Item | Value |
---|---|
geneid | 84295 |
ensemblid | ENSG00000156531.18 |
hgncid | 18145 |
symbol | PHF6 |
name | PHD finger protein 6 |
refseq_nuc | NM_001015877.2 |
refseq_prot | NP_001015877.1 |
ensembl_nuc | ENST00000370803.8 |
ensembl_prot | ENSP00000359839.4 |
mane_status | MANE Select |
chr | chrX |
start | 134373312 |
end | 134428790 |
strand | + |
ver | v1.2 |
region | chrX:134373312-134428790 |
region5000 | chrX:134368312-134433790 |
regionname0 | PHF6_chrX_134373312_134428790 |
regionname5000 | PHF6_chrX_134368312_134433790 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1095 | 281 | 58 | 51 | 135 | 9 | 28 | PHF6_chrX_134368312_134433790 | PHF6 | ATGTC others(1090): Show |
chrX | 134368312 | 134433790 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4432 | 102 | 20 | 19 | 50 | 1 | 12 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4427): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0002 | 0/0 | 4430 | 96 | 15 | 17 | 48 | 4 | 12 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4425): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0003 | 0/0 | 4431 | 34 | 2 | 2 | 27 | 2 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4426): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0004 | 0/0 | 4431 | 32 | 20 | 10 | 0 | 0 | 2 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4426): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0005 | 0/0 | 4430 | 12 | 0 | 2 | 7 | 2 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4425): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0006 | 0/0 | 4431 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4426): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0007 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4425): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0008 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4426): Show |
chrX | 134368312 | 134433790 |
a0001c0001t0009 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | AAGGG others(4425): Show |
chrX | 134368312 | 134433790 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0005 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0208 | EUR | GBR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0123 | EUR | GBR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0223 | EUR | FIN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | FIN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | CHS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0218 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01975 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0221 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0236 | SAS | STU | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | STU | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18941 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | LWK | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | LWK | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | YRI | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0109 | EUR | TSI | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | GIH | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | USA | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | USA | PHF6_chrX_134368312_134433790 | PHF6 | chrX | 134368312 | 134433790 |
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 |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:134426091 | A | AT | 2 | a0001c0001t0001 a0001c0001t0004 |
134 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*440dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 771 | INFO_REALIGN_3_PRIME | chrX | 134426091 | |||||
chrX:134426271 | A | G | 2 | a0001c0001t0005 a0001c0001t0009 |
13 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*611A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 941 | chrX | 134426271 | ||||||
chrX:134426556 | T | C | 1 | a0001c0001t0007 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 1226 | chrX | 134426556 | ||||||
chrX:134427062 | A | AT | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(1): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1411dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 1742 | INFO_REALIGN_3_PRIME | chrX | 134427062 | |||||
chrX:134427114 | C | A | 1 | a0001c0001t0009 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 1784 | chrX | 134427114 | ||||||
chrX:134427212 | G | A | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(1): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1552G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 1882 | chrX | 134427212 | ||||||
chrX:134428174 | C | T | 1 | a0001c0001t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2514C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 2844 | chrX | 134428174 | ||||||
chrX:134428767 | T | C | 1 | a0001c0001t0006 | 2 | NA18941.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3107T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 11/11 | 3437 | chrX | 134428767 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:134373706 | A | AG | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-47+244dupG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134373706 | ||||||
chrX:134373785 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47+318G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134373785 | |||||||
chrX:134374244 | T | TA | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-47+783dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134374244 | ||||||
chrX:134374461 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-47+994T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134374461 | |||||||
chrX:134375192 | C | A | 5 | a0001c0001t0003g0008 a0001c0001t0003g0027 a0001c0001t0003g0028 others(2): Show |
6 | HG02027.hp1 NA18940.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+1725C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134375192 | |||||||
chrX:134376281 | AT | A | 1 | a0001c0001t0002g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-46-1283delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134376281 | ||||||
chrX:134376542 | C | CT | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-1023dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134376542 | ||||||
chrX:134376916 | G | A | 1 | a0001c0001t0006g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-46-656G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134376916 | |||||||
chrX:134376921 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0245 |
3 | HG02572.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-46-651A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134376921 | |||||||
chrX:134376922 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-46-650C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134376922 | |||||||
chrX:134376930 | GT | G | 1 | a0001c0001t0002g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-46-638delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134376930 | ||||||
chrX:134377233 | TTATC | T | 1 | a0001c0001t0004g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-46-329_-46-326del others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 134377233 | ||||||
chrX:134377327 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-245C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134377327 | |||||||
chrX:134377480 | A | T | 1 | a0001c0001t0003g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-46-92A>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 1/10 | chrX | 134377480 | |||||||
chrX:134377958 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(209): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.139-47G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 2/10 | chrX | 134377958 | |||||||
chrX:134377981 | AT | A | 1 | a0001c0001t0002g0031 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.139-16delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 134377981 | ||||||
chrX:134378628 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+522C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134378628 | |||||||
chrX:134379054 | GCGTT | G | 2 | a0001c0001t0003g0109 a0001c0001t0003g0241 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.240+949_240+952del others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134379054 | |||||||
chrX:134379055 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(119): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.240+949C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134379055 | |||||||
chrX:134379427 | CTTTTCTT others(1): Show |
C | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.240+1326_240+1333d others(10): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379427 | CTTTTCTT others(2): Show |
C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01496.hp1 HG01934.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+1326_240+1334d others(11): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379427 | CTTTTCTT others(3): Show |
C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
68 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.240+1326_240+1335d others(12): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379427 | CTTTTCTT others(4): Show |
C | 40 | a0001c0001t0001g0015 a0001c0001t0001g0116 a0001c0001t0001g0117 others(37): Show |
47 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.240+1326_240+1336d others(13): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379427 | CTTTTCTT others(5): Show |
C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(11): Show |
15 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.240+1326_240+1337d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379427 | CTTTTCTT others(6): Show |
C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.240+1326_240+1338d others(15): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379427 | ||||||
chrX:134379432 | C | CT | 2 | a0001c0001t0002g0108 a0001c0001t0004g0240 |
2 | HG02109.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.240+1353dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379432 | ||||||
chrX:134379432 | CT | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.240+1353delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379432 | ||||||
chrX:134379432 | CTT | C | 6 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
6 | HG02280.hp2 HG02683.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+1352_240+1353d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379432 | ||||||
chrX:134379433 | T | TTTTC | 1 | a0001c0001t0002g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.240+1330_240+1331i others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134379433 | ||||||
chrX:134380028 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.240+1922G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134380028 | |||||||
chrX:134380149 | C | CT | 21 | a0001c0001t0001g0026 a0001c0001t0001g0139 a0001c0001t0001g0140 others(18): Show |
21 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+2060dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134380149 | ||||||
chrX:134380149 | CT | C | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.240+2060delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134380149 | ||||||
chrX:134380169 | CAG | C | 1 | a0001c0001t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.240+2066_240+2067d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134380169 | ||||||
chrX:134380238 | C | G | 1 | a0001c0001t0004g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.240+2132C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134380238 | |||||||
chrX:134380297 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.240+2191T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134380297 | |||||||
chrX:134380810 | A | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+2704A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134380810 | |||||||
chrX:134381149 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.240+3043G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381149 | |||||||
chrX:134381180 | C | T | 8 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(5): Show |
8 | HG01496.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.240+3074C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381180 | |||||||
chrX:134381213 | C | T | 33 | a0001c0001t0001g0112 a0001c0001t0003g0004 a0001c0001t0003g0008 others(30): Show |
39 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.240+3107C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381213 | |||||||
chrX:134381495 | A | AT | 2 | a0001c0001t0001g0201 a0001c0001t0002g0098 |
2 | HG00438.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.240+3405dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134381495 | ||||||
chrX:134381495 | AT | A | 39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.240+3405delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134381495 | ||||||
chrX:134381643 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.240+3537T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381643 | |||||||
chrX:134381673 | T | G | 1 | a0001c0001t0004g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.240+3567T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381673 | |||||||
chrX:134381711 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.240+3605G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381711 | |||||||
chrX:134381750 | C | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0092 a0001c0001t0002g0093 others(4): Show |
10 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.240+3644C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134381750 | |||||||
chrX:134382560 | ATTC | A | 2 | a0001c0001t0004g0236 a0001c0001t0004g0237 |
2 | HG01993.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.240+4460_240+4462d others(5): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134382560 | ||||||
chrX:134382566 | C | CT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(80): Show |
93 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.240+4479dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134382566 | ||||||
chrX:134382566 | C | CTT | 32 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0111 others(29): Show |
38 | HG00423.hp2 HG01361.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.240+4478_240+4479d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134382566 | ||||||
chrX:134382566 | CT | C | 9 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(6): Show |
9 | HG01099.hp1 HG01255.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+4479delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134382566 | ||||||
chrX:134382569 | T | C | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.240+4463T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134382569 | |||||||
chrX:134382606 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.240+4500T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134382606 | |||||||
chrX:134382947 | CAAGAT | C | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.240+4847_240+4851d others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134382947 | ||||||
chrX:134383066 | AC | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
10 | HG00408.hp1 HG00558.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+4964delC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134383066 | ||||||
chrX:134383242 | C | CA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(81): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.240+5147dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134383242 | ||||||
chrX:134383242 | CA | C | 1 | a0001c0001t0003g0137 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.240+5147delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134383242 | ||||||
chrX:134383305 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.240+5199G>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134383305 | |||||||
chrX:134383768 | C | A | 1 | a0001c0001t0002g0051 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.240+5662C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134383768 | |||||||
chrX:134384385 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.240+6279C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384385 | |||||||
chrX:134384515 | A | AC | 6 | a0001c0001t0001g0149 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
6 | HG00544.hp1 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+6413dupC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134384515 | ||||||
chrX:134384520 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.240+6414G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384520 | |||||||
chrX:134384634 | C | CTTCT | 9 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0149 others(6): Show |
9 | HG00544.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+6547_240+6550d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134384634 | ||||||
chrX:134384634 | CTTCT | C | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.240+6547_240+6550d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134384634 | ||||||
chrX:134384634 | CTTCTTTC others(5): Show |
C | 83 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(80): Show |
98 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.240+6539_240+6550d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134384634 | ||||||
chrX:134384675 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.240+6569G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384675 | |||||||
chrX:134384691 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.240+6585G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384691 | |||||||
chrX:134384744 | T | C | 1 | a0001c0001t0004g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.240+6638T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384744 | |||||||
chrX:134384807 | G | A | 4 | a0001c0001t0003g0123 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG00140.hp1 HG01361.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+6701G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384807 | |||||||
chrX:134384808 | C | T | 4 | a0001c0001t0003g0123 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG00140.hp1 HG01361.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+6702C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384808 | |||||||
chrX:134384809 | T | G | 4 | a0001c0001t0003g0123 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG00140.hp1 HG01361.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+6703T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384809 | |||||||
chrX:134384812 | T | C | 4 | a0001c0001t0003g0123 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG00140.hp1 HG01361.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+6706T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384812 | |||||||
chrX:134384813 | G | A | 4 | a0001c0001t0003g0123 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG00140.hp1 HG01361.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+6707G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384813 | |||||||
chrX:134384842 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.240+6736G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384842 | |||||||
chrX:134384843 | C | G | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.240+6737C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384843 | |||||||
chrX:134384853 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.240+6747G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384853 | |||||||
chrX:134384902 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.240+6796T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384902 | |||||||
chrX:134384930 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.240+6824C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384930 | |||||||
chrX:134384942 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.240+6836C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134384942 | |||||||
chrX:134385730 | C | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(144): Show |
166 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.240+7624C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134385730 | |||||||
chrX:134385996 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.241-7505A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134385996 | |||||||
chrX:134386035 | A | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0122 |
2 | NA18962.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.241-7466A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134386035 | |||||||
chrX:134386142 | C | CA | 1 | a0001c0001t0001g0151 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.241-7353dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134386142 | ||||||
chrX:134386414 | A | AT | 25 | a0001c0001t0002g0097 a0001c0001t0004g0005 a0001c0001t0004g0054 others(22): Show |
28 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.241-7071dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134386414 | ||||||
chrX:134386414 | A | ATT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(120): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.241-7072_241-7071d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134386414 | ||||||
chrX:134386414 | A | ATTT | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241-7073_241-7071d others(5): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134386414 | ||||||
chrX:134386713 | G | T | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241-6788G>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134386713 | |||||||
chrX:134387045 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.241-6456A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387045 | |||||||
chrX:134387083 | TA | T | 1 | a0001c0001t0002g0101 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.241-6414delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134387083 | ||||||
chrX:134387107 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.241-6394G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387107 | |||||||
chrX:134387413 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.241-6088T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387413 | |||||||
chrX:134387452 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.241-6049T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387452 | |||||||
chrX:134387659 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
5 | HG02572.hp1 HG02922.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-5842G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387659 | |||||||
chrX:134387704 | G | A | 1 | a0001c0001t0008g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.241-5797G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387704 | |||||||
chrX:134387949 | T | C | 1 | a0001c0001t0004g0211 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.241-5552T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387949 | |||||||
chrX:134387989 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.241-5512G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134387989 | |||||||
chrX:134388121 | T | A | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5380T>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134388121 | |||||||
chrX:134388336 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.241-5165C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134388336 | |||||||
chrX:134388426 | T | C | 3 | a0001c0001t0004g0052 a0001c0001t0004g0054 a0001c0001t0004g0103 |
3 | HG02886.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.241-5075T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134388426 | |||||||
chrX:134388599 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.241-4902G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134388599 | |||||||
chrX:134388694 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.241-4807C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134388694 | |||||||
chrX:134389163 | C | T | 33 | a0001c0001t0001g0112 a0001c0001t0003g0004 a0001c0001t0003g0008 others(30): Show |
39 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.241-4338C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134389163 | |||||||
chrX:134389442 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.241-4059A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134389442 | |||||||
chrX:134390016 | T | TATAAAG | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.241-3481_241-3480i others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134390016 | ||||||
chrX:134390487 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.241-3014A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134390487 | |||||||
chrX:134390812 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.241-2689C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134390812 | |||||||
chrX:134390966 | C | CT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(73): Show |
85 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.241-2525dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134390966 | ||||||
chrX:134390976 | T | TTC | 2 | a0001c0001t0001g0026 a0001c0001t0001g0183 |
2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.241-2525_241-2524i others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134390976 | |||||||
chrX:134390977 | C | CT | 3 | a0001c0001t0003g0030 a0001c0001t0004g0219 a0001c0001t0005g0230 |
3 | HG00738.hp1 HG01884.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.241-2510dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134390977 | ||||||
chrX:134390977 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0183 |
3 | HG03834.hp1 NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.241-2524C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134390977 | |||||||
chrX:134390977 | CT | C | 1 | a0001c0001t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.241-2510delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134390977 | ||||||
chrX:134390978 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.241-2523T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134390978 | |||||||
chrX:134391051 | C | T | 39 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(36): Show |
46 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.241-2450C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134391051 | |||||||
chrX:134391189 | GTCTTGAA others(1): Show |
G | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241-2309_241-2302d others(10): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134391189 | ||||||
chrX:134391216 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.241-2285C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134391216 | |||||||
chrX:134391233 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241-2268C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134391233 | |||||||
chrX:134392270 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.241-1231T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134392270 | |||||||
chrX:134392570 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
5 | HG02572.hp1 HG02922.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-931C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134392570 | |||||||
chrX:134392698 | C | G | 7 | a0001c0001t0004g0217 a0001c0001t0004g0233 a0001c0001t0004g0234 others(4): Show |
7 | HG00639.hp1 HG01261.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-803C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134392698 | |||||||
chrX:134392801 | A | AT | 8 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
8 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.241-683dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134392801 | ||||||
chrX:134392801 | AT | A | 15 | a0001c0001t0001g0153 a0001c0001t0002g0034 a0001c0001t0002g0036 others(12): Show |
18 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-683delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 134392801 | ||||||
chrX:134393449 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.241-52A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 3/10 | chrX | 134393449 | |||||||
chrX:134393676 | ATACT | A | 1 | a0001c0001t0004g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.374+44_374+47delAC others(2): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 134393676 | ||||||
chrX:134393710 | A | G | 7 | a0001c0001t0002g0226 a0001c0001t0005g0022 a0001c0001t0005g0053 others(4): Show |
8 | NA18939.hp1 NA18949.hp2 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.374+76A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 4/10 | chrX | 134393710 | |||||||
chrX:134393756 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.374+122A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 4/10 | chrX | 134393756 | |||||||
chrX:134394086 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+134A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134394086 | |||||||
chrX:134394133 | C | CT | 2 | a0001c0001t0002g0040 a0001c0001t0003g0247 |
2 | HG03098.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.418+196dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134394133 | ||||||
chrX:134394156 | C | T | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+204C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134394156 | |||||||
chrX:134394543 | G | GT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0141 a0001c0001t0001g0182 others(5): Show |
8 | HG00558.hp2 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.418+604dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134394543 | ||||||
chrX:134394756 | G | GTCTTGAT others(1): Show |
1 | a0001c0001t0001g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.418+811_418+818dup others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134394756 | ||||||
chrX:134394796 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.418+844C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134394796 | |||||||
chrX:134394834 | C | T | 2 | a0001c0001t0003g0109 a0001c0001t0003g0241 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.418+882C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134394834 | |||||||
chrX:134394863 | C | CT | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.418+923dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134394863 | ||||||
chrX:134394914 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+962A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134394914 | |||||||
chrX:134395286 | C | CT | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.418+1337dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134395286 | ||||||
chrX:134395335 | CT | C | 1 | a0001c0001t0004g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.418+1386delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134395335 | ||||||
chrX:134395505 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+1553T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134395505 | |||||||
chrX:134395756 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0087 |
4 | NA18945.hp1 NA18955.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+1804C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134395756 | |||||||
chrX:134395769 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+1817C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134395769 | |||||||
chrX:134396053 | G | GT | 1 | a0001c0001t0001g0120 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.418+2108dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134396053 | ||||||
chrX:134396132 | C | G | 1 | a0001c0001t0002g0042 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.418+2180C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134396132 | |||||||
chrX:134396598 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.418+2646C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134396598 | |||||||
chrX:134396885 | T | TA | 32 | a0001c0001t0001g0191 a0001c0001t0002g0055 a0001c0001t0002g0073 others(29): Show |
38 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.418+2949dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134396885 | ||||||
chrX:134396885 | T | TAA | 1 | a0001c0001t0003g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+2948_418+2949d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134396885 | ||||||
chrX:134396885 | TA | T | 2 | a0001c0001t0001g0180 a0001c0001t0004g0213 |
2 | HG02895.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.418+2949delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134396885 | ||||||
chrX:134397114 | AT | A | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+3166delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134397114 | ||||||
chrX:134397406 | TG | T | 1 | a0001c0001t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.418+3457delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134397406 | ||||||
chrX:134397519 | C | T | 1 | a0001c0001t0004g0211 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+3567C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134397519 | |||||||
chrX:134398016 | A | G | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+4064A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134398016 | |||||||
chrX:134398025 | G | GA | 1 | a0001c0001t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.418+4075dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134398025 | ||||||
chrX:134398213 | C | A | 5 | a0001c0001t0001g0116 a0001c0001t0001g0143 a0001c0001t0001g0154 others(2): Show |
5 | NA18951.hp1 NA18964.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+4261C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134398213 | |||||||
chrX:134398296 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.418+4344A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134398296 | |||||||
chrX:134398458 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(123): Show |
142 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.418+4506A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134398458 | |||||||
chrX:134399652 | T | TACAC | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(33): Show |
43 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.418+5714_418+5717d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399652 | ||||||
chrX:134399652 | T | TACACAC | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.418+5712_418+5717d others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399652 | ||||||
chrX:134399652 | TACACAC | T | 1 | a0001c0001t0003g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.418+5712_418+5717d others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399652 | ||||||
chrX:134399664 | C | CACACAG | 1 | a0001c0001t0001g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.418+5718_418+5723d others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399664 | ||||||
chrX:134399670 | G | GAC | 1 | a0001c0001t0004g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.418+5732_418+5733d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399670 | ||||||
chrX:134399674 | CACACACA others(5): Show |
C | 7 | a0001c0001t0004g0217 a0001c0001t0004g0233 a0001c0001t0004g0234 others(4): Show |
7 | HG00639.hp1 HG01261.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+5734_418+5745d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399674 | ||||||
chrX:134399686 | G | GAC | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0004g0035 |
3 | HG02922.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.418+5756_418+5757d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134399686 | ||||||
chrX:134399825 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.418+5873G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134399825 | |||||||
chrX:134399864 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.418+5912C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134399864 | |||||||
chrX:134400016 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+6064G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400016 | |||||||
chrX:134400085 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.418+6133A>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400085 | |||||||
chrX:134400119 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+6167C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400119 | |||||||
chrX:134400120 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.418+6168G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400120 | |||||||
chrX:134400206 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.418+6254G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400206 | |||||||
chrX:134400304 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.418+6352T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400304 | |||||||
chrX:134400390 | C | CT | 10 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0181 others(7): Show |
12 | HG01175.hp2 HG01346.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.418+6462dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134400390 | ||||||
chrX:134400390 | CT | C | 32 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(29): Show |
36 | HG00639.hp1 HG01123.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.418+6462delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134400390 | ||||||
chrX:134400655 | C | T | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+6703C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400655 | |||||||
chrX:134400672 | C | G | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+6720C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400672 | |||||||
chrX:134400729 | A | C | 1 | a0001c0001t0004g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.418+6777A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134400729 | |||||||
chrX:134401070 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(2): Show |
6 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+7118C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134401070 | |||||||
chrX:134401968 | G | A | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+8016G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134401968 | |||||||
chrX:134401974 | T | TTTTG | 1 | a0001c0001t0002g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.418+8050_418+8053d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134401974 | ||||||
chrX:134401974 | TTTTG | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(127): Show |
147 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.418+8050_418+8053d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134401974 | ||||||
chrX:134402213 | C | G | 1 | a0001c0001t0004g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.418+8261C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402213 | |||||||
chrX:134402283 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.418+8331C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402283 | |||||||
chrX:134402284 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.418+8332G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402284 | |||||||
chrX:134402562 | AT | A | 1 | a0001c0001t0003g0137 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.418+8617delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134402562 | ||||||
chrX:134402569 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+8617T>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402569 | |||||||
chrX:134402582 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.418+8630C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402582 | |||||||
chrX:134402690 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.418+8738C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402690 | |||||||
chrX:134402887 | A | G | 2 | a0001c0001t0004g0210 a0001c0001t0004g0216 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.418+8935A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134402887 | |||||||
chrX:134403018 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+9066G>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403018 | |||||||
chrX:134403359 | T | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.418+9407T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403359 | |||||||
chrX:134403404 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 |
3 | HG00323.hp1 HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.418+9452A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403404 | |||||||
chrX:134403475 | T | G | 1 | a0001c0001t0002g0087 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.418+9523T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403475 | |||||||
chrX:134403615 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.418+9663T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403615 | |||||||
chrX:134403681 | G | T | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.418+9729G>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403681 | |||||||
chrX:134403810 | CTG | C | 1 | a0001c0001t0004g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.419-9679_419-9678d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134403810 | ||||||
chrX:134403888 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.419-9603A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403888 | |||||||
chrX:134403919 | A | G | 70 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(67): Show |
84 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.419-9572A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134403919 | |||||||
chrX:134404117 | A | AT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.419-9373dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134404117 | ||||||
chrX:134404239 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.419-9252C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134404239 | |||||||
chrX:134404267 | C | CT | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.419-9224_419-9223i others(3): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134404267 | |||||||
chrX:134405355 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0071 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.419-8136C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405355 | |||||||
chrX:134405685 | G | A | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-7806G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405685 | |||||||
chrX:134405806 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.419-7685A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405806 | |||||||
chrX:134405807 | T | C | 1 | a0001c0001t0006g0136 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.419-7684T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405807 | |||||||
chrX:134405816 | A | AT | 45 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(42): Show |
52 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.419-7675_419-7674i others(3): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405816 | |||||||
chrX:134405816 | A | ATAT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0019 others(68): Show |
79 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.419-7675_419-7674i others(5): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405816 | |||||||
chrX:134405816 | A | ATATAT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0159 others(6): Show |
10 | HG00621.hp1 HG01496.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.419-7675_419-7674i others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405816 | |||||||
chrX:134405897 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.419-7594G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405897 | |||||||
chrX:134405963 | G | A | 1 | a0001c0001t0008g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.419-7528G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134405963 | |||||||
chrX:134406062 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.419-7429T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406062 | |||||||
chrX:134406062 | T | TTCTCTTT others(1): Show |
1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.419-7428_419-7427i others(10): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTC | 63 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0117 others(60): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.419-7381_419-7378d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTCTTT others(1): Show |
55 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0026 others(52): Show |
62 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.419-7385_419-7378d others(10): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTCTTT others(5): Show |
22 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0147 others(19): Show |
22 | HG00438.hp1 HG00621.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.419-7389_419-7378d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTCTTT others(9): Show |
10 | a0001c0001t0001g0120 a0001c0001t0001g0164 a0001c0001t0001g0201 others(7): Show |
10 | HG01069.hp1 HG02280.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.419-7393_419-7378d others(18): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTCTTT others(13): Show |
3 | a0001c0001t0001g0202 a0001c0001t0002g0070 a0001c0001t0002g0102 |
3 | HG00323.hp1 HG01346.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.419-7397_419-7378d others(22): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | T | TTTTCTTT others(17): Show |
1 | a0001c0001t0001g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.419-7401_419-7378d others(26): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | TTTTC | T | 15 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0176 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.419-7381_419-7378d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | TTTTCTTT others(1): Show |
T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(16): Show |
20 | HG00639.hp1 HG00639.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.419-7385_419-7378d others(10): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | TTTTCTTT others(5): Show |
T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0112 a0001c0001t0002g0058 others(2): Show |
5 | HG02257.hp2 HG02886.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-7389_419-7378d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | TTTTCTTT others(9): Show |
T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0232 |
2 | HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.419-7393_419-7378d others(18): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406062 | TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0002g0083 a0001c0001t0004g0005 |
5 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-7397_419-7378d others(22): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406062 | ||||||
chrX:134406068 | TTC | T | 1 | a0001c0001t0004g0237 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.419-7421_419-7420d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406068 | ||||||
chrX:134406086 | C | CTTTCTTT others(2): Show |
1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.419-7402_419-7394d others(11): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406086 | ||||||
chrX:134406102 | CTTTCTTT others(2): Show |
C | 1 | a0001c0001t0004g0233 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.419-7385_419-7377d others(11): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406102 | ||||||
chrX:134406110 | C | CT | 1 | a0001c0001t0002g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.419-7370dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406110 | ||||||
chrX:134406110 | C | CTTTCT | 2 | a0001c0001t0002g0082 a0001c0001t0003g0135 |
2 | HG02056.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.419-7378_419-7377i others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406110 | ||||||
chrX:134406110 | C | CTTTCTTT others(2): Show |
1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(11): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406110 | ||||||
chrX:134406110 | C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.419-7378_419-7377i others(15): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406110 | ||||||
chrX:134406110 | CTTT | C | 1 | a0001c0001t0001g0178 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.419-7372_419-7370d others(5): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406110 | ||||||
chrX:134406111 | T | TTTC | 1 | a0001c0001t0002g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(5): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406111 | ||||||
chrX:134406111 | T | TTTCTTTC | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.419-7378_419-7377i others(9): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406111 | ||||||
chrX:134406111 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.419-7378_419-7377i others(13): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406111 | ||||||
chrX:134406111 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0002g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(17): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406111 | ||||||
chrX:134406112 | T | TTCTTTC | 2 | a0001c0001t0001g0158 a0001c0001t0003g0186 |
2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.419-7378_419-7377i others(8): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406112 | ||||||
chrX:134406112 | T | TTCTTTCT others(2): Show |
1 | a0001c0001t0002g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(11): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406112 | ||||||
chrX:134406112 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(12): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406112 | ||||||
chrX:134406112 | T | TTCTTTCT others(7): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0163 |
2 | HG00438.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.419-7378_419-7377i others(16): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406112 | ||||||
chrX:134406113 | T | TCTTTC | 1 | a0001c0001t0003g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.419-7378_419-7377i others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406113 | |||||||
chrX:134406113 | T | TCTTTCTT others(6): Show |
1 | a0001c0001t0005g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.419-7378_419-7377i others(15): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406113 | |||||||
chrX:134406113 | T | TCTTTCTT others(10): Show |
1 | a0001c0001t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.419-7378_419-7377i others(19): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406113 | |||||||
chrX:134406114 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.419-7377T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406114 | |||||||
chrX:134406352 | TG | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0128 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.419-7137delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134406352 | ||||||
chrX:134406386 | G | A | 3 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0238 |
3 | HG02886.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419-7105G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406386 | |||||||
chrX:134406839 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0182 others(1): Show |
4 | HG01891.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-6652C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406839 | |||||||
chrX:134406851 | A | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0201 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.419-6640A>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134406851 | |||||||
chrX:134407055 | T | C | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-6436T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407055 | |||||||
chrX:134407238 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.419-6253G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407238 | |||||||
chrX:134407314 | A | G | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-6177A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407314 | |||||||
chrX:134407494 | G | C | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.419-5997G>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407494 | |||||||
chrX:134407585 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-5906T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407585 | |||||||
chrX:134407947 | AT | A | 1 | a0001c0001t0003g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-5540delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134407947 | ||||||
chrX:134407966 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.419-5525C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134407966 | |||||||
chrX:134408088 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.419-5403C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408088 | |||||||
chrX:134408102 | AT | A | 1 | a0001c0001t0003g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-5384delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134408102 | ||||||
chrX:134408195 | TG | T | 1 | a0001c0001t0003g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-5293delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134408195 | ||||||
chrX:134408207 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419-5284C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408207 | |||||||
chrX:134408299 | TC | T | 1 | a0001c0001t0003g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-5189delC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134408299 | ||||||
chrX:134408348 | TA | T | 1 | a0001c0001t0003g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-5139delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134408348 | ||||||
chrX:134408457 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(231): Show |
268 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.419-5034T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408457 | |||||||
chrX:134408560 | C | A | 1 | a0001c0001t0004g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.419-4931C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408560 | |||||||
chrX:134408570 | G | GT | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-4914dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134408570 | ||||||
chrX:134408755 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.419-4736C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408755 | |||||||
chrX:134408943 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.419-4548A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134408943 | |||||||
chrX:134409009 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.419-4482G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409009 | |||||||
chrX:134409079 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.419-4412A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409079 | |||||||
chrX:134409148 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.419-4343G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409148 | |||||||
chrX:134409242 | A | G | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-4249A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409242 | |||||||
chrX:134409269 | T | C | 8 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(5): Show |
8 | HG01496.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-4222T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409269 | |||||||
chrX:134409585 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.419-3906T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409585 | |||||||
chrX:134409593 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.419-3898C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409593 | |||||||
chrX:134409625 | T | TA | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3864dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134409625 | ||||||
chrX:134409654 | CT | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0082 |
2 | NA18953.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.419-3825delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134409654 | ||||||
chrX:134409720 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0068 |
2 | NA18747.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.419-3771T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409720 | |||||||
chrX:134409847 | G | GC | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3642dupC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134409847 | ||||||
chrX:134409935 | CT | C | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3554delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134409935 | ||||||
chrX:134409998 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.419-3493G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134409998 | |||||||
chrX:134410007 | C | CA | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3483dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410007 | ||||||
chrX:134410044 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.419-3447C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410044 | |||||||
chrX:134410075 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
5 | HG02572.hp1 HG02922.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-3416A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410075 | |||||||
chrX:134410128 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.419-3363C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410128 | |||||||
chrX:134410226 | A | C | 1 | a0001c0001t0002g0106 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.419-3265A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410226 | |||||||
chrX:134410275 | C | CT | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3212dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410275 | ||||||
chrX:134410305 | GT | G | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3180delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410305 | ||||||
chrX:134410413 | T | TG | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-3077dupG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410413 | ||||||
chrX:134410580 | AAT | A | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-2910_419-2909d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410580 | |||||||
chrX:134410584 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-2907C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410584 | |||||||
chrX:134410621 | G | GTTTAT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.419-2831_419-2827d others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410621 | ||||||
chrX:134410621 | G | GTTTATTT others(3): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0182 a0001c0001t0001g0187 |
3 | HG01891.hp2 HG03041.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.419-2836_419-2827d others(12): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410621 | ||||||
chrX:134410621 | GTTTAT | G | 61 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(58): Show |
71 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.419-2831_419-2827d others(7): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410621 | ||||||
chrX:134410621 | GTTTATTT others(3): Show |
G | 1 | a0001c0001t0002g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.419-2836_419-2827d others(12): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410621 | ||||||
chrX:134410671 | A | G | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.419-2820A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410671 | |||||||
chrX:134410721 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(244): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.419-2770T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410721 | |||||||
chrX:134410827 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-2664T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410827 | |||||||
chrX:134410848 | A | AC | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-2641dupC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410848 | ||||||
chrX:134410913 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.419-2578C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134410913 | |||||||
chrX:134410955 | C | CT | 18 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0031 others(15): Show |
20 | HG00558.hp1 HG00673.hp1 HG04199.hp1 others(17): Show |
intron_variant | MODIFIER | c.419-2521dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410955 | ||||||
chrX:134410955 | CT | C | 3 | a0001c0001t0001g0146 a0001c0001t0002g0093 a0001c0001t0003g0247 |
3 | HG02004.hp1 HG04115.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.419-2521delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134410955 | ||||||
chrX:134411076 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.419-2415C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134411076 | |||||||
chrX:134411134 | TG | T | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-2355delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134411134 | ||||||
chrX:134411135 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.419-2356G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134411135 | |||||||
chrX:134411219 | TG | T | 1 | a0001c0001t0002g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.419-2269delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134411219 | ||||||
chrX:134411244 | A | AC | 1 | a0001c0001t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.419-2244dupC | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 134411244 | ||||||
chrX:134411414 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.419-2077T>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134411414 | |||||||
chrX:134411882 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-1609G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134411882 | |||||||
chrX:134411975 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.419-1516G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134411975 | |||||||
chrX:134412009 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-1482G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134412009 | |||||||
chrX:134412111 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(121): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.419-1380G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134412111 | |||||||
chrX:134412136 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419-1355G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134412136 | |||||||
chrX:134412993 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.419-498A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134412993 | |||||||
chrX:134413249 | A | C | 29 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0016 others(26): Show |
35 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.419-242A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134413249 | |||||||
chrX:134413346 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0150 others(3): Show |
11 | HG00733.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-145T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 5/10 | chrX | 134413346 | |||||||
chrX:134413730 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.585+73A>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 6/10 | chrX | 134413730 | |||||||
chrX:134414049 | AT | A | 1 | a0001c0001t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.729+93delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 134414049 | ||||||
chrX:134414075 | A | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0128 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.729+109A>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | chrX | 134414075 | |||||||
chrX:134414238 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+272G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | chrX | 134414238 | |||||||
chrX:134414323 | AT | A | 1 | a0001c0001t0004g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.729+359delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 134414323 | ||||||
chrX:134414644 | GA | G | 6 | a0001c0001t0001g0150 a0001c0001t0004g0220 a0001c0001t0004g0232 others(3): Show |
6 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-361delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 134414644 | ||||||
chrX:134414965 | TTCTC | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
26 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.730-48_730-45delTC others(2): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 134414965 | ||||||
chrX:134415005 | T | G | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.730-11T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 7/10 | chrX | 134415005 | |||||||
chrX:134415208 | GA | G | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.834+92delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 134415208 | ||||||
chrX:134415372 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0088 |
4 | NA18948.hp1 NA18959.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+252C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134415372 | |||||||
chrX:134415373 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.834+253G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134415373 | |||||||
chrX:134415632 | C | T | 1 | a0001c0001t0005g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.834+512C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134415632 | |||||||
chrX:134415727 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0088 |
4 | NA18948.hp1 NA18959.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+607A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134415727 | |||||||
chrX:134415746 | T | C | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.834+626T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134415746 | |||||||
chrX:134415783 | AT | A | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.834+666delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 134415783 | ||||||
chrX:134415929 | CATT | C | 1 | a0001c0001t0002g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.834+812_834+814del others(3): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 134415929 | ||||||
chrX:134416070 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.834+950G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416070 | |||||||
chrX:134416092 | TG | T | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.834+975delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 134416092 | ||||||
chrX:134416096 | A | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0174 |
2 | HG00609.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.834+976A>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416096 | |||||||
chrX:134416227 | TG | T | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.835-939delG | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 134416227 | ||||||
chrX:134416241 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.835-928T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416241 | |||||||
chrX:134416277 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.835-892G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416277 | |||||||
chrX:134416353 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.835-816A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416353 | |||||||
chrX:134416379 | A | G | 1 | a0001c0001t0002g0108 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.835-790A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416379 | |||||||
chrX:134416614 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0184 |
2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.835-555A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416614 | |||||||
chrX:134416696 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.835-473A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 8/10 | chrX | 134416696 | |||||||
chrX:134417581 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0245 |
3 | HG02572.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.968+279C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134417581 | |||||||
chrX:134417784 | A | G | 1 | a0001c0001t0004g0237 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.968+482A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134417784 | |||||||
chrX:134418047 | T | C | 1 | a0001c0001t0005g0230 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.968+745T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134418047 | |||||||
chrX:134418236 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.968+934T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134418236 | |||||||
chrX:134418329 | G | A | 4 | a0001c0001t0004g0035 a0001c0001t0004g0052 a0001c0001t0004g0054 others(1): Show |
4 | HG02886.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.968+1027G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134418329 | |||||||
chrX:134418471 | A | G | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.968+1169A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134418471 | |||||||
chrX:134418839 | C | CT | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(41): Show |
51 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.968+1553dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134418839 | ||||||
chrX:134418839 | C | CTT | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.968+1552_968+1553d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134418839 | ||||||
chrX:134418839 | CT | C | 3 | a0001c0001t0001g0153 a0001c0001t0002g0092 a0001c0001t0002g0102 |
3 | HG00323.hp1 HG01943.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.968+1553delT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134418839 | ||||||
chrX:134418840 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.968+1538T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134418840 | |||||||
chrX:134419041 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(149): Show |
171 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.968+1739A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134419041 | |||||||
chrX:134419668 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.968+2366A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134419668 | |||||||
chrX:134419699 | G | A | 1 | a0001c0001t0008g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.968+2397G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134419699 | |||||||
chrX:134419919 | G | A | 1 | a0001c0001t0003g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.968+2617G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134419919 | |||||||
chrX:134420171 | G | A | 10 | a0001c0001t0001g0026 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
10 | HG00408.hp1 HG00558.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.968+2869G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420171 | |||||||
chrX:134420307 | C | CA | 6 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0064 others(3): Show |
6 | HG00438.hp1 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.968+3021dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134420307 | ||||||
chrX:134420307 | CA | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(118): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.968+3021delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134420307 | ||||||
chrX:134420328 | T | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(122): Show |
141 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.968+3026T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420328 | |||||||
chrX:134420332 | T | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(120): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.968+3030T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420332 | |||||||
chrX:134420340 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0016 others(29): Show |
38 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.968+3038A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420340 | |||||||
chrX:134420468 | TA | T | 1 | a0001c0001t0002g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.968+3172delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134420468 | ||||||
chrX:134420529 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.968+3227C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420529 | |||||||
chrX:134420568 | T | TA | 2 | a0001c0001t0002g0084 a0001c0001t0002g0086 |
2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.968+3276dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134420568 | ||||||
chrX:134420661 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.968+3359C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420661 | |||||||
chrX:134420972 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0016 others(29): Show |
38 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.968+3670A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134420972 | |||||||
chrX:134421097 | TA | T | 1 | a0001c0001t0002g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.968+3797delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421097 | ||||||
chrX:134421813 | T | TA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(79): Show |
91 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.969-3374dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421813 | ||||||
chrX:134421813 | T | TAA | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.969-3375_969-3374d others(4): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421813 | ||||||
chrX:134421813 | TA | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0051 |
2 | NA18941.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.969-3374delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421813 | ||||||
chrX:134421916 | G | GT | 1 | a0001c0001t0004g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.969-3279dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421916 | ||||||
chrX:134421919 | TTTTG | T | 29 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0016 others(26): Show |
35 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.969-3258_969-3255d others(6): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421919 | ||||||
chrX:134421919 | TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0005g0230 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.969-3266_969-3255d others(14): Show |
PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134421919 | ||||||
chrX:134421953 | C | A | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.969-3248C>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134421953 | |||||||
chrX:134422160 | C | G | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0110 others(35): Show |
45 | HG00140.hp1 HG00423.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.969-3041C>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134422160 | |||||||
chrX:134422169 | C | T | 1 | a0001c0001t0008g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.969-3032C>T | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134422169 | |||||||
chrX:134422716 | A | AT | 1 | a0001c0001t0004g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.969-2478dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134422716 | ||||||
chrX:134423108 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(76): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.969-2093A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134423108 | |||||||
chrX:134423146 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.969-2055A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134423146 | |||||||
chrX:134423287 | C | CT | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.969-1913dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134423287 | ||||||
chrX:134423558 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.969-1643G>A | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134423558 | |||||||
chrX:134423742 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | NA18951.hp1 NA18968.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.969-1459T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134423742 | |||||||
chrX:134423778 | A | AT | 1 | a0001c0001t0002g0107 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.969-1416dupT | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134423778 | ||||||
chrX:134423853 | T | C | 10 | a0001c0001t0005g0022 a0001c0001t0005g0053 a0001c0001t0005g0208 others(7): Show |
11 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.969-1348T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134423853 | |||||||
chrX:134424111 | T | TA | 2 | a0001c0001t0004g0234 a0001c0001t0004g0240 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.969-1080dupA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 134424111 | ||||||
chrX:134424744 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
5 | HG02572.hp1 HG02922.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.969-457A>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134424744 | |||||||
chrX:134424934 | CA | C | 1 | a0001c0001t0004g0005 | 4 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.969-266delA | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134424934 | |||||||
chrX:134424936 | T | C | 1 | a0001c0001t0004g0005 | 4 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.969-265T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134424936 | |||||||
chrX:134425185 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.969-16T>G | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 9/10 | chrX | 134425185 | |||||||
chrX:134425429 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1098+99T>C | PHF6 | ENSG00000156531.18 | transcript | ENST00000370803.8 | protein_coding | 10/10 | chrX | 134425429 |