Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54891 |
| ensemblid | ENSG00000114933.16 |
| hgncid | 25997 |
| symbol | INO80D |
| name | INO80 complex subunit D |
| refseq_nuc | NM_017759.5 |
| refseq_prot | NP_060229.3 |
| ensembl_nuc | ENST00000403263.6 |
| ensembl_prot | ENSP00000384198.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 205993721 |
| end | 206086174 |
| strand | - |
| ver | v1.2 |
| region | chr2:205993721-206086174 |
| region5000 | chr2:205988721-206091174 |
| regionname0 | INO80D_chr2_205993721_206086174 |
| regionname5000 | INO80D_chr2_205988721_206091174 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1027 | 221 | 58 | 50 | 80 | 11 | 20 | 63 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0002 | 0/0 | 1027 | 105 | 20 | 19 | 42 | 5 | 19 | 35 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0003 | 0/0 | 1027 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0004 | 0/0 | 1027 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0005 | 0/0 | 1027 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0006 | 0/0 | 1027 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| a0007 | 0/0 | 1027 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | MYEGK others(1022): Show |
chr2 | 205988721 | 206091174 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3081 | 127 | 27 | 35 | 45 | 8 | 11 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0003 | 1/0 | 3081 | 77 | 29 | 10 | 29 | 2 | 6 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0004 | 0/0 | 3081 | 10 | 0 | 4 | 3 | 1 | 2 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0006 | 0/0 | 3081 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0008 | 0/0 | 3081 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0011 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0001c0013 | 0/0 | 3081 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0002c0002 | 0/0 | 3081 | 97 | 16 | 19 | 41 | 5 | 16 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0002c0005 | 0/0 | 3081 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0002c0010 | 0/0 | 3081 | 2 | 0 | 0 | 0 | 0 | 2 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0002c0016 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0002c0017 | 0/0 | 3081 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0003c0007 | 0/0 | 3081 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0004c0009 | 0/0 | 3081 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0005c0015 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0006c0012 | 0/0 | 3081 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 | ||
| a0007c0014 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | ATGTA others(3076): Show |
chr2 | 205988721 | 206091174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 14128 | 3 | 2 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0003 | 0/0 | 14126 | 43 | 2 | 9 | 22 | 5 | 5 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0004 | 0/0 | 14128 | 19 | 0 | 14 | 0 | 3 | 2 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0005 | 0/0 | 14126 | 13 | 0 | 0 | 13 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0008 | 0/0 | 14129 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0009 | 0/0 | 14127 | 6 | 6 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0012 | 0/0 | 14127 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0013 | 0/0 | 14128 | 4 | 4 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0015 | 0/0 | 14128 | 3 | 0 | 3 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0016 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0018 | 0/0 | 14129 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0020 | 0/0 | 14126 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0021 | 0/0 | 14126 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0022 | 0/0 | 14127 | 2 | 1 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0024 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0025 | 0/0 | 14127 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0026 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0027 | 0/0 | 14127 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0028 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0029 | 0/0 | 14127 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0030 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14107): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0031 | 0/0 | 14125 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14120): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0032 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0034 | 0/0 | 14126 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0038 | 0/0 | 14126 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0041 | 0/0 | 14127 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0042 | 0/0 | 14127 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0050 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0053 | 0/1 | 14126 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0001c0001t0064 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0002 | 1/0 | 14128 | 48 | 21 | 6 | 14 | 2 | 4 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0006 | 0/0 | 14129 | 12 | 2 | 3 | 7 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0007 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0011 | 0/0 | 14129 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0014 | 0/0 | 14128 | 4 | 0 | 0 | 4 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0017 | 0/0 | 14128 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0023 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0054 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0059 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0061 | 0/0 | 14139 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14134): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0062 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0003t0063 | 0/0 | 14129 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0004t0007 | 0/0 | 14128 | 7 | 0 | 4 | 1 | 1 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0004t0011 | 0/0 | 14129 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0001c0004t0037 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0006t0001 | 0/0 | 14128 | 3 | 0 | 0 | 3 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0008t0019 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0001c0011t0043 | 0/0 | 14127 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0001c0013t0005 | 0/0 | 14126 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0001 | 0/0 | 14128 | 79 | 12 | 18 | 32 | 4 | 13 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0010 | 0/0 | 14129 | 5 | 1 | 1 | 2 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0033 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0035 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0039 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0044 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0046 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14122): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0047 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0048 | 0/0 | 14129 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0049 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0051 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0056 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0057 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0058 | 0/0 | 14129 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0002c0002t0060 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0005t0002 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0005t0006 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0002c0005t0040 | 0/0 | 14126 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| a0002c0010t0001 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0010t0055 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0016t0036 | 0/0 | 14128 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0002c0017t0052 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0003c0007t0001 | 0/0 | 14128 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0003c0007t0045 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0004c0009t0007 | 0/0 | 14128 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0004c0009t0011 | 0/0 | 14129 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14124): Show |
chr2 | 205988721 | 206091174 |
| a0005c0015t0016 | 0/0 | 14128 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0006c0012t0002 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14123): Show |
chr2 | 205988721 | 206091174 |
| a0007c0014t0003 | 0/0 | 14126 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | GTACA others(14121): Show |
chr2 | 205988721 | 206091174 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0015g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0015g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0016g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0016g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0018g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0020g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0020g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0021g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0022g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0024g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0025g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0026g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0027g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0028g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0029g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0030g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0031g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0032g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0034g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0038g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0041g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0042g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0050g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0053g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0001t0064g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0014g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0017g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0017g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0023g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0054g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0059g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0061g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0062g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0003t0063g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0011g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0011g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0004t0037g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0008t0019g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0008t0019g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0011t0043g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0001c0013t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0010g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0010g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0010g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0033g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0035g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0039g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0044g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0046g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0047g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0048g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0049g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0051g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0056g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0057g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0058g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0002t0060g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0005t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0005t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0005t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0005t0040g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0010t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0010t0055g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0016t0036g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0002c0017t0052g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0003c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0003c0007t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0003c0007t0045g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0004c0009t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0004c0009t0011g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0005c0015t0016g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0006c0012t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| a0007c0014t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0057 | g0175 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0234 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0197 | EUR | GBR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0185 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0069 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0148 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0050 | EUR | FIN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0310 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00438 | hp1 | a0001 | c0003 | t0014 | g0275 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00621 | hp2 | a0001 | c0003 | t0006 | g0244 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00639 | hp2 | a0001 | c0004 | t0007 | g0295 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00642 | hp1 | a0001 | c0013 | t0005 | g0307 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00673 | hp1 | a0001 | c0003 | t0006 | g0252 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0011 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0216 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0007 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0006 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01106 | hp1 | a0001 | c0001 | t0030 | g0063 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0008 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01109 | hp2 | a0001 | c0001 | t0022 | g0033 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01168 | hp1 | a0001 | c0001 | t0021 | g0047 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01169 | hp1 | a0001 | c0001 | t0021 | g0054 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01175 | hp1 | a0001 | c0004 | t0007 | g0297 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0253 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01243 | hp1 | a0001 | c0004 | t0007 | g0299 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01243 | hp2 | a0001 | c0003 | t0007 | g0237 | AMR | PUR | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0249 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01255 | hp2 | a0001 | c0001 | t0025 | g0030 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01256 | hp2 | a0001 | c0001 | t0027 | g0010 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01257 | hp2 | a0004 | c0009 | t0007 | g0296 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0260 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0029 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0250 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0019 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0060 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0222 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01891 | hp1 | a0001 | c0003 | t0011 | g0220 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01891 | hp2 | a0004 | c0009 | t0011 | g0294 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01928 | hp2 | a0001 | c0003 | t0006 | g0211 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0232 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01978 | hp1 | a0001 | c0001 | t0024 | g0014 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01981 | hp1 | a0001 | c0003 | t0006 | g0257 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02055 | hp2 | a0001 | c0003 | t0011 | g0273 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0315 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0127 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02135 | hp1 | a0001 | c0004 | t0011 | g0293 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0302 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02148 | hp2 | a0002 | c0002 | t0010 | g0138 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | CDX | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | CDX | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02257 | hp1 | a0005 | c0015 | t0016 | g0283 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02257 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0226 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02258 | hp2 | a0002 | c0005 | t0002 | g0326 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0242 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02293 | hp2 | a0001 | c0003 | t0006 | g0276 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0229 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02451 | hp1 | a0001 | c0001 | t0050 | g0318 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02451 | hp2 | a0002 | c0002 | t0049 | g0147 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0215 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0320 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0217 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02683 | hp2 | a0001 | c0011 | t0043 | g0248 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02698 | hp2 | a0002 | c0002 | t0047 | g0120 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0225 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0230 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02809 | hp2 | a0002 | c0002 | t0051 | g0154 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02886 | hp1 | a0001 | c0003 | t0062 | g0210 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0301 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0282 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0274 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0319 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0281 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02970 | hp2 | a0001 | c0001 | t0041 | g0291 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03098 | hp1 | a0002 | c0005 | t0006 | g0327 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03098 | hp2 | a0001 | c0003 | t0006 | g0269 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0223 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03139 | hp1 | a0001 | c0008 | t0019 | g0285 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0286 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0317 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03209 | hp2 | a0002 | c0002 | t0056 | g0178 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0218 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0289 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03239 | hp2 | a0002 | c0010 | t0055 | g0177 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0233 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03453 | hp2 | a0001 | c0001 | t0042 | g0031 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03486 | hp1 | a0001 | c0003 | t0059 | g0231 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0224 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03492 | hp2 | a0001 | c0003 | t0054 | g0261 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03516 | hp1 | a0002 | c0002 | t0010 | g0174 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03516 | hp2 | a0001 | c0008 | t0019 | g0284 | AFR | ESN | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0219 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0037 | AFR | GWD | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03579 | hp1 | a0001 | c0001 | t0022 | g0035 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0121 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0258 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03654 | hp2 | a0002 | c0002 | t0035 | g0118 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0205 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03704 | hp1 | a0001 | c0001 | t0029 | g0064 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03704 | hp2 | a0001 | c0003 | t0063 | g0329 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03710 | hp2 | a0001 | c0004 | t0007 | g0292 | SAS | PJL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0262 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0246 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | BEB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04199 | hp1 | a0002 | c0002 | t0010 | g0110 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04199 | hp2 | a0001 | c0004 | t0037 | g0280 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04204 | hp2 | a0001 | c0001 | t0034 | g0304 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04228 | hp1 | a0001 | c0001 | t0064 | g0330 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG04228 | hp2 | a0002 | c0010 | t0001 | g0117 | SAS | STU | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0235 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0213 | EAS | CHB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0221 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0271 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18943 | hp2 | a0001 | c0004 | t0007 | g0300 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18944 | hp2 | a0001 | c0003 | t0017 | g0267 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18945 | hp2 | a0001 | c0003 | t0014 | g0204 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18947 | hp2 | a0002 | c0002 | t0033 | g0181 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18948 | hp2 | a0001 | c0003 | t0017 | g0265 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18951 | hp2 | a0001 | c0006 | t0001 | g0111 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18954 | hp2 | a0001 | c0003 | t0006 | g0254 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18957 | hp1 | a0002 | c0002 | t0060 | g0166 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18961 | hp1 | a0002 | c0002 | t0010 | g0141 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0203 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0264 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18966 | hp1 | a0002 | c0017 | t0052 | g0100 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18966 | hp2 | a0001 | c0003 | t0014 | g0207 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18967 | hp1 | a0001 | c0003 | t0006 | g0277 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18967 | hp2 | a0001 | c0001 | t0028 | g0053 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18968 | hp1 | a0002 | c0002 | t0039 | g0131 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18968 | hp2 | a0001 | c0003 | t0017 | g0263 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18970 | hp1 | a0001 | c0003 | t0006 | g0255 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18970 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18971 | hp1 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18975 | hp2 | a0001 | c0003 | t0006 | g0247 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18977 | hp1 | a0001 | c0006 | t0001 | g0123 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18979 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18980 | hp2 | a0001 | c0001 | t0012 | g0083 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0206 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18984 | hp1 | a0002 | c0002 | t0044 | g0152 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18986 | hp2 | a0003 | c0007 | t0001 | g0182 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18988 | hp1 | a0001 | c0001 | t0020 | g0039 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18988 | hp2 | a0001 | c0001 | t0038 | g0243 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18989 | hp2 | a0002 | c0002 | t0046 | g0323 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0241 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19001 | hp1 | a0001 | c0001 | t0026 | g0005 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0189 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19002 | hp1 | a0002 | c0002 | t0010 | g0322 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19004 | hp2 | a0001 | c0003 | t0014 | g0209 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19005 | hp2 | a0002 | c0002 | t0058 | g0103 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19009 | hp1 | a0001 | c0003 | t0006 | g0251 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0087 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0240 | AFR | LWK | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0239 | AFR | LWK | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19055 | hp1 | a0001 | c0001 | t0020 | g0038 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19056 | hp1 | a0001 | c0003 | t0061 | g0212 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19057 | hp2 | a0001 | c0004 | t0011 | g0298 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19058 | hp1 | a0001 | c0003 | t0002 | g0266 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19058 | hp2 | a0003 | c0007 | t0001 | g0164 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19066 | hp2 | a0001 | c0001 | t0032 | g0046 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19070 | hp2 | a0002 | c0002 | t0048 | g0119 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19074 | hp1 | a0003 | c0007 | t0045 | g0160 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19077 | hp1 | a0006 | c0012 | t0002 | g0208 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20129 | hp1 | a0001 | c0003 | t0023 | g0228 | AFR | ASW | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20129 | hp2 | a0002 | c0005 | t0002 | g0191 | AFR | ASW | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20805 | hp1 | a0001 | c0004 | t0007 | g0278 | EUR | TSI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0136 | EUR | TSI | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20905 | hp1 | a0002 | c0016 | t0036 | g0113 | SAS | GIH | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20905 | hp2 | a0007 | c0014 | t0003 | g0076 | SAS | GIH | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG01123 | hp2 | a0001 | c0004 | t0007 | g0279 | AMR | CLM | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02109 | hp1 | a0002 | c0005 | t0040 | g0325 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0236 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0328 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02486 | hp2 | a0001 | c0003 | t0006 | g0268 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0245 | AFR | ACB | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0321 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0270 | AFR | MSL | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0227 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| HG06807 | hp2 | a0001 | c0003 | t0023 | g0214 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| NA20300 | hp2 | a0001 | c0001 | t0031 | g0324 | AFR | USA | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0053 | g0305 | REF | REF | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0116 | REF | REF | INO80D_chr2_205988721_206091174 | INO80D | chr2 | 205988721 | 206091174 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206004381 | G | C | 1 | a0007 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3071C>G | p.Pro1024Arg | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3468/14128 | 3071/3084 | 1024/1027 | chr2 | 206004381 | |||
| chr2:206009583 | T | C | 1 | a0004 | 2 | HG01257.hp2 HG01891.hp2 |
missense_variant | MODERATE | c.1754A>G | p.His585Arg | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2151/14128 | 1754/3084 | 585/1027 | chr2 | 206009583 | |||
| chr2:206028250 | G | A | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1159C>T | p.Arg387Cys | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/11 | 1556/14128 | 1159/3084 | 387/1027 | chr2 | 206028250 | |||
| chr2:206028318 | G | A | 2 | a0003 a0006 |
4 | NA18986.hp2 NA19058.hp2 NA19074.hp1 others(1): Show |
missense_variant | MODERATE | c.1091C>T | p.Ala364Val | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/11 | 1488/14128 | 1091/3084 | 364/1027 | chr2 | 206028318 | |||
| chr2:206046504 | G | A | 2 | a0002 a0003 |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
missense_variant&splice_region_variant | MODERATE | c.1073C>T | p.Ala358Val | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/11 | 1470/14128 | 1073/3084 | 358/1027 | chr2 | 206046504 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206005046 | C | T | 1 | a0002c0010 | 2 | HG03239.hp2 HG04228.hp2 |
synonymous_variant | LOW | c.2406G>A | p.Leu802Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2803/14128 | 2406/3084 | 802/1027 | chr2 | 206005046 | |||
| chr2:206005085 | G | A | 1 | a0001c0008 | 2 | HG03139.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.2367C>T | p.Asp789Asp | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2764/14128 | 2367/3084 | 789/1027 | chr2 | 206005085 | |||
| chr2:206005229 | C | T | 1 | a0002c0016 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.2223G>A | p.Leu741Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2620/14128 | 2223/3084 | 741/1027 | chr2 | 206005229 | |||
| chr2:206009615 | G | A | 7 | a0001c0006 a0001c0011 a0002c0002 others(4): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
synonymous_variant | LOW | c.1722C>T | p.Pro574Pro | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2119/14128 | 1722/3084 | 574/1027 | chr2 | 206009615 | |||
| chr2:206009642 | T | A | 1 | a0002c0017 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1695A>T | p.Ala565Ala | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/11 | 2092/14128 | 1695/3084 | 565/1027 | chr2 | 206009642 | |||
| chr2:206017716 | A | G | 1 | a0001c0013 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1506T>C | p.His502His | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/11 | 1903/14128 | 1506/3084 | 502/1027 | chr2 | 206017716 | |||
| chr2:206017806 | G | C | 2 | a0001c0004 a0004c0009 |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
synonymous_variant | LOW | c.1416C>G | p.Leu472Leu | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/11 | 1813/14128 | 1416/3084 | 472/1027 | chr2 | 206017806 | |||
| chr2:206056727 | G | A | 14 | a0001c0001 a0001c0004 a0001c0006 others(11): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
synonymous_variant | LOW | c.435C>T | p.Thr145Thr | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/11 | 832/14128 | 435/3084 | 145/1027 | chr2 | 206056727 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:205994481 | T | A | 1 | a0001c0008t0019 | 2 | HG03139.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9887A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9887 | chr2 | 205994481 | ||||||
| chr2:205994594 | T | A | 1 | a0002c0002t0047 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9774A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9774 | chr2 | 205994594 | ||||||
| chr2:205994609 | C | A | 1 | a0001c0001t0042 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9759G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9759 | chr2 | 205994609 | ||||||
| chr2:205994795 | T | C | 1 | a0001c0003t0017 | 3 | NA18944.hp2 NA18948.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9573A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9573 | chr2 | 205994795 | ||||||
| chr2:205994859 | G | A | 3 | a0001c0001t0016 a0001c0008t0019 a0005c0015t0016 |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9509C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9509 | chr2 | 205994859 | ||||||
| chr2:205994874 | C | CA | 9 | a0001c0001t0041 a0001c0001t0042 a0001c0003t0006 others(6): Show |
20 | HG00621.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*9493dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9493 | chr2 | 205994874 | ||||||
| chr2:205994874 | CA | C | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(20): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*9493delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9493 | chr2 | 205994874 | ||||||
| chr2:205994967 | C | G | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9401G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9401 | chr2 | 205994967 | ||||||
| chr2:205994999 | G | T | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9369C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9369 | chr2 | 205994999 | ||||||
| chr2:205995126 | C | G | 1 | a0001c0001t0020 | 2 | NA18988.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9242G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 9242 | chr2 | 205995126 | ||||||
| chr2:205995942 | G | A | 1 | a0001c0003t0054 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8426C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8426 | chr2 | 205995942 | ||||||
| chr2:205996326 | A | AT | 26 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(23): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*8041dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8041 | chr2 | 205996326 | ||||||
| chr2:205996346 | T | C | 1 | a0002c0002t0049 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8022A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 8022 | chr2 | 205996346 | ||||||
| chr2:205996512 | C | T | 1 | a0003c0007t0045 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7856G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7856 | chr2 | 205996512 | ||||||
| chr2:205996915 | T | TA | 16 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(13): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*7452dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7452 | chr2 | 205996915 | ||||||
| chr2:205996920 | A | AC | 7 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 others(4): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*7447_*7448insG | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7447 | chr2 | 205996920 | ||||||
| chr2:205996974 | G | A | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7394C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7394 | chr2 | 205996974 | ||||||
| chr2:205997280 | T | C | 1 | a0001c0003t0014 | 4 | HG00438.hp1 NA18945.hp2 NA18966.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7088A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7088 | chr2 | 205997280 | ||||||
| chr2:205997291 | G | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(20): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*7077C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 7077 | chr2 | 205997291 | ||||||
| chr2:205997458 | A | T | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6910T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 6910 | chr2 | 205997458 | ||||||
| chr2:205998166 | T | C | 1 | a0002c0002t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6202A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 6202 | chr2 | 205998166 | ||||||
| chr2:205998450 | C | CA | 2 | a0002c0002t0010 a0002c0002t0058 |
6 | HG02148.hp2 HG03516.hp1 HG04199.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5917dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5917 | chr2 | 205998450 | ||||||
| chr2:205998450 | CA | C | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(19): Show |
75 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*5917delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5917 | chr2 | 205998450 | ||||||
| chr2:205998450 | CAA | C | 12 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0021 others(9): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5916_*5917delTT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5916 | chr2 | 205998450 | ||||||
| chr2:205999150 | C | T | 51 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(48): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5218G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5218 | chr2 | 205999150 | ||||||
| chr2:205999178 | AAAAAACA others(7): Show |
A | 1 | a0001c0001t0030 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5176_*5189delGTTT others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5176 | chr2 | 205999178 | ||||||
| chr2:205999254 | G | C | 1 | a0002c0017t0052 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5114C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5114 | chr2 | 205999254 | ||||||
| chr2:205999262 | G | A | 2 | a0001c0001t0013 a0001c0001t0022 |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5106C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 5106 | chr2 | 205999262 | ||||||
| chr2:205999557 | CA | C | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(18): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*4810delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4810 | chr2 | 205999557 | ||||||
| chr2:205999595 | G | C | 2 | a0001c0001t0016 a0005c0015t0016 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4773C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4773 | chr2 | 205999595 | ||||||
| chr2:206000040 | C | T | 51 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(48): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*4328G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4328 | chr2 | 206000040 | ||||||
| chr2:206000140 | G | A | 10 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0020 others(7): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4228C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4228 | chr2 | 206000140 | ||||||
| chr2:206000305 | C | T | 1 | a0002c0002t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4063G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 4063 | chr2 | 206000305 | ||||||
| chr2:206000522 | A | G | 7 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 others(4): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3846T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3846 | chr2 | 206000522 | ||||||
| chr2:206000573 | C | G | 1 | a0001c0001t0038 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3795G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3795 | chr2 | 206000573 | ||||||
| chr2:206000638 | G | T | 1 | a0001c0004t0037 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3730C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3730 | chr2 | 206000638 | ||||||
| chr2:206000739 | A | G | 1 | a0002c0016t0036 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3629T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3629 | chr2 | 206000739 | ||||||
| chr2:206000886 | T | A | 1 | a0002c0010t0055 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3482A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3482 | chr2 | 206000886 | ||||||
| chr2:206001023 | T | C | 1 | a0002c0002t0056 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3345A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3345 | chr2 | 206001023 | ||||||
| chr2:206001234 | T | C | 1 | a0002c0002t0057 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3134A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 3134 | chr2 | 206001234 | ||||||
| chr2:206001378 | G | A | 1 | a0002c0002t0058 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2990 | chr2 | 206001378 | ||||||
| chr2:206001476 | T | C | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2892A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2892 | chr2 | 206001476 | ||||||
| chr2:206002056 | C | T | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(15): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2312G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2312 | chr2 | 206002056 | ||||||
| chr2:206002109 | T | C | 1 | a0001c0003t0059 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2259A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2259 | chr2 | 206002109 | ||||||
| chr2:206002362 | T | C | 1 | a0002c0002t0060 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 2006 | chr2 | 206002362 | ||||||
| chr2:206002731 | A | T | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1637 | chr2 | 206002731 | ||||||
| chr2:206002734 | C | CTATTTAT others(3): Show |
1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633_*1634insCTTA others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1633 | chr2 | 206002734 | ||||||
| chr2:206002735 | A | G | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1633 | chr2 | 206002735 | ||||||
| chr2:206002736 | C | A | 1 | a0001c0003t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1632 | chr2 | 206002736 | ||||||
| chr2:206002997 | C | T | 1 | a0002c0002t0035 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1371 | chr2 | 206002997 | ||||||
| chr2:206003038 | A | G | 4 | a0001c0001t0004 a0001c0001t0024 a0001c0001t0025 others(1): Show |
22 | HG00738.hp1 HG01123.hp1 HG01255.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1330T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1330 | chr2 | 206003038 | ||||||
| chr2:206003126 | G | C | 1 | a0001c0003t0023 | 2 | HG06807.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1242C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1242 | chr2 | 206003126 | ||||||
| chr2:206003603 | G | A | 1 | a0001c0001t0021 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*765C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 765 | chr2 | 206003603 | ||||||
| chr2:206003616 | C | T | 1 | a0001c0001t0034 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 752 | chr2 | 206003616 | ||||||
| chr2:206003649 | G | A | 1 | a0001c0001t0032 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 719 | chr2 | 206003649 | ||||||
| chr2:206003652 | C | G | 1 | a0002c0002t0033 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 716 | chr2 | 206003652 | ||||||
| chr2:206003714 | T | C | 1 | a0001c0003t0062 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 654 | chr2 | 206003714 | ||||||
| chr2:206003998 | C | T | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0012 others(18): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*370G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 370 | chr2 | 206003998 | ||||||
| chr2:206004367 | C | T | 1 | a0001c0001t0024 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 11/11 | 1 | chr2 | 206004367 | ||||||
| chr2:206085904 | T | A | 1 | a0001c0003t0063 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22888 | chr2 | 206085904 | ||||||
| chr2:206085911 | C | CT | 8 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0018 others(5): Show |
29 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-135dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22896 | chr2 | 206085911 | ||||||
| chr2:206085980 | T | G | 1 | a0001c0001t0064 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/11 | 22964 | chr2 | 206085980 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206005554 | G | A | 1 | a0001c0003t0002g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1919-21C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005554 | |||||||
| chr2:206005584 | A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1919-51T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005584 | |||||||
| chr2:206005765 | T | A | 95 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1919-232A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005765 | |||||||
| chr2:206005810 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1919-277A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005810 | |||||||
| chr2:206005857 | G | A | 2 | a0001c0003t0002g0240 a0002c0002t0001g0003 |
3 | HG02630.hp1 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1919-324C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005857 | |||||||
| chr2:206005883 | C | G | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1919-350G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005883 | |||||||
| chr2:206005887 | A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1919-354T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005887 | |||||||
| chr2:206005895 | A | T | 1 | a0001c0003t0002g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1919-362T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206005895 | |||||||
| chr2:206006039 | C | G | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1919-506G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006039 | |||||||
| chr2:206006060 | C | T | 265 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(262): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1919-527G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006060 | |||||||
| chr2:206006277 | C | CCTGAAAT others(3): Show |
1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1919-745_1919-744i others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006277 | |||||||
| chr2:206006291 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1919-758C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006291 | |||||||
| chr2:206006316 | C | T | 3 | a0001c0001t0002g0309 a0001c0001t0005g0311 a0001c0001t0005g0312 |
3 | HG04115.hp2 NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1919-783G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006316 | |||||||
| chr2:206006343 | A | C | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1919-810T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006343 | |||||||
| chr2:206006437 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1918+847G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006437 | |||||||
| chr2:206006477 | G | A | 107 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1918+807C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006477 | |||||||
| chr2:206006575 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0029g0064 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1918+709G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006575 | |||||||
| chr2:206006576 | G | A | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1918+708C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006576 | |||||||
| chr2:206006640 | G | A | 1 | a0001c0001t0009g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1918+644C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006640 | |||||||
| chr2:206006661 | C | T | 1 | a0001c0003t0002g0203 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1918+623G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006661 | |||||||
| chr2:206006678 | A | T | 1 | a0003c0007t0001g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1918+606T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006678 | |||||||
| chr2:206006682 | C | CA | 30 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(27): Show |
30 | HG00423.hp2 HG00558.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1918+601dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006682 | |||||||
| chr2:206006682 | CA | C | 29 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(26): Show |
30 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1918+601delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006682 | |||||||
| chr2:206006734 | C | T | 236 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(233): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1918+550G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006734 | |||||||
| chr2:206006746 | C | T | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1918+538G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006746 | |||||||
| chr2:206006791 | A | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1918+493T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006791 | |||||||
| chr2:206006818 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1918+466C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006818 | |||||||
| chr2:206006867 | C | T | 20 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1918+417G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006867 | |||||||
| chr2:206006939 | C | T | 1 | a0002c0010t0055g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1918+345G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206006939 | |||||||
| chr2:206007093 | T | C | 9 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(6): Show |
9 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.1918+191A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 10/10 | chr2 | 206007093 | |||||||
| chr2:206007754 | G | A | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1761-313C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007754 | |||||||
| chr2:206007765 | T | C | 107 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1761-324A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007765 | |||||||
| chr2:206007832 | AC | A | 211 | a0001c0001t0002g0034 a0001c0001t0002g0309 a0001c0001t0003g0002 others(208): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1761-392delG | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007832 | |||||||
| chr2:206007833 | C | A | 105 | a0001c0001t0002g0287 a0001c0001t0003g0070 a0001c0001t0003g0091 others(102): Show |
106 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1761-392G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007833 | |||||||
| chr2:206007835 | A | C | 3 | a0002c0005t0002g0191 a0002c0005t0002g0326 a0002c0005t0006g0327 |
3 | HG02258.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1761-394T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007835 | |||||||
| chr2:206007877 | T | A | 108 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1761-436A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007877 | |||||||
| chr2:206007893 | A | G | 1 | a0001c0004t0007g0300 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1761-452T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007893 | |||||||
| chr2:206007899 | G | A | 1 | a0001c0003t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1761-458C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007899 | |||||||
| chr2:206007938 | A | T | 1 | a0001c0003t0006g0247 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1761-497T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206007938 | |||||||
| chr2:206008003 | CAG | C | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1761-564_1761-563d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008003 | |||||||
| chr2:206008045 | A | G | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1761-604T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008045 | |||||||
| chr2:206008203 | C | T | 1 | a0001c0003t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1761-762G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008203 | |||||||
| chr2:206008282 | C | CT | 113 | a0001c0001t0003g0058 a0001c0001t0003g0068 a0001c0001t0003g0091 others(110): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1761-842dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008282 | |||||||
| chr2:206008282 | C | CTT | 6 | a0002c0002t0001g0142 a0002c0002t0001g0151 a0002c0002t0001g0171 others(3): Show |
6 | HG02145.hp2 HG03516.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761-843_1761-842d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008282 | |||||||
| chr2:206008429 | C | T | 1 | a0001c0001t0009g0302 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1761-988G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008429 | |||||||
| chr2:206008487 | G | A | 1 | a0005c0015t0016g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1761-1046C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008487 | |||||||
| chr2:206008789 | C | T | 1 | a0001c0001t0050g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1760+788G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008789 | |||||||
| chr2:206008801 | T | C | 95 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1760+776A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008801 | |||||||
| chr2:206008841 | G | A | 20 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1760+736C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008841 | |||||||
| chr2:206008993 | A | G | 4 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0060 others(1): Show |
4 | HG00323.hp2 HG00741.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+584T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206008993 | |||||||
| chr2:206009042 | G | T | 3 | a0002c0005t0002g0191 a0002c0005t0002g0326 a0002c0005t0006g0327 |
3 | HG02258.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1760+535C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009042 | |||||||
| chr2:206009171 | G | A | 3 | a0002c0002t0001g0128 a0002c0002t0001g0171 a0002c0002t0049g0147 |
3 | HG02145.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1760+406C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009171 | |||||||
| chr2:206009277 | G | A | 249 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(246): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1760+300C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009277 | |||||||
| chr2:206009358 | C | CA | 215 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1760+218_1760+219i others(3): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009358 | |||||||
| chr2:206009482 | C | T | 1 | a0001c0001t0026g0005 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1760+95G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 9/10 | chr2 | 206009482 | |||||||
| chr2:206009842 | A | G | 1 | a0002c0002t0058g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1543-48T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206009842 | |||||||
| chr2:206009856 | T | C | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-62A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206009856 | |||||||
| chr2:206010062 | T | TAC | 17 | a0001c0001t0041g0291 a0001c0001t0042g0031 a0001c0003t0002g0203 others(14): Show |
17 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1543-270_1543-269d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | |||||||
| chr2:206010062 | T | TACAC | 4 | a0001c0001t0009g0288 a0001c0001t0009g0290 a0001c0003t0002g0242 others(1): Show |
4 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-272_1543-269d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | |||||||
| chr2:206010062 | TACACACA others(3): Show |
T | 1 | a0002c0002t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1543-278_1543-269d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010062 | |||||||
| chr2:206010083 | A | ACACACAC others(19): Show |
1 | a0001c0008t0019g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1543-290_1543-289i others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(15): Show |
2 | a0001c0001t0003g0238 a0001c0008t0019g0284 |
2 | HG02165.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-290_1543-289i others(24): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(11): Show |
1 | a0001c0001t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1543-290_1543-289i others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(9): Show |
35 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(32): Show |
36 | HG00673.hp2 HG00741.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(7): Show |
17 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0058 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(11): Show |
1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-290_1543-289i others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(5): Show |
6 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0004g0022 others(3): Show |
6 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010083 | A | ACACACAC others(3): Show |
26 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(23): Show |
27 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1543-290_1543-289i others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010083 | |||||||
| chr2:206010122 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-328C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010122 | |||||||
| chr2:206010285 | A | G | 1 | a0001c0001t0013g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1543-491T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010285 | |||||||
| chr2:206010397 | C | T | 1 | a0001c0003t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1543-603G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010397 | |||||||
| chr2:206010839 | G | A | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1543-1045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010839 | |||||||
| chr2:206010844 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1543-1050C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010844 | |||||||
| chr2:206010937 | G | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-1143C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206010937 | |||||||
| chr2:206011078 | C | CA | 9 | a0001c0001t0002g0309 a0001c0001t0041g0291 a0001c0003t0002g0250 others(6): Show |
9 | HG00621.hp1 HG00642.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1543-1285dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011078 | |||||||
| chr2:206011078 | CA | C | 87 | a0001c0001t0003g0002 a0001c0001t0003g0041 a0001c0001t0003g0043 others(84): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1543-1285delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011078 | |||||||
| chr2:206011101 | A | G | 1 | a0001c0003t0002g0274 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1543-1307T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011101 | |||||||
| chr2:206011205 | G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1543-1411C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011205 | |||||||
| chr2:206011208 | C | G | 3 | a0001c0001t0009g0288 a0001c0001t0009g0289 a0001c0001t0009g0290 |
3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1543-1414G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011208 | |||||||
| chr2:206011241 | C | G | 83 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(80): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1543-1447G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011241 | |||||||
| chr2:206011304 | A | G | 4 | a0001c0003t0002g0250 a0001c0003t0002g0258 a0001c0003t0002g0260 others(1): Show |
4 | HG01361.hp1 HG01515.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-1510T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011304 | |||||||
| chr2:206011535 | A | G | 108 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1543-1741T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011535 | |||||||
| chr2:206011944 | T | C | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-2150A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011944 | |||||||
| chr2:206011967 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2173A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011967 | |||||||
| chr2:206011977 | G | A | 2 | a0001c0003t0002g0215 a0001c0003t0002g0245 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1543-2183C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206011977 | |||||||
| chr2:206012002 | C | A | 13 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(10): Show |
13 | HG00423.hp2 HG00558.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.1543-2208G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012002 | |||||||
| chr2:206012003 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2209C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012003 | |||||||
| chr2:206012007 | A | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-2213T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012007 | |||||||
| chr2:206012032 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1543-2238C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012032 | |||||||
| chr2:206012089 | G | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1543-2295C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012089 | |||||||
| chr2:206012202 | A | G | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1543-2408T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012202 | |||||||
| chr2:206012277 | A | C | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1543-2483T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012277 | |||||||
| chr2:206012347 | G | A | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1543-2553C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012347 | |||||||
| chr2:206012436 | C | A | 1 | a0001c0003t0002g0250 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1543-2642G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012436 | |||||||
| chr2:206012476 | A | T | 7 | a0002c0002t0001g0108 a0002c0002t0001g0124 a0002c0002t0001g0140 others(4): Show |
7 | HG00642.hp2 HG01346.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543-2682T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012476 | |||||||
| chr2:206012574 | T | C | 1 | a0001c0003t0002g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1543-2780A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012574 | |||||||
| chr2:206012588 | T | C | 324 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(321): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1543-2794A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012588 | |||||||
| chr2:206012605 | C | T | 1 | a0001c0004t0037g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1543-2811G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012605 | |||||||
| chr2:206012867 | C | CA | 40 | a0001c0001t0002g0034 a0001c0001t0002g0309 a0001c0001t0005g0088 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1543-3074dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | |||||||
| chr2:206012867 | C | CAA | 33 | a0001c0001t0002g0287 a0001c0001t0004g0001 a0001c0001t0004g0012 others(30): Show |
34 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1543-3075_1543-307 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | |||||||
| chr2:206012867 | C | CAAA | 58 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(55): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1543-3076_1543-307 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | |||||||
| chr2:206012867 | C | CAAAA | 9 | a0001c0001t0003g0045 a0001c0001t0003g0057 a0001c0001t0003g0066 others(6): Show |
9 | HG01081.hp1 HG02523.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543-3077_1543-307 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012867 | |||||||
| chr2:206012976 | CTT | C | 23 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1543-3184_1543-318 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012976 | |||||||
| chr2:206012993 | C | T | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1543-3199G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206012993 | |||||||
| chr2:206013056 | C | A | 2 | a0001c0003t0002g0235 a0001c0003t0002g0241 |
2 | NA18612.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1543-3262G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013056 | |||||||
| chr2:206013276 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1543-3482T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013276 | |||||||
| chr2:206013289 | T | C | 2 | a0001c0001t0003g0045 a0002c0002t0001g0136 |
2 | NA19010.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1543-3495A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013289 | |||||||
| chr2:206013456 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1543-3662T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013456 | |||||||
| chr2:206013551 | C | CA | 108 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1543-3758dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013551 | |||||||
| chr2:206013628 | T | G | 1 | a0001c0003t0002g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1543-3834A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013628 | |||||||
| chr2:206013726 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1543-3932C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013726 | |||||||
| chr2:206013848 | T | TA | 34 | a0001c0001t0002g0309 a0001c0001t0005g0311 a0001c0001t0005g0312 others(31): Show |
34 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1542+3831dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | |||||||
| chr2:206013848 | TA | T | 16 | a0001c0001t0002g0034 a0001c0001t0003g0042 a0001c0001t0013g0032 others(13): Show |
16 | HG01070.hp2 HG01109.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542+3831delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | |||||||
| chr2:206013848 | TAA | T | 91 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(88): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1542+3830_1542+383 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013848 | |||||||
| chr2:206013923 | C | T | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1542+3757G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013923 | |||||||
| chr2:206013943 | G | A | 94 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(91): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1542+3737C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206013943 | |||||||
| chr2:206014089 | C | T | 1 | a0002c0002t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1542+3591G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014089 | |||||||
| chr2:206014157 | CA | C | 41 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(38): Show |
41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1542+3522delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | |||||||
| chr2:206014157 | CAA | C | 130 | a0001c0001t0002g0034 a0001c0001t0009g0289 a0001c0001t0013g0032 others(127): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1542+3521_1542+352 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | |||||||
| chr2:206014157 | CAAA | C | 92 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(89): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1542+3520_1542+352 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | |||||||
| chr2:206014157 | CAAAA | C | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+3519_1542+352 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014157 | |||||||
| chr2:206014237 | T | C | 1 | a0002c0002t0001g0140 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+3443A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014237 | |||||||
| chr2:206014541 | C | T | 1 | a0001c0001t0027g0010 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1542+3139G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014541 | |||||||
| chr2:206014729 | T | C | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1542+2951A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014729 | |||||||
| chr2:206014742 | C | A | 1 | a0002c0005t0002g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1542+2938G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014742 | |||||||
| chr2:206014820 | A | G | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1542+2860T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014820 | |||||||
| chr2:206014836 | T | C | 1 | a0002c0002t0001g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1542+2844A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014836 | |||||||
| chr2:206014937 | A | G | 22 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1542+2743T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206014937 | |||||||
| chr2:206015110 | T | C | 1 | a0001c0001t0018g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1542+2570A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015110 | |||||||
| chr2:206015387 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1542+2293C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015387 | |||||||
| chr2:206015404 | A | G | 95 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1542+2276T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015404 | |||||||
| chr2:206015622 | C | G | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+2058G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015622 | |||||||
| chr2:206015647 | G | C | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1542+2033C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015647 | |||||||
| chr2:206015655 | C | T | 1 | a0001c0004t0011g0298 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1542+2025G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015655 | |||||||
| chr2:206015747 | C | A | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+1933G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015747 | |||||||
| chr2:206015759 | C | T | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1542+1921G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015759 | |||||||
| chr2:206015800 | T | G | 2 | a0002c0002t0001g0170 a0002c0002t0001g0173 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1542+1880A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015800 | |||||||
| chr2:206015869 | A | G | 111 | a0001c0003t0014g0275 a0001c0006t0001g0111 a0001c0006t0001g0123 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1542+1811T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015869 | |||||||
| chr2:206015941 | G | A | 109 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1542+1739C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206015941 | |||||||
| chr2:206016003 | C | T | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1542+1677G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016003 | |||||||
| chr2:206016071 | A | T | 1 | a0001c0001t0064g0330 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1542+1609T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016071 | |||||||
| chr2:206016166 | C | CTA | 20 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1542+1512_1542+151 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016166 | |||||||
| chr2:206016373 | C | T | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1542+1307G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016373 | |||||||
| chr2:206016529 | C | T | 88 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1542+1151G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016529 | |||||||
| chr2:206016626 | C | G | 1 | a0001c0003t0002g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+1054G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016626 | |||||||
| chr2:206016643 | C | T | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1542+1037G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016643 | |||||||
| chr2:206016758 | G | A | 1 | a0001c0003t0002g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+922C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206016758 | |||||||
| chr2:206017204 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1542+476G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017204 | |||||||
| chr2:206017306 | G | T | 4 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0003g0062 others(1): Show |
4 | HG01099.hp2 HG01109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542+374C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017306 | |||||||
| chr2:206017504 | C | A | 1 | a0002c0002t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1542+176G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017504 | |||||||
| chr2:206017526 | C | T | 1 | a0001c0003t0002g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1542+154G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 8/10 | chr2 | 206017526 | |||||||
| chr2:206018236 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-423C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018236 | |||||||
| chr2:206018245 | A | G | 109 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1409-432T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018245 | |||||||
| chr2:206018270 | G | A | 1 | a0001c0001t0005g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1409-457C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018270 | |||||||
| chr2:206018486 | T | G | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-673A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018486 | |||||||
| chr2:206018654 | C | G | 3 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 |
3 | HG01123.hp2 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1409-841G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206018654 | |||||||
| chr2:206019124 | T | C | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1408+612A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019124 | |||||||
| chr2:206019196 | A | G | 1 | a0001c0001t0009g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1408+540T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019196 | |||||||
| chr2:206019403 | A | G | 1 | a0001c0001t0003g0041 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1408+333T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019403 | |||||||
| chr2:206019571 | G | C | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1408+165C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019571 | |||||||
| chr2:206019588 | A | T | 1 | a0001c0003t0014g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1408+148T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 7/10 | chr2 | 206019588 | |||||||
| chr2:206019850 | G | C | 1 | a0001c0003t0006g0251 | 1 | NA19009.hp1 | splice_region_variant&intron_variant | LOW | c.1299-5C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206019850 | |||||||
| chr2:206019871 | AT | A | 88 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1299-27delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206019871 | |||||||
| chr2:206020002 | G | A | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1299-157C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020002 | |||||||
| chr2:206020068 | G | C | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1299-223C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020068 | |||||||
| chr2:206020089 | G | GT | 243 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(240): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1299-245dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020089 | |||||||
| chr2:206020115 | T | C | 1 | a0001c0001t0004g0018 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1299-270A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020115 | |||||||
| chr2:206020469 | C | A | 213 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1299-624G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020469 | |||||||
| chr2:206020704 | A | C | 2 | a0004c0009t0007g0296 a0004c0009t0011g0294 |
2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1299-859T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020704 | |||||||
| chr2:206020791 | A | C | 1 | a0002c0005t0002g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1299-946T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206020791 | |||||||
| chr2:206021006 | C | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1299-1161G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021006 | |||||||
| chr2:206021329 | G | A | 109 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1299-1484C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021329 | |||||||
| chr2:206021497 | T | C | 2 | a0001c0001t0003g0068 a0007c0014t0003g0076 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1299-1652A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021497 | |||||||
| chr2:206021693 | A | G | 5 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0001c0008t0019g0284 others(2): Show |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-1848T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021693 | |||||||
| chr2:206021776 | T | C | 2 | a0002c0002t0001g0126 a0002c0002t0001g0143 |
2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1299-1931A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021776 | |||||||
| chr2:206021889 | C | G | 1 | a0001c0003t0002g0236 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1299-2044G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206021889 | |||||||
| chr2:206022041 | C | A | 203 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(200): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1299-2196G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022041 | |||||||
| chr2:206022250 | C | T | 3 | a0001c0001t0005g0303 a0001c0001t0005g0306 a0001c0001t0005g0313 |
3 | NA18984.hp2 NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1299-2405G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022250 | |||||||
| chr2:206022375 | A | G | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1299-2530T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022375 | |||||||
| chr2:206022465 | C | G | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1299-2620G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022465 | |||||||
| chr2:206022509 | A | T | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299-2664T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022509 | |||||||
| chr2:206022615 | A | G | 1 | a0001c0001t0005g0090 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1299-2770T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022615 | |||||||
| chr2:206022771 | T | C | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1299-2926A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022771 | |||||||
| chr2:206022773 | G | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0029 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1299-2928C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022773 | |||||||
| chr2:206022787 | C | T | 1 | a0006c0012t0002g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1299-2942G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022787 | |||||||
| chr2:206022798 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1299-2953G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022798 | |||||||
| chr2:206022862 | T | G | 5 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(2): Show |
5 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-3017A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022862 | |||||||
| chr2:206022968 | G | T | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1299-3123C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206022968 | |||||||
| chr2:206023125 | C | T | 1 | a0001c0004t0037g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1299-3280G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023125 | |||||||
| chr2:206023126 | G | A | 107 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1299-3281C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023126 | |||||||
| chr2:206023141 | C | A | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299-3296G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023141 | |||||||
| chr2:206023255 | T | C | 1 | a0001c0001t0004g0020 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1299-3410A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023255 | |||||||
| chr2:206023438 | C | T | 1 | a0001c0001t0026g0005 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1299-3593G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023438 | |||||||
| chr2:206023540 | G | A | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1299-3695C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023540 | |||||||
| chr2:206023554 | A | G | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1299-3709T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023554 | |||||||
| chr2:206023631 | C | T | 17 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(14): Show |
17 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.1299-3786G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023631 | |||||||
| chr2:206023680 | T | TA | 45 | a0001c0001t0003g0042 a0001c0001t0004g0001 a0001c0001t0004g0012 others(42): Show |
46 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1299-3836dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023680 | |||||||
| chr2:206023680 | TA | T | 12 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(9): Show |
13 | HG01070.hp2 HG01255.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1299-3836delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023680 | |||||||
| chr2:206023871 | T | C | 5 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0001c0008t0019g0284 others(2): Show |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299-4026A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206023871 | |||||||
| chr2:206024128 | A | G | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+3983T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024128 | |||||||
| chr2:206024295 | G | C | 1 | a0001c0004t0011g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1298+3816C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024295 | |||||||
| chr2:206024409 | A | C | 3 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 |
3 | HG00735.hp2 HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1298+3702T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024409 | |||||||
| chr2:206024778 | C | T | 43 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(40): Show |
44 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1298+3333G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206024778 | |||||||
| chr2:206025090 | G | T | 109 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(106): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1298+3021C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025090 | |||||||
| chr2:206025386 | A | G | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1298+2725T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025386 | |||||||
| chr2:206025389 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1298+2722C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025389 | |||||||
| chr2:206025397 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1298+2714C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025397 | |||||||
| chr2:206025472 | G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1298+2639C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025472 | |||||||
| chr2:206025506 | C | T | 21 | a0001c0003t0002g0127 a0001c0003t0002g0161 a0001c0003t0002g0172 others(18): Show |
21 | HG00438.hp1 HG02071.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1298+2605G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025506 | |||||||
| chr2:206025528 | C | CAA | 10 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(7): Show |
11 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1298+2581_1298+258 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | |||||||
| chr2:206025528 | C | CAAAAA | 14 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(11): Show |
15 | HG00738.hp1 HG01123.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1298+2578_1298+258 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | |||||||
| chr2:206025528 | C | CAAAAAA | 6 | a0001c0001t0004g0020 a0001c0001t0015g0007 a0001c0001t0015g0008 others(3): Show |
6 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+2577_1298+258 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | |||||||
| chr2:206025528 | C | CAAAAAAA others(5): Show |
2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1298+2571_1298+258 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | |||||||
| chr2:206025528 | CAA | C | 9 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(6): Show |
9 | HG01123.hp2 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1298+2581_1298+258 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025528 | |||||||
| chr2:206025538 | A | AATATATA others(5): Show |
1 | a0002c0016t0036g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1298+2572_1298+257 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025538 | |||||||
| chr2:206025538 | A | AATATATA others(9): Show |
1 | a0002c0002t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1298+2572_1298+257 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025538 | |||||||
| chr2:206025540 | A | AATATATA others(3): Show |
3 | a0002c0002t0001g0095 a0002c0002t0001g0137 a0002c0002t0001g0150 |
3 | NA19004.hp1 NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1298+2570_1298+257 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | |||||||
| chr2:206025540 | A | AATATATA others(5): Show |
3 | a0002c0002t0001g0104 a0002c0002t0001g0124 a0002c0002t0001g0185 |
3 | HG00280.hp1 HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1298+2570_1298+257 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | |||||||
| chr2:206025540 | A | AATATATA others(7): Show |
1 | a0002c0005t0002g0326 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1298+2570_1298+257 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | |||||||
| chr2:206025540 | A | AATATATA others(21): Show |
1 | a0002c0002t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1298+2570_1298+257 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | |||||||
| chr2:206025540 | A | T | 5 | a0001c0001t0003g0068 a0001c0001t0012g0085 a0001c0001t0012g0087 others(2): Show |
5 | HG00621.hp1 HG02738.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298+2571T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025540 | |||||||
| chr2:206025542 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0004g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAAAAAA others(17): Show |
2 | a0001c0001t0004g0015 a0001c0001t0004g0029 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0064g0330 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0025g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAAAAAA others(9): Show |
3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(1): Show |
15 | a0001c0003t0002g0253 a0001c0003t0002g0259 a0002c0002t0001g0003 others(12): Show |
16 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(3): Show |
4 | a0002c0002t0001g0093 a0002c0002t0001g0099 a0002c0002t0001g0101 others(1): Show |
4 | HG02165.hp1 HG02523.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(5): Show |
2 | a0002c0002t0001g0121 a0002c0002t0001g0151 |
2 | HG03579.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(7): Show |
1 | a0002c0002t0039g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(9): Show |
2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(11): Show |
1 | a0002c0002t0047g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(22): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAAATATA others(15): Show |
1 | a0002c0002t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(26): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAATATAT others(4): Show |
1 | a0002c0002t0001g0188 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAATATAT others(14): Show |
1 | a0002c0002t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1298+2568_1298+256 others(25): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AAT | 12 | a0001c0001t0003g0084 a0001c0001t0003g0096 a0001c0001t0003g0238 others(9): Show |
12 | HG01070.hp2 HG01255.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1298+2567_1298+256 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATAT | 12 | a0001c0001t0003g0040 a0001c0001t0003g0057 a0001c0001t0003g0061 others(9): Show |
12 | HG00099.hp2 HG00673.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1298+2565_1298+256 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATAT | 7 | a0001c0001t0031g0324 a0001c0003t0006g0211 a0001c0003t0006g0255 others(4): Show |
7 | HG01928.hp2 HG02293.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1298+2563_1298+256 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATATA others(1): Show |
37 | a0001c0001t0028g0053 a0001c0003t0002g0232 a0001c0003t0002g0266 others(34): Show |
37 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1298+2561_1298+256 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATATA others(3): Show |
15 | a0001c0003t0002g0264 a0001c0003t0017g0263 a0002c0002t0001g0097 others(12): Show |
15 | HG00423.hp1 HG01168.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.1298+2559_1298+256 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATATA others(5): Show |
6 | a0001c0003t0002g0229 a0002c0002t0001g0157 a0002c0002t0001g0184 others(3): Show |
6 | HG00099.hp1 HG00735.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+2557_1298+256 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATATA others(7): Show |
4 | a0002c0002t0001g0149 a0002c0002t0001g0168 a0002c0005t0006g0327 others(1): Show |
4 | HG03098.hp1 NA18945.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2555_1298+256 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | AATATATA others(9): Show |
3 | a0002c0002t0001g0107 a0002c0002t0001g0197 a0002c0002t0010g0110 |
3 | HG00140.hp2 HG04199.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1298+2553_1298+256 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0153 a0002c0002t0001g0199 |
2 | HG02735.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1298+2568_1298+256 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | A | T | 23 | a0001c0001t0003g0044 a0001c0001t0003g0068 a0001c0001t0012g0085 others(20): Show |
23 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1298+2569T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025542 | AATAT | A | 13 | a0001c0001t0005g0090 a0001c0001t0005g0303 a0001c0001t0005g0306 others(10): Show |
13 | HG00423.hp2 HG00642.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1298+2565_1298+256 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025542 | |||||||
| chr2:206025543 | AT | A | 11 | a0001c0001t0003g0066 a0001c0001t0003g0077 a0001c0001t0003g0086 others(8): Show |
11 | HG00673.hp2 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298+2567delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025543 | |||||||
| chr2:206025543 | ATATAT | A | 5 | a0001c0001t0005g0088 a0001c0001t0005g0089 a0001c0001t0005g0312 others(2): Show |
5 | HG00558.hp1 NA18960.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298+2563_1298+256 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025543 | |||||||
| chr2:206025544 | T | A | 48 | a0001c0001t0002g0034 a0001c0001t0003g0048 a0001c0001t0003g0049 others(45): Show |
50 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1298+2567A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025544 | |||||||
| chr2:206025546 | T | A | 40 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0004g0001 others(37): Show |
42 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1298+2565A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025546 | |||||||
| chr2:206025548 | T | A | 43 | a0001c0001t0002g0034 a0001c0001t0004g0001 a0001c0001t0004g0012 others(40): Show |
45 | HG00423.hp2 HG00642.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1298+2563A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025548 | |||||||
| chr2:206025550 | T | A | 25 | a0001c0001t0002g0034 a0001c0001t0004g0001 a0001c0001t0004g0012 others(22): Show |
26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1298+2561A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025550 | |||||||
| chr2:206025552 | T | A | 23 | a0001c0001t0002g0034 a0001c0001t0004g0001 a0001c0001t0004g0012 others(20): Show |
24 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1298+2559A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025552 | |||||||
| chr2:206025554 | T | A | 15 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(12): Show |
16 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1298+2557A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025554 | |||||||
| chr2:206025556 | T | A | 4 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0026 others(1): Show |
4 | HG01256.hp2 HG01516.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+2555A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025556 | |||||||
| chr2:206025568 | T | TATATATA others(9): Show |
1 | a0002c0002t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1298+2542_1298+254 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025568 | |||||||
| chr2:206025568 | TAA | T | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+2541_1298+254 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025568 | |||||||
| chr2:206025570 | A | T | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1298+2541T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025570 | |||||||
| chr2:206025636 | C | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298+2475G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025636 | |||||||
| chr2:206025721 | G | A | 2 | a0002c0010t0001g0117 a0002c0010t0055g0177 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1298+2390C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025721 | |||||||
| chr2:206025892 | T | C | 36 | a0001c0003t0002g0213 a0001c0003t0002g0216 a0001c0003t0002g0229 others(33): Show |
36 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1298+2219A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206025892 | |||||||
| chr2:206026090 | G | T | 2 | a0004c0009t0007g0296 a0004c0009t0011g0294 |
2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1298+2021C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026090 | |||||||
| chr2:206026124 | C | T | 88 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1298+1987G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026124 | |||||||
| chr2:206026272 | G | A | 1 | a0001c0001t0038g0243 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1298+1839C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026272 | |||||||
| chr2:206026285 | C | T | 1 | a0001c0003t0002g0260 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1298+1826G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026285 | |||||||
| chr2:206026312 | A | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1298+1799T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026312 | |||||||
| chr2:206026414 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1298+1697G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026414 | |||||||
| chr2:206026428 | C | T | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1298+1683G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026428 | |||||||
| chr2:206026557 | A | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1298+1554T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206026557 | |||||||
| chr2:206027112 | A | C | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+999T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027112 | |||||||
| chr2:206027145 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1298+966G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027145 | |||||||
| chr2:206027156 | G | GCA | 65 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(62): Show |
67 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1298+953_1298+954d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027156 | G | GCACA | 4 | a0001c0001t0003g0069 a0001c0003t0002g0246 a0001c0003t0002g0253 others(1): Show |
4 | HG00280.hp2 HG01175.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1298+951_1298+954d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027156 | G | GCACACA | 8 | a0001c0001t0003g0048 a0001c0001t0003g0070 a0001c0001t0003g0071 others(5): Show |
8 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298+949_1298+954d others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027156 | GCA | G | 155 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(152): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1298+953_1298+954d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027156 | GCACA | G | 14 | a0001c0001t0031g0324 a0001c0004t0007g0278 a0001c0004t0007g0279 others(11): Show |
14 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1298+951_1298+954d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027156 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+945_1298+954d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027156 | |||||||
| chr2:206027160 | A | G | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1298+951T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027160 | |||||||
| chr2:206027224 | TTCTC | T | 21 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(18): Show |
21 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1298+883_1298+886d others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027224 | |||||||
| chr2:206027597 | A | G | 1 | a0001c0001t0013g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1298+514T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027597 | |||||||
| chr2:206027682 | C | T | 95 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1298+429G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027682 | |||||||
| chr2:206027754 | T | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1298+357A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027754 | |||||||
| chr2:206027780 | T | C | 1 | a0001c0003t0006g0244 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1298+331A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 6/10 | chr2 | 206027780 | |||||||
| chr2:206028565 | T | C | 1 | a0002c0010t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1074-230A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028565 | |||||||
| chr2:206028884 | G | T | 1 | a0002c0002t0047g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1074-549C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028884 | |||||||
| chr2:206028888 | T | G | 1 | a0001c0001t0022g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1074-553A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028888 | |||||||
| chr2:206028894 | T | G | 57 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(54): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1074-559A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028894 | |||||||
| chr2:206028895 | T | G | 1 | a0001c0001t0009g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1074-560A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206028895 | |||||||
| chr2:206029005 | A | G | 1 | a0001c0003t0006g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1074-670T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029005 | |||||||
| chr2:206029236 | A | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074-901T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029236 | |||||||
| chr2:206029591 | ATTC | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074-1259_1074-125 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029591 | |||||||
| chr2:206029602 | C | T | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-1267G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029602 | |||||||
| chr2:206029845 | G | C | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-1510C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206029845 | |||||||
| chr2:206030078 | G | A | 1 | a0001c0001t0009g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-1743C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030078 | |||||||
| chr2:206030265 | A | T | 4 | a0001c0003t0002g0270 a0001c0003t0002g0271 a0001c0003t0006g0268 others(1): Show |
4 | HG02486.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-1930T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030265 | |||||||
| chr2:206030462 | C | CA | 113 | a0001c0001t0005g0303 a0001c0001t0005g0313 a0001c0003t0002g0161 others(110): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1074-2128dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030462 | |||||||
| chr2:206030616 | G | GT | 3 | a0001c0001t0004g0015 a0001c0001t0004g0024 a0001c0001t0004g0029 |
3 | HG01515.hp1 HG01517.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1074-2282dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030616 | |||||||
| chr2:206030783 | T | A | 5 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0001c0008t0019g0284 others(2): Show |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-2448A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206030783 | |||||||
| chr2:206031149 | G | T | 1 | a0002c0002t0001g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1074-2814C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031149 | |||||||
| chr2:206031486 | A | G | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-3151T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031486 | |||||||
| chr2:206031597 | G | A | 1 | a0001c0001t0022g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1074-3262C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031597 | |||||||
| chr2:206031676 | C | T | 2 | a0001c0001t0016g0281 a0001c0001t0016g0282 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-3341G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031676 | |||||||
| chr2:206031711 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-3376C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031711 | |||||||
| chr2:206031904 | G | A | 1 | a0001c0003t0002g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074-3569C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206031904 | |||||||
| chr2:206032138 | T | G | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-3803A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032138 | |||||||
| chr2:206032255 | C | G | 2 | a0001c0003t0002g0236 a0001c0003t0002g0239 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1074-3920G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032255 | |||||||
| chr2:206032333 | G | A | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-3998C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032333 | |||||||
| chr2:206032564 | G | C | 1 | a0002c0002t0010g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1074-4229C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032564 | |||||||
| chr2:206032665 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1074-4330G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206032665 | |||||||
| chr2:206033150 | A | T | 1 | a0001c0001t0003g0044 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1074-4815T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033150 | |||||||
| chr2:206033228 | G | C | 1 | a0001c0013t0005g0307 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1074-4893C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033228 | |||||||
| chr2:206033321 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1074-4986A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033321 | |||||||
| chr2:206033425 | C | T | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1074-5090G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033425 | |||||||
| chr2:206033447 | T | A | 1 | a0001c0001t0004g0012 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1074-5112A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033447 | |||||||
| chr2:206033783 | A | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-5448T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033783 | |||||||
| chr2:206033980 | C | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1074-5645G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206033980 | |||||||
| chr2:206034073 | C | A | 2 | a0002c0010t0001g0117 a0002c0010t0055g0177 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1074-5738G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034073 | |||||||
| chr2:206034287 | C | T | 1 | a0002c0002t0001g0162 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1074-5952G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034287 | |||||||
| chr2:206034583 | G | A | 86 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1074-6248C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034583 | |||||||
| chr2:206034605 | A | T | 1 | a0002c0002t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1074-6270T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034605 | |||||||
| chr2:206034674 | GAACTGGA others(36): Show |
G | 9 | a0002c0002t0001g0094 a0002c0002t0001g0098 a0002c0002t0001g0135 others(6): Show |
9 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-6382_1074-634 others(47): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034674 | |||||||
| chr2:206034746 | C | G | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074-6411G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034746 | |||||||
| chr2:206034861 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1074-6526T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206034861 | |||||||
| chr2:206035018 | A | C | 2 | a0002c0010t0001g0117 a0002c0010t0055g0177 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1074-6683T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035018 | |||||||
| chr2:206035041 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074-6706G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035041 | |||||||
| chr2:206035072 | A | G | 1 | a0001c0003t0062g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1074-6737T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035072 | |||||||
| chr2:206035098 | C | G | 1 | a0002c0002t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1074-6763G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035098 | |||||||
| chr2:206035116 | T | A | 1 | a0002c0010t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1074-6781A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035116 | |||||||
| chr2:206035134 | G | A | 20 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1074-6799C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035134 | |||||||
| chr2:206035386 | AAAT | A | 88 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1074-7054_1074-705 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035386 | |||||||
| chr2:206035487 | A | G | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074-7152T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035487 | |||||||
| chr2:206035536 | A | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-7201T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206035536 | |||||||
| chr2:206036166 | A | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-7831T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036166 | |||||||
| chr2:206036220 | T | C | 95 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1074-7885A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036220 | |||||||
| chr2:206036237 | C | T | 105 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(102): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1074-7902G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036237 | |||||||
| chr2:206036301 | T | C | 1 | a0001c0003t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1074-7966A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036301 | |||||||
| chr2:206036488 | A | C | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074-8153T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206036488 | |||||||
| chr2:206037001 | T | C | 101 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(98): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1074-8666A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037001 | |||||||
| chr2:206037365 | C | T | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1074-9030G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037365 | |||||||
| chr2:206037509 | A | G | 216 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1073+8995T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037509 | |||||||
| chr2:206037532 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1073+8972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037532 | |||||||
| chr2:206037635 | A | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+8869T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037635 | |||||||
| chr2:206037771 | G | A | 22 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1073+8733C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037771 | |||||||
| chr2:206037886 | G | A | 1 | a0002c0002t0057g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1073+8618C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206037886 | |||||||
| chr2:206038124 | C | T | 206 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1073+8380G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038124 | |||||||
| chr2:206038181 | T | C | 3 | a0001c0003t0002g0224 a0001c0003t0002g0236 a0001c0003t0002g0239 |
3 | HG02109.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1073+8323A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038181 | |||||||
| chr2:206038214 | A | G | 1 | a0001c0001t0038g0243 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1073+8290T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038214 | |||||||
| chr2:206038485 | T | C | 2 | a0001c0001t0003g0048 a0001c0001t0003g0077 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1073+8019A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038485 | |||||||
| chr2:206038578 | T | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+7926A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038578 | |||||||
| chr2:206038726 | G | A | 88 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1073+7778C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038726 | |||||||
| chr2:206038792 | C | A | 107 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1073+7712G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206038792 | |||||||
| chr2:206039053 | A | G | 102 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1073+7451T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039053 | |||||||
| chr2:206039060 | G | A | 2 | a0002c0002t0010g0322 a0002c0002t0046g0323 |
2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1073+7444C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039060 | |||||||
| chr2:206039168 | C | T | 20 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1073+7336G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039168 | |||||||
| chr2:206039337 | C | T | 134 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(131): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1073+7167G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039337 | |||||||
| chr2:206039354 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+7150C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039354 | |||||||
| chr2:206039366 | C | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0134 |
2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1073+7138G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039366 | |||||||
| chr2:206039414 | A | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+7090T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039414 | |||||||
| chr2:206039477 | C | T | 16 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(13): Show |
17 | HG00738.hp1 HG01123.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1073+7027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039477 | |||||||
| chr2:206039530 | T | C | 3 | a0001c0004t0007g0295 a0001c0004t0007g0297 a0001c0004t0007g0299 |
3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1073+6974A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039530 | |||||||
| chr2:206039577 | T | C | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1073+6927A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039577 | |||||||
| chr2:206039608 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1073+6896G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039608 | |||||||
| chr2:206039609 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1073+6895C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039609 | |||||||
| chr2:206039810 | CA | C | 104 | a0001c0001t0003g0041 a0001c0001t0004g0021 a0001c0001t0024g0014 others(101): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1073+6693delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039810 | |||||||
| chr2:206039810 | CAA | C | 98 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1073+6692_1073+669 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039810 | |||||||
| chr2:206039841 | G | A | 1 | a0001c0003t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+6663C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039841 | |||||||
| chr2:206039842 | A | G | 1 | a0001c0003t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+6662T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039842 | |||||||
| chr2:206039969 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+6535C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039969 | |||||||
| chr2:206039972 | A | C | 1 | a0001c0001t0034g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1073+6532T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206039972 | |||||||
| chr2:206040020 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+6484G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040020 | |||||||
| chr2:206040021 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1073+6483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040021 | |||||||
| chr2:206040118 | C | A | 1 | a0001c0001t0004g0022 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1073+6386G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040118 | |||||||
| chr2:206040154 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+6350C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040154 | |||||||
| chr2:206040206 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+6298A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040206 | |||||||
| chr2:206040244 | C | G | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1073+6260G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040244 | |||||||
| chr2:206040279 | C | T | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1073+6225G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040279 | |||||||
| chr2:206040285 | C | CA | 67 | a0001c0001t0003g0002 a0001c0001t0003g0041 a0001c0001t0003g0042 others(64): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1073+6218dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040285 | |||||||
| chr2:206040285 | C | CAA | 37 | a0001c0001t0002g0034 a0001c0001t0003g0091 a0001c0001t0003g0096 others(34): Show |
38 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1073+6217_1073+621 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040285 | |||||||
| chr2:206040381 | A | C | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1073+6123T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040381 | |||||||
| chr2:206040385 | A | G | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+6119T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040385 | |||||||
| chr2:206040426 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+6078C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040426 | |||||||
| chr2:206040674 | T | G | 2 | a0001c0003t0002g0226 a0001c0003t0023g0214 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1073+5830A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040674 | |||||||
| chr2:206040676 | C | G | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+5828G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040676 | |||||||
| chr2:206040697 | A | G | 94 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(91): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1073+5807T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040697 | |||||||
| chr2:206040762 | T | G | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1073+5742A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040762 | |||||||
| chr2:206040806 | G | A | 1 | a0001c0001t0013g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1073+5698C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040806 | |||||||
| chr2:206040808 | G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1073+5696C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040808 | |||||||
| chr2:206040826 | T | C | 1 | a0001c0001t0003g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1073+5678A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040826 | |||||||
| chr2:206040879 | A | G | 1 | a0001c0001t0003g0055 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1073+5625T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040879 | |||||||
| chr2:206040964 | G | A | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1073+5540C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206040964 | |||||||
| chr2:206041006 | C | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073+5498G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041006 | |||||||
| chr2:206041009 | G | T | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1073+5495C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041009 | |||||||
| chr2:206041023 | C | T | 1 | a0001c0001t0013g0032 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1073+5481G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041023 | |||||||
| chr2:206041204 | C | T | 1 | a0001c0003t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1073+5300G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041204 | |||||||
| chr2:206041208 | TA | T | 212 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1073+5295delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041208 | |||||||
| chr2:206041421 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1073+5083C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041421 | |||||||
| chr2:206041459 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+5045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041459 | |||||||
| chr2:206041721 | C | T | 95 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1073+4783G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041721 | |||||||
| chr2:206041879 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+4625C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206041879 | |||||||
| chr2:206042073 | G | A | 1 | a0002c0002t0048g0119 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1073+4431C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042073 | |||||||
| chr2:206042210 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1073+4294C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042210 | |||||||
| chr2:206042508 | C | G | 8 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(5): Show |
8 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1073+3996G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042508 | |||||||
| chr2:206042532 | G | A | 149 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1073+3972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042532 | |||||||
| chr2:206042611 | G | A | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1073+3893C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042611 | |||||||
| chr2:206042656 | G | C | 2 | a0002c0002t0001g0168 a0002c0002t0001g0186 |
2 | NA18945.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1073+3848C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042656 | |||||||
| chr2:206042679 | T | A | 1 | a0002c0002t0046g0323 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1073+3825A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042679 | |||||||
| chr2:206042680 | C | A | 1 | a0002c0002t0046g0323 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1073+3824G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | |||||||
| chr2:206042680 | C | CA | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1073+3823dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | |||||||
| chr2:206042680 | C | CAA | 87 | a0001c0001t0003g0072 a0001c0001t0003g0091 a0001c0001t0003g0146 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1073+3822_1073+382 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | |||||||
| chr2:206042680 | C | CAAA | 21 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1073+3821_1073+382 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042680 | |||||||
| chr2:206042882 | G | A | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1073+3622C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042882 | |||||||
| chr2:206042907 | G | C | 38 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1073+3597C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206042907 | |||||||
| chr2:206043263 | C | T | 23 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0095 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1073+3241G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043263 | |||||||
| chr2:206043330 | C | T | 5 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0021g0047 others(2): Show |
5 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+3174G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043330 | |||||||
| chr2:206043391 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1073+3113G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043391 | |||||||
| chr2:206043422 | G | A | 38 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1073+3082C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043422 | |||||||
| chr2:206043519 | G | A | 19 | a0001c0003t0002g0127 a0001c0003t0002g0161 a0001c0003t0002g0172 others(16): Show |
19 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1073+2985C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043519 | |||||||
| chr2:206043544 | GTGGCACG others(12): Show |
G | 1 | a0002c0002t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1073+2941_1073+295 others(23): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043544 | |||||||
| chr2:206043598 | C | T | 7 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0061 others(4): Show |
7 | HG02132.hp1 HG02523.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073+2906G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043598 | |||||||
| chr2:206043690 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1073+2814G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043690 | |||||||
| chr2:206043767 | G | A | 111 | a0001c0001t0031g0324 a0001c0006t0001g0111 a0001c0006t0001g0123 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1073+2737C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206043767 | |||||||
| chr2:206044086 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+2418C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044086 | |||||||
| chr2:206044265 | T | C | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1073+2239A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044265 | |||||||
| chr2:206044271 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1073+2233C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044271 | |||||||
| chr2:206044481 | T | TA | 25 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(22): Show |
27 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1073+2022dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | |||||||
| chr2:206044481 | T | TAA | 32 | a0001c0001t0041g0291 a0001c0003t0002g0242 a0002c0002t0001g0092 others(29): Show |
32 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1073+2021_1073+202 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | |||||||
| chr2:206044481 | T | TAAA | 78 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(75): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1073+2020_1073+202 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | |||||||
| chr2:206044481 | TA | T | 31 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0004g0029 others(28): Show |
31 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073+2022delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044481 | |||||||
| chr2:206044546 | G | A | 1 | a0001c0003t0002g0274 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1073+1958C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044546 | |||||||
| chr2:206044663 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+1841A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044663 | |||||||
| chr2:206044773 | C | T | 4 | a0001c0001t0009g0288 a0001c0001t0009g0290 a0001c0001t0041g0291 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+1731G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044773 | |||||||
| chr2:206044852 | G | C | 1 | a0001c0003t0002g0256 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1073+1652C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206044852 | |||||||
| chr2:206045602 | C | T | 5 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0001c0008t0019g0284 others(2): Show |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+902G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045602 | |||||||
| chr2:206045760 | A | G | 1 | a0002c0016t0036g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1073+744T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045760 | |||||||
| chr2:206045850 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+654C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045850 | |||||||
| chr2:206045903 | T | C | 2 | a0001c0003t0002g0203 a0001c0003t0002g0206 |
2 | NA18961.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1073+601A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045903 | |||||||
| chr2:206045931 | G | A | 4 | a0001c0001t0009g0288 a0001c0001t0009g0290 a0001c0001t0041g0291 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+573C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045931 | |||||||
| chr2:206045983 | T | C | 5 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0061 others(2): Show |
5 | HG02523.hp1 NA18951.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+521A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206045983 | |||||||
| chr2:206046259 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1073+245C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046259 | |||||||
| chr2:206046324 | A | G | 4 | a0001c0001t0009g0288 a0001c0001t0009g0290 a0001c0001t0041g0291 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+180T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046324 | |||||||
| chr2:206046343 | C | T | 1 | a0001c0001t0038g0243 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1073+161G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046343 | |||||||
| chr2:206046467 | C | CA | 250 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(247): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1073+36dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 5/10 | chr2 | 206046467 | |||||||
| chr2:206046782 | GTTTGTT | G | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.965-176_965-171del others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046782 | |||||||
| chr2:206046787 | T | C | 4 | a0001c0001t0009g0288 a0001c0001t0009g0290 a0001c0001t0041g0291 others(1): Show |
4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-175A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046787 | |||||||
| chr2:206046824 | C | A | 1 | a0001c0004t0011g0298 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.965-212G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206046824 | |||||||
| chr2:206047001 | G | C | 1 | a0001c0003t0002g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.965-389C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047001 | |||||||
| chr2:206047165 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.965-553C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047165 | |||||||
| chr2:206047167 | G | A | 5 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0001c0008t0019g0284 others(2): Show |
5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-555C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047167 | |||||||
| chr2:206047300 | C | A | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.965-688G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047300 | |||||||
| chr2:206047431 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.965-819G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047431 | |||||||
| chr2:206047432 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.965-820A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047432 | |||||||
| chr2:206047498 | C | T | 3 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 |
3 | HG00735.hp2 HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.965-886G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047498 | |||||||
| chr2:206047665 | A | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-1053T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047665 | |||||||
| chr2:206047856 | A | ATTTTTTT | 88 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.965-1251_965-1245d others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | |||||||
| chr2:206047856 | A | ATTTTTTT others(1): Show |
10 | a0001c0001t0003g0068 a0001c0001t0003g0071 a0001c0001t0003g0086 others(7): Show |
10 | HG00673.hp2 HG01981.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.965-1252_965-1245d others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | |||||||
| chr2:206047856 | A | ATTTTTTT others(2): Show |
101 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(98): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.965-1253_965-1245d others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | |||||||
| chr2:206047856 | A | ATTTTTTT others(3): Show |
6 | a0002c0002t0001g0133 a0002c0002t0001g0149 a0002c0002t0001g0169 others(3): Show |
6 | HG00140.hp2 HG02145.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-1254_965-1245d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | |||||||
| chr2:206047856 | A | G | 3 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 |
3 | HG01123.hp2 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.965-1244T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047856 | |||||||
| chr2:206047937 | G | A | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-1325C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206047937 | |||||||
| chr2:206048090 | T | C | 206 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(203): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.965-1478A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048090 | |||||||
| chr2:206048127 | T | G | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.965-1515A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048127 | |||||||
| chr2:206048145 | G | A | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.965-1533C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048145 | |||||||
| chr2:206048150 | C | A | 45 | a0001c0003t0002g0213 a0001c0003t0002g0216 a0001c0003t0002g0225 others(42): Show |
45 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-1538G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048150 | |||||||
| chr2:206048154 | C | T | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.965-1542G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048154 | |||||||
| chr2:206048423 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.965-1811C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048423 | |||||||
| chr2:206048438 | G | A | 1 | a0001c0001t0003g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.965-1826C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048438 | |||||||
| chr2:206048452 | C | T | 1 | a0001c0001t0013g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965-1840G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048452 | |||||||
| chr2:206048624 | C | T | 2 | a0001c0003t0014g0275 a0002c0005t0002g0326 |
2 | HG00438.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.965-2012G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206048624 | |||||||
| chr2:206049152 | G | A | 5 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-2540C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049152 | |||||||
| chr2:206049247 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2635C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049247 | |||||||
| chr2:206049290 | G | A | 2 | a0001c0003t0002g0226 a0001c0003t0023g0214 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.965-2678C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049290 | |||||||
| chr2:206049304 | T | C | 102 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(99): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.965-2692A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049304 | |||||||
| chr2:206049370 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.965-2758C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049370 | |||||||
| chr2:206049530 | A | T | 1 | a0002c0002t0001g0132 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.965-2918T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049530 | |||||||
| chr2:206049668 | T | C | 9 | a0001c0001t0003g0048 a0001c0001t0003g0069 a0001c0001t0003g0070 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-3056A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049668 | |||||||
| chr2:206049718 | C | T | 2 | a0001c0003t0002g0270 a0001c0003t0006g0269 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.965-3106G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049718 | |||||||
| chr2:206049839 | T | C | 1 | a0001c0001t0003g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.965-3227A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049839 | |||||||
| chr2:206049867 | C | T | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.965-3255G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049867 | |||||||
| chr2:206049992 | G | T | 1 | a0002c0002t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.965-3380C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206049992 | |||||||
| chr2:206050095 | G | A | 3 | a0002c0002t0001g0128 a0002c0002t0001g0171 a0002c0002t0049g0147 |
3 | HG02145.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.965-3483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050095 | |||||||
| chr2:206050106 | C | G | 1 | a0001c0008t0019g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.965-3494G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050106 | |||||||
| chr2:206050139 | A | G | 1 | a0002c0002t0039g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.965-3527T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050139 | |||||||
| chr2:206050140 | G | A | 1 | a0002c0002t0039g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.965-3528C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050140 | |||||||
| chr2:206050316 | C | T | 95 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.965-3704G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050316 | |||||||
| chr2:206050399 | G | A | 1 | a0001c0001t0013g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965-3787C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050399 | |||||||
| chr2:206050485 | C | A | 3 | a0001c0001t0009g0288 a0001c0001t0009g0289 a0001c0001t0009g0290 |
3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.965-3873G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050485 | |||||||
| chr2:206050496 | G | GA | 20 | a0001c0001t0009g0290 a0001c0001t0022g0033 a0001c0003t0002g0200 others(17): Show |
20 | HG01109.hp2 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.965-3885dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GA | G | 19 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(16): Show |
19 | HG00423.hp2 HG00558.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.965-3885delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAA | G | 6 | a0002c0002t0001g0129 a0002c0002t0001g0167 a0002c0005t0002g0326 others(3): Show |
6 | HG02109.hp1 HG02165.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-3890_965-3885d others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA | G | 101 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.965-3891_965-3885d others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA others(3): Show |
G | 53 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(50): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.965-3894_965-3885d others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA others(4): Show |
G | 5 | a0001c0001t0003g0061 a0001c0001t0003g0068 a0001c0001t0005g0313 others(2): Show |
5 | HG02622.hp1 HG02738.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-3895_965-3885d others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA others(5): Show |
G | 6 | a0001c0001t0008g0004 a0001c0001t0008g0319 a0001c0001t0008g0321 others(3): Show |
7 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-3896_965-3885d others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA others(6): Show |
G | 23 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(20): Show |
24 | HG00738.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.965-3897_965-3885d others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050496 | GAAAAAAA others(7): Show |
G | 7 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 others(4): Show |
7 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-3898_965-3885d others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050496 | |||||||
| chr2:206050682 | T | C | 2 | a0002c0002t0001g0126 a0002c0002t0001g0143 |
2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.965-4070A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050682 | |||||||
| chr2:206050862 | G | T | 2 | a0001c0003t0002g0127 a0001c0003t0002g0200 |
2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.965-4250C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050862 | |||||||
| chr2:206050896 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.965-4284C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050896 | |||||||
| chr2:206050924 | C | G | 238 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(235): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.965-4312G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050924 | |||||||
| chr2:206050931 | T | C | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-4319A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050931 | |||||||
| chr2:206050980 | C | CAAAAATT others(314): Show |
2 | a0001c0004t0007g0278 a0001c0004t0007g0292 |
2 | HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(323): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206050980 | C | CAAAAATT others(315): Show |
2 | a0001c0004t0007g0279 a0001c0004t0037g0280 |
2 | HG01123.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(324): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206050980 | C | CAAAAATT others(321): Show |
2 | a0001c0004t0011g0298 a0004c0009t0007g0296 |
2 | HG01257.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(330): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206050980 | C | CAAAAATT others(322): Show |
3 | a0001c0004t0007g0295 a0001c0004t0011g0293 a0004c0009t0011g0294 |
3 | HG00639.hp2 HG01891.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(331): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206050980 | C | CAAAAATT others(323): Show |
2 | a0001c0004t0007g0297 a0001c0004t0007g0300 |
2 | HG01175.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.965-4369_965-4368i others(332): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206050980 | C | CAAAAATT others(324): Show |
1 | a0001c0004t0007g0299 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.965-4369_965-4368i others(333): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206050980 | |||||||
| chr2:206051215 | ATTTCT | A | 5 | a0002c0002t0001g0094 a0002c0002t0001g0102 a0002c0002t0001g0180 others(2): Show |
5 | HG01074.hp1 NA18947.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-4608_965-4604d others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051215 | |||||||
| chr2:206051219 | C | T | 5 | a0001c0003t0002g0249 a0001c0003t0002g0256 a0001c0003t0054g0261 others(2): Show |
5 | HG01255.hp1 HG02683.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-4607G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051219 | |||||||
| chr2:206051239 | T | C | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.965-4627A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051239 | |||||||
| chr2:206051245 | C | T | 2 | a0001c0001t0005g0311 a0001c0001t0005g0312 |
2 | NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.965-4633G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051245 | |||||||
| chr2:206051304 | G | A | 1 | a0001c0003t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.965-4692C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051304 | |||||||
| chr2:206051485 | A | G | 1 | a0001c0001t0027g0010 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.964+4713T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051485 | |||||||
| chr2:206051562 | T | C | 1 | a0001c0004t0037g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964+4636A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051562 | |||||||
| chr2:206051671 | A | T | 1 | a0002c0002t0039g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.964+4527T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051671 | |||||||
| chr2:206051701 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.964+4497T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051701 | |||||||
| chr2:206051715 | G | A | 2 | a0002c0002t0001g0126 a0002c0002t0001g0143 |
2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.964+4483C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051715 | |||||||
| chr2:206051999 | A | C | 1 | a0003c0007t0001g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.964+4199T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206051999 | |||||||
| chr2:206052058 | T | G | 1 | a0001c0003t0059g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.964+4140A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052058 | |||||||
| chr2:206052154 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.964+4044A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052154 | |||||||
| chr2:206052257 | G | A | 111 | a0001c0001t0031g0324 a0001c0006t0001g0111 a0001c0006t0001g0123 others(108): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.964+3941C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052257 | |||||||
| chr2:206052293 | A | G | 1 | a0001c0003t0002g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.964+3905T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052293 | |||||||
| chr2:206052661 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+3537C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052661 | |||||||
| chr2:206052732 | C | T | 1 | a0001c0001t0004g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964+3466G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052732 | |||||||
| chr2:206052791 | C | CA | 83 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(80): Show |
86 | HG00323.hp2 HG00673.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.964+3406dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052791 | |||||||
| chr2:206052791 | C | CAA | 9 | a0001c0001t0003g0048 a0001c0001t0003g0069 a0001c0001t0003g0070 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+3405_964+3406d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052791 | |||||||
| chr2:206052953 | A | C | 2 | a0001c0001t0008g0321 a0001c0001t0050g0318 |
2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.964+3245T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206052953 | |||||||
| chr2:206053004 | C | A | 205 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(202): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.964+3194G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053004 | |||||||
| chr2:206053380 | T | C | 110 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.964+2818A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053380 | |||||||
| chr2:206053456 | G | A | 95 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.964+2742C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053456 | |||||||
| chr2:206053513 | C | T | 59 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(56): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.964+2685G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053513 | |||||||
| chr2:206053593 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.964+2605A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053593 | |||||||
| chr2:206053842 | A | AT | 108 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.964+2355dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053842 | |||||||
| chr2:206053869 | C | T | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+2329G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206053869 | |||||||
| chr2:206054012 | G | A | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.964+2186C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054012 | |||||||
| chr2:206054041 | T | C | 2 | a0001c0003t0006g0247 a0001c0003t0006g0252 |
2 | HG00673.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.964+2157A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054041 | |||||||
| chr2:206054188 | T | C | 1 | a0001c0001t0008g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.964+2010A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054188 | |||||||
| chr2:206054583 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0060 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.964+1615C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054583 | |||||||
| chr2:206054607 | AG | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.964+1590delC | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054607 | |||||||
| chr2:206054784 | G | C | 1 | a0001c0003t0062g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.964+1414C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206054784 | |||||||
| chr2:206055372 | G | A | 1 | a0001c0004t0007g0295 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.964+826C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055372 | |||||||
| chr2:206055435 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.964+763C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055435 | |||||||
| chr2:206055469 | T | C | 10 | a0002c0002t0001g0092 a0002c0002t0001g0105 a0002c0002t0001g0114 others(7): Show |
10 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.964+729A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055469 | |||||||
| chr2:206055628 | G | A | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.964+570C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055628 | |||||||
| chr2:206055643 | C | T | 1 | a0001c0003t0002g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964+555G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055643 | |||||||
| chr2:206055692 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.964+506C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055692 | |||||||
| chr2:206055875 | G | A | 59 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(56): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.964+323C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206055875 | |||||||
| chr2:206056111 | T | C | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.964+87A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056111 | |||||||
| chr2:206056145 | G | A | 2 | a0001c0003t0002g0271 a0001c0003t0006g0268 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.964+53C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056145 | |||||||
| chr2:206056169 | T | C | 1 | a0001c0003t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964+29A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 4/10 | chr2 | 206056169 | |||||||
| chr2:206057039 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-96G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057039 | |||||||
| chr2:206057413 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0195 |
2 | HG00621.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.219-470G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057413 | |||||||
| chr2:206057421 | C | G | 1 | a0002c0016t0036g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.219-478G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057421 | |||||||
| chr2:206057485 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.219-542A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057485 | |||||||
| chr2:206057665 | A | G | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-722T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057665 | |||||||
| chr2:206057778 | G | A | 314 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.219-835C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057778 | |||||||
| chr2:206057899 | TA | T | 11 | a0001c0001t0003g0050 a0001c0001t0005g0314 a0001c0001t0008g0321 others(8): Show |
11 | HG00323.hp2 HG00558.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-957delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057899 | |||||||
| chr2:206057939 | T | G | 1 | a0001c0001t0013g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219-996A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206057939 | |||||||
| chr2:206058149 | A | G | 212 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.219-1206T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058149 | |||||||
| chr2:206058150 | A | G | 212 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.219-1207T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058150 | |||||||
| chr2:206058194 | C | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-1251G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058194 | |||||||
| chr2:206058311 | C | T | 3 | a0001c0004t0007g0295 a0001c0004t0007g0297 a0001c0004t0007g0299 |
3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.219-1368G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058311 | |||||||
| chr2:206058329 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-1386C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058329 | |||||||
| chr2:206058368 | G | A | 5 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 others(2): Show |
5 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1425C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058368 | |||||||
| chr2:206058381 | T | G | 1 | a0002c0002t0001g0196 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.219-1438A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058381 | |||||||
| chr2:206058418 | C | CA | 55 | a0001c0001t0002g0287 a0001c0001t0005g0090 a0001c0001t0005g0303 others(52): Show |
55 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.219-1476dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | |||||||
| chr2:206058418 | C | CAA | 11 | a0001c0001t0002g0309 a0001c0001t0005g0088 a0001c0001t0005g0089 others(8): Show |
11 | HG02055.hp1 HG02135.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.219-1477_219-1476d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | |||||||
| chr2:206058418 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0003g0080 a0001c0001t0029g0064 a0002c0005t0002g0326 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-1486_219-1476d others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | |||||||
| chr2:206058418 | CAAAAAAA others(5): Show |
C | 207 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(204): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.219-1487_219-1476d others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058418 | |||||||
| chr2:206058507 | G | C | 17 | a0001c0003t0002g0127 a0001c0003t0002g0161 a0001c0003t0002g0172 others(14): Show |
17 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-1564C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058507 | |||||||
| chr2:206058660 | G | A | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-1717C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058660 | |||||||
| chr2:206058861 | T | G | 1 | a0001c0001t0025g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.219-1918A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206058861 | |||||||
| chr2:206059062 | TA | T | 14 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(11): Show |
14 | HG00323.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-2120delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059062 | |||||||
| chr2:206059237 | C | T | 1 | a0001c0004t0007g0300 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.219-2294G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059237 | |||||||
| chr2:206059303 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.219-2360G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059303 | |||||||
| chr2:206059363 | AG | A | 19 | a0001c0003t0002g0127 a0001c0003t0002g0161 a0001c0003t0002g0172 others(16): Show |
19 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-2421delC | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059363 | |||||||
| chr2:206059740 | C | CGT | 9 | a0001c0001t0003g0048 a0001c0001t0003g0069 a0001c0001t0003g0070 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-2799_219-2798d others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206059740 | |||||||
| chr2:206060017 | A | C | 1 | a0001c0003t0002g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218+2782T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060017 | |||||||
| chr2:206060056 | C | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218+2743G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060056 | |||||||
| chr2:206060155 | C | T | 25 | a0001c0001t0003g0002 a0001c0001t0003g0049 a0001c0001t0003g0052 others(22): Show |
26 | HG00673.hp2 HG02132.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.218+2644G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060155 | |||||||
| chr2:206060156 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218+2643C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060156 | |||||||
| chr2:206060313 | A | C | 2 | a0002c0002t0001g0104 a0002c0002t0001g0196 |
2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.218+2486T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060313 | |||||||
| chr2:206060394 | G | A | 4 | a0002c0002t0001g0098 a0002c0002t0001g0145 a0002c0002t0001g0155 others(1): Show |
4 | HG01081.hp2 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+2405C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060394 | |||||||
| chr2:206060472 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.218+2327G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060472 | |||||||
| chr2:206060532 | CA | C | 115 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(112): Show |
115 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.218+2266delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060532 | |||||||
| chr2:206060542 | A | C | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+2257T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060542 | |||||||
| chr2:206060564 | C | CT | 100 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(97): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.218+2234dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060564 | |||||||
| chr2:206060582 | C | T | 10 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(7): Show |
10 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+2217G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060582 | |||||||
| chr2:206060588 | T | C | 3 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 |
3 | NA18951.hp2 NA18977.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.218+2211A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060588 | |||||||
| chr2:206060621 | C | T | 1 | a0003c0007t0045g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.218+2178G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060621 | |||||||
| chr2:206060646 | C | T | 1 | a0001c0003t0002g0274 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.218+2153G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060646 | |||||||
| chr2:206060752 | G | T | 2 | a0001c0003t0014g0204 a0001c0003t0014g0207 |
2 | NA18945.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.218+2047C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060752 | |||||||
| chr2:206060825 | G | T | 3 | a0001c0001t0009g0288 a0001c0001t0009g0289 a0001c0001t0009g0290 |
3 | HG02055.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218+1974C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206060825 | |||||||
| chr2:206061021 | C | CT | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1777dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061021 | |||||||
| chr2:206061030 | T | A | 114 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(111): Show |
114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.218+1769A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061030 | |||||||
| chr2:206061051 | T | C | 1 | a0002c0002t0001g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.218+1748A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061051 | |||||||
| chr2:206061138 | A | G | 89 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(86): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.218+1661T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061138 | |||||||
| chr2:206061223 | G | C | 1 | a0001c0001t0004g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.218+1576C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061223 | |||||||
| chr2:206061234 | ACTC | A | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.218+1562_218+1564d others(5): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206061234 | |||||||
| chr2:206062075 | A | G | 1 | a0001c0001t0038g0243 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.218+724T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062075 | |||||||
| chr2:206062105 | G | C | 1 | a0002c0002t0001g0106 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.218+694C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062105 | |||||||
| chr2:206062186 | A | G | 10 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(7): Show |
11 | HG02451.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+613T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062186 | |||||||
| chr2:206062316 | T | C | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+483A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062316 | |||||||
| chr2:206062495 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.218+304A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062495 | |||||||
| chr2:206062633 | T | C | 1 | a0002c0016t0036g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.218+166A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062633 | |||||||
| chr2:206062671 | T | C | 2 | a0001c0001t0003g0070 a0001c0001t0003g0073 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.218+128A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062671 | |||||||
| chr2:206062711 | CAGAAGAA others(3): Show |
C | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.218+78_218+87delCT others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 3/10 | chr2 | 206062711 | |||||||
| chr2:206063091 | A | C | 1 | a0001c0001t0013g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29-46T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 2/10 | chr2 | 206063091 | |||||||
| chr2:206063126 | G | A | 86 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(83): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-30+25C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 2/10 | chr2 | 206063126 | |||||||
| chr2:206063429 | C | T | 1 | a0001c0003t0002g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-123-185G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063429 | |||||||
| chr2:206063438 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123-194G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063438 | |||||||
| chr2:206063439 | G | A | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-195C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063439 | |||||||
| chr2:206063452 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-208C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063452 | |||||||
| chr2:206063528 | T | C | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-284A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063528 | |||||||
| chr2:206063544 | C | A | 220 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-123-300G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063544 | |||||||
| chr2:206063668 | T | C | 4 | a0001c0003t0002g0250 a0001c0003t0002g0258 a0001c0003t0002g0260 others(1): Show |
4 | HG01361.hp1 HG01515.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123-424A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063668 | |||||||
| chr2:206063856 | T | C | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-612A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063856 | |||||||
| chr2:206063892 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-123-648T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206063892 | |||||||
| chr2:206064078 | A | G | 78 | a0001c0003t0002g0127 a0001c0003t0002g0161 a0001c0003t0002g0172 others(75): Show |
78 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-123-834T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064078 | |||||||
| chr2:206064446 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-1202A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064446 | |||||||
| chr2:206064817 | GA | G | 86 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(83): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-123-1574delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064817 | |||||||
| chr2:206064878 | GA | G | 45 | a0001c0003t0002g0213 a0001c0003t0002g0216 a0001c0003t0002g0225 others(42): Show |
45 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-123-1635delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206064878 | |||||||
| chr2:206065220 | CAGCACTT others(5243): Show |
C | 1 | a0001c0001t0018g0009 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-123-7226_-123-197 others(4): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065220 | |||||||
| chr2:206065267 | G | A | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-123-2023C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065267 | |||||||
| chr2:206065426 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0024g0014 |
2 | HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-123-2182C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065426 | |||||||
| chr2:206065536 | T | A | 1 | a0001c0001t0022g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-123-2292A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065536 | |||||||
| chr2:206065974 | C | T | 320 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(317): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-123-2730G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065974 | |||||||
| chr2:206065998 | G | A | 116 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(113): Show |
116 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-123-2754C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206065998 | |||||||
| chr2:206066048 | T | G | 3 | a0001c0004t0007g0295 a0001c0004t0007g0297 a0001c0004t0007g0299 |
3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-123-2804A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066048 | |||||||
| chr2:206066093 | C | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(23): Show |
27 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-123-2849G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066093 | |||||||
| chr2:206066132 | C | T | 2 | a0001c0001t0003g0072 a0001c0001t0003g0079 |
2 | HG00140.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-123-2888G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066132 | |||||||
| chr2:206066154 | A | G | 217 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(214): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-123-2910T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066154 | |||||||
| chr2:206066207 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123-2963C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066207 | |||||||
| chr2:206066250 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-3006A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066250 | |||||||
| chr2:206066322 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-123-3078G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066322 | |||||||
| chr2:206066534 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(23): Show |
27 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-123-3290C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066534 | |||||||
| chr2:206066760 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-3516C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066760 | |||||||
| chr2:206066804 | C | CA | 105 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(102): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-123-3561dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066804 | |||||||
| chr2:206066804 | CA | C | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-3561delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066804 | |||||||
| chr2:206066949 | CAT | C | 100 | a0001c0001t0002g0034 a0001c0001t0003g0002 a0001c0001t0003g0040 others(97): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-123-3707_-123-370 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206066949 | |||||||
| chr2:206067030 | T | A | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-123-3786A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067030 | |||||||
| chr2:206067093 | C | CA | 217 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(214): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-123-3850dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067093 | |||||||
| chr2:206067219 | C | T | 1 | a0002c0002t0001g0095 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-123-3975G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067219 | |||||||
| chr2:206067312 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-4068A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067312 | |||||||
| chr2:206067451 | G | A | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-123-4207C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067451 | |||||||
| chr2:206067597 | TA | T | 86 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0001c0006t0001g0189 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-123-4354delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067597 | |||||||
| chr2:206067716 | T | G | 220 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.-123-4472A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067716 | |||||||
| chr2:206067756 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0055 a0001c0001t0003g0075 |
4 | NA18977.hp2 NA18983.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123-4512G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067756 | |||||||
| chr2:206067759 | A | G | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-123-4515T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206067759 | |||||||
| chr2:206068040 | T | C | 2 | a0002c0002t0001g0097 a0002c0002t0001g0139 |
2 | HG00423.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-123-4796A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068040 | |||||||
| chr2:206068132 | C | T | 5 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(2): Show |
5 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-4888G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068132 | |||||||
| chr2:206068200 | A | G | 160 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(157): Show |
162 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-123-4956T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068200 | |||||||
| chr2:206068291 | G | C | 3 | a0001c0001t0009g0301 a0001c0001t0009g0302 a0001c0001t0009g0328 |
3 | HG02145.hp1 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-123-5047C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068291 | |||||||
| chr2:206068506 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-123-5262G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068506 | |||||||
| chr2:206068795 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-123-5551C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206068795 | |||||||
| chr2:206069266 | A | G | 1 | a0002c0010t0055g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-123-6022T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069266 | |||||||
| chr2:206069463 | T | C | 1 | a0001c0003t0002g0253 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-123-6219A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069463 | |||||||
| chr2:206069731 | C | T | 3 | a0001c0001t0031g0324 a0001c0001t0041g0291 a0001c0001t0042g0031 |
3 | HG02970.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123-6487G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206069731 | |||||||
| chr2:206070006 | G | A | 80 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(77): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-123-6762C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070006 | |||||||
| chr2:206070007 | T | A | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6763A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070007 | |||||||
| chr2:206070009 | C | A | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6765G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070009 | |||||||
| chr2:206070010 | A | T | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6766T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070010 | |||||||
| chr2:206070014 | C | G | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6770G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070014 | |||||||
| chr2:206070022 | C | T | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-123-6778G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070022 | |||||||
| chr2:206070177 | G | A | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-6933C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070177 | |||||||
| chr2:206070449 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-7205C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070449 | |||||||
| chr2:206070470 | T | C | 211 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(208): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-123-7226A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070470 | |||||||
| chr2:206070775 | G | T | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-7531C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070775 | |||||||
| chr2:206070880 | G | A | 87 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(84): Show |
87 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-123-7636C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070880 | |||||||
| chr2:206070889 | A | AT | 97 | a0001c0001t0002g0034 a0001c0001t0002g0309 a0001c0001t0003g0238 others(94): Show |
99 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.-123-7646dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | |||||||
| chr2:206070889 | A | ATT | 12 | a0001c0001t0009g0302 a0001c0001t0009g0328 a0001c0001t0013g0032 others(9): Show |
12 | HG01978.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-123-7647_-123-764 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | |||||||
| chr2:206070889 | AT | A | 14 | a0001c0001t0005g0303 a0001c0004t0007g0278 a0001c0004t0007g0279 others(11): Show |
14 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-123-7646delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | |||||||
| chr2:206070889 | ATTT | A | 51 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-123-7648_-123-764 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206070889 | |||||||
| chr2:206071011 | G | A | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-123-7767C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071011 | |||||||
| chr2:206071254 | G | A | 2 | a0001c0001t0012g0085 a0001c0001t0012g0087 |
2 | NA18971.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-123-8010C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071254 | |||||||
| chr2:206071257 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0012g0087 a0002c0002t0001g0186 a0002c0002t0010g0110 others(2): Show |
5 | HG03239.hp2 HG04199.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-8023_-123-801 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(4): Show |
C | 5 | a0002c0002t0001g0092 a0002c0002t0001g0095 a0002c0002t0001g0107 others(2): Show |
5 | HG01069.hp2 HG01168.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8024_-123-801 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(5): Show |
C | 4 | a0002c0002t0001g0093 a0002c0002t0001g0104 a0002c0002t0001g0197 others(1): Show |
4 | HG00140.hp2 HG01346.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123-8025_-123-801 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0012g0085 a0002c0002t0001g0106 a0002c0002t0035g0118 others(2): Show |
5 | HG02698.hp2 HG03654.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8026_-123-801 others(17): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0003g0052 a0001c0001t0012g0081 a0001c0001t0022g0035 others(2): Show |
5 | HG01074.hp1 HG03579.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123-8027_-123-801 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(8): Show |
C | 6 | a0001c0006t0001g0111 a0001c0006t0001g0123 a0002c0002t0001g0122 others(3): Show |
6 | HG00738.hp2 NA18944.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-123-8028_-123-801 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0003t0002g0200 others(6): Show |
9 | HG01071.hp2 HG01081.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123-8029_-123-801 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(10): Show |
C | 46 | a0001c0001t0003g0049 a0001c0001t0021g0047 a0001c0001t0021g0054 others(43): Show |
47 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-123-8030_-123-801 others(21): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(11): Show |
C | 33 | a0001c0001t0003g0051 a0001c0001t0003g0055 a0001c0001t0003g0056 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.-123-8031_-123-801 others(22): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(12): Show |
C | 19 | a0001c0001t0003g0002 a0001c0001t0003g0041 a0001c0001t0003g0042 others(16): Show |
20 | HG00741.hp2 HG01099.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-123-8032_-123-801 others(23): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(13): Show |
C | 12 | a0001c0001t0003g0040 a0001c0001t0003g0043 a0001c0001t0003g0048 others(9): Show |
12 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.-123-8033_-123-801 others(24): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(14): Show |
C | 4 | a0001c0001t0013g0032 a0002c0002t0001g0157 a0002c0002t0001g0184 others(1): Show |
4 | HG00735.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123-8034_-123-801 others(25): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0034 a0002c0002t0001g0185 |
2 | HG00280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-123-8035_-123-801 others(26): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0013g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-123-8036_-123-801 others(27): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0016g0281 a0001c0001t0016g0282 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-8037_-123-801 others(28): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(18): Show |
C | 3 | a0002c0002t0001g0099 a0002c0002t0001g0194 a0002c0002t0001g0199 |
3 | HG02559.hp1 HG02735.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-123-8038_-123-801 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(22): Show |
C | 2 | a0002c0002t0001g0176 a0002c0002t0001g0187 |
2 | HG00438.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-123-8042_-123-801 others(33): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(23): Show |
C | 1 | a0002c0002t0001g0202 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-123-8043_-123-801 others(34): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(25): Show |
C | 8 | a0001c0001t0041g0291 a0001c0001t0042g0031 a0001c0003t0002g0206 others(5): Show |
8 | HG02486.hp2 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-123-8045_-123-801 others(36): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(26): Show |
C | 17 | a0001c0001t0008g0317 a0001c0001t0030g0063 a0001c0003t0002g0203 others(14): Show |
17 | HG00673.hp1 HG01106.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-123-8046_-123-801 others(37): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(27): Show |
C | 65 | a0001c0001t0003g0238 a0001c0001t0008g0004 a0001c0001t0008g0319 others(62): Show |
66 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123-8047_-123-801 others(38): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(28): Show |
C | 5 | a0001c0001t0004g0027 a0001c0003t0002g0258 a0001c0003t0017g0263 others(2): Show |
5 | HG01891.hp2 HG02148.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123-8048_-123-801 others(39): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(29): Show |
C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(32): Show |
36 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-123-8049_-123-801 others(40): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(30): Show |
C | 3 | a0001c0001t0027g0010 a0002c0002t0001g0167 a0002c0016t0036g0113 |
3 | HG01256.hp2 HG02165.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-123-8050_-123-801 others(41): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(33): Show |
C | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-8053_-123-801 others(44): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(35): Show |
C | 1 | a0002c0002t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-123-8055_-123-801 others(46): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(37): Show |
C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-123-8057_-123-801 others(48): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071257 | CTTTTTTT others(38): Show |
C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-8058_-123-801 others(49): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071257 | |||||||
| chr2:206071746 | C | T | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-123-8502G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071746 | |||||||
| chr2:206071820 | C | T | 1 | a0001c0001t0022g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-123-8576G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206071820 | |||||||
| chr2:206072270 | G | A | 2 | a0001c0003t0002g0258 a0001c0003t0002g0260 |
2 | HG01361.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-123-9026C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072270 | |||||||
| chr2:206072285 | G | GT | 26 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0003g0091 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-123-9042dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072285 | |||||||
| chr2:206072364 | C | T | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-9120G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072364 | |||||||
| chr2:206072533 | C | T | 2 | a0001c0003t0002g0233 a0001c0003t0007g0237 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-123-9289G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072533 | |||||||
| chr2:206072570 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123-9326C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072570 | |||||||
| chr2:206072763 | C | T | 2 | a0002c0002t0010g0322 a0002c0002t0046g0323 |
2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-123-9519G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072763 | |||||||
| chr2:206072846 | C | CTT | 84 | a0001c0001t0003g0238 a0001c0003t0002g0161 a0001c0003t0002g0205 others(81): Show |
84 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-123-9604_-123-960 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072846 | |||||||
| chr2:206072846 | CT | C | 21 | a0001c0001t0002g0034 a0001c0001t0003g0040 a0001c0001t0003g0050 others(18): Show |
21 | HG00323.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-123-9603delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072846 | |||||||
| chr2:206072896 | G | A | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-123-9652C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206072896 | |||||||
| chr2:206073454 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-123-10210T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073454 | |||||||
| chr2:206073481 | T | A | 84 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-123-10237A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073481 | |||||||
| chr2:206073551 | G | T | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10307C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073551 | |||||||
| chr2:206073799 | G | A | 2 | a0001c0003t0002g0236 a0001c0003t0002g0239 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-123-10555C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073799 | |||||||
| chr2:206073915 | T | C | 1 | a0002c0002t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-123-10671A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073915 | |||||||
| chr2:206073984 | C | T | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-10740G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206073984 | |||||||
| chr2:206074033 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-123-10789C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074033 | |||||||
| chr2:206074061 | C | A | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10817G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074061 | |||||||
| chr2:206074115 | AGAC | A | 3 | a0001c0004t0007g0295 a0001c0004t0007g0297 a0001c0004t0007g0299 |
3 | HG00639.hp2 HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-123-10874_-123-10 others(9): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074115 | |||||||
| chr2:206074183 | C | T | 3 | a0001c0001t0016g0281 a0001c0001t0016g0282 a0005c0015t0016g0283 |
3 | HG02257.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-123-10939G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074183 | |||||||
| chr2:206074271 | C | T | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-123-11027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074271 | |||||||
| chr2:206074278 | A | C | 1 | a0002c0016t0036g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-123-11034T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074278 | |||||||
| chr2:206074352 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-123-11108C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074352 | |||||||
| chr2:206074563 | G | A | 1 | a0003c0007t0045g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-123-11319C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074563 | |||||||
| chr2:206074671 | G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-124+11230C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074671 | |||||||
| chr2:206074726 | G | A | 2 | a0001c0001t0041g0291 a0001c0001t0042g0031 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-124+11175C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206074726 | |||||||
| chr2:206075039 | C | CAAAAA | 96 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0003g0002 others(93): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-124+10857_-124+10 others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAA | 16 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0005g0088 others(13): Show |
16 | HG00558.hp1 HG00642.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-124+10856_-124+10 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA | 67 | a0001c0001t0003g0238 a0001c0001t0005g0308 a0001c0001t0005g0310 others(64): Show |
67 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-124+10855_-124+10 others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(1): Show |
7 | a0001c0003t0002g0233 a0001c0003t0002g0245 a0001c0003t0006g0211 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10854_-124+10 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(3): Show |
1 | a0001c0004t0037g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-124+10852_-124+10 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0013g0037 a0001c0001t0041g0291 a0001c0001t0042g0031 |
3 | HG02970.hp2 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-124+10850_-124+10 others(18): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10849_-124+10 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0013g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-124+10848_-124+10 others(20): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(27): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(16): Show |
2 | a0004c0009t0007g0296 a0004c0009t0011g0294 |
2 | HG01257.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(29): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(17): Show |
2 | a0001c0004t0007g0295 a0001c0004t0007g0297 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(30): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(19): Show |
1 | a0001c0004t0011g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(32): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(22): Show |
2 | a0001c0004t0007g0278 a0001c0004t0007g0292 |
2 | HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(35): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(24): Show |
1 | a0001c0004t0007g0279 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-124+10861_-124+10 others(37): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075039 | C | CAAAAAAA others(25): Show |
2 | a0001c0004t0007g0299 a0001c0004t0011g0298 |
2 | HG01243.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-124+10861_-124+10 others(38): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075039 | |||||||
| chr2:206075094 | T | C | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+10807A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075094 | |||||||
| chr2:206075438 | A | AT | 78 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(75): Show |
81 | HG00323.hp2 HG00673.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.-124+10462dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075438 | |||||||
| chr2:206075438 | AT | A | 6 | a0001c0003t0002g0223 a0002c0002t0001g0162 a0002c0002t0001g0163 others(3): Show |
6 | HG00558.hp2 HG00639.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+10462delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075438 | |||||||
| chr2:206075499 | C | T | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-124+10402G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075499 | |||||||
| chr2:206075505 | T | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+10396A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075505 | |||||||
| chr2:206075524 | C | T | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+10377G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075524 | |||||||
| chr2:206075547 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-124+10354G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075547 | |||||||
| chr2:206075626 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+10275C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075626 | |||||||
| chr2:206075690 | G | A | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+10211C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075690 | |||||||
| chr2:206075829 | G | A | 1 | a0001c0001t0022g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-124+10072C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206075829 | |||||||
| chr2:206076051 | C | CA | 6 | a0001c0001t0002g0309 a0001c0001t0005g0089 a0001c0001t0009g0302 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+9849dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | |||||||
| chr2:206076051 | CA | C | 66 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(63): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-124+9849delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | |||||||
| chr2:206076051 | CAA | C | 29 | a0001c0001t0003g0051 a0001c0001t0004g0001 a0001c0001t0004g0012 others(26): Show |
30 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-124+9848_-124+984 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076051 | |||||||
| chr2:206076114 | G | A | 1 | a0001c0001t0042g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-124+9787C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076114 | |||||||
| chr2:206076155 | T | C | 1 | a0001c0001t0022g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-124+9746A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076155 | |||||||
| chr2:206076298 | G | A | 9 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(6): Show |
9 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-124+9603C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076298 | |||||||
| chr2:206076498 | A | T | 1 | a0001c0003t0002g0216 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-124+9403T>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076498 | |||||||
| chr2:206076646 | C | T | 1 | a0001c0006t0001g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-124+9255G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076646 | |||||||
| chr2:206076856 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG01081.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-124+9045C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076856 | |||||||
| chr2:206076937 | T | G | 1 | a0001c0001t0008g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-124+8964A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076937 | |||||||
| chr2:206076961 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+8940A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076961 | |||||||
| chr2:206076977 | T | C | 90 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(87): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-124+8924A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206076977 | |||||||
| chr2:206077056 | G | A | 87 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(84): Show |
87 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.-124+8845C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077056 | |||||||
| chr2:206077072 | G | A | 1 | a0001c0003t0002g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-124+8829C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077072 | |||||||
| chr2:206077253 | T | C | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+8648A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077253 | |||||||
| chr2:206077262 | C | T | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-124+8639G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077262 | |||||||
| chr2:206077308 | C | T | 1 | a0002c0002t0010g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-124+8593G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077308 | |||||||
| chr2:206077334 | T | C | 1 | a0001c0003t0014g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+8567A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077334 | |||||||
| chr2:206077339 | C | CA | 28 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0238 others(25): Show |
29 | HG00438.hp1 HG01981.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.-124+8561dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077339 | |||||||
| chr2:206077353 | C | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+8548G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077353 | |||||||
| chr2:206077801 | G | A | 1 | a0002c0002t0056g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-124+8100C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206077801 | |||||||
| chr2:206078061 | C | CA | 55 | a0001c0001t0002g0034 a0001c0001t0004g0001 a0001c0001t0004g0012 others(52): Show |
57 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+7839dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAA | 11 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0074 others(8): Show |
11 | HG00323.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-124+7838_-124+783 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAA | 39 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0042 others(36): Show |
40 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-124+7837_-124+783 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAA | 13 | a0001c0001t0003g0041 a0001c0001t0003g0043 a0001c0001t0003g0069 others(10): Show |
13 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-124+7836_-124+783 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAA | 8 | a0001c0003t0061g0212 a0001c0004t0007g0278 a0001c0004t0007g0292 others(5): Show |
8 | HG01175.hp1 HG01243.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-124+7834_-124+783 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA | 8 | a0001c0003t0002g0225 a0001c0003t0002g0226 a0001c0003t0002g0227 others(5): Show |
8 | HG01891.hp2 HG02135.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-124+7833_-124+783 others(11): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA others(1): Show |
20 | a0001c0003t0002g0213 a0001c0003t0002g0216 a0001c0003t0002g0229 others(17): Show |
20 | HG00621.hp2 HG01070.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-124+7832_-124+783 others(12): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA others(2): Show |
27 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(24): Show |
27 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-124+7831_-124+783 others(13): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA others(3): Show |
14 | a0001c0003t0002g0206 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG01884.hp1 HG01981.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-124+7830_-124+783 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA others(4): Show |
5 | a0001c0003t0002g0258 a0001c0003t0002g0271 a0001c0003t0006g0269 others(2): Show |
5 | HG03098.hp2 HG03654.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-124+7829_-124+783 others(15): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | C | CAAAAAAA others(5): Show |
1 | a0001c0003t0002g0270 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-124+7828_-124+783 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | CA | C | 9 | a0001c0001t0005g0090 a0001c0001t0005g0310 a0001c0001t0009g0302 others(6): Show |
9 | HG00423.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-124+7839delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | CAA | C | 17 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(14): Show |
17 | HG00558.hp1 HG00642.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-124+7838_-124+783 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0016g0281 a0001c0001t0016g0282 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-124+7830_-124+783 others(14): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078061 | CAAAAAAA others(8): Show |
C | 1 | a0002c0017t0052g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-124+7825_-124+783 others(19): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078061 | |||||||
| chr2:206078211 | A | G | 1 | a0002c0002t0001g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-124+7690T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078211 | |||||||
| chr2:206078275 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-124+7626C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078275 | |||||||
| chr2:206078290 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+7611C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078290 | |||||||
| chr2:206078341 | G | A | 4 | a0002c0002t0001g0102 a0002c0002t0001g0180 a0002c0002t0001g0188 others(1): Show |
4 | NA18947.hp2 NA18964.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+7560C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078341 | |||||||
| chr2:206078520 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-124+7381C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078520 | |||||||
| chr2:206078521 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-124+7380C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078521 | |||||||
| chr2:206078648 | CA | C | 88 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(85): Show |
88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+7252delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078648 | |||||||
| chr2:206078685 | G | A | 88 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(85): Show |
88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+7216C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078685 | |||||||
| chr2:206078874 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0077 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-124+7027G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078874 | |||||||
| chr2:206078895 | C | G | 1 | a0001c0003t0014g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+7006G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078895 | |||||||
| chr2:206078898 | A | G | 1 | a0001c0003t0014g0275 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-124+7003T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206078898 | |||||||
| chr2:206079226 | C | T | 1 | a0001c0011t0043g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-124+6675G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079226 | |||||||
| chr2:206079269 | C | T | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+6632G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079269 | |||||||
| chr2:206079305 | T | C | 88 | a0001c0001t0003g0238 a0001c0003t0002g0203 a0001c0003t0002g0205 others(85): Show |
88 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-124+6596A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079305 | |||||||
| chr2:206079813 | C | T | 1 | a0001c0003t0006g0247 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-124+6088G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206079813 | |||||||
| chr2:206080089 | C | T | 1 | a0002c0002t0001g0107 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-124+5812G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080089 | |||||||
| chr2:206080304 | G | A | 24 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+5597C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080304 | |||||||
| chr2:206080345 | C | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+5556G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080345 | |||||||
| chr2:206080351 | G | C | 214 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(211): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-124+5550C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080351 | |||||||
| chr2:206080390 | G | A | 1 | a0001c0001t0012g0087 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-124+5511C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080390 | |||||||
| chr2:206080630 | G | A | 89 | a0001c0001t0003g0238 a0001c0001t0038g0243 a0001c0003t0002g0203 others(86): Show |
89 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-124+5271C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080630 | |||||||
| chr2:206080652 | T | A | 4 | a0001c0001t0003g0075 a0001c0001t0005g0311 a0001c0001t0005g0312 others(1): Show |
4 | HG00621.hp2 NA18947.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5249A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080652 | |||||||
| chr2:206080692 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-124+5209C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080692 | |||||||
| chr2:206080702 | C | T | 1 | a0001c0001t0032g0046 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-124+5199G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080702 | |||||||
| chr2:206080724 | G | A | 67 | a0001c0001t0003g0002 a0001c0001t0003g0238 a0001c0001t0038g0243 others(64): Show |
68 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-124+5177C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080724 | |||||||
| chr2:206080724 | G | C | 1 | a0001c0001t0005g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-124+5177C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080724 | |||||||
| chr2:206080735 | G | A | 1 | a0007c0014t0003g0076 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-124+5166C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080735 | |||||||
| chr2:206080858 | G | C | 4 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(1): Show |
4 | HG01123.hp2 HG03710.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5043C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080858 | |||||||
| chr2:206080859 | T | C | 4 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(1): Show |
4 | HG01123.hp2 HG03710.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-124+5042A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080859 | |||||||
| chr2:206080879 | G | A | 1 | a0001c0001t0005g0313 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-124+5022C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080879 | |||||||
| chr2:206080902 | C | CA | 24 | a0001c0001t0005g0303 a0001c0003t0002g0200 a0001c0003t0002g0245 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.-124+4998dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | |||||||
| chr2:206080902 | C | CAA | 18 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(15): Show |
18 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.-124+4997_-124+499 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | |||||||
| chr2:206080902 | C | CAAA | 12 | a0001c0001t0002g0034 a0001c0001t0005g0089 a0001c0001t0005g0090 others(9): Show |
13 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-124+4996_-124+499 others(7): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | |||||||
| chr2:206080902 | C | CAAAA | 6 | a0001c0001t0008g0321 a0001c0001t0013g0036 a0001c0001t0022g0033 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+4995_-124+499 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | |||||||
| chr2:206080902 | CA | C | 79 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(76): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-124+4998delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080902 | |||||||
| chr2:206080928 | G | A | 23 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-124+4973C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080928 | |||||||
| chr2:206080931 | T | A | 2 | a0001c0001t0005g0314 a0001c0001t0005g0316 |
2 | HG00558.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-124+4970A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206080931 | |||||||
| chr2:206081177 | A | G | 1 | a0002c0005t0040g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-124+4724T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081177 | |||||||
| chr2:206081363 | T | C | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-124+4538A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081363 | |||||||
| chr2:206081528 | G | A | 1 | a0001c0006t0001g0189 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-124+4373C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081528 | |||||||
| chr2:206081612 | G | T | 54 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(51): Show |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-124+4289C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081612 | |||||||
| chr2:206081672 | A | C | 12 | a0001c0004t0007g0278 a0001c0004t0007g0279 a0001c0004t0007g0292 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-124+4229T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081672 | |||||||
| chr2:206081688 | T | G | 6 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+4213A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081688 | |||||||
| chr2:206081756 | C | CA | 33 | a0001c0001t0004g0001 a0001c0001t0004g0013 a0001c0001t0004g0015 others(30): Show |
34 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-124+4144dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081756 | |||||||
| chr2:206081768 | A | AAAAG | 50 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.-124+4129_-124+413 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081768 | |||||||
| chr2:206081768 | AAAAGAAA others(5): Show |
A | 23 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-124+4121_-124+413 others(16): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081768 | |||||||
| chr2:206081817 | T | G | 77 | a0001c0001t0003g0238 a0001c0001t0038g0243 a0001c0003t0002g0203 others(74): Show |
77 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-124+4084A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081817 | |||||||
| chr2:206081838 | A | G | 1 | a0002c0002t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-124+4063T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081838 | |||||||
| chr2:206081873 | A | G | 2 | a0002c0002t0001g0104 a0002c0002t0001g0196 |
2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-124+4028T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081873 | |||||||
| chr2:206081935 | C | T | 54 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(51): Show |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-124+3966G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081935 | |||||||
| chr2:206081970 | A | G | 3 | a0001c0003t0002g0213 a0001c0003t0061g0212 a0002c0002t0001g0195 |
3 | HG00621.hp1 NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-124+3931T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206081970 | |||||||
| chr2:206082107 | G | A | 1 | a0001c0004t0037g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-124+3794C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082107 | |||||||
| chr2:206082247 | G | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+3654C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082247 | |||||||
| chr2:206082332 | T | C | 1 | a0001c0001t0041g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-124+3569A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082332 | |||||||
| chr2:206082387 | C | T | 6 | a0001c0001t0015g0007 a0001c0001t0015g0008 a0001c0001t0015g0011 others(3): Show |
6 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-124+3514G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082387 | |||||||
| chr2:206082442 | T | C | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+3459A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082442 | |||||||
| chr2:206082697 | C | A | 1 | a0001c0003t0054g0261 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-124+3204G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082697 | |||||||
| chr2:206082847 | A | G | 23 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0005g0088 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-124+3054T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082847 | |||||||
| chr2:206082929 | T | A | 1 | a0001c0004t0011g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-124+2972A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206082929 | |||||||
| chr2:206083400 | G | T | 88 | a0001c0001t0003g0238 a0001c0001t0038g0243 a0001c0003t0002g0203 others(85): Show |
88 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.-124+2501C>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083400 | |||||||
| chr2:206083440 | T | C | 1 | a0001c0003t0002g0272 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-124+2461A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083440 | |||||||
| chr2:206083530 | C | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-124+2371G>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083530 | |||||||
| chr2:206083535 | C | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+2366G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083535 | |||||||
| chr2:206083627 | A | G | 2 | a0001c0008t0019g0284 a0001c0008t0019g0285 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-124+2274T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083627 | |||||||
| chr2:206083682 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-124+2219G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083682 | |||||||
| chr2:206083824 | A | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+2077T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083824 | |||||||
| chr2:206083860 | C | CA | 73 | a0001c0001t0003g0091 a0001c0001t0003g0238 a0001c0001t0013g0037 others(70): Show |
73 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-124+2040dupT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | |||||||
| chr2:206083860 | C | CAA | 19 | a0001c0003t0002g0249 a0001c0003t0002g0250 a0001c0003t0002g0253 others(16): Show |
19 | HG00673.hp1 HG01175.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-124+2039_-124+204 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | |||||||
| chr2:206083860 | CA | C | 54 | a0001c0001t0002g0287 a0001c0001t0002g0309 a0001c0001t0004g0001 others(51): Show |
55 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-124+2040delT | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206083860 | |||||||
| chr2:206084074 | C | CT | 28 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(25): Show |
29 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-124+1826dupA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084074 | |||||||
| chr2:206084086 | T | G | 1 | a0001c0003t0002g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-124+1815A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084086 | |||||||
| chr2:206084213 | AT | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0012 a0001c0001t0004g0013 others(24): Show |
28 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-124+1687delA | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084213 | |||||||
| chr2:206084215 | T | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+1686A>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084215 | |||||||
| chr2:206084238 | CAT | C | 3 | a0001c0001t0022g0033 a0001c0001t0041g0291 a0001c0001t0042g0031 |
3 | HG01109.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-124+1661_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084238 | |||||||
| chr2:206084240 | T | C | 4 | a0001c0001t0002g0034 a0001c0001t0013g0036 a0001c0001t0013g0037 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-124+1661A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084240 | T | TAC | 12 | a0001c0001t0005g0315 a0001c0003t0002g0200 a0001c0004t0011g0293 others(9): Show |
12 | HG00140.hp2 HG00621.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-124+1659_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084240 | T | TACAC | 9 | a0001c0004t0007g0295 a0001c0004t0007g0297 a0001c0004t0007g0299 others(6): Show |
9 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-124+1657_-124+166 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084240 | TAC | T | 38 | a0001c0001t0002g0287 a0001c0001t0003g0086 a0001c0001t0004g0001 others(35): Show |
39 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-124+1659_-124+166 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084240 | TACAC | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+1657_-124+166 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084240 | TACACAC | T | 13 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(10): Show |
14 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-124+1655_-124+166 others(10): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084240 | |||||||
| chr2:206084271 | A | ACC | 7 | a0001c0003t0002g0203 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG03669.hp2 NA18945.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+1629_-124+163 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084271 | |||||||
| chr2:206084273 | A | ACACC | 13 | a0001c0003t0002g0264 a0001c0003t0002g0266 a0001c0003t0002g0270 others(10): Show |
13 | HG01123.hp2 HG02486.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.-124+1627_-124+162 others(8): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | |||||||
| chr2:206084273 | A | ACC | 55 | a0001c0001t0003g0238 a0001c0001t0038g0243 a0001c0003t0002g0213 others(52): Show |
55 | HG00099.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-124+1626_-124+162 others(6): Show |
INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | |||||||
| chr2:206084273 | A | C | 10 | a0001c0003t0002g0203 a0001c0003t0002g0205 a0001c0003t0002g0206 others(7): Show |
10 | HG01074.hp1 HG02523.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-124+1628T>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084273 | |||||||
| chr2:206084354 | T | C | 1 | a0001c0003t0006g0277 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-124+1547A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084354 | |||||||
| chr2:206084527 | A | G | 76 | a0001c0001t0003g0238 a0001c0001t0038g0243 a0001c0003t0002g0203 others(73): Show |
76 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-124+1374T>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084527 | |||||||
| chr2:206084617 | G | A | 1 | a0001c0001t0003g0091 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-124+1284C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084617 | |||||||
| chr2:206084684 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-124+1217G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084684 | |||||||
| chr2:206084819 | T | C | 1 | a0001c0001t0005g0316 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-124+1082A>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084819 | |||||||
| chr2:206084929 | G | A | 16 | a0001c0001t0002g0309 a0001c0001t0005g0303 a0001c0001t0005g0306 others(13): Show |
16 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.-124+972C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206084929 | |||||||
| chr2:206085136 | G | A | 6 | a0001c0001t0008g0004 a0001c0001t0008g0317 a0001c0001t0008g0319 others(3): Show |
7 | HG02451.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+765C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085136 | |||||||
| chr2:206085163 | G | A | 215 | a0001c0001t0002g0034 a0001c0001t0002g0287 a0001c0001t0002g0309 others(212): Show |
218 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-124+738C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085163 | |||||||
| chr2:206085308 | T | G | 2 | a0002c0002t0010g0322 a0002c0002t0046g0323 |
2 | NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-124+593A>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085308 | |||||||
| chr2:206085366 | G | A | 1 | a0001c0001t0031g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-124+535C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085366 | |||||||
| chr2:206085445 | C | T | 8 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(5): Show |
8 | HG02135.hp2 NA18940.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.-124+456G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085445 | |||||||
| chr2:206085512 | G | C | 107 | a0001c0001t0003g0238 a0001c0001t0004g0001 a0001c0001t0004g0012 others(104): Show |
108 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.-124+389C>G | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085512 | |||||||
| chr2:206085526 | G | A | 3 | a0002c0005t0002g0326 a0002c0005t0006g0327 a0002c0005t0040g0325 |
3 | HG02109.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-124+375C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085526 | |||||||
| chr2:206085560 | G | A | 1 | a0001c0001t0009g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-124+341C>T | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085560 | |||||||
| chr2:206085594 | C | G | 56 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0041 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-124+307G>C | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085594 | |||||||
| chr2:206085602 | C | T | 7 | a0001c0001t0002g0034 a0001c0001t0013g0032 a0001c0001t0013g0036 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-124+299G>A | INO80D | ENSG00000114933.16 | transcript | ENST00000403263.6 | protein_coding | 1/10 | chr2 | 206085602 |