| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs1878548 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322983 | ATAATCTGTATTCTA[A/G]AGAGGGTCCTCCTGG | 84108 |
| rs1878549 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323043 | AGTCTTCTGCTTTTA[A/G]AAATAACAGGCTGTT | 84108 |
| rs2945128 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347780 | atccacctaagccta[A/G]gaagtggaggctgca | 84108 |
| rs3004636 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314827 | cggtggtaatcatgg[G/T]gcctgtaatcccagc | 84108 |
| rs3062789 | in-del | -/C/CA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322836 | tcaCACACACACACA[-/C/CA]AAAAGTCCAGCCTGG | 84108 |
| rs3062791 | snp | A/C | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316013 | tctctctctctctct[A/C]tATATATATATATAT | 84108 |
| rs3106997 | snp | C/T | 0.0058479 | 0.0537564 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305579 | CCCGGCCCTAGACTT[C/T]TTAATAGACTATTTA | 84108 |
| rs4420190 | snp | C/T | 0.264358 | 0.249587 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325434 | AATTTTTGTATTTTT[C/T]AGTAGAGATAGGGTT | 84108 |
| rs4917387 | snp | C/T | 0.499614 | 0.013886 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348698 | AAAATACAATTGTAA[C/T]TTATATATTCTTCTT | 84108 |
| rs4918007 | snp | A/G | 0.477004 | 0.104734 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347713 | GTGTGTGTGTGACAA[A/G]GTCTCACTTTTGTCA | 84108 |
| rs5787487 | in-del | -/A | 0.499609 | 0.0139722 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306088 | ACCAAGGCTGCATCC[-/A]GCAAGCAATCCACCT | 84108 |
| rs5787488 | in-del | -/GAGA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316041 | AGAGAGAGAGAGAGA[-/GAGA]TATCTCACTTAACTG | 84108 |
| rs5787491 | in-del | -/C | 0.0919752 | 0.193722 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348006 | ACTGTTAGTATTTTT[-/C]CCTCTCTTAAGAAAC | 84108 |
| rs6584547 | snp | C/T | 0.499965 | 0.00419314 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305652 | TCGCAGATCTGTTCA[C/T]TTCCACATAAATGCA | 84108 |
| rs7082576 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340198 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 84108 |
| rs7085765 | snp | A/G | 0.371177 | 0.218669 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315996 | tgtgtgtgtgtgtgt[A/G]tATATATATATATAT | 84108 |
| rs7093667 | snp | C/T | 0.4582 | 0.138394 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320818 | GTTAGTAAATAACCA[C/T]AAATGAAGGTCACAT | 84108 |
| rs7096008 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348302 | ttaaaagaatATGTA[A/G]TTCCCTTTTAATTTT | 84108 |
| rs7902377 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308794 | gggagaatcacttga[C/G]cctgggaggcagagg | 84108 |
| rs7908588 | snp | C/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328067 | TGAGGTGTAGGAGGT[C/G]ATAAGTAGATGACAG | 84108 |
| rs7923496 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340200 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 84108 |
| rs7923497 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340202 | aaaaaaaaaaaaata[A/T]atatatatatatata | 84108 |
| rs10615985 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315994 | tgtgtgtgtgtgtgt[A/G]tATATATATATATAT | 84108 |
| rs10687554 | in-del | -/GT/TG | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342920 | GGGGACATAACAAAT[-/GT/TG]CTCTTGCCTTTTAGG | 84108 |
| rs10883855 | snp | C/T | 0.457737 | 0.139088 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332690 | TGGTAGCATATATCC[C/T]GGTGCTTAAACCATA | 84108 |
| rs11191649 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307280 | agacccccatttcta[C/T]gaaaaataaaaaaat | 84108 |
| rs11191650 | snp | C/G | 0.0995161 | 0.199636 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309482 | CTTCAGCCATGATTG[C/G]AAGCTAAGCTGCTAT | 84108 |
| rs11191652 | snp | G/T | 0.111576 | 0.20818 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315979 | TTATAtgtgtgtgtg[G/T]gtgtgtgtgtgtgtg | 84108 |
| rs11191653 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315983 | Atgtgtgtgtgtgtg[G/T]gtgtgtgtgtgtata | 84108 |
| rs11191654 | snp | A/C | 0.499451 | 0.0165644 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317367 | TTAGTGGGCTTTATA[A/C]CACGTGGTATACATT | 84108 |
| rs11191655 | snp | C/T | 0.153665 | 0.230694 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319036 | ATGAAAGTAGTCTTA[C/T]TAAAAGGAGAAAAAG | 84108 |
| rs11191656 | snp | C/T | 0.103438 | 0.202533 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325539 | aggcatgagccactg[C/T]gcctggccGAGCTTG | 84108 |
| rs11191657 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335827 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGCATGCC | 84108 |
| rs11191658 | snp | A/G | 0.423413 | 0.180077 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336264 | AAAAAAAATAAATAA[A/G]TAAAAAGAAAAAAGT | 84108 |
| rs11191659 | snp | C/T | 0.151668 | 0.229849 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341944 | TGCCATTAATATGTT[C/T]TTTTTTTTTTCTCAG | 84108 |
| rs11191660 | snp | A/G | 0.422315 | 0.181128 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343208 | GCTGGGATTATAGGC[A/G]TGAGCCACCGCGCCC | 84108 |
| rs11191661 | snp | A/G | 0.0275645 | 0.114116 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351162 | GCGCGGCAGCCTGAG[A/G]GGCTCGCCGGGAAAT | 84108 |
| rs11287016 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305217 | GAGCTTCAAGCAATA[-/C]CCCCATCTTGGCTTC | 84108 |
| rs11300480 | in-del | -/T | 0.204803 | 0.245881 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351644 | TTGAATTCGAAAAGC[-/T]TTTTTTTTTTTTTTT | 84108 |
| rs11345505 | in-del | -/T | 0.335788 | 0.23482 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327842 | ACTACGCCCAACTAA[-/T]TTTTTTTTTTTTTTT | 84108 |
| rs11450842 | in-del | -/T/TT/TTT | 0.493613 | 0.0561475 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349479 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GAGAGGGAGTCTGCC | 84108 |
| rs11498782 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316015 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 84108 |
| rs11594626 | snp | C/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335742 | ggaggccaaggtggg[C/T]agataatgaggtcag | 84108 |
| rs11599068 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335734 | gcactttgggaggcc[A/G]aggtgggcagataat | 84108 |
| rs11599069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335743 | gaggccaaggtgggc[A/G]gataatgaggtcagg | 84108 |
| rs12219982 | snp | A/G | 0.00332778 | 0.0406548 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345467 | tgcatcatctcattc[A/G]tccttactatagtcc | 84108 |
| rs12220267 | snp | C/T | 0.422787 | 0.180679 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315955 | AAATGGGGTTAGAGC[C/T]TCAACAGCTTATATG | 84108 |
| rs12220933 | snp | A/G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308899 | ataaataaataaaaa[A/G/T]aaaaaaattaatggc | 84108 |
| rs12252283 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305850 | accgggagttcaaga[A/C]cagcctgggcaacat | 84108 |
| rs12253433 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331645 | ttatatgtcccttaa[A/G]ttacttttctcaata | 84108 |
| rs12254444 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306828 | TAAACTCAAggccag[A/G]tgcaggggctcatgc | 84108 |
| rs12254510 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306958 | aaaatacaaaaatta[C/G]ccaggtgtggtggca | 84108 |
| rs12258092 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344326 | acccagactggagtg[C/T]ggtggcacgacctcg | 84108 |
| rs12260079 | snp | A/G | 0.00385355 | 0.0437256 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315001 | TTAAAAGGTATTAAT[A/G]CTTAAAAAGGCAATC | 84108 |
| rs12261012 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331631 | acaatgtaattaatt[A/T]atatgtcccttaagt | 84108 |
| rs12268583 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319405 | ATGTGCCCGCCTCGG[C/T]CTCCCAAAGTGCTGG | 84108 |
| rs12356928 | snp | C/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305768 | AAAGAATGCCCTCag[C/G]tggatgcagtggctc | 84108 |
| rs12414225 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304274 | cccaagtagctggga[C/T]tacaggcacccgcca | 84108 |
| rs12763259 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341457 | gtttttgtatttttc[A/G]agacggagtttggcc | 84108 |
| rs12774390 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309139 | aatgagttaagactt[G/T]gggggactattggga | 84108 |
| rs12778277 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330864 | aacctgggaggcaga[A/G]gttgcagtgagccca | 84108 |
| rs28510637 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327863 | TTTTTTTTTTCATTA[C/G]AGATAGGGTTTCACT | 84108 |
| rs28666634 | snp | C/G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315484 | CCTGCCTCAGCCTCC[C/G/T]GAATAGCTGGAACTA | 84108 |
| rs34099936 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332111 | CATCTCTGTGTCCCC[-/C]TGTATTTCTTGTAAA | 84108 |
| rs34156353 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312326 | TGAACCCGGGAGGCA[A/G]AGGTTGTAGTGAGCT | 84108 |
| rs34158009 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321520 | AGATCGAGATCATCC[C/T]GGCTAAATGGTGAAA | 84108 |
| rs34250994 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344329 | CAGACTGGAGTGCGG[G/T]GGCACGACCTCGGTT | 84108 |
| rs34273036 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335742 | GGAGGCCAAGGTGGG[CA/TG]GATAATGAGGTCAGG | 84108 |
| rs34389346 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336872 | GAGCCAGACTCCATC[-/C]TCAAAAAAGCAAAAA | 84108 |
| rs34403112 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304672 | TTTTTTTTTTTTTTT[-/T]GAAGACAGGGTCTTG | 84108 |
| rs34467688 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306190 | CAATCTCCGCCTCCC[-/C]GGGTTCAAGCGATTC | 84108 |
| rs34719186 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312120 | AGTCACGGTTGGGCA[-/C]TGGTGGCTCACGCCT | 84108 |
| rs34724815 | snp | A/C | 0 | 0 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351366 | TTCTGTTTGCATCAC[A/C]TAATTCACAGAGCAC | 84108 |
| rs34732054 | in-del | -/T | 0.488302 | 0.0755777 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304140 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 84108 |
| rs34738935 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322840 | ACACACACACAAAAA[-/A]GTCCAGCCTGGGCAA | 84108 |
| rs34900995 | snp | C/T | 0.0209036 | 0.100074 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303493 | GCTTTGAATCTTCCA[C/T]TCAAAAGCACACTTC | 84108 |
| rs35035891 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303697 | TTTCCCCTGAGCTTT[C/G]GCTGCTTTTTATATA | 84108 |
| rs35048058 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328878 | GCCTCAGCCTCCCAA[-/A]GTAGCTGGGACTACA | 84108 |
| rs35051041 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324329 | TAAATTTGACTAATG[-/A]AAAAAAAAAAAAGAA | 84108 |
| rs35108621 | snp | A/C | 0.0292618 | 0.117366 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353094 | TCAAAAAATTAAAAT[A/C]CAATAAAATAAAATA | 84108 |
| rs35225295 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316011 | ATATATATATATATA[G/T]ATAGAGAGAGAGAGA | 84108 |
| rs35560089 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303484 | CAAAGACTGGCTTTG[A/G]ATCTTCCACTCAAAA | 84108 |
| rs35648329 | in-del | -/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344860 | AGGCGTGAGCCACTG[-/G]CACCCGGCCCTTTAT | 84108 |
| rs35655182 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303455 | GGTCTTTGAGAGTAC[A/G]CCCTGCAGTTTAACA | 84108 |
| rs35672281 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303519 | ACTTCTCTTCCAAAA[A/G]GATGACTGCCCAACT | 84108 |
| rs35713672 | in-del | -/TT | 0.152334 | 0.230133 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305141 | TTCAAAATTTTTTTT[-/TT]CCCAGTATAAACGAG | 84108 |
| rs35839501 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338064 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs35844802 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303762 | AGTTGTACTTATAAA[C/T]GCTATAATTCTTGGT | 84108 |
| rs35888221 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303285 | CTTATTACACTGAAA[G/T]TTTATGGCACAGATC | 84108 |
| rs35956583 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345094 | ATTCTAGGACTTTTT[-/T]AGATCTTCCTTTGCT | 84108 |
| rs35977730 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303299 | ATTTTATGGCACAGA[C/T]CATAAACTCAGAGTC | 84108 |
| rs36067043 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303391 | CTAGTATAAAAAAAG[A/G]TACAAGTTCAAAATA | 84108 |
| rs36122679 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303163 | TTCAGAAGCAATACT[A/T]TTGCAAGGTATCAAC | 84108 |
| rs41287490 | snp | C/T | 0.147656 | 0.228091 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303522 | TCTCTTCCAAAAAGA[C/T]GACTGCCCAACTGAT | 84108 |
| rs55722610 | in-del | -/A | 0.464735 | 0.128019 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333138 | AAAAAAAAAAAAAAA[-/A]TCATGAGGACTTAAA | 84108 |
| rs55873511 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348585 | TCACCTCGGCCTCCC[A/C]AAGTGCTGGGATTAT | 84108 |
| rs56060736 | snp | C/T | 0.259951 | 0.249802 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310496 | ATATCATATGTACAT[C/T]ATGCACATATAACTA | 84108 |
| rs56777926 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324340 | AATGAAAAAAAAAAA[-/AA]GAAAAAGCAAAGCTA | 84108 |
| rs57037263 | in-del | -/GTGTAT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315992 | TGTGTGTGTGTGTGT[-/GTGTAT]ATATATATATATATA | 84108 |
| rs57407443 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335179 | AGCCTACCTGAGCAG[C/T]TGGGAGTACAGATAT | 84108 |
| rs57497944 | in-del | -/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309206 | TTGGTGGGGGGGGGG[-/G]CATGATTTGGGTGGA | 84108 |
| rs57906915 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326302 | GCTGACGCAGAAGAA[A/T]GGCGTGAACCCGGGA | 84108 |
| rs58312332 | in-del | -/AAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340196 | AAAAAAAAAAAAAAA[-/AAAA]TATATATATATATAT | 84108 |
| rs58927608 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339766 | CGCGCCACTGCCCTC[C/T]AGCCTGGGGAACAAA | 84108 |
| rs59117304 | in-del | -/GA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316043 | AGAGAGAGAGAGAGA[-/GA]TATCTCACTTAACTG | 84108 |
| rs59567810 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313628 | ATAGAAAAAAAAAAA[-/A]TCTCATCACGTTTTA | 84108 |
| rs59658888 | in-del | -/AACACACACACACA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339810 | CTGTCTCAAAAAAAA[-/AACACACACACACA]CACACACACACACAC | 84108 |
| rs59709249 | snp | C/G/T | 0.0109346 | 0.0731292 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303879 | AAGCCTCCTTTGTTT[C/G/T]CCTCCTCATAATGTG | 84108 |
| rs59855380 | snp | C/T | 0.0192964 | 0.0963112 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326655 | AACAGACAGATAAAA[C/T]TATTTTTAGGTTAAA | 84108 |
| rs59937825 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306773 | GAATGTTGAAGACCA[A/G]TGGTAAACCAGAGAG | 84108 |
| rs60182387 | in-del | -/A | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314982 | AAAAAAAAAAAAAAA[-/A]TCATTAAAAGGTATT | 84108 |
| rs60211186 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340030 | AAAAAAAAAAAAAAA[-/AA]TTCAGGCATGGTGGT | 84108 |
| rs60388741 | snp | G/T | 0.499942 | 0.00539106 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344668 | CCTAGGTTCAAGAGA[G/T]TCTCCTGCCTCAGCC | 84108 |
| rs60406996 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345682 | AAAATACAAAAATTA[C/G]CCAGGCATGGTGGCA | 84108 |
| rs60968810 | in-del | -/AGGCGG | | | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350997 | AGGAGGCGGAGGCGG[-/AGGCGG]CAAGGCTGCAGCTCC | 84108 |
| rs61284665 | in-del | -/AAAACA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339808 | GTCTGTCTCAAAAAA[-/AAAACA]CACACACACACACAC | 84108 |
| rs61350103 | snp | A/C | 0.499653 | 0.0131743 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309363 | AATTTCCCTTTGGTA[A/C]TGTCCTCACAAAAGT | 84108 |
| rs61400102 | snp | A/G | 0.103438 | 0.202533 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302929 | TCTGCTGTTAAACAG[A/G]ATTTATAAAATATTT | 84108 |
| rs61760880 | snp | C/T | 0.00143298 | 0.026729 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345062 | CATATCAAGTTCAGG[C/T]GGAATACGAAACACT | 84108 |
| rs61869822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304758 | CCACCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 84108 |
| rs61869823 | snp | A/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305895 | TCTCTACTTATATAA[A/T]TTAAAAAAAAAAAAA | 84108 |
| rs61869825 | snp | C/T | 0.422944 | 0.180528 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313313 | CTCACCCCTGTAATC[C/T]CAGCCCTTTGGGAGG | 84108 |
| rs61869826 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319436 | GATTACAAGCGTGAG[C/T]CACCGGACCTGGCCA | 84108 |
| rs61869827 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319682 | CTAAGGTCAAATACA[C/T]AGACCCTCAATTTAG | 84108 |
| rs61869828 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320012 | GGGGTTTCACCATGT[G/T]GGCCAGGATGGTCTC | 84108 |
| rs61869829 | snp | C/T | 0.48955 | 0.071525 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325083 | GAAGTTGCAGAGAGC[C/T]GAGATCACGCCATTG | 84108 |
| rs61869830 | snp | A/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327840 | CCACTACGCCCAACT[A/T]ATTTTTTTTTTTTTT | 84108 |
| rs61869831 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329772 | GCCACCGTGCCCGGC[C/T]AGTTTTTTTGTTGTT | 84108 |
| rs61869832 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335447 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 84108 |
| rs61869833 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335638 | AGTGCTAGGATTACA[A/G]GAGTGAGCCACGGTG | 84108 |
| rs61869834 | snp | C/T | 0.226188 | 0.248863 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335941 | CACTACACTCCAGCC[C/T]GGTGACAGTGCGAGA | 84108 |
| rs71019676 | in-del | -/TGTGTTT | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339811 | GTGTGTGTGTGTGTG[-/TGTGTTT]TTTTTTTTTTGAGAC | 84108 |
| rs71019677 | in-del | -/TTTTTTTTTT | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343850 | AGTTAGATACCTTTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 84108 |
| rs71229632 | multinucleotide-polymorphism | AATCTTCCAC/GATCTTCCAT | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303484 | CAAAGACTGGCTTTG[AATCTTCCAC/GATCTTCCAT]TCAAAAGCACACTTC | 84108 |
| rs71471279 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322895 | AAAAAAAAACAAAAA[A/C]CAAAAAACAAAAAAA | 84108 |
| rs71471280 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340006 | GCCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA | 84108 |
| rs71471281 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340042 | AAAATTCAGGCATGG[G/T]GGTATGCGCCTGTAA | 84108 |
| rs71471282 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346746 | GTTGCGGTGAGCTGA[A/G]ATCACAGCATTGCAC | 84108 |
| rs71474584 | in-del | -/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317263 | GATCCGCCCACCTCA[-/G]GGCTCCCAAAGTGCT | 84108 |
| rs71474585 | in-del | -/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321434 | ATAATATATTGTAGG[-/C]TGGGCGCGGTGGCTC | 84108 |
| rs71474587 | in-del | -/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346554 | GCTTGAGCCCAGAAG[-/G]CGGAGGTTGCAGTGA | 84108 |
| rs72262877 | in-del | -/TGTGTA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315991 | GTGTGTGTGTGTGTG[-/TGTGTA]TATATATATATATAT | 84108 |
| rs72357106 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340181 | GACTCTGTCTCAGGG[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs72505130 | in-del | -/TG | 0.0876345 | 0.190099 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342919 | TGGGGACATAACAAA[-/TG]TCTCTTGCCTTTTAG | 84108 |
| rs72846190 | snp | C/T | 0.260227 | 0.249791 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319660 | ATTTTGTCTCATCTT[C/T]GTACTCCTAAGGTCA | 84108 |
| rs72846191 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322174 | GTGCTGGGATTACAG[A/G]GTGAGCCACCTTGCC | 84108 |
| rs72846192 | snp | A/C | 0.258288 | 0.249863 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331702 | TCTCTTTCCTTTTTA[A/C]TTTATTTGCTGAAGA | 84108 |
| rs72846195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334409 | AGCAATTTTCAAGTA[C/T]ATAATACATTATTAA | 84108 |
| rs72846196 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337508 | ACATCCCAAGGGTTA[C/T]CTACTCTGAGTTAGT | 84108 |
| rs72846198 | snp | A/G | 0.420574 | 0.182769 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338267 | CAAAAAAACCGGTCA[A/G]GTGCAGTGGCTCATG | 84108 |
| rs73334808 | snp | A/T | 0.103438 | 0.202533 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311084 | CAAATGATCCTCCCA[A/T]CTTGGCCCCACAAAA | 84108 |
| rs73334819 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329446 | AAATATAACCAGTAA[C/T]GGGCTTAAACAAAAA | 84108 |
| rs73334821 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332216 | CATGTTTTTTCATGT[G/T]TAAGAACCACAACTA | 84108 |
| rs73334824 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339733 | AGACTGAGGACTGAG[A/G]TTGCAGTAAGCCAAG | 84108 |
| rs74154321 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332568 | GATGTGAGCCAACGA[A/C]CCCGGCCTAATATTT | 84108 |
| rs74233813 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332579 | ACGAACCCGGCCTAA[C/T]ATTTCAATTCATTCT | 84108 |
| rs74398240 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304748 | GAATTGCTTGAACCC[A/G]GGAAGCAGAGGTTGC | 84108 |
| rs74674688 | snp | A/T | 0.00518234 | 0.0506391 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347707 | TTTTGTGTGTGTGTG[A/T]GACAAGGTCTCACTT | 84108 |
| rs74678577 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326390 | CAAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 84108 |
| rs74693936 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318868 | GCAGGCCTAGTTCCT[C/T]GATAGCCAAAGGCCA | 84108 |
| rs74729149 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321914 | ACTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 84108 |
| rs74745496 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323314 | GTCACTTTTTTTTTT[G/T]AGTTGGAGTTTTGCT | 84108 |
| rs74816205 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341798 | AAGATATTACTCCAG[C/T]CTTCTTTTGATTAGT | 84108 |
| rs74948498 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318744 | GCGAGACTCTGTCTG[A/G]AAAAAAAAAAGAAAA | 84108 |
| rs75051428 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333114 | CAGAGGAAGACTCCA[-/AAA]TTTAAAAAAAAAAAA | 84108 |
| rs75079768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342282 | CTCATTGCCCAGGCT[A/G]GAGTGCAACAGCATA | 84108 |
| rs75202703 | snp | C/T | 0.00015188 | 0.00871302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345155 | ATAGTCAAACAAAAA[C/T]GTTAATTAAGAATAA | 84108 |
| rs75266352 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347885 | CCCTTCATAAGAATA[C/T]GAGTTGAGGGCAGAG | 84108 |
| rs75358623 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341705 | CACCTAAGCCTCCCA[A/G]AATGCTGGGATTACA | 84108 |
| rs75383465 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330088 | TTTGTTTGTTTGTTT[G/T]TTTTTTGAGATGAAG | 84108 |
| rs75435276 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346512 | GCCTGTAGCCCCAGC[C/T]ACTCAGGAGGCTGAG | 84108 |
| rs75477360 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330384 | CTGGACAAGCATATA[A/T]TGTTTCAACCAGATA | 84108 |
| rs75692102 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322883 | TCCTTGCCACCAAAA[A/C]AAAAACAAAAAACAA | 84108 |
| rs75890466 | snp | C/T | 0.093777 | 0.195178 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316626 | TGCCATCTCAGGGGT[C/T]GGCAAACCGTTTCTG | 84108 |
| rs75964205 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337537 | GTCTTCAAAACCTAT[A/G]CTCTTTCAACATACC | 84108 |
| rs76196456 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323313 | AGTCACTTTTTTTTT[G/T]GAGTTGGAGTTTTGC | 84108 |
| rs76197128 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350049 | GATCGCGCCACTGCA[A/C]TCCAGCCTGGGCGAC | 84108 |
| rs76304782 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343851 | AAAAAAAAAAAAAAA[A/G]AAAGGTATCTAACTA | 84108 |
| rs76448540 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318743 | AGCGAGACTCTGTCT[A/G]AAAAAAAAAAAGAAA | 84108 |
| rs76636588 | snp | A/C | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322903 | ACAAAAAACAAAAAA[A/C]AAAAAAAAAAACAAC | 84108 |
| rs76695159 | snp | C/T | 0.152001 | 0.229992 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311080 | GGGTCAAATGATCCT[C/T]CCATCTTGGCCCCAC | 84108 |
| rs76751118 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348006 | ACTGTTAGTATTTTT[C/T]CCTCTCTTAAGAAAC | 84108 |
| rs76792309 | snp | A/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309760 | CATGGCAAAACCCCA[A/T]CTCTACAAAAAATTA | 84108 |
| rs76923115 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304155 | CTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 84108 |
| rs76980333 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313618 | AACAGTAGCTGATAG[A/G]AAAAAAAAAATCTCA | 84108 |
| rs77328741 | snp | C/T | 0.152334 | 0.230133 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306557 | TGCTGCTCTGGCTAT[C/T]ACTCTCCTTCGCTTC | 84108 |
| rs77376583 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307450 | GCAAGACCCTGTCTC[A/C]AAAAAAAAAGAAAGA | 84108 |
| rs77406134 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311461 | TCTTTTTTTTTTTTT[G/T]TGAGACATGGTCCTG | 84108 |
| rs78042626 | snp | A/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327843 | CTACGCCCAACTAAT[A/T]TTTTTTTTTTTTTTC | 84108 |
| rs78097464 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306758 | TGTGAAGTCAATAGG[C/G]AATGTTGAAGACCAG | 84108 |
| rs78214896 | snp | G/T | 0 | 0 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351658 | CTTTTTTTTTTTTTT[G/T]TTGAGACAGTTTCGC | 84108 |
| rs78300470 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350083 | GCGAGACTCCGTCTC[A/C]AAAACAAAACAAAAC | 84108 |
| rs78382105 | in-del | -/AAAAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340194 | GGAAAAAAAAAAAAA[-/AAAAAA]TATATATATATATAT | 84108 |
| rs78514319 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317774 | TTCTGTTTTTTTTTT[G/T]AGACAGAGTTTCGCT | 84108 |
| rs78629417 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324450 | GAAGTTTGAGGTTTC[C/T]ATCGTACAACAAGAA | 84108 |
| rs78742461 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316237 | ATCATACCTTTCAAC[C/T]ACTGCCCATAGACTT | 84108 |
| rs78743011 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305290 | GACTTTTTTTTTTTT[G/T]AAACACAGTCTGGCT | 84108 |
| rs78779345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334613 | AAAATTTCTTACAAG[A/G]AGGCTGCTATGCTTC | 84108 |
| rs78883680 | snp | A/C | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309767 | AAACCCCATCTCTAC[A/C]AAAAATTAAAAAAAA | 84108 |
| rs79099624 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322799 | ACTGCACTCCAGCAT[G/T]GGTGACAGAGCAAGA | 84108 |
| rs79113102 | snp | A/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335683 | CTTTGTAAGAAAAAA[A/T]TAGGCTGGGCGAGGT | 84108 |
| rs79160225 | snp | C/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346737 | AAGGTGGAGGTTGCG[C/G]TGAGCTGAGATCACA | 84108 |
| rs79173927 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318771 | AAAAAAGAAAAAAAA[-/A]GTTGGTTTTGTTGGC | 84108 |
| rs79424133 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351273 | AAAGGAATCTCACCA[A/G]ATTTTCTCCTTGGAA | 84108 |
| rs79560233 | snp | A/C | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309765 | CAAAACCCCATCTCT[A/C]CAAAAAATTAAAAAA | 84108 |
| rs79627327 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338546 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAG | 84108 |
| rs79679985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327875 | TTAGAGATAGGGTTT[C/T]ACTGTTAGCCAGCAT | 84108 |
| rs79911753 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350050 | ATCGCGCCACTGCAC[C/T]CCAGCCTGGGCGACA | 84108 |
| rs80089818 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326388 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 84108 |
| rs80163985 | snp | A/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322836 | ATCACACACACACAC[A/C]AAAAGTCCAGCCTGG | 84108 |
| rs80198203 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342776 | TAACCTACTCCCTTA[C/T]AGAGATATAAATTGC | 84108 |
| rs111267368 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333568 | TCAGTGAATAATTGA[A/G]GTAACAAGTAGGGCA | 84108 |
| rs111322127 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326465 | CATGAAATCCTACAG[A/G]GTTCTTTCTACAGTG | 84108 |
| rs111328752 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342346 | TCAAGTAATTCTCCC[A/G]CCTCAGCCTCCTGGG | 84108 |
| rs111367561 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343152 | CCAGGATGGTCTTGA[A/T]CTTCTGACCTCATGA | 84108 |
| rs111410909 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345644 | ACCAGCCTGGCCAAC[A/G]TCGCAAAACCCTGCC | 84108 |
| rs111413235 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310272 | ATGTCTTAAAAAAAA[A/G]AAAAGAAAGAAAGAA | 84108 |
| rs111570160 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306564 | CTGGCTATTACTCTC[C/T]TTCGCTTCTTTGCTA | 84108 |
| rs111576817 | in-del | -/C | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339812 | GTCTCAAAAAAAAAA[-/C]ACACACACACACACA | 84108 |
| rs111614962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320401 | TTTCTTAAGAACACA[C/T]GATGGCCGGGCGCGG | 84108 |
| rs111643278 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324453 | GTTTGAGGTTTCCAT[C/T]GTACAACAAGAAGAA | 84108 |
| rs111649652 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350176 | GGCAACGTGGCTCAC[A/G]CATGTAATCTTTCGG | 84108 |
| rs111668776 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330487 | CTTGGCTTAGGTATT[-/A]AAAAAAAAATCAACA | 84108 |
| rs111776557 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315585 | AGGATGGTCTAGATC[C/T]CCTGACCTGATGATC | 84108 |
| rs111923042 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330143 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAGCCT | 84108 |
| rs111932595 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316794 | CAATTTAAAAGCTAG[C/T]AAGTCTAAAATCCAA | 84108 |
| rs111954061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337659 | AAAGCTGGGCACGGT[A/G]GCTCACGCCTGTAAT | 84108 |
| rs111989721 | snp | C/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342921 | GGGGACATAACAAAT[C/G]TCTTGCCTTTTAGGG | 84108 |
| rs112037177 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333672 | CAAAAATGCTTTGAG[A/G]CATTTTTTATCACCA | 84108 |
| rs112141020 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346790 | CAAGAGCAAAACTCC[A/G]TCTCAAAATAAAAAG | 84108 |
| rs112184148 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349590 | GATTCAAGTGATTCT[C/T]CTACCTCAGCCTCCT | 84108 |
| rs112184880 | snp | C/T | 0.103438 | 0.202533 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308510 | TTCAAGCAATTCTCC[C/T]ACCTCAGCCTCCCAA | 84108 |
| rs112186664 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316581 | ATAAACCCAGGTCTG[C/T]CCAAGATCTAATTTT | 84108 |
| rs112288997 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314797 | TCTACTAAAAATACA[A/G]AAACTAACCAGGCAC | 84108 |
| rs112297898 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318116 | CACTATGTGTGCATG[G/T]GGGTTTTTCTGTTAT | 84108 |
| rs112303434 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332165 | AGTCACCTTCCTATA[A/T]GTCTTGGCAAGAACA | 84108 |
| rs112303838 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339562 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT | 84108 |
| rs112512798 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323114 | AGCTTTGTCTCTAAC[A/G]AAAACCTAAGAATAA | 84108 |
| rs112559381 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342964 | TTGAGACGGAGTCTC[C/T]GCCGCCCAGGCTGGA | 84108 |
| rs112611617 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325414 | GTGTGCCAACAGGTC[C/T]GGCTAATTTTTGTAT | 84108 |
| rs112643532 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334033 | ACATATATAAATATT[C/T]GAGAAACATCAATTC | 84108 |
| rs112645902 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337792 | ATTAGCGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 84108 |
| rs112756264 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330555 | CCCTTTAAAAGTGTA[C/G]GATTAAATGGATTTT | 84108 |
| rs112803498 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310112 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 84108 |
| rs112869295 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315992 | TGTGTGTGTGTGTGT[A/G]TGTATATATATATAT | 84108 |
| rs112896267 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349829 | GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA | 84108 |
| rs112906825 | in-del | -/A | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338874 | ACTCCGTCTCAAAAG[-/A]AAAAAAAAATGCATA | 84108 |
| rs112940311 | snp | C/T | 0.499609 | 0.0139722 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304537 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 84108 |
| rs112974857 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345953 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGTG | 84108 |
| rs112993242 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311812 | CATGACTGTCAGCCA[C/G]GTGTGGTGGCTCATG | 84108 |
| rs113018538 | in-del | -/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348341 | TCAAGAGTTTTTTTG[-/T]TTTTTTTTTTTTTGA | 84108 |
| rs113035424 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327625 | ATACTATTCTGCCTA[C/T]TTTTGTATAAGTTTT | 84108 |
| rs113076508 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334345 | GCTAAGCATGTGAGG[C/T]GATGGATATGTTGAT | 84108 |
| rs113077861 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315560 | GAGACGGGGTTTCAG[C/T]GTGTTAGCCAGGATG | 84108 |
| rs113103280 | in-del | -/T | 0.499767 | 0.0107802 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345509 | TACCAGTGCTACTGC[-/T]TTTTTTTTTTTTCTT | 84108 |
| rs113185487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316488 | ACTACAATTCTGATT[C/T]TACAGATAGGGAAAC | 84108 |
| rs113207546 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322426 | GCCCAGGCTGGTCTC[A/G]AACTCCTGGGCTCAA | 84108 |
| rs113278560 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304803 | TGGGAAAATAGACAC[G/T]CACCACCACCAGACT | 84108 |
| rs113359610 | in-del | -/GGAGGC | 0.498198 | 0.0327153 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350983 | GCGGGCGGGGAGACA[-/GGAGGC]GGAGGCGGAGGCGGC | 84108 |
| rs113365678 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331283 | TTTGAGACAGAGGTT[C/T]GCTCTTTTGCCCAGG | 84108 |
| rs113470381 | snp | C/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315993 | GTGTGTGTGTGTGTG[C/T]GTATATATATATATA | 84108 |
| rs113555008 | snp | A/G | 0.093777 | 0.195178 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319373 | GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTTGT | 84108 |
| rs113683594 | snp | C/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313232 | ATCTTTTGGCTTCCC[C/T]GGGCCACACTGGAAG | 84108 |
| rs113758605 | snp | A/G | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340742 | GATGGGACTACAGGT[A/G]CATGCCACCATGGCC | 84108 |
| rs113775258 | snp | G/T | 0.5 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316961 | TGCACAGAGAACTTA[G/T]ATCCATAAAAAGTTA | 84108 |
| rs113861465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346850 | TGTCCATTCCGTGAC[A/G]TTACATCATCATAAA | 84108 |
| rs113877615 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323422 | CTGCCTCAGCCTCTC[A/G]AGTAGCTGGGATTAC | 84108 |
| rs113966337 | snp | C/T | 0.103794 | 0.20279 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320624 | CCCAGGAGGCGGAGG[C/T]TGCGGTGAGCCGACA | 84108 |
| rs113968420 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325050 | TGAGGCAGGAGAATC[A/G]CCTGAACCCGGGGGG | 84108 |
| rs114387999 | snp | G/T | 0.0573587 | 0.15934 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309140 | ATGAGTTAAGACTTT[G/T]GGGGACTATTGGGAA | 84108 |
| rs115433926 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342018 | TCAGCTCACTGCAAC[A/G]TCCACCTCCCAATTC | 84108 |
| rs115729984 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323175 | ATAAGTCATTTCTAG[C/T]TTTCAGCTGCCATGA | 84108 |
| rs115960857 | snp | A/G/T | 0.00795532 | 0.062565 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340755 | GTGCATGCCACCATG[A/G/T]CCAATTAATTTTCTT | 84108 |
| rs116092894 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313677 | TGTTGGGCCCCATTC[A/G]CAGCTATCCTGGGCC | 84108 |
| rs116120213 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342223 | TTAAGAGTGAGCCAC[C/T]GCACCCGGACTTTTT | 84108 |
| rs116442807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305559 | TACAAGTGTGACCCG[C/T]TGCACCCGGCCCTAG | 84108 |
| rs116501581 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340396 | GGTAATGACTGCCTT[C/G]AGCAGTGTGGTCAAG | 84108 |
| rs116718848 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335091 | GAGATAGGGTCTTGC[A/T]CTATCACCCAGGCAG | 84108 |
| rs116877190 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315093 | ATCATAGTACAACAC[C/T]GACTTGAAGTTCACA | 84108 |
| rs116889583 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345547 | AAAGAAACTGAGACC[A/G]CCAGTCGCCATGGCT | 84108 |
| rs116935979 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321348 | TGATGTAAGCAAAAA[A/G]GAAACCCACATTTTT | 84108 |
| rs117127192 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333814 | ATATTATTAAATGTA[C/T]TTCATATTTAAATAA | 84108 |
| rs117163338 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310903 | ATGGGGTTTCATCAC[A/G]TTGTCTAAGCTGGTC | 84108 |
| rs117254468 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318775 | AAGAAAAAAAAAGTT[C/G]GTTTTGTTGGCACTC | 84108 |
| rs117294680 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347681 | CACTAAACTGTTTCA[C/T]GTGCATTGTTTTTTG | 84108 |
| rs117502120 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343941 | CTCGTGGAGAACTAT[C/G]TATCTCACATATACA | 84108 |
| rs117502386 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337274 | CTGTATCACACATCT[C/G]CTAAGACTCTATTTT | 84108 |
| rs117576475 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318944 | ACGTTAACTCTTTTG[C/T]GCATAATATCTTACC | 84108 |
| rs117618769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318837 | AAACTTTTCACATTA[A/G]TGTAGGAAACTTTTT | 84108 |
| rs117720914 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320930 | CACCAAGAATTGTAG[A/T]CTGATGACTAGCAAA | 84108 |
| rs117807544 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329990 | TAGCCAGGATGGTAT[C/T]GATCTCCTGACTCGT | 84108 |
| rs117848719 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315314 | CCTTAGCAACCCAAG[C/T]AGCTGGGACTAGAGG | 84108 |
| rs117870499 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306981 | TGGTGGCACATGTCT[A/G]TATTTCCAGCTACTC | 84108 |
| rs117927731 | snp | A/C | 0.0962929 | 0.197165 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353095 | CAAAAAATTAAAATA[A/C]AATAAAATAAAATAA | 84108 |
| rs118037730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315214 | CCCCCCAGACAGGGT[A/G]TCACTCTGTCACTCA | 84108 |
| rs118129511 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307517 | AGGGTCTTGCTCTGT[C/T]GCACAGGCTGGCATG | 84108 |
| rs137888444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346844 | ATTTCATGTCCATTC[C/T]GTGACATTACATCAT | 84108 |
| rs137910892 | snp | C/T | 0.000379047 | 0.0137615 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345069 | AGTTCAGGTGGAATA[C/T]GAAACACTGATTCTA | 84108 |
| rs137911538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308098 | TCACAGAGAACCTCT[A/G]CTAGGGCAGTGCGGA | 84108 |
| rs138123250 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327825 | GACTACAGGCGTGCA[C/G]CACTACGCCCAACTA | 84108 |
| rs138164731 | in-del | -/AAGT | 0.0232847 | 0.105357 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307466 | AAAAAAAAAGAAAGA[-/AAGT]TTGTTTATTTCATTC | 84108 |
| rs138298802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316841 | GAGATTATATAGAAT[C/T]ATGAGATAGAACCCG | 84108 |
| rs138390062 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322717 | TAATCCCAGCTACCT[C/G]GGAGGCTGAGGCAGG | 84108 |
| rs138538313 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308476 | TGATCTCTGCTCACT[A/G]CAACCTCTGCCTCCC | 84108 |
| rs138643798 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346131 | AACCTGGAGGCGGAG[G/T]TTGCAGTGAGCCAAG | 84108 |
| rs138727250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323592 | GAGCCACCGCGTCCG[A/G]CCCCTTTTCTTTTTT | 84108 |
| rs138884621 | snp | G/T | 4.95291e-05 | 0.00497615 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345028 | AGGGTACTCACCCAA[G/T]GAACTCCAGTAATAA | 84108 |
| rs138892856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316512 | GGGAAACTAAGAAGT[A/G]AAGACATTAAACTTT | 84108 |
| rs138924959 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332542 | TGGCCTCCCAAAGTA[A/C]TGGGATTACAGATGT | 84108 |
| rs138962841 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338277 | GGTCAGGTGCAGTGG[C/T]TCATGCCTCTAATCC | 84108 |
| rs139134128 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333373 | GTCACCTATTCCTTG[C/T]ATATTTACCTCCCAA | 84108 |
| rs139160000 | snp | A/G/T | 8.17762e-05 | 0.00639386 | stop-gained, missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350723 | TCCTCCTCGTCCTCC[A/G/T]AGTCCTGCCGGCCTC | 84108 |
| rs139397712 | snp | C/T | 0.00177786 | 0.0297619 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348946 | ATCTATTAAGTAACC[C/T]TTGCAAATGGAACAC | 84108 |
| rs139523191 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310443 | AACAAATAGGTATTT[C/G]TTGAAACTCATGCAT | 84108 |
| rs139753052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304854 | GAGACAGAGTTTCAC[C/T]GTATTGCATAGGCTG | 84108 |
| rs139788971 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329661 | TTTTTTTAGTAGAGA[C/T]AGGGTTTCACCATGT | 84108 |
| rs139834723 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335423 | CAGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 84108 |
| rs139965356 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310756 | GCCCAGGCTGGAGTG[A/C]AGTGGTGTGATCATG | 84108 |
| rs139995358 | snp | C/T | 1.6528e-05 | 0.00287467 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348777 | TTGGACATCTGTTGC[C/T]GTAGTAAAAATGTCT | 84108 |
| rs140474107 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325067 | CTGAACCCGGGGGGC[A/G]GAAGTTGCAGAGAGC | 84108 |
| rs140513317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328281 | ACACATTTGTTCCAT[A/G]TTACAGCACTCAGCT | 84108 |
| rs140526272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337206 | GCACAGAGTGGGATA[C/T]TACTCTCGGGTTTAC | 84108 |
| rs140574602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322158 | ACCTCGGCCTCTGAA[A/G]GTGCTGGGATTACAG | 84108 |
| rs140753308 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350105 | AAACAAAACAAAACA[A/G]AACAAAAGGATCTTT | 84108 |
| rs141063087 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306830 | AACTCAAGGCCAGGT[G/T]CAGGGGCTCATGCCT | 84108 |
| rs141194778 | in-del | -/G | 0.162909 | 0.23434 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309196 | GACATGAGATTTGGT[-/G]GGGGGGGGGGCATGA | 84108 |
| rs141329235 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327129 | CCGTCTCTACTAAAA[A/G]TACAAATTAGCTGGG | 84108 |
| rs141429823 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327522 | TATCATTAATTTAAA[A/T]AACTGTAGTATCATT | 84108 |
| rs141464281 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339186 | TTGGGAGGCCAAGGC[A/G]GGTAGATTGCTTGAG | 84108 |
| rs141479146 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308660 | AAAGATTGCCTGAGC[C/G]CAGGGGTTTGAGACC | 84108 |
| rs141568985 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341609 | CACATCCAGCTTTTT[C/T]TTTTTTTGTATTTTT | 84108 |
| rs141623952 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347886 | CCTTCATAAGAATAC[A/G]AGTTGAGGGCAGAGA | 84108 |
| rs141637930 | snp | C/T | 0.000208863 | 0.010217 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350785 | CTCCTCCTCCTCCTC[C/T]TCTTCCTCCTCCAGC | 84108 |
| rs141659810 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346408 | AGGAGGGCAGATCAC[A/G]AGGTCAAGAGATTGA | 84108 |
| rs141731476 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339752 | CAGTAAGCCAAGATC[A/G]CGCCACTGCCCTCCA | 84108 |
| rs141803239 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349931 | ACTAAAAATACAAAA[A/C]ATAAGCCGGGCGTGG | 84108 |
| rs142048246 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320262 | AACAAAGCAAAATAC[A/G]ATAAGACATCAAAGA | 84108 |
| rs142207313 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348778 | TGGACATCTGTTGCT[A/G]TAGTAAAAATGTCTT | 84108 |
| rs142222668 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318351 | AGGAGGCTGAGGCAG[A/G]AGGATCACTCAAACC | 84108 |
| rs142259379 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349919 | AACCCCGTCTCTACT[A/C]AAAATACAAAAAATA | 84108 |
| rs142360344 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347291 | TCATGCATTTGCTTT[C/T]TTTCTCCTAAAAAAT | 84108 |
| rs142373672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337638 | AAGAGTCTATCTTAA[A/G]ATCATAAAGCTGGGC | 84108 |
| rs142438546 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336806 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 84108 |
| rs142546763 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329204 | GCCACCAACGTCTGG[C/T]TAATTTTGTATTTTT | 84108 |
| rs142568730 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313495 | GCTTGAACCTGGGAG[G/T]CAGAGGCTGCAGTGA | 84108 |
| rs142750192 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349928 | TCTACTAAAAATACA[A/C]AAAATAAGCCGGGCG | 84108 |
| rs142799511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328432 | ATAAATGGTCTGCCC[A/G]TTATTACCACAGTAC | 84108 |
| rs142803954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316967 | GAGAACTTAGATCCA[C/T]AAAAAGTTAAAGAAT | 84108 |
| rs142876938 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323469 | GCCCGGCTGATTTTA[C/T]ATTTTTAGTAGAGAT | 84108 |
| rs142899135 | in-del | -/AGAG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316014 | TATATATATATATAT[-/AGAG]AGAGAGAGAGAGAGA | 84108 |
| rs143121244 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306876 | TGGGAGGCCAAGGCA[A/G]GTGGATCACCTGAGC | 84108 |
| rs143378454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308111 | CTACTAGGGCAGTGC[A/G]GAGGGGAAAAGTGGG | 84108 |
| rs143379829 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310010 | AGGCTGGAGTGCAAT[C/G]GTGCAATTTCAGCTC | 84108 |
| rs143397830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321496 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 84108 |
| rs143579566 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339287 | CCCAGCTGCTCAGGA[A/G]GCTGAGGCGAGAGGA | 84108 |
| rs143694918 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331616 | CCAAATAATGTGCAC[A/T]CAATGTAATTAATTT | 84108 |
| rs143921941 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334261 | TATTAGGGGATAATA[G/T]ACAAATTAAAATTGT | 84108 |
| rs144007263 | in-del | -/A | 0.103794 | 0.20279 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322878 | GTTATCCTTGCCACC[-/A]AAAAAAAAAACAAAA | 84108 |
| rs144077726 | in-del | -/CAAAAA | 0.474964 | 0.109046 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312960 | AGCGAGACTCCGTCT[-/CAAAAA]CAAAAACAAAAACAA | 84108 |
| rs144196198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310630 | TTATAATATTCACAT[A/C]TTCTTTTGAGCAGTT | 84108 |
| rs144233646 | in-del | -/CC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324774 | CAAAAAAAAAAAAAA[-/CC]AAAAAAAAAAAAAAA | 84108 |
| rs144269311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320409 | GAACACATGATGGCC[A/G]GGCGCGGTGGCTCAC | 84108 |
| rs144329368 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308568 | CATGCCTGGCTAATT[C/T]TGAGCTTTAAGATTT | 84108 |
| rs144379995 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339812 | GTCTCAAAAAAAAAA[A/C]ACACACACACACACA | 84108 |
| rs144517794 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328855 | CTTCCGGATTCAAGC[G/T]ATTCTCTTGCCTCAG | 84108 |
| rs144520083 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329768 | GTGAGCCACCGTGCC[C/T]GGCCAGTTTTTTTGT | 84108 |
| rs144650057 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324562 | AGGAGATGGAGGCCA[C/G]CCTGACCAACAACAT | 84108 |
| rs144683689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343377 | TCAGTGATACAACAT[C/G]AGAAATCTAGATTTT | 84108 |
| rs144763128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345496 | CCCATGATATAGGTA[C/T]CAGTGCTACTGCTTT | 84108 |
| rs144817957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342467 | TTGAACTCCTGACCT[C/T]GGGTAATCTGCCCGC | 84108 |
| rs145078114 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327204 | GCAGGAGAATCGCTT[C/G]AACCTGGGAGGCAGA | 84108 |
| rs145097540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330825 | TACCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA | 84108 |
| rs145263159 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324692 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 84108 |
| rs145577572 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313303 | GGCAGAGGGGCTCAC[C/T]CCTGTAATCCCAGCC | 84108 |
| rs145743192 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315318 | AGCAACCCAAGTAGC[C/T]GGGACTAGAGGTGTG | 84108 |
| rs145779481 | snp | C/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 10:103330993 | GCCTCTTCCCCAAGC[C/G]TCTGACAACCACTAA | 84108 |
| rs145874150 | snp | A/T | 1.7177e-05 | 0.00293056 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326650 | ACAAAAACAGACAGA[A/T]AAAACTATTTTTAGG | 84108 |
| rs145885038 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325605 | GTCCTATAAAGAAAG[C/T]GGATGATAAGCAATA | 84108 |
| rs145936308 | snp | C/T | 0.000132225 | 0.00812988 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348776 | TTTGGACATCTGTTG[C/T]TGTAGTAAAAATGTC | 84108 |
| rs146065302 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317693 | CAAACTTAAAAAAAA[C/T]TGTAGAAAGTAGAAT | 84108 |
| rs146078372 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323531 | AACTCCTGACCTCAG[A/G]TGATCCACCTGCCTT | 84108 |
| rs146198396 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346710 | TGAGGCAGGAGAATT[A/G]CTCAAACCCAGAAGG | 84108 |
| rs146238814 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332464 | TATTTTTGATAGAGA[C/G]AGGGTATTCCTGTGT | 84108 |
| rs146311930 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350088 | ACTCCGTCTCAAAAA[C/G]AAAACAAAACAAAAC | 84108 |
| rs146458474 | in-del | -/AA | 0.0248432 | 0.108648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305611 | GCATTAGATTCTCCT[-/AA]AAAAGACTCAACTAC | 84108 |
| rs146526515 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310734 | TGAAAAAGGGTCTTA[C/T]TCTGTCGCCCAGGCT | 84108 |
| rs146603622 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349921 | CCCCGTCTCTACTAA[A/C]AATACAAAAAATAAG | 84108 |
| rs146608563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327009 | AACAACTTTGAGGCC[A/G]GGCATGGTGGCTCAC | 84108 |
| rs146614498 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349934 | AAAAATACAAAAAAT[A/T]AGCCGGGCGTGGTGG | 84108 |
| rs146633399 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329771 | AGCCACCGTGCCCGG[A/C/T]CAGTTTTTTTGTTGT | 84108 |
| rs147124747 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308462 | GGAGTGCAGTGGTGT[A/G]ATCTCTGCTCACTGC | 84108 |
| rs147206314 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328086 | AGTAGATGACAGAGT[A/T]TGAAAGTAAAAACTA | 84108 |
| rs147524494 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304046 | GCTGGCTTACTTTTT[C/T]TTAATAATCTAACAC | 84108 |
| rs147586253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314401 | TTAGACTGATTAAAC[A/G]CTCTTGAAAAGAGAG | 84108 |
| rs147595971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319718 | ATATATAATAAATGG[C/T]ATGGAAACATCATAT | 84108 |
| rs147690464 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337608 | TACACATAGAAACTA[C/T]AGAACAAAAAGGATA | 84108 |
| rs147700101 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343007 | CACCTCGGCTCACTG[A/C]AAGCTCTGCCTCCTG | 84108 |
| rs147878062 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343797 | GAGATTGCACCACTG[C/T]ACTCCAGCCTGGGCG | 84108 |
| rs147901614 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351943 | CCCAACAAACATTTA[C/T]TGAGGGCCTACTGTA | 84108 |
| rs147906472 | snp | A/T | 0.000743448 | 0.0192658 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350766 | ACGAGAAGTGACTCA[A/T]GTCCTCCTCCTCCTC | 84108 |
| rs148087439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332057 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAAGCT | 84108 |
| rs148324210 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327439 | GAATCCTGATTGAAA[A/T]ACTATCAACAATTTT | 84108 |
| rs148422723 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329189 | GGACTACAGGTACCC[A/G]CCACCAACGTCTGGC | 84108 |
| rs148476176 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324637 | TGGTGGCACAGGCCT[A/G]TAATCCCAGCTACTC | 84108 |
| rs148570344 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342685 | CTTTTCCCACTTAAT[A/C]CATCTTGGAGACTAT | 84108 |
| rs148596323 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350093 | GTCTCAAAAACAAAA[A/C]AAAACAAAACAAAAC | 84108 |
| rs148760963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308622 | CACGCCTGTAATCCC[A/C]GCACTTTGGAAAGCT | 84108 |
| rs148810960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320631 | GGCGGAGGTTGCGGT[G/T]AGCCGACATCATCGC | 84108 |
| rs148959046 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331020 | CTAATCTGCTTTCTG[C/G]TCCTGTGGATTTTCT | 84108 |
| rs149093167 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345392 | ATTAGAACAGCAACA[C/T]GTGTAGACAACCCTG | 84108 |
| rs149348369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324127 | ATTTTTTAGTAGAGA[C/T]AGGGTTTCACCGTGT | 84108 |
| rs149394518 | snp | G/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345060 | GACATATCAAGTTCA[G/T]GTGGAATACGAAACA | 84108 |
| rs149485183 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333444 | CTTTTCCTGATGACT[C/T]ACATTATAGTAGTAA | 84108 |
| rs149623159 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349404 | TGCAACATGGAAACA[A/T]ACACCTCCAACCCAT | 84108 |
| rs149736811 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313154 | AAACATCAAAATAGT[A/T]ACCTTGAGTTCTTAT | 84108 |
| rs149780885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304855 | AGACAGAGTTTCACC[A/G]TATTGCATAGGCTGG | 84108 |
| rs149919157 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350724 | CCTCCTCGTCCTCCG[A/C]GTCCTGCCGGCCTCC | 84108 |
| rs150011972 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337428 | ATTCTTACAACAATC[C/G]TTTGAGTTGCTATTG | 84108 |
| rs150316450 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307847 | ACATATCCCTATTGT[G/T]AAGTGACGCATAACT | 84108 |
| rs150548479 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340538 | ACTTTTCAAAAAAGG[C/T]ATAAAAAGTGGATCC | 84108 |
| rs150766911 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333032 | GGCTGGGTTCAAGAA[C/T]TGCTTGAACCCAGAC | 84108 |
| rs150787616 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319189 | GAGTCTCACTCTGCC[A/G]CCCAGGCTGGAATGC | 84108 |
| rs150838317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309157 | GGGACTATTGGGAAA[C/T]CATGATTGTCTTTTG | 84108 |
| rs150916738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348627 | CTGAACCCATCCTGA[A/G]AGGTCAATAATTTAT | 84108 |
| rs150937875 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329541 | GGAGTGGAATGGCGC[A/G]GTCTTGGCTCACTGC | 84108 |
| rs151158247 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325124 | TGGGCAACAGAGTGG[C/G]ACTCAGTCTCAAAAT | 84108 |
| rs151178975 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307190 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGAAAG | 84108 |
| rs151305863 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336970 | GCCTTCTGGTATTGT[C/G]AATCAGACCAATTTT | 84108 |
| rs180741028 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310116 | CCACCATGCCCGGCT[A/G]ATTTTTTGTATTTTT | 84108 |
| rs180783269 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308129 | GGGGAAAAGTGGGGT[G/T]GGAGCCCCCACATAG | 84108 |
| rs180979046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337103 | CGTATTTTCAAACTT[C/T]TACCATTCCAGTTAT | 84108 |
| rs180986666 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327140 | AAAAATACAAATTAG[C/T]TGGGCAAGGTGGCAC | 84108 |
| rs181000032 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314482 | GAGGATACAGCAGGA[C/G]AACAGCACAGTATAA | 84108 |
| rs181027313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348377 | TCTCATCAGTCTGTC[A/G]CCCAGGCTGGAATAC | 84108 |
| rs181226469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310678 | GAACATAGGCAATTA[C/T]ACCAAAAAAAAAAAT | 84108 |
| rs181227659 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331789 | TTCAGTGTCATTTAA[A/T]ACATCTCTCTCTCTC | 84108 |
| rs181320495 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343185 | CGCCCGCCTCGGCCT[C/G]CCAAAGTGCTGGGAT | 84108 |
| rs181400104 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321415 | AAGATGGTGACTATA[C/T]GTAATAATATATTGT | 84108 |
| rs181409121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305058 | GCCTCAATCTCCCAG[A/G]CTCAAGTGATCCTCC | 84108 |
| rs181419881 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326433 | ACATCATAAAACAAA[A/G]ATAACAAAAATAATT | 84108 |
| rs181435667 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347572 | GAGGTGAGTTACTTT[A/T]AAGTAGCATTTACAG | 84108 |
| rs181563473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314932 | TGCATTCCAGCCTGG[A/G]CCACAGAGCGAGACT | 84108 |
| rs181632718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322384 | CTAATTTTGGTATTT[C/T]TTGTAGAGCTGGGGT | 84108 |
| rs181637073 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343533 | TATGCTACAGTGTAT[A/G]AAAGAAGCAATTTAT | 84108 |
| rs181699737 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337738 | TTCAAGACCAGCCTG[A/G]CCAACAAGGAGAAAC | 84108 |
| rs181830112 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329334 | CGTGAGCCACCGCAC[A/C]CGGCCCCAATTTCTT | 84108 |
| rs181936796 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313233 | TCTTTTGGCTTCCCT[G/T]GGCCACACTGGAAGA | 84108 |
| rs182047625 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311877 | GCAGATCACTTGAGG[C/T]CAAGAGTTTGAGATT | 84108 |
| rs182059624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347819 | CCTCAGCCTCCTTAA[C/T]AGCTGGGACTAAAGG | 84108 |
| rs182062449 | snp | A/C | 3.7219e-05 | 0.00431371 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333889 | TGTGTGCTACAGAGT[A/C]CTCTTGTGAAATGAA | 84108 |
| rs182083335 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352826 | GGTGGCTCATGCCTG[A/T]AATCCCAATGCTTTG | 84108 |
| rs182168968 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305838 | AGGTCACTTGAGACC[A/G]GGAGTTCAAGACCAG | 84108 |
| rs182194353 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309400 | GGTCTTGTGTGATAT[A/G]GTTGTTTAAAAGTGT | 84108 |
| rs182398733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306313 | ATGTTGGTCAGGCTG[A/G]TCTTGAACTCGCGAC | 84108 |
| rs182434433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326776 | TGAAAAAACTTACTA[C/T]GAAACAAGTTAATAC | 84108 |
| rs182467410 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322952 | ACACACACACAGACA[C/T]ATAAATAGCCATAGA | 84108 |
| rs182606104 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343811 | GCACTCCAGCCTGGG[C/T]GACAGAGTAAAACTC | 84108 |
| rs182625674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339150 | TGAGGTGCAGTGGCT[C/T]ACGCCTGTAATCCCA | 84108 |
| rs182664731 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323660 | TGCAGTGGCATGATC[C/T]TGACTCACTGCAATC | 84108 |
| rs182862560 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327799 | CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGACTA | 84108 |
| rs182865427 | snp | C/T | 0.000217979 | 0.0104375 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348687 | AAAGTATATTTAAAA[C/T]ACAATTGTAATTTAT | 84108 |
| rs182940261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306970 | TTAGCCAGGTGTGGT[A/G]GCACATGTCTATATT | 84108 |
| rs182979232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344928 | TAATTTTCCAAGGGG[A/G]TGTCAGAAAACTTGA | 84108 |
| rs182987426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317817 | GCTGGAGGGCAATGA[C/T]GCAACCTTGGCTCAC | 84108 |
| rs183077654 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324709 | AGGTTGCAGTGAGCC[A/G]GGACCGCCCCACTGC | 84108 |
| rs183093304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345851 | AAAAAGAAACTGAGG[C/T]TTAGAGAGAGTAAGC | 84108 |
| rs183208897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316118 | TCTCATTGTCTTCCA[C/T]ACCAGAATGTCACCT | 84108 |
| rs183211513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338205 | GAGATCATGCCACTG[C/T]ACTCCAGCCTTGACA | 84108 |
| rs183244899 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318838 | AACTTTTCACATTAG[A/T]GTAGGAAACTTTTTG | 84108 |
| rs183493840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341004 | GGGGTCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 84108 |
| rs183580214 | snp | C/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333047 | TTGCTTGAACCCAGA[C/T]GGCGGAAGTTGCAGT | 84108 |
| rs183661838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308275 | ACTCAACACCAGCTC[A/G]TGAGAGAAGCCATGG | 84108 |
| rs183669364 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328967 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 84108 |
| rs183686714 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352104 | GGGAGGCCGAGGCGC[A/G]CAGATCATGAGGTCA | 84108 |
| rs183791228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311389 | TCAAATGATCTGCCC[A/G]TCTCTGCCTTCCAAA | 84108 |
| rs183850317 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307460 | GTCTCAAAAAAAAAA[C/G]AAAGAAAGTTTGTTT | 84108 |
| rs183875716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349638 | GGCGCGTGCCACCAC[A/G]CCCCGCTACTTTTTG | 84108 |
| rs183891009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304759 | CACCTGGGCTCAAGC[A/G]ATCCTCCCACCTCAG | 84108 |
| rs183904830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326292 | TACTCGGGAGGCTGA[C/T]GCAGAAGAATGGCGT | 84108 |
| rs183908150 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347176 | GGAACTTCAAAGGGC[A/C]TATATTTTATTGTTA | 84108 |
| rs184041572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328117 | ATGCTTACCCAGCTC[C/T]GATCTGAGACAACTA | 84108 |
| rs184129855 | snp | A/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352729 | CGGTGAGCCGAGATC[A/T]CACCACTGCACTCCA | 84108 |
| rs184138065 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325184 | AATAAAATAAAATAA[A/T]ATAATAGGGTCCCTA | 84108 |
| rs184206254 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329150 | ATTCAAGTGATTCTC[C/T]TATCTCAGCCTCCCA | 84108 |
| rs184291197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345976 | GGTGGGTGGATCACT[A/T]CAGGTCAGGAGTTCG | 84108 |
| rs184332806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347636 | AGTAAATATATGTAA[C/T]CATAAGTATTCACAG | 84108 |
| rs184421187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326436 | TCATAAAACAAAAAT[A/G]ACAAAAATAATTGCA | 84108 |
| rs184436238 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341688 | ATGTCAAGTAATCTG[C/T]CCACCTAAGCCTCCC | 84108 |
| rs184564851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320757 | AAATTTGATCTGCCA[C/T]AAAAAACTTTAAAGT | 84108 |
| rs184752043 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312561 | CACTCACAGCAGAAG[A/C]CCTTTTTTCCCCAAG | 84108 |
| rs184799986 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335709 | GAGGTGGCTGATGCC[C/T]GTAATCCCAGCACTT | 84108 |
| rs184814733 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320625 | CCAGGAGGCGGAGGT[G/T]GCGGTGAGCCGACAT | 84108 |
| rs184822886 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341624 | TTTTTTTTGTATTTT[C/T]AGTAAAGACGGGTTT | 84108 |
| rs185068767 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313575 | GTCTCAAAAAAATGA[A/T]TAAATAAAAATACAA | 84108 |
| rs185070813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336520 | CAGCTTCTACCTGAA[A/T]ATCTAAAGACAGCTT | 84108 |
| rs185127642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309070 | ACAGGCTCATAGGCA[G/T]AAGGGACTAGCCTTG | 84108 |
| rs185244717 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336248 | CCAAAAAAAAAATTT[A/T]AAAAAAAATAAATAA | 84108 |
| rs185323638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330157 | TCGGCTCACTGCAGC[A/C]TCTGCCTCCCGGGTT | 84108 |
| rs185357513 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312910 | AGCTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 84108 |
| rs185403269 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310158 | GGTTTCACCATGTTA[A/G]CCAGGCTGGTCTTGA | 84108 |
| rs185481928 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309775 | TCTCTACAAAAAATT[A/T]AAAAAAATAGCCAGA | 84108 |
| rs185492760 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352858 | GAGGCTGAGTTGGGC[A/G]GGTAACGAGGTCAGG | 84108 |
| rs185557454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327449 | TGAAAAACTATCAAC[A/T]ATTTTCAGGGGACAA | 84108 |
| rs185574658 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348457 | TTCTCCTGCCTCAAC[C/T]TCCCAAGTAGCTGGG | 84108 |
| rs185617009 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329335 | GTGAGCCACCGCACC[A/C]GGCCCCAATTTCTTA | 84108 |
| rs185637329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321842 | CCATCCCACAATGTA[C/T]ACATATTTCAAAACA | 84108 |
| rs185646432 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306657 | CAATTACAGTAAAAA[C/T]TCACCAGAATTCTAG | 84108 |
| rs185874768 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315261 | CCCAATCATAGCTCA[C/T]TGCAGCCTCAAACTC | 84108 |
| rs185990799 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343970 | CACAGGAGATACATA[C/T]GAATTTGTTTACGGC | 84108 |
| rs186104045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323195 | AGCTGCCATGAGATA[C/T]AACCAGGATATGTCA | 84108 |
| rs186115677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343566 | GTATCTAGCAGGGCA[C/T]GGTGGCTCACGTCTG | 84108 |
| rs186277549 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314511 | AATTGATATTCAAAA[G/T]GATTTCCCTGAATCT | 84108 |
| rs186447712 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316855 | TTATGAGATAGAACC[C/T]GGGTTGGCATACTCA | 84108 |
| rs186452605 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338740 | GGGCATGGTGGCACA[C/T]GCCTGTAATCCCAGC | 84108 |
| rs186455503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337408 | CTTAAGAATATCACA[C/T]GTTGATTCTTACAAC | 84108 |
| rs186523346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332341 | CTAGAGTGTAGTGAC[A/G]CAATCACAGCTCACT | 84108 |
| rs186691786 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312034 | GAGGTGCAGTGAGCC[A/G]AAATCACGCCACTGC | 84108 |
| rs186696079 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335488 | TTGCCTCAGCCTCCC[A/G]AATAGGTGGGACTAC | 84108 |
| rs186737214 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343219 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTTAGGGG | 84108 |
| rs186749056 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311019 | TTTTCTATCCTTTGT[A/G]AAGACGGGACTCGCT | 84108 |
| rs186778740 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337831 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 84108 |
| rs186828053 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352410 | GCCAGCTAATGTCAC[A/G]ATGCCTGCAAGAAAG | 84108 |
| rs186845977 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305553 | TGGGATTACAAGTGT[G/T]ACCCGCTGCACCCGG | 84108 |
| rs186895501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308866 | ACAGAGAGAGAGAGA[C/G]TCCATCTCAAAAAAT | 84108 |
| rs186913494 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329000 | TCTACCGGCCTCAGC[A/G]TCCCGAAGTGCTGGG | 84108 |
| rs187264073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324394 | CTGGACCACAGAACT[A/C]GAACTATGAGTATAT | 84108 |
| rs187267435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345273 | CTGTCTTTAATGACA[C/T]TGGCTAATCTGTCAA | 84108 |
| rs187399874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326953 | AGTACTGAACTTACA[C/G]TTTAAAGACACAGAG | 84108 |
| rs187482675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319855 | TCTGTCGCCAGGCTG[C/T]AGTGCAGTGGTGCGA | 84108 |
| rs187488741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341342 | GCTCACCACAACCTC[C/T]GCCTCCCGGGTTCAA | 84108 |
| rs187545384 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348890 | TCAGAAATGTGATCG[A/G]TATGCTTACAGGTAT | 84108 |
| rs187575588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346024 | ATGGTGAAACCCCAT[C/T]TCTACTAAAAATACA | 84108 |
| rs187653375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305994 | TATGATTCCAGATGC[G/T]ATGTGTCCAAGTCTT | 84108 |
| rs187665797 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347847 | AGGCGCGTGACACCA[C/T]GCCTGGTTAATTTGA | 84108 |
| rs187782779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324910 | GAGGCCGAGGTAGGC[A/G]GATCACCTGAGGTCA | 84108 |
| rs187784942 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345940 | GCTCATGCCAGTAAT[C/T]CCAGCACTTTGGGAG | 84108 |
| rs187857863 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317889 | TCAGCCTCCCAAGTA[G/T]CTGGGATTACAGGCA | 84108 |
| rs188107086 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335936 | CGTGTCACTACACTC[C/T]AGCCCGGTGACAGTG | 84108 |
| rs188139941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339753 | AGTAAGCCAAGATCG[C/T]GCCACTGCCCTCCAG | 84108 |
| rs188266618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313858 | CTTTTAGAATCAAAC[C/T]GCCTAGAGTCTGAGC | 84108 |
| rs188271050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336845 | GTGCCACTGCACTCC[A/T]GCCTGGGTGACAGAG | 84108 |
| rs188375930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312687 | ATTTTCATGGCCGGG[C/T]GCGGTGGCTCACACC | 84108 |
| rs188408459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307182 | GGCTCATGGCTCATG[C/T]CTGTAATCCCAGCAC | 84108 |
| rs188599429 | snp | G/T | 0.000314906 | 0.0125441 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347460 | TCCAACCTAATAAAA[G/T]GAAAGGATGGAGAAT | 84108 |
| rs188628726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311769 | ACAGCCCTAAGAGGG[A/G]GCAGAAACCTGGATT | 84108 |
| rs188669231 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304897 | CTGCCTGTCTCAGAC[C/T]CCCAAAGTGCTGGGA | 84108 |
| rs188683814 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326385 | CAGAGCAAGACTCCA[C/T]CTCAAAAAAAAAAAA | 84108 |
| rs188692564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327910 | TCAATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 84108 |
| rs188892159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328736 | TGCTCTTTATGTACA[C/G]GATTTTAACTTTTTT | 84108 |
| rs188921034 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333807 | ATCTATAATATTATT[A/G]AATGTACTTCATATT | 84108 |
| rs188929453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321898 | TTATTTATTTCATTT[C/T]ACTTTTTTTTTTTTT | 84108 |
| rs188931494 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343257 | TAACAGTTGAGAGCA[A/C/T]GAAGTGGATATACAA | 84108 |
| rs189132771 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302771 | ATTTTTTTTTTAACC[C/T]ACAGTAAACACTAAC | 84108 |
| rs189159344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347694 | CATGTGCATTGTTTT[G/T]TGTGTGTGTGTGTGA | 84108 |
| rs189167809 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307976 | CATGCTGGCTCACGC[C/G]TGGAATCCCAGCAGT | 84108 |
| rs189176402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350020 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 84108 |
| rs189364532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313047 | ATGTGGTCCTATTTT[A/C]TCTTCATTAAACTTG | 84108 |
| rs189381801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320924 | GCAGGACACCAAGAA[C/T]TGTAGTCTGATGACT | 84108 |
| rs189413286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325186 | TAAAATAAAATAAAA[C/T]AATAGGGTCCCTATT | 84108 |
| rs189588849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320654 | ATCATCGCACCATTG[C/T]ACTCCATCCTGGGCA | 84108 |
| rs189603392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309936 | AGGCTGGGCAAAACA[C/G]AGTGAGACCTTGTCT | 84108 |
| rs189603807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341663 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGATGTCA | 84108 |
| rs189631589 | snp | A/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317386 | GTGGTATACATTCAC[A/G]GTATTATTACTATAT | 84108 |
| rs189645428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337718 | GGATAACCTGAGGTC[A/G]GGAGTTCAAGACCAG | 84108 |
| rs189645887 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338765 | CCCAGCTACTTGGGA[A/G]GCTAAGGCAGGAGAA | 84108 |
| rs189667743 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341955 | TGTTCTTTTTTTTTT[C/G]TCAGCAGTCTTTCTC | 84108 |
| rs189959058 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309197 | GACATGAGATTTGGT[G/T]GGGGGGGGGCATGAT | 84108 |
| rs189974470 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352747 | CCACTGCACTCCAGC[C/T]TGGGCAACAAGAGCA | 84108 |
| rs190076923 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310229 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCACA | 84108 |
| rs190080988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331337 | AGCTCACTTCGCCAA[G/T]TTCTCTGCCCTCCGG | 84108 |
| rs190209704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326739 | AAGAAAATTTTATAG[C/T]GAAGATGATTCAATA | 84108 |
| rs190210337 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329166 | TATCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 84108 |
| rs190311305 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306767 | AATAGGGAATGTTGA[A/G]GACCAGTGGTAAACC | 84108 |
| rs190330517 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327545 | GTATCATTATTATGT[G/T]GCCATAAAAGGACAC | 84108 |
| rs190338298 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348515 | CTAATAGTGGAGATG[G/T]GGTTTCACCATGTTG | 84108 |
| rs190440666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329540 | TGGAGTGGAATGGCG[C/T]GGTCTTGGCTCACTG | 84108 |
| rs190445615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336345 | ATTTTATATGAAATT[A/G]TATCAATATATAAAT | 84108 |
| rs190453698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305781 | AGCTGGATGCAGTGG[C/T]TCATGCCTGTAATCC | 84108 |
| rs190702381 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352864 | GAGTTGGGCGGGTAA[C/T]GAGGTCAGGAGTTTG | 84108 |
| rs190727906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315328 | GTAGCTGGGACTAGA[A/G]GTGTGCACCACCACA | 84108 |
| rs190745158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338155 | CTGAGACAGGAGAAC[C/T]GCTTGAACCTAGGAG | 84108 |
| rs190780559 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306275 | GCTAATTTTTGTATT[C/T]TGAGTAGAGATGGGG | 84108 |
| rs190936826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327024 | GGGCATGGTGGCTCA[A/C]GCCTGCAATCCCAGC | 84108 |
| rs190966124 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343696 | AAATTAGCCAGGCGT[G/T]GTGGCATGTGCCTGC | 84108 |
| rs190981045 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333868 | GTTGCTAATCTGACT[C/T]GAATTTGTGTGCTAC | 84108 |
| rs191187823 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344758 | TAATTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT | 84108 |
| rs191207823 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308078 | CTGCTGTAGTGGCAG[A/T]GCCCTCACAGAGAAC | 84108 |
| rs191293251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341664 | GGCCAGGCTGGTCTC[A/G]AACTCTTGATGTCAA | 84108 |
| rs191446237 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312272 | GTGGCAGGCACCTAT[A/G]GTCCCAGCTACCTGG | 84108 |
| rs191450603 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335631 | CTCCCAAAGTGCTAG[A/G]ATTACAGGAGTGAGC | 84108 |
| rs191466012 | snp | A/C | 6.59011e-05 | 0.00573988 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303936 | GGAGAAACCACAAGA[A/C]CATAATGAAGGACAA | 84108 |
| rs191482019 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314520 | TCAAAATGATTTCCC[G/T]GAATCTCAAAGAAAT | 84108 |
| rs191493162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311025 | ATCCTTTGTAAAGAC[A/G]GGACTCGCTATACTG | 84108 |
| rs191686902 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308957 | GGGACATATAGCCTC[A/C]TTCTTTTGGCCAATT | 84108 |
| rs191703638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329145 | CTTGGATTCAAGTGA[C/T]TCTCCTATCTCAGCC | 84108 |
| rs191708444 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352640 | AGCCGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 84108 |
| rs191744158 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327922 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 84108 |
| rs191755516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332983 | GCTGGGCGTGGTGGT[A/G]CATGCCTGTAATCCT | 84108 |
| rs192043148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307226 | GGTTGGAGTATCACT[C/T]GAGCTCAGGAGTTCA | 84108 |
| rs192059984 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349190 | GTAGCTGGGATTACA[A/G]GCGCGCACAACCACG | 84108 |
| rs192085460 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324599 | ACCCCGTCTCTACTA[A/T]AAATACAAAAATTAG | 84108 |
| rs192100249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345705 | TGGTGGCATGTGCCT[A/G]TAATCCCAGCTATTT | 84108 |
| rs192191442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320746 | TCTTGTTTTTAAAAT[C/T]TGATCTGCCACAAAA | 84108 |
| rs192263924 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351771 | AAGCAGCTGGGACTA[C/T]TGGCGCCTGCCACCA | 84108 |
| rs192333151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341456 | TGTTTTTGTATTTTT[C/T]GAGACGGAGTTTGGC | 84108 |
| rs192372611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322461 | TCCATCCACTTTGGC[C/T]TCCCAAAGTGCTGGG | 84108 |
| rs192515408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326125 | AACAATGTCCAGGCG[C/T]GGTGGCTCATGCCTG | 84108 |
| rs192547347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336354 | GAAATTATATCAATA[C/T]ATAAATGTAAACTGT | 84108 |
| rs192666818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328933 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACTGT | 84108 |
| rs192706922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339888 | ATCTTATGAGGCCAG[A/G]TGCAGTGGCTCATGC | 84108 |
| rs192812413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346231 | GCGCGGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 84108 |
| rs192878492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312689 | TTTCATGGCCGGGCG[C/T]GGTGGCTCACACCTG | 84108 |
| rs192960827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317917 | GCATGCATCACCACG[A/C]ATGGCTAATTTTGTA | 84108 |
| rs193036899 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336247 | TCCAAAAAAAAAATT[A/T]AAAAAAAAATAAATA | 84108 |
| rs193101285 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345949 | AGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 84108 |
| rs193255918 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325060 | GAATCGCCTGAACCC[A/G]GGGGGCGGAAGTTGC | 84108 |
| rs199536332 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351645 | TGAATTCGAAAAGCT[C/T]TTTTTTTTTTTTTTT | 84108 |
| rs199583634 | in-del | -/AAC | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352360 | AACAAAACAAAACAA[-/AAC]AAAACAAAAAAACCA | 84108 |
| rs199615301 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339810 | CTGTCTCAAAAAAAA[A/C]ACACACACACACACA | 84108 |
| rs199750074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350461 | TAACAGAACGAATGA[C/G]TTGGACTCGCAGAGC | 84108 |
| rs199802435 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326407 | AAAAAAAAAAAAAAA[G/T]AATGTCTACAACATC | 84108 |
| rs199837522 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342356 | CTCCCGCCTCAGCCT[C/T]CTGGGTAGCTGGGAC | 84108 |
| rs199856362 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317763 | AGTTTCTTTTTTCTG[-/T]TTTTTTTTTTGAGAC | 84108 |
| rs199872878 | snp | A/G | 0.000544433 | 0.01649 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348999 | AGAGATTAATCAGGC[A/G]CTGCAAATAAACGGA | 84108 |
| rs199907212 | snp | C/T | 0.00145429 | 0.0269264 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351099 | GGCGAGGCGAGGCGG[C/T]GGGAGAGCGCGGGAG | 84108 |
| rs200037917 | in-del | -/AAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339808 | AATTCTGTCTGTCTC[-/AAAA]AAAAAACACACACAC | 84108 |
| rs200146344 | snp | C/T | 1.97502e-05 | 0.0031424 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333987 | TTAATCAATATTTAA[C/T]ACTTTAAGCTATATG | 84108 |
| rs200225923 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348340 | GTCAAGAGTTTTTTT[G/T]TTTTTTTTTTTTTTG | 84108 |
| rs200230704 | snp | C/G/T | 5.02032e-05 | 0.00500994 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348720 | ATTCTTCTTACCTTA[C/G/T]GTTATAAAGAGGTTG | 84108 |
| rs200346904 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348005 | TACTGTTAGTATTTT[-/T]CCCTCTCTTAAGAAA | 84108 |
| rs200373033 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342234 | CCACTGCACCCGGAC[-/T]TTTTTTTTTTTTCCT | 84108 |
| rs200564910 | snp | C/T | 0.00199802 | 0.0315439 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347428 | CTAATTTGTACACTA[C/T]GTCTTGTAACTGTCG | 84108 |
| rs200577684 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303944 | CACAAGACCATAATG[A/G]AGGACAAGCAGACCA | 84108 |
| rs200681272 | snp | A/G | 0.00123364 | 0.0248052 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350684 | GCTTGGGCCCAGCGG[A/G]GTCGCGCGGGGGCTC | 84108 |
| rs200854681 | snp | C/T | 0.00199805 | 0.0315441 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303891 | TTTCCCTCCTCATAA[C/T]GTGCCTAGAATCTTC | 84108 |
| rs200858964 | snp | A/G | | | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350981 | AGGGCGGGCGGGGAG[A/G]CAGGAGGCGGAGGCG | 84108 |
| rs200864871 | snp | A/G/T | 0.000609595 | 0.017448 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348894 | AAATGTGATCGGTAT[A/G/T]CTTACAGGTATGAAG | 84108 |
| rs200906770 | in-del | -/CT | 0.0240643 | 0.107019 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326023 | CAACAGAAACAGACC[-/CT]GTCTCAAAAAAAGAA | 84108 |
| rs200968246 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341941 | ACTGCCATTAATATG[-/T]TTCTTTTTTTTTTCT | 84108 |
| rs201068069 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340204 | AAAAAAAAAAATATA[A/T]ATATATATATATATA | 84108 |
| rs201172053 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315998 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 84108 |
| rs201188184 | snp | C/T | 0.000264249 | 0.0114915 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347330 | ACAGACTAAATTACA[C/T]TTAAAATGTAACTAC | 84108 |
| rs201230559 | snp | C/T | 0.000214789 | 0.0103609 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348798 | AAAAATGTCTTACGA[C/T]GCAGCTTTTACAAAC | 84108 |
| rs201427417 | snp | C/G | 0.000478165 | 0.0154549 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348878 | CTGAAAAATTATTCA[C/G]AAATGTGATCGGTAT | 84108 |
| rs201454866 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313752 | GCCTAATAAGTACTT[G/T]CAAGTTTTTCTTGAA | 84108 |
| rs201471553 | snp | A/G | 0.000302069 | 0.0122859 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350675 | CCTGACGCCGCTTGG[A/G]CCCAGCGGGGTCGCG | 84108 |
| rs201660003 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339810 | TGTCTCAAAAAAAAA[-/C]ACACACACACACACA | 84108 |
| rs201686526 | snp | A/C | 6.50146e-05 | 0.00570115 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351059 | GTCACCACCGCGACC[A/C]CCTCCATGGTCGGGA | 84108 |
| rs201702163 | snp | A/C | 0.000352933 | 0.0132794 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350983 | GGCGGGCGGGGAGAC[A/C]GGAGGCGGAGGCGGC | 84108 |
| rs201738694 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344245 | CGTGGCAACCACATG[-/A]AAAAAAAAGGCATGG | 84108 |
| rs201745256 | in-del | -/AAAAAAC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322883 | TCCTTGCCACCAAAA[-/AAAAAAC]AAAAAACAAAAAACA | 84108 |
| rs201765840 | in-del | -/CA | 0.103438 | 0.202533 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326201 | AGGAGATCGAGACCA[-/CA]GTGAAACCCCTTCTC | 84108 |
| rs201782538 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339808 | GTCTGTCTCAAAAAA[A/C]AAACACACACACACA | 84108 |
| rs202037510 | in-del | -/AAATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325143 | CAGTCTCAAAATAAT[-/AAATA]AAATAAAATAAAATA | 84108 |
| rs202047483 | in-del | -/ATTA | 0.0111196 | 0.0737302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314575 | GAAATTCATTTTGAC[-/ATTA]ATTAAGAAATTAAGT | 84108 |
| rs202127192 | snp | A/G | 0.000462626 | 0.0152019 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348781 | ACATCTGTTGCTGTA[A/G]TAAAAATGTCTTACG | 84108 |
| rs202146858 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341944 | TGCCATTAATATGTT[-/C]TTTTTTTTTTCTCAG | 84108 |
| rs367557204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321441 | ATTGTAGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 84108 |
| rs367564774 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304024 | TAATGCAAATGATCA[A/G]GTCAAAGCTGGCTTA | 84108 |
| rs367596760 | in-del | -/AAATA/AAATAAAATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325142 | CAGTCTCAAAATAAT[-/AAATA/AAATAAAATA]AAATAAAATAAAATA | 84108 |
| rs367623798 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315979 | TTATATGTGTGTGTG[-/T]GTGTGTGTGTGTGTG | 84108 |
| rs367688783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338961 | AGGCTGAACCCACCT[C/T]AGTGTTTTTCCTCCT | 84108 |
| rs367758876 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320452 | AGCACTTTGGGAGGC[A/C]GAGGTGGGCAGATTG | 84108 |
| rs367923482 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330810 | GGGGCGCACCTGTAA[C/T]ACCAGCTACTTGGGA | 84108 |
| rs368079512 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351926 | TGAGCCAGGGCGCCG[A/G]GCCCAACAAACATTT | 84108 |
| rs368081578 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335049 | CATCTCCAAAGTATT[A/C]TTTTTTTCTTTCATT | 84108 |
| rs368131712 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340689 | GCAGCCTCAAACTCC[A/C/T]GGGCTCAGTCGATCC | 84108 |
| rs368134765 | snp | A/G | 5.11086e-05 | 0.00505487 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326521 | CCTATTCTTTTACAT[A/G]TATGTACTGTACCTG | 84108 |
| rs368173239 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320306 | AATCAACCACAGTAA[C/G]CCTGAGACACTGGAG | 84108 |
| rs368209648 | in-del | -/CA | 0.0185938 | 0.0946107 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322822 | AGCAAGACTCTGTAT[-/CA]CACACACACACACAA | 84108 |
| rs368280164 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332834 | TCATGGGGATTTATG[C/G]TCGGGCGCAGTGGCT | 84108 |
| rs368290354 | snp | C/T | 3.33067e-05 | 0.00408072 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314155 | TCACTAAGTAACTTA[C/T]CTGTTAGACATGGGT | 84108 |
| rs368301725 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322903 | ACAAAAAACAAAAAA[-/C]AAAAAAAAAAACAAC | 84108 |
| rs368320032 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305185 | TGCTATGTAACCCAG[C/G]CTGGTCTCAAACTCT | 84108 |
| rs368386622 | snp | A/G | 3.31928e-05 | 0.00407373 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347466 | CTAATAAAAGGAAAG[A/G]ATGGAGAATACCTCA | 84108 |
| rs368422277 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314358 | AATCAACATAAATTG[C/T]TTCCAAACTAGATTT | 84108 |
| rs368427447 | snp | C/G/T | 7.05995e-05 | 0.005941 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326488 | CTACAGTGTGCTAAA[C/G/T]GTAAGCTCACAACTT | 84108 |
| rs368508870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346538 | CTGAGGCAGGAGAAT[C/T]GCTTGAGCCCAGAAG | 84108 |
| rs368617067 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305221 | TTCAAGCAATACCCC[A/C]ATCTTGGCTTCCCAA | 84108 |
| rs368717175 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340402 | GACTGCCTTGAGCAG[C/T]GTGGTCAAGTCTCAT | 84108 |
| rs368732479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322398 | TTTTGTAGAGCTGGG[G/T]TTTCGCTATGTTGCC | 84108 |
| rs368750443 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317010 | TTGTTTTATTAATTT[A/T]ATTTTATTTTATTTT | 84108 |
| rs368774098 | snp | A/C | 1.65181e-05 | 0.00287381 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347329 | CACAGACTAAATTAC[A/C]CTTAAAATGTAACTA | 84108 |
| rs368790939 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305425 | ACAGGGGCCCGCCAT[C/G]ACGCCTGGCTAATTT | 84108 |
| rs368793629 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321942 | ACTCTGTCACCCAGG[A/C]TGGAGTGCAGTGGCA | 84108 |
| rs368830334 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302833 | AAATGTTAGAATAAA[C/T]TTATACACAATTCAC | 84108 |
| rs368924394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328156 | ACGACCTCATGCAAA[C/T]AAAAAGCTGAAGTAA | 84108 |
| rs368938158 | snp | A/G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305026 | GGAGTGCAATGGCGC[A/G/T]ATCATAGCTCACTGT | 84108 |
| rs368962085 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352576 | TTGGGAGTTAGAGAC[C/T]AGCCTGACCAACATG | 84108 |
| rs369009172 | in-del | -/AA | 0.265275 | 0.249533 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324329 | TAAATTTGACTAATG[-/AA]AAAAAAAAAAAGAAA | 84108 |
| rs369050456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315654 | GTGAGCCACCGTGCC[C/T]GGCCAATTGTGTGGT | 84108 |
| rs369138880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335952 | AGCCCGGTGACAGTG[C/T]GAGACTCCATCTCAA | 84108 |
| rs369209294 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343803 | GCACCACTGCACTCC[A/G]GCCTGGGCGACAGAG | 84108 |
| rs369374259 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312354 | GCTGAGATCGCACCA[C/T]TGCACTCCAGCCTGT | 84108 |
| rs369499715 | in-del | -/A | 0.374 | 0.217081 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338544 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs369501380 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335792 | CCAACATAATGAAAC[C/T]CCGTCTCTCCTAAAA | 84108 |
| rs369513496 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311325 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAG | 84108 |
| rs369536966 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347788 | CCACTTCCTAGGCTT[A/C/G]GGTGGATTTTTCCCA | 84108 |
| rs369550958 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337075 | TATTTTTGTTCCTTC[C/T]GCTACCACATGACGT | 84108 |
| rs369554797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306340 | CGACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTC | 84108 |
| rs369569318 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312321 | TCCCTTGAACCCGGG[A/G]GGCAGAGGTTGTAGT | 84108 |
| rs369725793 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343983 | TATGAATTTGTTTAC[A/G]GCAACATTGTTTAAA | 84108 |
| rs369763488 | snp | C/G | 9.10042e-05 | 0.00674491 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350808 | CCTCCAGCTCCTCTT[C/G]TTCTTCCAACTCCTC | 84108 |
| rs369800754 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304940 | GCCATCTAGACCAGC[C/T]TGTCAATGTGTCTTT | 84108 |
| rs369914306 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314814 | AACTAACCAGGCACG[A/G]TGGTAATCATGGTGC | 84108 |
| rs369977135 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345058 | AAGACATATCAAGTT[C/T]AGGTGGAATACGAAA | 84108 |
| rs370011390 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331350 | AAGTTCTCTGCCCTC[C/T]GGGTTCAAGTGATTC | 84108 |
| rs370083174 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325488 | TTCCTGACCTCGTGA[A/T]CCACCCACCTCAGCC | 84108 |
| rs370086225 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348696 | TTAAAATACAATTGT[A/C]ATTTATATATTCTTC | 84108 |
| rs370087649 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320415 | ATGATGGCCGGGCGC[A/C/G]GTGGCTCACACTTGT | 84108 |
| rs370087928 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332277 | GAAGCAGTAGACTAA[C/T]ACTTTATCTTTTCTG | 84108 |
| rs370151370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329736 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTATAGG | 84108 |
| rs370166132 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306619 | CACTCCTCAACTCAC[C/T]GCAATCTGGTTTGTG | 84108 |
| rs370168918 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305734 | AAAGCCTAAAATATA[C/T]ATGTTTTACTTCTGC | 84108 |
| rs370275744 | snp | C/T | 4.9498e-05 | 0.00497459 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348998 | GAGAGATTAATCAGG[C/T]GCTGCAAATAAACGG | 84108 |
| rs370360147 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304001 | ATTTTGCAGTTCTTT[C/G]AAACCAGTAATGCAA | 84108 |
| rs370389084 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324584 | CAACAACATGGTGAA[A/C]CCCCGTCTCTACTAA | 84108 |
| rs370391569 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312391 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs370398748 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344191 | CCATTTCAAGTTTGG[-/C]AAAAACAATGCTACA | 84108 |
| rs370470160 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327675 | AATTCTTTTTTTTTT[-/T]CTTTTCTTTTCTTTT | 84108 |
| rs370508104 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339306 | GAGGCGAGAGGATTG[C/T]TTGAGTATAGGAGGC | 84108 |
| rs370614848 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341713 | CCTCCCAGAATGCTG[A/G]GATTACAGGCGAGAG | 84108 |
| rs370662888 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342379 | GCTGGGACTACAGGC[A/C]CCTGCCACAACACCT | 84108 |
| rs370800785 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320001 | TTAGTAGAGATGGGG[C/T]TTCACCATGTGGGCC | 84108 |
| rs370883260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309708 | GGCTGAGATGGCTGA[C/T]TGCTTGATCTCAGGA | 84108 |
| rs370912131 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337440 | ATCCTTTGAGTTGCT[A/G]TTGTAACCTCCAGTT | 84108 |
| rs370923613 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324257 | ATACACAGTATTTTA[A/G]ATAAAAAATTATTCT | 84108 |
| rs370929916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313570 | ACCTTGTCTCAAAAA[A/C]ATGAATAAATAAAAA | 84108 |
| rs371161960 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325417 | TGCCAACAGGTCCGG[C/G]TAATTTTTGTATTTT | 84108 |
| rs371197801 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348944 | GCATCTATTAAGTAA[C/T]CTTTGCAAATGGAAC | 84108 |
| rs371258592 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315981 | ATATGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTA | 84108 |
| rs371331034 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310629 | CTTATAATATTCACA[C/T]CTTCTTTTGAGCAGT | 84108 |
| rs371427587 | snp | A/G | 1.65759e-05 | 0.00287883 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314173 | GTTAGACATGGGTAT[A/G]TCTATAACCTACCTG | 84108 |
| rs371454652 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316228 | TGAATTCATATCATA[A/C]CTTTCAACTACTGCC | 84108 |
| rs371619249 | in-del | -/AAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340181 | GACTCTGTCTCAGGG[-/AAAA]AAAAAAAAAAAAAAA | 84108 |
| rs371726949 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326388 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs371771625 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335163 | GTGAACTTCTTGCCT[C/T]AGCCTACCTGAGCAG | 84108 |
| rs371784501 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331018 | CACTAATCTGCTTTC[C/T]GCTCCTGTGGATTTT | 84108 |
| rs371883279 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322790 | GACTGTGCCACTGCA[C/G]TCCAGCATGGGTGAC | 84108 |
| rs372097002 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310956 | TCCCTCTGCCTCAGC[A/C]TCCCCAGGTAACTGG | 84108 |
| rs372099259 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343033 | TCCTGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 84108 |
| rs372100995 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325918 | GTCCTAACTACTCAG[A/G]AGGCTGAGACAGGAG | 84108 |
| rs372106066 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343297 | TACAATAAAGCACAC[A/G]CTAGATAATAAATGA | 84108 |
| rs372112602 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339802 | AATTCTGTCTGTCTC[-/A]AAAAAAAAACACACA | 84108 |
| rs372120883 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320515 | AACATGGAGAAACTC[C/T]GTCTACTAAAAAAAC | 84108 |
| rs372123041 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312844 | CGCATGCCTGTAAAC[C/T]CAGCTACTCGGGAGG | 84108 |
| rs372190098 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322466 | CCACTTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 84108 |
| rs372270368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342967 | AGACGGAGTCTCTGC[C/T]GCCCAGGCTGGAGTG | 84108 |
| rs372298007 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344865 | GTGAGCCACTGCACC[C/G]GGCCCTTTATACCTT | 84108 |
| rs372340928 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305222 | TCAAGCAATACCCCC[A/T]TCTTGGCTTCCCAAA | 84108 |
| rs372427350 | snp | A/C/T | 1.68838e-05 | 0.00290544 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347497 | GAATTCAGAAAAATG[A/C/T]ATTTTGGTACAGAGT | 84108 |
| rs372526847 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349303 | TCCACCCGCCAAGGC[C/T]TCCCAAAGTGCTAGG | 84108 |
| rs372538289 | snp | A/G | 1.82577e-05 | 0.00302134 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326682 | TAAATATACCTGTAC[A/G]TGCATGACGTATGTG | 84108 |
| rs372569146 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326932 | AAAATTTATTCATTC[A/G]TTTCAAGTACTGAAC | 84108 |
| rs372617447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335650 | ACAGGAGTGAGCCAC[A/G]GTGCCCAGCAAAGTA | 84108 |
| rs372634771 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322910 | ACAAAAAACAAAAAA[A/C]AAAACAACCCACAAA | 84108 |
| rs372662689 | in-del | -/CAAAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312959 | AGCGAGACTCCGTCT[-/CAAAAA]CAAAAACAAAAACAA | 84108 |
| rs372664700 | snp | G/T | 0.000164867 | 0.00907779 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345096 | TCTAGGACTTTTTTA[G/T]ATCTTCCTTTGCTTG | 84108 |
| rs372679274 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341244 | CAAAAACAAAAAAAA[A/G]TCCTTTTAATTTTCT | 84108 |
| rs372823840 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335691 | GAAAAAAATAGGCTG[A/G]GCGAGGTGGCTGATG | 84108 |
| rs372831803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331977 | TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 84108 |
| rs372862460 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346145 | GGTTGCAGTGAGCCA[A/G]GATCATGCCACTGCA | 84108 |
| rs372914895 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312506 | TGAAATCTCTTGATG[C/T]TGATTCTGGCACCAA | 84108 |
| rs372984226 | snp | A/T | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345050 | CAGTAATAAAGACAT[A/T]TCAAGTTCAGGTGGA | 84108 |
| rs373084595 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338477 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84108 |
| rs373089608 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353006 | GAATCACTTGAACCC[A/G]GGAGGCGAAGGTTGC | 84108 |
| rs373201875 | snp | C/T | 0.000197795 | 0.00994274 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348888 | ATTCAGAAATGTGAT[C/T]GGTATGCTTACAGGT | 84108 |
| rs373228139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318602 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCGGTC | 84108 |
| rs373240952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311883 | CACTTGAGGCCAAGA[A/G]TTTGAGATTAGCCTC | 84108 |
| rs373256836 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339814 | CTCAAAAAAAAAACA[A/C]ACACACACACACACA | 84108 |
| rs373304714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349230 | TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA | 84108 |
| rs373348911 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340958 | ATTCCTTACAGGCGC[A/G]GTGGCTCACGCCTGT | 84108 |
| rs373396209 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319523 | TGTTCTTCAAACCCA[A/T]TCCTGAGTTAAATCA | 84108 |
| rs373470024 | snp | C/G | 0.000264053 | 0.0114872 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303970 | GACCATCCTGAAAAG[C/G]GGAGAAAAAAAGACG | 84108 |
| rs373470595 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331540 | TAGGATTACAGGCAT[A/G]ACCCAATGTCCCCAG | 84108 |
| rs373634981 | snp | C/T | 8.51444e-05 | 0.00652418 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348689 | AGTATATTTAAAATA[C/T]AATTGTAATTTATAT | 84108 |
| rs373714369 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327966 | AGGTATGAGCCACTG[C/T]GCCCAGCCAGGGATT | 84108 |
| rs373876509 | snp | C/T | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302309 | AGCTGGGAATACAGG[C/T]ACACACCACCATGCC | 84108 |
| rs373983716 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339614 | GCCAACATGGTGAAA[A/C]CCCATCTCTACTAAA | 84108 |
| rs374036374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328134 | ATCTGAGACAACTAA[C/T]GATGCTACGACCTCA | 84108 |
| rs374067663 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350267 | GAGCCCTCCTCGCTA[A/C]AAAAAAAAAAAAAAA | 84108 |
| rs374125579 | snp | C/T | 0.000131887 | 0.00811949 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314211 | GCATCACCTATTGCA[C/T]GTCGGATTTCCCTTA | 84108 |
| rs374324384 | snp | C/T | 1.6691e-05 | 0.00288881 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304009 | GTTCTTTCAAACCAG[C/T]AATGCAAATGATCAA | 84108 |
| rs374430014 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332329 | CTGTCACCTAGGCTA[C/G]AGTGTAGTGACGCAA | 84108 |
| rs374449550 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306764 | GTCAATAGGGAATGT[C/T]GAAGACCAGTGGTAA | 84108 |
| rs374505986 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346119 | GAGAATTGCTTGAAC[C/T]TGGAGGCGGAGGTTG | 84108 |
| rs374509878 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341900 | CCATCCCAGACTCAA[C/T]AGACTCCAGTGCCGC | 84108 |
| rs374711599 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341923 | AGTGCCGCTTCCTAG[A/G]GGCACTGCCATTAAT | 84108 |
| rs374766975 | in-del | -/AAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307456 | CCCTGTCTCAAAAAA[-/AAAA]GAAAGAAAGTTTGTT | 84108 |
| rs374769152 | in-del | -/AAAAC/AAAACAAAAC/AAAC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350083 | CGAGACTCCGTCTCA[-/AAAAC/AAAACAAAAC/AAAC]AAAACAAAACAAAAC | 84108 |
| rs374799115 | in-del | -/AG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308853 | TCTAACCTGAGTGAC[-/AG]AGAGAGAGAGACTCC | 84108 |
| rs374832057 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323282 | ATATCGGTACTAAAA[A/G]CACTAGCAAACTTTC | 84108 |
| rs374860985 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323030 | TATAATAAGGGCAAG[C/T]CTTCTGCTTTTAGAA | 84108 |
| rs374863872 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311026 | TCCTTTGTAAAGACG[A/G]GACTCGCTATACTGC | 84108 |
| rs374870135 | snp | A/C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329810 | TTTTGAGACAGTCTC[A/C/G]CTCTGTCGCCTGGGC | 84108 |
| rs375024627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348837 | AAGAATGTTGAAGTC[A/G]GGATGCTTTCAAGAC | 84108 |
| rs375025758 | snp | C/T | 3.33089e-05 | 0.00408085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347200 | ATTGTTAGTATTCTT[C/T]AATCTGTAAGTACAT | 84108 |
| rs375065378 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328485 | TGTAGGCACTCCAGG[A/C]AGACACCTGGGCTCA | 84108 |
| rs375140167 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344380 | GATTTCAAGTGATTC[G/T]CCTGCCTCAGCCTCC | 84108 |
| rs375159026 | in-del | -/AAAAACACACACAC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339807 | TGTCTGTCTCAAAAA[-/AAAAACACACACAC]ACACACACACACACA | 84108 |
| rs375201614 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334852 | AATAGCCCTGCAAAT[A/G]AGGTATTAGTACCCC | 84108 |
| rs375235284 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310432 | GGTTTGAGTTAAACA[A/G]ATAGGTATTTGTTGA | 84108 |
| rs375269864 | snp | C/G | 6.60088e-05 | 0.00574457 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347404 | ACTTACTTTCCTCTA[C/G]ATTGATCACTAATTT | 84108 |
| rs375327410 | snp | C/T | 0.000321234 | 0.0126694 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350797 | CTCTTCTTCCTCCTC[C/T]AGCTCCTCTTCTTCT | 84108 |
| rs375383456 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316695 | CATAGCATCTCTGTT[A/G]TATCTCTTCAATTCA | 84108 |
| rs375384815 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334642 | TCCTATTGCTTTTTT[G/T]GCAGAATAATTACCT | 84108 |
| rs375512667 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322900 | AAAACAAAAAACAAA[A/C]AACAAAAAAAAAAAC | 84108 |
| rs375539031 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349104 | CCCAAGCTGAGTGCA[C/G]TGATGTCATCTCGGT | 84108 |
| rs375713112 | in-del | -/GTT | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328672 | AGTAAGCACTGAAGA[-/GTT]GTTAGTGTTGTGAGC | 84108 |
| rs375765869 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313888 | CCCTGTCTCACCCAC[C/T]GACTGTAGGAAGTTA | 84108 |
| rs375793340 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331019 | ACTAATCTGCTTTCT[A/G]CTCCTGTGGATTTTC | 84108 |
| rs375871260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350587 | AGGTCGGGGGAGGTC[C/T]GCTCCAGTGCTCCGC | 84108 |
| rs375871607 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320503 | ACCAGCCTGGCCAAC[A/G]TGGAGAAACTCTGTC | 84108 |
| rs375908829 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323895 | TGGCCAGTCACTGTT[A/T]TAACATATCTATTAA | 84108 |
| rs375913559 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312318 | GAATCCCTTGAACCC[A/G]GGAGGCAGAGGTTGT | 84108 |
| rs375964723 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349053 | GCCTTTTACAAATTC[-/T]TTTTTTTTTTTTTGA | 84108 |
| rs376004812 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335725 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGTGG | 84108 |
| rs376040698 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324139 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 84108 |
| rs376079509 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332162 | CATAGTCACCTTCCT[A/G]TATGTCTTGGCAAGA | 84108 |
| rs376092042 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306567 | GCTATTACTCTCCTT[C/T]GCTTCTTTGCTAAGC | 84108 |
| rs376104907 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313411 | TTTGACTAAAAATAC[A/G]AAAATCAGCCGGGTG | 84108 |
| rs376126907 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338502 | GTGAGCTGAGATCGC[C/G]CCACTGCACTCCAGC | 84108 |
| rs376138205 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306016 | CCAAGTCTTTTTATC[C/T]ACTTTTTGTGGCGTT | 84108 |
| rs376224050 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336768 | TAATCCTAGCTACTC[A/G]AGAGGCTGAGGCAGG | 84108 |
| rs376236247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332562 | ATTACAGATGTGAGC[C/T]AACGAACCCGGCCTA | 84108 |
| rs376306313 | in-del | -/TATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315995 | GTGTGTGTGTGTGTG[-/TATA]TATATATATATATAT | 84108 |
| rs376319280 | snp | A/G | 2.07316e-05 | 0.00321953 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348691 | TATATTTAAAATACA[A/G]TTGTAATTTATATAT | 84108 |
| rs376321728 | snp | A/T | 3.29973e-05 | 0.00406172 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345109 | TAGATCTTCCTTTGC[A/T]TGAAGGGACTGGCTG | 84108 |
| rs376357621 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318046 | ACAGGCATGAGCCAC[C/T]GCACCCAGCTGGGGT | 84108 |
| rs376408461 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322899 | AAAACAAAAAACAAA[-/C]AAACAAAAAAAAAAA | 84108 |
| rs376411290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343916 | TACCCTAAGACTCAG[C/T]AAATCTACACTCGTG | 84108 |
| rs376414688 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327078 | GATTGTTTGAGGTCA[C/G]GAGTTCGAGACCAGC | 84108 |
| rs376425436 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320834 | AAATGAAGGTCACAT[A/G]TCTGTAAACCATGCA | 84108 |
| rs376674913 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350267 | AGCCCTCCTCGCTAC[-/A]AAAAAAAAAAAAAAA | 84108 |
| rs376774773 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325831 | TGAGACCAGCCTGGA[C/G]AAAAGCAAGACCGCA | 84108 |
| rs376791795 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339801 | AATTCTGTCTGTCTC[-/AAA]AAAAAAAAAACACAC | 84108 |
| rs376882943 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312939 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 84108 |
| rs376912505 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311219 | CGATCTTGGCTCACC[A/G]CAAACTCTGCCTCCC | 84108 |
| rs376952529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346556 | TTGAGCCCAGAAGGC[A/G]GAGGTTGCAGTGAGC | 84108 |
| rs376961850 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328996 | ATGATCTACCGGCCT[C/T]AGCGTCCCGAAGTGC | 84108 |
| rs376964380 | snp | C/T | 9.93657e-05 | 0.00704791 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347235 | GTATACACCCAAACT[C/T]ACCAGGTTTAGGTAC | 84108 |
| rs377018836 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305031 | GCAATGGCGCGATCA[C/T]AGCTCACTGTAGCCT | 84108 |
| rs377064184 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320903 | CAGCATAGCAGGCTC[A/G]TGACTGCAGGACACC | 84108 |
| rs377074950 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305811 | CCAACACTTTGAGAG[C/T]CCGAGGTGGGCAGGT | 84108 |
| rs377350224 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340710 | CAGTCGATCCTCCCC[A/C]ATCAGCCTCCCTAGT | 84108 |
| rs377367828 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344155 | CAGGGATGAATCACA[A/C]AATACTGAGTGAAAA | 84108 |
| rs377377192 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321395 | TTAGAAGAGAAATAC[C/T]GTACAAGATGGTGAC | 84108 |
| rs377420968 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318723 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 84108 |
| rs377572246 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302873 | ACAAAGAATTGCCAA[A/T]CTTTTTCCAATTTTG | 84108 |
| rs377577221 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350531 | AGACCCAGGCCGGGC[C/T]GGAGGCCTGTCGGCG | 84108 |
| rs377690898 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338209 | TCATGCCACTGCACT[C/T]CAGCCTTGACAACAA | 84108 |
| rs377716041 | in-del | -/T/TT | 0.451856 | 0.147493 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304656 | GACACCCAGCCCCAC[-/T/TT]TTTTTTTTTTTTTTT | 84108 |
| rs377749632 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308329 | GAGGTGGAGCTGCTC[A/T]AGGCCTTGGGAACCC | 84108 |
| rs377759999 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328140 | GACAACTAACGATGC[C/T]ACGACCTCATGCAAA | 84108 |
| rs397727020 | in-del | -/T | 0 | 0 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351660 | TTTTTTTTTTTTTTT[-/T]GAGACAGTTTCGCTC | 84108 |
| rs397802168 | in-del | -/A | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338084 | AAAAAAAAAAAAAAA[-/A]TACAAAATTAGCTGA | 84108 |
| rs397818005 | in-del | -/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327857 | TTTTTTTTTTTTTTT[-/T]CATTAGAGATAGGGT | 84108 |
| rs397845563 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325872 | AAAAAAAAAAAAAAA[-/A]ATTAGCTGGGCATGG | 84108 |
| rs397845812 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325873 | AAAAAAAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 84108 |
| rs397846417 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304154 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 84108 |
| rs397945972 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312406 | AAAAAAAAAAAAAAA[-/AA]GTCACAACTGTCTAA | 84108 |
| rs397961509 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314982 | AAAAAAAAAAAAAAA[-/A]TCATTAAAAGGTATT | 84108 |
| rs398014677 | in-del | -/G | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348008 | CAGTTTCTTAAGAGA[-/G]GGAAAAATACTAACA | 84108 |
| rs527273347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321958 | TGGAGTGCAGTGGCA[G/T]GGTCTCAGCTCACTG | 84108 |
| rs527274722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329067 | ACTTTTGAGATGGAG[C/T]CTCGCTCTGTCACCC | 84108 |
| rs527329987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322763 | CGGGAGGTAGAGACC[A/G]CAGTGAGTCAAGACT | 84108 |
| rs527334276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314753 | TCAGGAGTTCCAGAC[C/G]AGCCTGGCCAACATG | 84108 |
| rs527339668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313716 | CCTGAGGGCCACAGG[C/T]TGGACAAACTTGGCT | 84108 |
| rs527349836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305552 | CTGGGATTACAAGTG[C/T]GACCCGCTGCACCCG | 84108 |
| rs527398369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306382 | GAATTATAGGTGTGA[A/G]CCACAACGCCTGGCC | 84108 |
| rs527506864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345391 | CATTAGAACAGCAAC[A/G]TGTGTAGACAACCCT | 84108 |
| rs527613124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345959 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 84108 |
| rs527619153 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341278 | TTATTTTTTTTGAGA[C/T]GGAGTTTCACTCCTG | 84108 |
| rs527680226 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337938 | GCGTAGTGGTGGGCG[C/T]CTGTAGTCCCAGCTA | 84108 |
| rs527694278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329899 | TTCTCCTGCCTCAGC[C/G]TCCCGAGTAGCTGGG | 84108 |
| rs527695658 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338387 | TCTCTACAAAAAAAC[A/C]AAAAAAAATTAGCCG | 84108 |
| rs527751756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323631 | GAGTCTCCCTCTTGT[C/T]GCCCAGGTTGGAGTG | 84108 |
| rs527754358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330698 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACCTGA | 84108 |
| rs527847353 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334283 | TAAAATTGTGTATAT[C/T]TATAGGTTTTGATAC | 84108 |
| rs527865219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315688 | CTTTTTTCAATTTTT[A/G]TAGAGACAGGGTCTC | 84108 |
| rs527946108 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317605 | GATCGTACCGCTCCA[A/C]CCCAAGCCTGGGCAA | 84108 |
| rs527992327 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348219 | TCAGGAAAAAGGCCT[A/G]TGCCTCTTTTAAGTC | 84108 |
| rs528163236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326923 | ACTCAGAGTAAAATT[C/T]ATTCATTCATTTCAA | 84108 |
| rs528165994 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348369 | TGAGATACTCTCATC[A/G]GTCTGTCGCCCAGGC | 84108 |
| rs528205072 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317172 | CACGCCACCACACTC[A/G]GCTAATTTTTGTATT | 84108 |
| rs528288853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327381 | AACATTAAGGGGTGT[A/G]AATGACAAATACATT | 84108 |
| rs528291561 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319649 | TGATGGCATGAATTT[A/T]GTCTCATCTTTGTAC | 84108 |
| rs528310715 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334063 | CATTGTAATTCTAGA[-/AC]ACAGTCACCTGAAGT | 84108 |
| rs528433981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346586 | CCAAGATCATGCCAC[C/T]GCACTCCAGCCTGGT | 84108 |
| rs528450752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350527 | GTAAAGACCCAGGCC[A/G]GGCCGGAGGCCTGTC | 84108 |
| rs528459501 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303764 | TTGTACTTATAAACG[C/T]TATAATTCTTGGTGC | 84108 |
| rs528468555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312829 | AGTTGGGCGTGGTGG[C/T]GCATGCCTGTAAACC | 84108 |
| rs528515143 | snp | C/G | 0.000173671 | 0.00931695 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350961 | CCGCTGCGGGTGCAG[C/G]GGTGAGGGCGGGCGG | 84108 |
| rs528581587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309655 | AGAAACAGAGTTCAG[C/G]CATGGTGGCTCACAC | 84108 |
| rs528681185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344214 | ATGCTACATATTGCT[C/T]AGGAATAGATATACA | 84108 |
| rs528729783 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328582 | ATTTGTAAAATAGAT[A/G]AAAATAGCACCTGCT | 84108 |
| rs528789756 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324118 | CTATTTTTCATTTTT[C/T]AGTAGAGACAGGGTT | 84108 |
| rs528840162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307394 | GTGAACCATATTCAT[A/G]CCACTGCACTCCAAC | 84108 |
| rs528868903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316260 | ATAGACTTAAACCAC[C/T]AAAACTACCTCCTAG | 84108 |
| rs528931365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308503 | TCCCAGGTTCAAGCA[A/G]TTCTCCTACCTCAGC | 84108 |
| rs528979486 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341686 | TGATGTCAAGTAATC[C/T]GCCCACCTAAGCCTC | 84108 |
| rs529021811 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344626 | GGAGTGCAATGGCGC[A/G]ATCTTGGCTCACTGC | 84108 |
| rs529040602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338725 | TACAAAAACTTAACC[A/G]GGCATGGTGGCACAC | 84108 |
| rs529071938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330790 | AAAAATTAGCTGGGC[A/G]TGGTGGGGCGCACCT | 84108 |
| rs529095048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339545 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 84108 |
| rs529109750 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313588 | GAATAAATAAAAATA[C/T]AATATACCAGTACGA | 84108 |
| rs529181211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331414 | AGGTGCCCACCACCA[C/T]GCCTGGCTAATTTTT | 84108 |
| rs529246030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325015 | GGCACCTGCCTGTAA[C/T]CCCAGCTACTCAGGA | 84108 |
| rs529259344 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344729 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTTGTA | 84108 |
| rs529295714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317886 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 84108 |
| rs529575563 | snp | C/T | 3.34079e-05 | 0.00408691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349034 | GTTTTAAAATACAAG[C/T]CCTTGCCTTTTACAA | 84108 |
| rs529626600 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321166 | AGAAAATTAAAGGTT[A/G]AAACAAATTTTATAT | 84108 |
| rs529631243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328077 | GAGGTGATAAGTAGA[C/T]GACAGAGTTTGAAAG | 84108 |
| rs529642940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328507 | CTGGGCTCAAACCCT[C/G]GTTCTGCCATTTTCT | 84108 |
| rs529680927 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323950 | TTATTTTATTTTACT[A/G]TTTTTTTGAGACAGA | 84108 |
| rs529769767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321837 | TTTTGCCATCCCACA[A/G]TGTATACATATTTCA | 84108 |
| rs529925468 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352096 | AGCACTTTGGGAGGC[C/T]GAGGCGCGCAGATCA | 84108 |
| rs529965357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305459 | TAATTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 84108 |
| rs529985015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344365 | CAACCTCCACTGCCC[A/G]ATTTCAAGTGATTCT | 84108 |
| rs530166334 | snp | C/G | 0.202343 | 0.245416 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337934 | CCGGGCGTAGTGGTG[C/G]GCGCCTGTAGTCCCA | 84108 |
| rs530170732 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330064 | TGAGCCACTGTGCCC[A/G]GCCTGTTTTTTGTTT | 84108 |
| rs530209254 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327620 | TCATTATACTATTCT[C/G]CCTACTTTTGTATAA | 84108 |
| rs530227675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322964 | ACACATAAATAGCCA[C/T]AGAATAATCTGTATT | 84108 |
| rs530327560 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323590 | GTGAGCCACCGCGTC[C/T]GGCCCCTTTTCTTTT | 84108 |
| rs530334707 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319893 | TCACCGCAACCTCCA[A/C]CTCCTGGATTCATGT | 84108 |
| rs530340302 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332746 | CCCACTACATGGCTA[C/T]GAGAATTTCCTAAAG | 84108 |
| rs530419696 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333126 | TCCATTTAAAAAAAA[A/T]AAAAAAAAAAAATCA | 84108 |
| rs530444772 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352097 | GCACTTTGGGAGGCC[A/G]AGGCGCGCAGATCAT | 84108 |
| rs530477520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320358 | TTTGGATAATTATTG[A/G]TCTCTAAATTTTAAA | 84108 |
| rs530649456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332509 | TTGAACTCCTGGCTC[C/T]AAGCAATCCTCCTGA | 84108 |
| rs530729902 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326018 | CTGGGCAACAGAAAC[A/C]GACCCTGTCTCAAAA | 84108 |
| rs530799074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311278 | TCCCGAGTAGCTGGG[A/C]TTACAGGCACCTGCC | 84108 |
| rs530862134 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334739 | TTTAAGCCATGAGGG[-/A]AGACAAGGGTATCTA | 84108 |
| rs530873684 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303533 | AAGATGACTGCCCAA[C/T]TGATGCCATCCCAGA | 84108 |
| rs530920293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320110 | CATGCCTGGCCAGCC[C/T]AACTTTTAAGATGGA | 84108 |
| rs530951016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350304 | ATTAGCCCGGCGTGG[C/T]GGCGCGTGCCTGTAG | 84108 |
| rs531026584 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327181 | TCCCAGCTACTCGGG[A/C]GGCTGAGGCAGGAGA | 84108 |
| rs531026931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334955 | ATAAAACTGAAATTC[A/G]CACTCAGGTGTGCCT | 84108 |
| rs531138204 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324530 | TTGGGAGGCCGAGGC[A/G]GGAGGATCACGAGGT | 84108 |
| rs531183850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314869 | CTGAGGCAGGAGAAT[C/T]ACTCGACCCCAGGAG | 84108 |
| rs531187611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329315 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 84108 |
| rs531243881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315609 | GATGATCCGCCCACC[C/T]CAGCCTCCCAAAATG | 84108 |
| rs531416325 | snp | C/T | 0.499732 | 0.0115784 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337955 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 84108 |
| rs531526731 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338470 | GAATGGCATGAACCC[G/T]GGAGGCGGAGCTTGC | 84108 |
| rs531585938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330757 | ACACGGTGAAACCCC[A/G]TTTCTACTAAAAATA | 84108 |
| rs531597819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331332 | ATCTCAGCTCACTTC[A/G]CCAAGTTCTCTGCCC | 84108 |
| rs531675804 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324891 | TGTAATCCCAGCACA[C/T]TGGGAGGCCGAGGTA | 84108 |
| rs531721261 | in-del | -/CATC | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303336 | CACATAATAACAATT[-/CATC]CATTTTGAAATGAGT | 84108 |
| rs531743376 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324517 | TAATCCCAGCACTTT[A/C/G]GGAGGCCGAGGCGGG | 84108 |
| rs531787645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317764 | AGTTTCTTTTTTCTG[A/T]TTTTTTTTTGAGACA | 84108 |
| rs531805307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316527 | AAAGACATTAAACTT[C/T]CCTGAGATCACAAAG | 84108 |
| rs531981241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309438 | TTCCCTCCTTATTCT[C/G]TCTCTTCTGGTTCCT | 84108 |
| rs532014419 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304529 | TATTTTTAGTAGAGA[C/T]AGGGTTTTGCCATGT | 84108 |
| rs532142750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335583 | GTTCAGGATGGCCTC[A/G]ATCTCTTGATCTCGT | 84108 |
| rs532206462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327921 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 84108 |
| rs532258847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304740 | GACTCACTGCAGCCT[C/T]GACCACCTGGGCTCA | 84108 |
| rs532344850 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351022 | AGCTCCCTCGGTTTT[A/G]GCAGCGCCTACGCTG | 84108 |
| rs532387512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312833 | GGGCGTGGTGGCGCA[C/T]GCCTGTAAACCCAGC | 84108 |
| rs532388669 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330136 | CTGGAATGCAGTGGC[A/G]CAATCTCGGCTCACT | 84108 |
| rs532399629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313410 | TTTTGACTAAAAATA[C/G]AAAAATCAGCCGGGT | 84108 |
| rs532450232 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305262 | TACAGGTGTGAGGCA[C/G/T]GCATCCAGCCCAGAC | 84108 |
| rs532511712 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314780 | CATGGTGAAACCCTG[C/T]CTCTACTAAAAATAC | 84108 |
| rs532574299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344297 | TTTTTTTTGAGACAG[A/T]GTCTCACTCTGTCAC | 84108 |
| rs532597272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328731 | ATTTTTGCTCTTTAT[G/T]TACAGGATTTTAACT | 84108 |
| rs532688884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345203 | ATCTTTGGAAAAATA[C/T]ACAAGTATTATAATT | 84108 |
| rs532752119 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337133 | TACCTGTTTACCAAT[A/C]TCTCTCTTAAAATAT | 84108 |
| rs532918342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347012 | ACTGGCTTGGCTTAA[C/G]TTATACACCTCATAA | 84108 |
| rs532991540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332353 | GACGCAATCACAGCT[C/T]ACTGCAGCCTCAATC | 84108 |
| rs533034027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344101 | TTAATGGAATGCCAA[A/G]TAATGGTGAAAATGA | 84108 |
| rs533044350 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325941 | GACAGGAGGGAGGAC[A/C/T]ACCCAAGCCCAGGAA | 84108 |
| rs533095860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339705 | TGAGGTGGCAGAATT[A/G]CTTGAAACCGGAAGA | 84108 |
| rs533135917 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318844 | TCACATTAGTGTAGG[A/C]AACTTTTTGCAGGCC | 84108 |
| rs533160258 | snp | G/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340572 | TTCCTGCTGTGATTA[G/T]TGGAAAGTGTTACAT | 84108 |
| rs533195448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319454 | CCGGACCTGGCCATA[C/T]ATACTCTTCTTTGCT | 84108 |
| rs533209495 | in-del | -/AAAAC | 0.00661423 | 0.0571259 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350084 | CGAGACTCCGTCTCA[-/AAAAC]AAAACAAAACAAAAC | 84108 |
| rs533209517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311122 | ATTATAGGAGCAAGC[G/T]ACTATGCCTGGCCAA | 84108 |
| rs533216537 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309316 | GAGGTGATTGGATCA[C/T]GGGGTTGGATTTCTC | 84108 |
| rs533307864 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313288 | TGCTAACACAGGCTG[A/G]GCAGAGGGGCTCACC | 84108 |
| rs533309345 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349117 | CAGTGATGTCATCTC[C/G]GTTCACTGCAACCTC | 84108 |
| rs533338385 | snp | A/G | 5.28863e-05 | 0.00514202 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326493 | GTGTGCTAAAGGTAA[A/G]CTCACAACTTTACCT | 84108 |
| rs533371555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350223 | AATCTCTTGAACCCA[A/G]GAGTTCGAGAACAGC | 84108 |
| rs533479879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342530 | TGAGCCACCATGCCT[A/G]GCCAAGATTTTCTTA | 84108 |
| rs533603756 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303463 | AGAGTACACCCTGCA[G/T]TTTAACAAAGACTGG | 84108 |
| rs533690323 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352172 | CGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 84108 |
| rs533699661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341509 | CACTGGTGTGATCTC[A/G]GCTCACTGCAACCTC | 84108 |
| rs533701403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344682 | AGTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 84108 |
| rs533728211 | snp | G/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352464 | ATCAAATAATGCCTG[G/T]CAAAGTCACATTTAA | 84108 |
| rs533762666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312947 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 84108 |
| rs533983957 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334124 | TTCTGCCACCTAGTG[C/G]TTAAGGCAAAGGCAG | 84108 |
| rs534015864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336792 | AGGCAGGAGAATCAC[C/T]TGAACCCGGGAGGCG | 84108 |
| rs534089678 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303292 | CACTGAAATTTTATG[A/G]CACAGATCATAAACT | 84108 |
| rs534186507 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314486 | ATACAGCAGGACAAC[A/C]GCACAGTATAATTGA | 84108 |
| rs534214788 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339913 | TCATGCCTGTAATCC[C/G]AGCACTCTGGGAGGC | 84108 |
| rs534362588 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353048 | ATCGCACCACTGCAC[C/G]CCAGCCTGGGCGACA | 84108 |
| rs534383019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306793 | AAACCAGAGAGAGCA[A/G]ATGTCTATCTAAAGA | 84108 |
| rs534480144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345612 | GTGGGTGGATCACCT[C/G]AGGTCAGGAGTTCGA | 84108 |
| rs534546123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346220 | AAAAAAGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 84108 |
| rs534600639 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336328 | CCTATAAATGATATA[C/T]TATTTTATATGAAAT | 84108 |
| rs534606355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332566 | CAGATGTGAGCCAAC[A/G]AACCCGGCCTAATAT | 84108 |
| rs534606856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326168 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 84108 |