Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11016 |
| ensemblid | ENSG00000170653.19 |
| hgncid | 792 |
| symbol | ATF7 |
| name | activating transcription factor 7 |
| refseq_nuc | NM_006856.3 |
| refseq_prot | NP_006847.1 |
| ensembl_nuc | ENST00000420353.7 |
| ensembl_prot | ENSP00000399465.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53512054 |
| end | 53626382 |
| strand | - |
| ver | v1.2 |
| region | chr12:53512054-53626382 |
| region5000 | chr12:53507054-53631382 |
| regionname0 | ATF7_chr12_53512054_53626382 |
| regionname5000 | ATF7_chr12_53507054_53631382 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 483 | 329 | 83 | 66 | 124 | 12 | 42 | 94 | ATF7_chr12_53507054_53631382 | ATF7 | MGDDR others(478): Show |
chr12 | 53507054 | 53631382 |
| a0002 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | MGDDR others(478): Show |
chr12 | 53507054 | 53631382 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1449 | 310 | 77 | 61 | 119 | 10 | 41 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 | ||
| a0001c0002 | 0/0 | 1449 | 11 | 0 | 5 | 4 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 | ||
| a0001c0003 | 0/0 | 1449 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 | ||
| a0001c0005 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 | ||
| a0001c0006 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 | ||
| a0002c0004 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | ATGGG others(1444): Show |
chr12 | 53507054 | 53631382 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6660 | 211 | 66 | 46 | 66 | 8 | 23 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0002 | 0/0 | 6660 | 36 | 0 | 4 | 22 | 1 | 9 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0003 | 0/0 | 6660 | 14 | 7 | 0 | 5 | 0 | 2 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0004 | 0/0 | 6660 | 10 | 0 | 0 | 10 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0006 | 0/0 | 6660 | 5 | 0 | 0 | 5 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0007 | 0/0 | 6660 | 5 | 0 | 4 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0009 | 0/0 | 6660 | 4 | 0 | 3 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0010 | 0/0 | 6660 | 3 | 1 | 2 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0011 | 0/0 | 6660 | 2 | 0 | 0 | 0 | 1 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0012 | 0/0 | 6660 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0013 | 0/0 | 6660 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0014 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0015 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0016 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0017 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0018 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0019 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0020 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0021 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0022 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0023 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0024 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0025 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0026 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0027 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0028 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0001t0029 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0002t0001 | 0/0 | 6660 | 4 | 0 | 0 | 4 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0002t0003 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0002t0005 | 0/0 | 6660 | 6 | 0 | 4 | 0 | 2 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0003t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0003t0008 | 0/0 | 6660 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0003t0030 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0005t0001 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0001c0006t0001 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| a0002c0004t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | GGACG others(6655): Show |
chr12 | 53507054 | 53631382 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0012g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0012g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0013g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0014g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0018g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0019g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0020g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0021g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0022g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0023g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0024g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0025g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0026g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0027g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0028g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0001t0029g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0003t0030g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0001c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| a0002c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0082 | EUR | GBR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0159 | EUR | FIN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00673 | hp2 | a0001 | c0001 | t0027 | g0194 | EAS | CHS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0166 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01070 | hp2 | a0001 | c0001 | t0025 | g0315 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01074 | hp2 | a0001 | c0001 | t0010 | g0076 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0075 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0171 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0172 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0189 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0137 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0100 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0042 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0181 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0235 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01934 | hp2 | a0001 | c0001 | t0023 | g0302 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0115 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02080 | hp1 | a0001 | c0006 | t0001 | g0083 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02135 | hp2 | a0001 | c0001 | t0013 | g0021 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0139 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | CDX | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0080 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02647 | hp2 | a0001 | c0001 | t0016 | g0308 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02735 | hp1 | a0001 | c0001 | t0024 | g0239 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03130 | hp2 | a0001 | c0003 | t0008 | g0228 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03195 | hp2 | a0001 | c0003 | t0030 | g0330 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0230 | AFR | GWD | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0104 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03710 | hp1 | a0001 | c0001 | t0019 | g0290 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0030 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04184 | hp1 | a0001 | c0001 | t0029 | g0236 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04199 | hp2 | a0001 | c0005 | t0001 | g0069 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0084 | SAS | STU | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0273 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18948 | hp1 | a0001 | c0001 | t0012 | g0254 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18962 | hp2 | a0001 | c0001 | t0012 | g0284 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18999 | hp1 | a0001 | c0001 | t0017 | g0174 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19002 | hp2 | a0001 | c0001 | t0022 | g0169 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19010 | hp2 | a0001 | c0001 | t0020 | g0316 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0032 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19062 | hp1 | a0001 | c0001 | t0026 | g0298 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19087 | hp1 | a0001 | c0001 | t0013 | g0020 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0227 | AFR | YRI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0182 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | GIH | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0078 | SAS | GIH | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02486 | hp1 | a0001 | c0001 | t0028 | g0224 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG02559 | hp2 | a0001 | c0003 | t0008 | g0225 | AFR | ACB | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0071 | AFR | USA | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0206 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0266 | REF | REF | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0039 | REF | REF | ATF7_chr12_53507054_53631382 | ATF7 | chr12 | 53507054 | 53631382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53537486 | G | T | 1 | a0002 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.331C>A | p.Pro111Thr | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/12 | 456/6660 | 331/1452 | 111/483 | chr12 | 53537486 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53524654 | T | C | 1 | a0001c0003 | 6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.1035A>G | p.Ala345Ala | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/12 | 1160/6660 | 1035/1452 | 345/483 | chr12 | 53524654 | |||
| chr12:53531789 | C | T | 1 | a0001c0005 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.882G>A | p.Gln294Gln | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/12 | 1007/6660 | 882/1452 | 294/483 | chr12 | 53531789 | |||
| chr12:53537538 | G | A | 1 | a0001c0006 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.279C>T | p.Pro93Pro | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/12 | 404/6660 | 279/1452 | 93/483 | chr12 | 53537538 | |||
| chr12:53552626 | G | A | 1 | a0001c0002 | 11 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(8): Show |
synonymous_variant | LOW | c.60C>T | p.Asn20Asn | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/12 | 185/6660 | 60/1452 | 20/483 | chr12 | 53552626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53512063 | C | T | 1 | a0001c0001t0020 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5074G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 5074 | chr12 | 53512063 | ||||||
| chr12:53512635 | T | C | 1 | a0001c0001t0009 | 4 | HG01261.hp2 HG01433.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4502A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4502 | chr12 | 53512635 | ||||||
| chr12:53512648 | A | G | 1 | a0001c0001t0009 | 4 | HG01261.hp2 HG01433.hp2 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4489T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4489 | chr12 | 53512648 | ||||||
| chr12:53512839 | A | C | 1 | a0001c0003t0008 | 4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4298T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 4298 | chr12 | 53512839 | ||||||
| chr12:53513226 | C | T | 1 | a0001c0001t0010 | 3 | HG01074.hp2 HG01081.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3911G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3911 | chr12 | 53513226 | ||||||
| chr12:53513283 | C | T | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0017 others(3): Show |
33 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3854G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3854 | chr12 | 53513283 | ||||||
| chr12:53513493 | G | A | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 |
43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3644C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3644 | chr12 | 53513493 | ||||||
| chr12:53513624 | A | G | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3513 | chr12 | 53513624 | ||||||
| chr12:53513707 | T | C | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3430A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3430 | chr12 | 53513707 | ||||||
| chr12:53513822 | C | T | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3315G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3315 | chr12 | 53513822 | ||||||
| chr12:53514041 | G | C | 2 | a0001c0001t0011 a0001c0001t0021 |
3 | HG00140.hp2 HG03688.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3096C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3096 | chr12 | 53514041 | ||||||
| chr12:53514130 | A | G | 1 | a0001c0001t0018 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3007T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 3007 | chr12 | 53514130 | ||||||
| chr12:53514215 | C | T | 1 | a0001c0001t0017 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2922G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2922 | chr12 | 53514215 | ||||||
| chr12:53514890 | T | C | 1 | a0001c0001t0022 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2247A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2247 | chr12 | 53514890 | ||||||
| chr12:53514968 | G | A | 1 | a0001c0001t0023 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2169C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2169 | chr12 | 53514968 | ||||||
| chr12:53515005 | G | A | 1 | a0001c0001t0006 | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2132C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2132 | chr12 | 53515005 | ||||||
| chr12:53515055 | C | T | 1 | a0001c0002t0005 | 6 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2082G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 2082 | chr12 | 53515055 | ||||||
| chr12:53515301 | A | G | 1 | a0001c0001t0007 | 5 | HG00621.hp2 HG01261.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1836T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1836 | chr12 | 53515301 | ||||||
| chr12:53515473 | C | T | 1 | a0001c0001t0006 | 5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1664 | chr12 | 53515473 | ||||||
| chr12:53515507 | A | G | 1 | a0001c0001t0016 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1630 | chr12 | 53515507 | ||||||
| chr12:53515635 | T | A | 1 | a0001c0001t0024 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1502A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1502 | chr12 | 53515635 | ||||||
| chr12:53515810 | C | T | 1 | a0001c0001t0015 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1327 | chr12 | 53515810 | ||||||
| chr12:53515981 | G | C | 1 | a0001c0001t0004 | 10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 1156 | chr12 | 53515981 | ||||||
| chr12:53516175 | G | A | 1 | a0001c0001t0025 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*962C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 962 | chr12 | 53516175 | ||||||
| chr12:53516227 | G | A | 1 | a0001c0001t0026 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 910 | chr12 | 53516227 | ||||||
| chr12:53516625 | A | C | 1 | a0001c0001t0014 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 512 | chr12 | 53516625 | ||||||
| chr12:53516657 | G | C | 1 | a0001c0001t0012 | 2 | NA18948.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*480C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 480 | chr12 | 53516657 | ||||||
| chr12:53516759 | G | A | 1 | a0001c0001t0027 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 378 | chr12 | 53516759 | ||||||
| chr12:53516935 | G | A | 1 | a0001c0001t0013 | 2 | HG02135.hp2 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*202C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 202 | chr12 | 53516935 | ||||||
| chr12:53516976 | C | A | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 161 | chr12 | 53516976 | ||||||
| chr12:53517097 | G | A | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 12/12 | 40 | chr12 | 53517097 | ||||||
| chr12:53626333 | T | C | 1 | a0001c0003t0030 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/12 | 25333 | chr12 | 53626333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53517480 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1235-126A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517480 | |||||||
| chr12:53517524 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1235-170G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517524 | |||||||
| chr12:53517761 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1235-407G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517761 | |||||||
| chr12:53517875 | T | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235-521A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517875 | |||||||
| chr12:53517974 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0001t0001g0200 |
3 | HG01358.hp1 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1235-620G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53517974 | |||||||
| chr12:53518028 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1235-674G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518028 | |||||||
| chr12:53518450 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1235-1096T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518450 | |||||||
| chr12:53518452 | T | C | 6 | a0001c0003t0001g0235 a0001c0003t0008g0225 a0001c0003t0008g0227 others(3): Show |
6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235-1098A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518452 | |||||||
| chr12:53518499 | C | G | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1145G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518499 | |||||||
| chr12:53518815 | C | G | 251 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(248): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1235-1461G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518815 | |||||||
| chr12:53518882 | C | CA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0057 a0001c0001t0001g0089 others(11): Show |
14 | HG00597.hp1 HG00621.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1235-1529dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518882 | |||||||
| chr12:53518958 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1235-1604C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53518958 | |||||||
| chr12:53519033 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1235-1679T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519033 | |||||||
| chr12:53519053 | C | CA | 8 | a0001c0001t0001g0064 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
8 | HG02145.hp1 HG03225.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-1700dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519053 | |||||||
| chr12:53519053 | CA | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1235-1700delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519053 | |||||||
| chr12:53519177 | G | T | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1235-1823C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519177 | |||||||
| chr12:53519246 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1235-1892C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519246 | |||||||
| chr12:53519443 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00738.hp2 HG01243.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1235-2089A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519443 | |||||||
| chr12:53519501 | A | G | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1235-2147T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519501 | |||||||
| chr12:53519563 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1235-2209C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519563 | |||||||
| chr12:53519642 | T | G | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1235-2288A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519642 | |||||||
| chr12:53519648 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0006g0141 a0001c0001t0006g0142 others(3): Show |
6 | HG01884.hp1 NA18947.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-2294A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519648 | |||||||
| chr12:53519950 | G | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1235-2596C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53519950 | |||||||
| chr12:53520161 | G | T | 1 | a0001c0001t0001g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1235-2807C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520161 | |||||||
| chr12:53520369 | G | A | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1234+2907C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520369 | |||||||
| chr12:53520527 | C | CA | 25 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0198 others(22): Show |
25 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1234+2748dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520527 | |||||||
| chr12:53520627 | A | T | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234+2649T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520627 | |||||||
| chr12:53520681 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+2595A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520681 | |||||||
| chr12:53520705 | T | G | 1 | a0001c0001t0022g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1234+2571A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520705 | |||||||
| chr12:53520765 | T | C | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1234+2511A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520765 | |||||||
| chr12:53520896 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234+2380G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520896 | |||||||
| chr12:53520993 | A | AT | 54 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(51): Show |
54 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1234+2282dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520993 | |||||||
| chr12:53520993 | AT | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234+2282delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53520993 | |||||||
| chr12:53521045 | C | T | 249 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(246): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1234+2231G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521045 | |||||||
| chr12:53521137 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+2139G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521137 | |||||||
| chr12:53521233 | A | C | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1234+2043T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521233 | |||||||
| chr12:53521234 | C | T | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1234+2042G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521234 | |||||||
| chr12:53521401 | G | A | 1 | a0001c0006t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1234+1875C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521401 | |||||||
| chr12:53521458 | G | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+1818C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521458 | |||||||
| chr12:53521681 | T | C | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1234+1595A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521681 | |||||||
| chr12:53521738 | C | G | 40 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1234+1538G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53521738 | |||||||
| chr12:53522052 | G | A | 24 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(21): Show |
24 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1234+1224C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522052 | |||||||
| chr12:53522170 | G | A | 2 | a0001c0001t0012g0254 a0001c0001t0012g0284 |
2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1234+1106C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522170 | |||||||
| chr12:53522449 | C | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+827G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522449 | |||||||
| chr12:53522503 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0129 |
2 | HG00423.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1234+773T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522503 | |||||||
| chr12:53522506 | C | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+770G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522506 | |||||||
| chr12:53522507 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0282 |
2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1234+769G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522507 | |||||||
| chr12:53522514 | G | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234+762C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522514 | |||||||
| chr12:53522677 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234+599G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522677 | |||||||
| chr12:53522695 | G | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0066 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1234+581C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522695 | |||||||
| chr12:53522846 | G | A | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1234+430C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522846 | |||||||
| chr12:53522931 | T | C | 23 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(20): Show |
23 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1234+345A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53522931 | |||||||
| chr12:53523019 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234+257A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523019 | |||||||
| chr12:53523100 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1234+176A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523100 | |||||||
| chr12:53523103 | C | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1234+173G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523103 | |||||||
| chr12:53523164 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1234+112G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 11/11 | chr12 | 53523164 | |||||||
| chr12:53523765 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1126-381T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53523765 | |||||||
| chr12:53524068 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1125+496A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524068 | |||||||
| chr12:53524162 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1125+402T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524162 | |||||||
| chr12:53524338 | G | A | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1125+226C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 10/11 | chr12 | 53524338 | |||||||
| chr12:53524865 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-104G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53524865 | |||||||
| chr12:53525065 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.928-304C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525065 | |||||||
| chr12:53525244 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-483A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525244 | |||||||
| chr12:53525310 | G | GC | 3 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0158 |
3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.928-550dupG | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525310 | |||||||
| chr12:53525424 | A | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-663T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525424 | |||||||
| chr12:53525554 | G | C | 1 | a0001c0001t0010g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.928-793C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525554 | |||||||
| chr12:53525852 | A | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1091T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525852 | |||||||
| chr12:53525916 | A | C | 52 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(49): Show |
52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.928-1155T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53525916 | |||||||
| chr12:53526107 | G | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1346C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526107 | |||||||
| chr12:53526163 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-1402C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526163 | |||||||
| chr12:53526174 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.928-1413G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526174 | |||||||
| chr12:53526203 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.928-1442C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526203 | |||||||
| chr12:53526208 | C | CA | 59 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0031 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.928-1448dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526208 | |||||||
| chr12:53526208 | CA | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0155 others(46): Show |
49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.928-1448delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526208 | |||||||
| chr12:53526249 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.928-1488G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526249 | |||||||
| chr12:53526296 | CT | C | 40 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.928-1536delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526296 | |||||||
| chr12:53526315 | CCCTCCTC others(2): Show |
C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-1563_928-1555d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526315 | |||||||
| chr12:53526416 | CTCTT | C | 6 | a0001c0003t0001g0235 a0001c0003t0008g0225 a0001c0003t0008g0227 others(3): Show |
6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-1659_928-1656d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526416 | |||||||
| chr12:53526424 | TATG | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0094 others(1): Show |
4 | HG01943.hp1 HG02683.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-1666_928-1664d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526424 | |||||||
| chr12:53526614 | G | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-1853C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526614 | |||||||
| chr12:53526632 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1871G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526632 | |||||||
| chr12:53526680 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.928-1919C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526680 | |||||||
| chr12:53526741 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.928-1980G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526741 | |||||||
| chr12:53526966 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.928-2205G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53526966 | |||||||
| chr12:53527107 | C | T | 53 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0034 others(50): Show |
53 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.928-2346G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527107 | |||||||
| chr12:53527146 | G | A | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00408.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.928-2385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527146 | |||||||
| chr12:53527405 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.928-2644G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527405 | |||||||
| chr12:53527587 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-2826A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527587 | |||||||
| chr12:53527986 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.928-3225G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53527986 | |||||||
| chr12:53528032 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928-3271T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528032 | |||||||
| chr12:53528042 | C | T | 6 | a0001c0001t0001g0303 a0001c0001t0006g0141 a0001c0001t0006g0142 others(3): Show |
6 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-3281G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528042 | |||||||
| chr12:53528064 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.928-3303T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528064 | |||||||
| chr12:53528071 | A | G | 256 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.928-3310T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528071 | |||||||
| chr12:53528076 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-3315A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528076 | |||||||
| chr12:53528092 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-3331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528092 | |||||||
| chr12:53528399 | G | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(49): Show |
52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.927+3345C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528399 | |||||||
| chr12:53528501 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+3243C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528501 | |||||||
| chr12:53528529 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.927+3215C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528529 | |||||||
| chr12:53528559 | T | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.927+3185A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528559 | |||||||
| chr12:53528619 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.927+3125A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528619 | |||||||
| chr12:53528749 | C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+2995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528749 | |||||||
| chr12:53528803 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.927+2941T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53528803 | |||||||
| chr12:53529060 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927+2684G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529060 | |||||||
| chr12:53529095 | A | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.927+2649T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529095 | |||||||
| chr12:53529279 | A | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.927+2465T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529279 | |||||||
| chr12:53529302 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.927+2442G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529302 | |||||||
| chr12:53529313 | C | A | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.927+2431G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529313 | |||||||
| chr12:53529619 | C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+2125G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529619 | |||||||
| chr12:53529654 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.927+2090A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529654 | |||||||
| chr12:53529664 | CAT | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2078_927+2079d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529664 | |||||||
| chr12:53529664 | CATATATA others(13): Show |
C | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+2060_927+2079d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529664 | |||||||
| chr12:53529694 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2050G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529694 | |||||||
| chr12:53529694 | CAT | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
13 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2048_927+2049d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529694 | |||||||
| chr12:53529700 | T | TACAC | 4 | a0001c0001t0006g0141 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+2043_927+2044i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529700 | |||||||
| chr12:53529700 | T | TACACATA others(11): Show |
1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.927+2043_927+2044i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529700 | |||||||
| chr12:53529702 | T | C | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.927+2042A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529702 | |||||||
| chr12:53529702 | T | TACAC | 5 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+2041_927+2042i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529702 | |||||||
| chr12:53529704 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2040A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529704 | |||||||
| chr12:53529704 | T | TATACACA others(11): Show |
1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.927+2039_927+2040i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529704 | |||||||
| chr12:53529710 | T | C | 13 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2034A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TAC | 7 | a0001c0001t0010g0071 a0001c0001t0010g0075 a0001c0001t0010g0076 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2032_927+2033d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(3): Show |
15 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0252 others(12): Show |
15 | HG00140.hp1 HG00738.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.927+2024_927+2033d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(5): Show |
43 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0167 others(40): Show |
43 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.927+2022_927+2033d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(7): Show |
63 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0057 others(60): Show |
63 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.927+2020_927+2033d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(9): Show |
49 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0197 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.927+2018_927+2033d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(11): Show |
9 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG00639.hp1 HG01934.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+2016_927+2033d others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(13): Show |
2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.927+2014_927+2033d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+2012_927+2033d others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TATACACA others(5): Show |
1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+2033_927+2034i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TATACACA others(7): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TATACACA others(9): Show |
20 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(17): Show |
20 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TATACACA others(11): Show |
13 | a0001c0001t0002g0040 a0001c0001t0002g0118 a0001c0001t0002g0121 others(10): Show |
13 | HG00423.hp2 HG00609.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2033_927+2034i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529710 | T | TATACACA others(13): Show |
2 | a0001c0001t0002g0122 a0001c0001t0002g0153 |
2 | HG03942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.927+2033_927+2034i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529710 | |||||||
| chr12:53529734 | C | CACACACA others(25): Show |
1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(23): Show |
1 | a0001c0001t0001g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(19): Show |
1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(21): Show |
5 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2009_927+2010i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(19): Show |
5 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0053 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+2009_927+2010i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(15): Show |
1 | a0001c0001t0001g0198 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.927+2009_927+2010i others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(13): Show |
1 | a0001c0001t0001g0213 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.927+2009_927+2010i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(11): Show |
2 | a0001c0001t0001g0047 a0001c0001t0014g0030 |
2 | HG02647.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(7): Show |
3 | a0001c0001t0006g0141 a0001c0001t0006g0143 a0001c0001t0006g0144 |
3 | NA18947.hp1 NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(9): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.927+2009_927+2010i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529734 | C | CACACACA others(5): Show |
1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+2009_927+2010i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529734 | |||||||
| chr12:53529736 | T | C | 102 | a0001c0001t0001g0038 a0001c0001t0001g0057 a0001c0001t0001g0167 others(99): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.927+2008A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529736 | |||||||
| chr12:53529738 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0018g0273 |
2 | HG02723.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.927+2006A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529738 | |||||||
| chr12:53529857 | C | T | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.927+1887G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529857 | |||||||
| chr12:53529912 | T | A | 171 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(168): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.927+1832A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529912 | |||||||
| chr12:53529982 | T | C | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.927+1762A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53529982 | |||||||
| chr12:53530383 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.927+1361A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530383 | |||||||
| chr12:53530404 | G | A | 1 | a0001c0001t0007g0114 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.927+1340C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530404 | |||||||
| chr12:53530426 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.927+1318A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530426 | |||||||
| chr12:53530509 | T | C | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.927+1235A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530509 | |||||||
| chr12:53530567 | T | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.927+1177A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530567 | |||||||
| chr12:53530568 | A | AT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1175dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530568 | |||||||
| chr12:53530575 | T | A | 39 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(36): Show |
39 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.927+1169A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53530575 | |||||||
| chr12:53531079 | G | C | 40 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.927+665C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531079 | |||||||
| chr12:53531156 | C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+588G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531156 | |||||||
| chr12:53531157 | A | G | 69 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(66): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.927+587T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531157 | |||||||
| chr12:53531175 | T | C | 69 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(66): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.927+569A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531175 | |||||||
| chr12:53531208 | G | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.927+536C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531208 | |||||||
| chr12:53531422 | C | CA | 17 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0150 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.927+321dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531422 | |||||||
| chr12:53531447 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.927+297G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531447 | |||||||
| chr12:53531461 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+283A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531461 | |||||||
| chr12:53531574 | A | G | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.927+170T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531574 | |||||||
| chr12:53531587 | G | A | 40 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.927+157C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 9/11 | chr12 | 53531587 | |||||||
| chr12:53531973 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.775-77T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53531973 | |||||||
| chr12:53532124 | G | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-228C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532124 | |||||||
| chr12:53532468 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.774+42A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532468 | |||||||
| chr12:53532478 | G | A | 85 | a0001c0001t0001g0057 a0001c0001t0001g0183 a0001c0001t0001g0237 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.774+32C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 8/11 | chr12 | 53532478 | |||||||
| chr12:53532639 | GA | G | 76 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0033 others(73): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.661-17delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532639 | |||||||
| chr12:53532705 | G | A | 19 | a0001c0001t0001g0195 a0001c0001t0001g0199 a0001c0001t0001g0200 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.661-82C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532705 | |||||||
| chr12:53532842 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.661-219C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532842 | |||||||
| chr12:53532872 | T | A | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.661-249A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532872 | |||||||
| chr12:53532990 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0157 |
3 | HG02145.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.660+170A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53532990 | |||||||
| chr12:53533066 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+94A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53533066 | |||||||
| chr12:53533105 | G | A | 40 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.660+55C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 7/11 | chr12 | 53533105 | |||||||
| chr12:53533419 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.561-160T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533419 | |||||||
| chr12:53533770 | C | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(49): Show |
52 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.561-511G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533770 | |||||||
| chr12:53533896 | C | T | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.560+606G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533896 | |||||||
| chr12:53533922 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.560+580T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533922 | |||||||
| chr12:53533977 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0003g0165 |
3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.560+525A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533977 | |||||||
| chr12:53533999 | T | C | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.560+503A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53533999 | |||||||
| chr12:53534080 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+422C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534080 | |||||||
| chr12:53534342 | TAAA | T | 14 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0262 others(11): Show |
14 | HG00140.hp1 HG00738.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.560+157_560+159del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534342 | |||||||
| chr12:53534360 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.560+142A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 6/11 | chr12 | 53534360 | |||||||
| chr12:53535008 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403-349G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535008 | |||||||
| chr12:53535149 | T | C | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-490A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535149 | |||||||
| chr12:53535328 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0098 a0001c0001t0014g0030 |
2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.403-679_403-670dup others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(4): Show |
15 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.403-680_403-670dup others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.403-681_403-670dup others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0015g0032 |
3 | HG02572.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-684_403-670dup others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(3): Show |
6 | HG02145.hp2 HG02523.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-685_403-670dup others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(10): Show |
19 | a0001c0001t0002g0001 a0001c0001t0002g0040 a0001c0001t0002g0111 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.403-686_403-670dup others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0002g0116 a0001c0001t0002g0119 a0001c0001t0002g0121 others(7): Show |
10 | HG02056.hp2 HG02300.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(12): Show |
10 | a0001c0001t0002g0024 a0001c0001t0002g0113 a0001c0001t0002g0117 others(7): Show |
10 | HG00423.hp2 HG00621.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.403-670_403-669ins others(20): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | NA18941.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.403-670_403-669ins others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(16): Show |
4 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(1): Show |
4 | NA18947.hp1 NA18984.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-670_403-669ins others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535328 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.403-670_403-669ins others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535328 | |||||||
| chr12:53535533 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403-874A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535533 | |||||||
| chr12:53535576 | G | A | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.403-917C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535576 | |||||||
| chr12:53535599 | G | T | 70 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(67): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.403-940C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535599 | |||||||
| chr12:53535652 | G | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.403-993C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535652 | |||||||
| chr12:53535684 | C | G | 1 | a0001c0001t0002g0154 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.403-1025G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535684 | |||||||
| chr12:53535758 | C | T | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.403-1099G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535758 | |||||||
| chr12:53535881 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.403-1222G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535881 | |||||||
| chr12:53535882 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.403-1223C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535882 | |||||||
| chr12:53535888 | C | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0009g0042 others(3): Show |
6 | HG01261.hp2 HG01433.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-1229G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53535888 | |||||||
| chr12:53536033 | A | C | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.403-1374T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536033 | |||||||
| chr12:53536226 | T | C | 6 | a0001c0003t0001g0235 a0001c0003t0008g0225 a0001c0003t0008g0227 others(3): Show |
6 | HG01891.hp2 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+1189A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536226 | |||||||
| chr12:53536299 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.402+1116G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536299 | |||||||
| chr12:53536315 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.402+1100G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536315 | |||||||
| chr12:53536316 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.402+1099C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536316 | |||||||
| chr12:53536615 | C | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.402+800G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536615 | |||||||
| chr12:53536616 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+799C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536616 | |||||||
| chr12:53536758 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.402+657G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53536758 | |||||||
| chr12:53537161 | T | C | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.402+254A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537161 | |||||||
| chr12:53537223 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.402+192G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537223 | |||||||
| chr12:53537263 | TTCTCCAT others(1): Show |
T | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.402+144_402+151del others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537263 | |||||||
| chr12:53537274 | GCCC | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.402+138_402+140del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 5/11 | chr12 | 53537274 | |||||||
| chr12:53537725 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265-173T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537725 | |||||||
| chr12:53537844 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.265-292G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537844 | |||||||
| chr12:53537991 | A | C | 70 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(67): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.265-439T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53537991 | |||||||
| chr12:53538149 | A | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.265-597T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538149 | |||||||
| chr12:53538241 | G | A | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-689C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538241 | |||||||
| chr12:53538535 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.265-983A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538535 | |||||||
| chr12:53538912 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0201 a0001c0001t0001g0202 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-1360A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538912 | |||||||
| chr12:53538972 | C | A | 5 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0153 others(2): Show |
5 | HG02698.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-1420G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53538972 | |||||||
| chr12:53539050 | A | G | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.265-1498T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539050 | |||||||
| chr12:53539229 | G | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.265-1677C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539229 | |||||||
| chr12:53539282 | A | G | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.265-1730T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539282 | |||||||
| chr12:53539561 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-2009G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539561 | |||||||
| chr12:53539686 | C | CAATG | 11 | a0001c0001t0001g0036 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
11 | HG01433.hp1 HG02135.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-2138_265-2135d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | |||||||
| chr12:53539686 | CAATG | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(6): Show |
9 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-2138_265-2135d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | |||||||
| chr12:53539686 | CAATGAAT others(5): Show |
C | 20 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.265-2146_265-2135d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | |||||||
| chr12:53539686 | CAATGAAT others(9): Show |
C | 177 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.265-2150_265-2135d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | |||||||
| chr12:53539686 | CAATGAAT others(17): Show |
C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.265-2158_265-2135d others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539686 | |||||||
| chr12:53539792 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.265-2240C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539792 | |||||||
| chr12:53539969 | C | G | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.265-2417G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539969 | |||||||
| chr12:53539976 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.265-2424C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53539976 | |||||||
| chr12:53540014 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-2462G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540014 | |||||||
| chr12:53540291 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2739G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540291 | |||||||
| chr12:53540348 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-2796C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540348 | |||||||
| chr12:53540352 | C | CA | 58 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(55): Show |
58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.265-2801dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540352 | |||||||
| chr12:53540352 | CA | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0170 others(5): Show |
8 | HG01099.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-2801delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540352 | |||||||
| chr12:53540590 | G | A | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.264+2740C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540590 | |||||||
| chr12:53540775 | G | C | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18941.hp1 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.264+2555C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53540775 | |||||||
| chr12:53541156 | A | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.264+2174T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541156 | |||||||
| chr12:53541257 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+2073C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541257 | |||||||
| chr12:53541311 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.264+2019A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541311 | |||||||
| chr12:53541516 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.264+1814G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541516 | |||||||
| chr12:53541537 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+1793C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541537 | |||||||
| chr12:53541730 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.264+1600G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541730 | |||||||
| chr12:53541744 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.264+1586C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541744 | |||||||
| chr12:53541859 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.264+1471A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53541859 | |||||||
| chr12:53542019 | G | A | 194 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.264+1311C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542019 | |||||||
| chr12:53542107 | G | GT | 7 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0090 others(4): Show |
7 | HG00741.hp2 HG01361.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+1222dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(1): Show |
13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
13 | HG01099.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.264+1215_264+1222d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(2): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0050 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+1214_264+1222d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0207 a0001c0003t0008g0227 a0001c0003t0008g0228 others(2): Show |
5 | HG01243.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1213_264+1222d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(4): Show |
95 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0193 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.264+1212_264+1222d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(5): Show |
29 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0195 others(26): Show |
29 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.264+1211_264+1222d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(6): Show |
4 | a0001c0001t0001g0251 a0001c0001t0001g0265 a0001c0001t0001g0283 others(1): Show |
4 | HG01192.hp1 HG01358.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+1210_264+1222d others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.264+1209_264+1222d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.264+1208_264+1222d others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0233 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.264+1207_264+1222d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542107 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0234 |
2 | HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.264+1206_264+1222d others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542107 | |||||||
| chr12:53542151 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0213 |
2 | NA18998.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.264+1179G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542151 | |||||||
| chr12:53542319 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(21): Show |
24 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.264+1011G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542319 | |||||||
| chr12:53542342 | G | A | 48 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.264+988C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542342 | |||||||
| chr12:53542391 | C | T | 246 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.264+939G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542391 | |||||||
| chr12:53542427 | C | CA | 12 | a0001c0001t0001g0249 a0001c0001t0001g0295 a0001c0001t0001g0297 others(9): Show |
12 | HG00140.hp1 HG00621.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.264+902dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542427 | |||||||
| chr12:53542461 | C | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.264+869G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542461 | |||||||
| chr12:53542495 | T | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.264+835A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542495 | |||||||
| chr12:53542754 | A | G | 10 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(7): Show |
10 | HG00423.hp1 HG02135.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+576T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53542754 | |||||||
| chr12:53543050 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.264+280A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543050 | |||||||
| chr12:53543055 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.264+275T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543055 | |||||||
| chr12:53543084 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0094 others(1): Show |
4 | HG01943.hp1 HG02683.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+246A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543084 | |||||||
| chr12:53543094 | G | T | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.264+236C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543094 | |||||||
| chr12:53543261 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.264+69G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543261 | |||||||
| chr12:53543323 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.264+7A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 4/11 | chr12 | 53543323 | |||||||
| chr12:53543668 | C | T | 258 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(255): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.146-220G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53543668 | |||||||
| chr12:53543835 | T | C | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-387A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53543835 | |||||||
| chr12:53544106 | C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-658G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544106 | |||||||
| chr12:53544163 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146-715G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544163 | |||||||
| chr12:53544692 | A | G | 310 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.146-1244T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544692 | |||||||
| chr12:53544694 | G | A | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.146-1246C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544694 | |||||||
| chr12:53544771 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.146-1323T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544771 | |||||||
| chr12:53544906 | CA | C | 255 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.146-1459delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544906 | |||||||
| chr12:53544979 | A | G | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-1531T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53544979 | |||||||
| chr12:53545024 | T | C | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-1576A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545024 | |||||||
| chr12:53545048 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146-1600A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545048 | |||||||
| chr12:53545129 | G | A | 255 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.146-1681C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545129 | |||||||
| chr12:53545235 | G | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0003g0165 |
3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.146-1787C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545235 | |||||||
| chr12:53545329 | T | A | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.146-1881A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545329 | |||||||
| chr12:53545432 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-1984C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545432 | |||||||
| chr12:53545481 | C | T | 1 | a0001c0001t0003g0173 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.146-2033G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545481 | |||||||
| chr12:53545485 | C | T | 39 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.146-2037G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545485 | |||||||
| chr12:53545499 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-2051C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545499 | |||||||
| chr12:53545505 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0003g0165 |
3 | NA18954.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.146-2057A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545505 | |||||||
| chr12:53545673 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.146-2225A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545673 | |||||||
| chr12:53545754 | G | A | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0153 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2306C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545754 | |||||||
| chr12:53545829 | C | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-2381G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545829 | |||||||
| chr12:53545920 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.146-2472G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53545920 | |||||||
| chr12:53546060 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0090 |
3 | HG03704.hp1 HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.146-2612G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546060 | |||||||
| chr12:53546065 | G | A | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.146-2617C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546065 | |||||||
| chr12:53546101 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.146-2653G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546101 | |||||||
| chr12:53546196 | A | AAAAC | 4 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0056 others(1): Show |
4 | HG00609.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2752_146-2749d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | |||||||
| chr12:53546196 | A | AAAACAAA others(1): Show |
16 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(13): Show |
16 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-2756_146-2749d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | |||||||
| chr12:53546196 | A | C | 3 | a0001c0001t0001g0198 a0001c0001t0003g0027 a0001c0001t0003g0028 |
3 | HG02922.hp2 HG03130.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.146-2748T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546196 | |||||||
| chr12:53546262 | T | C | 255 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.146-2814A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546262 | |||||||
| chr12:53546313 | T | C | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-2865A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546313 | |||||||
| chr12:53546375 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0004g0188 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.146-2928_146-2927i others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546375 | |||||||
| chr12:53546375 | A | AAAAAAAC others(7): Show |
193 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.146-2941_146-2928d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546375 | |||||||
| chr12:53546383 | A | AAAAAACA others(7): Show |
3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-2936_146-2935i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546383 | |||||||
| chr12:53546456 | CT | C | 6 | a0001c0001t0001g0063 a0001c0001t0006g0141 a0001c0001t0006g0142 others(3): Show |
6 | HG01515.hp2 NA18947.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-3009delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546456 | |||||||
| chr12:53546460 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3012A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546460 | |||||||
| chr12:53546463 | T | C | 4 | a0001c0002t0001g0324 a0001c0002t0001g0325 a0001c0002t0001g0326 others(1): Show |
4 | NA18962.hp1 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3015A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546463 | |||||||
| chr12:53546473 | C | CAG | 255 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.146-3027_146-3026d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546473 | |||||||
| chr12:53546558 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146-3110G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546558 | |||||||
| chr12:53546633 | A | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.146-3185T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546633 | |||||||
| chr12:53546692 | T | C | 313 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(310): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.146-3244A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546692 | |||||||
| chr12:53546694 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146-3246G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546694 | |||||||
| chr12:53546732 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3284C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546732 | |||||||
| chr12:53546747 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3299C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546747 | |||||||
| chr12:53546820 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146-3372G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546820 | |||||||
| chr12:53546872 | C | G | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3424G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546872 | |||||||
| chr12:53546977 | C | CT | 17 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0167 others(14): Show |
17 | HG00738.hp2 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-3530dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546977 | |||||||
| chr12:53546977 | CTTTTTTT others(4): Show |
C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.146-3540_146-3530d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546977 | |||||||
| chr12:53546998 | T | C | 12 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-3550A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53546998 | |||||||
| chr12:53547078 | G | A | 15 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0262 others(12): Show |
15 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.146-3630C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547078 | |||||||
| chr12:53547132 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.146-3684G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547132 | |||||||
| chr12:53547133 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.146-3685G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547133 | |||||||
| chr12:53547283 | C | CT | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.146-3836dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | |||||||
| chr12:53547283 | C | CTT | 21 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0241 others(18): Show |
21 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-3837_146-3836d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | |||||||
| chr12:53547283 | C | CTTT | 9 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(6): Show |
9 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-3838_146-3836d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | |||||||
| chr12:53547283 | C | CTTTT | 7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3839_146-3836d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | |||||||
| chr12:53547283 | CT | C | 49 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0041 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.146-3836delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547283 | |||||||
| chr12:53547475 | A | G | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146-4027T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547475 | |||||||
| chr12:53547644 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.146-4196G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547644 | |||||||
| chr12:53547747 | T | TTATG | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0061 others(15): Show |
18 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.146-4303_146-4300d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | |||||||
| chr12:53547747 | TTATG | T | 67 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0079 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.146-4303_146-4300d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | |||||||
| chr12:53547747 | TTATGTAT others(1): Show |
T | 24 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(21): Show |
24 | HG01099.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.146-4307_146-4300d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | |||||||
| chr12:53547747 | TTATGTAT others(5): Show |
T | 127 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(124): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.146-4311_146-4300d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | |||||||
| chr12:53547747 | TTATGTAT others(9): Show |
T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0102 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.146-4315_146-4300d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547747 | |||||||
| chr12:53547752 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.146-4304A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547752 | |||||||
| chr12:53547910 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-4462C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53547910 | |||||||
| chr12:53548037 | AT | A | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.145+4503delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548037 | |||||||
| chr12:53548191 | G | A | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+4350C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548191 | |||||||
| chr12:53548535 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0052 |
3 | HG01109.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.145+4006C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548535 | |||||||
| chr12:53548611 | G | A | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.145+3930C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548611 | |||||||
| chr12:53548773 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.145+3768T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548773 | |||||||
| chr12:53548878 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.145+3663C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53548878 | |||||||
| chr12:53549005 | G | A | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.145+3536C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549005 | |||||||
| chr12:53549008 | C | T | 1 | a0001c0001t0021g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.145+3533G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549008 | |||||||
| chr12:53549153 | G | A | 3 | a0001c0001t0011g0082 a0001c0001t0011g0084 a0001c0001t0021g0104 |
3 | HG00140.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.145+3388C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549153 | |||||||
| chr12:53549187 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.145+3354A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549187 | |||||||
| chr12:53549273 | C | T | 59 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.145+3268G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549273 | |||||||
| chr12:53549282 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.145+3259C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549282 | |||||||
| chr12:53549297 | AAG | A | 189 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.145+3242_145+3243d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549297 | |||||||
| chr12:53549298 | AG | A | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+3242delC | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549298 | |||||||
| chr12:53549490 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.145+3051C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549490 | |||||||
| chr12:53549575 | G | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+2966C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549575 | |||||||
| chr12:53549723 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG02622.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.145+2818G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549723 | |||||||
| chr12:53549879 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.145+2662G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549879 | |||||||
| chr12:53549880 | G | A | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.145+2661C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549880 | |||||||
| chr12:53549998 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.145+2543C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53549998 | |||||||
| chr12:53550061 | G | A | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.145+2480C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550061 | |||||||
| chr12:53550076 | A | G | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+2465T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550076 | |||||||
| chr12:53550093 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.145+2448G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550093 | |||||||
| chr12:53550094 | A | G | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145+2447T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550094 | |||||||
| chr12:53550151 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0014g0030 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.145+2390G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550151 | |||||||
| chr12:53550184 | G | A | 1 | a0001c0001t0009g0080 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.145+2357C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550184 | |||||||
| chr12:53550244 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.145+2297T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550244 | |||||||
| chr12:53550323 | C | CA | 9 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0002t0003g0189 others(6): Show |
9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+2217dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550323 | |||||||
| chr12:53550323 | CAAAA | C | 70 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.145+2214_145+2217d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550323 | |||||||
| chr12:53550327 | A | AAAAT | 31 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0058 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.145+2213_145+2214i others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | |||||||
| chr12:53550327 | A | AAAATAAA others(1): Show |
11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0070 others(8): Show |
11 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.145+2213_145+2214i others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | |||||||
| chr12:53550327 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.145+2202_145+2213d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | |||||||
| chr12:53550327 | AAAAAAAA others(9): Show |
A | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145+2198_145+2213d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550327 | |||||||
| chr12:53550331 | A | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0034 others(62): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.145+2210T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550331 | |||||||
| chr12:53550331 | AAAAT | A | 78 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(75): Show |
78 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.145+2206_145+2209d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550331 | |||||||
| chr12:53550334 | AT | A | 42 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.145+2206delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550334 | |||||||
| chr12:53550335 | T | A | 42 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0106 others(39): Show |
42 | HG00280.hp2 HG00408.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.145+2206A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550335 | |||||||
| chr12:53550337 | A | T | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.145+2204T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550337 | |||||||
| chr12:53550339 | T | A | 56 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0179 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.145+2202A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550339 | |||||||
| chr12:53550343 | T | A | 18 | a0001c0001t0001g0170 a0001c0001t0001g0183 a0001c0001t0001g0191 others(15): Show |
18 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+2198A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550343 | |||||||
| chr12:53550347 | T | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0003g0178 |
3 | HG01993.hp1 HG02886.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.145+2194A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550347 | |||||||
| chr12:53550465 | T | A | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+2076A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550465 | |||||||
| chr12:53550569 | G | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+1972C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53550569 | |||||||
| chr12:53551646 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.145+895T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551646 | |||||||
| chr12:53551761 | A | G | 180 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.145+780T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551761 | |||||||
| chr12:53551969 | C | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0134 |
3 | HG00408.hp1 NA18955.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.145+572G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53551969 | |||||||
| chr12:53552020 | C | T | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.145+521G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552020 | |||||||
| chr12:53552088 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0157 |
3 | HG02145.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.145+453T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552088 | |||||||
| chr12:53552107 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.145+434G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552107 | |||||||
| chr12:53552140 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.145+401A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552140 | |||||||
| chr12:53552148 | A | G | 1 | a0001c0006t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.145+393T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552148 | |||||||
| chr12:53552262 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.145+279T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552262 | |||||||
| chr12:53552270 | A | G | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.145+271T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552270 | |||||||
| chr12:53552302 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.145+239G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552302 | |||||||
| chr12:53552435 | C | G | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.145+106G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 3/11 | chr12 | 53552435 | |||||||
| chr12:53552811 | C | G | 178 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.49-174G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53552811 | |||||||
| chr12:53552992 | A | G | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-355T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53552992 | |||||||
| chr12:53553022 | T | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-385A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553022 | |||||||
| chr12:53553205 | T | C | 1 | a0001c0003t0001g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-568A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553205 | |||||||
| chr12:53553278 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-641A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553278 | |||||||
| chr12:53553388 | G | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-751C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553388 | |||||||
| chr12:53553456 | T | G | 1 | a0001c0001t0002g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.49-819A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553456 | |||||||
| chr12:53553843 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49-1206G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53553843 | |||||||
| chr12:53554013 | G | A | 1 | a0001c0001t0026g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49-1376C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554013 | |||||||
| chr12:53554127 | TTTTA | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-1494_49-1491del others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554127 | |||||||
| chr12:53554331 | A | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-1694T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554331 | |||||||
| chr12:53554384 | G | A | 3 | a0001c0001t0001g0300 a0001c0001t0001g0317 a0001c0001t0020g0316 |
3 | HG00544.hp1 HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-1747C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554384 | |||||||
| chr12:53554634 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-1997C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554634 | |||||||
| chr12:53554660 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.49-2023G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554660 | |||||||
| chr12:53554770 | C | A | 23 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0199 others(20): Show |
23 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.49-2133G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554770 | |||||||
| chr12:53554870 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0027g0194 |
2 | HG00673.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.49-2233C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | |||||||
| chr12:53554870 | G | GA | 18 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(15): Show |
18 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-2234dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | |||||||
| chr12:53554870 | G | GAA | 192 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(189): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.49-2235_49-2234dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | |||||||
| chr12:53554870 | G | GAAA | 20 | a0001c0001t0001g0049 a0001c0001t0001g0102 a0001c0001t0001g0149 others(17): Show |
20 | HG00140.hp1 HG00544.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.49-2236_49-2234dup others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | |||||||
| chr12:53554870 | G | GAAAA | 17 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-2237_49-2234dup others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53554870 | |||||||
| chr12:53555002 | A | G | 15 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0262 others(12): Show |
15 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.49-2365T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555002 | |||||||
| chr12:53555078 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.49-2441C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555078 | |||||||
| chr12:53555101 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49-2464G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555101 | |||||||
| chr12:53555176 | G | A | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-2539C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555176 | |||||||
| chr12:53555325 | C | CA | 50 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(47): Show |
50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-2689dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555325 | |||||||
| chr12:53555398 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0158 |
3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-2761C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555398 | |||||||
| chr12:53555437 | A | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-2800T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555437 | |||||||
| chr12:53555490 | A | AT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(30): Show |
33 | HG00544.hp2 HG00621.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-2854dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | AT | A | 14 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-2854delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTT | A | 41 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0158 others(38): Show |
41 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.49-2856_49-2854del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTTT | A | 110 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0038 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.49-2857_49-2854del others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTTTT | A | 26 | a0001c0001t0001g0167 a0001c0001t0001g0183 a0001c0001t0001g0191 others(23): Show |
26 | HG02165.hp1 HG02258.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.49-2858_49-2854del others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49-2863_49-2854del others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-2864_49-2854del others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555490 | ATTTTTTT others(5): Show |
A | 25 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0058 others(22): Show |
25 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.49-2865_49-2854del others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555490 | |||||||
| chr12:53555534 | G | A | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-2897C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555534 | |||||||
| chr12:53555671 | C | T | 178 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.49-3034G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555671 | |||||||
| chr12:53555737 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49-3100G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555737 | |||||||
| chr12:53555753 | G | A | 1 | a0001c0005t0001g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49-3116C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53555753 | |||||||
| chr12:53556074 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0158 |
3 | HG02723.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-3437G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556074 | |||||||
| chr12:53556312 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49-3675C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556312 | |||||||
| chr12:53556479 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.49-3842A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556479 | |||||||
| chr12:53556524 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.49-3887C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556524 | |||||||
| chr12:53556593 | A | G | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-3956T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556593 | |||||||
| chr12:53556671 | C | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-4034G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556671 | |||||||
| chr12:53556784 | A | G | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-4147T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556784 | |||||||
| chr12:53556821 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0301 |
2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.49-4184G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556821 | |||||||
| chr12:53556965 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49-4328G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53556965 | |||||||
| chr12:53557092 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.49-4455G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557092 | |||||||
| chr12:53557184 | T | A | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-4547A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557184 | |||||||
| chr12:53557265 | G | T | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-4628C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557265 | |||||||
| chr12:53557462 | C | A | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-4825G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557462 | |||||||
| chr12:53557541 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49-4904G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557541 | |||||||
| chr12:53557632 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-4995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557632 | |||||||
| chr12:53557663 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.49-5026G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557663 | |||||||
| chr12:53557977 | T | C | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-5340A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53557977 | |||||||
| chr12:53558517 | A | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-5880T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558517 | |||||||
| chr12:53558629 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-5992G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558629 | |||||||
| chr12:53558757 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-6120C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558757 | |||||||
| chr12:53558940 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49-6303A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558940 | |||||||
| chr12:53558979 | G | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-6342C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53558979 | |||||||
| chr12:53559101 | G | A | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49-6464C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559101 | |||||||
| chr12:53559121 | TA | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0256 a0001c0001t0001g0295 others(4): Show |
7 | HG01168.hp2 HG02647.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-6485delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559121 | |||||||
| chr12:53559169 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-6532A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559169 | |||||||
| chr12:53559220 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-6583A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559220 | |||||||
| chr12:53559237 | C | CT | 180 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.49-6601dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559237 | |||||||
| chr12:53559548 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.49-6911C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559548 | |||||||
| chr12:53559556 | G | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-6919C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559556 | |||||||
| chr12:53559590 | A | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-6953T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559590 | |||||||
| chr12:53559656 | G | C | 22 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0066 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-7019C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559656 | |||||||
| chr12:53559678 | C | CA | 177 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.49-7042dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559678 | |||||||
| chr12:53559678 | C | CAA | 30 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(27): Show |
30 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.49-7043_49-7042dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559678 | |||||||
| chr12:53559750 | A | T | 199 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.49-7113T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559750 | |||||||
| chr12:53559963 | C | T | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.49-7326G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53559963 | |||||||
| chr12:53560083 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-7446G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560083 | |||||||
| chr12:53560220 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49-7583G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560220 | |||||||
| chr12:53560424 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.49-7787C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560424 | |||||||
| chr12:53560424 | G | GT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-7788dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560424 | |||||||
| chr12:53560948 | CT | C | 50 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(47): Show |
50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-8312delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560948 | |||||||
| chr12:53560972 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-8335C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560972 | |||||||
| chr12:53560992 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-8355G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53560992 | |||||||
| chr12:53561013 | T | A | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.49-8376A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561013 | |||||||
| chr12:53561092 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.49-8455G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561092 | |||||||
| chr12:53561231 | C | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-8594G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561231 | |||||||
| chr12:53561282 | C | T | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-8645G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561282 | |||||||
| chr12:53561329 | T | TA | 58 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0033 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.49-8693dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | |||||||
| chr12:53561329 | TA | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.49-8693delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | |||||||
| chr12:53561329 | TAA | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0248 a0001c0001t0001g0251 others(3): Show |
6 | HG01515.hp1 HG01884.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-8694_49-8693del others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561329 | |||||||
| chr12:53561389 | A | T | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-8752T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561389 | |||||||
| chr12:53561701 | A | C | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-9064T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561701 | |||||||
| chr12:53561922 | C | T | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-9285G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561922 | |||||||
| chr12:53561958 | TGAA | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-9324_49-9322del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53561958 | |||||||
| chr12:53562121 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.49-9484C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562121 | |||||||
| chr12:53562181 | A | G | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-9544T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562181 | |||||||
| chr12:53562250 | G | A | 1 | a0001c0001t0009g0042 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49-9613C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562250 | |||||||
| chr12:53562255 | C | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0261 |
2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.49-9618G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562255 | |||||||
| chr12:53562258 | T | C | 1 | a0001c0001t0006g0142 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49-9621A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562258 | |||||||
| chr12:53562306 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.49-9669G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562306 | |||||||
| chr12:53562321 | C | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-9684G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562321 | |||||||
| chr12:53562635 | C | CA | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.49-9999dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562635 | |||||||
| chr12:53562635 | CA | C | 12 | a0001c0001t0001g0072 a0001c0001t0006g0141 a0001c0001t0006g0142 others(9): Show |
12 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.49-9999delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562635 | |||||||
| chr12:53562659 | C | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0261 |
2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.49-10022G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562659 | |||||||
| chr12:53562662 | A | G | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.49-10025T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562662 | |||||||
| chr12:53562730 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49-10093G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562730 | |||||||
| chr12:53562797 | C | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-10160G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53562797 | |||||||
| chr12:53563026 | T | C | 314 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.49-10389A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563026 | |||||||
| chr12:53563043 | C | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-10406G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563043 | |||||||
| chr12:53563058 | G | A | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.49-10421C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563058 | |||||||
| chr12:53563177 | T | C | 45 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0193 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.49-10540A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563177 | |||||||
| chr12:53563459 | GA | G | 194 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.49-10823delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563459 | |||||||
| chr12:53563546 | G | T | 28 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0003g0165 others(25): Show |
28 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.49-10909C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563546 | |||||||
| chr12:53563570 | T | C | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-10933A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563570 | |||||||
| chr12:53563702 | T | A | 66 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(63): Show |
66 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.49-11065A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563702 | |||||||
| chr12:53563744 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49-11107C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563744 | |||||||
| chr12:53563798 | G | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-11161C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563798 | |||||||
| chr12:53563802 | T | C | 28 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0003g0165 others(25): Show |
28 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.49-11165A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563802 | |||||||
| chr12:53563843 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.49-11206C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563843 | |||||||
| chr12:53563886 | A | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-11249T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563886 | |||||||
| chr12:53563939 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-11302T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53563939 | |||||||
| chr12:53564175 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-11538C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564175 | |||||||
| chr12:53564259 | C | T | 43 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(40): Show |
43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-11622G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564259 | |||||||
| chr12:53564293 | C | T | 254 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.49-11656G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564293 | |||||||
| chr12:53564301 | A | G | 198 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(195): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.49-11664T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564301 | |||||||
| chr12:53564386 | C | G | 1 | a0001c0001t0003g0173 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.49-11749G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564386 | |||||||
| chr12:53564471 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-11834G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564471 | |||||||
| chr12:53564475 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.49-11838A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564475 | |||||||
| chr12:53564680 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0179 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-12043T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564680 | |||||||
| chr12:53564689 | G | T | 4 | a0001c0001t0004g0160 a0001c0001t0004g0162 a0001c0001t0004g0163 others(1): Show |
4 | HG02074.hp1 NA18971.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-12052C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564689 | |||||||
| chr12:53564921 | G | A | 177 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.49-12284C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53564921 | |||||||
| chr12:53565035 | C | T | 1 | a0001c0001t0006g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.49-12398G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565035 | |||||||
| chr12:53565302 | GT | G | 20 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
20 | HG01099.hp1 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-12666delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565302 | |||||||
| chr12:53565493 | C | CG | 26 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0086 others(23): Show |
26 | HG00673.hp2 HG00735.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.49-12857dupC | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565493 | |||||||
| chr12:53565493 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.49-12856G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565493 | |||||||
| chr12:53565501 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-12864T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565501 | |||||||
| chr12:53565602 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0020g0316 |
2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-12965G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565602 | |||||||
| chr12:53565905 | A | G | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.49-13268T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53565905 | |||||||
| chr12:53566142 | A | G | 3 | a0001c0001t0003g0184 a0001c0001t0017g0174 a0001c0001t0022g0169 |
3 | NA18999.hp1 NA19002.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.49-13505T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566142 | |||||||
| chr12:53566405 | A | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.49-13768T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566405 | |||||||
| chr12:53566449 | A | G | 1 | a0001c0002t0003g0189 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.49-13812T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566449 | |||||||
| chr12:53566700 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.49-14063C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566700 | |||||||
| chr12:53566740 | G | GT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-14104dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566740 | |||||||
| chr12:53566753 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-14116A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566753 | |||||||
| chr12:53566767 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-14130C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566767 | |||||||
| chr12:53566836 | C | T | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49-14199G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566836 | |||||||
| chr12:53566952 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.49-14315G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566952 | |||||||
| chr12:53566998 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49-14361G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53566998 | |||||||
| chr12:53567103 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-14466G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567103 | |||||||
| chr12:53567159 | G | A | 6 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0179 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-14522C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567159 | |||||||
| chr12:53567178 | A | G | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-14541T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567178 | |||||||
| chr12:53567232 | T | G | 1 | a0001c0001t0002g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.49-14595A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567232 | |||||||
| chr12:53567509 | C | A | 2 | a0001c0001t0003g0322 a0001c0001t0003g0323 |
2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.49-14872G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567509 | |||||||
| chr12:53567671 | G | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-15034C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567671 | |||||||
| chr12:53567693 | A | AATTGCTT others(3): Show |
1 | a0001c0001t0002g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.49-15066_49-15057d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567693 | |||||||
| chr12:53567709 | G | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-15072C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53567709 | |||||||
| chr12:53568225 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.49-15588G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568225 | |||||||
| chr12:53568392 | G | GCA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-15757_49-15756d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568392 | |||||||
| chr12:53568644 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0015 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49-16007A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568644 | |||||||
| chr12:53568789 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.49-16152T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568789 | |||||||
| chr12:53568793 | G | C | 1 | a0001c0006t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.49-16156C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568793 | |||||||
| chr12:53568827 | G | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.49-16190C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53568827 | |||||||
| chr12:53569129 | G | A | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-16492C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569129 | |||||||
| chr12:53569518 | G | A | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-16881C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569518 | |||||||
| chr12:53569670 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.49-17033T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569670 | |||||||
| chr12:53569679 | T | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0099 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49-17042A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569679 | |||||||
| chr12:53569681 | A | AT | 98 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.49-17045dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569681 | |||||||
| chr12:53569714 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-17077C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569714 | |||||||
| chr12:53569824 | A | G | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-17187T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53569824 | |||||||
| chr12:53570030 | G | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-17393C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570030 | |||||||
| chr12:53570267 | A | G | 4 | a0001c0001t0001g0196 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG00597.hp2 NA18959.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-17630T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570267 | |||||||
| chr12:53570268 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0329 |
2 | HG01943.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.49-17631A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570268 | |||||||
| chr12:53570349 | G | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.49-17712C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570349 | |||||||
| chr12:53570729 | CTGTGTGC others(1): Show |
C | 6 | a0001c0001t0002g0001 a0001c0001t0002g0116 a0001c0001t0002g0122 others(3): Show |
6 | HG00741.hp2 HG02135.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-18100_49-18093d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | |||||||
| chr12:53570729 | CTGTGTGC others(5): Show |
C | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-18104_49-18093d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | |||||||
| chr12:53570729 | CTGTGTGC others(13): Show |
C | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0137 others(1): Show |
4 | HG01261.hp1 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18112_49-18093d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570729 | |||||||
| chr12:53570730 | TGTGTGC | T | 12 | a0001c0001t0002g0026 a0001c0001t0002g0040 a0001c0001t0002g0111 others(9): Show |
12 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-18099_49-18094d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570730 | |||||||
| chr12:53570732 | TGTGC | T | 13 | a0001c0001t0002g0022 a0001c0001t0002g0110 a0001c0001t0002g0117 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.49-18099_49-18096d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570732 | |||||||
| chr12:53570734 | TGC | T | 7 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0118 others(4): Show |
7 | HG02698.hp2 NA18941.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-18099_49-18098d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570734 | |||||||
| chr12:53570736 | C | CGT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0150 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-18101_49-18100d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGT | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
74 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.49-18101_49-18100d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGTGT | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0074 others(5): Show |
8 | HG01361.hp1 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-18103_49-18100d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGTGTGT | C | 54 | a0001c0001t0001g0038 a0001c0001t0001g0149 a0001c0001t0001g0158 others(51): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.49-18105_49-18100d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGTGTGTG others(1): Show |
C | 120 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0168 others(117): Show |
120 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.49-18107_49-18100d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0003g0173 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.49-18109_49-18100d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570736 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.49-18111_49-18100d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570736 | |||||||
| chr12:53570777 | A | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(40): Show |
43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-18140T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570777 | |||||||
| chr12:53570850 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.49-18213T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53570850 | |||||||
| chr12:53571078 | G | A | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-18441C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571078 | |||||||
| chr12:53571084 | C | A | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-18447G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571084 | |||||||
| chr12:53571411 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0309 others(1): Show |
4 | HG00735.hp2 HG01934.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-18774A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571411 | |||||||
| chr12:53571552 | A | G | 3 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0178 |
3 | HG02622.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.49-18915T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571552 | |||||||
| chr12:53571638 | TA | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0217 others(4): Show |
7 | HG00639.hp2 HG01167.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-19002delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571638 | |||||||
| chr12:53571639 | A | T | 228 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(225): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.49-19002T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571639 | |||||||
| chr12:53571640 | A | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0233 a0001c0001t0001g0295 others(1): Show |
4 | HG01167.hp1 HG02698.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-19003T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571640 | |||||||
| chr12:53571770 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.49-19133A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571770 | |||||||
| chr12:53571935 | C | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.49-19298G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53571935 | |||||||
| chr12:53572071 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.49-19434T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572071 | |||||||
| chr12:53572264 | A | C | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49-19627T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572264 | |||||||
| chr12:53572273 | C | A | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49-19636G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572273 | |||||||
| chr12:53572562 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0297 |
2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.49-19925C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572562 | |||||||
| chr12:53572669 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.49-20032C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572669 | |||||||
| chr12:53572699 | C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.49-20062G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572699 | |||||||
| chr12:53572787 | A | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-20150T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572787 | |||||||
| chr12:53572803 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.49-20166A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572803 | |||||||
| chr12:53572853 | T | G | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-20216A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53572853 | |||||||
| chr12:53573084 | C | CA | 22 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(19): Show |
22 | HG01099.hp1 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.49-20448dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573084 | |||||||
| chr12:53573282 | C | T | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.49-20645G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573282 | |||||||
| chr12:53573374 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49-20737A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573374 | |||||||
| chr12:53573599 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.49-20962G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573599 | |||||||
| chr12:53573616 | T | C | 1 | a0001c0001t0003g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.49-20979A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573616 | |||||||
| chr12:53573644 | T | G | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-21007A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573644 | |||||||
| chr12:53573658 | T | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-21021A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573658 | |||||||
| chr12:53573777 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-21140G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573777 | |||||||
| chr12:53573811 | G | T | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.49-21174C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573811 | |||||||
| chr12:53573944 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0056 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.49-21307G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53573944 | |||||||
| chr12:53574487 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-21850G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574487 | |||||||
| chr12:53574718 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49-22081C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574718 | |||||||
| chr12:53574800 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49-22163C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574800 | |||||||
| chr12:53574915 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49-22278C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574915 | |||||||
| chr12:53574932 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.49-22295A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574932 | |||||||
| chr12:53574953 | C | CA | 92 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(89): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.49-22317dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574953 | |||||||
| chr12:53574953 | CA | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.49-22317delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574953 | |||||||
| chr12:53574974 | G | A | 4 | a0001c0001t0001g0251 a0001c0001t0001g0278 a0001c0001t0001g0283 others(1): Show |
4 | HG01192.hp1 HG01515.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-22337C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53574974 | |||||||
| chr12:53575174 | G | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-22537C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575174 | |||||||
| chr12:53575179 | A | G | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22542T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575179 | |||||||
| chr12:53575182 | C | T | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22545G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575182 | |||||||
| chr12:53575187 | C | A | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22550G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575187 | |||||||
| chr12:53575197 | T | C | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22560A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575197 | |||||||
| chr12:53575198 | G | A | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22561C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575198 | |||||||
| chr12:53575199 | A | G | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22562T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575199 | |||||||
| chr12:53575206 | G | A | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22569C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575206 | |||||||
| chr12:53575208 | G | C | 1 | a0001c0001t0011g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.49-22571C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575208 | |||||||
| chr12:53575407 | T | TA | 56 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0055 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49-22771dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575407 | |||||||
| chr12:53575407 | TA | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp1 HG01074.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.49-22771delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575407 | |||||||
| chr12:53575574 | C | CA | 7 | a0001c0001t0001g0057 a0001c0001t0001g0087 a0001c0001t0001g0234 others(4): Show |
7 | HG00597.hp1 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-22938dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | |||||||
| chr12:53575574 | C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(47): Show |
50 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.49-22947_49-22938d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | |||||||
| chr12:53575574 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0122 a0001c0001t0002g0129 a0001c0001t0002g0132 |
3 | HG00423.hp2 HG01433.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.49-22948_49-22938d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575574 | |||||||
| chr12:53575682 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-23045A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575682 | |||||||
| chr12:53575988 | A | G | 1 | a0001c0001t0025g0315 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.49-23351T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53575988 | |||||||
| chr12:53576102 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.49-23465T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576102 | |||||||
| chr12:53576140 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-23503A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576140 | |||||||
| chr12:53576377 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.49-23740A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576377 | |||||||
| chr12:53576409 | T | A | 1 | a0001c0001t0006g0145 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.49-23772A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576409 | |||||||
| chr12:53576701 | AAAAC | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-24068_49-24065d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53576701 | |||||||
| chr12:53577023 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+23930A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577023 | |||||||
| chr12:53577212 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.48+23741G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577212 | |||||||
| chr12:53577411 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.48+23542A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577411 | |||||||
| chr12:53577413 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+23540C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577413 | |||||||
| chr12:53577426 | AAC | A | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+23525_48+23526d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577426 | |||||||
| chr12:53577444 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0014g0030 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.48+23509G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577444 | |||||||
| chr12:53577471 | C | T | 179 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.48+23482G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577471 | |||||||
| chr12:53577513 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.48+23440C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577513 | |||||||
| chr12:53577542 | C | T | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.48+23411G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577542 | |||||||
| chr12:53577702 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+23251G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577702 | |||||||
| chr12:53577717 | G | GA | 45 | a0001c0001t0001g0218 a0001c0001t0002g0001 a0001c0001t0002g0022 others(42): Show |
45 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.48+23235dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577717 | |||||||
| chr12:53577728 | A | AAAAG | 52 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(49): Show |
52 | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+23221_48+23224d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577728 | |||||||
| chr12:53577728 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48+23225T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577728 | |||||||
| chr12:53577730 | AAG | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+23221_48+23222d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577730 | |||||||
| chr12:53577732 | G | A | 49 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(46): Show |
49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+23221C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577732 | |||||||
| chr12:53577736 | G | A | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.48+23217C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577736 | |||||||
| chr12:53577771 | G | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+23182C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53577771 | |||||||
| chr12:53578048 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+22905C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578048 | |||||||
| chr12:53578124 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+22829C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578124 | |||||||
| chr12:53578367 | C | CA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.48+22585dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | |||||||
| chr12:53578367 | CA | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(8): Show |
11 | HG01258.hp2 HG01433.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+22585delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | |||||||
| chr12:53578367 | CAA | C | 210 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(207): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.48+22584_48+22585d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | |||||||
| chr12:53578367 | CAAA | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(8): Show |
11 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+22583_48+22585d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578367 | |||||||
| chr12:53578783 | C | CA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0101 a0001c0001t0001g0151 others(4): Show |
7 | HG02145.hp1 HG03688.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+22169dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578783 | |||||||
| chr12:53578783 | CA | C | 133 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0033 others(130): Show |
133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.48+22169delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53578783 | |||||||
| chr12:53579344 | CCAAAATA others(12): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.48+21590_48+21608d others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579344 | |||||||
| chr12:53579444 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.48+21509G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579444 | |||||||
| chr12:53579551 | C | CA | 22 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
22 | HG00597.hp2 HG00738.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+21401dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579551 | |||||||
| chr12:53579842 | C | CCT | 44 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0022 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+21109_48+21110d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579842 | |||||||
| chr12:53579843 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+21110G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579843 | |||||||
| chr12:53579958 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+20995G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579958 | |||||||
| chr12:53579990 | G | C | 179 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.48+20963C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53579990 | |||||||
| chr12:53580075 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.48+20878G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580075 | |||||||
| chr12:53580210 | C | T | 40 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(37): Show |
40 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.48+20743G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580210 | |||||||
| chr12:53580235 | A | T | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.48+20718T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580235 | |||||||
| chr12:53580267 | CA | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.48+20685delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580267 | |||||||
| chr12:53580332 | G | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.48+20621C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580332 | |||||||
| chr12:53580387 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+20566C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580387 | |||||||
| chr12:53580559 | A | G | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+20394T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580559 | |||||||
| chr12:53580621 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.48+20332C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580621 | |||||||
| chr12:53580663 | C | CA | 10 | a0001c0001t0001g0091 a0001c0001t0001g0108 a0001c0001t0001g0200 others(7): Show |
10 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+20289dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580663 | |||||||
| chr12:53580663 | CA | C | 52 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0149 others(49): Show |
52 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+20289delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580663 | |||||||
| chr12:53580845 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+20108G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53580845 | |||||||
| chr12:53581021 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.48+19932T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581021 | |||||||
| chr12:53581022 | G | C | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+19931C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581022 | |||||||
| chr12:53581029 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+19924A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581029 | |||||||
| chr12:53581111 | CA | C | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.48+19841delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581111 | |||||||
| chr12:53581119 | A | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+19834T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581119 | |||||||
| chr12:53581223 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.48+19730A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581223 | |||||||
| chr12:53581541 | C | G | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.48+19412G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581541 | |||||||
| chr12:53581604 | G | T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0291 others(1): Show |
4 | HG02135.hp1 HG02523.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+19349C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581604 | |||||||
| chr12:53581704 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.48+19249A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581704 | |||||||
| chr12:53581774 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+19179G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581774 | |||||||
| chr12:53581874 | G | A | 1 | a0001c0001t0014g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.48+19079C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581874 | |||||||
| chr12:53581930 | C | T | 70 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.48+19023G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581930 | |||||||
| chr12:53581967 | A | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+18986T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53581967 | |||||||
| chr12:53582122 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+18831T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582122 | |||||||
| chr12:53582197 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+18756G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582197 | |||||||
| chr12:53582198 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.48+18755C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582198 | |||||||
| chr12:53582199 | C | T | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+18754G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582199 | |||||||
| chr12:53582200 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0197 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.48+18753C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582200 | |||||||
| chr12:53582212 | C | T | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+18741G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582212 | |||||||
| chr12:53582306 | C | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+18647G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582306 | |||||||
| chr12:53582326 | T | TA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0214 others(5): Show |
8 | HG00423.hp1 HG01169.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+18626dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582326 | |||||||
| chr12:53582483 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.48+18470G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582483 | |||||||
| chr12:53582494 | GA | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+18458delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582494 | |||||||
| chr12:53582563 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.48+18390T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582563 | |||||||
| chr12:53582664 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.48+18289G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53582664 | |||||||
| chr12:53583041 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.48+17912T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583041 | |||||||
| chr12:53583066 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.48+17887A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583066 | |||||||
| chr12:53583244 | C | G | 1 | a0001c0001t0001g0269 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.48+17709G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583244 | |||||||
| chr12:53583460 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.48+17493A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583460 | |||||||
| chr12:53583533 | T | G | 228 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(225): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.48+17420A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583533 | |||||||
| chr12:53583640 | C | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.48+17313G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583640 | |||||||
| chr12:53583641 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48+17312C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583641 | |||||||
| chr12:53583705 | G | T | 11 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(8): Show |
11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+17248C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583705 | |||||||
| chr12:53583926 | C | CAAATAAG others(9): Show |
1 | a0001c0001t0001g0012 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.48+17011_48+17026d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53583926 | |||||||
| chr12:53584197 | T | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16756A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584197 | |||||||
| chr12:53584229 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.48+16724C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584229 | |||||||
| chr12:53584312 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+16641G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584312 | |||||||
| chr12:53584365 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16588A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584365 | |||||||
| chr12:53584504 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+16449G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584504 | |||||||
| chr12:53584517 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+16436A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584517 | |||||||
| chr12:53584931 | A | G | 240 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(237): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.48+16022T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53584931 | |||||||
| chr12:53585048 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+15905G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585048 | |||||||
| chr12:53585131 | C | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
4 | NA18941.hp1 NA18973.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+15822G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585131 | |||||||
| chr12:53585465 | C | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(35): Show |
38 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.48+15488G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585465 | |||||||
| chr12:53585465 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48+15488G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585465 | |||||||
| chr12:53585552 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.48+15401T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585552 | |||||||
| chr12:53585632 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+15321T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585632 | |||||||
| chr12:53585721 | A | C | 239 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(236): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.48+15232T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585721 | |||||||
| chr12:53585721 | ACACTGAT others(5): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+15220_48+15231d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53585721 | |||||||
| chr12:53586002 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.48+14951G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586002 | |||||||
| chr12:53586148 | C | T | 1 | a0001c0001t0009g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.48+14805G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586148 | |||||||
| chr12:53586307 | C | T | 212 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(209): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.48+14646G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586307 | |||||||
| chr12:53586410 | TA | T | 194 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.48+14542delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586410 | |||||||
| chr12:53586650 | A | G | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+14303T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586650 | |||||||
| chr12:53586783 | T | A | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+14170A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586783 | |||||||
| chr12:53586801 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+14152T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586801 | |||||||
| chr12:53586810 | C | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+14143G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586810 | |||||||
| chr12:53586832 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+14121G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53586832 | |||||||
| chr12:53587037 | C | T | 217 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(214): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.48+13916G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587037 | |||||||
| chr12:53587093 | A | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+13860T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587093 | |||||||
| chr12:53587104 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.48+13849G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587104 | |||||||
| chr12:53587204 | T | C | 1 | a0001c0001t0028g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+13749A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587204 | |||||||
| chr12:53587275 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0098 |
2 | HG01099.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.48+13678C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587275 | |||||||
| chr12:53587353 | C | T | 7 | a0001c0001t0002g0110 a0001c0001t0002g0119 a0001c0001t0002g0120 others(4): Show |
7 | HG00408.hp1 HG02056.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13600G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587353 | |||||||
| chr12:53587366 | C | CAA | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+13585_48+13586d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(5): Show |
63 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0180 others(60): Show |
63 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.48+13575_48+13586d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(6): Show |
36 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0265 others(33): Show |
36 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.48+13574_48+13586d others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0197 a0001c0001t0001g0245 a0001c0001t0001g0294 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+13573_48+13586d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0176 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48+13572_48+13586d others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0280 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.48+13571_48+13586d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(16): Show |
9 | a0001c0001t0001g0243 a0001c0001t0001g0248 a0001c0001t0001g0252 others(6): Show |
9 | HG01256.hp2 HG03195.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(17): Show |
30 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0211 others(27): Show |
30 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(18): Show |
34 | a0001c0001t0001g0057 a0001c0001t0001g0193 a0001c0001t0001g0195 others(31): Show |
34 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(27): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(19): Show |
11 | a0001c0001t0001g0210 a0001c0001t0001g0216 a0001c0001t0001g0277 others(8): Show |
11 | HG00408.hp2 HG00735.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(20): Show |
5 | a0001c0001t0001g0238 a0001c0001t0001g0257 a0001c0001t0001g0258 others(2): Show |
5 | HG00423.hp1 HG00621.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0207 a0001c0001t0001g0215 a0001c0001t0001g0261 |
3 | HG01243.hp2 HG02015.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.48+13586_48+13587i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(22): Show |
7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0219 others(4): Show |
7 | HG00099.hp2 HG00609.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13586_48+13587i others(31): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0202 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.48+13586_48+13587i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.48+13586_48+13587i others(33): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0237 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.48+13586_48+13587i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.48+13586_48+13587i others(37): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587366 | C | CAAAAAAA others(29): Show |
3 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0027g0194 |
3 | HG00673.hp2 NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.48+13586_48+13587i others(38): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587366 | |||||||
| chr12:53587568 | G | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(36): Show |
39 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.48+13385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587568 | |||||||
| chr12:53587589 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.48+13364G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587589 | |||||||
| chr12:53587642 | G | C | 239 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(236): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.48+13311C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587642 | |||||||
| chr12:53587671 | CA | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(11): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.48+13281delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587671 | |||||||
| chr12:53587820 | C | CATATATA others(1): Show |
4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0091 others(1): Show |
4 | HG00639.hp2 HG01099.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13125_48+13132d others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0245 |
2 | HG01070.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.48+13123_48+13132d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(5): Show |
3 | a0001c0001t0001g0247 a0001c0001t0001g0319 a0001c0001t0010g0071 |
3 | HG00639.hp1 NA18941.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.48+13121_48+13132d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(7): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0255 a0001c0001t0025g0315 |
3 | HG01070.hp2 HG03017.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.48+13119_48+13132d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(9): Show |
1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.48+13117_48+13132d others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(13): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0092 a0001c0006t0001g0083 |
3 | HG02080.hp1 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.48+13113_48+13132d others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(17): Show |
1 | a0001c0001t0001g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.48+13109_48+13132d others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(19): Show |
1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.48+13132_48+13133i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587820 | C | CATATATA others(13): Show |
2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.48+13132_48+13133i others(22): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587820 | |||||||
| chr12:53587824 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.48+13129A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587824 | |||||||
| chr12:53587839 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.48+13114T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587839 | |||||||
| chr12:53587839 | ATATATT | A | 35 | a0001c0001t0001g0149 a0001c0001t0001g0195 a0001c0001t0001g0196 others(32): Show |
35 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+13108_48+13113d others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587839 | |||||||
| chr12:53587840 | TATA | T | 21 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(18): Show |
21 | HG00408.hp1 HG00621.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.48+13110_48+13112d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587840 | |||||||
| chr12:53587841 | A | AT | 3 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 |
3 | NA18947.hp1 NA18984.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.48+13111dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587841 | |||||||
| chr12:53587841 | ATAT | A | 14 | a0001c0001t0001g0170 a0001c0001t0001g0183 a0001c0001t0001g0190 others(11): Show |
14 | HG02056.hp2 HG02165.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13109_48+13111d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587841 | |||||||
| chr12:53587843 | A | AT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
6 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+13109dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0263 a0001c0001t0001g0297 |
2 | HG00140.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0232 |
2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0002t0005g0171 |
3 | HG01168.hp1 HG01168.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(25): Show |
1 | a0001c0001t0009g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(34): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(32): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(19): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0086 others(1): Show |
4 | HG00735.hp1 HG01261.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(20): Show |
1 | a0001c0001t0011g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(21): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0066 a0001c0001t0001g0085 others(2): Show |
5 | HG01943.hp1 HG02148.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0095 a0001c0001t0009g0080 |
2 | HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(30): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0101 |
2 | NA18943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(24): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0079 |
2 | HG02257.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0157 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0146 a0001c0001t0009g0042 |
2 | HG01433.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(26): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0088 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(28): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+13109_48+13110i others(25): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0061 a0001c0005t0001g0069 |
2 | HG02559.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0313 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 |
3 | HG00099.hp1 HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+13109_48+13110i others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(1): Show |
6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG01074.hp2 HG01081.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATATAT others(3): Show |
8 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
8 | HG01109.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+13109_48+13110i others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | ATATTTTT others(6): Show |
1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+13109_48+13110i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | A | T | 7 | a0001c0001t0001g0012 a0001c0001t0002g0117 a0001c0001t0006g0141 others(4): Show |
7 | HG02897.hp1 HG03195.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+13110T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | AT | A | 17 | a0001c0001t0002g0040 a0001c0001t0002g0122 a0001c0001t0002g0123 others(14): Show |
17 | HG00423.hp2 HG00544.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.48+13109delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587843 | ATTT | A | 13 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0179 others(10): Show |
13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.48+13107_48+13109d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587843 | |||||||
| chr12:53587844 | T | TA | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0033 others(11): Show |
14 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATA | 3 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0014g0030 |
3 | HG02257.hp1 HG03831.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.48+13108_48+13109i others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(2): Show |
12 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0250 others(9): Show |
12 | HG00408.hp2 HG00423.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(4): Show |
14 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0259 others(11): Show |
14 | HG02135.hp1 HG02293.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(6): Show |
16 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0257 others(13): Show |
16 | HG01192.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(15): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(8): Show |
7 | a0001c0001t0001g0057 a0001c0001t0001g0253 a0001c0001t0001g0256 others(4): Show |
7 | HG00597.hp1 HG00735.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(17): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(10): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0292 others(1): Show |
4 | HG03654.hp2 HG03710.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(12): Show |
8 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0265 others(5): Show |
8 | HG01255.hp2 HG01358.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(21): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(14): Show |
4 | a0001c0001t0001g0280 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG04228.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13108_48+13109i others(23): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(20): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0301 a0001c0001t0001g0304 |
3 | HG02683.hp1 NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.48+13108_48+13109i others(29): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587844 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.48+13108_48+13109i others(18): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587844 | |||||||
| chr12:53587845 | T | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0245 a0001c0001t0001g0247 others(6): Show |
9 | HG00639.hp1 HG01070.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13108A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587845 | |||||||
| chr12:53587846 | T | A | 67 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.48+13107A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587846 | |||||||
| chr12:53587847 | T | A | 7 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0319 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+13106A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587847 | |||||||
| chr12:53587848 | T | A | 40 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.48+13105A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587848 | |||||||
| chr12:53587849 | T | A | 2 | a0001c0001t0001g0245 a0001c0001t0012g0254 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.48+13104A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587849 | |||||||
| chr12:53587850 | T | A | 14 | a0001c0001t0001g0253 a0001c0001t0001g0280 a0001c0001t0001g0281 others(11): Show |
14 | HG00673.hp1 HG00735.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+13103A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587850 | |||||||
| chr12:53587851 | T | A | 1 | a0001c0001t0012g0254 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.48+13102A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587851 | |||||||
| chr12:53587852 | T | A | 9 | a0001c0001t0001g0253 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG00735.hp2 HG01934.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+13101A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587852 | |||||||
| chr12:53587854 | T | A | 1 | a0001c0001t0004g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.48+13099A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587854 | |||||||
| chr12:53587866 | ACACGAAG others(7): Show |
A | 1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.48+13073_48+13086d others(16): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53587866 | |||||||
| chr12:53588747 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.48+12206G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588747 | |||||||
| chr12:53588850 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0001c0001t0001g0077 others(2): Show |
5 | HG00733.hp1 HG01256.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+12103T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588850 | |||||||
| chr12:53588903 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+12050C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53588903 | |||||||
| chr12:53589756 | C | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0329 |
2 | HG01943.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.48+11197G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53589756 | |||||||
| chr12:53590106 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+10847C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590106 | |||||||
| chr12:53590130 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.48+10823G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590130 | |||||||
| chr12:53590367 | G | A | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+10586C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590367 | |||||||
| chr12:53590724 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.48+10229A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590724 | |||||||
| chr12:53590750 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.48+10203T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590750 | |||||||
| chr12:53590959 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+9994A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53590959 | |||||||
| chr12:53591124 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.48+9829A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591124 | |||||||
| chr12:53591249 | CACGGCTA others(3): Show |
C | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+9694_48+9703del others(10): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591249 | |||||||
| chr12:53591633 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+9320A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591633 | |||||||
| chr12:53591789 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+9164A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53591789 | |||||||
| chr12:53592002 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.48+8951C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592002 | |||||||
| chr12:53592267 | A | G | 5 | a0001c0001t0002g0110 a0001c0001t0002g0119 a0001c0001t0002g0120 others(2): Show |
5 | HG00408.hp1 HG02056.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+8686T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592267 | |||||||
| chr12:53592570 | A | AATAGATT others(5): Show |
1 | a0001c0001t0001g0255 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.48+8371_48+8382dup others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592570 | |||||||
| chr12:53592619 | G | A | 1 | a0001c0001t0003g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.48+8334C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592619 | |||||||
| chr12:53592984 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+7969G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53592984 | |||||||
| chr12:53593140 | A | G | 44 | a0001c0001t0001g0043 a0001c0001t0001g0193 a0001c0001t0001g0195 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+7813T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53593140 | |||||||
| chr12:53593231 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.48+7722G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53593231 | |||||||
| chr12:53594045 | G | A | 314 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.48+6908C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594045 | |||||||
| chr12:53594242 | A | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+6711T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594242 | |||||||
| chr12:53594568 | G | A | 1 | a0001c0001t0004g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.48+6385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594568 | |||||||
| chr12:53594625 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.48+6328G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594625 | |||||||
| chr12:53594807 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.48+6146C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594807 | |||||||
| chr12:53594825 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+6128A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594825 | |||||||
| chr12:53594874 | C | A | 1 | a0001c0001t0007g0137 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.48+6079G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594874 | |||||||
| chr12:53594880 | C | T | 327 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(324): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.48+6073G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594880 | |||||||
| chr12:53594887 | C | CA | 18 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
18 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.48+6065dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594887 | |||||||
| chr12:53594887 | CA | C | 6 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0179 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+6065delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594887 | |||||||
| chr12:53594901 | G | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6052C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594901 | |||||||
| chr12:53594901 | GA | G | 10 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(7): Show |
10 | HG00423.hp1 HG02135.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+6051delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594901 | |||||||
| chr12:53594902 | A | G | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6051T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53594902 | |||||||
| chr12:53595000 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5953A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595000 | |||||||
| chr12:53595054 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+5899C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595054 | |||||||
| chr12:53595159 | T | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+5794A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595159 | |||||||
| chr12:53595720 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+5233A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53595720 | |||||||
| chr12:53596019 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4934G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596019 | |||||||
| chr12:53596087 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+4866A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596087 | |||||||
| chr12:53596110 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48+4843A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596110 | |||||||
| chr12:53596129 | C | G | 1 | a0001c0001t0024g0239 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.48+4824G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596129 | |||||||
| chr12:53596157 | G | A | 1 | a0001c0001t0007g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.48+4796C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596157 | |||||||
| chr12:53596396 | TGAG | T | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+4554_48+4556del others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596396 | |||||||
| chr12:53596422 | C | T | 6 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0009g0042 others(3): Show |
6 | HG01261.hp2 HG01433.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+4531G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596422 | |||||||
| chr12:53596540 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+4413G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596540 | |||||||
| chr12:53596565 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.48+4388G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596565 | |||||||
| chr12:53596847 | T | C | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+4106A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596847 | |||||||
| chr12:53596866 | T | C | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.48+4087A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596866 | |||||||
| chr12:53596872 | C | T | 91 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(88): Show |
91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.48+4081G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53596872 | |||||||
| chr12:53597020 | A | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+3933T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597020 | |||||||
| chr12:53597035 | G | C | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+3918C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597035 | |||||||
| chr12:53597111 | T | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.48+3842A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597111 | |||||||
| chr12:53597186 | G | GT | 10 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0202 others(7): Show |
10 | HG01167.hp2 HG02970.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+3766dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597186 | |||||||
| chr12:53597380 | C | T | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3573G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597380 | |||||||
| chr12:53597385 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.48+3568A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597385 | |||||||
| chr12:53597537 | C | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.48+3416G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597537 | |||||||
| chr12:53597678 | G | A | 17 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): Show |
17 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+3275C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597678 | |||||||
| chr12:53597737 | A | G | 1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.48+3216T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597737 | |||||||
| chr12:53597782 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3171A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597782 | |||||||
| chr12:53597787 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.48+3166G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597787 | |||||||
| chr12:53597788 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.48+3165C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597788 | |||||||
| chr12:53597808 | C | CA | 44 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.48+3144dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | |||||||
| chr12:53597808 | C | CAA | 6 | a0001c0001t0001g0109 a0001c0001t0001g0195 a0001c0002t0001g0324 others(3): Show |
6 | HG01934.hp1 HG02896.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+3143_48+3144dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | |||||||
| chr12:53597808 | C | CAAA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+3142_48+3144dup others(3): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53597808 | |||||||
| chr12:53598725 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+2228A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598725 | |||||||
| chr12:53598794 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+2159A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598794 | |||||||
| chr12:53598867 | A | G | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+2086T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53598867 | |||||||
| chr12:53599053 | A | ACAGTGTC others(12): Show |
1 | a0001c0001t0022g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.48+1881_48+1899dup others(19): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599053 | |||||||
| chr12:53599123 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.48+1830G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599123 | |||||||
| chr12:53599138 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG00423.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.48+1815T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599138 | |||||||
| chr12:53599339 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.48+1614C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599339 | |||||||
| chr12:53599457 | G | GAT | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.48+1494_48+1495dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599457 | |||||||
| chr12:53599471 | C | CTA | 16 | a0001c0001t0001g0043 a0001c0001t0001g0106 a0001c0001t0001g0107 others(13): Show |
16 | HG01891.hp1 HG02486.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.48+1480_48+1481dup others(2): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | |||||||
| chr12:53599471 | C | CTATA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1478_48+1481dup others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | |||||||
| chr12:53599471 | C | CTATATA | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1476_48+1481dup others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599471 | |||||||
| chr12:53599779 | C | A | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.48+1174G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599779 | |||||||
| chr12:53599874 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1079C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53599874 | |||||||
| chr12:53600226 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.48+727T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600226 | |||||||
| chr12:53600584 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48+369C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600584 | |||||||
| chr12:53600627 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+326G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600627 | |||||||
| chr12:53600633 | G | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.48+320C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600633 | |||||||
| chr12:53600867 | C | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.48+86G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600867 | |||||||
| chr12:53600901 | G | A | 1 | a0001c0001t0009g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.48+52C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 2/11 | chr12 | 53600901 | |||||||
| chr12:53601052 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-31A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601052 | |||||||
| chr12:53601069 | C | CA | 33 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0090 others(30): Show |
33 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-21-49dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601069 | |||||||
| chr12:53601293 | T | C | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-272A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601293 | |||||||
| chr12:53601412 | T | C | 1 | a0001c0006t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-21-391A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601412 | |||||||
| chr12:53601707 | A | G | 91 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(88): Show |
91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-21-686T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601707 | |||||||
| chr12:53601754 | C | T | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-733G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53601754 | |||||||
| chr12:53602147 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21-1126G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602147 | |||||||
| chr12:53602222 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0282 |
2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-21-1201C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602222 | |||||||
| chr12:53602235 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21-1214T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602235 | |||||||
| chr12:53602274 | A | C | 1 | a0001c0002t0001g0326 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-21-1253T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602274 | |||||||
| chr12:53602495 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-21-1474G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602495 | |||||||
| chr12:53602793 | G | T | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-1772C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602793 | |||||||
| chr12:53602797 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-1776A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602797 | |||||||
| chr12:53602859 | A | G | 91 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(88): Show |
91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-21-1838T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602859 | |||||||
| chr12:53602860 | C | A | 4 | a0001c0003t0008g0225 a0001c0003t0008g0227 a0001c0003t0008g0228 others(1): Show |
4 | HG02559.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-1839G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53602860 | |||||||
| chr12:53603039 | C | T | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-2018G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603039 | |||||||
| chr12:53603063 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-21-2042G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603063 | |||||||
| chr12:53603388 | A | C | 2 | a0001c0001t0001g0220 a0001c0001t0003g0221 |
2 | HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-21-2367T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603388 | |||||||
| chr12:53603796 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-21-2775G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603796 | |||||||
| chr12:53603867 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-21-2846A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53603867 | |||||||
| chr12:53604073 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-21-3052T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604073 | |||||||
| chr12:53604214 | C | A | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-21-3193G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604214 | |||||||
| chr12:53604297 | C | G | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-3276G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604297 | |||||||
| chr12:53604892 | G | A | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-3871C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53604892 | |||||||
| chr12:53605272 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21-4251G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605272 | |||||||
| chr12:53605295 | A | G | 2 | a0001c0003t0001g0235 a0001c0003t0030g0330 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-4274T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605295 | |||||||
| chr12:53605337 | T | C | 239 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(236): Show |
239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-21-4316A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605337 | |||||||
| chr12:53605356 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-21-4335A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605356 | |||||||
| chr12:53605375 | G | A | 2 | a0001c0001t0012g0254 a0001c0001t0012g0284 |
2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-21-4354C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605375 | |||||||
| chr12:53605389 | C | CA | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-21-4369dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | |||||||
| chr12:53605389 | C | CAA | 17 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
17 | HG00423.hp2 HG00733.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-4370_-21-4369d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | |||||||
| chr12:53605389 | CA | C | 11 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(8): Show |
11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-4369delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605389 | |||||||
| chr12:53605474 | G | T | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-4453C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605474 | |||||||
| chr12:53605575 | T | C | 314 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-21-4554A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605575 | |||||||
| chr12:53605844 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-4823A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53605844 | |||||||
| chr12:53606035 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-5014T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606035 | |||||||
| chr12:53606050 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-5029G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606050 | |||||||
| chr12:53606090 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-21-5069A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606090 | |||||||
| chr12:53606128 | G | A | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-21-5107C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606128 | |||||||
| chr12:53606139 | A | G | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-21-5118T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606139 | |||||||
| chr12:53606247 | G | A | 217 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(214): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-21-5226C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606247 | |||||||
| chr12:53606318 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-21-5297C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606318 | |||||||
| chr12:53606352 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-21-5331C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606352 | |||||||
| chr12:53606406 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0134 |
3 | HG00408.hp1 NA18955.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-21-5385C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606406 | |||||||
| chr12:53606498 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-21-5477A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606498 | |||||||
| chr12:53606546 | C | A | 11 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(8): Show |
11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-5525G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606546 | |||||||
| chr12:53606554 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-21-5533C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606554 | |||||||
| chr12:53606564 | A | T | 1 | a0001c0001t0002g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-21-5543T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606564 | |||||||
| chr12:53606809 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-21-5788G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606809 | |||||||
| chr12:53606842 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-5821G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53606842 | |||||||
| chr12:53607012 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-5991C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607012 | |||||||
| chr12:53607065 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-21-6044A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607065 | |||||||
| chr12:53607093 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-21-6072C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607093 | |||||||
| chr12:53607271 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-21-6250C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607271 | |||||||
| chr12:53607352 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-6331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607352 | |||||||
| chr12:53607437 | A | C | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-21-6416T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607437 | |||||||
| chr12:53607453 | G | A | 174 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(171): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-21-6432C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607453 | |||||||
| chr12:53607481 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6460A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607481 | |||||||
| chr12:53607660 | A | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-6639T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607660 | |||||||
| chr12:53607668 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-6647A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607668 | |||||||
| chr12:53607679 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-6658T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607679 | |||||||
| chr12:53607763 | A | G | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-6742T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607763 | |||||||
| chr12:53607886 | A | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG02257.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-21-6865T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607886 | |||||||
| chr12:53607986 | G | A | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-6965C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53607986 | |||||||
| chr12:53608015 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-6994G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608015 | |||||||
| chr12:53608200 | T | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-7179A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608200 | |||||||
| chr12:53608218 | C | CA | 20 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(17): Show |
20 | HG01109.hp2 HG02055.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21-7198dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | |||||||
| chr12:53608218 | CA | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0018 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-21-7198delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | |||||||
| chr12:53608218 | CAA | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
32 | HG00609.hp1 HG01070.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-21-7199_-21-7198d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608218 | |||||||
| chr12:53608316 | A | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21-7295T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608316 | |||||||
| chr12:53608550 | C | T | 309 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-21-7529G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608550 | |||||||
| chr12:53608815 | C | T | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-21-7794G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53608815 | |||||||
| chr12:53609157 | C | CT | 85 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-21-8137dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609157 | |||||||
| chr12:53609157 | C | CTTTT | 15 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01891.hp1 HG02486.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21-8140_-21-8137d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609157 | |||||||
| chr12:53609381 | C | T | 13 | a0001c0001t0001g0197 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21-8360G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609381 | |||||||
| chr12:53609424 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-21-8403C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609424 | |||||||
| chr12:53609470 | TA | T | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-21-8450delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609470 | |||||||
| chr12:53609470 | TAA | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0059 others(12): Show |
15 | HG00735.hp1 HG01515.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21-8451_-21-8450d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609470 | |||||||
| chr12:53609641 | TA | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0034 others(34): Show |
37 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21-8621delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609641 | |||||||
| chr12:53609742 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21-8721C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609742 | |||||||
| chr12:53609821 | C | CTTTGTTT others(4): Show |
1 | a0001c0001t0014g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-21-8801_-21-8800i others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | |||||||
| chr12:53609821 | C | CTTTTTTT others(3): Show |
141 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0029 others(138): Show |
141 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-21-8810_-21-8801d others(12): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | |||||||
| chr12:53609821 | C | CTTTTTTT others(4): Show |
102 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(99): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-21-8811_-21-8801d others(13): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | |||||||
| chr12:53609821 | C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0246 others(8): Show |
11 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-8812_-21-8801d others(14): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609821 | |||||||
| chr12:53609822 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-8801A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609822 | |||||||
| chr12:53609915 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-8894G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609915 | |||||||
| chr12:53609964 | G | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0066 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-8943C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609964 | |||||||
| chr12:53609973 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00735.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-8952G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53609973 | |||||||
| chr12:53610005 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-21-8984G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610005 | |||||||
| chr12:53610037 | G | A | 4 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-9016C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610037 | |||||||
| chr12:53610052 | A | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21-9031T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610052 | |||||||
| chr12:53610220 | G | A | 1 | a0001c0001t0003g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-21-9199C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610220 | |||||||
| chr12:53610325 | G | C | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-21-9304C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610325 | |||||||
| chr12:53610327 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-21-9306G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610327 | |||||||
| chr12:53610441 | T | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0066 others(19): Show |
22 | HG00140.hp2 HG00738.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-9420A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610441 | |||||||
| chr12:53610497 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-21-9476C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610497 | |||||||
| chr12:53610564 | C | CA | 37 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(34): Show |
37 | HG00408.hp1 HG01099.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-21-9544dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610564 | |||||||
| chr12:53610564 | CA | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0155 others(11): Show |
14 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-9544delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610564 | |||||||
| chr12:53610614 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-21-9593T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610614 | |||||||
| chr12:53610671 | G | A | 11 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(8): Show |
11 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-9650C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610671 | |||||||
| chr12:53610687 | T | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG01099.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-9666A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610687 | |||||||
| chr12:53610902 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0158 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21-9881T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610902 | |||||||
| chr12:53610993 | A | AT | 10 | a0001c0001t0001g0029 a0001c0001t0001g0155 a0001c0001t0001g0195 others(7): Show |
10 | HG00140.hp1 HG00733.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-9973dupA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53610993 | |||||||
| chr12:53611091 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-21-10070C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611091 | |||||||
| chr12:53611220 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-10199G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611220 | |||||||
| chr12:53611229 | G | C | 1 | a0001c0001t0021g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-21-10208C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611229 | |||||||
| chr12:53611314 | C | G | 69 | a0001c0001t0001g0106 a0001c0001t0001g0167 a0001c0001t0001g0168 others(66): Show |
69 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-10293G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611314 | |||||||
| chr12:53611328 | G | A | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-10307C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611328 | |||||||
| chr12:53611452 | A | AAAAC | 90 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(87): Show |
90 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-21-10435_-21-1043 others(8): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611452 | |||||||
| chr12:53611558 | A | G | 1 | a0001c0001t0015g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21-10537T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611558 | |||||||
| chr12:53611711 | C | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA18959.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-21-10690G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611711 | |||||||
| chr12:53611945 | GAT | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-10926_-21-1092 others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611945 | |||||||
| chr12:53611949 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-10928A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53611949 | |||||||
| chr12:53612100 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-11079G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612100 | |||||||
| chr12:53612116 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-21-11095G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612116 | |||||||
| chr12:53612385 | C | G | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21-11364G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612385 | |||||||
| chr12:53612392 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-11371A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612392 | |||||||
| chr12:53612518 | C | T | 5 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0306 others(2): Show |
5 | HG00544.hp1 HG00673.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-11497G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612518 | |||||||
| chr12:53612741 | C | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0041 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-21-11720G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612741 | |||||||
| chr12:53612786 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21-11765G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612786 | |||||||
| chr12:53612872 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-11851G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612872 | |||||||
| chr12:53612880 | T | G | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-21-11859A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612880 | |||||||
| chr12:53612918 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG02145.hp1 HG02970.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-11897G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53612918 | |||||||
| chr12:53613005 | A | C | 1 | a0001c0001t0021g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-21-11984T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613005 | |||||||
| chr12:53613040 | T | A | 86 | a0001c0001t0001g0057 a0001c0001t0001g0237 a0001c0001t0001g0238 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-21-12019A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613040 | |||||||
| chr12:53613196 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-21-12175A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613196 | |||||||
| chr12:53613255 | T | TAAAAC | 256 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(253): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-21-12235_-21-1223 others(9): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613255 | |||||||
| chr12:53613339 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-21-12318G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53613339 | |||||||
| chr12:53614432 | G | A | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22+11847C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614432 | |||||||
| chr12:53614574 | G | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22+11705C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614574 | |||||||
| chr12:53614593 | A | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+11686T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614593 | |||||||
| chr12:53614843 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-22+11436C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614843 | |||||||
| chr12:53614955 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG02145.hp1 HG02970.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+11324G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53614955 | |||||||
| chr12:53615046 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01175.hp2 HG01515.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+11233G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615046 | |||||||
| chr12:53615064 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-22+11215C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615064 | |||||||
| chr12:53615154 | C | A | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+11125G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615154 | |||||||
| chr12:53615154 | C | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+11125G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615154 | |||||||
| chr12:53615310 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-22+10969C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615310 | |||||||
| chr12:53615315 | C | T | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22+10964G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615315 | |||||||
| chr12:53615611 | C | T | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22+10668G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615611 | |||||||
| chr12:53615777 | G | A | 3 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0145 |
3 | NA18947.hp1 NA18965.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-22+10502C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53615777 | |||||||
| chr12:53616087 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-22+10192G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616087 | |||||||
| chr12:53616193 | T | A | 78 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(75): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22+10086A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616193 | |||||||
| chr12:53616337 | G | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+9942C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616337 | |||||||
| chr12:53616415 | G | T | 6 | a0001c0001t0001g0155 a0001c0001t0002g0147 a0001c0001t0002g0148 others(3): Show |
6 | HG02698.hp2 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+9864C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616415 | |||||||
| chr12:53616572 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-22+9707T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616572 | |||||||
| chr12:53616761 | A | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+9518T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616761 | |||||||
| chr12:53616763 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0003g0221 |
2 | HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-22+9516A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616763 | |||||||
| chr12:53616783 | G | A | 28 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(25): Show |
28 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+9496C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616783 | |||||||
| chr12:53616894 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-22+9385C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616894 | |||||||
| chr12:53616914 | C | T | 1 | a0001c0002t0001g0324 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-22+9365G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616914 | |||||||
| chr12:53616945 | C | CA | 57 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-22+9333dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53616945 | |||||||
| chr12:53617082 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+9197G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617082 | |||||||
| chr12:53617124 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-22+9155C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617124 | |||||||
| chr12:53617143 | C | T | 1 | a0001c0001t0003g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-22+9136G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617143 | |||||||
| chr12:53617252 | G | C | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-22+9027C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617252 | |||||||
| chr12:53617414 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-22+8865C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617414 | |||||||
| chr12:53617636 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22+8643T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617636 | |||||||
| chr12:53617703 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0297 |
3 | HG00140.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-22+8576G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617703 | |||||||
| chr12:53617804 | G | T | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22+8475C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617804 | |||||||
| chr12:53617889 | C | CA | 97 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-22+8389dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | |||||||
| chr12:53617889 | CA | C | 18 | a0001c0001t0001g0062 a0001c0001t0001g0149 a0001c0001t0001g0150 others(15): Show |
18 | HG02145.hp1 HG02683.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22+8389delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | |||||||
| chr12:53617889 | CAAAA | C | 43 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-22+8386_-22+8389d others(6): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617889 | |||||||
| chr12:53617945 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-22+8334T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53617945 | |||||||
| chr12:53618221 | A | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-22+8058T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618221 | |||||||
| chr12:53618380 | T | C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01167.hp1 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-22+7899A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618380 | |||||||
| chr12:53618426 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-22+7853C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618426 | |||||||
| chr12:53618577 | TAA | T | 10 | a0001c0001t0004g0025 a0001c0001t0004g0160 a0001c0001t0004g0161 others(7): Show |
10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+7700_-22+7701d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618577 | |||||||
| chr12:53618702 | A | ATT | 87 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-22+7575_-22+7576d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618702 | |||||||
| chr12:53618703 | TTG | T | 18 | a0001c0001t0001g0102 a0001c0001t0001g0149 a0001c0001t0001g0150 others(15): Show |
18 | HG01884.hp1 HG02145.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22+7574_-22+7575d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618703 | |||||||
| chr12:53618717 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-22+7562C>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618717 | |||||||
| chr12:53618845 | C | T | 10 | a0001c0001t0004g0025 a0001c0001t0004g0160 a0001c0001t0004g0161 others(7): Show |
10 | HG02074.hp1 NA18946.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+7434G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618845 | |||||||
| chr12:53618935 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0153 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+7344G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53618935 | |||||||
| chr12:53619292 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0138 |
2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-22+6987G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619292 | |||||||
| chr12:53619359 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-22+6920C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619359 | |||||||
| chr12:53619419 | A | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | NA18994.hp2 NA19002.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-22+6860T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619419 | |||||||
| chr12:53619480 | C | A | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6799G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619480 | |||||||
| chr12:53619486 | C | CA | 89 | a0001c0001t0001g0015 a0001c0001t0001g0099 a0001c0001t0001g0102 others(86): Show |
89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-22+6792dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619486 | |||||||
| chr12:53619486 | C | CAA | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
17 | HG01433.hp1 HG02074.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6791_-22+6792d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619486 | |||||||
| chr12:53619570 | T | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22+6709A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619570 | |||||||
| chr12:53619577 | C | T | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+6702G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619577 | |||||||
| chr12:53619594 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22+6685G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619594 | |||||||
| chr12:53619668 | T | C | 183 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(180): Show |
183 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-22+6611A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619668 | |||||||
| chr12:53619673 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-22+6606T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53619673 | |||||||
| chr12:53620347 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-22+5932G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620347 | |||||||
| chr12:53620377 | C | A | 1 | a0001c0001t0016g0308 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-22+5902G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620377 | |||||||
| chr12:53620500 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22+5779G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620500 | |||||||
| chr12:53620575 | C | CA | 94 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-22+5703dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | |||||||
| chr12:53620575 | C | CAA | 9 | a0001c0001t0001g0297 a0001c0001t0002g0026 a0001c0001t0002g0133 others(6): Show |
9 | HG00140.hp1 HG01175.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+5702_-22+5703d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | |||||||
| chr12:53620575 | CA | C | 68 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0038 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-22+5703delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620575 | |||||||
| chr12:53620621 | T | C | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+5658A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620621 | |||||||
| chr12:53620735 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-22+5544G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620735 | |||||||
| chr12:53620813 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-22+5466G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620813 | |||||||
| chr12:53620863 | G | GA | 102 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-22+5415dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53620863 | |||||||
| chr12:53621055 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-22+5224T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621055 | |||||||
| chr12:53621313 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-22+4966G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621313 | |||||||
| chr12:53621452 | A | G | 262 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(259): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-22+4827T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621452 | |||||||
| chr12:53621475 | TA | T | 17 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
17 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+4803delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621475 | |||||||
| chr12:53621627 | C | CA | 21 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(18): Show |
21 | HG01175.hp1 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+4651dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621627 | |||||||
| chr12:53621652 | G | A | 1 | a0001c0001t0025g0315 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-22+4627C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621652 | |||||||
| chr12:53621707 | T | C | 1 | a0001c0001t0026g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-22+4572A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621707 | |||||||
| chr12:53621721 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+4558C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621721 | |||||||
| chr12:53621730 | A | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+4549T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621730 | |||||||
| chr12:53621758 | C | T | 44 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+4521G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621758 | |||||||
| chr12:53621766 | G | A | 1 | a0001c0001t0007g0137 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-22+4513C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621766 | |||||||
| chr12:53621786 | C | T | 1 | a0001c0001t0009g0042 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-22+4493G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621786 | |||||||
| chr12:53621788 | C | CA | 34 | a0001c0001t0001g0015 a0001c0001t0001g0098 a0001c0001t0001g0099 others(31): Show |
34 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+4490dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | |||||||
| chr12:53621788 | CA | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
61 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-22+4490delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | |||||||
| chr12:53621788 | CAA | C | 40 | a0001c0001t0001g0190 a0001c0001t0002g0001 a0001c0001t0002g0022 others(37): Show |
40 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-22+4489_-22+4490d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | |||||||
| chr12:53621788 | CAAA | C | 34 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(31): Show |
34 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.-22+4488_-22+4490d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53621788 | |||||||
| chr12:53622226 | C | T | 1 | a0001c0001t0029g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-22+4053G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622226 | |||||||
| chr12:53622304 | AAAT | A | 296 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-22+3972_-22+3974d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622304 | |||||||
| chr12:53622304 | AAATAATA others(2): Show |
A | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+3966_-22+3974d others(11): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622304 | |||||||
| chr12:53622529 | G | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+3750C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622529 | |||||||
| chr12:53622652 | C | CA | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0102 others(14): Show |
17 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+3626dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | |||||||
| chr12:53622652 | C | CAA | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+3625_-22+3626d others(4): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | |||||||
| chr12:53622652 | CA | C | 45 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+3626delT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | |||||||
| chr12:53622652 | CAAA | C | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(13): Show |
16 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22+3624_-22+3626d others(5): Show |
ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622652 | |||||||
| chr12:53622663 | A | G | 44 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+3616T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622663 | |||||||
| chr12:53622669 | AT | A | 77 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(74): Show |
77 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-22+3609delA | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622669 | |||||||
| chr12:53622670 | T | A | 1 | a0001c0001t0002g0040 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-22+3609A>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622670 | |||||||
| chr12:53622784 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-22+3495C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622784 | |||||||
| chr12:53622809 | C | CA | 5 | a0001c0001t0006g0141 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | NA18947.hp1 NA18965.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+3469dupT | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622809 | |||||||
| chr12:53622948 | C | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+3331G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53622948 | |||||||
| chr12:53623000 | T | C | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+3279A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623000 | |||||||
| chr12:53623032 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-22+3247C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623032 | |||||||
| chr12:53623077 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-22+3202G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623077 | |||||||
| chr12:53623099 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-22+3180G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623099 | |||||||
| chr12:53623276 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22+3003T>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623276 | |||||||
| chr12:53623537 | T | G | 44 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2742A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623537 | |||||||
| chr12:53623781 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0014g0030 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-22+2498G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623781 | |||||||
| chr12:53623827 | G | A | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+2452C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623827 | |||||||
| chr12:53623828 | T | C | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02145.hp1 HG02698.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+2451A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623828 | |||||||
| chr12:53623863 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(34): Show |
37 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22+2416C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623863 | |||||||
| chr12:53623891 | G | A | 44 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(41): Show |
44 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2388C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53623891 | |||||||
| chr12:53624095 | A | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-22+2184T>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624095 | |||||||
| chr12:53624241 | G | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-22+2038C>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624241 | |||||||
| chr12:53624366 | T | C | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1913A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624366 | |||||||
| chr12:53624864 | C | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
2 | HG02135.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-22+1415G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53624864 | |||||||
| chr12:53625022 | C | A | 85 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-22+1257G>T | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625022 | |||||||
| chr12:53625147 | T | C | 2 | a0001c0001t0003g0322 a0001c0001t0003g0323 |
2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-22+1132A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625147 | |||||||
| chr12:53625161 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-22+1118G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625161 | |||||||
| chr12:53625172 | A | G | 1 | a0001c0001t0004g0025 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-22+1107T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625172 | |||||||
| chr12:53625455 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(11): Show |
14 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22+824G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625455 | |||||||
| chr12:53625458 | T | C | 4 | a0001c0002t0001g0324 a0001c0002t0001g0325 a0001c0002t0001g0326 others(1): Show |
4 | NA18962.hp1 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+821A>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625458 | |||||||
| chr12:53625691 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | NA18941.hp1 NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-22+588T>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625691 | |||||||
| chr12:53625793 | T | G | 1 | a0001c0001t0001g0328 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-22+486A>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625793 | |||||||
| chr12:53625834 | C | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0021 |
2 | HG02135.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-22+445G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625834 | |||||||
| chr12:53625937 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-22+342G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53625937 | |||||||
| chr12:53626056 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
17 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-22+223G>A | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626056 | |||||||
| chr12:53626130 | C | G | 1 | a0001c0001t0002g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-22+149G>C | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626130 | |||||||
| chr12:53626142 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-22+137C>G | ATF7 | ENSG00000170653.19 | transcript | ENST00000420353.7 | protein_coding | 1/11 | chr12 | 53626142 |