Item | Value |
---|---|
geneid | 55813 |
ensemblid | ENSG00000108651.10 |
hgncid | 18279 |
symbol | UTP6 |
name | UTP6 small subunit processome component |
refseq_nuc | NM_018428.3 |
refseq_prot | NP_060898.2 |
ensembl_nuc | ENST00000261708.9 |
ensembl_prot | ENSP00000261708.4 |
mane_status | MANE Select |
chr | chr17 |
start | 31860904 |
end | 31901708 |
strand | - |
ver | v1.2 |
region | chr17:31860904-31901708 |
region5000 | chr17:31855904-31906708 |
regionname0 | UTP6_chr17_31860904_31901708 |
regionname5000 | UTP6_chr17_31855904_31906708 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 597 | 222 | 87 | 40 | 61 | 7 | 25 | 45 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0002 | 0/0 | 597 | 89 | 5 | 15 | 54 | 5 | 10 | 40 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0003 | 0/0 | 597 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0004 | 0/0 | 597 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0005 | 0/0 | 597 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0006 | 0/0 | 597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0007 | 0/0 | 597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0008 | 0/0 | 597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0009 | 0/0 | 597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
a0010 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(573): Show |
chr17 | 31855904 | 31906708 |
a0011 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | MAEII others(592): Show |
chr17 | 31855904 | 31906708 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1791 | 205 | 75 | 37 | 59 | 7 | 25 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0001c0003 | 0/0 | 1791 | 7 | 7 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0001c0004 | 0/0 | 1791 | 5 | 5 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0001c0005 | 0/0 | 1791 | 3 | 0 | 3 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0001c0007 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0002c0002 | 0/0 | 1791 | 89 | 5 | 15 | 54 | 5 | 10 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0003c0006 | 0/0 | 1791 | 3 | 3 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0004c0008 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0005c0009 | 0/0 | 1791 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0006c0012 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0007c0015 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0008c0013 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0009c0011 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0010c0014 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 | ||
a0011c0010 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | ATGGC others(1786): Show |
chr17 | 31855904 | 31906708 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4330 | 85 | 36 | 12 | 25 | 4 | 8 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0002 | 0/0 | 4330 | 46 | 6 | 5 | 27 | 2 | 6 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0003 | 0/0 | 4331 | 20 | 10 | 7 | 1 | 0 | 2 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0004 | 0/0 | 4330 | 17 | 2 | 7 | 0 | 1 | 7 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0005 | 0/0 | 4329 | 11 | 9 | 2 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4324): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0006 | 0/0 | 4330 | 6 | 6 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0007 | 0/0 | 4330 | 5 | 0 | 0 | 5 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0009 | 0/0 | 4330 | 3 | 2 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0010 | 0/0 | 4331 | 3 | 3 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0011 | 1/0 | 4330 | 2 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0013 | 0/0 | 4330 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0014 | 0/0 | 3601 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(3596): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0015 | 0/1 | 4331 | 1 | 0 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0016 | 0/0 | 4330 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0017 | 0/0 | 4330 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0020 | 0/0 | 4330 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0001t0021 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0003t0003 | 0/0 | 4331 | 7 | 7 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0001c0004t0002 | 0/0 | 4330 | 5 | 5 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0001c0005t0003 | 0/0 | 4331 | 3 | 0 | 3 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0001c0007t0001 | 0/0 | 4330 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0002c0002t0001 | 0/0 | 4330 | 87 | 5 | 15 | 52 | 5 | 10 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0002c0002t0012 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0002c0002t0019 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0003c0006t0008 | 0/0 | 4330 | 3 | 3 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0004c0008t0002 | 0/0 | 4330 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0005c0009t0001 | 0/0 | 4330 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0006c0012t0001 | 0/0 | 4330 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0007c0015t0008 | 0/0 | 4330 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0008c0013t0001 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
a0009c0011t0003 | 0/0 | 4331 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0010c0014t0018 | 0/0 | 4331 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4326): Show |
chr17 | 31855904 | 31906708 |
a0011c0010t0002 | 0/0 | 4330 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | GTCTC others(4325): Show |
chr17 | 31855904 | 31906708 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0005 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0011g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0013g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0015g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0016g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0017g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0020g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0001t0021g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0004t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0004t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0005t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0005t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0005t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0001c0007t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0012g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0002c0002t0019g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0003c0006t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0003c0006t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0003c0006t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0004c0008t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0004c0008t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0005c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0005c0009t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0006c0012t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0007c0015t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0008c0013t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0009c0011t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0010c0014t0018g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
a0011c0010t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0040 | EUR | GBR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0170 | EUR | GBR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0172 | EUR | FIN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | FIN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | FIN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00738 | hp2 | a0006 | c0012 | t0001 | g0124 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG00741 | hp2 | a0001 | c0001 | t0016 | g0076 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0284 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0256 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01192 | hp2 | a0001 | c0001 | t0009 | g0188 | AMR | PUR | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01261 | hp1 | a0001 | c0001 | t0013 | g0092 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01978 | hp1 | a0001 | c0005 | t0003 | g0272 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01981 | hp1 | a0001 | c0005 | t0003 | g0271 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02004 | hp2 | a0001 | c0001 | t0020 | g0213 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02015 | hp2 | a0002 | c0002 | t0012 | g0019 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02056 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0209 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0230 | EAS | CDX | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0195 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02300 | hp2 | a0001 | c0005 | t0003 | g0273 | AMR | PEL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02451 | hp2 | a0001 | c0004 | t0002 | g0246 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0244 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02622 | hp2 | a0001 | c0004 | t0002 | g0243 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0287 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02647 | hp1 | a0001 | c0004 | t0002 | g0242 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0275 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03098 | hp1 | a0001 | c0003 | t0003 | g0192 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03098 | hp2 | a0007 | c0015 | t0008 | g0250 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03130 | hp2 | a0003 | c0006 | t0008 | g0257 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0193 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03239 | hp1 | a0001 | c0001 | t0014 | g0084 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03453 | hp1 | a0003 | c0006 | t0008 | g0251 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03453 | hp2 | a0003 | c0006 | t0008 | g0258 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0196 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ESN | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0276 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0236 | SAS | PJL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG04115 | hp2 | a0001 | c0001 | t0017 | g0066 | SAS | STU | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | BEB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | CHB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18906 | hp2 | a0001 | c0003 | t0003 | g0012 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18942 | hp1 | a0002 | c0002 | t0019 | g0123 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0214 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18963 | hp2 | a0004 | c0008 | t0002 | g0225 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18966 | hp1 | a0008 | c0013 | t0001 | g0132 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18966 | hp2 | a0004 | c0008 | t0002 | g0207 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18968 | hp2 | a0005 | c0009 | t0001 | g0047 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18975 | hp1 | a0005 | c0009 | t0001 | g0046 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18980 | hp2 | a0001 | c0007 | t0001 | g0057 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19003 | hp2 | a0001 | c0007 | t0001 | g0176 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19060 | hp1 | a0009 | c0011 | t0003 | g0286 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19089 | hp1 | a0001 | c0001 | t0021 | g0291 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19089 | hp2 | a0010 | c0014 | t0018 | g0031 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | ASW | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ASW | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | TSI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0217 | EUR | TSI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0136 | EUR | TSI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | GIH | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20905 | hp2 | a0011 | c0010 | t0002 | g0224 | SAS | GIH | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02109 | hp1 | a0001 | c0003 | t0003 | g0194 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
HG06807 | hp2 | a0001 | c0004 | t0002 | g0245 | AFR | USA | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | USA | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
homoSapiens | chm13v2 | a0001 | c0001 | t0015 | g0056 | REF | REF | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0108 | REF | REF | UTP6_chr17_31855904_31906708 | UTP6 | chr17 | 31855904 | 31906708 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:31863418 | C | A | 1 | a0010 | 1 | NA19089.hp2 | stop_gained | HIGH | c.1735G>T | p.Gly579* | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1816/4330 | 1735/1794 | 579/597 | chr17 | 31863418 | |||
chr17:31863456 | C | T | 1 | a0008 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.1697G>A | p.Cys566Tyr | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1778/4330 | 1697/1794 | 566/597 | chr17 | 31863456 | |||
chr17:31880573 | C | T | 1 | a0007 | 1 | HG03098.hp2 | missense_variant&splice_region_variant | MODERATE | c.967G>A | p.Glu323Lys | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/19 | 1048/4330 | 967/1794 | 323/597 | chr17 | 31880573 | |||
chr17:31880694 | T | A | 1 | a0004 | 2 | NA18963.hp2 NA18966.hp2 |
missense_variant | MODERATE | c.846A>T | p.Leu282Phe | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/19 | 927/4330 | 846/1794 | 282/597 | chr17 | 31880694 | |||
chr17:31886025 | C | T | 2 | a0003 a0007 |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.658G>A | p.Glu220Lys | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/19 | 739/4330 | 658/1794 | 220/597 | chr17 | 31886025 | |||
chr17:31886039 | T | C | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.644A>G | p.Glu215Gly | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/19 | 725/4330 | 644/1794 | 215/597 | chr17 | 31886039 | |||
chr17:31887266 | C | G | 1 | a0006 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.591G>C | p.Lys197Asn | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/19 | 672/4330 | 591/1794 | 197/597 | chr17 | 31887266 | |||
chr17:31889320 | G | A | 1 | a0005 | 2 | NA18968.hp2 NA18975.hp1 |
missense_variant | MODERATE | c.508C>T | p.Arg170Cys | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/19 | 589/4330 | 508/1794 | 170/597 | chr17 | 31889320 | |||
chr17:31894695 | T | G | 1 | a0009 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.262A>C | p.Ile88Leu | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/19 | 343/4330 | 262/1794 | 88/597 | chr17 | 31894695 | |||
chr17:31894983 | T | C | 4 | a0002 a0006 a0008 others(1): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
missense_variant | MODERATE | c.206A>G | p.Gln69Arg | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 3/19 | 287/4330 | 206/1794 | 69/597 | chr17 | 31894983 | |||
chr17:31899719 | T | C | 2 | a0003 a0007 |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.104A>G | p.Lys35Arg | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/19 | 185/4330 | 104/1794 | 35/597 | chr17 | 31899719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:31884477 | C | T | 1 | a0001c0007 | 2 | NA18980.hp2 NA19003.hp2 |
synonymous_variant | LOW | c.732G>A | p.Ser244Ser | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/19 | 813/4330 | 732/1794 | 244/597 | chr17 | 31884477 | |||
chr17:31887284 | T | C | 1 | a0001c0004 | 5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.573A>G | p.Glu191Glu | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/19 | 654/4330 | 573/1794 | 191/597 | chr17 | 31887284 | |||
chr17:31895006 | T | C | 1 | a0001c0005 | 3 | HG01978.hp1 HG01981.hp1 HG02300.hp2 |
synonymous_variant | LOW | c.183A>G | p.Glu61Glu | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 3/19 | 264/4330 | 183/1794 | 61/597 | chr17 | 31895006 | |||
chr17:31901571 | C | T | 1 | a0001c0003 | 7 | HG02109.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
synonymous_variant | LOW | c.57G>A | p.Leu19Leu | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 138/4330 | 57/1794 | 19/597 | chr17 | 31901571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:31860979 | T | C | 1 | a0001c0001t0002 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2380A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 2380 | chr17 | 31860979 | ||||||
chr17:31861233 | C | CA | 6 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0017 others(3): Show |
46 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2125dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 2125 | chr17 | 31861233 | ||||||
chr17:31861283 | C | T | 1 | a0001c0001t0002 | 5 | NA18941.hp1 NA18993.hp2 NA19005.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2076G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 2076 | chr17 | 31861283 | ||||||
chr17:31861368 | C | T | 1 | a0002c0002t0001 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1991G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1991 | chr17 | 31861368 | ||||||
chr17:31861392 | T | C | 1 | a0001c0001t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1967A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1967 | chr17 | 31861392 | ||||||
chr17:31861406 | C | A | 1 | a0001c0001t0010 | 2 | HG02717.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1953G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1953 | chr17 | 31861406 | ||||||
chr17:31861618 | T | A | 3 | a0001c0001t0004 a0003c0006t0008 a0007c0015t0008 |
14 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1741A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1741 | chr17 | 31861618 | ||||||
chr17:31861658 | T | A | 2 | a0003c0006t0008 a0007c0015t0008 |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1701A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1701 | chr17 | 31861658 | ||||||
chr17:31861703 | C | T | 1 | a0001c0001t0007 | 5 | HG00673.hp1 HG02056.hp1 HG02074.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1656G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1656 | chr17 | 31861703 | ||||||
chr17:31861915 | A | G | 1 | a0001c0001t0013 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1444T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1444 | chr17 | 31861915 | ||||||
chr17:31861973 | G | A | 1 | a0001c0001t0016 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1386 | chr17 | 31861973 | ||||||
chr17:31862005 | G | C | 1 | a0001c0001t0017 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1354 | chr17 | 31862005 | ||||||
chr17:31862294 | C | CA | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(4): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1064dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 1064 | chr17 | 31862294 | ||||||
chr17:31862416 | C | T | 1 | a0001c0001t0009 | 3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*943G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 943 | chr17 | 31862416 | ||||||
chr17:31862604 | CTT | C | 1 | a0001c0001t0005 | 11 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*754delAA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 753 | chr17 | 31862604 | ||||||
chr17:31862659 | T | C | 1 | a0002c0002t0019 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 700 | chr17 | 31862659 | ||||||
chr17:31862852 | C | A | 1 | a0001c0001t0006 | 6 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 507 | chr17 | 31862852 | ||||||
chr17:31862931 | C | T | 1 | a0001c0001t0020 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 428 | chr17 | 31862931 | ||||||
chr17:31863064 | T | A | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(15): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*295A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 295 | chr17 | 31863064 | ||||||
chr17:31863329 | A | G | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0003 others(2): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 19/19 | 30 | chr17 | 31863329 | ||||||
chr17:31901637 | G | A | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
127 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(124): Show |
5_prime_UTR_variant | MODIFIER | c.-10C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 10 | chr17 | 31901637 | ||||||
chr17:31901650 | G | C | 1 | a0001c0001t0021 | 1 | NA19089.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 23 | chr17 | 31901650 | ||||||
chr17:31901651 | C | G | 1 | a0001c0001t0021 | 1 | NA19089.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 24 | chr17 | 31901651 | ||||||
chr17:31901652 | G | C | 1 | a0001c0001t0021 | 1 | NA19089.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 25 | chr17 | 31901652 | ||||||
chr17:31901690 | C | G | 1 | a0002c0002t0012 | 1 | HG02015.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/19 | 63 | chr17 | 31901690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:31863609 | TTAAC | T | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637-97_1637-94del others(4): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31863609 | |||||||
chr17:31863637 | C | T | 2 | a0001c0001t0009g0020 a0001c0001t0009g0187 |
2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1637-121G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31863637 | |||||||
chr17:31863970 | G | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1637-454C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31863970 | |||||||
chr17:31864013 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1637-497A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864013 | |||||||
chr17:31864064 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1637-548A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864064 | |||||||
chr17:31864256 | G | A | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1637-740C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864256 | |||||||
chr17:31864442 | T | A | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636+924A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864442 | |||||||
chr17:31864697 | T | C | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636+669A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864697 | |||||||
chr17:31864781 | C | T | 1 | a0011c0010t0002g0224 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1636+585G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864781 | |||||||
chr17:31864810 | T | C | 1 | a0001c0001t0010g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1636+556A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864810 | |||||||
chr17:31864829 | A | T | 37 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(34): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1636+537T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864829 | |||||||
chr17:31864935 | G | C | 244 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(241): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1636+431C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31864935 | |||||||
chr17:31865104 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0090 others(6): Show |
9 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1636+262G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31865104 | |||||||
chr17:31865225 | C | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1636+141G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31865225 | |||||||
chr17:31865226 | T | G | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(178): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1636+140A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31865226 | |||||||
chr17:31865230 | C | T | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(178): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1636+136G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 18/18 | chr17 | 31865230 | |||||||
chr17:31865884 | T | C | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564-446A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31865884 | |||||||
chr17:31865907 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1564-469A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31865907 | |||||||
chr17:31865923 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1564-485T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31865923 | |||||||
chr17:31865936 | C | T | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1564-498G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31865936 | |||||||
chr17:31866169 | C | A | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-731G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866169 | |||||||
chr17:31866180 | A | G | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-742T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866180 | |||||||
chr17:31866185 | G | A | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-747C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866185 | |||||||
chr17:31866190 | G | A | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-752C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866190 | |||||||
chr17:31866200 | C | T | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-762G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866200 | |||||||
chr17:31866201 | G | A | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1564-763C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866201 | |||||||
chr17:31866204 | G | A | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-766C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866204 | |||||||
chr17:31866212 | A | G | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-774T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866212 | |||||||
chr17:31866218 | T | C | 2 | a0001c0001t0003g0264 a0001c0001t0003g0269 |
2 | HG01123.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1564-780A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866218 | |||||||
chr17:31866266 | G | A | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564-828C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866266 | |||||||
chr17:31866286 | C | CA | 17 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0096 others(14): Show |
17 | HG00140.hp1 HG01123.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1564-849dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866286 | |||||||
chr17:31866286 | CA | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0055 others(12): Show |
15 | HG01069.hp1 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1564-849delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866286 | |||||||
chr17:31866286 | CAA | C | 6 | a0001c0001t0001g0189 a0001c0001t0006g0021 a0001c0001t0006g0022 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1564-850_1564-849d others(4): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866286 | |||||||
chr17:31866286 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1564-859_1564-849d others(13): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866286 | |||||||
chr17:31866291 | A | C | 1 | a0001c0001t0002g0239 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1564-853T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866291 | |||||||
chr17:31866454 | C | T | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1564-1016G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866454 | |||||||
chr17:31866456 | C | T | 1 | a0001c0001t0003g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1564-1018G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866456 | |||||||
chr17:31866457 | G | A | 2 | a0002c0002t0001g0113 a0002c0002t0001g0136 |
2 | HG02280.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1564-1019C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866457 | |||||||
chr17:31866560 | T | C | 1 | a0002c0002t0001g0137 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1564-1122A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866560 | |||||||
chr17:31866710 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1564-1272G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866710 | |||||||
chr17:31866717 | T | TAA | 12 | a0001c0001t0001g0055 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
14 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1564-1281_1564-128 others(6): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866717 | |||||||
chr17:31866717 | T | TAAA | 217 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(214): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1564-1282_1564-128 others(7): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866717 | |||||||
chr17:31866717 | T | TAAAA | 17 | a0001c0001t0001g0073 a0001c0001t0001g0085 a0001c0001t0001g0174 others(14): Show |
20 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1564-1283_1564-128 others(8): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866717 | |||||||
chr17:31866764 | A | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1563+1282T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866764 | |||||||
chr17:31866817 | A | G | 45 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(42): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1563+1229T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866817 | |||||||
chr17:31866841 | C | T | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563+1205G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866841 | |||||||
chr17:31866887 | C | CA | 25 | a0001c0001t0001g0101 a0001c0001t0003g0288 a0001c0001t0004g0205 others(22): Show |
29 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1563+1158dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866887 | |||||||
chr17:31866887 | C | CAA | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(145): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1563+1157_1563+115 others(6): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866887 | |||||||
chr17:31866887 | C | CAAA | 51 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0048 others(48): Show |
52 | HG00423.hp1 HG00423.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1563+1156_1563+115 others(7): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866887 | |||||||
chr17:31866887 | C | CAAAA | 9 | a0001c0001t0003g0262 a0001c0001t0003g0280 a0001c0001t0004g0007 others(6): Show |
11 | HG00642.hp2 HG01433.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1563+1155_1563+115 others(8): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866887 | |||||||
chr17:31866887 | CA | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(34): Show |
45 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1563+1158delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31866887 | |||||||
chr17:31867092 | A | G | 1 | a0007c0015t0008g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1563+954T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867092 | |||||||
chr17:31867174 | T | A | 1 | a0002c0002t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1563+872A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867174 | |||||||
chr17:31867306 | G | T | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1563+740C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867306 | |||||||
chr17:31867579 | G | A | 1 | a0002c0002t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1563+467C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867579 | |||||||
chr17:31867817 | A | C | 2 | a0001c0007t0001g0057 a0001c0007t0001g0176 |
2 | NA18980.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1563+229T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867817 | |||||||
chr17:31867849 | C | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0102 others(4): Show |
7 | HG02615.hp1 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563+197G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867849 | |||||||
chr17:31867893 | G | A | 1 | a0001c0001t0014g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1563+153C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867893 | |||||||
chr17:31867894 | T | C | 1 | a0010c0014t0018g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1563+152A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867894 | |||||||
chr17:31867959 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1563+87T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 17/18 | chr17 | 31867959 | |||||||
chr17:31868273 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0048 others(42): Show |
47 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1497-161C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868273 | |||||||
chr17:31868322 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497-210A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868322 | |||||||
chr17:31868324 | G | GTT | 3 | a0001c0004t0002g0243 a0001c0004t0002g0244 a0001c0004t0002g0245 |
3 | HG02572.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1497-213_1497-212i others(4): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868324 | |||||||
chr17:31868325 | G | GT | 23 | a0001c0001t0002g0202 a0001c0001t0002g0210 a0001c0001t0002g0219 others(20): Show |
27 | HG00438.hp2 HG00673.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1497-214dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868325 | |||||||
chr17:31868325 | G | GTT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(118): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1497-215_1497-214d others(4): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868325 | |||||||
chr17:31868325 | G | GTTT | 71 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1497-216_1497-214d others(5): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868325 | |||||||
chr17:31868325 | G | T | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1497-213C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868325 | |||||||
chr17:31868406 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1497-294A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868406 | |||||||
chr17:31868483 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1497-371G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868483 | |||||||
chr17:31868596 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1497-484C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868596 | |||||||
chr17:31868617 | C | T | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1497-505G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868617 | |||||||
chr17:31868668 | G | C | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1497-556C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868668 | |||||||
chr17:31868789 | C | A | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497-677G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868789 | |||||||
chr17:31868822 | C | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1497-710G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868822 | |||||||
chr17:31868842 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02647.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1497-730C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868842 | |||||||
chr17:31868859 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1497-747T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31868859 | |||||||
chr17:31869488 | T | A | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1497-1376A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31869488 | |||||||
chr17:31869841 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG01074.hp1 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1497-1729G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31869841 | |||||||
chr17:31869850 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1497-1738A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31869850 | |||||||
chr17:31869927 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1497-1815A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31869927 | |||||||
chr17:31870304 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1497-2192A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870304 | |||||||
chr17:31870494 | T | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1497-2382A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870494 | |||||||
chr17:31870515 | G | GT | 8 | a0001c0001t0001g0064 a0001c0001t0001g0104 a0001c0001t0003g0270 others(5): Show |
8 | HG01257.hp2 HG01934.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497-2404dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870515 | |||||||
chr17:31870560 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1497-2448G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870560 | |||||||
chr17:31870589 | T | G | 1 | a0002c0002t0001g0139 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1497-2477A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870589 | |||||||
chr17:31870766 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1496+2612C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870766 | |||||||
chr17:31870866 | A | C | 30 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(27): Show |
34 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1496+2512T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870866 | |||||||
chr17:31870987 | G | GT | 6 | a0001c0001t0002g0210 a0001c0001t0002g0219 a0001c0001t0002g0237 others(3): Show |
6 | HG00438.hp2 HG01496.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1496+2390dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870987 | |||||||
chr17:31870987 | GT | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0098 a0001c0001t0001g0111 others(22): Show |
27 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1496+2390delA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870987 | |||||||
chr17:31870987 | GTT | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(171): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1496+2389_1496+239 others(6): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870987 | |||||||
chr17:31870988 | T | G | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496+2390A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31870988 | |||||||
chr17:31871182 | C | A | 1 | a0002c0002t0001g0140 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1496+2196G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871182 | |||||||
chr17:31871225 | C | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(193): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1496+2153G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871225 | |||||||
chr17:31871238 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0091 |
2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1496+2140G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871238 | |||||||
chr17:31871245 | G | A | 2 | a0002c0002t0001g0154 a0002c0002t0001g0155 |
2 | HG01099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1496+2133C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871245 | |||||||
chr17:31871353 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1496+2025C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871353 | |||||||
chr17:31871473 | C | G | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1496+1905G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871473 | |||||||
chr17:31871597 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1496+1781C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871597 | |||||||
chr17:31871646 | C | A | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1496+1732G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871646 | |||||||
chr17:31871796 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1496+1582G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871796 | |||||||
chr17:31871965 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1496+1413C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871965 | |||||||
chr17:31871992 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0048 others(42): Show |
47 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1496+1386C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31871992 | |||||||
chr17:31872104 | A | G | 2 | a0005c0009t0001g0046 a0005c0009t0001g0047 |
2 | NA18968.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1496+1274T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872104 | |||||||
chr17:31872209 | A | T | 1 | a0001c0001t0003g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1496+1169T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872209 | |||||||
chr17:31872505 | C | CA | 40 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0052 others(37): Show |
40 | HG00642.hp2 HG00673.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1496+872dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872505 | |||||||
chr17:31872518 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(215): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1496+860A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872518 | |||||||
chr17:31872570 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1496+808C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872570 | |||||||
chr17:31872585 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00423.hp2 HG00597.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496+793G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872585 | |||||||
chr17:31872689 | A | C | 1 | a0008c0013t0001g0132 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1496+689T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872689 | |||||||
chr17:31872775 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1496+603G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872775 | |||||||
chr17:31872825 | A | ATTACAAA others(11): Show |
1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+552_1496+553i others(20): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872825 | |||||||
chr17:31872826 | C | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+552G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872826 | |||||||
chr17:31872827 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+551G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872827 | |||||||
chr17:31872829 | T | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+549A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872829 | |||||||
chr17:31872830 | C | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+548G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872830 | |||||||
chr17:31872831 | T | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+547A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872831 | |||||||
chr17:31872832 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1496+546G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872832 | |||||||
chr17:31872853 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1496+525G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872853 | |||||||
chr17:31872857 | C | T | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1496+521G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872857 | |||||||
chr17:31872919 | CAAAAAAA others(4): Show |
C | 1 | a0003c0006t0008g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1496+448_1496+458d others(13): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872919 | |||||||
chr17:31872927 | C | CA | 9 | a0001c0001t0001g0112 a0001c0001t0002g0239 a0001c0001t0006g0021 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1496+450dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31872927 | |||||||
chr17:31873178 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1496+200G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31873178 | |||||||
chr17:31873237 | G | GAGCA | 4 | a0003c0006t0008g0251 a0003c0006t0008g0257 a0003c0006t0008g0258 others(1): Show |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1496+137_1496+140d others(6): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31873237 | |||||||
chr17:31873344 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1496+34C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 16/18 | chr17 | 31873344 | |||||||
chr17:31873533 | T | C | 4 | a0003c0006t0008g0251 a0003c0006t0008g0257 a0003c0006t0008g0258 others(1): Show |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-46A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 15/18 | chr17 | 31873533 | |||||||
chr17:31873625 | C | G | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+48G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 15/18 | chr17 | 31873625 | |||||||
chr17:31873625 | C | T | 2 | a0001c0001t0003g0278 a0001c0001t0003g0280 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1386+48G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 15/18 | chr17 | 31873625 | |||||||
chr17:31873805 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1306-52G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31873805 | |||||||
chr17:31873805 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1306-52G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31873805 | |||||||
chr17:31873850 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1306-97A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31873850 | |||||||
chr17:31874156 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1306-403G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874156 | |||||||
chr17:31874290 | C | T | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(231): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1306-537G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874290 | |||||||
chr17:31874293 | TC | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(183): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1306-541delG | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874293 | |||||||
chr17:31874472 | G | T | 1 | a0002c0002t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1306-719C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874472 | |||||||
chr17:31874507 | C | G | 2 | a0003c0006t0008g0257 a0003c0006t0008g0258 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1305+727G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874507 | |||||||
chr17:31874559 | A | AAAC | 222 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(219): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1305+674_1305+675i others(5): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874559 | |||||||
chr17:31874559 | A | AACC | 8 | a0001c0001t0001g0174 a0001c0001t0001g0189 a0001c0001t0006g0021 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+672_1305+674d others(5): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874559 | |||||||
chr17:31874587 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1305+647G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874587 | |||||||
chr17:31874755 | T | A | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1305+479A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874755 | |||||||
chr17:31874889 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1305+345C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874889 | |||||||
chr17:31874931 | TA | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(224): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1305+302delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874931 | |||||||
chr17:31874941 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1305+293T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31874941 | |||||||
chr17:31875037 | T | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(234): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1305+197A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31875037 | |||||||
chr17:31875060 | A | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0075 others(7): Show |
10 | HG02027.hp1 HG02083.hp2 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.1305+174T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31875060 | |||||||
chr17:31875072 | T | C | 9 | a0002c0002t0001g0011 a0002c0002t0001g0038 a0002c0002t0001g0141 others(6): Show |
10 | HG00558.hp2 HG02040.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+162A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 14/18 | chr17 | 31875072 | |||||||
chr17:31875631 | C | T | 1 | a0001c0004t0002g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1126-218G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31875631 | |||||||
chr17:31875682 | G | A | 2 | a0001c0001t0004g0235 a0001c0001t0004g0236 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1126-269C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31875682 | |||||||
chr17:31875687 | G | A | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1126-274C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31875687 | |||||||
chr17:31875820 | C | CA | 10 | a0001c0001t0001g0069 a0001c0001t0002g0015 a0001c0001t0004g0205 others(7): Show |
11 | HG01106.hp1 HG01257.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1126-408dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31875820 | |||||||
chr17:31875834 | A | G | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1126-421T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31875834 | |||||||
chr17:31876053 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0070 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1126-640T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876053 | |||||||
chr17:31876124 | A | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1126-711T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876124 | |||||||
chr17:31876182 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1126-769C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876182 | |||||||
chr17:31876289 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1126-876C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876289 | |||||||
chr17:31876334 | G | A | 1 | a0002c0002t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1126-921C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876334 | |||||||
chr17:31876377 | G | A | 1 | a0002c0002t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1126-964C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876377 | |||||||
chr17:31876529 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(234): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1126-1116C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876529 | |||||||
chr17:31876638 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1126-1225G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876638 | |||||||
chr17:31876639 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1126-1226G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876639 | |||||||
chr17:31876696 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
7 | HG01192.hp2 HG02055.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-1283A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876696 | |||||||
chr17:31876836 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1414T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876836 | |||||||
chr17:31876837 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1413G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876837 | |||||||
chr17:31876841 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0247 |
3 | HG02559.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1125+1409C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876841 | |||||||
chr17:31876844 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1406A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876844 | |||||||
chr17:31876846 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1404A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876846 | |||||||
chr17:31876849 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1401A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876849 | |||||||
chr17:31876850 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1400T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876850 | |||||||
chr17:31876855 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1395A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876855 | |||||||
chr17:31876859 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1391T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876859 | |||||||
chr17:31876860 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1390T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876860 | |||||||
chr17:31876873 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1377C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876873 | |||||||
chr17:31876874 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1376A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876874 | |||||||
chr17:31876875 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1375C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876875 | |||||||
chr17:31876877 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1373A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876877 | |||||||
chr17:31876878 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1372C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876878 | |||||||
chr17:31876885 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1365C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876885 | |||||||
chr17:31876890 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1360A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876890 | |||||||
chr17:31876896 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1354G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876896 | |||||||
chr17:31876897 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1353T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876897 | |||||||
chr17:31876899 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1351G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876899 | |||||||
chr17:31876900 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1350A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876900 | |||||||
chr17:31876903 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1347A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876903 | |||||||
chr17:31876907 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1343C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876907 | |||||||
chr17:31876909 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1341C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876909 | |||||||
chr17:31876912 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1338A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876912 | |||||||
chr17:31876913 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1337C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876913 | |||||||
chr17:31876915 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1335C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876915 | |||||||
chr17:31876917 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1333A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876917 | |||||||
chr17:31876918 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1332C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876918 | |||||||
chr17:31876919 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1331C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876919 | |||||||
chr17:31876920 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1330C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876920 | |||||||
chr17:31876921 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1329T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876921 | |||||||
chr17:31876922 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1328C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876922 | |||||||
chr17:31876923 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1327T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876923 | |||||||
chr17:31876929 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1321A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876929 | |||||||
chr17:31876930 | T | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1320A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876930 | |||||||
chr17:31876931 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1319T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876931 | |||||||
chr17:31876937 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1313C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876937 | |||||||
chr17:31876938 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1312C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876938 | |||||||
chr17:31876939 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1311C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876939 | |||||||
chr17:31876940 | A | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1310T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876940 | |||||||
chr17:31876941 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1309C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876941 | |||||||
chr17:31876944 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1306C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876944 | |||||||
chr17:31876945 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1305C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876945 | |||||||
chr17:31876947 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1303T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876947 | |||||||
chr17:31876948 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1302C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876948 | |||||||
chr17:31876951 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1299C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876951 | |||||||
chr17:31876954 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1296C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876954 | |||||||
chr17:31876957 | G | C | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1293C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876957 | |||||||
chr17:31876958 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1292C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876958 | |||||||
chr17:31876959 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1291G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876959 | |||||||
chr17:31876960 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1290G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876960 | |||||||
chr17:31876961 | A | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1289T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876961 | |||||||
chr17:31876964 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1286T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876964 | |||||||
chr17:31876967 | A | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1283T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876967 | |||||||
chr17:31876969 | G | T | 1 | a0001c0001t0002g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1125+1281C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31876969 | |||||||
chr17:31877469 | T | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0167 |
2 | HG00642.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1125+781A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877469 | |||||||
chr17:31877508 | C | A | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1125+742G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877508 | |||||||
chr17:31877550 | G | C | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1125+700C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877550 | |||||||
chr17:31877664 | C | G | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1125+586G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877664 | |||||||
chr17:31877724 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+526A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877724 | |||||||
chr17:31877765 | G | C | 1 | a0001c0001t0003g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1125+485C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877765 | |||||||
chr17:31877899 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0070 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1125+351T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877899 | |||||||
chr17:31877966 | C | CA | 9 | a0001c0001t0001g0052 a0002c0002t0001g0116 a0002c0002t0001g0117 others(6): Show |
9 | HG00438.hp1 HG00673.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1125+283dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31877966 | |||||||
chr17:31878111 | C | T | 37 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(34): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1125+139G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31878111 | |||||||
chr17:31878206 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1125+44T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 13/18 | chr17 | 31878206 | |||||||
chr17:31878411 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1048-84C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 12/18 | chr17 | 31878411 | |||||||
chr17:31878439 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0070 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1048-112A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 12/18 | chr17 | 31878439 | |||||||
chr17:31878491 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1048-164G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 12/18 | chr17 | 31878491 | |||||||
chr17:31878807 | G | C | 1 | a0007c0015t0008g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.968-26C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31878807 | |||||||
chr17:31879040 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.968-259A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879040 | |||||||
chr17:31879076 | A | G | 1 | a0002c0002t0001g0150 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.968-295T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879076 | |||||||
chr17:31879228 | A | G | 4 | a0002c0002t0001g0121 a0002c0002t0001g0125 a0002c0002t0001g0130 others(1): Show |
4 | HG02074.hp2 NA18612.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-447T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879228 | |||||||
chr17:31879333 | T | C | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.968-552A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879333 | |||||||
chr17:31879374 | C | A | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.968-593G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879374 | |||||||
chr17:31879407 | T | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.968-626A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879407 | |||||||
chr17:31879583 | G | A | 1 | a0001c0001t0010g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.968-802C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879583 | |||||||
chr17:31879683 | T | C | 1 | a0001c0005t0003g0272 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.967+890A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879683 | |||||||
chr17:31879750 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.967+823C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879750 | |||||||
chr17:31879798 | C | T | 9 | a0001c0001t0003g0283 a0001c0001t0005g0008 a0001c0001t0005g0018 others(6): Show |
12 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.967+775G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879798 | |||||||
chr17:31879923 | T | C | 3 | a0002c0002t0001g0115 a0002c0002t0001g0145 a0002c0002t0001g0164 |
3 | HG01496.hp2 NA18747.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.967+650A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31879923 | |||||||
chr17:31880105 | C | CA | 5 | a0001c0001t0007g0209 a0002c0002t0001g0113 a0002c0002t0001g0150 others(2): Show |
5 | HG01099.hp2 HG02074.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+467dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31880105 | |||||||
chr17:31880125 | A | G | 1 | a0003c0006t0008g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.967+448T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31880125 | |||||||
chr17:31880136 | G | C | 1 | a0002c0002t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.967+437C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31880136 | |||||||
chr17:31880137 | C | A | 1 | a0002c0002t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.967+436G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31880137 | |||||||
chr17:31880338 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.967+235A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 11/18 | chr17 | 31880338 | |||||||
chr17:31880769 | T | C | 1 | a0001c0001t0005g0285 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.786-15A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31880769 | |||||||
chr17:31880820 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.786-66T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31880820 | |||||||
chr17:31880849 | G | A | 1 | a0001c0001t0005g0282 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786-95C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31880849 | |||||||
chr17:31880978 | C | T | 1 | a0002c0002t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.786-224G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31880978 | |||||||
chr17:31881130 | C | T | 6 | a0001c0001t0003g0267 a0001c0004t0002g0242 a0001c0004t0002g0243 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.786-376G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881130 | |||||||
chr17:31881169 | T | A | 1 | a0003c0006t0008g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.786-415A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881169 | |||||||
chr17:31881171 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18986.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.786-417T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881171 | |||||||
chr17:31881183 | A | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0016g0076 |
3 | HG00735.hp1 HG00741.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.786-429T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881183 | |||||||
chr17:31881251 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.786-497A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881251 | |||||||
chr17:31881267 | C | CT | 8 | a0001c0001t0001g0058 a0001c0001t0002g0231 a0001c0001t0004g0203 others(5): Show |
8 | HG01123.hp1 HG01358.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.786-514dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881267 | |||||||
chr17:31881267 | CT | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0189 others(46): Show |
56 | HG00438.hp2 HG00738.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.786-514delA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881267 | |||||||
chr17:31881308 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.786-554G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881308 | |||||||
chr17:31881464 | T | C | 1 | a0001c0001t0003g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.786-710A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881464 | |||||||
chr17:31881493 | T | G | 1 | a0002c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.786-739A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881493 | |||||||
chr17:31881501 | T | A | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.786-747A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881501 | |||||||
chr17:31881502 | C | A | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.786-748G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881502 | |||||||
chr17:31881617 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0222 |
2 | HG00280.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.786-863A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881617 | |||||||
chr17:31881839 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.786-1085C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31881839 | |||||||
chr17:31882220 | G | A | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.786-1466C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882220 | |||||||
chr17:31882327 | G | GT | 42 | a0001c0001t0001g0174 a0001c0001t0002g0237 a0001c0001t0003g0017 others(39): Show |
47 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.786-1574dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882327 | |||||||
chr17:31882381 | G | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.786-1627C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882381 | |||||||
chr17:31882456 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.786-1702C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882456 | |||||||
chr17:31882509 | C | T | 8 | a0001c0001t0001g0174 a0001c0001t0001g0189 a0001c0001t0006g0021 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.786-1755G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882509 | |||||||
chr17:31882735 | G | C | 1 | a0003c0006t0008g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785+1689C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882735 | |||||||
chr17:31882756 | C | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(4): Show |
9 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.785+1668G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882756 | |||||||
chr17:31882812 | G | T | 1 | a0004c0008t0002g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.785+1612C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882812 | |||||||
chr17:31882841 | A | T | 1 | a0002c0002t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.785+1583T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882841 | |||||||
chr17:31882861 | C | T | 2 | a0001c0001t0006g0025 a0001c0001t0006g0026 |
2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.785+1563G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882861 | |||||||
chr17:31882997 | A | G | 3 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0009c0011t0003g0286 |
3 | HG02630.hp2 NA19030.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.785+1427T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31882997 | |||||||
chr17:31883171 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.785+1253T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883171 | |||||||
chr17:31883316 | A | AT | 49 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(46): Show |
55 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.785+1107dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883316 | |||||||
chr17:31883316 | AT | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0101 a0001c0001t0002g0223 others(3): Show |
6 | HG01074.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+1107delA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883316 | |||||||
chr17:31883357 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.785+1067G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883357 | |||||||
chr17:31883564 | C | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0247 |
3 | HG02559.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.785+860G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883564 | |||||||
chr17:31883894 | CCT | C | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.785+528_785+529del others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31883894 | |||||||
chr17:31884002 | A | AT | 219 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(216): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.785+421dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884002 | |||||||
chr17:31884056 | T | C | 1 | a0002c0002t0001g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.785+368A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884056 | |||||||
chr17:31884180 | T | A | 39 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(36): Show |
44 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.785+244A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884180 | |||||||
chr17:31884186 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG01167.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.785+238G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884186 | |||||||
chr17:31884190 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.785+234C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884190 | |||||||
chr17:31884396 | T | C | 1 | a0002c0002t0001g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.785+28A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 10/18 | chr17 | 31884396 | |||||||
chr17:31884742 | C | CAT | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(235): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.704-238_704-237ins others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884742 | |||||||
chr17:31884742 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.704-237G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884742 | |||||||
chr17:31884743 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-238C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884743 | |||||||
chr17:31884812 | G | T | 9 | a0001c0001t0001g0027 a0001c0001t0001g0174 a0001c0001t0001g0189 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-307C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884812 | |||||||
chr17:31884859 | G | A | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.704-354C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884859 | |||||||
chr17:31884860 | C | A | 1 | a0002c0002t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.704-355G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884860 | |||||||
chr17:31884886 | TCTA | T | 37 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(34): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.704-384_704-382del others(3): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884886 | |||||||
chr17:31884997 | A | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(234): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.704-492T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31884997 | |||||||
chr17:31885019 | G | A | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.704-514C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885019 | |||||||
chr17:31885102 | G | A | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-597C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885102 | |||||||
chr17:31885170 | T | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0102 others(4): Show |
7 | HG02615.hp1 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-665A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885170 | |||||||
chr17:31885262 | G | A | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.703+718C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885262 | |||||||
chr17:31885382 | T | G | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.703+598A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885382 | |||||||
chr17:31885585 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.703+395G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885585 | |||||||
chr17:31885599 | C | G | 2 | a0004c0008t0002g0207 a0004c0008t0002g0225 |
2 | NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.703+381G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885599 | |||||||
chr17:31885631 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG00597.hp2 NA18955.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+349A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885631 | |||||||
chr17:31885737 | G | A | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.703+243C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885737 | |||||||
chr17:31885744 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.703+236G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885744 | |||||||
chr17:31885784 | T | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0186 |
2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.703+196A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885784 | |||||||
chr17:31885912 | C | G | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.703+68G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 9/18 | chr17 | 31885912 | |||||||
chr17:31886105 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-44C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886105 | |||||||
chr17:31886123 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.622-62C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886123 | |||||||
chr17:31886331 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.622-270G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886331 | |||||||
chr17:31886450 | G | C | 1 | a0002c0002t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.622-389C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886450 | |||||||
chr17:31886500 | C | A | 39 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(36): Show |
44 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.622-439G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886500 | |||||||
chr17:31886520 | C | T | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.622-459G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886520 | |||||||
chr17:31886557 | C | T | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.622-496G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886557 | |||||||
chr17:31886840 | T | C | 2 | a0002c0002t0001g0039 a0002c0002t0001g0152 |
2 | HG02683.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.621+396A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886840 | |||||||
chr17:31886964 | T | G | 1 | a0004c0008t0002g0225 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.621+272A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31886964 | |||||||
chr17:31887201 | G | A | 1 | a0003c0006t0008g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.621+35C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 8/18 | chr17 | 31887201 | |||||||
chr17:31887408 | G | A | 1 | a0002c0002t0012g0019 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.544-95C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887408 | |||||||
chr17:31887426 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.544-113G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887426 | |||||||
chr17:31887523 | T | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(172): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.544-210A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887523 | |||||||
chr17:31887712 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.544-399T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887712 | |||||||
chr17:31887817 | G | A | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.544-504C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887817 | |||||||
chr17:31887863 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.544-550T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887863 | |||||||
chr17:31887961 | C | CAA | 29 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(26): Show |
34 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.544-650_544-649dup others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887961 | |||||||
chr17:31887961 | C | CAAA | 9 | a0001c0001t0003g0262 a0001c0001t0003g0265 a0001c0001t0003g0266 others(6): Show |
9 | HG01258.hp1 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-651_544-649dup others(3): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887961 | |||||||
chr17:31887961 | CA | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.544-649delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887961 | |||||||
chr17:31887961 | CAA | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0109 others(5): Show |
8 | HG00099.hp2 HG01934.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-650_544-649del others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31887961 | |||||||
chr17:31888247 | A | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.544-934T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888247 | |||||||
chr17:31888286 | G | A | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-973C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888286 | |||||||
chr17:31888334 | T | C | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+951A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888334 | |||||||
chr17:31888356 | G | T | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.543+929C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888356 | |||||||
chr17:31888394 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+891T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888394 | |||||||
chr17:31888430 | C | A | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.543+855G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888430 | |||||||
chr17:31888506 | T | C | 193 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(190): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.543+779A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888506 | |||||||
chr17:31888650 | G | A | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.543+635C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888650 | |||||||
chr17:31888847 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(174): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.543+438C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888847 | |||||||
chr17:31888929 | A | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(234): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.543+356T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31888929 | |||||||
chr17:31889069 | C | CA | 38 | a0001c0001t0002g0239 a0001c0001t0003g0017 a0001c0001t0003g0260 others(35): Show |
43 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.543+215dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31889069 | |||||||
chr17:31889155 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02723.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.543+130G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 7/18 | chr17 | 31889155 | |||||||
chr17:31889495 | A | AT | 23 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(20): Show |
26 | HG00642.hp2 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.425-93dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889495 | |||||||
chr17:31889495 | AT | A | 25 | a0001c0001t0002g0241 a0001c0001t0003g0283 a0001c0001t0003g0288 others(22): Show |
29 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.425-93delA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889495 | |||||||
chr17:31889621 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.425-218G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889621 | |||||||
chr17:31889625 | T | C | 2 | a0001c0001t0004g0249 a0001c0001t0004g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.425-222A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889625 | |||||||
chr17:31889745 | G | A | 2 | a0001c0001t0002g0199 a0001c0001t0002g0226 |
2 | NA18960.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.425-342C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889745 | |||||||
chr17:31889789 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.425-386G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889789 | |||||||
chr17:31889849 | A | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.425-446T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889849 | |||||||
chr17:31889881 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.425-478C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889881 | |||||||
chr17:31889934 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.425-531A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31889934 | |||||||
chr17:31890012 | C | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02723.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.425-609G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890012 | |||||||
chr17:31890248 | G | A | 1 | a0003c0006t0008g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-845C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890248 | |||||||
chr17:31890287 | T | G | 4 | a0003c0006t0008g0251 a0003c0006t0008g0257 a0003c0006t0008g0258 others(1): Show |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-884A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890287 | |||||||
chr17:31890488 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.425-1085G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890488 | |||||||
chr17:31890577 | G | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.425-1174C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890577 | |||||||
chr17:31890628 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-1225C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890628 | |||||||
chr17:31890743 | T | C | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425-1340A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890743 | |||||||
chr17:31890759 | A | G | 230 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(227): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.425-1356T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890759 | |||||||
chr17:31890890 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.424+1370C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890890 | |||||||
chr17:31890897 | G | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(184): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.424+1363C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890897 | |||||||
chr17:31890937 | A | G | 5 | a0001c0001t0002g0231 a0001c0001t0002g0233 a0001c0001t0002g0239 others(2): Show |
5 | NA18941.hp1 NA18993.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+1323T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31890937 | |||||||
chr17:31891095 | A | T | 3 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0118 |
3 | NA18971.hp1 NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.424+1165T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31891095 | |||||||
chr17:31891298 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(172): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.424+962G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31891298 | |||||||
chr17:31891517 | T | TG | 3 | a0001c0001t0001g0027 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02647.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.424+742dupC | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31891517 | |||||||
chr17:31891574 | C | T | 1 | a0002c0002t0001g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.424+686G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31891574 | |||||||
chr17:31891641 | T | C | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.424+619A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31891641 | |||||||
chr17:31892008 | G | A | 1 | a0001c0003t0003g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.424+252C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31892008 | |||||||
chr17:31892009 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.424+251G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31892009 | |||||||
chr17:31892022 | C | CA | 6 | a0001c0001t0021g0291 a0001c0004t0002g0242 a0001c0004t0002g0243 others(3): Show |
6 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+237dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 6/18 | chr17 | 31892022 | |||||||
chr17:31892355 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.361-32G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892355 | |||||||
chr17:31892407 | C | G | 1 | a0002c0002t0001g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.361-84G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892407 | |||||||
chr17:31892481 | C | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(56): Show |
68 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.361-158G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892481 | |||||||
chr17:31892550 | G | A | 54 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(51): Show |
63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.360+197C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892550 | |||||||
chr17:31892613 | T | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 |
3 | NA18939.hp2 NA18949.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.360+134A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892613 | |||||||
chr17:31892640 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.360+107A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892640 | |||||||
chr17:31892668 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.360+79T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892668 | |||||||
chr17:31892684 | G | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0249 a0001c0001t0004g0252 others(5): Show |
10 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.360+63C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 5/18 | chr17 | 31892684 | |||||||
chr17:31892938 | C | T | 4 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0274 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-144G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31892938 | |||||||
chr17:31893015 | T | C | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-221A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893015 | |||||||
chr17:31893133 | C | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(56): Show |
68 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.313-339G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893133 | |||||||
chr17:31893134 | T | G | 114 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(111): Show |
130 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.313-340A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893134 | |||||||
chr17:31893171 | G | C | 1 | a0001c0001t0003g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.313-377C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893171 | |||||||
chr17:31893205 | C | T | 59 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(56): Show |
68 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.313-411G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893205 | |||||||
chr17:31893240 | T | C | 41 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(38): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.313-446A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893240 | |||||||
chr17:31893430 | C | CA | 65 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(62): Show |
71 | HG00673.hp1 HG01071.hp1 HG01257.hp1 others(68): Show |
intron_variant | MODIFIER | c.313-637dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893430 | |||||||
chr17:31893430 | C | CAA | 6 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(3): Show |
6 | HG00738.hp1 HG01123.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-638_313-637dup others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893430 | |||||||
chr17:31893523 | G | A | 39 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(36): Show |
44 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.313-729C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893523 | |||||||
chr17:31893734 | C | CA | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00642.hp1 HG00741.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+910dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893734 | |||||||
chr17:31893734 | CA | C | 12 | a0001c0001t0001g0054 a0001c0001t0004g0007 a0001c0001t0004g0253 others(9): Show |
14 | HG00642.hp2 HG01106.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+910delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893734 | |||||||
chr17:31893734 | CAA | C | 95 | a0001c0001t0001g0175 a0001c0001t0002g0003 a0001c0001t0002g0006 others(92): Show |
109 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.312+909_312+910del others(2): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893734 | |||||||
chr17:31893757 | A | C | 50 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(47): Show |
57 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.312+888T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893757 | |||||||
chr17:31893820 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.312+825C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893820 | |||||||
chr17:31893836 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02647.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.312+809A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893836 | |||||||
chr17:31893933 | G | T | 1 | a0001c0001t0002g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.312+712C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893933 | |||||||
chr17:31893951 | T | G | 1 | a0001c0001t0003g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.312+694A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893951 | |||||||
chr17:31893959 | A | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(98): Show |
115 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.312+686T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893959 | |||||||
chr17:31893963 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.312+682T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31893963 | |||||||
chr17:31894089 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.312+556G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894089 | |||||||
chr17:31894285 | G | A | 12 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0004g0007 others(9): Show |
14 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+360C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894285 | |||||||
chr17:31894285 | GA | G | 97 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0002g0003 others(94): Show |
111 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.312+359delT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894285 | |||||||
chr17:31894286 | A | G | 16 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0232 others(13): Show |
18 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.312+359T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894286 | |||||||
chr17:31894287 | A | G | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.312+358T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894287 | |||||||
chr17:31894547 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0011g0183 |
3 | HG03540.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.312+98G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894547 | |||||||
chr17:31894559 | T | C | 7 | a0001c0001t0001g0189 a0001c0001t0006g0021 a0001c0001t0006g0022 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+86A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894559 | |||||||
chr17:31894586 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.312+59G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894586 | |||||||
chr17:31894596 | A | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.312+49T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 4/18 | chr17 | 31894596 | |||||||
chr17:31894888 | C | G | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.219+82G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 3/18 | chr17 | 31894888 | |||||||
chr17:31894918 | A | G | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.219+52T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 3/18 | chr17 | 31894918 | |||||||
chr17:31895168 | T | G | 1 | a0001c0001t0002g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.178-157A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895168 | |||||||
chr17:31895256 | A | G | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-245T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895256 | |||||||
chr17:31895271 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-260G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895271 | |||||||
chr17:31895572 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-561G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895572 | |||||||
chr17:31895669 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178-658C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895669 | |||||||
chr17:31895684 | C | T | 2 | a0005c0009t0001g0046 a0005c0009t0001g0047 |
2 | NA18968.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.178-673G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895684 | |||||||
chr17:31895854 | C | T | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-843G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895854 | |||||||
chr17:31895908 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02647.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-897C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31895908 | |||||||
chr17:31896017 | G | GA | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-1007dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896017 | |||||||
chr17:31896017 | GAA | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0249 a0001c0001t0004g0252 others(5): Show |
10 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-1008_178-1007d others(4): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896017 | |||||||
chr17:31896109 | G | A | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-1098C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896109 | |||||||
chr17:31896171 | G | T | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.178-1160C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896171 | |||||||
chr17:31896173 | A | T | 1 | a0001c0001t0003g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.178-1162T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896173 | |||||||
chr17:31896197 | C | T | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.178-1186G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896197 | |||||||
chr17:31896233 | G | A | 59 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(56): Show |
68 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-1222C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896233 | |||||||
chr17:31896284 | A | T | 1 | a0001c0001t0004g0249 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-1273T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896284 | |||||||
chr17:31896291 | T | C | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1280A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896291 | |||||||
chr17:31896368 | G | A | 2 | a0001c0001t0010g0275 a0001c0001t0010g0276 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.178-1357C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896368 | |||||||
chr17:31896385 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0048 others(42): Show |
47 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.178-1374G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896385 | |||||||
chr17:31896637 | G | GA | 56 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(53): Show |
65 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.178-1627dupT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896637 | |||||||
chr17:31896643 | A | AT | 29 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(26): Show |
31 | HG00738.hp1 HG01123.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.178-1633_178-1632i others(3): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896643 | |||||||
chr17:31896644 | A | AT | 31 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0174 others(28): Show |
36 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.178-1634dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896644 | |||||||
chr17:31896644 | A | T | 30 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(27): Show |
32 | HG00738.hp1 HG01123.hp2 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.178-1633T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896644 | |||||||
chr17:31896645 | T | A | 2 | a0001c0001t0001g0171 a0001c0001t0002g0198 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.178-1634A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896645 | |||||||
chr17:31896891 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.178-1880G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896891 | |||||||
chr17:31896917 | T | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.178-1906A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896917 | |||||||
chr17:31896966 | G | C | 1 | a0002c0002t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.178-1955C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31896966 | |||||||
chr17:31897043 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.178-2032G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897043 | |||||||
chr17:31897049 | C | G | 114 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(111): Show |
130 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-2038G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897049 | |||||||
chr17:31897204 | T | C | 1 | a0001c0001t0002g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.178-2193A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897204 | |||||||
chr17:31897268 | G | C | 1 | a0001c0004t0002g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.178-2257C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897268 | |||||||
chr17:31897386 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.177+2260A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897386 | |||||||
chr17:31897400 | G | A | 123 | a0001c0001t0001g0027 a0001c0001t0001g0174 a0001c0001t0001g0189 others(120): Show |
139 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.177+2246C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897400 | |||||||
chr17:31897402 | CTGTCTTT | C | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+2237_177+2243d others(9): Show |
UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897402 | |||||||
chr17:31897443 | C | CT | 80 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.177+2202dupA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897443 | |||||||
chr17:31897443 | CT | C | 13 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG02027.hp1 HG02083.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+2202delA | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897443 | |||||||
chr17:31897574 | A | G | 1 | a0001c0001t0005g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.177+2072T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897574 | |||||||
chr17:31897584 | A | G | 3 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0010c0014t0018g0031 |
3 | HG01081.hp1 NA19084.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.177+2062T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897584 | |||||||
chr17:31897808 | G | A | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.177+1838C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897808 | |||||||
chr17:31897852 | T | G | 39 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(36): Show |
44 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.177+1794A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897852 | |||||||
chr17:31897907 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.177+1739A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897907 | |||||||
chr17:31897982 | A | G | 1 | a0002c0002t0001g0030 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.177+1664T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31897982 | |||||||
chr17:31898241 | A | T | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.177+1405T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898241 | |||||||
chr17:31898276 | C | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0197 a0001c0001t0002g0198 |
4 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1370G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898276 | |||||||
chr17:31898539 | A | T | 5 | a0001c0004t0002g0242 a0001c0004t0002g0243 a0001c0004t0002g0244 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+1107T>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898539 | |||||||
chr17:31898635 | T | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0248 |
3 | HG01884.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.177+1011A>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898635 | |||||||
chr17:31898650 | G | A | 3 | a0001c0001t0009g0020 a0001c0001t0009g0187 a0001c0001t0009g0188 |
3 | HG01192.hp2 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.177+996C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898650 | |||||||
chr17:31898700 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+946A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898700 | |||||||
chr17:31898794 | G | A | 114 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(111): Show |
130 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.177+852C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898794 | |||||||
chr17:31898931 | A | C | 99 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(96): Show |
113 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.177+715T>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898931 | |||||||
chr17:31898988 | C | T | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.177+658G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31898988 | |||||||
chr17:31899091 | C | A | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+555G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31899091 | |||||||
chr17:31899233 | G | T | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+413C>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31899233 | |||||||
chr17:31899618 | A | G | 1 | a0002c0002t0001g0029 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.177+28T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 2/18 | chr17 | 31899618 | |||||||
chr17:31899765 | C | T | 1 | a0002c0002t0001g0028 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.93-35G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31899765 | |||||||
chr17:31899900 | C | G | 40 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(37): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.93-170G>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31899900 | |||||||
chr17:31899955 | T | C | 114 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(111): Show |
130 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.93-225A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31899955 | |||||||
chr17:31900014 | C | T | 4 | a0001c0003t0003g0012 a0001c0003t0003g0192 a0001c0003t0003g0193 others(1): Show |
5 | HG02109.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-284G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900014 | |||||||
chr17:31900037 | G | A | 3 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | NA18941.hp1 NA18993.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.93-307C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900037 | |||||||
chr17:31900323 | G | A | 1 | a0001c0001t0009g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.93-593C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900323 | |||||||
chr17:31900343 | G | A | 6 | a0001c0001t0004g0007 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
8 | HG00642.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-613C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900343 | |||||||
chr17:31900385 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93-655C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900385 | |||||||
chr17:31900504 | C | A | 1 | a0001c0001t0003g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.93-774G>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900504 | |||||||
chr17:31900526 | G | A | 2 | a0003c0006t0008g0257 a0003c0006t0008g0258 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.93-796C>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900526 | |||||||
chr17:31900531 | C | T | 50 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(47): Show |
57 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.93-801G>A | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900531 | |||||||
chr17:31900634 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02647.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92+902T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900634 | |||||||
chr17:31900699 | T | A | 39 | a0001c0001t0003g0017 a0001c0001t0003g0260 a0001c0001t0003g0261 others(36): Show |
44 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.92+837A>T | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900699 | |||||||
chr17:31900712 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.92+824A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900712 | |||||||
chr17:31900763 | CAG | C | 2 | a0002c0002t0001g0011 a0002c0002t0001g0191 |
3 | NA18954.hp2 NA18998.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.92+771_92+772delCT | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900763 | |||||||
chr17:31900777 | A | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+759T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900777 | |||||||
chr17:31900871 | A | G | 1 | a0001c0001t0009g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92+665T>C | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900871 | |||||||
chr17:31900986 | G | C | 1 | a0001c0001t0004g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92+550C>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31900986 | |||||||
chr17:31901227 | T | C | 1 | a0001c0001t0010g0290 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92+309A>G | UTP6 | ENSG00000108651.10 | transcript | ENST00000261708.9 | protein_coding | 1/18 | chr17 | 31901227 |