Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55212 |
| ensemblid | ENSG00000138686.10 |
| hgncid | 18758 |
| symbol | BBS7 |
| name | Bardet-Biedl syndrome 7 |
| refseq_nuc | NM_176824.3 |
| refseq_prot | NP_789794.1 |
| ensembl_nuc | ENST00000264499.9 |
| ensembl_prot | ENSP00000264499.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 121824329 |
| end | 121870474 |
| strand | - |
| ver | v1.2 |
| region | chr4:121824329-121870474 |
| region5000 | chr4:121819329-121875474 |
| regionname0 | BBS7_chr4_121824329_121870474 |
| regionname5000 | BBS7_chr4_121819329_121875474 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 715 | 372 | 88 | 67 | 162 | 14 | 39 | 122 | BBS7_chr4_121819329_121875474 | BBS7 | MDLIL others(710): Show |
chr4 | 121819329 | 121875474 |
| a0002 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | MDLIL others(710): Show |
chr4 | 121819329 | 121875474 |
| a0003 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | MDLIL others(710): Show |
chr4 | 121819329 | 121875474 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2145 | 364 | 83 | 67 | 161 | 14 | 37 | BBS7_chr4_121819329_121875474 | BBS7 | ATGGA others(2140): Show |
chr4 | 121819329 | 121875474 | ||
| a0001c0002 | 0/0 | 2145 | 5 | 5 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | ATGGA others(2140): Show |
chr4 | 121819329 | 121875474 | ||
| a0001c0003 | 0/0 | 2145 | 3 | 0 | 0 | 1 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | ATGGA others(2140): Show |
chr4 | 121819329 | 121875474 | ||
| a0002c0005 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | ATGGA others(2140): Show |
chr4 | 121819329 | 121875474 | ||
| a0003c0004 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | ATGGA others(2140): Show |
chr4 | 121819329 | 121875474 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3840 | 164 | 64 | 25 | 56 | 6 | 11 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0002 | 0/0 | 3839 | 86 | 2 | 15 | 52 | 5 | 12 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3834): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0003 | 0/0 | 3840 | 62 | 7 | 15 | 31 | 2 | 7 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0004 | 0/0 | 3839 | 15 | 0 | 6 | 9 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3834): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0005 | 0/0 | 3840 | 10 | 1 | 3 | 2 | 1 | 3 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0006 | 0/0 | 3840 | 9 | 0 | 2 | 7 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0007 | 0/0 | 3840 | 6 | 5 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0008 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0009 | 0/0 | 3840 | 3 | 0 | 0 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0010 | 0/0 | 3840 | 3 | 0 | 0 | 0 | 0 | 3 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0011 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0012 | 0/0 | 3839 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3834): Show |
chr4 | 121819329 | 121875474 |
| a0001c0001t0013 | 0/0 | 3839 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3834): Show |
chr4 | 121819329 | 121875474 |
| a0001c0002t0001 | 0/0 | 3840 | 5 | 5 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0001c0003t0002 | 0/0 | 3839 | 2 | 0 | 0 | 0 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3834): Show |
chr4 | 121819329 | 121875474 |
| a0001c0003t0003 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0002c0005t0001 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| a0003c0004t0001 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | CCTGT others(3835): Show |
chr4 | 121819329 | 121875474 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0001 | 0/0 | 12 | 0 | 0 | 10 | 1 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0002 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0003 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0004 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0006g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0006g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0009g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0010g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0001t0013g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0003t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0002c0005t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| a0003c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0115 | EUR | GBR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0120 | EUR | FIN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | FIN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0140 | EUR | FIN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | CHS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0100 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0138 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01081 | hp2 | a0002 | c0005 | t0001 | g0154 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01099 | hp2 | a0001 | c0001 | t0012 | g0226 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0248 | EUR | IBS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02523 | hp1 | a0001 | c0001 | t0009 | g0029 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0116 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0256 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0265 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0272 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0203 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03490 | hp2 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0048 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0048 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | PJL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04199 | hp2 | a0003 | c0004 | t0001 | g0071 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CHB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CHB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18997 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0029 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19059 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0132 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ASW | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | GIH | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | LWK | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0169 | REF | REF | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0199 | REF | REF | BBS7_chr4_121819329_121875474 | BBS7 | chr4 | 121819329 | 121875474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:121839665 | C | T | 1 | a0003 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1337G>A | p.Arg446Gln | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/19 | 1498/3840 | 1337/2148 | 446/715 | chr4 | 121839665 | |||
| chr4:121843997 | T | C | 1 | a0002 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1235A>G | p.Asp412Gly | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/19 | 1396/3840 | 1235/2148 | 412/715 | chr4 | 121843997 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:121839691 | G | A | 1 | a0001c0003 | 3 | HG03491.hp2 HG03492.hp1 NA18997.hp2 |
synonymous_variant | LOW | c.1311C>T | p.Asn437Asn | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/19 | 1472/3840 | 1311/2148 | 437/715 | chr4 | 121839691 | |||
| chr4:121861659 | G | A | 1 | a0001c0002 | 5 | HG02559.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.186C>T | p.Pro62Pro | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/19 | 347/3840 | 186/2148 | 62/715 | chr4 | 121861659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:121824536 | C | T | 1 | a0001c0001t0009 | 3 | HG02523.hp1 NA19005.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1324G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 1324 | chr4 | 121824536 | ||||||
| chr4:121824574 | C | T | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0003t0003 |
66 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1286G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 1286 | chr4 | 121824574 | ||||||
| chr4:121824658 | C | T | 1 | a0001c0001t0004 | 15 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1202G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 1202 | chr4 | 121824658 | ||||||
| chr4:121824928 | A | C | 1 | a0001c0001t0010 | 3 | HG03239.hp2 HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 932 | chr4 | 121824928 | ||||||
| chr4:121825130 | TC | T | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(2): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*729delG | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 729 | chr4 | 121825130 | ||||||
| chr4:121825170 | A | G | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(3): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*690T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 690 | chr4 | 121825170 | ||||||
| chr4:121825233 | C | T | 1 | a0001c0001t0008 | 3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*627G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 627 | chr4 | 121825233 | ||||||
| chr4:121825441 | A | T | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(2): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*419T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 419 | chr4 | 121825441 | ||||||
| chr4:121825507 | C | T | 1 | a0001c0001t0013 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 353 | chr4 | 121825507 | ||||||
| chr4:121825610 | A | C | 1 | a0001c0001t0006 | 9 | HG01943.hp1 HG01981.hp2 NA18942.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 250 | chr4 | 121825610 | ||||||
| chr4:121825690 | A | T | 1 | a0001c0001t0012 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 19/19 | 170 | chr4 | 121825690 | ||||||
| chr4:121870435 | A | T | 1 | a0001c0001t0011 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/19 | 122 | chr4 | 121870435 | ||||||
| chr4:121870446 | G | C | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(4): Show |
112 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-133C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/19 | 133 | chr4 | 121870446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:121826027 | A | C | 1 | a0001c0001t0002g0243 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2015-34T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826027 | |||||||
| chr4:121826370 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2015-377T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826370 | |||||||
| chr4:121826506 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(26): Show |
38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2015-513G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826506 | |||||||
| chr4:121826799 | T | C | 5 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0271 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2015-806A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826799 | |||||||
| chr4:121826959 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2015-966C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826959 | |||||||
| chr4:121826970 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2015-977C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121826970 | |||||||
| chr4:121827000 | A | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2015-1007T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827000 | |||||||
| chr4:121827153 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.2014+993C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827153 | |||||||
| chr4:121827248 | A | G | 1 | a0001c0001t0010g0032 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2014+898T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827248 | |||||||
| chr4:121827376 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2014+770C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827376 | |||||||
| chr4:121827608 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0164 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2014+538G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827608 | |||||||
| chr4:121827790 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2014+356T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827790 | |||||||
| chr4:121827841 | A | C | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(74): Show |
115 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2014+305T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827841 | |||||||
| chr4:121827928 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2014+218A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121827928 | |||||||
| chr4:121828066 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2014+80G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 18/18 | chr4 | 121828066 | |||||||
| chr4:121828281 | G | T | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1891-12C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 17/18 | chr4 | 121828281 | |||||||
| chr4:121828386 | C | T | 96 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(93): Show |
129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1890+16G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 17/18 | chr4 | 121828386 | |||||||
| chr4:121828585 | ACAT | A | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1786+31_1786+33del others(3): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 16/18 | chr4 | 121828585 | |||||||
| chr4:121828850 | A | G | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1677-122T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121828850 | |||||||
| chr4:121828899 | T | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(9): Show |
18 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1677-171A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121828899 | |||||||
| chr4:121828924 | C | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(74): Show |
111 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1677-196G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121828924 | |||||||
| chr4:121828985 | T | TA | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1677-258dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121828985 | |||||||
| chr4:121829048 | T | C | 2 | a0001c0001t0002g0047 a0001c0003t0002g0048 |
4 | HG03491.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1677-320A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829048 | |||||||
| chr4:121829185 | T | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
36 | HG00544.hp2 HG00642.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1677-457A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829185 | |||||||
| chr4:121829237 | C | CT | 22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
25 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1677-510dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829237 | |||||||
| chr4:121829237 | CT | C | 61 | a0001c0001t0002g0215 a0001c0001t0002g0228 a0001c0001t0003g0003 others(58): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1677-510delA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829237 | |||||||
| chr4:121829295 | C | T | 52 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0025 others(49): Show |
70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1677-567G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829295 | |||||||
| chr4:121829319 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(26): Show |
38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1677-591G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829319 | |||||||
| chr4:121829516 | A | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0036 others(12): Show |
20 | HG00544.hp2 HG01261.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1677-788T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829516 | |||||||
| chr4:121829540 | G | A | 265 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(262): Show |
360 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.1677-812C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829540 | |||||||
| chr4:121829549 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1677-821G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829549 | |||||||
| chr4:121829553 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1677-825G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829553 | |||||||
| chr4:121829734 | T | C | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1677-1006A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829734 | |||||||
| chr4:121829906 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(68): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1677-1178C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829906 | |||||||
| chr4:121829927 | CTTTTAAG others(1): Show |
C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0160 |
5 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1677-1207_1677-120 others(12): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121829927 | |||||||
| chr4:121830173 | G | A | 1 | a0001c0001t0005g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1677-1445C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121830173 | |||||||
| chr4:121831024 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0246 |
4 | NA18977.hp1 NA18993.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676+2207C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831024 | |||||||
| chr4:121831142 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1676+2089A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831142 | |||||||
| chr4:121831353 | G | T | 1 | a0001c0001t0002g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1676+1878C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831353 | |||||||
| chr4:121831354 | G | C | 1 | a0001c0001t0002g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1676+1877C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831354 | |||||||
| chr4:121831355 | A | C | 1 | a0001c0001t0002g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1676+1876T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831355 | |||||||
| chr4:121831499 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1676+1732C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831499 | |||||||
| chr4:121831901 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1676+1330T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121831901 | |||||||
| chr4:121832007 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1676+1224T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832007 | |||||||
| chr4:121832009 | A | AAC | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(26): Show |
37 | HG00544.hp1 HG00558.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1676+1220_1676+122 others(6): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACAC | 9 | a0001c0001t0001g0190 a0001c0001t0002g0264 a0001c0001t0003g0008 others(6): Show |
12 | HG00741.hp1 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1676+1218_1676+122 others(8): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACAC | 56 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(53): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1676+1216_1676+122 others(10): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACACA others(1): Show |
30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
35 | HG00408.hp1 HG00558.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1676+1214_1676+122 others(12): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACACA others(3): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0067 others(6): Show |
9 | HG01192.hp1 HG02055.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676+1212_1676+122 others(14): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACACA others(5): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0095 a0001c0001t0001g0143 others(4): Show |
8 | HG01069.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1676+1210_1676+122 others(16): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACACA others(7): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0151 a0001c0001t0001g0179 |
4 | HG02145.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1676+1208_1676+122 others(18): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | AACACACA others(9): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0191 a0001c0001t0011g0210 |
3 | HG02280.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1676+1206_1676+122 others(20): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1676+1222T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | AAC | A | 30 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(27): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.1676+1220_1676+122 others(6): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | AACACAC | A | 3 | a0001c0001t0003g0125 a0001c0001t0003g0128 a0001c0001t0010g0203 |
3 | HG00597.hp2 HG03239.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1676+1216_1676+122 others(10): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | AACACACA others(1): Show |
A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0075 |
3 | HG01884.hp2 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1676+1214_1676+122 others(12): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832009 | AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1676+1206_1676+122 others(20): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832009 | |||||||
| chr4:121832011 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1676+1220G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832011 | |||||||
| chr4:121832042 | ACAAAAC | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0158 a0001c0001t0001g0162 others(2): Show |
6 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1676+1183_1676+118 others(10): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832042 | |||||||
| chr4:121832265 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1676+966A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832265 | |||||||
| chr4:121832277 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1676+954T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832277 | |||||||
| chr4:121832601 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1676+630C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832601 | |||||||
| chr4:121832629 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0206 |
2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1676+602C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832629 | |||||||
| chr4:121832636 | A | T | 1 | a0001c0001t0005g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1676+595T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832636 | |||||||
| chr4:121832730 | A | G | 60 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(57): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1676+501T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832730 | |||||||
| chr4:121832980 | T | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0257 |
2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1676+251A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 15/18 | chr4 | 121832980 | |||||||
| chr4:121833402 | T | A | 1 | a0001c0001t0007g0271 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.1512-7A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833402 | |||||||
| chr4:121833416 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1512-21G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833416 | |||||||
| chr4:121833482 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1512-87A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833482 | |||||||
| chr4:121833734 | A | G | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1512-339T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833734 | |||||||
| chr4:121833747 | G | A | 1 | a0001c0001t0006g0108 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1512-352C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833747 | |||||||
| chr4:121833765 | A | G | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1512-370T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833765 | |||||||
| chr4:121833986 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1512-591A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121833986 | |||||||
| chr4:121834007 | T | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(68): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1512-612A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834007 | |||||||
| chr4:121834090 | A | G | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(74): Show |
111 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1512-695T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834090 | |||||||
| chr4:121834422 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1511+722A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834422 | |||||||
| chr4:121834429 | G | T | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1511+715C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834429 | |||||||
| chr4:121834449 | A | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(22): Show |
31 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1511+695T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834449 | |||||||
| chr4:121834505 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1511+639A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834505 | |||||||
| chr4:121834516 | T | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0019 others(33): Show |
45 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1511+628A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834516 | |||||||
| chr4:121834863 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1511+281A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834863 | |||||||
| chr4:121834909 | A | G | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1511+235T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121834909 | |||||||
| chr4:121835018 | T | C | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1511+126A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121835018 | |||||||
| chr4:121835119 | G | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(22): Show |
31 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1511+25C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 14/18 | chr4 | 121835119 | |||||||
| chr4:121835352 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1372-69T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121835352 | |||||||
| chr4:121835486 | T | C | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG02040.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1372-203A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121835486 | |||||||
| chr4:121835492 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1372-209T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121835492 | |||||||
| chr4:121835515 | A | C | 1 | a0001c0001t0002g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1372-232T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121835515 | |||||||
| chr4:121835751 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1372-468A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121835751 | |||||||
| chr4:121836069 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1372-786T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836069 | |||||||
| chr4:121836092 | A | G | 1 | a0001c0001t0006g0096 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1372-809T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836092 | |||||||
| chr4:121836262 | A | T | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1372-979T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836262 | |||||||
| chr4:121836343 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1372-1060G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836343 | |||||||
| chr4:121836361 | T | C | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1372-1078A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836361 | |||||||
| chr4:121836714 | C | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0220 a0001c0001t0002g0229 others(9): Show |
20 | HG00323.hp1 HG01884.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1372-1431G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836714 | |||||||
| chr4:121836836 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(42): Show |
57 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1372-1553A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836836 | |||||||
| chr4:121836943 | C | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1372-1660G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836943 | |||||||
| chr4:121836960 | T | G | 1 | a0001c0001t0002g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1372-1677A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836960 | |||||||
| chr4:121836968 | G | GT | 58 | a0001c0001t0001g0149 a0001c0001t0003g0003 a0001c0001t0003g0004 others(55): Show |
83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1372-1686dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836968 | |||||||
| chr4:121836968 | G | T | 1 | a0001c0001t0003g0129 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1372-1685C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121836968 | |||||||
| chr4:121837046 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1372-1763C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837046 | |||||||
| chr4:121837067 | A | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1372-1784T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837067 | |||||||
| chr4:121837209 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(9): Show |
18 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1372-1926G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837209 | |||||||
| chr4:121837374 | G | A | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1372-2091C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837374 | |||||||
| chr4:121837764 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1371+1867G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837764 | |||||||
| chr4:121837976 | T | C | 272 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(269): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.1371+1655A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121837976 | |||||||
| chr4:121838011 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(69): Show |
106 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1371+1620G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838011 | |||||||
| chr4:121838102 | T | TA | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(69): Show |
106 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1371+1528dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838102 | |||||||
| chr4:121838189 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1371+1442A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838189 | |||||||
| chr4:121838316 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1371+1315G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838316 | |||||||
| chr4:121838364 | G | GA | 74 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0062 others(71): Show |
109 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1371+1266dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838364 | |||||||
| chr4:121838364 | G | GAA | 10 | a0001c0001t0001g0075 a0001c0001t0002g0220 a0001c0001t0002g0225 others(7): Show |
10 | HG02572.hp1 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1371+1265_1371+126 others(6): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838364 | |||||||
| chr4:121838419 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0164 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1371+1212C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838419 | |||||||
| chr4:121838425 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1371+1206C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838425 | |||||||
| chr4:121838677 | G | T | 1 | a0001c0001t0002g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1371+954C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838677 | |||||||
| chr4:121838717 | C | T | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1371+914G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838717 | |||||||
| chr4:121838723 | T | TA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(27): Show |
39 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1371+907dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838723 | |||||||
| chr4:121838756 | G | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG01361.hp2 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1371+875C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838756 | |||||||
| chr4:121838792 | G | C | 1 | a0001c0001t0004g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1371+839C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838792 | |||||||
| chr4:121838836 | G | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(74): Show |
111 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1371+795C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838836 | |||||||
| chr4:121838903 | C | CA | 9 | a0001c0001t0001g0017 a0001c0001t0003g0129 a0001c0001t0003g0130 others(6): Show |
10 | HG00438.hp1 HG00735.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1371+727dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838903 | |||||||
| chr4:121838903 | CA | C | 72 | a0001c0001t0001g0198 a0001c0001t0002g0001 a0001c0001t0002g0002 others(69): Show |
106 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1371+727delT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838903 | |||||||
| chr4:121838985 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1371+646T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121838985 | |||||||
| chr4:121839160 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1371+471G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121839160 | |||||||
| chr4:121839244 | A | C | 3 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0012g0226 |
3 | HG01099.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1371+387T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 13/18 | chr4 | 121839244 | |||||||
| chr4:121839813 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(68): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1306-117C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121839813 | |||||||
| chr4:121839826 | G | A | 1 | a0001c0001t0008g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1306-130C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121839826 | |||||||
| chr4:121840181 | T | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1306-485A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840181 | |||||||
| chr4:121840254 | C | T | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1306-558G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840254 | |||||||
| chr4:121840283 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1306-587C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840283 | |||||||
| chr4:121840485 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1306-789C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840485 | |||||||
| chr4:121840641 | T | C | 1 | a0001c0001t0008g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306-945A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840641 | |||||||
| chr4:121840699 | T | C | 218 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(215): Show |
297 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.1306-1003A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840699 | |||||||
| chr4:121840840 | CT | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(23): Show |
36 | HG00544.hp2 HG01261.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.1306-1145delA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840840 | |||||||
| chr4:121840982 | T | G | 1 | a0001c0001t0001g0037 | 2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1306-1286A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121840982 | |||||||
| chr4:121841139 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG00544.hp2 NA18995.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1306-1443G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841139 | |||||||
| chr4:121841140 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0001g0189 |
4 | HG01884.hp2 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-1444C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841140 | |||||||
| chr4:121841172 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA18944.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1306-1476C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841172 | |||||||
| chr4:121841561 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1306-1865G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841561 | |||||||
| chr4:121841569 | A | T | 172 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(169): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1306-1873T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841569 | |||||||
| chr4:121841570 | A | T | 96 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(93): Show |
129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1306-1874T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841570 | |||||||
| chr4:121841571 | A | T | 1 | a0001c0001t0003g0119 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1306-1875T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841571 | |||||||
| chr4:121841662 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1306-1966G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841662 | |||||||
| chr4:121841669 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(22): Show |
31 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1306-1973G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841669 | |||||||
| chr4:121841776 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1306-2080A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841776 | |||||||
| chr4:121841858 | G | A | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1305+2069C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841858 | |||||||
| chr4:121841903 | TAATAC | T | 3 | a0001c0001t0007g0271 a0001c0001t0007g0272 a0001c0001t0007g0273 |
3 | HG02257.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1305+2019_1305+202 others(9): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841903 | |||||||
| chr4:121841968 | C | T | 173 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(170): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1305+1959G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121841968 | |||||||
| chr4:121842018 | A | T | 1 | a0001c0001t0005g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1305+1909T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842018 | |||||||
| chr4:121842052 | G | A | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1305+1875C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842052 | |||||||
| chr4:121842108 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1305+1819G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842108 | |||||||
| chr4:121842248 | T | A | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+1679A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842248 | |||||||
| chr4:121842251 | C | CA | 20 | a0001c0001t0001g0196 a0001c0001t0002g0046 a0001c0001t0002g0216 others(17): Show |
25 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1305+1675dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842251 | |||||||
| chr4:121842251 | CA | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0021 others(39): Show |
50 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1305+1675delT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842251 | |||||||
| chr4:121842251 | CAAAAAA | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
11 | HG01884.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+1670_1305+167 others(10): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842251 | |||||||
| chr4:121842727 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1305+1200A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842727 | |||||||
| chr4:121842847 | C | G | 1 | a0001c0001t0003g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1305+1080G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121842847 | |||||||
| chr4:121843231 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1305+696T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843231 | |||||||
| chr4:121843301 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1305+626A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843301 | |||||||
| chr4:121843315 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0086 |
4 | HG02257.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+612T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843315 | |||||||
| chr4:121843360 | A | C | 1 | a0001c0001t0002g0263 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1305+567T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843360 | |||||||
| chr4:121843398 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1305+529C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843398 | |||||||
| chr4:121843570 | A | C | 60 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(57): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1305+357T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843570 | |||||||
| chr4:121843605 | C | A | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+322G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843605 | |||||||
| chr4:121843757 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1305+170C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 12/18 | chr4 | 121843757 | |||||||
| chr4:121844316 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1231-315C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844316 | |||||||
| chr4:121844494 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(68): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1231-493G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844494 | |||||||
| chr4:121844533 | G | GT | 163 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(160): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1231-533dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844533 | |||||||
| chr4:121844533 | G | GTT | 9 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-534_1231-533d others(4): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844533 | |||||||
| chr4:121844831 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1230+673C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844831 | |||||||
| chr4:121844841 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1230+663T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121844841 | |||||||
| chr4:121845106 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1230+398G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845106 | |||||||
| chr4:121845139 | C | T | 1 | a0001c0001t0003g0117 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1230+365G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845139 | |||||||
| chr4:121845198 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1230+306C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845198 | |||||||
| chr4:121845223 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1230+281G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845223 | |||||||
| chr4:121845254 | G | A | 1 | a0001c0001t0007g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1230+250C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845254 | |||||||
| chr4:121845260 | C | T | 2 | a0001c0001t0001g0153 a0002c0005t0001g0154 |
2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1230+244G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845260 | |||||||
| chr4:121845300 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1230+204C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 11/18 | chr4 | 121845300 | |||||||
| chr4:121846381 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1038-685C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121846381 | |||||||
| chr4:121846586 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1037+818C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121846586 | |||||||
| chr4:121846804 | C | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1037+600G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121846804 | |||||||
| chr4:121846862 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1037+542G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121846862 | |||||||
| chr4:121847144 | A | C | 1 | a0001c0001t0005g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037+260T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121847144 | |||||||
| chr4:121847177 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1037+227A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121847177 | |||||||
| chr4:121847255 | G | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1037+149C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 10/18 | chr4 | 121847255 | |||||||
| chr4:121847533 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.935-27G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847533 | |||||||
| chr4:121847592 | T | C | 1 | a0001c0001t0009g0132 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.935-86A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847592 | |||||||
| chr4:121847720 | A | AT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(12): Show |
21 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.935-215dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847720 | |||||||
| chr4:121847772 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.935-266A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847772 | |||||||
| chr4:121847830 | A | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0163 a0001c0001t0001g0195 others(1): Show |
5 | HG00280.hp1 HG01256.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.935-324T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847830 | |||||||
| chr4:121847918 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.935-412T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121847918 | |||||||
| chr4:121848094 | C | G | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.935-588G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848094 | |||||||
| chr4:121848230 | T | A | 1 | a0001c0001t0003g0133 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.934+614A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848230 | |||||||
| chr4:121848464 | A | C | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.934+380T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848464 | |||||||
| chr4:121848580 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02145.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.934+264G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848580 | |||||||
| chr4:121848665 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.934+179A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848665 | |||||||
| chr4:121848809 | CTCTT | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.934+31_934+34delAA others(2): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848809 | |||||||
| chr4:121848812 | T | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(42): Show |
66 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.934+32A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 9/18 | chr4 | 121848812 | |||||||
| chr4:121849253 | A | C | 218 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(215): Show |
297 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.850-325T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849253 | |||||||
| chr4:121849362 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-434C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849362 | |||||||
| chr4:121849522 | G | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(68): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.850-594C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849522 | |||||||
| chr4:121849583 | CT | C | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.850-656delA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849583 | |||||||
| chr4:121849594 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-666G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849594 | |||||||
| chr4:121849595 | G | C | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-667C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849595 | |||||||
| chr4:121849604 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0231 |
3 | HG03834.hp1 HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.850-676C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849604 | |||||||
| chr4:121849734 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-806C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849734 | |||||||
| chr4:121849844 | A | T | 1 | a0001c0001t0008g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.850-916T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849844 | |||||||
| chr4:121849873 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850-945G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121849873 | |||||||
| chr4:121850115 | T | A | 2 | a0001c0001t0002g0275 a0001c0001t0005g0105 |
2 | HG00609.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.850-1187A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850115 | |||||||
| chr4:121850127 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850-1199T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850127 | |||||||
| chr4:121850174 | G | T | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.850-1246C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850174 | |||||||
| chr4:121850276 | C | T | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-1348G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850276 | |||||||
| chr4:121850320 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.850-1392T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850320 | |||||||
| chr4:121850475 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.850-1547C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850475 | |||||||
| chr4:121850500 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(12): Show |
21 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-1572G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850500 | |||||||
| chr4:121850798 | A | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(12): Show |
21 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-1870T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850798 | |||||||
| chr4:121850904 | C | T | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-1976G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121850904 | |||||||
| chr4:121851158 | G | A | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(38): Show |
61 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.849+1798C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851158 | |||||||
| chr4:121851213 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(42): Show |
57 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+1743A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851213 | |||||||
| chr4:121851288 | A | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(18): Show |
28 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.849+1668T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851288 | |||||||
| chr4:121851373 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849+1583C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851373 | |||||||
| chr4:121851379 | G | GA | 78 | a0001c0001t0001g0055 a0001c0001t0001g0147 a0001c0001t0001g0156 others(75): Show |
112 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.849+1576dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851379 | |||||||
| chr4:121851788 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.849+1168A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851788 | |||||||
| chr4:121851903 | C | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(22): Show |
31 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.849+1053G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121851903 | |||||||
| chr4:121852047 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.849+909T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121852047 | |||||||
| chr4:121852607 | T | G | 1 | a0001c0001t0007g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.849+349A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121852607 | |||||||
| chr4:121852712 | T | TATTATTA others(28): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02165.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.849+243_849+244ins others(35): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 8/18 | chr4 | 121852712 | |||||||
| chr4:121853127 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.719-41A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853127 | |||||||
| chr4:121853154 | A | G | 5 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0271 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-68T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853154 | |||||||
| chr4:121853190 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.719-104C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853190 | |||||||
| chr4:121853600 | T | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(23): Show |
32 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.719-514A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853600 | |||||||
| chr4:121853638 | G | T | 2 | a0001c0001t0002g0248 a0001c0001t0002g0267 |
2 | HG01516.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.719-552C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853638 | |||||||
| chr4:121853681 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0163 others(2): Show |
7 | HG00280.hp1 HG01256.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.719-595A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853681 | |||||||
| chr4:121853748 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.719-662C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853748 | |||||||
| chr4:121853762 | G | A | 199 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0018 others(196): Show |
271 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.719-676C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853762 | |||||||
| chr4:121853810 | G | A | 4 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 others(1): Show |
4 | HG00642.hp2 HG01516.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-724C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121853810 | |||||||
| chr4:121854087 | C | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0234 a0001c0001t0002g0235 |
4 | HG03831.hp2 NA18612.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+617G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121854087 | |||||||
| chr4:121854095 | A | T | 1 | a0001c0001t0003g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.718+609T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121854095 | |||||||
| chr4:121854321 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.718+383A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121854321 | |||||||
| chr4:121854385 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0099 a0001c0001t0001g0165 others(3): Show |
9 | HG02451.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+319G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121854385 | |||||||
| chr4:121854528 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718+176T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 7/18 | chr4 | 121854528 | |||||||
| chr4:121854893 | A | T | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.602-73T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 6/18 | chr4 | 121854893 | |||||||
| chr4:121854912 | A | G | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(69): Show |
106 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.602-92T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 6/18 | chr4 | 121854912 | |||||||
| chr4:121855300 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.601+189G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 6/18 | chr4 | 121855300 | |||||||
| chr4:121855405 | T | A | 1 | a0001c0001t0002g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.601+84A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 6/18 | chr4 | 121855405 | |||||||
| chr4:121855406 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601+83T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 6/18 | chr4 | 121855406 | |||||||
| chr4:121855580 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.529-19T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855580 | |||||||
| chr4:121855633 | C | T | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.529-72G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855633 | |||||||
| chr4:121855658 | T | C | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.529-97A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855658 | |||||||
| chr4:121855704 | C | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.529-143G>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855704 | |||||||
| chr4:121855775 | AATGTATA others(1): Show |
A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0094 others(4): Show |
9 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-222_529-215del others(8): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855775 | |||||||
| chr4:121855778 | G | A | 213 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(210): Show |
290 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.529-217C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855778 | |||||||
| chr4:121855792 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0094 others(4): Show |
9 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-231C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855792 | |||||||
| chr4:121855851 | C | CACATGTA others(33): Show |
58 | a0001c0001t0002g0233 a0001c0001t0003g0003 a0001c0001t0003g0004 others(55): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.529-330_529-291dup others(40): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855851 | |||||||
| chr4:121855851 | C | CACATGTA others(73): Show |
6 | a0001c0001t0005g0107 a0001c0001t0006g0007 a0001c0001t0006g0026 others(3): Show |
10 | HG01943.hp1 HG01981.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.529-291_529-290ins others(80): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855851 | |||||||
| chr4:121855851 | CACATGTA others(33): Show |
C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(26): Show |
38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.529-330_529-291del others(40): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855851 | |||||||
| chr4:121855887 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.529-326A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855887 | |||||||
| chr4:121855896 | GTATGTGT others(11): Show |
G | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.529-353_529-336del others(18): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855896 | |||||||
| chr4:121855910 | GTATA | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(13): Show |
22 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.529-353_529-350del others(4): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855910 | |||||||
| chr4:121855914 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.529-353T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855914 | |||||||
| chr4:121855916 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.529-355T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855916 | |||||||
| chr4:121855922 | A | G | 1 | a0001c0003t0003g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.529-361T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855922 | |||||||
| chr4:121855962 | GTA | G | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.529-403_529-402del others(2): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855962 | |||||||
| chr4:121855962 | GTATA | G | 193 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0018 others(190): Show |
265 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.529-405_529-402del others(4): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121855962 | |||||||
| chr4:121856297 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.529-736A>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121856297 | |||||||
| chr4:121856387 | T | C | 5 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0271 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-826A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121856387 | |||||||
| chr4:121856423 | C | T | 1 | a0001c0001t0001g0011 | 3 | HG02083.hp1 NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.529-862G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121856423 | |||||||
| chr4:121856822 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.529-1261A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121856822 | |||||||
| chr4:121857121 | C | CT | 194 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(191): Show |
267 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.529-1561dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857121 | |||||||
| chr4:121857121 | C | CTT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(29): Show |
41 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.529-1562_529-1561d others(4): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857121 | |||||||
| chr4:121857182 | G | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.529-1621C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857182 | |||||||
| chr4:121857265 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(5): Show |
10 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.529-1704A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857265 | |||||||
| chr4:121857436 | A | G | 1 | a0001c0001t0002g0212 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.528+1556T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857436 | |||||||
| chr4:121857470 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG00544.hp2 NA18995.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.528+1522C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857470 | |||||||
| chr4:121857621 | G | A | 1 | a0001c0001t0005g0138 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.528+1371C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857621 | |||||||
| chr4:121857808 | C | CT | 8 | a0001c0001t0001g0080 a0001c0001t0001g0147 a0001c0001t0001g0156 others(5): Show |
8 | HG00733.hp1 HG01168.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+1183dupA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857808 | |||||||
| chr4:121857808 | C | CTT | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(205): Show |
287 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.528+1182_528+1183d others(4): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857808 | |||||||
| chr4:121857830 | G | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(69): Show |
106 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.528+1162C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121857830 | |||||||
| chr4:121858046 | T | A | 1 | a0001c0001t0004g0044 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.528+946A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858046 | |||||||
| chr4:121858139 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.528+853C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858139 | |||||||
| chr4:121858223 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.528+769G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858223 | |||||||
| chr4:121858282 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(30): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.528+710G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858282 | |||||||
| chr4:121858296 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.528+696C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858296 | |||||||
| chr4:121858365 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.528+627T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858365 | |||||||
| chr4:121858369 | AGT | A | 213 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(210): Show |
291 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+621_528+622del others(2): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858369 | |||||||
| chr4:121858515 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.528+477A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858515 | |||||||
| chr4:121858544 | A | C | 1 | a0001c0001t0001g0021 | 2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.528+448T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858544 | |||||||
| chr4:121858602 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.528+390A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858602 | |||||||
| chr4:121858611 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.528+381T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858611 | |||||||
| chr4:121858715 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.528+277A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858715 | |||||||
| chr4:121858819 | C | G | 220 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(217): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.528+173G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 5/18 | chr4 | 121858819 | |||||||
| chr4:121859236 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.342-58C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121859236 | |||||||
| chr4:121859277 | A | T | 3 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0012g0226 |
3 | HG01099.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.342-99T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121859277 | |||||||
| chr4:121859768 | GA | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0099 a0001c0001t0001g0165 others(3): Show |
9 | HG02451.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-591delT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121859768 | |||||||
| chr4:121859796 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0164 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.342-618A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121859796 | |||||||
| chr4:121859830 | T | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-652A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121859830 | |||||||
| chr4:121860080 | A | G | 1 | a0001c0001t0005g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.342-902T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121860080 | |||||||
| chr4:121860108 | A | C | 218 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(215): Show |
297 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.342-930T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121860108 | |||||||
| chr4:121860247 | T | C | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0016 others(74): Show |
111 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.342-1069A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121860247 | |||||||
| chr4:121860734 | G | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(8): Show |
14 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+770C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121860734 | |||||||
| chr4:121861208 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0176 |
3 | HG01123.hp2 HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.341+296C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 4/18 | chr4 | 121861208 | |||||||
| chr4:121861724 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.166-45C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121861724 | |||||||
| chr4:121861816 | A | C | 2 | a0001c0001t0003g0103 a0001c0001t0003g0104 |
2 | NA19059.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.166-137T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121861816 | |||||||
| chr4:121861823 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.166-144A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121861823 | |||||||
| chr4:121862066 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-387G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862066 | |||||||
| chr4:121862078 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(60): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.166-399C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862078 | |||||||
| chr4:121862220 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.166-541A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862220 | |||||||
| chr4:121862289 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.166-610T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862289 | |||||||
| chr4:121862413 | G | C | 2 | a0001c0001t0002g0047 a0001c0003t0002g0048 |
4 | HG03491.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-734C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862413 | |||||||
| chr4:121862606 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.165+611C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862606 | |||||||
| chr4:121862743 | T | C | 5 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0271 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+474A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 3/18 | chr4 | 121862743 | |||||||
| chr4:121863351 | G | C | 2 | a0001c0001t0007g0255 a0001c0001t0007g0256 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.103-72C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863351 | |||||||
| chr4:121863482 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.103-203A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863482 | |||||||
| chr4:121863524 | A | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0102 |
2 | HG00408.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.103-245T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863524 | |||||||
| chr4:121863527 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-248T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863527 | |||||||
| chr4:121863591 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.103-312G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863591 | |||||||
| chr4:121863700 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.103-421A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863700 | |||||||
| chr4:121863905 | T | C | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.103-626A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863905 | |||||||
| chr4:121863937 | G | A | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103-658C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121863937 | |||||||
| chr4:121864147 | C | G | 1 | a0001c0001t0002g0225 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.103-868G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864147 | |||||||
| chr4:121864302 | A | G | 173 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(170): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.103-1023T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864302 | |||||||
| chr4:121864323 | T | C | 2 | a0001c0001t0002g0217 a0001c0001t0002g0257 |
2 | NA18979.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.103-1044A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864323 | |||||||
| chr4:121864689 | G | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-1410C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864689 | |||||||
| chr4:121864811 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.103-1532A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864811 | |||||||
| chr4:121864821 | T | C | 2 | a0001c0002t0001g0089 a0001c0002t0001g0090 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.103-1542A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121864821 | |||||||
| chr4:121865046 | C | T | 8 | a0001c0001t0004g0005 a0001c0001t0004g0044 a0001c0001t0004g0049 others(5): Show |
15 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.103-1767G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865046 | |||||||
| chr4:121865241 | CT | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0039 others(164): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.103-1963delA | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865241 | |||||||
| chr4:121865246 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0086 |
4 | HG02257.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1967A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865246 | |||||||
| chr4:121865277 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103-1998G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865277 | |||||||
| chr4:121865486 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.103-2207C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865486 | |||||||
| chr4:121865599 | T | A | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103-2320A>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865599 | |||||||
| chr4:121865872 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+2109A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865872 | |||||||
| chr4:121865975 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.102+2006C>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121865975 | |||||||
| chr4:121866094 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0056 |
4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1887C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866094 | |||||||
| chr4:121866170 | T | C | 1 | a0001c0001t0001g0017 | 2 | NA18973.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.102+1811A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866170 | |||||||
| chr4:121866289 | A | G | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+1692T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866289 | |||||||
| chr4:121866395 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.102+1586A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866395 | |||||||
| chr4:121866612 | G | A | 1 | a0001c0003t0003g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.102+1369C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866612 | |||||||
| chr4:121866654 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.102+1327T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866654 | |||||||
| chr4:121866655 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.102+1326C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866655 | |||||||
| chr4:121866687 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102+1294G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866687 | |||||||
| chr4:121866945 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.102+1036A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121866945 | |||||||
| chr4:121867152 | T | C | 1 | a0003c0004t0001g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.102+829A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867152 | |||||||
| chr4:121867284 | T | C | 1 | a0001c0001t0002g0259 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.102+697A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867284 | |||||||
| chr4:121867389 | C | G | 1 | a0001c0001t0002g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.102+592G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867389 | |||||||
| chr4:121867578 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102+403T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867578 | |||||||
| chr4:121867659 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102+322T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867659 | |||||||
| chr4:121867671 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.102+310T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867671 | |||||||
| chr4:121867727 | C | T | 161 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(158): Show |
222 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.102+254G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867727 | |||||||
| chr4:121867866 | T | C | 2 | a0001c0001t0004g0049 a0001c0001t0004g0219 |
3 | NA18959.hp2 NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.102+115A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867866 | |||||||
| chr4:121867918 | A | C | 1 | a0001c0001t0002g0220 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.102+63T>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867918 | |||||||
| chr4:121867920 | A | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(18): Show |
28 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.102+61T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 2/18 | chr4 | 121867920 | |||||||
| chr4:121868113 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG03831.hp1 NA18946.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-67A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868113 | |||||||
| chr4:121868239 | C | G | 1 | a0001c0001t0005g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.37-193G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868239 | |||||||
| chr4:121868397 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
11 | HG01884.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-351C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868397 | |||||||
| chr4:121868684 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0037 others(20): Show |
30 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.37-639dupT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | C | CAA | 11 | a0001c0001t0001g0042 a0001c0001t0001g0178 a0001c0001t0001g0179 others(8): Show |
12 | HG01192.hp1 HG02074.hp1 HG03195.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-640_37-639dupTT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | C | CAAA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0186 others(5): Show |
13 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-641_37-639dupTT others(1): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | C | CAAAA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0191 others(3): Show |
9 | HG00544.hp2 HG00735.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.37-642_37-639dupTT others(2): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.37-648_37-639dupTT others(8): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CA | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0078 others(24): Show |
30 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.37-639delT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CAA | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(77): Show |
122 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.37-640_37-639delTT | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CAAA | C | 13 | a0001c0001t0001g0057 a0001c0001t0001g0142 a0001c0001t0001g0143 others(10): Show |
13 | HG00558.hp1 HG00673.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.37-641_37-639delTT others(1): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CAAAAAAA others(2): Show |
C | 58 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0008 others(55): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.37-647_37-639delTT others(7): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0099 others(4): Show |
8 | HG01099.hp1 HG01243.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-648_37-639delTT others(8): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868684 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0093 others(2): Show |
7 | HG01069.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-649_37-639delTT others(9): Show |
BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868684 | |||||||
| chr4:121868752 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.37-706G>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868752 | |||||||
| chr4:121868802 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0195 a0001c0001t0001g0209 |
4 | HG00280.hp1 HG01256.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-756C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868802 | |||||||
| chr4:121868829 | G | C | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.37-783C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121868829 | |||||||
| chr4:121869241 | A | G | 262 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(259): Show |
356 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.36+1037T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869241 | |||||||
| chr4:121869304 | A | T | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.36+974T>A | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869304 | |||||||
| chr4:121869330 | A | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(43): Show |
58 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.36+948T>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869330 | |||||||
| chr4:121869559 | G | A | 1 | a0001c0001t0003g0205 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.36+719C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869559 | |||||||
| chr4:121869823 | G | A | 1 | a0001c0001t0004g0274 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.36+455C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869823 | |||||||
| chr4:121869839 | C | G | 3 | a0001c0001t0008g0052 a0001c0001t0008g0053 a0001c0001t0008g0054 |
3 | HG02630.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.36+439G>C | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869839 | |||||||
| chr4:121869876 | G | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0206 a0001c0001t0001g0207 |
4 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+402C>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869876 | |||||||
| chr4:121869904 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.36+374A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869904 | |||||||
| chr4:121869941 | T | C | 1 | a0001c0001t0011g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.36+337A>G | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869941 | |||||||
| chr4:121869945 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.36+333C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121869945 | |||||||
| chr4:121870160 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.36+118C>T | BBS7 | ENSG00000138686.10 | transcript | ENST00000264499.9 | protein_coding | 1/18 | chr4 | 121870160 |