SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs534616535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318218 | GAGGCCGAGACGGGC[A/G]GATCACCTGAGGTCA | 84108 |
rs534618505 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310611 | CAAGAAAAAAAGATA[A/C]TTCTTATAATATTCA | 84108 |
rs534668132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342162 | GCTGGTCTCAAACTC[C/T]TAATCTCAAGTGATC | 84108 |
rs534697372 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320748 | TTGTTTTTAAAATTT[C/G]ATCTGCCACAAAAAA | 84108 |
rs534730262 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333834 | TATTTAAATAACTTA[A/T]TTATACAATCTCCAT | 84108 |
rs534819833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327167 | GCACATGCCTATAAT[C/T]CCAGCTACTCGGGAG | 84108 |
rs534837903 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331451 | TTAATAGAGATAGAG[G/T]TTTGGCATGTTGGCC | 84108 |
rs534889329 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302696 | GTGATCCACCTGCCT[C/T]GGTCTTCCAAAGTGC | 84108 |
rs534892502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320557 | CCAGGCATGGTGGCG[C/T]ATGCCTGTAATCCCA | 84108 |
rs534953720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321192 | TATATCTTTCTTTTT[C/G]AGACAGGGTCTCATC | 84108 |
rs534960890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349283 | GAACCCCTGGCCTCA[C/G]GTGATCCACCCGCCA | 84108 |
rs534975559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312432 | TCTAATTTACACAAC[A/G]AGTAAGGGCTACAGG | 84108 |
rs535036902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342788 | TTATAGAGATATAAA[C/T]TGCAACACTCTTTAA | 84108 |
rs535120002 | in-del | -/CAAAA | 0.0131196 | 0.0799228 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352332 | GACTCCATCTCAAAA[-/CAAAA]CAAAACAAAACAAAA | 84108 |
rs535152046 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318707 | TGAGATGGCACCACT[A/G]CACTCCAGCCTGGGC | 84108 |
rs535228751 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338042 | GCACTCCAGCCTGGG[A/T]GACAGAGCGAGACTC | 84108 |
rs535234572 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310076 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 84108 |
rs535264420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330135 | GCTGGAATGCAGTGG[C/T]GCAATCTCGGCTCAC | 84108 |
rs535387071 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345581 | GCCTGTAATTCCAAC[A/C]CTTTGGGAGGCCAAG | 84108 |
rs535391683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324540 | GAGGCGGGAGGATCA[C/T]GAGGTCAGGAGATGG | 84108 |
rs535405705 | in-del | -/GG | 0.00517822 | 0.0506191 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351237 | TCCGGGGCAGGCTGC[-/GG]GGCGCGCGGGCCGCA | 84108 |
rs535453242 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337835 | TTTGGGAGGCCGAGG[A/C]GGGCGGATCACGAGG | 84108 |
rs535477136 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316621 | CTAAATGCCATCTCA[C/G]GGGTCGGCAAACCGT | 84108 |
rs535489850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308870 | AGAGAGAGAGACTCC[A/T]TCTCAAAAAATAAAT | 84108 |
rs535535949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306575 | TCTCCTTCGCTTCTT[C/T]GCTAAGCTTTTCCAT | 84108 |
rs535673225 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349175 | GTCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 84108 |
rs535689170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339784 | CCTGGGGAACAAAAG[C/T]GAAATTCTGTCTGTC | 84108 |
rs535772210 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318479 | TGCGGGTGCGGTGGC[A/G]CACACCTGTAATCCT | 84108 |
rs535773350 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315844 | GAGAGAATATTGTTG[C/T]ATATATACATTTTAT | 84108 |
rs535837732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308053 | CCGGCCTGGATGTCT[A/G]GGCAGAAGCCTGCTG | 84108 |
rs535866053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311611 | CCACCGCACCTAGCC[A/G]CATTTCTTGTCTTTA | 84108 |
rs535887691 | in-del | -/T | 0.18989 | 0.242666 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306102 | CGCAAGCAATCCACC[-/T]TTTTTTTTTTTTTGA | 84108 |
rs536002928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339113 | GCGGTAACATAAATG[C/T]TTTTCTATGTAATAA | 84108 |
rs536008047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350611 | GCTCCGCGCGGCGGC[G/T]GCGCACTAGGATCGG | 84108 |
rs536013754 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346479 | AAATACAAAAATTAG[C/T]TTGGCGTAGTGGCGG | 84108 |
rs536198869 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324798 | AAAAAAAAGAAAATA[C/T]TACATAGCTAGAACA | 84108 |
rs536240720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320465 | GCCGAGGTGGGCAGA[C/T]TGCCTGAGGCTGGGA | 84108 |
rs536270118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321495 | AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 84108 |
rs536412857 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351150 | ACCACTGCGCAGGCG[C/T]GGCAGCCTGAGGGGC | 84108 |
rs536437333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304802 | CTGGGAAAATAGACA[C/T]GCACCACCACCAGAC | 84108 |
rs536455094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314904 | TGGTTGCAATGAGCC[A/G]AGATCATGCCATTGC | 84108 |
rs536516832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306731 | AACATAAATGAATAC[A/G]TAAGTTAGGTATGTG | 84108 |
rs536526396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343669 | AAAACCCTGTCTCTA[A/C]TAAAACTACAAAAAT | 84108 |
rs536530757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338741 | GGCATGGTGGCACAC[A/G]CCTGTAATCCCAGCT | 84108 |
rs536605467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328221 | AAGTGTTTTTTTAGG[A/G]CTTACAGACTGGGAG | 84108 |
rs536605504 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336627 | CACCTGTAATTTCAG[A/C]ACTCTGGGAGGCTGA | 84108 |
rs536620780 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322681 | ACAAACAATTTAGCC[A/G]GGCATGGTGGCATGC | 84108 |
rs536851163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318171 | GGATCAACTGGGTGC[A/G]GTGGCTCACGCCTGT | 84108 |
rs536860409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309848 | GGGAGGCTGAGGTGG[A/G]AAGAGATCAATTGAG | 84108 |
rs536929898 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352432 | GCAAGAAAGATTCGG[A/G]AAGTCAAATGCTCCT | 84108 |
rs536991399 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352944 | AAATTAGCCGGGCAT[A/G]GTGGTGCACACTTGT | 84108 |
rs536999508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330970 | TCTTGGTAGTCACTC[C/T]CCATTCAGCCTCTTC | 84108 |
rs537072068 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324679 | GCAGGAGAATCACTT[G/T]AACCCGGGAGGCGGA | 84108 |
rs537190175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332854 | GCGCAGTGGCTCACA[C/G]CTGTAATCCCAGCAC | 84108 |
rs537202649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333704 | ATTAACATAGCATTT[G/T]GTTTTAGTTTTAAAA | 84108 |
rs537259977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318907 | AGCAGGCCCTTCTAA[C/T]GACAGCAGCCTCAAG | 84108 |
rs537378325 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319926 | TTCTCCTGCCTCATC[A/T]TCCCGAGTAGCTGGG | 84108 |
rs537426098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305597 | AATAGACTATTTAAG[C/T]ATTAGATTCTCCTAA | 84108 |
rs537427740 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350040 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 84108 |
rs537523419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344766 | GTAGAGACGGGGTTT[C/T]GCCATGTTAGCCAGG | 84108 |
rs537530117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321644 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84108 |
rs537533278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349205 | GGCGCGCACAACCAC[A/G]CCTGGCTAATTTTTG | 84108 |
rs537588480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336830 | CAGTGAGCCGAGGTC[A/G]TGCCACTGCACTCCA | 84108 |
rs537656794 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328276 | GAGGCACACATTTGT[C/T]CCATGTTACAGCACT | 84108 |
rs537777343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330015 | ACTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 84108 |
rs537811105 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352363 | CAAAACAAAACAAAA[A/C]ACAAAAAAACCATTA | 84108 |
rs537850756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323696 | CTCCCGGGTAATAGC[A/G]ATTCTCTTGCCTCAG | 84108 |
rs538058921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329385 | TTATTGTTTTATAGG[A/G]CTGTCATTACTAAAA | 84108 |
rs538137549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347141 | AATCTCTCTGATCAT[A/G]TAATAAGCTACCCCC | 84108 |
rs538175906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323225 | AAGCTCAGTTAGAGA[A/T]GTCATATTTCACTGG | 84108 |
rs538220522 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322946 | AAACATACACACACA[C/G]AGACACATAAATAGC | 84108 |
rs538240310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315286 | AAACTCCTAGGCTGA[A/G]GCAATCCTCCCACCT | 84108 |
rs538254676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315718 | CGGTATATTGCCCAG[A/G]CTGGTCTCAAACTCC | 84108 |
rs538357268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336484 | AGAATTATCTCTGTA[A/G]AATACTTGGTACATG | 84108 |
rs538402963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346245 | GCCTGTAATCCTAGC[A/T]CTTTGGGAGGCCAAG | 84108 |
rs538417909 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349510 | TTTTGAGAGGGAGTC[G/T]GCCTCTGTCGCCCAG | 84108 |
rs538426406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308706 | GTAAAACCCCATCTC[C/T]ACAAAAAAATACAAA | 84108 |
rs538536722 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325377 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 84108 |
rs538581484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339020 | CAAATTTGCCCCTGT[C/G]CTTCCATCAGACTAA | 84108 |
rs538616998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327012 | AACTTTGAGGCCGGG[C/T]ATGGTGGCTCACGCC | 84108 |
rs538626771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319211 | CTGGAATGCAGTGGT[C/G]GGATCTCGGCTCACT | 84108 |
rs538669655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327659 | ATTTTCATAATAAAG[A/G]GAATTCTTTTTTTTT | 84108 |
rs538672287 | in-del | -/CACACACACACA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339856 | ACACACACACACACA[-/CACACACACACA]AAAGCATCTTATGAG | 84108 |
rs538703650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311539 | CTGCGACCTCCCGGG[C/T]TTGAAGCGATTCTCC | 84108 |
rs538811364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312121 | AGTCACGGTTGGGCA[C/T]GGTGGCTCACGCCTG | 84108 |
rs538902073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350581 | GGGCAGAGGTCGGGG[G/T]AGGTCCGCTCCAGTG | 84108 |
rs538910653 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313868 | CAAACTGCCTAGAGT[A/C]TGAGCCCTGTCTCAC | 84108 |
rs538919006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304901 | CTGTCTCAGACTCCC[A/G]AAGTGCTGGGATTAC | 84108 |
rs538974353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342912 | GGGCTTCTTGGGGAC[A/G]TAACAAATCTCTTGC | 84108 |
rs538984474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335294 | CCTGGCCTCAAGCCA[C/T]CCTTCTGCCTTAGCC | 84108 |
rs539049540 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335806 | CCCCGTCTCTCCTAA[A/C]AATACAAAAAATTAG | 84108 |
rs539084063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338791 | GAGAATCGCTTGAAC[C/T]CTAGAGGCAGAGGTA | 84108 |
rs539172898 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324100 | GTGTGCCACCATGCC[A/T]AGCTATTTTTCATTT | 84108 |
rs539193490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330943 | CCAACAAGAAAAAAA[A/G]AAACCTGTACCTCTT | 84108 |
rs539222861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321383 | AACAAAATCAACTTA[A/G]AAGAGAAATACTGTA | 84108 |
rs539313274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317984 | CTGGTCTCGAACTCC[C/T]GAACTCAGGCAATCC | 84108 |
rs539430073 | in-del | -/AA | 0.49941 | 0.0171624 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337909 | CTCTACTAAAAATAC[-/AA]AAAATTAGCCGGGCG | 84108 |
rs539442668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330284 | TTTCCCCATGTTGCC[A/G]AGGCTGGTCTCAACT | 84108 |
rs539530589 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335251 | AAGAGATAGGGTCTC[A/G]CTGTGTTGGCCAGGC | 84108 |
rs539567818 | snp | C/T | 0.000166005 | 0.00910907 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303988 | AGAAAAAAAGACGAT[C/T]TTGCAGTTCTTTCAA | 84108 |
rs539593323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348576 | GTGATCCACTCACCT[C/T]GGCCTCCCAAAGTGC | 84108 |
rs539605357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341144 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 84108 |
rs539661792 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306345 | TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 84108 |
rs539669650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332641 | TGTTGGACTGACTAC[C/T]ACAGGTTATTAGACA | 84108 |
rs539732511 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311181 | GAGTCTTGCTCTGCC[A/G]TCCAGGCTGATGTGC | 84108 |
rs539741848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345714 | GTGCCTGTAATCCCA[C/G]CTATTTGGGAGGCTG | 84108 |
rs539771510 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314453 | GTAAATAAGGTAACA[A/T]GGGAAGAGCATTAGA | 84108 |
rs539814853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350640 | GGGCCGGCGCCCGGC[A/G]GACGAGGGCCAGCTA | 84108 |
rs539853170 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326314 | GAATGGCGTGAACCC[A/G]GGAGGCTGAGCTTGC | 84108 |
rs539924694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343054 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 84108 |
rs539972865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332082 | CAAGCTTGAGCCACC[A/G]CGCCCGGCCTAATAC | 84108 |
rs540012939 | in-del | -/T | 0.00119737 | 0.0244387 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302421 | CCCAAAGTGCTGGGA[-/T]TTACAGGCATGAGCC | 84108 |
rs540025668 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342597 | TATACGTGTACTTGC[A/G]TATTTTCCACCATCC | 84108 |
rs540077378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328341 | GAACTTTCCCAACTA[A/C]AACTCAGAGTCTATA | 84108 |
rs540163017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333488 | GTTACCTGTGATTTC[A/G]GAATCTTTAAATCAA | 84108 |
rs540185729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312831 | TTGGGCGTGGTGGCG[C/G]ATGCCTGTAAACCCA | 84108 |
rs540304001 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329004 | CCGGCCTCAGCGTCC[C/T]GAAGTGCTGGGATTA | 84108 |
rs540331594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306179 | CTCGGCTCACTGCAA[G/T]CTCCGCCTCCCGGGT | 84108 |
rs540373133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335551 | TATTTTTAGTATAGA[C/T]GGGGTTTCACCATGT | 84108 |
rs540394850 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332760 | ACGAGAATTTCCTAA[A/G]GCTGAACACCACCGG | 84108 |
rs540400254 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310189 | ACTCCTGACCTTAGG[C/T]GATCCCCCCACCTCG | 84108 |
rs540436051 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327693 | TTTCTTTTCTTTTTT[A/G]AGACAGAGTCTCACT | 84108 |
rs540560300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321636 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 84108 |
rs540618602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337905 | CCGTCTCTACTAAAA[A/T]TACAAAAAATTAGCC | 84108 |
rs540621701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305184 | TTGCTATGTAACCCA[C/G]GCTGGTCTCAAACTC | 84108 |
rs540661043 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317449 | TTTTTGTAAAAAGCT[A/T]TACAAAAATCTTTAC | 84108 |
rs540677138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309333 | GGGTTGGATTTCTCA[C/T]GAATGGTTTAGCACA | 84108 |
rs540720152 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351823 | TTCAGTAGAGACAGG[G/T]TTTCACCATGTTGAC | 84108 |
rs540732585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344219 | ACATATTGCTTAGGA[A/G]TAGATATACACGTGG | 84108 |
rs540855721 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332774 | AAGCTGAACACCACC[A/G]GTTTGATGTTTTACA | 84108 |
rs540896742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337099 | ATGACGTATTTTCAA[A/G]CTTTTACCATTCCAG | 84108 |
rs540914927 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305024 | CTGGAGTGCAATGGC[A/G]CGATCATAGCTCACT | 84108 |
rs540952303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340505 | CACACGTTTACCATC[A/G]TTGTATTACAATATC | 84108 |
rs540959756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329121 | CTCGGCTCACTGCAA[C/T]CTCTGCCTCTTGGAT | 84108 |
rs540979268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325891 | AGCTGGGCATGGTGG[C/T]ATGTGCCTCTAGTCC | 84108 |
rs541015566 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332337 | TAGGCTAGAGTGTAG[C/T]GACGCAATCACAGCT | 84108 |
rs541091211 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308214 | CAGATCCCAGAATGG[C/T]AGACCCACTGAGAGC | 84108 |
rs541137296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347638 | TAAATATATGTAATC[A/G]TAAGTATTCACAGAT | 84108 |
rs541202530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347994 | TAACAGTAATCTACT[A/G]TTAGTATTTTTCCCT | 84108 |
rs541217590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319979 | TGCCCAGCTAATTTT[C/T]GTATTTTTAGTAGAG | 84108 |
rs541311763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341402 | GGTAGGACTAAAGGC[A/G]CGCACCACCATGCCT | 84108 |
rs541383773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328536 | CTAATAGTGAGTCTT[A/T]GGGCAAGTTCCTGAA | 84108 |
rs541444831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346873 | ATCATAAAAACTAAC[A/G]TTTGAACAGTTACTG | 84108 |
rs541445233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329005 | CGGCCTCAGCGTCCC[A/G]AAGTGCTGGGATTAC | 84108 |
rs541470795 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304594 | GATCCTCCTGCCTCA[A/G]CCTCCCACAGTGCTG | 84108 |
rs541528780 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315500 | GAATAGCTGGAACTA[A/C]AGGCACCCACCACCA | 84108 |
rs541617723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311752 | ACAGTGCATCACACC[A/G]CACAGCCCTAAGAGG | 84108 |
rs541678938 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303339 | ATAATAACAATTCAT[A/C]CATTTTGAAATGAGT | 84108 |
rs541725844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306996 | ATATTTCCAGCTACT[C/T]AAGAGGCTGAGGTGG | 84108 |
rs542000819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314628 | ATCAGGTAGCAAAGG[A/G]AAGTATATCTTTTTA | 84108 |
rs542011131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306341 | GACCTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC | 84108 |
rs542028511 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312167 | GGGAGGCTGATGCAG[A/G]CAGATCAGGAGGTCA | 84108 |
rs542226589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347029 | TATACACCTCATAAA[A/G]TGGCAGGGCTAGGAA | 84108 |
rs542255106 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341020 | GGATCACCTGAGGTC[A/G]GGAGATTGAGACCAG | 84108 |
rs542294235 | snp | A/G | 0.499741 | 0.0113788 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337935 | CGGGCGTAGTGGTGG[A/G]CGCCTGTAGTCCCAG | 84108 |
rs542339635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341560 | TTCTCCTCCCTCAGC[C/T]TCCTGAATAGCTGGG | 84108 |
rs542462654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331147 | CATGTCAGACCATGT[A/G]TCAGTACTTCATTCC | 84108 |
rs542539327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316359 | AAAACTTTTAGCATG[G/T]TTGGGAAAGAACAGT | 84108 |
rs542585477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320201 | TCAATGTGAGGTGTA[G/T]GTTCTAAATTTCATC | 84108 |
rs542683602 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345828 | GAGAAACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 84108 |
rs542745912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304483 | GTAGCTGCAATTACA[C/T]GTGCGTGCTACCAGG | 84108 |
rs542760901 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306246 | GGGATTACAGGCAGG[C/T]GTCAACACCCACCGC | 84108 |
rs542761311 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350806 | CTCCTCCAGCTCCTC[C/T]TCTTCTTCCAACTCC | 84108 |
rs542785878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313300 | CTGGGCAGAGGGGCT[C/T]ACCCCTGTAATCCCA | 84108 |
rs542800528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334101 | AAATAAACAAATGTA[A/G]TTGTCATTTCTGCCA | 84108 |
rs542809283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305110 | TGGGACCACACACAC[A/G]CATGTGCCACCATGC | 84108 |
rs542850706 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316797 | TTTAAAAGCTAGTAA[A/G]TCTAAAATCCAAAAG | 84108 |
rs542861863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327318 | CAAAAAACCCAAAAA[A/T]CTGCAAGGAAGAAAA | 84108 |
rs542965025 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320745 | GTCTTGTTTTTAAAA[G/T]TTGATCTGCCACAAA | 84108 |
rs542973403 | in-del | -/CAAAA | 0.0629927 | 0.165916 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352328 | AGTGAGACTCCATCT[-/CAAAA]CAAAACAAAACAAAA | 84108 |
rs542998177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344947 | CAGAAAACTTGATTT[A/T]ACCTGAGTTCACAAT | 84108 |
rs543010482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324194 | TCCACCTGCCTTGGC[C/T]TCCCAAAGTACTGGG | 84108 |
rs543214254 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351734 | CGCCTCCCGGGTCCA[A/G]GCGATTCTGCCTCAG | 84108 |
rs543317626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339414 | AAAACAGATAAAGGA[C/T]TGTCTTAGGAGGTAC | 84108 |
rs543343704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347579 | GTTACTTTTAAGTAG[C/T]ATTTACAGTTCCTAA | 84108 |
rs543491399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332209 | TTGCTACCATGTTTT[C/T]TCATGTGTAAGAACC | 84108 |
rs543539041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317181 | ACACTCGGCTAATTT[C/T]TGTATTTTTAGTGGA | 84108 |
rs543585013 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339408 | GAGGAAAAAACAGAT[-/A]AAGGACTGTCTTAGG | 84108 |
rs543596828 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325606 | TCCTATAAAGAAAGC[G/T]GATGATAAGCAATAT | 84108 |
rs543608899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318650 | CTCAGGAGGCTGAGG[C/G]AGAGAATGGCTTGAA | 84108 |
rs543659618 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319924 | GATTCTCCTGCCTCA[-/T]CTTCCCGAGTAGCTG | 84108 |
rs543880446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336229 | ACAGAGTGAGACTGC[A/G]TCTCCAAAAAAAAAA | 84108 |
rs543953494 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326367 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 84108 |
rs543957870 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323800 | ACGTTGGCCAGACTG[G/T]TCTTGAACTCCTGAC | 84108 |
rs544015734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319372 | TGGCCAGGATGGTCT[C/T]GATCTCTTGACCTTG | 84108 |
rs544030283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328994 | TCATGATCTACCGGC[A/C]TCAGCGTCCCGAAGT | 84108 |
rs544052297 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310198 | CTTAGGTGATCCCCC[A/C]ACCTCGGCCTCTCAA | 84108 |
rs544057775 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335216 | CATGCATGGCTAATT[-/A]AAAAAAAAAAAAAAA | 84108 |
rs544097610 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322537 | TGTCAATTAAAAAAA[C/T]AGGCTGGGCACAGTG | 84108 |
rs544334589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328362 | AGAGTCTATATTAGA[C/T]AGGTATTTTATTTTT | 84108 |
rs544370104 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325874 | AAAAAAAAAAAAAAA[G/T]TAGCTGGGCATGGTG | 84108 |
rs544575166 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330452 | TACAAACAATGTTTC[C/T]ATTCAAAGTTTCTAT | 84108 |
rs544623747 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352664 | GTAATCCCAGCTACT[C/T]GAGAGGCTGAGGCAG | 84108 |
rs544684926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345205 | CTTTGGAAAAATACA[C/T]AAGTATTATAATTAT | 84108 |
rs544689942 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351877 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 84108 |
rs544766182 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346061 | ATTAGCTGGGTGTGG[G/T]GGCACATGCCTGTAA | 84108 |
rs544782759 | snp | A/G | 0.202035 | 0.245356 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337925 | AAAAATTAGCCGGGC[A/G]TAGTGGTGGGCGCCT | 84108 |
rs544790414 | in-del | -/A/AA | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326229 | CTCTACTAAAAATAC[-/A/AA]AAAAAAAAAATCAGC | 84108 |
rs544806896 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323264 | TATATTTACTACCAG[C/T]AAATATCGGTACTAA | 84108 |
rs544934697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323558 | CCTTGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 84108 |
rs545021529 | snp | A/G | 3.30398e-05 | 0.00406434 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326595 | ACATGTCCAATAGTT[A/G]CTTCTCCTGAAACTC | 84108 |
rs545025064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320060 | ATCCGCCCGCCTCAG[A/C]CTCCCAAAATGCTGA | 84108 |
rs545112524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348313 | TGTAGTTCCCTTTTA[A/C]TTTTGAGAGAGGTCA | 84108 |
rs545126603 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340631 | AGACAGGGTCTTGCT[C/G]TGTCACCCAGGTTGG | 84108 |
rs545302187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342265 | TCAGACAGAGTTTCG[C/T]TCTCATTGCCCAGGC | 84108 |
rs545302868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350248 | AACAGCCTGGGAACA[C/T]AGGGAGCCCTCCTCG | 84108 |
rs545326362 | snp | A/G | 3.72578e-05 | 0.00431596 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333966 | CACTGAAAAATGAGA[A/G]CAAAATTAATCAATA | 84108 |
rs545346909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327246 | GCCAAGATCGTGCCA[C/T]TGTACTCCAGTCTGG | 84108 |
rs545383506 | snp | A/C | 0 | 0 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351592 | AATCACTACTCAAAG[A/C]TCATCCATGTCACCC | 84108 |
rs545593511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304329 | TATGTATCATATGCA[C/T]GTATGTATGTATACA | 84108 |
rs545692793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346555 | CTTGAGCCCAGAAGG[C/T]GGAGGTTGCAGTGAG | 84108 |
rs545754329 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338402 | AAAAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 84108 |
rs545758110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347524 | GAGTGAGTTAATTGT[A/G]TTTTCTCTTGAGAGT | 84108 |
rs545789322 | in-del | -/AAAT | 0.472522 | 0.113946 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340197 | AAAAAAAAAAAAAAA[-/AAAT]ATATATATATATATA | 84108 |
rs545817220 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332069 | AGTGCTGGGATTACA[A/G]GCTTGAGCCACCGCG | 84108 |
rs545867262 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336302 | ATACAGAAATATTTA[C/T]ATATTATAAACCTAT | 84108 |
rs545951802 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305417 | CTGGAACGACAGGGG[C/T]CCGCCATCACGCCTG | 84108 |
rs546019410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331187 | TCAAATAATACTCTA[G/T]TATATGAAAATACAT | 84108 |
rs546043587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324812 | ATTACATAGCTAGAA[C/T]AGGAGATCTCTTTTA | 84108 |
rs546043850 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340700 | CTCCCGGGCTCAGTC[A/C/G]ATCCTCCCCCATCAG | 84108 |
rs546254868 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330736 | AGTTCAAGACCAGCC[C/T]GGCTAACACGGTGAA | 84108 |
rs546326688 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322746 | GGAGAATTGCTGGAA[A/C]CCGGGAGGTAGAGAC | 84108 |
rs546430109 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311414 | TCCAAAGTGCTGGGA[C/T]TACAGGTGTGAGCCA | 84108 |
rs546482380 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346990 | GAAACAGACATTTAC[A/G]TATGTAACTGGCTTG | 84108 |
rs546543299 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323988 | TCTGTCGCCCAGGCT[A/G]GAGTGCAATGGCATG | 84108 |
rs546549371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333455 | GACTCACATTATAGT[A/G]GTAACACTGTATACA | 84108 |
rs546554500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309404 | TTGTGTGATATGGTT[A/G]TTTAAAAGTGTGTAG | 84108 |
rs546556312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318529 | GCAGGCGGATCACAA[G/T]GTCAGCAGTTCAAGA | 84108 |
rs546629631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327632 | TCTGCCTACTTTTGT[A/G]TAAGTTTTAAAATTT | 84108 |
rs546665445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304576 | GAACTCCTAATCTCA[C/G]ATGATCCTCCTGCCT | 84108 |
rs546668217 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330084 | TTTTTTGTTTGTTTG[-/T]TTTTTTTTTTGAGAT | 84108 |
rs546756098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327400 | GACAAATACATTAAC[C/T]AATTACAATGTATGG | 84108 |
rs546756141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319792 | GCTTAATATCATACA[C/T]CAAATAAGTAATAAT | 84108 |
rs546768228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320381 | ATTTTAAATGAACTT[A/C]AATCTTTCTTAAGAA | 84108 |
rs546787560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312042 | GTGAGCCGAAATCAC[A/G]CCACTGCACTCCAGC | 84108 |
rs546876118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321216 | TCTCATCATGCACTG[C/T]CGCCTTGACCTCCCA | 84108 |
rs546899833 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303765 | TGTACTTATAAACGC[A/T]ATAATTCTTGGTGCT | 84108 |
rs546929970 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350533 | ACCCAGGCCGGGCCG[C/G]AGGCCTGTCGGCGCC | 84108 |
rs546939403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322148 | TGATCCACCCACCTC[G/T]GCCTCTGAAAGTGCT | 84108 |
rs546953515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328686 | AGTTGTTAGTGTTGT[A/G]AGCCATTTGTCTCTA | 84108 |
rs547042650 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342858 | TTCTTCTAATTTTTC[A/C]AAAGGGATCTTTATG | 84108 |
rs547044665 | snp | A/G | 8.23757e-05 | 0.00641725 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350975 | GGGGTGAGGGCGGGC[A/G]GGGAGACAGGAGGCG | 84108 |
rs547072236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335765 | GAGGTCAGGAGTTCA[A/G]GAGCAGCCGGGCCAA | 84108 |
rs547105817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343301 | ATAAAGCACACACTA[A/G]ATAATAAATGATACA | 84108 |
rs547110827 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309871 | CAATTGAGCCCCCCA[A/G]GTTGAGGCTACACTG | 84108 |
rs547333326 | in-del | -/GC | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322540 | CAATTAAAAAAACAG[-/GC]TGGGCACAGTGGCTC | 84108 |
rs547404251 | snp | C/T | 0 | 0 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346186 | TGCGACAGAGCAAGT[C/T]CATCTCATTTAAAAA | 84108 |
rs547441704 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309118 | GAATTTTGAGTTAAT[A/G]CTGAAAATGAGTTAA | 84108 |
rs547486577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309660 | CAGAGTTCAGGCATG[A/G]TGGCTCACACCTATA | 84108 |
rs547544129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339605 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 84108 |
rs547567083 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334298 | CTATAGGTTTTGATA[C/T]GTATATACTGTAAAC | 84108 |
rs547647679 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306135 | TGGAGTTTTGCTCTC[C/T]TGCCCAGGTTGGAGT | 84108 |
rs547652450 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337782 | AAAATACAAAATTAG[C/T]GGCCGGGCGCGGTGG | 84108 |
rs547655954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331446 | TATTTTTAATAGAGA[C/T]AGAGTTTTGGCATGT | 84108 |
rs547683395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349060 | TACAAATTCTTTTTT[C/T]TTTTTTGAGACAGAG | 84108 |
rs547734275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317627 | CCTGGGCAACAAAAC[A/G]AAACCTCATCTCAAA | 84108 |
rs547896551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310249 | GAGCCACCACACCTG[A/G]CCCAACCATGTCTTA | 84108 |
rs548077290 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352758 | CAGCCTGGGCAACAA[A/G]AGCAAGACTCCATCT | 84108 |
rs548123554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320975 | TGTTCATATTAGAAG[A/T]AACTCTTAATTACTT | 84108 |
rs548184128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312917 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 84108 |
rs548199772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345342 | CAATGGAAGGCAGAC[A/G]TGTGGCTGGCTTATT | 84108 |
rs548246400 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336925 | CAAACACGCTTCACC[C/T]TGTAACATATACCTA | 84108 |
rs548340535 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305814 | ACACTTTGAGAGTCC[A/G]AGGTGGGCAGGTCAC | 84108 |
rs548397644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305472 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 84108 |
rs548465253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344609 | CTCTTGTCGCCTAGG[C/T]TGGAGTGCAATGGCG | 84108 |
rs548485164 | snp | C/T | | | splice-acceptor-variant, intron-variant | PCGF6 | GRCh38.p7 | 10:103333953 | GTGCCTTCATTAGCA[C/T]TGAAAAATGAGAGCA | 84108 |
rs548514894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315655 | TGAGCCACCGTGCCC[A/G]GCCAATTGTGTGGTT | 84108 |
rs548521486 | snp | G/T | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302398 | TCAAATGATCTGCCC[G/T]TCTGGCCTCCCAAAG | 84108 |
rs548632913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333697 | TCACCAAATTAACAT[A/G]GCATTTGGTTTTAGT | 84108 |
rs548741146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323060 | AATAACAGGCTGTTA[C/T]GGGATCACTCATAAT | 84108 |
rs548747460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329842 | GCAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 84108 |
rs548756180 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320086 | GCTGAGATTACAGGT[A/G]TGAGCCACCATGCCT | 84108 |
rs548861676 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313763 | ACTTGCAAGTTTTTC[C/T]TGAAATGTCCTTCTG | 84108 |
rs548968948 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303602 | AAAGAAAACTAACCA[A/T]TTACTTCAAAGATGG | 84108 |
rs549006120 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341913 | AATAGACTCCAGTGC[C/T]GCTTCCTAGGGGCAC | 84108 |
rs549042844 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310093 | GTAGCTGGGATTACA[C/G]GCACCCGCCACCATG | 84108 |
rs549100199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311899 | TTTGAGATTAGCCTC[A/G]CCAACACGGTGAAAC | 84108 |
rs549144231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333226 | GAGAATTACCTATCT[A/G]TTCCTATGCTTTAAT | 84108 |
rs549248792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335693 | AAAAAATAGGCTGGG[C/T]GAGGTGGCTGATGCC | 84108 |
rs549280187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343233 | GCGCCCGGCCTTAGG[A/G]GTTCTTAATAACAGT | 84108 |
rs549288496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311322 | AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 84108 |
rs549362382 | in-del | -/TTTTT/TTTTTTTTTTTTTTTTTTTTTTTTTTTT | 0.497829 | 0.0328757 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302452 | CAGTGCCTGACCTGG[lengthTooLong]TTTTTTTTTTTTTTT | 84108 |
rs549385063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307299 | AAATAAAAAAATTAG[A/C]CAGTGGCACACCTCT | 84108 |
rs549440765 | in-del | -/AAAAC | 0.0717427 | 0.175284 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350088 | CTCCGTCTCAAAAAC[-/AAAAC]AAAACAAAACAAAAC | 84108 |
rs549456254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350363 | AGGATCGCCTGAGGC[A/C]AGGAGTTGGAGGCTG | 84108 |
rs549466725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342701 | CATCTTGGAGACTAT[C/T]CCACATCATCACACA | 84108 |
rs549534362 | snp | C/T | 0.499732 | 0.0115784 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337956 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 84108 |
rs549644565 | in-del | -/GA | 0.00160032 | 0.0282418 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347707 | TTTGTGTGTGTGTGT[-/GA]GACAAGGTCTCACTT | 84108 |
rs549647077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338558 | TCAAAAAAAAAAAAA[A/G]AAGAAGACCATAAAA | 84108 |
rs549708356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330772 | GTTTCTACTAAAAAT[A/G]CAAAAAATTAGCTGG | 84108 |
rs549709759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315620 | CACCTCAGCCTCCCA[A/G]AATGCTGGGATTACA | 84108 |
rs549781084 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352879 | CGAGGTCAGGAGTTT[A/G]AGACCAGCCTGACCA | 84108 |
rs549862732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324524 | AGCACTTTGGGAGGC[C/T]GAGGCGGGAGGATCA | 84108 |
rs549925683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316567 | AGCAAAGTTCAGATA[C/T]AAACCCAGGTCTGTC | 84108 |
rs550087710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313306 | AGAGGGGCTCACCCC[C/T]GTAATCCCAGCCCTT | 84108 |
rs550121068 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318346 | TACTCAGGAGGCTGA[A/G]GCAGGAGGATCACTC | 84108 |
rs550156036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336746 | CAGGTGTGTTGGCAC[A/G]TGCCTGTAATCCTAG | 84108 |
rs550202290 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347721 | GTGACAAGGTCTCAC[A/T]TTTGTCACCCAGGCT | 84108 |
rs550222837 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348835 | AAAAGAATGTTGAAG[A/T]CAGGATGCTTTCAAG | 84108 |
rs550230111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324893 | TAATCCCAGCACATT[A/G]GGAGGCCGAGGTAGG | 84108 |
rs550327919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308783 | GAGGCTGAGGTGGGA[A/G]AATCACTTGAGCCTG | 84108 |
rs550333604 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348419 | CTTGGCTCCTGCAAC[C/T]TCTGCCTCCCAGGTT | 84108 |
rs550449299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320897 | GAAAGTCAGCATAGC[A/G]GGCTCGTGACTGCAG | 84108 |
rs550455966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348430 | CAACCTCTGCCTCCC[A/T]GGTTCAAGCGATTCT | 84108 |
rs550597466 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320626 | CAGGAGGCGGAGGTT[G/T]CGGTGAGCCGACATC | 84108 |
rs550752391 | snp | G/T | 1.64904e-05 | 0.00287139 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303866 | TGCAGTCCTGCAGAA[G/T]CCTCCTTTGTTTCCC | 84108 |
rs550754035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312854 | TAAACCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 84108 |
rs550816212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325043 | GGAAGGCTGAGGCAG[A/G]AGAATCGCCTGAACC | 84108 |
rs550906405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314874 | GCAGGAGAATCACTC[A/G]ACCCCAGGAGGTGTT | 84108 |
rs550931297 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305409 | TTGACCAGCTGGAAC[A/G]ACAGGGGCCCGCCAT | 84108 |
rs551000450 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314393 | ATTTTATTTTAGACT[A/G]ATTAAACGCTCTTGA | 84108 |
rs551010622 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348437 | TGCCTCCCAGGTTCA[A/G]GCGATTCTCCTGCCT | 84108 |
rs551013393 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314955 | GCGAGACTCTGTCAT[A/T]AAAAAAAAAAAAAAA | 84108 |
rs551039258 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317305 | CATGAGCCAAATCAC[C/T]GGGCCTATGTTTCAT | 84108 |
rs551084810 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335001 | GTTCTTTCTTCCTTA[G/T]GTTGTGAAGATTAGA | 84108 |
rs551096364 | in-del | -/AGTC | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320885 | AACTGGTTCAAAGAA[-/AGTC]AGCATAGCAGGCTCG | 84108 |
rs551122363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322175 | TGCTGGGATTACAGG[A/G]TGAGCCACCTTGCCT | 84108 |
rs551259467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325066 | CCTGAACCCGGGGGG[A/C]GGAAGTTGCAGAGAG | 84108 |
rs551385431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311205 | GATGTGCAGTAGTGC[A/G]ATCTTGGCTCACCGC | 84108 |
rs551424746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338812 | GGCAGAGGTAGCAGT[A/G]AGCCGAGATCACACC | 84108 |
rs551493476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339714 | AGAATTGCTTGAAAC[C/T]GGAAGACTGAGGACT | 84108 |
rs551539554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348597 | CCCAAAGTGCTGGGA[C/T]TATGGCATTAGCCAC | 84108 |
rs551638174 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325967 | AGGAAAACCTCAAGG[A/C/T]TGTAGTGAGCCATGA | 84108 |
rs551651373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333610 | GCAAAAAATGTTACA[G/T]GCAAATAAAATTTTA | 84108 |
rs551651526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342543 | CTGGCCAAGATTTTC[C/T]TATATGGCCTTTCAG | 84108 |
rs551717017 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313760 | AGTACTTGCAAGTTT[C/T]TCTTGAAATGTCCTT | 84108 |
rs551810993 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352241 | GGCTAAGGCAGAAGA[A/C]TCACTTGAGCCCAGG | 84108 |
rs551868341 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352841 | TAATCCCAATGCTTT[A/G]GGAGGCTGAGTTGGG | 84108 |
rs551869218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349133 | GTTCACTGCAACCTC[C/T]GCCTCCTGGATTAAA | 84108 |
rs552002852 | in-del | -/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351645 | TGAATTCGAAAAGCT[-/T]TTTTTTTTTTTTTTT | 84108 |
rs552013865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306398 | CCACAACGCCTGGCC[A/G]CAATCCACCTTTTTA | 84108 |
rs552055881 | snp | A/G | 0.202343 | 0.245416 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337944 | TGGTGGGCGCCTGTA[A/G]TCCCAGCTACTTGGG | 84108 |
rs552078980 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326740 | AGAAAATTTTATAGC[A/G]AAGATGATTCAATAG | 84108 |
rs552114511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330756 | AACACGGTGAAACCC[C/T]GTTTCTACTAAAAAT | 84108 |
rs552202570 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333493 | CTGTGATTTCGGAAT[C/T]TTTAAATCAACTCTG | 84108 |
rs552253200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329914 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCTGC | 84108 |
rs552312935 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348577 | TGATCCACTCACCTC[C/G]GCCTCCCAAAGTGCT | 84108 |
rs552375990 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335598 | GATCTCTTGATCTCG[A/T]GATCTGCCCACCTTG | 84108 |
rs552687481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324460 | GTTTCCATCGTACAA[C/G]AAGAAGAAAATATTA | 84108 |
rs552699834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307681 | TTTCAGCATGTTGCC[A/C]AGGCTGGTCTCAAAC | 84108 |
rs552713733 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313101 | ATTTTGACTAAGAGA[A/C]TTCACATTATATTCC | 84108 |
rs552752007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315703 | GTAGAGACAGGGTCT[C/T]GGTATATTGCCCAGG | 84108 |
rs552766440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316495 | TTCTGATTTTACAGA[C/T]AGGGAAACTAAGAAG | 84108 |
rs552778212 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310099 | GGGATTACAGGCACC[C/T]GCCACCATGCCCGGC | 84108 |
rs552779462 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336655 | TGAGGTAGGTGGATC[A/G]CTTGAGGTCAGGAGT | 84108 |
rs552907122 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302730 | GATTACAGGCGTGAG[C/T]CACTGCACCCAGCCC | 84108 |
rs552946078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341349 | ACAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 84108 |
rs552979197 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326280 | TGTAGTCCCAGCTAC[G/T]CGGGAGGCTGACGCA | 84108 |
rs553007088 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322843 | ACACACACAAAAAGT[C/G]CAGCCTGGGCAACAC | 84108 |
rs553008089 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318984 | ATCAAGAAGAGATAA[-/C]AAAAATATTTTTGAA | 84108 |
rs553032868 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321702 | GGGTGACAGAGACTC[C/T]GTCTCAAAAACAAAG | 84108 |
rs553047673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327177 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 84108 |
rs553059922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320000 | TTTAGTAGAGATGGG[A/G]TTTCACCATGTGGGC | 84108 |
rs553079937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310741 | GGGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTGC | 84108 |
rs553091330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319157 | CTTTGATCATACATA[C/T]TCTTCTTTTCGAGAT | 84108 |
rs553121939 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314073 | ATATAATTATTATTT[A/C]TAGTGTAGGTAATTT | 84108 |
rs553123429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320587 | AGCTACTCAGGAGGC[C/T]GAGGCAGGATAATCG | 84108 |
rs553182757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335104 | GCTCTATCACCCAGG[C/G]AGGAGTGTAGTGGCT | 84108 |
rs553239564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312445 | ACAAGTAAGGGCTAC[A/G]GGACCAATGATCACC | 84108 |
rs553255173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349384 | CCATAATCTCAAAAT[A/G]TCATTGCAACATGGA | 84108 |
rs553300292 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308241 | GAGCTTGCACCCTGA[A/G]TTTGAAAATGCCATA | 84108 |
rs553318442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342202 | CGGCCTCCTCAAGTG[C/T]TGGGATTAAGAGTGA | 84108 |
rs553438150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329616 | CCAAGTAGCTGGGAC[C/T]ACAGGCGTGAGCCAC | 84108 |
rs553462583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323445 | GGGATTACAAGCATG[C/T]GCCACCACGCCCGGC | 84108 |
rs553513602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323808 | CAGACTGGTCTTGAA[A/C]TCCTGACCTCAGGTG | 84108 |
rs553514444 | snp | C/T | 0.202035 | 0.245356 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337891 | AAAACGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 84108 |
rs553642723 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310693 | TACCAAAAAAAAAAA[-/T]ATTATTTCTTTTCTT | 84108 |
rs553678141 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304194 | CAGGCTGGAGTGCAG[G/T]GGTGCAATCTCAGCT | 84108 |
rs553724206 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303506 | CACTCAAAAGCACAC[C/T]TCTCTTCCAAAAAGA | 84108 |
rs553831251 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338043 | CACTCCAGCCTGGGT[A/G]ACAGAGCGAGACTCC | 84108 |
rs553863706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347804 | GGTGGATTTTTCCCA[C/T]CTCAGCCTCCTTAAT | 84108 |
rs553917980 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331770 | ATCTGGCTTATTATA[C/T]TCCTTCAGTGTCATT | 84108 |
rs553970128 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339957 | TCATGAGGTCAAGAG[A/T]TCGAGACCAGCCTGG | 84108 |
rs554057231 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342567 | CTTTCAGGAATGGCC[G/T]GTACACATAAAAAGT | 84108 |
rs554088588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308900 | TAAATAAATAAAAAT[A/T]AAAAAATTAATGGCT | 84108 |
rs554097888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331162 | ATCAGTACTTCATTC[C/G]TTTTTACTGTCAAAT | 84108 |
rs554204317 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350624 | GCGGCGCACTAGGAT[C/G]GGGCCGGCGCCCGGC | 84108 |
rs554222506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312369 | CTGCACTCCAGCCTG[C/T]TGACAGAGCAAGACT | 84108 |
rs554267717 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351151 | CCACTGCGCAGGCGC[A/G]GCAGCCTGAGGGGCT | 84108 |
rs554435943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332028 | TGATCTCCTGACCTC[A/G]TAATCTGCCCACCTC | 84108 |
rs554502496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343767 | GAACCTGGGAGGCAG[C/T]AGTTGCAATAAGCTG | 84108 |
rs554532983 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339985 | TGGTTAACAAGGTGA[A/G]ACCCCGCCTCTACTA | 84108 |
rs554555206 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303099 | CTAAGAAAACAATGA[A/G]TAAGTAATTCTGTAA | 84108 |
rs554567721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335921 | GCAGTGAGCTGAGAT[C/T]GTGTCACTACACTCC | 84108 |
rs554705597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328354 | TAAAACTCAGAGTCT[A/G]TATTAGATAGGTATT | 84108 |
rs554728089 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326399 | ATCTCAAAAAAAAAA[A/C]AAAAAAACAATGTCT | 84108 |
rs554804643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314412 | AAACGCTCTTGAAAA[C/G]AGAGTTTTAGAAACT | 84108 |
rs554814800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305947 | GAGTAAAGAATGCCC[C/T]AGGGCAGTTAGGCAA | 84108 |
rs554914282 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328235 | GACTTACAGACTGGG[A/G]GCCTAGAATGGCTAC | 84108 |
rs554977658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345585 | GTAATTCCAACCCTT[C/T]GGGAGGCCAAGGTGG | 84108 |
rs555028839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324685 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 84108 |
rs555098318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309877 | AGCCCCCCAGGTTGA[A/G]GCTACACTGAGCCAT | 84108 |
rs555197349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344986 | ATTAGGACTTTTAAC[A/C]TTCTTTAAGTTAAAA | 84108 |
rs555240861 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352521 | CTCCCGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 84108 |
rs555333308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347927 | AACTTCTGTCTATCA[C/T]CTGCAAAGCACTCCT | 84108 |
rs555420153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325091 | AGAGAGCCGAGATCA[C/T]GCCATTGCACTCCAG | 84108 |
rs555439876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332882 | CACTTTGGGAGGCCC[A/G]GGTGGGTGGGTCACC | 84108 |
rs555479096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318209 | GCACTTTGGGAGGCC[A/G]AGACGGGCAGATCAC | 84108 |
rs555827613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320531 | GTCTACTAAAAAAAC[C/T]AGAAAATTAGCCAGG | 84108 |
rs555846533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337727 | GAGGTCAGGAGTTCA[A/G]GACCAGCCTGACCAA | 84108 |
rs555848525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328999 | ATCTACCGGCCTCAG[C/T]GTCCCGAAGTGCTGG | 84108 |
rs555918658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344879 | CCGGCCCTTTATACC[C/T]TTTTCTAATTATTTC | 84108 |
rs555968508 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318573 | GATGGTAAAACCCTG[A/T]CTCTACCAAAAATAC | 84108 |
rs556003096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319928 | CTCCTGCCTCATCTT[C/T]CCGAGTAGCTGGGAC | 84108 |
rs556063243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311662 | TTTTCTATACTTAAG[A/T]TACACAAAATGTTTG | 84108 |
rs556096344 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352893 | TGAGACCAGCCTGAC[A/C/G]AACATGGTGAAACTC | 84108 |
rs556120325 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332084 | AGCTTGAGCCACCGC[A/G]CCCGGCCTAATACAT | 84108 |
rs556164339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323249 | TCACTGGATTTAGTA[C/T]ATATTTACTACCAGT | 84108 |
rs556290392 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322538 | GTCAATTAAAAAAAC[A/T]GGCTGGGCACAGTGG | 84108 |
rs556353414 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306490 | ATGTGCCACAGACCT[A/G]AACTGAGCAACACAG | 84108 |
rs556373629 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311536 | CAGCTGCGACCTCCC[A/G]GGCTTGAAGCGATTC | 84108 |
rs556405482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346283 | GATCACCTGAGGTCA[A/G]GAGTTCAAGACCAGC | 84108 |
rs556464325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323741 | AGGACTACAGGTGTG[C/T]GCCACCATACCTGGC | 84108 |
rs556476442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315794 | TGAGCCAGTGTGCTC[C/T]GGCCAATATACTGAC | 84108 |
rs556544138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323773 | AATTTTTGGTAGAGA[C/T]GGGGTTTCGCCACGT | 84108 |
rs556613923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307974 | GGCATGCTGGCTCAC[A/G]CCTGGAATCCCAGCA | 84108 |
rs556653226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319882 | GCGATCTCGGCTCAC[C/T]GCAACCTCCACCTCC | 84108 |
rs556746061 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346383 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGAGG | 84108 |
rs556748482 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347142 | ATCTCTCTGATCATA[A/T]AATAAGCTACCCCCA | 84108 |
rs556830682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338261 | AACAAACAAAAAAAC[C/T]GGTCAGGTGCAGTGG | 84108 |
rs556891726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339054 | TCCCCTTGTCCTGTC[A/T]TGAAAACAGTTTCCT | 84108 |
rs556893792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330402 | TTTCAACCAGATACA[C/T]TTTTATATCCCCAAA | 84108 |
rs556910514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350585 | AGAGGTCGGGGGAGG[C/T]CCGCTCCAGTGCTCC | 84108 |
rs556967663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311001 | ACAACCATGTCTGCT[A/T]ATTTTTCTATCCTTT | 84108 |
rs556980456 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350152 | TAGCTTCAATAATTA[C/T]ACAGGACAGGCAACG | 84108 |
rs557074930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312623 | GAGAGTTCATCAAAT[C/T]TTCATTAGTACTTCA | 84108 |
rs557075126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311547 | TCCCGGGCTTGAAGC[A/G]ATTCTCCCACCCTGC | 84108 |
rs557103381 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313203 | TATGTGAATCTCTAA[A/G]GCAGGGGTGTCCAAT | 84108 |
rs557168006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328205 | TTACAGGAAAAGCAC[A/G]AAGTGTTTTTTTAGG | 84108 |
rs557213886 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313950 | CTTTAAAATGGGAAA[A/T]AAAAAACTGCCTGCT | 84108 |
rs557215700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305040 | CGATCATAGCTCACT[A/G]TAGCCTCAATCTCCC | 84108 |
rs557283168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310616 | AAAAAAGATAATTCT[C/T]ATAATATTCACATCT | 84108 |
rs557289733 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342959 | TCTTTTTGAGACGGA[C/G]TCTCTGCCGCCCAGG | 84108 |
rs557293262 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310274 | GTCTTAAAAAAAAAA[-/AAAG]AAAGAAAGAAAAGAG | 84108 |
rs557300275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335413 | GTCACCCAGGCAGGA[A/G]TGCAGTGGCGTGATC | 84108 |
rs557357377 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320319 | AACCCTGAGACACTG[A/G]AGTCTCTATGAGAAA | 84108 |
rs557388779 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352373 | CAAAAAACAAAAAAA[A/C]CATTATCCTTGCTAA | 84108 |
rs557407651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320635 | GAGGTTGCGGTGAGC[C/T]GACATCATCGCACCA | 84108 |
rs557497120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330296 | GCCGAGGCTGGTCTC[A/G]ACTCCTAACTTCAAG | 84108 |
rs557588982 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351657 | GCTTTTTTTTTTTTT[C/T]TTTGAGACAGTTTCG | 84108 |
rs557618389 | in-del | -/CAAAACAAAA | 0.0283853 | 0.115702 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352337 | CATCTCAAAACAAAA[-/CAAAACAAAA]CAAAACAAAACAAAA | 84108 |
rs557654381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343968 | TACACAGGAGATACA[C/T]ATGAATTTGTTTACG | 84108 |
rs557675659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309740 | TTCAAAACCAGCCTG[A/G]GCAACATGGCAAAAC | 84108 |
rs557771798 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347839 | GGGACTAAAGGCGCG[G/T]GACACCACGCCTGGT | 84108 |
rs557780578 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350125 | AAAGGATCTTTACTG[C/T]CTAGTAAGCAGTAGC | 84108 |
rs557785906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340049 | AGGCATGGTGGTATG[C/T]GCCTGTAATCCCAGC | 84108 |
rs557825666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330948 | AAGAAAAAAAGAAAC[C/T]TGTACCTCTTGGTAG | 84108 |
rs557847543 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341178 | AGGTTGCGGTGAGCC[A/G]AGATTGCGCCATTGC | 84108 |
rs557988528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332088 | TGAGCCACCGCGCCC[A/G]GCCTAATACATCTCT | 84108 |
rs558172867 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351315 | CTTCGCCGCCTTTTA[A/C]AAACAGCAAAATTGC | 84108 |
rs558185363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343897 | GTAAAGTTGAAGAGG[A/G]ACATACCCTAAGACT | 84108 |
rs558209162 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349870 | GGCGGATCACGAGGT[C/G]AGGAGATCGAGACCA | 84108 |
rs558219514 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315777 | CTCCCAAAACACAGG[C/T]GTGAGCCAGTGTGCT | 84108 |
rs558248392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344720 | GGCACCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 84108 |
rs558345549 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321531 | ATCCTGGCTAAATGG[A/T]GAAACCCTGTCTCTA | 84108 |
rs558421959 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326305 | GACGCAGAAGAATGG[C/T]GTGAACCCGGGAGGC | 84108 |
rs558449053 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328215 | AGCACAAAGTGTTTT[A/T]TTAGGACTTACAGAC | 84108 |
rs558495328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319319 | TGCCCAGCTAATTTT[G/T]TTTTTGTATTTTTAG | 84108 |
rs558516439 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321074 | TAACATTTTGGTTAA[A/G]TAATAATTTATGAAC | 84108 |
rs558564856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328947 | AGACAGGGTTTCACT[A/G]TGTTAGCCAGGATGG | 84108 |
rs558637174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336041 | GGAGGCAAGGTGGGT[A/G]GATTGCCTGAGCTCA | 84108 |
rs558794046 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341733 | ACAGGCGAGAGCCAC[C/T]GCGCCCGGCCAACTC | 84108 |
rs558821897 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330166 | TGCAGCCTCTGCCTC[A/C]CGGGTTCAAGCAATT | 84108 |
rs558966308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314498 | AACAGCACAGTATAA[C/T]TGATATTCAAAATGA | 84108 |
rs559033943 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348180 | TAGCCTCATTAACCT[C/G]AGTAAGTGATGGGAT | 84108 |
rs559079544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315250 | GAGTGCAGTGGCCCA[A/G]TCATAGCTCATTGCA | 84108 |
rs559121606 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351622 | CCATCCCATAAAGCC[C/T]ATTATATTGAATTCG | 84108 |
rs559243175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325921 | CTAACTACTCAGGAG[A/G]CTGAGACAGGAGGGA | 84108 |
rs559247768 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346224 | AAGCCAGGCGCGGTG[A/G]CTCACGCCTGTAATC | 84108 |
rs559251429 | snp | C/T | 0.202035 | 0.245356 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337920 | ATACAAAAAATTAGC[C/T]GGGCGTAGTGGTGGG | 84108 |
rs559260919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339646 | AATACAAAAATTAGC[G/T]GGGTGTGGAGGAGGG | 84108 |
rs559271203 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317043 | TAGACAAGAGTCTCA[A/C]TCTGTCGCCCAGGCT | 84108 |
rs559310604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338186 | GCAGAGGTTGCAGTG[A/G]GTCGAGATCATGCCA | 84108 |
rs559355836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326452 | ACAAAAATAATTGCA[G/T]GAAATCCTACAGAGT | 84108 |
rs559402943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332993 | GTGGTGCATGCCTGT[A/C]ATCCTAGCTATTCAG | 84108 |
rs559418851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319433 | TGGGATTACAAGCGT[C/G]AGCCACCGGACCTGG | 84108 |
rs559458682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347677 | GGGTCACTAAACTGT[G/T]TCATGTGCATTGTTT | 84108 |
rs559525100 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349073 | TTTTTTTTTGAGACA[C/G]AGTCTCACTCTGTAG | 84108 |
rs559567084 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347999 | GTAATCTACTGTTAG[G/T]ATTTTTCCCTCTCTT | 84108 |
rs559741899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329024 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 84108 |
rs559781486 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349169 | CTCCTGTCTCAGCCT[-/C]CCCGAGTAGCTGGGA | 84108 |
rs559782084 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303458 | CTTTGAGAGTACACC[C/T]TGCAGTTTAACAAAG | 84108 |
rs559814945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322762 | CCGGGAGGTAGAGAC[C/T]GCAGTGAGTCAAGAC | 84108 |
rs559921288 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352785 | ATCTCAAAAAAAAAA[A/T]AAATTTTAAAAATAT | 84108 |
rs560002759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314670 | TAAAAATCATTAAGG[C/T]CGGGAGCAGTGGCTC | 84108 |
rs560063082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306355 | CGCCCGCCTTGGCCT[C/T]CCAAAGTGCTGGAAT | 84108 |
rs560101292 | in-del | -/CAGCCTCCCGAGTAGCTGGGATTACAGGAGTGTGCCACCATGCCA | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324056 | GCAATTCTCCAGCCT[lengthTooLong]AGCTATTTTTCATTT | 84108 |
rs560179122 | in-del | -/C | 0.00714227 | 0.0593306 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326512 | ACAACTTTACCTATT[-/C]TTTTACATATATGTA | 84108 |
rs560267723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315514 | ACAGGCACCCACCAC[A/C]ATGCCCAGCTTATTT | 84108 |
rs560268867 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346418 | ATCACGAGGTCAAGA[G/T]ATTGAGACCATCCTG | 84108 |
rs560323918 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337936 | GGGCGTAGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 84108 |
rs560337971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329891 | TCACGCCATTCTCCT[C/G]CCTCAGCCTCCCGAG | 84108 |
rs560373142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307170 | GCCAGGTGTGGTGGC[A/T]CATGGCTCATGCCTG | 84108 |
rs560586082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338314 | TTTAGGAGGCCAAGG[C/T]AGGCAGACCACGAGG | 84108 |
rs560595290 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347836 | GCTGGGACTAAAGGC[A/G/T]CGTGACACCACGCCT | 84108 |
rs560635205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308517 | AATTCTCCTACCTCA[A/G]CCTCCCAAGTAGCTG | 84108 |
rs560649409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330628 | TCAGAATATTTTCAT[A/T]ACCCTAAAAAGACGC | 84108 |
rs560724623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334282 | TTAAAATTGTGTATA[C/T]CTATAGGTTTTGATA | 84108 |
rs560761743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349938 | ATACAAAAAATAAGC[C/T]GGGCGTGGTGGCGGG | 84108 |
rs560764372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316364 | TTTTAGCATGGTTGG[C/G]AAAGAACAGTAATAG | 84108 |
rs560766053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324714 | GCAGTGAGCCGGGAC[C/T]GCCCCACTGCACTCC | 84108 |
rs560773813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342424 | TTTTTAGTAGAGACA[C/G]GGTTTCATCATGTTG | 84108 |
rs560778720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317598 | GAGATATGATCGTAC[C/T]GCTCCACCCCAAGCC | 84108 |
rs560837710 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326199 | TCAGGAGATCGAGAC[C/T]ACAGTGAAACCCCTT | 84108 |
rs560915879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333418 | TGATTTACCCCTTTT[C/T]AAAAAGTTACCTTTT | 84108 |
rs560964660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306323 | GGCTGGTCTTGAACT[C/T]GCGACCTCAGGTGAT | 84108 |
rs560969530 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323940 | CAGTATTTTATTATT[G/T]TATTTTACTATTTTT | 84108 |
rs560979210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334214 | TCTTTTTTTGATGGA[A/G]AATATGAGAATTTAC | 84108 |
rs561025618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304488 | TGCAATTACACGTGC[A/G]TGCTACCAGGCCCAG | 84108 |
rs561089680 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312773 | TAGAGACCAGCCTGA[C/T]CAACACAGAGAAACC | 84108 |
rs561090858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327354 | GATGGAGAAGGAATG[G/T]CGAGACTAAAAAACA | 84108 |
rs561166720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327851 | AACTAATTTTTTTTT[C/T]TTTTTTCATTAGAGA | 84108 |
rs561237499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311934 | TCTGTATTAAAAATA[C/G]AAAAATTAGCTGGTG | 84108 |
rs561260363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328577 | TCTCTATTTGTAAAA[C/T]AGATAAAAATAGCAC | 84108 |
rs561311144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307311 | TAGCCAGTGGCACAC[C/T]TCTGGTAACCAGCCA | 84108 |
rs561330452 | snp | A/G | 0.000123206 | 0.00784779 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350841 | CCTCGTCCTCGAAGC[A/G]GCCTCTGAAGCGGCC | 84108 |
rs561363901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344140 | GGCTATATATTTCAA[C/G]AGGGATGAATCACAC | 84108 |
rs561422819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103308501 | CCTCCCAGGTTCAAG[C/T]AATTCTCCTACCTCA | 84108 |
rs561472511 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305140 | CCTGGCTACTTCAAA[A/T]TTTTTTTTTTCCCAG | 84108 |
rs561488522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309278 | GAATTGTAATCCCCA[A/G]TGTTGGAGGTGGGGC | 84108 |
rs561639503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336989 | CAGACCAATTTTTCT[C/T]TTATTTGGTAACCCT | 84108 |
rs561671862 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331402 | AGCTGGGATTATAGG[A/T]GCCCACCACCACGCC | 84108 |
rs561689648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316252 | TACTGCCCATAGACT[C/T]AAACCACTAAAACTA | 84108 |
rs561835666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325642 | TCTACTACCAAAATG[A/G]AAAGAGCTGGAACTG | 84108 |
rs561966893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347598 | TACAGTTCCTAAAAT[A/G]TAACTCACTCAAGAA | 84108 |
rs561979290 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339431 | GTCTTAGGAGGTACA[A/C]TGAATACCCATCATA | 84108 |
rs562017674 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337534 | TTAGTCTTCAAAACC[C/T]ATACTCTTTCAACAT | 84108 |
rs562053132 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341162 | TGAACCCGGGAGGTG[A/G]AGGTTGCGGTGAGCC | 84108 |
rs562178425 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336245 | TCTCCAAAAAAAAAA[A/T]TTAAAAAAAAATAAA | 84108 |
rs562212782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318658 | GCTGAGGCAGAGAAT[A/G]GCTTGAACCTGGGAG | 84108 |
rs562220527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311031 | TGTAAAGACGGGACT[C/T]GCTATACTGCCCAGG | 84108 |
rs562227339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312232 | CCCCGTCTCTATTAA[A/G]AATACAAAAAATTAG | 84108 |
rs562271361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310203 | GTGATCCCCCCACCT[C/T]GGCCTCTCAAAGTGC | 84108 |
rs562446901 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321690 | GTACTCCAGCCTGGG[A/T]GACAGAGACTCCGTC | 84108 |
rs562537566 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328035 | CACATGTGGCTGGAA[C/T]GTGGGACCCAATAGT | 84108 |
rs562638781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313546 | CTCCAGCCTGGGCAA[A/C]AGATCAAGACCTTGT | 84108 |
rs562649852 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305551 | GCTGGGATTACAAGT[A/G]TGACCCGCTGCACCC | 84108 |
rs562737557 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307725 | TGACCCTCCCGCCTC[A/G]GCCTCCCAGAATACG | 84108 |
rs562751213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305442 | CGCCTGGCTAATTTT[C/T]GTAATTTTAGTAGAG | 84108 |
rs562775087 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351972 | TAGCAGAAACTCAGA[C/T]CCACCCAGGTACAAC | 84108 |
rs562780893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314553 | AGTCATTTTAGACTT[A/T]AATTAAGAAATTCAT | 84108 |
rs562789664 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345218 | CACAAGTATTATAAT[G/T]ATGTTGAGTATTTAA | 84108 |
rs562849727 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346696 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 84108 |
rs562882652 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333577 | AATTGAAGTAACAAG[C/T]AGGGCAAAATAACTT | 84108 |
rs562912679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332023 | GGTCTTGATCTCCTG[A/G]CCTCGTAATCTGCCC | 84108 |
rs562962918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345776 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 84108 |
rs562992375 | snp | A/G | 0.202651 | 0.245475 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337927 | AAATTAGCCGGGCGT[A/G]GTGGTGGGCGCCTGT | 84108 |
rs563030334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323564 | CCTCCCAAAGTGTTG[G/T]GATTACAGGTGTGAG | 84108 |
rs563042656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315625 | CAGCCTCCCAAAATG[C/T]TGGGATTACAGGCGT | 84108 |
rs563111062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329769 | TGAGCCACCGTGCCC[A/G]GCCAGTTTTTTTGTT | 84108 |
rs563199887 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324269 | TTAGATAAAAAATTA[C/T]TCTATAAAACTTAAC | 84108 |
rs563311515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311235 | CAAACTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 84108 |
rs563332259 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344353 | CTCGGTTCACTTCAA[C/T]CTCCACTGCCCGATT | 84108 |
rs563341080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348337 | GAGGTCAAGAGTTTT[C/T]TTGTTTTTTTTTTTT | 84108 |
rs563394609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341508 | GCACTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 84108 |
rs563394663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332467 | TTTTGATAGAGACAG[A/G]GTATTCCTGTGTTGC | 84108 |
rs563440020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327271 | GTCTGGGCAACAAGA[G/T]CAAAACTCCGTCTAA | 84108 |
rs563494862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304342 | CATGTATGTATGTAT[A/G]CATTTATTTATTTTT | 84108 |
rs563507928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333104 | AGCCTGGGCAACAGA[A/G]GAAGACTCCATTTAA | 84108 |
rs563530517 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347828 | CCTTAATAGCTGGGA[C/T]TAAAGGCGCGTGACA | 84108 |
rs563604136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319600 | TTAGTTAGTTGTTTA[C/T]TTATATATCTTTCCT | 84108 |
rs563662395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335645 | GGATTACAGGAGTGA[A/G]CCACGGTGCCCAGCA | 84108 |
rs563662772 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318379 | ACCTGGGAGTCAGAA[A/C/G]TTGTAGTGAACCGAG | 84108 |
rs563771024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314861 | TTGGGAGGCTGAGGC[A/C]GGAGAATCACTCGAC | 84108 |
rs563778297 | snp | A/G | 0.00136231 | 0.0260634 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350692 | CCAGCGGGGTCGCGC[A/G]GGGGCTCTAAATACC | 84108 |
rs563892211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350296 | AATGTTTAATTAGCC[C/T]GGCGTGGTGGCGCGT | 84108 |
rs563983850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346022 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 84108 |
rs564059530 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338469 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 84108 |
rs564142228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323487 | TTTTAGTAGAGATGC[A/G]GTTTACCATGTTGGT | 84108 |
rs564345726 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341600 | GCAAGCCACCACATC[C/T]AGCTTTTTTTTTTTT | 84108 |
rs564383875 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309148 | AGACTTTGGGGGACT[A/G]TTGGGAAATCATGAT | 84108 |
rs564384814 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350038 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 84108 |
rs564417226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324487 | ATTATGGCTGGGCGC[A/G]GTGGCTTATGCCTGT | 84108 |
rs564470294 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313195 | AGAAAAGCTATGTGA[A/T]TCTCTAAAGCAGGGG | 84108 |
rs564518277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342480 | CTCGGGTAATCTGCC[C/T]GCCTCGGCCTCCCAA | 84108 |
rs564581491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343057 | CCTCAGCCTCCCGAG[G/T]AGCTGGGACTATAGG | 84108 |
rs564599123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331242 | TAGGTTATATACACT[A/G]TTTCCAGTTTGGGGT | 84108 |
rs564611410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324825 | AACAGGAGATCTCTT[G/T]TAATCCATAAAAAAA | 84108 |
rs564638557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317685 | TATAGTAACAAACTT[A/G]AAAAAAATTGTAGAA | 84108 |
rs564705919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348439 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 84108 |
rs564735045 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323647 | GCCCAGGTTGGAGTG[C/T]AGTGGCATGATCTTG | 84108 |
rs564750295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309436 | ACTTCCCTCCTTATT[C/T]TCTCTCTTCTGGTTC | 84108 |
rs564782376 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329481 | AACATAAGCATATAC[-/AT]ATATATGTTTTTGAG | 84108 |
rs564782578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335576 | CCATGTTGTTCAGGA[G/T]GGCCTCGATCTCTTG | 84108 |
rs564804292 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332414 | CTTCCTGAGTAGCTG[C/G]AACTGCCCATGCCAA | 84108 |
rs564846048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327911 | CAATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 84108 |
rs564937534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334299 | TATAGGTTTTGATAC[A/G]TATATACTGTAAACT | 84108 |
rs564951449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327409 | ATTAACCAATTACAA[C/T]GTATGGACCTTACTG | 84108 |
rs564959113 | snp | A/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352092 | TCCCAGCACTTTGGG[A/T]GGCCGAGGCGCGCAG | 84108 |
rs565109737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320786 | GTTTAACAGTCCCGT[A/G]GGAATTACTCGTTCC | 84108 |
rs565175111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312832 | TGGGCGTGGTGGCGC[A/G]TGCCTGTAAACCCAG | 84108 |
rs565187224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313328 | CCAGCCCTTTGGGAG[C/G]CCAAGGTGGGCGGAT | 84108 |
rs565191934 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304738 | TGGACTCACTGCAGC[C/G]TTGACCACCTGGGCT | 84108 |
rs565229476 | in-del | -/CAAAAA/CAAAAACAAAAA | 0.375873 | 0.228068 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312965 | ACTCCGTCTCAAAAA[-/CAAAAA/CAAAAACAAAAA]CAAAAACAAAAACAA | 84108 |
rs565256008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322837 | TCACACACACACACA[A/G]AAAGTCCAGCCTGGG | 84108 |
rs565262670 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314650 | ATCTTTTTAAATATC[C/T]GTGATAAAAATCATT | 84108 |
rs565326159 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351849 | TTGACCAGGCTAGTC[C/T]CAAACTTCTGATCTC | 84108 |
rs565336707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344230 | AGGAATAGATATACA[C/T]GTGGCAACCACATGA | 84108 |
rs565346403 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352624 | CTAAAAATACAAAAT[A/T]AGCCGGGCATGGTGG | 84108 |
rs565347057 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328183 | GTAATCAGAACTAAA[C/T]AGTCCCTTACAGGAA | 84108 |
rs565399182 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344730 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTTTGTAA | 84108 |
rs565399302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336456 | TATAAAATAAAACAT[C/T]CCATTCATTGTAAGA | 84108 |
rs565544663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338143 | TTACCCGGGAGGCTG[A/C]GACAGGAGAACTGCT | 84108 |
rs565548172 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327084 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 84108 |
rs565584265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324589 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 84108 |
rs565585112 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329260 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 84108 |
rs565594808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316754 | GTGGCTGTGCTTTCA[A/G]TTCATTTTGCAAATA | 84108 |
rs565671379 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346196 | CAAGTCCATCTCATT[A/T]AAAAAAAAAAAAAAG | 84108 |
rs565683538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346999 | ATTTACGTATGTAAC[C/T]GGCTTGGCTTAAGTT | 84108 |
rs565768166 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314018 | ACATAAATTACTTAG[A/G]ACAGTACCTGACACA | 84108 |
rs565847761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330915 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCCA | 84108 |
rs565919441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348531 | GGTTTCACCATGTTG[A/G]CCAGGTTGGTCTTGA | 84108 |
rs565924537 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328750 | AGGATTTTAACTTTT[-/TTTG]TTTGTTTTTTGTTTT | 84108 |
rs566036547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310426 | AGGAGGGGTTTGAGT[C/T]AAACAAATAGGTATT | 84108 |
rs566097040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309689 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGATGGC | 84108 |
rs566129090 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318613 | AGCCGGGCATGGTGG[C/T]GGTCGCCTGTAATCC | 84108 |
rs566216296 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349445 | CTGAAAGTTACAATA[A/G]TAACACAATATAAAT | 84108 |
rs566350428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321435 | TAATATATTGTAGGC[C/T]GGGCGCGGTGGCTCA | 84108 |
rs566380357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312944 | CCAGCCTGGGCGACA[C/G]AGCGAGACTCCGTCT | 84108 |
rs566444032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304821 | CCACCACCAGACTCA[C/T]TTTTGTATTTTTTGT | 84108 |
rs566572166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305498 | CTGGTCCCGAACTCC[C/T]GACCTCAGGTGATCT | 84108 |
rs566614872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336772 | CCTAGCTACTCGAGA[A/G]GCTGAGGCAGGAGAA | 84108 |
rs566727516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345377 | ACGCAGAGAGAGCTC[A/T]TTAGAACAGCAACAT | 84108 |
rs566912260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329330 | CAGGCGTGAGCCACC[A/G]CACCCGGCCCCAATT | 84108 |
rs566993370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323614 | TTCTTTTTTTTGATA[C/T]AGAGTCTCCCTCTTG | 84108 |
rs567002396 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320518 | ATGGAGAAACTCTGT[C/T]TACTAAAAAAACTAG | 84108 |
rs567088542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315685 | TTTCTTTTTTCAATT[C/T]TTGTAGAGACAGGGT | 84108 |
rs567126348 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340840 | GCTCCTGGACTCCAG[A/C/T]GGTTCTCCTACCTCT | 84108 |
rs567151882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307511 | TGAGACAGGGTCTTG[C/T]TCTGTCGCACAGGCT | 84108 |
rs567232639 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302591 | CTGGGATTACAGGTA[C/T]CTGCTACCACACCCA | 84108 |
rs567287649 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303691 | GAAAAATTTCCCCTG[A/C]GCTTTGGCTGCTTTT | 84108 |
rs567330665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326164 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 84108 |
rs567384878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319689 | CAAATACATAGACCC[C/T]CAATTTAGTAACAAT | 84108 |
rs567560084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327597 | TGGAGTGGTGTGTAC[A/G]TGGGAGTTCATTATA | 84108 |
rs567572731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328112 | AACTAATGCTTACCC[A/T]GCTCCGATCTGAGAC | 84108 |
rs567580457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320556 | GCCAGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 84108 |
rs567641375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321106 | TTACCAGCTATACAG[C/T]AGCTGAGTGGTAGAA | 84108 |
rs567657924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349244 | GTAGAGATGGGGTTT[C/T]ACCATGTTGGCCAGG | 84108 |
rs567736547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335085 | CTTTAAGAGATAGGG[A/T]CTTGCTCTATCACCC | 84108 |
rs567890649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338020 | AGTGAGCCGAGATCC[C/T]GCCACTGCACTCCAG | 84108 |
rs567976417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330789 | AAAAAATTAGCTGGG[C/T]GTGGTGGGGCGCACC | 84108 |
rs568112804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346094 | CCAGCTACTCAGGAG[A/G]CCAAGGCAGGAGAAT | 84108 |
rs568226340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323743 | GACTACAGGTGTGCG[C/T]CACCATACCTGGCTA | 84108 |
rs568228438 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334106 | AACAAATGTAATTGT[C/T]ATTTCTGCCACCTAG | 84108 |
rs568265093 | snp | C/T | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302686 | CTGACCTCAGGTGAT[C/T]CACCTGCCTCGGTCT | 84108 |
rs568287664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315838 | TCTCTAGAGAGAATA[C/T]TGTTGTATATATACA | 84108 |
rs568433165 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306029 | TCTACTTTTTGTGGC[A/G]TTCTATCTCCTTTCT | 84108 |
rs568434751 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329072 | TGAGATGGAGTCTCG[-/CT]CTGTCACCCAGGCTG | 84108 |
rs568463659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309651 | TTTAAGAAACAGAGT[A/T]CAGGCATGGTGGCTC | 84108 |
rs568639235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347737 | TTTGTCACCCAGGCT[A/G]GAGTGCAGTGGCTCA | 84108 |
rs568702255 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339778 | CTCCAGCCTGGGGAA[A/C]AAAAGCGAAATTCTG | 84108 |
rs568786102 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338664 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 84108 |
rs568787673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320453 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATTGC | 84108 |
rs568871567 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313243 | TCCCTGGGCCACACT[-/G]GAAGAACTGTCTTTG | 84108 |
rs568961381 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312253 | AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCACC | 84108 |
rs568966969 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351131 | TCGGCCGGCCTCGGA[C/G]GCCACCACTGCGCAG | 84108 |
rs568977685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312909 | GAGCTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 84108 |
rs569062840 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330799 | CTGGGCGTGGTGGGG[C/T]GCACCTGTAATACCA | 84108 |
rs569101090 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328245 | CTGGGAGCCTAGAAT[A/G]GCTACCTAGGGAACC | 84108 |
rs569220389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344364 | TCAACCTCCACTGCC[C/T]GATTTCAAGTGATTC | 84108 |
rs569262389 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335864 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 84108 |
rs569266996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322349 | TAGGATTACAGGTGT[A/G]CGCTTAATTTTGTGT | 84108 |
rs569323429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328209 | AGGAAAAGCACAAAG[G/T]GTTTTTTTAGGACTT | 84108 |
rs569323536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336581 | TGACTTTGTTAGAAA[C/T]TGCTTGCTTGCGGCC | 84108 |
rs569335505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328818 | GTGCAGTGGAGCGAT[C/T]GTGGCTCACTGCAAC | 84108 |
rs569376661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314035 | CAGTACCTGACACAC[A/G]GCAAGAATTTGATAA | 84108 |
rs569522459 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317787 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGTCCAGG | 84108 |
rs569523476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314895 | AGGAGGTGTTGGTTG[C/T]AATGAGCCGAGATCA | 84108 |
rs569543345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318078 | GGTCAGTTTCTAAGA[A/G]TTTGATGTGTATGGT | 84108 |
rs569597408 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330966 | TACCTCTTGGTAGTC[A/C]CTCCCCATTCAGCCT | 84108 |
rs569617713 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338500 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 84108 |
rs569621134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310575 | ATTAAGAAAATAATT[A/C]TTGGGAACAGATTGT | 84108 |
rs569737055 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341634 | ATTTTTAGTAAAGAC[A/G]GGTTTCACCATATTG | 84108 |
rs569779392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103325980 | GGTTGTAGTGAGCCA[C/T]GATCGTGTCAATGTA | 84108 |
rs569789456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341190 | GCCGAGATTGCGCCA[C/T]TGCACTCCAGCATGA | 84108 |
rs569843523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318884 | GATAGCCAAAGGCCA[A/G]CTTTGTAAGCAGGCC | 84108 |
rs570026874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349154 | CTGGATTAAAGCGAT[C/T]CTCCTGTCTCAGCCT | 84108 |
rs570041506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348608 | GGGATTATGGCATTA[A/G]CCACTGAACCCATCC | 84108 |
rs570281299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327116 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 84108 |
rs570294922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345422 | GCATAAGCACTACTA[C/T]GTGTCAGGGCTCATA | 84108 |
rs570300982 | in-del | -/AG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349072 | TTTTTTTTTTGAGAC[-/AG]AGTCTCACTCTGTAG | 84108 |
rs570331393 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318473 | AAAAAGTGCGGGTGC[A/G]GTGGCGCACACCTGT | 84108 |
rs570359782 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352353 | CAAAACAAAACAAAA[A/C]AAAACAAAAAACAAA | 84108 |
rs570373315 | snp | C/T | 0.202343 | 0.245416 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337951 | CGCCTGTAGTCCCAG[C/T]TACTTGGGAGGCTGA | 84108 |
rs570523133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306532 | CAGCTCATATATCCT[A/G]TATTTCCAGTGCTGC | 84108 |
rs570607520 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334465 | ATCTCCAGGAAAAAG[C/T]ATATTCTTAAATATT | 84108 |
rs570612865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329352 | GCCCCAATTTCTTAA[A/G]CCTAGTAGAAAATGA | 84108 |
rs570672813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323223 | TCAAGCTCAGTTAGA[A/G]AAGTCATATTTCACT | 84108 |
rs570766755 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342596 | GTATACGTGTACTTG[C/T]GTATTTTCCACCATC | 84108 |
rs570854529 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345549 | AGAAACTGAGACCGC[C/T]AGTCGCCATGGCTAA | 84108 |
rs570854921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323678 | ACTCACTGCAATCTC[C/T]ACCTCCCGGGTAATA | 84108 |
rs570894290 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314400 | TTTAGACTGATTAAA[C/T]GCTCTTGAAAAGAGA | 84108 |
rs570951056 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315704 | TAGAGACAGGGTCTC[C/G/T]GTATATTGCCCAGGC | 84108 |
rs570951485 | in-del | -/A | 0.110872 | 0.20771 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313617 | AACAGTAGCTGATAG[-/A]AAAAAAAAAAATCTC | 84108 |
rs570961234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103307739 | CGGCCTCCCAGAATA[C/T]GGGGATTACAGGTGT | 84108 |
rs570963974 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335892 | GAACTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 84108 |
rs571006078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319151 | TCATTCCTTTGATCA[C/T]ACATACTCTTCTTTT | 84108 |
rs571025234 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322887 | TGCCACCAAAAAAAA[A/C]ACAAAAAACAAAAAA | 84108 |
rs571133799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347039 | ATAAAGTGGCAGGGC[C/T]AGGAACAAACTCAGA | 84108 |
rs571136680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333478 | TGTATACAATGTTAC[C/T]TGTGATTTCGGAATC | 84108 |
rs571323268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319823 | AATAACCTAACTTTT[C/T]TGAGATGGAGTCTTG | 84108 |
rs571385552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311432 | CAGGTGTGAGCCACT[A/G]TGCCCGGCCTCTCTC | 84108 |
rs571446385 | snp | A/G/T | 0.00239393 | 0.0345281 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303766 | GTACTTATAAACGCT[A/G/T]TAATTCTTGGTGCTA | 84108 |
rs571452010 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302770 | TATTTTTTTTTTAAC[C/T]CACAGTAAACACTAA | 84108 |
rs571502186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312112 | AAAAAAAAAAGTCAC[A/G]GTTGGGCATGGTGGC | 84108 |
rs571536445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350544 | GCCGGAGGCCTGTCG[A/G]CGCCACACGCCTAGG | 84108 |
rs571600520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313124 | TATATTCCCACTCAC[A/G]TTATAGGTTAATTAA | 84108 |
rs571607096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335795 | ACATAATGAAACCCC[C/G]TCTCTCCTAAAAATA | 84108 |
rs571651624 | snp | C/G | 0.000612783 | 0.0174933 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351017 | GCTGCAGCTCCCTCG[C/G]TTTTGGCAGCGCCTA | 84108 |
rs571653442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342910 | ATGGGCTTCTTGGGG[A/G]CATAACAAATCTCTT | 84108 |
rs571658909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335197 | GGAGTACAGATATGT[G/T]CCACCATGCATGGCT | 84108 |
rs571715410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343339 | TAGAGTTATAAAGAG[A/G]TGACTGAGAAGTAAA | 84108 |
rs571778187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323446 | GGATTACAAGCATGC[A/G]CCACCACGCCCGGCT | 84108 |
rs571814411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321637 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 84108 |
rs571824716 | in-del | -/CAAAA | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352327 | AGTGAGACTCCATCT[-/CAAAA]CAAAACAAAACAAAA | 84108 |
rs571841782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328714 | CTAAGATTATTTGCA[C/T]CATTTTTGCTCTTTA | 84108 |
rs571851578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324454 | TTTGAGGTTTCCATC[A/G]TACAACAAGAAGAAA | 84108 |
rs571892261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324012 | TGGCATGATCTAGGC[C/T]AACTGCAACCTCCGT | 84108 |
rs571892293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103315550 | ATTTTTAGTAGAGAC[A/G]GGGTTTCAGTGTGTT | 84108 |
rs571908291 | in-del | -/CAAAACAAAA | 0.00323624 | 0.0400955 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352328 | AGTGAGACTCCATCT[-/CAAAACAAAA]CAAAACAAAACAAAA | 84108 |
rs572000870 | snp | C/G | 0.202343 | 0.245416 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337894 | ACGGCGAAACCCCGT[C/G]TCTACTAAAAATACA | 84108 |
rs572013387 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330267 | TTTCAGTGGAGACAG[G/T]GTTTCCCCATGTTGC | 84108 |
rs572013877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329622 | AGCTGGGACTACAGG[C/T]GTGAGCCACCACACT | 84108 |
rs572102206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346539 | TGAGGCAGGAGAATC[A/G]CTTGAGCCCAGAAGG | 84108 |
rs572116263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347520 | TACAGAGTGAGTTAA[C/T]TGTGTTTTCTCTTGA | 84108 |
rs572471807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339185 | TTTGGGAGGCCAAGG[C/T]GGGTAGATTGCTTGA | 84108 |
rs572494442 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343220 | GGCGTGAGCCACCGC[A/G]CCCGGCCTTAGGGGT | 84108 |
rs572504489 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319315 | ACCATGCCCAGCTAA[-/T]TTTTTTTTTGTATTT | 84108 |
rs572523147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350625 | CGGCGCACTAGGATC[C/G]GGCCGGCGCCCGGCA | 84108 |
rs572524852 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346828 | ATTTAAATCCAAATC[C/T]ATTTCATGTCCATTC | 84108 |
rs572581770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331179 | TTTTACTGTCAAATA[A/G]TACTCTATTATATGA | 84108 |
rs572632399 | snp | A/C | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351633 | AGCCCATTATATTGA[A/C]TTCGAAAAGCTTTTT | 84108 |
rs572720187 | snp | A/G | 0.367503 | 0.220665 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324791 | AAAAAAAAAAAAAAA[A/G]AAAATATTACATAGC | 84108 |
rs572739137 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351317 | TCGCCGCCTTTTAAA[A/G]ACAGCAAAATTGCTA | 84108 |
rs572760761 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323046 | TTCTGCTTTTAGAAA[-/T]TAACAGGCTGTTATG | 84108 |
rs572814403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342427 | TTAGTAGAGACAGGG[C/T]TTCATCATGTTGGTC | 84108 |
rs572848936 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325242 | GTGTCCTGAGCTTTG[C/T]TTGTTTTTTTGTTTG | 84108 |
rs572880599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343048 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 84108 |
rs572882420 | in-del | -/A | 0.499617 | 0.0138261 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324330 | AAATTTGACTAATGA[-/A]AAAAAAAAAAAGAAA | 84108 |
rs572946342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103335549 | TGTATTTTTAGTATA[A/G]ACGGGGTTTCACCAT | 84108 |
rs572987796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327501 | ATGAATATCTGATCA[A/C]GGGATTATCATTAAT | 84108 |
rs573111408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340417 | TGTGGTCAAGTCTCA[A/T]CAGGAAAGCCTGCTA | 84108 |
rs573213270 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305141 | CTGGCTACTTCAAAA[A/T]TTTTTTTTTCCCAGT | 84108 |
rs573320425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322403 | TAGAGCTGGGGTTTC[A/G]CTATGTTGCCCAGGC | 84108 |
rs573407528 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351787 | TGGCGCCTGCCACCA[C/T]GCCCAGCTAACTTTT | 84108 |
rs573416291 | in-del | -/TGCA | 0.0123036 | 0.0774623 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329825 | CTCTGTCGCCTGGGC[-/TGCA]TGCAGTGCAGTGGCA | 84108 |
rs573428766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337044 | GGACTTACCATTGCT[G/T]TATTTCCAAACAAAA | 84108 |
rs573472540 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352561 | GCGGATTGCCTGAGG[C/T]TGGGAGTTAGAGACC | 84108 |
rs573486356 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353012 | CTTGAACCCGGGAGG[C/T]GAAGGTTGCAGTGAG | 84108 |
rs573509844 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342953 | TTCTTTTCTTTTTGA[C/G]ACGGAGTCTCTGCCG | 84108 |
rs573540841 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | PCGF6 | GRCh38.p7 | 10:103305894 | TCTCTACTTATATAA[-/T]TTTAAAAAAAAAAAA | 84108 |
rs573609122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345610 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 84108 |
rs573614365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318213 | TTTGGGAGGCCGAGA[C/T]GGGCAGATCACCTGA | 84108 |
rs573643371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309317 | AGGTGATTGGATCAC[A/G]GGGTTGGATTTCTCA | 84108 |
rs573679253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103309892 | GGCTACACTGAGCCA[C/T]GATTGTGCCACTGCA | 84108 |
rs573689821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332308 | TTTTTAAGACAGAGT[C/T]TTACTCTGTCACCTA | 84108 |
rs573700915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332897 | AGGTGGGTGGGTCAC[C/T]GGAGGTCAGGAGTTT | 84108 |
rs573798614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347942 | TCTGCAAAGCACTCC[C/T]GTGTGAAGGTAGTAA | 84108 |
rs573879756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327162 | AGGTGGCACATGCCT[A/G]TAATCCCAGCTACTC | 84108 |
rs573907533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340467 | GCTACAAGTAAAGAA[A/G]GAAGAAATGGTGGCA | 84108 |
rs573941581 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319930 | CCTGCCTCATCTTCC[A/C/T]GAGTAGCTGGGACTA | 84108 |
rs573942563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103341319 | TGGAGTGCAATGGCA[C/T]TATCTCGGCTCACCA | 84108 |
rs574098067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336881 | CTCCATCTCAAAAAA[C/G]CAAAAAAAATTACTT | 84108 |
rs574159775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319402 | GTGATGTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 84108 |
rs574212494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311714 | CAACATTTAATACAA[C/T]AAACCAATCACATAA | 84108 |
rs574220629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311039 | CGGGACTCGCTATAC[C/T]GCCCAGGCAAGTCTT | 84108 |
rs574230488 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331632 | CAATGTAATTAATTT[A/C]TATGTCCCTTAAGTT | 84108 |
rs574291100 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343271 | ACGAAGTGGATATAC[A/G]AGGAGATAAATACAA | 84108 |
rs574300359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312386 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 84108 |
rs574351588 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340197 | AAAAAAAAAAAAAAA[-/AAA]TATATATATATATAT | 84108 |
rs574410007 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303273 | TATTGAAGAAGTCTT[A/G]TTACACTGAAATTTT | 84108 |
rs574486054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328897 | GCTGGGACTACAGGC[A/G]TGTACCACCACGCTA | 84108 |
rs574533119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322623 | GCCAGGAGTTTGAGA[C/T]CAGCCTGGGCAAAAT | 84108 |
rs574594647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314623 | TCAACATCAGGTAGC[A/C]AAGGAAAGTATATCT | 84108 |
rs574624493 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF6 | GRCh38.p7 | 10:103323303 | GCAAACTTTCAGTCA[C/T]TTTTTTTTTTGAGTT | 84108 |
rs574777384 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346808 | TCAAAATAAAAAGAA[C/T]CAGGATTTAAATCCA | 84108 |
rs574843652 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339772 | ACTGCCCTCCAGCCT[A/G]GGGAACAAAAGCGAA | 84108 |
rs574907468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103346392 | GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC | 84108 |
rs574937048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339112 | TGCGGTAACATAAAT[G/T]CTTTTCTATGTAATA | 84108 |
rs575037875 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323787 | ACGGGGTTTCGCCAC[A/G]TTGGCCAGACTGGTC | 84108 |
rs575075230 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325775 | TATAATCCTAGTGCT[G/T]TGGGAAGCTGAGGCA | 84108 |
rs575079845 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304843 | TTTTTTGTAGGAGAC[-/A]AGAGTTTCACCGTAT | 84108 |
rs575098143 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333821 | TAAATGTACTTCATA[-/T]TTAAATAACTTATTT | 84108 |
rs575158149 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324327 | TTTAAATTTGACTAA[A/T]GAAAAAAAAAAAAAG | 84108 |
rs575169096 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331924 | CAGCCTCCCGGGTAG[C/G]TGGGACAACAGGCAC | 84108 |
rs575178327 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324535 | AGGCCGAGGCGGGAG[A/G]ATCACGAGGTCAGGA | 84108 |
rs575186395 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305898 | CTACTTATATAATTT[A/T]AAAAAAAAAAAAAGG | 84108 |
rs575203749 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339313 | GAGGATTGCTTGAGT[A/G]TAGGAGGCAGAGGCT | 84108 |
rs575271961 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349818 | CTGGGCGCAGTGGCT[A/C]ACGCCTGTAATCCCA | 84108 |
rs575337775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311610 | ACCACCGCACCTAGC[C/T]GCATTTCTTGTCTTT | 84108 |
rs575348818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304364 | TTTATTTTTTGAGTC[A/G]GAATCTTGCTCTGTT | 84108 |
rs575400088 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302881 | TTGCCAATCTTTTTC[C/T]AATTTTGTAGTAGTC | 84108 |
rs575469487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327310 | CAAACAAACAAAAAA[A/C]CCAAAAAACTGCAAG | 84108 |
rs575498477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103342345 | TTCAAGTAATTCTCC[C/T]GCCTCAGCCTCCTGG | 84108 |
rs575511978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103334064 | ATTGTAATTCTAGAA[A/C]ACAGTCACCTGAAGT | 84108 |
rs575685217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103316186 | CAATCAATTACAAAG[C/T]CCTATTGCTTCTTTC | 84108 |
rs575707212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103313266 | TGTCTTTGGCCAACA[C/T]AAAATATGCTAACAC | 84108 |
rs575762042 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351717 | CGCTCACTTGCAACC[C/T]CCGCCTCCCGGGTCC | 84108 |
rs575887989 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332087 | TTGAGCCACCGCGCC[C/T]GGCCTAATACATCTC | 84108 |
rs575976757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103330342 | GGTCTCCTAAAGTGC[C/T]GGGATTACAGGCGTT | 84108 |
rs576007240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324668 | AGGAGCCTGAGGCAG[A/G]AGAATCACTTGAACC | 84108 |
rs576016717 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103339355 | AGATCGCGCCACTGC[A/T]GTCCAGCCTGGGCAG | 84108 |
rs576027276 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103324130 | TTTTAGTAGAGACAG[G/T]GTTTCACCGTGTTGG | 84108 |
rs576040408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340299 | CAGCAGAGCTACGAC[C/T]TAAATCCAGATCTCC | 84108 |
rs576215870 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF6 | GRCh38.p7 | 10:103332808 | TAGAAGAGGTTCAAC[A/G]CTATCAAAAATCATG | 84108 |
rs576312546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347578 | AGTTACTTTTAAGTA[A/G]CATTTACAGTTCCTA | 84108 |
rs576377119 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315353 | ACCACATCTGGCAAA[C/T]TGTGTGTTTTTTAGT | 84108 |
rs576410974 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF6 | GRCh38.p7 | 10:103340848 | ACTCCAGCGGTTCTC[C/T]TACCTCTGCTTTCCA | 84108 |
rs576429158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103343134 | GGGGTTTCACCGTGT[C/T]AGCCAGGATGGTCTT | 84108 |
rs576460222 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103317082 | TGGCGCAATCTCAGC[-/A]ACACTGCAACCCTTG | 84108 |
rs576502203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336103 | GCAAGGTGTGGTGGC[A/G]TGCACCTGTAGTCCC | 84108 |
rs576556549 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311607 | GCCACCACCGCACCT[A/G]GCCGCATTTCTTGTC | 84108 |
rs576609521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103319342 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 84108 |
rs576612663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103336812 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGG | 84108 |
rs576615136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103318618 | GGCATGGTGGCGGTC[A/G]CCTGTAATCCCAGCT | 84108 |
rs576624330 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315203 | ATCTTTTTATTCCCC[C/T]CAGACAGGGTGTCAC | 84108 |
rs576772790 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351360 | ACAATATTCTGTTTG[C/T]ATCACCTAATTCACA | 84108 |
rs576946661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328355 | AAAACTCAGAGTCTA[C/T]ATTAGATAGGTATTT | 84108 |
rs576967898 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336286 | GAAAAAAGTAATAGA[A/G]ATACAGAAATATTTA | 84108 |
rs576970617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103331950 | GGCACGCGCCACCGC[A/G]CCTGGCTAATTTTTT | 84108 |
rs577003939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103321638 | AATGGCATGAACCCG[C/G]GAGGCGGAGCTTGCA | 84108 |
rs577020829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103322525 | ATATTTTGTTTCTGT[C/G]AATTAAAAAAACAGG | 84108 |
rs577223180 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308170 | GGGGAACTGCCCAGT[A/G]GTGCTGTGAGAAGAG | 84108 |
rs577303158 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353130 | GCTGAATGTGTGCCA[C/G]GGGTGGTAGCTCATT | 84108 |
rs577340854 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF6 | GRCh38.p7 | 10:103306282 | TTTGTATTTTGAGTA[C/G]AGATGGGGTTTCTCC | 84108 |
rs577405328 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342655 | AGGTACATGGGCTTG[A/C]CTTTCTGCACCTTGC | 84108 |
rs577417244 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PCGF6 | GRCh38.p7 | 10:103328879 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 84108 |
rs577440905 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PCGF6 | GRCh38.p7 | 10:103329741 | GCCTCCCAAAGTGCT[C/G]GGATTATAGGTGTGA | 84108 |
rs577524702 | snp | A/G | 0.202343 | 0.245416 | intron-variant | PCGF6 | GRCh38.p7 | 10:103337922 | ACAAAAAATTAGCCG[A/G]GCGTAGTGGTGGGCG | 84108 |
rs577585175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103338189 | GAGGTTGCAGTGAGT[C/T]GAGATCATGCCACTG | 84108 |
rs577596390 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF6 | GRCh38.p7 | 10:103310107 | AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTT | 84108 |
rs577669492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103320030 | CCAGGATGGTCTCCA[C/T]CTCTTGACCTCGTGA | 84108 |
rs577733632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103311791 | ACCTGGATTTACCCA[A/G]TAGGCCATGACTGTC | 84108 |
rs577844520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103312482 | CCAAGTACCAAAAAA[G/T]TATGCTTCTGAAATC | 84108 |
rs577939961 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349877 | CACGAGGTCAGGAGA[G/T]CGAGACCATCCTGGC | 84108 |
rs578014126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103327644 | TGTATAAGTTTTAAA[A/T]TTTTCATAATAAAGG | 84108 |
rs578181713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304286 | GGATTACAGGCACCC[A/G]CCACCATACTCAGCT | 84108 |
rs578199889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF6 | GRCh38.p7 | 10:103304888 | TCAAACAATCTGCCT[A/G]TCTCAGACTCCCAAA | 84108 |
rs578213979 | snp | C/T | 0.000301477 | 0.0122739 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350676 | CTGACGCCGCTTGGG[C/T]CCAGCGGGGTCGCGC | 84108 |
rs745361108 | in-del | -/CTC | 1.72104e-05 | 0.00293341 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350800 | TTCTTCCTCCTCCAG[-/CTC]CTCTTCTTCTTCCAA | 84108 |
rs745371451 | snp | A/G | 2.15557e-05 | 0.00328289 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351095 | ACCAGGCGAGGCGAG[A/G]CGGCGGGAGAGCGCG | 84108 |
rs745373135 | snp | A/G | 3.35132e-05 | 0.00409334 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345001 | ATTCTTTAAGTTAAA[A/G]GGTAAATTTTTAGGG | 84108 |
rs745384130 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317353 | AAAAACTATCACTCT[C/T]AGTGGGCTTTATACC | 84108 |
rs745428639 | snp | C/T | 0.000169223 | 0.0091969 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351024 | CTCCCTCGGTTTTGG[C/T]AGCGCCTACGCTGCC | 84108 |
rs745471630 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345991 | TCAGGTCAGGAGTTC[A/G]GGACCAGCCTGGCCA | 84108 |
rs745482899 | in-del | -/A | 0.0138882 | 0.0821658 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333907 | CTTGTGAAATGAATG[-/A]AAAAAAAAGTAAAAT | 84108 |
rs745519821 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330354 | TGCTGGGATTACAGG[C/T]GTTAGCCACCGTGCC | 84108 |
rs745533329 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316017 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 84108 |
rs745569169 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329228 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATCATAT | 84108 |
rs745649319 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348593 | GCCTCCCAAAGTGCT[A/G]GGATTATGGCATTAG | 84108 |
rs745667767 | snp | A/G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319732 | GTATGGAAACATCAT[A/G/T]TATTAGTCCTTAAAA | 84108 |
rs745789174 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307119 | AAAAACAAACAAAAA[A/G]TAAAAAATAAAAAAA | 84108 |
rs745842478 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305696 | ATAATTGCTAAAGCT[A/C]TGAAACACTTACTCA | 84108 |
rs745967766 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320460 | GGGAGGCCGAGGTGG[A/G]CAGATTGCCTGAGGC | 84108 |
rs745969670 | snp | C/T | 1.67705e-05 | 0.00289568 | splice-acceptor-variant | PCGF6 | GRCh38.p7 | 10:103326634 | TTCTTTTCCAATGGC[C/T]ACAAAAACAGACAGA | 84108 |
rs745986534 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334670 | CCTGGACATAATTTT[A/C]CTCAGTTTCCTTTTC | 84108 |
rs746014554 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332974 | GCAAAATTAGCTGGG[C/T]GTGGTGGTGCATGCC | 84108 |
rs746046234 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338624 | GTAATCCCAATACTT[C/T]GGGAGGCTGAGGTGG | 84108 |
rs746115350 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314707 | GTAATCCCAGCACTT[C/T]GGGAGGCAGAGGCGG | 84108 |
rs746258633 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311847 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGTGGG | 84108 |
rs746296762 | snp | C/G | 1.76176e-05 | 0.00296791 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326494 | TGTGCTAAAGGTAAG[C/G]TCACAACTTTACCTA | 84108 |
rs746411319 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325974 | CCTCAAGGTTGTAGT[A/G]AGCCATGATCGTGTC | 84108 |
rs746488571 | snp | A/G | 0.000235156 | 0.0108408 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350948 | GGTCCCTCCTCACCC[A/G]CTGCGGGTGCAGGGG | 84108 |
rs746509117 | in-del | -/ACAG | 3.38241e-05 | 0.00411229 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326641 | CCAATGGCTACAAAA[-/ACAG]ACAGATAAAACTATT | 84108 |
rs746657966 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319264 | AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 84108 |
rs746791844 | snp | C/G | 1.65776e-05 | 0.00287898 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347461 | CCAACCTAATAAAAG[C/G]AAAGGATGGAGAATA | 84108 |
rs746881981 | snp | C/T | 1.72695e-05 | 0.00293845 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348702 | TACAATTGTAATTTA[C/T]ATATTCTTCTTACCT | 84108 |
rs746962405 | in-del | -/CACACACACACACACAC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339812 | GTCTCAAAAAAAAAA[-/CACACACACACACACAC]ACACACACACACACA | 84108 |
rs746968922 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325853 | AAGACCGCATCTCTT[-/AAA]AAAAAAAAAAAAAAA | 84108 |
rs747077388 | snp | A/G | 1.66067e-05 | 0.00288151 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314167 | TTATCTGTTAGACAT[A/G]GGTATGTCTATAACC | 84108 |
rs747081523 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307163 | ACACAAGGCCAGGTG[C/T]GGTGGCTCATGGCTC | 84108 |
rs747134111 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323530 | GAACTCCTGACCTCA[C/G]GTGATCCACCTGCCT | 84108 |
rs747149199 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332024 | GTCTTGATCTCCTGA[A/C]CTCGTAATCTGCCCA | 84108 |
rs747164074 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335953 | GCCCGGTGACAGTGC[A/G]AGACTCCATCTCAAA | 84108 |
rs747164839 | snp | C/T | 7.00452e-05 | 0.00591757 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350736 | CCGAGTCCTGCCGGC[C/T]TCCCTCCAGCCTCAA | 84108 |
rs747338259 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103353035 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACCCC | 84108 |
rs747406397 | snp | C/G | 1.66651e-05 | 0.00288657 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349033 | AGTTTTAAAATACAA[C/G]TCCTTGCCTTTTACA | 84108 |
rs747451032 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306086 | TCACCAAGGCTGCAT[-/C]CCGCAAGCAATCCAC | 84108 |
rs747461274 | snp | C/G | | | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350861 | CTGAAGCGGCCCAGG[C/G]TGCGCTCCGGCTCCA | 84108 |
rs747564100 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342227 | GAGTGAGCCACTGCA[-/C]CCGGACTTTTTTTTT | 84108 |
rs747566373 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312235 | CGTCTCTATTAAAAA[C/T]ACAAAAAATTAGCCA | 84108 |
rs747606747 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352509 | CAGGCACAGTGGCTC[C/T]CGCCTGTAATCCCAG | 84108 |
rs747633467 | snp | A/G | 3.30458e-05 | 0.0040647 | stop-gained, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347443 | TGTCTTGTAACTGTC[A/G]GTCCAACCTAATAAA | 84108 |
rs747639452 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341462 | TGTATTTTTCGAGAC[A/G]GAGTTTGGCCCTTGT | 84108 |
rs747680000 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323781 | GTAGAGACGGGGTTT[C/T]GCCACGTTGGCCAGA | 84108 |
rs747781725 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305025 | TGGAGTGCAATGGCG[C/T]GATCATAGCTCACTG | 84108 |
rs747836612 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302859 | TTCACAAATTCTTTA[C/T]AAAGAATTGCCAATC | 84108 |
rs747966040 | snp | A/G | 8.30282e-05 | 0.00644261 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314316 | ATTTCTTGCTTCAAA[A/G]TACCATCTGAAGAAA | 84108 |
rs748051195 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317542 | ATAATCTTAGCTGCT[C/T]GGGAAGCTGAGGCAG | 84108 |
rs748153076 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347696 | TGTGCATTGTTTTTT[G/T]TGTGTGTGTGTGACA | 84108 |
rs748208147 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344742 | TAATTTTTTTTTTTT[A/G]TAATTTTAGTAGAGA | 84108 |
rs748221339 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303938 | AGAAACCACAAGACC[A/G]TAATGAAGGACAAGC | 84108 |
rs748221575 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349014 | GCTGCAAATAAACGG[A/G]AACAGTTTTAAAATA | 84108 |
rs748270020 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309730 | ATCTCAGGAGTTCAA[A/C]ACCAGCCTGGGCAAC | 84108 |
rs748276554 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348902 | TCGGTATGCTTACAG[C/G]TATGAAGACATTCTG | 84108 |
rs748465392 | in-del | -/GAAGCGGCCTCT | 3.83988e-05 | 0.00438154 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350836 | CTCGTCCTCGTCCTC[-/GAAGCGGCCTCT]GAAGCGGCCCAGGCT | 84108 |
rs748531897 | in-del | -/AATT | 1.87492e-05 | 0.00306174 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333970 | GAAAAATGAGAGCAA[-/AATT]AATCAATATTTAATA | 84108 |
rs748542716 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336120 | GCACCTGTAGTCCCA[G/T]CTACTCGGGAGGCTG | 84108 |
rs748564620 | snp | A/G | 6.04321e-05 | 0.00549658 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333993 | AATATTTAATACTTT[A/G]AGCTATATGTTTAAT | 84108 |
rs748743394 | snp | C/G | 6.61682e-05 | 0.0057515 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347250 | TACCAGGTTTAGGTA[C/G]TTCTAGACCTCTTTC | 84108 |
rs748879383 | snp | C/G | 0.000214707 | 0.0103589 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345121 | TGCTTGAAGGGACTG[C/G]CTGTGGAACAGCTAT | 84108 |
rs748879817 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320260 | CAAACAAAGCAAAAT[A/C]CAATAAGACATCAAA | 84108 |
rs748892129 | snp | C/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351776 | GCTGGGACTACTGGC[C/G]CCTGCCACCACGCCC | 84108 |
rs748901642 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328506 | CCTGGGCTCAAACCC[C/T]GGTTCTGCCATTTTC | 84108 |
rs748992355 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344048 | ACAAACCTAAATATT[-/C]AACAGAACAGGAAAA | 84108 |
rs748998217 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341683 | TCTTGATGTCAAGTA[A/G]TCTGCCCACCTAAGC | 84108 |
rs749004942 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340679 | AAACCTCACTGCAGC[C/T]TCAAACTCCCGGGCT | 84108 |
rs749059991 | snp | C/G | 9.88566e-05 | 0.00702983 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303895 | CCTCCTCATAATGTG[C/G]CTAGAATCTTCAAGT | 84108 |
rs749077282 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322973 | TAGCCATAGAATAAT[C/G]TGTATTCTAGAGAGG | 84108 |
rs749105756 | in-del | -/CTCT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311441 | GCCACTGTGCCCGGC[-/CTCT]CTCTTTTTTTTTTTT | 84108 |
rs749210655 | snp | A/C/G | 0.000259976 | 0.0113986 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351105 | GCGAGGCGGCGGGAG[A/C/G]GCGCGGGAGTTCGGC | 84108 |
rs749341896 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342527 | GTGTGAGCCACCATG[C/G]CTGGCCAAGATTTTC | 84108 |
rs749356581 | snp | C/T | 1.65726e-05 | 0.00287855 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348745 | AGGTTGTGTCTGATG[C/T]ACTACTATATTGCAT | 84108 |
rs749374359 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335217 | CATGCATGGCTAATT[-/A]AAAAAAAAAAAAAAT | 84108 |
rs749402375 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312643 | TTAGTACTTCATAAG[C/T]TTCTCAGAGTCATAT | 84108 |
rs749412533 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347738 | TTGTCACCCAGGCTG[C/G]AGTGCAGTGGCTCAA | 84108 |
rs749610887 | snp | C/T | 5.17063e-05 | 0.00508434 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351006 | GAGGCGGCAAGGCTG[C/T]AGCTCCCTCGGTTTT | 84108 |
rs749689156 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325687 | TTTCTATCTTCAGCT[A/T]TTCTATGACACTAAT | 84108 |
rs749709522 | snp | A/G | 0.000165879 | 0.00910559 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350928 | CCGTCTCAGACAGAG[A/G]CGCCGGTCCCTCCTC | 84108 |
rs749897717 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332340 | GCTAGAGTGTAGTGA[C/T]GCAATCACAGCTCAC | 84108 |
rs749911332 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318989 | GAAGAGATAACAAAA[A/G]TATTTTTGAATCTCA | 84108 |
rs749952645 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331459 | GATAGAGTTTTGGCA[C/T]GTTGGCCAGGCTAGT | 84108 |
rs750013302 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334866 | TGAGGTATTAGTACC[C/G]CTTTCTACAGATGAA | 84108 |
rs750031313 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337039 | TTGAGGGACTTACCA[C/T]TGCTTTATTTCCAAA | 84108 |
rs750113337 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307607 | TCTCCCAAGTAGCTG[A/G]GACTACAGGTGCATG | 84108 |
rs750128956 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345300 | TCAAAGCCAGTGAAA[C/T]GAGAGGCAAGCCTGG | 84108 |
rs750203193 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309367 | TCCCTTTGGTAATGT[A/C]CTCACAAAAGTGAAT | 84108 |
rs750248331 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308040 | CAGGAGTTCAAGACC[A/G]GCCTGGATGTCTAGG | 84108 |
rs750248718 | snp | A/C | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351347 | ACCGTTCCAAGCAAC[A/C]ATATTCTGTTTGCAT | 84108 |
rs750269866 | snp | C/T | 0.000346258 | 0.0131533 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348993 | GCTCAGAGAGATTAA[C/T]CAGGCGCTGCAAATA | 84108 |
rs750367218 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336829 | GCAGTGAGCCGAGGT[C/T]GTGCCACTGCACTCC | 84108 |
rs750371620 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335836 | GCTGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 84108 |
rs750374896 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323420 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT | 84108 |
rs750473360 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316846 | TATATAGAATTATGA[C/G]ATAGAACCCGGGTTG | 84108 |
rs750497639 | snp | C/T | 4.30858e-05 | 0.00464123 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351066 | CCGCGACCCCCTCCA[C/T]GGTCGGGAGAGACAC | 84108 |
rs750499699 | snp | A/G | 1.83199e-05 | 0.00302648 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333955 | GCCTTCATTAGCACT[A/G]AAAAATGAGAGCAAA | 84108 |
rs750554716 | snp | A/G | 5.41477e-05 | 0.00520297 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351001 | AGGCGGAGGCGGCAA[A/G]GCTGCAGCTCCCTCG | 84108 |
rs750595150 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352790 | AAAAAAAAAATAAAT[C/T]TTAAAAATATGGCCA | 84108 |
rs750604369 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339830 | ACACACACACACACA[A/C]ACACACACACACACA | 84108 |
rs750643940 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315639 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 84108 |
rs750659244 | in-del | -/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348355 | GTTTTTTTTTTTTTT[-/G]AGATACTCTCATCAG | 84108 |
rs750783063 | snp | C/T | 2.29745e-05 | 0.00338921 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348676 | AGCTTTCAGAAAAAG[C/T]ATATTTAAAATACAA | 84108 |
rs750831463 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312504 | TCTGAAATCTCTTGA[C/T]GTTGATTCTGGCACC | 84108 |
rs750838740 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328260 | GGCTACCTAGGGAAC[C/T]GAGGCACACATTTGT | 84108 |
rs750890096 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341322 | AGTGCAATGGCACTA[C/T]CTCGGCTCACCACAA | 84108 |
rs751026476 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320790 | AACAGTCCCGTGGGA[A/T]TTACTCGTTCCTGTT | 84108 |
rs751137139 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330885 | AGTGAGCCCAGATTG[C/T]GCCACTGCACTCCAG | 84108 |
rs751139730 | snp | A/T | 1.65165e-05 | 0.00287367 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348841 | ATGTTGAAGTCAGGA[A/T]GCTTTCAAGACATTT | 84108 |
rs751163929 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332500 | AGACTGGTCTTGAAC[C/T]CCTGGCTCCAAGCAA | 84108 |
rs751201815 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323273 | TACCAGTAAATATCG[A/G]TACTAAAAACACTAG | 84108 |
rs751317850 | snp | A/G | 0.000298295 | 0.0122089 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303974 | ATCCTGAAAAGGGGA[A/G]AAAAAAAGACGATTT | 84108 |
rs751371873 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310950 | AAACAATCCCTCTGC[C/T]TCAGCCTCCCCAGGT | 84108 |
rs751396644 | snp | C/T | 1.6693e-05 | 0.00288898 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347485 | GAGAATACCTCAGAA[C/T]TCAGAAAAATGCATT | 84108 |
rs751404603 | snp | C/T | 3.6249e-05 | 0.00425713 | missense, intron-variant | PCGF6 | GRCh38.p7 | 10:103333932 | TAAAATACCTTAAAA[C/T]GTCCCGTGCCTTCAT | 84108 |
rs751408599 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303741 | CAGATGCATTCCATC[A/G]TTCCAAGTTGTACTT | 84108 |
rs751435764 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309511 | ATGATTCCTGTACAG[A/C]CTGCAGAACTGTGAG | 84108 |
rs751465948 | in-del | -/TCC | 0.00219263 | 0.0330379 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350767 | GAGAAGTGACTCATG[-/TCC]TCCTCCTCCTCCTCC | 84108 |
rs751498394 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326939 | ATTCATTCATTTCAA[A/G]TACTGAACTTACACT | 84108 |
rs751537134 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339153 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCATCA | 84108 |
rs751566762 | snp | C/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351225 | AAACCCTGCAGCTCC[C/G]GGGCAGGCTGCGGGG | 84108 |
rs751589625 | snp | A/G | 0.000165989 | 0.00910862 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350893 | CTCAGGGGGCCGGGA[A/G]CCGGAGCAGCCGGGA | 84108 |
rs751657830 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337068 | AACAAAATATTTTTG[C/T]TCCTTCTGCTACCAC | 84108 |
rs751677395 | snp | C/T | 6.66167e-05 | 0.00577095 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326626 | GAACAAACTTCTTTT[C/T]CAATGGCTACAAAAA | 84108 |
rs751733177 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321845 | TCCCACAATGTATAC[A/C]TATTTCAAAACATCA | 84108 |
rs751750682 | snp | A/G | 2.77489e-05 | 0.00372474 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350987 | GGCGGGGAGACAGGA[A/G]GCGGAGGCGGCAAGG | 84108 |
rs751929126 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316963 | CACAGAGAACTTAGA[G/T]CCATAAAAAGTTAAA | 84108 |
rs751946307 | snp | A/G | 1.66333e-05 | 0.00288381 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347210 | TTCTTTAATCTGTAA[A/G]TACATTATAGTATAC | 84108 |
rs751984271 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329880 | GCCTCCTGAGTTCAC[A/G]CCATTCTCCTGCCTC | 84108 |
rs752120464 | snp | C/T | 1.67809e-05 | 0.00289658 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347495 | CAGAATTCAGAAAAA[C/T]GCATTTTGGTACAGA | 84108 |
rs752204266 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306777 | GTTGAAGACCAGTGG[C/T]AAACCAGAGAGAGCA | 84108 |
rs752275029 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321056 | CTGTATATTTGATAA[C/T]TCTAACATTTTGGTT | 84108 |
rs752308460 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341604 | GCCACCACATCCAGC[-/T]TTTTTTTTTTTTGTA | 84108 |
rs752463812 | snp | C/T | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326610 | GCTTCTCCTGAAACT[C/T]GAACAAACTTCTTTT | 84108 |
rs752521668 | in-del | -/AGT | 1.65482e-05 | 0.00287643 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314288 | TATGGACATGAAGAG[-/AGT]AGTATTAGATTGATT | 84108 |
rs752559283 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332669 | ACAGGCGTCTTCAGG[C/G]AACACTGGTAGCATA | 84108 |
rs752562539 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352430 | CTGCAAGAAAGATTC[A/G]GGAAGTCAAATGCTC | 84108 |
rs752565427 | snp | G/T | 0.000152311 | 0.00872539 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350879 | CGCTCCGGCTCCAGC[G/T]CAGGGGGCCGGGAGC | 84108 |
rs752600564 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330470 | TCAAAGTTTCTATCG[A/G]ATCTTGGCTTAGGTA | 84108 |
rs752609361 | in-del | -/TTCT | 3.6152e-05 | 0.00425143 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349051 | CTTGCCTTTTACAAA[-/TTCT]TTTTTTTTTTTTGAG | 84108 |
rs752611111 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314010 | GCTAATCTACATAAA[C/T]TACTTAGAACAGTAC | 84108 |
rs752613513 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348972 | AACACAAGATGTATG[G/T]GGTCAGCTCAGAGAG | 84108 |
rs752639754 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302894 | TCCAATTTTGTAGTA[A/G]TCTCTACACATTCAG | 84108 |
rs752687730 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTT | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302454 | GTGCCTGACCTGGTT[-/TTTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 84108 |
rs752692805 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333906 | TCTTGTGAAATGAAT[G/T]AAAAAAAAAGTAAAA | 84108 |
rs752753299 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347350 | AATGTAACTACTAGA[A/G]TCAGAGATTCTGGGA | 84108 |
rs752938574 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304465 | CCTGCCTCAGCCTAC[C/G]GAGTAGCTGCAATTA | 84108 |
rs752960234 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339295 | CTCAGGAGGCTGAGG[C/T]GAGAGGATTGCTTGA | 84108 |
rs753079254 | snp | A/G | 2.14968e-05 | 0.00327841 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351084 | TCGGGAGAGACACCA[A/G]GCGAGGCGAGGCGGC | 84108 |
rs753131315 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331318 | AGTGAAGTGGCATGA[C/T]CTCAGCTCACTTCGC | 84108 |
rs753193198 | snp | A/C | 1.6666e-05 | 0.00288664 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347197 | TTTATTGTTAGTATT[A/C]TTTAATCTGTAAGTA | 84108 |
rs753244804 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346751 | GGTGAGCTGAGATCA[C/T]AGCATTGCACTCCAG | 84108 |
rs753354271 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340886 | AGGATTACAGGCATA[A/G]GCCACCATGCCTGAC | 84108 |
rs753391432 | snp | G/T | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326585 | GAATTTTTCTACATG[G/T]CCAATAGTTGCTTCT | 84108 |
rs753411425 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307854 | CCTATTGTTAAGTGA[C/T]GCATAACTGCATATA | 84108 |
rs753421010 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342662 | TGGGCTTGCCTTTCT[A/G]CACCTTGCTTTTCCC | 84108 |
rs753439075 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308288 | TCGTGAGAGAAGCCA[C/T]GGGGGCCAAACCCTG | 84108 |
rs753456796 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309287 | TCCCCAATGTTGGAG[A/G]TGGGGCCTGGTGGGA | 84108 |
rs753473267 | snp | A/G | 1.65053e-05 | 0.0028727 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347424 | ATCACTAATTTGTAC[A/G]CTATGTCTTGTAACT | 84108 |
rs753494001 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311282 | GAGTAGCTGGGATTA[C/G]AGGCACCTGCCACCA | 84108 |
rs753599183 | snp | C/G | 1.66499e-05 | 0.00288525 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350713 | TCTAAATACCTCCTC[C/G]TCGTCCTCCGAGTCC | 84108 |
rs753708581 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327768 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCTATTCT | 84108 |
rs753776566 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314248 | GATACTGCTCCAACA[A/G]GTGATCACCACAGAT | 84108 |
rs753822743 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334364 | CACATACTTATTTTA[C/T]TGTAGTGAGAACATT | 84108 |
rs753921253 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314451 | AAGTAAATAAGGTAA[A/C]ATGGGAAGAGCATTA | 84108 |
rs754001394 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345059 | AGACATATCAAGTTC[A/G]GGTGGAATACGAAAC | 84108 |
rs754015290 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346126 | GCTTGAACCTGGAGG[C/T]GGAGGTTGCAGTGAG | 84108 |
rs754046791 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339804 | TTCTGTCTGTCTCAA[-/AA]AAAAAACACACACAC | 84108 |
rs754082376 | in-del | -/TCT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323030 | TATAATAAGGGCAAG[-/TCT]TCTGCTTTTAGAAAT | 84108 |
rs754133452 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341005 | GGGTCCAAGGTGGGC[A/G]GATCACCTGAGGTCG | 84108 |
rs754176949 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339403 | TCAAGGAGGAAAAAA[C/T]AGATAAAGGACTGTC | 84108 |
rs754194919 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319091 | CATGCTAGAGCTTCC[A/G]AGTTAAGATTTTTCA | 84108 |
rs754279114 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319875 | CAGTGGTGCGATCTC[A/G]GCTCACCGCAACCTC | 84108 |
rs754313162 | snp | C/G | 4.29286e-05 | 0.00463276 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351072 | CCCCCTCCATGGTCG[C/G]GAGAGACACCAGGCG | 84108 |
rs754426213 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308452 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC | 84108 |
rs754524947 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340295 | AAAACAGCAGAGCTA[C/T]GACTTAAATCCAGAT | 84108 |
rs754589710 | snp | C/T | 3.30147e-05 | 0.00406279 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347426 | CACTAATTTGTACAC[C/T]ATGTCTTGTAACTGT | 84108 |
rs754660039 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332565 | ACAGATGTGAGCCAA[C/T]GAACCCGGCCTAATA | 84108 |
rs754712308 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331637 | TAATTAATTTATATG[C/T]CCCTTAAGTTACTTT | 84108 |
rs754767403 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347629 | AACCTTAAGTAAATA[C/T]ATGTAATCATAAGTA | 84108 |
rs754796004 | snp | C/T | 1.66771e-05 | 0.00288761 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314140 | TAACATGGATAACTT[C/T]CACTAAGTAACTTAT | 84108 |
rs754797620 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327769 | AAGCTCCGCCTCCCG[C/G]GTTCACGCTATTCTC | 84108 |
rs754810375 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311024 | TATCCTTTGTAAAGA[C/T]GGGACTCGCTATACT | 84108 |
rs754834358 | snp | G/T | 9.10539e-05 | 0.00674675 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350714 | CTAAATACCTCCTCC[G/T]CGTCCTCCGAGTCCT | 84108 |
rs754839699 | in-del | -/T | 3.30082e-05 | 0.00406239 | frameshift-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314267 | TCACCACAGATTATA[-/T]TCTACCTATGGACAT | 84108 |
rs754921073 | snp | A/G | 1.65261e-05 | 0.0028745 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314277 | ATTATATCTACCTAT[A/G]GACATGAAGAGAGTA | 84108 |
rs755020947 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342537 | CCATGCCTGGCCAAG[A/G]TTTTCTTATATGGCC | 84108 |
rs755123174 | snp | A/G | 5.10912e-05 | 0.00505401 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345165 | AAAAATGTTAATTAA[A/G]AATAAAAATGCCATA | 84108 |
rs755168684 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349003 | ATTAATCAGGCGCTG[C/T]AAATAAACGGAAACA | 84108 |
rs755203281 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335992 | GGAAAAGAGGCCAGG[C/T]GCGGTGGCTCACGCC | 84108 |
rs755266439 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347616 | ACTCACTCAAGAAAA[C/T]CTTAAGTAAATATAT | 84108 |
rs755281103 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346197 | AAGTCCATCTCATTT[A/T]AAAAAAAAAAAAAGC | 84108 |
rs755347999 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319188 | GGAGTCTCACTCTGC[C/T]GCCCAGGCTGGAATG | 84108 |
rs755427741 | snp | A/C/G/T | 0.000755701 | 0.019425 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351009 | GCGGCAAGGCTGCAG[A/C/G/T]TCCCTCGGTTTTGGC | 84108 |
rs755440858 | snp | A/T | 4.28706e-05 | 0.00462963 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351076 | CTCCATGGTCGGGAG[A/T]GACACCAGGCGAGGC | 84108 |
rs755462396 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329969 | ATTTTTAGTAGAGAC[A/G]GGTGTTAGCCAGGAT | 84108 |
rs755492356 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315870 | TTTATTAAGACTCTA[C/T]TATACTTACTTGCTA | 84108 |
rs755512294 | snp | A/C | 1.65206e-05 | 0.00287403 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333989 | AATCAATATTTAATA[A/C]TTTAAGCTATATGTT | 84108 |
rs755546249 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306968 | ATTAGCCAGGTGTGG[-/C]TGGCACATGTCTATA | 84108 |
rs755606997 | in-del | -/TGTG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315969 | CCTCAACAGCTTATA[-/TGTG]TGTGTGTGTGTGTGT | 84108 |
rs755618927 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314214 | TCACCTATTGCACGT[C/T]GGATTTCCCTTAGAG | 84108 |
rs755627382 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349040 | AAATACAAGTCCTTG[A/C]CTTTTACAAATTCTT | 84108 |
rs755627753 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334925 | TTTCTTTGGGACACA[C/T]AAATATGGTAGGTAA | 84108 |
rs755689702 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341521 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCTCGGAT | 84108 |
rs755742582 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347218 | TCTGTAAGTACATTA[C/T]AGTATACACCCAAAC | 84108 |
rs755820249 | in-del | -/TCT | 0.000170765 | 0.00923869 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350804 | TCCTCCTCCAGCTCC[-/TCT]TCTTCTTCCAACTCC | 84108 |
rs755842214 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351554 | AAGGAATTATATAGT[A/G]TATTGATACAAGGTG | 84108 |
rs755872329 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322687 | AATTTAGCCGGGCAT[A/G]GTGGCATGCACCTCT | 84108 |
rs755919995 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348889 | TTCAGAAATGTGATC[A/G]GTATGCTTACAGGTA | 84108 |
rs755952922 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334009 | AGCTATATGTTTAAT[A/C]ATAAAACAACATATA | 84108 |
rs756031558 | snp | C/T | 1.66021e-05 | 0.0028811 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303989 | GAAAAAAAGACGATT[C/T]TGCAGTTCTTTCAAA | 84108 |
rs756083927 | snp | A/G | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348997 | AGAGAGATTAATCAG[A/G]CGCTGCAAATAAACG | 84108 |
rs756104849 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314324 | CTTCAAAATACCATC[A/T]GAAGAAATGAGGAAA | 84108 |
rs756129552 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339805 | CTGTCTGTCTCAAAA[-/AAA]AAAAAACACACACAC | 84108 |
rs756133871 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349150 | CCTCCTGGATTAAAG[C/T]GATTCTCCTGTCTCA | 84108 |
rs756142418 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324711 | GTTGCAGTGAGCCGG[C/G]ACCGCCCCACTGCAC | 84108 |
rs756159930 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311124 | TATAGGAGCAAGCGA[C/G]TATGCCTGGCCAAGA | 84108 |
rs756173699 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310104 | TACAGGCACCCGCCA[-/C]CATGCCCGGCTAATT | 84108 |
rs756191698 | in-del | -/CA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322823 | AGCAAGACTCTGTAT[-/CA]CACACACACACAAAA | 84108 |
rs756217339 | in-del | -/TG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315971 | TCAACAGCTTATATG[-/TG]TGTGTGTGTGTGTGT | 84108 |
rs756282828 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327085 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 84108 |
rs756296447 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339344 | GCAGTAACCTGAGAT[C/T]GCGCCACTGCAGTCC | 84108 |
rs756330029 | snp | A/G | 1.84384e-05 | 0.00303626 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333958 | TTCATTAGCACTGAA[A/G]AATGAGAGCAAAATT | 84108 |
rs756417949 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345055 | ATAAAGACATATCAA[A/G]TTCAGGTGGAATACG | 84108 |
rs756419318 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312530 | GCACCAAGAGCAAAC[A/G]ATGCCCTATGTGTGC | 84108 |
rs756472905 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315963 | TTAGAGCCTCAACAG[C/G]TTATATGTGTGTGTG | 84108 |
rs756486132 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337287 | CTCCTAAGACTCTAT[A/T]TTCTTTGGTATGCAG | 84108 |
rs756651298 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317218 | ATTTCCCCATGTTGG[C/T]CAGCCTGGTCTCAAA | 84108 |
rs756669304 | snp | C/G | 5.13452e-05 | 0.00506656 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351002 | GGCGGAGGCGGCAAG[C/G]CTGCAGCTCCCTCGG | 84108 |
rs756711163 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103344273 | GGGAATGACAAACAC[-/T]TTTTTTTTTTTTTTT | 84108 |
rs756721881 | snp | A/C | 1.83798e-05 | 0.00303143 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350923 | AGCCCCCGTCTCAGA[A/C]AGAGGCGCCGGTCCC | 84108 |
rs756734514 | in-del | -/AGACAG | 1.6971e-05 | 0.00291294 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326642 | AATGGCTACAAAAAC[-/AGACAG]AGACAGATAAAACTA | 84108 |
rs756749618 | in-del | -/TCT | 1.68295e-05 | 0.00290077 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350783 | TCCTCCTCCTCCTCC[-/TCT]TCTTCCTCCTCCAGC | 84108 |
rs756864870 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345188 | ATGCCATAAATTGAG[A/T]TCTTTGGAAAAATAC | 84108 |
rs756878812 | snp | A/C | 0.000150442 | 0.0086717 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351086 | GGGAGAGACACCAGG[A/C]GAGGCGAGGCGGCGG | 84108 |
rs756895748 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329196 | AGGTACCCGCCACCA[A/G]CGTCTGGCTAATTTT | 84108 |
rs756898122 | snp | C/T | 1.64893e-05 | 0.0028713 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303868 | CAGTCCTGCAGAAGC[C/T]TCCTTTGTTTCCCTC | 84108 |
rs756976682 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303744 | ATGCATTCCATCGTT[C/T]CAAGTTGTACTTATA | 84108 |
rs756986229 | snp | A/G | 1.65329e-05 | 0.0028751 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303975 | TCCTGAAAAGGGGAG[A/G]AAAAAAGACGATTTT | 84108 |
rs756994061 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307855 | CTATTGTTAAGTGAC[A/G]CATAACTGCATATAT | 84108 |
rs757012983 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334549 | TTTCATATTTTTCTT[C/T]TAATCATAATCAATG | 84108 |
rs757021368 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348488 | ATTACAGGCATGTGC[C/T]GCCACTCCTGGCTAA | 84108 |
rs757088004 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323160 | GGCTACAAGGTAAAA[A/C]TAAGTCATTTCTAGT | 84108 |
rs757243151 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348851 | CAGGATGCTTTCAAG[A/G]CATTTCAAAAACTGA | 84108 |
rs757265833 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334390 | ACATTTAGGATCTAC[C/T]TTTAGCAATTTTCAA | 84108 |
rs757290578 | in-del | -/GCGGGGCGC | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351234 | GCTCCGGGGCAGGCT[-/GCGGGGCGC]GCGGGGCGCGCGGGC | 84108 |
rs757294430 | snp | C/T | 1.70049e-05 | 0.00291585 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348708 | TGTAATTTATATATT[C/T]TTCTTACCTTATGTT | 84108 |
rs757321089 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349292 | GCCTCAGGTGATCCA[C/T]CCGCCAAGGCCTCCC | 84108 |
rs757359219 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321863 | TTTCAAAACATCATG[A/T]TGTATACAATAAATA | 84108 |
rs757373996 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant | PCGF6 | GRCh38.p7 | 10:103333937 | TACCTTAAAATGTCC[C/T]GTGCCTTCATTAGCA | 84108 |
rs757376835 | in-del | -/TGC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337654 | TCATAAAGCTGGGCA[-/TGC]CGGTGGCTCACGCCT | 84108 |
rs757473906 | snp | A/G | 0.00016735 | 0.00914587 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350896 | AGGGGGCCGGGAGCC[A/G]GAGCAGCCGGGAGCC | 84108 |
rs757488653 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328068 | GAGGTGTAGGAGGTG[A/G]TAAGTAGATGACAGA | 84108 |
rs757509424 | snp | A/G | 1.66857e-05 | 0.00288835 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326629 | CAAACTTCTTTTCCA[A/G]TGGCTACAAAAACAG | 84108 |
rs757557365 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338405 | AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCACC | 84108 |
rs757557974 | snp | A/G | 2.76178e-05 | 0.00371593 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350988 | GCGGGGAGACAGGAG[A/G]CGGAGGCGGCAAGGC | 84108 |
rs757620321 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327355 | ATGGAGAAGGAATGG[C/T]GAGACTAAAAAACAT | 84108 |
rs757648828 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308547 | GGGATTACAGTAGTG[C/T]ACCACCATGCCTGGC | 84108 |
rs757676607 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341028 | TGAGGTCGGGAGATT[A/G]AGACCAGCCTGACTG | 84108 |
rs757686183 | snp | G/T | 1.65029e-05 | 0.00287248 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347408 | ACTTTCCTCTAGATT[G/T]ATCACTAATTTGTAC | 84108 |
rs757724474 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304569 | TGGTCTTGAACTCCT[A/G]ATCTCAGATGATCCT | 84108 |
rs757766957 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312317 | AGAATCCCTTGAACC[C/T]GGGAGGCAGAGGTTG | 84108 |
rs757803177 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339635 | CTCTACTAAAAAATA[C/G]AAAAATTAGCTGGGT | 84108 |
rs757999191 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331481 | CAGGCTAGTCTCGAA[C/T]TCCTGAACTCAGGAG | 84108 |
rs758025044 | snp | A/G | 3.29919e-05 | 0.00406138 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303855 | CTTTGGTGAGATGCA[A/G]TCCTGCAGAAGCCTC | 84108 |
rs758078202 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347220 | TGTAAGTACATTATA[A/G]TATACACCCAAACTT | 84108 |
rs758106888 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328110 | AAAACTAATGCTTAC[C/G]CAGCTCCGATCTGAG | 84108 |
rs758112383 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330606 | CAACCATCACTGCTA[C/T]GTAATTTCAGAATAT | 84108 |
rs758118413 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345329 | GGGGACCACTCCACA[A/G]TGGAAGGCAGACATG | 84108 |
rs758134557 | snp | G/T | 1.65201e-05 | 0.00287398 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348817 | GCTTTTACAAACTGT[G/T]GAAAAAGAATGTTGA | 84108 |
rs758149811 | in-del | -/GCCTCAACGAGAAGTGACTCAT | 6.59826e-05 | 0.00574343 | frameshift-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350745 | GCCGGCCTCCCTCCA[-/GCCTCAACGAGAAGTGACTCAT]GTCCTCCTCCTCCTC | 84108 |
rs758234610 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309383 | CTCACAAAAGTGAAT[A/G]AGGTCTTGTGTGATA | 84108 |
rs758260563 | snp | A/G | 1.65501e-05 | 0.00287659 | stop-gained, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326611 | CTTCTCCTGAAACTC[A/G]AACAAACTTCTTTTC | 84108 |
rs758329276 | in-del | -/A | 1.76359e-05 | 0.00296945 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326485 | TTTCTACAGTGTGCT[-/A]AAGGTAAGCTCACAA | 84108 |
rs758489382 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335910 | AGGCGGAGGTTGCAG[C/T]GAGCTGAGATCGTGT | 84108 |
rs758492833 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347874 | TTGATTTTATTCCCT[C/T]CATAAGAATACGAGT | 84108 |
rs758497413 | snp | A/G | 2.11459e-05 | 0.00325154 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350889 | CCAGCTCAGGGGGCC[A/G]GGAGCCGGAGCAGCC | 84108 |
rs758511555 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334809 | TAGGTATTCATGTGC[A/G]TATGCATGCTTTTCA | 84108 |
rs758563514 | snp | A/C | 1.66313e-05 | 0.00288364 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314319 | TCTTGCTTCAAAATA[A/C]CATCTGAAGAAATGA | 84108 |
rs758636326 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352860 | GGCTGAGTTGGGCGG[A/G]TAACGAGGTCAGGAG | 84108 |
rs758647632 | snp | A/C | 0.000154154 | 0.00877801 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350728 | CTCGTCCTCCGAGTC[A/C]TGCCGGCCTCCCTCC | 84108 |
rs758753513 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321671 | GAGCCGAGATCGCGC[C/G]ACTGTACTCCAGCCT | 84108 |
rs758810902 | in-del | -/TTG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348354 | GTTTTTTTTTTTTTT[-/TTG]GAGATACTCTCATCA | 84108 |
rs758860265 | snp | C/T | 4.94491e-05 | 0.00497213 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345076 | GTGGAATACGAAACA[C/T]TGATTCTAGGACTTT | 84108 |
rs758866975 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337649 | TTAAGATCATAAAGC[C/T]GGGCACGGTGGCTCA | 84108 |
rs758931946 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342468 | TGAACTCCTGACCTC[A/G]GGTAATCTGCCCGCC | 84108 |
rs758932215 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328337 | TTGAGAACTTTCCCA[A/G]CTAAAACTCAGAGTC | 84108 |
rs758970590 | in-del | -/AG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343325 | TGATACAAGTAGCCT[-/AG]AGTTATAAAGAGATG | 84108 |
rs758985193 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341433 | GGCTAATTTTTGTAT[A/T]TTTTGTTTGTTTTTG | 84108 |
rs758991880 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340601 | ATTTCCCCAAAATAA[-/T]TTTTTTTTTTTTTGA | 84108 |
rs759012161 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320796 | CCCGTGGGAATTACT[C/T]GTTCCTGTTAGTAAA | 84108 |
rs759070169 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340956 | TAATTCCTTACAGGC[A/G]CGGTGGCTCACGCCT | 84108 |
rs759091966 | snp | G/T | 1.86353e-05 | 0.00305243 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333874 | AATCTGACTCGAATT[G/T]GTGTGCTACAGAGTC | 84108 |
rs759359678 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328845 | CAACCTCTGCCTTCC[A/G]GATTCAAGCGATTCT | 84108 |
rs759425497 | snp | A/G | 0.000102865 | 0.0071709 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350959 | ACCCGCTGCGGGTGC[A/G]GGGGTGAGGGCGGGC | 84108 |
rs759478488 | snp | A/G | 4.2372e-05 | 0.00460263 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350871 | CCAGGCTGCGCTCCG[A/G]CTCCAGCTCAGGGGG | 84108 |
rs759518623 | snp | A/G/T | 6.60648e-05 | 0.00574706 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347338 | AATTACACTTAAAAT[A/G/T]TAACTACTAGAGTCA | 84108 |
rs759535603 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340724 | CCATCAGCCTCCCTA[A/G]TAGATGGGACTACAG | 84108 |
rs759588542 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339174 | AATCCCATCATTTTG[A/G]GAGGCCAAGGCGGGT | 84108 |
rs759601538 | in-del | -/AC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305293 | TTTTTTTTTTTTGAA[-/AC]ACAGTCTGGCTCTGT | 84108 |
rs759637811 | snp | C/T | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302425 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACAG | 84108 |
rs759687310 | in-del | -/CA | 7.97395e-05 | 0.00631375 | frameshift-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350998 | AGGAGGCGGAGGCGG[-/CA]AGGCTGCAGCTCCCT | 84108 |
rs759714064 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304074 | CACTAAGGTGAAATT[A/C]TTTAATTTAAAGAAA | 84108 |
rs759804389 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349579 | TCCGCCTCCCAGATT[C/T]AAGTGATTCTCCTAC | 84108 |
rs759851688 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321595 | TGGGTGCCTGTAGTC[A/G]CAGCTACTCAGGAGG | 84108 |
rs759856769 | in-del | -/TTT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327984 | CCAGCCAGGGATTTC[-/TTT]TTTAAGTGAAAAATA | 84108 |
rs759861210 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332043 | GTAATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 84108 |
rs759862305 | snp | A/G/T | 3.30503e-05 | 0.00406501 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303973 | CATCCTGAAAAGGGG[A/G/T]GAAAAAAAGACGATT | 84108 |
rs759875700 | in-del | -/TT | 5.78709e-05 | 0.00537886 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348698 | AAAATACAATTGTAA[-/TT]TATATATTCTTCTTA | 84108 |
rs759909443 | in-del | -/AG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320897 | GAAAGTCAGCATAGC[-/AG]GCTCGTGACTGCAGG | 84108 |
rs759913090 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346641 | AAATAAATAAAAATA[C/T]AAAATTAGCCAGGTG | 84108 |
rs759958175 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310434 | TTTGAGTTAAACAAA[C/T]AGGTATTTGTTGAAA | 84108 |
rs760032852 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323948 | TATTATTTTATTTTA[C/T]TATTTTTTTGAGACA | 84108 |
rs760136271 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307518 | GGGTCTTGCTCTGTC[A/G]CACAGGCTGGCATGA | 84108 |
rs760177122 | snp | G/T | 5.25371e-05 | 0.00512502 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326666 | AAAACTATTTTTAGG[G/T]TAAATATACCTGTAC | 84108 |
rs760191299 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322725 | GCTACCTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 84108 |
rs760218812 | snp | A/T | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326557 | CTGGATCAAGACCCA[A/T]TTTTCTTCTGAGGAA | 84108 |
rs760267796 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324411 | AACTATGAGTATATT[C/T]TACTTTTATGTTCAA | 84108 |
rs760271743 | snp | A/G | 4.11041e-05 | 0.00453325 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350853 | AGCGGCCTCTGAAGC[A/G]GCCCAGGCTGCGCTC | 84108 |
rs760272387 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305698 | ATTGCTAAAGCTCTG[-/A]AAACACTTACTCATT | 84108 |
rs760346270 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336653 | GCTGAGGTAGGTGGA[C/T]CGCTTGAGGTCAGGA | 84108 |
rs760435068 | in-del | -/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309197 | GACATGAGATTTGGT[-/G]GGGGGGGGGCATGAT | 84108 |
rs760472848 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335599 | ATCTCTTGATCTCGT[A/G]ATCTGCCCACCTTGG | 84108 |
rs760539430 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315428 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 84108 |
rs760570732 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313816 | CAAAATTGTATTATA[C/G]CACTGGACAGGCGGA | 84108 |
rs760650475 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352493 | AAGAGCTGAATGTGA[C/T]CAGGCACAGTGGCTC | 84108 |
rs760659212 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327506 | TATCTGATCAAGGGA[C/T]TATCATTAATTTAAA | 84108 |
rs760679921 | in-del | -/TA | 0.000124218 | 0.00787996 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333997 | TTTAATACTTTAAGC[-/TA]TATGTTTAATCATAA | 84108 |
rs760793800 | in-del | GAGA/TGAGACAGAGTCTCACTGTCACCCAGGCAGGAGTG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335381 | ATTTTTTTTTTTTTT[lengthTooLong]CAGTGGCGTGATCTC | 84108 |
rs760902287 | snp | A/G | 2.15334e-05 | 0.00328119 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351067 | CGCGACCCCCTCCAT[A/G]GTCGGGAGAGACACC | 84108 |
rs760979550 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346948 | TTTTAAATGAAGTGG[A/T]ATGATTATCATTATT | 84108 |
rs760985653 | snp | C/T | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348788 | TTGCTGTAGTAAAAA[C/T]GTCTTACGATGCAGC | 84108 |
rs760990476 | snp | A/G/T | 6.57662e-05 | 0.00573406 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351118 | AGAGCGCGGGAGTTC[A/G/T]GCCGGCCTCGGACGC | 84108 |
rs761007875 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320595 | AGGAGGCTGAGGCAG[C/G]ATAATCGCTTGAACC | 84108 |
rs761083408 | snp | A/C/G | 3.29507e-05 | 0.00405887 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348929 | TCTGTGATGGTAGTT[A/C/G]CATCTATTAAGTAAC | 84108 |
rs761111831 | in-del | -/TG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347694 | ATGTGCATTGTTTTT[-/TG]TGTGTGTGTGTGTGA | 84108 |
rs761115895 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332234 | AGAACCACAACTATA[G/T]ATTCTGGGTTGCACA | 84108 |
rs761147436 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333118 | AGGAAGACTCCATTT[-/AA]AAAAAAAAAAAAAAA | 84108 |
rs761175184 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303956 | ATGAAGGACAAGCAG[A/G]CCATCCTGAAAAGGG | 84108 |
rs761291548 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347002 | TACGTATGTAACTGG[C/G]TTGGCTTAAGTTATA | 84108 |
rs761300554 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348980 | ATGTATGGGGTCAGC[C/T]CAGAGAGATTAATCA | 84108 |
rs761316215 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331351 | AGTTCTCTGCCCTCC[A/G]GGTTCAAGTGATTCT | 84108 |
rs761333383 | snp | C/T | 9.35585e-05 | 0.0068389 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350811 | CCAGCTCCTCTTCTT[C/T]TTCCAACTCCTCGTC | 84108 |
rs761431386 | in-del | -/TGTGTATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315991 | GTGTGTGTGTGTGTG[-/TGTGTATA]TATATATATATATAT | 84108 |
rs761491102 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309344 | CTCATGAATGGTTTA[C/G]CACAATTTCCCTTTG | 84108 |
rs761497338 | snp | A/G | | | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326584 | GGAATTTTTCTACAT[A/G]TCCAATAGTTGCTTC | 84108 |
rs761500951 | snp | C/T | 6.66856e-05 | 0.00577394 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345141 | GGAACAGCTATTTAA[C/T]AGTCAAACAAAAATG | 84108 |
rs761519604 | snp | C/T | 9.8943e-05 | 0.0070329 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314206 | TTGCTGCATCACCTA[C/T]TGCACGTCGGATTTC | 84108 |
rs761541083 | snp | C/G | 1.68672e-05 | 0.00290402 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350681 | GCCGCTTGGGCCCAG[C/G]GGGGTCGCGCGGGGG | 84108 |
rs761597152 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310580 | GAAAATAATTCTTGG[A/G]AACAGATTGTGAGGA | 84108 |
rs761689400 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336371 | TAAATGTAAACTGTA[A/T]ATCCGTAAATGTACA | 84108 |
rs761707647 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340284 | TACAAAGCTAGAAAA[C/G]AGCAGAGCTACGACT | 84108 |
rs761742573 | snp | A/G | 2.17697e-05 | 0.00329914 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351113 | GCGGGAGAGCGCGGG[A/G]GTTCGGCCGGCCTCG | 84108 |
rs762114227 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306465 | AGCTAAAAGGAAAGG[G/T]CATTGGGAAATGTGC | 84108 |
rs762196431 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342027 | TGCAACGTCCACCTC[C/G]CAATTCAAGCGATTC | 84108 |
rs762250347 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320661 | CACCATTGCACTCCA[C/T]CCTGGGCAAAAACAG | 84108 |
rs762350830 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343698 | ATTAGCCAGGCGTGG[G/T]GGCATGTGCCTGCAG | 84108 |
rs762370984 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333052 | TGAACCCAGACGGCG[A/G]AAGTTGCAGTGAGCC | 84108 |
rs762398145 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318546 | TCAGCAGTTCAAGAC[C/T]AGCCTGGCCAAGATG | 84108 |
rs762438871 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346859 | CGTGACATTACATCA[C/T]CATAAAAACTAACGT | 84108 |
rs762499587 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351481 | CACCTCCATCCAAGA[C/T]TATTTCCCTTAGGAA | 84108 |
rs762625139 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312691 | TCATGGCCGGGCGCG[A/G]TGGCTCACACCTGTA | 84108 |
rs762679800 | in-del | -/GCGGGAGAGC | 2.15743e-05 | 0.00328431 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351097 | AGGCGAGGCGAGGCG[-/GCGGGAGAGC]GCGGGAGAGCGCGGG | 84108 |
rs762751723 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310773 | GTGGTGTGATCATGG[A/G]TCACTGCAACCTCAA | 84108 |
rs762764285 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333119 | GGAAGACTCCATTTA[-/A]AAAAAAAAAAAAAAA | 84108 |
rs762802243 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336854 | CACTCCAGCCTGGGT[A/G]ACAGAGCCAGACTCC | 84108 |
rs762815332 | snp | A/C | 2.245e-05 | 0.0033503 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351043 | GCCTACGCTGCCCGC[A/C]GTCACCACCGCGACC | 84108 |
rs762840265 | snp | A/G | 3.31796e-05 | 0.00407292 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345014 | AAAGGTAAATTTTTA[A/G]GGTACTCACCCAATG | 84108 |
rs762876078 | snp | C/G | 8.14365e-05 | 0.00638057 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350980 | GAGGGCGGGCGGGGA[C/G]ACAGGAGGCGGAGGC | 84108 |
rs762895847 | snp | A/T | 1.9993e-05 | 0.00316166 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333907 | CTTGTGAAATGAATG[A/T]AAAAAAAAGTAAAAT | 84108 |
rs762896275 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338986 | CCTCCTCCAAGTCAA[C/G]CAGAGTCAAGCACTG | 84108 |
rs762932653 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303109 | AATGAATAAGTAATT[A/C]TGTAAACTTCTCAAA | 84108 |
rs762939454 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303057 | CAGTGATGAAATAAT[A/G]AGAAAAATAAACATT | 84108 |
rs762971252 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317614 | GCTCCACCCCAAGCC[C/T]GGGCAACAAAACGAA | 84108 |
rs762985752 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306868 | TAGCACTTTGGGAGG[C/G]CAAGGCAGGTGGATC | 84108 |
rs763061574 | snp | A/G | 3.33606e-05 | 0.00408401 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347482 | ATGGAGAATACCTCA[A/G]AATTCAGAAAAATGC | 84108 |
rs763140046 | in-del | -/ATC | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352280 | TTGCAGTGAGCTAAG[-/ATC]ATCGTGCCACTGCAC | 84108 |
rs763154366 | snp | A/G | | | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350957 | TCACCCGCTGCGGGT[A/G]CAGGGGTGAGGGCGG | 84108 |
rs763173929 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316936 | ACTTGAAAGTAATGA[C/T]ATGAGATCTTGCACA | 84108 |
rs763209635 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330916 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCCAA | 84108 |
rs763300699 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345997 | CAGGAGTTCGGGACC[A/G]GCCTGGCCAACATGG | 84108 |
rs763334245 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308942 | TTTCAGACTTACATG[G/T]GGACATATAGCCTCA | 84108 |
rs763381186 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307445 | ACACAGCAAGACCCT[A/G]TCTCAAAAAAAAAAG | 84108 |
rs763382874 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324051 | TTCATGCAATTCTCC[A/T]GCCTCAGCCTCCCGA | 84108 |
rs763418431 | in-del | -/AGA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326295 | TCGGGAGGCTGACGC[-/AGA]AGAATGGCGTGAACC | 84108 |
rs763460907 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326519 | TACCTATTCTTTTAC[A/G]TATATGTACTGTACC | 84108 |
rs763472004 | snp | A/G | 1.65083e-05 | 0.00287296 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347357 | CTACTAGAGTCAGAG[A/G]TTCTGGGATTCACAA | 84108 |
rs763500798 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309170 | AATCATGATTGTCTT[C/T]TGAAATGTGAGGACA | 84108 |
rs763524223 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318603 | CAAAAAAATTAGCCG[A/G]GCATGGTGGCGGTCG | 84108 |
rs763570187 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322350 | AGGATTACAGGTGTG[C/T]GCTTAATTTTGTGTG | 84108 |
rs763628123 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348828 | CTGTTGAAAAAGAAT[A/G]TTGAAGTCAGGATGC | 84108 |
rs763702962 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307709 | AACTCCTGGGCTCAA[G/T]TGACCCTCCCGCCTC | 84108 |
rs763732740 | snp | A/G | 1.82647e-05 | 0.00302192 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333915 | ATGAATGAAAAAAAA[A/G]GTAAAATACCTTAAA | 84108 |
rs763751536 | in-del | -/ATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333796 | TTTATTCATAAATCT[-/ATA]ATATTATTAAATGTA | 84108 |
rs763890537 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348966 | AAATGGAACACAAGA[G/T]GTATGGGGTCAGCTC | 84108 |
rs763916725 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335614 | GATCTGCCCACCTTG[G/T]CCTCCCAAAGTGCTA | 84108 |
rs763954493 | in-del | -/TCC | 0.00219263 | 0.0330379 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350768 | GAGAAGTGACTCATG[-/TCC]TCCTCCTCCTCCTCT | 84108 |
rs764039809 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334259 | TTTATTAGGGGATAA[C/T]AGACAAATTAAAATT | 84108 |
rs764092821 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352715 | CGAGGTGGAGGTTGC[A/G]GTGAGCCGAGATCAC | 84108 |
rs764115744 | snp | A/C | 3.30344e-05 | 0.004064 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345026 | TTAGGGTACTCACCC[A/C]ATGAACTCCAGTAAT | 84108 |
rs764155753 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314332 | TACCATCTGAAGAAA[G/T]GAGGAAAACAAATCA | 84108 |
rs764234108 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328887 | CTCCCAAGTAGCTGG[C/G]ACTACAGGCGTGTAC | 84108 |
rs764255216 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340901 | AGCCACCATGCCTGA[A/C]CCTCAAAATAATTTT | 84108 |
rs764285503 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341983 | CTCTGTCACCCAGGC[C/T]GGAGTGCAGTGGCAC | 84108 |
rs764380692 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311447 | TGCCCGGCCTCTCTC[-/T]TTTTTTTTTTTTTTT | 84108 |
rs764409769 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321740 | CAATAATAATAATAA[C/T]AATATATTGTAATTG | 84108 |
rs764418443 | snp | A/G | 0.000330688 | 0.0128544 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350892 | GCTCAGGGGGCCGGG[A/G]GCCGGAGCAGCCGGG | 84108 |
rs764561446 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319868 | TGTAGTGCAGTGGTG[C/T]GATCTCGGCTCACCG | 84108 |
rs764588152 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311528 | GGTCATTGCAGCTGC[A/G]ACCTCCCGGGCTTGA | 84108 |
rs764637934 | snp | A/T | 3.30066e-05 | 0.00406229 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347383 | CACAACCATGTAATA[A/T]AAGAAACTTACTTTC | 84108 |
rs764663594 | in-del | -/AATT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334044 | TATTTGAGAAACATC[-/AATT]CATTGTAATTCTAGA | 84108 |
rs764664491 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331403 | GCTGGGATTATAGGT[A/G]CCCACCACCACGCCT | 84108 |
rs764664608 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348247 | GTCCTCAGCAGATAT[C/T]ACAGTGCCTAGTACA | 84108 |
rs764760484 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343493 | CAGTCTGTTTAACAT[C/T]GCTGCACTAAAATGG | 84108 |
rs764772777 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317397 | TCACGGTATTATTAC[C/T]ATATTTTCAACTTTG | 84108 |
rs764789146 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347100 | TTTTTATAAATAAAT[G/T]GGATTACACACAGCA | 84108 |
rs764879760 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310656 | CAGTTGTTCCATTGA[A/G]ACAAAGGAACATAGG | 84108 |
rs764933678 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314854 | CAGCTACTTGGGAGG[C/T]TGAGGCAGGAGAATC | 84108 |
rs764935670 | snp | A/G | 1.65241e-05 | 0.00287433 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348796 | GTAAAAATGTCTTAC[A/G]ATGCAGCTTTTACAA | 84108 |
rs764940684 | snp | C/G | 2.14016e-05 | 0.00327114 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350877 | TGCGCTCCGGCTCCA[C/G]CTCAGGGGGCCGGGA | 84108 |
rs765121004 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324473 | AACAAGAAGAAAATA[C/T]TATGGCTGGGCGCGG | 84108 |
rs765178393 | snp | A/C | 1.6546e-05 | 0.00287624 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326606 | AGTTGCTTCTCCTGA[A/C]ACTCGAACAAACTTC | 84108 |
rs765262655 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302828 | TTATTAAATGTTAGA[A/G]TAAATTTATACACAA | 84108 |
rs765281123 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315601 | CCTGACCTGATGATC[C/T]GCCCACCTCAGCCTC | 84108 |
rs765355208 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316766 | TCAATTCATTTTGCA[A/G]ATACCACTCTGTCAA | 84108 |
rs765514003 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338064 | GCGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 84108 |
rs765546418 | in-del | -/GCTCAGAGAGATTAATCAGGCGCT | 1.64789e-05 | 0.0028704 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348977 | AGATGTATGGGGTCA[-/GCTCAGAGAGATTAATCAGGCGCT]GCTCAGAGAGATTAA | 84108 |
rs765565066 | in-del | -/A | 4.28835e-05 | 0.00463032 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351074 | CCCTCCATGGTCGGG[-/A]GAGACACCAGGCGAG | 84108 |
rs765568876 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350688 | GGGCCCAGCGGGGTC[A/G]CGCGGGGGCTCTAAA | 84108 |
rs765572236 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321615 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATGGCAT | 84108 |
rs765641622 | snp | C/T | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314191 | TATAACCTACCTGCA[C/T]TGCTGCATCACCTAT | 84108 |
rs765654686 | snp | A/T | 8.58583e-05 | 0.00655147 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345172 | TTAATTAAGAATAAA[A/T]ATGCCATAAATTGAG | 84108 |
rs765736389 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333206 | TGTATAATATGCTTC[A/G]CCCAGAGAATTACCT | 84108 |
rs765746959 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326572 | TTTTTCTTCTGAGGA[A/G]TTTTTCTACATGTCC | 84108 |
rs765757198 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337211 | GAGTGGGATACTACT[C/T]TCGGGTTTACTAAAC | 84108 |
rs765768542 | in-del | -/AAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339802 | AATTCTGTCTGTCTC[-/AAA]AAAAAAACACACACA | 84108 |
rs765860898 | snp | C/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351582 | GTGAAAATCTAATCA[C/G]TACTCAAAGATCATC | 84108 |
rs765861837 | in-del | -/TA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315995 | GTGTGTGTGTGTGTG[-/TA]TATATATATATATAT | 84108 |
rs765929531 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332371 | TGCAGCCTCAATCTC[C/T]TAGGCTCACGTGATC | 84108 |
rs766035234 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347246 | AACTTACCAGGTTTA[C/G]GTACTTCTAGACCTC | 84108 |
rs766080097 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310881 | TTAATTTTTGTATTT[C/T]GTAGAGATGGGGTTT | 84108 |
rs766132902 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326896 | ATTTTAATGTTTCAT[C/T]GAAAAAACAAAACTC | 84108 |
rs766298294 | snp | A/C | 0.000142076 | 0.0084272 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350864 | AAGCGGCCCAGGCTG[A/C]GCTCCGGCTCCAGCT | 84108 |
rs766318390 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327542 | GTAGTATCATTATTA[C/T]GTTGCCATAAAAGGA | 84108 |
rs766334588 | snp | C/T | 0.000148345 | 0.00861106 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314235 | TCCCTTAGAGTTTGA[C/T]ACTGCTCCAACAGGT | 84108 |
rs766334745 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339134 | TATGTAATAAAAAGG[A/G]TGAGGTGCAGTGGCT | 84108 |
rs766351223 | snp | A/G | 0.000116638 | 0.00763581 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350695 | GCGGGGTCGCGCGGG[A/G]GCTCTAAATACCTCC | 84108 |
rs766383999 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337006 | TATTTGGTAACCCTT[C/T]AAAGATTTTAAACTA | 84108 |
rs766428726 | in-del | -/AG | 1.65121e-05 | 0.00287329 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347353 | GTAACTACTAGAGTC[-/AG]AGATTCTGGGATTCA | 84108 |
rs766602941 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317780 | TTTTTTTTTGAGACA[G/T]AGTTTCGCTCTTGTT | 84108 |
rs766628831 | in-del | -/CCTCCC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348424 | CTCCTGCAACCTCTG[-/CCTCCC]AGGTTCAAGCGATTC | 84108 |
rs766701916 | in-del | -/GCA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306089 | ACCAAGGCTGCATCC[-/GCA]AGCAATCCACCTTTT | 84108 |
rs766718552 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347026 | AGTTATACACCTCAT[A/G]AAGTGGCAGGGCTAG | 84108 |
rs766725590 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316950 | ATATGAGATCTTGCA[C/T]AGAGAACTTAGATCC | 84108 |
rs766729438 | snp | A/C | 1.67959e-05 | 0.00289787 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345149 | TATTTAATAGTCAAA[A/C]AAAAATGTTAATTAA | 84108 |
rs766781705 | snp | C/G | 2.1476e-05 | 0.00327682 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351071 | ACCCCCTCCATGGTC[C/G]GGAGAGACACCAGGC | 84108 |
rs766823431 | snp | C/G | 1.64863e-05 | 0.00287104 | splice-acceptor-variant | PCGF6 | GRCh38.p7 | 10:103303962 | GACAAGCAGACCATC[C/G]TGAAAAGGGGAGAAA | 84108 |
rs766826631 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328319 | CTGTACAGTAGTTTG[-/T]TCTTGAGAACTTTCC | 84108 |
rs766872682 | snp | A/G | 0.000138591 | 0.00832322 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350683 | CGCTTGGGCCCAGCG[A/G]GGTCGCGCGGGGGCT | 84108 |
rs766889295 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307465 | AAAAAAAAAAGAAAG[A/T]AAGTTTGTTTATTTC | 84108 |
rs766934125 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322552 | CAGGCTGGGCACAGT[A/G]GCTCATGCCTGTAAT | 84108 |
rs766983162 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335568 | GGGTTTCACCATGTT[A/G]TTCAGGATGGCCTCG | 84108 |
rs767071686 | snp | C/T | 4.97244e-05 | 0.00498596 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303984 | GGGGAGAAAAAAAGA[C/T]GATTTTGCAGTTCTT | 84108 |
rs767229576 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333442 | ACCTTTTCCTGATGA[C/T]TCACATTATAGTAGT | 84108 |
rs767260792 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313676 | GTGTTGGGCCCCATT[A/C]GCAGCTATCCTGGGC | 84108 |
rs767276405 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334635 | TATGCTTCCTATTGC[-/T]TTTTTTTGCAGAATA | 84108 |
rs767284797 | snp | A/G | 1.66941e-05 | 0.00288908 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345143 | AACAGCTATTTAATA[A/G]TCAAACAAAAATGTT | 84108 |
rs767300911 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314208 | GCTGCATCACCTATT[A/G]CACGTCGGATTTCCC | 84108 |
rs767320097 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338065 | CGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 84108 |
rs767484912 | snp | C/T | | | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348947 | TCTATTAAGTAACCT[C/T]TGCAAATGGAACACA | 84108 |
rs767516789 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327062 | GAGGCAGAGGCAGGC[A/G]GATTGTTTGAGGTCA | 84108 |
rs767572606 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314955 | GCGAGACTCTGTCAT[-/AA]AAAAAAAAAAAAAAA | 84108 |
rs767573141 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324588 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 84108 |
rs767606115 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326993 | AATACCAAATGTCTG[A/C]AACAACTTTGAGGCC | 84108 |
rs767629086 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345049 | CCAGTAATAAAGACA[C/T]ATCAAGTTCAGGTGG | 84108 |
rs767639784 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339199 | GCGGGTAGATTGCTT[C/G]AGCCAGGAGTTCAAG | 84108 |
rs767666414 | snp | A/C | 2.79936e-05 | 0.00374112 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350999 | GGAGGCGGAGGCGGC[A/C]AGGCTGCAGCTCCCT | 84108 |
rs767801267 | snp | A/G | 2.3088e-05 | 0.00339757 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348670 | ACTTCAAGCTTTCAG[A/G]AAAAGTATATTTAAA | 84108 |
rs767809961 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304460 | ATTCTCCTGCCTCAG[C/T]CTACCGAGTAGCTGC | 84108 |
rs767902294 | snp | C/G | 0.000151556 | 0.00870374 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351060 | TCACCACCGCGACCC[C/G]CTCCATGGTCGGGAG | 84108 |
rs767912001 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330272 | GTGGAGACAGGGTTT[-/C]CCCATGTTGCCGAGG | 84108 |
rs767929883 | snp | A/T | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348780 | GACATCTGTTGCTGT[A/T]GTAAAAATGTCTTAC | 84108 |
rs767942212 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330029 | CGCCTCAGCCTCCCA[A/C]AGTGCTGGGATTACA | 84108 |
rs767974461 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331201 | ATTATATGAAAATAC[A/G]TTTTGTTTATCCATT | 84108 |
rs768011993 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343912 | AACATACCCTAAGAC[C/T]CAGTAAATCTACACT | 84108 |
rs768028512 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346891 | TGAACAGTTACTGTG[G/T]GCCAGGCACTGTTTT | 84108 |
rs768116287 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349194 | CTGGGATTACAGGCG[C/G]GCACAACCACGCCTG | 84108 |
rs768247280 | snp | C/G | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302752 | ACCCAGCCCTGGCCT[C/G]GTTATTTTTTTTTTA | 84108 |
rs768269986 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326123 | TTAACAATGTCCAGG[C/T]GCGGTGGCTCATGCC | 84108 |
rs768270811 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347251 | ACCAGGTTTAGGTAC[C/T]TCTAGACCTCTTTCT | 84108 |
rs768275749 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352320 | GGCTACAGAGTGAGA[C/T]TCCATCTCAAAACAA | 84108 |
rs768325110 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338758 | CTGTAATCCCAGCTA[C/G]TTGGGAGGCTAAGGC | 84108 |
rs768337075 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322977 | CATAGAATAATCTGT[A/G]TTCTAGAGAGGGTCC | 84108 |
rs768421648 | snp | A/C/G | 2.53152e-05 | 0.00355768 | intron-variant | PCGF6 | GRCh38.p7 | 10:103350680 | CGCCGCTTGGGCCCA[A/C/G]CGGGGTCGCGCGGGG | 84108 |
rs768431972 | snp | G/T | 2.23746e-05 | 0.00334467 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351044 | CCTACGCTGCCCGCC[G/T]TCACCACCGCGACCC | 84108 |
rs768448211 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336699 | GGCCAACATGGTAAA[C/T]TTATGTCTCCAATAA | 84108 |
rs768449004 | snp | A/G | 1.65247e-05 | 0.00287438 | stop-gained, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345124 | TTGAAGGGACTGGCT[A/G]TGGAACAGCTATTTA | 84108 |
rs768534171 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330707 | CCAAGGCGGGTGGAT[C/G]ACCTGAGGTCAGAAG | 84108 |
rs768538328 | in-del | -/AAAAAAAAAA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343832 | GTAAAACTCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 84108 |
rs768542102 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316379 | GAAAGAACAGTAATA[A/G]CAGCTGCATTTAAAT | 84108 |
rs768666697 | snp | C/T | 9.91998e-05 | 0.00704202 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348769 | ATTGCATTTTGGACA[C/T]CTGTTGCTGTAGTAA | 84108 |
rs768698461 | in-del | -/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305494 | CAGGCTGGTCCCGAA[-/C]TCCTGACCTCAGGTG | 84108 |
rs768793721 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312758 | CTGAGGTCGGGAGTT[-/A]AGAGACCAGCCTGAC | 84108 |
rs768896693 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320619 | TTGAACCCAGGAGGC[A/G]GAGGTTGCGGTGAGC | 84108 |
rs768900276 | snp | A/C | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303928 | TCTTCAGAGGAGAAA[A/C]CACAAGACCATAATG | 84108 |
rs768934906 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321995 | CCGCTTCCTAGGTTC[A/G]AGGGATCCTCCCACC | 84108 |
rs769055045 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333022 | AGGAGGCTGAGGCTG[G/T]GTTCAAGAATTGCTT | 84108 |
rs769177933 | snp | C/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351428 | AATAATAATCATTTC[C/T]ACTTGAGTACCAATT | 84108 |
rs769201537 | snp | A/C | 3.4475e-05 | 0.00415167 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326654 | AAACAGACAGATAAA[A/C]CTATTTTTAGGTTAA | 84108 |
rs769240846 | snp | A/G | 1.6743e-05 | 0.0028933 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345002 | TTCTTTAAGTTAAAA[A/G]GTAAATTTTTAGGGT | 84108 |
rs769287642 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315229 | GTCACTCTGTCACTC[A/T]GGCTGGAGTGCAGTG | 84108 |
rs769329537 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328461 | ACAGCATACAGAATA[A/G]GTGTTGAGTGTAGGC | 84108 |
rs769350284 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340500 | CCCATCACACGTTTA[C/T]CATCGTTGTATTACA | 84108 |
rs769376995 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103318472 | AAAAAAGTGCGGGTG[C/T]GGTGGCGCACACCTG | 84108 |
rs769406543 | in-del | -/A | 0.0138882 | 0.0821658 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333906 | CTTGTGAAATGAATG[-/A]AAAAAAAAAGTAAAA | 84108 |
rs769414203 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312284 | TATAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 84108 |
rs769438818 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325854 | AGACCGCATCTCTTA[-/AA]AAAAAAAAAAAAAAA | 84108 |
rs769467663 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327538 | AACTGTAGTATCATT[A/G]TTATGTTGCCATAAA | 84108 |
rs769470053 | snp | A/T | 1.64898e-05 | 0.00287135 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345098 | TAGGACTTTTTTAGA[A/T]CTTCCTTTGCTTGAA | 84108 |
rs769562635 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338822 | GCAGTGAGCCGAGAT[C/G]ACACCACTACACTCC | 84108 |
rs769624721 | snp | A/G | 1.64784e-05 | 0.00287035 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303887 | TTTGTTTCCCTCCTC[A/G]TAATGTGCCTAGAAT | 84108 |
rs769628856 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317543 | TAATCTTAGCTGCTT[A/G]GGAAGCTGAGGCAGG | 84108 |
rs769721696 | snp | C/G | 2.40503e-05 | 0.00346765 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351026 | CCCTCGGTTTTGGCA[C/G]CGCCTACGCTGCCCG | 84108 |
rs769727139 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319431 | GCTGGGATTACAAGC[A/G]TGAGCCACCGGACCT | 84108 |
rs769866330 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331859 | GTGCAGTGGTGAGGT[C/G]TTGGCTCACTGCAAG | 84108 |
rs769878283 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308402 | AGGAGATTTTAGAGC[-/T]TTTTTTTTTTTTCTG | 84108 |
rs769936386 | snp | A/G | 1.66454e-05 | 0.00288486 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347471 | AAAAGGAAAGGATGG[A/G]GAATACCTCAGAATT | 84108 |
rs769986019 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330801 | GGGCGTGGTGGGGCG[A/C]ACCTGTAATACCAGC | 84108 |
rs769990046 | in-del | -/TT | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351644 | TTGAATTCGAAAAGC[-/TT]TTTTTTTTTTTTTTT | 84108 |
rs770003545 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308717 | TCTCTACAAAAAAAT[A/G]CAAAAATTAGCCAGG | 84108 |
rs770039380 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345846 | AAAAAAAAAAGAAAC[C/T]GAGGCTTAGAGAGAG | 84108 |
rs770094284 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336127 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 84108 |
rs770126835 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323721 | CCTCAGCCTCCTGAG[C/T]AGCCAGGACTACAGG | 84108 |
rs770181581 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322161 | TCGGCCTCTGAAAGT[A/G]CTGGGATTACAGGGT | 84108 |
rs770190695 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324040 | CGTCTCCCAGGTTCA[C/T]GCAATTCTCCAGCCT | 84108 |
rs770365835 | snp | C/G | 0.000114857 | 0.00757728 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350953 | CTCCTCACCCGCTGC[C/G]GGTGCAGGGGTGAGG | 84108 |
rs770395488 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325932 | GGAGGCTGAGACAGG[A/T]GGGAGGACCACCCAA | 84108 |
rs770402263 | snp | A/C | 1.68721e-05 | 0.00290444 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326636 | CTTTTCCAATGGCTA[A/C]AAAAACAGACAGATA | 84108 |
rs770444791 | in-del | -/ATGT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304327 | GTATGTATCATATGC[-/ATGT]ATGTATGTATGTATA | 84108 |
rs770446244 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315270 | AGCTCATTGCAGCCT[C/G]AAACTCCTAGGCTGA | 84108 |
rs770457009 | snp | A/C | 0.000123206 | 0.00784779 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326496 | TGCTAAAGGTAAGCT[A/C]ACAACTTTACCTATT | 84108 |
rs770464250 | snp | C/T | 1.70093e-05 | 0.00291622 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344973 | ACAATGATTTCCTAT[C/T]AGGACTTTTAACATT | 84108 |
rs770501089 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328573 | TGTGTCTCTATTTGT[A/C]AAATAGATAAAAATA | 84108 |
rs770508818 | in-del | -/CA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349554 | GGCAAGATCTCGGCT[-/CA]CTGCAACCTCCGCCT | 84108 |
rs770598636 | snp | C/T | 2.471e-05 | 0.00351488 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351015 | AGGCTGCAGCTCCCT[C/T]GGTTTTGGCAGCGCC | 84108 |
rs770644881 | snp | A/T | 7.06327e-05 | 0.00594234 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326670 | CTATTTTTAGGTTAA[A/T]TATACCTGTACATGC | 84108 |
rs770740913 | in-del | -/TCT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310628 | CTTATAATATTCACA[-/TCT]TCTTCTTTTGAGCAG | 84108 |
rs770810993 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314363 | ACATAAATTGTTTCC[A/C]AACTAGATTTTGTAA | 84108 |
rs770855461 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305636 | CAACTACTACAACGC[A/G]TCGCAGATCTGTTCA | 84108 |
rs770866148 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317916 | GGCATGCATCACCAC[C/G]CATGGCTAATTTTGT | 84108 |
rs771000914 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320440 | ACTTGTAATCCCAGC[A/T]CTTTGGGAGGCCGAG | 84108 |
rs771121683 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332852 | GGGCGCAGTGGCTCA[C/T]ACCTGTAATCCCAGC | 84108 |
rs771125408 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319483 | CTACTAAGTTCTTTT[C/T]TTCTGTGTCTGGCAA | 84108 |
rs771134605 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346320 | AACATGGAGAAACCC[A/C]GTCTCTATTAAAAAT | 84108 |
rs771267058 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310111 | ACCCGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 84108 |
rs771299363 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331009 | TCTGACAACCACTAA[C/T]CTGCTTTCTGCTCCT | 84108 |
rs771314642 | snp | A/T | 6.19675e-05 | 0.00556596 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350763 | TCAACGAGAAGTGAC[A/T]CATGTCCTCCTCCTC | 84108 |
rs771355613 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338295 | ATGCCTCTAATCCCA[A/G]CACTTTAGGAGGCCA | 84108 |
rs771391806 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309001 | ATGAGAGTTATTTGC[C/T]CAATGTTTATACCCC | 84108 |
rs771498453 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325554 | CGCCTGGCCGAGCTT[A/G]CTTGTTATACTTGAA | 84108 |
rs771504736 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337802 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 84108 |
rs771572556 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323883 | AGCCACTACACATGG[C/T]CAGTCACTGTTTTAA | 84108 |
rs771592448 | snp | A/C | 3.63603e-05 | 0.00426367 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350929 | CGTCTCAGACAGAGG[A/C]GCCGGTCCCTCCTCA | 84108 |
rs771781093 | snp | A/G | 0.000121426 | 0.00779089 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350839 | GTCCTCGTCCTCGAA[A/G]CGGCCTCTGAAGCGG | 84108 |
rs771889710 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315340 | AGAGGTGTGCACCAC[C/T]ACATCTGGCAAATTG | 84108 |
rs771942860 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342968 | GACGGAGTCTCTGCC[A/G]CCCAGGCTGGAGTGC | 84108 |
rs772097703 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349016 | TGCAAATAAACGGAA[A/G]CAGTTTTAAAATACA | 84108 |
rs772112687 | snp | A/G | 1.65389e-05 | 0.00287562 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347449 | GTAACTGTCGGTCCA[A/G]CCTAATAAAAGGAAA | 84108 |
rs772158847 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349054 | GCCTTTTACAAATTC[-/T]TTTTTTTTTTTTGAG | 84108 |
rs772165800 | snp | C/T | 1.65321e-05 | 0.00287502 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347293 | ATGCATTTGCTTTTT[C/T]TCTCCTAAAAAATGA | 84108 |
rs772195361 | snp | C/T | 6.59011e-05 | 0.00573988 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303942 | ACCACAAGACCATAA[C/T]GAAGGACAAGCAGAC | 84108 |
rs772204654 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307120 | AAAACAAACAAAAAA[C/T]AAAAAATAAAAAAAT | 84108 |
rs772228744 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319545 | GTTAAATCATTCACT[G/T]TTGTGTTATCTCCAC | 84108 |
rs772231430 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317270 | CCCACCTCAGGCTCC[C/G]AAAGTGCTGGGATTA | 84108 |
rs772257970 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305722 | ACTCATTTAATGAAA[A/G]CCTAAAATATATATG | 84108 |
rs772258968 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331942 | GGACAACAGGCACGC[A/G]CCACCGCGCCTGGCT | 84108 |
rs772298227 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320547 | AGAAAATTAGCCAGG[C/T]ATGGTGGCGCATGCC | 84108 |
rs772355689 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332975 | CAAAATTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 84108 |
rs772396607 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329125 | GCTCACTGCAACCTC[C/T]GCCTCTTGGATTCAA | 84108 |
rs772411616 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311907 | TAGCCTCGCCAACAC[A/G]GTGAAACCTCATCTG | 84108 |
rs772416621 | snp | C/T | 2.19802e-05 | 0.00331506 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351116 | GGAGAGCGCGGGAGT[C/T]CGGCCGGCCTCGGAC | 84108 |
rs772425460 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350438 | TGTCTCAAAATAATT[A/G]TAATTATTAACAGAA | 84108 |
rs772475992 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103347869 | TTAATTTGATTTTAT[C/T]CCCTTCATAAGAATA | 84108 |
rs772519622 | in-del | -/CA | 1.8973e-05 | 0.00307996 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333977 | GAGAGCAAAATTAAT[-/CA]ATATTTAATACTTTA | 84108 |
rs772600171 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348909 | GCTTACAGGTATGAA[A/G]ACATTCTGTGATGGT | 84108 |
rs772712403 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327496 | AGTACATGAATATCT[C/G]ATCAAGGGATTATCA | 84108 |
rs772734429 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325852 | AAGACCGCATCTCTT[-/A]AAAAAAAAAAAAAAA | 84108 |
rs772787964 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315239 | CACTCAGGCTGGAGT[A/G]CAGTGGCCCAATCAT | 84108 |
rs772805762 | snp | C/T | 5.05404e-05 | 0.00502669 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326529 | TTTACATATATGTAC[C/T]GTACCTGACAAGCTG | 84108 |
rs772842390 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326686 | TATACCTGTACATGC[A/G]TGACGTATGTGTATA | 84108 |
rs772891758 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338860 | ACAAGAAGAGTGAAA[C/T]TCCGTCTCAAAAGAA | 84108 |
rs772898787 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327624 | TATACTATTCTGCCT[A/T]CTTTTGTATAAGTTT | 84108 |
rs772921229 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312684 | ACAATTTTCATGGCC[A/G]GGCGCGGTGGCTCAC | 84108 |
rs772974671 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310691 | TATACCAAAAAAAAA[A/T]ATATTATTTCTTTTC | 84108 |
rs772983688 | snp | C/T | 0.000144854 | 0.00850917 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350937 | ACAGAGGCGCCGGTC[C/T]CTCCTCACCCGCTGC | 84108 |
rs773091034 | snp | A/G | 1.65326e-05 | 0.00287507 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347300 | TGCTTTTTTTCTCCT[A/G]AAAAATGATAAAACA | 84108 |
rs773145991 | snp | C/G/T | 3.34517e-05 | 0.00408961 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345145 | CAGCTATTTAATAGT[C/G/T]AAACAAAAATGTTAA | 84108 |
rs773209293 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310652 | TGAGCAGTTGTTCCA[C/T]TGAGACAAAGGAACA | 84108 |
rs773231678 | snp | C/T | 4.98691e-05 | 0.0049932 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314164 | AACTTATCTGTTAGA[C/T]ATGGGTATGTCTATA | 84108 |
rs773430519 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330845 | GAGGCAGGAGAACTG[C/T]TTGAACCTGGGAGGC | 84108 |
rs773503879 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308808 | AGCCTGGGAGGCAGA[A/G]GTTGCAGTGAGCCTA | 84108 |
rs773513645 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331946 | AACAGGCACGCGCCA[C/T]CGCGCCTGGCTAATT | 84108 |
rs773553407 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345987 | CACTTCAGGTCAGGA[A/G]TTCGGGACCAGCCTG | 84108 |
rs773606304 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343605 | GCACTTTGGGAGGCT[C/G]AGGTGGGTGGATCAC | 84108 |
rs773625016 | snp | A/C | 2.19957e-05 | 0.00331623 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351117 | GAGAGCGCGGGAGTT[A/C]GGCCGGCCTCGGACG | 84108 |
rs773628751 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307330 | GGTAACCAGCCACAC[A/G]GGAGGCTGAGGCAGG | 84108 |
rs773630626 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323873 | TACAGGCATGAGCCA[C/T]TACACATGGCCAGTC | 84108 |
rs773644670 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346929 | TATATTACTCAATAT[A/G]TTTTTTTAAATGAAG | 84108 |
rs773655928 | snp | A/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348916 | GGTATGAAGACATTC[A/T]GTGATGGTAGTTGCA | 84108 |
rs773694691 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335513 | GACTACAGGCACCCA[C/T]CACCACACCCGGCTA | 84108 |
rs773699775 | in-del | -/A | 2.00515e-05 | 0.00316629 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333992 | AATATTTAATACTTT[-/A]AAGCTATATGTTTAA | 84108 |
rs773892225 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329062 | TTTTAACTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 84108 |
rs773924534 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103333274 | TGTGTTCATAAAACA[A/G]TACAGTATATCCAAC | 84108 |
rs773969968 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323202 | ATGAGATATAACCAG[A/G]ATATGTCAAGCTCAG | 84108 |
rs773997289 | snp | A/G | 1.65127e-05 | 0.00287334 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345027 | TAGGGTACTCACCCA[A/G]TGAACTCCAGTAATA | 84108 |
rs773998619 | snp | A/C/G | 8.24246e-05 | 0.00641915 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348987 | GGGTCAGCTCAGAGA[A/C/G]ATTAATCAGGCGCTG | 84108 |
rs774018104 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327740 | AGTGCAATGGTGCAA[C/T]CTCAGCTCACTGCAA | 84108 |
rs774046455 | snp | A/G | 2.18787e-05 | 0.0033074 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351053 | CCCGCCGTCACCACC[A/G]CGACCCCCTCCATGG | 84108 |
rs774066829 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338066 | GAGACTCCGTCTCAA[-/A]AAAAAAAAAAAAAAA | 84108 |
rs774083266 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336361 | TATCAATATATAAAT[A/G]TAAACTGTAAATCCG | 84108 |
rs774150055 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328632 | ATAAGTTAATGTATG[G/T]AAATAATAAAAATAC | 84108 |
rs774266896 | snp | C/T | 2.1755e-05 | 0.00329803 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351107 | GAGGCGGCGGGAGAG[C/T]GCGGGAGTTCGGCCG | 84108 |
rs774277983 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319038 | GAAAGTAGTCTTATT[-/A]AAAGGAGAAAAAGTC | 84108 |
rs774288846 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340050 | GGCATGGTGGTATGC[A/G]CCTGTAATCCCAGCT | 84108 |
rs774363786 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348895 | AATGTGATCGGTATG[C/T]TTACAGGTATGAAGA | 84108 |
rs774413592 | snp | A/G | 4.96553e-05 | 0.00498249 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345129 | GGGACTGGCTGTGGA[A/G]CAGCTATTTAATAGT | 84108 |
rs774518268 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103304048 | TGGCTTACTTTTTTT[A/T]AATAATCTAACACTA | 84108 |
rs774656906 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335367 | ACTCCAAAGCACTCA[-/T]TTTTTTTTTTTTTTG | 84108 |
rs774695987 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317915 | AGGCATGCATCACCA[C/T]GCATGGCTAATTTTG | 84108 |
rs774745603 | in-del | -/AA | 2.01546e-05 | 0.00317441 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333907 | CTTGTGAAATGAATG[-/AA]AAAAAAAGTAAAATA | 84108 |
rs774817904 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324129 | TTTTTAGTAGAGACA[C/G]GGTTTCACCGTGTTG | 84108 |
rs774891099 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325965 | CCAGGAAAACCTCAA[G/T]GTTGTAGTGAGCCAT | 84108 |
rs774988597 | snp | A/C | 1.66999e-05 | 0.00288958 | intron-variant | PCGF6 | GRCh38.p7 | 10:103345005 | TTTAAGTTAAAAGGT[A/C]AATTTTTAGGGTACT | 84108 |
rs775008047 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320255 | AATATCAAACAAAGC[A/G]AAATACAATAAGACA | 84108 |
rs775145518 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336492 | CTCTGTAGAATACTT[C/G]GTACATGGGCATCAG | 84108 |
rs775207678 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316139 | AATGTCACCTCTGCT[C/T]CCTCTTTCTCCTTTT | 84108 |
rs775316303 | in-del | -/TT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309954 | GAGACCTTGTCTTTC[-/TT]TTTTTTTTTTTTTTG | 84108 |
rs775334541 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315399 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 84108 |
rs775334682 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329284 | ACCTCAGGTGATCCA[A/C]CCGCCTTGGCCTCCC | 84108 |
rs775383934 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328877 | TTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 84108 |
rs775448155 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340841 | CTCCTGGACTCCAGC[A/G]GTTCTCCTACCTCTG | 84108 |
rs775523475 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335965 | GCGAGACTCCATCTC[-/A]AAAAAAATAAAGGAA | 84108 |
rs775546184 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320555 | AGCCAGGCATGGTGG[C/T]GCATGCCTGTAATCC | 84108 |
rs775558277 | snp | C/T | 2.2872e-05 | 0.00338164 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351039 | CAGCGCCTACGCTGC[C/T]CGCCGTCACCACCGC | 84108 |
rs775589676 | in-del | -/AATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103313986 | AGAATAATTATGAAG[-/AATA]AATAAGCTAATCTAC | 84108 |
rs775610614 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306849 | GGGCTCATGCCTATA[A/G]TCCTAGCACTTTGGG | 84108 |
rs775621402 | snp | A/T | 3.3284e-05 | 0.00407932 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347474 | AGGAAAGGATGGAGA[A/T]TACCTCAGAATTCAG | 84108 |
rs775642285 | snp | A/G | 1.66668e-05 | 0.00288672 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103348727 | TTACCTTATGTTATA[A/G]AGAGGTTGTGTCTGA | 84108 |
rs775653037 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307148 | AATAAAAAAATTTAA[A/G]CACAAGGCCAGGTGT | 84108 |
rs775771605 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305755 | TTACTTCTGCCTTAA[A/G]GAATGCCCTCAGCTG | 84108 |
rs775800450 | in-del | -/AGGCG | 0.000107254 | 0.00732225 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351082 | GTCGGGAGAGACACC[-/AGGCG]AGGCGAGGCGAGGCG | 84108 |
rs775839692 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103350529 | AAAGACCCAGGCCGG[A/G]CCGGAGGCCTGTCGG | 84108 |
rs775946846 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310587 | ATTCTTGGGAACAGA[C/T]TGTGAGGACAAGAAA | 84108 |
rs775949616 | snp | C/G | 1.74087e-05 | 0.00295026 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326507 | AGCTCACAACTTTAC[C/G]TATTCTTTTACATAT | 84108 |
rs776004397 | snp | A/C | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103314197 | CTACCTGCATTGCTG[A/C]ATCACCTATTGCACG | 84108 |
rs776067926 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103324043 | CTCCCAGGTTCATGC[A/C]ATTCTCCAGCCTCAG | 84108 |
rs776093659 | in-del | -/AAATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325147 | TCAAAATAATAAATA[-/AAATA]AAATAAAATAAAATA | 84108 |
rs776119730 | snp | A/G | 9.69321e-05 | 0.00696108 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350955 | CCTCACCCGCTGCGG[A/G]TGCAGGGGTGAGGGC | 84108 |
rs776123223 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326246 | AAAAAAAAATCAGCC[A/G]GGTGCAGTGGCAGGT | 84108 |
rs776175666 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345796 | TCATGCCACTGCACT[C/T]CAGCCTAGGTGACAA | 84108 |
rs776298773 | snp | A/C/G | 3.32332e-05 | 0.00407624 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347470 | TAAAAGGAAAGGATG[A/C/G]AGAATACCTCAGAAT | 84108 |
rs776355047 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317457 | AAAAGCTTTACAAAA[A/G]TCTTTACAAAATAAT | 84108 |
rs776383200 | snp | C/G | 3.40449e-05 | 0.00412568 | intron-variant | PCGF6 | GRCh38.p7 | 10:103344978 | GATTTCCTATTAGGA[C/G]TTTTAACATTCTTTA | 84108 |
rs776406512 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330745 | CCAGCCTGGCTAACA[C/T]GGTGAAACCCCGTTT | 84108 |
rs776531375 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336703 | AACATGGTAAACTTA[C/T]GTCTCCAATAAAAAT | 84108 |
rs776581484 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328946 | GAGACAGGGTTTCAC[A/T]GTGTTAGCCAGGATG | 84108 |
rs776607617 | snp | C/G | 0.000145381 | 0.00852462 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350868 | GGCCCAGGCTGCGCT[C/G]CGGCTCCAGCTCAGG | 84108 |
rs776730175 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332081 | ACAAGCTTGAGCCAC[C/T]GCGCCCGGCCTAATA | 84108 |
rs776782766 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103343224 | TGAGCCACCGCGCCC[A/G]GCCTTAGGGGTTCTT | 84108 |
rs776911757 | in-del | -/AGGCGC | 2.80281e-05 | 0.00374343 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350985 | GGGCGGGGAGACAGG[-/AGGCGC]AGGCGGAGGCGGCAA | 84108 |
rs776931057 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322014 | GATCCTCCCACCTCA[A/G]CTTCCCAAGTAGCTG | 84108 |
rs776975731 | snp | C/T | 1.65165e-05 | 0.00287367 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347337 | AAATTACACTTAAAA[C/T]GTAACTACTAGAGTC | 84108 |
rs777004315 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103306279 | ATTTTTGTATTTTGA[A/G]TAGAGATGGGGTTTC | 84108 |
rs777009485 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323947 | TTATTATTTTATTTT[A/T]CTATTTTTTTGAGAC | 84108 |
rs777022098 | in-del | -/AA | 3.30077e-05 | 0.00406236 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347387 | ACCATGTAATAAAAG[-/AA]ACTTACTTTCCTCTA | 84108 |
rs777039993 | snp | C/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351476 | CAAATCACCTCCATC[C/G]AAGATTATTTCCCTT | 84108 |
rs777074820 | snp | A/C/T | 4.95916e-05 | 0.00497933 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314183 | GGTATGTCTATAACC[A/C/T]ACCTGCATTGCTGCA | 84108 |
rs777120557 | in-del | -/CT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349514 | GAGAGGGAGTCTGCC[-/CT]TGTCGCCCAGACTGG | 84108 |
rs777147422 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321539 | TAAATGGTGAAACCC[A/T]GTCTCTACTAAAAAT | 84108 |
rs777211644 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328494 | TCCAGGCAGACACCT[G/T]GGCTCAAACCCTGGT | 84108 |
rs777268829 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341533 | CAACCTCCGCCTCTC[A/G]GATTCAAGTGATTCT | 84108 |
rs777275874 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337804 | GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 84108 |
rs777283199 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328142 | CAACTAACGATGCTA[C/T]GACCTCATGCAAATA | 84108 |
rs777344357 | snp | A/G | 1.64923e-05 | 0.00287156 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303862 | GAGATGCAGTCCTGC[A/G]GAAGCCTCCTTTGTT | 84108 |
rs777401442 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325648 | ACCAAAATGGAAAGA[C/G]CTGGAACTGAGGCCT | 84108 |
rs777407496 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342660 | CATGGGCTTGCCTTT[C/T]TGCACCTTGCTTTTC | 84108 |
rs777561268 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305109 | CTGGGACCACACACA[C/T]GCATGTGCCACCATG | 84108 |
rs777672917 | snp | A/G | 7.21735e-05 | 0.00600679 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350733 | CCTCCGAGTCCTGCC[A/G]GCCTCCCTCCAGCCT | 84108 |
rs777683982 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320399 | TCTTTCTTAAGAACA[C/T]ATGATGGCCGGGCGC | 84108 |
rs777821031 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332712 | TAAACCATACAAAAA[C/T]GTATCTGCCACTATC | 84108 |
rs777837671 | snp | C/T | 5.212e-05 | 0.00510463 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348700 | AATACAATTGTAATT[C/T]ATATATTCTTCTTAC | 84108 |
rs777839435 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345405 | CATGTGTAGACAACC[C/G]TGCATAAGCACTACT | 84108 |
rs777854116 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103348087 | ATGGGCTTTACTAAA[A/G]AGGCCAGTTGTTTCA | 84108 |
rs777891823 | in-del | -/AGAGAGAG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316014 | TATATATATATATAT[-/AGAGAGAG]AGAGAGAGAGAGAGA | 84108 |
rs777917956 | snp | A/C | 1.65877e-05 | 0.00287986 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349027 | GGAAACAGTTTTAAA[A/C]TACAAGTCCTTGCCT | 84108 |
rs777950137 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349218 | ACGCCTGGCTAATTT[C/T]TGTATTTTTAGTAGA | 84108 |
rs778006358 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310064 | TCAGGCAATTCCCTG[A/C]CTCAGCCTCCCGAGT | 84108 |
rs778014961 | snp | A/G | 1.76344e-05 | 0.00296932 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326485 | TTTCTACAGTGTGCT[A/G]AAGGTAAGCTCACAA | 84108 |
rs778046260 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335578 | ATGTTGTTCAGGATG[A/G]CCTCGATCTCTTGAT | 84108 |
rs778046845 | snp | A/C | 3.31967e-05 | 0.00407397 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326621 | AACTCGAACAAACTT[A/C]TTTTCCAATGGCTAC | 84108 |
rs778057661 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325597 | GCAAGGATGTCCTAT[A/G]AAGAAAGCGGATGAT | 84108 |
rs778074109 | snp | A/G | 3.32751e-05 | 0.00407878 | intron-variant | PCGF6 | GRCh38.p7 | 10:103347208 | TATTCTTTAATCTGT[A/G]AGTACATTATAGTAT | 84108 |
rs778091549 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327180 | ATCCCAGCTACTCGG[G/T]AGGCTGAGGCAGGAG | 84108 |
rs778127531 | snp | C/G | 1.64857e-05 | 0.00287099 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103345086 | AAACACTGATTCTAG[C/G]ACTTTTTTAGATCTT | 84108 |
rs778142496 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339347 | GTAACCTGAGATCGC[A/G]CCACTGCAGTCCAGC | 84108 |
rs778299421 | snp | C/T | 1.65353e-05 | 0.00287531 | missense, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347270 | AGACCTCTTTCTTTA[C/T]AGAAATCATGCATTT | 84108 |
rs778336936 | in-del | -/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338262 | ACAAACAAAAAAACC[-/G]GTCAGGTGCAGTGGC | 84108 |
rs778422890 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317253 | TAACCTTAGGTGATC[C/T]GCCCACCTCAGGCTC | 84108 |
rs778444995 | snp | A/G | 1.65192e-05 | 0.00287391 | stop-gained, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347440 | CTATGTCTTGTAACT[A/G]TCGGTCCAACCTAAT | 84108 |
rs778452449 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330120 | TTTGCTTTAGCCCAG[A/G]CTGGAATGCAGTGGC | 84108 |
rs778526068 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321901 | TTTATTTCATTTCAC[-/T]TTTTTTTTTTTTGAG | 84108 |
rs778526793 | in-del | -/C | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352321 | CTACAGAGTGAGACT[-/C]CCATCTCAAAACAAA | 84108 |
rs778568769 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325253 | TTTGCTTGTTTTTTT[A/G]TTTGTTTTGTTTTGT | 84108 |
rs778609828 | snp | A/C | 1.65312e-05 | 0.00287495 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314279 | TATATCTACCTATGG[A/C]CATGAAGAGAGTATT | 84108 |
rs778630263 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342761 | GGGTATACCATTATT[C/T]AACCTACTCCCTTAT | 84108 |
rs778804386 | snp | A/C | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103334452 | TGATGTACAATAGAT[A/C]TCCAGGAAAAAGTAT | 84108 |
rs778807441 | in-del | -/AG | 1.65395e-05 | 0.00287567 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314285 | TACCTATGGACATGA[-/AG]AGAGTATTAGATTGA | 84108 |
rs778901667 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323239 | AAGTCATATTTCACT[G/T]GATTTAGTATATATT | 84108 |
rs778903396 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307022 | GGTGGGAGGATCACT[G/T]GAGCCTGGGAGGCAA | 84108 |
rs778915637 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310869 | ACCACACCTGGTTAA[-/T]TTTTTGTATTTCGTA | 84108 |
rs778929195 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352762 | CTGGGCAACAAGAGC[A/G]AGACTCCATCTCAAA | 84108 |
rs779025973 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321442 | TTGTAGGCTGGGCGC[A/G]GTGGCTCATGCCTGT | 84108 |
rs779026015 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342586 | CACATAAAAAGTATA[C/T]GTGTACTTGCGTATT | 84108 |
rs779081416 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320443 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 84108 |
rs779082408 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103311699 | TGTTATAATCACCCA[C/T]AACATTTAATACAAC | 84108 |
rs779090040 | snp | A/C | 9.06577e-05 | 0.00673206 | stop-gained, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350715 | TAAATACCTCCTCCT[A/C]GTCCTCCGAGTCCTG | 84108 |
rs779092277 | snp | A/C/G | 5.00049e-05 | 0.00500003 | intron-variant | PCGF6 | GRCh38.p7 | 10:103314147 | GATAACTTTCACTAA[A/C/G]TAACTTATCTGTTAG | 84108 |
rs779105135 | snp | C/T | 1.98253e-05 | 0.00314838 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333990 | ATCAATATTTAATAC[C/T]TTAAGCTATATGTTT | 84108 |
rs779115752 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332943 | AACATGGTGAAACAC[C/T]GTCTCTACTAAAAAT | 84108 |
rs779145930 | snp | C/T | 6.61244e-05 | 0.0057496 | intron-variant | PCGF6 | GRCh38.p7 | 10:103349011 | GGCGCTGCAAATAAA[C/T]GGAAACAGTTTTAAA | 84108 |
rs779175900 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349325 | AGTGCTAGGATTACA[A/T]GCATGAGCCACCGCG | 84108 |
rs779201493 | in-del | -/CA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103322824 | CAAGACTCTGTATCA[-/CA]CACACACACACAAAA | 84108 |
rs779205326 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327395 | TAAATGACAAATACA[C/T]TAACCAATTACAATG | 84108 |
rs779218928 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314531 | TCCCTGAATCTCAAA[C/G]AAATTAAGTCATTTT | 84108 |
rs779292553 | snp | C/T | 8.58047e-05 | 0.00654943 | utr-variant-5-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351082 | GGTCGGGAGAGACAC[C/T]AGGCGAGGCGAGGCG | 84108 |
rs779304541 | in-del | -/CACACACACACAC | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103339812 | GTCTCAAAAAAAAAA[-/CACACACACACAC]ACACACACACACACA | 84108 |
rs779439029 | snp | A/G | 4.33482e-05 | 0.00465534 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351104 | GGCGAGGCGGCGGGA[A/G]AGCGCGGGAGTTCGG | 84108 |
rs779479458 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335318 | CTTAGCCTCCCCAAA[C/T]GCTGGAATTACAGGT | 84108 |
rs779669244 | snp | C/T | 0.000181517 | 0.00952499 | synonymous-codon, intron-variant, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103347414 | CTCTAGATTGATCAC[C/T]AATTTGTACACTATG | 84108 |
rs779675045 | in-del | -/TCCTCGTCCTCG | 1.82844e-05 | 0.00302355 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350819 | TCTTCTTCTTCCAAC[-/TCCTCGTCCTCG]TCCTCGAAGCGGCCT | 84108 |
rs779714007 | snp | G/T | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351593 | ATCACTACTCAAAGA[G/T]CATCCATGTCACCCC | 84108 |
rs779714140 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317385 | CGTGGTATACATTCA[C/T]GGTATTATTACTATA | 84108 |
rs779769268 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103330511 | ATCAACAGCTTTATT[A/G]AGATGTAATTCACAT | 84108 |
rs779860006 | snp | G/T | 1.6477e-05 | 0.00287024 | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303892 | TTCCCTCCTCATAAT[G/T]TGCCTAGAATCTTCA | 84108 |
rs779905592 | snp | A/G | 1.66164e-05 | 0.00288235 | intron-variant | PCGF6 | GRCh38.p7 | 10:103303994 | AAAGACGATTTTGCA[A/G]TTCTTTCAAACCAGT | 84108 |
rs779938442 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323470 | CCCGGCTGATTTTAT[A/T]TTTTTAGTAGAGATG | 84108 |
rs780042363 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338865 | AAGAGTGAAACTCCG[C/T]CTCAAAAGAAAAAAA | 84108 |
rs780170954 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308192 | TGAGAAGAGGGCCAC[A/T]GTCCTCCAGATCCCA | 84108 |
rs780234620 | snp | A/G | 3.65764e-05 | 0.00427632 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350925 | CCCCCGTCTCAGACA[A/G]AGGCGCCGGTCCCTC | 84108 |
rs780239478 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103321728 | CAAAGAAACAAACAA[C/T]AATAATAATAATAAT | 84108 |
rs780312884 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103342481 | TCGGGTAATCTGCCC[A/G]CCTCGGCCTCCCAAA | 84108 |
rs780352185 | snp | A/C | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352942 | GAAAATTAGCCGGGC[A/C]TGGTGGTGCACACTT | 84108 |
rs780620725 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103314870 | TGAGGCAGGAGAATC[A/G]CTCGACCCCAGGAGG | 84108 |
rs780648314 | snp | G/T | 7.82748e-05 | 0.0062555 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103351004 | CGGAGGCGGCAAGGC[G/T]GCAGCTCCCTCGGTT | 84108 |
rs780722312 | in-del | -/TCC | 0.000285124 | 0.0119365 | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350789 | TCCTCCTCCTCTTCT[-/TCC]TCCTCCAGCTCCTCT | 84108 |
rs780735361 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103320232 | TCATAAAAGCAAAAT[A/G]AGGTCTGAATATCAA | 84108 |
rs780741270 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328764 | TTTTGTTTGTTTTTT[A/G]TTTTTGAGATGGAGT | 84108 |
rs780747366 | snp | A/C | 1.6971e-05 | 0.00291294 | intron-variant | PCGF6 | GRCh38.p7 | 10:103326642 | CAATGGCTACAAAAA[A/C]AGACAGATAAAACTA | 84108 |
rs780792676 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332598 | TCAATTCATTCTCTA[C/G]TTCTTTCTTCATGAG | 84108 |
rs780846963 | in-del | -/AC | 5.59571e-05 | 0.00528918 | intron-variant | PCGF6 | GRCh38.p7 | 10:103333882 | TCGAATTTGTGTGCT[-/AC]AGAGTCCTCTTGTGA | 84108 |
rs780851366 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340296 | AAACAGCAGAGCTAC[A/G]ACTTAAATCCAGATC | 84108 |
rs780852877 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103302808 | AAATAGGTTAAAATA[C/T]ATTTTTATTAAATGT | 84108 |
rs780891869 | snp | C/T | 2.15186e-05 | 0.00328006 | utr-variant-5-prime, upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351091 | AGACACCAGGCGAGG[C/T]GAGGCGGCGGGAGAG | 84108 |
rs780902423 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103331478 | GGCCAGGCTAGTCTC[A/G]AACTCCTGAACTCAG | 84108 |
rs780981518 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319398 | CCTTGTGATGTGCCC[A/G]CCTCGGCCTCCCAAA | 84108 |
rs780982707 | snp | A/C | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103351268 | ACTTTAAAGGAATCT[A/C]ACCAGATTTTCTCCT | 84108 |
rs780993608 | snp | C/T | 1.69112e-05 | 0.0029078 | intron-variant | PCGF6 | GRCh38.p7 | 10:103348711 | AATTTATATATTCTT[C/T]TTACCTTATGTTATA | 84108 |
rs781062594 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309693 | CCCAGCACTTTGGGA[C/G]GCTGAGATGGCTGAT | 84108 |
rs781093373 | snp | A/G | 1.67055e-05 | 0.00289006 | missense, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103326631 | AACTTCTTTTCCAAT[A/G]GCTACAAAAACAGAC | 84108 |
rs781157259 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103319703 | CTCAATTTAGTAACA[A/G]TATATAATAAATGGT | 84108 |
rs781204617 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103340583 | TTAGTGGAAAGTGTT[-/A]ACATTTCCCCAAAAT | 84108 |
rs781304202 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325415 | TGTGCCAACAGGTCC[A/G]GCTAATTTTTGTATT | 84108 |
rs781308191 | in-del | -/CTC | | | cds-indel, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103303360 | TGAAATGAGTAACTT[-/CTC]CTTTGTAGTGTTGCT | 84108 |
rs781357285 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103323685 | GCAATCTCCACCTCC[C/T]GGGTAATAGCGATTC | 84108 |
rs781361295 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103337148 | ATCTCTCTTAAAATA[C/T]GGTACCCAGAGCTGA | 84108 |
rs781375869 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103335775 | GTTCAAGAGCAGCCG[A/G]GCCAACATAATGAAA | 84108 |
rs781376807 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103345587 | AATTCCAACCCTTTG[A/G]GAGGCCAAGGTGGGT | 84108 |
rs781394095 | snp | G/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103338406 | AAAAATTAGCCGGGC[G/T]TGGTGGCAGGCACCT | 84108 |
rs781435923 | snp | A/C/T | 1.8842e-05 | 0.00306932 | synonymous-codon, nc-transcript-variant | PCGF6 | GRCh38.p7 | 10:103350914 | GCAGCCGGGAGCCCC[A/C/T]GTCTCAGACAGAGGC | 84108 |
rs781482238 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103308679 | GGGTTTGAGACCAGC[C/T]GGGGCAACATGGTAA | 84108 |
rs781486321 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103336064 | TGAGCTCAGGAGCTC[A/G]AGACCAGCCTGGGCA | 84108 |
rs781528375 | snp | A/G | 0.000217604 | 0.0104286 | missense, intron-variant | PCGF6 | GRCh38.p7 | 10:103333938 | ACCTTAAAATGTCCC[A/G]TGCCTTCATTAGCAC | 84108 |
rs781590202 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103341904 | CCCAGACTCAATAGA[C/T]TCCAGTGCCGCTTCC | 84108 |
rs781638792 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103312347 | GTAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 84108 |
rs781647133 | in-del | -/TTGT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103329783 | CGGCCAGTTTTTTTG[-/TTGT]TTGTTTGTTTTTGAG | 84108 |
rs781725194 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103317125 | AAGCGATTCTCATGC[C/T]TCACCCTCCCAAGTA | 84108 |
rs796073265 | in-del | -/CA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103326199 | TCAGGAGATCGAGAC[-/CA]CAGTGAAACCCCTTC | 84108 |
rs796206064 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307837 | ATTTCTCAGAACATA[C/T]CCCTATTGTTAAGTG | 84108 |
rs796232789 | in-del | -/TA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103315965 | AGAGCCTCAACAGCT[-/TA]TATGTGTGTGTGTGT | 84108 |
rs796275438 | in-del | -/AA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325872 | AAAAAAAAAAAAAAA[-/AA]TTAGCTGGGCATGGT | 84108 |
rs796300797 | in-del | -/CT | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103349515 | AGAGGGAGTCTGCCT[-/CT]GTCGCCCAGACTGGA | 84108 |
rs796334813 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103332196 | CTTCAAGGTGATATT[A/G]CTACCATGTTTTTTC | 84108 |
rs796346519 | in-del | -/AATA | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103346623 | TCAAAAAATAATCAT[-/AATA]AATAAATAAAAATAC | 84108 |
rs796373038 | in-del | -/ATATAGAGAG | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103316010 | TATATATATATATAT[-/ATATAGAGAG]AGAGAGAGAGAGAGA | 84108 |
rs796525581 | snp | C/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103328688 | TTGTTAGTGTTGTGA[C/G]CCATTTGTCTCTAAG | 84108 |
rs796535534 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103309955 | GAGACCTTGTCTTTC[-/T]TTTTTTTTTTTTTGA | 84108 |
rs796637000 | in-del | -/A | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103325853 | AGACCGCATCTCTTA[-/A]AAAAAAAAAAAAAAA | 84108 |
rs796769821 | snp | A/G | | | upstream-variant-2KB | PCGF6 | GRCh38.p7 | 10:103352324 | ACAGAGTGAGACTCC[A/G]TCTCAAAACAAAACA | 84108 |
rs796853194 | in-del | -/T | | | downstream-variant-500B | PCGF6 | GRCh38.p7 | 10:103302453 | CAGTGCCTGACCTGG[-/T]TTTTTTTTTTTTTTT | 84108 |
rs796868355 | in-del | -/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103327666 | TAATAAAGGGAATTC[-/T]TTTTTTTTTCTTTTC | 84108 |
rs796910532 | snp | A/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103307469 | AAAAAAGAAAGAAAG[A/T]TTGTTTATTTCATTC | 84108 |
rs796938264 | snp | A/G | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103305216 | TGAGCTTCAAGCAAT[A/G]CCCCCATCTTGGCTT | 84108 |
rs797004292 | snp | C/T | | | intron-variant | PCGF6 | GRCh38.p7 | 10:103310148 | GTAGAGATGGGGTTT[C/T]ACCATGTTAGCCAGG | 84108 |