Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25923 |
| ensemblid | ENSG00000184743.13 |
| hgncid | 24526 |
| symbol | ATL3 |
| name | atlastin GTPase 3 |
| refseq_nuc | NM_015459.5 |
| refseq_prot | NP_056274.3 |
| ensembl_nuc | ENST00000398868.8 |
| ensembl_prot | ENSP00000381844.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 63624087 |
| end | 63671376 |
| strand | - |
| ver | v1.2 |
| region | chr11:63624087-63671376 |
| region5000 | chr11:63619087-63676376 |
| regionname0 | ATL3_chr11_63624087_63671376 |
| regionname5000 | ATL3_chr11_63619087_63676376 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 541 | 240 | 81 | 56 | 57 | 10 | 34 | 34 | ATL3_chr11_63619087_63676376 | ATL3 | MLSPQ others(536): Show |
chr11 | 63619087 | 63676376 |
| a0002 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | MLSPQ others(536): Show |
chr11 | 63619087 | 63676376 |
| a0003 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | MLSPQ others(536): Show |
chr11 | 63619087 | 63676376 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1623 | 234 | 78 | 55 | 57 | 10 | 32 | ATL3_chr11_63619087_63676376 | ATL3 | ATGTT others(1618): Show |
chr11 | 63619087 | 63676376 | ||
| a0001c0002 | 0/0 | 1623 | 4 | 3 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | ATGTT others(1618): Show |
chr11 | 63619087 | 63676376 | ||
| a0001c0003 | 0/0 | 1623 | 2 | 0 | 0 | 0 | 0 | 2 | ATL3_chr11_63619087_63676376 | ATL3 | ATGTT others(1618): Show |
chr11 | 63619087 | 63676376 | ||
| a0002c0004 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | ATGTT others(1618): Show |
chr11 | 63619087 | 63676376 | ||
| a0003c0005 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | ATGTT others(1618): Show |
chr11 | 63619087 | 63676376 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6899 | 149 | 45 | 41 | 37 | 7 | 18 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0002 | 0/0 | 6900 | 11 | 1 | 5 | 3 | 0 | 2 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6895): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0003 | 0/0 | 6898 | 9 | 0 | 0 | 7 | 2 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0004 | 0/0 | 6886 | 8 | 2 | 2 | 0 | 0 | 4 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6881): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0005 | 0/0 | 6899 | 7 | 0 | 3 | 0 | 0 | 4 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0006 | 0/0 | 6899 | 6 | 0 | 0 | 6 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0007 | 0/0 | 6895 | 5 | 4 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6890): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0008 | 0/0 | 6899 | 5 | 4 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0009 | 0/0 | 6892 | 4 | 4 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6887): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0011 | 0/0 | 6896 | 3 | 3 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6891): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0012 | 0/0 | 6898 | 3 | 3 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0013 | 0/0 | 6900 | 3 | 0 | 2 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6895): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0014 | 0/0 | 6893 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6888): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0015 | 0/0 | 6887 | 2 | 0 | 0 | 0 | 0 | 2 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6882): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0016 | 0/0 | 6898 | 2 | 0 | 0 | 2 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0017 | 0/0 | 6897 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6892): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0018 | 0/0 | 6886 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6881): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0019 | 0/0 | 6898 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0020 | 0/0 | 6899 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0021 | 0/0 | 6899 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0022 | 0/0 | 6899 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0023 | 0/0 | 6900 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6895): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0024 | 0/0 | 6891 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6886): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0025 | 0/0 | 6899 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0026 | 0/0 | 6898 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0027 | 0/0 | 6899 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0028 | 0/1 | 6897 | 1 | 0 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6892): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0029 | 0/0 | 6899 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0001t0030 | 0/0 | 6898 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0001c0002t0010 | 0/0 | 6899 | 4 | 3 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0001c0003t0001 | 0/0 | 6899 | 2 | 0 | 0 | 0 | 0 | 2 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6894): Show |
chr11 | 63619087 | 63676376 |
| a0002c0004t0003 | 0/0 | 6898 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6893): Show |
chr11 | 63619087 | 63676376 |
| a0003c0005t0009 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | CTCTG others(6887): Show |
chr11 | 63619087 | 63676376 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0013g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0014g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0015g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0015g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0016g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0018g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0019g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0021g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0024g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0026g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0027g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0028g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0001t0030g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0002t0010g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0002t0010g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0002t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0002c0004t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| a0003c0005t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | FIN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | FIN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00408 | hp2 | a0001 | c0001 | t0016 | g0126 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00673 | hp2 | a0002 | c0004 | t0003 | g0154 | EAS | CHS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0032 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01496 | hp2 | a0001 | c0002 | t0010 | g0016 | AMR | CLM | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01516 | hp1 | a0001 | c0001 | t0025 | g0130 | EUR | IBS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01993 | hp1 | a0001 | c0001 | t0013 | g0157 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02257 | hp1 | a0001 | c0001 | t0030 | g0135 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02258 | hp2 | a0001 | c0002 | t0010 | g0007 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02293 | hp2 | a0001 | c0001 | t0013 | g0069 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02523 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | KHV | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0114 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02615 | hp2 | a0003 | c0005 | t0009 | g0210 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02723 | hp2 | a0001 | c0002 | t0010 | g0018 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0132 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0131 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02809 | hp1 | a0001 | c0002 | t0010 | g0007 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0201 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0211 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03041 | hp2 | a0001 | c0001 | t0022 | g0046 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0047 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0037 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03195 | hp2 | a0001 | c0001 | t0020 | g0048 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0141 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0049 | AFR | ESN | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03654 | hp2 | a0001 | c0001 | t0015 | g0022 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03927 | hp2 | a0001 | c0001 | t0015 | g0024 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0208 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04184 | hp2 | a0001 | c0001 | t0018 | g0017 | SAS | BEB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0129 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04228 | hp1 | a0001 | c0001 | t0029 | g0162 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18747 | hp2 | a0001 | c0001 | t0026 | g0145 | EAS | CHB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | YRI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0051 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | ASW | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ASW | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0209 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02486 | hp2 | a0001 | c0001 | t0017 | g0140 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | MSL | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | USA | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | USA | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0205 | AFR | USA | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0040 | AFR | LWK | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0028 | g0071 | REF | REF | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0142 | REF | REF | ATL3_chr11_63619087_63676376 | ATL3 | chr11 | 63619087 | 63676376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63631056 | G | A | 1 | a0003 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1523C>T | p.Ala508Val | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/13 | 1564/6899 | 1523/1626 | 508/541 | chr11 | 63631056 | |||
| chr11:63658876 | C | G | 1 | a0002 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.290G>C | p.Gly97Ala | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/13 | 331/6899 | 290/1626 | 97/541 | chr11 | 63658876 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63629346 | T | C | 1 | a0001c0003 | 2 | HG02602.hp1 HG02738.hp2 |
synonymous_variant | LOW | c.1599A>G | p.Arg533Arg | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1640/6899 | 1599/1626 | 533/541 | chr11 | 63629346 | |||
| chr11:63631205 | T | C | 1 | a0001c0002 | 4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1374A>G | p.Ser458Ser | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/13 | 1415/6899 | 1374/1626 | 458/541 | chr11 | 63631205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63624131 | G | C | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5188C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 5188 | chr11 | 63624131 | ||||||
| chr11:63624480 | T | C | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4839A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 4839 | chr11 | 63624480 | ||||||
| chr11:63625188 | TCA | T | 1 | a0001c0001t0011 | 3 | HG02717.hp1 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4129_*4130delTG | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 4129 | chr11 | 63625188 | ||||||
| chr11:63625195 | AAT | A | 2 | a0001c0001t0007 a0001c0001t0014 |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4122_*4123delAT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 4122 | chr11 | 63625195 | ||||||
| chr11:63625356 | G | A | 1 | a0001c0001t0007 | 5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3963C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 3963 | chr11 | 63625356 | ||||||
| chr11:63625508 | A | G | 1 | a0001c0001t0016 | 2 | HG00408.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3811T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 3811 | chr11 | 63625508 | ||||||
| chr11:63625771 | A | G | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
38 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3548T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 3548 | chr11 | 63625771 | ||||||
| chr11:63625981 | CA | C | 2 | a0001c0001t0007 a0001c0001t0014 |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3337delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 3337 | chr11 | 63625981 | ||||||
| chr11:63626313 | G | A | 1 | a0001c0001t0022 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3006C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 3006 | chr11 | 63626313 | ||||||
| chr11:63626539 | ATT | A | 2 | a0001c0001t0017 a0001c0001t0030 |
3 | HG02257.hp1 HG02486.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2778_*2779delAA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 2778 | chr11 | 63626539 | ||||||
| chr11:63626679 | G | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2640C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 2640 | chr11 | 63626679 | ||||||
| chr11:63626699 | G | A | 3 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0019 |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2620C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 2620 | chr11 | 63626699 | ||||||
| chr11:63626942 | GA | G | 4 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0019 others(1): Show |
8 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2376delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 2376 | chr11 | 63626942 | ||||||
| chr11:63627619 | A | G | 1 | a0001c0001t0018 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1700 | chr11 | 63627619 | ||||||
| chr11:63627641 | T | G | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1678A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1678 | chr11 | 63627641 | ||||||
| chr11:63627699 | CAAT | C | 1 | a0001c0001t0014 | 2 | HG03209.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1617_*1619delATT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1617 | chr11 | 63627699 | ||||||
| chr11:63627905 | T | C | 4 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0022 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1414A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1414 | chr11 | 63627905 | ||||||
| chr11:63628068 | T | C | 1 | a0001c0001t0029 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1251 | chr11 | 63628068 | ||||||
| chr11:63628145 | G | A | 1 | a0001c0001t0005 | 7 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1174C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1174 | chr11 | 63628145 | ||||||
| chr11:63628154 | C | A | 1 | a0001c0001t0012 | 3 | HG02622.hp1 HG03139.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1165G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1165 | chr11 | 63628154 | ||||||
| chr11:63628167 | C | T | 3 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 1152 | chr11 | 63628167 | ||||||
| chr11:63628319 | C | CA | 7 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0013 others(4): Show |
13 | HG01993.hp1 HG02293.hp2 HG02523.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*999dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 999 | chr11 | 63628319 | ||||||
| chr11:63628319 | CAAAAAAA | C | 3 | a0001c0001t0009 a0001c0001t0024 a0003c0005t0009 |
6 | HG02109.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*993_*999delTTTTTT others(1): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 993 | chr11 | 63628319 | ||||||
| chr11:63628569 | C | G | 1 | a0001c0001t0025 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750G>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 750 | chr11 | 63628569 | ||||||
| chr11:63628570 | G | A | 3 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0019 |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*749C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 749 | chr11 | 63628570 | ||||||
| chr11:63628705 | G | A | 1 | a0001c0001t0006 | 6 | HG00597.hp1 HG02015.hp1 HG02080.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*614C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 614 | chr11 | 63628705 | ||||||
| chr11:63628759 | C | T | 1 | a0001c0001t0007 | 5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*560G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 560 | chr11 | 63628759 | ||||||
| chr11:63628778 | G | C | 1 | a0001c0002t0010 | 4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*541C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 541 | chr11 | 63628778 | ||||||
| chr11:63628834 | C | CA | 2 | a0001c0001t0002 a0001c0001t0030 |
12 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*484dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 484 | chr11 | 63628834 | ||||||
| chr11:63628834 | CA | C | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(7): Show |
27 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*484delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 484 | chr11 | 63628834 | ||||||
| chr11:63628834 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0015 | 2 | HG03654.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*473_*484delTTTTTT others(6): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 473 | chr11 | 63628834 | ||||||
| chr11:63628834 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0004 a0001c0001t0018 |
9 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*472_*484delTTTTTT others(7): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 472 | chr11 | 63628834 | ||||||
| chr11:63628912 | C | T | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*407G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 407 | chr11 | 63628912 | ||||||
| chr11:63629193 | A | G | 2 | a0001c0001t0007 a0001c0001t0014 |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*126T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 13/13 | 126 | chr11 | 63629193 | ||||||
| chr11:63671364 | C | T | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
38 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-29G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/13 | 29 | chr11 | 63671364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:63629431 | A | G | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-26T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63629431 | |||||||
| chr11:63629447 | C | A | 2 | a0001c0001t0009g0015 a0001c0001t0024g0201 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1540-42G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63629447 | |||||||
| chr11:63629521 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1540-116C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63629521 | |||||||
| chr11:63629733 | T | A | 1 | a0001c0001t0022g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1540-328A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63629733 | |||||||
| chr11:63629795 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0101 |
3 | HG01516.hp2 HG01517.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1540-390C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63629795 | |||||||
| chr11:63630032 | A | T | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1540-627T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630032 | |||||||
| chr11:63630167 | C | A | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1540-762G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630167 | |||||||
| chr11:63630426 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0002g0164 |
2 | NA18964.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1539+614G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630426 | |||||||
| chr11:63630426 | C | CA | 11 | a0001c0001t0001g0074 a0001c0001t0001g0100 a0001c0001t0001g0179 others(8): Show |
11 | HG01934.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1539+613dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630426 | |||||||
| chr11:63630426 | CA | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0077 others(5): Show |
8 | HG00323.hp1 HG00558.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1539+613delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630426 | |||||||
| chr11:63630448 | A | AG | 70 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
77 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1539+591dupC | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630448 | |||||||
| chr11:63630448 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0152 a0001c0001t0006g0112 |
3 | HG00597.hp1 HG01975.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1539+592T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630448 | |||||||
| chr11:63630474 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1539+566T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630474 | |||||||
| chr11:63630652 | G | A | 1 | a0001c0001t0014g0008 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1539+388C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630652 | |||||||
| chr11:63630800 | CA | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1539+239delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63630800 | |||||||
| chr11:63631023 | TCAG | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1539+14_1539+16del others(3): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 12/12 | chr11 | 63631023 | |||||||
| chr11:63631678 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(69): Show |
78 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1108-207T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631678 | |||||||
| chr11:63631703 | C | T | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-232G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631703 | |||||||
| chr11:63631740 | C | T | 1 | a0002c0004t0003g0154 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1108-269G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631740 | |||||||
| chr11:63631936 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0098 |
4 | NA18943.hp2 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-465G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631936 | |||||||
| chr11:63631946 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1108-475G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631946 | |||||||
| chr11:63631983 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1108-512T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63631983 | |||||||
| chr11:63632000 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(73): Show |
83 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1108-529C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63632000 | |||||||
| chr11:63632499 | C | T | 1 | a0001c0001t0014g0008 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1107+527G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63632499 | |||||||
| chr11:63632820 | T | TCAAAA | 8 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(5): Show |
8 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107+201_1107+205d others(7): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63632820 | |||||||
| chr11:63633021 | C | T | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1107+5G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 11/12 | chr11 | 63633021 | |||||||
| chr11:63633369 | ATAT | A | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-275_1036-273d others(5): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633369 | |||||||
| chr11:63633502 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1036-405A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633502 | |||||||
| chr11:63633727 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0061 others(16): Show |
20 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.1036-630T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633727 | |||||||
| chr11:63633733 | AG | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
154 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1036-637delC | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633733 | |||||||
| chr11:63633734 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1036-637C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633734 | |||||||
| chr11:63633803 | G | C | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036-706C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63633803 | |||||||
| chr11:63634021 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1036-924G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634021 | |||||||
| chr11:63634038 | C | CA | 27 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0057 others(24): Show |
30 | HG00673.hp1 HG01109.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1036-942dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634038 | |||||||
| chr11:63634038 | CA | C | 19 | a0001c0001t0001g0062 a0001c0001t0001g0081 a0001c0001t0004g0019 others(16): Show |
20 | HG00642.hp1 HG00738.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1036-942delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634038 | |||||||
| chr11:63634059 | G | C | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-962C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634059 | |||||||
| chr11:63634089 | G | A | 2 | a0001c0001t0007g0028 a0001c0001t0007g0029 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1036-992C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634089 | |||||||
| chr11:63634185 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1036-1088A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634185 | |||||||
| chr11:63634185 | T | TA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0094 others(3): Show |
6 | HG00642.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036-1089dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634185 | |||||||
| chr11:63634185 | T | TAA | 6 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036-1090_1036-108 others(6): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634185 | |||||||
| chr11:63634185 | TA | T | 17 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0152 others(14): Show |
17 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1036-1089delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634185 | |||||||
| chr11:63634187 | A | T | 2 | a0001c0001t0004g0021 a0001c0001t0004g0027 |
2 | HG00642.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1036-1090T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634187 | |||||||
| chr11:63634201 | A | G | 4 | a0001c0001t0001g0139 a0001c0001t0020g0048 a0001c0001t0021g0049 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036-1104T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634201 | |||||||
| chr11:63634201 | AAAG | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
15 | HG01346.hp1 HG02145.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1036-1107_1036-110 others(7): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634201 | |||||||
| chr11:63634215 | A | G | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036-1118T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634215 | |||||||
| chr11:63634233 | G | A | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0208 |
3 | HG01433.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1036-1136C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634233 | |||||||
| chr11:63634235 | G | A | 2 | a0001c0001t0009g0211 a0003c0005t0009g0210 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1036-1138C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634235 | |||||||
| chr11:63634412 | C | A | 1 | a0001c0001t0008g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1035+1122G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634412 | |||||||
| chr11:63634800 | G | A | 1 | a0002c0004t0003g0154 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1035+734C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634800 | |||||||
| chr11:63634813 | T | C | 1 | a0001c0001t0004g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1035+721A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634813 | |||||||
| chr11:63634932 | C | T | 1 | a0001c0001t0027g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1035+602G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634932 | |||||||
| chr11:63634974 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1035+560G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63634974 | |||||||
| chr11:63635016 | G | T | 1 | a0001c0001t0019g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1035+518C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63635016 | |||||||
| chr11:63635018 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035+516G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63635018 | |||||||
| chr11:63635194 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1035+340T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63635194 | |||||||
| chr11:63635326 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1035+208G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63635326 | |||||||
| chr11:63635397 | T | TA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(75): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1035+136dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 10/12 | chr11 | 63635397 | |||||||
| chr11:63635813 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.979-223A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 9/12 | chr11 | 63635813 | |||||||
| chr11:63635900 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.978+307C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 9/12 | chr11 | 63635900 | |||||||
| chr11:63636004 | G | A | 1 | a0001c0001t0007g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.978+203C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 9/12 | chr11 | 63636004 | |||||||
| chr11:63636198 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.978+9G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 9/12 | chr11 | 63636198 | |||||||
| chr11:63636401 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.851-67G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636401 | |||||||
| chr11:63636536 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.851-202G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636536 | |||||||
| chr11:63636683 | G | A | 1 | a0001c0001t0014g0008 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.851-349C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636683 | |||||||
| chr11:63636707 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0121 |
3 | HG01952.hp1 HG02273.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.851-373G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636707 | |||||||
| chr11:63636742 | GA | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
235 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.851-409delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636742 | |||||||
| chr11:63636893 | A | G | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0208 |
3 | HG01433.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.851-559T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636893 | |||||||
| chr11:63636954 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.851-620G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63636954 | |||||||
| chr11:63637032 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.851-698T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637032 | |||||||
| chr11:63637225 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.851-891C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637225 | |||||||
| chr11:63637272 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0193 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.851-938A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637272 | |||||||
| chr11:63637277 | G | GAAAA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(75): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.851-947_851-944dup others(4): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637277 | |||||||
| chr11:63637457 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.851-1123C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637457 | |||||||
| chr11:63637458 | C | A | 1 | a0001c0001t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.851-1124G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637458 | |||||||
| chr11:63637845 | T | A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-1511A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637845 | |||||||
| chr11:63637974 | T | C | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-1640A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637974 | |||||||
| chr11:63637995 | T | C | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-1661A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63637995 | |||||||
| chr11:63638078 | C | T | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-1744G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638078 | |||||||
| chr11:63638084 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
7 | NA18612.hp2 NA18943.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-1750T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638084 | |||||||
| chr11:63638286 | T | C | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-1952A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638286 | |||||||
| chr11:63638403 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.851-2069G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638403 | |||||||
| chr11:63638597 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.851-2263G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638597 | |||||||
| chr11:63638727 | C | CA | 9 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0075 others(6): Show |
9 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-2394dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638727 | |||||||
| chr11:63638732 | A | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0177 a0001c0001t0001g0195 others(1): Show |
4 | NA19009.hp2 NA19065.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-2398T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638732 | |||||||
| chr11:63638781 | C | T | 3 | a0001c0001t0012g0034 a0001c0001t0012g0036 a0001c0001t0012g0037 |
3 | HG02622.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.851-2447G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638781 | |||||||
| chr11:63638790 | AGTTATAC others(15): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.851-2478_851-2457d others(24): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638790 | |||||||
| chr11:63638891 | T | C | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.851-2557A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63638891 | |||||||
| chr11:63639153 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0177 |
2 | NA19077.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.851-2819G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639153 | |||||||
| chr11:63639302 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.851-2968A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639302 | |||||||
| chr11:63639473 | G | A | 4 | a0001c0001t0001g0171 a0001c0002t0010g0007 a0001c0002t0010g0016 others(1): Show |
5 | HG01496.hp2 HG02027.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-3139C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639473 | |||||||
| chr11:63639590 | CA | C | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.851-3257delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639590 | |||||||
| chr11:63639746 | C | A | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.851-3412G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639746 | |||||||
| chr11:63639913 | A | C | 1 | a0001c0002t0010g0018 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.850+3444T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639913 | |||||||
| chr11:63639934 | C | CT | 9 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(6): Show |
9 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.850+3422dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639934 | |||||||
| chr11:63639945 | T | G | 1 | a0001c0002t0010g0016 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.850+3412A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639945 | |||||||
| chr11:63639959 | G | A | 11 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
11 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+3398C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639959 | |||||||
| chr11:63639999 | G | C | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+3358C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63639999 | |||||||
| chr11:63640032 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(119): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.850+3325T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640032 | |||||||
| chr11:63640097 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850+3260A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640097 | |||||||
| chr11:63640221 | G | A | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+3136C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640221 | |||||||
| chr11:63640314 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG01074.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.850+3043C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640314 | |||||||
| chr11:63640474 | A | T | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2883T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640474 | |||||||
| chr11:63640549 | T | C | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+2808A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640549 | |||||||
| chr11:63640594 | C | CT | 29 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0105 others(26): Show |
30 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.850+2762dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640594 | |||||||
| chr11:63640594 | CT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0054 others(17): Show |
24 | HG01168.hp2 HG01517.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.850+2762delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640594 | |||||||
| chr11:63640594 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0200 |
2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.850+2751_850+2762d others(14): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640594 | |||||||
| chr11:63640712 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.850+2645G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640712 | |||||||
| chr11:63640750 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
52 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.850+2607T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63640750 | |||||||
| chr11:63641228 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.850+2129T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63641228 | |||||||
| chr11:63641697 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.850+1660G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63641697 | |||||||
| chr11:63641742 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.850+1615G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63641742 | |||||||
| chr11:63641897 | T | C | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.850+1460A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63641897 | |||||||
| chr11:63642192 | C | T | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.850+1165G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63642192 | |||||||
| chr11:63642417 | T | C | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+940A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63642417 | |||||||
| chr11:63642549 | T | G | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.850+808A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63642549 | |||||||
| chr11:63642717 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.850+640C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63642717 | |||||||
| chr11:63642884 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0081 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.850+473C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63642884 | |||||||
| chr11:63643124 | C | T | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+233G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 8/12 | chr11 | 63643124 | |||||||
| chr11:63643513 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(47): Show |
59 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.712-18C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 7/12 | chr11 | 63643513 | |||||||
| chr11:63643605 | T | C | 4 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0022g0046 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-110A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 7/12 | chr11 | 63643605 | |||||||
| chr11:63644279 | G | A | 2 | a0001c0001t0007g0028 a0001c0001t0007g0029 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.619-18C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644279 | |||||||
| chr11:63644367 | A | AGATAC | 20 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(17): Show |
22 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.619-107_619-106ins others(5): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644367 | |||||||
| chr11:63644370 | A | ACT | 20 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(17): Show |
22 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.619-110_619-109ins others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644370 | |||||||
| chr11:63644382 | C | CT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0088 others(10): Show |
15 | HG01109.hp1 HG01516.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.619-122dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644382 | |||||||
| chr11:63644382 | CT | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0062 others(9): Show |
13 | HG01168.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-122delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644382 | |||||||
| chr11:63644562 | T | A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-301A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644562 | |||||||
| chr11:63644599 | C | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.619-338G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644599 | |||||||
| chr11:63644739 | G | A | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.619-478C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63644739 | |||||||
| chr11:63645268 | G | A | 3 | a0001c0001t0009g0209 a0001c0001t0009g0211 a0003c0005t0009g0210 |
3 | HG02109.hp1 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.619-1007C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645268 | |||||||
| chr11:63645408 | A | T | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.618+1099T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645408 | |||||||
| chr11:63645513 | G | A | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+994C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645513 | |||||||
| chr11:63645540 | C | CAG | 2 | a0001c0001t0001g0010 a0001c0001t0014g0008 |
4 | HG02895.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+965_618+966dup others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645540 | |||||||
| chr11:63645552 | G | C | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+955C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645552 | |||||||
| chr11:63645556 | G | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.618+951C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645556 | |||||||
| chr11:63645849 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.618+658G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63645849 | |||||||
| chr11:63646066 | A | AT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.618+440dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646066 | |||||||
| chr11:63646073 | T | TA | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+433dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646073 | |||||||
| chr11:63646079 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0193 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.618+428T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646079 | |||||||
| chr11:63646240 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.618+267C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646240 | |||||||
| chr11:63646309 | C | T | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(25): Show |
30 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.618+198G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646309 | |||||||
| chr11:63646465 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.618+42T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646465 | |||||||
| chr11:63646490 | AAAAT | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.618+13_618+16delAT others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 6/12 | chr11 | 63646490 | |||||||
| chr11:63646680 | G | T | 1 | a0001c0001t0014g0008 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.562-117C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63646680 | |||||||
| chr11:63646979 | C | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-416G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63646979 | |||||||
| chr11:63647203 | A | AT | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-641dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647203 | |||||||
| chr11:63647279 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
8 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-716G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647279 | |||||||
| chr11:63647473 | G | A | 1 | a0001c0001t0011g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.562-910C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647473 | |||||||
| chr11:63647557 | G | A | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.562-994C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647557 | |||||||
| chr11:63647593 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.562-1030C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647593 | |||||||
| chr11:63647868 | T | A | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-1305A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63647868 | |||||||
| chr11:63648015 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.562-1452C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63648015 | |||||||
| chr11:63648387 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0070 others(14): Show |
19 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-1824T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63648387 | |||||||
| chr11:63648548 | G | A | 1 | a0001c0001t0022g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.562-1985C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63648548 | |||||||
| chr11:63648757 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.562-2194G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63648757 | |||||||
| chr11:63648841 | G | C | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-2278C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63648841 | |||||||
| chr11:63649232 | T | C | 1 | a0001c0001t0022g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.562-2669A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63649232 | |||||||
| chr11:63649308 | G | C | 7 | a0001c0001t0001g0166 a0001c0001t0006g0112 a0001c0001t0006g0116 others(4): Show |
7 | HG00597.hp1 HG02015.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+2628C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63649308 | |||||||
| chr11:63649779 | C | G | 1 | a0001c0001t0004g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.561+2157G>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63649779 | |||||||
| chr11:63649974 | C | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0086 a0001c0001t0002g0087 |
3 | HG00735.hp1 HG01261.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.561+1962G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63649974 | |||||||
| chr11:63650037 | AT | A | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+1898delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650037 | |||||||
| chr11:63650252 | G | A | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+1684C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650252 | |||||||
| chr11:63650262 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.561+1674T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650262 | |||||||
| chr11:63650333 | T | G | 8 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(5): Show |
8 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+1603A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650333 | |||||||
| chr11:63650397 | G | T | 1 | a0001c0001t0004g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.561+1539C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650397 | |||||||
| chr11:63650502 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.561+1434G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650502 | |||||||
| chr11:63650657 | T | C | 3 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 |
3 | HG02717.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561+1279A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650657 | |||||||
| chr11:63650661 | G | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
14 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.561+1275C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650661 | |||||||
| chr11:63650688 | G | A | 1 | a0001c0001t0014g0008 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.561+1248C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650688 | |||||||
| chr11:63650758 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.561+1178C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650758 | |||||||
| chr11:63650809 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.561+1127A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63650809 | |||||||
| chr11:63651067 | G | T | 1 | a0001c0001t0003g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.561+869C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651067 | |||||||
| chr11:63651241 | G | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0132 |
3 | HG00738.hp2 HG01099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.561+695C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651241 | |||||||
| chr11:63651450 | T | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.561+486A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651450 | |||||||
| chr11:63651529 | A | C | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+407T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651529 | |||||||
| chr11:63651692 | G | A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+244C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651692 | |||||||
| chr11:63651778 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0193 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.561+158G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651778 | |||||||
| chr11:63651802 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.561+134A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 5/12 | chr11 | 63651802 | |||||||
| chr11:63651997 | A | G | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-11T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 4/12 | chr11 | 63651997 | |||||||
| chr11:63652182 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.511-196C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 4/12 | chr11 | 63652182 | |||||||
| chr11:63652234 | T | C | 2 | a0001c0001t0003g0197 a0001c0001t0003g0199 |
2 | NA18960.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.510+237A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 4/12 | chr11 | 63652234 | |||||||
| chr11:63652359 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.510+112T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 4/12 | chr11 | 63652359 | |||||||
| chr11:63652408 | C | T | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+63G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 4/12 | chr11 | 63652408 | |||||||
| chr11:63652864 | T | C | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-289A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63652864 | |||||||
| chr11:63652971 | G | T | 25 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(22): Show |
27 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.406-396C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63652971 | |||||||
| chr11:63652986 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.406-411A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63652986 | |||||||
| chr11:63653105 | T | C | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-530A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653105 | |||||||
| chr11:63653305 | A | G | 1 | a0001c0001t0004g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.406-730T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653305 | |||||||
| chr11:63653325 | C | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-750G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653325 | |||||||
| chr11:63653425 | A | G | 23 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(20): Show |
25 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.406-850T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653425 | |||||||
| chr11:63653464 | C | CA | 19 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0109 others(16): Show |
19 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-890dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653464 | |||||||
| chr11:63653551 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
8 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.406-976T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653551 | |||||||
| chr11:63653551 | A | T | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-976T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653551 | |||||||
| chr11:63653771 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.406-1196A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63653771 | |||||||
| chr11:63654027 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.406-1452C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654027 | |||||||
| chr11:63654127 | A | C | 16 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0105 others(13): Show |
16 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.406-1552T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654127 | |||||||
| chr11:63654149 | G | GT | 22 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0079 others(19): Show |
23 | HG00597.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.406-1575dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654149 | |||||||
| chr11:63654149 | G | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-1574C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654149 | |||||||
| chr11:63654247 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1672G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654247 | |||||||
| chr11:63654289 | GACGCCCG others(5): Show |
G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.406-1726_406-1715d others(14): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654289 | |||||||
| chr11:63654295 | C | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-1720G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654295 | |||||||
| chr11:63654321 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0002g0084 a0001c0001t0002g0086 others(1): Show |
4 | HG00735.hp1 HG01261.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-1746T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654321 | |||||||
| chr11:63654367 | G | C | 1 | a0001c0001t0027g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.406-1792C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654367 | |||||||
| chr11:63654391 | C | T | 1 | a0001c0001t0017g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.406-1816G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654391 | |||||||
| chr11:63654404 | C | T | 9 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(6): Show |
10 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.406-1829G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654404 | |||||||
| chr11:63654452 | C | A | 9 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(6): Show |
10 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.406-1877G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654452 | |||||||
| chr11:63654587 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
14 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.406-2012T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654587 | |||||||
| chr11:63654699 | A | AT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(20): Show |
25 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.406-2125dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654699 | |||||||
| chr11:63654699 | AT | A | 24 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0001t0001g0143 others(21): Show |
25 | HG00408.hp1 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.406-2125delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654699 | |||||||
| chr11:63654732 | C | CTT | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.406-2158_406-2157i others(4): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654732 | |||||||
| chr11:63654786 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406-2211A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654786 | |||||||
| chr11:63654853 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.406-2278A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654853 | |||||||
| chr11:63654894 | TA | T | 26 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(23): Show |
28 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.406-2320delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63654894 | |||||||
| chr11:63655096 | T | G | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-2521A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655096 | |||||||
| chr11:63655198 | G | T | 2 | a0001c0001t0009g0015 a0001c0001t0024g0201 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.406-2623C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655198 | |||||||
| chr11:63655236 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.406-2661G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655236 | |||||||
| chr11:63655441 | G | A | 4 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0022g0046 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-2866C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655441 | |||||||
| chr11:63655443 | A | G | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-2868T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655443 | |||||||
| chr11:63655450 | C | CT | 10 | a0001c0001t0001g0056 a0001c0001t0001g0105 a0001c0001t0001g0139 others(7): Show |
10 | HG00735.hp2 HG01109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.406-2876dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655450 | |||||||
| chr11:63655558 | C | T | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-2983G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655558 | |||||||
| chr11:63655737 | C | T | 5 | a0001c0001t0009g0015 a0001c0001t0009g0209 a0001c0001t0009g0211 others(2): Show |
6 | HG02109.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+3024G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655737 | |||||||
| chr11:63655741 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02258.hp1 HG02717.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+3020C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655741 | |||||||
| chr11:63655950 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.405+2811G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655950 | |||||||
| chr11:63655962 | C | T | 9 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(6): Show |
10 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.405+2799G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655962 | |||||||
| chr11:63655963 | G | A | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.405+2798C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63655963 | |||||||
| chr11:63656021 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.405+2740C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656021 | |||||||
| chr11:63656096 | C | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.405+2665G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656096 | |||||||
| chr11:63656148 | C | A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+2613G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656148 | |||||||
| chr11:63656149 | G | A | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+2612C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656149 | |||||||
| chr11:63656223 | C | CA | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.405+2537dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656223 | |||||||
| chr11:63656223 | CA | C | 17 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0083 others(14): Show |
17 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.405+2537delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656223 | |||||||
| chr11:63656346 | T | A | 1 | a0001c0001t0013g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.405+2415A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656346 | |||||||
| chr11:63656715 | CAG | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+2044_405+2045d others(4): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656715 | |||||||
| chr11:63656731 | C | CA | 19 | a0001c0001t0005g0014 a0001c0001t0005g0132 a0001c0001t0007g0028 others(16): Show |
22 | HG00738.hp2 HG01099.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.405+2029dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656731 | |||||||
| chr11:63656838 | T | C | 2 | a0001c0001t0003g0172 a0002c0004t0003g0154 |
2 | HG00673.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.405+1923A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63656838 | |||||||
| chr11:63657073 | G | A | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+1688C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657073 | |||||||
| chr11:63657208 | C | CA | 15 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0118 others(12): Show |
15 | HG00408.hp2 HG00597.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+1552dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAA | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.405+1549_405+1552d others(6): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0019g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.405+1535_405+1552d others(20): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0007g0028 a0001c0001t0007g0029 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.405+1552_405+1553i others(22): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0011g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405+1552_405+1553i others(24): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0011g0038 |
3 | HG02486.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.405+1552_405+1553i others(25): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0011g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.405+1552_405+1553i others(27): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657208 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0007g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.405+1552_405+1553i others(32): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657208 | |||||||
| chr11:63657359 | C | T | 4 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+1402G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657359 | |||||||
| chr11:63657405 | T | G | 1 | a0001c0001t0006g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.405+1356A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657405 | |||||||
| chr11:63657538 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.405+1223C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657538 | |||||||
| chr11:63657735 | T | C | 1 | a0001c0001t0007g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405+1026A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657735 | |||||||
| chr11:63657857 | C | CT | 18 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0147 others(15): Show |
19 | HG00735.hp1 HG01109.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.405+903dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657857 | |||||||
| chr11:63657976 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(81): Show |
91 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.405+785G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63657976 | |||||||
| chr11:63658002 | A | G | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+759T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63658002 | |||||||
| chr11:63658332 | T | A | 1 | a0001c0001t0006g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.405+429A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63658332 | |||||||
| chr11:63658625 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.405+136C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 3/12 | chr11 | 63658625 | |||||||
| chr11:63659281 | T | A | 1 | a0001c0001t0004g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.47-29A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63659281 | |||||||
| chr11:63659456 | G | A | 1 | a0001c0001t0008g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47-204C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63659456 | |||||||
| chr11:63659707 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.47-455C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63659707 | |||||||
| chr11:63659813 | G | GT | 2 | a0001c0001t0001g0153 a0001c0001t0001g0193 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.47-562dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63659813 | |||||||
| chr11:63660111 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.47-859C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63660111 | |||||||
| chr11:63660253 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.47-1001A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63660253 | |||||||
| chr11:63660648 | T | C | 3 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0007g0032 |
3 | HG01109.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.47-1396A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63660648 | |||||||
| chr11:63660813 | A | T | 15 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0105 others(12): Show |
15 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-1561T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63660813 | |||||||
| chr11:63660840 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.47-1588T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63660840 | |||||||
| chr11:63661031 | T | G | 1 | a0001c0001t0025g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.47-1779A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661031 | |||||||
| chr11:63661196 | TG | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-1945delC | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661196 | |||||||
| chr11:63661201 | G | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-1949C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661201 | |||||||
| chr11:63661311 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0200 |
2 | HG02523.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.47-2059C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661311 | |||||||
| chr11:63661524 | G | C | 3 | a0001c0001t0012g0034 a0001c0001t0012g0036 a0001c0001t0012g0037 |
3 | HG02622.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.47-2272C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661524 | |||||||
| chr11:63661578 | AAAGAG | A | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-2331_47-2327del others(5): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661578 | |||||||
| chr11:63661578 | AAAGAGAA others(3): Show |
A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-2336_47-2327del others(10): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661578 | |||||||
| chr11:63661719 | A | C | 1 | a0001c0001t0026g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.47-2467T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661719 | |||||||
| chr11:63661812 | CCAG | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-2563_47-2561del others(3): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661812 | |||||||
| chr11:63661884 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47-2632C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661884 | |||||||
| chr11:63661888 | C | CA | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-2637dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63661888 | |||||||
| chr11:63662030 | T | C | 1 | a0001c0001t0022g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.47-2778A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63662030 | |||||||
| chr11:63662043 | T | C | 5 | a0001c0001t0009g0015 a0001c0001t0009g0209 a0001c0001t0009g0211 others(2): Show |
6 | HG02109.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-2791A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63662043 | |||||||
| chr11:63662152 | G | T | 1 | a0001c0001t0003g0144 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.47-2900C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63662152 | |||||||
| chr11:63662212 | C | CA | 12 | a0001c0001t0001g0203 a0001c0001t0001g0212 a0001c0001t0011g0035 others(9): Show |
13 | HG01496.hp2 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.47-2961dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63662212 | |||||||
| chr11:63662491 | T | C | 1 | a0001c0001t0005g0129 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.47-3239A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63662491 | |||||||
| chr11:63663105 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
8 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-3853G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663105 | |||||||
| chr11:63663112 | G | A | 1 | a0001c0001t0025g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.47-3860C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663112 | |||||||
| chr11:63663122 | C | CT | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-3871dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663122 | |||||||
| chr11:63663345 | T | A | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-4093A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663345 | |||||||
| chr11:63663345 | T | C | 11 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-4093A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663345 | |||||||
| chr11:63663595 | T | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01106.hp1 HG01192.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-4343A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63663595 | |||||||
| chr11:63664054 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.47-4802C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664054 | |||||||
| chr11:63664084 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47-4832G>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664084 | |||||||
| chr11:63664171 | A | G | 4 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(1): Show |
4 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-4919T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664171 | |||||||
| chr11:63664265 | T | A | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.47-5013A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664265 | |||||||
| chr11:63664366 | C | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-5114G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664366 | |||||||
| chr11:63664397 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
14 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.47-5145C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664397 | |||||||
| chr11:63664401 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.47-5149C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664401 | |||||||
| chr11:63664703 | A | G | 4 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0022g0046 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-5451T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664703 | |||||||
| chr11:63664780 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.47-5528C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664780 | |||||||
| chr11:63664832 | T | C | 1 | a0001c0001t0004g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.47-5580A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63664832 | |||||||
| chr11:63665267 | C | A | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-6015G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665267 | |||||||
| chr11:63665278 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46+6012C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665278 | |||||||
| chr11:63665327 | CAG | C | 3 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 |
3 | HG02717.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.46+5961_46+5962del others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665327 | |||||||
| chr11:63665345 | C | CA | 9 | a0001c0001t0001g0052 a0001c0001t0001g0190 a0001c0001t0001g0203 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.46+5944dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665345 | |||||||
| chr11:63665345 | CA | C | 25 | a0001c0001t0001g0101 a0001c0001t0001g0137 a0001c0001t0004g0019 others(22): Show |
27 | HG00642.hp1 HG01496.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.46+5944delT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665345 | |||||||
| chr11:63665362 | A | T | 3 | a0001c0002t0010g0007 a0001c0002t0010g0016 a0001c0002t0010g0018 |
4 | HG01496.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+5928T>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665362 | |||||||
| chr11:63665463 | C | T | 4 | a0001c0001t0009g0015 a0001c0001t0009g0209 a0001c0001t0024g0201 others(1): Show |
5 | HG02109.hp1 HG02615.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+5827G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665463 | |||||||
| chr11:63665476 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46+5814C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665476 | |||||||
| chr11:63665527 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
8 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+5763C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665527 | |||||||
| chr11:63665618 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.46+5672C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665618 | |||||||
| chr11:63665762 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.46+5528G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665762 | |||||||
| chr11:63665763 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0191 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.46+5527C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665763 | |||||||
| chr11:63665767 | G | A | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.46+5523C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665767 | |||||||
| chr11:63665837 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.46+5453T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63665837 | |||||||
| chr11:63666199 | C | T | 1 | a0001c0001t0030g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.46+5091G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666199 | |||||||
| chr11:63666258 | C | T | 6 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(3): Show |
7 | HG01109.hp1 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+5032G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666258 | |||||||
| chr11:63666273 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.46+5017T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666273 | |||||||
| chr11:63666331 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0068 others(5): Show |
9 | HG03669.hp1 NA18612.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.46+4959C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666331 | |||||||
| chr11:63666468 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46+4822G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666468 | |||||||
| chr11:63666543 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0070 others(14): Show |
19 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.46+4747G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666543 | |||||||
| chr11:63666584 | C | T | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+4706G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63666584 | |||||||
| chr11:63667465 | G | T | 1 | a0001c0001t0013g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.46+3825C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667465 | |||||||
| chr11:63667492 | T | A | 3 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0007g0032 |
3 | HG01109.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46+3798A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667492 | |||||||
| chr11:63667533 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.46+3757C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667533 | |||||||
| chr11:63667691 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.46+3599C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667691 | |||||||
| chr11:63667696 | G | T | 3 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 |
3 | HG02717.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.46+3594C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667696 | |||||||
| chr11:63667750 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46+3540G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667750 | |||||||
| chr11:63667763 | C | CA | 10 | a0001c0001t0001g0100 a0001c0001t0001g0133 a0001c0001t0001g0194 others(7): Show |
11 | HG01192.hp1 HG01346.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+3526dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667763 | |||||||
| chr11:63667782 | T | A | 3 | a0001c0001t0004g0033 a0001c0001t0015g0022 a0001c0001t0015g0024 |
3 | HG03130.hp2 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.46+3508A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667782 | |||||||
| chr11:63667906 | C | T | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.46+3384G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63667906 | |||||||
| chr11:63668541 | C | A | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+2749G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668541 | |||||||
| chr11:63668560 | T | C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0200 others(3): Show |
6 | HG02523.hp1 NA18954.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+2730A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668560 | |||||||
| chr11:63668790 | C | CT | 50 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0101 others(47): Show |
52 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.46+2499dupA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668790 | |||||||
| chr11:63668790 | C | CTT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(37): Show |
45 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.46+2498_46+2499dup others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668790 | |||||||
| chr11:63668790 | C | CTTT | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG03492.hp2 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+2497_46+2499dup others(3): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668790 | |||||||
| chr11:63668790 | CT | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
27 | HG00558.hp2 HG00642.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.46+2499delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668790 | |||||||
| chr11:63668790 | CTT | C | 5 | a0001c0001t0008g0041 a0001c0001t0008g0042 a0001c0001t0008g0043 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2498_46+2499del others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668790 | |||||||
| chr11:63668902 | C | T | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.46+2388G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668902 | |||||||
| chr11:63668958 | A | G | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+2332T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668958 | |||||||
| chr11:63668999 | T | A | 1 | a0001c0001t0022g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46+2291A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63668999 | |||||||
| chr11:63669010 | T | TG | 7 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 others(4): Show |
7 | HG00642.hp1 HG02622.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+2279dupC | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669010 | |||||||
| chr11:63669011 | G | T | 7 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(4): Show |
7 | HG01109.hp1 HG01496.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+2279C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669011 | |||||||
| chr11:63669013 | GT | G | 5 | a0001c0001t0011g0038 a0001c0001t0011g0039 a0001c0001t0014g0008 others(2): Show |
6 | HG02717.hp1 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+2276delA | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669013 | |||||||
| chr11:63669014 | T | G | 22 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(19): Show |
23 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.46+2276A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669014 | |||||||
| chr11:63669014 | T | TG | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(31): Show |
40 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.46+2275dupC | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669014 | |||||||
| chr11:63669015 | G | T | 1 | a0003c0005t0009g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46+2275C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669015 | |||||||
| chr11:63669017 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.46+2273C>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669017 | |||||||
| chr11:63669024 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.46+2266G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669024 | |||||||
| chr11:63669033 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.46+2257T>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669033 | |||||||
| chr11:63669125 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46+2165A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669125 | |||||||
| chr11:63669127 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46+2163G>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669127 | |||||||
| chr11:63669491 | C | T | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+1799G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669491 | |||||||
| chr11:63669569 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.46+1721A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669569 | |||||||
| chr11:63669677 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+1613A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669677 | |||||||
| chr11:63669685 | G | C | 1 | a0001c0001t0004g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+1605C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669685 | |||||||
| chr11:63669924 | G | A | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.46+1366C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669924 | |||||||
| chr11:63669948 | C | CA | 10 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+1341dupT | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63669948 | |||||||
| chr11:63670159 | T | C | 3 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0023g0047 |
3 | HG03098.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.46+1131A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670159 | |||||||
| chr11:63670172 | T | G | 1 | a0001c0001t0027g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.46+1118A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670172 | |||||||
| chr11:63670204 | G | C | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0208 |
3 | HG01433.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.46+1086C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670204 | |||||||
| chr11:63670223 | T | C | 2 | a0001c0001t0009g0211 a0003c0005t0009g0210 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.46+1067A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670223 | |||||||
| chr11:63670315 | C | T | 14 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(11): Show |
15 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.46+975G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670315 | |||||||
| chr11:63670334 | T | G | 3 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0007g0032 |
3 | HG01109.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46+956A>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670334 | |||||||
| chr11:63670387 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46+903T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670387 | |||||||
| chr11:63670454 | T | C | 3 | a0001c0001t0009g0209 a0001c0001t0009g0211 a0003c0005t0009g0210 |
3 | HG02109.hp1 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.46+836A>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670454 | |||||||
| chr11:63670468 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.46+822G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670468 | |||||||
| chr11:63670746 | G | C | 1 | a0001c0001t0004g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+544C>G | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670746 | |||||||
| chr11:63670802 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
14 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.46+488T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670802 | |||||||
| chr11:63670827 | T | A | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01106.hp1 HG01192.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+463A>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670827 | |||||||
| chr11:63670885 | G | A | 7 | a0001c0001t0011g0035 a0001c0001t0011g0038 a0001c0001t0011g0039 others(4): Show |
7 | HG02622.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+405C>T | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63670885 | |||||||
| chr11:63671035 | A | G | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
29 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.46+255T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671035 | |||||||
| chr11:63671038 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46+252T>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671038 | |||||||
| chr11:63671074 | AAAGT | A | 4 | a0001c0001t0020g0048 a0001c0001t0021g0049 a0001c0001t0022g0046 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+212_46+215delAC others(2): Show |
ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671074 | |||||||
| chr11:63671130 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.46+160G>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671130 | |||||||
| chr11:63671132 | C | G | 1 | a0001c0001t0016g0051 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.46+158G>C | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671132 | |||||||
| chr11:63671259 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.46+31G>A | ATL3 | ENSG00000184743.13 | transcript | ENST00000398868.8 | protein_coding | 1/12 | chr11 | 63671259 |