Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54540 |
| ensemblid | ENSG00000146067.17 |
| hgncid | 25524 |
| symbol | FAM193B |
| name | family with sequence similarity 193 member B |
| refseq_nuc | NM_001190946.3 |
| refseq_prot | NP_001177875.1 |
| ensembl_nuc | ENST00000514747.6 |
| ensembl_prot | ENSP00000422131.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 177519789 |
| end | 177554563 |
| strand | - |
| ver | v1.2 |
| region | chr5:177519789-177554563 |
| region5000 | chr5:177514789-177559563 |
| regionname0 | FAM193B_chr5_177519789_177554563 |
| regionname5000 | FAM193B_chr5_177514789_177559563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 822 | 350 | 71 | 66 | 164 | 12 | 36 | 125 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0002 | 1/0 | 822 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0003 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0004 | 0/0 | 822 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0005 | 0/0 | 822 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0006 | 0/0 | 822 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0007 | 0/0 | 822 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0009 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0010 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| a0011 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | MTRRR others(817): Show |
chr5 | 177514789 | 177559563 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2466 | 343 | 70 | 66 | 161 | 12 | 33 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0005 | 0/0 | 2466 | 2 | 0 | 0 | 0 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0007 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0009 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0010 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0011 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0001c0014 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0002c0002 | 1/0 | 2466 | 5 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0003c0003 | 0/0 | 2466 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0004c0004 | 0/0 | 2466 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0005c0006 | 0/0 | 2466 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0006c0017 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0007c0016 | 0/0 | 2466 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0008c0013 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0009c0015 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0010c0008 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 | ||
| a0011c0012 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATGAC others(2461): Show |
chr5 | 177514789 | 177559563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2967 | 85 | 8 | 21 | 40 | 5 | 11 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0002 | 0/0 | 2967 | 56 | 0 | 9 | 44 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0003 | 0/0 | 2973 | 24 | 10 | 10 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2968): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0004 | 0/0 | 2979 | 15 | 1 | 0 | 14 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2974): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0005 | 0/0 | 2985 | 12 | 2 | 2 | 8 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2980): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0006 | 0/0 | 2979 | 10 | 0 | 5 | 2 | 1 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2974): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0007 | 0/0 | 2988 | 11 | 0 | 2 | 7 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2983): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0008 | 0/0 | 2964 | 7 | 6 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2959): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0009 | 0/0 | 2976 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0010 | 0/0 | 2964 | 5 | 0 | 4 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2959): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0011 | 0/0 | 2970 | 6 | 3 | 2 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2965): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0012 | 0/0 | 2973 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2968): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0013 | 0/0 | 2976 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0014 | 0/0 | 2982 | 6 | 1 | 0 | 1 | 0 | 4 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2977): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0015 | 0/0 | 2991 | 5 | 2 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2986): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0016 | 0/0 | 2970 | 5 | 3 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2965): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0017 | 0/0 | 2979 | 5 | 3 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2974): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0018 | 0/0 | 2982 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2977): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0019 | 0/0 | 2982 | 4 | 0 | 1 | 2 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2977): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0020 | 0/0 | 3003 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2998): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0022 | 0/0 | 2976 | 3 | 1 | 0 | 0 | 2 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0023 | 0/0 | 2994 | 4 | 1 | 0 | 2 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2989): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0024 | 0/0 | 2967 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0025 | 0/1 | 2970 | 3 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2965): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0026 | 0/0 | 2985 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2980): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0027 | 0/0 | 2994 | 3 | 0 | 0 | 2 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2989): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0028 | 0/0 | 2997 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2992): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0029 | 0/0 | 3006 | 3 | 1 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3001): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0032 | 0/0 | 2958 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2953): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0033 | 0/0 | 2964 | 2 | 0 | 0 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2959): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0034 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2983): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0035 | 0/0 | 2991 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2986): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0036 | 0/0 | 2991 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2986): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0037 | 0/0 | 3000 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2995): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0038 | 0/0 | 3021 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3016): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0039 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0040 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0041 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2965): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0042 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2968): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0043 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2968): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0044 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2980): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0045 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2983): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0047 | 0/0 | 2994 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2989): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0048 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2995): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0049 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2995): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0050 | 0/0 | 3003 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2998): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0051 | 0/0 | 3006 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3001): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0052 | 0/0 | 3009 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3004): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0053 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3007): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0054 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3007): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0055 | 0/0 | 3015 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3010): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0056 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3010): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0057 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3016): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0058 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3019): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0059 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3028): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0060 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3031): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0061 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(3046): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0062 | 0/0 | 2968 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2963): Show |
chr5 | 177514789 | 177559563 |
| a0001c0001t0063 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0001c0005t0006 | 0/0 | 2979 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2974): Show |
chr5 | 177514789 | 177559563 |
| a0001c0005t0022 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0001c0007t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0009t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0010t0019 | 0/0 | 2982 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2977): Show |
chr5 | 177514789 | 177559563 |
| a0001c0011t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0001c0014t0046 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2983): Show |
chr5 | 177514789 | 177559563 |
| a0002c0002t0030 | 1/0 | 2968 | 2 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2963): Show |
chr5 | 177514789 | 177559563 |
| a0002c0002t0031 | 0/0 | 2962 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2957): Show |
chr5 | 177514789 | 177559563 |
| a0003c0003t0021 | 0/0 | 2970 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2965): Show |
chr5 | 177514789 | 177559563 |
| a0004c0004t0015 | 0/0 | 2991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2986): Show |
chr5 | 177514789 | 177559563 |
| a0004c0004t0020 | 0/0 | 3003 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2998): Show |
chr5 | 177514789 | 177559563 |
| a0005c0006t0002 | 0/0 | 2967 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2962): Show |
chr5 | 177514789 | 177559563 |
| a0006c0017t0003 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2968): Show |
chr5 | 177514789 | 177559563 |
| a0007c0016t0010 | 0/0 | 2964 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2959): Show |
chr5 | 177514789 | 177559563 |
| a0008c0013t0020 | 0/0 | 3003 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2998): Show |
chr5 | 177514789 | 177559563 |
| a0009c0015t0030 | 0/0 | 2968 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2963): Show |
chr5 | 177514789 | 177559563 |
| a0010c0008t0009 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2971): Show |
chr5 | 177514789 | 177559563 |
| a0011c0012t0018 | 0/0 | 2982 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | ATATT others(2977): Show |
chr5 | 177514789 | 177559563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0001 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0039 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0020g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0020g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0022g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0022g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0027g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0027g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0032g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0032g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0033g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0033g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0034g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0034g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0035g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0035g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0036g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0036g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0037g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0037g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0038g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0038g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0039g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0040g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0041g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0042g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0043g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0044g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0045g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0047g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0048g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0049g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0050g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0051g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0052g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0053g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0054g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0055g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0056g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0057g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0058g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0059g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0060g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0061g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0062g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0063g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0005t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0005t0022g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0009t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0010t0019g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0014t0046g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0030g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0030g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0031g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0031g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0003c0003t0021g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0003c0003t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0020g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0005c0006t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0005c0006t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0006c0017t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0007c0016t0010g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0008c0013t0020g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0009c0015t0030g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0010c0008t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0011c0012t0018g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0043 | g0145 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00099 | hp2 | a0001 | c0001 | t0033 | g0047 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00140 | hp2 | a0001 | c0001 | t0037 | g0239 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0042 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0174 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00423 | hp1 | a0001 | c0001 | t0061 | g0261 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00438 | hp2 | a0001 | c0001 | t0015 | g0228 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00558 | hp1 | a0001 | c0001 | t0011 | g0129 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00558 | hp2 | a0001 | c0001 | t0015 | g0227 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00609 | hp2 | a0001 | c0001 | t0023 | g0232 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0198 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0162 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01081 | hp2 | a0005 | c0006 | t0002 | g0059 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01106 | hp1 | a0006 | c0017 | t0003 | g0141 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0024 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01175 | hp2 | a0001 | c0001 | t0052 | g0250 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0054 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0034 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0205 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01261 | hp2 | a0001 | c0001 | t0016 | g0132 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01346 | hp2 | a0001 | c0001 | t0053 | g0251 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0189 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01516 | hp2 | a0001 | c0001 | t0022 | g0036 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01517 | hp2 | a0001 | c0001 | t0022 | g0036 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01884 | hp1 | a0001 | c0001 | t0040 | g0079 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0180 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0161 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01928 | hp1 | a0001 | c0001 | t0010 | g0024 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01928 | hp2 | a0001 | c0001 | t0025 | g0122 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01934 | hp1 | a0005 | c0006 | t0002 | g0058 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0159 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01978 | hp2 | a0007 | c0016 | t0010 | g0049 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01981 | hp2 | a0001 | c0001 | t0016 | g0131 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0050 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02027 | hp1 | a0001 | c0001 | t0054 | g0252 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0051 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02055 | hp1 | a0002 | c0002 | t0031 | g0043 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02071 | hp1 | a0008 | c0013 | t0020 | g0244 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02129 | hp1 | a0001 | c0001 | t0015 | g0226 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0215 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02135 | hp2 | a0001 | c0001 | t0019 | g0194 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0130 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02165 | hp1 | a0001 | c0001 | t0055 | g0253 | EAS | CDX | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0113 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02258 | hp2 | a0001 | c0001 | t0023 | g0231 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0160 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0192 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0163 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0155 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02572 | hp1 | a0004 | c0004 | t0015 | g0219 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0245 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02615 | hp2 | a0001 | c0001 | t0056 | g0254 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0124 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02622 | hp2 | a0002 | c0002 | t0031 | g0266 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02630 | hp1 | a0003 | c0003 | t0021 | g0020 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02630 | hp2 | a0009 | c0015 | t0030 | g0264 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02647 | hp1 | a0001 | c0001 | t0034 | g0210 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0147 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02698 | hp1 | a0001 | c0001 | t0049 | g0236 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02717 | hp2 | a0003 | c0003 | t0021 | g0020 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0127 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0039 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02735 | hp1 | a0001 | c0001 | t0027 | g0041 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0223 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02818 | hp2 | a0001 | c0001 | t0044 | g0209 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02886 | hp1 | a0003 | c0003 | t0021 | g0020 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02886 | hp2 | a0010 | c0008 | t0009 | g0157 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02895 | hp2 | a0001 | c0001 | t0058 | g0258 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0173 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02896 | hp2 | a0004 | c0004 | t0020 | g0240 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02897 | hp2 | a0004 | c0004 | t0020 | g0241 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02965 | hp2 | a0002 | c0002 | t0031 | g0043 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0224 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0211 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0120 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0126 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03130 | hp1 | a0003 | c0003 | t0021 | g0134 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0177 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03453 | hp1 | a0001 | c0014 | t0046 | g0218 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0166 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03486 | hp1 | a0001 | c0001 | t0029 | g0249 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03490 | hp2 | a0001 | c0001 | t0017 | g0170 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03491 | hp2 | a0001 | c0001 | t0033 | g0048 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0191 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03669 | hp1 | a0001 | c0001 | t0028 | g0234 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0178 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0176 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0023 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0213 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0023 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0216 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04115 | hp2 | a0001 | c0001 | t0014 | g0023 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04184 | hp1 | a0001 | c0001 | t0025 | g0121 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0197 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04199 | hp1 | a0001 | c0010 | t0019 | g0193 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04199 | hp2 | a0001 | c0001 | t0036 | g0222 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04204 | hp1 | a0001 | c0001 | t0038 | g0257 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04204 | hp2 | a0001 | c0005 | t0022 | g0156 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04228 | hp2 | a0001 | c0001 | t0024 | g0076 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18612 | hp2 | a0001 | c0001 | t0020 | g0243 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18942 | hp1 | a0011 | c0012 | t0018 | g0190 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18943 | hp1 | a0001 | c0011 | t0001 | g0098 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18944 | hp1 | a0001 | c0001 | t0027 | g0041 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18947 | hp1 | a0001 | c0001 | t0028 | g0235 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18949 | hp1 | a0001 | c0009 | t0001 | g0093 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18949 | hp2 | a0001 | c0001 | t0019 | g0195 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18957 | hp2 | a0001 | c0001 | t0039 | g0056 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18959 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18968 | hp2 | a0001 | c0001 | t0051 | g0246 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18969 | hp1 | a0001 | c0001 | t0029 | g0248 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18970 | hp2 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18971 | hp1 | a0001 | c0001 | t0035 | g0225 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0214 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18977 | hp1 | a0001 | c0001 | t0036 | g0220 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18979 | hp2 | a0001 | c0001 | t0035 | g0221 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18982 | hp2 | a0001 | c0001 | t0063 | g0267 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18984 | hp1 | a0001 | c0001 | t0026 | g0201 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18984 | hp2 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18989 | hp1 | a0001 | c0001 | t0060 | g0260 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18992 | hp1 | a0001 | c0001 | t0018 | g0196 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18999 | hp2 | a0001 | c0001 | t0029 | g0247 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19010 | hp2 | a0001 | c0001 | t0027 | g0229 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19011 | hp2 | a0001 | c0001 | t0032 | g0044 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19043 | hp1 | a0002 | c0002 | t0030 | g0265 | AFR | LWK | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0133 | AFR | LWK | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19057 | hp2 | a0001 | c0001 | t0062 | g0262 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19058 | hp1 | a0001 | c0001 | t0042 | g0135 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19058 | hp2 | a0001 | c0001 | t0038 | g0255 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19060 | hp2 | a0001 | c0007 | t0001 | g0075 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19062 | hp1 | a0001 | c0001 | t0050 | g0242 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19068 | hp1 | a0001 | c0001 | t0026 | g0200 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19079 | hp1 | a0001 | c0001 | t0041 | g0119 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19079 | hp2 | a0001 | c0001 | t0026 | g0207 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19081 | hp2 | a0001 | c0001 | t0057 | g0256 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19083 | hp2 | a0001 | c0001 | t0037 | g0238 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19087 | hp1 | a0001 | c0001 | t0024 | g0077 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19240 | hp1 | a0001 | c0001 | t0047 | g0230 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0175 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20805 | hp2 | a0001 | c0001 | t0023 | g0042 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20905 | hp1 | a0001 | c0001 | t0045 | g0212 | SAS | GIH | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20905 | hp2 | a0001 | c0005 | t0006 | g0169 | SAS | GIH | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0168 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02109 | hp2 | a0001 | c0001 | t0059 | g0259 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03471 | hp2 | a0001 | c0001 | t0028 | g0233 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG06807 | hp1 | a0001 | c0001 | t0048 | g0237 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20300 | hp1 | a0001 | c0001 | t0032 | g0045 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0037 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0025 | g0123 | REF | REF | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0030 | g0263 | REF | REF | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177524275 | A | G | 8 | a0001 a0004 a0005 others(5): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
missense_variant | MODERATE | c.2206T>C | p.Ser736Pro | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 2311/2968 | 2206/2469 | 736/822 | chr5 | 177524275 | |||
| chr5:177524629 | G | A | 1 | a0011 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.1852C>T | p.Pro618Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1957/2968 | 1852/2469 | 618/822 | chr5 | 177524629 | |||
| chr5:177524706 | T | C | 1 | a0008 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1775A>G | p.Asn592Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1880/2968 | 1775/2469 | 592/822 | chr5 | 177524706 | |||
| chr5:177524712 | A | G | 1 | a0003 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.1769T>C | p.Val590Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1874/2968 | 1769/2469 | 590/822 | chr5 | 177524712 | |||
| chr5:177524715 | G | T | 1 | a0004 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1766C>A | p.Thr589Asn | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1871/2968 | 1766/2469 | 589/822 | chr5 | 177524715 | |||
| chr5:177524913 | G | A | 1 | a0005 | 2 | HG01081.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.1568C>T | p.Ser523Phe | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1673/2968 | 1568/2469 | 523/822 | chr5 | 177524913 | |||
| chr5:177525177 | T | G | 1 | a0009 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1304A>C | p.Glu435Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1409/2968 | 1304/2469 | 435/822 | chr5 | 177525177 | |||
| chr5:177536530 | G | A | 1 | a0007 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.904C>T | p.His302Tyr | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/9 | 1009/2968 | 904/2469 | 302/822 | chr5 | 177536530 | |||
| chr5:177539137 | G | C | 1 | a0006 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.221C>G | p.Ala74Gly | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/9 | 326/2968 | 221/2469 | 74/822 | chr5 | 177539137 | |||
| chr5:177554281 | C | T | 1 | a0010 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.178G>A | p.Asp60Asn | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 283/2968 | 178/2469 | 60/822 | chr5 | 177554281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177523962 | A | G | 1 | a0001c0011 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.2367T>C | p.Phe789Phe | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/9 | 2472/2968 | 2367/2469 | 789/822 | chr5 | 177523962 | |||
| chr5:177524993 | G | A | 1 | a0001c0014 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1488C>T | p.Ser496Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1593/2968 | 1488/2469 | 496/822 | chr5 | 177524993 | |||
| chr5:177525107 | C | T | 1 | a0001c0010 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1374G>A | p.Glu458Glu | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1479/2968 | 1374/2469 | 458/822 | chr5 | 177525107 | |||
| chr5:177536636 | G | T | 1 | a0001c0009 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.798C>A | p.Pro266Pro | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/9 | 903/2968 | 798/2469 | 266/822 | chr5 | 177536636 | |||
| chr5:177554315 | C | T | 1 | a0001c0005 | 2 | HG04204.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.144G>A | p.Ala48Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 249/2968 | 144/2469 | 48/822 | chr5 | 177554315 | |||
| chr5:177554369 | C | T | 1 | a0001c0007 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.90G>A | p.Glu30Glu | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 195/2968 | 90/2469 | 30/822 | chr5 | 177554369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177519961 | G | A | 1 | a0001c0014t0046 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 2014 | chr5 | 177519961 | ||||||
| chr5:177520069 | G | A | 1 | a0003c0003t0021 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*114C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1906 | chr5 | 177520069 | ||||||
| chr5:177520088 | C | T | 1 | a0001c0001t0040 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1887 | chr5 | 177520088 | ||||||
| chr5:177520106 | G | A | 20 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0019 others(17): Show |
54 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1869 | chr5 | 177520106 | ||||||
| chr5:177520152 | C | T | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1823 | chr5 | 177520152 | ||||||
| chr5:177554468 | C | T | 6 | a0001c0001t0002 a0001c0001t0039 a0001c0001t0041 others(3): Show |
62 | HG00544.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 10 | chr5 | 177554468 | ||||||
| chr5:177554489 | A | ACGCCG | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0042 others(2): Show |
33 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-32dupCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(1): Show |
6 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0022 others(3): Show |
18 | HG01081.hp1 HG01516.hp2 HG01517.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(4): Show |
4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0017 others(1): Show |
31 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGCG others(3): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(7): Show |
5 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0019 others(2): Show |
16 | HG00741.hp1 HG02135.hp2 HG02300.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(10): Show |
3 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0044 |
16 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(9): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(13): Show |
4 | a0001c0001t0007 a0001c0001t0034 a0001c0001t0045 others(1): Show |
15 | HG01496.hp2 HG01943.hp1 HG02132.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(12): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(16): Show |
4 | a0001c0001t0015 a0001c0001t0035 a0001c0001t0036 others(1): Show |
10 | HG00438.hp2 HG00558.hp2 HG02129.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(15): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(19): Show |
3 | a0001c0001t0023 a0001c0001t0027 a0001c0001t0047 |
8 | HG00408.hp1 HG00609.hp2 HG02258.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(18): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(22): Show |
1 | a0001c0001t0028 | 3 | HG03471.hp2 HG03669.hp1 NA18947.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(21): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(25): Show |
3 | a0001c0001t0037 a0001c0001t0048 a0001c0001t0049 |
4 | HG00140.hp2 HG02698.hp1 HG06807.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(24): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(28): Show |
4 | a0001c0001t0020 a0001c0001t0050 a0004c0004t0020 others(1): Show |
6 | HG02071.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(27): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(31): Show |
2 | a0001c0001t0029 a0001c0001t0051 |
4 | HG03486.hp1 NA18968.hp2 NA18969.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(30): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(34): Show |
1 | a0001c0001t0052 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(33): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(37): Show |
2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG01346.hp2 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(36): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(40): Show |
2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG02165.hp1 HG02615.hp2 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(39): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(46): Show |
2 | a0001c0001t0038 a0001c0001t0057 |
3 | HG04204.hp1 NA19058.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(45): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(49): Show |
1 | a0001c0001t0058 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(48): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(58): Show |
1 | a0001c0001t0059 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(57): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(61): Show |
1 | a0001c0001t0060 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(60): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | A | ACGCCGCG others(76): Show |
1 | a0001c0001t0061 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(75): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554489 | ACGCCGC | A | 1 | a0002c0002t0031 | 3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37_-32delGCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | ||||||
| chr5:177554492 | C | CCG | 5 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0025 others(2): Show |
18 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-35dupCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 35 | chr5 | 177554492 | ||||||
| chr5:177554494 | GC | G | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0024 others(6): Show |
151 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-37delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | ||||||
| chr5:177554494 | GCCGC | G | 4 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0033 others(1): Show |
15 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-40_-37delGCGG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | ||||||
| chr5:177554494 | GCCGCCGC others(3): Show |
G | 1 | a0001c0001t0032 | 2 | NA19011.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-46_-37delGCGGCGGC others(2): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | ||||||
| chr5:177554532 | T | C | 1 | a0001c0001t0063 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 74 | chr5 | 177554532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177520194 | AAAAG | A | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-17_*2-14delCTTT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520194 | |||||||
| chr5:177520298 | T | C | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-117A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520298 | |||||||
| chr5:177520365 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.*2-184C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520365 | |||||||
| chr5:177520403 | G | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(260): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.*2-222C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520403 | |||||||
| chr5:177520507 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0099 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.*2-326G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520507 | |||||||
| chr5:177520599 | G | A | 1 | a0001c0001t0019g0192 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*2-418C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520599 | |||||||
| chr5:177521120 | G | T | 61 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(58): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.*1+854C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521120 | |||||||
| chr5:177521170 | G | A | 2 | a0001c0001t0006g0175 a0001c0001t0006g0189 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.*1+804C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521170 | |||||||
| chr5:177521257 | A | G | 1 | a0001c0001t0063g0267 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.*1+717T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521257 | |||||||
| chr5:177521518 | T | C | 1 | a0001c0001t0011g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*1+456A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521518 | |||||||
| chr5:177521533 | G | A | 1 | a0001c0001t0010g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.*1+441C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521533 | |||||||
| chr5:177521567 | G | A | 1 | a0001c0001t0024g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*1+407C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521567 | |||||||
| chr5:177521715 | T | G | 61 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(58): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.*1+259A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521715 | |||||||
| chr5:177521716 | T | C | 79 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0136 others(76): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.*1+258A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521716 | |||||||
| chr5:177521746 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.*1+228C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521746 | |||||||
| chr5:177521776 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.*1+198C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521776 | |||||||
| chr5:177521788 | A | C | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*1+186T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521788 | |||||||
| chr5:177522321 | T | C | 79 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0136 others(76): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2373-250A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522321 | |||||||
| chr5:177522351 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2373-280C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522351 | |||||||
| chr5:177522475 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2373-404C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522475 | |||||||
| chr5:177522497 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2373-426A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522497 | |||||||
| chr5:177522610 | G | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2373-539C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522610 | |||||||
| chr5:177522679 | A | G | 4 | a0001c0001t0015g0223 a0001c0001t0023g0231 a0001c0001t0028g0233 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2373-608T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522679 | |||||||
| chr5:177522887 | G | T | 1 | a0001c0001t0032g0044 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2373-816C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522887 | |||||||
| chr5:177523095 | G | A | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372+862C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523095 | |||||||
| chr5:177523171 | T | C | 1 | a0001c0001t0041g0119 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2372+786A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523171 | |||||||
| chr5:177523251 | C | T | 1 | a0001c0001t0040g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+706G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523251 | |||||||
| chr5:177523291 | C | T | 1 | a0001c0001t0040g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+666G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523291 | |||||||
| chr5:177523326 | CATT | C | 2 | a0001c0001t0012g0034 a0001c0001t0016g0120 |
3 | HG01243.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2372+628_2372+630d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523326 | |||||||
| chr5:177523413 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0089 others(7): Show |
14 | HG00423.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.2372+544G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523413 | |||||||
| chr5:177523638 | T | C | 1 | a0001c0001t0053g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2372+319A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523638 | |||||||
| chr5:177523822 | G | C | 62 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(59): Show |
77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.2372+135C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523822 | |||||||
| chr5:177525215 | C | T | 1 | a0001c0001t0029g0249 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1276-10G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525215 | |||||||
| chr5:177525342 | C | G | 1 | a0009c0015t0030g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1276-137G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525342 | |||||||
| chr5:177525431 | C | T | 1 | a0001c0001t0008g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1276-226G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525431 | |||||||
| chr5:177525639 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0018g0198 |
2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1276-434C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525639 | |||||||
| chr5:177525697 | G | A | 5 | a0001c0001t0012g0147 a0001c0001t0012g0148 a0001c0001t0016g0124 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-492C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525697 | |||||||
| chr5:177525823 | C | T | 1 | a0001c0001t0010g0050 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1276-618G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525823 | |||||||
| chr5:177525918 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1276-713G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525918 | |||||||
| chr5:177525951 | C | G | 1 | a0001c0001t0001g0011 | 4 | HG02145.hp1 HG02559.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-746G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525951 | |||||||
| chr5:177526017 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(180): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1276-812C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526017 | |||||||
| chr5:177526130 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1276-925G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526130 | |||||||
| chr5:177526131 | G | A | 5 | a0001c0001t0012g0147 a0001c0001t0012g0148 a0001c0001t0016g0124 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-926C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526131 | |||||||
| chr5:177526293 | C | T | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(258): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1276-1088G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526293 | |||||||
| chr5:177526414 | C | T | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-1209G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526414 | |||||||
| chr5:177526465 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1276-1260G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526465 | |||||||
| chr5:177526524 | T | C | 2 | a0001c0001t0011g0128 a0001c0001t0011g0130 |
2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1276-1319A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526524 | |||||||
| chr5:177526813 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1276-1608T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526813 | |||||||
| chr5:177526851 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0080 |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-1646A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526851 | |||||||
| chr5:177526906 | C | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-1701G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526906 | |||||||
| chr5:177526924 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0083 a0001c0001t0001g0085 others(1): Show |
6 | NA18952.hp1 NA18961.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-1719T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526924 | |||||||
| chr5:177527121 | G | GC | 62 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(59): Show |
77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1276-1917dupG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527121 | |||||||
| chr5:177527240 | T | C | 1 | a0001c0001t0001g0031 | 2 | NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1276-2035A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527240 | |||||||
| chr5:177527416 | C | T | 3 | a0001c0001t0011g0128 a0001c0001t0011g0130 a0001c0001t0053g0251 |
3 | HG01346.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1276-2211G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527416 | |||||||
| chr5:177527647 | G | A | 1 | a0001c0001t0007g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1276-2442C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527647 | |||||||
| chr5:177527790 | T | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(260): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1276-2585A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527790 | |||||||
| chr5:177527828 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0064 others(2): Show |
11 | NA18939.hp2 NA18942.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.1276-2623A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527828 | |||||||
| chr5:177527926 | C | A | 1 | a0002c0002t0031g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1276-2721G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527926 | |||||||
| chr5:177528085 | C | T | 1 | a0001c0001t0033g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1276-2880G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528085 | |||||||
| chr5:177528155 | A | T | 4 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0022g0036 others(1): Show |
5 | HG01255.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-2950T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528155 | |||||||
| chr5:177528201 | G | A | 1 | a0001c0001t0002g0027 | 2 | NA18962.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1276-2996C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528201 | |||||||
| chr5:177528223 | C | T | 1 | a0001c0001t0025g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1276-3018G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528223 | |||||||
| chr5:177528475 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1276-3270C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528475 | |||||||
| chr5:177528531 | GGTCAAGA others(7): Show |
G | 1 | a0001c0001t0018g0196 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1276-3340_1276-332 others(18): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528531 | |||||||
| chr5:177528597 | T | A | 74 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0136 others(71): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1276-3392A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528597 | |||||||
| chr5:177528717 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1276-3512C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528717 | |||||||
| chr5:177528794 | TGA | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0033 |
5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-3591_1276-359 others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528794 | |||||||
| chr5:177528840 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1275+3603G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528840 | |||||||
| chr5:177529034 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0013g0037 a0001c0001t0017g0180 |
4 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+3409G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529034 | |||||||
| chr5:177529083 | A | T | 1 | a0001c0001t0002g0067 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1275+3360T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529083 | |||||||
| chr5:177529090 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0011g0126 |
2 | HG01099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1275+3353C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529090 | |||||||
| chr5:177529131 | G | T | 1 | a0001c0001t0007g0215 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1275+3312C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529131 | |||||||
| chr5:177529225 | C | T | 41 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(38): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1275+3218G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529225 | |||||||
| chr5:177529506 | G | T | 2 | a0002c0002t0031g0043 a0002c0002t0031g0266 |
3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1275+2937C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529506 | |||||||
| chr5:177529547 | G | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+2896C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529547 | |||||||
| chr5:177529598 | G | C | 3 | a0001c0001t0003g0006 a0001c0001t0003g0151 a0001c0001t0003g0152 |
7 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+2845C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529598 | |||||||
| chr5:177530125 | T | C | 62 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(59): Show |
77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1275+2318A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530125 | |||||||
| chr5:177530429 | A | T | 1 | a0001c0001t0002g0061 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1275+2014T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530429 | |||||||
| chr5:177530534 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1275+1909G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530534 | |||||||
| chr5:177530791 | C | T | 6 | a0001c0001t0024g0076 a0001c0001t0033g0048 a0001c0001t0049g0236 others(3): Show |
6 | HG02698.hp1 HG03491.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+1652G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530791 | |||||||
| chr5:177531106 | T | C | 1 | a0003c0003t0021g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1275+1337A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531106 | |||||||
| chr5:177531167 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1275+1276C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531167 | |||||||
| chr5:177531396 | G | A | 35 | a0001c0001t0001g0078 a0001c0001t0002g0001 a0001c0001t0002g0004 others(32): Show |
66 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1275+1047C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531396 | |||||||
| chr5:177531612 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1275+831C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531612 | |||||||
| chr5:177531613 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1275+830G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531613 | |||||||
| chr5:177531807 | A | G | 5 | a0001c0001t0015g0223 a0001c0001t0015g0224 a0001c0001t0023g0231 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275+636T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531807 | |||||||
| chr5:177531935 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0071 |
5 | HG00544.hp1 HG00673.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275+508G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531935 | |||||||
| chr5:177532024 | T | C | 8 | a0001c0001t0004g0188 a0001c0001t0009g0165 a0001c0001t0009g0166 others(5): Show |
8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1275+419A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532024 | |||||||
| chr5:177532031 | G | A | 1 | a0002c0002t0030g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1275+412C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532031 | |||||||
| chr5:177532054 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0142 a0001c0001t0003g0143 others(7): Show |
12 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1275+389G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532054 | |||||||
| chr5:177532295 | T | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(106): Show |
177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1275+148A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532295 | |||||||
| chr5:177532711 | C | T | 1 | a0001c0001t0005g0204 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1077-70G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177532711 | |||||||
| chr5:177533295 | C | T | 1 | a0001c0001t0023g0232 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1077-654G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533295 | |||||||
| chr5:177533306 | A | AT | 9 | a0001c0001t0005g0203 a0001c0001t0009g0165 a0001c0001t0012g0154 others(6): Show |
9 | HG00099.hp1 HG00558.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077-666dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533306 | |||||||
| chr5:177533449 | C | T | 1 | a0001c0001t0022g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1077-808G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533449 | |||||||
| chr5:177533450 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(106): Show |
177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-809C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533450 | |||||||
| chr5:177533495 | T | C | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-854A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533495 | |||||||
| chr5:177533646 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(106): Show |
177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-1005A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533646 | |||||||
| chr5:177533942 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(258): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1077-1301C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533942 | |||||||
| chr5:177534046 | T | C | 2 | a0001c0001t0003g0143 a0001c0001t0005g0199 |
2 | HG02922.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1077-1405A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534046 | |||||||
| chr5:177534067 | G | T | 1 | a0001c0001t0002g0067 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1077-1426C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534067 | |||||||
| chr5:177534165 | C | T | 1 | a0001c0001t0054g0252 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1077-1524G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534165 | |||||||
| chr5:177534187 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1077-1546A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534187 | |||||||
| chr5:177534192 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0080 |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077-1551G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534192 | |||||||
| chr5:177534248 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1077-1607C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534248 | |||||||
| chr5:177534291 | A | AT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(178): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1077-1651dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534291 | |||||||
| chr5:177534291 | A | ATT | 10 | a0001c0001t0001g0082 a0001c0001t0001g0094 a0001c0001t0001g0103 others(7): Show |
13 | HG00673.hp1 HG03831.hp2 HG03942.hp1 others(10): Show |
intron_variant | MODIFIER | c.1077-1652_1077-165 others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534291 | |||||||
| chr5:177534316 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1077-1675C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534316 | |||||||
| chr5:177534624 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1076+1734T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534624 | |||||||
| chr5:177534686 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1076+1672G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534686 | |||||||
| chr5:177534688 | G | T | 1 | a0001c0001t0003g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1076+1670C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534688 | |||||||
| chr5:177534944 | T | G | 1 | a0001c0001t0013g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1076+1414A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534944 | |||||||
| chr5:177535303 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1076+1055C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535303 | |||||||
| chr5:177535306 | G | T | 1 | a0001c0001t0010g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1076+1052C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535306 | |||||||
| chr5:177535328 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1076+1030C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535328 | |||||||
| chr5:177535387 | T | C | 1 | a0001c0001t0017g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1076+971A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535387 | |||||||
| chr5:177535395 | T | C | 6 | a0001c0001t0017g0170 a0001c0001t0033g0048 a0001c0001t0049g0236 others(3): Show |
6 | HG02698.hp1 HG03490.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+963A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535395 | |||||||
| chr5:177535651 | C | A | 2 | a0002c0002t0031g0043 a0002c0002t0031g0266 |
3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1076+707G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535651 | |||||||
| chr5:177535753 | C | T | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076+605G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535753 | |||||||
| chr5:177535759 | G | T | 2 | a0001c0001t0003g0146 a0001c0001t0010g0046 |
2 | HG01167.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1076+599C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535759 | |||||||
| chr5:177535779 | T | C | 1 | a0001c0001t0006g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1076+579A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535779 | |||||||
| chr5:177535921 | AT | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(258): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1076+436delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535921 | |||||||
| chr5:177536100 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1076+258C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536100 | |||||||
| chr5:177536173 | A | G | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+185T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536173 | |||||||
| chr5:177536332 | G | C | 41 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(38): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076+26C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536332 | |||||||
| chr5:177536348 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1076+10C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536348 | |||||||
| chr5:177536873 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.689-128G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177536873 | |||||||
| chr5:177536994 | G | A | 3 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 |
4 | HG02055.hp1 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-249C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177536994 | |||||||
| chr5:177537046 | T | G | 3 | a0001c0001t0003g0144 a0001c0001t0013g0162 a0006c0017t0003g0141 |
3 | HG00639.hp1 HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.689-301A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537046 | |||||||
| chr5:177537133 | C | A | 1 | a0001c0001t0006g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.689-388G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537133 | |||||||
| chr5:177537410 | A | G | 1 | a0001c0001t0010g0050 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.688+463T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537410 | |||||||
| chr5:177537540 | G | A | 3 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 |
4 | HG02055.hp1 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+333C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537540 | |||||||
| chr5:177538160 | G | A | 1 | a0001c0001t0043g0145 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.454-53C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538160 | |||||||
| chr5:177538168 | G | A | 1 | a0001c0001t0037g0239 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.454-61C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538168 | |||||||
| chr5:177538292 | C | T | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(258): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.454-185G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538292 | |||||||
| chr5:177538372 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0118 |
5 | HG01517.hp1 HG01981.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-265C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538372 | |||||||
| chr5:177538398 | T | C | 2 | a0001c0001t0001g0089 a0001c0007t0001g0075 |
2 | NA19057.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.454-291A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538398 | |||||||
| chr5:177538440 | G | C | 1 | a0001c0001t0023g0231 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-333C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538440 | |||||||
| chr5:177539236 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211-89G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539236 | |||||||
| chr5:177539500 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-353A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539500 | |||||||
| chr5:177539622 | T | C | 67 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(64): Show |
84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.211-475A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539622 | |||||||
| chr5:177539662 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211-515C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539662 | |||||||
| chr5:177539768 | C | T | 1 | a0001c0001t0011g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.211-621G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539768 | |||||||
| chr5:177539978 | CTTTTT | C | 8 | a0001c0001t0004g0188 a0001c0001t0009g0165 a0001c0001t0009g0166 others(5): Show |
8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-836_211-832del others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539978 | |||||||
| chr5:177540238 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.211-1091G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540238 | |||||||
| chr5:177540276 | C | T | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-1129G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540276 | |||||||
| chr5:177540306 | C | CA | 13 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0104 others(10): Show |
15 | HG00423.hp2 HG00673.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.211-1160dupT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540306 | |||||||
| chr5:177540306 | CA | C | 137 | a0001c0001t0001g0011 a0001c0001t0001g0110 a0001c0001t0002g0064 others(134): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.211-1160delT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540306 | |||||||
| chr5:177540335 | A | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(106): Show |
177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.211-1188T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540335 | |||||||
| chr5:177540337 | A | G | 1 | a0001c0001t0011g0128 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-1190T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540337 | |||||||
| chr5:177540478 | G | T | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-1331C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540478 | |||||||
| chr5:177540661 | G | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(181): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.211-1514C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540661 | |||||||
| chr5:177540736 | T | C | 1 | a0001c0001t0016g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211-1589A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540736 | |||||||
| chr5:177540864 | C | T | 2 | a0001c0001t0014g0023 a0001c0001t0014g0197 |
4 | HG03704.hp2 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1717G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540864 | |||||||
| chr5:177541156 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0080 |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-2009T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541156 | |||||||
| chr5:177541395 | C | A | 1 | a0001c0001t0003g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211-2248G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541395 | |||||||
| chr5:177541442 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211-2295C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541442 | |||||||
| chr5:177541445 | G | A | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2298C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541445 | |||||||
| chr5:177541520 | G | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0073 |
6 | HG01192.hp1 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-2373C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541520 | |||||||
| chr5:177541539 | C | T | 59 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(56): Show |
74 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.211-2392G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541539 | |||||||
| chr5:177541652 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.211-2505G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541652 | |||||||
| chr5:177541654 | C | T | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2507G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541654 | |||||||
| chr5:177541698 | C | T | 33 | a0001c0001t0001g0078 a0001c0001t0002g0001 a0001c0001t0002g0004 others(30): Show |
63 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.211-2551G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541698 | |||||||
| chr5:177541742 | A | G | 1 | a0001c0001t0007g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.211-2595T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541742 | |||||||
| chr5:177541989 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.211-2842A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541989 | |||||||
| chr5:177542092 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.211-2945G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542092 | |||||||
| chr5:177542214 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.211-3067A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542214 | |||||||
| chr5:177542271 | T | C | 3 | a0001c0001t0006g0171 a0001c0001t0019g0194 a0001c0001t0027g0229 |
3 | HG02135.hp2 NA18951.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.211-3124A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542271 | |||||||
| chr5:177542298 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3151C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542298 | |||||||
| chr5:177542299 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3152G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542299 | |||||||
| chr5:177542624 | G | A | 76 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0003g0021 others(73): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.211-3477C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542624 | |||||||
| chr5:177542733 | C | G | 5 | a0001c0001t0015g0223 a0001c0001t0015g0224 a0001c0001t0023g0231 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-3586G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542733 | |||||||
| chr5:177542734 | G | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3587C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542734 | |||||||
| chr5:177542793 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0033 others(1): Show |
10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3646C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542793 | |||||||
| chr5:177542823 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.211-3676G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542823 | |||||||
| chr5:177542925 | T | C | 1 | a0001c0001t0009g0167 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.211-3778A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542925 | |||||||
| chr5:177542942 | A | G | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3795T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542942 | |||||||
| chr5:177542995 | T | C | 1 | a0001c0001t0007g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211-3848A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542995 | |||||||
| chr5:177543241 | C | T | 1 | a0009c0015t0030g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.211-4094G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543241 | |||||||
| chr5:177543304 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.211-4157G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543304 | |||||||
| chr5:177543434 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.211-4287A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543434 | |||||||
| chr5:177543801 | C | T | 1 | a0001c0001t0015g0224 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.211-4654G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543801 | |||||||
| chr5:177543802 | G | A | 74 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0136 others(71): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.211-4655C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543802 | |||||||
| chr5:177543854 | G | A | 1 | a0001c0001t0015g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.211-4707C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543854 | |||||||
| chr5:177544072 | G | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(181): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.211-4925C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544072 | |||||||
| chr5:177544144 | T | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0106 |
2 | HG02132.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.211-4997A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544144 | |||||||
| chr5:177544633 | T | TG | 41 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0002g0001 others(38): Show |
71 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.211-5487dupC | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544633 | |||||||
| chr5:177544752 | AC | A | 2 | a0001c0001t0012g0034 a0001c0001t0016g0120 |
3 | HG01243.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.211-5606delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544752 | |||||||
| chr5:177544951 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG02145.hp1 HG02559.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-5804C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544951 | |||||||
| chr5:177545020 | T | C | 1 | a0001c0001t0008g0054 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-5873A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545020 | |||||||
| chr5:177545042 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.211-5895T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545042 | |||||||
| chr5:177545074 | C | T | 1 | a0006c0017t0003g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211-5927G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545074 | |||||||
| chr5:177545146 | C | T | 41 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(38): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.211-5999G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545146 | |||||||
| chr5:177545200 | C | T | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-6053G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545200 | |||||||
| chr5:177545258 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(181): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.211-6111C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545258 | |||||||
| chr5:177545400 | A | G | 1 | a0001c0001t0004g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.211-6253T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545400 | |||||||
| chr5:177545404 | T | G | 1 | a0001c0001t0004g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.211-6257A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545404 | |||||||
| chr5:177545486 | T | A | 1 | a0001c0001t0013g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-6339A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545486 | |||||||
| chr5:177545583 | C | T | 2 | a0005c0006t0002g0058 a0005c0006t0002g0059 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.211-6436G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545583 | |||||||
| chr5:177545619 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(181): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.211-6472G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545619 | |||||||
| chr5:177545658 | C | CAA | 49 | a0001c0001t0004g0003 a0001c0001t0004g0182 a0001c0001t0004g0183 others(46): Show |
64 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.211-6513_211-6512d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | |||||||
| chr5:177545658 | C | CAAA | 8 | a0001c0001t0004g0188 a0001c0001t0009g0165 a0001c0001t0009g0166 others(5): Show |
8 | HG02145.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-6514_211-6512d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | |||||||
| chr5:177545658 | CA | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(170): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.211-6512delT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | |||||||
| chr5:177545658 | CAA | C | 10 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(7): Show |
10 | HG00741.hp2 HG02132.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-6513_211-6512d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | |||||||
| chr5:177545898 | C | T | 1 | a0001c0001t0002g0025 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.211-6751G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545898 | |||||||
| chr5:177546010 | C | CGTGTT | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-6864_211-6863i others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546010 | |||||||
| chr5:177546150 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(192): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.211-7003C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546150 | |||||||
| chr5:177546196 | A | G | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-7049T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546196 | |||||||
| chr5:177546358 | G | C | 1 | a0001c0001t0001g0032 | 2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.211-7211C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546358 | |||||||
| chr5:177546422 | G | A | 4 | a0001c0001t0015g0223 a0001c0001t0023g0231 a0001c0001t0028g0233 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-7275C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546422 | |||||||
| chr5:177546791 | G | C | 4 | a0001c0001t0012g0147 a0001c0001t0012g0148 a0001c0001t0044g0209 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+7458C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546791 | |||||||
| chr5:177546910 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0004g0188 others(17): Show |
24 | HG01243.hp2 HG01261.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+7339C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546910 | |||||||
| chr5:177546948 | G | A | 1 | a0001c0001t0047g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210+7301C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546948 | |||||||
| chr5:177546959 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.210+7290G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546959 | |||||||
| chr5:177547006 | C | T | 2 | a0001c0001t0012g0147 a0001c0001t0012g0148 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.210+7243G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547006 | |||||||
| chr5:177547018 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.210+7231A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547018 | |||||||
| chr5:177547119 | A | G | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01109.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210+7130T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547119 | |||||||
| chr5:177547277 | A | AATTT | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6968_210+6971d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547277 | |||||||
| chr5:177547286 | C | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6963G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
9 | HG01069.hp1 HG01099.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.210+6957_210+6962d others(8): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
14 | HG01081.hp2 HG01258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+6955_210+6962d others(10): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTTT others(2): Show |
85 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0035 others(82): Show |
99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.210+6954_210+6962d others(11): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTTT others(3): Show |
50 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(47): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.210+6953_210+6962d others(12): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTTT others(4): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0004g0182 others(10): Show |
18 | HG01175.hp2 HG01261.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+6952_210+6962d others(13): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547286 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0004g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.210+6951_210+6962d others(14): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | |||||||
| chr5:177547290 | T | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6959A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547290 | |||||||
| chr5:177547378 | G | A | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6871C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547378 | |||||||
| chr5:177547496 | G | C | 62 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(59): Show |
77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.210+6753C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547496 | |||||||
| chr5:177547526 | C | T | 2 | a0001c0005t0006g0169 a0001c0005t0022g0156 |
2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.210+6723G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547526 | |||||||
| chr5:177547530 | C | T | 4 | a0001c0001t0026g0200 a0001c0001t0026g0201 a0001c0001t0050g0242 others(1): Show |
4 | NA18942.hp1 NA18984.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+6719G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547530 | |||||||
| chr5:177547579 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(102): Show |
173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.210+6670G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547579 | |||||||
| chr5:177547680 | C | T | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6569G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547680 | |||||||
| chr5:177547966 | G | GCA | 62 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(59): Show |
77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.210+6281_210+6282d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547966 | |||||||
| chr5:177548022 | C | G | 1 | a0001c0001t0026g0200 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.210+6227G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548022 | |||||||
| chr5:177548139 | C | G | 79 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0136 others(76): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.210+6110G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548139 | |||||||
| chr5:177548243 | T | C | 1 | a0001c0001t0005g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.210+6006A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548243 | |||||||
| chr5:177548358 | G | GT | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+5890dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548358 | |||||||
| chr5:177548692 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(180): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.210+5557T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548692 | |||||||
| chr5:177548918 | G | C | 1 | a0001c0001t0009g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.210+5331C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548918 | |||||||
| chr5:177548967 | CCTTT | C | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+5278_210+5281d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548967 | |||||||
| chr5:177548990 | C | G | 3 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 |
3 | HG01109.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210+5259G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548990 | |||||||
| chr5:177549134 | A | C | 1 | a0005c0006t0002g0058 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.210+5115T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549134 | |||||||
| chr5:177549187 | CT | C | 11 | a0001c0001t0008g0015 a0001c0001t0008g0054 a0001c0001t0008g0055 others(8): Show |
12 | HG00140.hp2 HG01243.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+5061delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | |||||||
| chr5:177549187 | CTT | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(176): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.210+5060_210+5061d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | |||||||
| chr5:177549187 | CTTT | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0110 others(8): Show |
12 | HG01074.hp1 HG01168.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.210+5059_210+5061d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | |||||||
| chr5:177549187 | CTTTTT | C | 6 | a0001c0001t0006g0022 a0001c0001t0009g0158 a0001c0001t0009g0159 others(3): Show |
6 | HG00735.hp1 HG01934.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+5057_210+5061d others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | |||||||
| chr5:177549192 | T | C | 3 | a0001c0014t0046g0218 a0003c0003t0021g0020 a0003c0003t0021g0134 |
5 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+5057A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549192 | |||||||
| chr5:177549193 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210+5056A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549193 | |||||||
| chr5:177549194 | T | C | 1 | a0001c0001t0002g0010 | 4 | NA18957.hp1 NA18990.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+5055A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549194 | |||||||
| chr5:177549195 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.210+5054A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549195 | |||||||
| chr5:177549338 | G | A | 1 | a0001c0001t0059g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+4911C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549338 | |||||||
| chr5:177549342 | G | A | 1 | a0001c0001t0015g0224 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.210+4907C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549342 | |||||||
| chr5:177549596 | A | G | 1 | a0001c0001t0005g0199 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.210+4653T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549596 | |||||||
| chr5:177549636 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02071.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.210+4613G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549636 | |||||||
| chr5:177549867 | TTATTA | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.210+4377_210+4381d others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549867 | |||||||
| chr5:177550051 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.210+4198C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550051 | |||||||
| chr5:177550096 | C | G | 1 | a0001c0001t0015g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.210+4153G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550096 | |||||||
| chr5:177550132 | T | C | 1 | a0001c0014t0046g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+4117A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550132 | |||||||
| chr5:177550154 | T | TAA | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+4093_210+4094d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550154 | |||||||
| chr5:177550202 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.210+4047C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550202 | |||||||
| chr5:177550296 | C | T | 1 | a0001c0001t0007g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.210+3953G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550296 | |||||||
| chr5:177550447 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.210+3802G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550447 | |||||||
| chr5:177550496 | C | T | 1 | a0001c0001t0008g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+3753G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550496 | |||||||
| chr5:177550564 | A | G | 1 | a0001c0001t0007g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.210+3685T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550564 | |||||||
| chr5:177550610 | C | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(44): Show |
72 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.210+3639G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550610 | |||||||
| chr5:177550850 | G | A | 4 | a0001c0001t0010g0024 a0001c0001t0010g0050 a0001c0001t0010g0051 others(1): Show |
5 | HG01106.hp2 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3399C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550850 | |||||||
| chr5:177550862 | C | T | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+3387G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550862 | |||||||
| chr5:177550865 | T | C | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3384A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550865 | |||||||
| chr5:177550979 | AC | A | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3269delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550979 | |||||||
| chr5:177550982 | C | T | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3267G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550982 | |||||||
| chr5:177551001 | A | AT | 79 | a0001c0001t0002g0057 a0001c0001t0003g0021 a0001c0001t0003g0035 others(76): Show |
91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.210+3247dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551001 | |||||||
| chr5:177551028 | TCTCA | T | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3217_210+3220d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551028 | |||||||
| chr5:177551048 | T | A | 1 | a0001c0001t0029g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3201A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551048 | |||||||
| chr5:177551108 | T | A | 1 | a0001c0001t0029g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3141A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551108 | |||||||
| chr5:177551109 | A | C | 1 | a0001c0001t0029g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3140T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551109 | |||||||
| chr5:177551151 | G | GTCAGAGA others(7): Show |
1 | a0001c0001t0029g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3097_210+3098i others(16): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551151 | |||||||
| chr5:177551152 | G | T | 1 | a0001c0001t0029g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3097C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551152 | |||||||
| chr5:177551172 | G | A | 2 | a0001c0001t0010g0050 a0001c0001t0010g0051 |
2 | HG01993.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.210+3077C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551172 | |||||||
| chr5:177551257 | C | CAGTT | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+2988_210+2991d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551257 | |||||||
| chr5:177551269 | AT | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(253): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.210+2979delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551269 | |||||||
| chr5:177551269 | ATT | A | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+2978_210+2979d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551269 | |||||||
| chr5:177551277 | T | G | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0012g0034 others(1): Show |
5 | HG01243.hp2 HG01934.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+2972A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551277 | |||||||
| chr5:177551284 | T | C | 1 | a0001c0001t0028g0235 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.210+2965A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551284 | |||||||
| chr5:177551405 | A | T | 1 | a0001c0014t0046g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+2844T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551405 | |||||||
| chr5:177551966 | G | A | 41 | a0001c0001t0004g0003 a0001c0001t0004g0181 a0001c0001t0004g0182 others(38): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.210+2283C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551966 | |||||||
| chr5:177551993 | G | A | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+2256C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551993 | |||||||
| chr5:177552222 | T | C | 8 | a0001c0001t0004g0188 a0001c0001t0009g0165 a0001c0001t0009g0166 others(5): Show |
8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+2027A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552222 | |||||||
| chr5:177552331 | T | C | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1918A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552331 | |||||||
| chr5:177552382 | C | G | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1867G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552382 | |||||||
| chr5:177552427 | A | G | 1 | a0001c0005t0022g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210+1822T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552427 | |||||||
| chr5:177553003 | T | C | 6 | a0001c0001t0008g0015 a0001c0001t0008g0052 a0001c0001t0008g0053 others(3): Show |
8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1246A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553003 | |||||||
| chr5:177553025 | T | C | 4 | a0002c0002t0030g0265 a0002c0002t0031g0043 a0002c0002t0031g0266 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1224A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553025 | |||||||
| chr5:177553307 | G | C | 2 | a0003c0003t0021g0020 a0003c0003t0021g0134 |
4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+942C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553307 | |||||||
| chr5:177553473 | T | G | 1 | a0001c0014t0046g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+776A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553473 | |||||||
| chr5:177553650 | A | G | 6 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0004c0004t0015g0219 others(3): Show |
6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+599T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553650 | |||||||
| chr5:177553808 | G | A | 1 | a0001c0001t0013g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.210+441C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553808 | |||||||
| chr5:177553903 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0018 others(15): Show |
30 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+346C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553903 | |||||||
| chr5:177553955 | G | GCCCAGT | 3 | a0001c0001t0012g0034 a0001c0001t0016g0120 a0001c0001t0049g0236 |
4 | HG01243.hp2 HG02698.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+288_210+293dup others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553955 | |||||||
| chr5:177554178 | G | A | 1 | a0001c0001t0041g0119 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.210+71C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177554178 |