Search by Gene
| Item | Value |
|---|---|
| geneid | 51096 |
| ensemblid | ENSG00000011260.14 |
| hgncid | 24274 |
| symbol | UTP18 |
| name | UTP18 small subunit processome component |
| refseq_nuc | NM_016001.3 |
| refseq_prot | NP_057085.2 |
| ensembl_nuc | ENST00000225298.12 |
| ensembl_prot | ENSP00000225298.7 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 51260546 |
| end | 51297933 |
| strand | + |
| ver | v1.2 |
| region | chr17:51260546-51297933 |
| region5000 | chr17:51255546-51302933 |
| regionname0 | UTP18_chr17_51260546_51297933 |
| regionname5000 | UTP18_chr17_51255546_51302933 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 556 | 358 | 93 | 75 | 132 | 14 | 42 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0002 | 0/0 | 556 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0003 | 0/0 | 556 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0004 | 0/0 | 556 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0005 | 0/0 | 556 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0006 | 0/0 | 556 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| a0007 | 0/0 | 556 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | MPPER others(551): Show |
chr17 | 51255546 | 51302933 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1668 | 138 | 26 | 35 | 57 | 7 | 12 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0002 | 0/0 | 1668 | 112 | 12 | 24 | 53 | 4 | 19 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0003 | 0/1 | 1668 | 34 | 17 | 11 | 0 | 1 | 4 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0004 | 0/0 | 1668 | 33 | 1 | 4 | 20 | 2 | 6 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0005 | 0/0 | 1668 | 17 | 17 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0006 | 0/0 | 1668 | 16 | 16 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0009 | 0/0 | 1668 | 2 | 1 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0010 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0011 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0012 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0017 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0018 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0001c0019 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0002c0007 | 0/0 | 1668 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0003c0008 | 0/0 | 1668 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0004c0014 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0005c0016 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0006c0013 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 | ||
| a0007c0015 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | ATGCC others(1663): Show |
chr17 | 51255546 | 51302933 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1876 | 138 | 26 | 35 | 57 | 7 | 12 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0002t0001 | 0/0 | 1876 | 112 | 12 | 24 | 53 | 4 | 19 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0003t0001 | 0/1 | 1876 | 34 | 17 | 11 | 0 | 1 | 4 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0004t0001 | 0/0 | 1876 | 33 | 1 | 4 | 20 | 2 | 6 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0005t0001 | 0/0 | 1876 | 17 | 17 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0006t0001 | 0/0 | 1876 | 16 | 16 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0009t0001 | 0/0 | 1876 | 2 | 1 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0010t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0011t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0012t0001 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0017t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0018t0001 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0001c0019t0001 | 0/0 | 1876 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0002c0007t0001 | 0/0 | 1876 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0003c0008t0001 | 0/0 | 1876 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0004c0014t0001 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0005c0016t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0006c0013t0001 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| a0007c0015t0001 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | GTTCC others(1871): Show |
chr17 | 51255546 | 51302933 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 5 | 9 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0015 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0011 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0006t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0009t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0010t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0011t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0012t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0017t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0018t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0001c0019t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0002c0007t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0002c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0003c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0003c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0004c0014t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0005c0016t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0006c0013t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| a0007c0015t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0282 | EUR | GBR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0106 | EUR | GBR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0187 | EUR | GBR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0061 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0276 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0262 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0266 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0275 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0272 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01099 | hp2 | a0004 | c0014 | t0001 | g0240 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0105 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0287 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0085 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0030 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01361 | hp1 | a0001 | c0018 | t0001 | g0127 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0253 | EUR | IBS | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0299 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01891 | hp1 | a0001 | c0006 | t0001 | g0044 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0139 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02083 | hp1 | a0002 | c0007 | t0001 | g0092 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02129 | hp1 | a0001 | c0009 | t0001 | g0023 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0071 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CDX | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02257 | hp1 | a0001 | c0009 | t0001 | g0023 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0151 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0290 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02280 | hp1 | a0001 | c0006 | t0001 | g0042 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0295 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0296 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02572 | hp1 | a0001 | c0006 | t0001 | g0257 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0043 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0138 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0049 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0294 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0291 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0297 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02683 | hp2 | a0001 | c0012 | t0001 | g0094 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0293 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02717 | hp2 | a0005 | c0016 | t0001 | g0058 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0050 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0265 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0045 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0047 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0283 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0164 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0048 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0285 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0277 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0003 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0077 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0055 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0163 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0003 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0298 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03195 | hp1 | a0001 | c0017 | t0001 | g0284 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0003 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0263 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0292 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0087 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0268 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0270 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0031 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | ESN | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0051 | AFR | GWD | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0278 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0031 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0300 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0066 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03831 | hp1 | a0006 | c0013 | t0001 | g0175 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0088 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0269 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04115 | hp2 | a0007 | c0015 | t0001 | g0036 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0185 | SAS | BEB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | STU | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0281 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | CHB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18945 | hp1 | a0003 | c0008 | t0001 | g0130 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18945 | hp2 | a0001 | c0004 | t0001 | g0136 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0078 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18954 | hp1 | a0002 | c0007 | t0001 | g0006 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18967 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0098 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0137 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18977 | hp2 | a0001 | c0019 | t0001 | g0027 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18988 | hp2 | a0003 | c0008 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0074 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18994 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0280 | AFR | LWK | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0108 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0109 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19076 | hp2 | a0001 | c0004 | t0001 | g0075 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19089 | hp1 | a0001 | c0004 | t0001 | g0110 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0003 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | YRI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | ASW | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0076 | EUR | TSI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0183 | EUR | TSI | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0112 | SAS | GIH | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0081 | SAS | GIH | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0273 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0150 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG02486 | hp2 | a0001 | c0011 | t0001 | g0084 | AFR | ACB | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0052 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0046 | AFR | USA | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0267 | REF | REF | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | UTP18_chr17_51255546_51302933 | UTP18 | chr17 | 51255546 | 51302933 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:51260760 | C | T | 1 | a0005 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.176C>T | p.Ala59Val | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/14 | 215/1876 | 176/1671 | 59/556 | chr17 | 51260760 | |||
| chr17:51260814 | G | A | 1 | a0002 | 2 | HG02083.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.230G>A | p.Arg77His | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/14 | 269/1876 | 230/1671 | 77/556 | chr17 | 51260814 | |||
| chr17:51266199 | A | G | 1 | a0007 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.473A>G | p.Asn158Ser | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/14 | 512/1876 | 473/1671 | 158/556 | chr17 | 51266199 | |||
| chr17:51275866 | A | G | 1 | a0004 | 1 | HG01099.hp2 | missense_variant&splice_region_variant | MODERATE | c.712A>G | p.Met238Val | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/14 | 751/1876 | 712/1671 | 238/556 | chr17 | 51275866 | |||
| chr17:51280103 | A | G | 1 | a0003 | 2 | NA18945.hp1 NA18988.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1111A>G | p.Lys371Glu | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 8/14 | 1150/1876 | 1111/1671 | 371/556 | chr17 | 51280103 | |||
| chr17:51285256 | G | A | 1 | a0006 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1216G>A | p.Val406Ile | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/14 | 1255/1876 | 1216/1671 | 406/556 | chr17 | 51285256 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:51260632 | A | G | 3 | a0001c0017a0001c0018a0001c0019 | 3 | HG01361.hp1 HG03195.hp1 NA18977.hp2 |
synonymous_variant | LOW | c.48A>G | p.Gly16Gly | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/14 | 87/1876 | 48/1671 | 16/556 | chr17 | 51260632 | |||
| chr17:51260896 | C | T | 1 | a0001c0004 | 33 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(30): Show |
synonymous_variant | LOW | c.312C>T | p.Asp104Asp | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/14 | 351/1876 | 312/1671 | 104/556 | chr17 | 51260896 | |||
| chr17:51260914 | G | A | 2 | a0001c0003a0001c0017 | 35 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(32): Show |
synonymous_variant | LOW | c.330G>A | p.Leu110Leu | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/14 | 369/1876 | 330/1671 | 110/556 | chr17 | 51260914 | |||
| chr17:51263276 | T | C | 2 | a0001c0005a0001c0010 | 18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
splice_region_variant&synonymous_variant | LOW | c.345T>C | p.Val115Val | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/14 | 384/1876 | 345/1671 | 115/556 | chr17 | 51263276 | |||
| chr17:51263294 | G | A | 1 | a0001c0011 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.363G>A | p.Ser121Ser | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/14 | 402/1876 | 363/1671 | 121/556 | chr17 | 51263294 | |||
| chr17:51273441 | A | C | 5 | a0001c0002a0001c0009a0001c0019others(2): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
synonymous_variant | LOW | c.702A>C | p.Gly234Gly | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/14 | 741/1876 | 702/1671 | 234/556 | chr17 | 51273441 | |||
| chr17:51275985 | A | G | 2 | a0001c0006a0001c0010 | 17 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(14): Show |
synonymous_variant | LOW | c.831A>G | p.Leu277Leu | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/14 | 870/1876 | 831/1671 | 277/556 | chr17 | 51275985 | |||
| chr17:51288197 | C | T | 1 | a0001c0009 | 2 | HG02129.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.1497C>T | p.Val499Val | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/14 | 1536/1876 | 1497/1671 | 499/556 | chr17 | 51288197 | |||
| chr17:51293974 | T | C | 1 | a0001c0012 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.1575T>C | p.His525His | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/14 | 1614/1876 | 1575/1671 | 525/556 | chr17 | 51293974 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:51260994 | G | C | 2 | a0001c0002t0001g0033a0001c0002t0001g0034 | 2 | HG03669.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.342+68G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51260994 | |||||||
| chr17:51261060 | G | T | 1 | a0001c0002t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.342+134G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261060 | |||||||
| chr17:51261386 | A | G | 1 | a0001c0003t0001g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.342+460A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261386 | |||||||
| chr17:51261463 | C | T | 12 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0290others(9): Show | 13 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+537C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261463 | |||||||
| chr17:51261736 | C | T | 32 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0030others(29): Show | 35 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.342+810C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261736 | |||||||
| chr17:51261787 | A | C | 3 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG02015.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.342+861A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261787 | |||||||
| chr17:51261837 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.342+911C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261837 | |||||||
| chr17:51261903 | C | T | 1 | a0001c0006t0001g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.342+977C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261903 | |||||||
| chr17:51261907 | A | G | 4 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0255others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+981A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51261907 | |||||||
| chr17:51262120 | C | T | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-1154C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262120 | |||||||
| chr17:51262185 | G | T | 96 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(93): Show | 111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.343-1089G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262185 | |||||||
| chr17:51262297 | G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-977G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262297 | |||||||
| chr17:51262355 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-919A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262355 | |||||||
| chr17:51262415 | G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0053others(13): Show | 20 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.343-859G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262415 | |||||||
| chr17:51262418 | T | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0053others(46): Show | 56 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.343-856T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262418 | |||||||
| chr17:51262557 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.343-717G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262557 | |||||||
| chr17:51262575 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-699C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262575 | |||||||
| chr17:51262582 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.343-692A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262582 | |||||||
| chr17:51262604 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.343-670C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262604 | |||||||
| chr17:51262641 | A | G | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02976.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.343-633A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262641 | |||||||
| chr17:51262740 | C | T | 100 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(97): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.343-534C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262740 | |||||||
| chr17:51262950 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.343-324A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262950 | |||||||
| chr17:51262994 | T | G | 1 | a0001c0002t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-280T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51262994 | |||||||
| chr17:51263072 | C | T | 2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.343-202C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 1/13 | chr17 | 51263072 | |||||||
| chr17:51263520 | C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.455+134C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51263520 | |||||||
| chr17:51263623 | A | G | 33 | a0001c0001t0001g0166a0001c0003t0001g0028a0001c0003t0001g0029others(30): Show | 36 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.455+237A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51263623 | |||||||
| chr17:51263755 | G | T | 1 | a0001c0004t0001g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.455+369G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51263755 | |||||||
| chr17:51263901 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.455+515T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51263901 | |||||||
| chr17:51264028 | C | T | 1 | a0001c0001t0001g0010 | 3 | HG00099.hp2 HG00733.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.455+642C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264028 | |||||||
| chr17:51264049 | T | A | 101 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(98): Show | 116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.455+663T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264049 | |||||||
| chr17:51264130 | G | A | 1 | a0006c0013t0001g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.455+744G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264130 | |||||||
| chr17:51264402 | T | C | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.455+1016T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264402 | |||||||
| chr17:51264533 | A | G | 2 | a0001c0005t0001g0163a0001c0005t0001g0164 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.455+1147A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264533 | |||||||
| chr17:51264607 | TC | T | 143 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(140): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.455+1223delC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51264607 | ||||||
| chr17:51264608 | C | T | 7 | a0001c0003t0001g0283a0001c0003t0001g0285a0001c0003t0001g0286others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.455+1222C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264608 | |||||||
| chr17:51264689 | TC | T | 3 | a0001c0002t0001g0176a0001c0003t0001g0262a0001c0003t0001g0283 | 3 | HG01070.hp1 HG01257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.455+1304delC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264689 | |||||||
| chr17:51264690 | C | T | 147 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(144): Show | 169 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.455+1304C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264690 | |||||||
| chr17:51264690 | CT | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.455+1318delT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51264690 | ||||||
| chr17:51264768 | C | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(97): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.455+1382C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264768 | |||||||
| chr17:51264785 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.456-1397C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264785 | |||||||
| chr17:51264902 | C | T | 190 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(187): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.456-1280C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264902 | |||||||
| chr17:51264934 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.456-1248C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264934 | |||||||
| chr17:51264935 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.456-1247G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51264935 | |||||||
| chr17:51265100 | G | A | 1 | a0001c0017t0001g0284 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.456-1082G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265100 | |||||||
| chr17:51265326 | C | T | 100 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(97): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.456-856C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265326 | |||||||
| chr17:51265553 | G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.456-629G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265553 | |||||||
| chr17:51265562 | C | CT | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(62): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.456-599dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265562 | C | CTT | 117 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0037others(114): Show | 135 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.456-600_456-599dup others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265562 | C | CTTT | 54 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0026others(51): Show | 60 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.456-601_456-599dup others(3): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265562 | C | CTTTT | 6 | a0001c0002t0001g0053a0001c0002t0001g0247a0001c0002t0001g0248others(3): Show | 6 | HG00099.hp1 HG00741.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.456-602_456-599dup others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265562 | C | CTTTTTTT others(13): Show |
1 | a0001c0002t0001g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.456-618_456-599dup others(20): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265562 | C | CTTTTTTT others(42): Show |
1 | a0001c0002t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.456-599_456-598ins others(49): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 51265562 | ||||||
| chr17:51265588 | C | CGG | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-594_456-593ins others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265588 | |||||||
| chr17:51265595 | A | G | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-587A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265595 | |||||||
| chr17:51265600 | T | G | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-582T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265600 | |||||||
| chr17:51265602 | T | C | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-580T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265602 | |||||||
| chr17:51265760 | C | T | 39 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.456-422C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265760 | |||||||
| chr17:51265788 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.456-394T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265788 | |||||||
| chr17:51265934 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.456-248T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 2/13 | chr17 | 51265934 | |||||||
| chr17:51266287 | G | T | 1 | a0001c0005t0001g0298 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.554+7G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266287 | |||||||
| chr17:51266294 | T | C | 15 | a0001c0001t0001g0013a0001c0002t0001g0053a0001c0006t0001g0003others(12): Show | 19 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.554+14T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266294 | |||||||
| chr17:51266297 | A | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0053others(46): Show | 56 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.554+17A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266297 | |||||||
| chr17:51266485 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.554+205A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266485 | |||||||
| chr17:51266731 | A | C | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+451A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266731 | |||||||
| chr17:51266815 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.554+535A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266815 | |||||||
| chr17:51266927 | T | G | 2 | a0001c0002t0001g0249a0001c0002t0001g0250 | 2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.554+647T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266927 | |||||||
| chr17:51266954 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.554+674G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266954 | |||||||
| chr17:51266991 | A | C | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+711A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266991 | |||||||
| chr17:51266993 | T | A | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+713T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266993 | |||||||
| chr17:51266998 | A | T | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+718A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51266998 | |||||||
| chr17:51267008 | T | G | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+728T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267008 | |||||||
| chr17:51267009 | G | A | 1 | a0001c0002t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.554+729G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267009 | |||||||
| chr17:51267197 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.554+917A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267197 | |||||||
| chr17:51267294 | G | T | 3 | a0001c0003t0001g0283a0001c0003t0001g0287a0001c0003t0001g0288 | 3 | HG01167.hp1 HG01169.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.554+1014G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267294 | |||||||
| chr17:51267382 | G | A | 15 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0163others(12): Show | 16 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.554+1102G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267382 | |||||||
| chr17:51267402 | AGT | A | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 25 | HG01943.hp1 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.554+1123_554+1124d others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267402 | |||||||
| chr17:51267429 | C | T | 3 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233 | 3 | NA18964.hp1 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.554+1149C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267429 | |||||||
| chr17:51267461 | G | GT | 105 | a0001c0001t0001g0142a0001c0002t0001g0002a0001c0002t0001g0011others(102): Show | 120 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.554+1194dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51267461 | ||||||
| chr17:51267461 | G | T | 1 | a0001c0004t0001g0110 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.554+1181G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267461 | |||||||
| chr17:51267514 | C | T | 1 | a0001c0002t0001g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.554+1234C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267514 | |||||||
| chr17:51267682 | C | T | 3 | a0001c0002t0001g0227a0001c0002t0001g0228a0001c0002t0001g0229 | 3 | HG01256.hp2 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.555-1155C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267682 | |||||||
| chr17:51267800 | C | T | 11 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0263others(8): Show | 13 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.555-1037C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267800 | |||||||
| chr17:51267959 | ACT | A | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.555-873_555-872del others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51267959 | ||||||
| chr17:51267978 | A | G | 3 | a0001c0002t0001g0229a0001c0004t0001g0105a0001c0004t0001g0106 | 3 | HG00140.hp1 HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.555-859A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51267978 | |||||||
| chr17:51268007 | G | GT | 16 | a0001c0002t0001g0025a0001c0002t0001g0171a0001c0002t0001g0220others(13): Show | 17 | HG00544.hp2 HG02074.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.555-824dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51268007 | ||||||
| chr17:51268007 | G | GTT | 27 | a0001c0003t0001g0030a0001c0003t0001g0262a0001c0003t0001g0271others(24): Show | 31 | HG00099.hp1 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.555-825_555-824dup others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51268007 | ||||||
| chr17:51268007 | G | GTTT | 10 | a0001c0001t0001g0054a0001c0003t0001g0264a0001c0003t0001g0277others(7): Show | 10 | HG02723.hp1 HG02970.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.555-826_555-824dup others(3): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51268007 | ||||||
| chr17:51268007 | G | GTTTT | 4 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0265others(1): Show | 6 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-827_555-824dup others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 51268007 | ||||||
| chr17:51268007 | G | T | 1 | a0001c0002t0001g0226 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.555-830G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268007 | |||||||
| chr17:51268014 | G | T | 143 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(140): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.555-823G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268014 | |||||||
| chr17:51268021 | T | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0144 | 4 | HG00423.hp2 NA18953.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-816T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268021 | |||||||
| chr17:51268031 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.555-806A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268031 | |||||||
| chr17:51268071 | G | A | 2 | a0001c0004t0001g0066a0001c0004t0001g0112 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.555-766G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268071 | |||||||
| chr17:51268114 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.555-723A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268114 | |||||||
| chr17:51268183 | G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(47): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.555-654G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268183 | |||||||
| chr17:51268296 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555-541G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268296 | |||||||
| chr17:51268314 | T | C | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.555-523T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268314 | |||||||
| chr17:51268316 | G | A | 149 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(146): Show | 171 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.555-521G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268316 | |||||||
| chr17:51268318 | G | T | 1 | a0001c0004t0001g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.555-519G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268318 | |||||||
| chr17:51268393 | G | C | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.555-444G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268393 | |||||||
| chr17:51268450 | T | A | 1 | a0001c0004t0001g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.555-387T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268450 | |||||||
| chr17:51268450 | T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.555-387T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268450 | |||||||
| chr17:51268536 | T | C | 190 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(187): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.555-301T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268536 | |||||||
| chr17:51268542 | G | A | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.555-295G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268542 | |||||||
| chr17:51268736 | C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0162 | 2 | HG01346.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.555-101C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268736 | |||||||
| chr17:51268815 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.555-22T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 3/13 | chr17 | 51268815 | |||||||
| chr17:51269052 | C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.622+148C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269052 | |||||||
| chr17:51269096 | G | A | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.622+192G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269096 | |||||||
| chr17:51269108 | G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0004t0001g0069others(14): Show | 21 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+204G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269108 | |||||||
| chr17:51269294 | C | CA | 24 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0086others(21): Show | 26 | HG00280.hp1 HG01255.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.622+422dupA | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | C | CAA | 22 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0083others(19): Show | 23 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.622+421_622+422dup others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | C | CAAA | 8 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0004t0001g0059others(5): Show | 8 | HG01952.hp2 HG02148.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.622+420_622+422dup others(3): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAA | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0152others(3): Show | 6 | HG02015.hp2 HG02129.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+421_622+422del others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAA | C | 20 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(17): Show | 20 | HG00558.hp2 HG00642.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.622+420_622+422del others(3): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAAA | C | 10 | a0001c0002t0001g0171a0001c0002t0001g0174a0001c0005t0001g0032others(7): Show | 11 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.622+419_622+422del others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAAAAA | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0016others(54): Show | 67 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.622+417_622+422del others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAAAAAA | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(104): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.622+416_622+422del others(7): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAAAAAA others(1): Show |
C | 27 | a0001c0001t0001g0056a0001c0001t0001g0143a0001c0001t0001g0149others(24): Show | 30 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.622+415_622+422del others(8): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269294 | CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0001g0277 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.622+410_622+422del others(13): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269294 | ||||||
| chr17:51269315 | A | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0102 | 4 | HG01069.hp1 HG01257.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+411A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269315 | |||||||
| chr17:51269324 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622+420A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269324 | |||||||
| chr17:51269342 | TTTTGACT others(5): Show |
T | 4 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(1): Show | 4 | NA18971.hp2 NA19054.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+442_622+453del others(12): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269342 | ||||||
| chr17:51269518 | C | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.622+614C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269518 | |||||||
| chr17:51269532 | G | A | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.622+628G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269532 | |||||||
| chr17:51269595 | T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(296): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.622+691T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269595 | |||||||
| chr17:51269688 | A | G | 32 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0030others(29): Show | 35 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.622+784A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269688 | |||||||
| chr17:51269838 | ATT | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(30): Show | 58 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.622+935_622+936del others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269838 | |||||||
| chr17:51269838 | ATTGT | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0063others(5): Show | 10 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.622+935_622+938del others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269838 | |||||||
| chr17:51269839 | T | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0119others(6): Show | 12 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.622+935T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269839 | |||||||
| chr17:51269839 | T | TTG | 101 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(98): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.622+965_622+966dup others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269839 | ||||||
| chr17:51269839 | T | TTGTG | 47 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0101others(44): Show | 52 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.622+963_622+966dup others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269839 | ||||||
| chr17:51269839 | T | TTGTGTG | 4 | a0001c0001t0001g0162a0001c0002t0001g0254a0001c0002t0001g0255others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+961_622+966dup others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269839 | ||||||
| chr17:51269839 | T | TTGTGTGT others(1): Show |
3 | a0001c0002t0001g0176a0001c0002t0001g0192a0001c0002t0001g0216 | 3 | HG01257.hp1 HG01258.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.622+959_622+966dup others(8): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269839 | ||||||
| chr17:51269839 | TTGTG | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.622+963_622+966del others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51269839 | ||||||
| chr17:51269907 | G | A | 39 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.622+1003G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51269907 | |||||||
| chr17:51270169 | T | C | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.622+1265T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270169 | |||||||
| chr17:51270174 | C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.622+1270C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270174 | |||||||
| chr17:51270188 | A | G | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.622+1284A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270188 | |||||||
| chr17:51270209 | T | A | 3 | a0001c0004t0001g0085a0001c0004t0001g0105a0001c0004t0001g0106 | 3 | HG00140.hp1 HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.622+1305T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270209 | |||||||
| chr17:51270259 | T | C | 190 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(187): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.622+1355T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270259 | |||||||
| chr17:51270280 | C | T | 150 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(147): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.622+1376C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270280 | |||||||
| chr17:51270308 | T | G | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.622+1404T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270308 | |||||||
| chr17:51270362 | T | C | 1 | a0001c0005t0001g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.622+1458T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270362 | |||||||
| chr17:51270473 | G | A | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.622+1569G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270473 | |||||||
| chr17:51270510 | A | G | 2 | a0001c0004t0001g0061a0001c0004t0001g0071 | 2 | HG00639.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.622+1606A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270510 | |||||||
| chr17:51270563 | G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0140 | 2 | HG01361.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.622+1659G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270563 | |||||||
| chr17:51270605 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.622+1701A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270605 | |||||||
| chr17:51270640 | G | A | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.622+1736G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270640 | |||||||
| chr17:51270646 | C | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.622+1742C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270646 | |||||||
| chr17:51270665 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.622+1761C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270665 | |||||||
| chr17:51270816 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.622+1912A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51270816 | |||||||
| chr17:51271187 | C | G | 1 | a0001c0002t0001g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.623-2175C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271187 | |||||||
| chr17:51271203 | T | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0253others(46): Show | 56 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.623-2159T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271203 | |||||||
| chr17:51271258 | C | T | 1 | a0001c0003t0001g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.623-2104C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271258 | |||||||
| chr17:51271427 | C | G | 1 | a0001c0002t0001g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.623-1935C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271427 | |||||||
| chr17:51271485 | A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0141 | 3 | HG01515.hp2 HG01517.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.623-1877A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271485 | |||||||
| chr17:51271581 | T | TCTGTACT others(9): Show |
12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-1781_623-1780i others(18): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271581 | |||||||
| chr17:51271582 | T | G | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-1780T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271582 | |||||||
| chr17:51271610 | C | A | 1 | a0001c0005t0001g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.623-1752C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271610 | |||||||
| chr17:51271618 | A | G | 1 | a0001c0006t0001g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.623-1744A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271618 | |||||||
| chr17:51271643 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.623-1719A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271643 | |||||||
| chr17:51271706 | C | T | 1 | a0001c0004t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.623-1656C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271706 | |||||||
| chr17:51271707 | G | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.623-1655G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271707 | |||||||
| chr17:51271880 | C | G | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.623-1482C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271880 | |||||||
| chr17:51271918 | T | C | 1 | a0001c0002t0001g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.623-1444T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271918 | |||||||
| chr17:51271992 | G | A | 2 | a0001c0005t0001g0291a0001c0005t0001g0292 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.623-1370G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51271992 | |||||||
| chr17:51272066 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.623-1296C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272066 | |||||||
| chr17:51272086 | T | A | 2 | a0001c0002t0001g0254a0001c0002t0001g0256 | 2 | HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.623-1276T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272086 | |||||||
| chr17:51272245 | T | C | 1 | a0001c0002t0001g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.623-1117T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272245 | |||||||
| chr17:51272291 | G | A | 32 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0030others(29): Show | 35 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.623-1071G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272291 | |||||||
| chr17:51272421 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.623-941T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272421 | |||||||
| chr17:51272437 | G | A | 1 | a0001c0005t0001g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.623-925G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272437 | |||||||
| chr17:51272533 | G | A | 3 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG02015.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.623-829G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272533 | |||||||
| chr17:51272585 | T | C | 1 | a0001c0002t0001g0194 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.623-777T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272585 | |||||||
| chr17:51272616 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.623-746A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272616 | |||||||
| chr17:51272688 | A | T | 1 | a0001c0002t0001g0221 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.623-674A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272688 | |||||||
| chr17:51272696 | A | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0248 | 2 | NA18982.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.623-666A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272696 | |||||||
| chr17:51272743 | C | T | 1 | a0001c0002t0001g0241 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.623-619C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272743 | |||||||
| chr17:51272809 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.623-553A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272809 | |||||||
| chr17:51272980 | A | G | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.623-382A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272980 | |||||||
| chr17:51272999 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.623-363C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51272999 | |||||||
| chr17:51273049 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.623-313C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51273049 | |||||||
| chr17:51273185 | AT | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(194): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.623-161delT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 51273185 | ||||||
| chr17:51273256 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.623-106C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51273256 | |||||||
| chr17:51273339 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.623-23C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 4/13 | chr17 | 51273339 | |||||||
| chr17:51273598 | G | GT | 117 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(114): Show | 136 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.711+160dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273598 | ||||||
| chr17:51273739 | T | TAATA | 16 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(13): Show | 18 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+321_711+324dup others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273739 | T | TAATAAAT others(1): Show |
31 | a0001c0001t0001g0035a0001c0002t0001g0024a0001c0002t0001g0027others(28): Show | 33 | HG00099.hp1 HG00558.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.711+317_711+324dup others(8): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273739 | T | TAATAAAT others(5): Show |
43 | a0001c0001t0001g0054a0001c0002t0001g0012a0001c0002t0001g0026others(40): Show | 49 | HG00642.hp2 HG01106.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.711+313_711+324dup others(12): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273739 | T | TAATAAAT others(9): Show |
61 | a0001c0001t0001g0013a0001c0002t0001g0002a0001c0002t0001g0011others(58): Show | 73 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.711+309_711+324dup others(16): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273739 | T | TAATAAAT others(13): Show |
7 | a0001c0002t0001g0186a0001c0002t0001g0189a0001c0002t0001g0195others(4): Show | 7 | HG00609.hp1 HG01433.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.711+305_711+324dup others(20): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273739 | TAATA | T | 16 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0150others(13): Show | 17 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.711+321_711+324del others(4): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51273739 | ||||||
| chr17:51273797 | C | T | 150 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(147): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.711+347C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51273797 | |||||||
| chr17:51273858 | C | T | 1 | a0001c0003t0001g0279 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.711+408C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51273858 | |||||||
| chr17:51273906 | C | T | 17 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0150others(14): Show | 18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+456C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51273906 | |||||||
| chr17:51274022 | C | T | 1 | a0001c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.711+572C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274022 | |||||||
| chr17:51274109 | C | T | 6 | a0001c0004t0001g0059a0001c0004t0001g0070a0001c0004t0001g0079others(3): Show | 6 | NA18944.hp1 NA18967.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.711+659C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274109 | |||||||
| chr17:51274138 | G | A | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.711+688G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274138 | |||||||
| chr17:51274139 | G | C | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.711+689G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274139 | |||||||
| chr17:51274185 | T | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0158 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.711+735T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274185 | |||||||
| chr17:51274302 | A | G | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.711+852A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274302 | |||||||
| chr17:51274377 | G | A | 187 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(184): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.711+927G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274377 | |||||||
| chr17:51274406 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01074.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.711+956A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274406 | |||||||
| chr17:51274477 | T | C | 17 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0150others(14): Show | 18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+1027T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274477 | |||||||
| chr17:51274695 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.712-1171G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274695 | |||||||
| chr17:51274920 | G | T | 33 | a0001c0004t0001g0059a0001c0004t0001g0060a0001c0004t0001g0061others(30): Show | 33 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.712-946G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274920 | |||||||
| chr17:51274969 | G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0063others(4): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.712-897G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51274969 | |||||||
| chr17:51275145 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.712-721C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275145 | |||||||
| chr17:51275197 | C | CA | 38 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(35): Show | 39 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.712-652dupA | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51275197 | ||||||
| chr17:51275239 | C | CT | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.712-625dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 51275239 | ||||||
| chr17:51275246 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.712-620G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275246 | |||||||
| chr17:51275295 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.712-571A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275295 | |||||||
| chr17:51275357 | C | T | 1 | a0001c0005t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.712-509C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275357 | |||||||
| chr17:51275469 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.712-397A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275469 | |||||||
| chr17:51275572 | G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.712-294G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275572 | |||||||
| chr17:51275667 | T | C | 1 | a0001c0002t0001g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.712-199T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275667 | |||||||
| chr17:51275769 | T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-97T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 5/13 | chr17 | 51275769 | |||||||
| chr17:51276140 | CAG | C | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.837+152_837+153del others(2): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 51276140 | ||||||
| chr17:51276330 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.837+339C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276330 | |||||||
| chr17:51276426 | G | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.837+435G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276426 | |||||||
| chr17:51276475 | G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0227a0001c0002t0001g0228others(1): Show | 4 | HG01074.hp1 HG01256.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+484G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276475 | |||||||
| chr17:51276535 | T | C | 1 | a0005c0016t0001g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.837+544T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276535 | |||||||
| chr17:51276616 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.838-514C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276616 | |||||||
| chr17:51276662 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.838-468A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276662 | |||||||
| chr17:51276721 | T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.838-409T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276721 | |||||||
| chr17:51276820 | C | G | 7 | a0001c0005t0001g0031a0001c0005t0001g0290a0001c0005t0001g0293others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-310C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276820 | |||||||
| chr17:51276882 | C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-248C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276882 | |||||||
| chr17:51276902 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.838-228C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276902 | |||||||
| chr17:51276916 | C | G | 1 | a0001c0002t0001g0188 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.838-214C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276916 | |||||||
| chr17:51276948 | C | T | 150 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(147): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.838-182C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 6/13 | chr17 | 51276948 | |||||||
| chr17:51277330 | A | ACCAGTCA others(6): Show |
1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1012+30_1012+42dup others(13): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 51277330 | ||||||
| chr17:51277662 | G | C | 1 | a0001c0005t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1012+358G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51277662 | |||||||
| chr17:51277842 | T | G | 1 | a0001c0018t0001g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1012+538T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51277842 | |||||||
| chr17:51278023 | A | T | 1 | a0001c0005t0001g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1012+719A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278023 | |||||||
| chr17:51278131 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1012+827C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278131 | |||||||
| chr17:51278136 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1012+832G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278136 | |||||||
| chr17:51278160 | A | G | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1012+856A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278160 | |||||||
| chr17:51278179 | C | A | 1 | a0001c0002t0001g0221 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1012+875C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278179 | |||||||
| chr17:51278226 | G | A | 3 | a0001c0003t0001g0262a0001c0003t0001g0272a0001c0003t0001g0275 | 3 | HG01070.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1012+922G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278226 | |||||||
| chr17:51278289 | A | G | 1 | a0001c0005t0001g0290 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1012+985A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278289 | |||||||
| chr17:51278805 | C | T | 1 | a0001c0002t0001g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1013-1200C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51278805 | |||||||
| chr17:51279084 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(47): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1013-921T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279084 | |||||||
| chr17:51279140 | C | T | 2 | a0001c0001t0001g0086a0001c0002t0001g0208 | 2 | HG02622.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1013-865C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279140 | |||||||
| chr17:51279307 | A | G | 2 | a0001c0005t0001g0032a0001c0005t0001g0295 | 3 | HG02280.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1013-698A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279307 | |||||||
| chr17:51279351 | C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1013-654C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279351 | |||||||
| chr17:51279425 | A | C | 1 | a0001c0004t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1013-580A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279425 | |||||||
| chr17:51279467 | G | C | 1 | a0001c0002t0001g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1013-538G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279467 | |||||||
| chr17:51279490 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1013-515G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279490 | |||||||
| chr17:51279506 | G | GT | 38 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(35): Show | 39 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1013-494dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 51279506 | ||||||
| chr17:51279512 | G | T | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1013-493G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279512 | |||||||
| chr17:51279550 | A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0132 | 2 | NA19081.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1013-455A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279550 | |||||||
| chr17:51279869 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1013-136C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 7/13 | chr17 | 51279869 | |||||||
| chr17:51280214 | G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+109G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 8/13 | chr17 | 51280214 | |||||||
| chr17:51280256 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1114-133G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 8/13 | chr17 | 51280256 | |||||||
| chr17:51280485 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.1204+6A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280485 | |||||||
| chr17:51280536 | A | G | 17 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0150others(14): Show | 18 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204+57A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280536 | |||||||
| chr17:51280822 | A | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG00558.hp2 NA18950.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+343A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280822 | |||||||
| chr17:51280823 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1204+344T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280823 | |||||||
| chr17:51280857 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1204+378C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280857 | |||||||
| chr17:51280899 | C | G | 1 | a0001c0004t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1204+420C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280899 | |||||||
| chr17:51280905 | C | T | 1 | a0001c0002t0001g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1204+426C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51280905 | |||||||
| chr17:51281141 | A | T | 1 | a0001c0003t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1204+662A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281141 | |||||||
| chr17:51281160 | A | AT | 4 | a0001c0002t0001g0169a0001c0005t0001g0163a0001c0005t0001g0292others(1): Show | 4 | HG02280.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+682dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281160 | ||||||
| chr17:51281160 | A | T | 2 | a0001c0004t0001g0078a0001c0012t0001g0094 | 2 | HG02683.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1204+681A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281160 | |||||||
| chr17:51281161 | TA | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0086others(4): Show | 7 | HG01943.hp1 HG02109.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204+683delA | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281161 | |||||||
| chr17:51281162 | A | AT | 24 | a0001c0001t0001g0173a0001c0002t0001g0033a0001c0002t0001g0170others(21): Show | 26 | HG00544.hp2 HG01099.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.1204+684dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281162 | ||||||
| chr17:51281162 | A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1204+683A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281162 | |||||||
| chr17:51281164 | A | AT | 83 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(80): Show | 97 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1204+693dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281164 | ||||||
| chr17:51281164 | A | ATATAT | 10 | a0001c0003t0001g0030a0001c0003t0001g0262a0001c0003t0001g0264others(7): Show | 11 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1204+686_1204+687i others(7): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281164 | ||||||
| chr17:51281164 | A | ATATATAT | 12 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0263others(9): Show | 17 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1204+686_1204+687i others(9): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281164 | ||||||
| chr17:51281164 | A | ATATATAT others(4): Show |
1 | a0001c0006t0001g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1204+686_1204+687i others(13): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281164 | ||||||
| chr17:51281164 | A | ATATATTT | 8 | a0001c0001t0001g0054a0001c0006t0001g0044a0001c0006t0001g0045others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1204+686_1204+687i others(9): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51281164 | ||||||
| chr17:51281164 | A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1204+685A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281164 | |||||||
| chr17:51281165 | T | TA | 5 | a0001c0002t0001g0053a0001c0002t0001g0174a0001c0002t0001g0197others(2): Show | 5 | HG00741.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204+686_1204+687i others(3): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281165 | |||||||
| chr17:51281165 | T | TATATA | 11 | a0001c0003t0001g0265a0001c0003t0001g0274a0001c0003t0001g0276others(8): Show | 11 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1204+686_1204+687i others(7): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281165 | |||||||
| chr17:51281165 | T | TATATATA others(8): Show |
1 | a0001c0003t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1204+686_1204+687i others(17): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281165 | |||||||
| chr17:51281167 | T | A | 2 | a0001c0003t0001g0285a0001c0003t0001g0299 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1204+688T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281167 | |||||||
| chr17:51281221 | C | G | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1204+742C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281221 | |||||||
| chr17:51281288 | A | G | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204+809A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281288 | |||||||
| chr17:51281364 | A | T | 1 | a0001c0002t0001g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1204+885A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281364 | |||||||
| chr17:51281411 | T | C | 3 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0078 | 3 | NA18949.hp2 NA18989.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1204+932T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281411 | |||||||
| chr17:51281796 | G | A | 32 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0030others(29): Show | 35 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1204+1317G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51281796 | |||||||
| chr17:51282067 | C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1204+1588C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282067 | |||||||
| chr17:51282156 | A | G | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1204+1677A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282156 | |||||||
| chr17:51282160 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1204+1681G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282160 | |||||||
| chr17:51282507 | TGGAA | T | 190 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(187): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1204+2045_1204+204 others(8): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282507 | ||||||
| chr17:51282577 | C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0131 | 2 | NA18953.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1204+2098C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282577 | |||||||
| chr17:51282617 | T | TTGGGGAG others(10): Show |
1 | a0001c0002t0001g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1204+2148_1204+216 others(21): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282617 | ||||||
| chr17:51282673 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1204+2194T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282673 | |||||||
| chr17:51282738 | A | G | 1 | a0001c0002t0001g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1204+2259A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282738 | |||||||
| chr17:51282836 | G | A | 7 | a0001c0003t0001g0283a0001c0003t0001g0285a0001c0003t0001g0286others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1204+2357G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282836 | |||||||
| chr17:51282867 | C | CT | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1205-2359dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282867 | ||||||
| chr17:51282867 | C | CTT | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01884.hp1 HG01943.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1205-2360_1205-235 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282867 | ||||||
| chr17:51282867 | C | CTTT | 16 | a0001c0001t0001g0161a0001c0005t0001g0031a0001c0005t0001g0032others(13): Show | 17 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1205-2361_1205-235 others(7): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282867 | ||||||
| chr17:51282867 | CTT | C | 98 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(95): Show | 113 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1205-2360_1205-235 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282867 | ||||||
| chr17:51282867 | CTTTTTTT others(3): Show |
C | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1205-2368_1205-235 others(14): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51282867 | ||||||
| chr17:51282938 | G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG02129.hp2 HG02615.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-2307G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51282938 | |||||||
| chr17:51283013 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1205-2232C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283013 | |||||||
| chr17:51283026 | A | G | 190 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(187): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1205-2219A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283026 | |||||||
| chr17:51283030 | A | G | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1205-2215A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283030 | |||||||
| chr17:51283057 | C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0093 | 2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1205-2188C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283057 | |||||||
| chr17:51283142 | T | C | 1 | a0002c0007t0001g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1205-2103T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283142 | |||||||
| chr17:51283148 | C | T | 12 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0290others(9): Show | 13 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1205-2097C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283148 | |||||||
| chr17:51283173 | C | CT | 8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1205-2059dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51283173 | ||||||
| chr17:51283299 | G | T | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1205-1946G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283299 | |||||||
| chr17:51283415 | G | A | 7 | a0001c0005t0001g0031a0001c0005t0001g0290a0001c0005t0001g0293others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-1830G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283415 | |||||||
| chr17:51283542 | A | C | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1205-1703A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283542 | |||||||
| chr17:51283617 | A | AT | 8 | a0001c0001t0001g0040a0001c0001t0001g0065a0001c0001t0001g0091others(5): Show | 8 | HG02145.hp1 HG02293.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.1205-1613dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51283617 | ||||||
| chr17:51283617 | A | ATT | 98 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(95): Show | 113 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1205-1614_1205-161 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 51283617 | ||||||
| chr17:51283740 | G | A | 1 | a0001c0004t0001g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1205-1505G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283740 | |||||||
| chr17:51283797 | T | C | 2 | a0001c0005t0001g0163a0001c0005t0001g0164 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1205-1448T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283797 | |||||||
| chr17:51283859 | C | A | 1 | a0001c0002t0001g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1205-1386C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51283859 | |||||||
| chr17:51284211 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1205-1034A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284211 | |||||||
| chr17:51284322 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1205-923T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284322 | |||||||
| chr17:51284467 | C | T | 1 | a0001c0005t0001g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1205-778C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284467 | |||||||
| chr17:51284589 | G | A | 1 | a0001c0002t0001g0181 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1205-656G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284589 | |||||||
| chr17:51284616 | C | G | 150 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(147): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1205-629C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284616 | |||||||
| chr17:51284749 | A | G | 1 | a0001c0002t0001g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1205-496A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284749 | |||||||
| chr17:51284960 | C | T | 1 | a0005c0016t0001g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1205-285C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51284960 | |||||||
| chr17:51285120 | G | A | 1 | a0001c0004t0001g0074 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1205-125G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51285120 | |||||||
| chr17:51285140 | A | G | 1 | a0001c0002t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1205-105A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51285140 | |||||||
| chr17:51285183 | G | C | 1 | a0001c0002t0001g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1205-62G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 9/13 | chr17 | 51285183 | |||||||
| chr17:51285497 | A | G | 1 | a0001c0004t0001g0080 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1328+129A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51285497 | |||||||
| chr17:51285561 | T | TC | 15 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1328+199dupC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 51285561 | ||||||
| chr17:51285829 | C | G | 3 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0078 | 3 | NA18949.hp2 NA18989.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1328+461C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51285829 | |||||||
| chr17:51285924 | T | C | 40 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 41 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1328+556T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51285924 | |||||||
| chr17:51285973 | G | C | 2 | a0001c0002t0001g0186a0001c0002t0001g0210 | 2 | NA18975.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1328+605G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51285973 | |||||||
| chr17:51286047 | A | C | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1328+679A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286047 | |||||||
| chr17:51286130 | G | A | 1 | a0001c0002t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1328+762G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286130 | |||||||
| chr17:51286186 | A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(90): Show | 108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1328+818A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286186 | |||||||
| chr17:51286239 | G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0119a0001c0001t0001g0120 | 5 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328+871G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286239 | |||||||
| chr17:51286376 | G | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0006t0001g0003others(12): Show | 19 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1328+1008G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286376 | |||||||
| chr17:51286458 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1328+1090C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286458 | |||||||
| chr17:51286667 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1328+1299C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286667 | |||||||
| chr17:51286675 | G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1328+1307G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286675 | |||||||
| chr17:51286779 | G | C | 1 | a0001c0002t0001g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1329-1250G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286779 | |||||||
| chr17:51286815 | A | G | 1 | a0001c0005t0001g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1329-1214A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286815 | |||||||
| chr17:51286828 | A | T | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1329-1201A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286828 | |||||||
| chr17:51286830 | AT | A | 16 | a0001c0001t0001g0054a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1329-1191delT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 51286830 | ||||||
| chr17:51286874 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1329-1155C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286874 | |||||||
| chr17:51286885 | G | A | 2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1329-1144G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286885 | |||||||
| chr17:51286978 | T | TC | 125 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(122): Show | 140 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1329-1043dupC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 51286978 | ||||||
| chr17:51286982 | C | CCG | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1329-1046_1329-104 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 51286982 | ||||||
| chr17:51286987 | G | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 25 | HG01943.hp1 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1329-1042G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51286987 | |||||||
| chr17:51287063 | A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0063others(5): Show | 10 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1329-966A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287063 | |||||||
| chr17:51287073 | A | G | 102 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(99): Show | 117 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1329-956A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287073 | |||||||
| chr17:51287094 | T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0158 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1329-935T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287094 | |||||||
| chr17:51287124 | A | C | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1329-905A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287124 | |||||||
| chr17:51287350 | G | A | 15 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1329-679G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287350 | |||||||
| chr17:51287381 | G | A | 1 | a0001c0003t0001g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1329-648G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287381 | |||||||
| chr17:51287481 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1329-548G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287481 | |||||||
| chr17:51287918 | G | T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1329-111G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 10/13 | chr17 | 51287918 | |||||||
| chr17:51288284 | C | T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1503+81C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51288284 | |||||||
| chr17:51288489 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1503+286A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51288489 | |||||||
| chr17:51288649 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503+446A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51288649 | |||||||
| chr17:51288691 | C | T | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 25 | HG01943.hp1 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1503+488C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51288691 | |||||||
| chr17:51289075 | T | C | 1 | a0001c0002t0001g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1503+872T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289075 | |||||||
| chr17:51289117 | G | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0122 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1503+914G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289117 | |||||||
| chr17:51289199 | TG | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01943.hp1 HG04115.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1503+997delG | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289199 | |||||||
| chr17:51289200 | G | GT | 14 | a0001c0001t0001g0082a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 14 | HG00558.hp2 HG00642.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1503+1011dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289200 | ||||||
| chr17:51289200 | GT | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0196others(66): Show | 77 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.1503+1011delT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289200 | ||||||
| chr17:51289200 | GTT | G | 98 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(95): Show | 113 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1503+1010_1503+101 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289200 | ||||||
| chr17:51289203 | T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0096 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1503+1000T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289203 | |||||||
| chr17:51289346 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1503+1143G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289346 | |||||||
| chr17:51289371 | A | AT | 44 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(41): Show | 44 | HG00558.hp2 HG00642.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.1503+1184dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289371 | ||||||
| chr17:51289371 | A | ATT | 141 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0002t0001g0002others(138): Show | 164 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1503+1183_1503+118 others(6): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289371 | ||||||
| chr17:51289371 | A | ATTT | 7 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0189others(4): Show | 7 | HG02735.hp1 HG02738.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1503+1182_1503+118 others(7): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51289371 | ||||||
| chr17:51289434 | C | T | 1 | a0001c0005t0001g0294 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1503+1231C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289434 | |||||||
| chr17:51289537 | C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1503+1334C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289537 | |||||||
| chr17:51289555 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1503+1352G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289555 | |||||||
| chr17:51289619 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1503+1416G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289619 | |||||||
| chr17:51289621 | G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0126others(1): Show | 7 | NA18944.hp2 NA18948.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503+1418G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289621 | |||||||
| chr17:51289670 | A | T | 1 | a0001c0006t0001g0046 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1503+1467A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289670 | |||||||
| chr17:51289736 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1503+1533C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51289736 | |||||||
| chr17:51290162 | TC | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1503+1962delC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51290162 | ||||||
| chr17:51290461 | G | T | 8 | a0001c0006t0001g0003a0001c0006t0001g0042a0001c0006t0001g0043others(5): Show | 11 | HG02280.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1503+2258G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51290461 | |||||||
| chr17:51290551 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1503+2348C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51290551 | |||||||
| chr17:51290776 | A | G | 101 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(98): Show | 116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1503+2573A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51290776 | |||||||
| chr17:51290866 | A | G | 1 | a0001c0006t0001g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1503+2663A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51290866 | |||||||
| chr17:51291270 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1504-2633G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51291270 | |||||||
| chr17:51291343 | T | G | 2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1504-2560T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51291343 | |||||||
| chr17:51291620 | A | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01943.hp1 HG02129.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1504-2283A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51291620 | |||||||
| chr17:51291738 | CA | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0134others(3): Show | 6 | HG01496.hp1 HG02129.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1504-2150delA | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51291738 | ||||||
| chr17:51291749 | A | G | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1504-2154A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51291749 | |||||||
| chr17:51292083 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1504-1820T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51292083 | |||||||
| chr17:51292277 | A | C | 1 | a0001c0002t0001g0201 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1504-1626A>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51292277 | |||||||
| chr17:51292601 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1504-1302C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51292601 | |||||||
| chr17:51292886 | T | C | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1504-1017T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51292886 | |||||||
| chr17:51292915 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1504-988C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51292915 | |||||||
| chr17:51293002 | T | C | 1 | a0001c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1504-901T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293002 | |||||||
| chr17:51293134 | A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1504-769A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293134 | |||||||
| chr17:51293252 | C | A | 1 | a0001c0002t0001g0199 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1504-651C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293252 | |||||||
| chr17:51293258 | T | TC | 4 | a0001c0005t0001g0031a0001c0005t0001g0293a0001c0005t0001g0298others(1): Show | 4 | HG02717.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1504-644dupC | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51293258 | ||||||
| chr17:51293386 | G | A | 1 | a0001c0003t0001g0277 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1504-517G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293386 | |||||||
| chr17:51293440 | C | T | 1 | a0001c0002t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1504-463C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293440 | |||||||
| chr17:51293483 | T | C | 11 | a0001c0003t0001g0271a0001c0003t0001g0274a0001c0003t0001g0277others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1504-420T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293483 | |||||||
| chr17:51293501 | TG | T | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1504-401delG | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293501 | |||||||
| chr17:51293502 | G | GT | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(46): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1504-387dupT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51293502 | ||||||
| chr17:51293502 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1504-401G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293502 | |||||||
| chr17:51293502 | GT | G | 155 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(152): Show | 177 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1504-387delT | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 51293502 | ||||||
| chr17:51293572 | C | A | 2 | a0001c0001t0001g0096a0001c0003t0001g0278 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1504-331C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293572 | |||||||
| chr17:51293625 | T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0131a0001c0001t0001g0133 | 3 | NA18953.hp2 NA18986.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1504-278T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293625 | |||||||
| chr17:51293816 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1504-87T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293816 | |||||||
| chr17:51293869 | G | C | 101 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(98): Show | 116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1504-34G>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 11/13 | chr17 | 51293869 | |||||||
| chr17:51294112 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1646+67C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294112 | |||||||
| chr17:51294144 | C | G | 189 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(186): Show | 212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1646+99C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294144 | |||||||
| chr17:51294155 | A | G | 1 | a0001c0005t0001g0164 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1646+110A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294155 | |||||||
| chr17:51294209 | A | T | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1646+164A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294209 | |||||||
| chr17:51294305 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1646+260C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294305 | |||||||
| chr17:51294425 | C | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0003t0001g0028others(45): Show | 55 | HG00099.hp1 HG00733.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1646+380C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294425 | |||||||
| chr17:51294463 | C | T | 1 | a0003c0008t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1646+418C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294463 | |||||||
| chr17:51294570 | G | A | 15 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0163others(12): Show | 16 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1646+525G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294570 | |||||||
| chr17:51294830 | G | A | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 25 | HG01943.hp1 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1646+785G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294830 | |||||||
| chr17:51294933 | T | A | 2 | a0001c0005t0001g0150a0001c0005t0001g0151 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1646+888T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51294933 | |||||||
| chr17:51295117 | A | G | 16 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0005t0001g0055others(13): Show | 20 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1646+1072A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295117 | |||||||
| chr17:51295123 | C | A | 3 | a0001c0005t0001g0291a0001c0005t0001g0292a0001c0005t0001g0294 | 3 | HG02630.hp2 HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1646+1078C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295123 | |||||||
| chr17:51295126 | C | A | 3 | a0001c0005t0001g0291a0001c0005t0001g0292a0001c0005t0001g0294 | 3 | HG02630.hp2 HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1646+1081C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295126 | |||||||
| chr17:51295157 | T | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 25 | HG01943.hp1 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1646+1112T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295157 | |||||||
| chr17:51295227 | G | T | 15 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1646+1182G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295227 | |||||||
| chr17:51295294 | T | C | 15 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1646+1249T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295294 | |||||||
| chr17:51295341 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(47): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1646+1296T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295341 | |||||||
| chr17:51295417 | T | A | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1646+1372T>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295417 | |||||||
| chr17:51295515 | T | C | 5 | a0001c0002t0001g0203a0001c0002t0001g0205a0001c0002t0001g0239others(2): Show | 5 | HG01099.hp2 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1647-1450T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295515 | |||||||
| chr17:51295534 | C | G | 1 | a0001c0003t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1647-1431C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295534 | |||||||
| chr17:51295582 | C | A | 4 | a0001c0002t0001g0249a0001c0002t0001g0250a0001c0002t0001g0251others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647-1383C>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295582 | |||||||
| chr17:51295593 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1647-1372G>A | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295593 | |||||||
| chr17:51295612 | A | G | 1 | a0001c0004t0001g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1647-1353A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295612 | |||||||
| chr17:51295664 | G | T | 1 | a0001c0002t0001g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1647-1301G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295664 | |||||||
| chr17:51295689 | T | G | 1 | a0001c0002t0001g0231 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1647-1276T>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295689 | |||||||
| chr17:51295739 | A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0173 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1647-1226A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295739 | |||||||
| chr17:51295804 | A | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0006t0001g0003others(12): Show | 19 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1647-1161A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51295804 | |||||||
| chr17:51295853 | ATATATT | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | HG00558.hp2 HG00642.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-1110_1647-110 others(10): Show |
UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr17 | 51295853 | ||||||
| chr17:51296090 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1647-875G>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51296090 | |||||||
| chr17:51296327 | C | T | 12 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1647-638C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51296327 | |||||||
| chr17:51296604 | C | G | 1 | a0001c0005t0001g0293 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1647-361C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51296604 | |||||||
| chr17:51296619 | C | G | 1 | a0001c0004t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1647-346C>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51296619 | |||||||
| chr17:51296949 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1647-16T>C | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 12/13 | chr17 | 51296949 | |||||||
| chr17:51297104 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*14+101C>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 13/13 | chr17 | 51297104 | |||||||
| chr17:51297448 | A | G | 15 | a0001c0005t0001g0031a0001c0005t0001g0032a0001c0005t0001g0163others(12): Show | 16 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.*15-334A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 13/13 | chr17 | 51297448 | |||||||
| chr17:51297462 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*15-320A>T | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 13/13 | chr17 | 51297462 | |||||||
| chr17:51297625 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.*15-157A>G | UTP18 | ENSG00000011260.14 | transcript | ENST00000225298.12 | protein_coding | 13/13 | chr17 | 51297625 |