Item | Value |
---|---|
geneid | 10745 |
ensemblid | ENSG00000116793.16 |
hgncid | 8939 |
symbol | PHTF1 |
name | putative homeodomain transcription factor 1 |
refseq_nuc | NM_001323043.2 |
refseq_prot | NP_001309972.1 |
ensembl_nuc | ENST00000369604.6 |
ensembl_prot | ENSP00000358617.1 |
mane_status | MANE Select |
chr | chr1 |
start | 113696831 |
end | 113759486 |
strand | - |
ver | v1.2 |
region | chr1:113696831-113759486 |
region5000 | chr1:113691831-113764486 |
regionname0 | PHTF1_chr1_113696831_113759486 |
regionname5000 | PHTF1_chr1_113691831_113764486 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 762 | 327 | 66 | 57 | 148 | 14 | 40 | 120 | PHTF1_chr1_113691831_113764486 | PHTF1 | MASNE others(757): Show |
chr1 | 113691831 | 113764486 |
a0002 | 0/0 | 762 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | MASNE others(757): Show |
chr1 | 113691831 | 113764486 |
a0003 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | MASNE others(757): Show |
chr1 | 113691831 | 113764486 |
a0004 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | MASNE others(508): Show |
chr1 | 113691831 | 113764486 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2286 | 299 | 53 | 55 | 136 | 14 | 39 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0001c0002 | 0/0 | 2286 | 18 | 5 | 1 | 12 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0001c0003 | 0/0 | 2286 | 5 | 4 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0001c0004 | 0/0 | 2286 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0001c0006 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0001c0008 | 0/0 | 2286 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0002c0007 | 0/0 | 2286 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0003c0009 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2281): Show |
chr1 | 113691831 | 113764486 | ||
a0004c0005 | 0/0 | 2027 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | ATGGC others(2022): Show |
chr1 | 113691831 | 113764486 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3655 | 177 | 34 | 34 | 70 | 7 | 31 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0002 | 0/0 | 3654 | 80 | 3 | 15 | 54 | 3 | 5 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3649): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0003 | 0/0 | 3654 | 16 | 1 | 2 | 8 | 2 | 3 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3649): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0004 | 0/0 | 3655 | 6 | 3 | 2 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0005 | 0/0 | 3654 | 6 | 6 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3649): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0006 | 0/0 | 3655 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0007 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3653): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0008 | 0/0 | 3655 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0009 | 0/0 | 3655 | 2 | 0 | 1 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0010 | 0/0 | 3655 | 2 | 2 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0011 | 1/0 | 3657 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3652): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0013 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3649): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0014 | 0/0 | 3655 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0001t0015 | 0/0 | 3655 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0002t0001 | 0/0 | 3655 | 16 | 3 | 1 | 12 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0002t0007 | 0/0 | 3658 | 2 | 2 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3653): Show |
chr1 | 113691831 | 113764486 |
a0001c0003t0003 | 0/0 | 3654 | 5 | 4 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3649): Show |
chr1 | 113691831 | 113764486 |
a0001c0004t0001 | 0/0 | 3655 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0006t0001 | 0/0 | 3655 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0001c0008t0001 | 0/0 | 3655 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0002c0007t0001 | 0/0 | 3655 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0003c0009t0001 | 0/0 | 3655 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3650): Show |
chr1 | 113691831 | 113764486 |
a0004c0005t0012 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | AGACG others(3394): Show |
chr1 | 113691831 | 113764486 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0009g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0010g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0011g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0014g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0001t0015g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0002t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0003t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0003t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0003t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0003t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0003t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0004t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0006t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0001c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0002c0007t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0003c0009t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
a0004c0005t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00099 | hp2 | a0001 | c0001 | t0015 | g0318 | EUR | GBR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | GBR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00738 | hp2 | a0001 | c0003 | t0003 | g0313 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01175 | hp2 | a0002 | c0007 | t0001 | g0179 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0202 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01192 | hp2 | a0001 | c0001 | t0009 | g0203 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02055 | hp2 | a0001 | c0003 | t0003 | g0315 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0298 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CDX | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | CDX | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0280 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02602 | hp2 | a0001 | c0008 | t0001 | g0208 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02615 | hp1 | a0001 | c0002 | t0007 | g0017 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0316 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0310 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0311 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0146 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03209 | hp2 | a0003 | c0009 | t0001 | g0317 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03225 | hp1 | a0001 | c0002 | t0007 | g0020 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03486 | hp1 | a0001 | c0003 | t0003 | g0260 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0324 | AFR | MSL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0319 | AFR | ESN | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0292 | SAS | PJL | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18906 | hp1 | a0004 | c0005 | t0012 | g0018 | AFR | YRI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | YRI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18942 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19066 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19084 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ASW | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | TSI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20805 | hp2 | a0001 | c0001 | t0009 | g0204 | EUR | TSI | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | GIH | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | GIH | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0312 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | USA | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA21309 | hp1 | a0001 | c0006 | t0001 | g0307 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0221 | REF | REF | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0016 | REF | REF | PHTF1_chr1_113691831_113764486 | PHTF1 | chr1 | 113691831 | 113764486 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113705236 | TCGAGACA others(905): Show |
T | 1 | a0004 | 1 | NA18906.hp1 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1413_1672-440del | p.Gln472fs | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/19 | 1413/2289 | 471/762 | chr1 | 113705236 | ||||
chr1:113706159 | T | A | 1 | a0002 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1402A>T | p.Asn468Tyr | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/19 | 1896/3657 | 1402/2289 | 468/762 | chr1 | 113706159 | |||
chr1:113758664 | T | C | 1 | a0003 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.40A>G | p.Lys14Glu | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/19 | 534/3657 | 40/2289 | 14/762 | chr1 | 113758664 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113706702 | C | T | 1 | a0001c0003 | 5 | HG00738.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.1290G>A | p.Gln430Gln | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 12/19 | 1784/3657 | 1290/2289 | 430/762 | chr1 | 113706702 | |||
chr1:113712015 | C | T | 1 | a0001c0006 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.882G>A | p.Val294Val | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 9/19 | 1376/3657 | 882/2289 | 294/762 | chr1 | 113712015 | |||
chr1:113724860 | G | A | 1 | a0001c0004 | 3 | HG02145.hp2 HG02630.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.522C>T | p.Ser174Ser | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/19 | 1016/3657 | 522/2289 | 174/762 | chr1 | 113724860 | |||
chr1:113738159 | A | G | 2 | a0001c0002 a0004c0005 |
19 | HG01123.hp2 HG02015.hp1 HG02572.hp1 others(16): Show |
synonymous_variant | LOW | c.282T>C | p.Val94Val | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/19 | 776/3657 | 282/2289 | 94/762 | chr1 | 113738159 | |||
chr1:113738234 | T | C | 1 | a0001c0008 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.207A>G | p.Pro69Pro | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/19 | 701/3657 | 207/2289 | 69/762 | chr1 | 113738234 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113696837 | A | G | 1 | a0001c0001t0009 | 2 | HG01192.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*868T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 868 | chr1 | 113696837 | ||||||
chr1:113696842 | G | A | 1 | a0001c0001t0014 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*863C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 863 | chr1 | 113696842 | ||||||
chr1:113696866 | T | C | 1 | a0001c0001t0010 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*839A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 839 | chr1 | 113696866 | ||||||
chr1:113697087 | A | G | 1 | a0004c0005t0012 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 618 | chr1 | 113697087 | ||||||
chr1:113697505 | A | C | 1 | a0001c0001t0013 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 200 | chr1 | 113697505 | ||||||
chr1:113697697 | T | TA | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(14): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*7dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 19/19 | 7 | chr1 | 113697697 | ||||||
chr1:113758713 | C | T | 3 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0013 |
83 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/19 | 10 | chr1 | 113758713 | ||||||
chr1:113759078 | G | A | 1 | a0001c0001t0006 | 3 | HG02257.hp2 HG02895.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-86C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/19 | 375 | chr1 | 113759078 | ||||||
chr1:113759092 | G | A | 1 | a0001c0001t0015 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-100C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/19 | 389 | chr1 | 113759092 | ||||||
chr1:113759425 | AGGC | A | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
5_prime_UTR_variant | MODIFIER | c.-436_-434delGCC | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/19 | 723 | chr1 | 113759425 | ||||||
chr1:113759444 | C | T | 2 | a0001c0001t0004 a0001c0001t0006 |
9 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-452G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/19 | 741 | chr1 | 113759444 | ||||||
chr1:113759465 | G | A | 1 | a0001c0001t0005 | 6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-473C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/19 | 762 | chr1 | 113759465 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:113697928 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2269-203C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113697928 | |||||||
chr1:113698152 | A | AAC | 3 | a0001c0001t0003g0006 a0001c0004t0001g0146 a0003c0009t0001g0317 |
4 | HG01515.hp2 HG01517.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+108_2268+109d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AAC | A | 81 | a0001c0001t0001g0163 a0001c0001t0002g0001 a0001c0001t0002g0002 others(78): Show |
83 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2268+108_2268+109d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AACAC | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(23): Show |
27 | HG00423.hp2 HG01070.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2268+106_2268+109d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AACACAC | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0136 others(80): Show |
84 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2268+104_2268+109d others(8): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AACACACA others(1): Show |
A | 87 | a0001c0001t0001g0021 a0001c0001t0001g0101 a0001c0001t0001g0104 others(84): Show |
87 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2268+102_2268+109d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AACACACA others(3): Show |
A | 23 | a0001c0001t0001g0297 a0001c0001t0002g0072 a0001c0001t0004g0010 others(20): Show |
24 | HG00621.hp1 HG01109.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.2268+100_2268+109d others(12): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698152 | AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2268+98_2268+109de others(13): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 18/18 | chr1 | 113698152 | |||||||
chr1:113698522 | C | A | 3 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0006t0001g0307 |
3 | HG02630.hp1 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2143-135G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698522 | |||||||
chr1:113698607 | TTA | T | 16 | a0001c0001t0001g0175 a0001c0001t0001g0261 a0001c0001t0001g0289 others(13): Show |
17 | HG01891.hp1 HG02145.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.2143-222_2143-221d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698607 | |||||||
chr1:113698607 | TTATA | T | 14 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(11): Show |
14 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.2143-224_2143-221d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698607 | |||||||
chr1:113698616 | TATATAC | T | 8 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0214 others(5): Show |
8 | HG00735.hp2 HG02145.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.2143-235_2143-230d others(8): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698616 | |||||||
chr1:113698616 | TATATACA others(1): Show |
T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0159 others(34): Show |
37 | HG00408.hp2 HG00642.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.2143-237_2143-230d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698616 | |||||||
chr1:113698616 | TATATACA others(3): Show |
T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2143-239_2143-230d others(12): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698616 | |||||||
chr1:113698616 | TATATACA others(5): Show |
T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0239 |
2 | HG00408.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.2143-241_2143-230d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698616 | |||||||
chr1:113698616 | TATATACA others(7): Show |
T | 1 | a0001c0002t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2143-243_2143-230d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698616 | |||||||
chr1:113698618 | T | C | 6 | a0001c0002t0001g0244 a0001c0002t0001g0259 a0001c0002t0001g0288 others(3): Show |
6 | HG01123.hp2 HG02015.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143-231A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698618 | |||||||
chr1:113698618 | TATAC | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0164 others(32): Show |
36 | HG00621.hp1 HG00642.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2143-235_2143-232d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698618 | |||||||
chr1:113698618 | TATACAC | T | 32 | a0001c0001t0001g0101 a0001c0001t0001g0163 a0001c0001t0001g0169 others(29): Show |
32 | HG01175.hp2 HG01433.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.2143-237_2143-232d others(8): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698618 | |||||||
chr1:113698618 | TATACACA others(3): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2143-241_2143-232d others(12): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698618 | |||||||
chr1:113698618 | TATACACA others(7): Show |
T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(43): Show |
47 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143-245_2143-232d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698618 | |||||||
chr1:113698620 | T | C | 24 | a0001c0001t0001g0187 a0001c0001t0001g0197 a0001c0001t0001g0242 others(21): Show |
25 | HG00738.hp1 HG01123.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.2143-233A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698620 | |||||||
chr1:113698620 | T | TACAC | 7 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(4): Show |
7 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2143-237_2143-234d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698620 | |||||||
chr1:113698620 | TAC | T | 17 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0026 others(14): Show |
17 | HG00597.hp2 HG01496.hp2 HG03239.hp2 others(14): Show |
intron_variant | MODIFIER | c.2143-235_2143-234d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698620 | |||||||
chr1:113698620 | TACAC | T | 14 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(11): Show |
14 | HG00741.hp1 HG02027.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2143-237_2143-234d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698620 | |||||||
chr1:113698620 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2143-247_2143-234d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698620 | |||||||
chr1:113698622 | C | T | 7 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0046 others(4): Show |
7 | HG00423.hp1 HG02083.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.2143-235G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698622 | |||||||
chr1:113698624 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0041 a0001c0001t0002g0044 others(1): Show |
4 | HG00597.hp2 HG01496.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-237G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698624 | |||||||
chr1:113698635 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2143-248T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698635 | |||||||
chr1:113698655 | A | G | 5 | a0001c0003t0003g0260 a0001c0003t0003g0312 a0001c0003t0003g0313 others(2): Show |
5 | HG00738.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2143-268T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698655 | |||||||
chr1:113698793 | A | G | 4 | a0001c0001t0001g0114 a0001c0001t0001g0160 a0001c0001t0001g0165 others(1): Show |
4 | HG00642.hp2 HG01928.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-406T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113698793 | |||||||
chr1:113699195 | C | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(18): Show |
21 | HG01175.hp2 HG02717.hp1 HG02895.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+509G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699195 | |||||||
chr1:113699233 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2142+471A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699233 | |||||||
chr1:113699254 | T | G | 14 | a0001c0001t0002g0075 a0001c0001t0002g0085 a0001c0001t0003g0123 others(11): Show |
15 | HG02015.hp1 HG02155.hp2 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.2142+450A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699254 | |||||||
chr1:113699256 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2142+448G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699256 | |||||||
chr1:113699341 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2142+363T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699341 | |||||||
chr1:113699378 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2142+326T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699378 | |||||||
chr1:113699500 | T | C | 62 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0128 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2142+204A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699500 | |||||||
chr1:113699628 | C | T | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0158 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.2142+76G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 17/18 | chr1 | 113699628 | |||||||
chr1:113699937 | T | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0247 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-138A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113699937 | |||||||
chr1:113700026 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2047-227A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700026 | |||||||
chr1:113700084 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(42): Show |
46 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2047-285C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700084 | |||||||
chr1:113700250 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(45): Show |
49 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2047-451G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700250 | |||||||
chr1:113700251 | A | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(45): Show |
49 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2047-452T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700251 | |||||||
chr1:113700260 | A | C | 7 | a0001c0001t0003g0117 a0001c0001t0003g0118 a0001c0001t0003g0121 others(4): Show |
7 | HG02132.hp2 HG02155.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.2047-461T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700260 | |||||||
chr1:113700574 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2046+220G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700574 | |||||||
chr1:113700576 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2046+218A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700576 | |||||||
chr1:113700774 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2046+20A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 16/18 | chr1 | 113700774 | |||||||
chr1:113701277 | C | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1891-328G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701277 | |||||||
chr1:113701555 | G | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1891-606C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701555 | |||||||
chr1:113701660 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1891-711T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701660 | |||||||
chr1:113701820 | T | A | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-871A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701820 | |||||||
chr1:113701821 | C | A | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-872G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701821 | |||||||
chr1:113701826 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-877A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TA | 50 | a0001c0001t0001g0164 a0001c0001t0001g0176 a0001c0001t0001g0182 others(47): Show |
50 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1891-878dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAA | 14 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0178 others(11): Show |
14 | HG01175.hp2 HG01433.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1891-879_1891-878d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(4): Show |
4 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0232 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-888_1891-878d others(13): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(5): Show |
11 | a0001c0001t0001g0159 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG00140.hp1 HG00408.hp2 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.1891-889_1891-878d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(6): Show |
5 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0250 others(2): Show |
5 | HG03942.hp2 HG04199.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1891-890_1891-878d others(15): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(7): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0223 a0001c0001t0001g0277 others(1): Show |
4 | HG03688.hp2 HG04115.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-891_1891-878d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0222 |
2 | HG01346.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1891-892_1891-878d others(17): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(9): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG00735.hp2 HG01261.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891-893_1891-878d others(18): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG00642.hp2 HG01243.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1891-894_1891-878d others(19): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(11): Show |
3 | a0001c0001t0001g0160 a0001c0001t0001g0234 a0001c0001t0001g0239 |
3 | HG00408.hp1 HG02293.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1891-895_1891-878d others(20): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1891-896_1891-878d others(21): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | T | TAAAAAAA others(20): Show |
1 | a0001c0001t0001g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1891-904_1891-878d others(29): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TA | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0185 others(18): Show |
22 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1891-878delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAA | T | 18 | a0001c0001t0001g0101 a0001c0001t0001g0192 a0001c0001t0001g0240 others(15): Show |
19 | HG02015.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1891-879_1891-878d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAAA | T | 6 | a0001c0001t0001g0163 a0001c0001t0003g0314 a0001c0001t0004g0010 others(3): Show |
6 | HG00621.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1891-880_1891-878d others(5): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAAAAAAA others(1): Show |
T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(47): Show |
51 | HG00423.hp2 HG00733.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1891-885_1891-878d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAAAAAAA others(6): Show |
T | 1 | a0001c0003t0003g0313 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1891-890_1891-878d others(15): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAAAAAAA others(7): Show |
T | 5 | a0001c0001t0001g0171 a0001c0003t0003g0260 a0001c0003t0003g0312 others(2): Show |
5 | HG02055.hp1 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891-891_1891-878d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701826 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0085 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1891-892_1891-878d others(17): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701826 | |||||||
chr1:113701830 | A | T | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-881T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701830 | |||||||
chr1:113701831 | A | T | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-882T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701831 | |||||||
chr1:113701832 | A | C | 1 | a0001c0001t0001g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1891-883T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701832 | |||||||
chr1:113701856 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0278 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1891-908_1891-907i others(15): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701856 | |||||||
chr1:113701937 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1891-988G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113701937 | |||||||
chr1:113702530 | T | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1890+1551A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702530 | |||||||
chr1:113702645 | G | GA | 97 | a0001c0001t0001g0101 a0001c0001t0001g0163 a0001c0001t0001g0164 others(94): Show |
98 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1890+1435dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702645 | |||||||
chr1:113702653 | AGG | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0185 |
4 | NA18952.hp1 NA18972.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890+1426_1890+142 others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702653 | |||||||
chr1:113702657 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0185 |
4 | NA18952.hp1 NA18972.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890+1424T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702657 | |||||||
chr1:113702676 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1890+1405T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702676 | |||||||
chr1:113702824 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1890+1257T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702824 | |||||||
chr1:113702855 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0223 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1890+1226C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113702855 | |||||||
chr1:113703345 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1890+736T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113703345 | |||||||
chr1:113703530 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1890+551A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113703530 | |||||||
chr1:113703831 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1890+250G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 15/18 | chr1 | 113703831 | |||||||
chr1:113704824 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0161 a0001c0001t0001g0210 others(9): Show |
12 | HG00735.hp2 HG01069.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1672-27C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/18 | chr1 | 113704824 | |||||||
chr1:113705177 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1672-380G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/18 | chr1 | 113705177 | |||||||
chr1:113705442 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1671+448T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/18 | chr1 | 113705442 | |||||||
chr1:113705642 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1671+248C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/18 | chr1 | 113705642 | |||||||
chr1:113705784 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1671+106A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 13/18 | chr1 | 113705784 | |||||||
chr1:113706188 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1399-26G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 12/18 | chr1 | 113706188 | |||||||
chr1:113706565 | G | T | 1 | a0001c0001t0002g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1398+29C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 12/18 | chr1 | 113706565 | |||||||
chr1:113706760 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1270-38G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113706760 | |||||||
chr1:113706851 | C | CT | 10 | a0001c0001t0001g0112 a0001c0001t0001g0119 a0001c0001t0001g0148 others(7): Show |
10 | HG00423.hp2 HG00733.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.1270-130dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113706851 | |||||||
chr1:113706851 | CT | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(99): Show |
104 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1270-130delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113706851 | |||||||
chr1:113706856 | T | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01891.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1270-134A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113706856 | |||||||
chr1:113706878 | G | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-156C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113706878 | |||||||
chr1:113707117 | TG | T | 7 | a0001c0001t0003g0006 a0001c0001t0003g0290 a0001c0001t0003g0291 others(4): Show |
8 | HG00735.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1270-396delC | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707117 | |||||||
chr1:113707145 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1270-423T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707145 | |||||||
chr1:113707281 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1270-559C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707281 | |||||||
chr1:113707294 | T | G | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1270-572A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707294 | |||||||
chr1:113707453 | G | A | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1270-731C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707453 | |||||||
chr1:113707586 | C | T | 2 | a0001c0006t0001g0307 a0003c0009t0001g0317 |
2 | HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1270-864G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707586 | |||||||
chr1:113707752 | T | G | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(8): Show |
11 | HG00741.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1270-1030A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707752 | |||||||
chr1:113707962 | C | CA | 162 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1270-1241dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113707962 | |||||||
chr1:113708397 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1270-1675C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113708397 | |||||||
chr1:113708725 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1269+1529G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113708725 | |||||||
chr1:113709688 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1269+566C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113709688 | |||||||
chr1:113709948 | T | C | 8 | a0001c0001t0001g0192 a0001c0001t0004g0007 a0001c0001t0004g0010 others(5): Show |
8 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1269+306A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113709948 | |||||||
chr1:113710099 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1269+155G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 11/18 | chr1 | 113710099 | |||||||
chr1:113710779 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1048-304G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710779 | |||||||
chr1:113710791 | G | GAT | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0102 others(116): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1048-318_1048-317d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710791 | |||||||
chr1:113710791 | G | GATAT | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0150 others(4): Show |
7 | HG02257.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048-320_1048-317d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710791 | |||||||
chr1:113710791 | G | GATATATA others(5): Show |
1 | a0001c0001t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1048-328_1048-317d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710791 | |||||||
chr1:113710810 | A | AT | 6 | a0001c0001t0001g0159 a0001c0001t0001g0215 a0001c0001t0001g0308 others(3): Show |
6 | HG01109.hp1 HG01261.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-336dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710810 | |||||||
chr1:113710810 | A | T | 3 | a0001c0001t0010g0310 a0001c0001t0010g0311 a0001c0006t0001g0307 |
3 | HG02896.hp2 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1048-335T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710810 | |||||||
chr1:113710810 | AT | A | 93 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0022 others(90): Show |
96 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1048-336delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710810 | |||||||
chr1:113710811 | T | TA | 55 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0114 others(52): Show |
55 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1048-337_1048-336i others(3): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710811 | |||||||
chr1:113710811 | T | TATA | 26 | a0001c0001t0001g0158 a0001c0001t0001g0199 a0001c0001t0001g0230 others(23): Show |
27 | HG01123.hp2 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1048-337_1048-336i others(5): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710811 | |||||||
chr1:113710811 | T | TATATATA others(4): Show |
1 | a0001c0002t0007g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1048-337_1048-336i others(13): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710811 | |||||||
chr1:113710812 | T | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(61): Show |
65 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1048-337A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710812 | |||||||
chr1:113710813 | T | A | 29 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0224 others(26): Show |
30 | HG01123.hp2 HG01928.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1048-338A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710813 | |||||||
chr1:113710814 | T | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG01175.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048-339A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710814 | |||||||
chr1:113710815 | T | A | 4 | a0001c0001t0001g0299 a0001c0004t0001g0146 a0001c0004t0001g0147 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-340A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710815 | |||||||
chr1:113710816 | T | A | 1 | a0001c0001t0004g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1048-341A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710816 | |||||||
chr1:113710817 | T | A | 4 | a0001c0001t0001g0299 a0001c0004t0001g0146 a0001c0004t0001g0147 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-342A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710817 | |||||||
chr1:113710928 | G | A | 6 | a0001c0001t0004g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-453C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710928 | |||||||
chr1:113710975 | A | T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1048-500T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113710975 | |||||||
chr1:113711017 | C | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1048-542G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113711017 | |||||||
chr1:113711228 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1047+518G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113711228 | |||||||
chr1:113711270 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1047+476T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113711270 | |||||||
chr1:113711296 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0009g0203 a0001c0001t0009g0204 |
3 | HG01192.hp2 HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1047+450G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113711296 | |||||||
chr1:113711653 | G | C | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1047+93C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 10/18 | chr1 | 113711653 | |||||||
chr1:113711930 | T | C | 1 | a0001c0002t0001g0288 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.957+10A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 9/18 | chr1 | 113711930 | |||||||
chr1:113712165 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.784-52A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712165 | |||||||
chr1:113712316 | T | C | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.784-203A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712316 | |||||||
chr1:113712508 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.784-395A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712508 | |||||||
chr1:113712784 | A | AT | 24 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.783+494dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712784 | |||||||
chr1:113712784 | AT | A | 19 | a0001c0001t0001g0192 a0001c0001t0001g0289 a0001c0001t0002g0048 others(16): Show |
19 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.783+494delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712784 | |||||||
chr1:113712784 | ATT | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(85): Show |
90 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.783+493_783+494del others(2): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712784 | |||||||
chr1:113712784 | ATTT | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.783+492_783+494del others(3): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712784 | |||||||
chr1:113712785 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.783+494A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712785 | |||||||
chr1:113712873 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.783+406T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712873 | |||||||
chr1:113712887 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.783+392A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113712887 | |||||||
chr1:113713042 | C | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.783+237G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113713042 | |||||||
chr1:113713153 | TGTG | T | 8 | a0001c0001t0001g0192 a0001c0001t0004g0007 a0001c0001t0004g0010 others(5): Show |
8 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+123_783+125del others(3): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113713153 | |||||||
chr1:113713206 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(55): Show |
59 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.783+73A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 8/18 | chr1 | 113713206 | |||||||
chr1:113713501 | T | G | 1 | a0001c0004t0001g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.624-63A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713501 | |||||||
chr1:113713517 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(89): Show |
94 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.624-79G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713517 | |||||||
chr1:113713545 | T | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01891.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.624-107A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713545 | |||||||
chr1:113713757 | C | G | 160 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.624-319G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713757 | |||||||
chr1:113713808 | G | A | 1 | a0002c0007t0001g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.624-370C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713808 | |||||||
chr1:113713835 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-397C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113713835 | |||||||
chr1:113714344 | G | A | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.624-906C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113714344 | |||||||
chr1:113714622 | A | G | 1 | a0001c0001t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-1184T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113714622 | |||||||
chr1:113714623 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.624-1185A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113714623 | |||||||
chr1:113714667 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.624-1229C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113714667 | |||||||
chr1:113714737 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.624-1299C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113714737 | |||||||
chr1:113715054 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.624-1616C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715054 | |||||||
chr1:113715129 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0074 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.624-1691A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715129 | |||||||
chr1:113715261 | G | C | 5 | a0001c0003t0003g0260 a0001c0003t0003g0312 a0001c0003t0003g0313 others(2): Show |
5 | HG00738.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.624-1823C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715261 | |||||||
chr1:113715301 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.624-1863T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715301 | |||||||
chr1:113715344 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01516.hp2 HG01517.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.624-1906C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715344 | |||||||
chr1:113715641 | C | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.624-2203G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715641 | |||||||
chr1:113715648 | C | CA | 10 | a0001c0001t0001g0158 a0001c0001t0002g0038 a0001c0001t0002g0042 others(7): Show |
10 | HG00423.hp1 HG00735.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.624-2211dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAA | 6 | a0001c0001t0001g0159 a0001c0001t0002g0023 a0001c0001t0002g0030 others(3): Show |
6 | NA18967.hp2 NA18972.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-2212_624-2211d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAA | 19 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(16): Show |
19 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.624-2216_624-2211d others(8): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA | 25 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0108 others(22): Show |
25 | HG01081.hp2 HG01943.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.624-2217_624-2211d others(9): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0001g0106 others(9): Show |
13 | HG00408.hp2 HG00423.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.624-2218_624-2211d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA others(2): Show |
21 | a0001c0001t0001g0021 a0001c0001t0001g0102 a0001c0001t0001g0114 others(18): Show |
21 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.624-2219_624-2211d others(11): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA others(3): Show |
25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(22): Show |
25 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.624-2220_624-2211d others(12): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0216 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp2 HG03688.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-2221_624-2211d others(13): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.624-2225_624-2211d others(17): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | CA | C | 54 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0172 others(51): Show |
56 | HG00597.hp2 HG00621.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.624-2211delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | CAA | C | 8 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0005g0320 others(5): Show |
8 | HG01891.hp2 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.624-2212_624-2211d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | CAAAA | C | 9 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0197 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.624-2214_624-2211d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | CAAAAA | C | 48 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0176 others(45): Show |
48 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.624-2215_624-2211d others(7): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715648 | CAAAAAA | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(31): Show |
36 | HG01123.hp2 HG01192.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.624-2216_624-2211d others(8): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715648 | |||||||
chr1:113715720 | G | A | 3 | a0001c0002t0007g0017 a0001c0002t0007g0020 a0004c0005t0012g0018 |
3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624-2282C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715720 | |||||||
chr1:113715720 | G | T | 1 | a0001c0003t0003g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.624-2282C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113715720 | |||||||
chr1:113716017 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0269 |
2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.624-2579G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716017 | |||||||
chr1:113716018 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.624-2580C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716018 | |||||||
chr1:113716169 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624-2731T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716169 | |||||||
chr1:113716260 | T | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.624-2822A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716260 | |||||||
chr1:113716342 | C | CT | 33 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0113 others(30): Show |
33 | HG00597.hp2 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.624-2905dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716342 | |||||||
chr1:113716342 | CT | C | 8 | a0001c0001t0001g0134 a0001c0001t0001g0157 a0001c0001t0001g0241 others(5): Show |
8 | HG01070.hp1 HG01943.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.624-2905delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716342 | |||||||
chr1:113716433 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.624-2995C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716433 | |||||||
chr1:113716447 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.624-3009G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716447 | |||||||
chr1:113716447 | C | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.624-3009G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716447 | |||||||
chr1:113716774 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.624-3336C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716774 | |||||||
chr1:113716935 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.624-3497A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113716935 | |||||||
chr1:113717003 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.624-3565A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717003 | |||||||
chr1:113717010 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0041 a0001c0001t0002g0044 others(1): Show |
4 | HG00597.hp2 HG01496.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-3572G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717010 | |||||||
chr1:113717132 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624-3694A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717132 | |||||||
chr1:113717261 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.624-3823G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717261 | |||||||
chr1:113717296 | G | A | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-3858C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717296 | |||||||
chr1:113717393 | T | C | 1 | a0001c0001t0004g0012 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.624-3955A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717393 | |||||||
chr1:113717422 | G | C | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(8): Show |
11 | HG00741.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.624-3984C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717422 | |||||||
chr1:113717445 | A | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | NA18939.hp2 NA18953.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-4007T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717445 | |||||||
chr1:113717605 | C | T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.624-4167G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717605 | |||||||
chr1:113717711 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-4273C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717711 | |||||||
chr1:113717747 | C | A | 3 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0004t0001g0298 |
3 | HG02145.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.624-4309G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717747 | |||||||
chr1:113717844 | C | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(9): Show |
12 | HG03491.hp1 HG03654.hp2 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.624-4406G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717844 | |||||||
chr1:113717935 | C | A | 7 | a0001c0001t0001g0193 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-4497G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113717935 | |||||||
chr1:113718493 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.624-5055G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113718493 | |||||||
chr1:113718526 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624-5088A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113718526 | |||||||
chr1:113718857 | A | G | 64 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(61): Show |
64 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.624-5419T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113718857 | |||||||
chr1:113718954 | C | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.624-5516G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113718954 | |||||||
chr1:113719049 | G | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0040 |
2 | NA18972.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.624-5611C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719049 | |||||||
chr1:113719272 | G | C | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623+5487C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719272 | |||||||
chr1:113719659 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.623+5100C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719659 | |||||||
chr1:113719934 | G | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.623+4825C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719934 | |||||||
chr1:113719936 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.623+4823A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719936 | |||||||
chr1:113719939 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.623+4820A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113719939 | |||||||
chr1:113720185 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.623+4574A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720185 | |||||||
chr1:113720312 | TAAAG | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+4443_623+4446d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720312 | |||||||
chr1:113720336 | C | T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.623+4423G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720336 | |||||||
chr1:113720411 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.623+4348A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720411 | |||||||
chr1:113720772 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.623+3987C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720772 | |||||||
chr1:113720773 | C | T | 1 | a0001c0001t0014g0202 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.623+3986G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113720773 | |||||||
chr1:113721094 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.623+3665C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721094 | |||||||
chr1:113721110 | T | C | 16 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0125 others(13): Show |
16 | HG01167.hp1 HG01433.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.623+3649A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721110 | |||||||
chr1:113721113 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.623+3646C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721113 | |||||||
chr1:113721159 | C | T | 7 | a0001c0001t0002g0023 a0001c0001t0002g0030 a0001c0001t0002g0032 others(4): Show |
7 | NA18949.hp1 NA18951.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+3600G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721159 | |||||||
chr1:113721210 | C | G | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+3549G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721210 | |||||||
chr1:113721263 | A | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0163 a0001c0001t0001g0240 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+3496T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721263 | |||||||
chr1:113721396 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.623+3363C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721396 | |||||||
chr1:113721405 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.623+3354A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721405 | |||||||
chr1:113721783 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.623+2976C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721783 | |||||||
chr1:113721861 | T | A | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.623+2898A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721861 | |||||||
chr1:113721941 | G | A | 3 | a0001c0004t0001g0146 a0001c0004t0001g0147 a0001c0004t0001g0298 |
3 | HG02145.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.623+2818C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113721941 | |||||||
chr1:113722003 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.623+2756A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722003 | |||||||
chr1:113722086 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2673T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722086 | |||||||
chr1:113722094 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2665T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722094 | |||||||
chr1:113722095 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2664C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722095 | |||||||
chr1:113722097 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2662T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722097 | |||||||
chr1:113722098 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2661T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722098 | |||||||
chr1:113722104 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2655G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722104 | |||||||
chr1:113722105 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2654T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722105 | |||||||
chr1:113722106 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2653T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722106 | |||||||
chr1:113722110 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2649T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722110 | |||||||
chr1:113722111 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2648C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722111 | |||||||
chr1:113722114 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2645T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722114 | |||||||
chr1:113722115 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2644T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722115 | |||||||
chr1:113722116 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2643T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722116 | |||||||
chr1:113722120 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2639G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722120 | |||||||
chr1:113722130 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2629T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722130 | |||||||
chr1:113722131 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2628T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722131 | |||||||
chr1:113722133 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2626T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722133 | |||||||
chr1:113722139 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2620T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722139 | |||||||
chr1:113722147 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2612T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722147 | |||||||
chr1:113722152 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2607T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722152 | |||||||
chr1:113722156 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2603T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722156 | |||||||
chr1:113722159 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2600C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722159 | |||||||
chr1:113722160 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2599T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722160 | |||||||
chr1:113722164 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2595C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722164 | |||||||
chr1:113722165 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2594T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722165 | |||||||
chr1:113722168 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2591C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722168 | |||||||
chr1:113722169 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2590G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722169 | |||||||
chr1:113722178 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.623+2581C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722178 | |||||||
chr1:113722215 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2544T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722215 | |||||||
chr1:113722221 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2538T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722221 | |||||||
chr1:113722227 | G | A | 1 | a0001c0001t0005g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.623+2532C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722227 | |||||||
chr1:113722245 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2514T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722245 | |||||||
chr1:113722247 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2512G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722247 | |||||||
chr1:113722267 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.623+2492T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722267 | |||||||
chr1:113722622 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.623+2137G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722622 | |||||||
chr1:113722869 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.623+1890C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722869 | |||||||
chr1:113722919 | C | CAAAT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0104 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.623+1836_623+1839d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722919 | C | CAAATAAA others(1): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0137 others(5): Show |
9 | HG01255.hp1 HG01952.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.623+1832_623+1839d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722919 | C | CAAATAAA others(9): Show |
1 | a0001c0001t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.623+1824_623+1839d others(18): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722919 | CAAAT | C | 17 | a0001c0001t0001g0107 a0001c0001t0001g0176 a0001c0001t0001g0200 others(14): Show |
17 | HG01243.hp2 HG01943.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.623+1836_623+1839d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722919 | CAAATAAA others(1): Show |
C | 10 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0004g0007 others(7): Show |
10 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.623+1832_623+1839d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722919 | CAAATAAA others(5): Show |
C | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623+1828_623+1839d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722919 | |||||||
chr1:113722963 | TAAAA | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+1792_623+1795d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113722963 | |||||||
chr1:113723097 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.623+1662A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723097 | |||||||
chr1:113723119 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.623+1640G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723119 | |||||||
chr1:113723177 | A | AT | 8 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0135 others(5): Show |
8 | HG00099.hp1 HG02717.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.623+1581dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723177 | |||||||
chr1:113723306 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.623+1453G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723306 | |||||||
chr1:113723341 | A | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+1418T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723341 | |||||||
chr1:113723378 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.623+1381T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723378 | |||||||
chr1:113723607 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.623+1152G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723607 | |||||||
chr1:113723924 | G | GA | 55 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.623+834dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113723924 | |||||||
chr1:113724207 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.623+552C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724207 | |||||||
chr1:113724404 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.623+355G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724404 | |||||||
chr1:113724540 | C | CA | 7 | a0001c0001t0001g0116 a0001c0001t0001g0192 a0001c0001t0001g0247 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.623+218dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724540 | |||||||
chr1:113724540 | C | CAA | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
10 | HG00741.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.623+217_623+218dup others(2): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724540 | |||||||
chr1:113724662 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.623+97G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724662 | |||||||
chr1:113724725 | C | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.623+34G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 7/18 | chr1 | 113724725 | |||||||
chr1:113725023 | C | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.489-130G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113725023 | |||||||
chr1:113725068 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01891.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.489-175A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113725068 | |||||||
chr1:113725302 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.489-409C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113725302 | |||||||
chr1:113725329 | T | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0104 others(97): Show |
102 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.489-436A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113725329 | |||||||
chr1:113725503 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.489-610T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113725503 | |||||||
chr1:113726056 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.488+362G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113726056 | |||||||
chr1:113726169 | A | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.488+249T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 6/18 | chr1 | 113726169 | |||||||
chr1:113726834 | A | G | 2 | a0001c0001t0001g0299 a0001c0004t0001g0298 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.332-260T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113726834 | |||||||
chr1:113726859 | T | C | 2 | a0001c0001t0001g0299 a0001c0004t0001g0298 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.332-285A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113726859 | |||||||
chr1:113726944 | T | C | 3 | a0001c0001t0002g0048 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | NA18974.hp2 NA18984.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.332-370A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113726944 | |||||||
chr1:113727042 | G | GTA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0185 others(11): Show |
15 | HG02723.hp1 HG02896.hp2 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.332-470_332-469dup others(2): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727042 | |||||||
chr1:113727042 | G | GTATA | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
10 | HG00741.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.332-472_332-469dup others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727042 | |||||||
chr1:113727044 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.332-470T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727044 | |||||||
chr1:113727046 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.332-472T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727046 | |||||||
chr1:113727355 | A | G | 164 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.332-781T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727355 | |||||||
chr1:113727438 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0090 |
2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.332-864A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727438 | |||||||
chr1:113727536 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.332-962G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727536 | |||||||
chr1:113727537 | G | A | 55 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(52): Show |
55 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.332-963C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727537 | |||||||
chr1:113727704 | C | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.332-1130G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727704 | |||||||
chr1:113727719 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.332-1145G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113727719 | |||||||
chr1:113728098 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-1524C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728098 | |||||||
chr1:113728116 | G | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.332-1542C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728116 | |||||||
chr1:113728284 | C | T | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.332-1710G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728284 | |||||||
chr1:113728285 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.332-1711T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728285 | |||||||
chr1:113728506 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(226): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.332-1932T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728506 | |||||||
chr1:113728801 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(237): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.332-2227A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728801 | |||||||
chr1:113728979 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-2405A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113728979 | |||||||
chr1:113729040 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.332-2466G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729040 | |||||||
chr1:113729106 | C | A | 1 | a0001c0001t0003g0290 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.332-2532G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729106 | |||||||
chr1:113729276 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.332-2702A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729276 | |||||||
chr1:113729541 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.332-2967G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729541 | |||||||
chr1:113729557 | A | T | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.332-2983T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729557 | |||||||
chr1:113729742 | G | A | 7 | a0001c0001t0003g0006 a0001c0001t0003g0290 a0001c0001t0003g0291 others(4): Show |
8 | HG00735.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-3168C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729742 | |||||||
chr1:113729805 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.332-3231C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729805 | |||||||
chr1:113729843 | G | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.332-3269C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729843 | |||||||
chr1:113729926 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.332-3352G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113729926 | |||||||
chr1:113730127 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.332-3553C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113730127 | |||||||
chr1:113730619 | G | A | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-4045C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113730619 | |||||||
chr1:113730631 | C | T | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-4057G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113730631 | |||||||
chr1:113730714 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332-4140A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113730714 | |||||||
chr1:113731005 | G | A | 6 | a0001c0001t0004g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-4431C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731005 | |||||||
chr1:113731055 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.332-4481T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731055 | |||||||
chr1:113731102 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.332-4528T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731102 | |||||||
chr1:113731226 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.332-4652A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731226 | |||||||
chr1:113731359 | C | A | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-4785G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731359 | |||||||
chr1:113731360 | C | A | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-4786G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731360 | |||||||
chr1:113731517 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.332-4943A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731517 | |||||||
chr1:113731536 | T | A | 321 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(318): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.332-4962A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731536 | |||||||
chr1:113731625 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(51): Show |
55 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.332-5051C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731625 | |||||||
chr1:113731846 | G | A | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-5272C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731846 | |||||||
chr1:113731882 | G | A | 6 | a0001c0001t0004g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-5308C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731882 | |||||||
chr1:113731891 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-5317G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731891 | |||||||
chr1:113731898 | AT | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0163 a0001c0001t0001g0240 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-5325delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731898 | |||||||
chr1:113731902 | T | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0246 a0001c0001t0001g0297 others(2): Show |
5 | HG01346.hp1 HG01928.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-5328A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731902 | |||||||
chr1:113731902 | T | TA | 6 | a0001c0001t0001g0129 a0001c0001t0001g0214 a0001c0001t0001g0218 others(3): Show |
6 | HG01167.hp2 HG03942.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-5329dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731902 | |||||||
chr1:113731902 | TA | T | 14 | a0001c0001t0001g0176 a0001c0001t0001g0190 a0001c0001t0001g0230 others(11): Show |
14 | HG00140.hp2 HG01069.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-5329delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113731902 | |||||||
chr1:113732188 | G | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0283 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-5614C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732188 | |||||||
chr1:113732422 | G | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.331+5688C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732422 | |||||||
chr1:113732509 | C | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+5601G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732509 | |||||||
chr1:113732812 | T | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0157 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.331+5298A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732812 | |||||||
chr1:113732815 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.331+5295A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732815 | |||||||
chr1:113732833 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.331+5277T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732833 | |||||||
chr1:113732835 | GA | G | 3 | a0001c0001t0002g0049 a0001c0001t0002g0083 a0001c0001t0002g0100 |
3 | NA18941.hp1 NA19078.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.331+5274delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732835 | |||||||
chr1:113732941 | A | G | 4 | a0001c0001t0001g0299 a0001c0004t0001g0146 a0001c0004t0001g0147 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+5169T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732941 | |||||||
chr1:113732979 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.331+5131A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113732979 | |||||||
chr1:113733060 | A | AT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0105 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.331+5049dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733060 | |||||||
chr1:113733060 | A | ATT | 22 | a0001c0001t0001g0021 a0001c0001t0001g0104 a0001c0001t0001g0106 others(19): Show |
22 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.331+5048_331+5049d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733060 | |||||||
chr1:113733060 | A | ATTT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0103 others(79): Show |
84 | HG00099.hp2 HG00621.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.331+5047_331+5049d others(5): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733060 | |||||||
chr1:113733060 | A | ATTTT | 19 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0001g0185 others(16): Show |
19 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.331+5046_331+5049d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733060 | |||||||
chr1:113733193 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0090 |
2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.331+4917G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733193 | |||||||
chr1:113733209 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.331+4901G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733209 | |||||||
chr1:113733479 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.331+4631A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733479 | |||||||
chr1:113733521 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0007g0019 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.331+4589C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733521 | |||||||
chr1:113733614 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.331+4496G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733614 | |||||||
chr1:113733878 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.331+4232C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113733878 | |||||||
chr1:113734087 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(51): Show |
55 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.331+4023G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734087 | |||||||
chr1:113734103 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(208): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.331+4007G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734103 | |||||||
chr1:113734143 | C | T | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331+3967G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734143 | |||||||
chr1:113734405 | T | G | 2 | a0001c0001t0003g0291 a0001c0001t0003g0295 |
2 | HG00735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.331+3705A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734405 | |||||||
chr1:113734708 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.331+3402T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734708 | |||||||
chr1:113734770 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.331+3340C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734770 | |||||||
chr1:113734773 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.331+3337A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113734773 | |||||||
chr1:113735038 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.331+3072G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735038 | |||||||
chr1:113735365 | C | CA | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(141): Show |
147 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.331+2744dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735365 | |||||||
chr1:113735365 | C | CAA | 63 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0115 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.331+2743_331+2744d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735365 | |||||||
chr1:113735365 | C | CAAA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0151 others(8): Show |
11 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+2742_331+2744d others(5): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735365 | |||||||
chr1:113735883 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.331+2227G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735883 | |||||||
chr1:113735945 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.331+2165A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113735945 | |||||||
chr1:113736007 | A | G | 8 | a0001c0001t0001g0178 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01175.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+2103T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736007 | |||||||
chr1:113736118 | G | A | 4 | a0001c0002t0001g0244 a0001c0002t0001g0245 a0001c0002t0001g0280 others(1): Show |
4 | HG01123.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+1992C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736118 | |||||||
chr1:113736211 | G | A | 1 | a0001c0003t0003g0313 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.331+1899C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736211 | |||||||
chr1:113736259 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.331+1851C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736259 | |||||||
chr1:113736300 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.331+1810G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736300 | |||||||
chr1:113736375 | T | A | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(17): Show |
20 | HG01175.hp2 HG02717.hp1 HG02895.hp2 others(17): Show |
intron_variant | MODIFIER | c.331+1735A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736375 | |||||||
chr1:113736447 | T | C | 1 | a0001c0001t0004g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.331+1663A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736447 | |||||||
chr1:113736644 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.331+1466A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736644 | |||||||
chr1:113736648 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331+1462C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736648 | |||||||
chr1:113736698 | T | C | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331+1412A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736698 | |||||||
chr1:113736783 | A | C | 1 | a0001c0002t0001g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.331+1327T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736783 | |||||||
chr1:113736806 | C | T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.331+1304G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736806 | |||||||
chr1:113736864 | G | A | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331+1246C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736864 | |||||||
chr1:113736893 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.331+1217T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113736893 | |||||||
chr1:113737141 | A | T | 2 | a0001c0004t0001g0146 a0001c0004t0001g0147 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.331+969T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113737141 | |||||||
chr1:113737513 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.331+597C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113737513 | |||||||
chr1:113737549 | G | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.331+561C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113737549 | |||||||
chr1:113737612 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.331+498C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113737612 | |||||||
chr1:113738095 | A | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.331+15T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 5/18 | chr1 | 113738095 | |||||||
chr1:113738491 | A | G | 2 | a0001c0001t0003g0291 a0001c0001t0003g0295 |
2 | HG00735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.173-223T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 4/18 | chr1 | 113738491 | |||||||
chr1:113739319 | T | G | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG01081.hp2 HG01943.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-520A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739319 | |||||||
chr1:113739353 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.103-554C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739353 | |||||||
chr1:113739552 | C | A | 1 | a0001c0001t0003g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.103-753G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739552 | |||||||
chr1:113739599 | C | A | 4 | a0001c0001t0001g0215 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-800G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739599 | |||||||
chr1:113739665 | C | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0163 others(94): Show |
99 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.103-866G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739665 | |||||||
chr1:113739748 | C | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(5): Show |
8 | HG00741.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-949G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113739748 | |||||||
chr1:113740134 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.103-1335A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740134 | |||||||
chr1:113740136 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(53): Show |
57 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.103-1337A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740136 | |||||||
chr1:113740292 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.103-1493G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740292 | |||||||
chr1:113740442 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.103-1643A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740442 | |||||||
chr1:113740749 | G | A | 4 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(1): Show |
4 | HG01258.hp2 HG01261.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1950C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740749 | |||||||
chr1:113740814 | TGAGGTCA others(1): Show |
T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(53): Show |
57 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.103-2023_103-2016d others(10): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113740814 | |||||||
chr1:113741161 | A | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 |
3 | HG00642.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.103-2362T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113741161 | |||||||
chr1:113741626 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0148 |
2 | HG00733.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.103-2827C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113741626 | |||||||
chr1:113741808 | G | A | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-3009C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113741808 | |||||||
chr1:113742024 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.103-3225A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742024 | |||||||
chr1:113742141 | T | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0196 |
3 | NA18953.hp1 NA18980.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.103-3342A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742141 | |||||||
chr1:113742198 | C | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0010 others(5): Show |
8 | HG00621.hp1 HG01109.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-3399G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742198 | |||||||
chr1:113742454 | G | A | 2 | a0001c0004t0001g0146 a0001c0004t0001g0147 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.103-3655C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742454 | |||||||
chr1:113742681 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.103-3882C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742681 | |||||||
chr1:113742867 | T | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 |
3 | HG02258.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.103-4068A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113742867 | |||||||
chr1:113743128 | T | C | 3 | a0001c0001t0003g0314 a0001c0001t0010g0310 a0001c0001t0010g0311 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-4329A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743128 | |||||||
chr1:113743144 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.103-4345C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743144 | |||||||
chr1:113743238 | T | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0038 a0001c0001t0002g0065 others(2): Show |
6 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-4439A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743238 | |||||||
chr1:113743628 | G | C | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG01081.hp1 HG01257.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.103-4829C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743628 | |||||||
chr1:113743738 | T | C | 3 | a0001c0001t0003g0314 a0001c0001t0010g0310 a0001c0001t0010g0311 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-4939A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743738 | |||||||
chr1:113743753 | C | T | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 |
3 | HG00642.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.103-4954G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743753 | |||||||
chr1:113743784 | C | G | 2 | a0001c0004t0001g0146 a0001c0004t0001g0147 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.103-4985G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113743784 | |||||||
chr1:113744045 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.103-5246C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744045 | |||||||
chr1:113744064 | T | C | 7 | a0001c0001t0001g0193 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG02145.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-5265A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744064 | |||||||
chr1:113744084 | A | T | 3 | a0001c0001t0003g0314 a0001c0001t0010g0310 a0001c0001t0010g0311 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-5285T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744084 | |||||||
chr1:113744143 | T | A | 1 | a0001c0002t0001g0259 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-5344A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744143 | |||||||
chr1:113744593 | T | C | 15 | a0001c0002t0001g0005 a0001c0002t0001g0244 a0001c0002t0001g0245 others(12): Show |
16 | HG01123.hp2 HG02015.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.103-5794A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744593 | |||||||
chr1:113744668 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.103-5869G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744668 | |||||||
chr1:113744743 | G | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG01257.hp1 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.103-5944C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744743 | |||||||
chr1:113744805 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-6006C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744805 | |||||||
chr1:113744807 | G | C | 1 | a0001c0001t0003g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.103-6008C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744807 | |||||||
chr1:113744893 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103-6094C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744893 | |||||||
chr1:113744900 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-6101C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744900 | |||||||
chr1:113744915 | C | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0034 |
2 | NA18942.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.103-6116G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744915 | |||||||
chr1:113744956 | G | A | 5 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(2): Show |
5 | HG01258.hp2 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-6157C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744956 | |||||||
chr1:113744971 | G | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-6172C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744971 | |||||||
chr1:113744994 | G | GGGGAAGG others(7): Show |
1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.103-6209_103-6196d others(16): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113744994 | |||||||
chr1:113745056 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.103-6257T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745056 | |||||||
chr1:113745180 | A | G | 7 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
7 | NA18950.hp2 NA18961.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-6381T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745180 | |||||||
chr1:113745195 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.103-6396C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745195 | |||||||
chr1:113745280 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.103-6481C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745280 | |||||||
chr1:113745354 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0196 |
2 | NA18980.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.103-6555C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745354 | |||||||
chr1:113745658 | G | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.103-6859C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745658 | |||||||
chr1:113745661 | T | G | 1 | a0001c0001t0001g0249 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.103-6862A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745661 | |||||||
chr1:113745697 | C | T | 5 | a0001c0003t0003g0260 a0001c0003t0003g0312 a0001c0003t0003g0313 others(2): Show |
5 | HG00738.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-6898G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745697 | |||||||
chr1:113745714 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.103-6915C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113745714 | |||||||
chr1:113746069 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.103-7270T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113746069 | |||||||
chr1:113746077 | A | T | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-7278T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113746077 | |||||||
chr1:113746125 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-7326C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113746125 | |||||||
chr1:113746215 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.103-7416T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113746215 | |||||||
chr1:113746801 | TA | T | 12 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0181 others(9): Show |
12 | HG03491.hp1 HG03654.hp2 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-8003delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113746801 | |||||||
chr1:113747139 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.103-8340C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113747139 | |||||||
chr1:113747143 | G | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0161 a0001c0001t0001g0210 others(7): Show |
10 | HG00735.hp2 HG01069.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-8344C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113747143 | |||||||
chr1:113747325 | C | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-8526G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113747325 | |||||||
chr1:113747441 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.103-8642A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113747441 | |||||||
chr1:113748046 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18747.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.103-9247G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748046 | |||||||
chr1:113748239 | A | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-9440T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748239 | |||||||
chr1:113748337 | A | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.102+9362T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748337 | |||||||
chr1:113748437 | A | G | 11 | a0001c0001t0002g0033 a0001c0001t0002g0041 a0001c0001t0002g0042 others(8): Show |
11 | HG00423.hp1 HG00597.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.102+9262T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748437 | |||||||
chr1:113748651 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.102+9048C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748651 | |||||||
chr1:113748784 | G | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.102+8915C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113748784 | |||||||
chr1:113749036 | G | A | 3 | a0001c0001t0002g0087 a0001c0001t0002g0097 a0001c0001t0003g0293 |
3 | HG02071.hp2 HG02074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.102+8663C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749036 | |||||||
chr1:113749158 | T | C | 1 | a0001c0001t0004g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.102+8541A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749158 | |||||||
chr1:113749185 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102+8514G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749185 | |||||||
chr1:113749234 | C | A | 1 | a0001c0001t0003g0314 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+8465G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749234 | |||||||
chr1:113749794 | A | G | 17 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(14): Show |
18 | HG00741.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+7905T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749794 | |||||||
chr1:113749922 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.102+7777G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113749922 | |||||||
chr1:113750187 | T | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0163 others(103): Show |
108 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.102+7512A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750187 | |||||||
chr1:113750261 | G | A | 1 | a0001c0006t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.102+7438C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750261 | |||||||
chr1:113750266 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(53): Show |
57 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.102+7433G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750266 | |||||||
chr1:113750418 | C | T | 1 | a0001c0002t0001g0282 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102+7281G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750418 | |||||||
chr1:113750466 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.102+7233A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750466 | |||||||
chr1:113750625 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.102+7074T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750625 | |||||||
chr1:113750822 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.102+6877G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750822 | |||||||
chr1:113750844 | C | CA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(68): Show |
73 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.102+6854dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750844 | |||||||
chr1:113750844 | CA | C | 12 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0001t0001g0300 others(9): Show |
12 | HG01255.hp2 HG02083.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+6854delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750844 | |||||||
chr1:113750904 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.102+6795C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750904 | |||||||
chr1:113750965 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.102+6734T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113750965 | |||||||
chr1:113751235 | G | C | 1 | a0001c0001t0005g0323 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.102+6464C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113751235 | |||||||
chr1:113751412 | T | C | 1 | a0001c0004t0001g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.102+6287A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113751412 | |||||||
chr1:113751958 | T | C | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.102+5741A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113751958 | |||||||
chr1:113752239 | CTAAG | C | 5 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0283 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+5456_102+5459d others(6): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752239 | |||||||
chr1:113752385 | A | AT | 61 | a0001c0001t0001g0021 a0001c0001t0001g0102 a0001c0001t0001g0103 others(58): Show |
62 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+5313dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752385 | |||||||
chr1:113752385 | A | ATT | 7 | a0001c0001t0001g0210 a0001c0001t0002g0025 a0001c0001t0002g0080 others(4): Show |
7 | HG01243.hp2 HG02145.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+5312_102+5313d others(4): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752385 | |||||||
chr1:113752385 | AT | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0111 a0001c0001t0001g0112 others(86): Show |
91 | HG00099.hp2 HG00597.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.102+5313delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752385 | |||||||
chr1:113752385 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.102+5302_102+5313d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752385 | |||||||
chr1:113752430 | C | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0169 others(79): Show |
84 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.102+5269G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752430 | |||||||
chr1:113752432 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.102+5267A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752432 | |||||||
chr1:113752530 | A | AGCTGGGA others(8): Show |
227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.102+5168_102+5169i others(17): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752530 | |||||||
chr1:113752816 | G | A | 161 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0101 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.102+4883C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752816 | |||||||
chr1:113752860 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.102+4839A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113752860 | |||||||
chr1:113753410 | T | A | 2 | a0001c0001t0010g0310 a0001c0001t0010g0311 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.102+4289A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113753410 | |||||||
chr1:113753426 | CT | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.102+4272delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113753426 | |||||||
chr1:113753486 | T | C | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+4213A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113753486 | |||||||
chr1:113753510 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+4189G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113753510 | |||||||
chr1:113753544 | CAGCCCCC others(5): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+4143_102+4154d others(14): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113753544 | |||||||
chr1:113754042 | T | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0101 others(237): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.102+3657A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754042 | |||||||
chr1:113754148 | T | A | 102 | a0001c0001t0001g0299 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
105 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.102+3551A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754148 | |||||||
chr1:113754148 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(57): Show |
61 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.102+3551A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754148 | |||||||
chr1:113754155 | A | C | 2 | a0001c0004t0001g0146 a0003c0009t0001g0317 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.102+3544T>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754155 | |||||||
chr1:113754230 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01891.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.102+3469C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754230 | |||||||
chr1:113754410 | C | CA | 56 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(53): Show |
57 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.102+3288dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754410 | |||||||
chr1:113754449 | T | G | 1 | a0001c0001t0002g0076 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.102+3250A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754449 | |||||||
chr1:113754873 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.102+2826G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113754873 | |||||||
chr1:113755153 | T | A | 102 | a0001c0001t0001g0299 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
105 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.102+2546A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755153 | |||||||
chr1:113755272 | T | A | 4 | a0001c0002t0001g0244 a0001c0002t0001g0245 a0001c0002t0001g0280 others(1): Show |
4 | HG01123.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2427A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755272 | |||||||
chr1:113755692 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102+2007A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755692 | |||||||
chr1:113755750 | T | C | 11 | a0001c0002t0001g0005 a0001c0002t0001g0251 a0001c0002t0001g0252 others(8): Show |
12 | HG02015.hp1 NA18950.hp1 NA18956.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+1949A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755750 | |||||||
chr1:113755798 | T | G | 102 | a0001c0001t0001g0299 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
105 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.102+1901A>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755798 | |||||||
chr1:113755887 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.102+1812G>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755887 | |||||||
chr1:113755896 | TA | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(160): Show |
167 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.102+1802delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755896 | |||||||
chr1:113755936 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102+1763C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113755936 | |||||||
chr1:113756066 | C | CA | 13 | a0001c0001t0001g0168 a0001c0001t0001g0247 a0001c0001t0001g0248 others(10): Show |
13 | HG00140.hp2 HG02129.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.102+1632dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756066 | |||||||
chr1:113756288 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102+1411G>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756288 | |||||||
chr1:113756290 | T | A | 3 | a0001c0001t0003g0314 a0001c0001t0010g0310 a0001c0001t0010g0311 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.102+1409A>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756290 | |||||||
chr1:113756337 | T | C | 11 | a0001c0002t0001g0005 a0001c0002t0001g0251 a0001c0002t0001g0252 others(8): Show |
12 | HG02015.hp1 NA18950.hp1 NA18956.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+1362A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756337 | |||||||
chr1:113756637 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.102+1062C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756637 | |||||||
chr1:113756807 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.102+892T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756807 | |||||||
chr1:113756894 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0022 others(78): Show |
83 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.102+805C>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113756894 | |||||||
chr1:113757096 | G | C | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102+603C>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113757096 | |||||||
chr1:113757190 | C | A | 1 | a0003c0009t0001g0317 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102+509G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113757190 | |||||||
chr1:113757448 | C | A | 3 | a0001c0001t0003g0314 a0001c0001t0010g0310 a0001c0001t0010g0311 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.102+251G>T | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113757448 | |||||||
chr1:113757653 | A | G | 6 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0321 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+46T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 3/18 | chr1 | 113757653 | |||||||
chr1:113757877 | T | C | 1 | a0001c0003t0003g0260 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.46-122A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113757877 | |||||||
chr1:113758041 | A | G | 7 | a0001c0001t0003g0006 a0001c0001t0003g0290 a0001c0001t0003g0291 others(4): Show |
8 | HG00735.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-286T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758041 | |||||||
chr1:113758231 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(77): Show |
81 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.45+427dupT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758231 | C | CAA | 14 | a0001c0001t0001g0113 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
14 | HG01070.hp2 HG01433.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+426_45+427dupTT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758231 | C | CAAA | 12 | a0001c0001t0001g0156 a0001c0001t0003g0314 a0001c0001t0005g0319 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+425_45+427dupTT others(1): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758231 | C | CAAAA | 58 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0022 others(55): Show |
60 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+424_45+427dupTT others(2): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758231 | C | CAAAAA | 25 | a0001c0001t0002g0024 a0001c0001t0002g0080 a0001c0001t0002g0081 others(22): Show |
26 | HG00621.hp2 HG00735.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+423_45+427dupTT others(3): Show |
PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758231 | CA | C | 18 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(15): Show |
18 | HG00621.hp1 HG00741.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+427delT | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758231 | |||||||
chr1:113758270 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(55): Show |
59 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.45+389T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758270 | |||||||
chr1:113758514 | C | CT | 52 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0119 others(49): Show |
52 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+144dupA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758514 | |||||||
chr1:113758514 | C | CTT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(11): Show |
15 | HG00597.hp1 HG01081.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+143_45+144dupAA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758514 | |||||||
chr1:113758514 | CT | C | 27 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0299 others(24): Show |
27 | HG00621.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.45+144delA | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758514 | |||||||
chr1:113758641 | A | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | NA18747.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.45+18T>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758641 | |||||||
chr1:113758644 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45+15T>C | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758644 | |||||||
chr1:113758647 | T | C | 1 | a0001c0002t0007g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+12A>G | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 2/18 | chr1 | 113758647 | |||||||
chr1:113758942 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-31+81C>A | PHTF1 | ENSG00000116793.16 | transcript | ENST00000369604.6 | protein_coding | 1/18 | chr1 | 113758942 |