Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84916 |
| ensemblid | ENSG00000141076.18 |
| hgncid | 1983 |
| symbol | UTP4 |
| name | UTP4 small subunit processome component |
| refseq_nuc | NM_032830.3 |
| refseq_prot | NP_116219.2 |
| ensembl_nuc | ENST00000314423.12 |
| ensembl_prot | ENSP00000327179.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 69132649 |
| end | 69169021 |
| strand | + |
| ver | v1.2 |
| region | chr16:69132649-69169021 |
| region5000 | chr16:69127649-69174021 |
| regionname0 | UTP4_chr16_69132649_69169021 |
| regionname5000 | UTP4_chr16_69127649_69174021 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 686 | 283 | 92 | 55 | 85 | 14 | 35 | 53 | UTP4_chr16_69127649_69174021 | UTP4 | MGEFK others(681): Show |
chr16 | 69127649 | 69174021 |
| a0002 | 0/0 | 686 | 5 | 1 | 1 | 1 | 0 | 2 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | MGEFK others(681): Show |
chr16 | 69127649 | 69174021 |
| a0003 | 0/0 | 686 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | MGEFK others(681): Show |
chr16 | 69127649 | 69174021 |
| a0004 | 0/0 | 686 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | MGEFK others(681): Show |
chr16 | 69127649 | 69174021 |
| a0005 | 0/0 | 686 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | MGEFK others(681): Show |
chr16 | 69127649 | 69174021 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2058 | 265 | 85 | 52 | 80 | 13 | 33 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0001c0002 | 0/0 | 2058 | 14 | 5 | 2 | 5 | 1 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0001c0005 | 0/0 | 2058 | 2 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0001c0008 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0001c0010 | 0/0 | 2058 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0002c0003 | 0/0 | 2058 | 4 | 0 | 1 | 1 | 0 | 2 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0002c0007 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0003c0004 | 0/0 | 2058 | 2 | 0 | 2 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0004c0009 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 | ||
| a0005c0006 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | ATGGG others(2053): Show |
chr16 | 69127649 | 69174021 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2188 | 262 | 85 | 51 | 80 | 11 | 33 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0001c0001t0002 | 0/0 | 2188 | 3 | 0 | 1 | 0 | 2 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0001c0002t0001 | 0/0 | 2188 | 14 | 5 | 2 | 5 | 1 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0001c0005t0001 | 0/0 | 2188 | 2 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0001c0008t0001 | 0/0 | 2188 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0001c0010t0001 | 0/0 | 2188 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0002c0003t0001 | 0/0 | 2188 | 4 | 0 | 1 | 1 | 0 | 2 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0002c0007t0001 | 0/0 | 2188 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0003c0004t0001 | 0/0 | 2188 | 2 | 0 | 2 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0004c0009t0001 | 0/0 | 2188 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| a0005c0006t0001 | 0/0 | 2188 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | GGAGA others(2183): Show |
chr16 | 69127649 | 69174021 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0002 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0001c0010t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0002c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0002c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0003c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0003c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0004c0009t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| a0005c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01099 | hp1 | a0001 | c0010 | t0001 | g0136 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0067 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01361 | hp2 | a0003 | c0004 | t0001 | g0206 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | IBS | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0246 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02886 | hp2 | a0002 | c0007 | t0001 | g0022 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0041 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0277 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0280 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03688 | hp2 | a0004 | c0009 | t0001 | g0201 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0056 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03927 | hp1 | a0001 | c0008 | t0001 | g0085 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | STU | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0281 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | TSI | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | USA | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20300 | hp1 | a0005 | c0006 | t0001 | g0116 | AFR | USA | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0091 | REF | REF | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | UTP4_chr16_69127649_69174021 | UTP4 | chr16 | 69127649 | 69174021 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69143319 | C | T | 1 | a0004 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.668C>T | p.Ser223Leu | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/17 | 711/2188 | 668/2061 | 223/686 | chr16 | 69143319 | |||
| chr16:69157109 | G | A | 1 | a0005 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1313G>A | p.Arg438His | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/17 | 1356/2188 | 1313/2061 | 438/686 | chr16 | 69157109 | |||
| chr16:69165386 | C | T | 1 | a0003 | 2 | HG01361.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.1693C>T | p.Arg565Trp | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/17 | 1736/2188 | 1693/2061 | 565/686 | chr16 | 69165386 | |||
| chr16:69167147 | C | T | 1 | a0002 | 4 | HG01346.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
missense_variant | MODERATE | c.1906C>T | p.Arg636Cys | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/17 | 1949/2188 | 1906/2061 | 636/686 | chr16 | 69167147 | |||
| chr16:69167148 | G | A | 1 | a0002 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1907G>A | p.Arg636His | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/17 | 1950/2188 | 1907/2061 | 636/686 | chr16 | 69167148 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69143266 | C | T | 1 | a0001c0010 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.615C>T | p.Ser205Ser | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/17 | 658/2188 | 615/2061 | 205/686 | chr16 | 69143266 | |||
| chr16:69143365 | C | T | 1 | a0001c0002 | 14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
synonymous_variant | LOW | c.714C>T | p.Asp238Asp | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/17 | 757/2188 | 714/2061 | 238/686 | chr16 | 69143365 | |||
| chr16:69150859 | A | G | 1 | a0001c0005 | 2 | HG03041.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.957A>G | p.Glu319Glu | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/17 | 1000/2188 | 957/2061 | 319/686 | chr16 | 69150859 | |||
| chr16:69153595 | C | T | 1 | a0001c0005 | 2 | HG03041.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1014C>T | p.Ile338Ile | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/17 | 1057/2188 | 1014/2061 | 338/686 | chr16 | 69153595 | |||
| chr16:69168829 | C | A | 1 | a0001c0008 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1953C>A | p.Leu651Leu | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 17/17 | 1996/2188 | 1953/2061 | 651/686 | chr16 | 69168829 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69169005 | A | G | 1 | a0001c0001t0002 | 3 | HG01243.hp1 HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 17/17 | 68 | chr16 | 69169005 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69132762 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG01496.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-3+73C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69132762 | |||||||
| chr16:69132770 | G | T | 1 | a0002c0003t0001g0281 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3+81G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69132770 | |||||||
| chr16:69132787 | C | G | 1 | a0002c0003t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-3+98C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69132787 | |||||||
| chr16:69132955 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3+266C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69132955 | |||||||
| chr16:69133002 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
30 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-3+313G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133002 | |||||||
| chr16:69133014 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-3+325T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133014 | |||||||
| chr16:69133094 | G | T | 1 | a0001c0002t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-2-364G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133094 | |||||||
| chr16:69133237 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-2-221T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133237 | |||||||
| chr16:69133260 | T | C | 1 | a0001c0005t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2-198T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133260 | |||||||
| chr16:69133268 | C | G | 1 | a0001c0005t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2-190C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133268 | |||||||
| chr16:69133306 | T | G | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-2-152T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133306 | |||||||
| chr16:69133393 | T | G | 1 | a0001c0005t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2-65T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 1/16 | chr16 | 69133393 | |||||||
| chr16:69133724 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.159+106C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69133724 | |||||||
| chr16:69133748 | C | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159+130C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69133748 | |||||||
| chr16:69133838 | C | G | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+220C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69133838 | |||||||
| chr16:69133907 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159+289A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69133907 | |||||||
| chr16:69134080 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.159+462T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134080 | |||||||
| chr16:69134304 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02735.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.159+686C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134304 | |||||||
| chr16:69134312 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159+694T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134312 | |||||||
| chr16:69134471 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+853G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134471 | |||||||
| chr16:69134485 | TTGAATTG others(19): Show |
T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.159+868_159+893del others(26): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134485 | |||||||
| chr16:69134486 | T | TGAATTGC others(21): Show |
1 | a0001c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.159+880_159+907dup others(28): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 69134486 | ||||||
| chr16:69134528 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+910T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134528 | |||||||
| chr16:69134587 | C | T | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+969C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134587 | |||||||
| chr16:69134634 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.159+1016C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134634 | |||||||
| chr16:69134643 | GAAGAACA | G | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1026_159+1032d others(9): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134643 | |||||||
| chr16:69134654 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.159+1036G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134654 | |||||||
| chr16:69134702 | C | CT | 14 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(11): Show |
14 | HG01261.hp1 HG03041.hp2 HG03225.hp2 others(11): Show |
intron_variant | MODIFIER | c.159+1101dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 69134702 | ||||||
| chr16:69134902 | G | T | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1284G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69134902 | |||||||
| chr16:69135017 | CT | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0103 others(4): Show |
7 | HG01169.hp1 HG02451.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1414delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 69135017 | ||||||
| chr16:69135088 | A | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02735.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.159+1470A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135088 | |||||||
| chr16:69135258 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.160-1438C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135258 | |||||||
| chr16:69135502 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.160-1194C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135502 | |||||||
| chr16:69135544 | C | A | 1 | a0001c0002t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160-1152C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135544 | |||||||
| chr16:69135551 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160-1145A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135551 | |||||||
| chr16:69135794 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.160-902G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135794 | |||||||
| chr16:69135798 | G | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.160-898G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135798 | |||||||
| chr16:69135890 | G | A | 1 | a0002c0003t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.160-806G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69135890 | |||||||
| chr16:69136024 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.160-672T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136024 | |||||||
| chr16:69136159 | T | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG02015.hp2 HG02155.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-537T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136159 | |||||||
| chr16:69136313 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160-383C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136313 | |||||||
| chr16:69136314 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160-382G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136314 | |||||||
| chr16:69136319 | C | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0240 a0001c0001t0001g0241 others(10): Show |
14 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.160-377C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136319 | |||||||
| chr16:69136655 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160-41T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136655 | |||||||
| chr16:69136665 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.160-31G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 2/16 | chr16 | 69136665 | |||||||
| chr16:69137177 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.351+290T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | chr16 | 69137177 | |||||||
| chr16:69137237 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.351+350A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | chr16 | 69137237 | |||||||
| chr16:69137507 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-294T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | chr16 | 69137507 | |||||||
| chr16:69137621 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-180A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | chr16 | 69137621 | |||||||
| chr16:69137727 | GGT | G | 9 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(6): Show |
9 | HG01346.hp1 HG01361.hp1 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-61_352-60delGT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 69137727 | ||||||
| chr16:69137750 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.352-51A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 3/16 | chr16 | 69137750 | |||||||
| chr16:69137969 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00544.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.436+84T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69137969 | |||||||
| chr16:69138235 | C | CT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
100 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.436+365dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69138235 | ||||||
| chr16:69138264 | G | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+379G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138264 | |||||||
| chr16:69138283 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.436+398T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138283 | |||||||
| chr16:69138284 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.436+399G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138284 | |||||||
| chr16:69138285 | G | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.436+400G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138285 | |||||||
| chr16:69138287 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.436+402A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138287 | |||||||
| chr16:69138290 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.436+405G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138290 | |||||||
| chr16:69138300 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.436+415T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138300 | |||||||
| chr16:69138307 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.436+422G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138307 | |||||||
| chr16:69138367 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.436+482G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138367 | |||||||
| chr16:69138451 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0005c0006t0001g0116 |
3 | HG02145.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.436+566T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138451 | |||||||
| chr16:69138477 | A | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+592A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138477 | |||||||
| chr16:69138575 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.436+690A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138575 | |||||||
| chr16:69138703 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.436+818C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138703 | |||||||
| chr16:69138756 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0062 others(31): Show |
35 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.436+871C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138756 | |||||||
| chr16:69138777 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.436+892T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138777 | |||||||
| chr16:69138789 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.436+904G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69138789 | |||||||
| chr16:69138958 | C | CT | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(38): Show |
41 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.437-842dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69138958 | ||||||
| chr16:69138958 | CT | C | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00544.hp2 HG01256.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.437-842delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69138958 | ||||||
| chr16:69139166 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
5 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-659A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69139166 | |||||||
| chr16:69139202 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-623C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69139202 | |||||||
| chr16:69139334 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-491A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69139334 | |||||||
| chr16:69139562 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-263C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69139562 | |||||||
| chr16:69139639 | A | AAAAT | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.437-142_437-139dup others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | A | AAAATAAA others(1): Show |
28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
29 | HG00642.hp2 HG01070.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.437-146_437-139dup others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | A | AAAATAAA others(5): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
5 | HG01081.hp2 HG02486.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-150_437-139dup others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | AAAAT | A | 10 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0065 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-142_437-139del others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | AAAATAAA others(1): Show |
A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
13 | HG00735.hp1 HG02055.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.437-146_437-139del others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | AAAATAAA others(5): Show |
A | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(10): Show |
13 | HG00621.hp2 HG00738.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-150_437-139del others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139639 | AAAATAAA others(9): Show |
A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-154_437-139del others(16): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 69139639 | ||||||
| chr16:69139776 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.437-49G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 4/16 | chr16 | 69139776 | |||||||
| chr16:69140238 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
43 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.526+324C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69140238 | |||||||
| chr16:69140448 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.526+534G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69140448 | |||||||
| chr16:69140505 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.526+591C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69140505 | |||||||
| chr16:69140819 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(17): Show |
21 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.526+905A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69140819 | |||||||
| chr16:69140940 | CTT | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+1028_526+1029d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 69140940 | ||||||
| chr16:69141021 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.526+1107G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141021 | |||||||
| chr16:69141137 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.526+1223C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141137 | |||||||
| chr16:69141171 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+1257C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141171 | |||||||
| chr16:69141195 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.526+1281C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141195 | |||||||
| chr16:69141244 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.526+1330A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141244 | |||||||
| chr16:69141259 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.526+1345T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141259 | |||||||
| chr16:69141271 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.526+1357C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141271 | |||||||
| chr16:69141275 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG02258.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+1361C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141275 | |||||||
| chr16:69141326 | G | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+1412G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141326 | |||||||
| chr16:69141374 | C | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0204 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1460C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141374 | |||||||
| chr16:69141813 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0226 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.527-1365C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141813 | |||||||
| chr16:69141988 | C | A | 2 | a0002c0003t0001g0067 a0002c0003t0001g0281 |
2 | HG01346.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.527-1190C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69141988 | |||||||
| chr16:69142335 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.527-843A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69142335 | |||||||
| chr16:69142512 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | NA18946.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.527-666C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69142512 | |||||||
| chr16:69142555 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-623A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69142555 | |||||||
| chr16:69142875 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.527-303C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69142875 | |||||||
| chr16:69142953 | A | C | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-225A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69142953 | |||||||
| chr16:69143073 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.527-105G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69143073 | |||||||
| chr16:69143096 | A | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-82A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69143096 | |||||||
| chr16:69143113 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.527-65C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69143113 | |||||||
| chr16:69143156 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.527-22G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 5/16 | chr16 | 69143156 | |||||||
| chr16:69143416 | T | C | 1 | a0002c0003t0001g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.738+27T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69143416 | |||||||
| chr16:69143624 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.738+235C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69143624 | |||||||
| chr16:69144073 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.738+684A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144073 | |||||||
| chr16:69144132 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.738+743C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144132 | |||||||
| chr16:69144149 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.738+760A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144149 | |||||||
| chr16:69144211 | T | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+822T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144211 | |||||||
| chr16:69144286 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.738+897C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144286 | |||||||
| chr16:69144503 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+1114C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144503 | |||||||
| chr16:69144992 | A | G | 14 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(11): Show |
14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+1603A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69144992 | |||||||
| chr16:69145084 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.738+1695G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145084 | |||||||
| chr16:69145120 | C | T | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+1731C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145120 | |||||||
| chr16:69145149 | C | CAATAAT | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0005c0006t0001g0116 |
3 | HG02145.hp1 HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.738+1776_738+1781d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69145149 | ||||||
| chr16:69145482 | A | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+2093A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145482 | |||||||
| chr16:69145550 | G | GCTTTTTC others(5): Show |
3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG03831.hp1 NA18946.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.738+2174_738+2185d others(14): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69145550 | ||||||
| chr16:69145618 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+2229T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145618 | |||||||
| chr16:69145748 | T | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+2359T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145748 | |||||||
| chr16:69145791 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738+2402G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145791 | |||||||
| chr16:69145813 | A | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.738+2424A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145813 | |||||||
| chr16:69145830 | G | A | 1 | a0003c0004t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.738+2441G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145830 | |||||||
| chr16:69145840 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.738+2451C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69145840 | |||||||
| chr16:69146050 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.738+2661G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146050 | |||||||
| chr16:69146096 | C | CA | 14 | a0001c0001t0001g0073 a0001c0002t0001g0014 a0001c0002t0001g0016 others(11): Show |
14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+2720dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69146096 | ||||||
| chr16:69146162 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.738+2773C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146162 | |||||||
| chr16:69146380 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.738+2991A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146380 | |||||||
| chr16:69146483 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0169 others(18): Show |
22 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.738+3094C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146483 | |||||||
| chr16:69146743 | T | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
30 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.738+3354T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146743 | |||||||
| chr16:69146859 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+3470C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146859 | |||||||
| chr16:69146949 | G | C | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG00621.hp2 HG02004.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+3560G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146949 | |||||||
| chr16:69146959 | G | A | 14 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(11): Show |
14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+3570G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69146959 | |||||||
| chr16:69147001 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
82 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.739-3517dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147001 | ||||||
| chr16:69147001 | C | CAA | 17 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(14): Show |
17 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.739-3518_739-3517d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147001 | ||||||
| chr16:69147001 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.739-3517_739-3516i others(30): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147001 | ||||||
| chr16:69147021 | T | A | 19 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0068 others(16): Show |
19 | HG00544.hp2 HG01109.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.739-3516T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147021 | |||||||
| chr16:69147023 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG01109.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.739-3514C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147023 | |||||||
| chr16:69147143 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.739-3394C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147143 | |||||||
| chr16:69147178 | A | AAAT | 42 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0050 others(39): Show |
43 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-3317_739-3315d others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | A | AAATAAT | 20 | a0001c0001t0001g0069 a0001c0001t0001g0102 a0001c0001t0001g0127 others(17): Show |
20 | HG00423.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.739-3320_739-3315d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | A | AAATAATA others(2): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0122 |
3 | HG02258.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.739-3323_739-3315d others(11): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | AAAT | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.739-3317_739-3315d others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | AAATAAT | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
26 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.739-3320_739-3315d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | AAATAATA others(2): Show |
A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0064 others(9): Show |
12 | HG00544.hp2 HG02976.hp1 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.739-3323_739-3315d others(11): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | AAATAATA others(5): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0104 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.739-3326_739-3315d others(14): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147178 | AAATAATA others(8): Show |
A | 1 | a0002c0003t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.739-3329_739-3315d others(17): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69147178 | ||||||
| chr16:69147220 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.739-3317T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147220 | |||||||
| chr16:69147220 | T | G | 2 | a0001c0001t0001g0093 a0001c0008t0001g0085 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.739-3317T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147220 | |||||||
| chr16:69147312 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.739-3225T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147312 | |||||||
| chr16:69147365 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.739-3172C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147365 | |||||||
| chr16:69147510 | A | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.739-3027A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147510 | |||||||
| chr16:69147511 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.739-3026A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147511 | |||||||
| chr16:69147518 | A | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-3019A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147518 | |||||||
| chr16:69147614 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.739-2923T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147614 | |||||||
| chr16:69147714 | C | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-2823C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147714 | |||||||
| chr16:69147742 | G | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2795G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147742 | |||||||
| chr16:69147827 | A | G | 4 | a0002c0003t0001g0056 a0002c0003t0001g0067 a0002c0003t0001g0280 others(1): Show |
4 | HG01346.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-2710A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147827 | |||||||
| chr16:69147971 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.739-2566C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69147971 | |||||||
| chr16:69148024 | G | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-2513G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148024 | |||||||
| chr16:69148117 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.739-2420G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148117 | |||||||
| chr16:69148132 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.739-2405T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148132 | |||||||
| chr16:69148204 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.739-2333G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148204 | |||||||
| chr16:69148216 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.739-2321C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148216 | |||||||
| chr16:69148255 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.739-2282C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148255 | |||||||
| chr16:69148328 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
103 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.739-2209T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148328 | |||||||
| chr16:69148339 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2198C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148339 | |||||||
| chr16:69148343 | C | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2194C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148343 | |||||||
| chr16:69148356 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-2181C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148356 | |||||||
| chr16:69148392 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2145C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148392 | |||||||
| chr16:69148459 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.739-2078C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148459 | |||||||
| chr16:69148516 | G | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-2021G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148516 | |||||||
| chr16:69148561 | T | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-1976T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148561 | |||||||
| chr16:69148613 | C | CT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG01346.hp2 HG01361.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.739-1907dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69148613 | ||||||
| chr16:69148751 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0114 others(10): Show |
15 | HG01109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-1786G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69148751 | |||||||
| chr16:69149058 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.739-1479A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149058 | |||||||
| chr16:69149174 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.739-1363G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149174 | |||||||
| chr16:69149252 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.739-1285C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149252 | |||||||
| chr16:69149380 | C | CA | 5 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0139 others(2): Show |
5 | HG00597.hp2 HG01261.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-1149dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69149380 | ||||||
| chr16:69149480 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.739-1057G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149480 | |||||||
| chr16:69149481 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.739-1056G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149481 | |||||||
| chr16:69149530 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.739-1007G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149530 | |||||||
| chr16:69149557 | TACAA | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.739-966_739-963del others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 69149557 | ||||||
| chr16:69149643 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.739-894C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149643 | |||||||
| chr16:69149752 | A | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG01433.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.739-785A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149752 | |||||||
| chr16:69149917 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.739-620C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149917 | |||||||
| chr16:69149918 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.739-619G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69149918 | |||||||
| chr16:69150059 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.739-478C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69150059 | |||||||
| chr16:69150422 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-115A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69150422 | |||||||
| chr16:69150436 | T | C | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG00621.hp2 HG02004.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.739-101T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 6/16 | chr16 | 69150436 | |||||||
| chr16:69150746 | G | T | 1 | a0001c0002t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.910+38G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 7/16 | chr16 | 69150746 | |||||||
| chr16:69150773 | T | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.911-40T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 7/16 | chr16 | 69150773 | |||||||
| chr16:69150994 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1002+90G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69150994 | |||||||
| chr16:69151109 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0083 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1002+205C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151109 | |||||||
| chr16:69151161 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1002+257C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151161 | |||||||
| chr16:69151161 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
42 | HG01346.hp1 HG02055.hp2 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.1002+257C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151161 | |||||||
| chr16:69151315 | CT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(17): Show |
21 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1002+420delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69151315 | ||||||
| chr16:69151325 | C | CT | 10 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
10 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002+436dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69151325 | ||||||
| chr16:69151346 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1002+442T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151346 | |||||||
| chr16:69151411 | TC | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1002+510delC | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69151411 | ||||||
| chr16:69151446 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+542C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151446 | |||||||
| chr16:69151569 | C | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002+665C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151569 | |||||||
| chr16:69151622 | T | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1002+718T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151622 | |||||||
| chr16:69151625 | CT | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
83 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1002+735delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69151625 | ||||||
| chr16:69151646 | C | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002+742C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151646 | |||||||
| chr16:69151712 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1002+808A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151712 | |||||||
| chr16:69151848 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0166 a0001c0001t0001g0255 |
3 | HG02027.hp1 NA18612.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1002+944A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151848 | |||||||
| chr16:69151863 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+959G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69151863 | |||||||
| chr16:69152009 | TATAG | T | 3 | a0001c0001t0001g0042 a0001c0005t0001g0041 a0001c0005t0001g0277 |
3 | HG03041.hp2 HG03225.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1002+1124_1002+112 others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69152009 | ||||||
| chr16:69152131 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1002+1227C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152131 | |||||||
| chr16:69152155 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+1251A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152155 | |||||||
| chr16:69152210 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1002+1306A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152210 | |||||||
| chr16:69152239 | G | C | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1002+1335G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152239 | |||||||
| chr16:69152464 | C | CT | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1003-1098dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69152464 | ||||||
| chr16:69152464 | CT | C | 26 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0075 others(23): Show |
26 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1003-1098delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69152464 | ||||||
| chr16:69152464 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-1108_1003-109 others(15): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69152464 | ||||||
| chr16:69152464 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0106 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1003-1109_1003-109 others(16): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69152464 | ||||||
| chr16:69152465 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1003-1119T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152465 | |||||||
| chr16:69152469 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0174 |
2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1003-1115T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152469 | |||||||
| chr16:69152472 | T | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-1112T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152472 | |||||||
| chr16:69152473 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1003-1111T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152473 | |||||||
| chr16:69152476 | T | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-1108T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152476 | |||||||
| chr16:69152512 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1003-1072C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152512 | |||||||
| chr16:69152515 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1003-1069G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152515 | |||||||
| chr16:69152520 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1003-1064A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152520 | |||||||
| chr16:69152527 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1003-1057T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152527 | |||||||
| chr16:69152545 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1003-1039C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152545 | |||||||
| chr16:69152548 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1003-1036C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152548 | |||||||
| chr16:69152564 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-1020G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152564 | |||||||
| chr16:69152627 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(25): Show |
29 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1003-957G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152627 | |||||||
| chr16:69152787 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1003-797T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152787 | |||||||
| chr16:69152869 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1003-715G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69152869 | |||||||
| chr16:69153012 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1003-572C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153012 | |||||||
| chr16:69153024 | T | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0222 |
3 | HG00639.hp1 HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1003-560T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153024 | |||||||
| chr16:69153109 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1003-475T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153109 | |||||||
| chr16:69153197 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1003-387C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153197 | |||||||
| chr16:69153274 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(8): Show |
12 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1003-310C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153274 | |||||||
| chr16:69153367 | CT | C | 4 | a0002c0003t0001g0056 a0002c0003t0001g0067 a0002c0003t0001g0280 others(1): Show |
4 | HG01346.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-214delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 69153367 | ||||||
| chr16:69153370 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1003-214T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153370 | |||||||
| chr16:69153415 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1003-169C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153415 | |||||||
| chr16:69153419 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1003-165A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 8/16 | chr16 | 69153419 | |||||||
| chr16:69153715 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1099+35C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69153715 | |||||||
| chr16:69153951 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099+271G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69153951 | |||||||
| chr16:69154099 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1100-294T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69154099 | |||||||
| chr16:69154198 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1100-195A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69154198 | |||||||
| chr16:69154209 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(97): Show |
102 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1100-184A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69154209 | |||||||
| chr16:69154214 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1100-179T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 9/16 | chr16 | 69154214 | |||||||
| chr16:69154492 | C | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+35C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154492 | |||||||
| chr16:69154595 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1164+138C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154595 | |||||||
| chr16:69154704 | T | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1164+247T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154704 | |||||||
| chr16:69154704 | T | TTTTA | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(41): Show |
46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1164+283_1164+286d others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 69154704 | ||||||
| chr16:69154704 | T | TTTTATTT others(1): Show |
18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0069 others(15): Show |
18 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1164+279_1164+286d others(10): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 69154704 | ||||||
| chr16:69154704 | T | TTTTATTT others(5): Show |
5 | a0001c0001t0001g0057 a0001c0001t0001g0071 a0001c0001t0001g0080 others(2): Show |
5 | HG00738.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1164+275_1164+286d others(14): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 69154704 | ||||||
| chr16:69154704 | TTTTA | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0103 others(7): Show |
10 | HG01123.hp2 HG02300.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164+283_1164+286d others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 69154704 | ||||||
| chr16:69154872 | G | T | 2 | a0001c0001t0001g0093 a0001c0008t0001g0085 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1164+415G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154872 | |||||||
| chr16:69154890 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(17): Show |
21 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1164+433G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154890 | |||||||
| chr16:69154945 | C | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+488C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69154945 | |||||||
| chr16:69155066 | G | GA | 9 | a0001c0001t0001g0102 a0001c0001t0001g0218 a0001c0001t0001g0270 others(6): Show |
9 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1164+618dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 69155066 | ||||||
| chr16:69155077 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1164+620C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155077 | |||||||
| chr16:69155190 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1165-681T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155190 | |||||||
| chr16:69155334 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1165-537C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155334 | |||||||
| chr16:69155384 | T | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0256 |
2 | HG01261.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1165-487T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155384 | |||||||
| chr16:69155401 | A | G | 1 | a0002c0003t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1165-470A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155401 | |||||||
| chr16:69155671 | G | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0105 others(7): Show |
13 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1165-200G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 10/16 | chr16 | 69155671 | |||||||
| chr16:69156071 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1287+78C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156071 | |||||||
| chr16:69156146 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1287+153C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156146 | |||||||
| chr16:69156154 | C | CT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0234 a0001c0005t0001g0041 others(4): Show |
7 | HG01346.hp2 HG03041.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1287+178dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 69156154 | ||||||
| chr16:69156154 | C | CTT | 23 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(20): Show |
23 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1287+177_1287+178d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 69156154 | ||||||
| chr16:69156154 | C | CTTT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(63): Show |
68 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1287+176_1287+178d others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 69156154 | ||||||
| chr16:69156154 | CT | C | 7 | a0001c0001t0001g0160 a0001c0001t0001g0181 a0001c0001t0001g0187 others(4): Show |
7 | HG01168.hp2 HG01256.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1287+178delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 69156154 | ||||||
| chr16:69156393 | G | C | 1 | a0002c0003t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1287+400G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156393 | |||||||
| chr16:69156463 | C | CT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0064 others(39): Show |
42 | HG00408.hp2 HG00642.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1287+484dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 69156463 | ||||||
| chr16:69156480 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1287+487C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156480 | |||||||
| chr16:69156481 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1287+488C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156481 | |||||||
| chr16:69156552 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1288-532G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156552 | |||||||
| chr16:69156748 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1288-336C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156748 | |||||||
| chr16:69156865 | G | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1288-219G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156865 | |||||||
| chr16:69156950 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1288-134A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 11/16 | chr16 | 69156950 | |||||||
| chr16:69157349 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1444+109G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157349 | |||||||
| chr16:69157397 | G | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1444+157G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157397 | |||||||
| chr16:69157403 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1444+163G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157403 | |||||||
| chr16:69157517 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(17): Show |
21 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1444+277A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157517 | |||||||
| chr16:69157579 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+339G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157579 | |||||||
| chr16:69157596 | T | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0040 others(86): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1444+356T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157596 | |||||||
| chr16:69157639 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1444+399T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157639 | |||||||
| chr16:69157717 | C | G | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+477C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157717 | |||||||
| chr16:69157891 | C | CCCAAAAG others(308): Show |
1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1444+665_1444+666i others(317): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(314): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0065 others(14): Show |
18 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1444+665_1444+666i others(323): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(315): Show |
5 | a0001c0002t0001g0030 a0001c0002t0001g0032 a0001c0002t0001g0034 others(2): Show |
5 | HG04199.hp2 NA18957.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444+665_1444+666i others(324): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(315): Show |
6 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0271 others(3): Show |
6 | HG00738.hp2 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1444+665_1444+666i others(324): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(316): Show |
3 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0036 |
3 | HG01361.hp1 NA19067.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1444+665_1444+666i others(325): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(316): Show |
11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(8): Show |
11 | HG00621.hp2 HG02004.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1444+665_1444+666i others(325): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(317): Show |
1 | a0001c0002t0001g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1444+665_1444+666i others(326): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157891 | C | CCCAAAAG others(317): Show |
3 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0002t0001g0033 |
3 | NA19030.hp1 NA19076.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1444+665_1444+666i others(326): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69157891 | ||||||
| chr16:69157957 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1444+717T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69157957 | |||||||
| chr16:69158079 | G | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1444+839G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158079 | |||||||
| chr16:69158161 | C | CT | 61 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(58): Show |
61 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1444+951dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTT | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0090 others(42): Show |
47 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1444+950_1444+951d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(16): Show |
19 | HG00280.hp2 HG01346.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1444+949_1444+951d others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(7): Show |
10 | HG00280.hp1 HG01361.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444+948_1444+951d others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTTT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0062 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444+947_1444+951d others(7): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTTTT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0047 others(5): Show |
8 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444+946_1444+951d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTTTTT | 11 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0082 others(8): Show |
11 | HG00738.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1444+945_1444+951d others(9): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0008t0001g0085 |
3 | HG03491.hp1 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1444+942_1444+951d others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG03017.hp1 HG03492.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1444+941_1444+951d others(13): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CT | C | 19 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0052 others(16): Show |
19 | HG00099.hp1 HG00544.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1444+951delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CTT | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1444+950_1444+951d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CTTTTTT | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG00621.hp2 HG02004.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1444+946_1444+951d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1444+942_1444+951d others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
5 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1444+939_1444+951d others(15): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158161 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1444+937_1444+951d others(17): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69158161 | ||||||
| chr16:69158234 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+994C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158234 | |||||||
| chr16:69158413 | C | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(25): Show |
29 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1444+1173C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158413 | |||||||
| chr16:69158869 | C | T | 14 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(11): Show |
14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1445-1487C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158869 | |||||||
| chr16:69158944 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1445-1412C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158944 | |||||||
| chr16:69158982 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1445-1374A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69158982 | |||||||
| chr16:69159047 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0138 a0001c0001t0001g0236 |
3 | HG02486.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1445-1309C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159047 | |||||||
| chr16:69159060 | T | TA | 4 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-1296_1445-129 others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159060 | |||||||
| chr16:69159416 | C | T | 4 | a0002c0003t0001g0056 a0002c0003t0001g0067 a0002c0003t0001g0280 others(1): Show |
4 | HG01346.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-940C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159416 | |||||||
| chr16:69159436 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0226 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1445-920T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159436 | |||||||
| chr16:69159456 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1445-900G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159456 | |||||||
| chr16:69159560 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1445-796C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159560 | |||||||
| chr16:69159565 | G | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-791G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159565 | |||||||
| chr16:69159984 | C | CA | 44 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0039 others(41): Show |
45 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1445-359dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69159984 | ||||||
| chr16:69159998 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0084 |
4 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-358C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69159998 | |||||||
| chr16:69160007 | G | GA | 6 | a0001c0001t0001g0074 a0001c0001t0001g0110 a0001c0001t0001g0159 others(3): Show |
6 | HG00621.hp2 HG01175.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1445-341dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 69160007 | ||||||
| chr16:69160128 | A | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0062 others(30): Show |
34 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1445-228A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69160128 | |||||||
| chr16:69160268 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1445-88G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 12/16 | chr16 | 69160268 | |||||||
| chr16:69160560 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1551+98A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160560 | |||||||
| chr16:69160583 | A | C | 9 | a0001c0001t0001g0103 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01123.hp2 HG01517.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+121A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160583 | |||||||
| chr16:69160598 | C | CT | 30 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(27): Show |
30 | HG00140.hp2 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1551+152dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 69160598 | ||||||
| chr16:69160598 | CT | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0146 others(5): Show |
9 | HG01109.hp2 HG02683.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+152delT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 69160598 | ||||||
| chr16:69160679 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1551+217C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160679 | |||||||
| chr16:69160687 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1551+225C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160687 | |||||||
| chr16:69160689 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
5 | HG02258.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+227C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160689 | |||||||
| chr16:69160769 | G | C | 5 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+307G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160769 | |||||||
| chr16:69160796 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0062 others(45): Show |
49 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1551+334G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160796 | |||||||
| chr16:69160940 | C | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1551+478C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160940 | |||||||
| chr16:69160962 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0084 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1551+500G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160962 | |||||||
| chr16:69160967 | C | G | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1551+505C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69160967 | |||||||
| chr16:69161185 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1551+723G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161185 | |||||||
| chr16:69161230 | G | A | 4 | a0002c0003t0001g0056 a0002c0003t0001g0067 a0002c0003t0001g0280 others(1): Show |
4 | HG01346.hp2 HG03669.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+768G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161230 | |||||||
| chr16:69161300 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1551+838G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161300 | |||||||
| chr16:69161404 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1551+942A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161404 | |||||||
| chr16:69161539 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1551+1077G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161539 | |||||||
| chr16:69161640 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1551+1178C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161640 | |||||||
| chr16:69161668 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1551+1206A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161668 | |||||||
| chr16:69161700 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1551+1238C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161700 | |||||||
| chr16:69161816 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1552-1267A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69161816 | |||||||
| chr16:69162024 | G | A | 1 | a0002c0003t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1552-1059G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162024 | |||||||
| chr16:69162104 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-979A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162104 | |||||||
| chr16:69162111 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-972G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162111 | |||||||
| chr16:69162112 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(97): Show |
102 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1552-971T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162112 | |||||||
| chr16:69162112 | T | G | 1 | a0001c0001t0001g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-971T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162112 | |||||||
| chr16:69162115 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-968A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162115 | |||||||
| chr16:69162117 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1552-966G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162117 | |||||||
| chr16:69162228 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1552-855A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162228 | |||||||
| chr16:69162296 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1552-787G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162296 | |||||||
| chr16:69162300 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1552-783T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162300 | |||||||
| chr16:69162315 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1552-768C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162315 | |||||||
| chr16:69162406 | T | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-677T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162406 | |||||||
| chr16:69162595 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1552-488C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162595 | |||||||
| chr16:69162660 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1552-423C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162660 | |||||||
| chr16:69162704 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1552-379T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162704 | |||||||
| chr16:69162711 | CA | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1552-357delA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 69162711 | ||||||
| chr16:69162745 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1552-338C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162745 | |||||||
| chr16:69162878 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1552-205G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162878 | |||||||
| chr16:69162890 | C | CA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
6 | HG02572.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552-179dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 69162890 | ||||||
| chr16:69162922 | A | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0062 others(23): Show |
27 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1552-161A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162922 | |||||||
| chr16:69162941 | A | C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG01884.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1552-142A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162941 | |||||||
| chr16:69162991 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1552-92G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69162991 | |||||||
| chr16:69163057 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0155 |
2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1552-26C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 13/16 | chr16 | 69163057 | |||||||
| chr16:69163631 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1647+453T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163631 | |||||||
| chr16:69163641 | T | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1647+463T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163641 | |||||||
| chr16:69163684 | T | TA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(57): Show |
62 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1647+519dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69163684 | ||||||
| chr16:69163691 | A | AC | 21 | a0001c0001t0001g0137 a0001c0001t0001g0153 a0001c0001t0001g0175 others(18): Show |
21 | HG00099.hp1 HG01081.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.1647+513_1647+514i others(3): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163691 | |||||||
| chr16:69163771 | T | G | 6 | a0001c0001t0001g0153 a0001c0002t0001g0014 a0001c0002t0001g0016 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1647+593T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163771 | |||||||
| chr16:69163880 | G | GT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0048 others(8): Show |
11 | HG02572.hp2 HG02723.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1647+705dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69163880 | ||||||
| chr16:69163880 | G | GTT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
17 | HG00621.hp2 HG00738.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1647+704_1647+705d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69163880 | ||||||
| chr16:69163880 | G | GTTT | 7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647+703_1647+705d others(5): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69163880 | ||||||
| chr16:69163883 | TG | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(8): Show |
11 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1647+706delG | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163883 | |||||||
| chr16:69163884 | G | GT | 21 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0110 others(18): Show |
21 | HG00735.hp2 HG00741.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1647+725dupT | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69163884 | ||||||
| chr16:69163884 | G | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
64 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1647+706G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163884 | |||||||
| chr16:69163889 | T | TG | 12 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(9): Show |
13 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1647+711_1647+712i others(3): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163889 | |||||||
| chr16:69163949 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1647+771G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163949 | |||||||
| chr16:69163973 | C | T | 15 | a0001c0001t0001g0153 a0001c0002t0001g0014 a0001c0002t0001g0016 others(12): Show |
15 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1647+795C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69163973 | |||||||
| chr16:69164074 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1647+896T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164074 | |||||||
| chr16:69164148 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1647+970T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164148 | |||||||
| chr16:69164164 | T | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1647+986T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164164 | |||||||
| chr16:69164175 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1647+997C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164175 | |||||||
| chr16:69164335 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1648-1006A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164335 | |||||||
| chr16:69164586 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1648-755_1648-754i others(13): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164586 | |||||||
| chr16:69164586 | T | TTA | 62 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0084 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1648-727_1648-726d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | T | TTATA | 14 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0142 others(11): Show |
14 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.1648-729_1648-726d others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | T | TTATATA | 8 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0083 others(5): Show |
8 | HG01934.hp2 HG02135.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648-731_1648-726d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1648-735_1648-726d others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1648-737_1648-726d others(14): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | TTA | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(22): Show |
25 | HG01243.hp1 HG01346.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1648-727_1648-726d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | TTATA | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(46): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1648-729_1648-726d others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | TTATATA | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1648-731_1648-726d others(8): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164586 | TTATATAT others(3): Show |
T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0002t0001g0029 others(8): Show |
12 | HG01346.hp1 HG01361.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1648-735_1648-726d others(12): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164586 | ||||||
| chr16:69164604 | ATATATAT others(5): Show |
A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-725_1648-714d others(14): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69164604 | ||||||
| chr16:69164610 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1648-731A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164610 | |||||||
| chr16:69164620 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-721A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164620 | |||||||
| chr16:69164641 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1648-700T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164641 | |||||||
| chr16:69164725 | C | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1648-616C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164725 | |||||||
| chr16:69164742 | A | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1648-599A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164742 | |||||||
| chr16:69164838 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1648-503G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164838 | |||||||
| chr16:69164876 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-465G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164876 | |||||||
| chr16:69164947 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1648-394G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69164947 | |||||||
| chr16:69165118 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1648-223C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | chr16 | 69165118 | |||||||
| chr16:69165194 | CA | C | 8 | a0001c0001t0001g0181 a0001c0001t0001g0227 a0001c0001t0001g0271 others(5): Show |
8 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648-133delA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr16 | 69165194 | ||||||
| chr16:69165706 | T | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0095 others(6): Show |
9 | HG00544.hp2 HG03654.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1833+180T>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69165706 | |||||||
| chr16:69165993 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1833+467T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69165993 | |||||||
| chr16:69166180 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1833+654G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166180 | |||||||
| chr16:69166194 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1833+668C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166194 | |||||||
| chr16:69166457 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1834-618C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166457 | |||||||
| chr16:69166518 | C | A | 1 | a0003c0004t0001g0246 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1834-557C>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166518 | |||||||
| chr16:69166552 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834-523C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166552 | |||||||
| chr16:69166573 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00738.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1834-502C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166573 | |||||||
| chr16:69166588 | A | G | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834-487A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166588 | |||||||
| chr16:69166652 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0155 |
2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1834-423T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166652 | |||||||
| chr16:69166656 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834-419G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69166656 | |||||||
| chr16:69167028 | A | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0072 others(4): Show |
8 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834-47A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 15/16 | chr16 | 69167028 | |||||||
| chr16:69167259 | G | A | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1944+74G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167259 | |||||||
| chr16:69167272 | A | G | 1 | a0004c0009t0001g0201 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1944+87A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167272 | |||||||
| chr16:69167275 | T | C | 1 | a0002c0007t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1944+90T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167275 | |||||||
| chr16:69167305 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1944+120G>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167305 | |||||||
| chr16:69167399 | C | T | 7 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(4): Show |
7 | HG00621.hp2 HG02004.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1944+214C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167399 | |||||||
| chr16:69167675 | TACTCAAA others(2): Show |
T | 14 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(11): Show |
14 | HG01346.hp1 HG01361.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1944+500_1944+508d others(11): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69167675 | ||||||
| chr16:69167789 | T | C | 7 | a0001c0001t0002g0210 a0001c0001t0002g0230 a0001c0001t0002g0231 others(4): Show |
7 | HG01243.hp1 HG01346.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1944+604T>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167789 | |||||||
| chr16:69167824 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0105 others(7): Show |
13 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1944+639A>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167824 | |||||||
| chr16:69167829 | G | A | 2 | a0001c0001t0002g0210 a0001c0001t0002g0230 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1944+644G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167829 | |||||||
| chr16:69167842 | CA | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(71): Show |
76 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1944+671delA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69167842 | ||||||
| chr16:69167855 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0070 others(6): Show |
9 | HG00099.hp2 HG00738.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1944+670A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167855 | |||||||
| chr16:69167929 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1944+744G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167929 | |||||||
| chr16:69167955 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944+770G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69167955 | |||||||
| chr16:69168029 | G | A | 15 | a0001c0001t0001g0066 a0001c0002t0001g0014 a0001c0002t0001g0016 others(12): Show |
15 | HG01346.hp1 HG01361.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-792G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168029 | |||||||
| chr16:69168222 | T | G | 2 | a0001c0005t0001g0041 a0001c0005t0001g0277 |
2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1945-599T>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168222 | |||||||
| chr16:69168245 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1945-576G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168245 | |||||||
| chr16:69168299 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945-522G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168299 | |||||||
| chr16:69168342 | G | A | 15 | a0001c0001t0001g0066 a0001c0002t0001g0014 a0001c0002t0001g0016 others(12): Show |
15 | HG01346.hp1 HG01361.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-479G>A | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168342 | |||||||
| chr16:69168426 | A | ACTCT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1945-393_1945-392i others(6): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69168426 | ||||||
| chr16:69168429 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-392G>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168429 | |||||||
| chr16:69168433 | C | CA | 68 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(65): Show |
69 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1945-364dupA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69168433 | ||||||
| chr16:69168433 | C | CAA | 21 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(18): Show |
21 | HG01243.hp1 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.1945-365_1945-364d others(4): Show |
UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69168433 | ||||||
| chr16:69168433 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-388C>G | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168433 | |||||||
| chr16:69168433 | CA | C | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG01168.hp1 HG01884.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1945-364delA | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 69168433 | ||||||
| chr16:69168434 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-387A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168434 | |||||||
| chr16:69168435 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-386A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168435 | |||||||
| chr16:69168436 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-385A>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168436 | |||||||
| chr16:69168437 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1945-384A>C | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168437 | |||||||
| chr16:69168463 | C | T | 5 | a0001c0002t0001g0032 a0001c0002t0001g0034 a0001c0002t0001g0035 others(2): Show |
5 | NA18957.hp2 NA18960.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945-358C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168463 | |||||||
| chr16:69168489 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1945-332C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168489 | |||||||
| chr16:69168751 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1945-70C>T | UTP4 | ENSG00000141076.18 | transcript | ENST00000314423.12 | protein_coding | 16/16 | chr16 | 69168751 |