Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55973 |
| ensemblid | ENSG00000075790.12 |
| hgncid | 24131 |
| symbol | BCAP29 |
| name | B cell receptor associated protein 29 |
| refseq_nuc | NM_018844.4 |
| refseq_prot | NP_061332.2 |
| ensembl_nuc | ENST00000005259.9 |
| ensembl_prot | ENSP00000005259.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 107580246 |
| end | 107620478 |
| strand | + |
| ver | v1.2 |
| region | chr7:107580246-107620478 |
| region5000 | chr7:107575246-107625478 |
| regionname0 | BCAP29_chr7_107580246_107620478 |
| regionname5000 | BCAP29_chr7_107575246_107625478 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 723 | 398 | 90 | 76 | 182 | 16 | 32 | BCAP29_chr7_107575246_107625478 | BCAP29 | ATGAC others(718): Show |
chr7 | 107575246 | 107625478 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2911 | 199 | 59 | 33 | 86 | 6 | 15 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0002 | 1/0 | 2911 | 95 | 7 | 19 | 58 | 3 | 7 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0003 | 0/1 | 2911 | 47 | 0 | 14 | 22 | 5 | 5 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0004 | 0/0 | 2911 | 16 | 0 | 0 | 16 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0005 | 0/0 | 2911 | 10 | 3 | 2 | 0 | 2 | 3 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0006 | 0/0 | 2911 | 7 | 6 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0007 | 0/0 | 2911 | 6 | 6 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0008 | 0/0 | 2911 | 3 | 0 | 3 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0009 | 0/0 | 2911 | 3 | 0 | 3 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0010 | 0/0 | 2911 | 2 | 0 | 0 | 0 | 0 | 2 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0011 | 0/0 | 2911 | 2 | 2 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0012 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0013 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0014 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0015 | 0/0 | 2911 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0016 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0017 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0018 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| a0001c0001t0019 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | GTCCC others(2906): Show |
chr7 | 107575246 | 107625478 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0007 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0008g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0012g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0013g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0015g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0017g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0018g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0352 | EUR | GBR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0208 | EUR | GBR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | GBR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | FIN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0354 | EUR | FIN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0351 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0161 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0162 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0180 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0163 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0214 | EUR | IBS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0353 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02145 | hp1 | a0001 | c0001 | t0019 | g0051 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CDX | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CDX | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CDX | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0179 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0323 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0348 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0357 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0244 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0346 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0322 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0336 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0324 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0172 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0356 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0358 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0350 | SAS | PJL | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0164 | SAS | STU | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | STU | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | CHB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0249 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0176 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0202 | EUR | TSI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0212 | EUR | TSI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0349 | SAS | GIH | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0136 | SAS | GIH | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0355 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0359 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0345 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | USA | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0092 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0216 | REF | REF | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0258 | REF | REF | BCAP29_chr7_107575246_107625478 | BCAP29 | chr7 | 107575246 | 107625478 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107580251 | G | A | 1 | a0001c0001t0012 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/8 | 522 | chr7 | 107580251 | ||||||
| chr7:107618411 | G | A | 1 | a0001c0001t0006 | 7 | HG01243.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 48 | chr7 | 107618411 | ||||||
| chr7:107618462 | T | C | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 |
8 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 99 | chr7 | 107618462 | ||||||
| chr7:107618465 | G | A | 1 | a0001c0001t0008 | 3 | HG00642.hp2 HG01081.hp1 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*102G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 102 | chr7 | 107618465 | ||||||
| chr7:107618748 | A | G | 1 | a0001c0001t0019 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 385 | chr7 | 107618748 | ||||||
| chr7:107618842 | C | T | 1 | a0001c0001t0009 | 3 | HG01167.hp2 HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*479C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 479 | chr7 | 107618842 | ||||||
| chr7:107619123 | A | C | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 760 | chr7 | 107619123 | ||||||
| chr7:107619276 | T | C | 1 | a0001c0001t0003 | 46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*913T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 913 | chr7 | 107619276 | ||||||
| chr7:107619286 | G | A | 1 | a0001c0001t0015 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 923 | chr7 | 107619286 | ||||||
| chr7:107619368 | T | C | 1 | a0001c0001t0010 | 2 | HG04228.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1005T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1005 | chr7 | 107619368 | ||||||
| chr7:107619733 | A | C | 1 | a0001c0001t0005 | 10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1370A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1370 | chr7 | 107619733 | ||||||
| chr7:107619833 | G | A | 1 | a0001c0001t0013 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1470G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1470 | chr7 | 107619833 | ||||||
| chr7:107619895 | A | G | 1 | a0001c0001t0004 | 16 | HG02083.hp2 NA18946.hp2 NA18954.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1532A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1532 | chr7 | 107619895 | ||||||
| chr7:107619915 | T | C | 1 | a0001c0001t0016 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1552 | chr7 | 107619915 | ||||||
| chr7:107620060 | C | G | 1 | a0001c0001t0017 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1697 | chr7 | 107620060 | ||||||
| chr7:107620333 | G | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*1970G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 1970 | chr7 | 107620333 | ||||||
| chr7:107620411 | A | G | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2048A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 8/8 | 2048 | chr7 | 107620411 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107580400 | A | ACCCGG | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+110_-15+114dup others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 107580400 | ||||||
| chr7:107580412 | C | T | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+111C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580412 | |||||||
| chr7:107580482 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+181T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580482 | |||||||
| chr7:107580518 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
8 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+217G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580518 | |||||||
| chr7:107580539 | C | T | 1 | a0001c0001t0003g0349 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-220C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580539 | |||||||
| chr7:107580590 | G | T | 4 | a0001c0001t0007g0345 a0001c0001t0007g0347 a0001c0001t0007g0348 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-169G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580590 | |||||||
| chr7:107580636 | G | C | 1 | a0001c0001t0003g0349 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-123G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580636 | |||||||
| chr7:107580647 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-14-112T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580647 | |||||||
| chr7:107580686 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-73C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 1/7 | chr7 | 107580686 | |||||||
| chr7:107580875 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.92+11T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107580875 | |||||||
| chr7:107580935 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+71G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107580935 | |||||||
| chr7:107581006 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.92+142A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581006 | |||||||
| chr7:107581090 | A | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
16 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.92+226A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581090 | |||||||
| chr7:107581179 | T | C | 1 | a0001c0001t0003g0349 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.92+315T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581179 | |||||||
| chr7:107581256 | A | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
10 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.92+392A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581256 | |||||||
| chr7:107581274 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92+410T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581274 | |||||||
| chr7:107581486 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.92+622A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581486 | |||||||
| chr7:107581588 | C | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0326 a0001c0001t0001g0327 others(5): Show |
9 | HG00408.hp1 HG00438.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+724C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581588 | |||||||
| chr7:107581678 | A | G | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.92+814A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581678 | |||||||
| chr7:107581822 | A | C | 4 | a0001c0001t0007g0345 a0001c0001t0007g0347 a0001c0001t0007g0348 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+958A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581822 | |||||||
| chr7:107581841 | T | G | 1 | a0001c0001t0002g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.92+977T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107581841 | |||||||
| chr7:107582143 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.92+1279A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582143 | |||||||
| chr7:107582280 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.92+1416G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582280 | |||||||
| chr7:107582296 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02055.hp1 HG02897.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+1432G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582296 | |||||||
| chr7:107582337 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
6 | HG02615.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+1473C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582337 | |||||||
| chr7:107582528 | G | C | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.93-1354G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582528 | |||||||
| chr7:107582590 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.93-1292C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582590 | |||||||
| chr7:107582617 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.93-1265G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582617 | |||||||
| chr7:107582840 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.93-1042T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582840 | |||||||
| chr7:107582896 | A | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0242 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-986A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582896 | |||||||
| chr7:107582956 | A | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
295 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.93-926A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582956 | |||||||
| chr7:107582981 | G | C | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG00280.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-901G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107582981 | |||||||
| chr7:107583300 | T | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
51 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.93-582T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107583300 | |||||||
| chr7:107583300 | T | TTA | 14 | a0001c0001t0001g0040 a0001c0001t0001g0231 a0001c0001t0001g0232 others(11): Show |
14 | HG00438.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.93-567_93-566dupTA | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 107583300 | ||||||
| chr7:107583611 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.93-271T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107583611 | |||||||
| chr7:107583809 | T | C | 1 | a0001c0001t0012g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.93-73T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 2/7 | chr7 | 107583809 | |||||||
| chr7:107584051 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.193+69G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584051 | |||||||
| chr7:107584120 | C | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.193+138C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584120 | |||||||
| chr7:107584122 | A | G | 3 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 |
3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.193+140A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584122 | |||||||
| chr7:107584209 | T | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+227T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584209 | |||||||
| chr7:107584222 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.193+240A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584222 | |||||||
| chr7:107584302 | T | C | 1 | a0001c0001t0002g0019 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.193+320T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584302 | |||||||
| chr7:107584480 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.193+498G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584480 | |||||||
| chr7:107584559 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193+577T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584559 | |||||||
| chr7:107584567 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.193+585G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584567 | |||||||
| chr7:107584598 | C | T | 41 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(38): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.193+616C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584598 | |||||||
| chr7:107584748 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.193+766G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584748 | |||||||
| chr7:107584784 | G | C | 1 | a0001c0001t0002g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.193+802G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107584784 | |||||||
| chr7:107585269 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.193+1287C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585269 | |||||||
| chr7:107585304 | A | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0188 a0001c0001t0001g0191 others(14): Show |
20 | HG02083.hp2 NA18946.hp2 NA18954.hp2 others(17): Show |
intron_variant | MODIFIER | c.193+1322A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585304 | |||||||
| chr7:107585442 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+1460A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585442 | |||||||
| chr7:107585488 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193+1506C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585488 | |||||||
| chr7:107585607 | C | T | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG00423.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.193+1625C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585607 | |||||||
| chr7:107585711 | C | T | 41 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(38): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.193+1729C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585711 | |||||||
| chr7:107585715 | C | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
88 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.193+1733C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585715 | |||||||
| chr7:107585787 | T | C | 1 | a0001c0001t0002g0252 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.193+1805T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585787 | |||||||
| chr7:107585836 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.193+1854C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585836 | |||||||
| chr7:107585861 | C | T | 4 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | HG01074.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+1879C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585861 | |||||||
| chr7:107585870 | A | C | 1 | a0001c0001t0004g0195 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.193+1888A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107585870 | |||||||
| chr7:107585991 | C | CA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02055.hp1 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+2018dupA | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107585991 | ||||||
| chr7:107586018 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.193+2036G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586018 | |||||||
| chr7:107586018 | G | T | 3 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG02027.hp1 NA18988.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.193+2036G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586018 | |||||||
| chr7:107586025 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.193+2043T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586025 | |||||||
| chr7:107586158 | A | G | 2 | a0001c0001t0002g0230 a0001c0001t0002g0316 |
2 | HG01106.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.193+2176A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586158 | |||||||
| chr7:107586167 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.193+2185T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586167 | |||||||
| chr7:107586347 | C | A | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+2365C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586347 | |||||||
| chr7:107586441 | G | C | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193+2459G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586441 | |||||||
| chr7:107586593 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.193+2611C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586593 | |||||||
| chr7:107586728 | C | CT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2763dupT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107586728 | ||||||
| chr7:107586728 | CT | C | 10 | a0001c0001t0001g0101 a0001c0001t0002g0254 a0001c0001t0003g0196 others(7): Show |
10 | HG01169.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+2763delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107586728 | ||||||
| chr7:107586729 | T | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0242 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+2747T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586729 | |||||||
| chr7:107586869 | A | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0058 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.193+2887A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586869 | |||||||
| chr7:107586885 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.193+2903C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586885 | |||||||
| chr7:107586935 | T | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+2953T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107586935 | |||||||
| chr7:107587259 | T | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG01261.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+3277T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587259 | |||||||
| chr7:107587382 | C | A | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG01943.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.193+3400C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587382 | |||||||
| chr7:107587435 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.193+3453G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587435 | |||||||
| chr7:107587473 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
11 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+3491G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587473 | |||||||
| chr7:107587618 | A | G | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193+3636A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587618 | |||||||
| chr7:107587632 | A | G | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG02723.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3650A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587632 | |||||||
| chr7:107587955 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.193+3973G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107587955 | |||||||
| chr7:107588063 | C | A | 1 | a0001c0001t0002g0313 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.193+4081C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588063 | |||||||
| chr7:107588107 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.193+4125A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588107 | |||||||
| chr7:107588117 | C | T | 30 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(27): Show |
33 | HG00438.hp2 HG00558.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.193+4135C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588117 | |||||||
| chr7:107588210 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+4228G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588210 | |||||||
| chr7:107588311 | TGTG | T | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+4331_193+4333d others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107588311 | ||||||
| chr7:107588317 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193+4335A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588317 | |||||||
| chr7:107588614 | C | T | 1 | a0001c0001t0010g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.193+4632C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588614 | |||||||
| chr7:107588638 | A | G | 2 | a0001c0001t0009g0162 a0001c0001t0009g0163 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.193+4656A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588638 | |||||||
| chr7:107588744 | A | G | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | NA18971.hp2 NA18999.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+4762A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588744 | |||||||
| chr7:107588772 | A | G | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193+4790A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588772 | |||||||
| chr7:107588891 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.193+4909G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588891 | |||||||
| chr7:107588975 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.194-4980C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107588975 | |||||||
| chr7:107589116 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.194-4839G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589116 | |||||||
| chr7:107589172 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4783C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589172 | |||||||
| chr7:107589173 | T | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.194-4782T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589173 | |||||||
| chr7:107589581 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.194-4374A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589581 | |||||||
| chr7:107589746 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.194-4209A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589746 | |||||||
| chr7:107589780 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-4175G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589780 | |||||||
| chr7:107589810 | A | G | 6 | a0001c0001t0007g0323 a0001c0001t0007g0324 a0001c0001t0007g0345 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-4145A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589810 | |||||||
| chr7:107589956 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.194-3999G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107589956 | |||||||
| chr7:107590119 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.194-3836C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590119 | |||||||
| chr7:107590164 | A | G | 2 | a0001c0001t0002g0317 a0001c0001t0002g0318 |
2 | HG00423.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.194-3791A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590164 | |||||||
| chr7:107590186 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.194-3769C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590186 | |||||||
| chr7:107590215 | T | C | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.194-3740T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590215 | |||||||
| chr7:107590283 | G | C | 2 | a0001c0001t0003g0196 a0001c0001t0003g0200 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.194-3672G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590283 | |||||||
| chr7:107590393 | C | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-3562C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590393 | |||||||
| chr7:107590829 | A | AAAAG | 46 | a0001c0001t0001g0045 a0001c0001t0001g0101 a0001c0001t0001g0109 others(43): Show |
48 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.194-3123_194-3122i others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107590829 | ||||||
| chr7:107590833 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.194-3122A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590833 | |||||||
| chr7:107590883 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.194-3072T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590883 | |||||||
| chr7:107590971 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.194-2984A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107590971 | |||||||
| chr7:107591119 | A | ATTAAAGA others(2): Show |
10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-2836_194-2835i others(11): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591119 | |||||||
| chr7:107591199 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-2756A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591199 | |||||||
| chr7:107591249 | C | G | 1 | a0001c0001t0015g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.194-2706C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591249 | |||||||
| chr7:107591584 | C | G | 1 | a0001c0001t0003g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.194-2371C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591584 | |||||||
| chr7:107591593 | T | A | 1 | a0001c0001t0004g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.194-2362T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591593 | |||||||
| chr7:107591631 | C | T | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | NA18999.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.194-2324C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591631 | |||||||
| chr7:107591641 | T | C | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.194-2314T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591641 | |||||||
| chr7:107591641 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.194-2309_194-2298d others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(13): Show |
6 | a0001c0001t0007g0323 a0001c0001t0007g0324 a0001c0001t0007g0345 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(22): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(15): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0007g0322 |
3 | HG02055.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(24): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(19): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(28): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(21): Show |
1 | a0001c0001t0016g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(30): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(23): Show |
1 | a0001c0001t0002g0230 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(32): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(25): Show |
1 | a0001c0001t0001g0093 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(34): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(27): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
8 | HG00408.hp1 HG00639.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(36): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(29): Show |
3 | a0001c0001t0001g0035 a0001c0001t0001g0339 a0001c0001t0008g0004 |
5 | HG00642.hp2 HG01074.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(38): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(31): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0330 a0001c0001t0011g0179 |
3 | HG02132.hp1 HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(40): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(33): Show |
5 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0243 others(2): Show |
5 | HG02559.hp2 HG02647.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(42): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(35): Show |
9 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0034 others(6): Show |
11 | HG02886.hp1 HG02922.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(44): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(37): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0031 others(12): Show |
17 | HG00438.hp1 HG01255.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(46): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(39): Show |
6 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02027.hp2 HG02615.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(48): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(41): Show |
12 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0060 others(9): Show |
13 | HG02622.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(50): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(43): Show |
7 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0096 others(4): Show |
7 | HG00735.hp1 HG03834.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(52): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(45): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG01884.hp1 HG02970.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(54): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591641 | T | TACACACA others(47): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0006g0063 |
3 | HG01243.hp1 NA18522.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(56): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591641 | ||||||
| chr7:107591656 | A | ACACACAC others(22): Show |
2 | a0001c0001t0003g0221 a0001c0001t0004g0193 |
2 | NA18945.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(31): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(24): Show |
7 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0124 others(4): Show |
7 | HG00544.hp2 HG02683.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(33): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(26): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0333 a0001c0001t0003g0224 |
3 | HG01109.hp2 HG01256.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(35): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(28): Show |
1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(37): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(40): Show |
2 | a0001c0001t0001g0173 a0001c0001t0003g0055 |
2 | HG00280.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(49): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(44): Show |
1 | a0001c0001t0001g0170 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(53): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(39): Show |
1 | a0001c0001t0003g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(48): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(40): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(49): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(37): Show |
1 | a0001c0001t0003g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(46): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(38): Show |
1 | a0001c0001t0001g0177 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(47): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(35): Show |
1 | a0001c0001t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(44): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(36): Show |
1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(45): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(33): Show |
4 | a0001c0001t0001g0027 a0001c0001t0003g0108 a0001c0001t0003g0202 others(1): Show |
4 | HG01358.hp2 HG02027.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(42): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(31): Show |
5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0003g0203 others(2): Show |
5 | HG00544.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(40): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(29): Show |
7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0167 others(4): Show |
8 | HG00621.hp1 HG01175.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(38): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(27): Show |
9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0199 others(6): Show |
9 | HG00642.hp1 HG01070.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(36): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(25): Show |
38 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0037 others(35): Show |
42 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(34): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(27): Show |
1 | a0001c0001t0004g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(36): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(23): Show |
58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(32): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(25): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | NA18944.hp2 NA18979.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(34): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(21): Show |
10 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0152 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(30): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(24): Show |
1 | a0001c0001t0001g0151 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(33): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(19): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0156 others(5): Show |
9 | HG01261.hp2 HG02976.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-2298_194-2297i others(28): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(17): Show |
2 | a0001c0001t0002g0343 a0001c0001t0003g0222 |
2 | HG02155.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(26): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(15): Show |
2 | a0001c0001t0001g0159 a0001c0001t0003g0223 |
2 | HG02132.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(24): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(13): Show |
1 | a0001c0001t0002g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(22): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591656 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0160 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591656 | ||||||
| chr7:107591657 | C | CACACACA others(26): Show |
1 | a0001c0001t0004g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.194-2298_194-2297i others(35): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591657 | |||||||
| chr7:107591657 | C | CACACACA others(36): Show |
1 | a0001c0001t0011g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(45): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591657 | |||||||
| chr7:107591657 | C | CACACACA others(38): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0325 |
2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.194-2298_194-2297i others(47): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591657 | |||||||
| chr7:107591657 | C | CACACACA others(42): Show |
1 | a0001c0001t0006g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194-2298_194-2297i others(51): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591657 | |||||||
| chr7:107591658 | C | A | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.194-2297C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591658 | |||||||
| chr7:107591853 | T | C | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.194-2102T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591853 | |||||||
| chr7:107591879 | A | C | 4 | a0001c0001t0002g0309 a0001c0001t0002g0310 a0001c0001t0002g0311 others(1): Show |
4 | HG02129.hp2 NA18977.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-2076A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591879 | |||||||
| chr7:107591924 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.194-2031T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107591924 | |||||||
| chr7:107591943 | C | CTTAT | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-2009_194-2006d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 107591943 | ||||||
| chr7:107592080 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.194-1875C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592080 | |||||||
| chr7:107592127 | T | G | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194-1828T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592127 | |||||||
| chr7:107592205 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-1750T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592205 | |||||||
| chr7:107592345 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.194-1610A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592345 | |||||||
| chr7:107592450 | T | C | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-1505T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592450 | |||||||
| chr7:107592507 | C | T | 1 | a0001c0001t0002g0308 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.194-1448C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592507 | |||||||
| chr7:107592597 | A | C | 1 | a0001c0001t0003g0349 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.194-1358A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592597 | |||||||
| chr7:107592647 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-1308G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592647 | |||||||
| chr7:107592686 | C | A | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.194-1269C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592686 | |||||||
| chr7:107592815 | A | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-1140A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592815 | |||||||
| chr7:107592868 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-1087G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107592868 | |||||||
| chr7:107593025 | A | C | 1 | a0001c0001t0002g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.194-930A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593025 | |||||||
| chr7:107593031 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG02055.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.194-924C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593031 | |||||||
| chr7:107593336 | G | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0031 others(30): Show |
35 | HG00408.hp1 HG00438.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.194-619G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593336 | |||||||
| chr7:107593363 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0237 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.194-592A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593363 | |||||||
| chr7:107593626 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18960.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.194-329A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593626 | |||||||
| chr7:107593664 | A | G | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-291A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593664 | |||||||
| chr7:107593836 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.194-119G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593836 | |||||||
| chr7:107593866 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0292 |
3 | NA18942.hp1 NA18953.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.194-89T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593866 | |||||||
| chr7:107593906 | C | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-49C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 3/7 | chr7 | 107593906 | |||||||
| chr7:107594188 | A | AT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0233 a0001c0001t0001g0234 others(6): Show |
9 | HG02055.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+97dupT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594188 | ||||||
| chr7:107594235 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0243 |
3 | HG02622.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.344+130C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594235 | |||||||
| chr7:107594275 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG02717.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.344+170A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594275 | |||||||
| chr7:107594380 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0242 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+275G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594380 | |||||||
| chr7:107594428 | TCCTC | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.344+326_344+329del others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594428 | ||||||
| chr7:107594455 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
16 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.344+350G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594455 | |||||||
| chr7:107594463 | C | CAGGCACA | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.344+360_344+361ins others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594463 | ||||||
| chr7:107594489 | T | TTTTG | 12 | a0001c0001t0001g0074 a0001c0001t0002g0256 a0001c0001t0002g0342 others(9): Show |
12 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.344+408_344+411dup others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594489 | ||||||
| chr7:107594489 | T | TTTTGTTT others(1): Show |
249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.344+404_344+411dup others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594489 | ||||||
| chr7:107594489 | T | TTTTGTTT others(5): Show |
4 | a0001c0001t0001g0046 a0001c0001t0003g0227 a0001c0001t0003g0228 others(1): Show |
4 | HG02027.hp1 NA18988.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+400_344+411dup others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594489 | ||||||
| chr7:107594489 | TTTTGTTT others(1): Show |
T | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.344+404_344+411del others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 107594489 | ||||||
| chr7:107594641 | A | G | 1 | a0001c0001t0005g0358 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.344+536A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594641 | |||||||
| chr7:107594642 | C | T | 9 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0255 others(6): Show |
11 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.344+537C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594642 | |||||||
| chr7:107594690 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.344+585G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594690 | |||||||
| chr7:107594790 | A | C | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.344+685A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594790 | |||||||
| chr7:107594798 | G | A | 1 | a0001c0001t0004g0190 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.344+693G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107594798 | |||||||
| chr7:107595005 | A | T | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.345-862A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107595005 | |||||||
| chr7:107595080 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0292 |
3 | NA18942.hp1 NA18953.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.345-787G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107595080 | |||||||
| chr7:107595227 | A | G | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.345-640A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107595227 | |||||||
| chr7:107595271 | T | G | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.345-596T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107595271 | |||||||
| chr7:107595659 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.345-208C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 4/7 | chr7 | 107595659 | |||||||
| chr7:107596251 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.480+249T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107596251 | |||||||
| chr7:107596572 | TAACTA | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.480+575_480+579del others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107596572 | ||||||
| chr7:107596850 | T | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+848T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107596850 | |||||||
| chr7:107596886 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.480+884T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107596886 | |||||||
| chr7:107596907 | G | C | 4 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | HG01074.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+905G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107596907 | |||||||
| chr7:107597051 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.480+1049A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597051 | |||||||
| chr7:107597075 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.480+1073G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597075 | |||||||
| chr7:107597078 | G | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
88 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.480+1076G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597078 | |||||||
| chr7:107597096 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+1094A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597096 | |||||||
| chr7:107597362 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
295 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.480+1360T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597362 | |||||||
| chr7:107597367 | C | T | 4 | a0001c0001t0004g0183 a0001c0001t0004g0192 a0001c0001t0004g0193 others(1): Show |
4 | NA18963.hp2 NA18969.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+1365C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597367 | |||||||
| chr7:107597395 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.480+1393C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597395 | |||||||
| chr7:107597427 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.480+1425C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597427 | |||||||
| chr7:107597437 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0155 |
3 | NA18977.hp2 NA19003.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.480+1435C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597437 | |||||||
| chr7:107597508 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG02717.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480+1506C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597508 | |||||||
| chr7:107597625 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG02717.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480+1623A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597625 | |||||||
| chr7:107597879 | A | T | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+1877A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597879 | |||||||
| chr7:107597914 | T | C | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+1912T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107597914 | |||||||
| chr7:107598002 | T | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.480+2000T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107598002 | |||||||
| chr7:107598021 | A | C | 1 | a0001c0001t0003g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.480+2019A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107598021 | |||||||
| chr7:107598300 | AT | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-2090delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598300 | ||||||
| chr7:107598337 | C | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.481-2060C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107598337 | |||||||
| chr7:107598523 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.481-1874G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107598523 | |||||||
| chr7:107598540 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.481-1857A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107598540 | |||||||
| chr7:107598706 | C | CCT | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
295 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.481-1688_481-1687d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598706 | ||||||
| chr7:107598894 | T | TACAC | 5 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-1468_481-1465d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598894 | ||||||
| chr7:107598894 | TAC | T | 74 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0020 others(71): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.481-1466_481-1465d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598894 | ||||||
| chr7:107598894 | TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG00140.hp1 HG00735.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1474_481-1465d others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598894 | ||||||
| chr7:107598894 | TACACACA others(5): Show |
T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.481-1476_481-1465d others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598894 | ||||||
| chr7:107598894 | TACACACA others(7): Show |
T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
137 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.481-1478_481-1465d others(16): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598894 | ||||||
| chr7:107598921 | ACACACAC others(5): Show |
A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0091 |
3 | HG02922.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.481-1472_481-1461d others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107598921 | ||||||
| chr7:107599002 | TCTA | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
257 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.481-1393_481-1391d others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599002 | ||||||
| chr7:107599003 | C | CAAA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0040 others(19): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1394_481-1393i others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599003 | |||||||
| chr7:107599005 | A | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0040 others(19): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1392A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599005 | |||||||
| chr7:107599006 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0040 others(19): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1391C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599006 | |||||||
| chr7:107599008 | A | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0040 others(19): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1389A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599008 | |||||||
| chr7:107599011 | T | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0040 others(19): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-1386T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599011 | |||||||
| chr7:107599011 | T | TTA | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
158 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.481-1377_481-1376d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599011 | ||||||
| chr7:107599011 | T | TTATA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
112 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.481-1379_481-1376d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599011 | ||||||
| chr7:107599040 | G | GTA | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-1348_481-1347d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599040 | ||||||
| chr7:107599052 | A | AATATATT others(7): Show |
3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.481-1339_481-1326d others(16): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599052 | ||||||
| chr7:107599052 | A | AATATATT others(42): Show |
1 | a0001c0001t0005g0358 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.481-1264_481-1216d others(51): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599052 | ||||||
| chr7:107599091 | T | TGTATATA others(64): Show |
6 | a0001c0001t0007g0323 a0001c0001t0007g0324 a0001c0001t0007g0345 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1284_481-1283i others(73): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599091 | ||||||
| chr7:107599103 | T | C | 2 | a0001c0001t0011g0176 a0001c0001t0011g0179 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.481-1294T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599103 | |||||||
| chr7:107599114 | A | G | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.481-1283A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599114 | |||||||
| chr7:107599128 | TA | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1264delA | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599128 | ||||||
| chr7:107599150 | T | C | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
51 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.481-1247T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599150 | |||||||
| chr7:107599162 | A | AGTATATA others(42): Show |
1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.481-1235_481-1234i others(51): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599162 | |||||||
| chr7:107599163 | A | G | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.481-1234A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599163 | |||||||
| chr7:107599172 | T | TAC | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1224_481-1223i others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599172 | ||||||
| chr7:107599176 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1221T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599176 | |||||||
| chr7:107599178 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1219A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599178 | |||||||
| chr7:107599180 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1217A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599180 | |||||||
| chr7:107599183 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1214T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599183 | |||||||
| chr7:107599187 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1210A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599187 | |||||||
| chr7:107599189 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1208G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599189 | |||||||
| chr7:107599200 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.481-1197C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599200 | |||||||
| chr7:107599203 | A | ATAATT | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1193_481-1192i others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599203 | ||||||
| chr7:107599205 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.481-1192T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599205 | |||||||
| chr7:107599210 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1187A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599210 | |||||||
| chr7:107599216 | T | TTTATATA others(3): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1181_481-1180i others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599216 | |||||||
| chr7:107599218 | T | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.481-1179T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599218 | |||||||
| chr7:107599220 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.481-1177T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599220 | |||||||
| chr7:107599221 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1176A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599221 | |||||||
| chr7:107599222 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1175C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599222 | |||||||
| chr7:107599225 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.481-1172A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599225 | |||||||
| chr7:107599227 | T | TTATATAT others(28): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0238 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.481-1138_481-1137i others(37): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(28): Show |
98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
113 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.481-1150_481-1116d others(37): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(61): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.481-1116_481-1115i others(70): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(63): Show |
13 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01074.hp1 HG01891.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.481-1116_481-1115i others(72): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(98): Show |
1 | a0001c0001t0003g0209 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.481-1116_481-1115i others(107): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(63): Show |
67 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0045 others(64): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.481-1116_481-1115i others(72): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(98): Show |
37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
41 | HG00423.hp2 HG02027.hp1 HG02027.hp2 others(38): Show |
intron_variant | MODIFIER | c.481-1116_481-1115i others(107): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATAT others(133): Show |
12 | a0001c0001t0003g0006 a0001c0001t0003g0055 a0001c0001t0003g0056 others(9): Show |
14 | HG00280.hp1 HG00544.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.481-1116_481-1115i others(142): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTATATTT others(24): Show |
1 | a0001c0001t0001g0140 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.481-1165_481-1164i others(33): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599227 | T | TTTTTA | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0141 |
4 | HG00544.hp2 NA18951.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1169_481-1168i others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599227 | ||||||
| chr7:107599248 | TATATATA | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.481-1146_481-1140d others(9): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599248 | ||||||
| chr7:107599258 | T | TTTTATAT others(5): Show |
2 | a0001c0001t0011g0176 a0001c0001t0011g0179 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.481-1128_481-1117d others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599258 | ||||||
| chr7:107599260 | T | A | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-1137T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599260 | |||||||
| chr7:107599260 | T | TTA | 5 | a0001c0001t0002g0021 a0001c0001t0002g0255 a0001c0001t0002g0280 others(2): Show |
6 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1127_481-1126d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599260 | ||||||
| chr7:107599260 | T | TTATATAT others(30): Show |
9 | a0001c0001t0001g0040 a0001c0001t0001g0233 a0001c0001t0001g0234 others(6): Show |
9 | HG02055.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-1116_481-1115i others(39): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599260 | ||||||
| chr7:107599260 | T | TTATATAT others(98): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0097 |
3 | NA18963.hp1 NA18989.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.481-1116_481-1115i others(107): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599260 | ||||||
| chr7:107599260 | T | TTATATAT others(133): Show |
1 | a0001c0001t0003g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.481-1116_481-1115i others(142): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599260 | ||||||
| chr7:107599262 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0148 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.481-1116_481-1115i others(35): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599262 | ||||||
| chr7:107599262 | A | ATATATAT others(61): Show |
1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.481-1116_481-1115i others(70): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599262 | ||||||
| chr7:107599270 | A | ATAATT | 5 | a0001c0001t0007g0322 a0001c0001t0007g0345 a0001c0001t0007g0347 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-1126_481-1125i others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599270 | ||||||
| chr7:107599280 | A | AAATATAT others(97): Show |
1 | a0001c0001t0008g0004 | 3 | HG00642.hp2 HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.481-1116_481-1115i others(106): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599280 | ||||||
| chr7:107599280 | A | AT | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1117_481-1116i others(3): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599280 | |||||||
| chr7:107599282 | T | A | 1 | a0001c0001t0008g0004 | 3 | HG00642.hp2 HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.481-1115T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599282 | |||||||
| chr7:107599283 | T | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1114T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599283 | |||||||
| chr7:107599285 | T | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.481-1112T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599285 | |||||||
| chr7:107599305 | AATTTT | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1089_481-1085d others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599305 | ||||||
| chr7:107599309 | T | TTA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
119 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.481-1073_481-1072d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599309 | ||||||
| chr7:107599309 | T | TTATA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0119 |
5 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-1075_481-1072d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599309 | ||||||
| chr7:107599309 | TTA | T | 13 | a0001c0001t0001g0027 a0001c0001t0002g0025 a0001c0001t0002g0294 others(10): Show |
13 | HG00733.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.481-1073_481-1072d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599309 | ||||||
| chr7:107599309 | TTATA | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
88 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.481-1075_481-1072d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599309 | ||||||
| chr7:107599342 | C | CAT | 7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0231 others(4): Show |
7 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1041_481-1040d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599342 | ||||||
| chr7:107599482 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.481-915T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599482 | |||||||
| chr7:107599521 | T | TA | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
85 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.481-863dupA | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 107599521 | ||||||
| chr7:107599574 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.481-823G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599574 | |||||||
| chr7:107599693 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0242 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-704G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599693 | |||||||
| chr7:107599769 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0242 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-628A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599769 | |||||||
| chr7:107599890 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-507A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599890 | |||||||
| chr7:107599973 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0243 |
3 | HG02622.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.481-424C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107599973 | |||||||
| chr7:107600037 | A | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
16 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-360A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107600037 | |||||||
| chr7:107600056 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.481-341A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107600056 | |||||||
| chr7:107600110 | C | T | 1 | a0001c0001t0002g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.481-287C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107600110 | |||||||
| chr7:107600279 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.481-118G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 5/7 | chr7 | 107600279 | |||||||
| chr7:107600782 | G | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
16 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.589+277G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107600782 | |||||||
| chr7:107600828 | G | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01261.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.589+323G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107600828 | |||||||
| chr7:107600835 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0147 others(1): Show |
4 | HG00741.hp1 HG01496.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+330C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107600835 | |||||||
| chr7:107600937 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.589+432C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107600937 | |||||||
| chr7:107601007 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.589+502G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601007 | |||||||
| chr7:107601015 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.589+510C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601015 | |||||||
| chr7:107601060 | C | G | 1 | a0001c0001t0006g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.589+555C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601060 | |||||||
| chr7:107601129 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+624C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601129 | |||||||
| chr7:107601340 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.589+835A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601340 | |||||||
| chr7:107601566 | A | C | 1 | a0001c0001t0002g0307 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.589+1061A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601566 | |||||||
| chr7:107601638 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.589+1133A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601638 | |||||||
| chr7:107601692 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+1187A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601692 | |||||||
| chr7:107601912 | T | C | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+1407T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107601912 | |||||||
| chr7:107602026 | A | T | 11 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(8): Show |
11 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+1521A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602026 | |||||||
| chr7:107602031 | T | C | 8 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+1526T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602031 | |||||||
| chr7:107602197 | G | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+1692G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602197 | |||||||
| chr7:107602246 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.589+1741G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602246 | |||||||
| chr7:107602311 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0096 |
2 | NA18960.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.589+1806C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602311 | |||||||
| chr7:107602464 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.589+1959G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602464 | |||||||
| chr7:107602550 | T | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.589+2045T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602550 | |||||||
| chr7:107602562 | AT | A | 17 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0170 others(14): Show |
18 | HG00408.hp1 HG00438.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.589+2068delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107602562 | ||||||
| chr7:107602697 | C | G | 1 | a0001c0001t0005g0358 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.589+2192C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602697 | |||||||
| chr7:107602843 | A | G | 8 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+2338A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602843 | |||||||
| chr7:107602885 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
10 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.589+2380C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602885 | |||||||
| chr7:107602905 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.589+2400T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602905 | |||||||
| chr7:107602915 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.589+2410C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602915 | |||||||
| chr7:107602931 | A | ACTT | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 |
3 | HG02965.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.589+2427_589+2429d others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107602931 | ||||||
| chr7:107602964 | C | CT | 9 | a0001c0001t0002g0230 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG01433.hp2 HG01952.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.589+2483dupT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107602964 | ||||||
| chr7:107602964 | CT | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(219): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.589+2483delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107602964 | ||||||
| chr7:107602964 | CTT | C | 17 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0141 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.589+2482_589+2483d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107602964 | ||||||
| chr7:107602999 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 |
3 | HG02965.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.589+2494C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107602999 | |||||||
| chr7:107603114 | C | T | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.589+2609C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603114 | |||||||
| chr7:107603197 | C | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.589+2692C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603197 | |||||||
| chr7:107603216 | C | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+2711C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603216 | |||||||
| chr7:107603456 | CT | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.589+2953delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107603456 | ||||||
| chr7:107603523 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.589+3018A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603523 | |||||||
| chr7:107603550 | G | T | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.589+3045G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603550 | |||||||
| chr7:107603604 | A | AT | 29 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0060 others(26): Show |
29 | HG00735.hp1 HG01243.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.589+3120dupT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107603604 | ||||||
| chr7:107603604 | A | ATT | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
34 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.589+3119_589+3120d others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107603604 | ||||||
| chr7:107603604 | A | ATTT | 6 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0076 others(3): Show |
6 | HG02027.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+3118_589+3120d others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107603604 | ||||||
| chr7:107603604 | AT | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.589+3120delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107603604 | ||||||
| chr7:107603756 | C | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0204 a0001c0001t0003g0210 |
5 | NA18955.hp2 NA18964.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+3251C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603756 | |||||||
| chr7:107603903 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.589+3398C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603903 | |||||||
| chr7:107603929 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.589+3424C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603929 | |||||||
| chr7:107603935 | ATTCAGT | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+3431_589+3436d others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603935 | |||||||
| chr7:107603942 | C | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+3437C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603942 | |||||||
| chr7:107603943 | G | T | 2 | a0001c0001t0002g0320 a0001c0001t0002g0321 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.589+3438G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107603943 | |||||||
| chr7:107604011 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.589+3506G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604011 | |||||||
| chr7:107604090 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.589+3585A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604090 | |||||||
| chr7:107604100 | C | T | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.589+3595C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604100 | |||||||
| chr7:107604196 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.589+3691A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604196 | |||||||
| chr7:107604229 | A | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.589+3724A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604229 | |||||||
| chr7:107604319 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0075 |
3 | NA18953.hp2 NA18981.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.589+3814A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604319 | |||||||
| chr7:107604503 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0238 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.589+3998T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604503 | |||||||
| chr7:107604572 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0066 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.589+4067A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604572 | |||||||
| chr7:107604667 | G | T | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.589+4162G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604667 | |||||||
| chr7:107604685 | GT | G | 18 | a0001c0001t0001g0084 a0001c0001t0001g0233 a0001c0001t0001g0234 others(15): Show |
18 | HG02129.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.589+4193delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107604685 | ||||||
| chr7:107604685 | GTTT | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0101 others(3): Show |
10 | HG01074.hp2 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.589+4191_589+4193d others(5): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107604685 | ||||||
| chr7:107604688 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(237): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.589+4183T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604688 | |||||||
| chr7:107604689 | T | G | 9 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(6): Show |
9 | HG02451.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.589+4184T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604689 | |||||||
| chr7:107604691 | T | G | 29 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0104 others(26): Show |
31 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.589+4186T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604691 | |||||||
| chr7:107604751 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.589+4246T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604751 | |||||||
| chr7:107604846 | T | C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0170 others(15): Show |
19 | HG00408.hp1 HG00438.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+4341T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107604846 | |||||||
| chr7:107605023 | A | G | 41 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(38): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.589+4518A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605023 | |||||||
| chr7:107605052 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589+4547T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605052 | |||||||
| chr7:107605070 | A | G | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.589+4565A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605070 | |||||||
| chr7:107605149 | G | C | 2 | a0001c0001t0002g0265 a0001c0001t0002g0275 |
2 | HG00558.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.589+4644G>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605149 | |||||||
| chr7:107605254 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.589+4749C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605254 | |||||||
| chr7:107605278 | A | G | 10 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.589+4773A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605278 | |||||||
| chr7:107605283 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.589+4778C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605283 | |||||||
| chr7:107605449 | T | C | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | NA18972.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.589+4944T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605449 | |||||||
| chr7:107605576 | C | G | 1 | a0001c0001t0003g0215 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.589+5071C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605576 | |||||||
| chr7:107605632 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.589+5127C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605632 | |||||||
| chr7:107605653 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.589+5148G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605653 | |||||||
| chr7:107605777 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.589+5272A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605777 | |||||||
| chr7:107605913 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.589+5408A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605913 | |||||||
| chr7:107605980 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
10 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.589+5475G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107605980 | |||||||
| chr7:107606168 | T | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG01261.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+5663T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107606168 | |||||||
| chr7:107606387 | A | G | 1 | a0001c0001t0006g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.589+5882A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107606387 | |||||||
| chr7:107606543 | A | G | 3 | a0001c0001t0002g0303 a0001c0001t0002g0306 a0001c0001t0002g0308 |
3 | HG02071.hp1 HG02165.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.589+6038A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107606543 | |||||||
| chr7:107606667 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.589+6162C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107606667 | |||||||
| chr7:107606920 | T | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02723.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.590-6412T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107606920 | |||||||
| chr7:107607053 | G | T | 5 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0004g0192 others(2): Show |
5 | NA18963.hp2 NA18969.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-6279G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607053 | |||||||
| chr7:107607060 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0001g0173 others(11): Show |
15 | HG00408.hp1 HG00438.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.590-6272A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607060 | |||||||
| chr7:107607083 | G | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.590-6249G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607083 | |||||||
| chr7:107607102 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0132 others(1): Show |
5 | HG02015.hp2 NA18969.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-6230C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607102 | |||||||
| chr7:107607457 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-5875G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607457 | |||||||
| chr7:107607511 | TATATC | T | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-5817_590-5813d others(7): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107607511 | ||||||
| chr7:107607536 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.590-5796A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607536 | |||||||
| chr7:107607635 | C | CT | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0115 others(4): Show |
7 | HG00642.hp1 HG02738.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.590-5680dupT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107607635 | ||||||
| chr7:107607635 | CT | C | 16 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0002g0268 others(13): Show |
16 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.590-5680delT | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107607635 | ||||||
| chr7:107607723 | G | A | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-5609G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607723 | |||||||
| chr7:107607841 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02055.hp1 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-5491T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107607841 | |||||||
| chr7:107608130 | C | T | 2 | a0001c0001t0011g0176 a0001c0001t0011g0179 |
2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.590-5202C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608130 | |||||||
| chr7:107608141 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-5191T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608141 | |||||||
| chr7:107608200 | TA | T | 16 | a0001c0001t0001g0047 a0001c0001t0001g0337 a0001c0001t0002g0342 others(13): Show |
16 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.590-5119delA | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107608200 | ||||||
| chr7:107608200 | TAAAA | T | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-5122_590-5119d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107608200 | ||||||
| chr7:107608211 | A | T | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-5121A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608211 | |||||||
| chr7:107608230 | C | T | 1 | a0001c0001t0016g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-5102C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608230 | |||||||
| chr7:107608350 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-4982G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608350 | |||||||
| chr7:107608387 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.590-4945T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608387 | |||||||
| chr7:107608458 | A | ATTTG | 3 | a0001c0001t0002g0259 a0001c0001t0002g0276 a0001c0001t0002g0313 |
3 | HG01346.hp2 HG01433.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.590-4846_590-4843d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107608458 | ||||||
| chr7:107608458 | ATTTG | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-4846_590-4843d others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107608458 | ||||||
| chr7:107608484 | T | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.590-4848T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608484 | |||||||
| chr7:107608542 | T | C | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-4790T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608542 | |||||||
| chr7:107608575 | A | G | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.590-4757A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608575 | |||||||
| chr7:107608603 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.590-4729G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107608603 | |||||||
| chr7:107609025 | A | G | 1 | a0001c0001t0016g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-4307A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609025 | |||||||
| chr7:107609153 | T | C | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.590-4179T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609153 | |||||||
| chr7:107609165 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0091 |
3 | HG02922.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.590-4167G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609165 | |||||||
| chr7:107609254 | G | T | 79 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
87 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.590-4078G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609254 | |||||||
| chr7:107609399 | C | T | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.590-3933C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609399 | |||||||
| chr7:107609410 | G | A | 42 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.590-3922G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609410 | |||||||
| chr7:107609431 | C | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0066 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.590-3901C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609431 | |||||||
| chr7:107609660 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.590-3672G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609660 | |||||||
| chr7:107609815 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.590-3517G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609815 | |||||||
| chr7:107609910 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.590-3422G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609910 | |||||||
| chr7:107609918 | A | G | 1 | a0001c0001t0016g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-3414A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609918 | |||||||
| chr7:107609944 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-3388G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609944 | |||||||
| chr7:107609969 | G | A | 3 | a0001c0001t0003g0108 a0001c0001t0003g0207 a0001c0001t0003g0224 |
3 | HG01109.hp2 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.590-3363G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107609969 | |||||||
| chr7:107610020 | C | A | 2 | a0001c0001t0005g0352 a0001c0001t0005g0353 |
2 | HG00099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.590-3312C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610020 | |||||||
| chr7:107610033 | C | T | 1 | a0001c0001t0003g0018 | 2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.590-3299C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610033 | |||||||
| chr7:107610039 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.590-3293A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610039 | |||||||
| chr7:107610109 | A | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-3223A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610109 | |||||||
| chr7:107610112 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-3220A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610112 | |||||||
| chr7:107610275 | C | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.590-3057C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610275 | |||||||
| chr7:107610326 | G | T | 1 | a0001c0001t0004g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.590-3006G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610326 | |||||||
| chr7:107610327 | C | G | 8 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.590-3005C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610327 | |||||||
| chr7:107610917 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.590-2415T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107610917 | |||||||
| chr7:107611135 | C | T | 8 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.590-2197C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611135 | |||||||
| chr7:107611189 | A | G | 1 | a0001c0001t0002g0314 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.590-2143A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611189 | |||||||
| chr7:107611519 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.590-1813G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611519 | |||||||
| chr7:107611535 | G | T | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.590-1797G>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611535 | |||||||
| chr7:107611868 | A | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-1464A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611868 | |||||||
| chr7:107611879 | A | C | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.590-1453A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107611879 | |||||||
| chr7:107612391 | T | TTA | 12 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0022 others(9): Show |
15 | HG00558.hp2 HG00597.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.590-893_590-892dup others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATA | 15 | a0001c0001t0002g0024 a0001c0001t0002g0042 a0001c0001t0002g0248 others(12): Show |
16 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.590-895_590-892dup others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATATA | 13 | a0001c0001t0002g0021 a0001c0001t0002g0250 a0001c0001t0002g0260 others(10): Show |
14 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.590-897_590-892dup others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATATAT others(1): Show |
11 | a0001c0001t0002g0252 a0001c0001t0002g0259 a0001c0001t0002g0277 others(8): Show |
11 | HG00558.hp1 HG00621.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.590-899_590-892dup others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATATAT others(3): Show |
3 | a0001c0001t0002g0270 a0001c0001t0002g0296 a0001c0001t0005g0352 |
3 | HG00099.hp1 NA18981.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.590-901_590-892dup others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0023 | 2 | NA18953.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.590-903_590-892dup others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTATATAT others(7): Show |
1 | a0001c0001t0002g0281 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.590-905_590-892dup others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | T | TTTTATAT others(5): Show |
1 | a0001c0001t0002g0269 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.590-940_590-939ins others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTA | T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0059 others(23): Show |
32 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.590-893_590-892del others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATA | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
36 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.590-895_590-892del others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATA | T | 3 | a0001c0001t0001g0081 a0001c0001t0002g0291 a0001c0001t0002g0301 |
3 | HG02083.hp1 NA18962.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.590-897_590-892del others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(1): Show |
T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0043 others(2): Show |
6 | HG00738.hp1 HG01433.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-899_590-892del others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(3): Show |
T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0130 others(2): Show |
5 | HG02258.hp1 HG02300.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-901_590-892del others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(7): Show |
T | 1 | a0001c0001t0007g0348 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.590-905_590-892del others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(9): Show |
T | 10 | a0001c0001t0002g0257 a0001c0001t0002g0261 a0001c0001t0002g0312 others(7): Show |
10 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-907_590-892del others(16): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(11): Show |
T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0113 a0001c0001t0001g0123 others(7): Show |
10 | HG02027.hp1 HG02132.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-909_590-892del others(18): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(13): Show |
T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.590-911_590-892del others(20): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612391 | TTATATAT others(15): Show |
T | 2 | a0001c0001t0002g0320 a0001c0001t0002g0321 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.590-913_590-892del others(22): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612391 | ||||||
| chr7:107612393 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.590-939A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612393 | |||||||
| chr7:107612395 | A | T | 1 | a0001c0001t0002g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.590-937A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612395 | |||||||
| chr7:107612397 | A | T | 2 | a0001c0001t0002g0342 a0001c0001t0002g0344 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.590-935A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612397 | |||||||
| chr7:107612425 | A | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0098 a0001c0001t0006g0068 |
3 | HG01255.hp2 HG02027.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.590-907A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612425 | |||||||
| chr7:107612429 | A | ATATT | 4 | a0001c0001t0001g0245 a0001c0001t0001g0326 a0001c0001t0001g0335 others(1): Show |
4 | HG01074.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-900_590-899ins others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612429 | ||||||
| chr7:107612429 | A | ATT | 3 | a0001c0001t0001g0062 a0001c0001t0001g0085 a0001c0001t0001g0246 |
3 | HG02922.hp2 HG03453.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.590-902_590-901ins others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612429 | ||||||
| chr7:107612429 | A | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): Show |
60 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.590-903A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612429 | |||||||
| chr7:107612433 | A | ATATTTAT others(1): Show |
3 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0241 |
3 | HG02976.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.590-896_590-895ins others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612433 | ||||||
| chr7:107612433 | A | ATATTTAT others(5): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0036 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.590-896_590-895ins others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612433 | ||||||
| chr7:107612433 | A | ATT | 5 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0003g0197 others(2): Show |
5 | HG01943.hp2 HG01981.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-898_590-897ins others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612433 | ||||||
| chr7:107612433 | A | ATTTATT | 3 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0338 |
3 | HG03139.hp2 HG03225.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.590-898_590-897ins others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612433 | ||||||
| chr7:107612433 | A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.590-898_590-897ins others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612433 | ||||||
| chr7:107612433 | A | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
200 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.590-899A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612433 | |||||||
| chr7:107612437 | A | ATATATAT others(11): Show |
1 | a0001c0001t0003g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.590-892_590-891ins others(18): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0174 |
2 | HG02897.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.590-892_590-891ins others(20): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.590-892_590-891ins others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0177 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.590-892_590-891ins others(18): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0225 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.590-892_590-891ins others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0239 |
2 | HG03540.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.590-892_590-891ins others(16): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(3): Show |
4 | a0001c0001t0003g0055 a0001c0001t0003g0201 a0001c0001t0003g0202 others(1): Show |
4 | HG00280.hp1 HG02040.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(7): Show |
6 | a0001c0001t0001g0049 a0001c0001t0001g0175 a0001c0001t0001g0178 others(3): Show |
6 | HG00438.hp1 HG02132.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(14): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(1): Show |
8 | a0001c0001t0001g0341 a0001c0001t0002g0256 a0001c0001t0003g0017 others(5): Show |
9 | HG00140.hp1 HG00621.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(8): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0247 others(1): Show |
4 | HG02723.hp1 HG03130.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0331 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.590-892_590-891ins others(16): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATT | 4 | a0001c0001t0003g0108 a0001c0001t0003g0212 a0001c0001t0003g0214 others(1): Show |
4 | HG00423.hp2 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATATTT others(3): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0034 others(2): Show |
6 | HG02809.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-892_590-891ins others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATT | 5 | a0001c0001t0003g0056 a0001c0001t0003g0203 a0001c0001t0003g0215 others(2): Show |
5 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.590-889_590-886dup others(4): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATATTTAT others(5): Show |
1 | a0001c0001t0001g0066 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.590-886_590-885ins others(12): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATT | 3 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0219 |
3 | HG01256.hp1 HG01258.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.590-894_590-893ins others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATTTATT | 2 | a0001c0001t0001g0026 a0001c0001t0001g0329 |
3 | NA18998.hp2 NA19075.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.590-894_590-893ins others(6): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | ATTTATTT others(3): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0060 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.590-894_590-893ins others(10): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 107612437 | ||||||
| chr7:107612437 | A | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
234 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.590-895A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612437 | |||||||
| chr7:107612464 | C | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-868C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612464 | |||||||
| chr7:107612481 | T | G | 4 | a0001c0001t0001g0085 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02723.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-851T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612481 | |||||||
| chr7:107612536 | T | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0204 a0001c0001t0003g0210 |
5 | NA18955.hp2 NA18964.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-796T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612536 | |||||||
| chr7:107612561 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.590-771A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612561 | |||||||
| chr7:107612636 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.590-696C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612636 | |||||||
| chr7:107612859 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
290 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.590-473A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612859 | |||||||
| chr7:107612944 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.590-388G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107612944 | |||||||
| chr7:107613056 | A | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-276A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107613056 | |||||||
| chr7:107613074 | A | G | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
50 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.590-258A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107613074 | |||||||
| chr7:107613195 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.590-137A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107613195 | |||||||
| chr7:107613276 | T | C | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-56T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107613276 | |||||||
| chr7:107613291 | A | G | 9 | a0001c0001t0002g0020 a0001c0001t0002g0042 a0001c0001t0002g0252 others(6): Show |
10 | HG00558.hp2 HG00597.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-41A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 6/7 | chr7 | 107613291 | |||||||
| chr7:107613453 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.690+21A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107613453 | |||||||
| chr7:107613649 | TACAGCAT others(43): Show |
T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(2): Show |
5 | HG01891.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+218_690+267del others(50): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107613649 | |||||||
| chr7:107614204 | T | C | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+772T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614204 | |||||||
| chr7:107614207 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.690+775C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614207 | |||||||
| chr7:107614263 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+831A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614263 | |||||||
| chr7:107614274 | T | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+842T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614274 | |||||||
| chr7:107614437 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.690+1005G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614437 | |||||||
| chr7:107614539 | T | A | 1 | a0001c0001t0004g0187 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.690+1107T>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614539 | |||||||
| chr7:107614773 | A | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.690+1341A>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614773 | |||||||
| chr7:107614839 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.690+1407G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614839 | |||||||
| chr7:107614977 | A | G | 10 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.690+1545A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107614977 | |||||||
| chr7:107615089 | C | T | 3 | a0001c0001t0002g0254 a0001c0001t0002g0297 a0001c0001t0002g0301 |
3 | NA18944.hp1 NA18962.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.690+1657C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615089 | |||||||
| chr7:107615103 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.690+1671T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615103 | |||||||
| chr7:107615111 | GTCCATTG others(9): Show |
G | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.690+1720_690+1735d others(18): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 107615111 | ||||||
| chr7:107615225 | C | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+1793C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615225 | |||||||
| chr7:107615453 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.690+2021G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615453 | |||||||
| chr7:107615544 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.690+2112C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615544 | |||||||
| chr7:107615724 | G | A | 1 | a0001c0001t0005g0353 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.690+2292G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615724 | |||||||
| chr7:107615782 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.690+2350T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615782 | |||||||
| chr7:107615850 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0114 a0001c0001t0001g0122 others(4): Show |
8 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+2418A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615850 | |||||||
| chr7:107615878 | G | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+2446G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107615878 | |||||||
| chr7:107616244 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.691-2084C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616244 | |||||||
| chr7:107616472 | T | C | 4 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1856T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616472 | |||||||
| chr7:107616597 | A | T | 1 | a0001c0001t0010g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.691-1731A>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616597 | |||||||
| chr7:107616620 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.691-1708A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616620 | |||||||
| chr7:107616691 | C | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0048 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-1637C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616691 | |||||||
| chr7:107616812 | C | A | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1516C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616812 | |||||||
| chr7:107616813 | G | A | 2 | a0001c0001t0005g0352 a0001c0001t0005g0353 |
2 | HG00099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.691-1515G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616813 | |||||||
| chr7:107616853 | C | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0031 others(29): Show |
34 | HG00408.hp1 HG00438.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.691-1475C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616853 | |||||||
| chr7:107616870 | C | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1458C>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616870 | |||||||
| chr7:107616976 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02723.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1352C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107616976 | |||||||
| chr7:107617045 | C | A | 12 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0066 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-1283C>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617045 | |||||||
| chr7:107617247 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.691-1081T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617247 | |||||||
| chr7:107617267 | C | T | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1061C>T | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617267 | |||||||
| chr7:107617407 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.691-921T>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617407 | |||||||
| chr7:107617586 | A | G | 11 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0048 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.691-742A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617586 | |||||||
| chr7:107617676 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.691-652T>C | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617676 | |||||||
| chr7:107617714 | A | G | 2 | a0001c0001t0004g0184 a0001c0001t0004g0189 |
2 | NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.691-614A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617714 | |||||||
| chr7:107617752 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0238 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.691-576G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617752 | |||||||
| chr7:107617771 | A | G | 1 | a0001c0001t0007g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.691-557A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617771 | |||||||
| chr7:107617776 | A | G | 20 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0253 others(17): Show |
22 | HG00438.hp2 HG00558.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.691-552A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617776 | |||||||
| chr7:107617817 | A | G | 4 | a0001c0001t0001g0085 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02723.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-511A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617817 | |||||||
| chr7:107617845 | CTT | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
16 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-482_691-481del others(2): Show |
BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617845 | |||||||
| chr7:107617922 | A | G | 7 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-406A>G | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617922 | |||||||
| chr7:107617923 | G | A | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.691-405G>A | BCAP29 | ENSG00000075790.12 | transcript | ENST00000005259.9 | protein_coding | 7/7 | chr7 | 107617923 |