Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 125476 |
| ensemblid | ENSG00000153391.16 |
| hgncid | 26994 |
| symbol | INO80C |
| name | INO80 complex subunit C |
| refseq_nuc | NM_194281.4 |
| refseq_prot | NP_919257.2 |
| ensembl_nuc | ENST00000334598.12 |
| ensembl_prot | ENSP00000334473.6 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 35468333 |
| end | 35497960 |
| strand | - |
| ver | v1.2 |
| region | chr18:35468333-35497960 |
| region5000 | chr18:35463333-35502960 |
| regionname0 | INO80C_chr18_35468333_35497960 |
| regionname5000 | INO80C_chr18_35463333_35502960 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 192 | 389 | 89 | 66 | 174 | 10 | 48 | 138 | INO80C_chr18_35463333_35502960 | INO80C | MAAQI others(187): Show |
chr18 | 35463333 | 35502960 |
| a0002 | 0/0 | 192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | MAAQI others(187): Show |
chr18 | 35463333 | 35502960 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 579 | 384 | 85 | 66 | 173 | 10 | 48 | INO80C_chr18_35463333_35502960 | INO80C | ATGGC others(574): Show |
chr18 | 35463333 | 35502960 | ||
| a0001c0002 | 0/0 | 579 | 3 | 3 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATGGC others(574): Show |
chr18 | 35463333 | 35502960 | ||
| a0001c0004 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATGGC others(574): Show |
chr18 | 35463333 | 35502960 | ||
| a0001c0005 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATGGC others(574): Show |
chr18 | 35463333 | 35502960 | ||
| a0002c0003 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATGGC others(574): Show |
chr18 | 35463333 | 35502960 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 942 | 193 | 56 | 32 | 70 | 4 | 31 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0002 | 1/0 | 943 | 97 | 8 | 1 | 81 | 0 | 6 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0003 | 0/1 | 943 | 44 | 1 | 28 | 5 | 5 | 4 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0004 | 0/0 | 942 | 25 | 10 | 2 | 8 | 0 | 5 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0005 | 0/0 | 942 | 8 | 8 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0006 | 0/0 | 944 | 6 | 0 | 0 | 6 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(939): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0007 | 0/0 | 944 | 5 | 0 | 3 | 1 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(939): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0008 | 0/0 | 942 | 2 | 1 | 0 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0009 | 0/0 | 943 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0010 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0011 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0001t0012 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| a0001c0002t0002 | 0/0 | 943 | 3 | 3 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0001c0004t0002 | 0/0 | 943 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0001c0005t0002 | 0/0 | 943 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(938): Show |
chr18 | 35463333 | 35502960 |
| a0002c0003t0004 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | ATCAA others(937): Show |
chr18 | 35463333 | 35502960 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 2 | 9 | 1 | 4 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0003 | 0/0 | 10 | 1 | 1 | 8 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0009 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0011g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0001t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| a0002c0003t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | CLM | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | IBS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0053 | EUR | IBS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0259 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0176 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02083 | hp1 | a0001 | c0001 | t0010 | g0203 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0189 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CDX | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0055 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0187 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0120 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02922 | hp2 | a0002 | c0003 | t0004 | g0056 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03098 | hp1 | a0001 | c0004 | t0002 | g0195 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0215 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | BEB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | YRI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19006 | hp2 | a0001 | c0001 | t0011 | g0159 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19087 | hp1 | a0001 | c0005 | t0002 | g0064 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | TSI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0252 | EUR | TSI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | TSI | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0201 | SAS | GIH | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | USA | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | USA | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | USA | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | LWK | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0188 | REF | REF | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0234 | REF | REF | INO80C_chr18_35463333_35502960 | INO80C | chr18 | 35463333 | 35502960 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35497855 | A | G | 1 | a0002 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.20T>C | p.Ile7Thr | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/5 | 106/943 | 20/579 | 7/192 | chr18 | 35497855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35468620 | G | A | 1 | a0001c0004 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.570C>T | p.Ile190Ile | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 656/943 | 570/579 | 190/192 | chr18 | 35468620 | |||
| chr18:35468653 | G | A | 2 | a0001c0002 a0001c0004 |
4 | HG02622.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.537C>T | p.Thr179Thr | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 623/943 | 537/579 | 179/192 | chr18 | 35468653 | |||
| chr18:35468662 | G | A | 1 | a0001c0005 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.528C>T | p.Asp176Asp | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 614/943 | 528/579 | 176/192 | chr18 | 35468662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35468423 | T | G | 1 | a0001c0001t0012 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 188 | chr18 | 35468423 | ||||||
| chr18:35468437 | A | G | 3 | a0001c0001t0004 a0001c0001t0010 a0002c0003t0004 |
27 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*174T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 174 | chr18 | 35468437 | ||||||
| chr18:35468448 | T | TA | 2 | a0001c0001t0006 a0001c0001t0007 |
11 | HG01934.hp2 HG01978.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*162dupT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 162 | chr18 | 35468448 | ||||||
| chr18:35468448 | TA | T | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(5): Show |
232 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*162delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 162 | chr18 | 35468448 | ||||||
| chr18:35468555 | A | T | 1 | a0001c0001t0010 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 56 | chr18 | 35468555 | ||||||
| chr18:35468585 | T | G | 1 | a0001c0001t0011 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 26 | chr18 | 35468585 | ||||||
| chr18:35468587 | C | T | 1 | a0001c0001t0011 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 24 | chr18 | 35468587 | ||||||
| chr18:35468590 | C | T | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(4): Show |
85 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 5/5 | 21 | chr18 | 35468590 | ||||||
| chr18:35497875 | C | T | 1 | a0001c0001t0009 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/5 | 1 | chr18 | 35497875 | ||||||
| chr18:35497948 | C | T | 1 | a0001c0001t0008 | 2 | HG01516.hp1 HG02109.hp1 |
5_prime_UTR_variant | MODIFIER | c.-74G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/5 | 74 | chr18 | 35497948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:35468938 | G | A | 1 | a0001c0002t0002g0047 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-196C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35468938 | |||||||
| chr18:35468968 | A | G | 2 | a0001c0001t0005g0048 a0001c0001t0005g0199 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.448-226T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35468968 | |||||||
| chr18:35469037 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.448-295C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469037 | |||||||
| chr18:35469201 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.448-459G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469201 | |||||||
| chr18:35469356 | C | T | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-614G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469356 | |||||||
| chr18:35469357 | T | C | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-615A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469357 | |||||||
| chr18:35469382 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0093 a0001c0001t0001g0101 others(1): Show |
5 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-640A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469382 | |||||||
| chr18:35469715 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.448-973G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469715 | |||||||
| chr18:35469724 | T | C | 1 | a0001c0001t0004g0049 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.448-982A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469724 | |||||||
| chr18:35469745 | A | G | 1 | a0001c0001t0012g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.448-1003T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35469745 | |||||||
| chr18:35470027 | G | A | 1 | a0001c0001t0004g0049 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.448-1285C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470027 | |||||||
| chr18:35470252 | G | A | 2 | a0001c0001t0005g0048 a0001c0001t0005g0199 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.448-1510C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470252 | |||||||
| chr18:35470280 | C | G | 4 | a0001c0001t0001g0124 a0001c0001t0003g0020 a0001c0001t0003g0184 others(1): Show |
6 | HG01106.hp1 HG01255.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1538G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470280 | |||||||
| chr18:35470352 | T | TATAAA | 140 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 others(137): Show |
204 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.448-1615_448-1611d others(7): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470352 | |||||||
| chr18:35470575 | T | C | 1 | a0001c0002t0002g0047 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-1833A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470575 | |||||||
| chr18:35470611 | G | A | 1 | a0001c0005t0002g0064 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.448-1869C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470611 | |||||||
| chr18:35470650 | C | G | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-1908G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470650 | |||||||
| chr18:35470651 | G | C | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-1909C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470651 | |||||||
| chr18:35470689 | T | TAAAC | 6 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1951_448-1948d others(6): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470689 | |||||||
| chr18:35470740 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.448-1998G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470740 | |||||||
| chr18:35470778 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.448-2036G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470778 | |||||||
| chr18:35470874 | C | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0099 a0001c0001t0001g0116 |
3 | HG02165.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.448-2132G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470874 | |||||||
| chr18:35470978 | G | A | 3 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 |
3 | HG02647.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.448-2236C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35470978 | |||||||
| chr18:35471341 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0258 |
5 | HG01891.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-2599T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471341 | |||||||
| chr18:35471481 | T | C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0080 a0001c0001t0002g0151 others(3): Show |
8 | NA18965.hp1 NA18972.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-2739A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471481 | |||||||
| chr18:35471552 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-2810G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471552 | |||||||
| chr18:35471610 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.448-2868A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471610 | |||||||
| chr18:35471709 | T | A | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-2967A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471709 | |||||||
| chr18:35471753 | C | A | 1 | a0001c0001t0002g0196 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.448-3011G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471753 | |||||||
| chr18:35471754 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.448-3012G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471754 | |||||||
| chr18:35471759 | T | C | 134 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 others(131): Show |
198 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.448-3017A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471759 | |||||||
| chr18:35471778 | C | T | 1 | a0001c0001t0004g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.448-3036G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471778 | |||||||
| chr18:35471833 | C | CTA | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
373 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(370): Show |
intron_variant | MODIFIER | c.448-3092_448-3091i others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471833 | |||||||
| chr18:35471848 | C | G | 1 | a0001c0002t0002g0047 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-3106G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471848 | |||||||
| chr18:35471944 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3202T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471944 | |||||||
| chr18:35471970 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.448-3228A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35471970 | |||||||
| chr18:35472012 | T | C | 1 | a0001c0001t0004g0208 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.448-3270A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472012 | |||||||
| chr18:35472172 | C | T | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.448-3430G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472172 | |||||||
| chr18:35472216 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.448-3474G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472216 | |||||||
| chr18:35472232 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.448-3490C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472232 | |||||||
| chr18:35472244 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.448-3502G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472244 | |||||||
| chr18:35472288 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.448-3546G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472288 | |||||||
| chr18:35472357 | T | G | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.448-3615A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472357 | |||||||
| chr18:35472433 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.448-3691G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472433 | |||||||
| chr18:35472540 | T | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3798A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472540 | |||||||
| chr18:35472541 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3799G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472541 | |||||||
| chr18:35472561 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
336 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(333): Show |
intron_variant | MODIFIER | c.448-3819C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472561 | |||||||
| chr18:35472651 | T | C | 38 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0002g0019 others(35): Show |
61 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.448-3909A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35472651 | |||||||
| chr18:35473059 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.448-4317A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473059 | |||||||
| chr18:35473133 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.448-4391G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473133 | |||||||
| chr18:35473318 | A | AC | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-4577dupG | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473318 | |||||||
| chr18:35473423 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-4681G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473423 | |||||||
| chr18:35473571 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.447+4711G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473571 | |||||||
| chr18:35473761 | T | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+4521A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473761 | |||||||
| chr18:35473823 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447+4459C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473823 | |||||||
| chr18:35473965 | C | T | 1 | a0001c0001t0002g0025 | 2 | NA19076.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.447+4317G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473965 | |||||||
| chr18:35473995 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.447+4287C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35473995 | |||||||
| chr18:35474073 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): Show |
intron_variant | MODIFIER | c.447+4209G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474073 | |||||||
| chr18:35474160 | C | CAT | 12 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
12 | HG02486.hp2 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+4120_447+4121d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474160 | |||||||
| chr18:35474160 | CAT | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0168 a0001c0001t0001g0258 others(30): Show |
57 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.447+4120_447+4121d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474160 | |||||||
| chr18:35474207 | C | CTA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(30): Show |
67 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.447+4073_447+4074d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATA | 23 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0071 others(20): Show |
31 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.447+4071_447+4074d others(6): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATA | 50 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(47): Show |
69 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.447+4069_447+4074d others(8): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATAT others(1): Show |
26 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0059 others(23): Show |
35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.447+4067_447+4074d others(10): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATAT others(3): Show |
18 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0060 others(15): Show |
20 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.447+4065_447+4074d others(12): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATAT others(5): Show |
5 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0136 others(2): Show |
5 | HG00280.hp2 HG01256.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+4063_447+4074d others(14): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATAT others(9): Show |
3 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0142 |
3 | HG02523.hp1 HG03017.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.447+4059_447+4074d others(18): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0108 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.447+4057_447+4074d others(20): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTA | C | 22 | a0001c0001t0001g0062 a0001c0001t0001g0122 a0001c0001t0001g0132 others(19): Show |
34 | HG00408.hp2 HG01074.hp2 HG02135.hp1 others(31): Show |
intron_variant | MODIFIER | c.447+4073_447+4074d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATA | C | 17 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0037 others(14): Show |
24 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.447+4071_447+4074d others(6): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATATA | C | 30 | a0001c0001t0001g0192 a0001c0001t0001g0217 a0001c0001t0001g0218 others(27): Show |
51 | HG02015.hp1 HG02027.hp2 HG02074.hp1 others(48): Show |
intron_variant | MODIFIER | c.447+4069_447+4074d others(8): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0236 a0001c0001t0002g0153 a0001c0004t0002g0195 |
3 | HG02976.hp2 HG03098.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.447+4067_447+4074d others(10): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATATAT others(3): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0248 |
4 | HG02015.hp2 HG02280.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+4065_447+4074d others(12): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATATAT others(5): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0258 |
6 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+4063_447+4074d others(14): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474207 | CTATATAT others(7): Show |
C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0004g0050 |
4 | HG02132.hp1 HG02615.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+4061_447+4074d others(16): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474207 | |||||||
| chr18:35474231 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.447+4050_447+4051i others(16): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474231 | |||||||
| chr18:35474297 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.447+3985C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474297 | |||||||
| chr18:35474390 | A | C | 1 | a0001c0002t0002g0047 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.447+3892T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474390 | |||||||
| chr18:35474418 | T | A | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.447+3864A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35474418 | |||||||
| chr18:35475099 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.447+3183T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475099 | |||||||
| chr18:35475130 | C | CAAT | 131 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 others(128): Show |
195 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(192): Show |
intron_variant | MODIFIER | c.447+3149_447+3151d others(5): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475130 | |||||||
| chr18:35475181 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 others(65): Show |
106 | HG00408.hp2 HG01243.hp2 HG02015.hp1 others(103): Show |
intron_variant | MODIFIER | c.447+3101A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475181 | |||||||
| chr18:35475318 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.447+2964C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475318 | |||||||
| chr18:35475596 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0229 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.447+2686C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475596 | |||||||
| chr18:35475659 | T | TAAGA | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+2619_447+2622d others(6): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475659 | |||||||
| chr18:35475672 | TA | T | 45 | a0001c0001t0001g0168 a0001c0001t0003g0008 a0001c0001t0003g0009 others(42): Show |
68 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.447+2609delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475672 | |||||||
| chr18:35475686 | T | A | 59 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 others(56): Show |
96 | HG00408.hp2 HG01243.hp2 HG02015.hp1 others(93): Show |
intron_variant | MODIFIER | c.447+2596A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475686 | |||||||
| chr18:35475772 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.447+2510T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475772 | |||||||
| chr18:35475820 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0229 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.447+2462C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475820 | |||||||
| chr18:35475905 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.447+2377C>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475905 | |||||||
| chr18:35475925 | T | C | 1 | a0001c0001t0005g0140 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.447+2357A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35475925 | |||||||
| chr18:35476082 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0229 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.447+2200A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35476082 | |||||||
| chr18:35476551 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.447+1731A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35476551 | |||||||
| chr18:35477177 | G | A | 25 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0087 others(22): Show |
27 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.447+1105C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477177 | |||||||
| chr18:35477243 | C | CA | 136 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0131 others(133): Show |
200 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.447+1038dupT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477243 | |||||||
| chr18:35477243 | C | CAA | 5 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(2): Show |
5 | HG02622.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1037_447+1038d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477243 | |||||||
| chr18:35477269 | G | GATATACC others(5): Show |
38 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0002g0019 others(35): Show |
61 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.447+1001_447+1012d others(14): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477269 | |||||||
| chr18:35477572 | G | GAAAAC | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0110 |
3 | HG00280.hp2 HG02040.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.447+705_447+709dup others(5): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477572 | |||||||
| chr18:35477572 | GAAAAC | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+705_447+709del others(5): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477572 | |||||||
| chr18:35477572 | GAAAACAA others(3): Show |
G | 4 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0128 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+700_447+709del others(10): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477572 | |||||||
| chr18:35477779 | T | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0229 a0001c0002t0002g0047 |
4 | HG02922.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+503A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477779 | |||||||
| chr18:35477797 | TG | T | 15 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0029 others(12): Show |
24 | HG00597.hp1 HG02027.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.447+484delC | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477797 | |||||||
| chr18:35477965 | T | C | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+317A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35477965 | |||||||
| chr18:35478115 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.447+167G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35478115 | |||||||
| chr18:35478239 | A | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0229 a0001c0001t0005g0139 others(3): Show |
7 | HG02723.hp1 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+43T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35478239 | |||||||
| chr18:35478256 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.447+26C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 4/4 | chr18 | 35478256 | |||||||
| chr18:35478354 | G | GA | 7 | a0001c0001t0002g0147 a0001c0001t0002g0228 a0001c0001t0005g0126 others(4): Show |
7 | HG02622.hp2 HG02647.hp1 HG02886.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.380-6dupT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478354 | |||||||
| chr18:35478355 | A | G | 47 | a0001c0001t0001g0111 a0001c0001t0002g0002 a0001c0001t0002g0005 others(44): Show |
83 | HG00408.hp2 HG00597.hp1 HG01243.hp2 others(80): Show |
splice_region_variant&intron_variant | LOW | c.380-6T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478355 | |||||||
| chr18:35478380 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.380-31T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478380 | |||||||
| chr18:35478473 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.380-124G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478473 | |||||||
| chr18:35478624 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.380-275T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478624 | |||||||
| chr18:35478742 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.380-393G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478742 | |||||||
| chr18:35478770 | C | G | 1 | a0001c0001t0012g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.380-421G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478770 | |||||||
| chr18:35478813 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0199 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.380-464A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478813 | |||||||
| chr18:35478841 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.379+459T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478841 | |||||||
| chr18:35478871 | C | A | 1 | a0001c0001t0004g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.379+429G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478871 | |||||||
| chr18:35478985 | A | G | 1 | a0001c0001t0002g0029 | 2 | NA18944.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.379+315T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35478985 | |||||||
| chr18:35479101 | A | C | 35 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0024 others(32): Show |
47 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.379+199T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 3/4 | chr18 | 35479101 | |||||||
| chr18:35479688 | C | G | 1 | a0001c0001t0004g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268-277G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35479688 | |||||||
| chr18:35479781 | A | G | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.268-370T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35479781 | |||||||
| chr18:35479869 | ACTCTTCT others(6): Show |
A | 3 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 |
3 | HG01891.hp1 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.268-471_268-459del others(13): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35479869 | |||||||
| chr18:35479969 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.267+484A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35479969 | |||||||
| chr18:35480062 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267+391G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480062 | |||||||
| chr18:35480135 | C | G | 1 | a0001c0001t0012g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.267+318G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480135 | |||||||
| chr18:35480152 | T | C | 6 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+301A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480152 | |||||||
| chr18:35480279 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
340 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.267+174T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480279 | |||||||
| chr18:35480312 | A | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02040.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.267+141T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480312 | |||||||
| chr18:35480322 | T | C | 38 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0002g0019 others(35): Show |
61 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.267+131A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480322 | |||||||
| chr18:35480376 | T | G | 1 | a0001c0001t0011g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.267+77A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 2/4 | chr18 | 35480376 | |||||||
| chr18:35480632 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0229 a0001c0001t0004g0202 others(1): Show |
5 | HG02922.hp1 HG03195.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-69T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35480632 | |||||||
| chr18:35480915 | C | A | 1 | a0001c0001t0003g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.157-352G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35480915 | |||||||
| chr18:35480993 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.157-430A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35480993 | |||||||
| chr18:35481012 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0148 others(11): Show |
19 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.157-449G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481012 | |||||||
| chr18:35481042 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157-479G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481042 | |||||||
| chr18:35481094 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18953.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.157-531C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481094 | |||||||
| chr18:35481212 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.157-649C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481212 | |||||||
| chr18:35481452 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157-889G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481452 | |||||||
| chr18:35481476 | C | A | 4 | a0001c0001t0004g0206 a0001c0001t0004g0207 a0001c0001t0004g0208 others(1): Show |
4 | HG02922.hp2 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-913G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481476 | |||||||
| chr18:35481659 | G | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG00735.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.157-1096C>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481659 | |||||||
| chr18:35481734 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.157-1171T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481734 | |||||||
| chr18:35481815 | C | T | 1 | a0001c0001t0003g0041 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.157-1252G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481815 | |||||||
| chr18:35481833 | G | A | 28 | a0001c0001t0001g0111 a0001c0001t0001g0156 a0001c0001t0002g0002 others(25): Show |
47 | HG00597.hp1 HG02027.hp2 HG02074.hp1 others(44): Show |
intron_variant | MODIFIER | c.157-1270C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35481833 | |||||||
| chr18:35482268 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.157-1705A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35482268 | |||||||
| chr18:35482527 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0143 |
3 | HG01884.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.157-1964A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35482527 | |||||||
| chr18:35482636 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.157-2073A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35482636 | |||||||
| chr18:35482736 | TCTTC | T | 2 | a0001c0001t0005g0048 a0001c0001t0005g0199 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.157-2177_157-2174d others(6): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35482736 | |||||||
| chr18:35482926 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.157-2363G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35482926 | |||||||
| chr18:35483057 | C | CCATTT | 5 | a0001c0001t0001g0125 a0001c0001t0005g0126 a0001c0001t0005g0127 others(2): Show |
5 | HG02622.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-2499_157-2495d others(7): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483057 | |||||||
| chr18:35483128 | T | C | 19 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0024 others(16): Show |
29 | HG00408.hp1 HG01074.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-2565A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483128 | |||||||
| chr18:35483178 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.157-2615A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483178 | |||||||
| chr18:35483229 | C | A | 49 | a0001c0001t0001g0168 a0001c0001t0002g0196 a0001c0001t0003g0008 others(46): Show |
73 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.157-2666G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483229 | |||||||
| chr18:35483255 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 |
3 | HG01891.hp1 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.157-2692G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483255 | |||||||
| chr18:35483377 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.157-2814T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483377 | |||||||
| chr18:35483404 | T | C | 51 | a0001c0001t0001g0168 a0001c0001t0002g0196 a0001c0001t0003g0008 others(48): Show |
75 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.157-2841A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483404 | |||||||
| chr18:35483601 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.157-3038T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35483601 | |||||||
| chr18:35484036 | T | G | 6 | a0001c0001t0001g0194 a0001c0001t0005g0139 a0001c0001t0005g0140 others(3): Show |
7 | HG02622.hp2 HG02723.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-3473A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484036 | |||||||
| chr18:35484153 | A | C | 1 | a0001c0001t0002g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.157-3590T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484153 | |||||||
| chr18:35484362 | A | C | 6 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-3799T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484362 | |||||||
| chr18:35484464 | T | C | 1 | a0001c0002t0002g0047 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.157-3901A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484464 | |||||||
| chr18:35484513 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0188 a0001c0001t0009g0055 |
4 | HG00642.hp2 HG01433.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-3950A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484513 | |||||||
| chr18:35484530 | C | T | 1 | a0001c0001t0003g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157-3967G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484530 | |||||||
| chr18:35484559 | T | C | 6 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-3996A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484559 | |||||||
| chr18:35484645 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.157-4082C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484645 | |||||||
| chr18:35484743 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157-4180A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484743 | |||||||
| chr18:35484815 | A | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-4252T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484815 | |||||||
| chr18:35484931 | T | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0162 |
2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.157-4368A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484931 | |||||||
| chr18:35484950 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.157-4387C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35484950 | |||||||
| chr18:35485002 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.157-4439C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485002 | |||||||
| chr18:35485065 | C | T | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157-4502G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485065 | |||||||
| chr18:35485079 | C | T | 3 | a0001c0001t0004g0088 a0001c0001t0004g0094 a0001c0001t0004g0115 |
3 | HG02132.hp2 NA18991.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.157-4516G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485079 | |||||||
| chr18:35485080 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
389 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(386): Show |
intron_variant | MODIFIER | c.157-4517T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485080 | |||||||
| chr18:35485171 | CA | C | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
10 | HG02258.hp1 HG02451.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-4609delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485171 | |||||||
| chr18:35485222 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157-4659A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485222 | |||||||
| chr18:35485325 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
288 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.157-4762A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485325 | |||||||
| chr18:35485434 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.157-4871A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485434 | |||||||
| chr18:35485465 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.157-4902C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485465 | |||||||
| chr18:35485480 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
372 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.157-4917A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485480 | |||||||
| chr18:35485503 | C | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.157-4940G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485503 | |||||||
| chr18:35485678 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.157-5115A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35485678 | |||||||
| chr18:35486302 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0002g0224 |
3 | HG03831.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.157-5739C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486302 | |||||||
| chr18:35486672 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.157-6109G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486672 | |||||||
| chr18:35486786 | T | TA | 20 | a0001c0001t0001g0037 a0001c0001t0001g0081 a0001c0001t0001g0083 others(17): Show |
22 | HG01884.hp2 HG02055.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-6224dupT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486786 | |||||||
| chr18:35486786 | TA | T | 34 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
46 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.157-6224delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486786 | |||||||
| chr18:35486813 | T | C | 51 | a0001c0001t0001g0066 a0001c0001t0001g0141 a0001c0001t0001g0142 others(48): Show |
86 | HG00408.hp2 HG01243.hp2 HG02015.hp1 others(83): Show |
intron_variant | MODIFIER | c.157-6250A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486813 | |||||||
| chr18:35486855 | G | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0223 others(14): Show |
22 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-6292C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486855 | |||||||
| chr18:35486952 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
339 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(336): Show |
intron_variant | MODIFIER | c.157-6389T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35486952 | |||||||
| chr18:35487128 | T | G | 1 | a0001c0001t0003g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.157-6565A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487128 | |||||||
| chr18:35487395 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.157-6832G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487395 | |||||||
| chr18:35487431 | G | A | 96 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0037 others(93): Show |
142 | HG00408.hp2 HG00639.hp2 HG01074.hp2 others(139): Show |
intron_variant | MODIFIER | c.157-6868C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487431 | |||||||
| chr18:35487438 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.157-6875C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487438 | |||||||
| chr18:35487516 | TGA | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0143 |
3 | HG01884.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.157-6955_157-6954d others(4): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487516 | |||||||
| chr18:35487525 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.157-6962A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487525 | |||||||
| chr18:35487583 | C | T | 1 | a0001c0001t0004g0087 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.157-7020G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487583 | |||||||
| chr18:35487647 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-7084C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487647 | |||||||
| chr18:35487668 | G | A | 2 | a0001c0001t0008g0053 a0001c0001t0008g0054 |
2 | HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.157-7105C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487668 | |||||||
| chr18:35487818 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.157-7255T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35487818 | |||||||
| chr18:35488076 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.157-7513C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488076 | |||||||
| chr18:35488188 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.157-7625A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488188 | |||||||
| chr18:35488218 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG02698.hp2 HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.157-7655G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488218 | |||||||
| chr18:35488235 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157-7672C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488235 | |||||||
| chr18:35488501 | A | AG | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
339 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(336): Show |
intron_variant | MODIFIER | c.157-7939_157-7938i others(3): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488501 | |||||||
| chr18:35488606 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
339 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(336): Show |
intron_variant | MODIFIER | c.157-8043A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488606 | |||||||
| chr18:35488762 | A | G | 1 | a0001c0001t0004g0210 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.157-8199T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488762 | |||||||
| chr18:35488778 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.157-8215C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488778 | |||||||
| chr18:35488800 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.157-8237G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488800 | |||||||
| chr18:35488879 | T | A | 35 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0148 others(32): Show |
60 | HG00408.hp2 HG01243.hp2 HG02027.hp2 others(57): Show |
intron_variant | MODIFIER | c.157-8316A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488879 | |||||||
| chr18:35488887 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0143 a0001c0001t0001g0192 others(1): Show |
5 | HG01884.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-8324T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488887 | |||||||
| chr18:35488936 | CA | C | 3 | a0001c0001t0001g0125 a0001c0001t0005g0126 a0001c0001t0005g0127 |
3 | HG02647.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.157-8374delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488936 | |||||||
| chr18:35488980 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
338 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(335): Show |
intron_variant | MODIFIER | c.157-8417T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35488980 | |||||||
| chr18:35489249 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
333 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(330): Show |
intron_variant | MODIFIER | c.156+8470C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489249 | |||||||
| chr18:35489295 | G | C | 38 | a0001c0001t0001g0168 a0001c0001t0001g0174 a0001c0001t0001g0180 others(35): Show |
60 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.156+8424C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489295 | |||||||
| chr18:35489347 | G | A | 6 | a0001c0001t0001g0125 a0001c0001t0002g0129 a0001c0001t0005g0126 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+8372C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489347 | |||||||
| chr18:35489384 | G | A | 7 | a0001c0001t0004g0050 a0001c0001t0004g0210 a0001c0001t0004g0211 others(4): Show |
8 | HG00639.hp2 HG03017.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+8335C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489384 | |||||||
| chr18:35489403 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0200 a0001c0001t0001g0216 others(5): Show |
9 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.156+8316T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489403 | |||||||
| chr18:35489417 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.156+8302C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489417 | |||||||
| chr18:35489419 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.156+8300T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489419 | |||||||
| chr18:35489680 | T | C | 38 | a0001c0001t0001g0168 a0001c0001t0001g0174 a0001c0001t0001g0180 others(35): Show |
60 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.156+8039A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489680 | |||||||
| chr18:35489756 | T | C | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+7963A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489756 | |||||||
| chr18:35489920 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.156+7799G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35489920 | |||||||
| chr18:35490047 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.156+7672C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490047 | |||||||
| chr18:35490048 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.156+7671G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490048 | |||||||
| chr18:35490129 | T | G | 6 | a0001c0001t0001g0125 a0001c0001t0002g0129 a0001c0001t0005g0126 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+7590A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490129 | |||||||
| chr18:35490133 | C | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+7586G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490133 | |||||||
| chr18:35490366 | G | C | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.156+7353C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490366 | |||||||
| chr18:35490515 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156+7204G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490515 | |||||||
| chr18:35490527 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
333 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(330): Show |
intron_variant | MODIFIER | c.156+7192C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490527 | |||||||
| chr18:35490541 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.156+7178A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490541 | |||||||
| chr18:35490567 | CCAATCTG others(7): Show |
C | 24 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0004g0049 others(21): Show |
27 | HG00639.hp2 HG01074.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.156+7138_156+7151d others(16): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490567 | |||||||
| chr18:35490599 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+7120G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490599 | |||||||
| chr18:35490630 | A | G | 2 | a0001c0001t0005g0139 a0001c0001t0005g0140 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.156+7089T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490630 | |||||||
| chr18:35490759 | T | TTTG | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
333 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(330): Show |
intron_variant | MODIFIER | c.156+6957_156+6959d others(5): Show |
INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490759 | |||||||
| chr18:35490782 | G | T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG03710.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.156+6937C>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490782 | |||||||
| chr18:35490961 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+6758A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35490961 | |||||||
| chr18:35491200 | G | T | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+6519C>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491200 | |||||||
| chr18:35491235 | G | A | 35 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0148 others(32): Show |
60 | HG00408.hp2 HG01243.hp2 HG02027.hp2 others(57): Show |
intron_variant | MODIFIER | c.156+6484C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491235 | |||||||
| chr18:35491253 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0258 |
6 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+6466T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491253 | |||||||
| chr18:35491396 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+6323G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491396 | |||||||
| chr18:35491436 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
331 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.156+6283C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491436 | |||||||
| chr18:35491459 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0122 |
2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.156+6260C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491459 | |||||||
| chr18:35491503 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.156+6216A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491503 | |||||||
| chr18:35491854 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0141 a0001c0001t0001g0142 others(34): Show |
63 | HG00408.hp2 HG01243.hp2 HG01884.hp2 others(60): Show |
intron_variant | MODIFIER | c.156+5865G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35491854 | |||||||
| chr18:35492010 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.156+5709T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492010 | |||||||
| chr18:35492096 | T | C | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+5623A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492096 | |||||||
| chr18:35492544 | GA | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
331 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.156+5174delT | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492544 | |||||||
| chr18:35492609 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
336 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(333): Show |
intron_variant | MODIFIER | c.156+5110A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492609 | |||||||
| chr18:35492625 | G | C | 1 | a0001c0001t0008g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+5094C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492625 | |||||||
| chr18:35492808 | G | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
7 | HG00280.hp1 HG01261.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+4911C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492808 | |||||||
| chr18:35492832 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0199 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.156+4887A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492832 | |||||||
| chr18:35492920 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
331 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.156+4799A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492920 | |||||||
| chr18:35492930 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
142 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.156+4789G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492930 | |||||||
| chr18:35492994 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
331 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.156+4725C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35492994 | |||||||
| chr18:35493166 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
25 | HG00558.hp2 HG00621.hp1 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.156+4553G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493166 | |||||||
| chr18:35493187 | T | C | 2 | a0001c0001t0001g0194 a0001c0002t0002g0047 |
3 | HG03195.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.156+4532A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493187 | |||||||
| chr18:35493331 | C | A | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+4388G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493331 | |||||||
| chr18:35493482 | G | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+4237C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493482 | |||||||
| chr18:35493541 | G | A | 1 | a0001c0001t0009g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.156+4178C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493541 | |||||||
| chr18:35493590 | G | C | 2 | a0001c0001t0005g0139 a0001c0001t0005g0140 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.156+4129C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493590 | |||||||
| chr18:35493921 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
335 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(332): Show |
intron_variant | MODIFIER | c.156+3798G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493921 | |||||||
| chr18:35493948 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.156+3771A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35493948 | |||||||
| chr18:35494067 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+3652A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494067 | |||||||
| chr18:35494256 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
335 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(332): Show |
intron_variant | MODIFIER | c.156+3463A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494256 | |||||||
| chr18:35494277 | C | G | 5 | a0001c0001t0001g0125 a0001c0001t0002g0129 a0001c0001t0005g0126 others(2): Show |
5 | HG02055.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+3442G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494277 | |||||||
| chr18:35494290 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156+3429T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494290 | |||||||
| chr18:35494464 | T | C | 50 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0141 others(47): Show |
86 | HG00408.hp2 HG01243.hp2 HG01884.hp2 others(83): Show |
intron_variant | MODIFIER | c.156+3255A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494464 | |||||||
| chr18:35494525 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.156+3194C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494525 | |||||||
| chr18:35494537 | C | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
337 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(334): Show |
intron_variant | MODIFIER | c.156+3182G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494537 | |||||||
| chr18:35494594 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
337 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(334): Show |
intron_variant | MODIFIER | c.156+3125A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494594 | |||||||
| chr18:35494605 | C | T | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+3114G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494605 | |||||||
| chr18:35494767 | C | T | 48 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0141 others(45): Show |
84 | HG00408.hp2 HG01243.hp2 HG01884.hp2 others(81): Show |
intron_variant | MODIFIER | c.156+2952G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494767 | |||||||
| chr18:35494853 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0256 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.156+2866A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494853 | |||||||
| chr18:35494950 | A | G | 2 | a0001c0001t0001g0131 a0001c0002t0002g0057 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.156+2769T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494950 | |||||||
| chr18:35494960 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+2759T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35494960 | |||||||
| chr18:35495135 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
335 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(332): Show |
intron_variant | MODIFIER | c.156+2584T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495135 | |||||||
| chr18:35495198 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.156+2521C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495198 | |||||||
| chr18:35495295 | G | A | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+2424C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495295 | |||||||
| chr18:35495399 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.156+2320T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495399 | |||||||
| chr18:35495405 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.156+2314G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495405 | |||||||
| chr18:35495654 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156+2065A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495654 | |||||||
| chr18:35495668 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.156+2051G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495668 | |||||||
| chr18:35495768 | T | A | 1 | a0001c0004t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.156+1951A>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495768 | |||||||
| chr18:35495789 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+1930T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495789 | |||||||
| chr18:35495969 | A | G | 24 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0004g0049 others(21): Show |
27 | HG00639.hp2 HG01074.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.156+1750T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35495969 | |||||||
| chr18:35496034 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.156+1685C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496034 | |||||||
| chr18:35496062 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0258 |
6 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+1657C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496062 | |||||||
| chr18:35496103 | T | G | 1 | a0001c0001t0002g0198 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.156+1616A>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496103 | |||||||
| chr18:35496241 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156+1478A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496241 | |||||||
| chr18:35496446 | G | C | 22 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0004g0049 others(19): Show |
25 | HG00639.hp2 HG01074.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.156+1273C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496446 | |||||||
| chr18:35496518 | T | C | 20 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0004g0049 others(17): Show |
22 | HG00639.hp2 HG01074.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.156+1201A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496518 | |||||||
| chr18:35496552 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+1167C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496552 | |||||||
| chr18:35496587 | C | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
328 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(325): Show |
intron_variant | MODIFIER | c.156+1132G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496587 | |||||||
| chr18:35496746 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02572.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.156+973C>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496746 | |||||||
| chr18:35496805 | G | T | 2 | a0001c0001t0005g0139 a0001c0001t0005g0140 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.156+914C>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496805 | |||||||
| chr18:35496830 | T | C | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+889A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496830 | |||||||
| chr18:35496869 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
339 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(336): Show |
intron_variant | MODIFIER | c.156+850G>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496869 | |||||||
| chr18:35496900 | A | C | 1 | a0001c0001t0001g0023 | 2 | NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.156+819T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496900 | |||||||
| chr18:35496928 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0138 |
3 | HG02027.hp2 NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.156+791T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35496928 | |||||||
| chr18:35497128 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
335 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(332): Show |
intron_variant | MODIFIER | c.156+591T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497128 | |||||||
| chr18:35497181 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156+538A>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497181 | |||||||
| chr18:35497197 | C | A | 1 | a0001c0001t0007g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.156+522G>T | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497197 | |||||||
| chr18:35497398 | A | C | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+321T>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497398 | |||||||
| chr18:35497573 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+146G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497573 | |||||||
| chr18:35497589 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.156+130G>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497589 | |||||||
| chr18:35497696 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
161 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.156+23T>C | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497696 | |||||||
| chr18:35497704 | A | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+15T>A | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497704 | |||||||
| chr18:35497709 | G | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.156+10C>G | INO80C | ENSG00000153391.16 | transcript | ENST00000334598.12 | protein_coding | 1/4 | chr18 | 35497709 |