Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 146556 |
| ensemblid | ENSG00000153446.16 |
| hgncid | 28687 |
| symbol | C16orf89 |
| name | chromosome 16 open reading frame 89 |
| refseq_nuc | NM_001098514.3 |
| refseq_prot | NP_001091984.2 |
| ensembl_nuc | ENST00000472572.8 |
| ensembl_prot | ENSP00000420566.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 5044122 |
| end | 5065956 |
| strand | - |
| ver | v1.2 |
| region | chr16:5044122-5065956 |
| region5000 | chr16:5039122-5070956 |
| regionname0 | C16orf89_chr16_5044122_5065956 |
| regionname5000 | C16orf89_chr16_5039122_5070956 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 308 | 88 | 41 | 131 | 12 | 34 | 92 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(356): Show |
chr16 | 5039122 | 5070956 |
| a0002 | 0/0 | 361 | 108 | 4 | 36 | 51 | 6 | 11 | 41 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(356): Show |
chr16 | 5039122 | 5070956 |
| a0003 | 0/0 | 148 | 10 | 0 | 1 | 9 | 0 | 0 | 8 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(143): Show |
chr16 | 5039122 | 5070956 |
| a0004 | 0/0 | 361 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(356): Show |
chr16 | 5039122 | 5070956 |
| a0005 | 0/0 | 301 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(296): Show |
chr16 | 5039122 | 5070956 |
| a0006 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(356): Show |
chr16 | 5039122 | 5070956 |
| a0007 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | MASLG others(356): Show |
chr16 | 5039122 | 5070956 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 181 | 52 | 30 | 66 | 7 | 24 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0001c0002 | 0/0 | 1083 | 124 | 33 | 11 | 65 | 5 | 10 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0001c0006 | 0/0 | 1083 | 3 | 3 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0002c0003 | 0/0 | 1083 | 106 | 3 | 35 | 51 | 6 | 11 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0002c0009 | 0/0 | 1083 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0002c0011 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0003c0004 | 0/0 | 814 | 8 | 0 | 1 | 7 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(809): Show |
chr16 | 5039122 | 5070956 | ||
| a0003c0007 | 0/0 | 814 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(809): Show |
chr16 | 5039122 | 5070956 | ||
| a0004c0005 | 0/0 | 1083 | 3 | 3 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0005c0012 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0006c0008 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 | ||
| a0007c0010 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | ATGGC others(1078): Show |
chr16 | 5039122 | 5070956 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1360 | 174 | 47 | 29 | 66 | 7 | 24 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0001t0002 | 0/0 | 1360 | 4 | 4 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0001t0003 | 1/0 | 1360 | 2 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0001t0005 | 0/0 | 1360 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0002t0001 | 0/0 | 1360 | 121 | 30 | 11 | 65 | 5 | 10 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0002t0002 | 0/0 | 1360 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0002t0006 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0001c0006t0001 | 0/0 | 1360 | 3 | 3 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0002c0003t0001 | 0/0 | 1360 | 106 | 3 | 35 | 51 | 6 | 11 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0002c0009t0001 | 0/0 | 1360 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0002c0011t0001 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0003c0004t0001 | 0/0 | 1091 | 8 | 0 | 1 | 7 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1086): Show |
chr16 | 5039122 | 5070956 |
| a0003c0007t0001 | 0/0 | 1091 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1086): Show |
chr16 | 5039122 | 5070956 |
| a0004c0005t0001 | 0/0 | 1360 | 3 | 3 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0005c0012t0004 | 0/0 | 1360 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0006c0008t0001 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| a0007c0010t0001 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | AGAGC others(1355): Show |
chr16 | 5039122 | 5070956 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 4 | 0 | 3 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 1 | 2 | 0 | 5 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0003g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0002t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0006t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0001c0006t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0003 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0018 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0009t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0002c0011t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0003c0007t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0004c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0004c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0004c0005t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0005c0012t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0006c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| a0007c0010t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0109 | EUR | GBR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | GBR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0267 | EUR | GBR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | FIN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | FIN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0090 | EUR | FIN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | CHS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0088 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0065 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0022 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0066 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0029 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0064 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01255 | hp1 | a0003 | c0004 | t0001 | g0133 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0069 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0260 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0085 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0015 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01433 | hp2 | a0002 | c0009 | t0001 | g0067 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0097 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0285 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0086 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0073 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0092 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0098 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0108 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0083 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0076 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0080 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0062 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0095 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02080 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0070 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | CDX | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | CDX | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | PEL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0263 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0016 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0023 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0027 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0063 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0104 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0075 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0101 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0268 | SAS | BEB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0025 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04204 | hp1 | a0005 | c0012 | t0004 | g0209 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18522 | hp2 | a0004 | c0005 | t0001 | g0272 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18612 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | CHB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | CHB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | CHB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18945 | hp2 | a0003 | c0004 | t0001 | g0132 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18953 | hp1 | a0003 | c0007 | t0001 | g0120 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18965 | hp2 | a0003 | c0004 | t0001 | g0125 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18972 | hp1 | a0003 | c0007 | t0001 | g0121 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18993 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0096 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0309 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0140 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19043 | hp1 | a0004 | c0005 | t0001 | g0271 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0310 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19060 | hp1 | a0006 | c0008 | t0001 | g0074 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19080 | hp1 | a0003 | c0004 | t0001 | g0131 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0291 | AFR | ASW | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0079 | EUR | TSI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | TSI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | TSI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0087 | EUR | TSI | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | GIH | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | GIH | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0196 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0288 | AMR | CLM | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0312 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | MSL | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA20300 | hp2 | a0002 | c0011 | t0001 | g0207 | AFR | USA | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA21309 | hp1 | a0007 | c0010 | t0001 | g0118 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0311 | AFR | LWK | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0284 | REF | REF | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0247 | REF | REF | C16orf89_chr16_5039122_5070956 | C16orf89 | chr16 | 5039122 | 5070956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5044460 | T | A | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.974A>T | p.Asn325Ile | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 1022/1360 | 974/1086 | 325/361 | chr16 | 5044460 | |||
| chr16:5044461 | T | G | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.973A>C | p.Asn325His | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 1021/1360 | 973/1086 | 325/361 | chr16 | 5044461 | |||
| chr16:5044462 | G | T | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.972C>A | p.His324Gln | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 1020/1360 | 972/1086 | 324/361 | chr16 | 5044462 | |||
| chr16:5047881 | G | A | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.952C>T | p.Pro318Ser | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/8 | 1000/1360 | 952/1086 | 318/361 | chr16 | 5047881 | |||
| chr16:5047927 | A | T | 1 | a0005 | 1 | HG04204.hp1 | stop_gained | HIGH | c.906T>A | p.Tyr302* | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/8 | 954/1360 | 906/1086 | 302/361 | chr16 | 5047927 | |||
| chr16:5047933 | A | C | 1 | a0004 | 3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.900T>G | p.Ile300Met | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/8 | 948/1360 | 900/1086 | 300/361 | chr16 | 5047933 | |||
| chr16:5047946 | A | G | 3 | a0002 a0003 a0006 |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
missense_variant | MODERATE | c.887T>C | p.Leu296Ser | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/8 | 935/1360 | 887/1086 | 296/361 | chr16 | 5047946 | |||
| chr16:5057216 | AACAGAGT others(4189): Show |
A | 1 | a0003 | 10 | HG01255.hp1 NA18612.hp2 NA18945.hp2 others(7): Show |
exon_loss_variant | HIGH | c.359-976_628-1029de others(1): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/8 | chr16 | 5057216 | |||||||
| chr16:5058569 | C | A | 1 | a0004 | 3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.551G>T | p.Arg184Met | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/8 | 599/1360 | 551/1086 | 184/361 | chr16 | 5058569 | |||
| chr16:5058588 | C | T | 1 | a0001 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.532G>A | p.Gly178Ser | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/8 | 580/1360 | 532/1086 | 178/361 | chr16 | 5058588 | |||
| chr16:5060287 | C | T | 1 | a0005 | 1 | HG04204.hp1 | missense_variant&splice_region_variant | MODERATE | c.508G>A | p.Gly170Arg | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/8 | 556/1360 | 508/1086 | 170/361 | chr16 | 5060287 | |||
| chr16:5060350 | C | T | 1 | a0002 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.445G>A | p.Gly149Arg | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/8 | 493/1360 | 445/1086 | 149/361 | chr16 | 5060350 | |||
| chr16:5060404 | T | A | 1 | a0002 | 1 | NA18983.hp1 | stop_gained | HIGH | c.391A>T | p.Lys131* | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/8 | 439/1360 | 391/1086 | 131/361 | chr16 | 5060404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5044357 | G | A | 1 | a0002c0009 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1077C>T | p.Ser359Ser | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 1125/1360 | 1077/1086 | 359/361 | chr16 | 5044357 | |||
| chr16:5056183 | C | T | 8 | a0001c0002 a0002c0003 a0002c0009 others(5): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
synonymous_variant | LOW | c.633G>A | p.Gly211Gly | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/8 | 681/1360 | 633/1086 | 211/361 | chr16 | 5056183 | |||
| chr16:5065810 | G | A | 1 | a0001c0006 | 3 | HG02486.hp2 NA19043.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.99C>T | p.Ala33Ala | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/8 | 147/1360 | 99/1086 | 33/361 | chr16 | 5065810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5044190 | T | C | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(13): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
3_prime_UTR_variant | MODIFIER | c.*158A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 158 | chr16 | 5044190 | ||||||
| chr16:5044221 | C | T | 1 | a0005c0012t0004 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 127 | chr16 | 5044221 | ||||||
| chr16:5044274 | C | T | 2 | a0001c0001t0002 a0001c0002t0002 |
6 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 74 | chr16 | 5044274 | ||||||
| chr16:5044334 | T | C | 1 | a0001c0001t0005 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 14 | chr16 | 5044334 | ||||||
| chr16:5044345 | G | A | 1 | a0001c0002t0006 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 8/8 | 3 | chr16 | 5044345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5044482 | G | A | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.956-4C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044482 | |||||||
| chr16:5044569 | G | A | 88 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(85): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.956-91C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044569 | |||||||
| chr16:5044571 | G | A | 6 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(3): Show |
6 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-93C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044571 | |||||||
| chr16:5044639 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.956-161G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044639 | |||||||
| chr16:5044700 | C | T | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.956-222G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044700 | |||||||
| chr16:5044705 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
137 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.956-227T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044705 | |||||||
| chr16:5044736 | C | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-258G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044736 | |||||||
| chr16:5044769 | A | C | 1 | a0002c0003t0001g0064 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.956-291T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044769 | |||||||
| chr16:5044849 | A | C | 6 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(3): Show |
6 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-371T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044849 | |||||||
| chr16:5044906 | C | T | 1 | a0002c0003t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.956-428G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5044906 | |||||||
| chr16:5045000 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.956-522T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045000 | |||||||
| chr16:5045028 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.956-550A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045028 | |||||||
| chr16:5045084 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.956-606G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045084 | |||||||
| chr16:5045119 | G | A | 1 | a0002c0003t0001g0024 | 2 | HG02071.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.956-641C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045119 | |||||||
| chr16:5045136 | T | C | 1 | a0001c0002t0001g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.956-658A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045136 | |||||||
| chr16:5045183 | C | T | 2 | a0001c0002t0001g0302 a0001c0002t0001g0305 |
2 | HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.956-705G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045183 | |||||||
| chr16:5045188 | C | A | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.956-710G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045188 | |||||||
| chr16:5045299 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.956-821G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045299 | |||||||
| chr16:5045346 | C | T | 11 | a0001c0001t0001g0236 a0001c0001t0002g0113 a0001c0001t0002g0114 others(8): Show |
11 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.956-868G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045346 | |||||||
| chr16:5045408 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.956-930C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045408 | |||||||
| chr16:5045447 | T | A | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-969A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045447 | |||||||
| chr16:5045598 | C | T | 111 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(108): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.956-1120G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045598 | |||||||
| chr16:5045620 | T | G | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1142A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045620 | |||||||
| chr16:5045670 | C | T | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-1192G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045670 | |||||||
| chr16:5045686 | C | T | 1 | a0001c0002t0006g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.956-1208G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045686 | |||||||
| chr16:5045735 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.956-1257G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045735 | |||||||
| chr16:5045789 | C | G | 1 | a0001c0002t0001g0178 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.956-1311G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045789 | |||||||
| chr16:5045810 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0278 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.956-1332T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045810 | |||||||
| chr16:5045824 | G | A | 1 | a0001c0002t0006g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.956-1346C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045824 | |||||||
| chr16:5045833 | G | A | 15 | a0001c0001t0001g0236 a0001c0001t0002g0113 a0001c0001t0002g0114 others(12): Show |
17 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.956-1355C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045833 | |||||||
| chr16:5045866 | C | A | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.956-1388G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045866 | |||||||
| chr16:5045968 | C | G | 1 | a0001c0002t0001g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.956-1490G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5045968 | |||||||
| chr16:5046078 | G | A | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.956-1600C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046078 | |||||||
| chr16:5046152 | G | T | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.956-1674C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046152 | |||||||
| chr16:5046223 | A | C | 1 | a0001c0001t0001g0217 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.955+1655T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046223 | |||||||
| chr16:5046330 | T | TTTTTA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(8): Show |
13 | HG01243.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.955+1543_955+1547d others(7): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046330 | |||||||
| chr16:5046330 | TTTTTATT others(3): Show |
T | 1 | a0001c0001t0001g0200 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.955+1538_955+1547d others(12): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046330 | |||||||
| chr16:5046336 | T | C | 6 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(3): Show |
6 | HG02055.hp1 HG02809.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.955+1542A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046336 | |||||||
| chr16:5046418 | C | G | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.955+1460G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046418 | |||||||
| chr16:5046434 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.955+1444G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046434 | |||||||
| chr16:5046483 | C | CT | 13 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0234 others(10): Show |
15 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.955+1394_955+1395i others(3): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046483 | |||||||
| chr16:5046558 | C | T | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.955+1320G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046558 | |||||||
| chr16:5046584 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.955+1294G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046584 | |||||||
| chr16:5046597 | C | T | 1 | a0003c0004t0001g0140 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.955+1281G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046597 | |||||||
| chr16:5046619 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
126 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.955+1259T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046619 | |||||||
| chr16:5046752 | C | A | 36 | a0001c0002t0001g0008 a0001c0002t0001g0030 a0001c0002t0001g0031 others(33): Show |
45 | HG00408.hp1 HG00558.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.955+1126G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046752 | |||||||
| chr16:5046756 | A | C | 14 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0234 others(11): Show |
16 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.955+1122T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046756 | |||||||
| chr16:5046764 | C | T | 1 | a0002c0003t0001g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.955+1114G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046764 | |||||||
| chr16:5046767 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(85): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.955+1111G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046767 | |||||||
| chr16:5046787 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.955+1091G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046787 | |||||||
| chr16:5046793 | C | G | 1 | a0002c0003t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.955+1085G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046793 | |||||||
| chr16:5046934 | C | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.955+944G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5046934 | |||||||
| chr16:5047032 | C | A | 1 | a0003c0004t0001g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.955+846G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047032 | |||||||
| chr16:5047093 | C | G | 7 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0234 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.955+785G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047093 | |||||||
| chr16:5047115 | G | C | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+763C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047115 | |||||||
| chr16:5047132 | T | C | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+746A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047132 | |||||||
| chr16:5047272 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.955+606C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047272 | |||||||
| chr16:5047340 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.955+538G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047340 | |||||||
| chr16:5047389 | G | A | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+489C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047389 | |||||||
| chr16:5047465 | T | C | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.955+413A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047465 | |||||||
| chr16:5047471 | C | CT | 80 | a0001c0001t0001g0282 a0001c0001t0001g0295 a0001c0002t0001g0126 others(77): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.955+406dupA | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047471 | |||||||
| chr16:5047592 | C | T | 64 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(61): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.955+286G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047592 | |||||||
| chr16:5047875 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.955+3A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 7/7 | chr16 | 5047875 | |||||||
| chr16:5048071 | C | T | 9 | a0001c0001t0001g0295 a0001c0002t0001g0034 a0001c0002t0001g0149 others(6): Show |
10 | HG00741.hp2 HG01243.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.869-107G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048071 | |||||||
| chr16:5048089 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.869-125C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048089 | |||||||
| chr16:5048101 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.869-137G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048101 | |||||||
| chr16:5048108 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.869-144T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048108 | |||||||
| chr16:5048130 | G | C | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-166C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048130 | |||||||
| chr16:5048138 | C | G | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.869-174G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048138 | |||||||
| chr16:5048165 | A | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.869-201T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048165 | |||||||
| chr16:5048204 | A | C | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-240T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048204 | |||||||
| chr16:5048206 | T | A | 2 | a0001c0001t0001g0254 a0007c0010t0001g0118 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.869-242A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048206 | |||||||
| chr16:5048220 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.869-256T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048220 | |||||||
| chr16:5048274 | A | G | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-310T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048274 | |||||||
| chr16:5048286 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.869-322A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048286 | |||||||
| chr16:5048333 | C | T | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.869-369G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048333 | |||||||
| chr16:5048339 | C | T | 1 | a0002c0003t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.869-375G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048339 | |||||||
| chr16:5048378 | A | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0060 a0001c0001t0001g0219 others(1): Show |
5 | HG01433.hp1 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-414T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048378 | |||||||
| chr16:5048591 | T | A | 4 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 others(1): Show |
4 | NA18522.hp2 NA19043.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-627A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048591 | |||||||
| chr16:5048610 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.869-646C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048610 | |||||||
| chr16:5048660 | A | G | 1 | a0001c0002t0001g0126 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.869-696T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048660 | |||||||
| chr16:5048705 | A | G | 1 | a0002c0003t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869-741T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048705 | |||||||
| chr16:5048745 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.869-781A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048745 | |||||||
| chr16:5048751 | T | C | 1 | a0001c0002t0001g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.869-787A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048751 | |||||||
| chr16:5048767 | C | A | 1 | a0002c0003t0001g0078 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.869-803G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048767 | |||||||
| chr16:5048767 | C | T | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-803G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048767 | |||||||
| chr16:5048774 | G | C | 1 | a0002c0003t0001g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.869-810C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048774 | |||||||
| chr16:5048818 | G | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.869-854C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048818 | |||||||
| chr16:5048846 | C | G | 1 | a0001c0002t0001g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.869-882G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048846 | |||||||
| chr16:5048891 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(6): Show |
11 | HG01243.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-927C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048891 | |||||||
| chr16:5048891 | G | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0282 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.869-927C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5048891 | |||||||
| chr16:5049140 | G | A | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-1176C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049140 | |||||||
| chr16:5049141 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.869-1177C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049141 | |||||||
| chr16:5049162 | C | G | 2 | a0003c0004t0001g0131 a0003c0004t0001g0309 |
2 | NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.869-1198G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049162 | |||||||
| chr16:5049281 | C | T | 1 | a0002c0003t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869-1317G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049281 | |||||||
| chr16:5049354 | T | G | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-1390A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049354 | |||||||
| chr16:5049382 | C | G | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.869-1418G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049382 | |||||||
| chr16:5049429 | C | T | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-1465G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049429 | |||||||
| chr16:5049478 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.869-1514T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049478 | |||||||
| chr16:5049543 | A | T | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-1579T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049543 | |||||||
| chr16:5049588 | A | G | 1 | a0001c0002t0006g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.869-1624T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049588 | |||||||
| chr16:5049905 | C | G | 1 | a0001c0002t0006g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.869-1941G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049905 | |||||||
| chr16:5049939 | A | C | 3 | a0002c0003t0001g0071 a0002c0003t0001g0077 a0002c0003t0001g0078 |
3 | NA18948.hp1 NA18961.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.869-1975T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049939 | |||||||
| chr16:5049974 | C | G | 1 | a0002c0003t0001g0092 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.869-2010G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5049974 | |||||||
| chr16:5050008 | T | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.869-2044A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050008 | |||||||
| chr16:5050052 | T | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0289 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.869-2088A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050052 | |||||||
| chr16:5050129 | A | T | 1 | a0001c0002t0001g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.869-2165T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050129 | |||||||
| chr16:5050162 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.869-2198C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050162 | |||||||
| chr16:5050223 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0180 |
3 | HG02145.hp1 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.869-2259G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050223 | |||||||
| chr16:5050240 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.869-2276G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050240 | |||||||
| chr16:5050332 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.869-2368G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050332 | |||||||
| chr16:5050385 | C | G | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869-2421G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050385 | |||||||
| chr16:5050415 | A | G | 2 | a0003c0004t0001g0131 a0003c0004t0001g0309 |
2 | NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.869-2451T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050415 | |||||||
| chr16:5050642 | T | G | 1 | a0002c0003t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.869-2678A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050642 | |||||||
| chr16:5050704 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869-2740C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050704 | |||||||
| chr16:5050829 | T | C | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2865A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050829 | |||||||
| chr16:5050832 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.869-2868T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050832 | |||||||
| chr16:5050877 | G | T | 1 | a0002c0003t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.869-2913C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050877 | |||||||
| chr16:5050959 | T | A | 87 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(84): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.869-2995A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050959 | |||||||
| chr16:5050978 | A | G | 3 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 |
4 | HG01106.hp1 HG01168.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3014T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5050978 | |||||||
| chr16:5051120 | G | A | 1 | a0002c0003t0001g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.869-3156C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051120 | |||||||
| chr16:5051179 | C | G | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.869-3215G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051179 | |||||||
| chr16:5051197 | A | T | 1 | a0002c0003t0001g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.869-3233T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051197 | |||||||
| chr16:5051220 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.869-3256T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051220 | |||||||
| chr16:5051290 | T | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-3326A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051290 | |||||||
| chr16:5051357 | G | T | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.869-3393C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051357 | |||||||
| chr16:5051378 | C | CA | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-3415dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051378 | |||||||
| chr16:5051496 | G | T | 80 | a0001c0001t0001g0236 a0001c0002t0001g0036 a0001c0002t0001g0037 others(77): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.869-3532C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051496 | |||||||
| chr16:5051607 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(5): Show |
10 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+3639C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051607 | |||||||
| chr16:5051654 | T | A | 1 | a0001c0002t0001g0126 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.868+3592A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051654 | |||||||
| chr16:5051655 | A | T | 1 | a0001c0002t0001g0126 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.868+3591T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051655 | |||||||
| chr16:5051656 | C | A | 1 | a0001c0002t0001g0126 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.868+3590G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051656 | |||||||
| chr16:5051738 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.868+3508G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051738 | |||||||
| chr16:5051783 | C | A | 1 | a0001c0002t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.868+3463G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051783 | |||||||
| chr16:5051818 | G | A | 7 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0234 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.868+3428C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5051818 | |||||||
| chr16:5052071 | C | A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.868+3175G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052071 | |||||||
| chr16:5052099 | C | CA | 9 | a0001c0001t0001g0295 a0001c0002t0006g0263 a0002c0003t0001g0022 others(6): Show |
11 | HG01106.hp1 HG01168.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.868+3146dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052099 | |||||||
| chr16:5052099 | CA | C | 50 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(47): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.868+3146delT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052099 | |||||||
| chr16:5052099 | CAA | C | 61 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(58): Show |
79 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.868+3145_868+3146d others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052099 | |||||||
| chr16:5052099 | CAAA | C | 9 | a0001c0001t0001g0179 a0001c0001t0001g0276 a0001c0001t0001g0297 others(6): Show |
9 | HG00639.hp2 HG01258.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.868+3144_868+3146d others(5): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052099 | |||||||
| chr16:5052118 | A | G | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.868+3128T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052118 | |||||||
| chr16:5052162 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.868+3084G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052162 | |||||||
| chr16:5052319 | TG | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(6): Show |
11 | HG01243.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+2926delC | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052319 | |||||||
| chr16:5052354 | C | T | 2 | a0002c0003t0001g0066 a0002c0003t0001g0196 |
2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.868+2892G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052354 | |||||||
| chr16:5052420 | T | C | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.868+2826A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052420 | |||||||
| chr16:5052554 | G | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | HG01099.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.868+2692C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052554 | |||||||
| chr16:5052603 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.868+2643C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052603 | |||||||
| chr16:5052603 | GA | G | 122 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(119): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.868+2642delT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052603 | |||||||
| chr16:5052608 | A | G | 92 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(89): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.868+2638T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052608 | |||||||
| chr16:5052638 | C | T | 2 | a0004c0005t0001g0271 a0004c0005t0001g0272 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.868+2608G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052638 | |||||||
| chr16:5052715 | A | G | 1 | a0002c0003t0001g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.868+2531T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052715 | |||||||
| chr16:5052725 | G | C | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.868+2521C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052725 | |||||||
| chr16:5052734 | C | T | 1 | a0001c0002t0001g0019 | 3 | HG00280.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.868+2512G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052734 | |||||||
| chr16:5052844 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.868+2402C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052844 | |||||||
| chr16:5052845 | C | G | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+2401G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052845 | |||||||
| chr16:5052881 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.868+2365G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052881 | |||||||
| chr16:5052912 | G | C | 1 | a0002c0003t0001g0087 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.868+2334C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052912 | |||||||
| chr16:5052929 | A | C | 4 | a0001c0002t0001g0034 a0001c0002t0001g0155 a0001c0002t0001g0168 others(1): Show |
5 | HG00741.hp2 HG01257.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+2317T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052929 | |||||||
| chr16:5052957 | A | G | 1 | a0001c0002t0001g0178 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.868+2289T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052957 | |||||||
| chr16:5052966 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.868+2280T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052966 | |||||||
| chr16:5052974 | C | T | 2 | a0001c0002t0001g0149 a0001c0002t0006g0263 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.868+2272G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052974 | |||||||
| chr16:5052981 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(6): Show |
11 | HG01243.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+2265C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5052981 | |||||||
| chr16:5053215 | C | G | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.868+2031G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053215 | |||||||
| chr16:5053230 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.868+2016G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053230 | |||||||
| chr16:5053270 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.868+1976A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053270 | |||||||
| chr16:5053290 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0273 a0001c0001t0001g0281 others(2): Show |
7 | HG01257.hp1 HG01258.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+1956A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053290 | |||||||
| chr16:5053356 | C | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.868+1890G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053356 | |||||||
| chr16:5053425 | G | C | 3 | a0001c0002t0001g0155 a0001c0002t0001g0168 a0001c0002t0001g0169 |
3 | HG01257.hp2 HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.868+1821C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053425 | |||||||
| chr16:5053541 | G | GT | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0002t0001g0148 others(7): Show |
10 | HG00597.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+1704dupA | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053541 | |||||||
| chr16:5053541 | G | T | 5 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(2): Show |
5 | HG02602.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+1705C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053541 | |||||||
| chr16:5053541 | GT | G | 40 | a0001c0001t0001g0218 a0001c0001t0001g0236 a0001c0001t0001g0275 others(37): Show |
49 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.868+1704delA | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053541 | |||||||
| chr16:5053542 | T | G | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.868+1704A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053542 | |||||||
| chr16:5053675 | C | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.868+1571G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053675 | |||||||
| chr16:5053705 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.868+1541C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053705 | |||||||
| chr16:5053760 | C | T | 1 | a0002c0003t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.868+1486G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053760 | |||||||
| chr16:5053761 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.868+1485C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053761 | |||||||
| chr16:5053828 | G | A | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+1418C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053828 | |||||||
| chr16:5053901 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.868+1345C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053901 | |||||||
| chr16:5053938 | C | A | 1 | a0001c0002t0006g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.868+1308G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053938 | |||||||
| chr16:5053949 | A | G | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.868+1297T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053949 | |||||||
| chr16:5053966 | A | G | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.868+1280T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5053966 | |||||||
| chr16:5054029 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.868+1217T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054029 | |||||||
| chr16:5054105 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.868+1141G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054105 | |||||||
| chr16:5054257 | G | A | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+989C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054257 | |||||||
| chr16:5054304 | G | A | 3 | a0002c0003t0001g0066 a0002c0003t0001g0196 a0002c0009t0001g0067 |
3 | HG01123.hp1 HG01175.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.868+942C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054304 | |||||||
| chr16:5054456 | C | T | 1 | a0002c0003t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.868+790G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054456 | |||||||
| chr16:5054557 | C | T | 2 | a0001c0001t0002g0298 a0001c0002t0002g0117 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.868+689G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054557 | |||||||
| chr16:5054692 | C | T | 6 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(3): Show |
6 | HG02055.hp1 HG02809.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+554G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054692 | |||||||
| chr16:5054856 | C | G | 1 | a0001c0002t0001g0019 | 3 | HG00280.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.868+390G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054856 | |||||||
| chr16:5054876 | A | T | 1 | a0002c0003t0001g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.868+370T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054876 | |||||||
| chr16:5054924 | C | G | 2 | a0001c0006t0001g0311 a0001c0006t0001g0312 |
2 | HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.868+322G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054924 | |||||||
| chr16:5054985 | A | G | 10 | a0001c0002t0001g0031 a0001c0002t0001g0056 a0001c0002t0001g0123 others(7): Show |
11 | NA18939.hp1 NA18975.hp1 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+261T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5054985 | |||||||
| chr16:5055012 | C | G | 1 | a0001c0001t0005g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.868+234G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5055012 | |||||||
| chr16:5055040 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.868+206G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5055040 | |||||||
| chr16:5055105 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0143 |
3 | NA18961.hp2 NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.868+141C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5055105 | |||||||
| chr16:5055119 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.868+127T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 6/7 | chr16 | 5055119 | |||||||
| chr16:5055358 | T | C | 15 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 others(12): Show |
15 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.764-8A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055358 | |||||||
| chr16:5055364 | C | T | 73 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(70): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764-14G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055364 | |||||||
| chr16:5055416 | G | A | 2 | a0001c0002t0001g0149 a0001c0002t0006g0263 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.764-66C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055416 | |||||||
| chr16:5055439 | T | C | 182 | a0001c0001t0001g0278 a0001c0001t0001g0295 a0001c0002t0001g0008 others(179): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.764-89A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055439 | |||||||
| chr16:5055485 | A | C | 182 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(179): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.764-135T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055485 | |||||||
| chr16:5055534 | G | C | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764-184C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055534 | |||||||
| chr16:5055545 | G | A | 1 | a0001c0002t0001g0160 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.764-195C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055545 | |||||||
| chr16:5055678 | G | T | 1 | a0005c0012t0004g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.764-328C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055678 | |||||||
| chr16:5055710 | G | A | 3 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0256 |
3 | HG02055.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.763+343C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055710 | |||||||
| chr16:5055754 | C | T | 1 | a0002c0009t0001g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.763+299G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055754 | |||||||
| chr16:5055766 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0202 |
2 | HG00423.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.763+287T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055766 | |||||||
| chr16:5055781 | A | C | 9 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(6): Show |
9 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.763+272T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055781 | |||||||
| chr16:5055833 | A | T | 1 | a0001c0001t0002g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.763+220T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055833 | |||||||
| chr16:5055938 | C | CGT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0043 others(8): Show |
19 | HG01071.hp1 HG01981.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.763+113_763+114dup others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGT | 10 | a0001c0001t0001g0171 a0001c0001t0001g0206 a0001c0001t0001g0208 others(7): Show |
10 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.763+111_763+114dup others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
9 | HG00597.hp1 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.763+109_763+114dup others(6): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0203 others(5): Show |
16 | HG02083.hp1 HG02083.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.763+107_763+114dup others(8): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(3): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0193 a0001c0001t0001g0202 others(1): Show |
5 | HG01891.hp2 NA18612.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.763+105_763+114dup others(10): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(5): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0201 a0001c0001t0001g0231 others(2): Show |
6 | HG02630.hp1 HG02976.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.763+103_763+114dup others(12): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(7): Show |
1 | a0001c0002t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.763+101_763+114dup others(14): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0200 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.763+99_763+114dupA others(15): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0199 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.763+97_763+114dupA others(17): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0001g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.763+95_763+114dupA others(19): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | C | CGTGTGTG others(15): Show |
1 | a0001c0001t0001g0197 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.763+93_763+114dupA others(21): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGT | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(22): Show |
38 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.763+113_763+114del others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGT | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0094 others(25): Show |
49 | HG00438.hp2 HG00621.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.763+111_763+114del others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGT | C | 42 | a0001c0001t0001g0047 a0001c0001t0001g0107 a0001c0001t0001g0221 others(39): Show |
59 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.763+109_763+114del others(6): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(1): Show |
C | 35 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0060 others(32): Show |
41 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.763+107_763+114del others(8): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(3): Show |
C | 47 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0058 others(44): Show |
57 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.763+105_763+114del others(10): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(5): Show |
C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(18): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.763+103_763+114del others(12): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(7): Show |
C | 18 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0057 others(15): Show |
21 | HG01255.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.763+101_763+114del others(14): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(9): Show |
C | 8 | a0001c0001t0001g0295 a0001c0002t0001g0032 a0001c0002t0001g0143 others(5): Show |
9 | HG00673.hp2 HG01243.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.763+99_763+114delA others(15): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(11): Show |
C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0262 a0002c0003t0001g0092 |
3 | HG01975.hp2 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.763+97_763+114delA others(17): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(13): Show |
C | 9 | a0001c0001t0001g0264 a0001c0002t0001g0019 a0001c0002t0001g0119 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.763+95_763+114delA others(19): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(15): Show |
C | 1 | a0001c0002t0001g0293 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.763+93_763+114delA others(21): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(17): Show |
C | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
4 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+91_763+114delA others(23): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(19): Show |
C | 1 | a0001c0002t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.763+89_763+114delA others(25): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055938 | CGTGTGTG others(21): Show |
C | 1 | a0001c0002t0001g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.763+87_763+114delA others(27): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055938 | |||||||
| chr16:5055987 | GTGTGTGT others(6): Show |
G | 1 | a0002c0003t0001g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.763+53_763+65delAC others(11): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055987 | |||||||
| chr16:5055995 | GTGTGT | G | 3 | a0001c0002t0001g0009 a0001c0002t0001g0037 a0002c0003t0001g0017 |
3 | HG01346.hp2 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.763+53_763+57delAC others(3): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5055995 | |||||||
| chr16:5056027 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.763+26G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5056027 | |||||||
| chr16:5056049 | A | G | 7 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.763+4T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 5/7 | chr16 | 5056049 | |||||||
| chr16:5056245 | G | A | 1 | a0001c0002t0002g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.628-57C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056245 | |||||||
| chr16:5056261 | G | T | 1 | a0001c0002t0001g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.628-73C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056261 | |||||||
| chr16:5056278 | C | A | 4 | a0001c0002t0001g0302 a0001c0002t0001g0303 a0001c0002t0001g0304 others(1): Show |
4 | HG00544.hp1 HG00673.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-90G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056278 | |||||||
| chr16:5056337 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.628-149C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056337 | |||||||
| chr16:5056338 | C | A | 1 | a0001c0002t0001g0293 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-150G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056338 | |||||||
| chr16:5056374 | G | A | 2 | a0001c0002t0001g0149 a0001c0002t0006g0263 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.628-186C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056374 | |||||||
| chr16:5056378 | C | T | 1 | a0004c0005t0001g0291 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.628-190G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056378 | |||||||
| chr16:5056462 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0276 |
3 | HG00639.hp1 HG00639.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.628-274C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056462 | |||||||
| chr16:5056607 | C | T | 1 | a0002c0003t0001g0070 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.628-419G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056607 | |||||||
| chr16:5056627 | C | CA | 7 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0256 others(4): Show |
7 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-440dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056627 | |||||||
| chr16:5056637 | G | T | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-449C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056637 | |||||||
| chr16:5056645 | C | G | 7 | a0001c0001t0001g0278 a0001c0002t0001g0292 a0001c0002t0001g0293 others(4): Show |
7 | HG02055.hp1 HG02809.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-457G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056645 | |||||||
| chr16:5056677 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.628-489C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056677 | |||||||
| chr16:5056679 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.628-491T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056679 | |||||||
| chr16:5056745 | A | G | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-557T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056745 | |||||||
| chr16:5056795 | A | G | 1 | a0002c0003t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.628-607T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5056795 | |||||||
| chr16:5057028 | CG | C | 9 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-841delC | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057028 | |||||||
| chr16:5057070 | T | A | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-882A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057070 | |||||||
| chr16:5057109 | G | A | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.628-921C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057109 | |||||||
| chr16:5057138 | T | A | 3 | a0004c0005t0001g0271 a0004c0005t0001g0272 a0004c0005t0001g0291 |
3 | NA18522.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.628-950A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057138 | |||||||
| chr16:5057159 | T | C | 90 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(87): Show |
113 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.628-971A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057159 | |||||||
| chr16:5057186 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-998C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057186 | |||||||
| chr16:5057187 | A | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-999T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057187 | |||||||
| chr16:5057191 | C | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1003G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057191 | |||||||
| chr16:5057191 | C | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.628-1003G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057191 | |||||||
| chr16:5057192 | G | C | 1 | a0002c0003t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.628-1004C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057192 | |||||||
| chr16:5057192 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1004C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057192 | |||||||
| chr16:5057193 | T | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1005A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057193 | |||||||
| chr16:5057194 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1006C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057194 | |||||||
| chr16:5057195 | C | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1007G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057195 | |||||||
| chr16:5057196 | C | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1008G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057196 | |||||||
| chr16:5057198 | C | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1010G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057198 | |||||||
| chr16:5057205 | C | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1017G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057205 | |||||||
| chr16:5057206 | C | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1018G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057206 | |||||||
| chr16:5057212 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1024C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057212 | |||||||
| chr16:5057213 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1025C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057213 | |||||||
| chr16:5057214 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1026C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057214 | |||||||
| chr16:5057216 | A | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1028T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057216 | |||||||
| chr16:5057220 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1032C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057220 | |||||||
| chr16:5057222 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1034C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057222 | |||||||
| chr16:5057223 | T | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1035A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057223 | |||||||
| chr16:5057224 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1036C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057224 | |||||||
| chr16:5057226 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1038C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057226 | |||||||
| chr16:5057229 | T | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1041A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057229 | |||||||
| chr16:5057234 | C | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1046G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057234 | |||||||
| chr16:5057236 | C | G | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1048G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057236 | |||||||
| chr16:5057237 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1049T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057237 | |||||||
| chr16:5057239 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1051T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057239 | |||||||
| chr16:5057241 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1053T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057241 | |||||||
| chr16:5057243 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1055T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057243 | |||||||
| chr16:5057245 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1057T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057245 | |||||||
| chr16:5057247 | A | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1059T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057247 | |||||||
| chr16:5057248 | A | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1060T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057248 | |||||||
| chr16:5057250 | G | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1062C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057250 | |||||||
| chr16:5057251 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1063T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057251 | |||||||
| chr16:5057253 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1065C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057253 | |||||||
| chr16:5057254 | G | A | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1066C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057254 | |||||||
| chr16:5057255 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1067T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057255 | |||||||
| chr16:5057257 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1069T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057257 | |||||||
| chr16:5057259 | G | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1071C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057259 | |||||||
| chr16:5057261 | A | T | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1073T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057261 | |||||||
| chr16:5057265 | T | C | 1 | a0002c0003t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.628-1077A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057265 | |||||||
| chr16:5057267 | C | CATATATA others(45): Show |
2 | a0001c0001t0001g0262 a0001c0002t0006g0263 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.628-1080_628-1079i others(54): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057267 | |||||||
| chr16:5057267 | C | CATATATA others(97): Show |
1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-1080_628-1079i others(106): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057267 | |||||||
| chr16:5057276 | ATGTATAT others(7): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.628-1102_628-1089d others(16): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057276 | |||||||
| chr16:5057292 | G | GTA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0002t0001g0019 others(9): Show |
14 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.628-1106_628-1105d others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057292 | |||||||
| chr16:5057292 | GTA | G | 81 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(78): Show |
102 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.628-1106_628-1105d others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057292 | |||||||
| chr16:5057334 | A | G | 1 | a0001c0002t0001g0034 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.628-1146T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057334 | |||||||
| chr16:5057370 | G | GAT | 9 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+1121_627+1122d others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057370 | |||||||
| chr16:5057371 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
3 | HG03017.hp1 HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.627+1108_627+1121d others(16): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057371 | |||||||
| chr16:5057405 | A | G | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+1088T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057405 | |||||||
| chr16:5057413 | G | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0010 |
3 | HG00558.hp1 HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.627+1080C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057413 | |||||||
| chr16:5057423 | A | G | 1 | a0001c0002t0001g0034 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.627+1070T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057423 | |||||||
| chr16:5057430 | G | A | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.627+1063C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057430 | |||||||
| chr16:5057479 | G | GTA | 31 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0030 others(28): Show |
38 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.627+1012_627+1013d others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057479 | |||||||
| chr16:5057658 | A | T | 3 | a0001c0001t0001g0262 a0001c0002t0001g0149 a0001c0002t0006g0263 |
3 | HG02622.hp1 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.627+835T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057658 | |||||||
| chr16:5057671 | G | A | 1 | a0002c0003t0001g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.627+822C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057671 | |||||||
| chr16:5057901 | T | C | 2 | a0001c0002t0001g0082 a0002c0003t0001g0003 |
2 | HG01071.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.627+592A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057901 | |||||||
| chr16:5057989 | C | A | 66 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(63): Show |
86 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.627+504G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5057989 | |||||||
| chr16:5058005 | C | T | 67 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(64): Show |
87 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.627+488G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058005 | |||||||
| chr16:5058087 | G | A | 3 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0307 |
3 | HG01884.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.627+406C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058087 | |||||||
| chr16:5058182 | C | T | 1 | a0002c0003t0001g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.627+311G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058182 | |||||||
| chr16:5058249 | C | A | 67 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(64): Show |
88 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.627+244G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058249 | |||||||
| chr16:5058259 | C | G | 12 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(9): Show |
14 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.627+234G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058259 | |||||||
| chr16:5058276 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.627+217G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058276 | |||||||
| chr16:5058298 | T | A | 9 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+195A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058298 | |||||||
| chr16:5058446 | T | C | 1 | a0001c0002t0002g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.627+47A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 4/7 | chr16 | 5058446 | |||||||
| chr16:5058719 | C | T | 9 | a0001c0001t0001g0057 a0001c0002t0001g0300 a0001c0002t0001g0301 others(6): Show |
9 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-109G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058719 | |||||||
| chr16:5058743 | G | A | 2 | a0002c0003t0001g0029 a0002c0003t0001g0260 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.510-133C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058743 | |||||||
| chr16:5058786 | C | T | 4 | a0001c0002t0001g0119 a0001c0002t0001g0266 a0001c0002t0001g0267 others(1): Show |
4 | HG00140.hp2 HG00642.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-176G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058786 | |||||||
| chr16:5058802 | A | G | 3 | a0001c0001t0001g0262 a0001c0002t0001g0149 a0001c0002t0006g0263 |
3 | HG02622.hp1 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.510-192T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058802 | |||||||
| chr16:5058806 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02886.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-196G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058806 | |||||||
| chr16:5058807 | G | A | 66 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(63): Show |
87 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.510-197C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058807 | |||||||
| chr16:5058855 | A | G | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.510-245T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058855 | |||||||
| chr16:5058920 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-310A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058920 | |||||||
| chr16:5058941 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510-331G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5058941 | |||||||
| chr16:5059095 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.510-485G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059095 | |||||||
| chr16:5059208 | A | T | 1 | a0001c0002t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.510-598T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059208 | |||||||
| chr16:5059211 | A | C | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-601T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059211 | |||||||
| chr16:5059237 | C | T | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-627G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059237 | |||||||
| chr16:5059272 | A | G | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.510-662T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059272 | |||||||
| chr16:5059322 | C | T | 67 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(64): Show |
88 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.510-712G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059322 | |||||||
| chr16:5059327 | A | G | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-717T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059327 | |||||||
| chr16:5059601 | G | A | 1 | a0001c0002t0001g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.509+685C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059601 | |||||||
| chr16:5059641 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.509+645G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059641 | |||||||
| chr16:5059650 | T | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG02280.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+636A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059650 | |||||||
| chr16:5059693 | G | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(297): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.509+593C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059693 | |||||||
| chr16:5059720 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.509+566G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059720 | |||||||
| chr16:5059782 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.509+504A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059782 | |||||||
| chr16:5059821 | T | C | 1 | a0001c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.509+465A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059821 | |||||||
| chr16:5059902 | C | A | 1 | a0007c0010t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+384G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059902 | |||||||
| chr16:5059998 | T | G | 2 | a0001c0001t0001g0262 a0001c0002t0006g0263 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.509+288A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5059998 | |||||||
| chr16:5060006 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509+280G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060006 | |||||||
| chr16:5060056 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.509+230G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060056 | |||||||
| chr16:5060117 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02886.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+169G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060117 | |||||||
| chr16:5060119 | C | G | 9 | a0001c0002t0001g0149 a0001c0002t0001g0300 a0001c0002t0001g0301 others(6): Show |
9 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+167G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060119 | |||||||
| chr16:5060119 | C | T | 2 | a0001c0002t0001g0008 a0001c0002t0001g0137 |
2 | NA18963.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.509+167G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060119 | |||||||
| chr16:5060131 | G | A | 2 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
2 | NA18944.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.509+155C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060131 | |||||||
| chr16:5060146 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.509+140C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060146 | |||||||
| chr16:5060252 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0013 |
2 | HG02056.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.509+34C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060252 | |||||||
| chr16:5060270 | C | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0171 others(67): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.509+16G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 3/7 | chr16 | 5060270 | |||||||
| chr16:5060625 | T | C | 19 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(16): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.359-189A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060625 | |||||||
| chr16:5060681 | C | T | 3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG02055.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359-245G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060681 | |||||||
| chr16:5060737 | C | T | 9 | a0001c0002t0001g0149 a0001c0002t0001g0300 a0001c0002t0001g0301 others(6): Show |
9 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-301G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060737 | |||||||
| chr16:5060945 | C | CT | 47 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0046 others(44): Show |
50 | HG00544.hp1 HG00673.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.359-510dupA | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060945 | |||||||
| chr16:5060945 | C | CTT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
130 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.359-511_359-510dup others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060945 | |||||||
| chr16:5060945 | C | CTTT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(49): Show |
66 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.359-512_359-510dup others(3): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060945 | |||||||
| chr16:5060945 | C | CTTTT | 7 | a0001c0001t0001g0295 a0001c0002t0001g0010 a0001c0002t0001g0012 others(4): Show |
7 | HG00438.hp1 HG01243.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-513_359-510dup others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060945 | |||||||
| chr16:5060945 | CT | C | 12 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0238 others(9): Show |
12 | HG00323.hp2 HG01168.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-510delA | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060945 | |||||||
| chr16:5060970 | A | G | 1 | a0002c0003t0001g0018 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.359-534T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060970 | |||||||
| chr16:5060981 | C | G | 1 | a0002c0003t0001g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359-545G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5060981 | |||||||
| chr16:5061031 | C | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0171 others(67): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.359-595G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061031 | |||||||
| chr16:5061099 | A | G | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-663T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061099 | |||||||
| chr16:5061201 | G | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0295 a0001c0002t0001g0270 |
3 | HG01243.hp1 HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.359-765C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061201 | |||||||
| chr16:5061264 | G | GA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
213 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.359-829dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061264 | |||||||
| chr16:5061264 | G | GAA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0043 others(28): Show |
33 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-830_359-829dup others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061264 | |||||||
| chr16:5061264 | GA | G | 11 | a0001c0001t0001g0051 a0002c0003t0001g0003 a0002c0003t0001g0015 others(8): Show |
13 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-829delT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061264 | |||||||
| chr16:5061338 | C | G | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-902G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061338 | |||||||
| chr16:5061432 | C | CA | 84 | a0001c0001t0001g0051 a0001c0001t0001g0094 a0001c0001t0001g0112 others(81): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.358+992dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061432 | C | CAA | 21 | a0001c0001t0001g0058 a0001c0001t0001g0256 a0001c0001t0002g0115 others(18): Show |
31 | HG00438.hp2 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.358+991_358+992dup others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061432 | CA | C | 69 | a0001c0001t0001g0035 a0001c0001t0001g0110 a0001c0001t0001g0175 others(66): Show |
91 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.358+992delT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061432 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.358+979_358+992del others(14): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061432 | CAAAAAAA others(8): Show |
C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
109 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.358+978_358+992del others(15): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061432 | CAAAAAAA others(9): Show |
C | 1 | a0002c0003t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.358+977_358+992del others(16): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061432 | |||||||
| chr16:5061458 | A | G | 1 | a0002c0003t0001g0062 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.358+967T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061458 | |||||||
| chr16:5061472 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.358+953C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061472 | |||||||
| chr16:5061484 | C | CA | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0249 others(4): Show |
9 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+940dupT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061484 | |||||||
| chr16:5061501 | A | AAAAAAAG | 7 | a0001c0001t0001g0180 a0001c0002t0001g0139 a0001c0002t0001g0142 others(4): Show |
7 | HG03098.hp1 NA18966.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+923_358+924ins others(7): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061501 | |||||||
| chr16:5061501 | A | AAAAAAG | 35 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0175 others(32): Show |
45 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.358+923_358+924ins others(6): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061501 | |||||||
| chr16:5061501 | A | AAAAAG | 39 | a0001c0001t0001g0171 a0001c0002t0001g0009 a0001c0002t0001g0010 others(36): Show |
51 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.358+923_358+924ins others(5): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061501 | |||||||
| chr16:5061501 | A | AAAAG | 6 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0300 others(3): Show |
6 | HG00140.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+923_358+924ins others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061501 | |||||||
| chr16:5061502 | A | AAAAG | 17 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+922_358+923ins others(4): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061502 | |||||||
| chr16:5061502 | A | AAAG | 97 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0052 others(94): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.358+922_358+923ins others(3): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061502 | |||||||
| chr16:5061502 | A | AAG | 11 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(8): Show |
11 | HG00323.hp1 HG00639.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+922_358+923ins others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061502 | |||||||
| chr16:5061503 | A | AAG | 11 | a0001c0001t0001g0058 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG01169.hp2 HG01928.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+921_358+922ins others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061503 | |||||||
| chr16:5061503 | A | AG | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
105 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.358+921_358+922ins others(1): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061503 | |||||||
| chr16:5061503 | A | G | 4 | a0001c0001t0001g0195 a0001c0002t0001g0053 a0001c0002t0001g0054 others(1): Show |
6 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+922T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061503 | |||||||
| chr16:5061505 | C | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
129 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.358+920G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061505 | |||||||
| chr16:5061506 | C | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
129 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.358+919G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061506 | |||||||
| chr16:5061511 | CAA | C | 88 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0153 others(85): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.358+912_358+913del others(2): Show |
C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061511 | |||||||
| chr16:5061512 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
135 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.358+913T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061512 | |||||||
| chr16:5061557 | T | C | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+868A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061557 | |||||||
| chr16:5061749 | C | G | 3 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.358+676G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061749 | |||||||
| chr16:5061957 | G | A | 1 | a0001c0002t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358+468C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5061957 | |||||||
| chr16:5062015 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.358+410T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062015 | |||||||
| chr16:5062107 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.358+318G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062107 | |||||||
| chr16:5062110 | C | G | 78 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0171 others(75): Show |
100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.358+315G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062110 | |||||||
| chr16:5062132 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0002c0003t0001g0192 |
3 | NA18941.hp2 NA18955.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.358+293G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062132 | |||||||
| chr16:5062171 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.358+254C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062171 | |||||||
| chr16:5062193 | C | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+232G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062193 | |||||||
| chr16:5062204 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.358+221G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062204 | |||||||
| chr16:5062261 | C | T | 2 | a0002c0003t0001g0066 a0002c0009t0001g0067 |
2 | HG01175.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.358+164G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062261 | |||||||
| chr16:5062307 | G | A | 1 | a0001c0002t0001g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.358+118C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062307 | |||||||
| chr16:5062316 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.358+109C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 2/7 | chr16 | 5062316 | |||||||
| chr16:5062589 | A | G | 2 | a0004c0005t0001g0271 a0004c0005t0001g0272 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.209-15T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062589 | |||||||
| chr16:5062600 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.209-26A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062600 | |||||||
| chr16:5062635 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.209-61C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062635 | |||||||
| chr16:5062641 | GA | G | 8 | a0001c0002t0001g0019 a0001c0002t0001g0119 a0001c0002t0001g0265 others(5): Show |
10 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-68delT | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062641 | |||||||
| chr16:5062682 | C | G | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209-108G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062682 | |||||||
| chr16:5062879 | A | G | 1 | a0002c0003t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.209-305T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062879 | |||||||
| chr16:5062950 | A | G | 76 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0001g0262 others(73): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.209-376T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5062950 | |||||||
| chr16:5063072 | C | T | 3 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 |
4 | HG01106.hp1 HG01168.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-498G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063072 | |||||||
| chr16:5063185 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.209-611C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063185 | |||||||
| chr16:5063283 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.209-709G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063283 | |||||||
| chr16:5063292 | C | T | 6 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(3): Show |
6 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-718G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063292 | |||||||
| chr16:5063330 | G | C | 1 | a0001c0002t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.209-756C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063330 | |||||||
| chr16:5063339 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.209-765C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063339 | |||||||
| chr16:5063419 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.209-845G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063419 | |||||||
| chr16:5063497 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209-923G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063497 | |||||||
| chr16:5063515 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-941A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063515 | |||||||
| chr16:5063581 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0190 |
3 | NA18966.hp2 NA19062.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.209-1007G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063581 | |||||||
| chr16:5063611 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.209-1037C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063611 | |||||||
| chr16:5063620 | C | T | 47 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0171 others(44): Show |
62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.209-1046G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063620 | |||||||
| chr16:5063754 | C | A | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | NA18965.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.209-1180G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063754 | |||||||
| chr16:5063778 | A | G | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0259 |
5 | HG02109.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-1204T>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063778 | |||||||
| chr16:5063790 | T | A | 2 | a0002c0003t0001g0108 a0002c0003t0001g0109 |
2 | HG00099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.209-1216A>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5063790 | |||||||
| chr16:5064004 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209-1430C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064004 | |||||||
| chr16:5064006 | A | C | 1 | a0002c0003t0001g0062 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.209-1432T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064006 | |||||||
| chr16:5064022 | G | T | 1 | a0002c0003t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.209-1448C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064022 | |||||||
| chr16:5064032 | A | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG02280.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-1458T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064032 | |||||||
| chr16:5064040 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.209-1466G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064040 | |||||||
| chr16:5064091 | C | T | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-1517G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064091 | |||||||
| chr16:5064111 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.209-1537G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064111 | |||||||
| chr16:5064119 | C | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-1545G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064119 | |||||||
| chr16:5064293 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+1408G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064293 | |||||||
| chr16:5064319 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+1382A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064319 | |||||||
| chr16:5064414 | G | C | 1 | a0001c0002t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208+1287C>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064414 | |||||||
| chr16:5064436 | T | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.208+1265A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064436 | |||||||
| chr16:5064498 | C | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.208+1203G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064498 | |||||||
| chr16:5064557 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0297 |
4 | HG01257.hp1 HG01258.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1144A>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064557 | |||||||
| chr16:5064645 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208+1056G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064645 | |||||||
| chr16:5064714 | A | C | 2 | a0003c0007t0001g0120 a0003c0007t0001g0121 |
2 | NA18953.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.208+987T>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064714 | |||||||
| chr16:5064729 | G | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+972C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064729 | |||||||
| chr16:5064915 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208+786C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5064915 | |||||||
| chr16:5065022 | C | A | 1 | a0001c0002t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208+679G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065022 | |||||||
| chr16:5065054 | G | T | 37 | a0001c0002t0001g0008 a0001c0002t0001g0030 a0001c0002t0001g0031 others(34): Show |
46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.208+647C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065054 | |||||||
| chr16:5065078 | C | T | 37 | a0001c0002t0001g0008 a0001c0002t0001g0030 a0001c0002t0001g0031 others(34): Show |
46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.208+623G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065078 | |||||||
| chr16:5065124 | G | A | 1 | a0001c0002t0001g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.208+577C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065124 | |||||||
| chr16:5065127 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+574G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065127 | |||||||
| chr16:5065165 | A | T | 1 | a0002c0003t0001g0059 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.208+536T>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065165 | |||||||
| chr16:5065215 | T | C | 8 | a0001c0002t0001g0300 a0001c0002t0001g0301 a0001c0002t0001g0302 others(5): Show |
8 | HG00544.hp1 HG00673.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+486A>G | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065215 | |||||||
| chr16:5065227 | C | T | 76 | a0001c0001t0001g0060 a0001c0001t0001g0094 a0001c0001t0001g0107 others(73): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.208+474G>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065227 | |||||||
| chr16:5065361 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+340G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065361 | |||||||
| chr16:5065494 | C | A | 1 | a0001c0002t0001g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.208+207G>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065494 | |||||||
| chr16:5065517 | G | A | 1 | a0003c0004t0001g0309 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.208+184C>T | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065517 | |||||||
| chr16:5065612 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208+89C>A | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065612 | |||||||
| chr16:5065665 | C | G | 1 | a0001c0002t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208+36G>C | C16orf89 | ENSG00000153446.16 | transcript | ENST00000472572.8 | protein_coding | 1/7 | chr16 | 5065665 |