Item | Value |
---|---|
geneid | 5538 |
ensemblid | ENSG00000131238.18 |
hgncid | 9325 |
symbol | PPT1 |
name | palmitoyl-protein thioesterase 1 |
refseq_nuc | NM_000310.4 |
refseq_prot | NP_000301.1 |
ensembl_nuc | ENST00000642050.2 |
ensembl_prot | ENSP00000493153.1 |
mane_status | MANE Select |
chr | chr1 |
start | 40072712 |
end | 40097252 |
strand | - |
ver | v1.2 |
region | chr1:40072712-40097252 |
region5000 | chr1:40067712-40102252 |
regionname0 | PPT1_chr1_40072712_40097252 |
regionname5000 | PPT1_chr1_40067712_40102252 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 306 | 357 | 84 | 53 | 162 | 17 | 39 | 129 | PPT1_chr1_40067712_40102252 | PPT1 | MASPG others(301): Show |
chr1 | 40067712 | 40102252 |
a0002 | 0/0 | 306 | 31 | 1 | 1 | 21 | 1 | 7 | 16 | PPT1_chr1_40067712_40102252 | PPT1 | MASPG others(301): Show |
chr1 | 40067712 | 40102252 |
a0003 | 0/0 | 306 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | MASPG others(301): Show |
chr1 | 40067712 | 40102252 |
a0004 | 0/0 | 306 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | MASPG others(301): Show |
chr1 | 40067712 | 40102252 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 918 | 357 | 84 | 53 | 162 | 17 | 39 | PPT1_chr1_40067712_40102252 | PPT1 | ATGGC others(913): Show |
chr1 | 40067712 | 40102252 | ||
a0002c0002 | 0/0 | 918 | 31 | 1 | 1 | 21 | 1 | 7 | PPT1_chr1_40067712_40102252 | PPT1 | ATGGC others(913): Show |
chr1 | 40067712 | 40102252 | ||
a0003c0003 | 0/0 | 918 | 7 | 7 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | ATGGC others(913): Show |
chr1 | 40067712 | 40102252 | ||
a0004c0004 | 0/0 | 918 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | ATGGC others(913): Show |
chr1 | 40067712 | 40102252 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2288 | 130 | 24 | 19 | 59 | 8 | 19 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0002 | 1/0 | 2284 | 117 | 27 | 26 | 49 | 6 | 8 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0003 | 0/0 | 2288 | 27 | 3 | 4 | 15 | 2 | 3 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0004 | 0/0 | 2284 | 35 | 0 | 1 | 27 | 1 | 6 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0005 | 0/0 | 2284 | 26 | 15 | 1 | 9 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0006 | 0/0 | 2281 | 9 | 9 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2276): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0007 | 0/0 | 2284 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0008 | 0/0 | 2284 | 2 | 0 | 2 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0009 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0010 | 0/0 | 2288 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0011 | 0/0 | 2288 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0012 | 0/0 | 2288 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0013 | 0/0 | 2288 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0014 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0015 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0001c0001t0016 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2279): Show |
chr1 | 40067712 | 40102252 |
a0002c0002t0001 | 0/0 | 2288 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0002c0002t0003 | 0/0 | 2288 | 30 | 1 | 1 | 21 | 1 | 6 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0003c0003t0003 | 0/0 | 2288 | 7 | 7 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
a0004c0004t0001 | 0/0 | 2288 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | GTGAC others(2283): Show |
chr1 | 40067712 | 40102252 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 16 | 3 | 5 | 5 | 2 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0002 | 0/0 | 9 | 2 | 2 | 2 | 1 | 2 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0012 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0004 | 0/0 | 7 | 1 | 1 | 2 | 3 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0005 | 0/0 | 7 | 2 | 0 | 4 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0017 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0055 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0057 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0019 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0006g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0006g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0007g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0013g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0014g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0015g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0001c0001t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0007 | 0/0 | 6 | 1 | 1 | 3 | 1 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0015 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0003c0003t0003g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0003c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0003c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0003c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0003c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
a0004c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0007 | EUR | GBR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | FIN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0215 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02055 | hp1 | a0003 | c0003 | t0003 | g0134 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02080 | hp2 | a0002 | c0002 | t0003 | g0138 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0222 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0223 | EAS | CDX | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02523 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | KHV | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0015 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0047 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0173 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02897 | hp2 | a0003 | c0003 | t0003 | g0131 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02922 | hp1 | a0003 | c0003 | t0003 | g0025 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0007 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02976 | hp2 | a0003 | c0003 | t0003 | g0129 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0193 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0237 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03453 | hp1 | a0003 | c0003 | t0003 | g0025 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | GWD | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03579 | hp1 | a0001 | c0001 | t0016 | g0251 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0015 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03831 | hp2 | a0001 | c0001 | t0013 | g0104 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0234 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03942 | hp2 | a0001 | c0001 | t0010 | g0073 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0047 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0229 | SAS | BEB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0045 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0015 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0098 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18961 | hp2 | a0002 | c0002 | t0003 | g0218 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18979 | hp1 | a0001 | c0001 | t0011 | g0236 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18985 | hp1 | a0001 | c0001 | t0015 | g0189 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18985 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19007 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19056 | hp2 | a0002 | c0002 | t0003 | g0217 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19072 | hp1 | a0001 | c0001 | t0014 | g0243 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19077 | hp1 | a0002 | c0002 | t0003 | g0224 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19091 | hp2 | a0004 | c0004 | t0001 | g0081 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19240 | hp1 | a0003 | c0003 | t0003 | g0132 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | YRI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ASW | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ASW | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | TSI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0247 | EUR | TSI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | GIH | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0015 | SAS | GIH | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG06807 | hp1 | a0003 | c0003 | t0003 | g0025 | AFR | USA | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | USA | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18955 | hp1 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | USA | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | USA | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0110 | REF | REF | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0057 | REF | REF | PPT1_chr1_40067712_40102252 | PPT1 | chr1 | 40067712 | 40102252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40074145 | C | G | 1 | a0003 | 7 | HG02055.hp1 HG02897.hp2 HG02922.hp1 others(4): Show |
missense_variant | MODERATE | c.837G>C | p.Gln279His | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 851/2284 | 837/921 | 279/306 | chr1 | 40074145 | |||
chr1:40091361 | A | G | 1 | a0002 | 31 | HG00140.hp1 HG01074.hp1 HG02027.hp2 others(28): Show |
missense_variant | MODERATE | c.401T>C | p.Ile134Thr | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/9 | 415/2284 | 401/921 | 134/306 | chr1 | 40091361 | |||
chr1:40092408 | G | T | 1 | a0004 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.224C>A | p.Thr75Asn | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 2/9 | 238/2284 | 224/921 | 75/306 | chr1 | 40092408 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40072769 | ACTT | A | 1 | a0001c0001t0006 | 9 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1289_*1291delAAG | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1289 | chr1 | 40072769 | ||||||
chr1:40072786 | C | T | 2 | a0001c0001t0005 a0001c0001t0012 |
27 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1275G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1275 | chr1 | 40072786 | ||||||
chr1:40072938 | A | C | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1123T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1123 | chr1 | 40072938 | ||||||
chr1:40072939 | G | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1122 | chr1 | 40072939 | ||||||
chr1:40072942 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1119 | chr1 | 40072942 | ||||||
chr1:40072943 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1118A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1118 | chr1 | 40072943 | ||||||
chr1:40072945 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1116 | chr1 | 40072945 | ||||||
chr1:40072958 | T | C | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1103A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1103 | chr1 | 40072958 | ||||||
chr1:40072960 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1101 | chr1 | 40072960 | ||||||
chr1:40072965 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1096A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1096 | chr1 | 40072965 | ||||||
chr1:40072966 | C | G | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1095 | chr1 | 40072966 | ||||||
chr1:40072976 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1085 | chr1 | 40072976 | ||||||
chr1:40072980 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1081A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1081 | chr1 | 40072980 | ||||||
chr1:40072981 | G | C | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1080C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1080 | chr1 | 40072981 | ||||||
chr1:40072982 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1079A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1079 | chr1 | 40072982 | ||||||
chr1:40072984 | G | C | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1077 | chr1 | 40072984 | ||||||
chr1:40072985 | G | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1076 | chr1 | 40072985 | ||||||
chr1:40072986 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1075T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1075 | chr1 | 40072986 | ||||||
chr1:40072988 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1073 | chr1 | 40072988 | ||||||
chr1:40072991 | G | C | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1070 | chr1 | 40072991 | ||||||
chr1:40072997 | T | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1064 | chr1 | 40072997 | ||||||
chr1:40072999 | C | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1062 | chr1 | 40072999 | ||||||
chr1:40073000 | G | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1061C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1061 | chr1 | 40073000 | ||||||
chr1:40073003 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1058T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1058 | chr1 | 40073003 | ||||||
chr1:40073011 | T | G | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1050A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1050 | chr1 | 40073011 | ||||||
chr1:40073013 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1048T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1048 | chr1 | 40073013 | ||||||
chr1:40073014 | C | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1047 | chr1 | 40073014 | ||||||
chr1:40073018 | A | G | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1043T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1043 | chr1 | 40073018 | ||||||
chr1:40073030 | C | A | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1031G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1031 | chr1 | 40073030 | ||||||
chr1:40073034 | A | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1027 | chr1 | 40073034 | ||||||
chr1:40073035 | G | T | 1 | a0001c0001t0014 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 1026 | chr1 | 40073035 | ||||||
chr1:40073070 | A | G | 1 | a0001c0001t0015 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*991T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 991 | chr1 | 40073070 | ||||||
chr1:40073092 | T | C | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*969A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 969 | chr1 | 40073092 | ||||||
chr1:40073155 | A | G | 1 | a0001c0001t0011 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*906T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 906 | chr1 | 40073155 | ||||||
chr1:40073160 | G | A | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 901 | chr1 | 40073160 | ||||||
chr1:40073183 | A | G | 2 | a0001c0001t0004 a0001c0001t0014 |
36 | HG01175.hp2 HG02015.hp1 HG02129.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*878T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 878 | chr1 | 40073183 | ||||||
chr1:40073404 | C | T | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(9): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 657 | chr1 | 40073404 | ||||||
chr1:40073531 | A | ATGAT | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(7): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*529dupATCA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 529 | chr1 | 40073531 | ||||||
chr1:40073556 | G | C | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 505 | chr1 | 40073556 | ||||||
chr1:40073605 | T | C | 2 | a0001c0001t0007 a0001c0001t0009 |
4 | HG02647.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*456A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 456 | chr1 | 40073605 | ||||||
chr1:40073673 | C | G | 1 | a0001c0001t0010 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 388 | chr1 | 40073673 | ||||||
chr1:40073776 | A | C | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(8): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 285 | chr1 | 40073776 | ||||||
chr1:40073900 | A | G | 3 | a0001c0001t0003 a0002c0002t0003 a0003c0003t0003 |
64 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*161T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 161 | chr1 | 40073900 | ||||||
chr1:40074049 | A | G | 1 | a0001c0001t0008 | 2 | HG01069.hp2 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 12 | chr1 | 40074049 | ||||||
chr1:40074058 | G | T | 1 | a0001c0001t0009 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 9/9 | 3 | chr1 | 40074058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40074336 | CCTA | C | 5 | a0001c0001t0006g0030 a0001c0001t0006g0036 a0001c0001t0006g0056 others(2): Show |
9 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-156_799-154del others(3): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074336 | |||||||
chr1:40074374 | TTCTC | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
5 | NA18961.hp1 NA18968.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-195_799-192del others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074374 | |||||||
chr1:40074386 | C | T | 5 | a0001c0001t0006g0030 a0001c0001t0006g0036 a0001c0001t0006g0056 others(2): Show |
9 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-203G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074386 | |||||||
chr1:40074422 | T | TC | 8 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0102 others(5): Show |
10 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-240dupG | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074422 | |||||||
chr1:40074428 | C | A | 2 | a0001c0001t0003g0177 a0001c0001t0003g0181 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.799-245G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074428 | |||||||
chr1:40074429 | CGCT | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0097 |
4 | NA18956.hp2 NA18979.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-249_799-247del others(3): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074429 | |||||||
chr1:40074430 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.799-247C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074430 | |||||||
chr1:40074433 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0097 |
4 | NA18956.hp2 NA18979.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-250A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074433 | |||||||
chr1:40074471 | CTCTT | C | 14 | a0001c0001t0005g0053 a0001c0001t0005g0062 a0001c0001t0005g0140 others(11): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-292_799-289del others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074471 | |||||||
chr1:40074513 | G | T | 42 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0032 others(39): Show |
64 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.799-330C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074513 | |||||||
chr1:40074641 | G | A | 1 | a0001c0001t0005g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.799-458C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074641 | |||||||
chr1:40074751 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.799-568C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074751 | |||||||
chr1:40074952 | A | T | 34 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0032 others(31): Show |
53 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.799-769T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074952 | |||||||
chr1:40074997 | A | C | 1 | a0001c0001t0015g0189 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.799-814T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40074997 | |||||||
chr1:40075059 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.799-876T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075059 | |||||||
chr1:40075472 | C | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
130 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.799-1289G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075472 | |||||||
chr1:40075477 | C | CT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.799-1295dupA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075477 | |||||||
chr1:40075618 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.798+1224C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075618 | |||||||
chr1:40075692 | G | C | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.798+1150C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075692 | |||||||
chr1:40075933 | C | A | 1 | a0001c0001t0001g0052 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.798+909G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075933 | |||||||
chr1:40075958 | CA | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0105 a0001c0001t0002g0004 others(23): Show |
44 | HG00140.hp2 HG00423.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+883delT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40075958 | CAA | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0070 others(23): Show |
36 | HG00408.hp1 HG00642.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.798+882_798+883del others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40075958 | CAAA | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0024 others(51): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.798+881_798+883del others(3): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40075958 | CAAAA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
123 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.798+880_798+883del others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40075958 | CAAAAA | C | 37 | a0001c0001t0001g0083 a0001c0001t0001g0113 a0001c0001t0001g0117 others(34): Show |
56 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.798+879_798+883del others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40075958 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0075 |
2 | HG00735.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.798+871_798+883del others(13): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40075958 | |||||||
chr1:40076171 | G | C | 5 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0148 others(2): Show |
9 | HG00408.hp2 HG00597.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+671C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40076171 | |||||||
chr1:40076394 | G | C | 8 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0045 others(5): Show |
11 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+448C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40076394 | |||||||
chr1:40076452 | G | A | 4 | a0001c0001t0004g0060 a0001c0001t0004g0240 a0001c0001t0004g0241 others(1): Show |
5 | NA18939.hp2 NA18940.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+390C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 8/8 | chr1 | 40076452 | |||||||
chr1:40076983 | T | C | 1 | a0001c0001t0003g0054 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.727-70A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40076983 | |||||||
chr1:40077229 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.727-316T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077229 | |||||||
chr1:40077265 | T | C | 1 | a0001c0001t0016g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.727-352A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077265 | |||||||
chr1:40077266 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.727-353C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077266 | |||||||
chr1:40077347 | T | C | 42 | a0001c0001t0003g0009 a0001c0001t0003g0021 a0001c0001t0003g0032 others(39): Show |
64 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.727-434A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077347 | |||||||
chr1:40077600 | T | C | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.727-687A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077600 | |||||||
chr1:40077616 | G | A | 1 | a0001c0001t0012g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727-703C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077616 | |||||||
chr1:40077635 | T | C | 5 | a0001c0001t0002g0020 a0001c0001t0002g0226 a0001c0001t0002g0250 others(2): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-722A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077635 | |||||||
chr1:40077753 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.726+807G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077753 | |||||||
chr1:40077829 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.726+731A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077829 | |||||||
chr1:40077864 | G | A | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.726+696C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077864 | |||||||
chr1:40077954 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0090 |
2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.726+606C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40077954 | |||||||
chr1:40078152 | G | GT | 4 | a0001c0001t0006g0030 a0001c0001t0006g0036 a0001c0001t0006g0056 others(1): Show |
8 | HG02145.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+407dupA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40078152 | |||||||
chr1:40078250 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
130 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.726+310A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40078250 | |||||||
chr1:40078359 | G | A | 1 | a0002c0002t0003g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.726+201C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 7/8 | chr1 | 40078359 | |||||||
chr1:40078774 | G | A | 3 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 |
3 | HG03195.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.628-116C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40078774 | |||||||
chr1:40078820 | C | CT | 8 | a0001c0001t0003g0046 a0001c0001t0003g0130 a0001c0001t0003g0133 others(5): Show |
11 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.628-163dupA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40078820 | |||||||
chr1:40078820 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.628-162G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40078820 | |||||||
chr1:40078898 | GGGTAT | G | 14 | a0001c0001t0002g0010 a0001c0001t0002g0041 a0001c0001t0002g0042 others(11): Show |
22 | HG01074.hp2 HG01099.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.628-245_628-241del others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40078898 | |||||||
chr1:40078904 | A | T | 14 | a0001c0001t0002g0010 a0001c0001t0002g0041 a0001c0001t0002g0042 others(11): Show |
22 | HG01074.hp2 HG01099.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.628-246T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40078904 | |||||||
chr1:40079000 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.628-342G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079000 | |||||||
chr1:40079242 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.628-584G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079242 | |||||||
chr1:40079304 | C | A | 5 | a0001c0001t0001g0199 a0001c0001t0002g0020 a0001c0001t0002g0226 others(2): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-646G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079304 | |||||||
chr1:40079392 | C | CT | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.628-735dupA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079392 | |||||||
chr1:40079392 | C | CTT | 38 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0077 others(35): Show |
56 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.628-736_628-735dup others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079392 | |||||||
chr1:40079394 | T | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.628-736A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079394 | |||||||
chr1:40079438 | C | T | 1 | a0001c0001t0006g0036 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.628-780G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079438 | |||||||
chr1:40079571 | T | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0099 others(6): Show |
12 | HG02040.hp1 HG02165.hp1 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.627+826A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079571 | |||||||
chr1:40079647 | C | T | 1 | a0003c0003t0003g0131 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.627+750G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079647 | |||||||
chr1:40079675 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0002g0182 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.627+722G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079675 | |||||||
chr1:40079786 | G | C | 1 | a0001c0001t0013g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.627+611C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40079786 | |||||||
chr1:40080046 | T | C | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.627+351A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40080046 | |||||||
chr1:40080292 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.627+105A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40080292 | |||||||
chr1:40080393 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03017.hp1 | splice_region_variant&intron_variant | LOW | c.627+4A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 6/8 | chr1 | 40080393 | |||||||
chr1:40080537 | C | T | 27 | a0001c0001t0003g0009 a0001c0001t0003g0089 a0001c0001t0003g0091 others(24): Show |
42 | HG00140.hp1 HG00609.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.537-50G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40080537 | |||||||
chr1:40080618 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.537-131C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40080618 | |||||||
chr1:40080735 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.537-248C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40080735 | |||||||
chr1:40080740 | G | A | 10 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0045 others(7): Show |
13 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.537-253C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40080740 | |||||||
chr1:40080805 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.537-318G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40080805 | |||||||
chr1:40081055 | G | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.537-568C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081055 | |||||||
chr1:40081242 | A | G | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.537-755T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081242 | |||||||
chr1:40081311 | A | G | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-824T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081311 | |||||||
chr1:40081565 | AATAG | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.537-1082_537-1079d others(6): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081565 | |||||||
chr1:40081569 | G | A | 48 | a0001c0001t0001g0199 a0001c0001t0002g0004 a0001c0001t0002g0005 others(45): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.537-1082C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081569 | |||||||
chr1:40081615 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.537-1128A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081615 | |||||||
chr1:40081644 | C | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.537-1157G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081644 | |||||||
chr1:40081854 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.537-1367G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081854 | |||||||
chr1:40081972 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.537-1485C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40081972 | |||||||
chr1:40082098 | G | A | 8 | a0001c0001t0003g0046 a0001c0001t0003g0130 a0001c0001t0003g0133 others(5): Show |
11 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-1611C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082098 | |||||||
chr1:40082108 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.537-1621T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082108 | |||||||
chr1:40082129 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.537-1642C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082129 | |||||||
chr1:40082234 | G | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.537-1747C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082234 | |||||||
chr1:40082240 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 |
6 | HG01069.hp1 HG01071.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-1753G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082240 | |||||||
chr1:40082241 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.537-1754C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082241 | |||||||
chr1:40082247 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.537-1760C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082247 | |||||||
chr1:40082278 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.537-1791G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082278 | |||||||
chr1:40082372 | A | G | 43 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(40): Show |
61 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.537-1885T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082372 | |||||||
chr1:40082422 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.537-1936dupT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082422 | |||||||
chr1:40082458 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.537-1971A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082458 | |||||||
chr1:40082563 | C | T | 6 | a0001c0001t0005g0062 a0001c0001t0005g0140 a0001c0001t0005g0141 others(3): Show |
6 | HG02258.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-2076G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082563 | |||||||
chr1:40082582 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.537-2095G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082582 | |||||||
chr1:40082652 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.537-2165A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082652 | |||||||
chr1:40082754 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.537-2267C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082754 | |||||||
chr1:40082930 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.537-2443G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40082930 | |||||||
chr1:40083018 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.537-2531C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083018 | |||||||
chr1:40083228 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.537-2741T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083228 | |||||||
chr1:40083296 | C | A | 3 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG02074.hp2 HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.537-2809G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083296 | |||||||
chr1:40083311 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.537-2824G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083311 | |||||||
chr1:40083379 | C | A | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.537-2892G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083379 | |||||||
chr1:40083385 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.537-2898C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083385 | |||||||
chr1:40083440 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.537-2953C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083440 | |||||||
chr1:40083497 | C | T | 4 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(1): Show |
6 | HG02074.hp2 HG02083.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.537-3010G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083497 | |||||||
chr1:40083568 | A | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0075 |
3 | HG00639.hp1 HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.537-3081T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083568 | |||||||
chr1:40083614 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.537-3127G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083614 | |||||||
chr1:40083683 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.537-3196A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083683 | |||||||
chr1:40083740 | A | G | 1 | a0001c0001t0005g0123 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.537-3253T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083740 | |||||||
chr1:40083782 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(29): Show |
47 | HG00544.hp1 HG01069.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.537-3295G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083782 | |||||||
chr1:40083891 | T | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.537-3404A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083891 | |||||||
chr1:40083945 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.537-3458G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40083945 | |||||||
chr1:40084001 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.537-3514A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084001 | |||||||
chr1:40084083 | C | T | 44 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(41): Show |
62 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.537-3596G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084083 | |||||||
chr1:40084126 | A | C | 1 | a0001c0001t0001g0035 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.537-3639T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084126 | |||||||
chr1:40084199 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.537-3712A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084199 | |||||||
chr1:40084258 | C | A | 43 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(40): Show |
61 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.537-3771G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084258 | |||||||
chr1:40084573 | G | A | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.537-4086C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084573 | |||||||
chr1:40084580 | G | A | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.537-4093C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084580 | |||||||
chr1:40084819 | C | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.537-4332G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084819 | |||||||
chr1:40084829 | C | T | 1 | a0001c0001t0003g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.537-4342G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084829 | |||||||
chr1:40084919 | T | C | 1 | a0002c0002t0001g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.537-4432A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084919 | |||||||
chr1:40084938 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0242 a0001c0001t0002g0244 others(25): Show |
43 | HG00544.hp1 HG01175.hp2 HG01981.hp2 others(40): Show |
intron_variant | MODIFIER | c.537-4451G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40084938 | |||||||
chr1:40085006 | T | A | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+4404A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085006 | |||||||
chr1:40085102 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.536+4308G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085102 | |||||||
chr1:40085196 | A | G | 30 | a0001c0001t0001g0199 a0001c0001t0002g0004 a0001c0001t0002g0005 others(27): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.536+4214T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085196 | |||||||
chr1:40085280 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.536+4130G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085280 | |||||||
chr1:40085421 | G | A | 40 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(37): Show |
58 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.536+3989C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085421 | |||||||
chr1:40085426 | C | T | 1 | a0001c0001t0002g0026 | 3 | NA18955.hp2 NA19006.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.536+3984G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085426 | |||||||
chr1:40085441 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.536+3969G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085441 | |||||||
chr1:40085485 | CTT | C | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+3923_536+3924d others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085485 | |||||||
chr1:40085546 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.536+3864G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085546 | |||||||
chr1:40085722 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.536+3688A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085722 | |||||||
chr1:40085855 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0088 |
4 | NA18977.hp2 NA19012.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+3555G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085855 | |||||||
chr1:40085891 | C | T | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.536+3519G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085891 | |||||||
chr1:40085921 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.536+3489C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085921 | |||||||
chr1:40085956 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.536+3454A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40085956 | |||||||
chr1:40086073 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(29): Show |
47 | HG00544.hp1 HG01069.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.536+3337G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086073 | |||||||
chr1:40086158 | C | T | 3 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG02074.hp2 HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.536+3252G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086158 | |||||||
chr1:40086185 | G | A | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+3225C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086185 | |||||||
chr1:40086215 | G | C | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+3195C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086215 | |||||||
chr1:40086267 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.536+3143C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086267 | |||||||
chr1:40086296 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.536+3114G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086296 | |||||||
chr1:40086424 | G | A | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+2986C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086424 | |||||||
chr1:40086603 | G | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.536+2807C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086603 | |||||||
chr1:40086686 | A | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2724T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086686 | |||||||
chr1:40086688 | T | G | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2722A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086688 | |||||||
chr1:40086689 | C | A | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2721G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086689 | |||||||
chr1:40086690 | T | C | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2720A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086690 | |||||||
chr1:40086691 | C | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2719G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086691 | |||||||
chr1:40086693 | TAACA | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2713_536+2716d others(6): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086693 | |||||||
chr1:40086703 | T | A | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2707A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086703 | |||||||
chr1:40086704 | T | C | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+2706A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086704 | |||||||
chr1:40086707 | ACATTTGG others(1254): Show |
A | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.536+1442_536+2702d others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086707 | |||||||
chr1:40086823 | G | C | 1 | a0001c0001t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.536+2587C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086823 | |||||||
chr1:40086849 | A | G | 1 | a0001c0001t0003g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.536+2561T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086849 | |||||||
chr1:40086874 | G | C | 3 | a0002c0002t0003g0059 a0002c0002t0003g0218 a0002c0002t0003g0220 |
4 | NA18961.hp2 NA18971.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+2536C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40086874 | |||||||
chr1:40087279 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.536+2131C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087279 | |||||||
chr1:40087319 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.536+2091A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087319 | |||||||
chr1:40087340 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
135 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.536+2070C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087340 | |||||||
chr1:40087480 | T | C | 1 | a0001c0001t0013g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.536+1930A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087480 | |||||||
chr1:40087583 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.536+1827G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087583 | |||||||
chr1:40087661 | G | T | 100 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(97): Show |
147 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.536+1749C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087661 | |||||||
chr1:40087698 | T | C | 3 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0005g0144 |
3 | HG03209.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.536+1712A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087698 | |||||||
chr1:40087702 | GGAA | G | 6 | a0001c0001t0005g0062 a0001c0001t0005g0140 a0001c0001t0005g0141 others(3): Show |
6 | HG02258.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+1705_536+1707d others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087702 | |||||||
chr1:40087772 | A | G | 60 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(57): Show |
89 | HG00140.hp1 HG00544.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.536+1638T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40087772 | |||||||
chr1:40088064 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.536+1346T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088064 | |||||||
chr1:40088143 | C | CT | 25 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(22): Show |
30 | HG00423.hp2 HG00735.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.536+1266dupA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088143 | |||||||
chr1:40088143 | CT | C | 6 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
6 | HG02074.hp2 HG02083.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+1266delA | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088143 | |||||||
chr1:40088230 | G | A | 1 | a0002c0002t0003g0059 | 2 | NA18971.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.536+1180C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088230 | |||||||
chr1:40088335 | C | T | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.536+1075G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088335 | |||||||
chr1:40088574 | T | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.536+836A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088574 | |||||||
chr1:40088575 | A | T | 60 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(57): Show |
89 | HG00140.hp1 HG00544.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.536+835T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088575 | |||||||
chr1:40088576 | A | T | 1 | a0001c0001t0004g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.536+834T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088576 | |||||||
chr1:40088771 | T | C | 6 | a0001c0001t0005g0062 a0001c0001t0005g0140 a0001c0001t0005g0141 others(3): Show |
6 | HG02258.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+639A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088771 | |||||||
chr1:40088927 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0009g0173 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.536+483A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40088927 | |||||||
chr1:40089008 | C | T | 2 | a0001c0001t0004g0230 a0001c0001t0004g0231 |
2 | NA18942.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.536+402G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089008 | |||||||
chr1:40089125 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.536+285A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089125 | |||||||
chr1:40089164 | G | A | 60 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(57): Show |
89 | HG00140.hp1 HG00544.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.536+246C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089164 | |||||||
chr1:40089286 | C | CAAAAAAA others(8): Show |
10 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
11 | HG00738.hp1 HG01169.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.536+123_536+124ins others(15): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089286 | C | CAAAAAAA others(9): Show |
129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.536+123_536+124ins others(16): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089286 | C | CAAAAAAA others(10): Show |
48 | a0001c0001t0001g0023 a0001c0001t0001g0075 a0001c0001t0001g0112 others(45): Show |
70 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.536+123_536+124ins others(17): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089286 | C | CAAAAAAA others(11): Show |
4 | a0001c0001t0002g0160 a0001c0001t0002g0166 a0001c0001t0002g0167 others(1): Show |
4 | HG02738.hp1 NA18950.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+123_536+124ins others(18): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089286 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
10 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.536+123_536+124ins others(19): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089286 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0005g0122 a0001c0001t0005g0127 |
2 | NA18949.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.536+123_536+124ins others(20): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089286 | |||||||
chr1:40089370 | C | T | 8 | a0001c0001t0003g0046 a0001c0001t0003g0130 a0001c0001t0003g0133 others(5): Show |
11 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.536+40G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089370 | |||||||
chr1:40089385 | A | G | 18 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0026 others(15): Show |
31 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.536+25T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 5/8 | chr1 | 40089385 | |||||||
chr1:40089602 | C | G | 30 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(27): Show |
45 | HG00544.hp1 HG01175.hp2 HG01981.hp2 others(42): Show |
intron_variant | MODIFIER | c.434-90G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40089602 | |||||||
chr1:40089649 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.434-137G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40089649 | |||||||
chr1:40089727 | C | T | 40 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(37): Show |
58 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.434-215G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40089727 | |||||||
chr1:40089792 | C | G | 3 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG02074.hp2 HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.434-280G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40089792 | |||||||
chr1:40090051 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.434-539A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090051 | |||||||
chr1:40090130 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
300 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.434-618C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090130 | |||||||
chr1:40090165 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.434-653C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090165 | |||||||
chr1:40090179 | CCTAGA | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0174 a0001c0001t0009g0173 |
4 | HG02257.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-672_434-668del others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090179 | |||||||
chr1:40090336 | G | GTA | 12 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(9): Show |
18 | HG01069.hp1 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.434-826_434-825dup others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090336 | |||||||
chr1:40090336 | G | GTATA | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.434-828_434-825dup others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090336 | |||||||
chr1:40090348 | A | ATG | 4 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(1): Show |
4 | HG02074.hp2 HG02083.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-838_434-837dup others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090348 | |||||||
chr1:40090350 | G | A | 40 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(37): Show |
58 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.434-838C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090350 | |||||||
chr1:40090440 | G | GTA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.433+887_433+888dup others(2): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090440 | |||||||
chr1:40090471 | T | C | 34 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
52 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.433+858A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090471 | |||||||
chr1:40090492 | A | G | 2 | a0001c0001t0004g0230 a0001c0001t0004g0231 |
2 | NA18942.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.433+837T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090492 | |||||||
chr1:40090606 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.433+723T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090606 | |||||||
chr1:40090631 | A | T | 1 | a0002c0002t0003g0218 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.433+698T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090631 | |||||||
chr1:40090648 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0005g0201 a0001c0001t0005g0202 |
3 | HG01891.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.433+681G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090648 | |||||||
chr1:40090845 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.433+483delT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090845 | |||||||
chr1:40090905 | G | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(26): Show |
44 | HG00544.hp1 HG01175.hp2 HG01981.hp2 others(41): Show |
intron_variant | MODIFIER | c.433+424C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40090905 | |||||||
chr1:40091096 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0004c0004t0001g0081 |
4 | HG00609.hp2 NA18947.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+233G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40091096 | |||||||
chr1:40091250 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.433+79A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40091250 | |||||||
chr1:40091270 | A | T | 34 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
52 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.433+59T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 4/8 | chr1 | 40091270 | |||||||
chr1:40091403 | C | T | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.363-4G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091403 | |||||||
chr1:40091417 | G | C | 2 | a0001c0001t0002g0018 a0001c0001t0002g0176 |
5 | HG02451.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-18C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091417 | |||||||
chr1:40091494 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.363-95A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091494 | |||||||
chr1:40091505 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.363-106C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091505 | |||||||
chr1:40091631 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.363-232T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091631 | |||||||
chr1:40091642 | C | T | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.363-243G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091642 | |||||||
chr1:40091734 | G | A | 1 | a0001c0001t0006g0030 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.362+311C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091734 | |||||||
chr1:40091865 | C | CA | 11 | a0001c0001t0002g0124 a0001c0001t0003g0130 a0001c0001t0005g0043 others(8): Show |
14 | HG00423.hp2 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+179dupT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091865 | |||||||
chr1:40091865 | CA | C | 62 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(59): Show |
86 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.362+179delT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091865 | |||||||
chr1:40091984 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.362+61C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 3/8 | chr1 | 40091984 | |||||||
chr1:40092309 | T | C | 1 | a0002c0002t0003g0138 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.234+89A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 2/8 | chr1 | 40092309 | |||||||
chr1:40092584 | C | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.125-77G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092584 | |||||||
chr1:40092619 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.125-112A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092619 | |||||||
chr1:40092673 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-166A>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092673 | |||||||
chr1:40092691 | CACTT | C | 9 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(6): Show |
9 | HG00280.hp2 HG01109.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-188_125-185del others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092691 | |||||||
chr1:40092787 | G | GGCATGTG others(4): Show |
207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.125-281_125-280ins others(11): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092787 | |||||||
chr1:40092839 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-332T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092839 | |||||||
chr1:40092986 | T | C | 1 | a0001c0001t0001g0024 | 3 | HG02451.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.125-479A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40092986 | |||||||
chr1:40093093 | T | G | 1 | a0001c0001t0004g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.125-586A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093093 | |||||||
chr1:40093122 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0003g0046 a0001c0001t0003g0130 others(6): Show |
12 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-615G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093122 | |||||||
chr1:40093127 | G | C | 1 | a0001c0001t0002g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.125-620C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093127 | |||||||
chr1:40093168 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.125-661G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093168 | |||||||
chr1:40093381 | AATAGG | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
309 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.125-879_125-875del others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093381 | |||||||
chr1:40093432 | A | AAGAG | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-926_125-925ins others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093432 | |||||||
chr1:40093481 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.125-974G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093481 | |||||||
chr1:40093535 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-1028G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093535 | |||||||
chr1:40093576 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-1069A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093576 | |||||||
chr1:40093616 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-1109T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093616 | |||||||
chr1:40093653 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(6): Show |
15 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-1146C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093653 | |||||||
chr1:40093769 | C | CA | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-1263_125-1262i others(3): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093769 | |||||||
chr1:40093806 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.125-1299T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093806 | |||||||
chr1:40093849 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.125-1342T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093849 | |||||||
chr1:40093865 | C | G | 5 | a0001c0001t0005g0062 a0001c0001t0005g0141 a0001c0001t0005g0142 others(2): Show |
5 | HG02258.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-1358G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093865 | |||||||
chr1:40093883 | C | CA | 8 | a0001c0001t0001g0199 a0001c0001t0002g0121 a0001c0001t0002g0166 others(5): Show |
8 | HG01891.hp1 HG02148.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1377dupT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093883 | |||||||
chr1:40093883 | C | CAAAA | 4 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(1): Show |
7 | HG01069.hp1 HG01071.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-1380_125-1377d others(6): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093883 | |||||||
chr1:40093883 | CA | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.125-1377delT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093883 | |||||||
chr1:40093883 | CAA | C | 32 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(29): Show |
46 | HG00544.hp1 HG01175.hp2 HG01981.hp2 others(43): Show |
intron_variant | MODIFIER | c.125-1378_125-1377d others(4): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093883 | |||||||
chr1:40093900 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.125-1393T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40093900 | |||||||
chr1:40094014 | G | A | 29 | a0001c0001t0001g0135 a0001c0001t0003g0046 a0001c0001t0003g0130 others(26): Show |
43 | HG00140.hp1 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.125-1507C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094014 | |||||||
chr1:40094033 | A | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(6): Show |
15 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-1526T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094033 | |||||||
chr1:40094071 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.125-1564A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094071 | |||||||
chr1:40094159 | G | A | 9 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(6): Show |
9 | HG00280.hp2 HG01109.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-1652C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094159 | |||||||
chr1:40094201 | G | A | 20 | a0002c0002t0001g0137 a0002c0002t0003g0007 a0002c0002t0003g0015 others(17): Show |
31 | HG00140.hp1 HG01074.hp1 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-1694C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094201 | |||||||
chr1:40094323 | C | A | 1 | a0002c0002t0003g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125-1816G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094323 | |||||||
chr1:40094439 | G | GC | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.125-1933dupG | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094439 | |||||||
chr1:40094562 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-2055A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094562 | |||||||
chr1:40094564 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-2057G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094564 | |||||||
chr1:40094648 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-2141T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094648 | |||||||
chr1:40094719 | T | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-2212A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094719 | |||||||
chr1:40094727 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-2220G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094727 | |||||||
chr1:40094734 | G | A | 10 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(7): Show |
10 | HG00280.hp2 HG01109.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-2227C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094734 | |||||||
chr1:40094786 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0066 others(10): Show |
17 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-2279T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094786 | |||||||
chr1:40094826 | G | A | 3 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 |
3 | HG02074.hp2 HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.124+2289C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094826 | |||||||
chr1:40094869 | C | T | 3 | a0001c0001t0003g0021 a0001c0001t0003g0032 a0001c0001t0003g0065 |
6 | HG00597.hp1 NA18943.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+2246G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094869 | |||||||
chr1:40094948 | T | C | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.124+2167A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094948 | |||||||
chr1:40094966 | G | A | 1 | a0001c0001t0001g0024 | 3 | HG02451.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.124+2149C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094966 | |||||||
chr1:40094992 | C | T | 41 | a0001c0001t0001g0162 a0001c0001t0002g0008 a0001c0001t0002g0016 others(38): Show |
59 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.124+2123G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094992 | |||||||
chr1:40094993 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.124+2122A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40094993 | |||||||
chr1:40095037 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.124+2078G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095037 | |||||||
chr1:40095084 | C | T | 9 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(6): Show |
15 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+2031G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095084 | |||||||
chr1:40095116 | T | C | 2 | a0001c0001t0002g0051 a0001c0001t0004g0169 |
3 | NA18939.hp1 NA18941.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.124+1999A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095116 | |||||||
chr1:40095159 | C | T | 41 | a0001c0001t0001g0162 a0001c0001t0002g0008 a0001c0001t0002g0016 others(38): Show |
59 | HG00408.hp2 HG00597.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.124+1956G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095159 | |||||||
chr1:40095261 | T | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0063 others(6): Show |
15 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+1854A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095261 | |||||||
chr1:40095461 | TACA | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1651_124+1653d others(5): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095461 | |||||||
chr1:40095504 | A | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1611T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095504 | |||||||
chr1:40095691 | A | G | 1 | a0001c0001t0004g0228 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.124+1424T>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095691 | |||||||
chr1:40095799 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.124+1316G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095799 | |||||||
chr1:40095809 | G | A | 2 | a0002c0002t0003g0224 a0002c0002t0003g0225 |
2 | HG02523.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.124+1306C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095809 | |||||||
chr1:40095809 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1306C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095809 | |||||||
chr1:40095826 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1289A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095826 | |||||||
chr1:40095844 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1271C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095844 | |||||||
chr1:40095860 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.124+1255C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095860 | |||||||
chr1:40095925 | A | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1190T>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095925 | |||||||
chr1:40095932 | C | A | 9 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(6): Show |
9 | HG00280.hp2 HG01109.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1183G>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40095932 | |||||||
chr1:40096005 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1110A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096005 | |||||||
chr1:40096106 | G | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+1009C>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096106 | |||||||
chr1:40096139 | C | G | 16 | a0001c0001t0001g0135 a0001c0001t0003g0046 a0001c0001t0003g0130 others(13): Show |
23 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+976G>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096139 | |||||||
chr1:40096141 | G | GGTACAAA others(1): Show |
16 | a0001c0001t0001g0135 a0001c0001t0003g0046 a0001c0001t0003g0130 others(13): Show |
23 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+973_124+974ins others(8): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096141 | |||||||
chr1:40096141 | G | T | 1 | a0001c0001t0004g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.124+974C>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096141 | |||||||
chr1:40096142 | A | C | 16 | a0001c0001t0001g0135 a0001c0001t0003g0046 a0001c0001t0003g0130 others(13): Show |
23 | HG00642.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+973T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096142 | |||||||
chr1:40096199 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.124+916G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096199 | |||||||
chr1:40096239 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.124+876A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096239 | |||||||
chr1:40096357 | A | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0242 others(42): Show |
67 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.124+758T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096357 | |||||||
chr1:40096363 | T | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+752A>C | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096363 | |||||||
chr1:40096420 | CTAATCTG others(15): Show |
C | 9 | a0001c0001t0002g0124 a0001c0001t0005g0043 a0001c0001t0005g0044 others(6): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+673_124+694del others(22): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096420 | |||||||
chr1:40096425 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.124+690G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096425 | |||||||
chr1:40096604 | C | T | 1 | a0002c0002t0003g0212 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.124+511G>A | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096604 | |||||||
chr1:40096648 | T | TA | 30 | a0001c0001t0001g0011 a0001c0001t0001g0242 a0001c0001t0002g0211 others(27): Show |
45 | HG00544.hp1 HG01175.hp2 HG01981.hp2 others(42): Show |
intron_variant | MODIFIER | c.124+466dupT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096648 | |||||||
chr1:40096648 | TA | T | 10 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(7): Show |
17 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.124+466delT | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096648 | |||||||
chr1:40096750 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.124+365A>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096750 | |||||||
chr1:40096779 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+336C>T | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096779 | |||||||
chr1:40096829 | A | ATGC | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+283_124+285dup others(3): Show |
PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40096829 | |||||||
chr1:40097097 | A | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0002g0020 others(1): Show |
7 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+18T>G | PPT1 | ENSG00000131238.18 | transcript | ENST00000642050.2 | protein_coding | 1/8 | chr1 | 40097097 |