |||||||
| chr14:31062969 | C | CA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0103 others(6): Show |
9 | HG01175.hp1 HG01433.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3143dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31062969 | ||||||
| chr14:31062977 | A | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3149A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062977 | |||||||
| chr14:31062997 | A | C | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-3129A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062997 | |||||||
| chr14:31063006 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-71-3120G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063006 | |||||||
| chr14:31063228 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0064 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-71-2898C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063228 | |||||||
| chr14:31063246 | C | G | 50 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-71-2880C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063246 | |||||||
| chr14:31063259 | A | G | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2867A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063259 | |||||||
| chr14:31063458 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-71-2668A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063458 | |||||||
| chr14:31063580 | A | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0142 |
3 | HG00099.hp2 HG00642.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-71-2546A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063580 | |||||||
| chr14:31063901 | T | C | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2225T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063901 | |||||||
| chr14:31063964 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2162C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063964 | |||||||
| chr14:31064070 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-71-2056A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064070 | |||||||
| chr14:31064275 | G | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0026 others(1): Show |
4 | HG02559.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-1851G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064275 | |||||||
| chr14:31064407 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-71-1719C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064407 | |||||||
| chr14:31064477 | A | G | 1 | a0001c0001t0035g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-71-1649A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064477 | |||||||
| chr14:31064506 | G | C | 1 | a0001c0001t0002g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-71-1620G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064506 | |||||||
| chr14:31065265 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-861T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065265 | |||||||
| chr14:31065418 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-71-708A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065418 | |||||||
| chr14:31065434 | G | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-692G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065434 | |||||||
| chr14:31065472 | TCAGAAGA others(3): Show |
T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-71-653_-71-644del others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065472 | |||||||
| chr14:31065500 | A | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(225): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-71-626A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065500 | |||||||
| chr14:31065531 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-595G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065531 | |||||||
| chr14:31065546 | A | AATGAATG others(3): Show |
1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-578_-71-569dup others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31065546 | ||||||
| chr14:31065574 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-71-552A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065574 | |||||||
| chr14:31065716 | A | G | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-410A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065716 | |||||||
| chr14:31065776 | T | G | 3 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0044 |
3 | HG00280.hp1 HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-71-350T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065776 | |||||||
| chr14:31065851 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(226): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-71-275A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065851 | |||||||
| chr14:31065911 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0008g0003 a0001c0001t0008g0244 |
3 | HG01081.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-71-215C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065911 | |||||||
| chr14:31065956 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-170G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065956 | |||||||
| chr14:31066397 | G | C | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.138+63G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066397 | |||||||
| chr14:31066550 | C | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.138+216C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066550 | |||||||
| chr14:31066750 | C | A | 1 | a0001c0001t0005g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.138+416C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066750 | |||||||
| chr14:31066790 | G | A | 51 | a0001c0001t0001g0118 a0001c0001t0001g0251 a0001c0001t0001g0252 others(48): Show |
51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.138+456G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066790 | |||||||
| chr14:31066969 | G | T | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.138+635G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066969 | |||||||
| chr14:31067112 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.138+778G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067112 | |||||||
| chr14:31067208 | C | CA | 50 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0251 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+888dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067208 | ||||||
| chr14:31067208 | CA | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(218): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.138+888delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067208 | ||||||
| chr14:31067209 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.138+875A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067209 | |||||||
| chr14:31067251 | C | T | 1 | a0001c0001t0005g0305 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.138+917C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067251 | |||||||
| chr14:31067256 | T | A | 1 | a0001c0001t0008g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+922T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067256 | |||||||
| chr14:31067424 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1090C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067424 | |||||||
| chr14:31067516 | A | AT | 54 | a0001c0001t0001g0060 a0001c0001t0001g0118 a0001c0001t0001g0251 others(51): Show |
54 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.138+1198dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067516 | ||||||
| chr14:31067516 | AT | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0175 others(3): Show |
6 | HG01891.hp2 HG02074.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1198delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067516 | ||||||
| chr14:31067739 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0047g0264 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.138+1405G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067739 | |||||||
| chr14:31067814 | A | G | 3 | a0001c0001t0005g0241 a0001c0001t0005g0242 a0001c0001t0029g0243 |
3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+1480A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067814 | |||||||
| chr14:31067876 | A | AT | 38 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(35): Show |
38 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.138+1554dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067876 | ||||||
| chr14:31068029 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.138+1695C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068029 | |||||||
| chr14:31068078 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.138+1744G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068078 | |||||||
| chr14:31068132 | T | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(229): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.139-1711T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068132 | |||||||
| chr14:31068163 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.139-1680C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068163 | |||||||
| chr14:31068210 | C | T | 1 | a0001c0001t0030g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.139-1633C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068210 | |||||||
| chr14:31068379 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.139-1464T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068379 | |||||||
| chr14:31068693 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.139-1150C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068693 | |||||||
| chr14:31068738 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0064 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-1105T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068738 | |||||||
| chr14:31068777 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.139-1066G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068777 | |||||||
| chr14:31069161 | C | T | 5 | a0001c0001t0007g0208 a0001c0001t0007g0266 a0001c0001t0007g0267 others(2): Show |
5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-682C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069161 | |||||||
| chr14:31069180 | G | A | 15 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.139-663G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069180 | |||||||
| chr14:31069258 | A | T | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139-585A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069258 | |||||||
| chr14:31069360 | G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.139-483G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069360 | |||||||
| chr14:31069422 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.139-421T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069422 | |||||||
| chr14:31069443 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.139-400A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069443 | |||||||
| chr14:31069568 | C | G | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-275C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069568 | |||||||
| chr14:31069694 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.139-149G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069694 | |||||||
| chr14:31069733 | A | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.139-110A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069733 | |||||||
| chr14:31069753 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0019g0007 a0001c0001t0019g0008 |
3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.139-90C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069753 | |||||||
| chr14:31069778 | C | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.139-65C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069778 | |||||||
| chr14:31070296 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.225+367A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070296 | |||||||
| chr14:31070569 | G | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.225+640G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070569 | |||||||
| chr14:31070631 | G | C | 6 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+702G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070631 | |||||||
| chr14:31070778 | C | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+849C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070778 | |||||||
| chr14:31071404 | C | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1475C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071404 | |||||||
| chr14:31071545 | T | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.226-1360T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071545 | |||||||
| chr14:31071554 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.226-1351A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071554 | |||||||
| chr14:31071578 | G | A | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226-1327G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071578 | |||||||
| chr14:31071626 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.226-1279G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071626 | |||||||
| chr14:31071683 | G | T | 1 | a0001c0001t0002g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.226-1222G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071683 | |||||||
| chr14:31071695 | G | A | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-1210G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071695 | |||||||
| chr14:31071887 | AC | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.226-1017delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071887 | |||||||
| chr14:31071922 | A | AT | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(248): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.226-975dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 31071922 | ||||||
| chr14:31071930 | T | G | 17 | a0001c0001t0001g0098 a0001c0001t0001g0144 a0001c0001t0003g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-975T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071930 | |||||||
| chr14:31071931 | G | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(183): Show |
186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.226-974G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071931 | |||||||
| chr14:31072061 | C | T | 2 | a0001c0001t0027g0164 a0001c0001t0028g0194 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.226-844C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072061 | |||||||
| chr14:31072088 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0005g0081 |
3 | NA18983.hp2 NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.226-817G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072088 | |||||||
| chr14:31072146 | G | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-759G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072146 | |||||||
| chr14:31072274 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG01346.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.226-631T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072274 | |||||||
| chr14:31072288 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.226-617C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072288 | |||||||
| chr14:31072344 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.226-561G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072344 | |||||||
| chr14:31072417 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0031 others(123): Show |
127 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-488C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072417 | |||||||
| chr14:31072473 | C | T | 5 | a0001c0001t0007g0208 a0001c0001t0007g0266 a0001c0001t0007g0267 others(2): Show |
5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-432C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072473 | |||||||
| chr14:31072543 | A | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.226-362A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072543 | |||||||
| chr14:31072560 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226-345A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072560 | |||||||
| chr14:31072670 | C | CA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.226-227dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 31072670 | ||||||
| chr14:31072678 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.226-227A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072678 | |||||||
| chr14:31072707 | C | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.226-198C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072707 | |||||||
| chr14:31072732 | CAAGT | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0337 others(26): Show |
29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.226-172_226-169del others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072732 | |||||||
| chr14:31072811 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.226-94G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072811 | |||||||
| chr14:31073046 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.294+73T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073046 | |||||||
| chr14:31073167 | G | T | 5 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(2): Show |
5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+194G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073167 | |||||||
| chr14:31073185 | G | GA | 68 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0036 others(65): Show |
68 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.294+227dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073185 | ||||||
| chr14:31073185 | G | GAA | 9 | a0001c0001t0001g0118 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
9 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+226_294+227dup others(2): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073185 | ||||||
| chr14:31073195 | A | AC | 8 | a0001c0001t0001g0061 a0001c0001t0005g0226 a0001c0001t0010g0271 others(5): Show |
8 | HG02074.hp2 HG03490.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+222_294+223ins others(1): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073195 | |||||||
| chr14:31073212 | A | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0063 others(11): Show |
14 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.294+239A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073212 | |||||||
| chr14:31073218 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.294+245C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073218 | |||||||
| chr14:31073220 | A | G | 21 | a0001c0001t0001g0132 a0001c0001t0005g0083 a0001c0001t0005g0241 others(18): Show |
21 | HG00639.hp2 HG01106.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.294+247A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073220 | |||||||
| chr14:31073226 | C | T | 2 | a0001c0001t0007g0208 a0001c0001t0007g0266 |
2 | HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.294+253C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073226 | |||||||
| chr14:31073256 | T | C | 77 | a0001c0001t0001g0045 a0001c0001t0001g0118 a0001c0001t0001g0127 others(74): Show |
78 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.294+283T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073256 | |||||||
| chr14:31073257 | A | G | 77 | a0001c0001t0001g0045 a0001c0001t0001g0118 a0001c0001t0001g0127 others(74): Show |
78 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.294+284A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073257 | |||||||
| chr14:31073261 | T | C | 2 | a0001c0001t0002g0196 a0001c0001t0030g0069 |
2 | HG02896.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.294+288T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073261 | |||||||
| chr14:31073266 | A | G | 3 | a0001c0001t0002g0182 a0001c0001t0002g0196 a0001c0001t0030g0069 |
3 | HG01192.hp2 HG02896.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.294+293A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073266 | |||||||
| chr14:31073269 | T | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.294+296T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073269 | |||||||
| chr14:31073273 | A | G | 87 | a0001c0001t0001g0045 a0001c0001t0001g0118 a0001c0001t0001g0127 others(84): Show |
88 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.294+300A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073273 | |||||||
| chr14:31073286 | G | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.294+313G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073286 | |||||||
| chr14:31073286 | G | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(4): Show |
7 | HG02630.hp1 HG02647.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+313G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073286 | |||||||
| chr14:31073290 | A | G | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.294+317A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073290 | |||||||
| chr14:31073293 | A | G | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(4): Show |
7 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+320A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073293 | |||||||
| chr14:31073294 | T | C | 3 | a0001c0001t0005g0084 a0001c0001t0008g0014 a0001c0001t0047g0264 |
3 | HG01109.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+321T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073294 | |||||||
| chr14:31073297 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0098 others(55): Show |
59 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.294+324T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073297 | |||||||
| chr14:31073301 | T | A | 1 | a0001c0001t0005g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294+328T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073301 | |||||||
| chr14:31073301 | T | C | 2 | a0001c0001t0002g0188 a0001c0001t0027g0164 |
2 | HG00438.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.294+328T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073301 | |||||||
| chr14:31073304 | T | C | 132 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(129): Show |
133 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.294+331T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073304 | |||||||
| chr14:31073306 | C | A | 1 | a0001c0001t0011g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.294+333C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073306 | |||||||
| chr14:31073306 | C | T | 7 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0012g0200 others(4): Show |
7 | HG01106.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+333C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073306 | |||||||
| chr14:31073306 | CGGTGAAA others(829): Show |
C | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.294+344_294+1179de others(1): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073306 | ||||||
| chr14:31073314 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.294+341C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073314 | |||||||
| chr14:31073317 | C | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0032 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.294+344C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073317 | |||||||
| chr14:31073317 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0126 a0001c0001t0002g0178 others(2): Show |
5 | HG00323.hp1 HG00408.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+344C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073317 | |||||||
| chr14:31073318 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+345G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073318 | |||||||
| chr14:31073320 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00639.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.294+347C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073320 | |||||||
| chr14:31073346 | T | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0028 others(130): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.294+373T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073346 | |||||||
| chr14:31073351 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.294+378G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073351 | |||||||
| chr14:31073353 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0015g0211 a0001c0001t0015g0263 |
3 | HG00140.hp1 HG03209.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.294+380G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073353 | |||||||
| chr14:31073356 | G | A | 64 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0055 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.294+383G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073356 | |||||||
| chr14:31073357 | G | T | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.294+384G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073357 | |||||||
| chr14:31073358 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.294+385T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073358 | |||||||
| chr14:31073360 | G | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0132 a0001c0001t0004g0203 others(1): Show |
4 | HG01891.hp2 HG03098.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+387G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073360 | |||||||
| chr14:31073361 | G | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0033 others(82): Show |
86 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.294+388G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073361 | |||||||
| chr14:31073362 | C | T | 3 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0047g0264 |
3 | HG01109.hp1 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.294+389C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073362 | |||||||
| chr14:31073363 | G | C | 3 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0047g0264 |
3 | HG01109.hp1 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.294+390G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073363 | |||||||
| chr14:31073364 | C | T | 26 | a0001c0001t0002g0173 a0001c0001t0003g0002 a0001c0001t0003g0024 others(23): Show |
27 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.294+391C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073364 | |||||||
| chr14:31073372 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.294+399C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073372 | |||||||
| chr14:31073382 | C | T | 3 | a0001c0001t0012g0200 a0001c0001t0012g0201 a0001c0001t0041g0227 |
3 | HG01891.hp1 HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.294+409C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073382 | |||||||
| chr14:31073383 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.294+410C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073383 | |||||||
| chr14:31073383 | C | G | 6 | a0001c0001t0001g0313 a0001c0001t0004g0256 a0001c0001t0004g0261 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+410C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073383 | |||||||
| chr14:31073419 | G | A | 2 | a0001c0001t0004g0209 a0001c0001t0015g0211 |
2 | HG00140.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.294+446G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073419 | |||||||
| chr14:31073427 | T | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0059 others(28): Show |
31 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.294+454T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073427 | |||||||
| chr14:31073433 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+460T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073433 | |||||||
| chr14:31073439 | G | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0126 a0001c0001t0002g0178 others(8): Show |
11 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.294+466G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073439 | |||||||
| chr14:31073445 | C | G | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.294+472C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073445 | |||||||
| chr14:31073446 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(228): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.294+473C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073446 | |||||||
| chr14:31073460 | A | T | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+487A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073460 | |||||||
| chr14:31073461 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.294+488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073461 | |||||||
| chr14:31073468 | C | T | 2 | a0001c0001t0004g0216 a0001c0001t0044g0131 |
2 | HG01255.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.294+495C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073468 | |||||||
| chr14:31073469 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.294+496A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073469 | |||||||
| chr14:31073473 | G | C | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+500G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073473 | |||||||
| chr14:31073476 | C | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.294+503C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073476 | |||||||
| chr14:31073485 | G | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.294+512G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073485 | |||||||
| chr14:31073487 | C | G | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.294+514C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073487 | |||||||
| chr14:31073491 | G | GA | 15 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0061 others(12): Show |
15 | HG02055.hp1 HG02074.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+530dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073491 | ||||||
| chr14:31073536 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.294+563T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073536 | |||||||
| chr14:31073633 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0005g0248 a0001c0001t0005g0249 others(1): Show |
4 | HG00733.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+660C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073633 | |||||||
| chr14:31073640 | G | A | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.294+667G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073640 | |||||||
| chr14:31073834 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.294+861G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073834 | |||||||
| chr14:31073854 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.294+881T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073854 | |||||||
| chr14:31073964 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.294+991G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073964 | |||||||
| chr14:31074097 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.294+1124T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074097 | |||||||
| chr14:31074153 | T | A | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.294+1180T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074153 | |||||||
| chr14:31074178 | T | G | 2 | a0001c0001t0004g0255 a0001c0001t0004g0278 |
2 | HG00733.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.294+1205T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074178 | |||||||
| chr14:31074270 | A | C | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.294+1297A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074270 | |||||||
| chr14:31074312 | G | A | 32 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
32 | HG00639.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.294+1339G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074312 | |||||||
| chr14:31074320 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0005g0226 |
2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.294+1347G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074320 | |||||||
| chr14:31074324 | C | CAAAT | 14 | a0001c0001t0001g0045 a0001c0001t0001g0115 a0001c0001t0001g0270 others(11): Show |
14 | HG01106.hp2 HG02040.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.294+1391_294+1394d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | ||||||
| chr14:31074324 | CAAAT | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.294+1391_294+1394d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | ||||||
| chr14:31074324 | CAAATAAA others(5): Show |
C | 58 | a0001c0001t0001g0093 a0001c0001t0001g0118 a0001c0001t0001g0141 others(55): Show |
58 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.294+1383_294+1394d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | ||||||
| chr14:31074364 | T | G | 5 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0063 others(2): Show |
5 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+1391T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074364 | |||||||
| chr14:31074365 | A | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0063 others(2): Show |
5 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+1392A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074365 | |||||||
| chr14:31074367 | A | G | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+1394A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074367 | |||||||
| chr14:31074377 | G | A | 9 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+1404G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074377 | |||||||
| chr14:31074419 | G | A | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.294+1446G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074419 | |||||||
| chr14:31074483 | T | G | 7 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+1510T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074483 | |||||||
| chr14:31074551 | G | A | 49 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0001g0251 others(46): Show |
49 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.294+1578G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074551 | |||||||
| chr14:31074555 | G | A | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.294+1582G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074555 | |||||||
| chr14:31074589 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.294+1616C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074589 | |||||||
| chr14:31074590 | G | A | 3 | a0001c0001t0015g0263 a0001c0001t0018g0205 a0001c0001t0047g0264 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.294+1617G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074590 | |||||||
| chr14:31074597 | T | C | 39 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(36): Show |
39 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.294+1624T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074597 | |||||||
| chr14:31074696 | G | A | 3 | a0001c0001t0019g0007 a0001c0001t0019g0008 a0001c0001t0039g0133 |
3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.294+1723G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074696 | |||||||
| chr14:31074826 | T | TC | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
128 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+1857dupC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074826 | ||||||
| chr14:31075083 | T | G | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+2110T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075083 | |||||||
| chr14:31075104 | T | A | 1 | a0001c0001t0005g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.294+2131T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075104 | |||||||
| chr14:31075336 | A | G | 2 | a0001c0001t0027g0164 a0001c0001t0043g0204 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.294+2363A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075336 | |||||||
| chr14:31075348 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0005g0226 |
2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.294+2375A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075348 | |||||||
| chr14:31075438 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.294+2465G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075438 | |||||||
| chr14:31075547 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.294+2574C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075547 | |||||||
| chr14:31075741 | A | AT | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.294+2783dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31075741 | ||||||
| chr14:31075741 | A | ATT | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0093 others(33): Show |
36 | HG00621.hp1 HG02040.hp2 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.294+2782_294+2783d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31075741 | ||||||
| chr14:31075801 | G | A | 7 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+2828G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075801 | |||||||
| chr14:31076002 | C | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0342 |
2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.294+3029C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076002 | |||||||
| chr14:31076104 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.294+3131C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076104 | |||||||
| chr14:31076121 | A | G | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+3148A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076121 | |||||||
| chr14:31076154 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.294+3181C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076154 | |||||||
| chr14:31076292 | T | C | 7 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+3319T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076292 | |||||||
| chr14:31076597 | C | G | 4 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0241 others(1): Show |
4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+3624C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076597 | |||||||
| chr14:31076665 | A | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+3692A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076665 | |||||||
| chr14:31076759 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.294+3786T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076759 | |||||||
| chr14:31076781 | A | G | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.295-3792A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076781 | |||||||
| chr14:31076815 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-3758G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076815 | |||||||
| chr14:31076872 | G | A | 4 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0241 others(1): Show |
4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-3701G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076872 | |||||||
| chr14:31076915 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(2): Show |
5 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-3658G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076915 | |||||||
| chr14:31077000 | C | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-3573C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077000 | |||||||
| chr14:31077018 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.295-3555G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077018 | |||||||
| chr14:31077087 | G | A | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-3486G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077087 | |||||||
| chr14:31077151 | C | G | 20 | a0001c0001t0001g0093 a0001c0001t0001g0315 a0001c0001t0005g0083 others(17): Show |
20 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-3422C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077151 | |||||||
| chr14:31077186 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.295-3387C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077186 | |||||||
| chr14:31077292 | A | G | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.295-3281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077292 | |||||||
| chr14:31077390 | A | G | 3 | a0001c0001t0015g0263 a0001c0001t0018g0205 a0001c0001t0047g0264 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.295-3183A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077390 | |||||||
| chr14:31077410 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.295-3163G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077410 | |||||||
| chr14:31077435 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0002g0182 |
3 | HG00741.hp2 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.295-3138G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077435 | |||||||
| chr14:31077578 | C | A | 3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 |
3 | HG02559.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.295-2995C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077578 | |||||||
| chr14:31077585 | A | G | 1 | a0001c0001t0005g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.295-2988A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077585 | |||||||
| chr14:31077587 | C | T | 11 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-2986C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077587 | |||||||
| chr14:31077629 | CTTCCAGG others(3): Show |
C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295-2930_295-2921d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077629 | ||||||
| chr14:31077683 | T | A | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-2890T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077683 | |||||||
| chr14:31077739 | C | CT | 50 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.295-2819dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077739 | ||||||
| chr14:31077739 | CT | C | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(23): Show |
26 | HG00621.hp1 HG02074.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-2819delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077739 | ||||||
| chr14:31077805 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.295-2768G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077805 | |||||||
| chr14:31077983 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-2590C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077983 | |||||||
| chr14:31078128 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295-2445G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078128 | |||||||
| chr14:31078406 | C | T | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.295-2167C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078406 | |||||||
| chr14:31078615 | G | T | 7 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-1958G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078615 | |||||||
| chr14:31078767 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.295-1806G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078767 | |||||||
| chr14:31078906 | C | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-1667C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078906 | |||||||
| chr14:31079136 | G | C | 9 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-1437G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079136 | |||||||
| chr14:31079245 | T | C | 5 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(2): Show |
5 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1328T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079245 | |||||||
| chr14:31079313 | T | C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-1260T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079313 | |||||||
| chr14:31079332 | G | A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.295-1241G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079332 | |||||||
| chr14:31079497 | A | G | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1076A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079497 | |||||||
| chr14:31079757 | T | C | 19 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(16): Show |
19 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.295-816T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079757 | |||||||
| chr14:31079900 | T | TTAC | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.295-671_295-669dup others(3): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31079900 | ||||||
| chr14:31080155 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-418C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080155 | |||||||
| chr14:31080237 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.295-336G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080237 | |||||||
| chr14:31080413 | T | C | 19 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(16): Show |
19 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.295-160T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080413 | |||||||
| chr14:31080460 | A | T | 3 | a0001c0001t0016g0197 a0001c0001t0016g0198 a0001c0001t0041g0227 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.295-113A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080460 | |||||||
| chr14:31080539 | T | G | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.295-34T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080539 | |||||||
| chr14:31080557 | T | C | 2 | a0001c0001t0010g0272 a0001c0001t0010g0274 |
2 | NA18971.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.295-16T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080557 | |||||||
| chr14:31080626 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0068 |
2 | HG02165.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.306+42G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31080626 | |||||||
| chr14:31080949 | G | A | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+365G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31080949 | |||||||
| chr14:31081072 | G | A | 8 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(5): Show |
8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081072 | |||||||
| chr14:31081089 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+505G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081089 | |||||||
| chr14:31081136 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.306+552C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081136 | |||||||
| chr14:31081388 | T | C | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+804T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081388 | |||||||
| chr14:31081463 | G | C | 4 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0241 others(1): Show |
4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+879G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081463 | |||||||
| chr14:31081517 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.306+933G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081517 | |||||||
| chr14:31081526 | G | A | 1 | a0001c0001t0012g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.306+942G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081526 | |||||||
| chr14:31081976 | C | T | 4 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(1): Show |
4 | HG02074.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1392C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081976 | |||||||
| chr14:31082341 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.306+1757A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082341 | |||||||
| chr14:31082357 | A | G | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+1773A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082357 | |||||||
| chr14:31082556 | T | A | 8 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(5): Show |
8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+1972T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082556 | |||||||
| chr14:31082569 | T | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
35 | HG00099.hp2 HG00642.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.306+1985T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082569 | |||||||
| chr14:31082654 | T | A | 1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.306+2070T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082654 | |||||||
| chr14:31082724 | G | A | 73 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0097 others(70): Show |
73 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.306+2140G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082724 | |||||||
| chr14:31082753 | G | A | 2 | a0001c0001t0005g0241 a0001c0001t0005g0242 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.306+2169G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082753 | |||||||
| chr14:31082765 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.306+2181G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082765 | |||||||
| chr14:31082778 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.306+2194C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082778 | |||||||
| chr14:31082788 | T | C | 8 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(5): Show |
8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+2204T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082788 | |||||||
| chr14:31082812 | C | T | 8 | a0001c0001t0001g0093 a0001c0001t0005g0083 a0001c0001t0005g0084 others(5): Show |
8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+2228C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082812 | |||||||
| chr14:31082813 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2229G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082813 | |||||||
| chr14:31082813 | G | T | 2 | a0001c0001t0015g0263 a0001c0001t0047g0264 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2229G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082813 | |||||||
| chr14:31082820 | C | T | 5 | a0001c0001t0007g0208 a0001c0001t0007g0266 a0001c0001t0007g0267 others(2): Show |
5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+2236C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082820 | |||||||
| chr14:31082825 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.306+2241G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082825 | |||||||
| chr14:31082846 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.306+2262A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082846 | |||||||
| chr14:31082850 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0015g0263 a0001c0001t0047g0264 |
3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2266T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082850 | |||||||
| chr14:31082862 | C | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2278C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082862 | |||||||
| chr14:31082883 | G | A | 3 | a0001c0001t0019g0007 a0001c0001t0019g0008 a0001c0001t0039g0133 |
3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.306+2299G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082883 | |||||||
| chr14:31082895 | C | CA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0074 others(3): Show |
6 | HG02165.hp2 HG03540.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2326dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31082895 | ||||||
| chr14:31082895 | C | CAA | 23 | a0001c0001t0001g0144 a0001c0001t0003g0002 a0001c0001t0003g0024 others(20): Show |
24 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.306+2325_306+2326d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31082895 | ||||||
| chr14:31083070 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0012g0199 a0001c0001t0012g0200 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.306+2486A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083070 | |||||||
| chr14:31083414 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
22 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.306+2830T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083414 | |||||||
| chr14:31083433 | A | AGTG | 3 | a0001c0001t0015g0263 a0001c0001t0018g0205 a0001c0001t0047g0264 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2852_306+2854d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083433 | ||||||
| chr14:31083467 | G | A | 7 | a0001c0001t0001g0331 a0001c0001t0001g0333 a0001c0001t0001g0334 others(4): Show |
7 | NA18939.hp1 NA18947.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2883G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083467 | |||||||
| chr14:31083494 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.306+2911_306+2912i others(21): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083494 | ||||||
| chr14:31083496 | C | CT | 57 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(54): Show |
57 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.306+2938dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTT | 68 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0039 others(65): Show |
68 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.306+2936_306+2938d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTT | 34 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(31): Show |
34 | HG01106.hp2 HG01175.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.306+2935_306+2938d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTT | 10 | a0001c0001t0001g0210 a0001c0001t0001g0220 a0001c0001t0001g0224 others(7): Show |
10 | HG00099.hp1 HG00621.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+2934_306+2938d others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
17 | HG00323.hp2 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.306+2933_306+2938d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT | 7 | a0001c0001t0003g0026 a0001c0001t0003g0130 a0001c0001t0003g0147 others(4): Show |
7 | HG01257.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2932_306+2938d others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0006g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.306+2928_306+2938d others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0005 a0001c0001t0006g0015 a0001c0001t0006g0018 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2927_306+2938d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0327 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+2926_306+2938d others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.306+2925_306+2938d others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0012g0199 a0001c0001t0018g0205 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.306+2924_306+2938d others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 others(4): Show |
7 | HG00099.hp2 HG02886.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2923_306+2938d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0139 a0001c0001t0005g0241 a0001c0001t0010g0272 others(2): Show |
5 | HG00642.hp2 HG02074.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+2922_306+2938d others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0142 a0001c0001t0005g0242 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.306+2921_306+2938d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.306+2920_306+2938d others(21): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0019g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+2917_306+2938d others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0093 a0001c0001t0019g0007 |
2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.306+2916_306+2938d others(25): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0049g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.306+2914_306+2938d others(27): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | ||||||
| chr14:31083496 | C | T | 1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.306+2912C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083496 | |||||||
| chr14:31083930 | T | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(68): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.306+3346T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083930 | |||||||
| chr14:31083934 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+3350G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083934 | |||||||
| chr14:31083940 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.306+3356G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083940 | |||||||
| chr14:31084055 | C | T | 5 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0014g0158 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+3471C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084055 | |||||||
| chr14:31084104 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0099 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.306+3520A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084104 | |||||||
| chr14:31084214 | G | T | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+3630G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084214 | |||||||
| chr14:31084373 | G | A | 1 | a0001c0001t0009g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.306+3789G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084373 | |||||||
| chr14:31084514 | T | G | 69 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.306+3930T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084514 | |||||||
| chr14:31084519 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.306+3935T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084519 | |||||||
| chr14:31084587 | C | T | 5 | a0001c0001t0001g0285 a0001c0001t0001g0311 a0001c0001t0001g0312 others(2): Show |
5 | HG03654.hp2 HG03834.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+4003C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084587 | |||||||
| chr14:31084903 | A | G | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.306+4319A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084903 | |||||||
| chr14:31084929 | C | G | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.306+4345C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084929 | |||||||
| chr14:31085076 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0322 |
2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.306+4492G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085076 | |||||||
| chr14:31085137 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.306+4553C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085137 | |||||||
| chr14:31085138 | G | T | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+4554G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085138 | |||||||
| chr14:31085270 | T | C | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.306+4686T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085270 | |||||||
| chr14:31085295 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.306+4711C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085295 | |||||||
| chr14:31085312 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.306+4728G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085312 | |||||||
| chr14:31085523 | C | T | 4 | a0001c0001t0011g0082 a0001c0001t0011g0088 a0001c0001t0011g0090 others(1): Show |
4 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+4939C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085523 | |||||||
| chr14:31085600 | C | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+5016C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085600 | |||||||
| chr14:31085664 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.306+5080T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085664 | |||||||
| chr14:31085957 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0006g0015 a0001c0001t0006g0016 others(19): Show |
22 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306+5373A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085957 | |||||||
| chr14:31085972 | G | A | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+5388G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085972 | |||||||
| chr14:31086198 | A | G | 1 | a0001c0001t0026g0192 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.306+5614A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086198 | |||||||
| chr14:31086314 | C | A | 16 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.306+5730C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086314 | |||||||
| chr14:31086377 | G | C | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+5793G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086377 | |||||||
| chr14:31086383 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0012g0199 a0001c0001t0012g0200 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+5799G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086383 | |||||||
| chr14:31086410 | A | ATTTG | 3 | a0001c0001t0001g0005 a0001c0001t0001g0240 a0001c0001t0005g0083 |
3 | HG02818.hp1 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.306+5850_306+5853d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31086410 | ||||||
| chr14:31086410 | ATTTG | A | 3 | a0001c0001t0019g0007 a0001c0001t0019g0008 a0001c0001t0039g0133 |
3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.306+5850_306+5853d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31086410 | ||||||
| chr14:31086583 | T | C | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+5999T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086583 | |||||||
| chr14:31086707 | C | T | 1 | a0001c0001t0005g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306+6123C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086707 | |||||||
| chr14:31086843 | C | T | 2 | a0001c0001t0005g0083 a0001c0001t0005g0084 |
2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-6064C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086843 | |||||||
| chr14:31087160 | C | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0228 |
2 | HG02129.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.307-5747C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087160 | |||||||
| chr14:31087380 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0029g0243 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.307-5527G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087380 | |||||||
| chr14:31087399 | C | T | 1 | a0001c0001t0024g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.307-5508C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087399 | |||||||
| chr14:31087601 | C | T | 1 | a0001c0001t0005g0108 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.307-5306C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087601 | |||||||
| chr14:31087673 | T | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(181): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.307-5234T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087673 | |||||||
| chr14:31087717 | A | G | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-5190A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087717 | |||||||
| chr14:31087754 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0029g0243 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.307-5153C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087754 | |||||||
| chr14:31087761 | T | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0008g0070 |
3 | HG01106.hp1 HG01256.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.307-5146T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087761 | |||||||
| chr14:31088123 | G | C | 178 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0032 others(175): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.307-4784G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088123 | |||||||
| chr14:31088129 | A | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0240 a0001c0001t0015g0263 |
3 | HG03041.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.307-4778A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088129 | |||||||
| chr14:31088178 | G | C | 2 | a0001c0001t0015g0263 a0001c0001t0018g0205 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.307-4729G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088178 | |||||||
| chr14:31088250 | T | C | 1 | a0001c0001t0026g0192 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307-4657T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088250 | |||||||
| chr14:31088487 | G | A | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-4420G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088487 | |||||||
| chr14:31088714 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.307-4193G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088714 | |||||||
| chr14:31088807 | C | CA | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.307-4077dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | ||||||
| chr14:31088807 | C | CAA | 29 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0096 others(26): Show |
29 | HG00621.hp1 HG02040.hp2 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.307-4078_307-4077d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | ||||||
| chr14:31088807 | CA | C | 31 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0104 others(28): Show |
31 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.307-4077delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | ||||||
| chr14:31088807 | CAA | C | 8 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-4078_307-4077d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | ||||||
| chr14:31088807 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307-4086_307-4077d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | ||||||
| chr14:31088886 | G | A | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-4021G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088886 | |||||||
| chr14:31088966 | A | T | 6 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(3): Show |
6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-3941A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088966 | |||||||
| chr14:31089027 | C | T | 18 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.307-3880C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089027 | |||||||
| chr14:31089163 | C | A | 12 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0007g0208 others(9): Show |
12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-3744C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089163 | |||||||
| chr14:31089163 | C | CA | 25 | a0001c0001t0001g0079 a0001c0001t0006g0015 a0001c0001t0006g0016 others(22): Show |
25 | HG00280.hp2 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.307-3726dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31089163 | ||||||
| chr14:31089163 | CA | C | 54 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0003g0002 others(51): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.307-3726delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31089163 | ||||||
| chr14:31089328 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.307-3579T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089328 | |||||||
| chr14:31089463 | A | G | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-3444A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089463 | |||||||
| chr14:31089465 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-3442T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089465 | |||||||
| chr14:31089584 | C | T | 51 | a0001c0001t0003g0002 a0001c0001t0003g0024 a0001c0001t0003g0025 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.307-3323C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089584 | |||||||
| chr14:31089642 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-3265T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089642 | |||||||
| chr14:31089746 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.307-3161G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089746 | |||||||
| chr14:31089914 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0027g0164 a0001c0001t0043g0204 |
3 | HG02280.hp2 HG02735.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.307-2993G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089914 | |||||||
| chr14:31090027 | T | G | 8 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-2880T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090027 | |||||||
| chr14:31090053 | G | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-2854G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090053 | |||||||
| chr14:31090081 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307-2826G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090081 | |||||||
| chr14:31090282 | G | C | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-2625G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090282 | |||||||
| chr14:31090402 | G | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(196): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.307-2505G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090402 | |||||||
| chr14:31090615 | A | G | 2 | a0001c0001t0036g0091 a0001c0001t0037g0041 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.307-2292A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090615 | |||||||
| chr14:31090632 | A | T | 9 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-2275A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090632 | |||||||
| chr14:31091199 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.307-1708G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091199 | |||||||
| chr14:31091219 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.307-1688T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091219 | |||||||
| chr14:31091362 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1545T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091362 | |||||||
| chr14:31091402 | G | T | 8 | a0001c0001t0012g0199 a0001c0001t0012g0200 a0001c0001t0012g0201 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1505G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091402 | |||||||
| chr14:31091525 | C | CT | 13 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0001t0002g0179 others(10): Show |
13 | HG01106.hp2 HG01175.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.307-1368dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31091525 | ||||||
| chr14:31091648 | C | G | 12 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0007g0208 others(9): Show |
12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-1259C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091648 | |||||||
| chr14:31091788 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.307-1119G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091788 | |||||||
| chr14:31091890 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1017A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091890 | |||||||
| chr14:31091933 | A | G | 1 | a0001c0001t0001g0313 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.307-974A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091933 | |||||||
| chr14:31091962 | C | G | 66 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0118 others(63): Show |
67 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.307-945C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091962 | |||||||
| chr14:31091969 | C | A | 24 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(21): Show |
24 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.307-938C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091969 | |||||||
| chr14:31092467 | AACAT | A | 3 | a0001c0001t0019g0007 a0001c0001t0019g0008 a0001c0001t0039g0133 |
3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.307-435_307-432del others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31092467 | ||||||
| chr14:31092496 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.307-411A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092496 | |||||||
| chr14:31092547 | TTAC | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0064 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-357_307-355del others(3): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31092547 | ||||||
| chr14:31092571 | A | T | 1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.307-336A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092571 | |||||||
| chr14:31092626 | A | G | 2 | a0001c0001t0005g0083 a0001c0001t0005g0084 |
2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092626 | |||||||
| chr14:31092684 | C | T | 99 | a0001c0001t0001g0093 a0001c0001t0003g0002 a0001c0001t0003g0024 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.307-223C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092684 | |||||||
| chr14:31092732 | T | A | 3 | a0001c0001t0003g0147 a0001c0001t0003g0148 a0001c0001t0003g0150 |
3 | HG00741.hp1 HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.307-175T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092732 | |||||||
| chr14:31092860 | T | TA | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-47_307-46insA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092860 | |||||||
| chr14:31092864 | A | T | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-43A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092864 | |||||||
| chr14:31092866 | T | A | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-41T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092866 | |||||||
| chr14:31092866 | T | C | 17 | a0001c0001t0010g0271 a0001c0001t0010g0272 a0001c0001t0010g0273 others(14): Show |
17 | HG01891.hp1 HG02074.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.307-41T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092866 | |||||||
| chr14:31092868 | A | G | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-39A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092868 | |||||||
| chr14:31092871 | T | A | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-36T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092871 | |||||||
| chr14:31092872 | T | A | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-35T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092872 | |||||||
| chr14:31092873 | T | A | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-34T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092873 | |||||||
| chr14:31092876 | C | T | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-31C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092876 | |||||||
| chr14:31092878 | T | G | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-29T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092878 | |||||||
| chr14:31092880 | A | T | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-27A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092880 | |||||||
| chr14:31092883 | CT | C | 10 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0017 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-23delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092883 | |||||||
| chr14:31092896 | T | C | 12 | a0001c0001t0007g0157 a0001c0001t0007g0161 a0001c0001t0007g0208 others(9): Show |
12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-11T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092896 |