SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2288 | snp | C/G | 0.35809 | 0.225425 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172612 | AGGAAGTGTTTAAAG[C/G]AGAGAGATGACCCAT | 84333 |
rs13675 | snp | C/T | 0.198634 | 0.244666 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284101 | TATTTTTTATTTTTG[C/T]GCTCAAATGTATTTT | 84333 |
rs14611 | snp | A/T | 0.225893 | 0.248835 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284172 | GTACTGTTGGGCTAG[A/T]TACTTTTTTTTTTTA | 84333 |
rs1057971 | snp | C/T | 0.206642 | 0.246211 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227753 | CTGGTTTCTGCCTAC[C/T]ACTTCCTCCCCTACC | 84333 |
rs1061292 | snp | A/T | 0 | 0 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278511 | CAAGTGCCATTCTGC[A/T]ACTGAACCATCTGCA | 84333 |
rs2254391 | snp | G/T | 0.498652 | 0.0259235 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258288 | TCCAGAAATGATGTT[G/T]GTATCACTACTTACA | 84333 |
rs2420802 | snp | C/T | 0.388964 | 0.20782 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195532 | GCACCACTGCACTCC[C/T]GTCTGAGTGACAGAG | 84333 |
rs2420803 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195483 | TCTCTCTCTCTCTAT[A/C]TATATATATATGCAT | 84333 |
rs2420804 | snp | A/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195453 | TGCATATATATATAT[A/G/T]CATATATATACATAT | 84333 |
rs2420805 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195452 | GCATATATATATATG[C/T]ATATATATACATATG | 84333 |
rs2421473 | snp | C/T | 0.275464 | 0.2487 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236313 | GAGGATAGTAACTGT[C/T]CATACTATAATCCAT | 84333 |
rs2421482 | snp | A/G | 0.484701 | 0.0861117 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212862 | TCTTTACAAAGAGAG[A/G]AGACATCAAGCTTAA | 84333 |
rs2421483 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206823 | GGACTAAACTGTGCA[A/G]GTAACTGGGGGAAGA | 84333 |
rs2421484 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205361 | GGATTTAGAGTGCCA[C/G]GTCTGACCTGGGGAA | 84333 |
rs2421485 | snp | C/T | 0.102726 | 0.202016 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202316 | ACAATCAGATCACAA[C/T]GGTGGTGGATTCAAA | 84333 |
rs2421486 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201310 | tacatgaagagagac[C/T]tgagctgacacactc | 84333 |
rs2421487 | snp | C/T | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193599 | GGTGGAGGGCCTTTC[C/T]GACCCTATCTCCTAC | 84333 |
rs2450444 | snp | C/T | 0.459574 | 0.136304 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250626 | ATCTGTTGAGTAGTT[C/T]TAACTATATGTTGGA | 84333 |
rs2450445 | snp | C/T | 0.456095 | 0.141508 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278773 | ACTTTTCTAAATATA[C/T]TTCCATACAAAATAA | 84333 |
rs2450446 | snp | C/T | 0.417845 | 0.185278 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245700 | caggcaggcagacag[C/T]gagtacatggtgcag | 84333 |
rs2454532 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253288 | TATTGACTATTATGC[C/T]TATTACCTGGGTGAC | 84333 |
rs2619614 | snp | A/G | 0 | 0 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284137 | ATACAGCTTTGTACA[A/G]AACATTCCATAGATC | 84333 |
rs2631676 | snp | A/G | 0.188316 | 0.242271 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277652 | CAAATCCAAATGTTT[A/G]TTAGTATCAACTGTT | 84333 |
rs2631677 | snp | A/G | 0.288127 | 0.247076 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277853 | GTTGATTTGTGATCT[A/G]GTGGGCTCTCACCAG | 84333 |
rs2631681 | snp | C/T | 0.455263 | 0.142713 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273186 | AGATCATTCTTCTCT[C/T]TATGCAGATAAGGGT | 84333 |
rs2648717 | snp | C/G | 0.187369 | 0.242028 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251984 | GAATCTCCATTTCTG[C/G]TACTGTTTTCCTCTG | 84333 |
rs2648718 | snp | A/C | 0.287606 | 0.247155 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252013 | TGCCTCTGCTAATTG[A/C]ATCTTTCCTTAGAGG | 84333 |
rs2648721 | snp | G/T | 0.297636 | 0.24542 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267239 | CTTAAATAATTTTGC[G/T]TCTACCTCACCTTCT | 84333 |
rs2648725 | snp | A/T | 0.197703 | 0.244469 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255322 | gtcacagccttttga[A/T]gctcctagggacatc | 84333 |
rs2901260 | snp | A/T | 0.472052 | 0.11486 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192083 | GGAAAGAGGATGACA[A/T]AACTATAAAGAAAAA | 84333 |
rs2901436 | snp | A/G | 0.103082 | 0.202275 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204516 | AAACAGGCTGTTTGT[A/G]AAAATGTGCCTGGAA | 84333 |
rs2936565 | snp | G/T | 0.402806 | 0.197864 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253211 | TTTTAGGTTCAGGAG[G/T]ACATGTGCAGGTTTC | 84333 |
rs3068500 | snp | A/C | 0.358303 | 0.225323 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195487 | TCTCTCTCTCTCTCT[A/C]TATATATATATATAT | 84333 |
rs3068529 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195471 | ATANtatatatatat[-/AT]ngcatgcatatatat | 84333 |
rs3074316 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249403 | tatatatatatatat[-/AT]GTATAAAATCTACAC | 84333 |
rs3758498 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279629 | ATTTTAAATCTTTTA[A/G]TATTTACAGTTTTCA | 84333 |
rs3847454 | snp | A/C | 0.417196 | 0.185864 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195485 | TCTCTCTCTCTCTCT[A/C]TATATATATATATGC | 84333 |
rs3858285 | snp | C/G | 0.496874 | 0.0394129 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195372 | TCTTCTAGGAGTCTA[C/G]ACAATGGATAGAAAG | 84333 |
rs3962051 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264884 | AATAACACCTTATCA[A/C]CCATTATCATTTAGG | 84333 |
rs3962086 | snp | C/T | 0.469642 | 0.119404 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179599 | GAACAGAATACCAAA[C/T]GCCACATGTTGTCAC | 84333 |
rs3980701 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264903 | TCCCTTTCCACACCA[A/G]AAATAACACCTTATC | 84333 |
rs3980838 | snp | A/G | 0.460925 | 0.134204 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184901 | TGGGAGTCCCATCCC[A/G]GGGAGTTATGGACCT | 84333 |
rs4278434 | snp | G/T | 0.236724 | 0.249647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262190 | AGCACTTGGGGAGGC[G/T]GAGGCTAGTGGGGTC | 84333 |
rs4297380 | snp | C/T | 0.358515 | 0.225221 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204662 | AAAGAAGGAGAGCTC[C/T]GAGGATAAAAATAGT | 84333 |
rs4300317 | snp | C/G | 0.469839 | 0.119042 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179947 | tccatggtggctgaa[C/G]taatttacaccccta | 84333 |
rs4443989 | snp | A/T | 0.358515 | 0.225221 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205074 | GTAACACAGTTTAGG[A/T]TGCTAATTCTTATGG | 84333 |
rs4451623 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262295 | GCCGGGTGTGGTGGC[A/G]GGTGCCTGTATTCTC | 84333 |
rs4462250 | snp | A/G | 0.102726 | 0.202016 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206806 | TTCTCTGCCTGGTAC[A/G]CTCTTCCCCCAGTTA | 84333 |
rs4631787 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275253 | acacaagaaggaaac[A/C]caatgggctaataaa | 84333 |
rs4933205 | snp | A/G | 0.101658 | 0.201233 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198024 | ACAGACAAAAAATAC[A/G]TGCCCTCACAGAGCT | 84333 |
rs4933649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182938 | gttttgagtgaattt[C/T]ttagtcttgagttct | 84333 |
rs4933650 | snp | A/G | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188076 | TGGTGTGCTGCACCC[A/G]TTAACTCCCCCGAAC | 84333 |
rs4933651 | snp | A/G | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198750 | AATTGCCAGGATGAC[A/G]TTTTGGCCTTGTCAT | 84333 |
rs4933652 | snp | C/T | 0.475702 | 0.107512 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205833 | TATCTCTGCTAAAAA[C/T]ACAAAAAGTAGCCAG | 84333 |
rs4933653 | snp | C/T | 0.324382 | 0.238678 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205914 | AGAATTGCTTGAACA[C/T]GGGAGGCTGAGGTGG | 84333 |
rs5786943 | in-del | -/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178396 | TTCTTTTTTTTTTTT[-/T]GAGATAGGGTCTTGC | 84333 |
rs5786944 | in-del | -/A | 0.493154 | 0.0581045 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178767 | TAGTAAAAAAAAAAA[-/A]TGTAATGATGATGAG | 84333 |
rs6583758 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186022 | agtcagccatcttgg[C/T]cgctcccTGCTTCAA | 84333 |
rs6583759 | snp | A/C | 0.282895 | 0.247826 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216813 | CCCCCTACCATTCAT[A/C]CATCATTGATTTTAG | 84333 |
rs6583760 | snp | C/T | 0.245346 | 0.249957 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217260 | ggatggtctcgatct[C/T]ctgaccttgtgacca | 84333 |
rs6583761 | snp | C/T | 0.245061 | 0.249951 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217268 | tcgatctcctgacct[C/T]gtgaccacccgcctc | 84333 |
rs6583762 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255196 | aaaggggcatttgtc[A/C]aaaacaattacaggc | 84333 |
rs7068527 | snp | C/T | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249645 | GGTGGATGAGATCTC[C/T]CTTTTTTAATCTGTA | 84333 |
rs7068817 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233436 | taaaaaaaaataaaG[C/T]GTTGTACTCGGTAGA | 84333 |
rs7069106 | snp | A/C | 0.100588 | 0.200439 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179142 | AACATCTTTTGTATT[A/C]TTCCCATCCTGTCCT | 84333 |
rs7069171 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178954 | TCTCAACATCTTTTG[A/G]gggagcttttagaaa | 84333 |
rs7070119 | snp | A/G | 0.235564 | 0.249583 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237511 | actttgggaggccga[A/G]gtgggcagattactt | 84333 |
rs7070494 | snp | A/G | 0.235564 | 0.249583 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237509 | gcactttgggaggcc[A/G]aagtgggcagattac | 84333 |
rs7070498 | snp | C/T | 0.228253 | 0.249052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258682 | GAGAAGATAGACGTG[C/T]ACATTTATCCCTTTG | 84333 |
rs7071503 | snp | A/G | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225026 | GGATGATGAGAAGAA[A/G]GCACAAACTCTCGCA | 84333 |
rs7074269 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194039 | aagatgcagaaaact[C/T]tgggtggagagatct | 84333 |
rs7074612 | snp | C/T | 0.127599 | 0.217986 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282112 | ATAGAAAAGACTTCA[C/T]TCTATGGGATTTATA | 84333 |
rs7075114 | snp | G/T | 0.236434 | 0.249632 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282494 | atctccaaaaaaaaT[G/T]CAACTCTTGGTCTTG | 84333 |
rs7075893 | snp | C/T | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216856 | TTAGAGTTATAATAT[C/T]CATGGTCATAAAATA | 84333 |
rs7077883 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186522 | TCAGGGAAAAACTTC[A/G]tatatatatgtgtgt | 84333 |
rs7078260 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221419 | CTCAGATATGAAACG[C/G]TTTGCTGAAGGTCAT | 84333 |
rs7078274 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221441 | GAAGGTCATACAGGG[C/G]TAAGGGCCAGAACCC | 84333 |
rs7078976 | snp | A/T | 0.0821764 | 0.185298 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239042 | aaatgtcaccaactt[A/T]ggggtcgctaagggg | 84333 |
rs7080584 | snp | C/G | 0.23786 | 0.254115 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226864 | CATATTTAGACTCTT[C/G]TTACCTACTAATACC | 84333 |
rs7081882 | snp | C/T | 0.499982 | 0.00299515 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177758 | agaccgtcggaaaag[C/T]gcagtattagggtgg | 84333 |
rs7082510 | snp | C/T | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245068 | gagtacagagaggca[C/T]gagtaaaggaccaag | 84333 |
rs7082516 | snp | G/T | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187157 | ATTATCTGAGGACTT[G/T]TAAAAAATACTGGTA | 84333 |
rs7084314 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270451 | ACCCTGTTTAGAATT[C/T]TCAATGTTATGCAAA | 84333 |
rs7085732 | snp | C/G | 0.225893 | 0.248835 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258004 | acatgctacaaaata[C/G]atgaatcttgaaaac | 84333 |
rs7085807 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258314 | CTGGAGATTCTTCCT[A/G]ATTTCTTGACAGATG | 84333 |
rs7086278 | snp | C/T | 0.226779 | 0.248919 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249412 | atatatatatatata[C/T]atatatatgtataAA | 84333 |
rs7087261 | snp | G/T | 0.100231 | 0.200173 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179183 | TTTGGTTTCAAGTCA[G/T]GTACTCTCTATCCTC | 84333 |
rs7088304 | snp | A/G | 0.336702 | 0.234484 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175860 | gggtcttgactcttt[A/G]tccagtttgccagtc | 84333 |
rs7089166 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224972 | CATTTGTTCATTGTT[C/T]TTAATTTTTGGATTC | 84333 |
rs7090340 | snp | C/T | 0.228253 | 0.249052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259015 | TTAGTATTCTGATAA[C/T]TTTTGAGGTTGTGGA | 84333 |
rs7091037 | snp | A/G | 0.0821764 | 0.185298 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282207 | AAGCAACTCTAggcc[A/G]ggcacagtggctcat | 84333 |
rs7092364 | snp | A/C | 0.081446 | 0.184634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247247 | AACACTGTCAAACTG[A/C]TGCAGAGCAATATAG | 84333 |
rs7095990 | snp | A/T | 0 | 0 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221405 | AGCCGAGACCCAGGC[A/T]CAGATATGAAACGGT | 84333 |
rs7096215 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244430 | tgagggacagaatac[C/T]gggcaacaagagcag | 84333 |
rs7096527 | snp | C/T | 0.236724 | 0.249647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180945 | ttgctttgggcagta[C/T]ggccattttcacaat | 84333 |
rs7097620 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177712 | ctccaagccaggtgc[A/G]ggatataatctcctg | 84333 |
rs7098133 | snp | A/G | 0.453818 | 0.144769 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235823 | tcctccttgccttct[A/G]ccttgattgtgaggc | 84333 |
rs7098290 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205793 | tcaggagtttgagac[C/T]agcctggccaacatg | 84333 |
rs7098577 | snp | A/G | 0.473451 | 0.112115 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178164 | TGGGAAAAAACATTG[A/G]CATAACTGTACAGTA | 84333 |
rs7099079 | snp | C/G | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236260 | gctgtgagcagccta[C/G]tcaggctctccagca | 84333 |
rs7100396 | snp | C/T | 0.421842 | 0.181577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187359 | GTGCAGATTTTGTAG[C/T]GATCTGGCAGGCACC | 84333 |
rs7894133 | snp | A/G | 0.248755 | 0.249997 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219419 | TGTGGTATATATACA[A/G]TAATATCCTCCAATG | 84333 |
rs7894606 | snp | A/G | 0.353803 | 0.227431 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206879 | ATGTCACCTAACTAA[A/G]TCCTTCTCTCACCTC | 84333 |
rs7894809 | snp | C/G | 0.353587 | 0.22753 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206786 | CCTTTGCCTTACATT[C/G]TGTATTCTCTGCCTG | 84333 |
rs7894925 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206825 | ttcccccagttacct[A/G]cacagtttagtccct | 84333 |
rs7896934 | snp | G/T | 0.226188 | 0.248863 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276478 | TAGTGTGGTGCCATT[G/T]TATTTCAGAAAACCA | 84333 |
rs7897104 | snp | C/T | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255644 | atatggtaaagaata[C/T]agactttatggaatt | 84333 |
rs7899233 | snp | A/G | 0.414245 | 0.188477 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173180 | AACACACACTGTGAT[A/G]TTTAAGAGCTTAATT | 84333 |
rs7899285 | snp | G/T | 0.475525 | 0.107882 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207822 | caggatagacatttt[G/T]ggcagaaacattaca | 84333 |
rs7900499 | snp | A/C | 0.235564 | 0.249583 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255804 | tatatgttggggatt[A/C]attccaggacccttc | 84333 |
rs7900890 | snp | A/G | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255961 | gcaaatgctatgtaa[A/G]tagttgttaatacta | 84333 |
rs7902517 | snp | A/G | 0.395818 | 0.203069 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186243 | CCTGGATTTTGCCCC[A/G]ACTCTCACAGCTGTG | 84333 |
rs7902531 | snp | A/G | 0.395635 | 0.2032 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186270 | TGTGGTGTACCAGGC[A/G]TTCATTCACCAGTAG | 84333 |
rs7902599 | snp | A/G | 0.496714 | 0.0404017 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186544 | TATGTGTGTGTGTGT[A/G]TATATATATATATAT | 84333 |
rs7902611 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186558 | TATATATATATATAT[A/G]TGTGTGTGTGTGTAT | 84333 |
rs7902729 | snp | C/T | 0.0839998 | 0.186933 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281638 | ACCATGTTGGAGAGA[C/T]GGTTTTAACAGTTTG | 84333 |
rs7902769 | snp | A/G | 0.378372 | 0.214524 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186425 | AAGGTTGGAAGTCTT[A/G]TTGCATTGAACTTTC | 84333 |
rs7903610 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268927 | AAATTTTTTCAGTTC[A/G]TATCAGTATTGCCAC | 84333 |
rs7904027 | snp | A/G | 0.469839 | 0.119042 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174169 | GTTGGATATGAAGTG[A/G]CATGAAGGATTCAGT | 84333 |
rs7904716 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199028 | TTATTGTTTTTGTTC[A/G]GAAACTGAAACTGCA | 84333 |
rs7904724 | snp | A/T | 0.311859 | 0.242226 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168957 | aaaaaaaaaaaaaaa[A/T]AGAAGGCTTGATAAC | 84333 |
rs7905513 | snp | A/G | 0.158962 | 0.232835 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257140 | ccaatttggaaaaag[A/G]caaaaggcttgaata | 84333 |
rs7906291 | snp | A/G | 0.462691 | 0.131387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186755 | CCAATGCCCTGCTCC[A/G]TATATTGATAGGACT | 84333 |
rs7907197 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215211 | ATACATGTAATTACT[C/T]CTCTTCCTTGGATTT | 84333 |
rs7907920 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239718 | AGTAGAAGCTTAGGT[A/G]AAAGATGAGAGAGAT | 84333 |
rs7908053 | snp | A/G | 0.144969 | 0.226867 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174836 | TTTGGTGGATGGAAC[A/G]CATGTGTTTACTGTC | 84333 |
rs7908154 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210085 | TGGGCAATTTCTAAC[A/G]TATAAATGATTTGCA | 84333 |
rs7908601 | snp | A/G | 0.110519 | 0.207473 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175289 | AAAGGTACAATGATC[A/G]ACTGAAAAAGGAATT | 84333 |
rs7908796 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199790 | GGAAGTGGAGTAAAT[A/G]AACAAAGGAGAATAA | 84333 |
rs7909865 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271920 | GAAATGTTAAGGCTA[C/T]TACTTATGAATCAGG | 84333 |
rs7911631 | snp | A/G | 0.393803 | 0.204501 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188445 | AAAATACAATTTTAT[A/G]TATATTAAAATTATG | 84333 |
rs7911817 | snp | A/C | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276665 | CCAAGCATTGCCAGT[A/C]AAGCCATTTTACTTC | 84333 |
rs7912140 | snp | C/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276634 | AAATCATTTTCAGCC[C/G]GAAACTGAGAAAATC | 84333 |
rs7912950 | snp | A/G | 0.228547 | 0.249078 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271525 | GGAAAGTGTTTATTT[A/G]CCATTAATCATGTTG | 84333 |
rs7915050 | snp | C/G | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252528 | TAGGTCTTATACATA[C/G]AAATAGTTAAGGTAA | 84333 |
rs7915347 | snp | A/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276958 | GCTCCCTCCCAGGTA[A/T]TCTGATTCAGGGGGA | 84333 |
rs7917134 | snp | C/G | 0.235273 | 0.249566 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234877 | ggcagtctgcctcaa[C/G]attatctggaacaac | 84333 |
rs7917178 | snp | A/G | 0.100944 | 0.200705 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177203 | CTGGGTATCAGCAGC[A/G]GAGGCTGCAGAACAG | 84333 |
rs7918759 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165284 | AGAAAGTATGTTACT[A/G]TGTAACTTCTGGATG | 84333 |
rs7919504 | snp | A/G | 0.105214 | 0.203807 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195657 | acccaggctagtctc[A/G]aactcctgggctcaa | 84333 |
rs7919961 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278067 | CTCTGCTGCATATTA[C/T]TGAAAACTTGACTGA | 84333 |
rs7920283 | snp | C/T | 0.234692 | 0.249531 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181381 | gccctggccggaact[C/T]tgaatactatgttga | 84333 |
rs7920860 | snp | G/T | 0.228253 | 0.249052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269614 | CATTGGCTAGATTCT[G/T]AGAAGTAGATTTTCA | 84333 |
rs7921621 | snp | C/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265917 | GGCCTTGAAGAACTT[C/G]TCATACATGTTTGTG | 84333 |
rs7921841 | snp | C/G | 0.145305 | 0.227022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178424 | AGATAGGGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 84333 |
rs9651430 | snp | A/G | 0.235273 | 0.249566 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232575 | aagatgtaagtgaaa[A/G]gggacaattacttga | 84333 |
rs9651431 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233844 | AGAAAAAATATGCAT[C/T]TAAGTTGACAGATAA | 84333 |
rs9651432 | snp | A/G | 0.228253 | 0.249052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272544 | ttgggagactgaggc[A/G]ggcagatctcttgag | 84333 |
rs9663247 | snp | C/T | 0.100944 | 0.200705 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182052 | GAAATTTATCAATTT[C/T]TTCTAGATTTTCTAG | 84333 |
rs9665492 | snp | A/G | 0.150667 | 0.229419 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176923 | tcaaagtctttctcc[A/G]tccagctttgttccg | 84333 |
rs10047356 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266529 | TCAGTAGCTATGGTT[C/T]ATCATTCAGGTGGAA | 84333 |
rs10160027 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275836 | tgaactagcagttcc[A/G]cttttaggaatctat | 84333 |
rs10437466 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185136 | ccagacagcaaagat[C/G]gtggcccacccctcc | 84333 |
rs10437467 | snp | A/G | 0.40263 | 0.198 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185432 | acagctccatgcaac[A/G]ctgttgtccgtgcct | 84333 |
rs10437468 | snp | C/T | 0.395635 | 0.2032 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185464 | gctggaattccaagc[C/T]agtgtgtcatcctgt | 84333 |
rs10437469 | snp | A/G | 0.395818 | 0.203069 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185812 | tccctgcttccctgg[A/G]caggggagattccct | 84333 |
rs10437470 | snp | A/G | 0.395635 | 0.2032 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185840 | ccttgactccgtgtg[A/G]ctccctggtgggcca | 84333 |
rs10509623 | snp | C/T | 0.214239 | 0.247429 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212671 | TTCTATAACGCATGC[C/T]CACTAATTCTGTTTG | 84333 |
rs10509624 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261887 | TTGTTTAGCAGTAGA[C/T]ATAACCAACATATTA | 84333 |
rs10559652 | snp | A/T | 0.158962 | 0.232835 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251098 | TTAATAAGTTTCCAA[A/T]TTTTTTTTTTTTTTT | 84333 |
rs10600191 | in-del | -/TTTAT | 0.220544 | 0.248259 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245524 | CAGCCAAGAAGGTTC[-/TTTAT]TTTGTTTTGATATAG | 84333 |
rs10648437 | in-del | -/TT | 0.498525 | 0.0271165 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250913 | TACTTATTTATAAAC[-/TT]GAGTATAATTTATAT | 84333 |
rs10657090 | in-del | -/T/TT | 0.254821 | 0.27323 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217039 | AATGAAAATTTCACC[-/T/TT]CTTTTTTTTTTGAGA | 84333 |
rs10686374 | in-del | -/AT | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274128 | TATGTATATATATAT[-/AT]GTAATAGTACATTAC | 84333 |
rs10705095 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209806 | AAAAAGAAAAACGAA[-/G]AAAGGAATTGGAGGA | 84333 |
rs10736060 | snp | A/C | 0.330016 | 0.236849 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167667 | TAGGACTATATTGTG[A/C]AGCATCTTGAATGCT | 84333 |
rs10736061 | snp | A/G | 0.329783 | 0.236927 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169766 | ATTTTGTAGATATTG[A/G]CAAACTGACTCTAAA | 84333 |
rs10736062 | snp | A/G | 0.110872 | 0.20771 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184231 | TCTCTACATAATCCC[A/G]TATTTCTTGGAGGTT | 84333 |
rs10748558 | snp | A/G | 0.475702 | 0.107512 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207212 | TTTAAGACCACTTTG[A/G]TGAGGGATGTGCAGC | 84333 |
rs10785991 | snp | C/G | 0.0991586 | 0.199366 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162041 | AGGAGCTGAGTCCAA[C/G]AAAGTTTGACAGGTG | 84333 |
rs10785992 | snp | A/G | 0.35809 | 0.225425 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175872 | TTTATCCAGTTTGCC[A/G]GTCTGTGTCTTTTAA | 84333 |
rs10785993 | snp | C/G | 0.356383 | 0.226236 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176295 | GCTGTTAGTCTGATG[C/G]GCTTCCCTTTGTGGG | 84333 |
rs10785994 | snp | C/T | 0.358303 | 0.225323 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178708 | GTTTCTCATTTTAAA[C/T]GTAGTAGTACACTTT | 84333 |
rs10785995 | snp | A/G | 0.408871 | 0.193029 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184467 | CTGCAATGTTTTAGC[A/G]TGATTTTTAGCTTCC | 84333 |
rs10785996 | snp | A/T | 0.472052 | 0.11486 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194742 | ATCACCAAGAGCATA[A/T]GTAGAGATAGAGAAG | 84333 |
rs10785997 | snp | G/T | 0.354665 | 0.227036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206064 | GGTATACCAACATTT[G/T]GGCAAATTTTGGCAA | 84333 |
rs10881893 | snp | A/G | 0.429688 | 0.173817 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167510 | ACTTCAATCGGCAAA[A/G]ATGTAGGGACCAGCC | 84333 |
rs10881894 | snp | C/T | 0.245916 | 0.249967 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168270 | TGGACTTGAGGGAGA[C/T]AGGAGGAGGTAGACA | 84333 |
rs10881895 | snp | C/T | 0.362104 | 0.223456 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178262 | ATTAATAAATCAAGA[C/T]GGCAGTTTAAACATT | 84333 |
rs10881896 | snp | A/G | 0.358303 | 0.225323 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178411 | ttttttttttttgag[A/G]tagggtcttgctctg | 84333 |
rs10881897 | snp | A/C | 0.242488 | 0.249887 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178732 | ACACTTTGAGTTTAA[A/C]CATAATTTTCATGGG | 84333 |
rs10881898 | snp | A/C | 0.488606 | 0.0746142 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181922 | tttcagttttttgga[A/C]tatttccagtaggaa | 84333 |
rs10881900 | snp | G/T | 0.471483 | 0.115954 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188721 | TCTGCCAGAGTCCTC[G/T]GTTATGGAGGTAGTA | 84333 |
rs10881901 | snp | G/T | 0.385932 | 0.209815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199233 | CTTGTCACAGGTTGG[G/T]TTCCCTGGGAAGCTG | 84333 |
rs10881902 | snp | C/T | 0.474 | 0.111014 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200136 | CCTGCATTTTTGCCT[C/T]ACTGTGGGAGAGGGC | 84333 |
rs10881903 | snp | A/G | 0.432357 | 0.171014 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213518 | TGCCCAGGCTGGAGT[A/G]CAATGGCGTGATCTT | 84333 |
rs10881904 | snp | G/T | 0.48491 | 0.0855403 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214972 | CTACTTAAAATTTCA[G/T]ACTTCACTGGTAAAA | 84333 |
rs10881905 | snp | C/T | 0.485324 | 0.0843964 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215276 | GTGATATTGAAATGA[C/T]CTGGTATCAAAGCCT | 84333 |
rs10881907 | snp | A/G | 0.485408 | 0.0841624 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240454 | GCGTTCATATGATGC[A/G]TTTTAACCTAACATC | 84333 |
rs10881908 | snp | A/G | 0.28052 | 0.24813 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253724 | TATTAAGTGTTTTCT[A/G]TACCCTTAATTTTTC | 84333 |
rs10881909 | snp | A/G | 0.228842 | 0.249103 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273256 | ATATCCGAGGTGTAT[A/G]GATGTTTCAGCTGCT | 84333 |
rs11186477 | snp | A/G | 0.236144 | 0.249616 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161457 | GATCAGACAGCGACA[A/G]ACCCACACTACCTAA | 84333 |
rs11186478 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166943 | cagcttaatctctca[A/G]aagtttcagtttttt | 84333 |
rs11186479 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169074 | AGGCTCTCCTCAAGC[A/C]GGAGAGATAGGATAG | 84333 |
rs11186480 | snp | A/G | 0.268995 | 0.249277 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171535 | AGAAAATTGGAAGTA[A/G]AGATGCTGTGAGTAT | 84333 |
rs11186482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175186 | ACCACAAGATGAAGT[C/T]TTTAACAGAGACTGG | 84333 |
rs11186484 | snp | A/G | 0.469642 | 0.119404 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176406 | ggagttgctcttctc[A/G]aggagtatctttgtg | 84333 |
rs11186485 | snp | A/G | 0.473543 | 0.111932 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176945 | tttgttccgttgctg[A/G]tgaggagctgtgttc | 84333 |
rs11186486 | snp | A/G | 0.469544 | 0.119585 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177615 | caatggtgggcgccc[A/G]tcccccagcctcact | 84333 |
rs11186487 | snp | A/C | 0.473543 | 0.111932 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179186 | GGTTTCAAGTCATGT[A/C]CTCTCTATCCTCAGA | 84333 |
rs11186488 | snp | C/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179255 | GAGGAAAGCAAGGGA[C/G]AGACATGGGAGAGGT | 84333 |
rs11186489 | snp | A/T | 0.474903 | 0.109173 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179333 | ATTTGTTTCTTTTTT[A/T]AAAAAAAATTAATCT | 84333 |
rs11186490 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186945 | AAGACCAGTGAAAAT[C/T]GCTAGGCCAGtgatt | 84333 |
rs11186491 | snp | A/C | 0.415235 | 0.18761 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193052 | ttggagagttgtggc[A/C]acagttggaatgatc | 84333 |
rs11186492 | snp | A/C | 0.388964 | 0.20782 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194415 | tggaggaagggggcc[A/C]ctggccaaggaatgt | 84333 |
rs11186493 | snp | C/T | 0.397633 | 0.201754 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194599 | ccactaagtttgtca[C/T]aatttgttatcacag | 84333 |
rs11186494 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195322 | AAAAGAAAATTTAGG[A/G]TGGAATTAGACAGGA | 84333 |
rs11186495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199635 | TCCAAAATATGATGC[A/G]GTATTTTAGTTAAGA | 84333 |
rs11186496 | snp | C/T | 0.474091 | 0.11083 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200327 | CTACTGACCAGGGTT[C/T]TTTATGCTGATTATT | 84333 |
rs11186497 | snp | A/G | 0.381113 | 0.21286 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200358 | AATATCTTCCTACTC[A/G]GTGCCCAAAATTGTT | 84333 |
rs11186498 | snp | A/G | 0.474363 | 0.110278 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200764 | CATTGGACAGTGGGC[A/G]AATTAAGCTTTGGTT | 84333 |
rs11186499 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202118 | tgtactcacccccta[A/G]gattattgtgagaaa | 84333 |
rs11186500 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202371 | CCTAATGATTTCAGT[A/G]AAACCCACCATTGTG | 84333 |
rs11186501 | snp | C/T | 0.471196 | 0.1165 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204720 | AACTCATTATTGCCA[C/T]GTCCTGCCCTTTTTC | 84333 |
rs11186502 | snp | A/G | 0.127944 | 0.218179 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216378 | GAAGAAGACCTATCT[A/G]TCTAGCTAGAGAGTA | 84333 |
rs11186503 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217126 | gcaagttccacctcc[C/T]gggttcacgccattc | 84333 |
rs11186504 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220790 | TTTCCTTCACTCTGA[A/G]GCCGGCGCGCTGGCG | 84333 |
rs11186505 | snp | A/G | 0.291235 | 0.246576 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223151 | CATTGGGTTGCCAGT[A/G]GCATGAAATTTTGCT | 84333 |
rs11186506 | snp | C/T | 0.29175 | 0.246489 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223376 | TTCCTAGACTAGCAG[C/T]ACCAGTGTCATTGCA | 84333 |
rs11186507 | snp | A/G | 0.193966 | 0.243639 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224074 | AATGGTTGAAATGGC[A/G]AATTTTATGTTACAT | 84333 |
rs11186508 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228173 | CTGTCTCTTTCACCA[A/G]GTGACCCTGGTGAAA | 84333 |
rs11186509 | snp | A/G | 0.29175 | 0.246489 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230069 | TTATGTGTATAGTTC[A/G]TTTAGCTTTTGAAAC | 84333 |
rs11186510 | snp | C/T | 0.46885 | 0.12085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231153 | ACTGCAATAGTAACA[C/T]GTGTAGGGTCTACAA | 84333 |
rs11186511 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233469 | AAAATGCTGTCCTTA[A/G]GGTTCTCTGTGAAAT | 84333 |
rs11186512 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234828 | cagaaacacaaagta[A/G]tttgcctaatggcag | 84333 |
rs11186513 | snp | A/C | 0.289165 | 0.246913 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236348 | AGTCCTGAGGCCAAG[A/C]CTGATATTTGGTTAG | 84333 |
rs11186514 | snp | A/G | 0.230896 | 0.249269 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236610 | GCAGTTAGAGAGTTT[A/G]GCATGAAATCTTTAA | 84333 |
rs11186515 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238635 | ttttttttttttGCC[C/T]CTTTCCCAAATTTCA | 84333 |
rs11186516 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238898 | TTTCTTTTTTTAAGG[G/T]TTTCTGATACTGTCT | 84333 |
rs11186517 | snp | A/G | 0.2768 | 0.248559 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245082 | acgagtaaaggacca[A/G]ggattgagccctgga | 84333 |
rs11186518 | snp | A/G | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250699 | TAATAGGTGAAATAC[A/G]TTTGTATATAATATA | 84333 |
rs11186519 | snp | A/C | 0.230037 | 0.250021 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266959 | TCACACAGCAGCCAG[A/C]GTGATCCTCTTAGGA | 84333 |
rs11186520 | snp | G/T | 0.00488995 | 0.0492043 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267391 | TATTTATGTTTATTG[G/T]TTGTCCTCCAAGTAA | 84333 |
rs11186522 | snp | A/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272250 | GATACATTTTAAAAA[A/T]TTGGGAAACAGACAA | 84333 |
rs11186523 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273393 | CTATGTATTTCCTTA[A/G]AAATGAAGATGTCCT | 84333 |
rs11186524 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274556 | CAGAAGTAAAAATGA[A/G]CACAAATCTTTTCTT | 84333 |
rs11186525 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274671 | AAATAGAATAGTTTT[A/G]ATAAGATAGCCAAGA | 84333 |
rs11186526 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277225 | CATAGCTATAGTAAG[C/T]ACTGAAATGGTCATT | 84333 |
rs11186527 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279621 | AAACTGTCATTTTAA[A/G]TCTTTTAATATTTAC | 84333 |
rs11288147 | in-del | -/C | 0.472147 | 0.114677 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197705 | CTCTGTCAACCGGTA[-/C]TGGACATCATCCTCT | 84333 |
rs11370726 | in-del | -/A | 0.234401 | 0.249513 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242419 | ATTTTTATTAAAATA[-/A]AAAAACTGTTAATAA | 84333 |
rs11385471 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236101 | AAATAATAATAAATT[-/A]TAAAAAAATATGATA | 84333 |
rs11392243 | in-del | -/T | 0.232359 | 0.249377 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224495 | AGGAAAACTAATTTT[-/T]AAAAATGCCATATTA | 84333 |
rs11400268 | in-del | -/A | 0.430434 | 0.173042 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270380 | TAGAAAAAAAAAAAA[-/A]GAATCACTTAGTGAA | 84333 |
rs11402069 | in-del | -/A | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237750 | TAAAAAAAAAAAAAA[-/A]TTGCATCAGAAAACC | 84333 |
rs11404081 | in-del | -/A | 0.4711 | 0.116682 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204334 | TCATTTAAAAAAAAA[-/A]CCCTTACATTAGTCT | 84333 |
rs11406829 | in-del | -/A | 0.149312 | 0.228828 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264559 | GTGTTTATTTAGTTA[-/A]TATACCATTATGTTA | 84333 |
rs11541126 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284094 | ATTTGAGCACAAAAA[A/T]AAAAAATATTTAAGG | 84333 |
rs11592412 | snp | A/T | 0.00947846 | 0.0681864 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283121 | AAATGTACAATACAG[A/T]GTTCAATAGTTTTTA | 84333 |
rs11592477 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262280 | aaaatataaaaatta[C/G]ccgggtgtggtggca | 84333 |
rs11593075 | snp | C/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232851 | aggtgtgaaatacta[C/G]caagaagcgtaatgg | 84333 |
rs11593954 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164691 | CAAAGATTAACTTGA[C/T]TCATTCCCACCTCAC | 84333 |
rs11594071 | snp | G/T | 0.469839 | 0.119042 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180276 | ataggttgcaaaaat[G/T]ttctcccattctgta | 84333 |
rs11596146 | snp | A/G | 0.491368 | 0.0651254 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173342 | AGTGAGATTAAGGCA[A/G]TGTGTTTCATGACAA | 84333 |
rs11597409 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240401 | AGTAGGTAGTTTTAA[A/G]GTCTGTTTCTAATTA | 84333 |
rs11597996 | snp | C/T | 0.45692 | 0.1403 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176270 | ttgtagagtttctgc[C/T]gagagatcagctgtt | 84333 |
rs11817842 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228726 | ACTCATGATGCTTTG[A/G]TATTCAATATTTGAA | 84333 |
rs12218424 | snp | C/G | 0.250732 | 0.249999 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199041 | TCAGAAACTGAAACT[C/G]CATCACATACATGCT | 84333 |
rs12218813 | snp | C/T | 0.243633 | 0.249919 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165586 | TCAACCTCCCAGGCT[C/T]AAGTGATCCAATATG | 84333 |
rs12220699 | snp | A/T | 0.471691 | 0.11677 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207801 | atgtttccaaatgat[A/T]atagtcaggatagac | 84333 |
rs12240806 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166971 | TTTCAATCGGAGAAT[A/T]GGTGGTCAGGATGGG | 84333 |
rs12241146 | snp | A/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246127 | agattagtcctaaat[A/T]gggctggaaggacag | 84333 |
rs12241814 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176227 | tttctttaagaatgt[C/T]gaatattggccccca | 84333 |
rs12241950 | snp | A/G | 0.226779 | 0.248919 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243445 | TGACACATGTAGcaa[A/G]aaatttaccttctat | 84333 |
rs12242498 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180534 | gtgtaaggaaggggt[A/C]cagtttcaatcttct | 84333 |
rs12242548 | snp | C/T | 0.226188 | 0.248863 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252102 | GTGTTACTTTAATAA[C/T]GTTTTCTACCTTTTT | 84333 |
rs12242723 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252375 | AAAACAATTTTTCAC[G/T]TCAGATTAAGTTTTC | 84333 |
rs12244087 | snp | C/G | 0.41275 | 0.189769 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186689 | CACCAGTTCCATCCC[C/G]GGCCTCCCTAGATTC | 84333 |
rs12244088 | snp | G/T | 0.412583 | 0.189912 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186690 | ACCAGTTCCATCCCG[G/T]GCCTCCCTAGATTCA | 84333 |
rs12244459 | snp | A/G | 0.228253 | 0.249052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261853 | AGTAATCACATTTCC[A/G]TGAAATGCAGAAGTG | 84333 |
rs12244653 | snp | G/T | 0.081446 | 0.184634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232097 | tcagtgagataggag[G/T]acaatgggaatagta | 84333 |
rs12245179 | snp | C/T | 0.101301 | 0.200969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217855 | gcaatggcgcgatct[C/T]ggctcactgcaacct | 84333 |
rs12245536 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257516 | ttgcaaccacagata[A/G]taccaaataatcctg | 84333 |
rs12247892 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178977 | tttagaaaattcaaa[C/T]gactctcctatctca | 84333 |
rs12249713 | snp | C/G | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259567 | ctacctgacttcaaa[C/G]tattctacaaggcta | 84333 |
rs12249777 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164596 | AGACTAGTTTTTTGA[C/G]GGTTTTTAAAAAGCC | 84333 |
rs12251037 | snp | G/T | 0.227664 | 0.249 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256313 | aaatgaaaattttac[G/T]ggtgaggctcaacag | 84333 |
rs12251417 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164968 | tgttcgctgctataa[C/T]cctagcacctagaac | 84333 |
rs12251527 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164958 | TGGGCTGTTTTGTTC[A/G]CTGCTATAACCCTAG | 84333 |
rs12253178 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206050 | aaaCTAAAAGACATG[A/G]TATACCAACATTTGG | 84333 |
rs12253468 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165854 | GTTTATATTATAAAT[A/C]AACTTTGGAGGCATG | 84333 |
rs12253484 | snp | A/G | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236702 | AGTGAGTTTTGTAGT[A/G]ATGAGAAGTTTTTTA | 84333 |
rs12253956 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261596 | ACTTAGGTAATATGT[A/G]TACTCTAATTGAACA | 84333 |
rs12255565 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167015 | cgatttctaagatct[C/T]gtccagctctATGGT | 84333 |
rs12255656 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166964 | tcagttttttcaatc[A/G]gagaataggtggtca | 84333 |
rs12255787 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167146 | TAGACCTTCTTAAGA[A/G]TTTGTCTAAATTAAC | 84333 |
rs12255971 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225502 | TGGCCTTTATCGTCA[A/G]CAGAGAACACAGAAA | 84333 |
rs12256740 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179892 | gctgggtcgaatggt[A/G]tttctatctttaggt | 84333 |
rs12256743 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179898 | tcgaatggtatttct[A/G]tctttaggtatttga | 84333 |
rs12256855 | snp | C/G/T | 0.00676848 | 0.0578101 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213589 | cctgcctcagcctcc[C/G/T]gagtagctgggatta | 84333 |
rs12256931 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258787 | AACTTCTGTTTTCTT[A/T]TAATGGATATTTTAT | 84333 |
rs12257267 | snp | G/T | 0.145978 | 0.227331 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208117 | TCCCTGGAGATTCTT[G/T]CCTGAATCAATTAAT | 84333 |
rs12257512 | snp | G/T | 0.108048 | 0.20579 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208518 | ctgtggaccctggct[G/T]aagtaacaAAGCTGT | 84333 |
rs12257732 | snp | A/G | 0.081446 | 0.184634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256101 | catacacaggaaaag[A/G]agcagtcaatagaaa | 84333 |
rs12257734 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168143 | GAGCCATTAAAAATA[C/G]AGAAAGATTTGGGGC | 84333 |
rs12259124 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164843 | aatactattttattt[C/T]cttcactgcgcttaa | 84333 |
rs12259394 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174280 | gggaagctaaggtgg[A/G]tggatcacttgaggc | 84333 |
rs12259585 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168760 | agtgaaaccccgtct[C/T]tactaaaaatacaaa | 84333 |
rs12259640 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168851 | gagaatcacatgaat[C/T]tgggaggcggaggtt | 84333 |
rs12259673 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161758 | GAGGTTTGCGGACCT[A/G]TCAGGAGAGCCTCTT | 84333 |
rs12259686 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168797 | gccgagtgtggtggt[A/G]tgtgtctgtaatctc | 84333 |
rs12260816 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275526 | gctcattgcagcctc[C/T]gtctcccaggttcaa | 84333 |
rs12261582 | snp | A/C | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175720 | TAAAAAtatcagaga[A/C]taggattgcaacccc | 84333 |
rs12261600 | snp | G/T | 0.425586 | 0.17796 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166558 | AGTTTTTTTTTAAAG[G/T]CTTAAAACTTGTAAG | 84333 |
rs12263099 | snp | G/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267696 | AGTGACATGGACGAA[G/T]GCAGCAGTATCACTA | 84333 |
rs12264135 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164271 | GGGACGCCCGGAGGG[A/G]CGGGGGAGACTTAGT | 84333 |
rs12264238 | snp | C/T | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252191 | GTCACTTTATCCTAG[C/T]AAATGTCAGCCACTG | 84333 |
rs12265165 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238605 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
rs12265261 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176915 | tcaactcatcaaagt[C/G]tttctccgtccagct | 84333 |
rs12265272 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167736 | CAGAAATATTTTAAA[C/T]GGGGGAATGATGTGA | 84333 |
rs12265514 | snp | A/C | 0.466927 | 0.124269 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177288 | tctcagaggggtacc[A/C]ggctgtgtgaggcgt | 84333 |
rs12265704 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168448 | ATCGTCAGTAGCCTT[C/T]GAGGAACAGAGTCAG | 84333 |
rs12266301 | snp | A/C | 0.226779 | 0.248919 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230351 | CAAGGGTTCAATATA[A/C]GCATTATAAACAATT | 84333 |
rs12267158 | snp | G/T | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248307 | agagctggggactgg[G/T]accatttttgttatc | 84333 |
rs12267225 | snp | A/G | 0.234982 | 0.249549 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248420 | TGTATTTTGTAACAT[A/G]TATAAGATTATACAT | 84333 |
rs12267809 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178615 | ggctggtctcaaacc[C/G]ctgggccagccagtc | 84333 |
rs12268274 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166135 | cttgcctaaggtaca[A/G]ggcaagagtcagaac | 84333 |
rs12268373 | snp | A/C | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254076 | TATTCAAGGCCCTTC[A/C]CTAACAAGCACCTCT | 84333 |
rs12416166 | snp | A/C | 0.415235 | 0.18761 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193269 | ccaaaaggaatacat[A/C]cctgctgtcacttgg | 84333 |
rs12416484 | snp | A/G | 0.415563 | 0.18732 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193915 | atatgtgttaaagac[A/G]aagtccatttctttg | 84333 |
rs12416527 | snp | A/G | 0.415235 | 0.18761 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194195 | ccagaaaatgtgaat[A/G]tgtcactttagggag | 84333 |
rs12416675 | snp | A/G | 0.459574 | 0.136304 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178955 | CTCAACATCTTTTGG[A/G]GGAGCTTTTAGAAAA | 84333 |
rs12569746 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180245 | agatgctggatatta[A/G]acatttgtcagatgc | 84333 |
rs12767642 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220391 | ATATGCCAGTCATTG[G/T]TATGATGTAAACAAC | 84333 |
rs12768356 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222481 | attagtatagaggtg[A/G]tagttgaggttccag | 84333 |
rs12768855 | snp | C/T | 0.389715 | 0.207315 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189246 | TTTTCCAGACATCCT[C/T]TCTTGACCCTCATGA | 84333 |
rs12772334 | snp | A/C | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221078 | CTCGCTCTCCCCGGC[A/C]TGAGCAgcgcgcccg | 84333 |
rs12772455 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213987 | ttgggctcttaattc[A/T]gtaagactcatgtcc | 84333 |
rs12772535 | snp | A/G | 0.336245 | 0.234652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177689 | cgaggctccataggc[A/G]taggaccctccaagc | 84333 |
rs12773006 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186594 | tgtgtgtgtatatat[A/G]tgtgtatatatacac | 84333 |
rs12773193 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186611 | gtgtatatatacaca[C/T]atatatatgtaACAA | 84333 |
rs12773528 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186586 | tatatatatgtgtgt[A/G]tatatatatgtgtat | 84333 |
rs12773541 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186598 | TGTGTATATATATGT[A/G]TATATATACACACAT | 84333 |
rs12773770 | snp | C/T | 0.337841 | 0.23406 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200122 | GAGATGCTAACTTCC[C/T]TGCATTTTTGCCTCA | 84333 |
rs12774655 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186605 | ATATATGTGTATATA[C/T]ACACACATATATATG | 84333 |
rs12774904 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231750 | gatttatgtttaaag[A/G]aatcactcagactac | 84333 |
rs12775660 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181097 | ttagctattttatta[A/T]ttttatggcaattgt | 84333 |
rs12775958 | snp | C/T | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253360 | tcaagtagggcctca[C/T]gtctgttgttctctt | 84333 |
rs12778694 | snp | A/G | 0.41507 | 0.187755 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197465 | GGCTTCCTGTGGTCC[A/G]GGCATTGTGCTAAGT | 84333 |
rs12778743 | snp | G/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227027 | TGGTTTACATGGCTG[G/T]GAGATAATTTTAATA | 84333 |
rs12781768 | snp | C/G | 0.46974 | 0.119223 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174970 | GTGGCAACTGCCTTA[C/G]TATAACAGAGGAAGT | 84333 |
rs12783854 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272482 | agacaaaaaaaaaTT[A/T]TTTTTTTAggccaga | 84333 |
rs12784538 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, intron-variant | PCGF5 | GRCh38.p7 | 10:91163075 | ATCGTGGCCTCTCGA[C/G]AGCAAGGTAAGGGCG | 84333 |
rs12785109 | snp | C/T | 0.448836 | 0.15154 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172001 | GATAAGGAAGTTGTT[C/T]CTTTATTTTAAAGAT | 84333 |
rs17106346 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179196 | CATGTACTCTCTATC[C/G]TCAGATCTGAACTAG | 84333 |
rs17106376 | snp | C/T | 0.135825 | 0.222405 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189065 | GTGGCTGCAGGAATA[C/T]AGGTGTGGAGAAGGT | 84333 |
rs17106383 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192294 | TAACTCAACAACTCA[A/C]GGTGTTTTGCTCGTA | 84333 |
rs17106432 | snp | C/T | 0.145305 | 0.227022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209192 | ACATAATTTCATTTA[C/T]TCATCTGTTACCTGA | 84333 |
rs17106435 | snp | A/G | 0.213937 | 0.247385 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211778 | TCACACTGTGTTCAA[A/G]GGATAGTGAGAAGCC | 84333 |
rs28398010 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177675 | GTGCTAGCAATGAGC[A/G]AGGCTCCATAGGCGT | 84333 |
rs28459398 | snp | C/T | 0.235564 | 0.249583 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233529 | AAACGTGCCAATATA[C/T]GGCACATTATGTAAT | 84333 |
rs28661426 | snp | C/T | 0.225301 | 0.248777 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233464 | AGAAGAAAATGCTGT[C/T]CTTAGGGTTCTCTGT | 84333 |
rs28709025 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206845 | GTTTAGTCCCTTACC[C/T]CATTCAGATCTGTGC | 84333 |
rs28843493 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260585 | ACAACGATAAACTGG[A/G]TTAAGAAAATGTGGC | 84333 |
rs34014288 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161536 | TCATGTCTACTTTTT[-/T]CATGATTTACTCTAT | 84333 |
rs34077206 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217904 | GATTCTCCTGCCTCA[-/C]GCCTCCCTAGTAGCT | 84333 |
rs34110278 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169358 | TTTGAAGATGACATG[-/C]ATTGTTTATGTAGAA | 84333 |
rs34169133 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224153 | GCTATTTAAGCATAC[A/G]CATGCTCAGGACCCT | 84333 |
rs34241298 | in-del | -/GTT | 0.236144 | 0.249616 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244928 | CAGAGAAGAGAGGAA[-/GTT]GGTAAGTGGATATAT | 84333 |
rs34258478 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199235 | GTCACAGGTTGGTTT[-/C]CCCTGGGAAGCTGAC | 84333 |
rs34265849 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235634 | ACTCCCACAATTTCC[-/C]ATGTGTTGTGGGAGG | 84333 |
rs34328644 | snp | A/G | 0.125874 | 0.217008 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234358 | ATGCATAATAGAAAA[A/G]CATTGGTCAATCTTG | 84333 |
rs34333335 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241731 | CTCTGGAACCTTTCA[-/A]TAACTCTCTTATCTG | 84333 |
rs34362692 | in-del | -/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282234 | CATGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC | 84333 |
rs34387066 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170845 | TCATAATTGCCAAAA[-/A]CTTGGAAGCAACCAA | 84333 |
rs34400681 | in-del | -/G | 0.227664 | 0.249 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257494 | GTTCCAAGACCCCCA[-/G]GGGATGTTGCAACCA | 84333 |
rs34447873 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185842 | TGACTCCGTGTGGCT[-/C]CCCTGGTGGGCCATC | 84333 |
rs34524616 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219316 | CCAATCACATTTAAG[-/C]CCCCTGGACTCCACT | 84333 |
rs34586205 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208480 | TGCATTCCTAACAAG[-/C]ATCCCTGCTGATGCT | 84333 |
rs34602274 | in-del | -/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281796 | TTTTCTTGCAATAAT[-/T]CAGAACACACTTCCT | 84333 |
rs34661087 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174509 | GAGACTGTCTCAAAA[A/G]ACAAAAAACTGTATT | 84333 |
rs34663905 | snp | A/G | 0.15665 | 0.231917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241224 | GGATTACAGGCATGC[A/G]CCACCACATTAATTT | 84333 |
rs34667308 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178152 | GCAATGTAGGCTGGG[-/A]AAAAAACATTGACAT | 84333 |
rs34701688 | in-del | -/ATATAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195482 | CATGCATATATATAT[-/ATATAG]AGAGAGAGAGAGAGA | 84333 |
rs34708998 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222283 | AACTTGGTTTGACTC[-/A]GTAACTGGATGAAGG | 84333 |
rs34771310 | snp | G/T | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253326 | TTTCAATCCTGTCTC[G/T]CCCCCTACCATTCCA | 84333 |
rs34772046 | in-del | -/TT | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251114 | TTTTTTTTTTTTTTT[-/TT]ACAAAATATTTCCAT | 84333 |
rs34786802 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263143 | GCTGCCTAGTATGCA[A/G]GGGGATTATTTAATG | 84333 |
rs34864359 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195285 | GCTATCACCTCCTTC[-/A]AAAAAAAAAAAGTCA | 84333 |
rs34865625 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252883 | AAAATTAACCACCCC[-/C]TGCTTGTTGTTCTCC | 84333 |
rs34867819 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91163380 | CTCTTCCCCAGAGGG[-/G]CGCCTTCCAGTCCTG | 84333 |
rs34885640 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250613 | GTATGATGTGTATCC[-/C]AACATATAGTTAGAA | 84333 |
rs34906871 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168082 | TATTGGTTTGGATTT[-/TG]GGATGTGTTAACTTG | 84333 |
rs34912755 | in-del | -/A | 0.261608 | 0.24973 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275308 | AGCAGTCAAGAAATG[-/A]AAAAAAAATACTATC | 84333 |
rs34957059 | in-del | -/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217040 | TCACCTTTTTTTTTT[-/T]GAGACAGAGTCTCTC | 84333 |
rs34966513 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228480 | TATGGCAGTAATCCC[-/C]TAACCTAAGAATAAA | 84333 |
rs34970816 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214742 | ATGATAACCAGAACA[-/G]GGGAGAAAGTTAATG | 84333 |
rs35084214 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269246 | AAATTGAGGATGCAG[-/G]AATTACAGAATCAGA | 84333 |
rs35112413 | snp | A/G | 0.160609 | 0.233472 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229831 | GCCAAAATAGAAATT[A/G]TATTTATCATCTCAG | 84333 |
rs35222869 | snp | A/C | 0.127944 | 0.218179 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271446 | GCTAAAATTACTTCA[A/C]GCTAAATTTTACCAG | 84333 |
rs35281303 | in-del | -/G | 0.422315 | 0.181128 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185208 | CCAGAAAACACCAGT[-/G]GGGGTGGCTGGAGGC | 84333 |
rs35284280 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170662 | TTTATTACTAGTGGG[-/G]AATGTCAAACAGTAC | 84333 |
rs35287131 | in-del | -/T | 0.465578 | 0.126594 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213472 | TTTCATTAAAAAAAA[-/T]TTTTTTTTTAAGATG | 84333 |
rs35288148 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170226 | TTGGTGATGACTTTT[-/T]AGATATGACATCATA | 84333 |
rs35304810 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182326 | TCAATTTCTTCTAGA[-/T]TTTTTTAGTTTATAA | 84333 |
rs35323355 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173598 | TTTTTTTTTTTTCCC[-/C]ACAGAAGCCATGAGT | 84333 |
rs35340206 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264890 | ATTAATGGTTGATAA[-/A]GGGTGTTTATTTTTG | 84333 |
rs35347329 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166077 | CAGTTCATTCCTTTT[-/T]AATCAATCCCTTCAC | 84333 |
rs35436177 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274466 | GTATTTCAAATTAAT[-/T]GCAGTAAAATGATTA | 84333 |
rs35472532 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186530 | AACTTCATATATATA[-/TG]TGTGTGTGTGTGTAT | 84333 |
rs35514090 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232508 | TTAGGGGGTTCTTTT[-/T]GAGCTGGGGAAATAT | 84333 |
rs35536495 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244091 | GACAGTCAATAAACC[-/C]ATATAATAAGTAATT | 84333 |
rs35552285 | snp | G/T | 0.127599 | 0.217986 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253619 | CGTCATCTTTGATCT[G/T]TTACTCTTTTCTTTC | 84333 |
rs35590053 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255043 | AGAGGTAGAGCTTTT[-/T]CAAAGCCTCATTGCC | 84333 |
rs35609498 | snp | A/G | 0.112916 | 0.209065 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271745 | TCATGACACCATGGC[A/G]GTGAGCACATTCATC | 84333 |
rs35684938 | in-del | -/AAAG | 0.236724 | 0.249647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263315 | ATTTACAAAAAAGAT[-/AAAG]AAAAATGAAATTATC | 84333 |
rs35699267 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231892 | GGTAAATTCATATTT[-/T]GCTAATGAATTGTAT | 84333 |
rs35720089 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246337 | GAGAGTACAGAGAGT[A/G]TTTGAGCCAGGATGT | 84333 |
rs35771688 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274426 | CTCAGCAACAGACCC[-/C]TAGTATGTATGAGTC | 84333 |
rs35807368 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166743 | AATAAGTAGAGCTTT[-/T]CCACAGCAAGTTACT | 84333 |
rs35809931 | in-del | -/TG | 0.348134 | 0.229934 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195636 | AGATGAGGTTCTCAC[-/TG]TGTTACCCAGGCTAG | 84333 |
rs35818406 | snp | C/G | 0.234109 | 0.249494 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237040 | ACATACATTGGTTAA[C/G]AAAATGGATTCAAAT | 84333 |
rs35832595 | snp | A/C | 0.169435 | 0.236663 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229767 | TAAATTGAACTTTAC[A/C]ATAATGTATTCTTAA | 84333 |
rs35843976 | snp | C/T | 0.235854 | 0.249599 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248026 | AGTCTAAAATGGCCT[C/T]AGCAGGGCAGCTTGG | 84333 |
rs35848051 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253603 | AAGTTCAAAAGCTTC[A/G]CGTCATCTTTGATCT | 84333 |
rs35901255 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166377 | GTTGGATAAATGGGT[-/G]TTTAAGTTGAAAATA | 84333 |
rs35923503 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266584 | CTACCTTTTACATTT[-/T]AGTGCAACAGTAAAG | 84333 |
rs35953673 | snp | A/C/G | 0.00716625 | 0.0594738 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264843 | ATGTATATGGAATGG[A/C/G]AGTGGGGGAAACTTA | 84333 |
rs35981490 | snp | C/T | 0.130351 | 0.219509 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259598 | CAGTAACCAAAACAG[C/T]ATGGTACTGGTACCA | 84333 |
rs35984384 | snp | A/G | 0.159292 | 0.232964 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224298 | AATTAGCAATTAACT[A/G]TGTACTATCTTGTAT | 84333 |
rs35996590 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224921 | AGCATGGAACCTGGA[C/G]CCAGTCCACAGTGTG | 84333 |
rs36034505 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205634 | ACTTTATGCCAGATT[-/C]CCTTGCCCTGCATCG | 84333 |
rs36056371 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235060 | CTGGAATGGGCACCC[-/C]TAACGATGGTACTAG | 84333 |
rs36111039 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274886 | GTAGGGCTTATTTTT[-/T]AATTAATTATACTGA | 84333 |
rs41286926 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264257 | GCATAGTAACAGTAT[A/G/T]TAAGTAACATATCCA | 84333 |
rs41286928 | snp | A/G | 0.039522 | 0.134904 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279369 | ACATTTCCAAACTAT[A/G]TGCATAAAATAGAAT | 84333 |
rs55763028 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197773 | CACTTTCATTTTGTT[A/G]TATTAAATTTCAATT | 84333 |
rs55816144 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209802 | AAAAAAAAAGAAAAA[A/C]GAAGAAAGGAATTGG | 84333 |
rs55837500 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242563 | TGTTTAATCAAACCC[A/G]CTCCCTTGGCTAAAG | 84333 |
rs55858066 | in-del | -/AC | 0.451483 | 0.148002 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205290 | CACACACACACACAC[-/AC]GGCCCAGCTAACATG | 84333 |
rs55909211 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221680 | CTTAGGAAAATCAAC[A/G]CCTTTCATGTTGTGT | 84333 |
rs56018537 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275486 | TTGCTCTGTTGCCAG[A/G]CTGGAATGCAGTGGT | 84333 |
rs56060706 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243041 | CTTTGACAGCTGGGA[G/T]AGCTCCTCATGATAG | 84333 |
rs56288334 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250512 | TTTTTTTTTTTTTTT[-/TT]TAGCTTGCCTTTATT | 84333 |
rs56693041 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277414 | TTCATTTTAAGAGAG[A/G]GTATCTACAGCTTTA | 84333 |
rs56896057 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195940 | CACTATTGTGGGCAA[C/G]TGGGACCTGTTCCCA | 84333 |
rs57050045 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221738 | TAAAAAAAAAAAAAA[-/A]CCTGAGACAGGAAAG | 84333 |
rs57152340 | snp | G/T | 0.199873 | 0.244923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193303 | CTGGCCTTGTGAGAC[G/T]AAGTAGAGGACCCAG | 84333 |
rs57232402 | snp | A/G | 0.00331291 | 0.0405645 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248501 | TTTCTCCCCCCTTTC[A/G]AAGGTTGGACAATAC | 84333 |
rs57318884 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197381 | GATGGCTGCACAGAC[A/G]TATATCTTTGGAAAA | 84333 |
rs57345364 | in-del | -/AA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168957 | AAAAAAAAAAAAAAA[-/AA]GAAGGCTTGATAACA | 84333 |
rs57550882 | in-del | -/A | 0.119978 | 0.213528 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181433 | TCCTTGTCTTGTGCC[-/A]AGTTTTCAAGGGGAA | 84333 |
rs57588243 | snp | G/T | 0.120326 | 0.21374 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173252 | ATTTGGTGGGGGATT[G/T]GTTTAGGCCCTTGAA | 84333 |
rs57633765 | in-del | -/GA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195508 | AGAGAGAGAGAGAGA[-/GA]CGCAGGGTCTCTGTC | 84333 |
rs57685367 | in-del | -/GT | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186586 | TATATATATGTGTGT[-/GT]ATATATATGTGTATA | 84333 |
rs58253030 | in-del | -/CTTTCTTTCTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238604 | TTTCTTTCTTTCTTT[-/CTTTCTTTCTT]TTTTTTTTTTTTTTT | 84333 |
rs58364744 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194088 | GAGGTCAGCTTGGAC[A/G]TACTGAGTGTGACAT | 84333 |
rs58400368 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250912 | TATACTTATTTATAA[A/T]CGAGTATAATTTATA | 84333 |
rs58795240 | in-del | -/ATATATATATAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249409 | TATATATATATATAT[-/ATATATATATAT]GTATAAAATCTACAC | 84333 |
rs58885299 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210169 | GGCCCCCACCTGTCT[G/T]CTGGGAGATTTGGAT | 84333 |
rs59147432 | snp | G/T | 0.119978 | 0.213528 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176101 | GCTCTTGTAGGGCAG[G/T]CCTGGTGGTGAAAAA | 84333 |
rs59254639 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173579 | CTAGAGGGAGTTGGC[-/T]TTTTTTTTTTTTTTT | 84333 |
rs59280736 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189880 | GTAGTTTTGAAAGGT[C/T]TTCCTCAACCATGTG | 84333 |
rs59475903 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249394 | ATATATATATATATA[C/T]ATATATATATATATA | 84333 |
rs59576804 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213026 | TTATACTTCCTAAGC[A/G]CTGCTCGTCTGTATC | 84333 |
rs59619411 | snp | C/T | 0.244205 | 0.249933 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165166 | TTTTCTTTTGATTCA[C/T]TTTCTGCTCTGTGAT | 84333 |
rs59663942 | snp | G/T | 0.030665 | 0.119967 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203376 | TTTTATTAGGATCCA[G/T]ATTCTATGAAGTTAG | 84333 |
rs59684573 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275626 | TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG | 84333 |
rs59837538 | snp | C/T | 0.119978 | 0.213528 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179769 | GGGCATTTAGTTTGA[C/T]TCCATGTCTTTGCTA | 84333 |
rs59862992 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167162 | TTTGTCTAAATTAAC[-/T]TTTATGATAAGTACA | 84333 |
rs59899683 | snp | A/G/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213714 | TGGTCTCAAACTCCC[A/G/T]ACCTCAGAGAGGTCC | 84333 |
rs59977249 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241055 | TCATATATATATATA[-/TA]ATATATATTTTATTT | 84333 |
rs59986921 | snp | A/C | 0.0792508 | 0.182605 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167496 | AAAAAATTGAGACGA[A/C]TTCAATCGGCAAAAA | 84333 |
rs60146527 | in-del | -/AAGTGA | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232775 | TTTCAGTAAAATAGA[-/AAGTGA]GGTCCTCAGTGGAGA | 84333 |
rs60196419 | in-del | -/CAAA | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199793 | AGTGGAGTAAATAAA[-/CAAA]GGAGAATAAATTTTA | 84333 |
rs60438346 | snp | G/T | 0.15698 | 0.23205 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183555 | TAATTGGGGCATTTA[G/T]CCCATTTGCATTTAA | 84333 |
rs60498216 | in-del | -/AG | 0.474363 | 0.110278 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200389 | CAACTAATCTAGTTA[-/AG]AGAGAGTGAGGGTAT | 84333 |
rs60596674 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254745 | TGGGATGTCAATAAA[A/G]AGAGTAGAGTAAGTA | 84333 |
rs60879476 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276116 | TTTTGAAAAAAAAAA[-/A]CGAATGTAGATAAAA | 84333 |
rs60974693 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212965 | CTATATGAAGAAATA[C/G]CATCTTCAAAGGATA | 84333 |
rs61008064 | in-del | -/ATTTT | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245527 | CCAAGAAGGTTCTTT[-/ATTTT]GTTTTGATATAGGAG | 84333 |
rs61046503 | in-del | -/GTT/TTG | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244929 | AGAGAAGAGAGGAAG[-/GTT/TTG]GTAAGTGGATATATG | 84333 |
rs61218065 | in-del | -/GT | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240152 | TTTTTATCTTTTTCT[-/GT]CCTACTTCTTTAAAT | 84333 |
rs61279719 | snp | A/G | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277412 | ATTTCATTTTAAGAG[A/G]GAGTATCTACAGCTT | 84333 |
rs61310014 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215492 | CTTCTCCTTAGGAGG[C/G]TGTCAGGTCTGATCT | 84333 |
rs61356648 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195486 | ATATATATATATATA[-/TA]GAGAGAGAGAGAGAG | 84333 |
rs61629471 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178767 | TTTGATTAAAAATAG[G/T]AAAAAAAAAAATGTA | 84333 |
rs61857950 | snp | A/G | 0.0681886 | 0.171594 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161603 | TCTCTGTAGAATTCA[A/G]TTTTATTCCTCAAGG | 84333 |
rs61857951 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164088 | ATCGCCCCGCGGACC[A/G]GGCCCCGATGATTCA | 84333 |
rs61857952 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164778 | TACTCAGCCAGGCCT[C/T]CTTGATCGCCTTCAT | 84333 |
rs61857953 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167848 | GAGAAATGATGAGAA[C/T]CTAAATTAGGGTGGA | 84333 |
rs61857954 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177003 | TTTAGAATTTTCAGT[A/T]TTTCTGCTCTGTTTT | 84333 |
rs61860167 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214325 | AAAAAAAAAAAAAAG[A/G]AGAGACAGACAGACA | 84333 |
rs61860168 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225378 | ATGACAGTTTAACTG[C/T]ACATGTCATCCTAGC | 84333 |
rs61860169 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226461 | CTCAGGCAGATAGTA[G/T]CCCTTGAGTAGTGGT | 84333 |
rs61875620 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237758 | AAAAAAAAAAAAAAT[A/T]GCATCAGAAAACCTG | 84333 |
rs61875621 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246965 | GATAGATGGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
rs61875622 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246969 | GATGGATAGATGGAT[A/G]GATAGATAGATAGAT | 84333 |
rs61875623 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246977 | GATGGATAGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
rs61875624 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260033 | GTGAACAGGCAACCT[A/G]CAGAATGGGAGAAAA | 84333 |
rs61875625 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260504 | TGCTATAAAGACACA[G/T]GCACACATATGTTTA | 84333 |
rs61875626 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282212 | ACTCTAGGCCGGGCA[C/T]AGTGGCTCATGCCTG | 84333 |
rs61875627 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282250 | AGCACTTTGGGAGGC[C/T]AAGGCAGGTGGATCA | 84333 |
rs61875628 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282256 | TTGGGAGGCCAAGGC[A/T]GGTGGATCACTTGAG | 84333 |
rs66464812 | snp | C/T | 0.127944 | 0.218179 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273467 | AAATTTCTAAATCCA[C/T]ACAAATTTCCTCTTC | 84333 |
rs66465569 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226290 | AAGTTAAGAAATGTA[-/A]AAAAAAAAAAAAAAA | 84333 |
rs66518918 | snp | A/G | 0.127944 | 0.218179 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271309 | AAGGGATGGAAGAAA[A/G]AGGATGTCCCTCGTG | 84333 |
rs66538532 | snp | C/T | 0.201727 | 0.245295 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271239 | TCTGATTTCCTTGAA[C/T]AGTATTACTTTCAGG | 84333 |
rs66727333 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273650 | ATATCATTCCTATGC[C/T]GTATCTATTGTTAAT | 84333 |
rs67392992 | in-del | -/AAAC | 0.343254 | 0.231956 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199790 | GGAAGTGGAGTAAAT[-/AAAC]AAAGGAGAATAAATT | 84333 |
rs67394295 | in-del | -/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275459 | TTATTTTATTTTTTT[-/T]TGAGATGGAATCTTG | 84333 |
rs67397753 | in-del | -/TATCTATCTATC | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246998 | AACATATAGGCAGAT[-/TATCTATCTATC]TATCTATCTATCTAT | 84333 |
rs67591355 | in-del | -/TG | 0.394904 | 0.203722 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186579 | GTGTGTGTATATATA[-/TG]TGTGTGTATATATAT | 84333 |
rs67708075 | in-del | -/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272482 | CTGGCCTAAAAAAAT[-/T]AATTTTTTTTTGTCT | 84333 |
rs67735817 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221724 | ACATATTTTACAGTT[-/A]AAAAAAAAAAAAAAC | 84333 |
rs68030127 | in-del | -/A | 0.236724 | 0.249647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265533 | GAAAATGTAAATCAT[-/A]AAAAAAAACAAAATT | 84333 |
rs68104135 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250914 | ACTTATTTATAAACG[-/TT]AGTATAATTTATATA | 84333 |
rs68172749 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271200 | CCTTACAGGTTGAGC[A/G]GAGTTCCACGTCCCT | 84333 |
rs71025342 | in-del | -/AAAAAAAAA | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173595 | CATGGCTTCTGTGGG[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 84333 |
rs71025345 | in-del | -/TCTATA | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195483 | CTCTCTCTCTCTCTC[-/TCTATA]TATATATATATGCAT | 84333 |
rs71025346 | in-del | -/T | 0.471004 | 0.116864 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214309 | TCTGTCTGTCTCTCC[-/T]TTTTTTTTTTTTTTA | 84333 |
rs71025349 | in-del | -/ATATATATATATAT | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249407 | GTGTAGATTTTATAC[-/ATATATATATATAT]ATATATATATATATA | 84333 |
rs71025350 | in-del | -/TTAAA | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261038 | AAAGAAAACATGAGC[-/TTAAA]TTAAAAAGAAAAAAA | 84333 |
rs71306843 | in-del | -/C/TTTC | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263318 | GGAGATAATTTCATT[-/C/TTTC]TTTATCTTTTTTGTA | 84333 |
rs71479077 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173871 | GATACTCATATGTCA[A/G]AAAAGTCCTCATGCT | 84333 |
rs71479078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173949 | AAGTAAAACAGCTAA[A/G]ACTCCAGTATTGATG | 84333 |
rs71479079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212502 | TTTGACCAGAAGTAG[C/T]TGGAAGTTTGGTTTG | 84333 |
rs71484259 | in-del | -/T/TT | 0.321292 | 0.23962 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250497 | TTGTCTGGTTTTTTC[-/T/TT]TTTTTTTTTTTTTTT | 84333 |
rs71485922 | multinucleotide-polymorphism | CTT/TTC | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237509 | AAGTAATCTGCCCAC[CTT/TTC]GGCCTCCCAAAGTGC | 84333 |
rs71487496 | in-del | CAAAAAAAAAAAAAAAAAAAAAAAAAAA/TAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAG | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238632 | AATTTGGGAAAGAGG[lengthTooLong]AAAGAAAGAAAGAAA | 84333 |
rs71881221 | in-del | -/CA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205300 | ACTGGACACACACAC[-/CA]ACACACACACGGCCC | 84333 |
rs71923551 | in-del | -/CA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186606 | GTATATATACACACA[-/CA]TATATATGTAACAAA | 84333 |
rs71942171 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274118 | TCAATCTGTGTATGT[-/TA]ATATATATATGTAAT | 84333 |
rs71986210 | in-del | -/AAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263316 | TTTACAAAAAAGATA[-/AAAG]AAAATGAAATTATCT | 84333 |
rs72134127 | in-del | -/GATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246966 | ATAGATGGATAGATG[-/GATA]GATAGATAGATAGAT | 84333 |
rs72439811 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275608 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 84333 |
rs72813400 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185341 | ATCCCTTCTGCCCCC[A/G]TGGGTTTGGACTCTC | 84333 |
rs72813402 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195648 | CACTGTGTTACCCAG[G/T]CTAGTCTCGAACTCC | 84333 |
rs72815404 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203236 | AATGTTTAGGAAAAT[C/T]ATCCAACATTTGGGA | 84333 |
rs72815408 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208830 | AGTGACACCTTCAGT[G/T]TTGGATGTGTCTCTA | 84333 |
rs72815411 | snp | C/G | 0.127254 | 0.217792 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219459 | AACACACTAGAAGTA[C/G]TGTGATTTTTCACAT | 84333 |
rs72815418 | snp | A/G | 0.224709 | 0.248717 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248220 | AGACCGTATTTCCAA[A/G]GCAGGGGAATAAACT | 84333 |
rs72815423 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253670 | AAAATTCCCCCAGTT[G/T]AGTGCTGCTCACCCT | 84333 |
rs72815431 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271396 | GAGGCCACCATTTTT[A/G]CATTTGCAGAATATT | 84333 |
rs72815434 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273610 | ATGGTTTTATGTTCT[A/G]AATTCTCTCTAATTT | 84333 |
rs73310412 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193225 | CAAAGACCCAAAGGA[A/G]CTTGGAAGGAGATCC | 84333 |
rs73310426 | snp | C/T | 0.23846 | 0.249734 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200224 | GCATGTAGAGATGAG[C/T]GTGGAGGAGATAAGA | 84333 |
rs73310432 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204471 | AGACTCTATGATGAC[C/T]AGGCCAGGTCTATTT | 84333 |
rs73310451 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212094 | AAATAATAAATGAAA[C/T]AATAATGATATAAAA | 84333 |
rs73310453 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212651 | GAAGAATTGTACAGC[A/C]TAACTTCTATAACGC | 84333 |
rs73310474 | snp | C/T | 0.276534 | 0.248588 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221016 | GAGCTGTGCCTACCT[C/T]GGCGGGGAGAGCGGC | 84333 |
rs73312405 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238779 | AAGATTATTTTGACT[C/T]GAGAAGACATTTAGA | 84333 |
rs73312452 | snp | C/G | 0.0916144 | 0.193427 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259115 | TTGGGTGTCCCTTCT[C/G]GATTGGTTCTTATAT | 84333 |
rs73312470 | snp | A/G | 0.077417 | 0.180873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268488 | AATTGGCATCTTTGC[A/G]GGTTTTTTATTCTAT | 84333 |
rs73312478 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270477 | GCAAAGTCTGATGGA[C/T]CAGAGCTTGGGGACT | 84333 |
rs73312480 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270737 | TTTGCTATGTTAGAA[A/G]TATCCTGGTTAATTT | 84333 |
rs73314513 | snp | C/T | 0.0792508 | 0.182605 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280744 | TAATACACTGTATTC[C/T]CCGTTAATTATCCCT | 84333 |
rs73325254 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166519 | TTTACAATAATGAAA[C/T]TACTGTTTAATTTTT | 84333 |
rs73325270 | snp | A/G | 0.120326 | 0.21374 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173984 | TTTTGGGCAGCAAAG[A/G]TCTTCTTGGAAAATG | 84333 |
rs73325272 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174725 | CATGTCTGTAAAATA[C/T]AGAAAAATTATGGCT | 84333 |
rs73325274 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175121 | AAAATGAGGGATAGG[C/T]GGAAAATCTGTAAGG | 84333 |
rs74149064 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171944 | TACACCTCCTAAAGC[C/T]TTTCTGAGCATTTAT | 84333 |
rs74149067 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173615 | CAGAAGCCATGAGTA[C/G]TAGCAGGAGGCAATT | 84333 |
rs74149072 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178121 | AGACAAAATGTTGAC[C/T]CTGGCCATAACTGAC | 84333 |
rs74149080 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197213 | GCCTGTCTCCATTCC[A/G]CTTGGCATCAGCAGG | 84333 |
rs74149082 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202169 | CACTGCTTAGAACCA[C/T]GCCTTCGTATAAAAT | 84333 |
rs74149083 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202307 | TAACCTGGATTTGAA[C/T]CCACCACCGTTGTGA | 84333 |
rs74149084 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203894 | TTTTGTGAACCTAAT[G/T]ATTTCAGTCAGGCCC | 84333 |
rs74149086 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208473 | CCAGATTCTGCATTC[C/T]TAACAAGATCCCTGC | 84333 |
rs74149087 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208688 | GTGTACCCCACCTGC[A/T]TGAGTCCCAGAAATC | 84333 |
rs74149088 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212597 | ATAGAGAATTGAATC[G/T]GAATAAATCAAAGTG | 84333 |
rs74150612 | snp | A/T | 0.0562307 | 0.157967 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218278 | GAAAGCTGAAGTACA[A/T]TATTGATAAGGGGAC | 84333 |
rs74150613 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231231 | ATAAATCATTACTAA[A/G]CACTTTGTCTTCCAG | 84333 |
rs74150614 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236139 | TGATTTTGATGCCAG[A/G]GACCAAATGTTACTA | 84333 |
rs74150616 | snp | A/G | 0.126219 | 0.217206 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238632 | TTTTTTTTTTTTTTT[A/G]CCTCTTTCCCAAATT | 84333 |
rs74150619 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258721 | CTGTCTAGAATATCC[A/G]TCTTCACATTTGAAA | 84333 |
rs74388588 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242093 | TATCAGTGCCTCTCA[A/G]CCAGGAGTGATTTTG | 84333 |
rs74449979 | snp | C/T | 0.0314385 | 0.121371 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161290 | TGCTGCATTAAATTA[C/T]TGCTATTGACTCGCT | 84333 |
rs74457866 | snp | G/T | 0.0414363 | 0.137845 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219899 | CACTTTAGTAAGAAG[G/T]TAACGCCTATCAGTT | 84333 |
rs74608992 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237742 | GAGTGAGAATCCATC[A/G/T]AAAAAAAAAAAAAAT | 84333 |
rs74620164 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196502 | TGTTCCTTTATTCTC[C/T]CAGATCTTTCCATGG | 84333 |
rs74696442 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275450 | ACTACATTTTATTTT[A/T]TTTTTTTTTGAGATG | 84333 |
rs74733302 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237190 | GATTATTAAATTGTA[C/T]TGAATTAAATATATG | 84333 |
rs74793315 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208127 | TTCTTGCCTGAATCA[A/G]TTAATAACATGGTTA | 84333 |
rs74793583 | snp | A/C | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237743 | AGTGAGAATCCATCT[A/C]AAAAAAAAAAAAATT | 84333 |
rs74832690 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246794 | TTAGTTTAAAAAAAG[C/T]GAGACAATGACTGGG | 84333 |
rs74846382 | snp | A/T | 0.0810805 | 0.184299 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226430 | GAAATTCCTGAAGCT[A/T]CAGACCATATGCCAT | 84333 |
rs74850402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272297 | ATTGTTGGGTACAGA[G/T]GTGATTGATGATCAG | 84333 |
rs74853449 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199497 | ATCTTTGCAGCTGAG[C/G]ACATGCCTGCAAGAG | 84333 |
rs75082454 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207381 | GAACATCCGTATATC[C/T]CTCACTTAGATTCAC | 84333 |
rs75157598 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262233 | GAGTTTGAGACCAAC[C/T]TGGCCAACATGGTAA | 84333 |
rs75227016 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185959 | AGTGCTGTATTTACT[C/T]GCCCCTTTCATTCCT | 84333 |
rs75234316 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264109 | GGCAGTCACAGAACT[A/G]TGCCTTAAACCTCTA | 84333 |
rs75240959 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201937 | TGTTTACTGGCACTA[G/T]GCTTTTGAAATTGTT | 84333 |
rs75273475 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185442 | GCAACACTGTTGTCC[A/G]TGCCTGGCTGGAATT | 84333 |
rs75273928 | in-del | -/C | 0.242775 | 0.249896 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175534 | ACCTTCCTCCCTCTT[-/C]CCCCCTACCCCTGTG | 84333 |
rs75283220 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195509 | AGAGAGAGAGAGAGA[C/T]GCAGGGTCTCTGTCA | 84333 |
rs75301571 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195402 | ATCACTTGCCTTAGA[A/G]GGTTAATAATATTCT | 84333 |
rs75317642 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193468 | ATTAAGCTGATAGTG[A/G]AGTAAGAATGTGTTC | 84333 |
rs75369883 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281337 | TAATGACTTTGCTCA[A/G]CTACATTACACACTC | 84333 |
rs75374522 | snp | A/C | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276116 | TTTTGAAAAAAAAAA[A/C]CGAATGTAGATAAAA | 84333 |
rs75425166 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272700 | GTCGCTTGAGCCCAG[A/G]AAATGGAGGTTGCAG | 84333 |
rs75441398 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202787 | AAAGATTGGCCATTT[A/G]TGCTATATAATATGC | 84333 |
rs75457828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231994 | CTTATGACTCCTGGA[A/G]TGATCAGCATATGCA | 84333 |
rs75492287 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270380 | CCAAAGAGATCAATA[A/G]AAAAAAAAAAAAGAA | 84333 |
rs75570626 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167774 | TATGCTTTAAGAGAT[C/T]AATCTTCATCACAGG | 84333 |
rs75582890 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198385 | CTTTTGATAACTATA[A/G]GACCAACTTCCTTAC | 84333 |
rs75600064 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237744 | GTGAGAATCCATCTA[A/T]AAAAAAAAAAAATTG | 84333 |
rs75619459 | snp | A/G | 0.000696922 | 0.0186541 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240441 | TAACATTAAATGAGC[A/G]TTCATATGATGCGTT | 84333 |
rs75636225 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217785 | ACAACAAAAAAAGTT[A/C]ATCTGTGTGTTTTTT | 84333 |
rs75708293 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270379 | ACCAAAGAGATCAAT[A/C]GAAAAAAAAAAAAGA | 84333 |
rs75713540 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222469 | GCTTTGGGTGTCATT[A/G]GTATAGAGGTGGTAG | 84333 |
rs75754021 | snp | C/G | 0.0387552 | 0.1337 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218492 | TAGGATAAGTAACTG[C/G]TAAGGAGCCCCAGGG | 84333 |
rs75795935 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211898 | CAGTGCTGCAGAGCA[A/G]AGTGGTCTGGAAGGT | 84333 |
rs75840641 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233373 | CTAACCCTGTTCAAG[C/T]AAGGTGTGCTTCGCT | 84333 |
rs75869966 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203926 | CATTTCTGAAATGAG[C/T]GTTATGTCAGTGTAA | 84333 |
rs75960472 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277612 | GAAAAACAATATGAA[C/T]CATTCAGTTATTTTA | 84333 |
rs75963066 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210583 | CCAGCAGAACCTGTG[G/T]TCTGTGGAGGCCACT | 84333 |
rs76055679 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191496 | ATATTTTTGGACTGA[A/G]GTTGACCATGGGTAA | 84333 |
rs76076532 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236178 | ATGCATTGCATAGTG[C/G]TTTGGATTTTAGGCC | 84333 |
rs76102475 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186067 | TGTTTTGCAGACAGT[A/G]GTTAAATTGATGACA | 84333 |
rs76107431 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164641 | ACCTCGGTTGCCATT[C/T]ATGAATACAGAATTT | 84333 |
rs76134049 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196028 | TGGTATTCATTATTT[G/T]TCCACTTTCTCGCAT | 84333 |
rs76157711 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229238 | CAACACAGCAATAAA[G/T]AGAACAGGCATAGTC | 84333 |
rs76195796 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212550 | ATATTTTATATTGTA[C/T]ACTCAGAGGCTACTC | 84333 |
rs76271374 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165676 | TGTTGTTGTTCATGT[C/T]GGTAATGCCACAGAA | 84333 |
rs76279057 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262001 | TTCCATGTTTAGAGA[A/C]TGTTTTTAATCCTAG | 84333 |
rs76314543 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174439 | TTGAACCCAGGAGGT[G/T]GAGATTGTAGTGAGC | 84333 |
rs76431120 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199306 | TGCCCTTTGAAGGGT[A/G]GGAAGGCAGCAAGGG | 84333 |
rs76456872 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250486 | CACATCCTGTATTTG[C/T]CTGGTTTTTTCTTTT | 84333 |
rs76499599 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249396 | ATATATATATATATA[C/T]ATATATATATATATA | 84333 |
rs76553784 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252454 | TATCCACTATGTGAA[C/G]AGTAGACAGTGAAGA | 84333 |
rs76680997 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234701 | AAGCTCACATTTATT[G/T]AATACTTACAAGTTA | 84333 |
rs76726228 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217049 | TTCACCTTTTTTTTT[G/T]GAGACAGAGTCTCTC | 84333 |
rs76731129 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187051 | GGTCTGAGATTCTGC[A/C/G]TTTCTGAGTTTCCCA | 84333 |
rs76755264 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255444 | CCTCACCTTGAGGTG[G/T]TCTGCACGAGTAGGA | 84333 |
rs76792462 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175096 | GGCTTTGGAGTGGGG[C/T]ATAAGCCTGAAAATG | 84333 |
rs76914655 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212873 | GTCTCCTCTCTTTGT[A/G]AAGATCTGAATAAGT | 84333 |
rs76916571 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197484 | ATTGTGCTAAGTGTT[C/T]TCCGTGTATTATATT | 84333 |
rs76917589 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221741 | AAAAAAAAAAAAACC[A/T]GAGACAGGAAAGTAG | 84333 |
rs76948440 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239109 | CTCCCAGCACCCTGT[C/T]TCTATCTTATTTTTG | 84333 |
rs76962304 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270377 | ATACCAAAGAGATCA[A/G]TAGAAAAAAAAAAAA | 84333 |
rs76976285 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166060 | CTTGAAATTACTTGG[C/T]GCAGTTCATTCCTTT | 84333 |
rs76998283 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172695 | AACTTTTGTGTTTGC[A/C]CCCAAGTTAAACTAA | 84333 |
rs77033468 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247593 | AGATGAGGCAGGAAG[C/G]GGGTGTTGTGGGGGC | 84333 |
rs77061487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186023 | GTCAGCCATCTTGGT[C/T]GCTCCCTGCTTCAAT | 84333 |
rs77068316 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250497 | TTTGTCTGGTTTTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
rs77133527 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267060 | TTTCTAGAGACCTAC[A/G]TATGTGGCCCCCATA | 84333 |
rs77164355 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186024 | TCAGCCATCTTGGTC[A/G]CTCCCTGCTTCAATA | 84333 |
rs77215169 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195628 | TTTTGTAGAGATGAG[G/T]TTCTCACTGTGTTAC | 84333 |
rs77223313 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234703 | GCTCACATTTATTGA[A/C]TACTTACAAGTTACC | 84333 |
rs77229469 | snp | C/T | 0.0314385 | 0.121371 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227587 | TCTTATTACATCTCA[C/T]CAAAGCCACTGCAGC | 84333 |
rs77259117 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198600 | GACCTGCCTACGGGC[C/T]GCAGAGTTCAAGCTT | 84333 |
rs77284033 | snp | C/T | 0.0193772 | 0.0965046 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281316 | ATGTGCCACATTTTA[C/T]AAACGTAATGACTTT | 84333 |
rs77294149 | snp | C/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190854 | TTAGAAACTATTTCA[C/G]ATCAGTTCCTGCTGT | 84333 |
rs77410927 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230193 | GTGAAATCTTCTATA[C/T]TGACTTATGAGAATA | 84333 |
rs77446815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191751 | CCTGTCCAGAACACT[C/G]CACCCAAAATGAGAC | 84333 |
rs77482803 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166236 | GGAGAAGAATGGTTT[A/C]TATCATTAGTTGATT | 84333 |
rs77566849 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245989 | TATCCAGCCATGGGT[A/G]CCAGTGCAGAGTTGA | 84333 |
rs77570369 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238902 | TTTTTTTAAGGTTTT[A/C]TGATACTGTCTTTTA | 84333 |
rs77580635 | snp | C/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233103 | TCGAAGTACAAAAGA[C/G]TGACACTATCAAGGG | 84333 |
rs77598522 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193405 | ACTTCATTAGTGGTA[A/T]TTTGTCATGGCAGCA | 84333 |
rs77659464 | in-del | -/AA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241682 | CTTAAAAAAAAAAAA[-/AA]GAAGCTACTCATCTA | 84333 |
rs77698815 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238604 | CTTTCTTTCTTTCTT[C/T]TTTTTTTTTTTTTTT | 84333 |
rs77724997 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183722 | TCCTTCTTTGCCATA[C/G/T]GTAGTGTGTCCTTCA | 84333 |
rs77746884 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167462 | GTAAGACTTAATTAG[A/G]GAATTTTGAGCAAGG | 84333 |
rs77772166 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186348 | ACTAGTTGTCTATGG[C/T]GAGAATTCTTAGGTG | 84333 |
rs77805456 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210131 | CTGCTCTCCCTTAAC[A/G]CTTCCTTCTTCCTAG | 84333 |
rs77840037 | snp | A/C/G | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197276 | GCTCGCGAGCTGACT[A/C/G]TCATGTCCTGGGTCT | 84333 |
rs77862552 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168959 | AAAAAAAAAAAAAAA[A/G]AAGGCTTGATAACAT | 84333 |
rs77936488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265071 | GCATATGGGAGAAAT[G/T]ATTCAAAGGAGAAAA | 84333 |
rs77966741 | snp | A/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237756 | CTAAAAAAAAAAAAA[A/T]TTGCATCAGAAAACC | 84333 |
rs77994166 | snp | G/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275460 | ATTTTTTTTTTTTTT[G/T]AGATGGAATCTTGCT | 84333 |
rs78006715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278061 | CTTGACCTCTGCTGC[A/G]TATTACTGAAAACTT | 84333 |
rs78010402 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218701 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACTT | 84333 |
rs78018121 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171251 | AGTTAGATGAAAACA[A/G]AAGGAAATTTTGAGT | 84333 |
rs78127446 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194166 | ATGGCCTCTAAAGAT[A/G]TTCATCCTAATCCCC | 84333 |
rs78132836 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252202 | CTAGCAAATGTCAGC[A/C]ACTGAGAATATTGTT | 84333 |
rs78141861 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225358 | AGCCTAAAGGGGTAA[A/G]TTAAATGACAGTTTA | 84333 |
rs78150289 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240899 | TGGTAGTAGAAAGAG[A/G]GAGAACTCATAGAAA | 84333 |
rs78207965 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183176 | CTGTCTCAATGATCT[A/G]ATATTGTCAGTGGGG | 84333 |
rs78228363 | snp | G/T | 0.081446 | 0.184634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207274 | GAGATGAGCCATTTG[G/T]CATTGCATTACTTTT | 84333 |
rs78253344 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265680 | ATAAAACAAGCCTCA[A/G]AAACTCATTGTCTTA | 84333 |
rs78320953 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201563 | GTGTTTGAAGGTGGA[A/G]TGGAGAACTATCTTC | 84333 |
rs78408685 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192558 | TGGAAAGATAAGTTC[A/C]TTTATTTATTCAAGA | 84333 |
rs78451039 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189819 | ATATTTTCATATTGA[A/G]CACGTCTATATTTTC | 84333 |
rs78530014 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191414 | ACCACATGAGATATC[A/G]TCACACTACTCAGAT | 84333 |
rs78554770 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170585 | ACACAATTGAAATGG[C/T]CAAAATTCAGAACAC | 84333 |
rs78572572 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209806 | AAAAAGAAAAACGAA[A/G]AAAGGAATTGGAGGA | 84333 |
rs78606902 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252352 | GGCATTTTCCTATTA[C/G]GAAGTGAAAAACAAT | 84333 |
rs78639249 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267505 | CAATACTTGTTCAAA[G/T]AATAAATTGAATGAA | 84333 |
rs78645702 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213629 | ACCACCACACCAGGC[C/T]TTTTTTTTTCTTTTT | 84333 |
rs78673759 | snp | A/C | 0.0345262 | 0.126772 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162092 | TGGCAGAGAACAGAG[A/C]AGGATCAAAATAAAG | 84333 |
rs78753737 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279968 | TCTGTTCCTTCTATC[C/T]TTTTTTGAGTCAAAA | 84333 |
rs78824294 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193395 | TTTTTAAGCTACTTC[A/G]TTAGTGGTAATTTGT | 84333 |
rs78830730 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181807 | TCAGGCCAATATCCC[C/T]GATGAATATAGATAT | 84333 |
rs78856060 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197978 | ACTAAGTGCCAGACA[C/T]TGGGGAAGTGAATCC | 84333 |
rs78883416 | snp | C/G | 0.281841 | 0.247964 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256968 | AGATAAATTGTAAAT[C/G]TAAAACTTCATTAAA | 84333 |
rs78966646 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270382 | AAAGAGATCAATAGA[A/G]AAAAAAAAAAGAATC | 84333 |
rs78992804 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186145 | TTTAACTTAAAATCA[C/T]TTTGGTATTTCTTTA | 84333 |
rs78998538 | snp | C/T | 0.077417 | 0.180873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165158 | CCTCCTGGTTTTCTT[C/T]TGATTCATTTTCTGC | 84333 |
rs79104078 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244259 | GAGACTTAAGCGAAG[A/G]CTTGGAGACTGTGAG | 84333 |
rs79117543 | snp | C/T | 0.144296 | 0.226554 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174569 | TAAATCCTATCATGC[C/T]TTAAGACTAAGTTAA | 84333 |
rs79245633 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186399 | GGAATATAAAAGCTG[A/C]ATGATTTCACAAGGT | 84333 |
rs79256982 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212211 | ATAGGTTAATTGAAG[C/T]TTGAGAAAGCTTTGT | 84333 |
rs79316299 | snp | A/G | 0.136166 | 0.22258 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197666 | CCTTGCTTCCAGAGG[A/G]AAAATGGGTTTCTTT | 84333 |
rs79358753 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205455 | AGGGTATATTCCAGC[A/G]TTCATTCATAAACTG | 84333 |
rs79397240 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211210 | CCCTGGCTGTTTATG[C/T]ACATGTATACAATAC | 84333 |
rs79481023 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214323 | TTAAAAAAAAAAAAA[A/G]GGAGAGACAGACAGA | 84333 |
rs79622762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206702 | CTGTGGGGGACTGCA[C/T]GGTCTCTGACTTCCT | 84333 |
rs79646171 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260822 | TTGTGGGGTGGGGGA[C/G/T]GGGGGAGGGATAGCA | 84333 |
rs79735338 | snp | A/C | 0.00645415 | 0.0564395 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197017 | TTTAAACAACAACAA[A/C]AAAAAAAACATGATG | 84333 |
rs79754569 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171191 | GTCCAAATCCCTAGA[A/T]TGTAGAAGAATACAA | 84333 |
rs79825821 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197505 | GTATTATATTATCTA[A/G]CCCCTGATGAGTGGG | 84333 |
rs79873997 | snp | A/C/G | 0.0825414 | 0.185628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240189 | GAACCTATTTTATGT[A/C/G]AATACACCAGCTTTT | 84333 |
rs79919488 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184457 | CTGTCAGCTCCTGCA[A/G]TGTTTTAGCGTGATT | 84333 |
rs80006613 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250022 | ACTCTATGGTTCTAC[A/G]TATCACAGTTTAACT | 84333 |
rs80069167 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277189 | TTACAGATTCCAACA[C/T]TGAGTCTTCCCAGTG | 84333 |
rs80136010 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271823 | GCTACAAAAACTTAT[A/C]TTTTCAACTTATATA | 84333 |
rs80213699 | snp | A/C | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221738 | TAAAAAAAAAAAAAA[A/C]CCTGAGACAGGAAAG | 84333 |
rs80253518 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228293 | AAAGGGGCTATGTTC[C/G]AGCAGCTCAAATGTG | 84333 |
rs80275462 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194329 | AGTAGAGTATCTTTC[C/T]CATGGTGGTCAGAGG | 84333 |
rs80301840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195198 | ATTAAAGGCCCACTT[A/G]AAGTTTGTGGTTATG | 84333 |
rs80352585 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243810 | GCAAAACATTAAAGT[G/T]AGTTTTATATAAAAA | 84333 |
rs111397423 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252735 | TTTAGCTCTCCAATA[C/T]ATGAGTTAGCTCATA | 84333 |
rs111413786 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191757 | CAGAACACTCCACCC[A/C]AAATGAGACATTTTG | 84333 |
rs111420386 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204009 | TGTTTATTGTTGAGT[G/T]TGTGAAGCATGACAC | 84333 |
rs111433491 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189312 | TCCATGCCATGAAAG[G/T]TGTCTGTTCATACCT | 84333 |
rs111473431 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207501 | ACCCTTTACCTCTAA[A/G]TACTTCAGGTTGTAT | 84333 |
rs111499914 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215871 | ATAATTGTTTCTTGT[A/G]GATAAGTCTGTACTC | 84333 |
rs111517172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165590 | CCTCCCAGGCTCAAG[C/T]GATCCAATATGAAGT | 84333 |
rs111576384 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228076 | TCTCCTAGGATCTAC[A/G]TAGGCATCTTTGGGG | 84333 |
rs111596678 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269256 | ATGCAGAATTACAGA[A/G]TCAGATCTCAGTTTG | 84333 |
rs111651451 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188947 | AGTGGTTTGGGAGAA[A/T]GGGAGAGTAGATAGC | 84333 |
rs111652837 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177707 | GGACCCTCCAAGCCA[G/T]GTGCAGGATATAATC | 84333 |
rs111663415 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171146 | AAACTACTCTGTGAT[A/G]TAACAGTGCATACAT | 84333 |
rs111675752 | snp | C/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188796 | TGTCATTTGGAGCCT[C/G]TTGACCTACCCAACC | 84333 |
rs111683353 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253605 | GTTCAAAAGCTTCGC[A/G]TCATCTTTGATCTGT | 84333 |
rs111706783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184528 | CAGAAAGTTTGGTTT[C/T]ATCCATATTCTGAAT | 84333 |
rs111722559 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209805 | AAAAAAGAAAAACGA[A/G]GAAAGGAATTGGAGG | 84333 |
rs111734236 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188233 | TGCAGCGCACCATGC[A/G]CGAGCTGAAGCAGGG | 84333 |
rs111753906 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168860 | ATGAATCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 84333 |
rs111763746 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204693 | TGTACATAACAAAAG[C/T]TCCCCACTGCCAACT | 84333 |
rs111787725 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230876 | GATCAATCTGCCTTG[A/C]CCTCCCAAAGTGCTG | 84333 |
rs111789275 | snp | G/T | 0.039522 | 0.134904 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196246 | GAGAAGTGATGTGAG[G/T]CAAAGATGTCCAATG | 84333 |
rs111796454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265455 | AAGATTCTGTGTTTA[C/T]GATACAATATGCCAT | 84333 |
rs111802530 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225418 | CCCTTGGTGGCCATC[A/G]AGCCCTTTTACTGAG | 84333 |
rs111815193 | in-del | -/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184724 | GAGGTTGCTGTTTTG[-/T]TTTTTTTTTTCCTAT | 84333 |
rs111819798 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222280 | TATCAACTTGGTTTG[A/T]CTCGTAACTGGATGA | 84333 |
rs111824461 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192211 | CACCCCAGAGGCATT[A/T]GTGGAATTTTTTTAA | 84333 |
rs111829921 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208949 | TTTTCTTGCTCTACA[A/G]GAGTGTGAGCTTTCT | 84333 |
rs111855064 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242156 | ATTTTTGGTTGTCAG[A/G]TCTGGGTGGGTGCTC | 84333 |
rs111945122 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179910 | TCTATCTTTAGGTAT[C/T]TGAGGAATCGCCATA | 84333 |
rs112022556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265390 | AAATATGAATTAAGA[C/T]TGGCTATAAGGTTGG | 84333 |
rs112045347 | snp | A/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177889 | CCTGCTTCAGCTCAC[A/T]CTTGGTGCACGGTGC | 84333 |
rs112087548 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252617 | AGAGAAATGACCACT[A/G]TACCTATTTATCCTT | 84333 |
rs112116472 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173686 | GGAGCAAGATCAAAA[G/T]TATAATATTAGTGTT | 84333 |
rs112123065 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215361 | TGTGTGAAACTCCCT[G/T]TTCACAGATTCTTCT | 84333 |
rs112132317 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265920 | CTTGAAGAACTTGTC[A/G]TACATGTTTGTGGCT | 84333 |
rs112217388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194738 | TGAGATCACCAAGAG[A/C]ATAAGTAGAGATAGA | 84333 |
rs112225201 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164770 | ACGGCATCTACTCAG[C/T]CAGGCCTTCTTGATC | 84333 |
rs112279441 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199320 | TGGGAAGGCAGCAAG[C/G/T]GGGGCAGAAAAGGAG | 84333 |
rs112314024 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260602 | TAAGAAAATGTGGCA[A/C]ATATACACCATGGAA | 84333 |
rs112316489 | snp | C/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207878 | GCATCATCTCAGCAG[C/G]TACATAATGTCAGAT | 84333 |
rs112344687 | in-del | -/GCTAA | 0.0146672 | 0.084371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258583 | GGCTTGTAAAAATGT[-/GCTAA]TGATTCTTTGTAAGC | 84333 |
rs112362937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235262 | TCTAATTAGTGATCA[C/T]GATGCCCATTTAAAT | 84333 |
rs112376393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196638 | TGCCCAGCTCCTTTC[C/T]ATTACACTGATGTGT | 84333 |
rs112385263 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197631 | GGAAAGGGCTAATGG[C/T]GGTAGAGAGTGCGTG | 84333 |
rs112393392 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202452 | AAATGAGGCAAATAA[C/T]ACAAAGTAGTTAACA | 84333 |
rs112554657 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182048 | TCCAGAAATTTATCA[A/G]TTTTTTCTAGATTTT | 84333 |
rs112562834 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166281 | TGTGAACTCTCAGAG[A/G]GAAAAATAATGTCTT | 84333 |
rs112574400 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199237 | TCACAGGTTGGGTTC[C/G]CTGGGAAGCTGACTC | 84333 |
rs112583471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202006 | TGGGAGCTACACTGT[C/T]CAGGATTATATCCAA | 84333 |
rs112591300 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226250 | TGCCCTTCTGGACTC[C/T]CTGGTCAAGTGAAGA | 84333 |
rs112600890 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240650 | TAATTTTTATTGTAT[C/G]TCATAATATTTCATG | 84333 |
rs112614511 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228489 | TAATCCCTAACCTAA[A/G]AATAAATTATTTGCA | 84333 |
rs112618748 | in-del | -/TA | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195488 | ATATATATATATAGA[-/TA]GAGAGAGAGAGAGAG | 84333 |
rs112689997 | snp | A/G | 0.0205511 | 0.0992634 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283768 | GATCATCAGTTTTAA[A/G]TAGAGTAGCCCTCAC | 84333 |
rs112714260 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251747 | TGGTGACCAACTTAG[A/G]CTTAGAGAATTTCAT | 84333 |
rs112741909 | snp | C/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199512 | GACATGCCTGCAAGA[C/G]GCCAACAACATCCCC | 84333 |
rs112779191 | snp | C/T | 0.0345262 | 0.126772 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161150 | AGCCCTCCAGGGTTC[C/T]GGCTGTCTCCTCTCT | 84333 |
rs112890248 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171034 | CTACACAACATTCTG[C/G]GCAAGCAAAACCATA | 84333 |
rs112897104 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168475 | TCAGTTGGGCAGTGG[A/G]GATTAGTGGGGACAA | 84333 |
rs112897917 | snp | A/C | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178099 | GTATAGCTGTACCAA[A/C]AGACACAGACAAAAT | 84333 |
rs112963059 | in-del | -/AA | 0.0744748 | 0.178019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257155 | GCAAAAGGCTTGAAT[-/AA]ACATTCCTCTAAAGA | 84333 |
rs112974539 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191073 | GGCCCCTAGTGGGTG[C/T]CTGATACCATGGATA | 84333 |
rs112985660 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206396 | TTTTTAATCTCAAAA[A/G]CCAAAGAGACAATTT | 84333 |
rs113006192 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177501 | TATGCCTTGCCCCCG[C/G]AGGTGGAGTCTACAG | 84333 |
rs113072152 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246975 | TAGATGGATAGATAG[A/G]TAGATAGATAGATAG | 84333 |
rs113121564 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177086 | CAGATGGGGTTTTGG[C/T]GTGGATGTCCTTTCT | 84333 |
rs113182954 | in-del | -/TT | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164242 | CCCTTCCACAATAAC[-/TT]GTGGGGGGGTCAGGG | 84333 |
rs113188295 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185750 | CCTGACCCGGGAGTT[G/T]CAAAGATTGGTGGGG | 84333 |
rs113214927 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191338 | GCTACTGAGTGACTA[A/C/G]GAATGGTGGCACAGA | 84333 |
rs113230553 | in-del | -/A | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188080 | GTGCTGCACCCGTTA[-/A]CTCCCCCGAACAGGA | 84333 |
rs113233061 | snp | C/T | 0.101658 | 0.201233 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188266 | AGGCATTGCCTCACT[C/T]GGGAAGCGCAAGGGG | 84333 |
rs113279340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189176 | TGAAACACATTCCTT[C/T]TCTTCTTTGCCTGGC | 84333 |
rs113330131 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278402 | AACGGTGTGTGGACT[A/C]GAGGAACACAACCAG | 84333 |
rs113443072 | in-del | -/AACTT | 0.0345262 | 0.126772 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161315 | TCGCTTGGGAAAGAA[-/AACTT]TACTTTCGCTGGATT | 84333 |
rs113478962 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164695 | GATTAACTTGACTCA[C/T]TCCCACCTCACATTA | 84333 |
rs113505404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183341 | ACCCTTTACCATTAT[A/G]TAATGCCCTTTGTCT | 84333 |
rs113533572 | snp | G/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168847 | GCAGGAGAATCACAT[G/T]AATCTGGGAGGCGGA | 84333 |
rs113557607 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239897 | CAATTTACCTCTCAT[C/G]CCTTTGTCCCAACTT | 84333 |
rs113585719 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242039 | CACTGGTCAACTCTG[A/G]TCTGTAATTCTGAGT | 84333 |
rs113617028 | snp | C/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168039 | GTAGTCTGCAATCAA[C/T]AAATATTTGTCTAAT | 84333 |
rs113640843 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188274 | CCTCACTCGGGAAGC[A/G]CAAGGGGTCAGGGAG | 84333 |
rs113641277 | snp | A/C | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178098 | GGTATAGCTGTACCA[A/C]AAGACACAGACAAAA | 84333 |
rs113642310 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189437 | AATAATATATGCTAG[A/G]TAAATGAATATAAGA | 84333 |
rs113696426 | snp | A/G | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255122 | ACTTACAAGATTGTC[A/G]GTATTCGACTTGACT | 84333 |
rs113812249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176375 | AAGTTTGGTGAATCT[G/T]ACAATTATGTGTCTT | 84333 |
rs113834545 | in-del | -/T | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213639 | AGGCTTTTTTTTTTC[-/T]TTTTTTTTTTTCTTT | 84333 |
rs113878545 | snp | A/G | 0.0368353 | 0.130617 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218335 | CTTTTTTTTTCCCCT[A/G]GTCCTATATCCAGTT | 84333 |
rs113880477 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227194 | TATTGAGCAAACTTA[C/T]ATGCCAAGAAGAAAT | 84333 |
rs113881380 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222503 | AGGTTCCAGGACTGG[A/G]TGAATTTGTCATTAT | 84333 |
rs113961384 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270530 | TGCTAAAAGAGAGCC[A/G]AGCTGAGCCCGCCTT | 84333 |
rs113977802 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185313 | TGGTAGAGCAGCTGT[A/G]CTGTGCTGGGGGATC | 84333 |
rs113993754 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172349 | ATTTGAACCCAGGAG[G/T]CGGAGGTTGTAGTAA | 84333 |
rs114039095 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258660 | TTGAGAAGGTGAACA[A/G]ATAACAGAGAAGATA | 84333 |
rs114052151 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232227 | AGCAATGCATAGGTC[A/G]TGGTGGTCTTTTCAA | 84333 |
rs114074106 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193548 | GTGTTTGAGGGGTGG[A/C]GAGGGGTAGTTGGAG | 84333 |
rs114118447 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165080 | TTTTTGACAGTTGAA[A/G]TTCAGTGCTTTTTTT | 84333 |
rs114224794 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262121 | CGAGTTCTGATAGTA[A/G]CATCTAGAAAATTAA | 84333 |
rs114226193 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235750 | GGTTTTAAAAAGAGG[A/T]GTTCCCTTGCACAAA | 84333 |
rs114226529 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268511 | TATTCTATTTGGCAC[C/T]ATGGGATGTCTCCTC | 84333 |
rs114265650 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189375 | GGGAGGTGATGTTTT[C/G]AAATCCCAGTTTACA | 84333 |
rs114529560 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198742 | TTAGCAGCAATTGCC[A/G]GGATGACGTTTTGGC | 84333 |
rs114614478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190848 | GTAAATTTAGAAACT[A/G]TTTCACATCAGTTCC | 84333 |
rs114619332 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233984 | ATTATTGTTTTATCA[C/T]CAGTGATAGCAGAAT | 84333 |
rs114733039 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274985 | TAAATATTTTAAATG[A/G]TACTATAAAAGATCA | 84333 |
rs114746026 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175117 | CCTGAAAATGAGGGA[C/T]AGGTGGAAAATCTGT | 84333 |
rs114845551 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219377 | TTCAGACACAAAATA[A/G]GAACATACCAAGTCT | 84333 |
rs114851043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241626 | CCAGTGAAAAGCACA[A/G]AAGGGGTCAATTCCG | 84333 |
rs114851135 | snp | A/C/T | 0.0757701 | 0.180052 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180324 | GCTGGTAGTTTCTTT[A/C/T]GCTGTACAGAAGCTC | 84333 |
rs114871446 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163950 | CCTCTCCTGGGTCTA[C/T]AGGTTTCTGGCCCCA | 84333 |
rs114977622 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204722 | CTCATTATTGCCACG[C/T]CCTGCCCTTTTTCTC | 84333 |
rs114996749 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236355 | AGGCCAAGCCTGATA[C/T]TTGGTTAGTGCTCAT | 84333 |
rs115050802 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253275 | GTAAGGTTATTTTGT[C/T]ACCCAGGTAATAGGC | 84333 |
rs115091137 | snp | C/T | 0.0452528 | 0.143452 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279519 | GAAATACAAAATGTC[C/T]TGTATTTTGCAGTTT | 84333 |
rs115106970 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274136 | ATATATATGTAATAG[C/T]ACATTACATTTTATA | 84333 |
rs115167971 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201729 | CCAGAAAACCTTTTT[C/T]TTTTTTTTTTAAGAA | 84333 |
rs115336884 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276379 | TTACATAATGAGCCT[C/T]GAGGACTAGAAACTG | 84333 |
rs115390531 | snp | C/T | 0.0142736 | 0.0832652 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284666 | AAAGCAAGACATTTA[C/T]GTCAGGAACACTGTG | 84333 |
rs115504314 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161681 | GGTGGGGAGGAGATA[C/T]AGAGACGCAGGAAAA | 84333 |
rs115540244 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282678 | GTAAAACTCATCTTA[C/T]GGAGTCTTTCTGATA | 84333 |
rs115574612 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162386 | CTGCGAGCTCTCGGG[C/T]GGAGGGCAGCTTATA | 84333 |
rs115604504 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238085 | AAAATGTAATTAATA[C/T]AAAATTATTGAGATT | 84333 |
rs115618334 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257644 | ACAACCTGGGCAGGA[C/T]GGAGTAGGATGGTGC | 84333 |
rs115710628 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278488 | TGTTGTTTCTATTAG[G/T]AGCAAACCAAGTGCC | 84333 |
rs115908287 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172777 | CTGAGAAAGGTTTGC[C/G]CATAGGTCCTTAGTT | 84333 |
rs116100773 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243420 | CTTCATTAGAAGCCT[A/T]AATTGCCTGTGACAC | 84333 |
rs116235886 | snp | A/G | 0.00400774 | 0.0445848 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248600 | AGACTTTTGTGTTTT[A/G]TGAAATCAACACTTC | 84333 |
rs116319715 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201547 | ACGTAAACAGAGTTA[G/T]GTGTTTGAAGGTGGA | 84333 |
rs116322091 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242790 | TTACATGTGTCATGG[A/C]CCCTTACTCTTAAAT | 84333 |
rs116550143 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242143 | AATATCTGGAGACAT[A/T]TTTGGTTGTCAGATC | 84333 |
rs116562715 | snp | A/T | 0.237882 | 0.249706 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275451 | CTACATTTTATTTTT[A/T]TTTTTTTTGAGATGG | 84333 |
rs116583691 | snp | A/C | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91220139 | ACTCACCCTCCCCCC[A/C]CCCTCAACCTCCACA | 84333 |
rs116667450 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233632 | CGAATTACAGCTATT[C/T]TGGATTTTTTAAATT | 84333 |
rs116706730 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269283 | TTTGGAAGGGACTTA[C/T]GTCATATCATCTGAT | 84333 |
rs116797180 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204146 | TAAACTTTTAGAATT[A/T]TGAATATAATGTTTA | 84333 |
rs116807590 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163815 | CGCCCCCTGCGGGCG[C/T]TGCCCGCGCGCGTGC | 84333 |
rs116897444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247853 | CAGACAACCCCTAAA[C/T]TGATGCTTGAAAAAG | 84333 |
rs116952601 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168351 | AGAAAGATAAGGAAG[A/G]AGATTTCGAAGGATC | 84333 |
rs116973187 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235181 | GTTATAGTCCTGGTG[C/T]GAATCTCCTAGATAT | 84333 |
rs116997468 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230846 | CAGCCTGGTCTTGAA[C/G]TCCTGGGCTCAAGTG | 84333 |
rs117050308 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260201 | TGCAGCCAACAGACA[C/T]GTGAAAAAATGCTCA | 84333 |
rs117060235 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281934 | AAAGTGAGAGAAATA[A/C]ATACTTTGAAAAGAA | 84333 |
rs117102647 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245815 | GTCAGTCAAAATTAA[A/G]GATAGAGGAAAGGGA | 84333 |
rs117113196 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215337 | GAACAGACCTCGGCC[C/T]TGGTGACTTGTGTGA | 84333 |
rs117186046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228996 | ACTAGCATCCTTTAA[A/C]GTAGGCAGTTTGTAT | 84333 |
rs117231376 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282647 | TTGGGAACTCATGCT[A/G]TGGGCTACCTTAAAG | 84333 |
rs117412740 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212831 | TAATTCATCTATTGG[C/G]ACGTTTGGATTTTTA | 84333 |
rs117451660 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265841 | CTTTGTGAGACTGAA[C/T]GCTTTCGCTAGCAGC | 84333 |
rs117454128 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169428 | CTAATAAGCAATTAC[A/G]GCAGGGTTGTAAGAG | 84333 |
rs117459325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245541 | TATTTTGTTTTGATA[C/T]AGGAGAAATAATGGC | 84333 |
rs117586017 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232860 | ATACTAGCAAGAAGC[A/G]TAATGGACTTGGGGC | 84333 |
rs117610098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170932 | ATAAATAGCTATCAA[C/G]CCATGAAAAGACATG | 84333 |
rs117714148 | snp | A/G | 0.0165278 | 0.0893908 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279760 | CACAATCTGTGTGTT[A/G]CACACATTTAGTTTT | 84333 |
rs117770123 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197137 | CGATTTCAAACAACA[A/G]TAATCATTTATCTCT | 84333 |
rs117792163 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263237 | TAAACGACATTAACA[A/G]ATGCAATATACCTGA | 84333 |
rs117827122 | snp | G/T | 0.0193772 | 0.0965046 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284448 | TCCCTCAAATACTAG[G/T]TAAGGTGTATACACA | 84333 |
rs117906088 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255098 | TCTGGTTGTTTCCTC[A/G]GAGACCCCACTTACA | 84333 |
rs117915234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215010 | AAGAATCAATGGTTA[C/T]GGAAATATTGTAAAG | 84333 |
rs117927248 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212307 | CTGTTCAAGAAGGCA[C/T]GGGAAGATACATGAA | 84333 |
rs117970702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236434 | CTTTGGTGAGCCTAA[C/T]TCCCTTTCTGACCCA | 84333 |
rs118000158 | snp | A/C/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182131 | TTCTGTGAGGTCAGC[A/C/G]GTAATGTCCCCCTTA | 84333 |
rs118016289 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253764 | CCAGGGCTAGGGCCA[C/T]TTGCCTGAGTGTGTG | 84333 |
rs118030613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232062 | AGGACTGAGCCCTGA[A/G]GTACCACTAAAAGGA | 84333 |
rs118081073 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273882 | ATATTTTATACATAT[A/G]TACTCTAGGTTAAAA | 84333 |
rs118156402 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237217 | TATGTTGATTAGGAC[A/G]TACATGGACATAGTA | 84333 |
rs137868349 | in-del | -/AG | 0.0166325 | 0.0896639 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262017 | TGTTTTTAATCCTAG[-/AG]TTATAACTAAAACAT | 84333 |
rs137894732 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188080 | GTGCTGCACCCGTTA[A/C]CTCCCCCGAACAGGA | 84333 |
rs137978540 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266327 | TTACAAGAACTCCTC[C/T]CAAAGTTGCCCCAGC | 84333 |
rs138006904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225628 | ATTTCTGTATTGTTT[A/G]TTTGTATTTATATTG | 84333 |
rs138011103 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177863 | GCTTCCTGGGTGAGG[C/T]GATGCCTCTCCCTGC | 84333 |
rs138050803 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180031 | TTTTACTTTTTAATA[A/G]TAGCCATTCTGACTG | 84333 |
rs138158752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168494 | TAGTGGGGACAAGTC[C/T]GCTAGTTACCTGAAG | 84333 |
rs138307285 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246542 | AGCAGGGAACTAACA[A/C]AATCAGATTAGCACT | 84333 |
rs138343939 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201409 | TCTAAATGCCATCAA[C/T]GTATGAATTTGAAGA | 84333 |
rs138392233 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231125 | TTGAAAATGTAAGCT[G/T]CTTTCCCACTTGACT | 84333 |
rs138392865 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252777 | ATCAATGGAAAGGCT[C/G]AATATCTTCTCATAA | 84333 |
rs138416652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183169 | TAATTTTCTGTCTCA[A/G]TGATCTAATATTGTC | 84333 |
rs138423836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197198 | CTGGTCAGCAGCGTA[A/G]CCTGTCTCCATTCCG | 84333 |
rs138453789 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176135 | TCTCGGCATTTGCTT[C/G]TCTGTAAAGTGTTTT | 84333 |
rs138492298 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265434 | TAAGATTATCTTTTG[A/G]ACATTAAGATTCTGT | 84333 |
rs138498467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177678 | CTAGCAATGAGCGAG[A/G]CTCCATAGGCGTAGG | 84333 |
rs138537431 | in-del | -/AAGTGA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232770 | TTTGTTTTCAGTAAA[-/AAGTGA]ATAGAGGTCCTCAGT | 84333 |
rs138593128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240754 | GAGTATTAAAAATAA[A/G]GTTTTACATCTTAAA | 84333 |
rs138601587 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163676 | AGCTCAGGTTATTAT[A/G]TAAGATGTCACGGAG | 84333 |
rs138670697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274462 | AGAGGGTATTTCAAA[G/T]TAATGCAGTAAAATG | 84333 |
rs138671662 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279999 | AGTCTATTAAATTTT[C/T]CTGTTGTTGTTCCAA | 84333 |
rs138716562 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278187 | GTAAATTATAACTCC[A/G]AATTCTTAAAATCTT | 84333 |
rs138729652 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197884 | CAAGATTTTCTTTGT[C/G]TGGATTCATTTTGCC | 84333 |
rs138751698 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219096 | GCTGCCTCTCCAGAC[A/C]CAAAGCACAGATTGC | 84333 |
rs138778190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191571 | ACTTTTTCCTACTAA[C/G]ATGTAGGTAATCTAG | 84333 |
rs138875960 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260183 | CTCAAAAGAAGACAT[A/T]TATGCAGCCAACAGA | 84333 |
rs138892283 | in-del | -/ATATATATGCATATATATATATGCATGC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195444 | ATATAAATCATATGT[-/ATATATATGCATATATATATATGCATGC]ATATATATATATATA | 84333 |
rs138906912 | snp | C/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263315 | AATTTACAAAAAAGA[C/G/T]AAAAATGAAATTATC | 84333 |
rs138960197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253381 | TTGTTCTCTTCTTTA[C/T]GCAAAGGACTTTTAA | 84333 |
rs139003824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254900 | GATGACTAACTATCA[A/G]TATAAAGGGTGAGCT | 84333 |
rs139012124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205535 | ATAAATGATGAGTTT[C/T]TCAGGCCAGGCCACA | 84333 |
rs139033161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210513 | GATAACTGGCTTAGC[C/T]TGGTAAGAGATCATT | 84333 |
rs139033222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171868 | GTCTTCGGGAACTAT[A/G]AGGCCAAAATATCAA | 84333 |
rs139036845 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198924 | TTCTCCTCCTCTCTC[A/G]GATGTTCTTCTCTTT | 84333 |
rs139168482 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245856 | TAGGGCGAGAAAAAA[C/G]CGTGTTGTCCAGGGG | 84333 |
rs139184610 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244376 | CTACGCCTTGTTGGA[C/T]GACCAGCAAGGAGAC | 84333 |
rs139293831 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269284 | TTGGAAGGGACTTAT[A/G]TCATATCATCTGATC | 84333 |
rs139301830 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228282 | AAACTAAGGACAAAG[G/T]GGCTATGTTCCAGCA | 84333 |
rs139315778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227532 | ACTTCTCAAATCTGT[A/C]CCTTTAGTTTCATCC | 84333 |
rs139423453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214600 | AAAGCAAAACAAAAC[A/G]CAGCATTAAGAACCC | 84333 |
rs139447442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203154 | ATTTAGGTCTCTAGA[A/G]CATGCCACTATCAAG | 84333 |
rs139449450 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275445 | ATAAAACTACATTTT[A/T]TTTTTTTTTTTTTTG | 84333 |
rs139494441 | in-del | -/AC | 0.467642 | 0.123012 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186605 | TATATGTGTATATAT[-/AC]ACACACATATATATG | 84333 |
rs139615394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221194 | GCAGAAAAGTTCCCC[C/G]TTGCCCCCGCCCCGT | 84333 |
rs139642862 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178640 | CCAGTCCTCCCACCT[C/T]GGCCTCCCAAAGTGC | 84333 |
rs139659649 | in-del | -/TT | 0.0422008 | 0.138995 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204008 | ATGTTTATTGTTGAG[-/TT]TGTGAAGCATGACAC | 84333 |
rs139660021 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247561 | TAGAAGAGTAATGTT[A/G]TTGAGCAGGATGAAG | 84333 |
rs139692445 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234246 | CAAAGGAATTGGGAA[A/G]CGGCAAAACAAAATA | 84333 |
rs139696985 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253615 | TTCGCGTCATCTTTG[A/T]TCTGTTACTCTTTTC | 84333 |
rs139708758 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172387 | TTGTGCCACTGCACT[C/G]CAGCCTGTGCCACAG | 84333 |
rs139768818 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184709 | TCTACCTTCAGTATT[G/T]GAGGTTGCTGTTTTG | 84333 |
rs139836914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248973 | GAGAAAAGGGAGATA[A/G]AAGAGAAGATTGGCT | 84333 |
rs139844669 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185488 | ATCCTGTGAGGTGCC[A/G]TGGAAGTGAGGCCCG | 84333 |
rs139846317 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243062 | CTCATGATAGGTTCT[C/G]AGTAAACACTTTTTA | 84333 |
rs139856387 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254821 | AAATGTTCAGTGTCA[C/G]CTTTTTCAGAGATCT | 84333 |
rs139879231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189229 | ATTGATAATTTTCTC[C/G]TTTTTCCAGACATCC | 84333 |
rs139894238 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165441 | CCCACTGCCTGGAAA[A/G]CAGCCTGAAGTTTAG | 84333 |
rs139899657 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275579 | CTTAGTAGCTGGGAT[C/T]ACAGGCATGCGCCAC | 84333 |
rs139923896 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184004 | TAATATTTTTTCTTC[A/G]TTTCGACCTTGGATA | 84333 |
rs140049332 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277253 | ATTTTCAGGATTGTT[A/C]AATCTCAGTCTAGCC | 84333 |
rs140071127 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281360 | ACACACTCAAATGTA[A/T]TCTAAATTTAAACTG | 84333 |
rs140116086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198537 | CAAACCACTATTTCA[A/G]CATGACCATTGGCAA | 84333 |
rs140142463 | in-del | -/GGTT/GGTTTTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184435 | ACTCTCTACTGGCTG[-/GGTT/GGTTTTT]TTTTGTCTGTCAGCT | 84333 |
rs140143292 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263311 | AATTAATTTACAAAA[A/T]AGATAAAAATGAAAT | 84333 |
rs140172345 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235511 | GAGTTTGAGACCAGC[C/G]TGGGCAATATGGGAA | 84333 |
rs140178713 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187306 | AACCACTGTTACAAG[A/C]TCTGCACACTTTTGC | 84333 |
rs140181079 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168713 | GTGGGCAGATCATGA[G/T]GTCAAGAGTTCCAGA | 84333 |
rs140217017 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284754 | AGTGAAACGTTGGAG[A/G]TAGCTAGAAACCCCA | 84333 |
rs140237483 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161529 | GACTGGGTTCATGTC[G/T]ACTTTTTCATGATTT | 84333 |
rs140255605 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263808 | GCAAATCACTGACCA[G/T]GCAAACCAGAGAAGC | 84333 |
rs140260432 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239666 | GGTACTGTAAATATT[A/G]TCTAAGGTTTTGGGG | 84333 |
rs140265931 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177301 | CCCGGCTGTGTGAGG[C/T]GTCACTCTGCCCCTA | 84333 |
rs140268573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267462 | AAATCTCCAGCACCT[A/G]GGGCAGTGCCCAGCA | 84333 |
rs140282281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165794 | GTAAAAAGGATGTGT[A/G]TGTCATATTTAATAA | 84333 |
rs140337846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245625 | TAGGGAATGCAATCT[C/T]ACAGCCTAAGAGGAG | 84333 |
rs140381946 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192110 | TTCCAGCCTTAAACT[A/G]GCTGAAGGCAATTAG | 84333 |
rs140421112 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258439 | CATTGTATATACTTA[C/G]AGTTGAACCTCCCAA | 84333 |
rs140476979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217481 | AGAACTACCTACCCA[C/T]CCATTGCCCAGCCAT | 84333 |
rs140592722 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277307 | AAAGTTCTCTATACC[A/G]TATTTTTATATTCAT | 84333 |
rs140595926 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262546 | TATGAATATCATGAA[A/G]AGTCATCATAGGAGA | 84333 |
rs140605492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178920 | TCATCCTCTACAACT[A/G]ATTTCAGCACTCACT | 84333 |
rs140669067 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251329 | ACCGAAAGTAGATGA[A/G]GAAGGTGATGAAAAT | 84333 |
rs140718105 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170183 | CTCCTAGAAGATAAC[A/G]TAGGAGAAAATCTGG | 84333 |
rs140757414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244752 | GCTGGTGGATTGGAT[A/G]TAGGATATGGGATAA | 84333 |
rs140767341 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230826 | CGGGGTTTGGCCATG[A/T]TGCCCAGCCTGGTCT | 84333 |
rs140812353 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208191 | ACATAAGTTGACATT[C/G]TCTTGAAAAGAAGGA | 84333 |
rs140850128 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191040 | AGTTCTCCCTGATCC[A/G]CAGGGAACATATTCC | 84333 |
rs140853826 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196974 | TTCTTTTTATCCTGT[A/G]CATGATGTGGAACCA | 84333 |
rs140873142 | snp | C/T | 0.077417 | 0.180873 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91162710 | ACGCTCCGGGAGCTG[C/T]GCGGCGGCGGCTCGA | 84333 |
rs140889126 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196218 | TCAGCAAGGGCTAGA[A/G]TGTCAGTGCCAAGAG | 84333 |
rs140917905 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179223 | CTAGTGTGGTCTCTT[C/T]TAAGTCAGAGGAATA | 84333 |
rs140935489 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263442 | ACATGTCTAATACAA[-/A]TTAACTGAAACTATA | 84333 |
rs141010258 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189402 | TACAACATGGTGCCT[C/G]GTACATAGTAGACAC | 84333 |
rs141048069 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195074 | AGGAAGCAGCTGAGA[G/T]TGAGGATGGGGAAGG | 84333 |
rs141085891 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223976 | TTGTTAGTAAGCCTC[A/G]TTTTTCAGCTATTCT | 84333 |
rs141128141 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180596 | TTATTTATGCTATTT[A/G]TGAATAGGGAATCCT | 84333 |
rs141136720 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240047 | TGCCAATAAAAGTAA[C/T]GCAAACAGGTTGAAA | 84333 |
rs141173563 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271199 | GCCTTACAGGTTGAG[C/T]GGAGTTCCACGTCCC | 84333 |
rs141268334 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209857 | GTCTCCCAGTTTAGT[A/T]GCTATCAATGGGCAT | 84333 |
rs141291296 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216479 | GAAATGGCCTTATTA[A/G]GTGTTTGGGCATTAT | 84333 |
rs141297721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200853 | TTCAATGAAGTAATT[A/G]ATGTAAAAATATTAA | 84333 |
rs141335980 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167494 | TTAAAAAATTGAGAC[A/G]ACTTCAATCGGCAAA | 84333 |
rs141368155 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192065 | TTGGCTCCAAAATTA[-/T]TTTTTTTCTTTATAG | 84333 |
rs141373502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226868 | TTTAGACTCTTCTTA[C/T]CTACTAATACCTCTT | 84333 |
rs141383146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203285 | GCATGTCTTTTTAGC[A/G]TTTTCTTGGAGCACT | 84333 |
rs141408031 | in-del | -/TA | 0.0763149 | 0.179815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183286 | TGTTCCTGTGTTGGG[-/TA]TATATATATATTTAG | 84333 |
rs141423867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170555 | CAAATCAAAACAACC[A/G]TGATATACCACTATA | 84333 |
rs141437321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201189 | AAATGTATTGCTTAC[A/G]TATCTGGAGGCTGGG | 84333 |
rs141498403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266292 | CACTGCACGACCTCT[A/G]CAAGTGGCTCACTTG | 84333 |
rs141603371 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220228 | ACAAGTTTGTCAGTC[A/G]TTTTCAGATAAGGTG | 84333 |
rs141697254 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184336 | TCTGAGATTCCTCTA[C/T]GTGGTCTATTCTGAT | 84333 |
rs141706758 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224951 | GTTTTGTTTTGCTTC[G/T]TTGAACATTTGTTCA | 84333 |
rs141746709 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280163 | TATCTAGCTACAGAA[A/G]TTATTTTTCTATGGT | 84333 |
rs141793573 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279819 | ATTTTCCAGTAAAAT[A/G]TATCAGAAATCAATG | 84333 |
rs141799479 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229896 | AATGATGTCATTGGT[A/G]TACTGATGTTACATA | 84333 |
rs141843170 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182116 | GATGGTTGTTTGTAT[A/T]TCTGTGAGGTCAGCG | 84333 |
rs141861865 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252915 | TTTTGACATCTTTGA[A/C]ACTTTGCTATTCTAG | 84333 |
rs141865792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171520 | TCTCCAGCAATGCTC[A/G]GAAAATTGGAAGTAG | 84333 |
rs141899418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234100 | CACACATACATCTAA[C/G]ATAGCAACAACAAAT | 84333 |
rs141924056 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212006 | TACTGGTTGTTGCAC[A/T]AACTCTCTGTACCAT | 84333 |
rs141936773 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247510 | TTTGGGGTTTTTTTT[-/T]AAGATGTGAGAAACC | 84333 |
rs141965279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198187 | CTTGGATTTCCGTCT[C/G]TCTAAATTGAACCCA | 84333 |