Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6910 |
| ensemblid | ENSG00000089225.20 |
| hgncid | 11604 |
| symbol | TBX5 |
| name | T-box transcription factor 5 |
| refseq_nuc | NM_181486.4 |
| refseq_prot | NP_852259.1 |
| ensembl_nuc | ENST00000405440.7 |
| ensembl_prot | ENSP00000384152.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 114353911 |
| end | 114406144 |
| strand | - |
| ver | v1.2 |
| region | chr12:114353911-114406144 |
| region5000 | chr12:114348911-114411144 |
| regionname0 | TBX5_chr12_114353911_114406144 |
| regionname5000 | TBX5_chr12_114348911_114411144 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 518 | 382 | 86 | 77 | 153 | 16 | 48 | 115 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0002 | 0/0 | 518 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0003 | 0/0 | 518 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0004 | 0/0 | 518 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0005 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0006 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| a0007 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | MADAD others(513): Show |
chr12 | 114348911 | 114411144 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1554 | 360 | 69 | 72 | 153 | 16 | 48 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0001c0002 | 0/0 | 1554 | 15 | 11 | 4 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0001c0003 | 0/0 | 1554 | 5 | 5 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0001c0006 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0001c0009 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0002c0005 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0003c0004 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0004c0008 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0005c0010 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0006c0011 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 | ||
| a0007c0007 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | ATGGC others(1549): Show |
chr12 | 114348911 | 114411144 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3732 | 125 | 29 | 22 | 49 | 9 | 16 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0002 | 0/1 | 3732 | 51 | 2 | 10 | 29 | 0 | 9 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0003 | 0/0 | 3732 | 42 | 0 | 0 | 41 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0004 | 1/0 | 3733 | 33 | 4 | 5 | 6 | 4 | 13 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0005 | 0/0 | 3733 | 24 | 1 | 11 | 12 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0006 | 0/0 | 3732 | 16 | 5 | 8 | 3 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0007 | 0/0 | 3733 | 12 | 9 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0008 | 0/0 | 3732 | 7 | 0 | 3 | 0 | 1 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0009 | 0/0 | 3733 | 5 | 1 | 2 | 0 | 1 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0010 | 0/0 | 3732 | 5 | 0 | 0 | 5 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0011 | 0/0 | 3732 | 4 | 0 | 1 | 0 | 0 | 3 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0012 | 0/0 | 3732 | 4 | 3 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0013 | 0/0 | 3732 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0014 | 0/0 | 3732 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0015 | 0/0 | 3732 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0016 | 0/0 | 3736 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3731): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0018 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0020 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0021 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0022 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0023 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0024 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0025 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0026 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0027 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0028 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0029 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0031 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0032 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0033 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0034 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0035 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3729): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0036 | 0/0 | 3732 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0037 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0038 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3739): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0039 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0040 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0041 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0042 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3731): Show |
chr12 | 114348911 | 114411144 |
| a0001c0001t0044 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3729): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0001 | 0/0 | 3732 | 7 | 6 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0002 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0004 | 0/0 | 3733 | 2 | 1 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0008 | 0/0 | 3732 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0017 | 0/0 | 3736 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3731): Show |
chr12 | 114348911 | 114411144 |
| a0001c0002t0043 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3731): Show |
chr12 | 114348911 | 114411144 |
| a0001c0003t0001 | 0/0 | 3732 | 5 | 5 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0006t0019 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0001c0009t0001 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0002c0005t0001 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0002c0005t0006 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0003c0004t0001 | 0/0 | 3732 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0004c0008t0030 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3728): Show |
chr12 | 114348911 | 114411144 |
| a0005c0010t0001 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0006c0011t0002 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| a0007c0007t0002 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | AGTAC others(3727): Show |
chr12 | 114348911 | 114411144 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0345 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0011g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0014g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0016g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0018g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0020g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0021g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0023g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0024g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0025g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0026g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0027g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0028g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0029g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0031g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0032g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0033g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0034g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0035g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0036g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0037g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0038g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0039g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0040g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0041g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0042g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0001t0044g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0017g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0017g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0002t0043g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0006t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0001c0009t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0002c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0002c0005t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0003c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0004c0008t0030g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0005c0010t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0006c0011t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| a0007c0007t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0025 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0114 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0327 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0322 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0115 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0113 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0188 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0348 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0321 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01099 | hp2 | a0001 | c0009 | t0001 | g0292 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0044 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01109 | hp1 | a0001 | c0001 | t0029 | g0340 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0142 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01168 | hp1 | a0001 | c0002 | t0008 | g0118 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01168 | hp2 | a0001 | c0001 | t0039 | g0359 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01169 | hp1 | a0001 | c0002 | t0008 | g0117 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01192 | hp1 | a0001 | c0001 | t0020 | g0024 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0306 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0299 | AMR | PUR | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0346 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0298 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0273 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0178 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01496 | hp2 | a0001 | c0001 | t0021 | g0019 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0336 | EUR | IBS | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01884 | hp1 | a0001 | c0001 | t0034 | g0286 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0039 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01928 | hp1 | a0001 | c0001 | t0044 | g0366 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0128 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01978 | hp1 | a0004 | c0008 | t0030 | g0318 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02015 | hp1 | a0001 | c0001 | t0040 | g0360 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02027 | hp1 | a0001 | c0001 | t0023 | g0041 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02055 | hp2 | a0005 | c0010 | t0001 | g0111 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0082 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0135 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02165 | hp1 | a0001 | c0001 | t0038 | g0234 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | CDX | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02257 | hp1 | a0001 | c0002 | t0017 | g0364 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02300 | hp1 | a0001 | c0001 | t0041 | g0361 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0307 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0297 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0149 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02683 | hp2 | a0001 | c0001 | t0011 | g0049 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0079 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0353 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02809 | hp1 | a0001 | c0001 | t0032 | g0088 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0143 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0017 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02965 | hp2 | a0002 | c0005 | t0001 | g0089 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02976 | hp1 | a0001 | c0001 | t0028 | g0194 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02976 | hp2 | a0002 | c0005 | t0006 | g0036 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0048 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0304 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0017 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0293 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03139 | hp2 | a0001 | c0002 | t0017 | g0365 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0080 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0095 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03209 | hp2 | a0001 | c0006 | t0019 | g0038 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0325 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0320 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03486 | hp2 | a0006 | c0011 | t0002 | g0311 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0081 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03540 | hp2 | a0001 | c0001 | t0025 | g0267 | AFR | GWD | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0042 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0302 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0027 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0099 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0100 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03927 | hp1 | a0001 | c0001 | t0036 | g0324 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0169 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0333 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0043 | SAS | STU | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0287 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18906 | hp1 | a0001 | c0002 | t0043 | g0363 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18949 | hp1 | a0001 | c0001 | t0024 | g0259 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18949 | hp2 | a0001 | c0001 | t0033 | g0261 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0244 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18973 | hp1 | a0007 | c0007 | t0002 | g0214 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0167 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18986 | hp1 | a0001 | c0001 | t0037 | g0062 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18988 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0252 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18991 | hp1 | a0001 | c0001 | t0031 | g0275 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0313 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0289 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19089 | hp1 | a0001 | c0001 | t0013 | g0032 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA19091 | hp2 | a0003 | c0004 | t0001 | g0166 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0037 | AFR | ASW | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0332 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | GIH | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | GIH | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0154 | AMR | CLM | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02109 | hp1 | a0001 | c0001 | t0042 | g0362 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0145 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0288 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0055 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0083 | AFR | MSL | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| HG06807 | hp2 | a0001 | c0001 | t0035 | g0278 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | USA | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | LWK | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0181 | REF | REF | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0345 | REF | REF | TBX5_chr12_114348911_114411144 | TBX5 | chr12 | 114348911 | 114411144 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114355855 | C | T | 1 | a0002 | 2 | HG02965.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1234G>A | p.Val412Ile | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1789/3733 | 1234/1557 | 412/518 | chr12 | 114355855 | |||
| chr12:114355938 | G | A | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1151C>T | p.Ala384Val | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1706/3733 | 1151/1557 | 384/518 | chr12 | 114355938 | |||
| chr12:114366356 | C | T | 1 | a0003 | 2 | NA18979.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.791G>A | p.Arg264Lys | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/9 | 1346/3733 | 791/1557 | 264/518 | chr12 | 114366356 | |||
| chr12:114385502 | C | A | 1 | a0007 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.729G>T | p.Glu243Asp | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/9 | 1284/3733 | 729/1557 | 243/518 | chr12 | 114385502 | |||
| chr12:114399544 | C | A | 1 | a0004 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.331G>T | p.Asp111Tyr | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/9 | 886/3733 | 331/1557 | 111/518 | chr12 | 114399544 | |||
| chr12:114403844 | C | A | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.55G>T | p.Ala19Ser | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/9 | 610/3733 | 55/1557 | 19/518 | chr12 | 114403844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114355808 | G | A | 2 | a0001c0003 a0001c0009 |
6 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
synonymous_variant | LOW | c.1281C>T | p.Ser427Ser | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1836/3733 | 1281/1557 | 427/518 | chr12 | 114355808 | |||
| chr12:114394786 | A | G | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.618T>C | p.Phe206Phe | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/9 | 1173/3733 | 618/1557 | 206/518 | chr12 | 114394786 | |||
| chr12:114399566 | G | A | 3 | a0001c0002 a0001c0009 a0005c0010 |
17 | HG01081.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
synonymous_variant | LOW | c.309C>T | p.Leu103Leu | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/9 | 864/3733 | 309/1557 | 103/518 | chr12 | 114399566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114354146 | GA | G | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*1385delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1385 | chr12 | 114354146 | ||||||
| chr12:114354152 | A | G | 1 | a0001c0001t0020 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1380 | chr12 | 114354152 | ||||||
| chr12:114354159 | C | A | 1 | a0001c0001t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1373 | chr12 | 114354159 | ||||||
| chr12:114354196 | GA | G | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0022 |
7 | HG01167.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1335delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1335 | chr12 | 114354196 | ||||||
| chr12:114354204 | C | CA | 5 | a0001c0001t0018 a0001c0001t0026 a0001c0001t0035 others(2): Show |
5 | HG01928.hp1 HG01978.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1327dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1327 | chr12 | 114354204 | ||||||
| chr12:114354431 | T | C | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 1101 | chr12 | 114354431 | ||||||
| chr12:114354696 | T | G | 1 | a0001c0001t0031 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 836 | chr12 | 114354696 | ||||||
| chr12:114354720 | G | A | 2 | a0001c0001t0015 a0001c0001t0022 |
3 | HG01884.hp2 HG02723.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*812C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 812 | chr12 | 114354720 | ||||||
| chr12:114354749 | G | A | 1 | a0001c0001t0036 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 783 | chr12 | 114354749 | ||||||
| chr12:114354774 | G | GAATAAGA others(5): Show |
1 | a0001c0001t0038 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*757_*758insTGGGCT others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 757 | chr12 | 114354774 | ||||||
| chr12:114354793 | A | G | 1 | a0001c0001t0010 | 5 | NA18952.hp1 NA18954.hp2 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*739T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 739 | chr12 | 114354793 | ||||||
| chr12:114354850 | C | G | 1 | a0001c0001t0027 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 682 | chr12 | 114354850 | ||||||
| chr12:114354931 | C | T | 5 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0026 others(2): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*601G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 601 | chr12 | 114354931 | ||||||
| chr12:114354969 | C | T | 1 | a0001c0001t0033 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 563 | chr12 | 114354969 | ||||||
| chr12:114355052 | C | T | 1 | a0001c0001t0025 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 480 | chr12 | 114355052 | ||||||
| chr12:114355148 | A | G | 3 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0044 |
26 | HG00408.hp2 HG01081.hp1 HG01256.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*384T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 384 | chr12 | 114355148 | ||||||
| chr12:114355237 | A | G | 1 | a0001c0001t0024 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 295 | chr12 | 114355237 | ||||||
| chr12:114355388 | G | A | 1 | a0001c0001t0032 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 144 | chr12 | 114355388 | ||||||
| chr12:114355435 | C | T | 28 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(25): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*97G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 97 | chr12 | 114355435 | ||||||
| chr12:114355455 | T | C | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0002t0008 |
13 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 77 | chr12 | 114355455 | ||||||
| chr12:114355492 | T | C | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0037 others(1): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 40 | chr12 | 114355492 | ||||||
| chr12:114355503 | G | A | 1 | a0001c0001t0023 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 9/9 | 29 | chr12 | 114355503 | ||||||
| chr12:114405655 | C | A | 1 | a0001c0001t0039 | 1 | HG01168.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | chr12 | 114405655 | |||||||
| chr12:114405731 | G | A | 1 | a0001c0001t0040 | 1 | HG02015.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | chr12 | 114405731 | |||||||
| chr12:114405757 | G | C | 1 | a0001c0001t0041 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-168C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1859 | chr12 | 114405757 | ||||||
| chr12:114405788 | G | A | 1 | a0001c0001t0042 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-199C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1890 | chr12 | 114405788 | ||||||
| chr12:114405801 | C | T | 11 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(8): Show |
34 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-212G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 1903 | chr12 | 114405801 | ||||||
| chr12:114405941 | C | T | 2 | a0001c0001t0016 a0001c0001t0042 |
3 | HG02109.hp1 HG02922.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-352G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2043 | chr12 | 114405941 | ||||||
| chr12:114406061 | T | TCTCC | 4 | a0001c0001t0016 a0001c0001t0042 a0001c0002t0017 others(1): Show |
6 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-476_-473dupGGAG | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2164 | chr12 | 114406061 | ||||||
| chr12:114406103 | G | A | 1 | a0001c0001t0044 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-514C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/9 | 2205 | chr12 | 114406103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:114356252 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(279): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.983-146A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356252 | |||||||
| chr12:114356398 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(29): Show |
37 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.983-292A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356398 | |||||||
| chr12:114356446 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.983-340G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356446 | |||||||
| chr12:114356794 | C | G | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-688G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356794 | |||||||
| chr12:114356852 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.983-746C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356852 | |||||||
| chr12:114356990 | C | CGATG | 35 | a0001c0001t0001g0073 a0001c0001t0001g0101 a0001c0001t0001g0108 others(32): Show |
35 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.983-888_983-885dup others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114356990 | C | CGATGGAT others(1): Show |
8 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0022g0039 others(5): Show |
8 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.983-892_983-885dup others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114356990 | C | CGATGGAT others(5): Show |
3 | a0001c0003t0001g0124 a0001c0003t0001g0287 a0001c0003t0001g0288 |
3 | HG02280.hp2 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.983-896_983-885dup others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114356990 | C | CGATGGAT others(9): Show |
1 | a0001c0003t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.983-900_983-885dup others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114356990 | CGATG | C | 129 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(126): Show |
135 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.983-888_983-885del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114356990 | CGATGGAT others(1): Show |
C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
106 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.983-892_983-885del others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114356990 | |||||||
| chr12:114357028 | A | G | 56 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(53): Show |
61 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.983-922T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357028 | |||||||
| chr12:114357221 | G | A | 22 | a0001c0001t0005g0003 a0001c0001t0005g0008 a0001c0001t0005g0060 others(19): Show |
25 | HG00408.hp2 HG01081.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.983-1115C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357221 | |||||||
| chr12:114357264 | C | T | 1 | a0001c0001t0006g0020 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.983-1158G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357264 | |||||||
| chr12:114357314 | A | G | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.983-1208T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357314 | |||||||
| chr12:114357549 | G | A | 1 | a0001c0001t0010g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.983-1443C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357549 | |||||||
| chr12:114357586 | T | C | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.983-1480A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357586 | |||||||
| chr12:114357614 | T | C | 1 | a0001c0002t0004g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.983-1508A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357614 | |||||||
| chr12:114357638 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(235): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.983-1532C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357638 | |||||||
| chr12:114357740 | C | G | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-1634G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357740 | |||||||
| chr12:114357931 | C | T | 1 | a0001c0001t0009g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.983-1825G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357931 | |||||||
| chr12:114357965 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.983-1859A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114357965 | |||||||
| chr12:114358122 | G | A | 5 | a0001c0001t0003g0202 a0001c0001t0003g0206 a0001c0001t0003g0212 others(2): Show |
5 | HG02056.hp2 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.983-2016C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358122 | |||||||
| chr12:114358272 | C | T | 1 | a0001c0001t0011g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.983-2166G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358272 | |||||||
| chr12:114358479 | G | T | 54 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
59 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.983-2373C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358479 | |||||||
| chr12:114358545 | A | C | 1 | a0006c0011t0002g0311 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.983-2439T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358545 | |||||||
| chr12:114358582 | T | G | 54 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
59 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.983-2476A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358582 | |||||||
| chr12:114358777 | T | TTTTG | 84 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(81): Show |
88 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.983-2675_983-2672d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | |||||||
| chr12:114358777 | T | TTTTGTTT others(1): Show |
54 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.983-2679_983-2672d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | |||||||
| chr12:114358777 | T | TTTTGTTT others(5): Show |
4 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0002g0219 others(1): Show |
4 | HG04115.hp2 NA18991.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-2683_983-2672d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | |||||||
| chr12:114358777 | TTTTGTTT others(1): Show |
T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
107 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.983-2679_983-2672d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358777 | |||||||
| chr12:114358781 | G | T | 1 | a0001c0001t0035g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.983-2675C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358781 | |||||||
| chr12:114358854 | C | A | 5 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0026g0083 others(2): Show |
5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-2748G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358854 | |||||||
| chr12:114358883 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.983-2777A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358883 | |||||||
| chr12:114358897 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG01515.hp1 HG02040.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-2791G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114358897 | |||||||
| chr12:114359136 | C | T | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.983-3030G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359136 | |||||||
| chr12:114359254 | G | C | 1 | a0001c0001t0040g0360 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.983-3148C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359254 | |||||||
| chr12:114359288 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.983-3182C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359288 | |||||||
| chr12:114359501 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(185): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.983-3395T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359501 | |||||||
| chr12:114359542 | A | G | 10 | a0001c0001t0007g0054 a0001c0001t0007g0074 a0001c0001t0007g0125 others(7): Show |
10 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3436T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359542 | |||||||
| chr12:114359624 | C | A | 1 | a0001c0001t0001g0352 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.983-3518G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359624 | |||||||
| chr12:114359756 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.983-3650C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359756 | |||||||
| chr12:114359760 | G | A | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-3654C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359760 | |||||||
| chr12:114359809 | T | C | 54 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
59 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.983-3703A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359809 | |||||||
| chr12:114359878 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0024g0259 |
2 | NA18949.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.983-3772T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359878 | |||||||
| chr12:114359922 | C | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0010 others(49): Show |
57 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.983-3816G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114359922 | |||||||
| chr12:114360060 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(94): Show |
108 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.983-3954A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360060 | |||||||
| chr12:114360068 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.983-3962T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360068 | |||||||
| chr12:114360124 | G | A | 6 | a0001c0003t0001g0124 a0001c0003t0001g0222 a0001c0003t0001g0287 others(3): Show |
6 | HG01099.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-4018C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360124 | |||||||
| chr12:114360194 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0338 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.983-4088C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360194 | |||||||
| chr12:114360277 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.983-4171G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360277 | |||||||
| chr12:114360284 | C | T | 2 | a0001c0001t0001g0342 a0001c0001t0006g0030 |
2 | HG00738.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.983-4178G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360284 | |||||||
| chr12:114360419 | G | A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0317 a0001c0001t0001g0355 others(1): Show |
4 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-4313C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360419 | |||||||
| chr12:114360570 | G | A | 1 | a0001c0001t0041g0361 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.983-4464C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360570 | |||||||
| chr12:114360668 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.983-4562C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360668 | |||||||
| chr12:114360679 | G | A | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.983-4573C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360679 | |||||||
| chr12:114360723 | A | G | 1 | a0001c0001t0004g0174 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.983-4617T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360723 | |||||||
| chr12:114360768 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0215 |
2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.983-4662C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360768 | |||||||
| chr12:114360840 | C | T | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.983-4734G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114360840 | |||||||
| chr12:114361049 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.983-4943G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361049 | |||||||
| chr12:114361191 | A | G | 1 | a0001c0001t0024g0259 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.982+4974T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361191 | |||||||
| chr12:114361235 | G | A | 1 | a0001c0001t0025g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.982+4930C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361235 | |||||||
| chr12:114361415 | T | C | 1 | a0003c0004t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.982+4750A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361415 | |||||||
| chr12:114361452 | A | G | 53 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(50): Show |
56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+4713T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361452 | |||||||
| chr12:114361599 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0148 a0001c0001t0016g0017 |
4 | HG02922.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+4566G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361599 | |||||||
| chr12:114361647 | C | T | 2 | a0001c0001t0007g0145 a0001c0001t0007g0348 |
2 | HG00639.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.982+4518G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361647 | |||||||
| chr12:114361651 | T | C | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+4514A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361651 | |||||||
| chr12:114361761 | C | A | 4 | a0001c0001t0003g0071 a0001c0001t0003g0227 a0001c0001t0003g0230 others(1): Show |
4 | HG00438.hp2 HG02135.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+4404G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361761 | |||||||
| chr12:114361883 | G | T | 4 | a0001c0001t0002g0126 a0001c0001t0002g0168 a0001c0001t0002g0200 others(1): Show |
4 | HG01123.hp1 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+4282C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361883 | |||||||
| chr12:114361986 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.982+4179G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114361986 | |||||||
| chr12:114362058 | A | T | 39 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0097 others(36): Show |
39 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.982+4107T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362058 | |||||||
| chr12:114362121 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.982+4044G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362121 | |||||||
| chr12:114362169 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.982+3996C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362169 | |||||||
| chr12:114362315 | T | C | 28 | a0001c0001t0001g0272 a0001c0001t0002g0057 a0001c0001t0002g0069 others(25): Show |
28 | HG00408.hp1 HG01123.hp1 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.982+3850A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362315 | |||||||
| chr12:114362575 | C | T | 1 | a0001c0001t0028g0194 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982+3590G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362575 | |||||||
| chr12:114362584 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+3581G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362584 | |||||||
| chr12:114362731 | C | T | 24 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(21): Show |
25 | HG01081.hp2 HG01943.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.982+3434G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362731 | |||||||
| chr12:114362749 | C | G | 1 | a0001c0001t0008g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.982+3416G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362749 | |||||||
| chr12:114362833 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 |
5 | HG01109.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.982+3332A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362833 | |||||||
| chr12:114362858 | T | A | 1 | a0001c0001t0009g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.982+3307A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114362858 | |||||||
| chr12:114363008 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.982+3157T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363008 | |||||||
| chr12:114363022 | C | T | 15 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(12): Show |
15 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.982+3143G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363022 | |||||||
| chr12:114363206 | C | T | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.982+2959G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363206 | |||||||
| chr12:114363420 | A | G | 53 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(50): Show |
56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+2745T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363420 | |||||||
| chr12:114363492 | C | G | 1 | a0001c0001t0003g0107 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.982+2673G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363492 | |||||||
| chr12:114363494 | T | C | 1 | a0001c0001t0003g0107 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.982+2671A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363494 | |||||||
| chr12:114363529 | C | T | 51 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(48): Show |
54 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.982+2636G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363529 | |||||||
| chr12:114363588 | T | G | 1 | a0001c0001t0002g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.982+2577A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363588 | |||||||
| chr12:114363670 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.982+2495C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363670 | |||||||
| chr12:114363728 | C | A | 2 | a0001c0001t0035g0278 a0001c0002t0004g0055 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.982+2437G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363728 | |||||||
| chr12:114363805 | T | C | 43 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0092 others(40): Show |
43 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.982+2360A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363805 | |||||||
| chr12:114363930 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982+2235C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363930 | |||||||
| chr12:114363967 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(173): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.982+2198C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114363967 | |||||||
| chr12:114364259 | G | A | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+1906C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364259 | |||||||
| chr12:114364290 | C | G | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+1875G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364290 | |||||||
| chr12:114364333 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(226): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.982+1832T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364333 | |||||||
| chr12:114364382 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+1783A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364382 | |||||||
| chr12:114364438 | C | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.982+1727G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364438 | |||||||
| chr12:114364468 | A | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+1697T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364468 | |||||||
| chr12:114364510 | T | G | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+1655A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364510 | |||||||
| chr12:114364525 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.982+1640A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364525 | |||||||
| chr12:114364556 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(224): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.982+1609T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364556 | |||||||
| chr12:114364568 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.982+1597A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364568 | |||||||
| chr12:114364584 | C | T | 3 | a0001c0001t0011g0042 a0001c0001t0011g0043 a0001c0001t0011g0049 |
3 | HG02683.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.982+1581G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364584 | |||||||
| chr12:114364753 | G | A | 1 | a0001c0001t0003g0296 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.982+1412C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364753 | |||||||
| chr12:114364928 | C | T | 15 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(12): Show |
15 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.982+1237G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364928 | |||||||
| chr12:114364955 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(173): Show |
188 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.982+1210C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114364955 | |||||||
| chr12:114365065 | GA | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(169): Show |
184 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.982+1099delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365065 | |||||||
| chr12:114365150 | C | T | 8 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(5): Show |
8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.982+1015G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365150 | |||||||
| chr12:114365167 | G | C | 1 | a0001c0001t0006g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.982+998C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365167 | |||||||
| chr12:114365168 | A | ATG | 7 | a0001c0001t0002g0203 a0001c0001t0004g0159 a0001c0001t0007g0054 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+995_982+996dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | |||||||
| chr12:114365168 | ATG | A | 43 | a0001c0001t0001g0221 a0001c0001t0003g0007 a0001c0001t0003g0011 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.982+995_982+996del others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | |||||||
| chr12:114365168 | ATGTG | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.982+993_982+996del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | |||||||
| chr12:114365168 | ATGTGTG | A | 63 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0073 others(60): Show |
64 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.982+991_982+996del others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365168 | |||||||
| chr12:114365198 | G | C | 51 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(48): Show |
54 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.982+967C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365198 | |||||||
| chr12:114365209 | GA | G | 53 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(50): Show |
56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.982+955delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365209 | |||||||
| chr12:114365539 | A | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0305 a0001c0001t0001g0312 others(4): Show |
7 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.982+626T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365539 | |||||||
| chr12:114365622 | A | T | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+543T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365622 | |||||||
| chr12:114365646 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.982+519G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365646 | |||||||
| chr12:114365759 | G | C | 1 | a0001c0001t0004g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.982+406C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365759 | |||||||
| chr12:114365829 | C | CA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(80): Show |
91 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.982+335dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | |||||||
| chr12:114365829 | C | CAA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0058 others(52): Show |
59 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.982+334_982+335dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | |||||||
| chr12:114365829 | CA | C | 64 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(61): Show |
67 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.982+335delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | |||||||
| chr12:114365829 | CAAAAAAA | C | 40 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0097 others(37): Show |
40 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.982+329_982+335del others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365829 | |||||||
| chr12:114365888 | C | T | 2 | a0001c0001t0003g0229 a0001c0001t0003g0231 |
2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.982+277G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114365888 | |||||||
| chr12:114366021 | T | A | 1 | a0001c0001t0014g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.982+144A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366021 | |||||||
| chr12:114366085 | C | G | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.982+80G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366085 | |||||||
| chr12:114366122 | A | G | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | NA18968.hp2 NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.982+43T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366122 | |||||||
| chr12:114366149 | G | A | 1 | a0001c0001t0008g0154 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.982+16C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 8/8 | chr12 | 114366149 | |||||||
| chr12:114366417 | C | A | 1 | a0001c0002t0004g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-26G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366417 | |||||||
| chr12:114366775 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(98): Show |
112 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.756-384T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366775 | |||||||
| chr12:114366881 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.756-490A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114366881 | |||||||
| chr12:114367093 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.756-702C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367093 | |||||||
| chr12:114367113 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.756-722C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367113 | |||||||
| chr12:114367252 | G | GGAAAGAA others(12): Show |
148 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(145): Show |
152 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.756-862_756-861ins others(19): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367252 | |||||||
| chr12:114367257 | G | GAAAGAAA others(13): Show |
94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(91): Show |
105 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.756-867_756-866ins others(20): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367257 | |||||||
| chr12:114367278 | T | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(313): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.756-887A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367278 | |||||||
| chr12:114367278 | T | G | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-887A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367278 | |||||||
| chr12:114367391 | G | C | 14 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0099 others(11): Show |
14 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-1000C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367391 | |||||||
| chr12:114367397 | T | A | 1 | a0001c0001t0027g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.756-1006A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367397 | |||||||
| chr12:114367400 | G | A | 1 | a0001c0001t0027g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.756-1009C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367400 | |||||||
| chr12:114367401 | C | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1010G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367401 | |||||||
| chr12:114367402 | A | G | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1011T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367402 | |||||||
| chr12:114367447 | G | A | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(11): Show |
14 | HG01943.hp2 HG02258.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-1056C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367447 | |||||||
| chr12:114367463 | C | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-1072G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367463 | |||||||
| chr12:114367738 | C | T | 1 | a0001c0001t0003g0096 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.756-1347G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367738 | |||||||
| chr12:114367788 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.756-1397A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367788 | |||||||
| chr12:114367820 | C | T | 3 | a0001c0001t0001g0342 a0001c0001t0006g0030 a0004c0008t0030g0318 |
3 | HG00738.hp1 HG01978.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.756-1429G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367820 | |||||||
| chr12:114367843 | T | C | 133 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(130): Show |
137 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.756-1452A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114367843 | |||||||
| chr12:114368014 | G | A | 1 | a0001c0003t0001g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.756-1623C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368014 | |||||||
| chr12:114368030 | A | G | 5 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0026g0083 others(2): Show |
5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-1639T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368030 | |||||||
| chr12:114368036 | A | C | 1 | a0001c0001t0039g0359 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.756-1645T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368036 | |||||||
| chr12:114368042 | T | C | 1 | a0001c0001t0005g0127 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.756-1651A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368042 | |||||||
| chr12:114368155 | G | A | 53 | a0001c0001t0001g0317 a0001c0001t0002g0004 a0001c0001t0002g0009 others(50): Show |
58 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.756-1764C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368155 | |||||||
| chr12:114368189 | T | A | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-1798A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368189 | |||||||
| chr12:114368196 | G | A | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.756-1805C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368196 | |||||||
| chr12:114368332 | C | CTCAA | 36 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(33): Show |
37 | HG00639.hp2 HG01081.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.756-1945_756-1942d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | |||||||
| chr12:114368332 | CTCAA | C | 3 | a0001c0001t0001g0279 a0001c0001t0018g0037 a0001c0001t0042g0362 |
3 | HG02109.hp1 HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.756-1945_756-1942d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | |||||||
| chr12:114368332 | CTCAATCA others(1): Show |
C | 5 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0026g0083 others(2): Show |
5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-1949_756-1942d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368332 | |||||||
| chr12:114368344 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.756-1953T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368344 | |||||||
| chr12:114368411 | G | A | 13 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0099 others(10): Show |
13 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.756-2020C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368411 | |||||||
| chr12:114368411 | G | T | 5 | a0001c0001t0007g0054 a0001c0001t0007g0125 a0001c0001t0007g0297 others(2): Show |
5 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-2020C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368411 | |||||||
| chr12:114368429 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-2038G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368429 | |||||||
| chr12:114368645 | T | G | 45 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(42): Show |
48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-2254A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368645 | |||||||
| chr12:114368716 | C | T | 11 | a0001c0001t0007g0054 a0001c0001t0007g0074 a0001c0001t0007g0125 others(8): Show |
11 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-2325G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368716 | |||||||
| chr12:114368730 | T | C | 16 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(13): Show |
17 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.756-2339A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368730 | |||||||
| chr12:114368736 | C | T | 53 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(50): Show |
56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.756-2345G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114368736 | |||||||
| chr12:114369079 | G | A | 1 | a0001c0002t0004g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-2688C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369079 | |||||||
| chr12:114369080 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(229): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.756-2689T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369080 | |||||||
| chr12:114369230 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(228): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.756-2839C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369230 | |||||||
| chr12:114369358 | T | A | 1 | a0006c0011t0002g0311 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.756-2967A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369358 | |||||||
| chr12:114369418 | T | A | 1 | a0001c0003t0001g0222 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.756-3027A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369418 | |||||||
| chr12:114369421 | C | T | 12 | a0001c0001t0007g0054 a0001c0001t0007g0074 a0001c0001t0007g0095 others(9): Show |
12 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.756-3030G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369421 | |||||||
| chr12:114369462 | G | A | 1 | a0001c0001t0022g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.756-3071C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369462 | |||||||
| chr12:114369498 | G | A | 1 | a0001c0002t0001g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.756-3107C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369498 | |||||||
| chr12:114369573 | A | C | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3182T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369573 | |||||||
| chr12:114369583 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0312 a0001c0001t0001g0338 |
3 | HG00741.hp1 HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.756-3192C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369583 | |||||||
| chr12:114369689 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0006g0026 |
2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.756-3298T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369689 | |||||||
| chr12:114369821 | A | G | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-3430T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369821 | |||||||
| chr12:114369850 | A | AG | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(229): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.756-3460_756-3459i others(3): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369850 | |||||||
| chr12:114369874 | G | A | 1 | a0001c0002t0004g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.756-3483C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369874 | |||||||
| chr12:114369995 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0195 others(5): Show |
11 | HG02027.hp2 NA18946.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.756-3604G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114369995 | |||||||
| chr12:114370060 | G | C | 1 | a0001c0001t0009g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.756-3669C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370060 | |||||||
| chr12:114370195 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.756-3804G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370195 | |||||||
| chr12:114370231 | C | CAGAAA | 13 | a0001c0001t0002g0215 a0001c0001t0004g0332 a0001c0001t0004g0353 others(10): Show |
13 | HG02071.hp1 HG02738.hp2 HG04228.hp1 others(10): Show |
intron_variant | MODIFIER | c.756-3845_756-3841d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(3): Show |
19 | a0001c0001t0002g0203 a0001c0001t0002g0210 a0001c0001t0002g0217 others(16): Show |
21 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.756-3850_756-3841d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(8): Show |
22 | a0001c0001t0002g0057 a0001c0001t0002g0069 a0001c0001t0002g0201 others(19): Show |
22 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.756-3855_756-3841d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(13): Show |
9 | a0001c0001t0002g0168 a0001c0001t0002g0200 a0001c0001t0002g0208 others(6): Show |
9 | HG01123.hp1 HG02027.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.756-3860_756-3841d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(18): Show |
4 | a0001c0001t0002g0126 a0001c0001t0002g0282 a0001c0001t0002g0300 others(1): Show |
4 | HG01993.hp1 HG02300.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-3865_756-3841d others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(23): Show |
1 | a0001c0001t0040g0360 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.756-3870_756-3841d others(32): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | C | CAGAAAAG others(28): Show |
1 | a0001c0001t0001g0314 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.756-3875_756-3841d others(37): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370231 | CAGAAAAG others(13): Show |
C | 42 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(39): Show |
45 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.756-3860_756-3841d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370231 | |||||||
| chr12:114370248 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
102 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.756-3857C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370248 | |||||||
| chr12:114370259 | A | C | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3868T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370259 | |||||||
| chr12:114370265 | AAAGAAAA others(20): Show |
A | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3901_756-3875d others(29): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370265 | |||||||
| chr12:114370267 | AGAAAAGA others(18): Show |
A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
103 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.756-3901_756-3877d others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370267 | |||||||
| chr12:114370272 | AGAAAAGA others(13): Show |
A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0319 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG01516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3901_756-3882d others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370272 | |||||||
| chr12:114370274 | AAAAGAAA others(7): Show |
A | 4 | a0001c0001t0004g0085 a0001c0001t0004g0163 a0001c0001t0004g0225 others(1): Show |
4 | HG01361.hp1 HG02965.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3897_756-3884d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370274 | |||||||
| chr12:114370277 | AGAAAAGA others(8): Show |
A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0002t0001g0116 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3901_756-3887d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370277 | |||||||
| chr12:114370278 | GA | G | 3 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 |
3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-3888delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370278 | |||||||
| chr12:114370279 | AAAAGAAA others(2): Show |
A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0099 a0001c0001t0004g0161 others(4): Show |
7 | HG02615.hp2 HG03017.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.756-3897_756-3889d others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370279 | |||||||
| chr12:114370281 | A | AAGAAAAG others(43): Show |
2 | a0001c0001t0015g0079 a0001c0001t0015g0080 |
2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.756-3940_756-3891d others(52): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370281 | |||||||
| chr12:114370282 | AGAAAAGA others(3): Show |
A | 18 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0109 others(15): Show |
18 | HG00544.hp1 HG00741.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.756-3901_756-3892d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370282 | |||||||
| chr12:114370284 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.756-3893T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370284 | |||||||
| chr12:114370284 | AAAAG | A | 3 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 |
3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-3897_756-3894d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370284 | |||||||
| chr12:114370287 | A | G | 1 | a0001c0001t0012g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-3896T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370287 | |||||||
| chr12:114370287 | AGAAAG | A | 18 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0241 others(15): Show |
18 | HG00735.hp1 HG01243.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.756-3901_756-3897d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370287 | |||||||
| chr12:114370288 | G | A | 1 | a0001c0001t0012g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.756-3897C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | C | 49 | a0001c0001t0001g0221 a0001c0001t0003g0007 a0001c0001t0003g0011 others(46): Show |
52 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.756-3897C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GA | 23 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0220 others(20): Show |
23 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.756-3898dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGA | 6 | a0001c0001t0001g0091 a0001c0001t0004g0159 a0001c0001t0042g0362 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(3): Show |
1 | a0001c0006t0019g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.756-3898_756-3897i others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(4): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0272 a0001c0001t0001g0291 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(8): Show |
2 | a0001c0001t0034g0286 a0001c0002t0004g0055 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(13): Show |
1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(18): Show |
3 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0021g0019 |
3 | HG01496.hp2 NA18946.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.756-3898_756-3897i others(27): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(13): Show |
4 | a0001c0001t0002g0098 a0001c0001t0002g0129 a0001c0001t0002g0193 others(1): Show |
4 | HG01070.hp2 HG01192.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(8): Show |
9 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0112 others(6): Show |
10 | HG01069.hp1 HG01168.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(13): Show |
1 | a0001c0001t0002g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.756-3898_756-3897i others(22): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(3): Show |
4 | a0001c0001t0002g0274 a0001c0001t0002g0330 a0001c0001t0002g0358 others(1): Show |
4 | HG00733.hp2 HG03654.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-3898_756-3897i others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAAGAA others(8): Show |
1 | a0001c0001t0002g0263 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.756-3898_756-3897i others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370288 | G | GAAAGA | 6 | a0001c0001t0001g0317 a0001c0001t0002g0010 a0001c0001t0002g0014 others(3): Show |
8 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-3902_756-3898d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370288 | |||||||
| chr12:114370289 | AAAGAAAA others(16): Show |
A | 1 | a0001c0001t0001g0053 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.756-3921_756-3899d others(25): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370289 | |||||||
| chr12:114370292 | G | A | 18 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
19 | HG00558.hp2 HG00642.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.756-3901C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370292 | |||||||
| chr12:114370293 | A | AAAAC | 29 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0091 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.756-3903_756-3902i others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | |||||||
| chr12:114370293 | A | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
167 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.756-3902T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | |||||||
| chr12:114370293 | A | G | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-3902T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370293 | |||||||
| chr12:114370311 | A | G | 13 | a0001c0001t0008g0100 a0001c0001t0008g0154 a0001c0001t0008g0178 others(10): Show |
14 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-3920T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370311 | |||||||
| chr12:114370312 | G | A | 13 | a0001c0001t0008g0100 a0001c0001t0008g0154 a0001c0001t0008g0178 others(10): Show |
14 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.756-3921C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370312 | |||||||
| chr12:114370312 | GAAAGA | G | 5 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0026g0083 others(2): Show |
5 | HG00140.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-3926_756-3922d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370312 | |||||||
| chr12:114370316 | G | A | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.756-3925C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370316 | |||||||
| chr12:114370317 | A | AAAAGAAA others(26): Show |
1 | a0001c0001t0018g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-3927_756-3926i others(35): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370317 | |||||||
| chr12:114370317 | A | G | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.756-3926T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370317 | |||||||
| chr12:114370528 | C | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-4137G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370528 | |||||||
| chr12:114370533 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0342 a0001c0001t0001g0355 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-4142T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370533 | |||||||
| chr12:114370627 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.756-4236C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370627 | |||||||
| chr12:114370638 | C | CCT | 78 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0097 others(75): Show |
81 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.756-4249_756-4248d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | |||||||
| chr12:114370638 | C | CCTCT | 43 | a0001c0001t0001g0053 a0001c0001t0001g0072 a0001c0001t0001g0076 others(40): Show |
44 | HG00558.hp2 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.756-4251_756-4248d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | |||||||
| chr12:114370638 | C | CCTCTCT | 4 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-4253_756-4248d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | |||||||
| chr12:114370638 | CCTCT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
99 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.756-4251_756-4248d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | |||||||
| chr12:114370638 | CCTCTCTC others(1): Show |
C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00733.hp1 HG01175.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-4255_756-4248d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370638 | |||||||
| chr12:114370741 | CT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
250 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.756-4351delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370741 | |||||||
| chr12:114370833 | G | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(283): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.756-4442C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370833 | |||||||
| chr12:114370894 | A | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0148 a0001c0001t0016g0017 |
4 | HG02922.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-4503T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370894 | |||||||
| chr12:114370918 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-4527G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370918 | |||||||
| chr12:114370979 | C | T | 53 | a0001c0001t0001g0317 a0001c0001t0002g0004 a0001c0001t0002g0009 others(50): Show |
58 | HG00408.hp1 HG00733.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.756-4588G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114370979 | |||||||
| chr12:114371125 | C | T | 1 | a0001c0001t0005g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.756-4734G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371125 | |||||||
| chr12:114371322 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.756-4931T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371322 | |||||||
| chr12:114371328 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 |
5 | HG01109.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.756-4937C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371328 | |||||||
| chr12:114371386 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.756-4995G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371386 | |||||||
| chr12:114371485 | C | A | 3 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 |
3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.756-5094G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371485 | |||||||
| chr12:114371587 | G | GT | 51 | a0001c0001t0001g0076 a0001c0001t0001g0108 a0001c0001t0001g0157 others(48): Show |
54 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.756-5197dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | |||||||
| chr12:114371587 | G | GTT | 6 | a0001c0001t0003g0071 a0001c0001t0003g0138 a0001c0001t0003g0202 others(3): Show |
6 | HG02135.hp1 HG02135.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.756-5198_756-5197d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | |||||||
| chr12:114371587 | GT | G | 69 | a0001c0001t0001g0050 a0001c0001t0001g0072 a0001c0001t0001g0172 others(66): Show |
74 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-5197delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371587 | |||||||
| chr12:114371589 | T | G | 1 | a0001c0001t0001g0005 | 3 | HG02486.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.756-5198A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371589 | |||||||
| chr12:114371606 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.756-5215A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371606 | |||||||
| chr12:114371664 | TG | T | 68 | a0001c0001t0001g0221 a0001c0001t0002g0207 a0001c0001t0002g0213 others(65): Show |
72 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.756-5274delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371664 | |||||||
| chr12:114371668 | G | C | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-5277C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371668 | |||||||
| chr12:114371669 | C | A | 1 | a0001c0001t0003g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756-5278G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371669 | |||||||
| chr12:114371844 | G | C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0001c0001t0001g0150 others(6): Show |
10 | HG01081.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.756-5453C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371844 | |||||||
| chr12:114371878 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
97 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.756-5487C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371878 | |||||||
| chr12:114371888 | G | C | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-5497C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114371888 | |||||||
| chr12:114372043 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.756-5652C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372043 | |||||||
| chr12:114372165 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.756-5774G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372165 | |||||||
| chr12:114372322 | T | C | 2 | a0001c0001t0005g0104 a0001c0001t0005g0188 |
2 | HG00408.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.756-5931A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372322 | |||||||
| chr12:114372417 | G | T | 7 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 others(4): Show |
7 | HG01167.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.756-6026C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372417 | |||||||
| chr12:114372479 | A | AT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0053 others(72): Show |
78 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.756-6089dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372479 | |||||||
| chr12:114372479 | AT | A | 68 | a0001c0001t0001g0221 a0001c0001t0002g0207 a0001c0001t0002g0213 others(65): Show |
72 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.756-6089delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372479 | |||||||
| chr12:114372591 | C | T | 61 | a0001c0001t0001g0221 a0001c0001t0002g0207 a0001c0001t0002g0213 others(58): Show |
65 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.756-6200G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372591 | |||||||
| chr12:114372628 | A | C | 1 | a0001c0001t0008g0169 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.756-6237T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372628 | |||||||
| chr12:114372819 | C | T | 1 | a0001c0002t0001g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.756-6428G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372819 | |||||||
| chr12:114372832 | G | C | 70 | a0001c0001t0001g0221 a0001c0001t0002g0207 a0001c0001t0002g0213 others(67): Show |
74 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-6441C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372832 | |||||||
| chr12:114372851 | A | G | 70 | a0001c0001t0001g0221 a0001c0001t0002g0207 a0001c0001t0002g0213 others(67): Show |
74 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.756-6460T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372851 | |||||||
| chr12:114372949 | A | T | 16 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(13): Show |
17 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.756-6558T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372949 | |||||||
| chr12:114372969 | AATATAT | A | 3 | a0001c0001t0003g0065 a0001c0001t0003g0296 a0001c0001t0038g0234 |
3 | HG02155.hp2 HG02165.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.756-6584_756-6579d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372969 | |||||||
| chr12:114372969 | AATATATA others(3): Show |
A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.756-6588_756-6579d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372969 | |||||||
| chr12:114372971 | TATATATA others(1): Show |
T | 38 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(35): Show |
41 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.756-6588_756-6581d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372971 | |||||||
| chr12:114372971 | TATATATA others(5): Show |
T | 2 | a0001c0001t0003g0138 a0001c0001t0003g0255 |
2 | HG00438.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.756-6592_756-6581d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372971 | |||||||
| chr12:114372977 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG00733.hp1 HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.756-6586A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372977 | |||||||
| chr12:114372981 | T | C | 45 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(42): Show |
48 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-6590A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | T | TAC | 19 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0291 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.756-6592_756-6591d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | T | TACAC | 3 | a0001c0001t0007g0125 a0001c0001t0007g0299 a0001c0001t0009g0025 |
3 | HG00099.hp1 HG01243.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.756-6594_756-6591d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TAC | T | 28 | a0001c0001t0001g0072 a0001c0001t0001g0097 a0001c0001t0001g0121 others(25): Show |
28 | HG00735.hp1 HG00741.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.756-6592_756-6591d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TACAC | T | 75 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0172 others(72): Show |
79 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.756-6594_756-6591d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TACACAC | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(66): Show |
73 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.756-6596_756-6591d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TACACACA others(1): Show |
T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(32): Show |
43 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.756-6598_756-6591d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0303 a0001c0001t0001g0323 others(4): Show |
7 | HG01943.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-6600_756-6591d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114372981 | TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0103 a0001c0001t0004g0084 a0001c0001t0004g0085 |
3 | HG02015.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.756-6602_756-6591d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114372981 | |||||||
| chr12:114373136 | A | G | 1 | a0001c0001t0003g0229 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.756-6745T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373136 | |||||||
| chr12:114373164 | G | C | 11 | a0001c0001t0007g0054 a0001c0001t0007g0074 a0001c0001t0007g0125 others(8): Show |
11 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-6773C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373164 | |||||||
| chr12:114373237 | A | G | 43 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0092 others(40): Show |
43 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.756-6846T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373237 | |||||||
| chr12:114373247 | C | T | 52 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-6856G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373247 | |||||||
| chr12:114373318 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-6927G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373318 | |||||||
| chr12:114373515 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0241 a0001c0001t0006g0031 others(1): Show |
4 | NA18963.hp2 NA18975.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-7124T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373515 | |||||||
| chr12:114373545 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.756-7154C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373545 | |||||||
| chr12:114373550 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(317): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.756-7159A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373550 | |||||||
| chr12:114373590 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-7199G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373590 | |||||||
| chr12:114373612 | T | C | 52 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7221A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373612 | |||||||
| chr12:114373615 | T | A | 52 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7224A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373615 | |||||||
| chr12:114373708 | C | T | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-7317G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373708 | |||||||
| chr12:114373815 | C | T | 52 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7424G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373815 | |||||||
| chr12:114373849 | T | C | 52 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.756-7458A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373849 | |||||||
| chr12:114373934 | G | C | 1 | a0001c0001t0001g0335 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.756-7543C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114373934 | |||||||
| chr12:114374045 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-7654A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374045 | |||||||
| chr12:114374089 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.756-7698C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374089 | |||||||
| chr12:114374385 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.756-7994T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374385 | |||||||
| chr12:114374429 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.756-8038C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374429 | |||||||
| chr12:114374582 | C | T | 45 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(42): Show |
48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.756-8191G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374582 | |||||||
| chr12:114374821 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
104 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.756-8430A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374821 | |||||||
| chr12:114374897 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.756-8506C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114374897 | |||||||
| chr12:114375287 | G | T | 43 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0012 others(40): Show |
46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.756-8896C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375287 | |||||||
| chr12:114375303 | T | C | 53 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(50): Show |
56 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.756-8912A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375303 | |||||||
| chr12:114375460 | T | C | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-9069A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375460 | |||||||
| chr12:114375508 | T | C | 43 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0092 others(40): Show |
43 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.756-9117A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375508 | |||||||
| chr12:114375706 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.756-9315C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375706 | |||||||
| chr12:114375731 | G | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.756-9340C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375731 | |||||||
| chr12:114375911 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.756-9520C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375911 | |||||||
| chr12:114375975 | G | T | 2 | a0001c0001t0001g0279 a0001c0001t0035g0278 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+9501C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375975 | |||||||
| chr12:114375984 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.755+9492C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114375984 | |||||||
| chr12:114376125 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755+9351A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376125 | |||||||
| chr12:114376188 | C | T | 8 | a0001c0001t0004g0099 a0001c0001t0004g0159 a0001c0001t0004g0161 others(5): Show |
8 | HG01981.hp1 HG03017.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.755+9288G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376188 | |||||||
| chr12:114376261 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9215C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376261 | |||||||
| chr12:114376262 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9214A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376262 | |||||||
| chr12:114376265 | GTA | G | 104 | a0001c0001t0001g0172 a0001c0001t0001g0279 a0001c0001t0001g0317 others(101): Show |
112 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.755+9209_755+9210d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376265 | |||||||
| chr12:114376267 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9209T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376267 | |||||||
| chr12:114376272 | T | TAC | 14 | a0001c0001t0001g0290 a0001c0001t0001g0315 a0001c0001t0001g0326 others(11): Show |
14 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.755+9203_755+9204i others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376272 | |||||||
| chr12:114376274 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(132): Show |
143 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.755+9202A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376274 | |||||||
| chr12:114376274 | TACAC | T | 24 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+9198_755+9201d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376274 | |||||||
| chr12:114376276 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.755+9200G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376276 | |||||||
| chr12:114376344 | C | G | 3 | a0001c0001t0001g0279 a0001c0001t0035g0278 a0001c0002t0004g0055 |
3 | HG02280.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+9132G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376344 | |||||||
| chr12:114376481 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.755+8995A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376481 | |||||||
| chr12:114376564 | G | C | 3 | a0001c0001t0001g0279 a0001c0001t0035g0278 a0001c0002t0004g0055 |
3 | HG02280.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.755+8912C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376564 | |||||||
| chr12:114376594 | GTT | G | 13 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0099 others(10): Show |
13 | HG01361.hp1 HG01981.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.755+8880_755+8881d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376594 | |||||||
| chr12:114376611 | G | A | 23 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 others(20): Show |
24 | HG01081.hp2 HG01943.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.755+8865C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376611 | |||||||
| chr12:114376720 | G | A | 2 | a0001c0001t0007g0146 a0001c0001t0007g0151 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.755+8756C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376720 | |||||||
| chr12:114376966 | T | C | 1 | a0001c0001t0020g0024 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.755+8510A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114376966 | |||||||
| chr12:114377256 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755+8220A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377256 | |||||||
| chr12:114377404 | T | A | 1 | a0001c0001t0002g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.755+8072A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377404 | |||||||
| chr12:114377459 | C | T | 24 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+8017G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377459 | |||||||
| chr12:114377512 | A | T | 8 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(5): Show |
8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7964T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377512 | |||||||
| chr12:114377513 | A | C | 8 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(5): Show |
8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7963T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377513 | |||||||
| chr12:114377514 | A | C | 8 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(5): Show |
8 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+7962T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377514 | |||||||
| chr12:114377539 | G | T | 24 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+7937C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377539 | |||||||
| chr12:114377559 | C | CT | 6 | a0001c0001t0001g0268 a0001c0001t0005g0133 a0001c0001t0006g0047 others(3): Show |
6 | HG00639.hp1 HG01074.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+7916dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377559 | |||||||
| chr12:114377559 | CT | C | 35 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0001g0314 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.755+7916delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377559 | |||||||
| chr12:114377564 | T | C | 45 | a0001c0001t0002g0207 a0001c0001t0002g0213 a0001c0001t0003g0007 others(42): Show |
48 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.755+7912A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377564 | |||||||
| chr12:114377617 | C | T | 25 | a0001c0001t0001g0221 a0001c0001t0002g0195 a0001c0001t0008g0100 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.755+7859G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377617 | |||||||
| chr12:114377618 | G | A | 3 | a0001c0001t0015g0079 a0001c0001t0015g0080 a0001c0001t0022g0039 |
3 | HG01884.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.755+7858C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377618 | |||||||
| chr12:114377670 | CA | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0305 a0001c0001t0001g0312 others(4): Show |
7 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+7805delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377670 | |||||||
| chr12:114377718 | G | A | 8 | a0001c0001t0004g0099 a0001c0001t0004g0159 a0001c0001t0004g0161 others(5): Show |
8 | HG01981.hp1 HG03017.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.755+7758C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377718 | |||||||
| chr12:114377719 | A | T | 60 | a0001c0001t0001g0108 a0001c0001t0001g0172 a0001c0001t0001g0279 others(57): Show |
65 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.755+7757T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377719 | |||||||
| chr12:114377720 | C | G | 24 | a0001c0001t0001g0221 a0001c0001t0008g0100 a0001c0001t0008g0154 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.755+7756G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377720 | |||||||
| chr12:114377951 | G | A | 7 | a0001c0001t0014g0082 a0001c0001t0014g0327 a0001c0001t0018g0037 others(4): Show |
7 | HG00140.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.755+7525C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114377951 | |||||||
| chr12:114378012 | C | A | 1 | a0001c0001t0004g0325 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.755+7464G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378012 | |||||||
| chr12:114378244 | G | A | 2 | a0001c0001t0003g0229 a0001c0001t0003g0231 |
2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.755+7232C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378244 | |||||||
| chr12:114378261 | C | T | 2 | a0001c0001t0034g0286 a0001c0006t0019g0038 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.755+7215G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378261 | |||||||
| chr12:114378555 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
167 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.755+6921G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378555 | |||||||
| chr12:114378558 | A | T | 58 | a0001c0001t0001g0108 a0001c0001t0001g0172 a0001c0001t0001g0317 others(55): Show |
63 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.755+6918T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378558 | |||||||
| chr12:114378631 | G | GTTTGT | 46 | a0001c0001t0001g0266 a0001c0001t0002g0207 a0001c0001t0002g0213 others(43): Show |
49 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.755+6840_755+6844d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378631 | |||||||
| chr12:114378743 | G | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(306): Show |
330 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.755+6733C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378743 | |||||||
| chr12:114378975 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.755+6501G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378975 | |||||||
| chr12:114378976 | G | A | 4 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 others(1): Show |
4 | HG01167.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+6500C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114378976 | |||||||
| chr12:114379015 | A | T | 59 | a0001c0001t0001g0097 a0001c0001t0001g0172 a0001c0001t0001g0279 others(56): Show |
64 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.755+6461T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379015 | |||||||
| chr12:114379044 | C | T | 2 | a0001c0003t0001g0124 a0001c0003t0001g0287 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.755+6432G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379044 | |||||||
| chr12:114379132 | C | T | 4 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 others(1): Show |
4 | HG01167.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+6344G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379132 | |||||||
| chr12:114379198 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.755+6278G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379198 | |||||||
| chr12:114379201 | A | T | 1 | a0001c0001t0010g0137 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.755+6275T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379201 | |||||||
| chr12:114379257 | A | G | 2 | a0001c0001t0001g0355 a0001c0001t0039g0359 |
2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.755+6219T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379257 | |||||||
| chr12:114379261 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.755+6215G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379261 | |||||||
| chr12:114379310 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.755+6166T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379310 | |||||||
| chr12:114379440 | C | T | 1 | a0001c0001t0007g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+6036G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379440 | |||||||
| chr12:114379515 | T | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(262): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.755+5961A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379515 | |||||||
| chr12:114379527 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0103 a0001c0001t0001g0106 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.755+5949C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379527 | |||||||
| chr12:114379703 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0317 |
2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.755+5773C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379703 | |||||||
| chr12:114379724 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(224): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.755+5752A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379724 | |||||||
| chr12:114379785 | G | A | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755+5691C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114379785 | |||||||
| chr12:114380009 | T | C | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+5467A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380009 | |||||||
| chr12:114380064 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0241 a0001c0001t0010g0152 others(3): Show |
6 | NA18952.hp1 NA18954.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+5412C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380064 | |||||||
| chr12:114380448 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(58): Show |
68 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.755+5028G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380448 | |||||||
| chr12:114380570 | T | C | 49 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(46): Show |
50 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.755+4906A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380570 | |||||||
| chr12:114380622 | G | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0034g0286 |
3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+4854C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380622 | |||||||
| chr12:114380656 | AG | A | 106 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(103): Show |
113 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.755+4819delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380656 | |||||||
| chr12:114380664 | T | A | 1 | a0001c0001t0010g0152 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.755+4812A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380664 | |||||||
| chr12:114380676 | A | G | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4800T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380676 | |||||||
| chr12:114380697 | G | A | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+4779C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380697 | |||||||
| chr12:114380850 | T | TA | 101 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(98): Show |
108 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.755+4625dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | |||||||
| chr12:114380850 | T | TAA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0103 a0001c0001t0001g0160 others(62): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.755+4624_755+4625d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | |||||||
| chr12:114380850 | T | TAAA | 40 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0077 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.755+4623_755+4625d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | |||||||
| chr12:114380850 | TA | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0339 a0001c0001t0012g0081 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+4625delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380850 | |||||||
| chr12:114380851 | A | T | 1 | a0001c0001t0003g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.755+4625T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380851 | |||||||
| chr12:114380921 | AT | A | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+4554delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380921 | |||||||
| chr12:114380933 | A | T | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.755+4543T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380933 | |||||||
| chr12:114380997 | G | A | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4479C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114380997 | |||||||
| chr12:114381136 | G | A | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755+4340C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381136 | |||||||
| chr12:114381139 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.755+4337C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381139 | |||||||
| chr12:114381173 | C | T | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+4303G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381173 | |||||||
| chr12:114381174 | A | C | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+4302T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381174 | |||||||
| chr12:114381207 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.755+4269C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381207 | |||||||
| chr12:114381594 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0007g0054 a0001c0001t0007g0297 others(3): Show |
7 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+3882G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381594 | |||||||
| chr12:114381826 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.755+3650G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381826 | |||||||
| chr12:114381955 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0073 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.755+3521T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114381955 | |||||||
| chr12:114382052 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0103 a0001c0001t0001g0192 others(23): Show |
31 | HG00408.hp2 HG00544.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.755+3424A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382052 | |||||||
| chr12:114382182 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.755+3294A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382182 | |||||||
| chr12:114382294 | A | G | 1 | a0001c0001t0031g0275 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.755+3182T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382294 | |||||||
| chr12:114382301 | G | A | 1 | a0001c0001t0008g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.755+3175C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382301 | |||||||
| chr12:114382445 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.755+3031G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382445 | |||||||
| chr12:114382458 | G | T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0323 a0001c0001t0004g0159 others(4): Show |
7 | HG01943.hp1 HG02683.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+3018C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382458 | |||||||
| chr12:114382475 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0073 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.755+3001C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382475 | |||||||
| chr12:114382537 | G | A | 106 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(103): Show |
113 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.755+2939C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382537 | |||||||
| chr12:114382643 | G | A | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+2833C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382643 | |||||||
| chr12:114382655 | G | C | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.755+2821C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382655 | |||||||
| chr12:114382751 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.755+2725G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382751 | |||||||
| chr12:114382758 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.755+2718G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382758 | |||||||
| chr12:114382791 | C | T | 16 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0092 others(13): Show |
16 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.755+2685G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382791 | |||||||
| chr12:114382903 | G | A | 1 | a0001c0001t0007g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+2573C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382903 | |||||||
| chr12:114382977 | C | CA | 6 | a0001c0001t0001g0087 a0001c0001t0001g0253 a0001c0001t0002g0284 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+2498dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | |||||||
| chr12:114382977 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0073 others(102): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.755+2498delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | |||||||
| chr12:114382977 | CAA | C | 12 | a0001c0001t0001g0160 a0001c0001t0001g0220 a0001c0001t0001g0323 others(9): Show |
12 | HG01943.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.755+2497_755+2498d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382977 | |||||||
| chr12:114382994 | AAG | A | 85 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(82): Show |
92 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.755+2480_755+2481d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382994 | |||||||
| chr12:114382995 | AG | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0349 a0001c0001t0001g0351 others(1): Show |
4 | HG01175.hp2 HG02148.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+2480delC | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114382995 | |||||||
| chr12:114383007 | A | G | 1 | a0001c0001t0006g0028 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.755+2469T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383007 | |||||||
| chr12:114383016 | C | T | 9 | a0001c0001t0001g0248 a0001c0001t0003g0007 a0001c0001t0003g0011 others(6): Show |
11 | HG00673.hp1 NA18944.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.755+2460G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383016 | |||||||
| chr12:114383133 | G | A | 1 | a0001c0001t0024g0259 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.755+2343C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383133 | |||||||
| chr12:114383180 | T | G | 1 | a0001c0001t0004g0161 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.755+2296A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383180 | |||||||
| chr12:114383341 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.755+2135G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383341 | |||||||
| chr12:114383425 | A | G | 5 | a0001c0001t0002g0069 a0001c0001t0002g0236 a0001c0001t0002g0247 others(2): Show |
5 | HG00408.hp1 HG02129.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+2051T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383425 | |||||||
| chr12:114383466 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(238): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.755+2010T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383466 | |||||||
| chr12:114383508 | A | T | 1 | a0001c0001t0040g0360 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.755+1968T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383508 | |||||||
| chr12:114383580 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.755+1896C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383580 | |||||||
| chr12:114383635 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.755+1841A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383635 | |||||||
| chr12:114383646 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(206): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.755+1830G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383646 | |||||||
| chr12:114383892 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.755+1584G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383892 | |||||||
| chr12:114383899 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.755+1577A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114383899 | |||||||
| chr12:114384006 | G | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0233 |
2 | HG00438.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.755+1470C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384006 | |||||||
| chr12:114384063 | G | T | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+1413C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384063 | |||||||
| chr12:114384273 | GT | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(352): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.755+1202delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384273 | |||||||
| chr12:114384395 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.755+1081G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384395 | |||||||
| chr12:114384487 | C | T | 12 | a0001c0001t0001g0160 a0001c0001t0001g0220 a0001c0001t0001g0323 others(9): Show |
12 | HG01943.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.755+989G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384487 | |||||||
| chr12:114384592 | T | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0034g0286 |
3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+884A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384592 | |||||||
| chr12:114384714 | A | AAC | 13 | a0001c0001t0001g0005 a0001c0001t0001g0090 a0001c0001t0001g0091 others(10): Show |
16 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.755+760_755+761dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACAC | 6 | a0001c0001t0001g0269 a0001c0001t0003g0066 a0001c0001t0004g0085 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+756_755+761dup others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACACA others(1): Show |
30 | a0001c0001t0001g0013 a0001c0001t0001g0103 a0001c0001t0001g0268 others(27): Show |
33 | HG00408.hp2 HG00639.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.755+754_755+761dup others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACACA others(3): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0001t0001g0182 others(34): Show |
40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.755+752_755+761dup others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACACA others(5): Show |
10 | a0001c0001t0001g0170 a0001c0001t0001g0305 a0001c0001t0004g0084 others(7): Show |
10 | HG00280.hp2 HG01106.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.755+750_755+761dup others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACACA others(7): Show |
1 | a0001c0001t0004g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.755+748_755+761dup others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | AACACACA others(9): Show |
2 | a0001c0002t0017g0364 a0001c0002t0017g0365 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.755+746_755+761dup others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0342 a0001c0001t0013g0032 |
2 | HG04204.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.755+761_755+762ins others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | AAC | A | 30 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0266 others(27): Show |
31 | HG00438.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+760_755+761del others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384714 | AACAC | A | 5 | a0001c0001t0001g0246 a0001c0001t0001g0253 a0001c0001t0007g0125 others(2): Show |
5 | HG01884.hp2 HG02071.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.755+758_755+761del others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384714 | |||||||
| chr12:114384724 | CACACACA others(14): Show |
C | 18 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.755+731_755+751del others(21): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384724 | |||||||
| chr12:114384726 | CACACACA others(12): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.755+731_755+749del others(19): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384726 | |||||||
| chr12:114384745 | A | ACACACAA others(3): Show |
1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.755+730_755+731ins others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(3): Show |
9 | a0001c0001t0001g0350 a0001c0001t0002g0010 a0001c0001t0002g0057 others(6): Show |
10 | HG01168.hp1 HG02132.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(5): Show |
6 | a0001c0001t0001g0323 a0001c0001t0004g0159 a0001c0001t0004g0161 others(3): Show |
6 | HG02683.hp1 NA18966.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(5): Show |
64 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0097 others(61): Show |
68 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0072 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.755+730_755+731ins others(11): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(7): Show |
19 | a0001c0001t0001g0075 a0001c0001t0001g0155 a0001c0001t0001g0157 others(16): Show |
19 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+730_755+731ins others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384745 | A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0349 a0001c0001t0002g0219 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.755+730_755+731ins others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384745 | |||||||
| chr12:114384914 | T | C | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.755+562A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384914 | |||||||
| chr12:114384927 | G | A | 1 | a0002c0005t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755+549C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114384927 | |||||||
| chr12:114385091 | C | T | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.755+385G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385091 | |||||||
| chr12:114385104 | C | CA | 151 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0097 others(148): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.755+371dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385104 | |||||||
| chr12:114385104 | CA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(137): Show |
151 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.755+371delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385104 | |||||||
| chr12:114385127 | C | T | 1 | a0001c0001t0027g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.755+349G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385127 | |||||||
| chr12:114385284 | G | A | 97 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(94): Show |
104 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.755+192C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385284 | |||||||
| chr12:114385286 | C | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0034g0286 |
3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.755+190G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385286 | |||||||
| chr12:114385293 | C | T | 54 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(51): Show |
54 | HG01070.hp1 HG01123.hp1 HG01192.hp1 others(51): Show |
intron_variant | MODIFIER | c.755+183G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385293 | |||||||
| chr12:114385382 | G | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(43): Show |
47 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.755+94C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385382 | |||||||
| chr12:114385389 | G | A | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755+87C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385389 | |||||||
| chr12:114385435 | G | A | 6 | a0001c0001t0001g0123 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG00323.hp2 HG00438.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.755+41C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 7/8 | chr12 | 114385435 | |||||||
| chr12:114385664 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.664-97C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385664 | |||||||
| chr12:114385666 | C | G | 1 | a0001c0001t0012g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.664-99G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385666 | |||||||
| chr12:114385670 | G | A | 1 | a0001c0001t0003g0231 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.664-103C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385670 | |||||||
| chr12:114385712 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.664-145G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385712 | |||||||
| chr12:114385728 | A | G | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.664-161T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385728 | |||||||
| chr12:114385840 | C | CT | 97 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(94): Show |
103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.664-274dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385840 | |||||||
| chr12:114385840 | C | CTT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0103 others(94): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.664-275_664-274dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385840 | |||||||
| chr12:114385962 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(59): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.664-395C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114385962 | |||||||
| chr12:114386086 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0007g0054 a0001c0001t0007g0297 others(3): Show |
7 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-519C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386086 | |||||||
| chr12:114386127 | C | T | 4 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0282 others(1): Show |
4 | HG02027.hp1 NA18957.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-560G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386127 | |||||||
| chr12:114386943 | AT | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(174): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.664-1377delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386943 | |||||||
| chr12:114386945 | TTA | T | 24 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0092 others(21): Show |
24 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-1380_664-1379d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386945 | |||||||
| chr12:114386946 | T | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0323 a0001c0001t0004g0159 others(5): Show |
8 | HG01243.hp1 HG01943.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-1379A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386946 | |||||||
| chr12:114386977 | G | C | 1 | a0001c0001t0024g0259 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.664-1410C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386977 | |||||||
| chr12:114386983 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.664-1416T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114386983 | |||||||
| chr12:114387108 | A | G | 1 | a0001c0001t0005g0131 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.664-1541T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387108 | |||||||
| chr12:114387114 | A | C | 107 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(104): Show |
114 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.664-1547T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387114 | |||||||
| chr12:114387115 | A | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(210): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.664-1548T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387115 | |||||||
| chr12:114387123 | CAAAA | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0001g0276 others(8): Show |
12 | HG00735.hp1 HG00738.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-1560_664-1557d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387123 | |||||||
| chr12:114387124 | A | C | 2 | a0001c0001t0004g0084 a0001c0001t0004g0085 |
2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.664-1557T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387124 | |||||||
| chr12:114387205 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.664-1638G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387205 | |||||||
| chr12:114387216 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.664-1649A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387216 | |||||||
| chr12:114387236 | GC | G | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-1670delG | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387236 | |||||||
| chr12:114387490 | T | C | 1 | a0001c0001t0005g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.664-1923A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387490 | |||||||
| chr12:114387492 | G | A | 1 | a0001c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-1925C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387492 | |||||||
| chr12:114387524 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.664-1957A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387524 | |||||||
| chr12:114387532 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.664-1965C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387532 | |||||||
| chr12:114387574 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.664-2007G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387574 | |||||||
| chr12:114387614 | C | T | 5 | a0001c0001t0006g0020 a0001c0001t0006g0021 a0001c0001t0006g0022 others(2): Show |
5 | HG01070.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-2047G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387614 | |||||||
| chr12:114387680 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.664-2113C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387680 | |||||||
| chr12:114387839 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0086 others(7): Show |
10 | HG01109.hp2 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.664-2272G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387839 | |||||||
| chr12:114387899 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664-2332G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387899 | |||||||
| chr12:114387915 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-2348G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387915 | |||||||
| chr12:114387962 | G | A | 2 | a0001c0001t0002g0219 a0001c0001t0007g0095 |
2 | HG03209.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.664-2395C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114387962 | |||||||
| chr12:114388056 | C | T | 20 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
20 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-2489G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388056 | |||||||
| chr12:114388097 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.664-2530G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388097 | |||||||
| chr12:114388239 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.664-2672G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388239 | |||||||
| chr12:114388292 | G | C | 1 | a0001c0001t0010g0238 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.664-2725C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388292 | |||||||
| chr12:114388318 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-2751A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388318 | |||||||
| chr12:114388472 | A | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-2905T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388472 | |||||||
| chr12:114388473 | A | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-2906T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388473 | |||||||
| chr12:114388569 | C | G | 1 | a0001c0001t0039g0359 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.664-3002G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388569 | |||||||
| chr12:114388675 | C | CGT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0073 others(40): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.664-3110_664-3109d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | C | CGTGT | 19 | a0001c0001t0001g0103 a0001c0001t0001g0155 a0001c0001t0001g0157 others(16): Show |
19 | HG00140.hp2 HG00738.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.664-3112_664-3109d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | C | CGTGTGT | 5 | a0001c0001t0001g0158 a0001c0001t0001g0342 a0001c0001t0004g0171 others(2): Show |
5 | HG00733.hp1 HG01934.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-3114_664-3109d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(106): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.664-3110_664-3109d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGT | C | 56 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(53): Show |
58 | HG00408.hp2 HG00673.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.664-3112_664-3109d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGTGT | C | 35 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0090 others(32): Show |
36 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.664-3114_664-3109d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGTGTG others(1): Show |
C | 27 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0086 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.664-3116_664-3109d others(10): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGTGTG others(3): Show |
C | 8 | a0001c0001t0001g0279 a0001c0001t0004g0225 a0001c0001t0004g0346 others(5): Show |
8 | HG01257.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-3118_664-3109d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0003g0063 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.664-3122_664-3109d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388675 | CGTGTGTG others(9): Show |
C | 23 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(20): Show |
23 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-3124_664-3109d others(18): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388675 | |||||||
| chr12:114388739 | C | CT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.664-3173dupA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388739 | |||||||
| chr12:114388765 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.664-3198C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388765 | |||||||
| chr12:114388843 | C | T | 5 | a0001c0001t0001g0220 a0001c0001t0004g0225 a0001c0001t0042g0362 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-3276G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388843 | |||||||
| chr12:114388928 | T | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0323 others(5): Show |
8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-3361A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388928 | |||||||
| chr12:114388974 | G | A | 93 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(90): Show |
100 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.664-3407C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388974 | |||||||
| chr12:114388990 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.664-3423C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114388990 | |||||||
| chr12:114389082 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-3515T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389082 | |||||||
| chr12:114389220 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664-3653C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389220 | |||||||
| chr12:114389230 | A | C | 24 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.664-3663T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389230 | |||||||
| chr12:114389409 | T | C | 1 | a0001c0001t0014g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.664-3842A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389409 | |||||||
| chr12:114389450 | T | A | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664-3883A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389450 | |||||||
| chr12:114389520 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.664-3953T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389520 | |||||||
| chr12:114389521 | G | A | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.664-3954C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389521 | |||||||
| chr12:114389531 | G | A | 1 | a0001c0001t0010g0152 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.664-3964C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389531 | |||||||
| chr12:114389547 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.664-3980C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389547 | |||||||
| chr12:114389550 | C | A | 1 | a0001c0001t0001g0232 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.664-3983G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389550 | |||||||
| chr12:114389627 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(237): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.664-4060T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389627 | |||||||
| chr12:114389711 | G | A | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664-4144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389711 | |||||||
| chr12:114389729 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0014 |
3 | HG02257.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.664-4162C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389729 | |||||||
| chr12:114389753 | C | CA | 20 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0272 others(17): Show |
23 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.664-4187dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | C | CAAAAA | 7 | a0001c0001t0001g0158 a0001c0001t0002g0265 a0001c0001t0008g0100 others(4): Show |
7 | HG00280.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-4191_664-4187d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.664-4196_664-4187d others(12): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | C | CAAAAAAA others(168): Show |
1 | a0001c0001t0004g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.664-4187_664-4186i others(177): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CA | C | 25 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0148 others(22): Show |
26 | HG01070.hp2 HG01243.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.664-4187delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAA | C | 5 | a0001c0001t0003g0139 a0001c0001t0007g0297 a0001c0001t0007g0298 others(2): Show |
6 | HG01346.hp2 HG02015.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-4188_664-4187d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAA | C | 14 | a0001c0001t0001g0165 a0001c0001t0001g0248 a0001c0001t0001g0251 others(11): Show |
14 | HG02071.hp2 HG02129.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.664-4189_664-4187d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAA | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(41): Show |
50 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.664-4190_664-4187d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAA | C | 17 | a0001c0001t0001g0150 a0001c0001t0001g0235 a0001c0001t0001g0260 others(14): Show |
17 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-4191_664-4187d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAA | C | 63 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(60): Show |
64 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.664-4192_664-4187d others(8): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA | C | 11 | a0001c0001t0001g0141 a0001c0001t0001g0266 a0001c0001t0001g0323 others(8): Show |
11 | HG02683.hp1 HG03017.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.664-4193_664-4187d others(9): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0192 a0001c0001t0001g0355 a0001c0001t0002g0190 others(4): Show |
7 | HG01256.hp1 HG02056.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-4197_664-4187d others(13): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(5): Show |
C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0103 others(71): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.664-4198_664-4187d others(14): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0170 a0001c0001t0005g0127 |
2 | HG01081.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.664-4199_664-4187d others(15): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(7): Show |
C | 10 | a0001c0001t0006g0045 a0001c0001t0008g0154 a0001c0001t0008g0320 others(7): Show |
11 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-4200_664-4187d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(8): Show |
C | 17 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(14): Show |
17 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-4201_664-4187d others(17): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389753 | CAAAAAAA others(11): Show |
C | 5 | a0001c0001t0001g0005 a0001c0001t0006g0040 a0001c0002t0001g0015 others(2): Show |
8 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-4204_664-4187d others(20): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389753 | |||||||
| chr12:114389857 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.664-4290C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389857 | |||||||
| chr12:114389878 | C | T | 94 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(91): Show |
101 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.664-4311G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389878 | |||||||
| chr12:114389902 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0103 a0001c0001t0001g0170 others(57): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.664-4335T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389902 | |||||||
| chr12:114389931 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(59): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.664-4364G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389931 | |||||||
| chr12:114389932 | A | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(358): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.664-4365T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114389932 | |||||||
| chr12:114390184 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0034g0286 |
2 | HG01884.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.663+4557G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390184 | |||||||
| chr12:114390566 | C | T | 2 | a0001c0002t0008g0117 a0001c0002t0008g0118 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.663+4175G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390566 | |||||||
| chr12:114390809 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0323 others(5): Show |
8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+3932C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390809 | |||||||
| chr12:114390876 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.663+3865G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390876 | |||||||
| chr12:114390877 | G | A | 95 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(92): Show |
102 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.663+3864C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390877 | |||||||
| chr12:114390898 | T | C | 1 | a0001c0001t0006g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.663+3843A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390898 | |||||||
| chr12:114390971 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.663+3770C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114390971 | |||||||
| chr12:114391020 | T | C | 5 | a0001c0001t0001g0123 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG00323.hp2 HG00438.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+3721A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391020 | |||||||
| chr12:114391067 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.663+3674C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391067 | |||||||
| chr12:114391130 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.663+3611C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391130 | |||||||
| chr12:114391146 | C | T | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.663+3595G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391146 | |||||||
| chr12:114391158 | G | A | 1 | a0001c0001t0004g0161 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663+3583C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391158 | |||||||
| chr12:114391166 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0323 others(5): Show |
8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+3575T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391166 | |||||||
| chr12:114391216 | G | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0268 a0001c0001t0001g0269 others(20): Show |
24 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.663+3525C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391216 | |||||||
| chr12:114391390 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.663+3351C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391390 | |||||||
| chr12:114391414 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0007g0313 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+3327C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391414 | |||||||
| chr12:114391490 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.663+3251G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391490 | |||||||
| chr12:114391512 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0034g0286 |
3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.663+3229G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391512 | |||||||
| chr12:114391586 | G | T | 1 | a0001c0001t0037g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.663+3155C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391586 | |||||||
| chr12:114391882 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+2859G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114391882 | |||||||
| chr12:114392022 | A | G | 1 | a0001c0001t0003g0357 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.663+2719T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392022 | |||||||
| chr12:114392099 | G | A | 1 | a0001c0001t0007g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.663+2642C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392099 | |||||||
| chr12:114392109 | A | G | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.663+2632T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392109 | |||||||
| chr12:114392178 | TA | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(81): Show |
88 | HG00438.hp2 HG00673.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.663+2562delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | |||||||
| chr12:114392178 | TAA | T | 99 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(96): Show |
107 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.663+2561_663+2562d others(4): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | |||||||
| chr12:114392178 | TAAA | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(56): Show |
65 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.663+2560_663+2562d others(5): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | |||||||
| chr12:114392178 | TAAAA | T | 56 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0076 others(53): Show |
57 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.663+2559_663+2562d others(6): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | |||||||
| chr12:114392178 | TAAAAA | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0103 a0001c0001t0001g0170 others(54): Show |
62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.663+2558_663+2562d others(7): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392178 | |||||||
| chr12:114392340 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.663+2401T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392340 | |||||||
| chr12:114392353 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.663+2388A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392353 | |||||||
| chr12:114392475 | C | G | 2 | a0001c0002t0017g0364 a0001c0002t0017g0365 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+2266G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392475 | |||||||
| chr12:114392477 | A | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0034g0286 |
3 | HG01884.hp1 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.663+2264T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392477 | |||||||
| chr12:114392542 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(209): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.663+2199T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392542 | |||||||
| chr12:114392563 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(209): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.663+2178G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392563 | |||||||
| chr12:114392722 | AT | A | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.663+2018delA | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392722 | |||||||
| chr12:114392843 | G | A | 1 | a0001c0001t0004g0332 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.663+1898C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392843 | |||||||
| chr12:114392856 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.663+1885C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392856 | |||||||
| chr12:114392895 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(233): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.663+1846C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392895 | |||||||
| chr12:114392957 | G | A | 22 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0277 others(19): Show |
22 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.663+1784C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392957 | |||||||
| chr12:114392969 | C | G | 19 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.663+1772G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392969 | |||||||
| chr12:114392976 | T | C | 1 | a0001c0001t0038g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.663+1765A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392976 | |||||||
| chr12:114392999 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.663+1742A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114392999 | |||||||
| chr12:114393091 | G | A | 3 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0013g0032 |
3 | NA18963.hp2 NA19062.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.663+1650C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393091 | |||||||
| chr12:114393165 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0316 a0001c0001t0029g0340 |
3 | HG01074.hp2 HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.663+1576C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393165 | |||||||
| chr12:114393184 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0323 others(5): Show |
8 | HG01943.hp1 HG02683.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+1557T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393184 | |||||||
| chr12:114393187 | C | T | 1 | a0001c0001t0022g0039 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.663+1554G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393187 | |||||||
| chr12:114393260 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.663+1481C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393260 | |||||||
| chr12:114393265 | TAAGAAAA others(7): Show |
T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(96): Show |
108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.663+1462_663+1475d others(16): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393265 | |||||||
| chr12:114393285 | C | T | 1 | a0001c0001t0027g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.663+1456G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393285 | |||||||
| chr12:114393377 | C | T | 3 | a0001c0001t0006g0028 a0001c0001t0012g0293 a0001c0002t0004g0055 |
3 | HG02559.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.663+1364G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393377 | |||||||
| chr12:114393414 | G | A | 2 | a0001c0002t0017g0364 a0001c0002t0017g0365 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+1327C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393414 | |||||||
| chr12:114393446 | C | G | 2 | a0001c0001t0006g0028 a0001c0002t0004g0055 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.663+1295G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393446 | |||||||
| chr12:114393497 | C | T | 13 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0220 others(10): Show |
13 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.663+1244G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393497 | |||||||
| chr12:114393653 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(57): Show |
67 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.663+1088G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393653 | |||||||
| chr12:114393739 | A | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.663+1002T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393739 | |||||||
| chr12:114393970 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0006g0040 a0001c0002t0001g0015 others(2): Show |
8 | HG01081.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+771T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114393970 | |||||||
| chr12:114394135 | C | T | 21 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0295 others(18): Show |
21 | HG00438.hp2 HG00673.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.663+606G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394135 | |||||||
| chr12:114394173 | A | G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0076 others(41): Show |
45 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.663+568T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394173 | |||||||
| chr12:114394222 | A | G | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.663+519T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394222 | |||||||
| chr12:114394247 | C | A | 1 | a0001c0001t0004g0333 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.663+494G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394247 | |||||||
| chr12:114394318 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.663+423G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394318 | |||||||
| chr12:114394460 | T | C | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.663+281A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394460 | |||||||
| chr12:114394527 | A | T | 1 | a0001c0001t0004g0225 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.663+214T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394527 | |||||||
| chr12:114394555 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(209): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.663+186A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394555 | |||||||
| chr12:114394705 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0058 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.663+36G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394705 | |||||||
| chr12:114394707 | G | A | 2 | a0001c0002t0017g0364 a0001c0002t0017g0365 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.663+34C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 6/8 | chr12 | 114394707 | |||||||
| chr12:114394981 | G | A | 1 | a0001c0001t0025g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-88C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114394981 | |||||||
| chr12:114395015 | T | C | 1 | a0004c0008t0030g0318 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.511-122A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395015 | |||||||
| chr12:114395033 | G | T | 1 | a0001c0001t0036g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.511-140C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395033 | |||||||
| chr12:114395389 | G | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0268 a0001c0001t0001g0269 others(21): Show |
25 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.511-496C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395389 | |||||||
| chr12:114395498 | C | T | 11 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0220 others(8): Show |
11 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-605G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395498 | |||||||
| chr12:114395579 | C | A | 2 | a0001c0001t0007g0313 a0001c0001t0042g0362 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.511-686G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395579 | |||||||
| chr12:114395579 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(158): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-686G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395579 | |||||||
| chr12:114395700 | T | C | 25 | a0001c0001t0001g0013 a0001c0001t0001g0268 a0001c0001t0001g0269 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.511-807A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395700 | |||||||
| chr12:114395810 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(158): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.511-917T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395810 | |||||||
| chr12:114395830 | G | C | 1 | a0001c0001t0006g0030 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.511-937C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395830 | |||||||
| chr12:114395847 | C | T | 3 | a0001c0001t0012g0081 a0001c0001t0012g0142 a0001c0001t0012g0143 |
3 | HG01167.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.511-954G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395847 | |||||||
| chr12:114395850 | C | T | 1 | a0001c0001t0018g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.511-957G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395850 | |||||||
| chr12:114395874 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(144): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.511-981G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395874 | |||||||
| chr12:114395879 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.511-986C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395879 | |||||||
| chr12:114395975 | T | G | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.511-1082A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114395975 | |||||||
| chr12:114396023 | C | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0001g0220 others(5): Show |
8 | HG01943.hp1 HG02257.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-1130G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396023 | |||||||
| chr12:114396032 | C | T | 6 | a0001c0001t0006g0045 a0001c0001t0008g0154 a0001c0001t0008g0320 others(3): Show |
7 | HG00099.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-1139G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396032 | |||||||
| chr12:114396037 | G | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0092 others(15): Show |
18 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.511-1144C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396037 | |||||||
| chr12:114396115 | A | G | 16 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-1222T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396115 | |||||||
| chr12:114396177 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0092 others(15): Show |
18 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.511-1284G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396177 | |||||||
| chr12:114396239 | G | C | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.511-1346C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396239 | |||||||
| chr12:114396261 | G | A | 1 | a0001c0001t0004g0273 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.511-1368C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396261 | |||||||
| chr12:114396502 | G | T | 1 | a0001c0001t0007g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-1609C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396502 | |||||||
| chr12:114396706 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.511-1813C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114396706 | |||||||
| chr12:114397117 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+1456G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397117 | |||||||
| chr12:114397123 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+1450A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397123 | |||||||
| chr12:114397240 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.510+1333T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397240 | |||||||
| chr12:114397325 | A | G | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(345): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.510+1248T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397325 | |||||||
| chr12:114397379 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+1194C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397379 | |||||||
| chr12:114397408 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(159): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.510+1165G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397408 | |||||||
| chr12:114397433 | T | A | 4 | a0001c0001t0001g0220 a0001c0001t0004g0273 a0001c0002t0017g0364 others(1): Show |
4 | HG01361.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1140A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397433 | |||||||
| chr12:114397433 | T | C | 5 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0027g0149 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+1140A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397433 | |||||||
| chr12:114397445 | C | T | 4 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0002t0001g0281 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1128G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397445 | |||||||
| chr12:114397511 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510+1062C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397511 | |||||||
| chr12:114397623 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0058 a0001c0001t0001g0059 others(157): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.510+950C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397623 | |||||||
| chr12:114397683 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.510+890G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397683 | |||||||
| chr12:114397778 | G | GA | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0006g0040 others(3): Show |
7 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+794dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114397778 | |||||||
| chr12:114398391 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0290 |
2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.510+182C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398391 | |||||||
| chr12:114398474 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.510+99A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398474 | |||||||
| chr12:114398497 | G | A | 1 | a0001c0001t0005g0110 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.510+76C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 5/8 | chr12 | 114398497 | |||||||
| chr12:114398771 | C | A | 1 | a0001c0001t0004g0346 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.363-51G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398771 | |||||||
| chr12:114398802 | C | T | 2 | a0001c0001t0034g0286 a0001c0002t0004g0055 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.363-82G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398802 | |||||||
| chr12:114398856 | C | T | 1 | a0001c0001t0010g0152 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.363-136G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398856 | |||||||
| chr12:114398864 | G | A | 2 | a0001c0001t0007g0151 a0001c0001t0007g0313 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.363-144C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114398864 | |||||||
| chr12:114399068 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.363-348C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399068 | |||||||
| chr12:114399188 | A | T | 1 | a0001c0001t0011g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.362+325T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399188 | |||||||
| chr12:114399247 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.362+266T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399247 | |||||||
| chr12:114399280 | G | A | 3 | a0001c0002t0017g0364 a0001c0002t0017g0365 a0001c0002t0043g0363 |
3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.362+233C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399280 | |||||||
| chr12:114399414 | T | A | 1 | a0001c0001t0006g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.362+99A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | |||||||
| chr12:114399414 | T | C | 1 | a0001c0001t0007g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362+99A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | |||||||
| chr12:114399414 | T | TA | 20 | a0001c0001t0001g0276 a0001c0001t0001g0291 a0001c0001t0001g0317 others(17): Show |
21 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.362+98dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | |||||||
| chr12:114399414 | TA | T | 30 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0148 others(27): Show |
31 | HG00323.hp1 HG00642.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.362+98delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 4/8 | chr12 | 114399414 | |||||||
| chr12:114399916 | A | G | 19 | a0001c0001t0001g0140 a0001c0001t0002g0126 a0001c0001t0002g0129 others(16): Show |
21 | HG00544.hp1 HG01081.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.243-284T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114399916 | |||||||
| chr12:114399956 | G | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(321): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.243-324C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114399956 | |||||||
| chr12:114400091 | A | G | 3 | a0001c0002t0017g0364 a0001c0002t0017g0365 a0001c0002t0043g0363 |
3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.243-459T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400091 | |||||||
| chr12:114400434 | C | A | 3 | a0001c0001t0001g0312 a0001c0001t0002g0347 a0001c0001t0007g0348 |
3 | HG00639.hp2 HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.243-802G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400434 | |||||||
| chr12:114400477 | C | A | 19 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.243-845G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400477 | |||||||
| chr12:114400601 | G | T | 2 | a0001c0001t0007g0125 a0001c0003t0001g0124 |
2 | HG02280.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.243-969C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400601 | |||||||
| chr12:114400602 | C | T | 2 | a0001c0001t0007g0125 a0001c0003t0001g0124 |
2 | HG02280.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.243-970G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400602 | |||||||
| chr12:114400813 | C | A | 1 | a0001c0001t0003g0007 | 2 | HG00673.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.242+1013G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400813 | |||||||
| chr12:114400891 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.242+935C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400891 | |||||||
| chr12:114400895 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0002g0280 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.242+931C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400895 | |||||||
| chr12:114400903 | G | C | 2 | a0001c0001t0001g0279 a0001c0001t0035g0278 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.242+923C>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400903 | |||||||
| chr12:114400931 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.242+895G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400931 | |||||||
| chr12:114400994 | A | G | 4 | a0001c0002t0001g0015 a0001c0002t0001g0307 a0001c0002t0001g0308 others(1): Show |
5 | HG01081.hp2 HG01243.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+832T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114400994 | |||||||
| chr12:114401183 | T | A | 1 | a0001c0001t0001g0349 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242+643A>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401183 | |||||||
| chr12:114401186 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0014 |
4 | HG01074.hp2 HG01358.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+640T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401186 | |||||||
| chr12:114401291 | T | G | 5 | a0001c0002t0001g0116 a0001c0002t0001g0119 a0001c0002t0008g0117 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.242+535A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401291 | |||||||
| chr12:114401328 | C | G | 1 | a0001c0001t0007g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242+498G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401328 | |||||||
| chr12:114401398 | T | G | 15 | a0001c0002t0001g0015 a0001c0002t0001g0116 a0001c0002t0001g0119 others(12): Show |
16 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.242+428A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401398 | |||||||
| chr12:114401409 | T | C | 1 | a0001c0001t0002g0282 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.242+417A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401409 | |||||||
| chr12:114401437 | A | T | 19 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.242+389T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401437 | |||||||
| chr12:114401451 | G | A | 13 | a0001c0002t0001g0015 a0001c0002t0001g0116 a0001c0002t0001g0119 others(10): Show |
14 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.242+375C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401451 | |||||||
| chr12:114401641 | C | T | 1 | a0001c0001t0005g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.242+185G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401641 | |||||||
| chr12:114401764 | T | C | 1 | a0006c0011t0002g0311 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.242+62A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 3/8 | chr12 | 114401764 | |||||||
| chr12:114401939 | A | T | 9 | a0001c0002t0001g0116 a0001c0002t0001g0119 a0001c0002t0004g0055 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-19T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114401939 | |||||||
| chr12:114402126 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0285 a0001c0001t0002g0284 others(13): Show |
18 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.148-206A>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402126 | |||||||
| chr12:114402151 | C | A | 4 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(1): Show |
4 | HG02148.hp2 HG02738.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-231G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402151 | |||||||
| chr12:114402151 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.148-231G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402151 | |||||||
| chr12:114402236 | C | G | 18 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 others(15): Show |
19 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.148-316G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402236 | |||||||
| chr12:114402262 | C | A | 2 | a0001c0001t0001g0309 a0001c0001t0003g0071 |
2 | HG01261.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.148-342G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402262 | |||||||
| chr12:114402270 | A | C | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 |
3 | HG00099.hp2 HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.148-350T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402270 | |||||||
| chr12:114402280 | C | CA | 37 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(34): Show |
38 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.148-361dupT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402280 | |||||||
| chr12:114402286 | A | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(228): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.148-366T>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402286 | |||||||
| chr12:114402287 | A | T | 5 | a0001c0001t0001g0097 a0001c0001t0007g0297 a0001c0001t0007g0298 others(2): Show |
6 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-367T>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402287 | |||||||
| chr12:114402330 | G | T | 19 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(16): Show |
20 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.148-410C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402330 | |||||||
| chr12:114402342 | T | C | 5 | a0001c0001t0002g0112 a0001c0001t0005g0008 a0001c0001t0042g0362 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-422A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402342 | |||||||
| chr12:114402642 | C | T | 5 | a0001c0001t0002g0112 a0001c0001t0005g0008 a0001c0001t0042g0362 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-722G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402642 | |||||||
| chr12:114402683 | T | C | 5 | a0001c0001t0001g0097 a0001c0001t0007g0297 a0001c0001t0007g0298 others(2): Show |
6 | HG01243.hp2 HG01346.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-763A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402683 | |||||||
| chr12:114402703 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0002g0300 |
2 | NA18747.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.148-783C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402703 | |||||||
| chr12:114402816 | GA | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
298 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.148-897delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402816 | |||||||
| chr12:114402934 | G | A | 8 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(5): Show |
9 | HG00642.hp1 HG01074.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+818C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402934 | |||||||
| chr12:114402991 | A | ACC | 28 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(25): Show |
28 | HG00621.hp1 HG01175.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.147+759_147+760dup others(2): Show |
TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114402991 | |||||||
| chr12:114403187 | C | A | 3 | a0001c0002t0017g0364 a0001c0002t0017g0365 a0001c0002t0043g0363 |
3 | HG02257.hp1 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.147+565G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403187 | |||||||
| chr12:114403187 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02809.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.147+565G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403187 | |||||||
| chr12:114403305 | G | A | 1 | a0001c0001t0009g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.147+447C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403305 | |||||||
| chr12:114403360 | C | T | 1 | a0001c0002t0004g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+392G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403360 | |||||||
| chr12:114403388 | G | T | 1 | a0001c0001t0008g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.147+364C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403388 | |||||||
| chr12:114403558 | C | T | 5 | a0001c0001t0042g0362 a0001c0002t0004g0055 a0001c0002t0017g0364 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+194G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403558 | |||||||
| chr12:114403583 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.147+169C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403583 | |||||||
| chr12:114403739 | G | T | 1 | a0001c0001t0004g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.147+13C>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 2/8 | chr12 | 114403739 | |||||||
| chr12:114404099 | G | A | 1 | a0006c0011t0002g0311 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-38-163C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404099 | |||||||
| chr12:114404147 | A | G | 6 | a0001c0001t0016g0017 a0001c0001t0042g0362 a0001c0002t0004g0055 others(3): Show |
7 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-211T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404147 | |||||||
| chr12:114404173 | C | A | 1 | a0001c0001t0016g0017 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-38-237G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404173 | |||||||
| chr12:114404191 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(318): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.-38-255T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404191 | |||||||
| chr12:114404382 | C | A | 1 | a0001c0001t0001g0354 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-38-446G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404382 | |||||||
| chr12:114404442 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-38-506C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404442 | |||||||
| chr12:114404453 | T | C | 1 | a0001c0001t0011g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-517A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404453 | |||||||
| chr12:114404462 | C | A | 1 | a0001c0001t0002g0356 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-38-526G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404462 | |||||||
| chr12:114404472 | CA | C | 36 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0006g0018 others(33): Show |
37 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-537delT | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404472 | |||||||
| chr12:114404479 | A | G | 36 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0006g0018 others(33): Show |
37 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38-543T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404479 | |||||||
| chr12:114404590 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-38-654T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404590 | |||||||
| chr12:114404603 | T | C | 5 | a0001c0001t0016g0017 a0001c0001t0042g0362 a0001c0002t0017g0364 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38-667A>G | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404603 | |||||||
| chr12:114404691 | A | G | 4 | a0001c0001t0042g0362 a0001c0002t0017g0364 a0001c0002t0017g0365 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-755T>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404691 | |||||||
| chr12:114404806 | C | T | 4 | a0001c0001t0042g0362 a0001c0002t0017g0364 a0001c0002t0017g0365 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+822G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404806 | |||||||
| chr12:114404922 | C | A | 1 | a0001c0001t0003g0357 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-39+706G>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114404922 | |||||||
| chr12:114405121 | C | G | 83 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0058 others(80): Show |
84 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-39+507G>C | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405121 | |||||||
| chr12:114405177 | G | A | 1 | a0001c0001t0042g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-39+451C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405177 | |||||||
| chr12:114405483 | G | A | 1 | a0001c0001t0002g0358 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-39+145C>T | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405483 | |||||||
| chr12:114405583 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0003g0007 |
4 | HG00558.hp1 HG00673.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+45G>A | TBX5 | ENSG00000089225.20 | transcript | ENST00000405440.7 | protein_coding | 1/8 | chr12 | 114405583 |