Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129880 |
| ensemblid | ENSG00000163093.12 |
| hgncid | 970 |
| symbol | BBS5 |
| name | Bardet-Biedl syndrome 5 |
| refseq_nuc | NM_152384.3 |
| refseq_prot | NP_689597.1 |
| ensembl_nuc | ENST00000295240.8 |
| ensembl_prot | ENSP00000295240.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 169479494 |
| end | 169506655 |
| strand | + |
| ver | v1.2 |
| region | chr2:169479494-169506655 |
| region5000 | chr2:169474494-169511655 |
| regionname0 | BBS5_chr2_169479494_169506655 |
| regionname5000 | BBS5_chr2_169474494_169511655 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 341 | 394 | 95 | 54 | 185 | 14 | 44 | 151 | BBS5_chr2_169474494_169511655 | BBS5 | MSVLD others(336): Show |
chr2 | 169474494 | 169511655 |
| a0002 | 0/0 | 341 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | MSVLD others(336): Show |
chr2 | 169474494 | 169511655 |
| a0003 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | MSVLD others(336): Show |
chr2 | 169474494 | 169511655 |
| a0004 | 0/0 | 341 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | MSVLD others(336): Show |
chr2 | 169474494 | 169511655 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1023 | 369 | 70 | 54 | 185 | 14 | 44 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0001c0002 | 0/0 | 1023 | 17 | 17 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0001c0003 | 0/0 | 1023 | 4 | 4 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0001c0004 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0001c0007 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0002c0005 | 0/0 | 1023 | 2 | 0 | 2 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0003c0006 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 | ||
| a0004c0008 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | ATGTC others(1018): Show |
chr2 | 169474494 | 169511655 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3110 | 111 | 17 | 24 | 52 | 6 | 12 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0002 | 0/0 | 3159 | 99 | 9 | 6 | 74 | 2 | 8 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0003 | 0/0 | 3159 | 29 | 9 | 8 | 9 | 0 | 3 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0004 | 0/0 | 3159 | 17 | 11 | 1 | 4 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0005 | 0/0 | 3161 | 15 | 0 | 1 | 13 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3156): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0006 | 1/0 | 3159 | 12 | 1 | 2 | 0 | 2 | 6 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0007 | 0/0 | 3159 | 11 | 2 | 4 | 1 | 1 | 3 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0009 | 0/0 | 3159 | 8 | 7 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0010 | 0/0 | 3159 | 7 | 3 | 0 | 0 | 1 | 3 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0011 | 0/0 | 3159 | 7 | 0 | 0 | 7 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0013 | 0/0 | 3161 | 5 | 0 | 0 | 5 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3156): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0014 | 0/0 | 3111 | 5 | 3 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3106): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0015 | 0/0 | 3110 | 5 | 0 | 0 | 5 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0016 | 0/0 | 3110 | 4 | 0 | 0 | 4 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0017 | 0/0 | 3158 | 3 | 2 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3153): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0018 | 0/0 | 3110 | 3 | 0 | 0 | 0 | 0 | 3 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0021 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0023 | 0/0 | 3159 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0024 | 0/0 | 3159 | 2 | 0 | 1 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0025 | 0/0 | 3159 | 2 | 0 | 0 | 0 | 1 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0026 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0027 | 0/0 | 3157 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3152): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0029 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0030 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0031 | 0/0 | 3199 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3194): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0032 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3155): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0033 | 0/1 | 3159 | 1 | 0 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0035 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0036 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3155): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0037 | 0/0 | 3159 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0038 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0039 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0040 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0041 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0042 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0043 | 0/0 | 3159 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0044 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0046 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0047 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3105): Show |
chr2 | 169474494 | 169511655 |
| a0001c0001t0048 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0002t0008 | 0/0 | 3159 | 9 | 9 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0002t0012 | 0/0 | 3159 | 5 | 5 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0002t0022 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0002t0034 | 0/0 | 3158 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3153): Show |
chr2 | 169474494 | 169511655 |
| a0001c0003t0020 | 0/0 | 3159 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0003t0028 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0001c0004t0019 | 0/0 | 3257 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3252): Show |
chr2 | 169474494 | 169511655 |
| a0001c0007t0045 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0002c0005t0002 | 0/0 | 3159 | 2 | 0 | 2 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0003c0006t0003 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| a0004c0008t0002 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | AGAGA others(3154): Show |
chr2 | 169474494 | 169511655 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 7 | 19 | 2 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0002 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 1 | 1 | 3 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 1 | 0 | 1 | 4 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0010 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0004 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0024 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0009g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0009g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0011g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0013g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0014g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0015g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0016g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0016g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0017g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0021g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0023g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0023g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0024g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0024g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0025g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0026g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0027g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0029g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0031g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0032g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0033g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0035g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0036g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0037g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0038g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0039g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0040g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0041g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0042g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0043g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0044g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0046g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0047g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0001t0048g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0012g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0022g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0022g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0002t0034g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0003t0020g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0003t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0003t0020g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0003t0028g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0004t0019g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0001c0007t0045g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0002c0005t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0002c0005t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0003c0006t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| a0004c0008t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0176 | EUR | GBR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0069 | EUR | GBR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0229 | EUR | FIN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | FIN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0233 | EUR | FIN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00438 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00639 | hp2 | a0002 | c0005 | t0002 | g0006 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01070 | hp1 | a0001 | c0001 | t0044 | g0162 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01099 | hp1 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01106 | hp2 | a0002 | c0005 | t0002 | g0103 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01109 | hp1 | a0001 | c0001 | t0024 | g0172 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01109 | hp2 | a0001 | c0001 | t0041 | g0167 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0155 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01255 | hp1 | a0001 | c0001 | t0048 | g0232 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0226 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01261 | hp1 | a0001 | c0001 | t0026 | g0036 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01496 | hp2 | a0001 | c0001 | t0017 | g0049 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01891 | hp2 | a0001 | c0007 | t0045 | g0211 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01978 | hp1 | a0001 | c0001 | t0038 | g0207 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0217 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02074 | hp1 | a0001 | c0001 | t0016 | g0187 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02132 | hp1 | a0001 | c0001 | t0031 | g0146 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02135 | hp2 | a0001 | c0001 | t0013 | g0071 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02145 | hp1 | a0001 | c0002 | t0008 | g0215 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0055 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02258 | hp2 | a0001 | c0002 | t0012 | g0241 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02280 | hp1 | a0001 | c0002 | t0008 | g0212 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02523 | hp2 | a0001 | c0001 | t0036 | g0014 | EAS | KHV | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02602 | hp2 | a0001 | c0001 | t0024 | g0016 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0045 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02630 | hp2 | a0001 | c0003 | t0020 | g0110 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02647 | hp1 | a0001 | c0003 | t0028 | g0209 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0024 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02723 | hp1 | a0001 | c0002 | t0034 | g0045 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0063 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02735 | hp1 | a0001 | c0001 | t0037 | g0136 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0039 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02886 | hp2 | a0003 | c0006 | t0003 | g0004 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0151 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0247 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0168 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02970 | hp2 | a0001 | c0002 | t0022 | g0219 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0165 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03098 | hp1 | a0001 | c0002 | t0022 | g0218 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0046 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0046 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03139 | hp2 | a0001 | c0002 | t0012 | g0047 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0049 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03195 | hp2 | a0001 | c0002 | t0012 | g0240 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03209 | hp1 | a0001 | c0004 | t0019 | g0020 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03225 | hp1 | a0001 | c0001 | t0021 | g0238 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03225 | hp2 | a0001 | c0004 | t0019 | g0020 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03239 | hp1 | a0001 | c0001 | t0025 | g0130 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0246 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03486 | hp2 | a0001 | c0003 | t0020 | g0111 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0016 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0239 | AFR | ESN | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0214 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0213 | AFR | MSL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0026 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03704 | hp2 | a0001 | c0001 | t0010 | g0026 | SAS | PJL | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0245 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03927 | hp1 | a0001 | c0001 | t0032 | g0084 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03927 | hp2 | a0001 | c0001 | t0018 | g0001 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG03942 | hp2 | a0001 | c0001 | t0043 | g0006 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04115 | hp1 | a0001 | c0001 | t0018 | g0196 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0061 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0024 | SAS | STU | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0216 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | CHB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18747 | hp2 | a0001 | c0001 | t0047 | g0001 | EAS | CHB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18906 | hp2 | a0001 | c0001 | t0035 | g0139 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18939 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18939 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18949 | hp2 | a0001 | c0001 | t0042 | g0133 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18952 | hp2 | a0001 | c0001 | t0027 | g0073 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18956 | hp1 | a0001 | c0001 | t0011 | g0104 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18960 | hp1 | a0001 | c0001 | t0015 | g0017 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18965 | hp2 | a0001 | c0001 | t0030 | g0129 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18970 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18981 | hp2 | a0001 | c0001 | t0013 | g0074 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18982 | hp2 | a0001 | c0001 | t0015 | g0005 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18986 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18987 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18994 | hp2 | a0001 | c0001 | t0016 | g0163 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18997 | hp1 | a0001 | c0001 | t0014 | g0203 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18997 | hp2 | a0001 | c0001 | t0023 | g0021 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18998 | hp1 | a0001 | c0001 | t0039 | g0188 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18998 | hp2 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19005 | hp2 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19055 | hp1 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19055 | hp2 | a0001 | c0001 | t0016 | g0189 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19066 | hp2 | a0001 | c0001 | t0013 | g0013 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19072 | hp1 | a0004 | c0008 | t0002 | g0082 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19074 | hp2 | a0001 | c0001 | t0013 | g0013 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19081 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19091 | hp1 | a0001 | c0001 | t0013 | g0013 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20129 | hp1 | a0001 | c0004 | t0019 | g0020 | AFR | ASW | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ASW | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20752 | hp1 | a0001 | c0001 | t0025 | g0003 | EUR | TSI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0152 | EUR | TSI | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0039 | SAS | GIH | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0001 | SAS | GIH | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02486 | hp2 | a0001 | c0003 | t0020 | g0109 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG02559 | hp2 | a0001 | c0002 | t0012 | g0047 | AFR | ACB | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG06807 | hp1 | a0001 | c0001 | t0029 | g0115 | AFR | USA | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | USA | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | USA | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0108 | AFR | LWK | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0033 | g0158 | REF | REF | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0024 | REF | REF | BBS5_chr2_169474494_169511655 | BBS5 | chr2 | 169474494 | 169511655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169482254 | A | T | 1 | a0004 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.63A>T | p.Gln21His | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/12 | 123/3159 | 63/1026 | 21/341 | chr2 | 169482254 | |||
| chr2:169488036 | G | A | 1 | a0003 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.308G>A | p.Ser103Asn | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/12 | 368/3159 | 308/1026 | 103/341 | chr2 | 169488036 | |||
| chr2:169497628 | G | A | 1 | a0002 | 2 | HG00639.hp2 HG01106.hp2 |
missense_variant&splice_region_variant | MODERATE | c.620G>A | p.Arg207His | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/12 | 680/3159 | 620/1026 | 207/341 | chr2 | 169497628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169479592 | C | G | 2 | a0001c0002 a0001c0004 |
20 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(17): Show |
synonymous_variant | LOW | c.39C>G | p.Val13Val | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/12 | 99/3159 | 39/1026 | 13/341 | chr2 | 169479592 | |||
| chr2:169482299 | C | T | 1 | a0001c0003 | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
synonymous_variant | LOW | c.108C>T | p.Ser36Ser | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/12 | 168/3159 | 108/1026 | 36/341 | chr2 | 169482299 | |||
| chr2:169488013 | C | T | 1 | a0001c0004 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.285C>T | p.Leu95Leu | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/12 | 345/3159 | 285/1026 | 95/341 | chr2 | 169488013 | |||
| chr2:169492988 | T | A | 1 | a0001c0004 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.501T>A | p.Val167Val | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 6/12 | 561/3159 | 501/1026 | 167/341 | chr2 | 169492988 | |||
| chr2:169499554 | C | T | 1 | a0001c0007 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.750C>T | p.Ile250Ile | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/12 | 810/3159 | 750/1026 | 250/341 | chr2 | 169499554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169479514 | G | C | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/12 | 40 | chr2 | 169479514 | ||||||
| chr2:169479532 | C | T | 1 | a0001c0003t0020 | 3 | HG02486.hp2 HG02630.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-22C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/12 | 22 | chr2 | 169479532 | ||||||
| chr2:169479552 | C | A | 1 | a0001c0001t0026 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/12 | 2 | chr2 | 169479552 | ||||||
| chr2:169504747 | TTTTCGGC others(35): Show |
T | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167_*208delTTCGGC others(36): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 167 | INFO_REALIGN_3_PRIME | chr2 | 169504747 | |||||
| chr2:169504802 | G | A | 2 | a0001c0003t0020 a0001c0003t0028 |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 220 | chr2 | 169504802 | ||||||
| chr2:169504805 | C | G | 1 | a0001c0001t0025 | 2 | HG03239.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*223C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 223 | chr2 | 169504805 | ||||||
| chr2:169504824 | A | G | 2 | a0001c0001t0007 a0001c0001t0024 |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*242A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 242 | chr2 | 169504824 | ||||||
| chr2:169504865 | A | G | 1 | a0001c0001t0047 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 283 | chr2 | 169504865 | ||||||
| chr2:169504899 | C | G | 1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*317C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 317 | chr2 | 169504899 | ||||||
| chr2:169504905 | A | G | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(41): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*323A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 323 | chr2 | 169504905 | ||||||
| chr2:169504916 | T | C | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
3_prime_UTR_variant | MODIFIER | c.*334T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 334 | chr2 | 169504916 | ||||||
| chr2:169504971 | A | G | 2 | a0001c0003t0020 a0001c0003t0028 |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 389 | chr2 | 169504971 | ||||||
| chr2:169505020 | A | G | 1 | a0001c0001t0046 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 438 | chr2 | 169505020 | ||||||
| chr2:169505080 | G | A | 1 | a0001c0001t0030 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 498 | chr2 | 169505080 | ||||||
| chr2:169505093 | T | C | 1 | a0001c0002t0012 | 5 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*511T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 511 | chr2 | 169505093 | ||||||
| chr2:169505189 | G | A | 1 | a0001c0001t0010 | 7 | HG00099.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*607G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 607 | chr2 | 169505189 | ||||||
| chr2:169505191 | G | C | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*609G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 609 | chr2 | 169505191 | ||||||
| chr2:169505200 | G | C | 2 | a0001c0002t0012 a0001c0002t0022 |
7 | HG02258.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*618G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 618 | chr2 | 169505200 | ||||||
| chr2:169505296 | C | T | 1 | a0001c0007t0045 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*714C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 714 | chr2 | 169505296 | ||||||
| chr2:169505367 | C | T | 1 | a0001c0001t0015 | 5 | NA18939.hp2 NA18960.hp1 NA18970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*785C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 785 | chr2 | 169505367 | ||||||
| chr2:169505372 | G | A | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*790G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 790 | chr2 | 169505372 | ||||||
| chr2:169505438 | C | T | 1 | a0001c0001t0044 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 856 | chr2 | 169505438 | ||||||
| chr2:169505485 | G | GCCGCCAT others(33): Show |
1 | a0001c0001t0031 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932_*971dupGCCTCT others(34): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 972 | INFO_REALIGN_3_PRIME | chr2 | 169505485 | |||||
| chr2:169505554 | T | G | 1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*972T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 972 | chr2 | 169505554 | ||||||
| chr2:169505563 | T | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(42): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*981T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 981 | chr2 | 169505563 | ||||||
| chr2:169505567 | C | T | 1 | a0001c0001t0018 | 3 | HG03927.hp2 HG04115.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*985C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 985 | chr2 | 169505567 | ||||||
| chr2:169505575 | G | A | 1 | a0001c0002t0022 | 2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*993G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 993 | chr2 | 169505575 | ||||||
| chr2:169505593 | A | G | 1 | a0001c0001t0043 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1011 | chr2 | 169505593 | ||||||
| chr2:169505603 | G | C | 1 | a0001c0001t0043 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1021 | chr2 | 169505603 | ||||||
| chr2:169505632 | C | A | 1 | a0001c0001t0013 | 5 | HG02135.hp2 NA18981.hp2 NA19066.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1050C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1050 | chr2 | 169505632 | ||||||
| chr2:169505660 | A | C | 1 | a0001c0001t0023 | 2 | NA18997.hp2 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1078A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1078 | chr2 | 169505660 | ||||||
| chr2:169505675 | C | T | 1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1093C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1093 | chr2 | 169505675 | ||||||
| chr2:169505684 | A | C | 1 | a0001c0001t0042 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1102 | chr2 | 169505684 | ||||||
| chr2:169505686 | C | T | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1104C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1104 | chr2 | 169505686 | ||||||
| chr2:169505786 | G | A | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1204 | chr2 | 169505786 | ||||||
| chr2:169505826 | T | TG | 7 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0031 others(4): Show |
36 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1251dupG | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1252 | INFO_REALIGN_3_PRIME | chr2 | 169505826 | |||||
| chr2:169505843 | C | T | 1 | a0001c0001t0029 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1261 | chr2 | 169505843 | ||||||
| chr2:169505856 | G | A | 2 | a0001c0002t0008 a0001c0002t0034 |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1274G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1274 | chr2 | 169505856 | ||||||
| chr2:169505864 | C | T | 1 | a0001c0001t0011 | 7 | HG00438.hp1 NA18939.hp1 NA18956.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1282 | chr2 | 169505864 | ||||||
| chr2:169505900 | C | G | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1318C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1318 | chr2 | 169505900 | ||||||
| chr2:169505934 | A | ACCCCGTC others(42): Show |
1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1377_*1425dupGGTC others(45): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1426 | INFO_REALIGN_3_PRIME | chr2 | 169505934 | |||||
| chr2:169505938 | C | T | 2 | a0001c0001t0040 a0001c0001t0041 |
2 | HG01109.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1356 | chr2 | 169505938 | ||||||
| chr2:169505942 | C | T | 2 | a0001c0003t0020 a0001c0003t0028 |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1360C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1360 | chr2 | 169505942 | ||||||
| chr2:169505959 | GGTCAGCC others(42): Show |
G | 9 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0015 others(6): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1378_*1426delGTCA others(45): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1378 | chr2 | 169505959 | ||||||
| chr2:169505970 | C | CGTCCGGC others(71): Show |
1 | a0001c0001t0005 | 2 | NA19001.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1389_*1390insTCCG others(74): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1390 | INFO_REALIGN_3_PRIME | chr2 | 169505970 | |||||
| chr2:169505975 | G | C | 1 | a0001c0001t0005 | 2 | NA19001.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1393G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1393 | chr2 | 169505975 | ||||||
| chr2:169505978 | CAGCCGCC others(41): Show |
C | 1 | a0001c0001t0044 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1416_*1463delGAGG others(44): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1416 | INFO_REALIGN_3_PRIME | chr2 | 169505978 | |||||
| chr2:169505982 | C | T | 1 | a0001c0001t0002 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1400C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1400 | chr2 | 169505982 | ||||||
| chr2:169506008 | A | G | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(28): Show |
207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1426A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1426 | chr2 | 169506008 | ||||||
| chr2:169506018 | C | T | 1 | a0001c0001t0039 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1436C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1436 | chr2 | 169506018 | ||||||
| chr2:169506019 | G | A | 1 | a0001c0001t0035 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1437G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1437 | chr2 | 169506019 | ||||||
| chr2:169506026 | T | C | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 others(1): Show |
24 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1444T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1444 | chr2 | 169506026 | ||||||
| chr2:169506082 | G | T | 1 | a0001c0001t0016 | 4 | HG02074.hp1 NA18987.hp1 NA18994.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1500G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1500 | chr2 | 169506082 | ||||||
| chr2:169506101 | G | GCCAGCCC others(31): Show |
1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1519_*1520insCCAG others(34): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1520 | chr2 | 169506101 | ||||||
| chr2:169506118 | A | AGGAGGGA others(42): Show |
1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1579_*1580insCGTC others(45): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1580 | INFO_REALIGN_3_PRIME | chr2 | 169506118 | |||||
| chr2:169506128 | T | G | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1546T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1546 | chr2 | 169506128 | ||||||
| chr2:169506140 | C | T | 1 | a0001c0001t0037 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1558C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1558 | chr2 | 169506140 | ||||||
| chr2:169506168 | G | T | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1586G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1586 | chr2 | 169506168 | ||||||
| chr2:169506170 | A | C | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1588A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1588 | chr2 | 169506170 | ||||||
| chr2:169506192 | C | A | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1610 | chr2 | 169506192 | ||||||
| chr2:169506194 | C | T | 4 | a0001c0001t0010 a0001c0001t0017 a0001c0002t0008 others(1): Show |
20 | HG00099.hp1 HG01496.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1612C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1612 | chr2 | 169506194 | ||||||
| chr2:169506200 | G | C | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1618 | chr2 | 169506200 | ||||||
| chr2:169506201 | C | G | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1619 | chr2 | 169506201 | ||||||
| chr2:169506204 | G | T | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1622G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1622 | chr2 | 169506204 | ||||||
| chr2:169506208 | C | G | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1626C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1626 | chr2 | 169506208 | ||||||
| chr2:169506227 | G | C | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1645G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1645 | chr2 | 169506227 | ||||||
| chr2:169506229 | C | G | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1647 | chr2 | 169506229 | ||||||
| chr2:169506230 | G | C | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1648 | chr2 | 169506230 | ||||||
| chr2:169506232 | C | G | 1 | a0001c0001t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1650C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1650 | chr2 | 169506232 | ||||||
| chr2:169506270 | T | A | 1 | a0001c0001t0048 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1688 | chr2 | 169506270 | ||||||
| chr2:169506290 | T | A | 1 | a0001c0001t0038 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1708T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1708 | chr2 | 169506290 | ||||||
| chr2:169506327 | G | C | 1 | a0001c0004t0019 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1745 | chr2 | 169506327 | ||||||
| chr2:169506344 | C | T | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 others(1): Show |
24 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1762C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1762 | chr2 | 169506344 | ||||||
| chr2:169506403 | G | T | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1821G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1821 | chr2 | 169506403 | ||||||
| chr2:169506464 | T | C | 1 | a0001c0001t0024 | 2 | HG01109.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1882T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1882 | chr2 | 169506464 | ||||||
| chr2:169506490 | T | TA | 2 | a0001c0001t0014 a0001c0001t0036 |
6 | HG02523.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1921dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1922 | INFO_REALIGN_3_PRIME | chr2 | 169506490 | |||||
| chr2:169506490 | T | TAA | 3 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0027 |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1920_*1921dupAA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1922 | INFO_REALIGN_3_PRIME | chr2 | 169506490 | |||||
| chr2:169506490 | TA | T | 8 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0023 others(5): Show |
39 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1921delA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 12/12 | 1921 | INFO_REALIGN_3_PRIME | chr2 | 169506490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169479664 | G | A | 1 | a0001c0001t0005g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.59+52G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169479664 | |||||||
| chr2:169479776 | G | A | 6 | a0001c0001t0003g0051 a0001c0001t0009g0012 a0001c0001t0009g0027 others(3): Show |
11 | HG01099.hp1 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.59+164G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169479776 | |||||||
| chr2:169479903 | A | T | 2 | a0001c0001t0017g0049 a0001c0001t0017g0247 |
3 | HG01496.hp2 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.59+291A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169479903 | |||||||
| chr2:169479925 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.59+313T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169479925 | |||||||
| chr2:169480131 | TACTA | T | 8 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0057 others(5): Show |
10 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.59+522_59+525delTA others(2): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480131 | ||||||
| chr2:169480139 | G | A | 24 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(21): Show |
28 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.59+527G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480139 | |||||||
| chr2:169480149 | T | C | 24 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(21): Show |
28 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.59+537T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480149 | |||||||
| chr2:169480187 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(218): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.59+575G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480187 | |||||||
| chr2:169480268 | G | A | 2 | a0001c0001t0002g0018 a0001c0001t0002g0080 |
4 | NA18906.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+656G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480268 | |||||||
| chr2:169480287 | G | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.59+675G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480287 | |||||||
| chr2:169480301 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.59+689A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480301 | |||||||
| chr2:169480335 | T | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.59+723T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480335 | |||||||
| chr2:169480498 | C | A | 1 | a0001c0001t0046g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59+886C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480498 | |||||||
| chr2:169480637 | T | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.59+1025T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480637 | |||||||
| chr2:169480670 | C | CT | 34 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0035 others(31): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.59+1086dupT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | C | CTT | 36 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0019 others(33): Show |
51 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.59+1085_59+1086dup others(2): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | C | CTTT | 16 | a0001c0001t0001g0140 a0001c0001t0002g0007 a0001c0001t0002g0009 others(13): Show |
28 | HG01106.hp2 HG01123.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.59+1084_59+1086dup others(3): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | CTT | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0204 others(23): Show |
31 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.59+1085_59+1086del others(2): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | CTTT | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(42): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.59+1084_59+1086del others(3): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | CTTTT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0022 others(43): Show |
71 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.59+1083_59+1086del others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | CTTTTT | C | 26 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0038 others(23): Show |
37 | HG00621.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+1082_59+1086del others(5): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480670 | CTTTTTTT | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0003t0020g0109 others(2): Show |
7 | HG02486.hp2 HG02630.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+1080_59+1086del others(7): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169480670 | ||||||
| chr2:169480806 | A | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.59+1194A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480806 | |||||||
| chr2:169480831 | A | C | 4 | a0001c0003t0020g0109 a0001c0003t0020g0110 a0001c0003t0020g0111 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+1219A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480831 | |||||||
| chr2:169480878 | T | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0175 |
3 | NA18980.hp2 NA19056.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.59+1266T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169480878 | |||||||
| chr2:169481128 | CGTTCTAG others(62): Show |
C | 1 | a0001c0001t0002g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.60-1122_60-1054del others(69): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481128 | |||||||
| chr2:169481132 | C | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.60-1119C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481132 | |||||||
| chr2:169481311 | T | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.60-940T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481311 | |||||||
| chr2:169481313 | G | C | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
72 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.60-938G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481313 | |||||||
| chr2:169481321 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.60-930A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481321 | |||||||
| chr2:169481499 | G | T | 8 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0057 others(5): Show |
10 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.60-752G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481499 | |||||||
| chr2:169481623 | G | GT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.60-617dupT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169481623 | ||||||
| chr2:169481623 | G | GTT | 42 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0006 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.60-618_60-617dupTT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169481623 | ||||||
| chr2:169481766 | A | G | 9 | a0001c0002t0008g0045 a0001c0002t0008g0046 a0001c0002t0008g0212 others(6): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-485A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169481766 | |||||||
| chr2:169482074 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.60-176dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169482074 | ||||||
| chr2:169482129 | AT | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
72 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.60-119delT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 169482129 | ||||||
| chr2:169482171 | A | G | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.60-80A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 1/11 | chr2 | 169482171 | |||||||
| chr2:169482394 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+61T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482394 | |||||||
| chr2:169482476 | C | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
72 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.142+143C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482476 | |||||||
| chr2:169482493 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(151): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.142+160C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482493 | |||||||
| chr2:169482914 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.142+581G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482914 | |||||||
| chr2:169482919 | G | A | 2 | a0001c0002t0022g0218 a0001c0002t0022g0219 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.142+586G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482919 | |||||||
| chr2:169482953 | C | T | 1 | a0001c0001t0040g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+620C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169482953 | |||||||
| chr2:169483082 | G | A | 5 | a0001c0001t0004g0220 a0001c0001t0004g0221 a0001c0001t0004g0222 others(2): Show |
5 | HG02027.hp1 HG03654.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+749G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483082 | |||||||
| chr2:169483408 | G | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(14): Show |
25 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.142+1075G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483408 | |||||||
| chr2:169483455 | T | C | 2 | a0001c0001t0021g0238 a0001c0001t0021g0239 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.142+1122T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483455 | |||||||
| chr2:169483742 | T | C | 63 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(60): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.142+1409T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483742 | |||||||
| chr2:169483744 | A | G | 37 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(34): Show |
48 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.142+1411A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483744 | |||||||
| chr2:169483813 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.142+1480G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169483813 | |||||||
| chr2:169484163 | G | C | 9 | a0001c0002t0008g0045 a0001c0002t0008g0046 a0001c0002t0008g0212 others(6): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+1830G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484163 | |||||||
| chr2:169484240 | A | G | 1 | a0001c0001t0001g0044 | 2 | NA18943.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.142+1907A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484240 | |||||||
| chr2:169484322 | T | G | 63 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(60): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.142+1989T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484322 | |||||||
| chr2:169484402 | C | CTG | 5 | a0001c0001t0002g0015 a0001c0001t0002g0081 a0001c0001t0002g0098 others(2): Show |
8 | HG01255.hp2 HG01943.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+2086_142+2087d others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484402 | ||||||
| chr2:169484402 | C | CTGTG | 37 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(34): Show |
48 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.142+2084_142+2087d others(6): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484402 | ||||||
| chr2:169484542 | G | T | 9 | a0001c0001t0002g0014 a0001c0001t0002g0034 a0001c0001t0002g0085 others(6): Show |
12 | HG02523.hp2 HG03927.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.142+2209G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484542 | |||||||
| chr2:169484829 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.143-2240G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484829 | |||||||
| chr2:169484879 | A | C | 4 | a0001c0002t0008g0046 a0001c0002t0008g0215 a0001c0002t0008g0216 others(1): Show |
5 | HG02055.hp1 HG02145.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-2190A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169484879 | |||||||
| chr2:169484989 | T | TAAAAATC others(630): Show |
2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.143-1745_143-1744i others(639): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484989 | ||||||
| chr2:169484989 | T | TAAAAATC others(631): Show |
12 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(9): Show |
20 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.143-1745_143-1744i others(640): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484989 | ||||||
| chr2:169484989 | T | TAAAAATC others(632): Show |
1 | a0001c0001t0003g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.143-1745_143-1744i others(641): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484989 | ||||||
| chr2:169484989 | T | TAAAAATC others(651): Show |
1 | a0001c0001t0044g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.143-1745_143-1744i others(660): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484989 | ||||||
| chr2:169484989 | T | TAAAAATC others(660): Show |
1 | a0001c0001t0003g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143-1745_143-1744i others(669): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 169484989 | ||||||
| chr2:169485200 | A | G | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.143-1869A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169485200 | |||||||
| chr2:169485409 | C | T | 41 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(38): Show |
69 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.143-1660C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169485409 | |||||||
| chr2:169485493 | A | G | 7 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0003t0020g0109 others(4): Show |
9 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-1576A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169485493 | |||||||
| chr2:169485807 | A | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-1262A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169485807 | |||||||
| chr2:169485810 | T | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-1259T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169485810 | |||||||
| chr2:169486017 | A | T | 3 | a0001c0001t0011g0008 a0001c0001t0011g0094 a0001c0001t0011g0104 |
7 | HG00438.hp1 NA18939.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-1052A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486017 | |||||||
| chr2:169486061 | G | T | 41 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(38): Show |
69 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.143-1008G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486061 | |||||||
| chr2:169486076 | G | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-993G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486076 | |||||||
| chr2:169486277 | G | C | 3 | a0001c0003t0020g0109 a0001c0003t0020g0110 a0001c0003t0028g0209 |
3 | HG02486.hp2 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.143-792G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486277 | |||||||
| chr2:169486363 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.143-706A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486363 | |||||||
| chr2:169486437 | G | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-632G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486437 | |||||||
| chr2:169486547 | A | C | 1 | a0001c0001t0002g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.143-522A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486547 | |||||||
| chr2:169486573 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.143-496T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486573 | |||||||
| chr2:169486817 | G | C | 2 | a0001c0001t0017g0049 a0001c0001t0017g0247 |
3 | HG01496.hp2 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.143-252G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486817 | |||||||
| chr2:169486903 | G | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-166G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169486903 | |||||||
| chr2:169487026 | G | A | 1 | a0001c0001t0014g0203 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.143-43G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 2/11 | chr2 | 169487026 | |||||||
| chr2:169487321 | G | A | 1 | a0001c0001t0005g0065 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.208+187G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487321 | |||||||
| chr2:169487420 | G | T | 10 | a0001c0001t0007g0016 a0001c0001t0007g0039 a0001c0001t0007g0152 others(7): Show |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+286G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487420 | |||||||
| chr2:169487436 | T | C | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.208+302T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487436 | |||||||
| chr2:169487447 | C | T | 1 | a0001c0002t0008g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.208+313C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487447 | |||||||
| chr2:169487451 | G | A | 1 | a0001c0001t0005g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.208+317G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487451 | |||||||
| chr2:169487550 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.209-256G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487550 | |||||||
| chr2:169487605 | G | T | 15 | a0001c0001t0010g0026 a0001c0001t0010g0056 a0001c0001t0010g0061 others(12): Show |
17 | HG00099.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-201G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487605 | |||||||
| chr2:169487683 | T | C | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.209-123T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 3/11 | chr2 | 169487683 | |||||||
| chr2:169488204 | A | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0202 |
2 | NA18964.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.386+90A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488204 | |||||||
| chr2:169488229 | C | G | 1 | a0001c0001t0002g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386+115C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488229 | |||||||
| chr2:169488464 | A | C | 1 | a0001c0001t0004g0236 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.386+350A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488464 | |||||||
| chr2:169488506 | T | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.386+392T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488506 | |||||||
| chr2:169488560 | C | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+446C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488560 | |||||||
| chr2:169488717 | C | G | 63 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(60): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.386+603C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488717 | |||||||
| chr2:169488804 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+690A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488804 | |||||||
| chr2:169488815 | A | C | 7 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0003t0020g0109 others(4): Show |
9 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+701A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488815 | |||||||
| chr2:169488999 | A | C | 9 | a0001c0002t0008g0045 a0001c0002t0008g0046 a0001c0002t0008g0212 others(6): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.386+885A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169488999 | |||||||
| chr2:169489122 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.386+1008G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489122 | |||||||
| chr2:169489297 | C | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+1183C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489297 | |||||||
| chr2:169489381 | T | G | 15 | a0001c0001t0010g0026 a0001c0001t0010g0056 a0001c0001t0010g0061 others(12): Show |
17 | HG00099.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.386+1267T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489381 | |||||||
| chr2:169489417 | C | T | 2 | a0001c0001t0007g0156 a0002c0005t0002g0103 |
2 | HG01106.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.386+1303C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489417 | |||||||
| chr2:169489420 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386+1306C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489420 | |||||||
| chr2:169489453 | ACT | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+1342_386+1343d others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489453 | ||||||
| chr2:169489462 | C | CA | 17 | a0001c0001t0010g0026 a0001c0001t0010g0056 a0001c0001t0010g0061 others(14): Show |
19 | HG00099.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.386+1360dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489462 | ||||||
| chr2:169489462 | CA | C | 22 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0197 others(19): Show |
25 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.386+1360delA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489462 | ||||||
| chr2:169489474 | A | AT | 43 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(40): Show |
71 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.386+1374dupT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489474 | ||||||
| chr2:169489475 | T | A | 1 | a0001c0001t0002g0114 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.386+1361T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489475 | |||||||
| chr2:169489494 | C | T | 43 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(40): Show |
71 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.386+1380C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489494 | |||||||
| chr2:169489517 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0199 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.386+1403G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489517 | |||||||
| chr2:169489564 | C | G | 1 | a0001c0001t0010g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386+1450C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489564 | |||||||
| chr2:169489667 | G | A | 10 | a0001c0001t0007g0016 a0001c0001t0007g0039 a0001c0001t0007g0152 others(7): Show |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+1553G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489667 | |||||||
| chr2:169489678 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.386+1564T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489678 | |||||||
| chr2:169489817 | TA | T | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.386+1704delA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169489817 | |||||||
| chr2:169489851 | C | CT | 14 | a0001c0001t0004g0025 a0001c0001t0004g0223 a0001c0001t0004g0231 others(11): Show |
19 | HG00323.hp2 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.386+1778dupT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | C | CTT | 6 | a0001c0001t0001g0170 a0001c0001t0004g0235 a0001c0001t0009g0027 others(3): Show |
8 | HG01099.hp1 HG01496.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.386+1777_386+1778d others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0155 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.386+1766_386+1778d others(15): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0024g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.386+1763_386+1778d others(18): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CT | C | 6 | a0001c0001t0002g0138 a0001c0001t0004g0220 a0001c0001t0006g0225 others(3): Show |
6 | HG01256.hp1 HG01891.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+1778delT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTT | C | 11 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.386+1775_386+1778d others(6): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTT | C | 13 | a0001c0001t0001g0140 a0001c0001t0002g0010 a0001c0001t0002g0035 others(10): Show |
19 | HG01261.hp1 HG01358.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.386+1774_386+1778d others(7): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTT | C | 9 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0118 others(6): Show |
15 | HG00423.hp1 HG01192.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.386+1773_386+1778d others(8): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(2): Show |
C | 11 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0143 others(8): Show |
17 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.386+1770_386+1778d others(11): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0002g0092 a0001c0001t0002g0102 a0001c0002t0008g0213 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+1769_386+1778d others(12): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0002g0009 a0001c0001t0002g0033 a0001c0001t0002g0034 others(17): Show |
28 | HG01106.hp2 HG02258.hp1 HG02615.hp1 others(25): Show |
intron_variant | MODIFIER | c.386+1768_386+1778d others(13): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(5): Show |
C | 27 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(24): Show |
47 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.386+1767_386+1778d others(14): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(6): Show |
C | 20 | a0001c0001t0001g0064 a0001c0001t0002g0086 a0001c0001t0002g0096 others(17): Show |
23 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.386+1766_386+1778d others(15): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0001g0067 a0001c0001t0003g0028 a0001c0001t0003g0029 others(4): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+1765_386+1778d others(16): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386+1764_386+1778d others(17): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0007g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.386+1762_386+1778d others(19): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(13): Show |
C | 4 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0001t0002g0114 others(1): Show |
6 | NA18906.hp1 NA19030.hp2 NA19075.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+1759_386+1778d others(22): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0014g0168 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.386+1758_386+1778d others(23): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0208 |
2 | HG01175.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.386+1757_386+1778d others(24): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(16): Show |
C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.386+1756_386+1778d others(25): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(17): Show |
C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0010g0026 others(2): Show |
6 | HG00099.hp1 HG03688.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+1755_386+1778d others(26): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489851 | CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0004g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386+1750_386+1778d others(31): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489851 | ||||||
| chr2:169489898 | CAG | C | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0057 others(4): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+1787_386+1788d others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169489898 | ||||||
| chr2:169490038 | G | T | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.386+1924G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490038 | |||||||
| chr2:169490110 | C | T | 2 | a0001c0001t0005g0072 a0001c0001t0005g0076 |
2 | NA18999.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.386+1996C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490110 | |||||||
| chr2:169490187 | A | AT | 44 | a0001c0001t0001g0011 a0001c0001t0001g0166 a0001c0001t0001g0195 others(41): Show |
59 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.386+2096dupT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169490187 | ||||||
| chr2:169490187 | A | ATT | 23 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(20): Show |
33 | HG00423.hp1 HG01261.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.386+2095_386+2096d others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169490187 | ||||||
| chr2:169490187 | A | ATTT | 10 | a0001c0001t0002g0035 a0001c0001t0002g0112 a0001c0001t0002g0119 others(7): Show |
11 | HG02135.hp1 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.386+2094_386+2096d others(5): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169490187 | ||||||
| chr2:169490187 | AT | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0064 others(27): Show |
41 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.386+2096delT | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169490187 | ||||||
| chr2:169490207 | T | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+2093T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490207 | |||||||
| chr2:169490338 | C | T | 6 | a0001c0002t0012g0047 a0001c0002t0012g0240 a0001c0002t0012g0241 others(3): Show |
7 | HG02258.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+2224C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490338 | |||||||
| chr2:169490341 | C | A | 1 | a0001c0001t0010g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386+2227C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490341 | |||||||
| chr2:169490342 | T | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+2228T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490342 | |||||||
| chr2:169490350 | C | T | 1 | a0001c0001t0003g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386+2236C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490350 | |||||||
| chr2:169490410 | G | A | 4 | a0001c0002t0012g0047 a0001c0002t0012g0240 a0001c0002t0012g0241 others(1): Show |
5 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+2296G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490410 | |||||||
| chr2:169490455 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386+2341A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490455 | |||||||
| chr2:169490650 | A | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.387-2224A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490650 | |||||||
| chr2:169490726 | A | G | 6 | a0001c0001t0010g0026 a0001c0001t0010g0056 a0001c0001t0010g0061 others(3): Show |
7 | HG00099.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-2148A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490726 | |||||||
| chr2:169490978 | G | A | 2 | a0001c0001t0005g0065 a0001c0001t0005g0068 |
2 | NA19007.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.387-1896G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169490978 | |||||||
| chr2:169490982 | C | CAGT | 10 | a0001c0001t0001g0040 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.387-1879_387-1877d others(5): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169490982 | ||||||
| chr2:169491188 | A | G | 1 | a0001c0001t0011g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.387-1686A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491188 | |||||||
| chr2:169491301 | C | T | 4 | a0001c0002t0012g0047 a0001c0002t0012g0240 a0001c0002t0012g0241 others(1): Show |
5 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.387-1573C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491301 | |||||||
| chr2:169491331 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.387-1543A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491331 | |||||||
| chr2:169491336 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.387-1538T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491336 | |||||||
| chr2:169491342 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.387-1532T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491342 | |||||||
| chr2:169491535 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.387-1339T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491535 | |||||||
| chr2:169491584 | T | A | 1 | a0001c0001t0002g0119 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.387-1290T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491584 | |||||||
| chr2:169491916 | T | C | 78 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(75): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.387-958T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491916 | |||||||
| chr2:169491957 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.387-917C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491957 | |||||||
| chr2:169491997 | A | G | 1 | a0001c0001t0005g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.387-877A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169491997 | |||||||
| chr2:169492040 | G | C | 1 | a0001c0001t0005g0077 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.387-834G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492040 | |||||||
| chr2:169492093 | G | A | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.387-781G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492093 | |||||||
| chr2:169492121 | G | A | 70 | a0001c0001t0001g0040 a0001c0001t0001g0169 a0001c0001t0001g0170 others(67): Show |
109 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.387-753G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492121 | |||||||
| chr2:169492204 | A | C | 1 | a0001c0001t0002g0124 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.387-670A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492204 | |||||||
| chr2:169492488 | C | CA | 22 | a0001c0001t0001g0042 a0001c0001t0001g0183 a0001c0001t0001g0204 others(19): Show |
27 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.387-371dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169492488 | ||||||
| chr2:169492488 | CA | C | 5 | a0001c0001t0002g0032 a0001c0001t0002g0088 a0001c0001t0002g0093 others(2): Show |
6 | HG02074.hp2 HG02132.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-371delA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 169492488 | ||||||
| chr2:169492611 | G | T | 10 | a0001c0001t0007g0016 a0001c0001t0007g0039 a0001c0001t0007g0152 others(7): Show |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.387-263G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492611 | |||||||
| chr2:169492633 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.387-241A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492633 | |||||||
| chr2:169492658 | C | T | 9 | a0001c0002t0008g0045 a0001c0002t0008g0046 a0001c0002t0008g0212 others(6): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-216C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492658 | |||||||
| chr2:169492689 | G | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.387-185G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492689 | |||||||
| chr2:169492739 | A | C | 2 | a0001c0001t0002g0091 a0001c0001t0002g0101 |
2 | NA19065.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.387-135A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492739 | |||||||
| chr2:169492752 | T | G | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0057 others(4): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-122T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492752 | |||||||
| chr2:169492795 | A | G | 6 | a0001c0001t0010g0026 a0001c0001t0010g0056 a0001c0001t0010g0061 others(3): Show |
7 | HG00099.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-79A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 5/11 | chr2 | 169492795 | |||||||
| chr2:169493355 | T | TTCTC | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.522+348_522+351dup others(4): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 169493355 | ||||||
| chr2:169493440 | A | G | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.523-301A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 6/11 | chr2 | 169493440 | |||||||
| chr2:169493557 | G | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.523-184G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 6/11 | chr2 | 169493557 | |||||||
| chr2:169493915 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.618+79T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169493915 | |||||||
| chr2:169493922 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.618+86T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169493922 | |||||||
| chr2:169493975 | T | C | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.618+139T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169493975 | |||||||
| chr2:169493990 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.618+154A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169493990 | |||||||
| chr2:169494172 | T | C | 2 | a0001c0001t0002g0123 a0001c0001t0002g0135 |
2 | NA18961.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.618+336T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494172 | |||||||
| chr2:169494192 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.618+356G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494192 | |||||||
| chr2:169494372 | G | T | 1 | a0001c0001t0006g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.618+536G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494372 | |||||||
| chr2:169494453 | A | G | 1 | a0001c0001t0005g0065 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.618+617A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494453 | |||||||
| chr2:169494555 | T | TA | 6 | a0001c0001t0001g0179 a0001c0001t0002g0087 a0001c0001t0002g0088 others(3): Show |
6 | HG02074.hp2 HG04115.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+733dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 169494555 | ||||||
| chr2:169494748 | A | G | 1 | a0001c0001t0006g0243 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.618+912A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494748 | |||||||
| chr2:169494794 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.618+958A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169494794 | |||||||
| chr2:169495043 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.618+1207A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495043 | |||||||
| chr2:169495149 | T | C | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.618+1313T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495149 | |||||||
| chr2:169495357 | T | C | 1 | a0001c0001t0007g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.618+1521T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495357 | |||||||
| chr2:169495741 | T | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-1886T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495741 | |||||||
| chr2:169495933 | G | A | 1 | a0001c0001t0004g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.619-1694G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495933 | |||||||
| chr2:169495941 | T | C | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.619-1686T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495941 | |||||||
| chr2:169495949 | C | A | 1 | a0001c0001t0003g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.619-1678C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169495949 | |||||||
| chr2:169496257 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0131 |
2 | NA19006.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.619-1370C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496257 | |||||||
| chr2:169496493 | T | C | 10 | a0001c0001t0007g0016 a0001c0001t0007g0039 a0001c0001t0007g0152 others(7): Show |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-1134T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496493 | |||||||
| chr2:169496518 | A | G | 5 | a0001c0003t0020g0109 a0001c0003t0020g0110 a0001c0003t0020g0111 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-1109A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496518 | |||||||
| chr2:169496565 | A | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-1062A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496565 | |||||||
| chr2:169496598 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | NA18992.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.619-1029G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496598 | |||||||
| chr2:169496636 | G | A | 1 | a0001c0001t0006g0243 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.619-991G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496636 | |||||||
| chr2:169496645 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.619-982G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496645 | |||||||
| chr2:169496786 | G | GTGAACCC others(173): Show |
1 | a0001c0001t0005g0079 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.619-835_619-834ins others(180): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 169496786 | ||||||
| chr2:169496786 | G | GTGAACCC others(172): Show |
19 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(16): Show |
22 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.619-835_619-834ins others(179): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 169496786 | ||||||
| chr2:169496786 | G | GTGAACCC others(169): Show |
1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-835_619-834ins others(176): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 169496786 | ||||||
| chr2:169496856 | G | A | 1 | a0001c0001t0003g0037 | 2 | NA18946.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.619-771G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169496856 | |||||||
| chr2:169496868 | C | CA | 6 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0177 others(3): Show |
6 | HG02135.hp1 HG02615.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-747dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 169496868 | ||||||
| chr2:169497082 | G | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-545G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497082 | |||||||
| chr2:169497179 | G | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-448G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497179 | |||||||
| chr2:169497184 | G | C | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.619-443G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497184 | |||||||
| chr2:169497194 | C | A | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.619-433C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497194 | |||||||
| chr2:169497235 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.619-392A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497235 | |||||||
| chr2:169497237 | C | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-390C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497237 | |||||||
| chr2:169497381 | C | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.619-246C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497381 | |||||||
| chr2:169497472 | C | T | 3 | a0001c0001t0014g0151 a0001c0001t0014g0165 a0001c0001t0014g0168 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.619-155C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497472 | |||||||
| chr2:169497486 | C | G | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.619-141C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 7/11 | chr2 | 169497486 | |||||||
| chr2:169497816 | A | G | 1 | a0001c0002t0022g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.681+127A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169497816 | |||||||
| chr2:169497880 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.681+191G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169497880 | |||||||
| chr2:169498214 | C | T | 17 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(14): Show |
25 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.681+525C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498214 | |||||||
| chr2:169498280 | A | G | 77 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(74): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.681+591A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498280 | |||||||
| chr2:169498367 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.681+678A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498367 | |||||||
| chr2:169498407 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.681+718T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498407 | |||||||
| chr2:169498479 | A | G | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.681+790A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498479 | |||||||
| chr2:169498488 | G | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+799G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498488 | |||||||
| chr2:169498578 | G | A | 1 | a0001c0001t0016g0187 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.681+889G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498578 | |||||||
| chr2:169498588 | C | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-898C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498588 | |||||||
| chr2:169498602 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-884A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498602 | |||||||
| chr2:169498736 | G | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-750G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498736 | |||||||
| chr2:169498761 | C | G | 2 | a0001c0001t0021g0238 a0001c0001t0021g0239 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.682-725C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498761 | |||||||
| chr2:169498784 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.682-702C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498784 | |||||||
| chr2:169498806 | C | CA | 82 | a0001c0001t0001g0140 a0001c0001t0001g0180 a0001c0001t0001g0195 others(79): Show |
123 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.682-662dupA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169498806 | ||||||
| chr2:169498806 | C | CAA | 10 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0093 others(7): Show |
13 | HG02055.hp1 HG02145.hp1 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-663_682-662dup others(2): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169498806 | ||||||
| chr2:169498806 | CA | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0186 a0001c0001t0003g0059 others(1): Show |
6 | HG00099.hp2 HG01070.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-662delA | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169498806 | ||||||
| chr2:169498821 | A | AAG | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(17): Show |
23 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.682-664_682-663ins others(2): Show |
BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169498821 | ||||||
| chr2:169498830 | G | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-656G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498830 | |||||||
| chr2:169498868 | G | A | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.682-618G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169498868 | |||||||
| chr2:169499068 | TC | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-416delC | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 169499068 | ||||||
| chr2:169499119 | T | A | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.682-367T>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499119 | |||||||
| chr2:169499144 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0041g0167 |
2 | HG01109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.682-342A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499144 | |||||||
| chr2:169499359 | T | C | 7 | a0001c0001t0010g0056 a0001c0002t0012g0047 a0001c0002t0012g0240 others(4): Show |
8 | HG02258.hp2 HG02559.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-127T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499359 | |||||||
| chr2:169499379 | C | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0080 |
4 | NA18906.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-107C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499379 | |||||||
| chr2:169499380 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0014g0203 a0001c0001t0039g0188 |
3 | NA18997.hp1 NA18998.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.682-106G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499380 | |||||||
| chr2:169499402 | C | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(39): Show |
70 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.682-84C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499402 | |||||||
| chr2:169499434 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.682-52A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499434 | |||||||
| chr2:169499460 | T | C | 1 | a0001c0007t0045g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.682-26T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 8/11 | chr2 | 169499460 | |||||||
| chr2:169499647 | G | T | 1 | a0001c0001t0007g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.816+27G>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169499647 | |||||||
| chr2:169499708 | T | G | 1 | a0001c0001t0009g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.816+88T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169499708 | |||||||
| chr2:169499759 | T | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.816+139T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169499759 | |||||||
| chr2:169500007 | C | T | 1 | a0001c0001t0006g0229 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.816+387C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500007 | |||||||
| chr2:169500083 | C | G | 18 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0050 others(15): Show |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.816+463C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500083 | |||||||
| chr2:169500161 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.816+541A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500161 | |||||||
| chr2:169500194 | T | G | 1 | a0001c0001t0003g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.816+574T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500194 | |||||||
| chr2:169500250 | T | G | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.816+630T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500250 | |||||||
| chr2:169500318 | C | T | 2 | a0001c0001t0006g0226 a0001c0001t0006g0228 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.816+698C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500318 | |||||||
| chr2:169500419 | T | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.816+799T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500419 | |||||||
| chr2:169500440 | G | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0224 a0001c0001t0004g0227 others(8): Show |
13 | HG00733.hp1 HG01255.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.816+820G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500440 | |||||||
| chr2:169500483 | G | A | 1 | a0001c0002t0022g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.816+863G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500483 | |||||||
| chr2:169500611 | G | C | 36 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
47 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.816+991G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500611 | |||||||
| chr2:169500620 | T | G | 1 | a0001c0001t0038g0207 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.816+1000T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500620 | |||||||
| chr2:169500651 | A | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.816+1031A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500651 | |||||||
| chr2:169500765 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.816+1145T>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500765 | |||||||
| chr2:169500831 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.816+1211A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500831 | |||||||
| chr2:169500994 | T | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.816+1374T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169500994 | |||||||
| chr2:169501068 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.816+1448T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501068 | |||||||
| chr2:169501231 | T | G | 1 | a0001c0001t0001g0022 | 3 | HG01192.hp1 HG01261.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.816+1611T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501231 | |||||||
| chr2:169501335 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.816+1715A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501335 | |||||||
| chr2:169501360 | A | C | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.817-1735A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501360 | |||||||
| chr2:169501393 | A | G | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.817-1702A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501393 | |||||||
| chr2:169501478 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.817-1617C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501478 | |||||||
| chr2:169501615 | G | A | 2 | a0001c0001t0002g0018 a0001c0001t0002g0080 |
4 | NA18906.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-1480G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501615 | |||||||
| chr2:169501683 | C | T | 18 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0050 others(15): Show |
21 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.817-1412C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501683 | |||||||
| chr2:169501856 | C | A | 35 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0010 others(32): Show |
46 | HG00423.hp1 HG01192.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.817-1239C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501856 | |||||||
| chr2:169501874 | T | G | 1 | a0001c0001t0004g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.817-1221T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169501874 | |||||||
| chr2:169502039 | C | G | 2 | a0001c0002t0022g0218 a0001c0002t0022g0219 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.817-1056C>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502039 | |||||||
| chr2:169502066 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG02132.hp2 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-1029C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502066 | |||||||
| chr2:169502090 | A | G | 6 | a0001c0001t0001g0183 a0001c0001t0004g0220 a0001c0001t0004g0221 others(3): Show |
6 | HG00741.hp1 HG02027.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1005A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502090 | |||||||
| chr2:169502185 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.817-910C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502185 | |||||||
| chr2:169502201 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.817-894C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502201 | |||||||
| chr2:169502236 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0003t0020g0109 others(3): Show |
8 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-859C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502236 | |||||||
| chr2:169502485 | T | G | 21 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0005g0013 others(18): Show |
26 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.817-610T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502485 | |||||||
| chr2:169502511 | G | A | 1 | a0001c0001t0016g0189 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.817-584G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502511 | |||||||
| chr2:169502535 | C | T | 7 | a0001c0001t0005g0013 a0001c0001t0005g0065 a0001c0001t0005g0066 others(4): Show |
9 | HG00558.hp1 HG02080.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-560C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502535 | |||||||
| chr2:169502603 | A | G | 10 | a0001c0001t0007g0016 a0001c0001t0007g0039 a0001c0001t0007g0152 others(7): Show |
13 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-492A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502603 | |||||||
| chr2:169502930 | A | T | 1 | a0001c0004t0019g0020 | 3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.817-165A>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502930 | |||||||
| chr2:169502982 | C | T | 1 | a0001c0001t0005g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.817-113C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502982 | |||||||
| chr2:169502983 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.817-112G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 9/11 | chr2 | 169502983 | |||||||
| chr2:169503248 | G | C | 17 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(14): Show |
25 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.900+70G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503248 | |||||||
| chr2:169503433 | G | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(14): Show |
25 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.900+255G>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503433 | |||||||
| chr2:169503467 | A | G | 19 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0050 others(16): Show |
24 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.900+289A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503467 | |||||||
| chr2:169503777 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.901-526A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503777 | |||||||
| chr2:169503887 | C | T | 19 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0050 others(16): Show |
24 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.901-416C>T | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503887 | |||||||
| chr2:169503913 | T | G | 4 | a0001c0002t0012g0047 a0001c0002t0012g0240 a0001c0002t0012g0241 others(1): Show |
5 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-390T>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169503913 | |||||||
| chr2:169504067 | C | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0021 a0001c0001t0003g0037 others(14): Show |
25 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.901-236C>A | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169504067 | |||||||
| chr2:169504184 | A | C | 1 | a0001c0001t0001g0040 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.901-119A>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169504184 | |||||||
| chr2:169504255 | G | C | 6 | a0001c0001t0007g0016 a0001c0001t0007g0152 a0001c0001t0007g0154 others(3): Show |
8 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-48G>C | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 10/11 | chr2 | 169504255 | |||||||
| chr2:169504359 | A | G | 1 | a0001c0001t0048g0232 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.924+33A>G | BBS5 | ENSG00000163093.12 | transcript | ENST00000295240.8 | protein_coding | 11/11 | chr2 | 169504359 |