Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55156 |
| ensemblid | ENSG00000104442.10 |
| hgncid | 17684 |
| symbol | ARMC1 |
| name | armadillo repeat containing 1 |
| refseq_nuc | NM_018120.6 |
| refseq_prot | NP_060590.1 |
| ensembl_nuc | ENST00000276569.8 |
| ensembl_prot | ENSP00000276569.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 65602458 |
| end | 65634177 |
| strand | - |
| ver | v1.2 |
| region | chr8:65602458-65634177 |
| region5000 | chr8:65597458-65639177 |
| regionname0 | ARMC1_chr8_65602458_65634177 |
| regionname5000 | ARMC1_chr8_65597458_65639177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 282 | 388 | 90 | 74 | 160 | 18 | 44 | 129 | ARMC1_chr8_65597458_65639177 | ARMC1 | MNSST others(277): Show |
chr8 | 65597458 | 65639177 |
| a0002 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | MNSST others(277): Show |
chr8 | 65597458 | 65639177 |
| a0003 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | MNSST others(277): Show |
chr8 | 65597458 | 65639177 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 846 | 233 | 76 | 42 | 76 | 6 | 32 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 | ||
| a0001c0002 | 0/1 | 846 | 135 | 12 | 27 | 73 | 11 | 11 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 | ||
| a0001c0003 | 0/0 | 846 | 16 | 2 | 5 | 7 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 | ||
| a0001c0004 | 0/0 | 846 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 | ||
| a0002c0006 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 | ||
| a0003c0005 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | ATGAA others(841): Show |
chr8 | 65597458 | 65639177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3000 | 102 | 9 | 10 | 61 | 0 | 22 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0003 | 0/0 | 3000 | 92 | 51 | 28 | 0 | 6 | 7 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0005 | 0/0 | 3000 | 20 | 5 | 2 | 13 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0006 | 0/0 | 3000 | 8 | 8 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0007 | 0/0 | 3000 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0008 | 0/0 | 3000 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0012 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0013 | 1/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0014 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0015 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0016 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0017 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0001t0018 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0002 | 0/0 | 3000 | 95 | 3 | 16 | 63 | 5 | 8 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0003 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0004 | 0/0 | 3000 | 36 | 8 | 10 | 9 | 6 | 3 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0009 | 0/1 | 3001 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2996): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0010 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0002t0011 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0003t0004 | 0/0 | 3000 | 16 | 2 | 5 | 7 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0001c0004t0004 | 0/0 | 3000 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0002c0006t0001 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| a0003c0005t0002 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | AGAGC others(2995): Show |
chr8 | 65597458 | 65639177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 5 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0003 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0013g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0014g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0015g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0016g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0017g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0001t0018g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0001 | 0/0 | 17 | 2 | 2 | 13 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0009g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0010g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0002t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0004t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0001c0004t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0002c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| a0003c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0213 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00099 | hp2 | a0001 | c0002 | t0004 | g0273 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0318 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00140 | hp2 | a0001 | c0003 | t0004 | g0292 | EUR | GBR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0279 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0107 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0274 | EUR | FIN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00642 | hp1 | a0001 | c0003 | t0004 | g0287 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0272 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0281 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0269 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0267 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0317 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0283 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0277 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01168 | hp2 | a0001 | c0003 | t0004 | g0296 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0280 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0261 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0275 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01346 | hp1 | a0001 | c0003 | t0004 | g0291 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01496 | hp2 | a0001 | c0003 | t0004 | g0011 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0014 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0103 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0235 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01516 | hp2 | a0001 | c0002 | t0004 | g0031 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0236 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0014 | EUR | IBS | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01928 | hp2 | a0001 | c0002 | t0004 | g0252 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01943 | hp2 | a0001 | c0002 | t0004 | g0259 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0260 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02027 | hp1 | a0002 | c0006 | t0001 | g0176 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0254 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0160 | EAS | CDX | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0276 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02293 | hp1 | a0001 | c0002 | t0010 | g0069 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02293 | hp2 | a0001 | c0003 | t0004 | g0290 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0207 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0031 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0268 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0030 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0074 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0304 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0271 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0265 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0321 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0285 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0309 | AFR | ESN | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0193 | SAS | PJL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0171 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0251 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04115 | hp2 | a0001 | c0003 | t0004 | g0293 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04204 | hp2 | a0001 | c0001 | t0015 | g0282 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0316 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18939 | hp2 | a0001 | c0003 | t0004 | g0298 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18942 | hp2 | a0001 | c0004 | t0004 | g0032 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18943 | hp1 | a0003 | c0005 | t0002 | g0047 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18946 | hp2 | a0001 | c0004 | t0004 | g0284 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18951 | hp2 | a0001 | c0003 | t0004 | g0294 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18960 | hp2 | a0001 | c0001 | t0016 | g0153 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18965 | hp2 | a0001 | c0003 | t0004 | g0289 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18967 | hp2 | a0001 | c0004 | t0004 | g0286 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18972 | hp2 | a0001 | c0002 | t0011 | g0060 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18977 | hp2 | a0001 | c0004 | t0004 | g0032 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0264 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19001 | hp2 | a0001 | c0003 | t0004 | g0288 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19056 | hp1 | a0001 | c0003 | t0004 | g0295 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0270 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0256 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19081 | hp1 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19086 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0250 | AFR | YRI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ASW | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ASW | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0278 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0297 | AFR | MSL | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | USA | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0009 | g0076 | REF | REF | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0086 | REF | REF | ARMC1_chr8_65597458_65639177 | ARMC1 | chr8 | 65597458 | 65639177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65604468 | C | T | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.775G>A | p.Gly259Ser | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 990/3000 | 775/849 | 259/282 | chr8 | 65604468 | |||
| chr8:65627376 | A | G | 1 | a0003 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.23T>C | p.Met8Thr | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/7 | 238/3000 | 23/849 | 8/282 | chr8 | 65627376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65604427 | A | T | 1 | a0001c0004 | 4 | NA18942.hp2 NA18946.hp2 NA18967.hp2 others(1): Show |
synonymous_variant | LOW | c.816T>A | p.Ala272Ala | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1031/3000 | 816/849 | 272/282 | chr8 | 65604427 | |||
| chr8:65605314 | T | C | 2 | a0001c0003 a0001c0004 |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
synonymous_variant | LOW | c.606A>G | p.Ser202Ser | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/7 | 821/3000 | 606/849 | 202/282 | chr8 | 65605314 | |||
| chr8:65613313 | T | C | 2 | a0001c0002 a0003c0005 |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
synonymous_variant | LOW | c.396A>G | p.Gln132Gln | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/7 | 611/3000 | 396/849 | 132/282 | chr8 | 65613313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65602534 | T | A | 1 | a0001c0002t0010 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1860 | chr8 | 65602534 | ||||||
| chr8:65602545 | A | G | 2 | a0001c0001t0005 a0001c0001t0014 |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1849T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1849 | chr8 | 65602545 | ||||||
| chr8:65602553 | T | C | 1 | a0001c0002t0011 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1841A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1841 | chr8 | 65602553 | ||||||
| chr8:65602619 | C | T | 1 | a0001c0001t0014 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1775 | chr8 | 65602619 | ||||||
| chr8:65602719 | T | C | 11 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(8): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*1675A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1675 | chr8 | 65602719 | ||||||
| chr8:65602730 | T | C | 9 | a0001c0001t0005 a0001c0001t0014 a0001c0002t0002 others(6): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1664 | chr8 | 65602730 | ||||||
| chr8:65602779 | T | C | 1 | a0001c0001t0012 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1615A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1615 | chr8 | 65602779 | ||||||
| chr8:65602828 | G | GT | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(7): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1565dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1565 | chr8 | 65602828 | ||||||
| chr8:65602828 | G | GTT | 3 | a0001c0001t0005 a0001c0002t0002 a0001c0002t0004 |
9 | HG00735.hp1 HG00741.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1564_*1565dupAA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1565 | chr8 | 65602828 | ||||||
| chr8:65602828 | G | T | 2 | a0001c0001t0007 a0001c0001t0015 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1566 | chr8 | 65602828 | ||||||
| chr8:65602851 | G | A | 2 | a0001c0001t0007 a0001c0001t0015 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1543C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1543 | chr8 | 65602851 | ||||||
| chr8:65603102 | C | G | 1 | a0001c0001t0016 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1292 | chr8 | 65603102 | ||||||
| chr8:65603333 | T | C | 1 | a0001c0001t0015 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 1061 | chr8 | 65603333 | ||||||
| chr8:65603548 | G | A | 11 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(8): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*846C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 846 | chr8 | 65603548 | ||||||
| chr8:65603630 | A | G | 11 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(8): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*764T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 764 | chr8 | 65603630 | ||||||
| chr8:65603753 | C | T | 11 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(8): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 641 | chr8 | 65603753 | ||||||
| chr8:65603831 | T | G | 2 | a0001c0001t0005 a0001c0001t0014 |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*563A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 563 | chr8 | 65603831 | ||||||
| chr8:65603839 | C | T | 1 | a0001c0001t0008 | 2 | HG02155.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*555G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 555 | chr8 | 65603839 | ||||||
| chr8:65603852 | G | T | 2 | a0001c0001t0005 a0001c0001t0014 |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*542C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 542 | chr8 | 65603852 | ||||||
| chr8:65604255 | C | T | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(14): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*139G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 7/7 | 139 | chr8 | 65604255 | ||||||
| chr8:65627405 | T | C | 1 | a0001c0001t0017 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/7 | 7 | chr8 | 65627405 | ||||||
| chr8:65634122 | G | A | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(12): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
5_prime_UTR_variant | MODIFIER | c.-160C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/7 | 6724 | chr8 | 65634122 | ||||||
| chr8:65634172 | G | A | 1 | a0001c0001t0018 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/7 | 6774 | chr8 | 65634172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65604854 | C | T | 1 | a0001c0001t0014g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.658-269G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65604854 | |||||||
| chr8:65605000 | G | A | 1 | a0001c0002t0011g0060 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.657+263C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605000 | |||||||
| chr8:65605219 | T | C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.657+44A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605219 | |||||||
| chr8:65605251 | C | T | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.657+12G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 6/6 | chr8 | 65605251 | |||||||
| chr8:65605619 | G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466-81C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605619 | |||||||
| chr8:65605778 | A | AT | 7 | a0001c0001t0003g0197 a0001c0001t0003g0198 a0001c0001t0003g0199 others(4): Show |
7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-241dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605778 | |||||||
| chr8:65605848 | A | G | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.466-310T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65605848 | |||||||
| chr8:65606227 | G | A | 141 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(138): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.466-689C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606227 | |||||||
| chr8:65606241 | G | A | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-703C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606241 | |||||||
| chr8:65606242 | T | G | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-704A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606242 | |||||||
| chr8:65606243 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-705G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606243 | |||||||
| chr8:65606360 | C | CA | 153 | a0001c0001t0001g0154 a0001c0001t0003g0009 a0001c0001t0003g0023 others(150): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.466-823dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606360 | |||||||
| chr8:65606371 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.466-833T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606371 | |||||||
| chr8:65606387 | A | G | 1 | a0001c0002t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466-849T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606387 | |||||||
| chr8:65606392 | T | G | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.466-854A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606392 | |||||||
| chr8:65606603 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.466-1065A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606603 | |||||||
| chr8:65606651 | G | A | 10 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0237 others(7): Show |
12 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-1113C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606651 | |||||||
| chr8:65606766 | A | G | 145 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(142): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.466-1228T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606766 | |||||||
| chr8:65606807 | C | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0013 a0001c0002t0002g0044 others(19): Show |
26 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.466-1269G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606807 | |||||||
| chr8:65606812 | T | C | 1 | a0001c0002t0002g0096 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.466-1274A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65606812 | |||||||
| chr8:65607024 | C | T | 145 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(142): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.466-1486G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607024 | |||||||
| chr8:65607157 | C | T | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.466-1619G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607157 | |||||||
| chr8:65607322 | T | G | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.466-1784A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607322 | |||||||
| chr8:65607454 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.466-1916G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607454 | |||||||
| chr8:65607636 | C | T | 1 | a0001c0001t0003g0188 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-2098G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607636 | |||||||
| chr8:65607804 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2266A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65607804 | |||||||
| chr8:65608017 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2479A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608017 | |||||||
| chr8:65608040 | G | A | 2 | a0001c0001t0006g0037 a0001c0001t0012g0036 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.466-2502C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608040 | |||||||
| chr8:65608239 | A | T | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.466-2701T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608239 | |||||||
| chr8:65608389 | C | T | 2 | a0001c0001t0003g0190 a0001c0001t0003g0205 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.466-2851G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608389 | |||||||
| chr8:65608455 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-2917C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608455 | |||||||
| chr8:65608486 | G | A | 1 | a0001c0001t0007g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.466-2948C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608486 | |||||||
| chr8:65608521 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466-2983A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608521 | |||||||
| chr8:65608626 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3088A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608626 | |||||||
| chr8:65608666 | G | C | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-3128C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608666 | |||||||
| chr8:65608698 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0161 others(1): Show |
5 | HG03017.hp1 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-3160T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608698 | |||||||
| chr8:65608715 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0167 others(1): Show |
4 | NA18957.hp2 NA18961.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-3177G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608715 | |||||||
| chr8:65608767 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3229C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608767 | |||||||
| chr8:65608787 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3249A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608787 | |||||||
| chr8:65608814 | CAGG | C | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.466-3279_466-3277d others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65608814 | |||||||
| chr8:65609037 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.466-3499G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609037 | |||||||
| chr8:65609074 | C | CT | 145 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(142): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.466-3537dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609074 | |||||||
| chr8:65609104 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3566G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609104 | |||||||
| chr8:65609106 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.466-3568A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609106 | |||||||
| chr8:65609133 | CT | C | 170 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0152 others(167): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.466-3596delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609133 | |||||||
| chr8:65609157 | G | A | 1 | a0001c0002t0004g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.466-3619C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609157 | |||||||
| chr8:65609176 | T | G | 145 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(142): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.466-3638A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609176 | |||||||
| chr8:65609204 | G | A | 6 | a0001c0001t0003g0010 a0001c0001t0003g0232 a0001c0001t0003g0233 others(3): Show |
8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-3666C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609204 | |||||||
| chr8:65609225 | C | A | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-3687G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609225 | |||||||
| chr8:65609236 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.466-3698C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609236 | |||||||
| chr8:65609237 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.466-3699T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609237 | |||||||
| chr8:65609261 | C | A | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.466-3723G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609261 | |||||||
| chr8:65609297 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.466-3759C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609297 | |||||||
| chr8:65609397 | A | G | 1 | a0001c0002t0002g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.465+3847T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609397 | |||||||
| chr8:65609409 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.465+3835T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609409 | |||||||
| chr8:65609534 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3710A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609534 | |||||||
| chr8:65609625 | C | A | 1 | a0001c0001t0003g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.465+3619G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609625 | |||||||
| chr8:65609631 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.465+3613C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609631 | |||||||
| chr8:65609655 | C | T | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+3589G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609655 | |||||||
| chr8:65609686 | C | T | 11 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0130 others(8): Show |
11 | HG02080.hp2 HG02135.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.465+3558G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609686 | |||||||
| chr8:65609716 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3528C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609716 | |||||||
| chr8:65609872 | A | AAAAG | 76 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(73): Show |
91 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | |||||||
| chr8:65609872 | A | AAAG | 8 | a0001c0001t0003g0235 a0001c0001t0007g0281 a0001c0001t0007g0283 others(5): Show |
8 | HG00733.hp2 HG01074.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | |||||||
| chr8:65609872 | A | AAG | 123 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0037 others(120): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | |||||||
| chr8:65609872 | A | AG | 23 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(20): Show |
24 | HG01069.hp1 HG01167.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.465+3371_465+3372i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | |||||||
| chr8:65609872 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.465+3372T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609872 | |||||||
| chr8:65609877 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.465+3367C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609877 | |||||||
| chr8:65609879 | A | AAAAG | 230 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(227): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.465+3364_465+3365i others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609879 | |||||||
| chr8:65609879 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.465+3365T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609879 | |||||||
| chr8:65609882 | G | A | 231 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(228): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.465+3362C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609882 | |||||||
| chr8:65609882 | G | GAAAAAGA others(2): Show |
5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0229 others(2): Show |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+3353_465+3361d others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609882 | |||||||
| chr8:65609888 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3356C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609888 | |||||||
| chr8:65609889 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3355T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65609889 | |||||||
| chr8:65610009 | T | C | 5 | a0001c0001t0006g0034 a0001c0001t0006g0039 a0001c0001t0006g0040 others(2): Show |
5 | HG02965.hp1 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+3235A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610009 | |||||||
| chr8:65610010 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465+3234A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610010 | |||||||
| chr8:65610090 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.465+3154C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610090 | |||||||
| chr8:65610102 | A | AT | 150 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(147): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.465+3141dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610102 | |||||||
| chr8:65610108 | T | TG | 3 | a0001c0004t0004g0032 a0001c0004t0004g0284 a0001c0004t0004g0286 |
4 | NA18942.hp2 NA18946.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+3135_465+3136i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610108 | |||||||
| chr8:65610120 | C | T | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.465+3124G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610120 | |||||||
| chr8:65610159 | G | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3085C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610159 | |||||||
| chr8:65610172 | A | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3072T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610172 | |||||||
| chr8:65610183 | C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3061G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610183 | |||||||
| chr8:65610191 | A | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3053T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610191 | |||||||
| chr8:65610200 | C | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3044G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610200 | |||||||
| chr8:65610201 | G | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3043C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610201 | |||||||
| chr8:65610202 | A | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3042T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610202 | |||||||
| chr8:65610204 | T | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3040A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610204 | |||||||
| chr8:65610211 | A | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3033T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610211 | |||||||
| chr8:65610222 | T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3022A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610222 | |||||||
| chr8:65610235 | T | C | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.465+3009A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610235 | |||||||
| chr8:65610242 | C | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3002G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610242 | |||||||
| chr8:65610243 | G | A | 2 | a0001c0002t0004g0275 a0001c0002t0004g0279 |
2 | HG00280.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.465+3001C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610243 | |||||||
| chr8:65610243 | G | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3001C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610243 | |||||||
| chr8:65610244 | T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+3000A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610244 | |||||||
| chr8:65610247 | A | C | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2997T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610247 | |||||||
| chr8:65610259 | T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2985A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610259 | |||||||
| chr8:65610263 | T | A | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+2981A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610263 | |||||||
| chr8:65610296 | A | G | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2948T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610296 | |||||||
| chr8:65610302 | T | A | 3 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0244 |
3 | HG02145.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.465+2942A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610302 | |||||||
| chr8:65610337 | T | A | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2907A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610337 | |||||||
| chr8:65610338 | C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2906G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610338 | |||||||
| chr8:65610348 | C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2896G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610348 | |||||||
| chr8:65610351 | C | T | 1 | a0001c0001t0005g0313 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.465+2893G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610351 | |||||||
| chr8:65610427 | G | A | 131 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0037 others(128): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.465+2817C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610427 | |||||||
| chr8:65610567 | C | T | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+2677G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610567 | |||||||
| chr8:65610606 | A | G | 16 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(13): Show |
17 | HG02027.hp2 HG02055.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+2638T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610606 | |||||||
| chr8:65610627 | G | A | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+2617C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610627 | |||||||
| chr8:65610657 | C | T | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.465+2587G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610657 | |||||||
| chr8:65610674 | A | C | 1 | a0001c0002t0002g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.465+2570T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610674 | |||||||
| chr8:65610744 | G | A | 7 | a0001c0001t0003g0197 a0001c0001t0003g0198 a0001c0001t0003g0199 others(4): Show |
7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+2500C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65610744 | |||||||
| chr8:65611036 | C | T | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+2208G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611036 | |||||||
| chr8:65611210 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+2034G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611210 | |||||||
| chr8:65611230 | G | A | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.465+2014C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611230 | |||||||
| chr8:65611326 | A | C | 1 | a0001c0001t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.465+1918T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611326 | |||||||
| chr8:65611444 | C | T | 1 | a0001c0001t0003g0028 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.465+1800G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611444 | |||||||
| chr8:65611482 | CT | C | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+1761delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611482 | |||||||
| chr8:65611517 | C | G | 231 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(228): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.465+1727G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611517 | |||||||
| chr8:65611564 | C | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.465+1680G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611564 | |||||||
| chr8:65611649 | T | C | 31 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0026 others(28): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.465+1595A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611649 | |||||||
| chr8:65611735 | A | G | 1 | a0001c0002t0004g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.465+1509T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611735 | |||||||
| chr8:65611810 | G | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.465+1434C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611810 | |||||||
| chr8:65611843 | A | G | 154 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(151): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465+1401T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611843 | |||||||
| chr8:65611889 | T | G | 1 | a0001c0002t0002g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.465+1355A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65611889 | |||||||
| chr8:65612028 | C | T | 71 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0005 others(68): Show |
98 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.465+1216G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612028 | |||||||
| chr8:65612211 | G | A | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465+1033C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612211 | |||||||
| chr8:65612554 | A | T | 1 | a0001c0002t0002g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.465+690T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612554 | |||||||
| chr8:65612669 | C | G | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+575G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612669 | |||||||
| chr8:65612948 | T | G | 1 | a0001c0001t0014g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.465+296A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612948 | |||||||
| chr8:65612960 | T | C | 6 | a0001c0002t0004g0254 a0001c0002t0004g0257 a0001c0002t0004g0263 others(3): Show |
6 | HG02055.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+284A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612960 | |||||||
| chr8:65612967 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.465+277A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 4/6 | chr8 | 65612967 | |||||||
| chr8:65613630 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-197G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613630 | |||||||
| chr8:65613712 | A | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.276-279T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613712 | |||||||
| chr8:65613889 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.276-456C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613889 | |||||||
| chr8:65613921 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.276-488G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613921 | |||||||
| chr8:65613959 | C | CA | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
206 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.276-527dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613959 | |||||||
| chr8:65613959 | CA | C | 71 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(68): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.276-527delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613959 | |||||||
| chr8:65613974 | C | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-541G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65613974 | |||||||
| chr8:65614243 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.276-810T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614243 | |||||||
| chr8:65614418 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.276-985T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614418 | |||||||
| chr8:65614425 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.276-992T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614425 | |||||||
| chr8:65614623 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.276-1190A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614623 | |||||||
| chr8:65614647 | T | G | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.276-1214A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614647 | |||||||
| chr8:65614849 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.276-1416C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65614849 | |||||||
| chr8:65615040 | TA | T | 15 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(12): Show |
17 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.276-1608delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615040 | |||||||
| chr8:65615105 | C | G | 2 | a0001c0002t0004g0256 a0001c0002t0004g0258 |
2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.276-1672G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615105 | |||||||
| chr8:65615119 | G | T | 1 | a0001c0001t0007g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.276-1686C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615119 | |||||||
| chr8:65615193 | A | C | 1 | a0001c0001t0006g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.276-1760T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615193 | |||||||
| chr8:65615219 | G | A | 2 | a0001c0003t0004g0288 a0001c0003t0004g0298 |
2 | NA18939.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.276-1786C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615219 | |||||||
| chr8:65615399 | T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1966A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615399 | |||||||
| chr8:65615400 | TA | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
110 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.276-1968delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615400 | |||||||
| chr8:65615400 | TAA | T | 154 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(151): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.276-1969_276-1968d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615400 | |||||||
| chr8:65615401 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1968T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615401 | |||||||
| chr8:65615413 | A | C | 1 | a0001c0002t0002g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.276-1980T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615413 | |||||||
| chr8:65615413 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1980T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615413 | |||||||
| chr8:65615416 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1983T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615416 | |||||||
| chr8:65615419 | A | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1986T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615419 | |||||||
| chr8:65615420 | C | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1987G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615420 | |||||||
| chr8:65615421 | A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-1988T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615421 | |||||||
| chr8:65615427 | G | A | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276-1994C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615427 | |||||||
| chr8:65615474 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.276-2041C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615474 | |||||||
| chr8:65615479 | T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2046A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615479 | |||||||
| chr8:65615480 | G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2047C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615480 | |||||||
| chr8:65615485 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2052T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615485 | |||||||
| chr8:65615525 | C | T | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.276-2092G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615525 | |||||||
| chr8:65615646 | G | T | 1 | a0001c0001t0003g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.276-2213C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615646 | |||||||
| chr8:65615666 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-2233C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615666 | |||||||
| chr8:65615826 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276-2393G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615826 | |||||||
| chr8:65615834 | G | A | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.276-2401C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615834 | |||||||
| chr8:65615891 | G | A | 1 | a0001c0001t0015g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.276-2458C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615891 | |||||||
| chr8:65615905 | A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2472T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615905 | |||||||
| chr8:65615906 | G | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2473C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615906 | |||||||
| chr8:65615908 | A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2475T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65615908 | |||||||
| chr8:65616021 | A | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2588T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616021 | |||||||
| chr8:65616031 | T | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2598A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616031 | |||||||
| chr8:65616093 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2660T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616093 | |||||||
| chr8:65616119 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2686T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616119 | |||||||
| chr8:65616128 | G | GT | 7 | a0001c0001t0003g0197 a0001c0001t0003g0198 a0001c0001t0003g0199 others(4): Show |
7 | HG01255.hp1 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.276-2696dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616128 | |||||||
| chr8:65616129 | T | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2696A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616129 | |||||||
| chr8:65616164 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.276-2731C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616164 | |||||||
| chr8:65616268 | G | A | 2 | a0001c0002t0004g0276 a0001c0002t0004g0278 |
2 | HG02280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.276-2835C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616268 | |||||||
| chr8:65616279 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0026 others(28): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.276-2846G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616279 | |||||||
| chr8:65616299 | G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-2866C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616299 | |||||||
| chr8:65616322 | A | G | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.276-2889T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616322 | |||||||
| chr8:65616323 | G | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-2890C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616323 | |||||||
| chr8:65616369 | G | A | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.276-2936C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616369 | |||||||
| chr8:65616395 | G | C | 1 | a0001c0001t0003g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.276-2962C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616395 | |||||||
| chr8:65616403 | G | A | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.276-2970C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616403 | |||||||
| chr8:65616422 | G | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-2989C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616422 | |||||||
| chr8:65616442 | G | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3009C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616442 | |||||||
| chr8:65616456 | G | A | 1 | a0001c0002t0002g0067 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.276-3023C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616456 | |||||||
| chr8:65616465 | C | T | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.276-3032G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616465 | |||||||
| chr8:65616492 | C | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3059G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616492 | |||||||
| chr8:65616553 | A | AC | 11 | a0001c0001t0001g0130 a0001c0001t0001g0142 a0001c0001t0005g0308 others(8): Show |
11 | HG00544.hp1 HG02135.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.276-3121dupG | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616553 | |||||||
| chr8:65616575 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.276-3142G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616575 | |||||||
| chr8:65616576 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.276-3143C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616576 | |||||||
| chr8:65616618 | T | C | 1 | a0001c0001t0003g0028 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.276-3185A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616618 | |||||||
| chr8:65616683 | G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3250C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616683 | |||||||
| chr8:65616692 | G | A | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3259C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616692 | |||||||
| chr8:65616701 | C | G | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3268G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616701 | |||||||
| chr8:65616702 | G | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3269C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616702 | |||||||
| chr8:65616710 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3277T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616710 | |||||||
| chr8:65616711 | T | A | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3278A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616711 | |||||||
| chr8:65616712 | A | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3279T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616712 | |||||||
| chr8:65616712 | A | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3279T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616712 | |||||||
| chr8:65616734 | T | C | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3301A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616734 | |||||||
| chr8:65616742 | G | A | 3 | a0001c0003t0004g0290 a0001c0003t0004g0291 a0001c0003t0004g0296 |
3 | HG01168.hp2 HG01346.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.276-3309C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616742 | |||||||
| chr8:65616821 | C | T | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-3388G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616821 | |||||||
| chr8:65616854 | C | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0182 others(15): Show |
21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3421G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616854 | |||||||
| chr8:65616855 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.276-3422C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616855 | |||||||
| chr8:65616866 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-3433A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616866 | |||||||
| chr8:65616902 | G | A | 3 | a0001c0002t0002g0082 a0001c0002t0002g0090 a0001c0002t0002g0101 |
3 | NA18961.hp2 NA19011.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.276-3469C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616902 | |||||||
| chr8:65616941 | T | C | 2 | a0001c0002t0002g0079 a0001c0002t0002g0083 |
2 | NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.276-3508A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616941 | |||||||
| chr8:65616966 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-3533A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616966 | |||||||
| chr8:65616970 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.276-3537G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616970 | |||||||
| chr8:65616981 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0174 |
3 | HG02257.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.276-3548G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65616981 | |||||||
| chr8:65617016 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-3583C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617016 | |||||||
| chr8:65617020 | G | A | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.276-3587C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617020 | |||||||
| chr8:65617032 | C | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-3599G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617032 | |||||||
| chr8:65617143 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.276-3710G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617143 | |||||||
| chr8:65617157 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-3724C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617157 | |||||||
| chr8:65617172 | G | A | 1 | a0001c0002t0002g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.276-3739C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617172 | |||||||
| chr8:65617172 | G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-3739C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617172 | |||||||
| chr8:65617226 | T | G | 1 | a0001c0001t0003g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.276-3793A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617226 | |||||||
| chr8:65617402 | A | G | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.276-3969T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617402 | |||||||
| chr8:65617408 | A | C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-3975T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617408 | |||||||
| chr8:65617467 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.276-4034A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617467 | |||||||
| chr8:65617482 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.276-4049G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617482 | |||||||
| chr8:65617568 | C | G | 54 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(51): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.276-4135G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617568 | |||||||
| chr8:65617593 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
202 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.276-4160C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617593 | |||||||
| chr8:65617617 | TA | T | 17 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(14): Show |
19 | HG01109.hp1 HG01169.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.276-4185delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617617 | |||||||
| chr8:65617677 | C | T | 1 | a0001c0001t0003g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.276-4244G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617677 | |||||||
| chr8:65617730 | G | T | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.276-4297C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617730 | |||||||
| chr8:65617763 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-4330G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617763 | |||||||
| chr8:65617834 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.276-4401A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617834 | |||||||
| chr8:65617850 | GA | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
218 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.275+4412delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617850 | |||||||
| chr8:65617857 | A | C | 1 | a0001c0003t0004g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.275+4406T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617857 | |||||||
| chr8:65617922 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.275+4341C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | |||||||
| chr8:65617922 | G | GT | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4340_275+4341i others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | |||||||
| chr8:65617922 | G | T | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.275+4341C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617922 | |||||||
| chr8:65617923 | G | C | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.275+4340C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65617923 | |||||||
| chr8:65618009 | G | A | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.275+4254C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618009 | |||||||
| chr8:65618063 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4200C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618063 | |||||||
| chr8:65618088 | A | T | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.275+4175T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618088 | |||||||
| chr8:65618104 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4159A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618104 | |||||||
| chr8:65618147 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4116G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618147 | |||||||
| chr8:65618150 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4113C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618150 | |||||||
| chr8:65618157 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+4106T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618157 | |||||||
| chr8:65618248 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0117 |
2 | NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.275+4015G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618248 | |||||||
| chr8:65618325 | A | G | 1 | a0001c0001t0005g0309 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.275+3938T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618325 | |||||||
| chr8:65618345 | A | G | 2 | a0001c0002t0002g0016 a0001c0002t0002g0045 |
3 | HG00738.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.275+3918T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618345 | |||||||
| chr8:65618386 | G | A | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.275+3877C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618386 | |||||||
| chr8:65618423 | G | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+3840C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618423 | |||||||
| chr8:65618447 | G | A | 18 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0182 others(15): Show |
21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+3816C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618447 | |||||||
| chr8:65618521 | C | CA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
140 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.275+3741dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | |||||||
| chr8:65618521 | C | CAA | 54 | a0001c0001t0001g0108 a0001c0001t0001g0143 a0001c0001t0003g0003 others(51): Show |
64 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.275+3740_275+3741d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | |||||||
| chr8:65618521 | CA | C | 8 | a0001c0001t0005g0308 a0001c0001t0006g0034 a0001c0002t0002g0071 others(5): Show |
8 | HG00099.hp2 HG02965.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.275+3741delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618521 | |||||||
| chr8:65618548 | T | C | 1 | a0001c0002t0002g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.275+3715A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618548 | |||||||
| chr8:65618573 | C | T | 1 | a0001c0002t0002g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.275+3690G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618573 | |||||||
| chr8:65618576 | G | C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.275+3687C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618576 | |||||||
| chr8:65618595 | A | AATTTCAG others(15): Show |
6 | a0001c0002t0002g0004 a0001c0002t0002g0053 a0001c0002t0002g0068 others(3): Show |
9 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+3646_275+3667d others(24): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618595 | |||||||
| chr8:65618674 | G | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0024 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.275+3589C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618674 | |||||||
| chr8:65618710 | T | C | 6 | a0001c0001t0003g0010 a0001c0001t0003g0232 a0001c0001t0003g0233 others(3): Show |
8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+3553A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618710 | |||||||
| chr8:65618772 | G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+3491C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618772 | |||||||
| chr8:65618857 | T | G | 7 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0184 others(4): Show |
9 | HG01109.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.275+3406A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618857 | |||||||
| chr8:65618903 | C | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+3360G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618903 | |||||||
| chr8:65618991 | C | T | 1 | a0001c0001t0006g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.275+3272G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618991 | |||||||
| chr8:65618997 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+3266G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65618997 | |||||||
| chr8:65619026 | G | C | 1 | a0001c0001t0003g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.275+3237C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619026 | |||||||
| chr8:65619394 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2869A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619394 | |||||||
| chr8:65619413 | A | G | 2 | a0001c0001t0003g0197 a0001c0001t0003g0199 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.275+2850T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619413 | |||||||
| chr8:65619542 | G | GA | 18 | a0001c0002t0002g0077 a0001c0003t0004g0011 a0001c0003t0004g0285 others(15): Show |
21 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.275+2720dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619542 | |||||||
| chr8:65619561 | G | A | 5 | a0001c0001t0006g0034 a0001c0001t0006g0039 a0001c0001t0006g0040 others(2): Show |
5 | HG02965.hp1 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+2702C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619561 | |||||||
| chr8:65619626 | C | A | 1 | a0001c0003t0004g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.275+2637G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619626 | |||||||
| chr8:65619626 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2637G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619626 | |||||||
| chr8:65619644 | C | T | 1 | a0003c0005t0002g0047 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.275+2619G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619644 | |||||||
| chr8:65619668 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+2595T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619668 | |||||||
| chr8:65619801 | T | C | 1 | a0001c0003t0004g0293 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.275+2462A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619801 | |||||||
| chr8:65619977 | C | CA | 16 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0173 others(13): Show |
16 | HG00673.hp2 HG01192.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.275+2285dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619977 | |||||||
| chr8:65619977 | CA | C | 7 | a0001c0001t0001g0152 a0001c0001t0003g0200 a0001c0001t0007g0281 others(4): Show |
7 | HG00733.hp2 HG01074.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+2285delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65619977 | |||||||
| chr8:65620294 | C | CT | 19 | a0001c0001t0005g0299 a0001c0001t0005g0306 a0001c0002t0002g0044 others(16): Show |
19 | HG00408.hp1 HG02135.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.275+1968dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | |||||||
| chr8:65620294 | CT | C | 13 | a0001c0001t0005g0305 a0001c0001t0006g0034 a0001c0001t0006g0035 others(10): Show |
13 | HG02486.hp1 HG02965.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.275+1968delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | |||||||
| chr8:65620294 | CTTTTT | C | 21 | a0001c0001t0001g0131 a0001c0001t0001g0166 a0001c0001t0003g0009 others(18): Show |
24 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.275+1964_275+1968d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | |||||||
| chr8:65620294 | CTTTTTT | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
161 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.275+1963_275+1968d others(8): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | |||||||
| chr8:65620294 | CTTTTTTT | C | 14 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0028 others(11): Show |
16 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.275+1962_275+1968d others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620294 | |||||||
| chr8:65620364 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.275+1899G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620364 | |||||||
| chr8:65620388 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1875C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620388 | |||||||
| chr8:65620455 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.275+1808G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620455 | |||||||
| chr8:65620503 | T | C | 9 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0037 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.275+1760A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620503 | |||||||
| chr8:65620530 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1733A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620530 | |||||||
| chr8:65620542 | T | TC | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1720dupG | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620542 | |||||||
| chr8:65620759 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275+1504G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620759 | |||||||
| chr8:65620798 | T | TAAAAAAA others(6): Show |
3 | a0001c0001t0003g0027 a0001c0001t0003g0186 a0001c0001t0003g0208 |
4 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1464_275+1465i others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620798 | |||||||
| chr8:65620799 | T | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0186 a0001c0001t0003g0208 |
4 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1464A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(3): Show |
4 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0150 others(1): Show |
4 | HG01975.hp1 HG04115.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(4): Show |
73 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(5): Show |
10 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0120 others(7): Show |
10 | HG01516.hp1 HG01517.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(14): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(6): Show |
32 | a0001c0001t0001g0121 a0001c0001t0003g0003 a0001c0001t0003g0010 others(29): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(7): Show |
38 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0024 others(35): Show |
45 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620799 | T | TAAAAAAA others(8): Show |
5 | a0001c0001t0003g0184 a0001c0001t0003g0197 a0001c0001t0003g0199 others(2): Show |
5 | HG01255.hp1 HG01433.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+1463_275+1464i others(17): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620799 | |||||||
| chr8:65620949 | T | G | 2 | a0001c0002t0002g0074 a0001c0002t0002g0106 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.275+1314A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65620949 | |||||||
| chr8:65621071 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+1192G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621071 | |||||||
| chr8:65621084 | C | T | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.275+1179G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621084 | |||||||
| chr8:65621391 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.275+872T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621391 | |||||||
| chr8:65621425 | C | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.275+838G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621425 | |||||||
| chr8:65621561 | T | G | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.275+702A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621561 | |||||||
| chr8:65621562 | G | A | 48 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0024 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.275+701C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621562 | |||||||
| chr8:65621670 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.275+593C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621670 | |||||||
| chr8:65621680 | T | C | 29 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(26): Show |
30 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.275+583A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621680 | |||||||
| chr8:65621683 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.275+580T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621683 | |||||||
| chr8:65621711 | G | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+552C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621711 | |||||||
| chr8:65621719 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.275+544G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621719 | |||||||
| chr8:65621820 | T | C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.275+443A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621820 | |||||||
| chr8:65621977 | G | A | 2 | a0001c0001t0001g0022 a0001c0002t0002g0043 |
3 | HG00673.hp2 HG02257.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.275+286C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65621977 | |||||||
| chr8:65622006 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.275+257G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 3/6 | chr8 | 65622006 | |||||||
| chr8:65622407 | G | T | 3 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0231 |
3 | HG02257.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.184-53C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622407 | |||||||
| chr8:65622454 | G | A | 2 | a0001c0001t0006g0037 a0001c0001t0012g0036 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-100C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622454 | |||||||
| chr8:65622552 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0137 |
3 | HG03491.hp1 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.184-198G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622552 | |||||||
| chr8:65622566 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.184-212G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622566 | |||||||
| chr8:65622712 | A | G | 1 | a0001c0001t0015g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184-358T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622712 | |||||||
| chr8:65622715 | G | GAA | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
200 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.184-363_184-362dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622715 | |||||||
| chr8:65622725 | A | C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-371T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622725 | |||||||
| chr8:65622740 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-386G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622740 | |||||||
| chr8:65622787 | G | A | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-433C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622787 | |||||||
| chr8:65622841 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.184-487T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622841 | |||||||
| chr8:65622897 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.184-543A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65622897 | |||||||
| chr8:65623012 | T | TA | 6 | a0001c0001t0001g0127 a0001c0001t0001g0177 a0001c0001t0005g0300 others(3): Show |
6 | HG02055.hp2 HG02523.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-659dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623012 | |||||||
| chr8:65623081 | G | A | 48 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0024 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.184-727C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623081 | |||||||
| chr8:65623165 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-811C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623165 | |||||||
| chr8:65623231 | C | T | 3 | a0001c0001t0006g0035 a0001c0001t0006g0037 a0001c0001t0012g0036 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-877G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623231 | |||||||
| chr8:65623271 | G | A | 1 | a0001c0002t0004g0270 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.184-917C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623271 | |||||||
| chr8:65623307 | C | CA | 11 | a0001c0002t0002g0053 a0001c0002t0002g0054 a0001c0002t0002g0061 others(8): Show |
11 | HG01928.hp1 HG02602.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-954dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(2): Show |
91 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(88): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.184-962_184-954dup others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(3): Show |
68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(65): Show |
77 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.184-963_184-954dup others(10): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0148 others(1): Show |
4 | HG02074.hp2 HG04204.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-964_184-954dup others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0159 a0001c0001t0006g0034 a0001c0001t0006g0039 others(2): Show |
5 | HG02965.hp1 HG03540.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-965_184-954dup others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0006g0035 a0001c0001t0006g0037 a0001c0001t0006g0038 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-966_184-954dup others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(7): Show |
23 | a0001c0001t0005g0033 a0001c0001t0005g0301 a0001c0001t0005g0304 others(20): Show |
25 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.184-967_184-954dup others(14): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(8): Show |
24 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0005g0302 others(21): Show |
25 | HG00323.hp2 HG00735.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.184-968_184-954dup others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623307 | C | CAAAAAAA others(9): Show |
5 | a0001c0001t0005g0307 a0001c0001t0005g0308 a0001c0001t0014g0316 others(2): Show |
5 | HG03834.hp2 NA18522.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-969_184-954dup others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623307 | |||||||
| chr8:65623324 | A | AAAAAAAA others(6): Show |
7 | a0001c0003t0004g0287 a0001c0003t0004g0288 a0001c0003t0004g0289 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-971_184-970ins others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623324 | |||||||
| chr8:65623324 | A | AAAAAAAA others(5): Show |
10 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0290 others(7): Show |
13 | HG01168.hp2 HG01346.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.184-971_184-970ins others(12): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623324 | |||||||
| chr8:65623499 | C | T | 3 | a0001c0001t0005g0302 a0001c0001t0005g0304 a0001c0001t0005g0312 |
3 | HG02486.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.184-1145G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623499 | |||||||
| chr8:65623504 | G | A | 3 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0244 |
3 | HG02145.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.184-1150C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623504 | |||||||
| chr8:65623721 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.184-1367T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623721 | |||||||
| chr8:65623732 | T | TA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1379dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623732 | |||||||
| chr8:65623755 | C | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0182 others(15): Show |
21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-1401G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623755 | |||||||
| chr8:65623786 | C | CT | 72 | a0001c0001t0005g0033 a0001c0001t0005g0304 a0001c0001t0005g0306 others(69): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-1433dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTT | 23 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0005g0301 others(20): Show |
23 | HG01175.hp1 HG01192.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.184-1434_184-1433d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTTTT | 34 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0025 others(31): Show |
44 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.184-1436_184-1433d others(6): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTTTTT | 40 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(37): Show |
45 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.184-1437_184-1433d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTTTTTT | 56 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.184-1438_184-1433d others(8): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTTTTTTT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
34 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.184-1439_184-1433d others(9): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0163 others(3): Show |
6 | HG00621.hp2 HG02027.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1440_184-1433d others(10): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623786 | CTTTTTTT others(10): Show |
C | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-1449_184-1433d others(19): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623786 | |||||||
| chr8:65623892 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1538T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623892 | |||||||
| chr8:65623900 | C | T | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.184-1546G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623900 | |||||||
| chr8:65623938 | T | C | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.184-1584A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623938 | |||||||
| chr8:65623956 | C | T | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.184-1602G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65623956 | |||||||
| chr8:65624049 | C | T | 9 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0037 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-1695G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624049 | |||||||
| chr8:65624090 | G | A | 1 | a0001c0002t0002g0096 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.184-1736C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624090 | |||||||
| chr8:65624175 | C | A | 1 | a0001c0002t0002g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.184-1821G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624175 | |||||||
| chr8:65624327 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.184-1973A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624327 | |||||||
| chr8:65624423 | C | T | 1 | a0001c0002t0004g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.184-2069G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624423 | |||||||
| chr8:65624434 | G | C | 1 | a0001c0002t0004g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184-2080C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624434 | |||||||
| chr8:65624456 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0137 a0001c0001t0001g0161 others(1): Show |
5 | HG03017.hp1 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2102C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624456 | |||||||
| chr8:65624466 | T | G | 3 | a0001c0003t0004g0289 a0001c0003t0004g0294 a0001c0003t0004g0295 |
3 | NA18951.hp2 NA18965.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.184-2112A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624466 | |||||||
| chr8:65624498 | C | CA | 28 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(25): Show |
31 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2145dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624498 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0228 |
3 | HG01070.hp2 HG02818.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.184-2157_184-2145d others(15): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624498 | C | CAAAAAAA others(7): Show |
23 | a0001c0001t0001g0119 a0001c0001t0001g0140 a0001c0001t0001g0177 others(20): Show |
31 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(16): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624498 | C | CAAAAAAA others(8): Show |
91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
112 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(17): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624498 | C | CAAAAAAA others(9): Show |
27 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0124 others(24): Show |
32 | HG00597.hp1 HG01106.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(18): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624498 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0003g0241 a0001c0001t0003g0243 a0001c0001t0003g0244 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-2145_184-2144i others(19): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624498 | |||||||
| chr8:65624757 | ATAAAT | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.184-2408_184-2404d others(7): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624757 | |||||||
| chr8:65624780 | TG | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-2427delC | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624780 | |||||||
| chr8:65624783 | A | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-2429T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624783 | |||||||
| chr8:65624848 | T | A | 1 | a0001c0003t0004g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+2368A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624848 | |||||||
| chr8:65624885 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+2331G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65624885 | |||||||
| chr8:65625027 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.183+2189T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625027 | |||||||
| chr8:65625291 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.183+1925G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625291 | |||||||
| chr8:65625298 | T | C | 1 | a0001c0002t0002g0072 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.183+1918A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625298 | |||||||
| chr8:65625321 | G | T | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1895C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625321 | |||||||
| chr8:65625358 | G | T | 17 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(14): Show |
20 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.183+1858C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625358 | |||||||
| chr8:65625385 | G | T | 2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.183+1831C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625385 | |||||||
| chr8:65625440 | C | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0182 others(15): Show |
21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.183+1776G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625440 | |||||||
| chr8:65625606 | C | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.183+1610G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625606 | |||||||
| chr8:65625664 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+1552T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625664 | |||||||
| chr8:65625739 | T | C | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183+1477A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625739 | |||||||
| chr8:65625798 | T | C | 16 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(13): Show |
18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+1418A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625798 | |||||||
| chr8:65625826 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.183+1390A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625826 | |||||||
| chr8:65625829 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183+1387G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625829 | |||||||
| chr8:65625887 | C | CT | 7 | a0001c0001t0001g0108 a0001c0001t0005g0299 a0001c0002t0002g0055 others(4): Show |
7 | HG02135.hp1 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+1328dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625887 | |||||||
| chr8:65625887 | CT | C | 8 | a0001c0001t0001g0114 a0001c0001t0003g0187 a0001c0001t0003g0215 others(5): Show |
8 | HG02486.hp1 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+1328delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625887 | |||||||
| chr8:65625910 | C | T | 1 | a0001c0001t0005g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.183+1306G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625910 | |||||||
| chr8:65625918 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.183+1298G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625918 | |||||||
| chr8:65625919 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.183+1297T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625919 | |||||||
| chr8:65625988 | A | C | 13 | a0001c0002t0002g0004 a0001c0002t0002g0013 a0001c0002t0002g0050 others(10): Show |
17 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+1228T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65625988 | |||||||
| chr8:65626009 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.183+1207G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626009 | |||||||
| chr8:65626357 | A | C | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+859T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626357 | |||||||
| chr8:65626417 | A | C | 1 | a0001c0002t0002g0064 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.183+799T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626417 | |||||||
| chr8:65626433 | A | G | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+783T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626433 | |||||||
| chr8:65626441 | T | TA | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.183+774dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626441 | |||||||
| chr8:65626441 | T | TAA | 32 | a0001c0001t0001g0108 a0001c0001t0003g0009 a0001c0001t0003g0023 others(29): Show |
37 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+773_183+774dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626441 | |||||||
| chr8:65626479 | A | G | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+737T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626479 | |||||||
| chr8:65626740 | G | A | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+476C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626740 | |||||||
| chr8:65626921 | C | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
186 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.183+295G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626921 | |||||||
| chr8:65626921 | C | T | 16 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(13): Show |
18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+295G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626921 | |||||||
| chr8:65626977 | C | T | 16 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0181 others(13): Show |
18 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+239G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65626977 | |||||||
| chr8:65627002 | CA | C | 74 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(71): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.183+213delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65627002 | |||||||
| chr8:65627023 | TA | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.183+192delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 2/6 | chr8 | 65627023 | |||||||
| chr8:65627435 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00621.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-35-2A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627435 | |||||||
| chr8:65627444 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0221 a0001c0001t0003g0222 others(5): Show |
10 | HG01070.hp1 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-11C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627444 | |||||||
| chr8:65627449 | G | T | 1 | a0001c0001t0018g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-35-16C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627449 | |||||||
| chr8:65627556 | C | T | 1 | a0001c0003t0004g0289 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-35-123G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627556 | |||||||
| chr8:65627563 | AT | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-35-131delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627563 | |||||||
| chr8:65627576 | CAGTTTGA others(4): Show |
C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-35-154_-35-144del others(11): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627576 | |||||||
| chr8:65627660 | T | G | 1 | a0001c0001t0005g0315 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-35-227A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627660 | |||||||
| chr8:65627670 | TTA | T | 3 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0003g0196 |
3 | HG01175.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-35-239_-35-238del others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627670 | |||||||
| chr8:65627672 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-35-239T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627672 | |||||||
| chr8:65627683 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-250G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627683 | |||||||
| chr8:65627818 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-35-385C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627818 | |||||||
| chr8:65627821 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-35-388C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65627821 | |||||||
| chr8:65628071 | G | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0237 a0001c0001t0003g0240 others(1): Show |
5 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-638C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628071 | |||||||
| chr8:65628204 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-35-771T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628204 | |||||||
| chr8:65628238 | T | C | 1 | a0001c0002t0004g0280 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-35-805A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628238 | |||||||
| chr8:65628247 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-814A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628247 | |||||||
| chr8:65628386 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-35-953C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628386 | |||||||
| chr8:65628391 | A | AT | 40 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0003g0186 others(37): Show |
44 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35-959dupA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | |||||||
| chr8:65628391 | A | ATT | 35 | a0001c0001t0007g0281 a0001c0001t0015g0282 a0001c0002t0002g0050 others(32): Show |
37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-35-960_-35-959dup others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | |||||||
| chr8:65628391 | A | ATTT | 8 | a0001c0002t0004g0250 a0001c0002t0004g0253 a0001c0002t0004g0254 others(5): Show |
8 | HG00733.hp1 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35-961_-35-959dup others(3): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | |||||||
| chr8:65628391 | AT | A | 65 | a0001c0001t0001g0017 a0001c0001t0001g0108 a0001c0001t0001g0110 others(62): Show |
75 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-35-959delA | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | |||||||
| chr8:65628391 | ATT | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
119 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-35-960_-35-959del others(2): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628391 | |||||||
| chr8:65628656 | G | A | 18 | a0001c0001t0003g0009 a0001c0001t0003g0023 a0001c0001t0003g0182 others(15): Show |
21 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35-1223C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628656 | |||||||
| chr8:65628801 | G | A | 1 | a0001c0002t0002g0014 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35-1368C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628801 | |||||||
| chr8:65628843 | A | C | 1 | a0001c0001t0003g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-35-1410T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628843 | |||||||
| chr8:65628853 | C | CA | 163 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
199 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.-35-1421dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628853 | |||||||
| chr8:65628865 | G | A | 1 | a0001c0001t0014g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-35-1432C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628865 | |||||||
| chr8:65628949 | T | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1516A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628949 | |||||||
| chr8:65628953 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1520T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628953 | |||||||
| chr8:65628956 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35-1523G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628956 | |||||||
| chr8:65628963 | G | C | 1 | a0001c0003t0004g0297 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35-1530C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65628963 | |||||||
| chr8:65629146 | C | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35-1713G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629146 | |||||||
| chr8:65629154 | C | CA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
7 | HG00140.hp1 HG02257.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35-1722dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629154 | |||||||
| chr8:65629328 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-1895T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629328 | |||||||
| chr8:65629401 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-35-1968T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629401 | |||||||
| chr8:65629555 | C | G | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2122G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629555 | |||||||
| chr8:65629556 | T | G | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2123A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629556 | |||||||
| chr8:65629557 | T | C | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2124A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629557 | |||||||
| chr8:65629558 | T | A | 1 | a0001c0002t0002g0015 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35-2125A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629558 | |||||||
| chr8:65629577 | G | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2144C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629577 | |||||||
| chr8:65629782 | G | C | 1 | a0001c0001t0003g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-35-2349C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629782 | |||||||
| chr8:65629798 | C | CA | 16 | a0001c0001t0005g0310 a0001c0001t0005g0311 a0001c0001t0005g0312 others(13): Show |
17 | HG00738.hp1 HG01069.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35-2366dupT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | |||||||
| chr8:65629798 | CA | C | 14 | a0001c0001t0001g0118 a0001c0001t0006g0034 a0001c0001t0006g0035 others(11): Show |
14 | HG00642.hp2 HG02027.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-35-2366delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | |||||||
| chr8:65629798 | CAA | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
197 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.-35-2367_-35-2366d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629798 | |||||||
| chr8:65629816 | A | C | 16 | a0001c0003t0004g0011 a0001c0003t0004g0285 a0001c0003t0004g0287 others(13): Show |
19 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-35-2383T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629816 | |||||||
| chr8:65629819 | T | A | 1 | a0001c0002t0002g0105 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-35-2386A>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629819 | |||||||
| chr8:65629842 | G | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-35-2409C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629842 | |||||||
| chr8:65629916 | G | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2483C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629916 | |||||||
| chr8:65629999 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-35-2566C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65629999 | |||||||
| chr8:65630042 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-2609C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630042 | |||||||
| chr8:65630202 | T | C | 9 | a0001c0002t0004g0272 a0001c0002t0004g0273 a0001c0002t0004g0274 others(6): Show |
9 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35-2769A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630202 | |||||||
| chr8:65630218 | GAT | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-35-2787_-35-2786d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630218 | |||||||
| chr8:65630504 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-35-3071A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630504 | |||||||
| chr8:65630509 | A | C | 3 | a0001c0001t0006g0035 a0001c0001t0006g0037 a0001c0001t0012g0036 |
3 | HG02486.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-35-3076T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630509 | |||||||
| chr8:65630536 | C | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
99 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-35-3103G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630536 | |||||||
| chr8:65630817 | T | TAA | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
196 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.-36+3179_-36+3180d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630817 | |||||||
| chr8:65630829 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+3169A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630829 | |||||||
| chr8:65630940 | T | TCCACAGG others(4): Show |
1 | a0001c0002t0002g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36+3047_-36+3057d others(13): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630940 | |||||||
| chr8:65630941 | C | A | 9 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0037 others(6): Show |
9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+3057G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65630941 | |||||||
| chr8:65631051 | G | A | 1 | a0001c0001t0007g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-36+2947C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631051 | |||||||
| chr8:65631099 | G | A | 1 | a0001c0001t0005g0315 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-36+2899C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631099 | |||||||
| chr8:65631246 | T | C | 20 | a0001c0001t0005g0033 a0001c0001t0005g0299 a0001c0001t0005g0300 others(17): Show |
21 | HG01069.hp1 HG01167.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36+2752A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631246 | |||||||
| chr8:65631290 | C | T | 2 | a0001c0001t0003g0248 a0001c0001t0003g0249 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+2708G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631290 | |||||||
| chr8:65631303 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2695G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631303 | |||||||
| chr8:65631334 | A | G | 1 | a0001c0001t0003g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-36+2664T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631334 | |||||||
| chr8:65631381 | C | T | 1 | a0003c0005t0002g0047 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-36+2617G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631381 | |||||||
| chr8:65631423 | G | A | 6 | a0001c0001t0003g0010 a0001c0001t0003g0232 a0001c0001t0003g0233 others(3): Show |
8 | HG00639.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-36+2575C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631423 | |||||||
| chr8:65631434 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2564C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631434 | |||||||
| chr8:65631525 | C | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
105 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-36+2473G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631525 | |||||||
| chr8:65631541 | G | T | 1 | a0001c0002t0002g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-36+2457C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631541 | |||||||
| chr8:65631742 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2256G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631742 | |||||||
| chr8:65631743 | G | A | 9 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0238 others(6): Show |
11 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36+2255C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631743 | |||||||
| chr8:65631883 | TA | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
213 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.-36+2114delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631883 | |||||||
| chr8:65631883 | TAA | T | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG02965.hp1 NA18939.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36+2113_-36+2114d others(4): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631883 | |||||||
| chr8:65631908 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-36+2090A>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631908 | |||||||
| chr8:65631915 | G | A | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-36+2083C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631915 | |||||||
| chr8:65631939 | ATAT | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+2056_-36+2058d others(5): Show |
ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65631939 | |||||||
| chr8:65632122 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36+1876A>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632122 | |||||||
| chr8:65632167 | C | T | 1 | a0001c0002t0002g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-36+1831G>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632167 | |||||||
| chr8:65632208 | G | C | 1 | a0001c0001t0003g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-36+1790C>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632208 | |||||||
| chr8:65632270 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-36+1728G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632270 | |||||||
| chr8:65632507 | G | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0283 a0001c0001t0015g0282 |
3 | HG00733.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-36+1491C>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632507 | |||||||
| chr8:65632554 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-36+1444T>G | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632554 | |||||||
| chr8:65632570 | G | A | 1 | a0001c0001t0014g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-36+1428C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632570 | |||||||
| chr8:65632825 | CA | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-36+1172delT | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65632825 | |||||||
| chr8:65633319 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-36+679T>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633319 | |||||||
| chr8:65633462 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-36+536T>A | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633462 | |||||||
| chr8:65633484 | G | A | 1 | a0001c0002t0002g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-36+514C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633484 | |||||||
| chr8:65633546 | C | G | 34 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0250 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.-36+452G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633546 | |||||||
| chr8:65633554 | G | A | 1 | a0001c0001t0005g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-36+444C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633554 | |||||||
| chr8:65633834 | G | A | 2 | a0001c0001t0003g0248 a0001c0001t0003g0249 |
2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+164C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633834 | |||||||
| chr8:65633891 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.-36+107G>C | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633891 | |||||||
| chr8:65633895 | C | A | 1 | a0001c0002t0004g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-36+103G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633895 | |||||||
| chr8:65633913 | C | A | 1 | a0001c0001t0001g0319 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-36+85G>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633913 | |||||||
| chr8:65633937 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-36+61C>T | ARMC1 | ENSG00000104442.10 | transcript | ENST00000276569.8 | protein_coding | 1/6 | chr8 | 65633937 |