SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs145426786 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428261 | ACAATACAAAGAGCA[C/T]GATCACTGTCTATAA | 115426 |
rs145440764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482851 | TCCACCTGCCTTGGC[C/T]TCCCATTACAGGCAT | 115426 |
rs145479628 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505716 | GCTCTGTTTAGAAAG[G/T]ACAGGGTTGAAATCT | 115426 |
rs145491796 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425656 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 115426 |
rs145494341 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461069 | CTCATAGGATTCTTA[C/T]AGATTGAACAAAACA | 115426 |
rs145505680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454632 | TGAGTTAGGTACACT[A/G]TTAGAGTCCTGAGCT | 115426 |
rs145554276 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490466 | AACTCCGTCTCTACT[A/G]AAAGTACAAAAATTA | 115426 |
rs145562532 | snp | C/G | 0.00261868 | 0.0360899 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504586 | TTATCCTTGGATACT[C/G]TTCTAGAATTTTCTG | 115426 |
rs145571998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452227 | TGATTGTTTTTAGAC[C/T]TGTTACAAATAGTGC | 115426 |
rs145578750 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489728 | TCTAATTGGGTTTTT[-/G]TTTTTTTTTTTTTTT | 115426 |
rs145644394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494281 | ACAAACTCCTTTTTA[C/G]AGTAAACTCAGTAAT | 115426 |
rs145645914 | snp | A/G | 0.00537581 | 0.0515655 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468671 | GGGCTTTGGTTGAAT[A/G]CTGGACTTCTGCTGG | 115426 |
rs145651451 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414735 | GGAATATTTTCCTCC[C/G]CTTCACAGGCTTAGT | 115426 |
rs145663611 | in-del | -/AAG | 0.322959 | 0.239117 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457393 | GTTGCTTATCACCTT[-/AAG]GAGATTTTGGGCTGA | 115426 |
rs145689540 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445127 | AAAACCCTATCTCTT[A/T]TTTAAAAAAAAAAAA | 115426 |
rs145697253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468498 | AGAATCTCATAAGGC[A/C]GGTAGCTTTGTAGTT | 115426 |
rs145719533 | snp | C/T | 0.124491 | 0.216211 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466294 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG | 115426 |
rs145755111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474934 | GTTACAGAATTATCC[C/T]ATATAATTACATTTT | 115426 |
rs145755482 | snp | A/G | 1.65337e-05 | 0.00287517 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497254 | TTGGAGCAGAGTCTC[A/G]GAATTGGAGAGCTGG | 115426 |
rs145759412 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504980 | TCTGTAATAGCTTAT[A/G]TGTTTTATATATTAT | 115426 |
rs145765420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419297 | TACCATGGATTAGGA[C/T]TTCAACCCATAACCC | 115426 |
rs145773258 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474176 | TCATTGGTGGTCACA[A/G]CGGATGTGCATGTTG | 115426 |
rs145773617 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502590 | AGTTTGCTCTGTTTC[A/G]TCAGTTATTACTATC | 115426 |
rs145801256 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491637 | CCTGATCTTGATGAT[A/G]GCAAGAATGTGAGCA | 115426 |
rs145804927 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418344 | TTACTGACTTGGAAT[A/T]CTACTTTGGCTTATT | 115426 |
rs145831581 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501964 | CCTATGGGTAGTGTC[C/G]CACTGGGACAGATTC | 115426 |
rs145911128 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437264 | TTTAGACAGAGTCTC[A/G]TTCTGTTGCTCAGTC | 115426 |
rs145934745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460454 | TATTTAAGGACACTT[C/T]AACCTATTTTACTCT | 115426 |
rs145962907 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423650 | TTTTTTTTTTTTTTT[-/T]AAAGAAAAGTCTCGG | 115426 |
rs145993374 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432689 | GTATGCCATCTATTA[C/G]ACACCTTAAGAGTGG | 115426 |
rs146001831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453760 | ATACAAAAAAACCAA[C/T]CAGGAGTGGTGGCAG | 115426 |
rs146002220 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420240 | CTTTGTATTTCTAGT[A/G]GAGACGGGGTTTCAC | 115426 |
rs146053564 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477211 | TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACT | 115426 |
rs146121976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437918 | CACCCGGCTAGTTTC[A/G]TTAGAAGTAAGATAC | 115426 |
rs146126056 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434574 | CTCCCAAGTAGCTGG[A/G]ATTACAGGTGCATAT | 115426 |
rs146126084 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466400 | AAAATGTTAGCTGGG[A/C]ATGCTGGTGCACGCC | 115426 |
rs146144257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463093 | TCGAGACCAGTCTGA[A/C]CAACTAGTGAAACCC | 115426 |
rs146175623 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487917 | AACTTACTATTTTGA[C/G]ATAGTTGTAGATTCA | 115426 |
rs146219181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461787 | TCACTCTTTTTCTGT[A/G]TCTGCTGCTTCTGAA | 115426 |
rs146240980 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450963 | AAAAGAACTAGGAAA[C/T]AATACTTAAATATAC | 115426 |
rs146261930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479405 | ACTTCACTGGCCTTT[C/T]CTTCTTAGTCTCTTG | 115426 |
rs146274440 | in-del | -/AG | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490015 | CTTTGTATATTTGTC[-/AG]AAATACAAAAGATGT | 115426 |
rs146295727 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501399 | TTTATAATACAATTA[C/T]TTTTCTGTTTTCTTT | 115426 |
rs146353135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487278 | CCCTGCAACCTCTGC[C/T]TTTGGGTTCAAGTGA | 115426 |
rs146360826 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462962 | TATAGTTAAGAGTGG[G/T]AACACACTGGCTTTA | 115426 |
rs146384515 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489927 | TACATTAACATGGCA[A/C]AGTAAATGGAAATGG | 115426 |
rs146417585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428703 | TACAGGTCTGTGCCA[A/C]CATACCCAGCTAATT | 115426 |
rs146437907 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458208 | GTCTATTTAGGGATT[C/T]GACTTCTTCCTGGTT | 115426 |
rs146493926 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494289 | TTTTTAGAGTAAACT[-/C]CAGTAATTTGAAATA | 115426 |
rs146509986 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417072 | ATAATACACACATAT[A/G]TAATATGTGATGGAT | 115426 |
rs146564956 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468739 | AGCAGTCTTAGAAGG[C/G]ATACACTGGATTTTA | 115426 |
rs146627660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431307 | ACTTACTATATTTAG[A/T]AGGATAATCCTTTTT | 115426 |
rs146661350 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435351 | GGCTGGTGTTGAACT[A/C]CTGGGCTCAAGTGAT | 115426 |
rs146666373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431510 | TCAGGAGTTTGAGTT[C/T]AGGAGTAGGAGGCTG | 115426 |
rs146745739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446431 | TACAGGCGTGAGCCA[C/T]CATGCCTGGCCTAAT | 115426 |
rs146783532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449022 | CAATTTTGTCTTTAC[C/G]TTTACCAGCACCTTT | 115426 |
rs146800305 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497686 | ATGATTTTAGTTGTA[A/G]TAGATTTTCAAAGCA | 115426 |
rs146801933 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446620 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGGG | 115426 |
rs146803792 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494612 | CTAATACCAATATTA[A/G]TAAGTAACCCAGACC | 115426 |
rs146804791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444828 | GGCTGGTCTTGAACC[A/C]TGACCTTAGGTGATT | 115426 |
rs146912578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478431 | TAATATTTACTAAAC[A/G]CTAACAAAGTGGTTT | 115426 |
rs146926614 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500023 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGAAAGAT | 115426 |
rs146962147 | snp | G/T | 0.000256737 | 0.0113271 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504631 | ATCTTTTATGTGCGT[G/T]TGCTGTCAGGAGCTA | 115426 |
rs147018675 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437373 | GAGTACCTGGGATGA[A/C/G]AGGTGCCTGCCACCA | 115426 |
rs147093674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418926 | CCCTTTACACTTTGC[C/T]GGAAATTTTCTTTCT | 115426 |
rs147106460 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502294 | TTATTTAAACATGCT[C/G]GACGTCTTGATACCC | 115426 |
rs147123011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450777 | CAAGTTTAAAGTGAC[A/G]TAATAGTTTTTGAAT | 115426 |
rs147141739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470533 | GAGGAATGAGATTCC[C/T]GATGGAACATCGAAA | 115426 |
rs147156650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500905 | CTTTAAACCTCTTAG[A/G]TGCTGGATTTTGACT | 115426 |
rs147173350 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412389 | TTATTTAAAACTGTT[A/T]CCCGCAAACCCGCAA | 115426 |
rs147186542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496542 | ACCATGCATTAATGC[A/G]TTATCAGTAAAATGT | 115426 |
rs147226390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430290 | GCTGGGATTACAGGC[A/G]TGAGCCCCTGTGCCT | 115426 |
rs147246598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483672 | TTATATTTTAAAAAC[A/G]CGCCCTACTTTTATC | 115426 |
rs147248725 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430641 | ACCAAGCCAATATTC[C/T]GCCCTGATCACCCAC | 115426 |
rs147265839 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428426 | CTAACTTTCTTATTA[A/G]TATTAACCTTTAACA | 115426 |
rs147326585 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505620 | ATTTTTTGAAGACTC[-/A]ACCATATGTGTTAAG | 115426 |
rs147354178 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445667 | GGTTCAAGTGATCCT[C/T]CTACCTCAGCCTCCT | 115426 |
rs147364584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496303 | CTTTTCACTTAAGAC[A/G]TAGGTGTCCTAGAGG | 115426 |
rs147370407 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442875 | TTCTCTTTATCCTCT[G/T]AAAACCAAGGATTTA | 115426 |
rs147474415 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487356 | ATCACACCTGGCTAA[C/T]TTTTGTATTTTTATG | 115426 |
rs147475929 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454388 | AGGCTGGCAGGGACA[A/T]TTAGGCTAAGTGTTA | 115426 |
rs147545006 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415773 | TTATTATAGATGTTC[A/T]GCTCACCCCAGAACT | 115426 |
rs147609518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463679 | TTTCACCTTGTTGTC[C/T]AGGCTGGTTTCGAAC | 115426 |
rs147625533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493323 | GTTAAGGTGAAGTTT[C/T]TAGGTAAATTTGCTT | 115426 |
rs147626053 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461664 | GGTATGAGCCACTGC[A/G]CCCAGCTTTCTATCA | 115426 |
rs147628950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490569 | GGAAGCAGAGGTTGC[A/G]GTGAGCCAAGATCAC | 115426 |
rs147715587 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425699 | ACCCAGGAAGCAGAG[A/G]TTACGGGGAGCCGAG | 115426 |
rs147731871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421537 | ATCTCCTGCCTTAGT[C/T]TCCTGATTAGCTGGG | 115426 |
rs147819446 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440603 | ATTTAAAGCAAAAAG[C/T]ACACACGCAACTTCT | 115426 |
rs147835559 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468026 | ACATAATGTGTCTTA[G/T]AGTTGCTGATTACCA | 115426 |
rs147942311 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450224 | TTAAAAATGTACTTA[A/G]GTTGTTCAAATAAGG | 115426 |
rs147942889 | snp | A/G/T | 0.00676848 | 0.0578101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482328 | TTACTGTTCTGTTAT[A/G/T]GTTGTGGTAGTAACC | 115426 |
rs147946411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480462 | AGATGACTTTAGGAT[A/G]GTATAATTAGAAGAG | 115426 |
rs147971931 | snp | A/C/T | 0.000247121 | 0.0111132 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6421018 | GCACATCTACACAGA[A/C/T]TGAGGCTAAACCCTG | 115426 |
rs147995438 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479122 | CAAACCTTCCTTGAT[C/T]CCATTTCTCCCACTG | 115426 |
rs147997364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422863 | TTTTGATGCAATTAT[A/T]ATATATGGTTATCTT | 115426 |
rs148011842 | snp | C/T | 0.00148967 | 0.027251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505983 | TAAGTTGCTGAGTAC[C/T]TACATGCTTTATGCT | 115426 |
rs148049391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427590 | CTTGGGAGGCTGAGA[C/T]GGGAGAATCACTTGA | 115426 |
rs148065984 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456724 | ATAAGGTGTAAGGAA[A/G]GGGTCCAGTTTCAGT | 115426 |
rs148099109 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441776 | ATAGACATAAATTAT[C/T]GGAACTAATTCTTTT | 115426 |
rs148151483 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445373 | GGTTCAAGCGATTCT[C/G]CTGCTTCAGCCTCCT | 115426 |
rs148155019 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474579 | GGTATGGTGGCGCAG[G/T]CCTGTAATCCCAGCT | 115426 |
rs148204629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419300 | CATGGATTAGGATTT[C/G]AACCCATAACCCTTA | 115426 |
rs148208174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450943 | TTTCTAGGTCTTTTC[A/G]TTGGAAAAGAACTAG | 115426 |
rs148219930 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502601 | TTTCATCAGTTATTA[C/T]TATCTGAAACAGTTT | 115426 |
rs148260226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453916 | TCTCAAAAAAAGAAA[A/G]AAAGTAGGGATTGAA | 115426 |
rs148277546 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483552 | GTTTATTTTTCCCAA[A/G]TATTTTTTACTCTCT | 115426 |
rs148292551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437503 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTATGAGT | 115426 |
rs148308870 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466120 | AAACTACAGATAAAG[G/T]CCGAGCATGGTGGCT | 115426 |
rs148359955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469179 | AATTATATGGAGATT[C/T]TAGAACTGAGAATTA | 115426 |
rs148362314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415050 | ATGTAATCGTTTGAT[A/G]CATTTTATTTTCTAG | 115426 |
rs148375888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499108 | ATGTCCCTGTTGAGA[A/G]CATTGTTCTAGATAG | 115426 |
rs148462349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472051 | ATACAGTGAACATTG[A/C]CAAATGGATATACGC | 115426 |
rs148479798 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501048 | TCAAAGTTACCTAAC[C/G/T]GCATAAGTCTTAAGC | 115426 |
rs148530971 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479750 | CTAATCATTTTATCT[A/G]CTTGTTCATGCCAAA | 115426 |
rs148539129 | snp | C/G | 0.000190531 | 0.00975853 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433872 | GTTTTTGAAGCAGTA[C/G]ACAAAATTAAGCTTC | 115426 |
rs148583564 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482374 | TCTAAACAGCCTTTC[C/G]TGCCAAAAATTTAGC | 115426 |
rs148589979 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438662 | GAAAGAAACCTGCCT[C/T]TGGAATTATTCTGGG | 115426 |
rs148614334 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486344 | CAGCAATCCTTGTAA[C/T]CAAAAGGGTTTGAGG | 115426 |
rs148643389 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414253 | CCTAGGTTTGGAATG[C/T]CTCGAGGGAGGTTAG | 115426 |
rs148656229 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496588 | CCAGAAGTCTTCATT[G/T]TCATTAGCACAGGCA | 115426 |
rs148673214 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446295 | AGATGGAATTACAGG[C/T]GTGTGCAACCACACT | 115426 |
rs148698153 | snp | A/T | 5.06761e-05 | 0.00503344 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460785 | TTCGTGTGAAAATTT[A/T]CCTGGGGTAAGATTG | 115426 |
rs148726344 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420744 | AGAGAATGTATTGGG[G/T]TCCAGAGAAGACACT | 115426 |
rs148739616 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504277 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 115426 |
rs148748544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459953 | ACTGCAGCCTAGGTG[A/G]CAGAGTGAGACCTTG | 115426 |
rs148797765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485299 | ACACTTTGTGTATTT[C/T]TAATTGCCTTATTTT | 115426 |
rs148845430 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505717 | CTCTGTTTAGAAAGG[A/G]CAGGGTTGAAATCTA | 115426 |
rs148848349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431681 | TGTGTTGATGTTCAA[A/G]CAATGGCAGTATTTT | 115426 |
rs148904576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465086 | GTCCTTATTCACCAG[C/T]TGGGCCCTGAATTAC | 115426 |
rs148921305 | snp | A/G | 0.000185753 | 0.00963545 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468510 | GGCAGGTAGCTTTGT[A/G]GTTGTGTTTTGCCCC | 115426 |
rs148988205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418413 | TAATTCCCTGACTGG[C/G]AAACTTGTGAAATTC | 115426 |
rs149001221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502208 | GTGATCAGCAGCCCT[A/G]CCTACATCTGTAGTC | 115426 |
rs149005808 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428576 | TTTTTTTTTTTGAAC[A/G]ATCTCATTCTGTCAC | 115426 |
rs149024205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450802 | TTGAATGTTTCTTTG[C/T]GTTCAGGTATAACAG | 115426 |
rs149053464 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480548 | ACCTGAAACTCCTTA[A/T]CCTTAAATCTTTTCT | 115426 |
rs149060698 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488415 | ACACTATACAGTCAG[A/G/T]CTGAACATTTATATT | 115426 |
rs149062453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437005 | TATAAAATATGAGAT[A/G]TATAACATAAATAAG | 115426 |
rs149114194 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441370 | CACGGTGAAAACCTG[C/T]CTCTACCCCTCCCAA | 115426 |
rs149128611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494533 | AGAAATACTAATGAC[A/G]TCTCAGCTCCCGTGG | 115426 |
rs149166782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414939 | TTGTAAGCTTTGCTT[C/T]TGAAATAATTGTACA | 115426 |
rs149182508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498665 | TTTTTCCCCTTTGCC[A/C]ATGCTCAGCTGTTAA | 115426 |
rs149227077 | snp | G/T | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493874 | GGTGGTAAAAATCTT[G/T]CTGGTAACAAAAGAA | 115426 |
rs149232533 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495813 | GTGGCAGTAATTATG[A/T]CTGAAGGTATCTGTG | 115426 |
rs149286030 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500930 | TTGACTTCTCTATGC[C/T]CAAAGTTACTTTACT | 115426 |
rs149287409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448458 | ATGGATTCTAGAGCC[A/C]GGTGATCAGTTTGAA | 115426 |
rs149353995 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507431 | ATTTTTAGTAAAGAC[A/G]GGGTTTCACCGTGTT | 115426 |
rs149372528 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433659 | AAGTCTAGTGTATAC[A/G]TCAGTAAGGCGTAAA | 115426 |
rs149441956 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466848 | TACTCATTTGACTTA[A/C]TCTGTCTCTTATTTC | 115426 |
rs149499782 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476283 | TTTTATCTGTTGATG[C/T]GTTTCTTGCTGTTTC | 115426 |
rs149528134 | snp | A/C/T | 6.59156e-05 | 0.00574056 | missense, synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460657 | ATGGAATGAACTAAA[A/C/T]GTTGGTGATGTGGTA | 115426 |
rs149531538 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482993 | GGGGATTGGTTCCAA[G/T]ATCCCCTATAGACAC | 115426 |
rs149532743 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430218 | TTTCGCCATGTTTGC[C/T]GGGCTGGTCTTGAAC | 115426 |
rs149568934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481253 | GAATTCTAATAACCA[A/G]TTTAGATGGGGAGTT | 115426 |
rs149583337 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459405 | CGGGTGCGGTGGCTC[A/G]TGCCTGTAATCCCAG | 115426 |
rs149598655 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489173 | GTATGTAGCATATTA[C/T]ATATTAACCTTTAGG | 115426 |
rs149601289 | in-del | -/ACCTCAGGTGATC | 0.485324 | 0.0843964 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426977 | GGTCTTGAACTCCTG[-/ACCTCAGGTGATC]ACCTCAGGTGATCAC | 115426 |
rs149619375 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485621 | CCACCCCCGCCCCCC[A/G]CCCCAAATTATTGTG | 115426 |
rs149651367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491884 | GCTGATTATTTTTCC[A/G]TAGGAAAAATATTTT | 115426 |
rs149672201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460926 | CATACTGAAGGAGAA[C/T]ATTTTTATAAATTCT | 115426 |
rs149702272 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490393 | AGCACTTTCGGAGTC[C/T]GAGGTGGGCTGATCA | 115426 |
rs149718620 | in-del | -/T | 0.0528381 | 0.153711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485576 | GCTGTCACCTTCTTG[-/T]TGGCTTCTAAAAGCT | 115426 |
rs149752305 | snp | C/T | 1.68046e-05 | 0.00289862 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493906 | TGGTGCACCTTCAGC[C/T]GATCAAACATTAACA | 115426 |
rs149755887 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443880 | TTTGCTCCCAGCATT[A/C]TTTAAGATTTCTGGA | 115426 |
rs149758949 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479670 | CAAAATTAGTCCAGA[C/T]GGAGTTCTTGATTTC | 115426 |
rs149762562 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425378 | TTTCTGGCACTACAA[C/T]ATGCTTCAGGTACAT | 115426 |
rs149771552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497499 | TGGAAATTGAACAGA[C/T]GCATAAAGCAAACTC | 115426 |
rs149814824 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428490 | CCTAATCCCTAATTT[G/T]CTGGTTTCTGAACTT | 115426 |
rs149822542 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501821 | CAGTTGTTAATCAGC[C/G]TAATTATTCTCTGAT | 115426 |
rs149965755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468242 | CATAAAGAGTGTCTT[C/G]ATAAGCCTTTAACAA | 115426 |
rs149967953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414464 | GGTGCATACTTGAAG[A/G]CTGTCTGTGGGCATC | 115426 |
rs150034325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477495 | CACGCCATTGCACTC[C/T]AGCCTGGGTAACAAG | 115426 |
rs150054333 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482079 | ATTCCTGTTGGATCA[A/G]CTTGGAGATTTAGAG | 115426 |
rs150055419 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431119 | CTGCCTTTAAAATCC[A/T]GGCTTTATAACACAG | 115426 |
rs150087216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452553 | ATCCTAAAGATGGGG[A/T]AGTGTGTTGGGCCTA | 115426 |
rs150094630 | snp | C/T | 0.000121115 | 0.00778091 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421117 | CTCGTGCCCGTCTTA[C/T]TGATCCTGGCTTTGG | 115426 |
rs150143611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487060 | AATCAGTTTTATACA[A/G]GTTAGAAAGTAAATC | 115426 |
rs150172022 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505283 | AATATATATATATGC[-/GT]GTGTGTGTGTGTATA | 115426 |
rs150196420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462251 | TAATTGCAACTGAGA[C/T]CATCTAGCCTGCAAA | 115426 |
rs150211241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491563 | TCATTGTGCTTTGGA[A/G]TTATTTATCTGATAG | 115426 |
rs150220371 | in-del | -/TTGTTG/TTGTTGTTG/TTGTTGTTGTTG | 0.364401 | 0.222289 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451773 | CCGCGCCCGGCCTGT[lengthTooLong]TTGTTGTTGTTGTTG | 115426 |
rs150223115 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442481 | TGTTTTGTTTTGTTT[G/T]TTTTGTTTTGTTTTT | 115426 |
rs150229067 | snp | A/C/T | 0.00597455 | 0.054357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417900 | TAGAAATACCCTCAA[A/C/T]GTCACTCTGACTCTG | 115426 |
rs150263839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495497 | ATACTCTTTGCCCAG[C/T]AGTGTATGGTTGAAT | 115426 |
rs150277848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445590 | TGAGACAGGGTCTTA[C/G]TGTGTCACACAGGTT | 115426 |
rs150280061 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421847 | TTACGTATATTTCTC[C/T]AGGCAGTATGTTTTG | 115426 |
rs150284414 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426667 | GGTATTCTGCCTTCA[C/G]AGAATTTTTATCACA | 115426 |
rs150296550 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480526 | TCGTATCAAGGTCTT[C/G/T]CGCTTCACCTGAAAC | 115426 |
rs150439124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446871 | AAACAAACAAATAAT[A/G]CTTATAAGTTTTATT | 115426 |
rs150475820 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469782 | TATATGTGTGTATAT[A/G]TATGTATATATGTGT | 115426 |
rs150511135 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439149 | TGCTTGTAAATGGTC[C/G]TTTTCTATAGATTTC | 115426 |
rs150522674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490235 | TAAAAAGAAGAAATA[A/G]TATTTTATGTGGAGA | 115426 |
rs150528914 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447941 | CTAAAAACAAGAGGA[C/T]TGGTTAATTTGTATT | 115426 |
rs150559930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479233 | ATTCATACTTCAGCA[C/T]TCCAGTCTAGCTTTC | 115426 |
rs150609270 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507320 | CGGCTCACTGCAAGC[C/T]CTGTCACCTGGGTTC | 115426 |
rs150612362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454306 | TTGATACAAGGATCC[A/G]AAACCTTGTCACATG | 115426 |
rs150678664 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487522 | CAAGTATGCACCACT[A/G]TGCCTGGCTAATTCT | 115426 |
rs150731108 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463145 | AATTAGCTGGGTGCG[A/C/G]TGTTGCATGCCTGTA | 115426 |
rs150734295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492704 | AATCACTATTTTGCT[A/G]GTGTTAGTAGGATTA | 115426 |
rs150737172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476034 | TCTTTATCCCCTGTC[C/G]CACTTCCCTTCCCAG | 115426 |
rs150753425 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419731 | ACAATGAAACATTTT[C/G]GGATTTATTTATTTA | 115426 |
rs150768199 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503061 | GTACAGTAGCATGAT[C/T]TCAGCTCACTGCAAC | 115426 |
rs150805484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425111 | ACTGTTGGAGAGAAA[A/G]TCACTGTACAGTCCA | 115426 |
rs150819696 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481100 | ACGAAATACAAGTTA[C/G]AGTAGGGTAATCAAT | 115426 |
rs150822477 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427678 | TGACAGAGCAAGACC[C/G]CATCTCAAAAAAAAG | 115426 |
rs150851832 | in-del | -/TTTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442474 | TTTGTTTTGTTTTGT[-/TTTG]TTTGTTTTGTTTTGT | 115426 |
rs150867774 | in-del | -/TG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469667 | GAAAGGTGTGTGTGT[-/TG]GTGTGTGTGTATGTA | 115426 |
rs150875044 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431012 | TTTAGCTAATTACTT[C/G]AGTTCTTAATTTGTA | 115426 |
rs150877993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460210 | GTGACTGAATAGATA[C/G]ATAACATATAGTTTA | 115426 |
rs150880672 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442157 | TTTAATAGAGACAAG[A/G]TTTCACCATGTTGTC | 115426 |
rs150978215 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431813 | CAGTACTTCATTTGT[A/G]CCGCCTCGTGTTCCT | 115426 |
rs150984562 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443192 | AGTCTTTAACTGTGG[A/G]CAAATGATCGCCAGG | 115426 |
rs151000697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472310 | CTTATGAAAATAAGC[A/G]AAAGGATCGATGTTA | 115426 |
rs151036770 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417405 | GCTTCTGACTCACAG[A/T]TGTTTGTGATTTCTA | 115426 |
rs151045215 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491045 | ATGTAATACTCTTGC[A/G]TACCTGCTGATAACT | 115426 |
rs151052515 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501784 | ACTCATTTTCACTTA[C/T]AGGAAATTAAGATAC | 115426 |
rs151053229 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449341 | ACACCTGAGCTTACC[A/G]TTAGACTGGCCAAGA | 115426 |
rs151137834 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455407 | GGTTTTTTGTACTTG[A/C]GATAGTTTGCTGAGA | 115426 |
rs151189520 | snp | A/G | 0.030665 | 0.119967 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458306 | TAGTATTCTCTGATG[A/G]TAGTTTGTATTTCTG | 115426 |
rs151197031 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414363 | CCGAAGTGAAAAGGA[A/G]TGTAAGACTGTTTGC | 115426 |
rs151202749 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467010 | TATCACCCCATTTGT[A/G]TTTAGTTTCCTATTG | 115426 |
rs151206738 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488682 | AATTTTTGTGTTTTT[A/G]CTAGAGATGGGGTTT | 115426 |
rs151263193 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477386 | AAAAAATTAGCCAGG[C/T]GTGGTGGCACATGCC | 115426 |
rs151266722 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421377 | TTGTGTAATTGCACC[A/G]AGGTTAAGAAGTAGA | 115426 |
rs151279412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504439 | ACATATAATAAATCA[A/G]GGTAATTGGAATGTT | 115426 |
rs151317843 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425854 | AGAGCCTTCAACAGA[C/G]AGCAAGGAAATAATA | 115426 |
rs180673166 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416874 | TTTAAAGGATTCTCT[C/G]TCGTCATTCTTTCAC | 115426 |
rs180680509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433189 | TTAAACCTTTCATTT[C/T]ATAACTCTTAATTCT | 115426 |
rs180688384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447976 | TTTTAACCACTTTTA[A/G]CCCTACCTAGTGTTT | 115426 |
rs180816332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489869 | TTTTCAGACAAATAG[A/G]AAAGCGTGCTGGCTT | 115426 |
rs180821983 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499172 | GCCCATCTGCTATGA[C/T]GAGTAATAGTCATTG | 115426 |
rs180825381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483437 | TACCTATAATACCTA[A/G]TAAAGTGTAAATGCT | 115426 |
rs180853991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474177 | CATTGGTGGTCACAA[C/T]GGATGTGCATGTTGA | 115426 |
rs180860849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460388 | ATATAGAAACTACCC[C/T]GTAGGTATCGCAGTA | 115426 |
rs180872655 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471705 | GCTAAGCTACTCCCA[C/G]ATTCCTGACCCACCC | 115426 |
rs180893956 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505309 | TGTATATATATATAT[A/T]TTTTTTGACGGAATC | 115426 |
rs180898402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493650 | TAGGTCAAGTTATAT[A/G]ACTTGAAAGTATACT | 115426 |
rs180898993 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503138 | TAGCTGGGATTGCAG[A/G]CACCCGCCACCACGC | 115426 |
rs180904018 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458238 | TTCGTCTTGGGAGGG[C/T]GTATGTGTCCAGGAA | 115426 |
rs180912953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450538 | ATCAGGAGACACATA[A/C]TACTTTTCTGTGGTA | 115426 |
rs180926227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429650 | CTCTGAGTTTTAATG[A/C]GTCTTAACATTGAAC | 115426 |
rs180929440 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463760 | ATAGGTATGAGCCAC[C/T]GTGTCTGGAGAAAAA | 115426 |
rs180932432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444530 | TGTAAGGTGTTTAAG[A/G]AACAGATTCCTGAGG | 115426 |
rs180942777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478645 | TTTTTAAACTATGTG[C/T]CATATTGCTACTGGT | 115426 |
rs180950847 | snp | A/G | 0.000148411 | 0.00861298 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421069 | TAAAGAAAGCTCCGA[A/G]GGTAGGACCTTCCAA | 115426 |
rs180996835 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436938 | AAAAATGAAAGATAA[C/G/T]AGAAGCTTAGTAACA | 115426 |
rs181205050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416209 | GCTGGGACTACAGGC[G/T]TGCGCCACCACTCCC | 115426 |
rs181300203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502705 | GAGTGCCTAGCACAT[C/T]GTAGCTACCTGTAAC | 115426 |
rs181366891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428790 | CTGGGTTCAAACAGT[C/G]CTCCTGCCACTTCCT | 115426 |
rs181368587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443409 | TAACTTGCTCAGTGT[C/T]AGAGAGCTAGTAAGT | 115426 |
rs181378067 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456774 | AGTTTTCCCAACACC[A/G]TTTATTAAATAGGGA | 115426 |
rs181392097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420404 | TGTAGTGAATATGGA[A/G]TAATTATTAAGAATT | 115426 |
rs181399347 | snp | C/G | 0.00795532 | 0.062565 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411781 | TACTGTACCTTTATG[C/G]GAATAATTAGCACCT | 115426 |
rs181402024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429075 | GAGGCTGAAGCAGGA[C/G]AATTGCTTGTACCTG | 115426 |
rs181411976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436870 | ATTTTACGTGATGGA[A/G]TTAAATGTTTCAATG | 115426 |
rs181414172 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486345 | AGCAATCCTTGTAAC[C/T]AAAAGGGTTTGAGGA | 115426 |
rs181423381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457797 | GTTCTGTTTATGTGA[C/T]GGATTATGTTTATTG | 115426 |
rs181488481 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437076 | GATACAAAGCATGTT[A/G]AAGTTTCATTCTTTG | 115426 |
rs181502358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501724 | TTTACTTGTATTTTA[C/G]CCAAGACACCCAGGC | 115426 |
rs181534751 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485397 | TAGTCTAAGATGACT[A/G]TGAGGTTGTTTTCCT | 115426 |
rs181539525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470778 | CCAATCTCTAATGCA[A/G]CTACTAAAAATAAAG | 115426 |
rs181540848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444237 | TAACCTGTCTGCTCT[A/G]TTGCTTCTTGGTTGT | 115426 |
rs181544069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471232 | AATAGCTGGTGGGAT[A/G]AACAGTGGAAAGCTT | 115426 |
rs181559123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498984 | GTCTTTTTAAACTCA[C/T]AGAATTGATTGTTGA | 115426 |
rs181565803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483030 | CTGTGGATGCTCAAA[C/T]TGCACACAAGCTCAG | 115426 |
rs181577063 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412060 | CAGGGAGGCTGAGGC[A/G]GGAGAATGGCGTGAA | 115426 |
rs181587633 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441035 | TGCCTTAGTTCATTG[A/G]TTCTCAAAATAATGG | 115426 |
rs181590784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454838 | AATTCCTGTATTTCT[A/G]TGGCACAGTGGGTTT | 115426 |
rs181598003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467278 | GTTGCTTCTCTTTGA[C/T]AGTTCTTTTTGTGGC | 115426 |
rs181613174 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425178 | TTGAGGGCAGAGTAT[C/G]TACAAAAAATTATTT | 115426 |
rs181616232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421500 | TGGCTCGCTATGACC[G/T]CTGCCTCCCAGGTTC | 115426 |
rs181717165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464692 | CATTGATCTTCAGTA[C/T]CACCTCTGTCATATC | 115426 |
rs181717402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494247 | TTGTCTACTACTCCA[C/T]TGGTCAAAGCTAAAA | 115426 |
rs181811892 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473889 | AAAAAACTGTTTAAC[C/T]CATACTTTGGGAATG | 115426 |
rs181813355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447189 | CCACCGCGCCCAGCC[A/G]GCACACGTACCTTTT | 115426 |
rs181822683 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506430 | GCCTCAGCTCTAGTT[C/G]ATATCCAAGTTATGA | 115426 |
rs181826412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490599 | CATCACTGTACTCCA[A/G]CCTGGATGACAAAGT | 115426 |
rs181851106 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450828 | AACAGAATGTTCCAG[A/C]CCTGGGTTCAGCCAT | 115426 |
rs181880880 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479357 | TTACTCTGTTTTATA[G/T]ATTTGAGATCAGGTA | 115426 |
rs181999825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448086 | TGTGGACCAGGCGTA[A/T]AGCCTACAAAGCCTA | 115426 |
rs182005182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460514 | GGTTTTTCTGTACAT[C/T]GCATAAAACTTTAGT | 115426 |
rs182011189 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424893 | GTCTGGGTTTGTTTT[A/G]GGGAGGAAGACCGCA | 115426 |
rs182024707 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474843 | ATTTGAAAGACTTTA[C/T]GAAAAGGGCATCTTA | 115426 |
rs182065867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432324 | GTTGATAGTTTTTGT[G/T]TAGTCTGTATTCTTT | 115426 |
rs182075247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460260 | AGCTCCCTCAAAGTA[A/G]ATGATTGTGGTTCTT | 115426 |
rs182137469 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475831 | AAATGATCAAATCTG[A/G]GAAACTGGGATATTC | 115426 |
rs182167936 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435405 | TGCTGGGATTAAAGG[C/G]GTGAGCCACTGTGCC | 115426 |
rs182173273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448949 | AAATCTTTAAACATC[A/G]CAGAACAAGCAGTAT | 115426 |
rs182180815 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462236 | CACAGTATTGTTGAA[C/T]AATTGCAACTGAGAC | 115426 |
rs182196484 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418483 | GTGTTTGAGATTGTG[C/G]TTGTTGGGTTCTTGG | 115426 |
rs182227158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495948 | GCCCTAGAGTTGATG[A/G]CTGTGTTTTTTTCTA | 115426 |
rs182234768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479987 | TGAATTAGATCATTC[A/G]TCTGTTTGAAACCCT | 115426 |
rs182253322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454531 | CTACGTGAACACAGA[A/G]TGGCTTTTCTTAGAG | 115426 |
rs182253631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433594 | TAGTGTCATTCTTAC[A/T]GGATGACTTGCAAGA | 115426 |
rs182270804 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482529 | GAAGTGCCAGCTAAT[C/G]CAAGAATAAAATAAT | 115426 |
rs182342065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413969 | TTCCCGCGCTCGGCG[A/G]GGCCTGGGGCCCCCA | 115426 |
rs182411039 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494968 | GCTGGTGAAAACATT[A/C]TTGAGACAGGAGCTT | 115426 |
rs182418775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479597 | AATTTATGTCTTCAT[A/G]TCTAATTTCCCCTGG | 115426 |
rs182488401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492038 | GCGCCTGGCCTTTCC[A/G]TAGGAAAAATAGCCT | 115426 |
rs182518375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440508 | AGCCAACTTTTCTAT[A/G]TTGCTGTCAGAGGTC | 115426 |
rs182523645 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417171 | CCCTCTCAGCCACTT[A/C]CACTTGGCATTTGCT | 115426 |
rs182527957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468067 | CAGCTTTATTTGGGA[A/G]TTCTTAGACTGCCTG | 115426 |
rs182529344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498295 | ATAAGATCATGCAAA[C/T]AGACAGAGGAAAAGA | 115426 |
rs182540734 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467042 | TGCTACAACAAATTA[C/T]CACAAACATAGTAGC | 115426 |
rs182557990 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441320 | TGGAGGTTGCAGTGA[C/G]TGAAGATTGTGCCAT | 115426 |
rs182603156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422050 | GTTTTAAACAGTGCT[A/G]TTTTGAACCTTCTGT | 115426 |
rs182615186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452014 | ATATACCCATATCTA[A/G]TGTATATATGTGTAT | 115426 |
rs182621724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437727 | GTTTCAAGTAATTCT[C/T]GTGCCTCAGCCTCCC | 115426 |
rs182633792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451137 | TAGTTTCAGACTAAC[A/G]ATACTTTCATATTGC | 115426 |
rs182639452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465119 | TGTTGAAAATAAGTA[C/G]TGATAACAGGCATCT | 115426 |
rs182660187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421578 | TGCACCACCACGCCC[A/G]GCTAATTTTTGTATT | 115426 |
rs182726376 | snp | A/G | 5.10321e-05 | 0.00505108 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504640 | GTGCGTTTGCTGTCA[A/G]GAGCTAGTTTACCAG | 115426 |
rs182731717 | snp | C/G/T | 0.00755907 | 0.0610114 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507482 | CCTGACCTCGTGATA[C/G/T]GCCTGCCTCGGCCTC | 115426 |
rs182832090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425921 | AATATTTATGTAACT[A/G]TCTGTATATTAAGTT | 115426 |
rs182848910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455070 | TTTTAAGAGTAAGAA[C/G]CAGATGTTACTCATT | 115426 |
rs182853024 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465469 | TTTTATGGTCAGTTC[A/G]GTTTCTGTAATGATC | 115426 |
rs182853963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459843 | CTGGGTGTGGTGGCA[C/T]GTGTCTGTAGTACCA | 115426 |
rs182866542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487961 | AAACAATACAGAGGG[C/T]CGAATCCAGTGGCTC | 115426 |
rs182887954 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439031 | TTTGTTTCCTAATTT[A/G]TCTCCACTATTCCTT | 115426 |
rs182962102 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503491 | TGATCATGTTTACAT[A/T]AGGTGGCTCTACTTT | 115426 |
rs182991101 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422765 | GGCGTGAGCCACCAT[A/G]CCCGGCTAACTTAGA | 115426 |
rs182997845 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458872 | CACATATACACCATG[C/G]AATACTATGCAGCCA | 115426 |
rs183012165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439324 | TGAGACACAGATGTG[C/T]ACCACCACGCCCGGC | 115426 |
rs183020766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487613 | CTCAGGTGATCCTCC[C/T]GCCTTGGCCTCCCAA | 115426 |
rs183027125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471904 | AAAGGAAAAAGGAGT[C/T]CGGTTAGAAATAGGG | 115426 |
rs183034523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430124 | CAAGTGATTGTCCTG[C/T]CTCAGCCTCCCAAGT | 115426 |
rs183037891 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444673 | ATGGCATAATCTCAG[C/T]TCACTGCAACCTCCC | 115426 |
rs183044313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456099 | CAGCCAAGTTACTGA[C/T]AGAATTTTTACATGG | 115426 |
rs183049123 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469195 | TAGAACTGAGAATTA[C/T]AGTTTCCTAAGACCT | 115426 |
rs183058712 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484195 | TCCACCTAGCTAGGA[C/G]TAAAGATGTAAAGAT | 115426 |
rs183063783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427386 | AAACATTTAAACAGT[A/G]TGTTAAGATGAAATT | 115426 |
rs183072231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442122 | GGTGCCTGGCACCAC[A/G]TCTGGCTAGTTTTGG | 115426 |
rs183126084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472429 | GTAAAGGAGAGCCAA[A/G]GATTTTAAGTCAAGC | 115426 |
rs183127004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430744 | TGTTTCCCCTGCCTT[A/G]CCTTTCCCATGGAAA | 115426 |
rs183137177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493228 | GATTGAACCTGGGAG[A/G]CAGAGGCTACAGCGA | 115426 |
rs183150139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476387 | TAATGAGATTTATTT[C/T]TACACGAGTAAAGCC | 115426 |
rs183152424 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445276 | ATTTATGTATTGATT[A/C/G]ATTGATTGATGGAGT | 115426 |
rs183154405 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462715 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 115426 |
rs183156547 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503660 | CTAGTGTTTTTTTTT[A/C]AGCTCCTAAAGACAA | 115426 |
rs183184816 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500109 | TCTGAAGTAGCCCAC[A/C/G]GCTGTACACCACCAC | 115426 |
rs183328844 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496213 | GAAGTATTTTATGTC[A/T]TATCTGCTTTCACCA | 115426 |
rs183358491 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466176 | GAGGCCAAGGTGGGC[A/G]GATCAGTTGAGGTCA | 115426 |
rs183376825 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414988 | GATTTGCTTTGCTGT[C/G/T]CCTCAAGTGGCTGAT | 115426 |
rs183410358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414566 | TAGCCACTCAGACCC[A/G]TCGTATTTTTCTTTG | 115426 |
rs183432680 | snp | C/T | 0.00250807 | 0.0353234 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475508 | GTTTTTAAGTATGGA[C/T]TTTTGTTTTTGGTCT | 115426 |
rs183461517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448373 | AACATGTAAAAAATA[C/T]TGATTTTACAAACTA | 115426 |
rs183463021 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507279 | TCTTGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 115426 |
rs183502092 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426829 | TCTCAGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 115426 |
rs183503071 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417922 | CTGACTCTGGTCCCT[C/G]AAACCTAAGTGGAAA | 115426 |
rs183507712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441378 | AAACCTGTCTCTACC[C/G]CTCCCAAAAAGAAAA | 115426 |
rs183577370 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480936 | TGAAATAGAAAGTAT[A/G]GGCAAAGAAATTTAA | 115426 |
rs183633752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459928 | CAGTGAGCTATTATC[A/G]TGTCACTGTACTGCA | 115426 |
rs183640432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452235 | TTTAGACCTGTTACA[A/G]ATAGTGCAGCTATAA | 115426 |
rs183653879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415629 | CTTTACTGCCACGTA[C/G]TGAAAAATGTCATAA | 115426 |
rs183656890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431536 | GGCTGCGGAGAGCTG[C/T]GATCACACCACTGCA | 115426 |
rs183697874 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483984 | GTGAGCCACTGCACC[C/T]GGCTTCATCATCATT | 115426 |
rs183701018 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463543 | TGGCACAATCCCGGC[C/T]CACTGCAACCTCCGC | 115426 |
rs183713557 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461756 | GAGTTACTTTTTTAC[A/G]CTTTGGAAAACATTA | 115426 |
rs183721037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477878 | GTATTTGAACCACCA[A/G]AAGTAGATTTCTAAA | 115426 |
rs183725363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420604 | CAGCTACTTCAGGGA[A/G]GCTGAGGCAGGAGAA | 115426 |
rs183725442 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436903 | GGCAACTTAAAGATA[C/T]GATAGCTGAACTTTC | 115426 |
rs183725730 | snp | A/T | 0.000419236 | 0.0144721 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500727 | ATGTGAAGATTTTTT[A/T]AAATAATAACATTCT | 115426 |
rs183735144 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450353 | ATTTGTCTTGTACAA[G/T]TTTCTCAGTCTGGAT | 115426 |
rs183746514 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434512 | GGCACAATCTCGCCT[C/T]ACTGCAACCTCAGCC | 115426 |
rs183772566 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473205 | GGAGTCAACTGGAAG[C/G]TCCCACTGGTCAAAG | 115426 |
rs183938193 | snp | C/T | 0.0449785 | 0.14306 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468775 | ACTGGTGTAATGGCT[C/T]CACAGAATATGTAGG | 115426 |
rs183951955 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499665 | GGATTTTAATAGTTG[C/T]CTGTGCTTTGAATTC | 115426 |
rs183966381 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497944 | GTTCTGGCAAAGATT[A/C]TTTTGATACCACTAA | 115426 |
rs183989192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497549 | TTTAAGGCTTATTTC[A/G]AGTTCCTAGGGGCAG | 115426 |
rs184014387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452689 | AAATTGGAGATAACT[C/G]TTACACTTCTAAGAG | 115426 |
rs184021116 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416412 | GACCTGCAATTCAGG[G/T]CTATAAGTTTTGGTT | 115426 |
rs184022355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455321 | AGGCCCGGGTGTGCG[A/G]TGTTCCCCTTCCTGT | 115426 |
rs184028792 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466535 | ACAGAGTGAGACTCT[A/G]TCTCAAAAAAAAAAG | 115426 |
rs184046939 | snp | C/T | 0.000450951 | 0.0150091 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481632 | CCTTCGTTCTTTTTT[C/T]TCTTTTAAAGGTATT | 115426 |
rs184047209 | snp | A/T | 0.141596 | 0.225274 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423949 | GACTCAGTATCAAAA[A/T]AAATAAATAAATAAA | 115426 |
rs184054883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440282 | GTTGTCTTATGTGCC[A/G]GACTCTGAGCATAAC | 115426 |
rs184242229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493454 | GTTGAAGTGGTATTA[C/T]CTATAAAGAACCTAC | 115426 |
rs184248460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442898 | AGGATTTAACATGTA[C/G]TGTCGGTCAGTCTTA | 115426 |
rs184266184 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469684 | TGTGTGTGTATGTAT[A/G]TATATACACGTATAT | 115426 |
rs184275168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504881 | GATAATAATTCAAAT[A/G]TGTGTCATTTGAGAT | 115426 |
rs184281053 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489052 | TGACCTCAAGTGACC[C/G]GCCTACCTCAGCCTC | 115426 |
rs184286455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473699 | AGTAAATAGTTTAAC[A/G]TGGGGGCCAGATGGT | 115426 |
rs184286762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460057 | TCCCCTACTTTCCCA[G/T]CTAGCAATGAACGTC | 115426 |
rs184368522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424278 | TCAAGGAATTAATGC[G/T]TGAATTAGAACAGGA | 115426 |
rs184404855 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456249 | GGCGTGATATGGTAT[C/G/T]TCAGTGTGGTTTTGA | 115426 |
rs184433515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428052 | GACTAAATAATGACT[A/G]TTTAGAATGATGATG | 115426 |
rs184494099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501952 | AAAGTTGTCTTCCCT[A/G]TGGGTAGTGTCCCAC | 115426 |
rs184496715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440476 | TCAGCACAGACATGG[A/T]ACATATAATTGATAA | 115426 |
rs184501897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482437 | ATTCTCATTGAATGT[C/T]GTGGAACTCTAAGCT | 115426 |
rs184503769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485969 | GTCATCCATTGAAGT[A/G]GAAATGGATAGCATG | 115426 |
rs184509496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457085 | CAGCATTGAATCTAT[A/C]AATTACTTTGGGCAG | 115426 |
rs184511581 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470845 | TAAATATTAGTCTAA[A/T]CCAAAATAAGGCAAT | 115426 |
rs184533036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454104 | ACCACCATATGAGAT[A/G]CAGTTACCATTAGGT | 115426 |
rs184538176 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420030 | TTGGGATTACAGATG[C/T]GAGGCCCGGAGCCCA | 115426 |
rs184554502 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489773 | GATATGTGGTCTTCA[A/G]GTATTTACTTGCTTT | 115426 |
rs184565381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443275 | TGTTAAAATAACACA[C/G]TGTGCCAAGCAGTAT | 115426 |
rs184573023 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460304 | ACACTTACTTGCCTG[A/C]CAACCTGCAAGCCAT | 115426 |
rs184578506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456567 | CAATTTTGGCTTCTG[C/T]TGCCGTTGCTTTTGG | 115426 |
rs184604332 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411210 | CCAACCTAAATATCA[C/T]CTCATTTACATATGT | 115426 |
rs184604704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428409 | CATTTCTTTGTTCTT[C/T]ACTAACTTTCTTATT | 115426 |
rs184610163 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433038 | TAGAGACGGGGTTTC[A/C]CTATGTTGGCCAGGC | 115426 |
rs184649461 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488174 | CTTGAGCTCAGGAGG[A/T]CGAGGCTGTAGTGAG | 115426 |
rs184672209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466918 | AATCACCCTTTTTAA[A/T]ATCACATACATACCA | 115426 |
rs184697063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473938 | ACTGTGAGAAACACT[A/G]TAGGACAAATGGTTG | 115426 |
rs184723733 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505064 | GCATCATGCCCAGAT[G/T]AATTGAATATTGTGT | 115426 |
rs184749288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447238 | CTACTATTAGCAAAA[C/T]AGATGTCAGGCGGTC | 115426 |
rs185002661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421608 | TTTTAGTAGAAACAG[C/G]GTTTCACCATGTAGG | 115426 |
rs185110261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447091 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 115426 |
rs185141281 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415956 | ATCCTCACGCCAGAC[A/C]TACTGAAGCTGACCT | 115426 |
rs185192609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449760 | TTCTGGGAGTCTGGA[A/G]TTCTGGTATGTGCTA | 115426 |
rs185210855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431899 | ACTATATGCTGCATT[C/G]TCTGCTATGCAATAT | 115426 |
rs185268510 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467481 | GTTCTGCCTGTCATA[C/G]CACTGGAATGTTAAT | 115426 |
rs185292030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436666 | AGTTTTAGGGGCTCT[C/T]AAAGTTGCTTTTGAA | 115426 |
rs185302458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441042 | GTTCATTGATTCTCA[A/G]AATAATGGTCCTTGG | 115426 |
rs185303868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499014 | AAAATAAGGCCATCA[A/G]CTGCTAAAACAACTA | 115426 |
rs185310366 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483055 | GCTCAGGCTGGTGTG[A/G]TGGCTCACACCTGTA | 115426 |
rs185312270 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454894 | ACTGAGGGGATTTGT[A/G]AATGTAGATTGCTGG | 115426 |
rs185330488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476795 | GGACGGGGTTTCACT[C/G]TGTTGGCCAGGTTGG | 115426 |
rs185384680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485346 | TATACCTGTCTGTCA[C/T]GTATTTATTTTCTAA | 115426 |
rs185442040 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435688 | CTTGGCTCACTGCAA[C/T]CTCTGCCTTTCAGGT | 115426 |
rs185465898 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463044 | CCCAGCACTTTGGGA[C/G]GCCAGGGTGGGTGGA | 115426 |
rs185468449 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460425 | AGAAACCAACATGAA[A/G]TAATAACACCTGCTA | 115426 |
rs185484692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416902 | CACTCCTTACCACTA[G/T]AGAGGTGGTCTTAAA | 115426 |
rs185489384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489945 | TAAATGGAAATGGAA[A/G]TATTTAGGTTCATCC | 115426 |
rs185495094 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474596 | CTGTAATCCCAGCTA[C/T]TTGGAAGGCTGAGGC | 115426 |
rs185499913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433332 | TTATATTTTATCTTT[C/G]TTCTTTGAGGTGGTA | 115426 |
rs185500371 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501241 | CTTTGTGTTAAGCTG[C/T]GTTTTGCAAACAAGC | 115426 |
rs185507061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447986 | TTTTAACCCTACCTA[C/G]TGTTTAAAACAGGAA | 115426 |
rs185548929 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438006 | TATTGTCCTCCAGCT[C/G]TCATGCCTTAAAAAC | 115426 |
rs185553168 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495688 | GGCAGATAGATTAAT[A/G]GAGGAGCTTTGTTGC | 115426 |
rs185559273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451340 | TCTCACATTTTGTTA[A/G]TTGTGTTTATAATTA | 115426 |
rs185560281 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469969 | CACAGTGGTATATCA[C/G]AAACAAGAATGCTAA | 115426 |
rs185563344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479738 | CATTAAATAGTACTA[A/G]TCATTTTATCTACTT | 115426 |
rs185569739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465303 | TAATTTTCCTATCTC[A/G]GTGTCCTTCACGGAT | 115426 |
rs185575302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449552 | AAAAAGGATTCTTTT[G/T]AGAGTTTGCAGAAAA | 115426 |
rs185613335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498377 | GCTTGGGAAAAGTTG[A/G]ACCTGTTAATTAAAA | 115426 |
rs185767798 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440551 | AAATATTTAATTGCA[A/C]GTATGAGCTGAAGAC | 115426 |
rs185780132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454602 | CACACAGGATTAATA[C/T]CTATTTAATCGAAAT | 115426 |
rs185807480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419777 | ACAGGGTCTCACTCT[G/T]TTGCCCAGACTTGAG | 115426 |
rs185815280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424985 | TTAGGTTTTACATCA[A/G]TGATAACATTAACAC | 115426 |
rs185866409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444275 | GTCTTTACCAAAGAC[G/T]TAGAGTATTTCCTCT | 115426 |
rs185899091 | snp | G/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412342 | CTAGTAGGGTCTTTG[G/T]AGTTCTTTCTTCGGA | 115426 |
rs185993675 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429571 | CCTGACCTCAGGTGC[C/T]CCACCTGCCTCGGCC | 115426 |
rs186008434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457826 | TGATTTGCATATGTT[A/G]AACCAGCCTTGCATC | 115426 |
rs186016035 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437236 | CAGATTTTTTATTTT[A/T]TTATTATTATTTTTT | 115426 |
rs186052547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421518 | GCCTCCCAGGTTCAA[C/G]CAAATCTCCTGCCTT | 115426 |
rs186064355 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483576 | ACTCTCTCGACTTGG[C/T]AGATGTGGAACCTGT | 115426 |
rs186068032 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505836 | ATAATTTACCTGAAG[G/T]CTCCCAATATCTGCC | 115426 |
rs186104611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426627 | ATTCCATAAATAGGT[A/G]GATATCTAGCATATG | 115426 |
rs186123189 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455083 | AACCAGATGTTACTC[A/G]TTTCTTTGTCCCTCT | 115426 |
rs186187392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499601 | TCTGAAACTTAAGAT[C/G]AGTGTATTATAAAAT | 115426 |
rs186215470 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468165 | GTGAAATAGGATATT[A/T]CTTGGGGAATGAATT | 115426 |
rs186248601 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441322 | GAGGTTGCAGTGAGT[C/G]AAGATTGTGCCATTG | 115426 |
rs186286787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479283 | TGTCAGGTTCACAGA[C/T]ACTTTTTATGTCTAA | 115426 |
rs186287648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458343 | CAGTGGTGATATCCC[C/T]TTTATCATTTTTTAT | 115426 |
rs186298839 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414230 | GGTCCCTCTCCCTCG[C/T]CGCCTTTCCTAGGTT | 115426 |
rs186301260 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429738 | TTGGCACGTTACATG[A/G]ATTTTCTCACTTTAT | 115426 |
rs186302987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471722 | TTCCTGACCCACCCC[C/T]ATATGAGTAAGTACA | 115426 |
rs186311236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493654 | TCAAGTTATATGACT[A/T]GAAAGTATACTACAC | 115426 |
rs186311271 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444553 | TCCTGAGGGGACCCT[C/T]TCTCTCCCTGCTTCC | 115426 |
rs186320695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491820 | TTTAGGCTACTGCCT[A/G]CCAGGCACAATTTAA | 115426 |
rs186326316 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475573 | TTTTACTGGTCAGTG[A/G]ATAACTTGGAAGGAA | 115426 |
rs186375334 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425235 | TTATTCAGACATTTA[C/T]ATCAGTATGAACTCA | 115426 |
rs186408463 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471447 | CTAGGGTGGCTCTTT[C/G]TGACCAATAGAATAT | 115426 |
rs186467923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502739 | AAATACCTGTATTAG[A/G]TATACCCGTATTATA | 115426 |
rs186508441 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506892 | CACTTCTCTACTAGT[A/C]GAACTGCTTTTAGTG | 115426 |
rs186510927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491307 | ACTGAACCTCTGCCA[C/T]ATCTGTAAAATAAGA | 115426 |
rs186617309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486379 | AGGGAGAAGAATGGG[A/G]CTAAAATAACTCCTG | 115426 |
rs186653248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417540 | GTAAATCATCTCAAC[A/G]CTTCACAGCTCTTCA | 115426 |
rs186674379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467164 | ATTCAGTTTTGTAGA[C/G]TCTAAGGGAGAACCC | 115426 |
rs186764162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435451 | TTTAAACAGCTTTTT[A/G]TTGAGATAGTTCACA | 115426 |
rs186769567 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507492 | TGATACGCCTGCCTC[A/G]GCCTCCCAAGGTGCT | 115426 |
rs186772741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449161 | AGAAAGACCTTTACT[C/G]ACCAGCTGCAAGTAG | 115426 |
rs186772742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492769 | TCAAGTACTGAATCA[G/T]ATAGAGACAATAATA | 115426 |
rs186781367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475890 | TGTGTGTTGGGAACA[C/T]TCTAAATCTATTCTT | 115426 |
rs186781563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462474 | CTTGAAACCCTGATA[C/T]GGATGCAAATCATGA | 115426 |
rs186807906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418839 | TAAAACAATAGAAAT[C/T]TACTGTCTCACAGTT | 115426 |
rs186864024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418233 | GTTTTTTTCCCTCCA[C/T]GGGAGTTCAAGACTA | 115426 |
rs186867822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434880 | TTGTTGCACATACTG[A/G]AGTACAGCAATGTGA | 115426 |
rs186881839 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433670 | ATACGTCAGTAAGGC[A/C/G]TAAAGAAAACACCTA | 115426 |
rs186899410 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479368 | TATAGATTTGAGATC[A/G]GGTAATCCCGATTTT | 115426 |
rs186939785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450942 | GTTTCTAGGTCTTTT[C/T]GTTGGAAAAGAACTA | 115426 |
rs186959343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428996 | ATGGTGAAACCCCAT[C/G]TCTGCTAAAAATATA | 115426 |
rs186982188 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411801 | AATTAGCACCTATGT[C/G]AATATTTAAGTTACC | 115426 |
rs187013004 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463778 | GTCTGGAGAAAAAAA[A/T]TTTTTTTTTTTAATG | 115426 |
rs187060467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436957 | AGCTTAGTAACAGGT[A/G]AATGTCACCTCTTTA | 115426 |
rs187081585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494498 | ACAAAAGAGCCACCG[G/T]GTGCTGATCTTTATT | 115426 |
rs187086021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415252 | AAACTAGGAAGCTCA[G/T]TCCAGATTCCAGGGA | 115426 |
rs187116931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484456 | TCCTCCCTCCTCCCC[A/C]CTCCTCCTGGATGCA | 115426 |
rs187138206 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464814 | ATAATACAACAGAGC[A/G]CATGATCCTGCCTTG | 115426 |
rs187145189 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469459 | GGAGACAGAGGTTGC[A/G]GTGAGCCAAGATTGC | 115426 |
rs187170569 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500273 | GCATCCAGCCAACAT[A/G]CTTTTTAATAAAGAG | 115426 |
rs187211046 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497714 | GCAGCACATCATAGT[A/G]ATAGATTTTCATTCT | 115426 |
rs187213859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450811 | TCTTTGTGTTCAGGT[A/G]TAACAGAATGTTCCA | 115426 |
rs187239411 | snp | A/G | 3.30338e-05 | 0.00406397 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421084 | GGGTAGGACCTTCCA[A/G]TCAGCCATCTACATC | 115426 |
rs187277780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448092 | CCAGGCGTAAAGCCT[A/G]CAAAGCCTACAATCT | 115426 |
rs187361452 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503202 | GTTTTGGCCATGTTG[A/G]CCAGGTTGGTCTAGC | 115426 |
rs187494255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485287 | TATAGTAAAAATACA[C/G]TTTGTGTATTTCTAA | 115426 |
rs187498183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482787 | ATTTGTAGTAGAGAC[A/G]AGGTTTCACCGTGTT | 115426 |
rs187550304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415824 | AGACCCCACGGGAGA[G/T]TCTGATAACACCAGA | 115426 |
rs187563825 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461224 | TGATTTTTCACCTTA[C/G]AGAATTTAAACTTAA | 115426 |
rs187607954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472047 | TTAAATACAGTGAAC[A/G]TTGACAAATGGATAT | 115426 |
rs187626547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459016 | AGTGGAAGTTGAACA[A/G]TGAGAACCCATGGAC | 115426 |
rs187627780 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423255 | AATTGTTTTAAACCT[A/G]TGAGGAGTAGATCAT | 115426 |
rs187629224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503509 | GTGGCTCTACTTTTT[A/G]TAATTTCCTCCTACT | 115426 |
rs187637201 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439474 | TTCTTGTGAATATTC[A/G]ATTGTCAGCCTTAAG | 115426 |
rs187640179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487791 | ATAGGCGTGAGCCAC[A/G]GTGCCCATCCTCTAT | 115426 |
rs187640223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452322 | AGGTGGAATTCCTGG[C/G]TCAGAAAGCAAATGT | 115426 |
rs187689704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456306 | GATGAGCTTTTTTTC[A/G]TATGTTTGTTGGCCG | 115426 |
rs187723094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496024 | GGTAACTTGGGAAGC[C/T]TCAACTCTTTGACCA | 115426 |
rs187740495 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431595 | TAAAAAAAAAAATTC[A/T]TACGTCCAGTTGTAA | 115426 |
rs187741284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500875 | AGGCAACACATATAC[A/G]TGCGCCTAAATTTAC | 115426 |
rs187747189 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446466 | TTTAATTTTTAGTAG[A/C]AGCAGGGTTTCGCCA | 115426 |
rs187747392 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488425 | GTCAGGCTGAACATT[C/T]ATATTACCACAGTTT | 115426 |
rs187752264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460014 | AAAAATGTAGAGCAA[A/G]AGCTTATGTTTTTAT | 115426 |
rs187755499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473350 | TTATTTTTAAAACTG[C/T]TAAGTCAGCATTTTA | 115426 |
rs187763164 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493245 | AGAGGCTACAGCGAG[A/C]CGAGATCGTGCCACC | 115426 |
rs187800341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461958 | ATTTGTTTTATTGAG[G/T]GCCGAGGGTTTTAGA | 115426 |
rs187807855 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442321 | AATAGATGTCAGATT[C/T]TTCCCTGATTGTAAA | 115426 |
rs187945518 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455452 | CTTCATCCCTGTCCC[C/T]ACAAAGGACATGCAC | 115426 |
rs187953936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468876 | GCCTTGACTCAGCAT[A/T]GATGCTGATTAAATG | 115426 |
rs187979234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427074 | GTTTTATATTTGCAT[C/T]GGGTTTTTTGTATTT | 115426 |
rs187984723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441759 | TTCCATTTTATTTCC[A/T]TATAGACATAAATTA | 115426 |
rs187986508 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469701 | ATATACACGTATATA[C/T]ATACATATACACACA | 115426 |
rs187992040 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503926 | ACTCTGATTTAAAAC[C/T]AATGTGTATGGAATG | 115426 |
rs188034708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445395 | CAGCCTCCTGAGTAA[C/T]GGATTACAGGGGCAT | 115426 |
rs188057815 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472846 | TGTCCTTAAGAACTG[A/G]GATTTTTCTGGTTGG | 115426 |
rs188074018 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448558 | TAATGCCAGACTGTC[C/T]TAAGGGTTGTTATAA | 115426 |
rs188080258 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427641 | AGTGAGCTTAGACCG[C/T]GCCACTGCACTCCTG | 115426 |
rs188145479 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478529 | AATCTATTTTTCTCC[C/T]ATGGCGTGGTGATAA | 115426 |
rs188164316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450423 | TTCTGTTATGTGTTA[A/G]TTTCCTGAGAAGCTA | 115426 |
rs188172537 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463673 | ACAGGGTTTCACCTT[A/G]TTGTCCAGGCTGGTT | 115426 |
rs188187084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493643 | AAAGTGTTAGGTCAA[C/G]TTATATGACTTGAAA | 115426 |
rs188284041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487962 | AACAATACAGAGGGC[C/T]GAATCCAGTGGCTCA | 115426 |
rs188325245 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459854 | GGCACGTGTCTGTAG[A/T]ACCAGCTACTCAGGC | 115426 |
rs188361864 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430906 | GTTGTCACTTAGTTA[C/T]ATCAATAAATTAAAA | 115426 |
rs188448352 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502574 | TTTATAGGCATGAGT[C/G]AGTTTGCTCTGTTTC | 115426 |
rs188460338 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486117 | GACTTGGGTTTGATA[C/G]TGTGTGACCACTTAA | 115426 |
rs188467593 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471056 | CAGAAGTTGAAAAGA[A/C/G]GTGGATGGTTGGGAT | 115426 |
rs188510238 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481437 | GGATTTATAAGTTAT[C/G]TAAAGGAATGACAAG | 115426 |
rs188534754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496662 | CCTTTAAAGAACATT[C/T]TCATACACCACTTAT | 115426 |
rs188540070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430267 | CATCCACCCTGGCCC[A/C]CTAAACTGCTGGGAT | 115426 |
rs188584996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439156 | AAATGGTCCTTTTCT[A/G]TAGATTTCTTGGTGA | 115426 |
rs188653422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420247 | TTTCTAGTAGAGACG[A/G]GGTTTCACCATGTTG | 115426 |
rs188667433 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436731 | GTTTGGTGTATCTTA[C/G]AGCACAAAACACAGT | 115426 |
rs188671967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449868 | CACAGTTGGTTGTTG[C/G]AGGCATTAAGCATGC | 115426 |
rs188682629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481934 | ACATCTCAGAATTAA[A/G]GGCTTTCATTAAAAT | 115426 |
rs188704894 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416819 | GGCGTGAGCCACCGC[G/T]CCCGGCCTAAATCTT | 115426 |
rs188706884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453899 | AACAGAGTAAGACTC[C/T]GTCTCAAAAAAAGAA | 115426 |
rs188708862 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433041 | AGACGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 115426 |
rs188714824 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466847 | ATACTCATTTGACTT[A/G]CTCTGTCTCTTATTT | 115426 |
rs188749620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440398 | TATAATTAGCCAAGG[G/T]TCACATCTATTAAAC | 115426 |
rs188753330 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465614 | TTTTAATGTGTTAAT[C/G]TGTTACGATGTTTTT | 115426 |
rs188767239 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466198 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 115426 |
rs188791988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476492 | TAGAATGCAGCTGTA[A/C]CTCTTCATTTAACGG | 115426 |
rs188796791 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504998 | TTTTATATATTATAG[C/T]GCAAACTGGAGTGTT | 115426 |
rs188800306 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489392 | GTGAACAGGTTTTTT[A/G]TAAACGTAAGTCTTT | 115426 |
rs188800759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499735 | CAGTTTGGGGAACGT[A/G]TAGTCTTCCCCTCCC | 115426 |
rs188810557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473830 | AAAGTTTTTTGACCT[A/C]CGCTCCAGATCAGCT | 115426 |
rs188818591 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441000 | TATGATTCTAATGTC[C/T]AGCCATGGTTGAGAA | 115426 |
rs188819204 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414876 | TTGTGTTTGCAGCCA[C/G]TTTTGTACTGACTTC | 115426 |
rs188829538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444750 | TGGGATTACAGGCAC[C/T]CACTACCACGCCTGC | 115426 |
rs188831153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454791 | TTAATGCTGCCTCAC[C/T]CTAGGATATGATATT | 115426 |
rs188839192 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467215 | TTTCAGACGCCTCCC[A/G]CATGCCTTAGCTTGT | 115426 |
rs188844159 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449583 | GAGTTAACATCAGAT[C/T]TGAGACTGGTATCCC | 115426 |
rs188859646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422422 | CTCCCCAATTTCTTT[A/C]CTCTTTCAGGGTCTC | 115426 |
rs188870657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419933 | TATTTATTTATTTTT[A/G]TTTTTTGTAGAGATG | 115426 |
rs188878394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452094 | CACCTTATTTTTTTT[A/G]AGTTCATATATCCTG | 115426 |
rs189019358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480256 | CATACCACTTCTAGT[C/T]ACTCTTGTCACATAT | 115426 |
rs189058456 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425065 | CACTATTAAACTACT[C/G]CCACACCTCCTTCCT | 115426 |
rs189082299 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462835 | GGCAGAGGAATCACT[G/T]GAACCCACGAGGCAG | 115426 |
rs189116022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436098 | GTAATACATTAATAT[A/G]TATGGAAAATATTAT | 115426 |
rs189136399 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484072 | TCTTATTTCTTTCTT[A/T]CTTTTTTTTTTTTTT | 115426 |
rs189312483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428087 | GCCTTTACAGTTTAG[C/T]TGAGCATGTGGCACT | 115426 |
rs189357086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443356 | AAGTGTAGATGTTTT[C/G]TTATGTGTAAAGTGG | 115426 |
rs189364099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485381 | TGAAAGCCTCCTTAT[A/G]TAGTCTAAGATGACT | 115426 |
rs189365776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456593 | TTTGGTGTTTTGGAC[A/G]TGGAGTCTTTGCCCA | 115426 |
rs189372232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470665 | GTGACAACAATAATG[C/G]AGAAGATGGGGTTGG | 115426 |
rs189390305 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411723 | GGATTTGTCTGTGCT[C/T]GTAATTATTTTAGCT | 115426 |
rs189394994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428751 | ACAGAGTTTCACTAT[A/G]TTGTCCAGGCTGGTC | 115426 |
rs189404525 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506298 | CTGAAGCAGCTAATC[C/G]TCTTTCCCACATAGC | 115426 |
rs189414819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490034 | ATACAAAAGATGTTA[C/T]ATAGTTTATTACAGT | 115426 |
rs189525001 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463440 | TAGGAACACAATAGC[C/T]AAAAAGGAACCAGTG | 115426 |
rs189529005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495865 | GTGACATGAATGAAA[C/G]TTACCCTAGCTCTTT | 115426 |
rs189531475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444185 | GAGTACAGGAGGGAA[C/G]TAGAATGAGTTGTTT | 115426 |
rs189535908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479935 | CTTCCATGTACTATC[C/T]GTTCTCCCATAGCAG | 115426 |
rs189546416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493352 | TTTTGTAGTACTTAT[G/T]TATTGTCAATGCCAG | 115426 |
rs189557489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443124 | TTCTTATGAAAGTTA[A/G]TATGTCTGTATCTGA | 115426 |
rs189568667 | snp | C/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420698 | GGCGACAGAGTGAGA[C/T]ACCGTCTCAAAAAAA | 115426 |
rs189569603 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412026 | GCGCGGTGGCGGGCG[C/T]CTGTAGTCCCAGCTA | 115426 |
rs189585313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451929 | AGTTTTTTAAGTAAC[A/G]ATGTTAGTTTGGTTT | 115426 |
rs189593162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465324 | CTTCACGGATTTATG[C/T]TAGTTTCACAAAATA | 115426 |
rs189609501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474135 | GGTGAGGGTTTCTGA[A/G]GTAGTTGATATTCCT | 115426 |
rs189628480 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447365 | CTCTCCCAAACACTC[A/T]ATATTTTGAACATGG | 115426 |
rs189641210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424113 | GTACTAGATAATGCA[A/G]TTAGGCAGGAGAACA | 115426 |
rs189736839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429627 | TGAGCCACTGCACCC[A/G]GGCTATACTCTGAGT | 115426 |
rs189766687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505208 | AATGGAAACAAATCT[A/G]CATACGAGTTTGTGC | 115426 |
rs189817565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457449 | CAATCATGTCATCTA[C/G]AAACAGGGACAATTT | 115426 |
rs189829638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477356 | ATGGAGAAACCCCAT[C/T]TCTACTAAAAAATAA | 115426 |
rs189847640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460323 | CCTGCAAGCCATGAA[G/T]AGATCCACATCTCCA | 115426 |
rs189876301 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489862 | TAGTATGTTTTCAGA[C/G]AAATAGAAAAGCGTG | 115426 |
rs189886000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482937 | GACCTTTAATACAAT[A/G]TAACATTTAGATAAC | 115426 |
rs189966962 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412453 | GTCTACGAACGGAAA[C/T]GTCCGGAGTTAGAGA | 115426 |
rs190038844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437671 | GGCCCAGGCTGGAGT[A/G]CAGTGGTGCGATCTC | 115426 |
rs190042940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451117 | TTGCTTTATCCTACT[C/T]ACGGTAGTTTCAGAC | 115426 |
rs190050452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464992 | ATGTAGATTGTTTCA[A/G]AATGTTTGGAATTAT | 115426 |
rs190071019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421577 | GTGCACCACCACGCC[C/T]GGCTAATTTTTGTAT | 115426 |
rs190090015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432132 | TATGTAATGTATAAC[A/G]TGCTCCATCTCTGAT | 115426 |
rs190110411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460195 | TTATAACAGTAATAC[A/G]TGACTGAATAGATAC | 115426 |
rs190119782 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418303 | AAGCAATATTCCCAT[C/G]CCTATCCTTATCAGG | 115426 |
rs190121956 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454910 | AATGTAGATTGCTGG[A/T]CCTCATTTCCAGAGT | 115426 |
rs190129933 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498497 | ACATTTATCCTAGAG[A/G]GCACAGGGGGTGTCT | 115426 |
rs190258079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499015 | AAATAAGGCCATCAA[C/T]TGCTAAAACAACTAC | 115426 |
rs190268936 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483273 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG | 115426 |
rs190281063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467572 | GATTTTCAGTACGGT[A/G]TTTCATAGATTCCGA | 115426 |
rs190283533 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435073 | GAGTACAGTGATGCA[A/T]CCTCCACCTCCCCAG | 115426 |
rs190286022 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448636 | GGAGGATGGAGGCAA[C/G]TGAACTGTATTTGGT | 115426 |
rs190299400 | snp | A/G | 0.000477311 | 0.0154411 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498149 | AAGGAGATTATGTCT[A/G]CGTTTACAGGTTAGA | 115426 |
rs190339544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440489 | GGTACATATAATTGA[C/T]AATAGCCAACTTTTC | 115426 |
rs190352134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447168 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC | 115426 |
rs190353225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467031 | TTTCCTATTGCTGCT[A/G]CAACAAATTACCACA | 115426 |
rs190383087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416065 | GACTCCACTTTTTTT[A/G]TTGTTGTTTTTGTTT | 115426 |
rs190392933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450824 | GTATAACAGAATGTT[C/T]CAGCCCTGGGTTCAG | 115426 |
rs190412192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479350 | TAGCTGGTTACTCTG[C/T]TTTATAGATTTGAGA | 115426 |
rs190419519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501271 | CCCTTCTTATCAAAT[A/C]CCTAAAGTTGGAGTC | 115426 |
rs190446627 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484077 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTAAGA | 115426 |
rs190450804 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506964 | GCTGACCTTTGAGAG[C/G]ATTTGAAATTGCTTC | 115426 |
rs190477852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469129 | ATATGCTGAAAACAT[A/G]GTGAATTTCAGCTGA | 115426 |
rs190485928 | snp | A/G | 0.00170223 | 0.0291242 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499928 | AAAAGGCCAATTTCA[A/G]ATGGTAGGTAATGAT | 115426 |
rs190561052 | snp | A/C/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482438 | TTCTCATTGAATGTC[A/C/G]TGGAACTCTAAGCTT | 115426 |
rs190592635 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454357 | AAATGGTTTGAATTA[A/G]GAAAGATGATGATTG | 115426 |
rs190624832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424365 | TTAAAACAGTGCTAT[A/C]TAGTGGTCACAATTA | 115426 |
rs190635284 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457983 | CTTTTTTTGTTGTGT[C/G]TCTGCCAGGTTTTGG | 115426 |
rs190643629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438638 | AGGGAGATGTATTGT[A/G]CATGAGATGAAAGAA | 115426 |
rs190652483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464566 | AGGTCTTTAATTGAC[C/T]TGGAGTAGATTTTTG | 115426 |
rs190665914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486673 | GGATCTTTAGGTACC[A/G]GGAGATTTAAAATGA | 115426 |
rs190678978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437058 | TGAGCCCGATATGGT[C/T]GTGATACAAAGCATG | 115426 |
rs190700657 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503556 | ATCAGGAAGGTATGG[A/G]ATTTTAGGATTGAGG | 115426 |
rs190709027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487915 | TAAACTTACTATTTT[C/G]AGATAGTTGTAGATT | 115426 |
rs190801045 | snp | A/G | 0.0053735 | 0.0515546 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493941 | TGAACAGGTACTACT[A/G]TAGACACTGTTTAGA | 115426 |
rs190859128 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503018 | GTTTGTTTTTGAGAC[A/G]GAGTTGTGGTCTGTC | 115426 |
rs190925256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471478 | GGTGTAAGTGATGCT[A/G]TACCACTTCAAGATG | 115426 |
rs190928074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421804 | CTGCTTATTCTTTTA[C/T]ACTCTTTTTGTTTTT | 115426 |
rs190944138 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474601 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 115426 |
rs190968369 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460482 | TCTTTCTCTTAGATG[A/G]TTAACTCAGCAAATT | 115426 |
rs190998107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417131 | CATCCCTAGTCAGTA[C/G]TTGCTTGGGAATGAC | 115426 |
rs191004982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433438 | TCTTTTTTTTATTGT[C/G]CATAATTCTCTCATT | 115426 |
rs191010836 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448052 | AGGAGGTAATGGAAG[G/T]AGATGCTAGCATGAA | 115426 |
rs191037242 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414518 | AGTCTAAGTTTTTTT[C/G/T]CTATTCCACAAGTCT | 115426 |
rs191052246 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430067 | TTGCCCTGAAGTGCA[A/T]TGGCACAATATTGGC | 115426 |
rs191054311 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444637 | ACTGAGTCTTGCTCT[C/T]GTTGCTTAGGCTGGA | 115426 |
rs191081432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444945 | CGCTGGCCATTAAGT[A/G]TACGGAGCAGTGGTT | 115426 |
rs191110201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472309 | TCTTATGAAAATAAG[C/T]GAAAGGATCGATGTT | 115426 |
rs191120550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494507 | CCACCGTGTGCTGAT[C/T]TTTATTCTATAGAAA | 115426 |
rs191121193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445695 | CCTAAGTAGCTGGGA[C/T]CACAGGTGCATGCCA | 115426 |
rs191150884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415621 | TCAAAATACTTTACT[A/G]CCACGTAGTGAAAAA | 115426 |
rs191151070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431530 | GTAGGAGGCTGCGGA[A/G]AGCTGTGATCACACC | 115426 |
rs191184358 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425315 | CTATGTCCCTTTGAC[A/T]TACCCCCATTATTGT | 115426 |
rs191186854 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487436 | CAGTGGCTCAGTCTC[C/G]GCTTACTGCAATCTC | 115426 |
rs191195034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471880 | AAGTAGGACCAGGAG[A/G]ATAGAGACAAAGGAA | 115426 |
rs191209509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458391 | TCTCTCTTTTCTTCT[A/G]TGTTAGTCTGGCTGG | 115426 |
rs191219867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503434 | ACCAGCCAAGATGAA[A/G]TGGAGCCAGTAATGG | 115426 |
rs191242447 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466899 | CTTCAGAGTTACCTT[G/T]CTTAATCACCCTTTT | 115426 |
rs191254724 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482264 | AGGTTAACAAAGGAA[C/G]ATACATCACAGAATT | 115426 |
rs191334260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459544 | AGTGGTGGCACATGC[C/T]TGTAATCCCAGCTAC | 115426 |
rs191341061 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492819 | GCTATAGAAGTAATT[A/G]GAGAGCTTTTGGCTT | 115426 |
rs191349165 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476257 | TTGTATATGTATATA[A/C]CATATTGTCTTTTTA | 115426 |
rs191359666 | snp | A/G/T | 0.00199529 | 0.0315338 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507442 | AGACGGGGTTTCACC[A/G/T]TGTTAGCCAGGTTGG | 115426 |
rs191364333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430686 | CAACTAGAGGCCACC[C/T]CTACAATCCAAAGCC | 115426 |
rs191368613 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479410 | ACTGGCCTTTCCTTC[G/T]TAGTCTCTTGTTGGG | 115426 |
rs191381753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475643 | ACAGTTTTGATCTAA[G/T]ATTCATTTTGTTTTA | 115426 |
rs191394666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497751 | AAAAAGAGGCATTTG[C/T]TGCCATCTTTACGAT | 115426 |
rs191401473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491392 | ATGCTTCTCCTAACA[C/T]CACCTAACCCACCAG | 115426 |
rs191432583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441222 | AGTCTCTACAAAAAA[A/C]ACTCAGCCACCTATG | 115426 |
rs191445678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461658 | ATTACAGGTATGAGC[C/T]ACTGCGCCCAGCTTT | 115426 |
rs191479066 | snp | A/G | 3.30218e-05 | 0.00406323 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434093 | AGAGAACACAAATAA[A/G]TTGGACAGTGTACCC | 115426 |
rs191612526 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491929 | ATAGAGACAAGGTCT[C/T]GCTATGTCACCCAGG | 115426 |
rs191619787 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462097 | CTTGGAACAATGATT[A/T]AAAATCTAAAGCGAG | 115426 |
rs191686641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448239 | GTAGATAAATTAATG[A/G]TAGGTACATAGTAAC | 115426 |
rs191701266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423878 | TGAACTTGGAGGGCA[G/T]AGGTTGCAGTGAGCC | 115426 |
rs191704766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439913 | AATGTTAAGGTAATA[C/G]AGGCAATTATAAATC | 115426 |
rs191713828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475182 | AATGAAGTCTGTATT[A/T]TTTTTCTCATATTAC | 115426 |
rs191716122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417686 | ATCTGGGTTTAAAAA[A/G]CCTGTCATAGCAAGC | 115426 |
rs191868559 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477481 | CAGTGAGCCAAGATC[A/C]CGCCATTGCACTCCA | 115426 |
rs191876482 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500331 | AAATGAAAGCAAAGG[A/T]TTTGGCTGGGGGGGC | 115426 |
rs191881491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484503 | CCCCTCCTGGGCTCA[A/G]GCTGTCCTTTACTCT | 115426 |
rs191888219 | snp | C/T | 0.000186759 | 0.0096615 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468714 | AAATGTAGTAAAAAG[C/T]GGCATTTTCAGCAGT | 115426 |
rs191888764 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463513 | TCTCGCTCTGTTGCC[C/G]AGGCTGCATAGCAGT | 115426 |
rs191906236 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499621 | TATTATAAAATGGAA[A/T]CTCTTAGCAGTCACA | 115426 |
rs191914500 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441357 | CCAGCTTGGGTGACA[C/T]GGTGAAAACCTGTCT | 115426 |
rs191927067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450075 | AGTCCTGTGAGTTCT[C/G]CTACATCATTGAACC | 115426 |
rs191983626 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456093 | TACGTACAGCCAAGT[G/T]ACTGATAGAATTTTT | 115426 |
rs192012396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427093 | TTTTTTGTATTTCCC[A/G]TAGTGCAAGTCTGAG | 115426 |
rs192028181 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442084 | ATTCTCATGCCTTAG[C/T]CTGTCGAGTAGCTGA | 115426 |
rs192116318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504999 | TTTATATATTATAGC[A/G]CAAACTGGAGTGTTT | 115426 |
rs192174226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459866 | TAGTACCAGCTACTC[A/G]GGCAGCTCAGGCTCG | 115426 |
rs192174472 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488068 | CAACGTGGCAAAGCC[C/G]TGTCCCTACCAAAAA | 115426 |
rs192181833 | snp | C/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440399 | ATAATTAGCCAAGGG[C/T]CACATCTATTAAACT | 115426 |
rs192211477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426711 | ACTAAACTGAAAACC[A/G]TTTAGAAGCTGCTAC | 115426 |
rs192213386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481486 | CTAACCATGTAAATA[C/T]TTTGAAAAGTTTAGT | 115426 |
rs192217552 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483804 | AAGCAATTCTCCTGC[C/G]TCAGCCTCCCAAGTA | 115426 |
rs192236514 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455320 | CAGGCCCGGGTGTGC[A/G]ATGTTCCCCTTCCTG | 115426 |
rs192237776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452430 | GAGAGTACTTGTTTT[C/T]CCATAGCCTGTCAAC | 115426 |
rs192246338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466237 | GAAACCTCATCTCTA[C/T]TAAAAATATAAAAAT | 115426 |
rs192398497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435515 | GTTTTTGACGTACTA[C/T]CACAAACTAATTTTA | 115426 |
rs192398679 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443141 | ATGTCTGTATCTGAT[C/G]TTAAGAATGAAGCTA | 115426 |
rs192403082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501220 | CACAGTTAATTAATG[C/T]GTGGGCTTTGTGTTA | 115426 |
rs192411873 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449498 | GTTACCTTCATCTTG[C/T]CGTCTGTTTCCCAGA | 115426 |
rs192417699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428317 | TAACAATACTCCCAG[A/G]AACTTACCAGGTGCC | 115426 |
rs192417923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462578 | GCATGTGTACACAGT[A/G]GGATAACAGCACACA | 115426 |
rs192418064 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469763 | ACGTATATATACACA[C/T]GTATATATGTGTGTA | 115426 |
rs192516179 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473199 | GATTTGGGAGTCAAC[C/T]GGAAGCTCCCACTGG | 115426 |
rs192518507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453951 | AGAAGAGTAGAACTA[C/T]AGACATAATTTTGTA | 115426 |
rs192552468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504322 | GAGCCACCGCGCCCG[A/G]CCTCTAAATAGAAGA | 115426 |
rs192561947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424179 | AGCCTATGGATACCT[C/G]GGAGAGCTGAGAAAA | 115426 |
rs192610583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504870 | AATTAGATAGTGATA[A/G]TAATTCAAATATGTG | 115426 |
rs192620875 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488867 | TTCCAGGCTACAGGG[C/G]AGTGATGCGATTTCG | 115426 |
rs192626274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473533 | GCATTAGTAGCTGCC[A/G]TCAGGAGAGGAAAAG | 115426 |
rs192655415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431700 | TGGCAGTATTTTGAG[A/G]TTGATTTAGGTGTCT | 115426 |
rs192656137 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414932 | TATTTAGTTGTAAGC[G/T]TTGCTTTTGAAATAA | 115426 |
rs192660359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446759 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCCAAGAA | 115426 |
rs192670752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460045 | CACCCTCCCCAGTCC[C/T]CTACTTTCCCAGCTA | 115426 |
rs192760052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456520 | TTCTTTTGCTGTGCA[A/G]CAGCTCTTTAGTTTA | 115426 |
rs192762451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485332 | TGCATCTTTTTTCGT[A/G]TACCTGTCTGTCACG | 115426 |
rs192784088 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456222 | GACTTTTTAATGATC[A/G]CCATTCTAACTGGCG | 115426 |
rs192800462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428001 | AAGCTTTTTATGATG[C/T]CAGAAAGATCGTACT | 115426 |
rs192805695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462922 | ACTCTGTCTAAAAAA[A/G]AAGTTTTCCCAAGTG | 115426 |
rs192819936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436602 | ATGGCACAACATAGA[C/G]ATAGAATAAGGAACT | 115426 |
rs192952200 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496706 | TAAACTTTAAGGATT[C/T]TCTATTGTCTGGAAT | 115426 |
rs192963100 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493417 | TGTAGATGTCAGTTG[A/G]AAATTTGGTTATGGA | 115426 |
rs192994973 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469682 | TGTGTGTGTGTATGT[A/G]TATATATACACGTAT | 115426 |
rs193010271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442376 | GTGGATGAAGCAGCT[C/T]AGTCTCTGGTCATTA | 115426 |
rs193026557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419966 | GTTACCCATACTGGT[C/G]TGGAGCTCCTGGGCT | 115426 |
rs193029979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476636 | TTTTGCTCTTGTTGC[A/C]CAGGCTGGAGTGCAG | 115426 |
rs193031823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449652 | GTTTGGAAACCTTAG[A/G]TTTCAGGAACATTCC | 115426 |
rs193076058 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419596 | TTATGAAAAATAAGG[A/C/T]CATAAAACAACTTTG | 115426 |
rs193145896 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422556 | AATCGACATCTTTAC[A/G]ATGTTGAGTCTTTTA | 115426 |
rs193149515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480845 | CTCCTATAGTGCTCA[A/G]CAAAGTATCTCATAA | 115426 |
rs193151230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452161 | ATAGGAGCACAATAT[G/T]CTATTATGTACCTGT | 115426 |
rs193175618 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489459 | TGGGTCATATGTGGC[A/G]GTTGCATGTTTAGTT | 115426 |
rs193291554 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466123 | CTACAGATAAAGGCC[A/G]AGCATGGTGGCTTGT | 115426 |
rs193296953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496210 | GAAGAAGTATTTTAT[C/G]TCATATCTGCTTTCA | 115426 |
rs193298951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439262 | TGATCTTGACTCACT[A/G]CAACTTCTGTCTCCC | 115426 |
rs193302649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415902 | ATTCAAAGTATGGTC[A/C]CTGGATTCTCAGGAC | 115426 |
rs199507879 | snp | G/T | 0.0105289 | 0.0717887 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486907 | TCTTGTACTGGCTGG[G/T]GGATTTGCGGATGAA | 115426 |
rs199531374 | in-del | -/TC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484787 | ATTCACTTCTTTCTT[-/TC]TTTTTTTTTTTTTTT | 115426 |
rs199556193 | snp | A/G | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434052 | TCTTGTAAAAGGACT[A/G]ATGGAAATATAAAGC | 115426 |
rs199558414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472377 | GGAACAGTATAACAT[A/G]CTTACAAGGAAAACA | 115426 |
rs199567263 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451950 | AGTTTGGTTTACGCT[C/T]CTGTTTTAATAAAAG | 115426 |
rs199593988 | snp | C/T | 1.65652e-05 | 0.0028779 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434147 | TGCTGCTGATGAAGA[C/T]GTTATTTACCATATC | 115426 |
rs199638493 | snp | A/C | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412184 | ATACATACATACATA[A/C]ATAATAAATAAAATA | 115426 |
rs199651739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486783 | ATGTATCTTAACTGT[G/T]CAGAGGTATTTTGAG | 115426 |
rs199666640 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452848 | TCTGAAAAGTTTAGG[C/T]GAGAGTGGAGCTTTA | 115426 |
rs199674453 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457357 | TTTGCACATTGATTT[A/G]TATCCTGAGACTTTG | 115426 |
rs199677162 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493879 | TAAAAATCTTGCTGG[C/T]AACAAAAGAATTGGT | 115426 |
rs199717946 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425772 | CTCAAAGTAAATAAA[A/T]TAAAAAAAAAAAAAT | 115426 |
rs199759757 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458613 | ATAGGAACGCTTTTA[C/T]ACTGTTGGTGGGAGT | 115426 |
rs199793502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459664 | ACAGAGTAAGACTCC[A/G]TCTCACAAAACAAAA | 115426 |
rs199795827 | snp | G/T | 0.171057 | 0.237209 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451479 | TTGTTTTTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 115426 |
rs199824870 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419604 | AATAAGGTCATAAAA[C/T]AACTTTGAAAATTCA | 115426 |
rs199832982 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448477 | GATCAGTTTGAAAAA[-/C]GTCTCTGTTTTTATT | 115426 |
rs199833332 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456769 | TAGCCAGTTTTCCCA[A/G]CACCATTTATTAAAT | 115426 |
rs199849002 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489728 | TCTAATTGGGTTTTT[G/T]TTTTTTTTTTTTTTT | 115426 |
rs199854102 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457413 | GATTTTGGGCTGAGA[C/T]GATGGGGTTTTCTAA | 115426 |
rs199871077 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438729 | AAAGCTGTTTTTTAT[A/G]GTAATCTACGTATCT | 115426 |
rs199872221 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503464 | GCTTTTGAAGAATAC[A/G]GGGTATCCATTTGAT | 115426 |
rs199920511 | snp | C/G | 0.00128798 | 0.0253458 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499829 | TCCCTCCTCCCCCCC[C/G]ATCAGTATCCAGCAG | 115426 |
rs199946730 | snp | C/T | 1.75452e-05 | 0.00296181 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413474 | CAAAGGGGACCGGTT[C/T]CTCTCTAGGCGCCAA | 115426 |
rs199974689 | in-del | -/TAAA/TAAATAAA | 0.00199561 | 0.0315249 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423968 | AAATAAATAAATAAA[-/TAAA/TAAATAAA]GGAACTCTTGATAAG | 115426 |
rs200009721 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505658 | GTAAAATATAAAATT[A/C/T]ATTTCTAAGCAAGGG | 115426 |
rs200011210 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504748 | GGCACACTAATTTCT[A/G]TACCTGTTTTTAGCA | 115426 |
rs200039927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490702 | TTTTGAATATACTTA[C/G]TGGTCAAACGTTAAA | 115426 |
rs200054497 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463285 | AAACTTCGTCTCAAT[A/T]AAAAAAAAAAGACTT | 115426 |
rs200073443 | snp | C/T | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477646 | ACCCTGAATGTGACC[C/T]GTGTGGTGGAGACCC | 115426 |
rs200081333 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469678 | TGTGTGTGTGTGTGT[A/G]TGTATATATATACAC | 115426 |
rs200084021 | in-del | -/T | 0.457504 | 0.139435 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418260 | ACTAGAGGATGTTCC[-/T]TTTTTTTTTTTTTTT | 115426 |
rs200084549 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455312 | CCCCACAACAGGCCC[A/G]GGTGTGCGATGTTCC | 115426 |
rs200090766 | in-del | -/AC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453954 | AGAGTAGAACTATAG[-/AC]ATAATTTTGTACTTG | 115426 |
rs200096114 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461914 | ATATGCATTTTTGTG[C/T]ATTTCTTTTCTTTAG | 115426 |
rs200112868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449029 | GTCTTTACCTTTACC[A/G]GCACCTTTGAGCACC | 115426 |
rs200113974 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506504 | TTTAAAAATCATTGA[A/G]TAACTAGTTAAATGA | 115426 |
rs200142361 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469027 | CCACATAATCAGAAA[A/G]CAGAAGGAATACCAA | 115426 |
rs200150728 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455509 | TTCCATGGTGTATAT[A/G]TGCCACATTTTCTTA | 115426 |
rs200152735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492151 | AAGTACAAATGAGTT[A/G]ATGGTACAGAATTTT | 115426 |
rs200169545 | snp | C/T | 0.00018167 | 0.009529 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506184 | AAGGACGATGATCTG[C/T]CTGCTTTCACTGTGT | 115426 |
rs200181004 | snp | C/T | 1.78976e-05 | 0.0029914 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500737 | TTTTTTAAATAATAA[C/T]ATTCTGATATTAACA | 115426 |
rs200183645 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426539 | ATGAACCTTAGTAAT[C/T]GTCATAGGTATTTGA | 115426 |
rs200195688 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476341 | AAGCCTGTTTCTGTA[A/G]TTTTGTTAGCCACCC | 115426 |
rs200209953 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458482 | TGAAGGGTTTTTCAT[C/G]TCTCTATCTCCTTCA | 115426 |
rs200220456 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495923 | AGGTATTCTGTAAGA[C/T]GTAATAGTAGCCCTA | 115426 |
rs200254341 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456382 | ACTTTTTGATGGGGT[A/G/T]GTTTGTTTTTTTCTT | 115426 |
rs200275830 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495999 | TCTTCCTTTTAGATT[-/A]AAAAAAAAAGGTAAC | 115426 |
rs200354850 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429670 | TAACATTGAACGTAT[A/G]TACTTAGTAAGGAGA | 115426 |
rs200358356 | snp | A/G | 0.000367924 | 0.0135583 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481808 | CTAATAGCAAGTTAT[A/G]ATATATAATGTTTTA | 115426 |
rs200374753 | snp | C/T | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506072 | GCACAGGTTTTCTCC[C/T]GCCCTGCTTGCCGGC | 115426 |
rs200388182 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431197 | TAGTATGTCTATCCA[A/G]TGTGCAGAAAGTTTT | 115426 |
rs200389512 | in-del | -/TTC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440924 | CAAAAGTTGTAATGA[-/TTC]TTCTAATCATTCCCT | 115426 |
rs200391411 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494658 | TCACATTATAGTTTG[C/T]CCTGCTGAAATTTTT | 115426 |
rs200424357 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416077 | TTTGTTGTTGTTTTT[-/G]TTTTTTTTTTAAGCC | 115426 |
rs200441638 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411803 | TTAGCACCTATGTGA[A/G]TATTTAAGTTACCGA | 115426 |
rs200462199 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452204 | TAAGGGTTTCTGTTA[C/T]GGACGTTTGATTGTT | 115426 |
rs200462631 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484988 | AGTAGAGATGGGGTT[A/T]CTCCATGTTGGTCAG | 115426 |
rs200468010 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424271 | TGATAGCTCAAGGAA[C/T]TAATGCGTGAATTAG | 115426 |
rs200477093 | snp | C/T | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433952 | AGATGTCGGCCTTGG[C/T]GCTTGGTTTGAAGCA | 115426 |
rs200507678 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441390 | ACCCCTCCCAAAAAG[A/G]AAAAAAAAAAAGCAG | 115426 |
rs200510932 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473323 | TCAGTATGGAAGTTG[G/T]TAGAGAATGATTTAT | 115426 |
rs200524960 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493294 | AGAGCAAGACTCTGT[-/C]TTAAAAAAAAAAAGT | 115426 |
rs200525197 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445974 | ATACTCTTCCCCCCC[C/G]GCCACCCTTTTTTTT | 115426 |
rs200537753 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503650 | TATTGTTTCCTAGTG[-/T]TTTTTTTTTAAGCTC | 115426 |
rs200539492 | in-del | -/CGTGG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463010 | GAGTGGGCCAGGTGC[-/CGTGG]CTCACGCCTGTAATC | 115426 |
rs200541263 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460116 | GCTCTGGGAAGTCAA[A/G]TCATGAGTGTATATC | 115426 |
rs200545633 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471276 | GTATCAGTGGCTGTG[C/G]AGGAGAAATATGTGT | 115426 |
rs200572714 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497639 | TTAAGTAACTGGCTG[G/T]TGTATAACTTGATTT | 115426 |
rs200587704 | snp | A/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412185 | TACATACATACATAC[A/T]TAATAAATAAAATAA | 115426 |
rs200597858 | in-del | -/C | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412187 | ATACATACATACATA[-/C]ATAAATAAAATAAAA | 115426 |
rs200602206 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413250 | TTCCTATCTTTGAGG[C/T]GGTGTCTGCGGCAGC | 115426 |
rs200605612 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434457 | AGGTGGGCTTTTTTT[G/T]AGATGGTCTCTCTCT | 115426 |
rs200612841 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456948 | AGGTAGCATGATGCC[A/T]CCAGCTTTGTTCTTT | 115426 |
rs200640661 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486740 | TGGGTCTTTAGGTAC[C/T]AAGAATATATATGAA | 115426 |
rs200680941 | snp | A/G | 0.00159766 | 0.0282184 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497378 | GCTCTATCTGGCATG[A/G]CATCTTGTTTGTCAT | 115426 |
rs200713057 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484788 | TTCACTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 115426 |
rs200728620 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455649 | CAGTGTGGACTGTTA[C/T]TGATTTCTTTGGTCT | 115426 |
rs200738549 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479710 | CCTAAAATCCTGCTC[C/G/T]TCCCCCAGTCTTCAT | 115426 |
rs200792089 | in-del | -/TGTT | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491539 | AAGGAGTTTGGAGAA[-/TGTT]TGTCTTCATTGTGCT | 115426 |
rs200815813 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422913 | GCTGATATAGAGAAA[C/T]GAAATTGATTTATTT | 115426 |
rs200820842 | snp | A/C | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434076 | ATAAAGCATAAATCC[A/C]AAGAGAACACAAATA | 115426 |
rs200835576 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466642 | TAAATTTTTTTCATA[C/G]TTAAGAAATTTCTAT | 115426 |
rs200844346 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430307 | GAGCCCCTGTGCCTG[A/G]CCCTTAATGTGGCTA | 115426 |
rs200854275 | snp | A/G | 0.000250955 | 0.0111989 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460806 | GGTAAGATTGTCTTC[A/G]CTGGTGCCATTTAAT | 115426 |
rs200890506 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424777 | GACAATTTCTCAGGA[-/T]TTTTTTTTTTTTTTT | 115426 |
rs200915846 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434718 | TGCTGGGATTACAGG[C/G]GTGAGCCACTGCGCC | 115426 |
rs200921548 | snp | C/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481699 | AGGCTGGTGAAAGAC[C/T]CAAGATGAGTAAAAA | 115426 |
rs200922099 | snp | C/T | 0.457388 | 0.139608 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424127 | AATTAGGCAGGAGAA[C/T]AAAATAAAGTGTAAA | 115426 |
rs200940806 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457448 | ACAATCATGTCATCT[A/G]CAAACAGGGACAATT | 115426 |
rs200956639 | snp | C/T | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477715 | GTGGGAAACATGAAC[C/T]CAACATGCAGCTTCT | 115426 |
rs200984339 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467975 | GAAGGTGTTCCTTAG[A/G]CACCTCATCACAGTC | 115426 |
rs200992720 | snp | A/G | 1.8851e-05 | 0.00307004 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500750 | AACATTCTGATATTA[A/G]CAAATGATAAATAAT | 115426 |
rs201002536 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448103 | GCCTACAAAGCCTAC[A/T]ATCTGGACAAAGCAA | 115426 |
rs201003330 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457389 | TGAAGTTGCTTATCA[C/G]CTTAAGGAGATTTTG | 115426 |
rs201009074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505811 | GGAAACTGATGCACA[A/C]ATTACATAAATAATT | 115426 |
rs201018616 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469680 | TGTGTGTGTGTGTAT[A/G]TATATATATACACGT | 115426 |
rs201033696 | snp | C/T | 1.67178e-05 | 0.00289113 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433907 | ACTGATTTTAAACTT[C/T]TTTTAGGTAAATGAA | 115426 |
rs201035695 | snp | C/T | 4.94711e-05 | 0.00497324 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421066 | AAGTAAAGAAAGCTC[C/T]GAGGGTAGGACCTTC | 115426 |
rs201065464 | snp | A/G | 0.0019981 | 0.0315446 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500533 | TAAGTCTGCTGATAC[A/G]TTTTTAAAATAAATC | 115426 |
rs201073230 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464975 | TACTAATTTTAATTT[A/C]CATGTAGATTGTTTC | 115426 |
rs201093090 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458606 | TGAAGAAATAGGAAC[A/G]CTTTTATACTGTTGG | 115426 |
rs201101140 | in-del | -/T | 0.248471 | 0.249995 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458454 | GATTTTTTTTTTTTT[-/T]GAAGGGTTTTTCATC | 115426 |
rs201123290 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450900 | GAGCACATAGTCTGT[G/T]CTGCTTACTGATATG | 115426 |
rs201155991 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456673 | GGTTTTAGGTCTTAC[A/G]TTTAAGTCTTTAATC | 115426 |
rs201172162 | in-del | -/T | 0.0952156 | 0.196321 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488822 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTGAGATAG | 115426 |
rs201199717 | snp | A/C/G | 1.65089e-05 | 0.00287301 | synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434066 | TAATGGAAATATAAA[A/C/G]CATAAATCCAAAGAG | 115426 |
rs201212995 | snp | G/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412951 | AAACGGCAACCGATG[G/T]GGTAGCCGCGCAATC | 115426 |
rs201215246 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455379 | CACCTATGAGTGAGA[A/G]CATGCGGTGTTTGGT | 115426 |
rs201224658 | in-del | -/AAAGTGTAAAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483439 | CCTATAATACCTAAT[-/AAAGTGTAAAT]GCTATGTAAATAGTT | 115426 |
rs201234807 | snp | C/G | 3.6708e-05 | 0.004284 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413449 | GCGGCGCCCAGAGCT[C/G]AGGGGGAGACAAAGG | 115426 |
rs201234847 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458371 | TATTGTGTCTATTTG[A/G]TTCTTCTCTCTTTTC | 115426 |
rs201243409 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418279 | TTTTTTTTTTTTTTT[A/T]AATCAAGGAAGCAAT | 115426 |
rs201249107 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485822 | AAAAAAAAAAAAAAA[A/C]AAAAAACAAAACCCA | 115426 |
rs201281173 | snp | A/G | 3.32696e-05 | 0.00407844 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497998 | AAATCTCAAACTGGC[A/G]CTGAAATATTGTGAT | 115426 |
rs201290316 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467685 | GACAGAAGTTGAATT[C/G]TTTCAAAGATTTGAA | 115426 |
rs201338584 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446440 | GAGCCACCATGCCTG[G/T]CCTAATTTTTTTTAA | 115426 |
rs201378069 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414540 | CACAAGTCTCTTACA[A/G]TCTATATCCCTAGCC | 115426 |
rs201384737 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452030 | TGTATATATGTGTAT[A/T]TATACATATATACAC | 115426 |
rs201386042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432785 | CCTTTTTAAGGGCTT[A/G]AAAAGAAAGTTGAAG | 115426 |
rs201389433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495266 | AAAATAATTGACAAG[C/T]AGTAAACATGTTTTC | 115426 |
rs201391704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491710 | AAGAATAGAGGTTGG[G/T]AATAACTGAAGAACT | 115426 |
rs201392999 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450160 | AAATTCCCAATGATT[C/T]CTTAACATCAAATAA | 115426 |
rs201394385 | snp | A/G | | | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421107 | TCTACATCAGCTCGT[A/G]CCCGTCTTATTGATC | 115426 |
rs201395060 | snp | C/G | 1.65405e-05 | 0.00287576 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460759 | GACAATCTCAAGGAC[C/G]AAAAAAGAACTTCGT | 115426 |
rs201426021 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441390 | ACCCCTCCCAAAAAG[-/A]AAAAAAAAAAAGCAG | 115426 |
rs201432601 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474483 | GGCCGAGGCGGGCAG[A/G]TCACCTGAGGTCAGG | 115426 |
rs201438339 | snp | C/G | 1.71731e-05 | 0.00293023 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477822 | TGGTATGATTATCAG[C/G]TTTTTGTTGTTGTTG | 115426 |
rs201460211 | in-del | -/TTCT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484778 | TTTAGTTGTATTCAC[-/TTCT]TTCTTTCTTTTTTTT | 115426 |
rs201466608 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445975 | TACTCTTCCCCCCCC[C/G]CCACCCTTTTTTTTT | 115426 |
rs201470363 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420473 | TTTGGGAGGTCGAGG[C/T]GGGTGGATCACGAGG | 115426 |
rs201477204 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481456 | AGGAATGACAAGGAT[A/G]TTTTTAAAGCCAGCC | 115426 |
rs201514730 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478521 | CTTGCCAAAATCTAT[C/T]TTTCTCCTATGGCGT | 115426 |
rs201556085 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436604 | GGCACAACATAGACA[C/T]AGAATAAGGAACTTT | 115426 |
rs201565204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452466 | GTAATCAAACTTCAT[A/G]AAATATTTTAAGTAG | 115426 |
rs201584672 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486799 | CAGAGGTATTTTGAG[A/T]CTCTCTTTAATTGTT | 115426 |
rs201598408 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424382 | AGTGGTCACAATTAA[A/G]AGAGAATTTTTAGCA | 115426 |
rs201601512 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459209 | ATCCAAGAACTTAAA[-/T]TTTTAAAAAAAGAAA | 115426 |
rs201601674 | snp | C/T | 4.96479e-05 | 0.00498212 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500594 | ACAAAGCATCAGATT[C/T]AGCAGAAGCAATTGA | 115426 |
rs201612556 | snp | G/T | 3.49229e-05 | 0.00417854 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497157 | GATTGTGTACTTGAA[G/T]AAAAATTACATGGTA | 115426 |
rs201615487 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462215 | TCTGTGGCTATTTTT[A/C]TGCTCCACAGTATTG | 115426 |
rs201629072 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451181 | CTGAAAAGTTACGTG[-/T]TTTTTTTTGTCTTTA | 115426 |
rs201647183 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426152 | TCTTCCCTCCCCAAT[A/C]GAATTCGGAAGAGCA | 115426 |
rs201659927 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457395 | TGCTTATCACCTTAA[G/T]GAGATTTTGGGCTGA | 115426 |
rs201669529 | snp | A/G | 6.6024e-05 | 0.00574523 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481730 | GAAAGCAAAGATGCC[A/G]TCAGCTAGTACTGAA | 115426 |
rs201711728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485008 | ATGTTGGTCAGGCTG[A/G]TCTCAAACTCCCGAC | 115426 |
rs201737696 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498632 | CCCTGCCCTGCCACC[A/G]CCTTTAGTGCTTTGT | 115426 |
rs201761591 | snp | A/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412186 | ACATACATACATACA[A/T]AATAAATAAAATAAA | 115426 |
rs201778353 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457686 | GATACATTCCATCAA[A/T]ACCTAGTTTATTGAG | 115426 |
rs201782192 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447468 | AAGGTAGAGGAGATA[C/T]TTTAGTTCCTGAAGG | 115426 |
rs201787064 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464383 | CTAATTCTGTGGCTT[G/T]TCTTTTTCTCCTTAC | 115426 |
rs201807679 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463148 | TAGCTGGGTGCGGTG[G/T]TGCATGCCTGTAATC | 115426 |
rs201872136 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458468 | GATTTTTTTTTTTTT[G/T]AAGGGTTTTTCATCT | 115426 |
rs201884765 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454239 | AGCTAAATTGGGAAT[C/G]TAAACCTAGGCAGAC | 115426 |
rs201894689 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474765 | AATCCACACCCGTAG[A/G/T]AGGAAACTTTGAAGA | 115426 |
rs201903063 | snp | A/G | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500602 | TCAGATTCAGCAGAA[A/G]CAATTGAGGCTTTTC | 115426 |
rs201933987 | snp | C/T | 3.29924e-05 | 0.00406142 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460739 | GCAGAAATTACCACA[C/T]TGAAGACAATCTCAA | 115426 |
rs201961543 | snp | G/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412954 | CGGCAACCGATGTGG[G/T]AGCCGCGCAATCTTC | 115426 |
rs201964876 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433787 | TCTAATCTTATTAAC[A/C]ACTTTAAACATGAGT | 115426 |
rs202043383 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505206 | AAAATGGAAACAAAT[A/C]TACATACGAGTTTGT | 115426 |
rs202053745 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445520 | CCTGCCTCGGCCTCC[A/C]AAAGTTCTGGAATTA | 115426 |
rs202154876 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495650 | TTTTATCAGGGCAGT[C/G]AGAGGCACCTGACTG | 115426 |
rs202162350 | snp | A/G | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477654 | TGTGACCTGTGTGGT[A/G]GAGACCCAGAAAAGA | 115426 |
rs202167670 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477233 | GTGAGACTCCATCTC[-/A]AAAAAAAAAGACTGG | 115426 |
rs202179265 | snp | C/G/T | 0.00501011 | 0.0498125 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413677 | GCCCCTAGCGAGGCT[C/G/T]GGGGCCGGAACAGCT | 115426 |
rs202185485 | in-del | -/GAAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469029 | CATAATCAGAAAACA[-/GAAG]GAAGGAATACCAATT | 115426 |
rs202203826 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458117 | CCTCTGGTAGAATTC[A/G]GCTGTGAATCCGTCT | 115426 |
rs202211992 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449450 | AGGGCTTTTACTGCC[G/T]AGTTCTCCTTTCTTT | 115426 |
rs202217487 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459221 | TAAATTTTAAAAAAA[-/G]AAAGAAAGAAACTGG | 115426 |
rs367623310 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476924 | AAAACCTCACACTTG[A/G]TTATTCTTTTTGGTT | 115426 |
rs367657466 | snp | C/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446788 | AAGTGGGGATTACAG[C/G/T]GAGCTGAAATGGCGC | 115426 |
rs367659794 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459598 | CACTTGAACCCAGGA[A/G]GTGGAAGTGGCAGTG | 115426 |
rs367671582 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437458 | GGCTGGTCTTGAACT[C/T]TGGACCTCAGGTGAT | 115426 |
rs367676322 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502912 | TTTGACTTTAATGAT[C/G]CATGTTCATAAATCA | 115426 |
rs367714500 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490195 | GCCAAATTATTTAAC[G/T]CTGGTAACTCAGTTT | 115426 |
rs367736356 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487370 | ATTTTTGTATTTTTA[A/T]GTATTTATTTTTTGA | 115426 |
rs367749349 | snp | C/T | 8.25743e-05 | 0.00642498 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481705 | GTGAAAGACTCAAGA[C/T]GAGTAAAAAGAAAGC | 115426 |
rs367769125 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468916 | CACATTATCTCTCCA[C/G]CAGTAGGAAGGTTGA | 115426 |
rs367799803 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432597 | TAGGAATTAAACTTC[G/T]TAGGGTTAGACATAT | 115426 |
rs367813173 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494358 | AACATAAGGTAACTT[A/T]ATCAGATCTGTACTG | 115426 |
rs367816833 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450522 | TATGGCATGGTATCC[C/T]ATCAGGAGACACATA | 115426 |
rs367825013 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440631 | TCTATTGAGCTAAAC[C/T]GTAGGTATGTCAACA | 115426 |
rs367892288 | snp | A/G/T | 3.64992e-05 | 0.00427183 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413452 | GCGCCCAGAGCTCAG[A/G/T]GGGAGACAAAGGGGA | 115426 |
rs367898591 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441735 | GTGGTTTGTGGCCGG[-/T]TTTTTTTTTTCCATT | 115426 |
rs367919732 | in-del | -/CCTCCTC | 0.0225045 | 0.103662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484404 | GCTTCTCCTCCTCCT[-/CCTCCTC]CCTCCTCCCTCCTCC | 115426 |
rs367956676 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497577 | AGAGTTGGGTTAAGG[-/T]TTTTTTTTTTTAAAA | 115426 |
rs367960067 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427988 | TTTTTGTGTATGGAA[A/G]CTTTTTATGATGCCA | 115426 |
rs367964372 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486418 | ACTTCACAAACTAGG[C/T]AGGCAACAGGGCCAC | 115426 |
rs368016600 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467071 | GCTTAAACAATAAAG[C/T]ATAGTACAGTTTGGA | 115426 |
rs368033475 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470048 | TTTAAGCTAGGAGAC[A/G]GTGGAATGGCATGTG | 115426 |
rs368077199 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419181 | AATTTTGGCAGGGAC[A/G]CAACTTAGCTCGTAA | 115426 |
rs368093815 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506118 | ATTACATCATGATTC[C/G]CAATGAGATTCTGCA | 115426 |
rs368133913 | in-del | -/ATT | 0.00225221 | 0.0334818 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486950 | TATACAACCTTACTC[-/ATT]AGTACCTGCCTTGAC | 115426 |
rs368141356 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432625 | TATCTAAGTAAAGAA[C/G]CTTGCATAATATCTG | 115426 |
rs368240469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486660 | AGACTCACTTCTTGG[A/G]TCTTTAGGTACCAGG | 115426 |
rs368303908 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413111 | CTGTAACCCTCTCCC[C/G]GGCCGCTTCCTCTTT | 115426 |
rs368316170 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449780 | GGTATGTGCTAGGCA[A/G]TACCTGTTATCAGCC | 115426 |
rs368371955 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504111 | GCTCACTGCAAGCTC[A/C/T]GCCTTCTTGGTTCAC | 115426 |
rs368378792 | snp | A/G | 1.65419e-05 | 0.00287588 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506198 | GCCTGCTTTCACTGT[A/G]TTGTTCATGGTGGCT | 115426 |
rs368404358 | snp | A/G | 4.99089e-05 | 0.00499519 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497373 | AAGGTGCTCTATCTG[A/G]CATGACATCTTGTTT | 115426 |
rs368413138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451946 | TGTTAGTTTGGTTTA[C/T]GCTTCTGTTTTAATA | 115426 |
rs368430664 | snp | A/G | 1.65378e-05 | 0.00287552 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433922 | TTTTTAGGTAAATGA[A/G]TTGGTGGATGCCAGA | 115426 |
rs368451864 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411779 | GGTACTGTACCTTTA[C/T]GGGAATAATTAGCAC | 115426 |
rs368493251 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451457 | TTGTTTCTTACCTAG[G/T]TTTTTTTTGTTTTTT | 115426 |
rs368536732 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442035 | CAGTGGCACGATCTT[C/G]GCTCACTGCAACCTC | 115426 |
rs368543251 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474853 | CTTTATGAAAAGGGC[A/G]TCTTATTTTTGCCTA | 115426 |
rs368560422 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474034 | AACACAGGCAAAACT[-/GT]TTTAGGGAGGTAGAC | 115426 |
rs368592033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424400 | AGAATTTTTAGCACT[A/G]AAAGCCAACTTGCCA | 115426 |
rs368630831 | snp | A/G | 3.34297e-05 | 0.00408824 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497392 | GACATCTTGTTTGTC[A/G]TTCTTCCTGGGCTTT | 115426 |
rs368717130 | snp | A/C/G | 1.65059e-05 | 0.00287275 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481983 | CAACGTTTGTTTTGC[A/C/G]TCTTGTAGGGAATGG | 115426 |
rs368726369 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503914 | TTCCTACCCAATACT[C/G]TGATTTAAAACTAAT | 115426 |
rs368870185 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485829 | AAAAAAAAAAAAAAA[-/C]AAAACCCAAAACCAA | 115426 |
rs368880762 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505051 | CAGTTTATACCTAGC[A/G]TCATGCCCAGATGAA | 115426 |
rs368890438 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414912 | GTTTGACTTGTAAAA[A/G]CAGGTATTTAGTTGT | 115426 |
rs368917032 | snp | A/G | 0.000175331 | 0.00936134 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500728 | TGTGAAGATTTTTTT[A/G]AATAATAACATTCTG | 115426 |
rs368932371 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447821 | ACTGAAACCTATGTA[C/T]GAGAAGCCAACAAAC | 115426 |
rs368935401 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422332 | TCATCTGCCCTCCTC[A/G]GTCTCCCAAAGTGCT | 115426 |
rs368943656 | snp | C/T | 1.68111e-05 | 0.00289918 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413534 | GCTCCAAGACGTGCA[C/T]CATTGAGGACGTGTC | 115426 |
rs369021483 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486464 | ATAAGAGAGAAACGG[A/T]ATAGACTGCTGGTAG | 115426 |
rs369074603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438864 | AACTTCTACTCCAGT[C/G]AGAGCAGAGTTAAAA | 115426 |
rs369082775 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423634 | TTTGAGTCATTAGTG[A/T]TTTTTTTTTTTTTTT | 115426 |
rs369120988 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425421 | CTGCTTCAGTCCTAG[A/C]ATCAACCATTTCTCC | 115426 |
rs369129216 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413716 | CTGGACGCACCGGTC[C/T]GAGGGCTCTGTGCGC | 115426 |
rs369164801 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501183 | TTTAAATTAATCACA[C/T]AATTTTAAAGTAAAA | 115426 |
rs369170103 | snp | C/G/T | 3.72837e-05 | 0.00431749 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486784 | TGTATCTTAACTGTT[C/G/T]AGAGGTATTTTGAGA | 115426 |
rs369182445 | snp | A/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420357 | ACCGCGCCCGGCCCA[A/T]TTTTTTTGTTTTAAT | 115426 |
rs369190704 | snp | A/G | 1.73546e-05 | 0.00294568 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493809 | GCTTTCTTAATAAAG[A/G]AAATCTTCTCTGACA | 115426 |
rs369220030 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414507 | TGGTCTGGCCAGTCT[-/T]AAGTTTTTTTCCTAT | 115426 |
rs369299223 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411921 | ATAAACCCACTTGGC[C/T]GGGCGCGGTGGCTCA | 115426 |
rs369368763 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499642 | AGCAGTCACAGCTAC[A/C]TAAATTGGGATTTTA | 115426 |
rs369389550 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448782 | ATGTGGTAGGTTGTG[G/T]CAGTAGACAGACTAC | 115426 |
rs369517540 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485545 | TTCAAAAGCCAAAAC[C/T]TTTCCAGGTTCTGTT | 115426 |
rs369521468 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506704 | CAGGTTCATTTTTTT[-/T]AGCCCACTTTGTGAA | 115426 |
rs369570622 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424938 | ACGTATATAGGGCAC[A/G]TACTATCAGTATTCT | 115426 |
rs369586401 | snp | A/C/G/T | 0.0028724 | 0.0377925 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499827 | TCTCCCTCCTCCCCC[A/C/G/T]CCATCAGTATCCAGC | 115426 |
rs369599038 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433224 | TACACCTGTTTTTTA[A/G]TACTCCTTCCTTTTG | 115426 |
rs369704050 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420518 | CCATCCTGGCAAACA[C/T]GGTGAAACCCCGTCT | 115426 |
rs369704159 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437741 | TCGTGCCTCAGCCTC[C/T]CAAGAAGCTAGGATT | 115426 |
rs369757332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442903 | TTAACATGTACTGTC[A/G]GTCAGTCTTACAGTT | 115426 |
rs369802742 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453706 | TCAGGAGATTGAGAC[C/G]ATCCTGGCTAACATG | 115426 |
rs369804671 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471517 | AAAAGATACCAGCTT[C/T]CATTTTGGGTGCGCC | 115426 |
rs369806441 | snp | C/G | 5.06718e-05 | 0.00503322 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460565 | CATATGGTTTTCTCT[C/G]TCCTCAGATACCCAG | 115426 |
rs369822991 | snp | A/T | 5.01869e-05 | 0.00500909 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497983 | ATAAGTCTAAATTTT[A/T]AATCTCAAACTGGCA | 115426 |
rs369862436 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426688 | TTTTATCACATACTG[A/G]CTTGTTGACTAAACT | 115426 |
rs369875848 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444172 | TCATGTCAGTCTTGA[G/T]TACAGGAGGGAACTA | 115426 |
rs369883333 | snp | C/G | 0.000324822 | 0.0127399 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500523 | GAACCACTTGTAAGT[C/G]TGCTGATACATTTTT | 115426 |
rs369924165 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467838 | TATCATTTAATTCTT[A/G]GAGGATGCTTTTTTT | 115426 |
rs369948466 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472002 | GGTATAACTTACATA[C/T]AGTAATATGTACTTA | 115426 |
rs369957591 | in-del | -/CTAA | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444289 | CTTAGAGTATTTCCT[-/CTAA]CTGTCTATGACTTGT | 115426 |
rs369962609 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476517 | TAACGGATTTTTCTT[A/G]CTTGATATCAAATAT | 115426 |
rs370001281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462637 | AAAAAAAGATTTCCT[A/G]GCTGGGTGCAGTGGC | 115426 |
rs370011744 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420432 | TTTATGGCCGGGTGC[-/G]GGTGCTCACGCTGTA | 115426 |
rs370070785 | snp | A/G | 3.30224e-05 | 0.00406326 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500630 | TTCAACTAACTCCTC[A/G]ACAGCAACATCTCAT | 115426 |
rs370091799 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416011 | CAAGATCTCCAGGTG[A/T]TCTGTATGTAGGTGA | 115426 |
rs370108137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450752 | CATCTTTAGCCTTTG[G/T]AAGATCCTTCAAGTT | 115426 |
rs370114057 | snp | A/G | 4.96537e-05 | 0.00498241 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481775 | GGGCAGGGTAAAGAA[A/G]AAATTCCCCTTTTCT | 115426 |
rs370120836 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484433 | CCTCCTCCCTCCTGT[C/G]TCTTCCCTCCTCCCT | 115426 |
rs370175283 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482376 | TAAACAGCCTTTCCT[A/G]CCAAAAATTTAGCAT | 115426 |
rs370244324 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464953 | GACTCAGTAGCTTTA[C/G]TAGATTTACTAATTT | 115426 |
rs370248990 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469971 | CAGTGGTATATCACA[A/G]ACAAGAATGCTAAAA | 115426 |
rs370253597 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482517 | CATTGGGCAGAGGAA[G/T]TGCCAGCTAATCCAA | 115426 |
rs370288267 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481016 | TTCCTTTGCTTGGTG[A/C]CATAAGAATAGCCTC | 115426 |
rs370333181 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414611 | TTAATACACTAAAAA[C/G]TTGGCATCCTGAGTT | 115426 |
rs370376269 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497164 | TACTTGAAGAAAAAT[C/T]ACATGGTATAAAGAC | 115426 |
rs370408971 | snp | A/C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417851 | GTATTTACTCCTGAC[A/C/T]GTCATTTAGTAGAAA | 115426 |
rs370426712 | snp | A/G | 0.000203955 | 0.0100963 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493938 | ACATGAACAGGTACT[A/G]CTATAGACACTGTTT | 115426 |
rs370440970 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433998 | ACTAGAGCTTCTGAT[C/G]GACAGTCACGTGGCA | 115426 |
rs370483193 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470943 | CAGCCTTTATATTAA[C/G]TGTGAGTCAAGCATT | 115426 |
rs370645110 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435629 | TTATTTATTTAGAGA[C/T]AGAGTCTTGCTCTGT | 115426 |
rs370716672 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501712 | CTTTGAGAAGTGTTT[A/G]CTTGTATTTTAGCCA | 115426 |
rs370723745 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421089 | GGACCTTCCAATCAG[C/T]CATCTACATCAGCTC | 115426 |
rs370727913 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427217 | GGTAAATATTTTTTT[C/T]TATACATGTAGAGCT | 115426 |
rs370744747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458278 | TTCTTCTAGATTTTC[C/T]AGTTTATTTGTGTAG | 115426 |
rs370767530 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490177 | GTTGTATTTGAGACT[G/T]GGGCCAAATTATTTA | 115426 |
rs370826189 | snp | A/G | 7.26401e-05 | 0.00602617 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413455 | CCCAGAGCTCAGGGG[A/G]AGACAAAGGGGACCG | 115426 |
rs370868130 | in-del | -/TAG | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492709 | CTATTTTGCTAGTGT[-/TAG]TAGGATTAATTGTGC | 115426 |
rs370882350 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431306 | TACTTACTATATTTA[A/G]TAGGATAATCCTTTT | 115426 |
rs370888224 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472893 | GACACATAATTTTTT[C/T]AAAAAGTAAATATCC | 115426 |
rs370973765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482880 | ATGAGCCACTGCGCC[C/T]GGCCTGGCTTTAATT | 115426 |
rs371116228 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477203 | GGCACCATTGCACTC[C/T]AGCCTGGGTGACAGA | 115426 |
rs371296968 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467306 | GGCTACATCCCCTTC[A/G]TATTCTCTCCTCTGC | 115426 |
rs371348703 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503243 | TCAAATGATCCACCC[A/G]CCTCAGCCTCCCAGA | 115426 |
rs371390558 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483453 | TAAAGTGTAAATGCT[A/C]TGTAAATAGTTGTTA | 115426 |
rs371458124 | snp | C/G | 0.000153808 | 0.00876814 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504668 | CAGCCTGTGACAACT[C/G]AGTGCTTCCACAATG | 115426 |
rs371470125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476888 | ATGAGCCACCACGCC[C/T]GGCCTCAGGCATTTA | 115426 |
rs371485202 | snp | G/T | 0.00248065 | 0.0351308 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413673 | CCGCGCCCCTAGCGA[G/T]GCTGGGGGCCGGAAC | 115426 |
rs371491767 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451538 | TTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 115426 |
rs371492593 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428698 | GGGACTACAGGTCTG[C/T]GCCACCATACCCAGC | 115426 |
rs371504516 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489530 | ATTTTATGTTCCTAT[A/C]GGCAGTATATGAGTG | 115426 |
rs371548870 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487177 | GAGCTTTTATTTTTT[-/A]TTTCCTTTTTTTTTT | 115426 |
rs371551368 | in-del | -/GTATAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469713 | TACATACATATACAC[-/GTATAT]ACATATATGTGCATA | 115426 |
rs371571470 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467648 | CTGAAATAAAAATGT[A/G]TCTTAAATTTGCTGT | 115426 |
rs371603337 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440642 | AAACCGTAGGTATGT[C/T]AACAACTTAGGGTAT | 115426 |
rs371604797 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424028 | AACACATTCTATACC[A/G]GTATTCCCTTTAAAG | 115426 |
rs371648083 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506175 | GCTACAGCAAAGGAC[A/G]ATGATCTGCCTGCTT | 115426 |
rs371658437 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481795 | TCCCCTTTTCTTCCT[A/T]ATAGCAAGTTATAAT | 115426 |
rs371683838 | in-del | -/ATAC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495369 | ACATCTGGTCAGTTT[-/ATAC]GTTAAGTTGTGAATA | 115426 |
rs371709418 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483132 | GGAATTCAAAACCAG[C/T]CTCGCCAACATGGTG | 115426 |
rs371768458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449822 | TGAATGCTCTAATCT[A/G]CCCTAGCAGACAATA | 115426 |
rs371780891 | snp | A/G | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434148 | GCTGCTGATGAAGAC[A/G]TTATTTACCATATCC | 115426 |
rs371787195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443301 | AGTATACAGATACTT[C/T]ACCTGGATTATCTCA | 115426 |
rs371821153 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471765 | TAAGATCTGAAGGGG[C/T]TAGAGTACTCTTTAA | 115426 |
rs371845988 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474211 | TTGGTTAAGCTATGC[A/C]TTTATGCAGTTTTTT | 115426 |
rs371929484 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481605 | TAGCTTTAATATGGT[A/G]TTGTGAAAATGCCTT | 115426 |
rs371932704 | snp | A/C | 1.68567e-05 | 0.00290312 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497410 | CTTCCTGGGCTTTCA[A/C]GGCAGGGTTGTTGCA | 115426 |
rs371951435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436883 | GAATTAAATGTTTCA[A/G]TGCTGGCAACTTAAA | 115426 |
rs371964620 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470115 | GTGGCTCACGCCTAT[A/G]TAATCGCAGCATTTT | 115426 |
rs372018153 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437007 | TAAAATATGAGATGT[A/G]TAACATAAATAAGCT | 115426 |
rs372036972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428328 | CCAGGAACTTACCAG[G/T]TGCCTCCTCCTGATT | 115426 |
rs372041814 | snp | A/C | 0.000149508 | 0.00864474 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481941 | AGAATTAAGGGCTTT[A/C]ATTAAAATTTAACAT | 115426 |
rs372045042 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460070 | CAGCTAGCAATGAAC[A/G]TCTTAATAAGACTTT | 115426 |
rs372060778 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504137 | TTCACTCCATTCTCC[A/T]GCCTCAGCCTCCCCA | 115426 |
rs372074149 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504475 | CTATAAACATCTTTT[A/G]TGCTGGGAACATTTG | 115426 |
rs372075143 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498532 | GGTAGGGGAAGGGTG[A/G]GGAGGTGGCTTTATA | 115426 |
rs372105977 | snp | A/T | 3.31972e-05 | 0.004074 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498004 | CAAACTGGCACTGAA[A/T]TATTGTGATTTAGGT | 115426 |
rs372122535 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429393 | TATGGTAATAAGACT[-/GT]ACTCTGAGGTTTTGT | 115426 |
rs372251101 | snp | C/T | 0.000597453 | 0.0172734 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504576 | TTTTCTTTCCTTATC[C/T]TTGGATACTGTTCTA | 115426 |
rs372268879 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425083 | ACACCTCCTTCCTGT[C/G]TTTCCATACTGTACT | 115426 |
rs372282086 | snp | A/G | 4.94311e-05 | 0.00497123 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482087 | TGGATCAACTTGGAG[A/G]TTTAGAGTTCAGGTA | 115426 |
rs372402596 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420950 | TGATTATGATGTTGG[A/G]CTGAATGATATAATT | 115426 |
rs372421813 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451478 | TTTGTTTTTTTTTTT[G/T]GTTTGTTTGTTTGTT | 115426 |
rs372454414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437743 | GTGCCTCAGCCTCCC[A/G]AGAAGCTAGGATTAT | 115426 |
rs372468061 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453746 | CGTCTCTACTAAAAA[C/T]ACAAAAAAACCAACC | 115426 |
rs372472488 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471699 | TACCCAGCTAAGCTA[A/C]TCCCAGATTCCTGAC | 115426 |
rs372490071 | snp | A/C | 0.000604822 | 0.0173794 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493777 | AATAAGAATTGATGA[A/C]ATTATACTTGGGTTT | 115426 |
rs372517892 | in-del | -/TGAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445283 | TATTGATTGATTGAT[-/TGAT]GGAGTCTTGCTCTGT | 115426 |
rs372538646 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500006 | AGACGGGGTCTCACT[C/G]TTGTCACCCAGGCTG | 115426 |
rs372580087 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443822 | AACTTAGGCTAGGCT[A/T]TAATTAAAAACTCAT | 115426 |
rs372580959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425673 | GAGGCTGAGGCAGGA[A/G]TATCACTTGAACCCA | 115426 |
rs372618340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500833 | CGGTTTTCTAATCCA[A/G]TGCCACTACCTTTCA | 115426 |
rs372623232 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469240 | AATAACAAATAAGGG[C/G]CAGGCACCATGGCAC | 115426 |
rs372640860 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461353 | CCTCCCTCTCTCTCT[-/C]CCCCCCCTCCTCCTC | 115426 |
rs372647241 | in-del | -/A/C | 0.00231242 | 0.0339243 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499829 | CCCTCCTCCCCCCCC[-/A/C]ATCAGTATCCAGCAG | 115426 |
rs372656910 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6460576 | CTCTCTCCTCAGATA[C/T]CCAGAAAGCGGTACT | 115426 |
rs372699476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452829 | GTGTAGATGGTTATA[A/T]GAATCTGAAAAGTTT | 115426 |
rs372721556 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415816 | ATTTAACAAGACCCC[A/G]CGGGAGATTCTGATA | 115426 |
rs372784676 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475107 | TTCATTTTAATTGAC[-/AG]AGTGCCATTTTATCT | 115426 |
rs372843767 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454291 | GTGAAGACACCAGGA[C/T]TGATACAAGGATCCA | 115426 |
rs372855215 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498694 | AACCCATAAAGACTT[C/T]GTTGATTTTGTGTGC | 115426 |
rs372883093 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499201 | GAGGCCTGAAACATA[-/A]CAGTGCTTTAAGCAT | 115426 |
rs372953359 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420100 | CTCCCTCTGTTGCCC[A/G]GGTTGGAGTGCAGTG | 115426 |
rs372976469 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491739 | CTGAGTTACTTTGGG[A/G]CAGTGCTGTGTCCCT | 115426 |
rs373027120 | snp | A/C/G/T | 0.000139336 | 0.0083458 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499828 | CTCCCTCCTCCCCCC[A/C/G/T]CATCAGTATCCAGCA | 115426 |
rs373076645 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451642 | CCCGCCACCACTCCC[A/G]GCTAATTTTTAGTTC | 115426 |
rs373077494 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463807 | TGATTAGAAATCTTT[C/G]ATCCTCACTGGTAAG | 115426 |
rs373140915 | snp | C/G | 1.65334e-05 | 0.00287514 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500603 | CAGATTCAGCAGAAG[C/G]AATTGAGGCTTTTCA | 115426 |
rs373146799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471057 | AATCCCAACCATCCA[C/T]CTCTTTTCAACTTCT | 115426 |
rs373150419 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435015 | TTTTTTTTTTTTTTA[A/T]TTTTAGTTTTGAGAC | 115426 |
rs373158878 | snp | C/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507473 | TCTTGATCTCCTGAC[C/T]TCGTGATACGCCTGC | 115426 |
rs373183506 | in-del | -/CT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414151 | GAATAAGAACCCTAA[-/CT]CTGCTTCCTGACTGT | 115426 |
rs373212943 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433851 | AATAACTTGAGTTAC[A/G]TTAAGGTTTTTGAAG | 115426 |
rs373251740 | snp | C/T | 0.000159375 | 0.00892537 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421135 | ATCCTGGCTTTGGAA[C/T]ATATAAGGTATGTTG | 115426 |
rs373257104 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420529 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 115426 |
rs373288503 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424016 | GTTAATATTTTAAAC[A/C]CATTCTATACCGGTA | 115426 |
rs373390457 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494805 | CCCCTTAATTTCTGA[A/T]TACTGTGTGATGTAA | 115426 |
rs373392942 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426939 | CTTTCAGTAGAGACA[A/G]GATTTCACCATGTTG | 115426 |
rs373417432 | snp | C/G | 0.000116751 | 0.0076395 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475396 | TTTTAAACAGGGGTT[C/G]TGAAGGAACATTAAA | 115426 |
rs373423841 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476872 | TGCTGGTATTACAGG[C/T]ATGAGCCACCACGCC | 115426 |
rs373432490 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501422 | TTTTCTTTCTCTCCA[A/C/G]AGTGTTGATGTGCCC | 115426 |
rs373500890 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449533 | CCAACGGACAAAATG[A/G]CTTAAAAAGGATTCT | 115426 |
rs373510684 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448098 | GTAAAGCCTACAAAG[C/T]CTACAATCTGGACAA | 115426 |
rs373535772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422472 | TACAAAAAACTGTAG[A/G]AATAGCATATAAAGC | 115426 |
rs373542394 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454957 | GAGATGGAGCCCAAG[A/G]ATTTGGATTTCCAGA | 115426 |
rs373549138 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505638 | CATATGTGTTAAGTG[C/G]TTTGGTAAAATATAA | 115426 |
rs373575073 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485564 | CCAGGTTCTGTTGCT[G/T]TCACCTTCTTGTTGG | 115426 |
rs373596604 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449031 | CTTTACCTTTACCAG[C/T]ACCTTTGAGCACCAC | 115426 |
rs373609576 | in-del | -/T/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423634 | TTGAGTCATTAGTGA[-/T/TT]TTTTTTTTTTTTTTT | 115426 |
rs373643276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456988 | ATAGTCTTGGCTATA[C/T]GGGCTCTTTTTTAGT | 115426 |
rs373663942 | in-del | -/CC | 0.00064779 | 0.0179854 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471716 | CCAGATTCCTGACCC[-/CC]ACCCCCATATGAGTA | 115426 |
rs373687928 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502544 | CCTCCCGCTTCAGCC[G/T]CCTAAGTAGCTGGGT | 115426 |
rs373696542 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414328 | TTACGAATGCCCTAT[A/G]TAAGCCAAGAGTTTT | 115426 |
rs373728296 | snp | C/T | 4.96676e-05 | 0.00498311 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505997 | CTTACATGCTTTATG[C/T]TCAGATTAAATTGGA | 115426 |
rs373733251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417156 | AATGACTTCCCACTG[C/T]CCTCTCAGCCACTTC | 115426 |
rs373736063 | in-del | -/T | 0.49645 | 0.0419827 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424776 | GACAATTTCTCAGGA[-/T]TTTTTTTTTTTTTTT | 115426 |
rs373738585 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469905 | AAAGATACAAGTTCA[A/G]GTCAAAGAAGTTCTG | 115426 |
rs373756256 | snp | C/T | 0.00447076 | 0.0470679 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481797 | CCCTTTTCTTCCTAA[C/T]AGCAAGTTATAATAT | 115426 |
rs373779568 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476923 | TAAAACCTCACACTT[A/G]ATTATTCTTTTTGGT | 115426 |
rs373783093 | snp | C/T | 0.000596952 | 0.0172661 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477844 | TTGTTGTTGTTCTTG[C/T]TGTGTAAACATGAAA | 115426 |
rs373857632 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435191 | TAGATATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 115426 |
rs373859645 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483890 | GACAGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 115426 |
rs373865020 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424069 | CAAGGAAGCCAATTC[A/G]TGCTTCCTTATTTGA | 115426 |
rs373866001 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453122 | TAGAATATATATAAT[A/C]CACTATATAATTCTC | 115426 |
rs373886120 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481881 | TATTTGTTAATATCA[A/G]TGGTACTTAAATTAC | 115426 |
rs373907147 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455856 | AGGCATAGTGGCATG[C/T]GTCTGTAGCCCCCGC | 115426 |
rs373908838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435293 | GCCACCACACCTGGC[C/T]GGCTAATTTTTTTGT | 115426 |
rs373914913 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451179 | CTACTGAAAAGTTAC[A/G]TGTTTTTTTTGTCTT | 115426 |
rs373927630 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504086 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 115426 |
rs374028713 | snp | G/T | 1.66062e-05 | 0.00288146 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500698 | GTGCTTTCACATCTT[G/T]TGGAAGGACCAGTAT | 115426 |
rs374043239 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431115 | GAACTGCCTTTAAAA[-/A]TCCAGGCTTTATAAC | 115426 |
rs374112042 | in-del | -/TAAGA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448724 | TGGAGGTAAATAAGA[-/TAAGA]ATGGAAAGTTTTCGC | 115426 |
rs374125089 | snp | C/T | 1.6715e-05 | 0.00289089 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475524 | TTTTGTTTTTGGTCT[C/T]AGACTACATGTGTTG | 115426 |
rs374177562 | snp | A/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419179 | AAAATTTTGGCAGGG[A/T]CGCAACTTAGCTCGT | 115426 |
rs374183977 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465129 | AAGTAGTGATAACAG[G/T]CATCTTTTTCCCCTG | 115426 |
rs374196193 | snp | A/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420540 | ACCCCGTCTCTACTA[A/T]AAATACAAAAAAAAA | 115426 |
rs374198531 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6413973 | CGCGCTCGGCGGGGC[C/G]TGGGGCCCCCAGAGG | 115426 |
rs374298093 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415007 | CAAGTGGCTGATACC[A/G]TTTCCTTTTGATCAC | 115426 |
rs374306000 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432060 | AAATGTCTTTAAATT[C/T]GTCAGTGATTAGTAT | 115426 |
rs374307103 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416302 | CTAGGACAGGACCTC[A/G]GGTGATGCGCCCACC | 115426 |
rs374310514 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473005 | TTTAAAATGTATAGG[A/G]TACAAACAGTAATCA | 115426 |
rs374374541 | snp | A/C/G | 9.97005e-05 | 0.0070599 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497368 | TTTATAAGGTGCTCT[A/C/G]TCTGGCATGACATCT | 115426 |
rs374448251 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455285 | TAATGCTATCCCTCC[C/T]CCCTCTCTCCACCCC | 115426 |
rs374481321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452788 | TGCTTTGCATTTGAG[C/G]TGCTTCTGGGACATT | 115426 |
rs374502598 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455479 | GCACTTATCCTTTTT[-/T]ATGGCTGCATAATAT | 115426 |
rs374516695 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418632 | TGAAAAGTAATACAT[A/G]TGAAGAGTAGAAAAT | 115426 |
rs374528074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435852 | GACCTCAAGTGATCC[A/G]CCCACCTTGGCCTCC | 115426 |
rs374577823 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471042 | TAAATATAAAATCAC[A/G]GAAGTTGAAAAGAGG | 115426 |
rs374660743 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501055 | TACCTAACCGCATAA[A/G]TCTTAAGCAGTTCAG | 115426 |
rs374670770 | in-del | -/AGGAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469036 | AGAAAACAGAAGGAA[-/AGGAA]TACCAATTATGGGAA | 115426 |
rs374671186 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439339 | CACCACCACGCCCGG[C/G]TAATTTTTGTGTTTA | 115426 |
rs374725166 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441605 | ACTGCTGCCAAATAG[C/T]AGTATAGGGGAAAGG | 115426 |
rs374732518 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482730 | GCCTCCAAAGTAGCT[A/G]GGACTACAGGCGCCT | 115426 |
rs374748506 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474482 | AGGCCGAGGCGGGCA[A/G]GTCACCTGAGGTCAG | 115426 |
rs374758504 | snp | C/G | 0.000116039 | 0.00761617 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481781 | GGTAAAGAAGAAATT[C/G]CCCTTTTCTTCCTAA | 115426 |
rs374764649 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413712 | TCCTCTGGACGCACC[C/G]GTCCGAGGGCTCTGT | 115426 |
rs374816778 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466800 | ATGCTCCTGCCTTGG[A/G]GCCTTTGTACTTGAT | 115426 |
rs374822595 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428764 | ATGTTGTCCAGGCTG[A/G]TCTTGAACTCCTGGG | 115426 |
rs374824143 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447671 | TCCTAAACCATCCTA[A/G]AAGACAGTAAAATAA | 115426 |
rs374844283 | snp | A/G | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434068 | ATGGAAATATAAAGC[A/G]TAAATCCAAAGAGAA | 115426 |
rs374852112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433092 | CCCCTGCCTTGGCCT[G/T]CCAAAGAGCTGGGAT | 115426 |
rs374854538 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451775 | CGCGCCCGGCCTGTT[G/T]GTTGTTGTTGTTGTT | 115426 |
rs374855910 | snp | A/G | 0.000215042 | 0.010367 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499978 | TAACATACTTTTGTT[A/G]TTGTTGTTGTTGAGA | 115426 |
rs374877168 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427612 | ATCACTTGAACCCAG[C/G]AGGTGGAGGTTTCAG | 115426 |
rs374895536 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478054 | GTTCATTCAAAAATG[C/T]AAATCTGATCATGTT | 115426 |
rs374901957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432459 | TATATCAAGGTTCAT[A/G]GTATGATGGCAAGAA | 115426 |
rs374910913 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466166 | AGCACTTTGGGAGGC[C/T]AAGGTGGGCGGATCA | 115426 |
rs374914653 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483358 | AAAAATCCTTTATAC[A/G]ATGGTGCAGTATTTT | 115426 |
rs374989545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502734 | ACTCAAAATACCTGT[A/G]TTAGATATACCCGTA | 115426 |
rs374993856 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458894 | TGCAGCCATAAAAAA[-/A]GGATGAGTTCCTGTC | 115426 |
rs375037129 | snp | C/G | 0.000117842 | 0.0076751 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481818 | GTTATAATATATAAT[C/G]TTTTAATACCAATAG | 115426 |
rs375042114 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458287 | ATTTTCTAGTTTATT[G/T]GTGTAGTATTCTCTG | 115426 |
rs375099235 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411888 | CTCCCTTCTTGAGAA[C/G]ACATATTTTCATTTA | 115426 |
rs375101849 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428481 | TTATGCAACCCTAAT[C/G]CCTAATTTTCTGGTT | 115426 |
rs375118392 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417181 | CACTTCCACTTGGCA[A/T]TTGCTTTCTAGTATT | 115426 |
rs375188028 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492126 | AATGTTTTTGTTGAT[A/G]TAATGATTAAAGTAC | 115426 |
rs375210038 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504008 | CTTGATTTTTTTAAA[-/T]AGAAGACTTTTTTTT | 115426 |
rs375218194 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456689 | TTTAAGTCTTTAATC[C/T]ATCTTGAGTTAATTT | 115426 |
rs375221076 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467806 | TTCAGGCCTCTGAAC[C/T]GGACTGAATCCTAGC | 115426 |
rs375388121 | in-del | -/TA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505296 | GCGTGTGTGTGTGTG[-/TA]TATATATATATATTT | 115426 |
rs375393419 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488540 | TTCTCTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 115426 |
rs375444688 | snp | C/T | 0.00022197 | 0.0105326 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460554 | TAATCATAAGCCATA[C/T]GGTTTTCTCTCTCCT | 115426 |
rs375449053 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446938 | CTGTCACCCAGGCTG[G/T]AGTGCAGTAGCACAA | 115426 |
rs375477715 | snp | A/T | 1.8069e-05 | 0.00300569 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413458 | AGAGCTCAGGGGGAG[A/T]CAAAGGGGACCGGTT | 115426 |
rs375577877 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425724 | GCCGAGATCGCGCCA[C/T]TGCACTCCAAGCCTG | 115426 |
rs375578973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454230 | TGAGGGAGAAGCTAA[A/G]TTGGGAATCTAAACC | 115426 |
rs375637633 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477215 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACTCCAT | 115426 |
rs375652289 | snp | C/G | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500611 | GCAGAAGCAATTGAG[C/G]CTTTTCAACTAACTC | 115426 |
rs375652988 | snp | G/T | 0.000437904 | 0.0147905 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411153 | AATGTAATTGTGGTT[G/T]TTGCCACCGAAAGAA | 115426 |
rs375666215 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442796 | GTGCCTGGCATGGCA[C/T]GAACTTCATGATGAT | 115426 |
rs375689652 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487171 | CTCTATAGAGCTTTT[A/T]TTTTTTTTTCCTTTT | 115426 |
rs375692855 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468212 | TTATTATGATCAATG[A/G]CATTTAGTTTTGTGC | 115426 |
rs375709301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466777 | TTGTGTTGCTTGATC[A/G]CGCAAACATGCTCCT | 115426 |
rs375782048 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460621 | CAAGGATCTTAGACC[A/G]CGAGCTAGAACCATT | 115426 |
rs375783512 | snp | C/G | 0.000379666 | 0.0137728 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482116 | TATGTTTTAACTTGG[C/G]CTTAGTTGAAAGGGG | 115426 |
rs375870696 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419767 | TTATTTTGAGACAGG[C/G]TCTCACTCTGTTGCC | 115426 |
rs375895177 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462635 | TTAAAAAAAGATTTC[C/T]TGGCTGGGTGCAGTG | 115426 |
rs375972887 | snp | A/G | 9.739e-05 | 0.0069775 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504583 | TCCTTATCCTTGGAT[A/G]CTGTTCTAGAATTTT | 115426 |
rs376067226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443445 | GCAGATTCCAAAAAG[C/T]GCATGCTTGCAACTA | 115426 |
rs376095023 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493944 | ACAGGTACTACTATA[A/G]ACACTGTTTAGAATT | 115426 |
rs376103286 | snp | A/C | 7.69897e-05 | 0.00620394 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504708 | TAAGTAGAATTCCTT[A/C]CTCACTTTCCCTGTT | 115426 |
rs376126514 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | UHRF2 | GRCh38.p7 | 9:6506011 | GCTCAGATTAAATTG[A/G]ATGTTTTTGTTTTTA | 115426 |
rs376134036 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433903 | ATTAACTGATTTTAA[A/C]CTTTTTTTAGGTAAA | 115426 |
rs376185954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460863 | TTTAGGTATTAAGCA[C/T]GTGTACCTTAGTAAA | 115426 |
rs376188749 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451288 | TAGGCTACCAGTTGT[A/G]TAGTTTCGTTCATTA | 115426 |
rs376273391 | snp | A/T | 0.000603771 | 0.0173644 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493782 | GAATTGATGAAATTA[A/T]ACTTGGGTTTAGCTT | 115426 |
rs376285362 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501533 | ATTATTATTAAGGAA[G/T]AATTTTTTAAATATG | 115426 |
rs376291172 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469923 | CAAAGAAGTTCTGTA[A/G]ATTCTAAGCAGGATA | 115426 |
rs376295849 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487614 | TCAGGTGATCCTCCC[A/G]CCTTGGCCTCCCAAA | 115426 |
rs376307010 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437809 | TTTTAGTTGAGACTG[A/G]GTTTCACCACGTTGG | 115426 |
rs376320991 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438571 | ACAATTGTGTCTGCA[A/C]ACCTCTTGAGTGTAG | 115426 |
rs376336139 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414427 | GTTCACGCTTTAAGC[A/G]TAGCACTGCAGCATA | 115426 |
rs376338143 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472553 | TTCAGGAGAACTAGG[G/T]TCAGACAATCAAGAT | 115426 |
rs376354776 | snp | A/G | 9.94497e-05 | 0.00705088 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475406 | GGGTTCTGAAGGAAC[A/G]TTAAATGACTGCAAG | 115426 |
rs376359410 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422944 | GGCTTTTGTAACCAG[C/G]AACCTTTTCAAATCT | 115426 |
rs376378212 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430438 | AATCTTTTAAAAATA[A/C/G]TTGTATATTTTATGA | 115426 |
rs376464258 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422827 | ATATTTAATATTTTG[C/G]TTTATTTCTGGTAGC | 115426 |
rs376475413 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472880 | AAAAAGGAAAAAAGA[C/G]ACATAATTTTTTTAA | 115426 |
rs376477707 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481608 | CTTTAATATGGTATT[C/G]TGAAAATGCCTTCGT | 115426 |
rs376478607 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492661 | TGTCTAAGTTGTCTA[A/C]ACTAATTAAAATGAT | 115426 |
rs376487736 | snp | A/G | 3.33128e-05 | 0.00408109 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497996 | TTAAATCTCAAACTG[A/G]CACTGAAATATTGTG | 115426 |
rs376511846 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488345 | CTCTACCCAGTTTCT[C/G]CCAGTGGTGACATCT | 115426 |
rs376520961 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450636 | TCTTTCAAAGGTTGA[C/G]CGGTGAGATTGATAC | 115426 |
rs376533131 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443858 | AAACGTCTTAAAATA[C/T]GTTGTCTTTGCTCCC | 115426 |
rs376577076 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502402 | CTGTATAAATAGATT[C/G]CTCAGAGAGATCTTC | 115426 |
rs376606673 | snp | A/G | 0.000131804 | 0.00811695 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6421013 | TCCTGGCACATCTAC[A/G]CAGATTGAGGCTAAA | 115426 |
rs376609946 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484862 | GCAGTGGCACAATCT[C/T]GGCTCACCGCAACCT | 115426 |
rs376646952 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423390 | GCTTCACTAACATTG[A/G]CATAAAACCTAAGTT | 115426 |
rs376655963 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481373 | GATAAGTTTAGAGTT[C/G]ATGGTATCATTTTGA | 115426 |
rs376701793 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425786 | ATTAAAAAAAAAAAA[A/T]TCAAGATCTCGGCTC | 115426 |
rs376760067 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439335 | TGTGCACCACCACGC[C/T]CGGCTAATTTTTGTG | 115426 |
rs376766865 | snp | G/T | 1.65523e-05 | 0.00287678 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498014 | CTGAAATATTGTGAT[G/T]TAGGTGGTGAAATAC | 115426 |
rs376770448 | in-del | -/TATTCATATG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464653 | TTTCCTAGCACTGTT[-/TATTCATATG]TATTGAAAAGCCCAT | 115426 |
rs376845496 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444803 | AGACAGGGTTTCACC[A/G/T]TGTTGGCCAGGCTGG | 115426 |
rs376874515 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435801 | TTTAGTAGAGACAGG[G/T]TTTCACTATGTTGGC | 115426 |
rs376906799 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425774 | CAAAGTAAATAAATT[A/T]AAAAAAAAAAAATCA | 115426 |
rs376952822 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420435 | TATGGCCGGGTGCGG[G/T]GCTCACGCTGTAATC | 115426 |
rs376962200 | snp | A/C | 0.00175047 | 0.0295325 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472078 | ACGCATGTCACCACT[A/C]ATCAAAACACAATGT | 115426 |
rs376967679 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453789 | AGGTACTTGTAGTCC[C/G]AGCTACTTGGGAGGC | 115426 |
rs376979824 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490930 | TAGGAAAAGGAAACC[C/T]GAATAAGCTTTTCAC | 115426 |
rs376982666 | snp | A/C/G | 3.31605e-05 | 0.00407177 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493846 | AGGTGATGAGTTCAC[A/C/G]TACACTGGAAGCGGT | 115426 |
rs377032931 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446251 | CGCCTCCCAGGTTCA[A/G]GCGATTCTCATACCT | 115426 |
rs377080816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422245 | TACCACCATGCCTGG[C/G]TAATTTTTATATTTC | 115426 |
rs377161749 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428946 | AGGACAAGTGGATCA[C/T]TTGAGGTCAGGAATT | 115426 |
rs377204864 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446024 | TGAGATAGAGTCTCA[C/G/T]TCCCGTCACCCAGGC | 115426 |
rs377210138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453689 | GCGGGCAGATCACGG[C/G]GTCAGGAGATTGAGA | 115426 |
rs377211746 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477395 | GCCAGGCGTGGTGGC[A/C]CATGCCTGTAATCCC | 115426 |
rs377215029 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471222 | ATAACCCCCAAATAG[C/G]TGGTGGGATAAACAG | 115426 |
rs377224704 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431061 | ATGGCAGGATCTTCT[C/G]TGTTCATATTAATCA | 115426 |
rs377272112 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463316 | GAGTGGAAATTATGG[A/G]TAGGCAAATACCGGC | 115426 |
rs377308216 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482233 | ATATTTTTTAGGATG[A/G]GTGTACTCTTCCTGG | 115426 |
rs377366755 | snp | A/T | 2.00882e-05 | 0.00316918 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421138 | CTGGCTTTGGAATAT[A/T]TAAGGTATGTTGTTT | 115426 |
rs377408902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427188 | TTTGTCTTGAATTCT[C/T]GGTTATGCCACTTGG | 115426 |
rs377444207 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464741 | GAATCCTTTTGACTT[C/G]TCTATTCTGTACCAT | 115426 |
rs377446685 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481953 | TTTCATTAAAATTTA[A/G]CATAACTGATTTCTC | 115426 |
rs377473113 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480981 | TAGCCATTAGATCTT[C/T]GTTAGAGTATTCCCA | 115426 |
rs377568200 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464647 | AAACATTTTTCCTAG[C/T]ACTGTTTATTGAAAA | 115426 |
rs377581357 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427488 | GGTCAGGCTTTTGCA[A/T]CCATCCTGGCCAACA | 115426 |
rs377584475 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441389 | TACCCCTCCCAAAAA[A/G]AAAAAAAAAAAAGCA | 115426 |
rs377635010 | snp | A/C/T | 3.36147e-05 | 0.00409957 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493823 | GAAAATCTTCTCTGA[A/C/T]AGGACCGAGGTGATG | 115426 |
rs377649887 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501213 | AAGGAATCACAGTTA[A/G]TTAATGTGTGGGCTT | 115426 |
rs377690357 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488540 | TTCTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 115426 |
rs386732104 | in-del | ATC/TG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425786 | ATTAAAAAAAAAAAA[ATC/TG]AAGATCTCGGCTCTA | 115426 |
rs386732105 | multinucleotide-polymorphism | AGC/TGT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458010 | TTGGTATCAGGATGA[AGC/TGT]TGGCCTCATAAAATG | 115426 |
rs397711607 | in-del | -/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412952 | ACGGCAACCGATGTG[-/G]GTAGCCGCGCAATCT | 115426 |
rs397751507 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424015 | GTTAATATTTTAAAC[-/C]ACATTCTATACCGGT | 115426 |
rs397776882 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434456 | AGGTGGGCTTTTTTT[-/T]GAGATGGTCTCTCTC | 115426 |
rs397830883 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450315 | CCTTCCCCCCCCCCC[-/C]ATTTATTTAAATAAA | 115426 |
rs397893297 | in-del | -/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412953 | CGGCAACCGATGTGG[-/G]TAGCCGCGCAATCTT | 115426 |
rs397893754 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445974 | ATACTCTTCCCCCCC[-/C]GCCACCCTTTTTTTT | 115426 |
rs397894178 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425786 | ATTAAAAAAAAAAAA[-/A]TCAAGATCTCGGCTC | 115426 |
rs397894573 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445126 | CAAAACCCTATCTCT[-/T]ATTTAAAAAAAAAAA | 115426 |
rs397894626 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442665 | TGATTTTTTTTTTTT[-/T]TGGGGGGGTAGAGAT | 115426 |
rs397894769 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454031 | AATTGACATTTACTT[-/T]ACCCCCATTATGTAC | 115426 |
rs397937182 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469677 | TGTGTGTGTGTGTGT[-/GT]ATGTATATATATACA | 115426 |
rs397962818 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503419 | GCTTAAAAAAAAAAA[-/A]CCAGCCAAGATGAAA | 115426 |
rs398010245 | in-del | -/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477526 | AACAGCATTTTTTTT[-/G]GAAATGGAGTTTTGC | 115426 |
rs398087117 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446171 | ATAATTTTTTTTTTT[-/T]TATACAGTCTTGCTC | 115426 |
rs398087118 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463294 | CTCAATAAAAAAAAA[-/A]AGACTTGAGTGGAAA | 115426 |
rs398087119 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465584 | TTGTCATAAATTTTT[-/T]TGGTACCTACATCTT | 115426 |
rs527263070 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441502 | GTGTTCTAATAAGTC[C/G]TTTGAGTGGCTCTGA | 115426 |
rs527273701 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467557 | GCACTAGTTACAATA[A/G]ATTTTCAGTACGGTA | 115426 |
rs527282060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473176 | GTCTGCTAAGTTCTC[A/G]TCAGAAGGATTTGGG | 115426 |
rs527306643 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433465 | CATTTTCAAGTTTTG[-/TT]TTCTTTTTAATACTT | 115426 |
rs527314485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478665 | TTGCTACTGGTGAGC[C/G]TTTTTAAGTAAGACG | 115426 |
rs527315536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472661 | CATAAAGGAGAAAGT[A/G]TAGTATGTACTGGCT | 115426 |
rs527391001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477412 | ATGCCTGTAATCCCA[C/G]CTACTCGAGAAGCTG | 115426 |
rs527444224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501069 | AGTCTTAAGCAGTTC[A/G]GCACAATTTTCAAAA | 115426 |
rs527444495 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494462 | AAGTGATCTTTTCTA[A/G]CTAAATCCCCTTAAG | 115426 |
rs527478278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462401 | GAACTTCTTACAAAC[A/G]AAAGTGTGATTCTAT | 115426 |
rs527490448 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461924 | TTGTGCATTTCTTTT[C/G]TTTAGAATAAATTGT | 115426 |
rs527527998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425548 | TCACTACAGGTCAGG[A/G]GTTTGAGATCAGCCT | 115426 |
rs527551331 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461358 | CTCTCTCTCTCCCCC[C/G]CCTCCTCCTCTCCCC | 115426 |
rs527594946 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430206 | GTAGAGACAGGGTTT[C/T]GCCATGTTTGCCGGG | 115426 |
rs527622544 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458332 | TTCTGTGGGATCAGT[A/G]GTGATATCCCCTTTA | 115426 |
rs527623981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505737 | GTTGAAATCTAACCC[A/G]GAAGATTAGGCTAGT | 115426 |
rs527642547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499305 | TGATAGATAGAATGT[A/G]TTACTTCAAATCTAA | 115426 |
rs527649153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492649 | ACAAAACATCATTGT[C/G]TAAGTTGTCTAAACT | 115426 |
rs527701608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466793 | CGCAAACATGCTCCT[G/T]CCTTGGGGCCTTTGT | 115426 |
rs527715911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429582 | GTGCTCCACCTGCCT[C/T]GGCCTCCCGAAGTGC | 115426 |
rs527779126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504513 | CTCTACTAGCTGTTT[C/T]GAAATACACAGTAGA | 115426 |
rs527780727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434855 | TGGGGGGTGGGGACC[A/G]GGTCCCACTTTGTTG | 115426 |
rs527781774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429168 | AGACTCTGTCTCAGG[A/G]AAAAAAAAAAAAGGA | 115426 |
rs527792320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434286 | ATCCTTTAGAGGTTA[C/T]GTTCATTTGTTACTT | 115426 |
rs527816050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504213 | TGTATTTTTAGTAGC[A/G]ATGGGGTTTCACTGT | 115426 |
rs527844017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445821 | CTTCCCCCTTGGCCT[C/G]CCAAAGTGCTGGGCT | 115426 |
rs527850862 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506477 | CTCAGGACAGAAAAG[A/G]TTTATGGGGATTTTA | 115426 |
rs527861444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414220 | CAGAACTTCTGGTCC[C/T]TCTCCCTCGCCGCCT | 115426 |
rs527862447 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450917 | TGCTTACTGATATGT[A/G]TTTGGTCATGTTTCT | 115426 |
rs527923282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419851 | GCTAAAGTGATCTCC[C/T]ACCTCAGCCTCCTGA | 115426 |
rs527928605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413750 | GCGCGCAGGGCTCAC[C/T]TGGCTCCGCTGCGGG | 115426 |
rs527934433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419270 | GTTTCCAAATAAGGT[C/T]ACATTCTCAAGTACC | 115426 |
rs527935359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482660 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 115426 |
rs527995590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418668 | ATTTAAAAATTGATT[A/G]TGTTTCTGGGAAAGT | 115426 |
rs528010692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493088 | GGATCACTTGAGACC[A/G]GGAGTTGGAGACCAA | 115426 |
rs528026372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455613 | TACTTGAGGAGCAGC[A/T]GGTCTTAATTTTATA | 115426 |
rs528031258 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454822 | TAATATCATAAATAC[C/T]AATTCCTGTATTTCT | 115426 |
rs528087251 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481331 | TTTTAATGACAGGAA[C/G]TTCAAATTTCTATTC | 115426 |
rs528111448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454505 | AGTACCTTCTCTTTC[C/G]TATGTCAGAACTACG | 115426 |
rs528116884 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412401 | GTTTCCCGCAAACCC[A/G]CAATCCCTTAGGCCA | 115426 |
rs528124262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417895 | GACTGTAGAAATACC[C/G]TCAACGTCACTCTGA | 115426 |
rs528128324 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486510 | GTTGAGCTGGAAGTT[C/G]CAATAGACATAAGAT | 115426 |
rs528166837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491582 | TTTATCTGATAGTCT[A/G]TAGGGAGGAGGCTGA | 115426 |
rs528188803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423010 | GCTTTATCCTTTCCT[A/C]TCTTTGTAACTTCCT | 115426 |
rs528207329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459573 | ACTTAGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 115426 |
rs528208035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497794 | TAATTAGCATAATCT[C/T]GTTACTCTATTAAAT | 115426 |
rs528212618 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448571 | TCCTAAGGGTTGTTA[C/T]AAGTATATGTGAACG | 115426 |
rs528214035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422455 | GGCTTTTAATATTTG[C/T]ATACAAAAAACTGTA | 115426 |
rs528231625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459779 | GGAGTTCTAAACCAG[C/T]GTCATGAACATAGTA | 115426 |
rs528265940 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439520 | TCAACTTTGTGGTTC[A/C]CACCTTTATGCAGAT | 115426 |
rs528282209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471513 | TTTAAAAAGATACCA[A/G]CTTCCATTTTGGGTG | 115426 |
rs528299709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476785 | TTTTTAGCAGGGACG[C/G]GGTTTCACTGTGTTG | 115426 |
rs528331990 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413366 | GTCCGGTCGGTCCGG[G/T]GGGCGCGCTCGCCCG | 115426 |
rs528336635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476249 | ATATTTTATTGTATA[C/T]GTATATACCATATTG | 115426 |
rs528376571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439004 | TGTAATTCTAAAATA[C/T]AACTGAAATAATTTG | 115426 |
rs528382417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444993 | GTTTAGGCACTAGAT[A/T]TAGAATTTGGGTTGA | 115426 |
rs528407133 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412914 | GAGGCACCCGCCCCC[C/T]CAGCTCTGAAACGAG | 115426 |
rs528416522 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438673 | GCCTCTGGAATTATT[C/T]TGGGGTATGCAATGT | 115426 |
rs528471916 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487963 | ACAATACAGAGGGCC[A/G]AATCCAGTGGCTCAT | 115426 |
rs528542995 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411566 | AATATTTTTAGTAGA[G/T]ATGGGGTTTCACCAT | 115426 |
rs528550735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443293 | TGCCAAGCAGTATAC[A/G]GATACTTTACCTGGA | 115426 |
rs528563186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480199 | TGCACTTAACTGTTT[C/G]TTTGCCAGGAATGCT | 115426 |
rs528607869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416807 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCGCCC | 115426 |
rs528658917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459190 | CCTGCACTTTCTGCA[C/G]AGGTATCCAAGAACT | 115426 |
rs528676557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464038 | GATAGAACCAAGTGT[C/T]TGTACCAGGTTACAG | 115426 |
rs528695419 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471345 | ACTAATTTGAAAATA[A/G]CAGCTATGGTAGCCA | 115426 |
rs528699715 | snp | C/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443303 | TATACAGATACTTTA[C/G/T]CTGGATTATCTCATG | 115426 |
rs528713497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463539 | GCAGTGGCACAATCC[C/T]GGCTCACTGCAACCT | 115426 |
rs528749178 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416992 | GTTTTCACACAGAAT[A/G]TAAAAGTACTTGCCT | 115426 |
rs528768636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438174 | GAGATTTCTGTATAA[C/T]ACAGAAGGGAAGTTT | 115426 |
rs528811189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501839 | ATTATTCTCTGATTG[A/G]GAAAGATAGGGCTTG | 115426 |
rs528827631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426158 | CTCCCCAATCGAATT[C/T]GGAAGAGCATCAGGA | 115426 |
rs528830775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502542 | ATCCTCCCGCTTCAG[C/T]CTCCTAAGTAGCTGG | 115426 |
rs528848841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431659 | CTTTGTGAGCTGATA[C/T]GTTCTATGTGTTGAT | 115426 |
rs528879828 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457192 | TTTCGTTGAGCAGTG[G/T]TTTGTAGTTCTTTTT | 115426 |
rs528906438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462509 | GGAGAAAGCCCCTAA[A/G]TAAACTGGCTATGTT | 115426 |
rs528949396 | snp | C/G | 0.000185891 | 0.00963903 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468680 | TTGAATACTGGACTT[C/G]TGCTGGACAAGAGGC | 115426 |
rs528959132 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485839 | AAAAACAAAACCCAA[A/T]ACCAATTGTATGACC | 115426 |
rs528961048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431206 | TATCCAATGTGCAGA[A/G]AGTTTTGAATTTAAG | 115426 |
rs528992181 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506639 | CTTCTAAAGTGTGCA[C/T]ATACTTTTTTAACGT | 115426 |
rs529019337 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504782 | TAAGAAGCATTTTCC[A/G]TGAAGCGGGATAGTT | 115426 |
rs529021288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436675 | GGCTCTTAAAGTTGC[A/T]TTTGAAGTAAGACTA | 115426 |
rs529046951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453039 | CCTTGGTTAGAATTT[A/G]AAAATGTATGCTTCA | 115426 |
rs529099159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452609 | AGGATATAGAGTTAC[A/G]TTAAACAGTCATTAA | 115426 |
rs529153246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489671 | ATTTGCCATCTGTAT[A/G]GCCTCTTTAGTAGTA | 115426 |
rs529155836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426887 | TTGAGTAGTTGGGAT[C/T]ACAGGCACCCGCCAC | 115426 |
rs529157868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420783 | AGGCCATTAAGTATT[A/G]AGAATGGTTTTAAAA | 115426 |
rs529187091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496028 | ACTTGGGAAGCTTCA[A/G]CTCTTTGACCACAGC | 115426 |
rs529226207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493514 | ATTGAATAAAATATA[A/G]TATTTAAATCCATAA | 115426 |
rs529286861 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488586 | GAATCTTGCCCTTGT[C/T]GCCCAGCTTGGAGTG | 115426 |
rs529294778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456468 | TTGCAAAAATGTTCT[C/G]TCGTTCTGTAGGTTG | 115426 |
rs529304827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420330 | AAAGTACTGAGATTA[C/T]AGGCGTGAGCCACCG | 115426 |
rs529310306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451390 | CTGTAGTTAAATCTC[C/T]AAAACAAAATATACT | 115426 |
rs529323944 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488056 | GACCAGCCTGGGCAA[C/T]GTGGCAAAGCCCTGT | 115426 |
rs529383501 | snp | C/T | 3.29984e-05 | 0.00406179 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500655 | TCTCATCAGAGAAGA[C/T]TGTCAAAACCAGAAG | 115426 |
rs529397406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425508 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 115426 |
rs529401220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493755 | TAATGAAATGTTTTG[A/G]CTCTGAAATAAGAAT | 115426 |
rs529408110 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484900 | CTGGTTTCAAGCAAT[C/T]CTCCTGCCTCAGCCT | 115426 |
rs529410414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425068 | TATTAAACTACTCCC[A/G]CACCTCCTTCCTGTC | 115426 |
rs529413239 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503816 | TGATTTTTTTATTTT[G/T]TAAGTGAAAAATAGT | 115426 |
rs529454640 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473740 | TACTTAACTCCCCTG[A/T]TAACAGCATGAAACC | 115426 |
rs529460460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436137 | ATTCTTAACAAGTAC[A/G]AGTTAGAAATCCTAG | 115426 |
rs529490268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479303 | TTTATGTCTAAACCT[A/C]AGGGTCAGTTCTCAT | 115426 |
rs529513364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483933 | ACCTCGGGTGATCTG[C/T]CTGTCTCAGCCTCCC | 115426 |
rs529525143 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437474 | TGGACCTCAGGTGAT[-/C]CACCTACCTCAACCT | 115426 |
rs529525400 | in-del | -/AAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462009 | TTTTAAAAAAAAAAA[-/AAT]AAGAGAAACAGCTAA | 115426 |
rs529597071 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441735 | GGTGGTTTGTGGCCG[G/T]TTTTTTTTTTCCATT | 115426 |
rs529606703 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414506 | ATGGTCTGGCCAGTC[-/T]TAAGTTTTTTTCCTA | 115426 |
rs529621683 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497138 | TTAATTGAGCTAATG[A/G]CTCGATTGTGTACTT | 115426 |
rs529648182 | snp | A/C | 0.000602538 | 0.0173466 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477578 | GATTCATAGATATAA[A/C]AAATGTTTTAAGACT | 115426 |
rs529655111 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445734 | GGCTAATTTAAAAAA[A/T]TTTTCTTTTTGTAGA | 115426 |
rs529658960 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458192 | TCGGAACTTGTTATT[A/G]GTCTATTTAGGGATT | 115426 |
rs529698633 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499994 | TGTTGTTGTTGAGAC[-/G]GGGGTCTCACTCTTG | 115426 |
rs529767220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450815 | TGTGTTCAGGTATAA[C/G]AGAATGTTCCAGCCC | 115426 |
rs529775072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419070 | TATTGGATTAGGGCC[C/T]TAATGACTTTGTTTT | 115426 |
rs529778554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482516 | ACATTGGGCAGAGGA[A/G]GTGCCAGCTAATCCA | 115426 |
rs529815356 | snp | A/G | 0.00029753 | 0.0121933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481972 | AACTGATTTCTCAAC[A/G]TTTGTTTTGCGTCTT | 115426 |
rs529819110 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413397 | CCTGCCGCTGAGGGC[C/T]CGAGCCGCAGGGAAA | 115426 |
rs529819533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487418 | GTCACCTAGACTGGA[A/G]TTCAGTGGCTCAGTC | 115426 |
rs529826045 | in-del | -/AGAC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6475291 | TCTCAATTTATAAAT[-/AGAC]AGATTTCAGTGAGAT | 115426 |
rs529835347 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472821 | AGTATTTGTAATATT[C/G]TAATTTTGGTGTCCT | 115426 |
rs529838749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461295 | CCTTCAGATATTTCT[A/G]TCATTTCTTTCTTTT | 115426 |
rs529896868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472580 | AGATGACTGAAGATA[A/C]TTTGAAATAAAGAGT | 115426 |
rs529928674 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452173 | TATTCTATTATGTAC[C/G]TGTATTATGTTATCT | 115426 |
rs529928988 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426445 | TAAAATTCTCAGAAG[C/G]TTGCTGTTCATACAA | 115426 |
rs529969220 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428219 | CAGTTCTTGATGTTT[A/G]ACCTTTTTGATTATG | 115426 |
rs529986928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440952 | CCTGTGATTCTATTT[A/C]ATTCCCTGTGATTCC | 115426 |
rs529995441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498007 | ACTGGCACTGAAATA[C/T]TGTGATTTAGGTGGT | 115426 |
rs529996569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429787 | TGCTGGGACAAATTA[A/C]GTAACTTGTTCATGG | 115426 |
rs530004048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428688 | CTGAGTAACCGGGAC[C/T]ACAGGTCTGTGCCAC | 115426 |
rs530041165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459686 | AAAACAAAACAAAAA[A/G]CTTGAGGCCTGACAT | 115426 |
rs530043691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504789 | CATTTTCCGTGAAGC[A/G]GGATAGTTGCGGAAC | 115426 |
rs530044830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435070 | TGGGAGTACAGTGAT[A/G]CAACCTCCACCTCCC | 115426 |
rs530048546 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445584 | TATTTTTGAGACAGG[G/T]TCTTACTGTGTCACA | 115426 |
rs530049208 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490773 | TAGTTAAGTCTGTTA[A/C]ATAATGTGAAGAAAA | 115426 |
rs530082001 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468082 | ATTCTTAGACTGCCT[G/T]ATTTCAGTCTAGTTT | 115426 |
rs530087110 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447847 | CAAACAAAGCAAGCA[A/G]ATTGGTGTTGGAGAA | 115426 |
rs530130731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465231 | TCTCCTAGATTTGGT[C/T]TGACAGTGTTTTGTG | 115426 |
rs530153268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471458 | CTTTGTGACCAATAG[A/C]ATATGGTGTAAGTGA | 115426 |
rs530168216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471003 | AATAAAAAAATCCAC[A/G]TGCTACTCTTAAGAA | 115426 |
rs530219681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455489 | TTTTTTATGGCTGCA[C/T]AATATTCCATGGTGT | 115426 |
rs530221162 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423305 | ACCTACAACATAAAG[A/G]AGGAAAGCTTCCTAT | 115426 |
rs530221339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450313 | TCCCCTTCCCCCCCC[C/T]CCATTTATTTAAATA | 115426 |
rs530274679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493060 | CCCAGCACTTTGGGA[A/G]GCCAAGGCGGGTGGA | 115426 |
rs530319787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423831 | GTGCCTGTAATCCCA[C/G]CTACTCCGGAGGCTG | 115426 |
rs530330689 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423180 | CTACATATGTATATA[A/C/G]AAAGATTAAGAAGAG | 115426 |
rs530353481 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418486 | TTTGAGATTGTGCTT[C/G]TTGGGTTCTTGGACC | 115426 |
rs530360384 | snp | C/T | 0.435263 | 0.167862 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487181 | CTTTTATTTTTTTTT[C/T]CTTTTTTTTTTTTTT | 115426 |
rs530392767 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440432 | CTGACTCAAGAGCCC[A/T]AGAGTTAACCAATAT | 115426 |
rs530400373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492516 | CAAAAGGTGAAAGTA[A/C]ATTTAAGGGTTTTGG | 115426 |
rs530434796 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494126 | TTATTTTTTAAATGC[C/T]ATAATTTCTAGTCTT | 115426 |
rs530438606 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498604 | TTTTCTCTCTTCCCC[C/T]GCAAAGCTGCTTCCC | 115426 |
rs530483855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463861 | GAACAAATGCATTCT[G/T]CTGTTGATAGGCATT | 115426 |
rs530517209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453873 | TCATGCCATTGTACT[C/G]CAACCTGGGCAACAG | 115426 |
rs530519532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421832 | TTTTATTTTTGCTAC[G/T]TACGTATATTTCTCT | 115426 |
rs530520186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453327 | ATGGAGGTGGTTCTT[C/T]TGCCACTGAAATATG | 115426 |
rs530574043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438418 | TCTCAAAGTCACATT[C/T]TTGTACTTTAACTAA | 115426 |
rs530601324 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499263 | CCACCCACCCCCTCA[A/G]AGAAGGTAGCCATTG | 115426 |
rs530608744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497143 | TGAGCTAATGACTCG[A/G]TTGTGTACTTGAAGA | 115426 |
rs530645908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475647 | TTTTGATCTAAGATT[A/C]ATTTTGTTTTAATGA | 115426 |
rs530647101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502863 | TAATTGCCATATTTT[A/T]AAAATGTGTTTATAA | 115426 |
rs530666787 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412794 | TCTCGGAAGTTTAGG[C/T]CGCACCCACCCGCGC | 115426 |
rs530668277 | snp | A/G | 0.000106661 | 0.00730199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477859 | CTGTGTAAACATGAA[A/G]TATGTATTTGAACCA | 115426 |
rs530675323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444563 | ACCCTCTCTCTCCCT[C/G]CTTCCTCATTGTGTG | 115426 |
rs530675988 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496714 | AAGGATTCTCTATTG[C/T]CTGGAATGTGGAAAG | 115426 |
rs530681170 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480702 | TAAAATACAGCTTTT[C/G]TTTAGGACAGTTTAT | 115426 |
rs530709310 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470140 | CATTTTGGAAGGCCA[A/G]GGCGGGCAGATCACT | 115426 |
rs530719335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485996 | CATGTTTGGGTAATA[C/T]TGAGTAGTTTTGGCT | 115426 |
rs530720673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476076 | CATCATCATTCTATT[C/T]TCCACCTGCACAAGA | 115426 |
rs530760959 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481107 | ACAAGTTACAGTAGG[G/T]TAATCAATTACAAAT | 115426 |
rs530762046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442840 | TAATTTTTAGGCCAT[A/T]GTTACCACACTACCA | 115426 |
rs530766938 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506071 | GGCACAGGTTTTCTC[C/T]TGCCCTGCTTGCCGG | 115426 |
rs530801259 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490677 | GAAGTTTATTTTCTT[A/G]TTTCCATGTTTTTGA | 115426 |
rs530814327 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462069 | ACTGGATTAGTGATA[A/C]AAGGTGACAAATCTT | 115426 |
rs530837067 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465466 | TTCTTTTATGGTCAG[A/T]TCGGTTTCTGTAATG | 115426 |
rs530857964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417259 | TTCAACTCAGTAAAA[C/T]TTCAAGAGTGGTCTG | 115426 |
rs530858200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479681 | CAGATGGAGTTCTTG[A/T]TTTCCACAAACTCCC | 115426 |
rs530870289 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443855 | GGCAAACGTCTTAAA[A/G]TATGTTGTCTTTGCT | 115426 |
rs530941197 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436592 | ATTATGCAGAATGGC[A/G]CAACATAGACATAGA | 115426 |
rs530957352 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438738 | TTTTATAGTAATCTA[C/T]GTATCTAATAGATTA | 115426 |
rs530963041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502471 | TAGTTTAAAAAGTCC[A/G]AACAGATGGGGTTAC | 115426 |
rs531010353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463501 | TGGGAGATGGGGTCT[C/T]GCTCTGTTGCCCAGG | 115426 |
rs531037867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483991 | ACTGCACCCGGCTTC[A/G]TCATCATTTTCTGTT | 115426 |
rs531050525 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415553 | GAATGGCATCACAGA[C/G]AGTCCCCGTCCTGTA | 115426 |
rs531058442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421383 | AATTGCACCAAGGTT[A/T]AGAAGTAGATTGATT | 115426 |
rs531072432 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423000 | TGGCAGTTTTGCTTT[A/T]TCCTTTCCTATCTTT | 115426 |
rs531084164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469368 | ACTGAAAATACAAAA[A/G]TTAGCTGGGCGTGGT | 115426 |
rs531089603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432253 | AGCTATTTCATTGCT[A/T]CCATGTTCATTACAT | 115426 |
rs531120580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474508 | GTCAGGAGTTCGAGA[C/T]GAGCCCAGCCAACAT | 115426 |
rs531147297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437155 | TTCAGTAAGTCATCA[A/C]ACAAGTTCTTCTTTG | 115426 |
rs531171494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430676 | AGGTACCAAACAACT[A/G]GAGGCCACCCCTACA | 115426 |
rs531173752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436610 | ACATAGACATAGAAT[A/G]AGGAACTTTAAATAG | 115426 |
rs531192325 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478534 | ATTTTTCTCCTATGG[C/T]GTGGTGATAACTACA | 115426 |
rs531229356 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454564 | AAAACTGCCCCCCAG[C/T]CCCCATCACCTACGT | 115426 |
rs531246080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480135 | CTTGGTCTCTACCCA[C/T]CTTTGTCTTCCTCAA | 115426 |
rs531279979 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443175 | TTGGCTAGGCAAGTT[G/T]CAGTCTTTAACTGTG | 115426 |
rs531292785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500813 | CAAAACTTCATCCTT[C/T]TACCCGGTTTTCTAA | 115426 |
rs531313296 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461997 | GACAATTTTTGTTTT[A/T]AAAAAAAAAAAAATA | 115426 |
rs531318054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478780 | CCTGTTGGGAAGGCA[A/G]TTGCTGTATTATGAC | 115426 |
rs531329304 | snp | A/G | 0.00130003 | 0.0254622 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468615 | CAGAGTTTTTGGCAG[A/G]TATTTGGGATGCCTC | 115426 |
rs531369912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473676 | TTTTCTTCTGTAAAG[A/T]GCCGGATAGTAAATA | 115426 |
rs531405648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432997 | AAGCATGCTCCACCA[C/T]GCCTGGCTAATTTTT | 115426 |
rs531406734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473204 | GGGAGTCAACTGGAA[A/G]CTCCCACTGGTCAAA | 115426 |
rs531407754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457154 | GCATGGAATGTTGTT[C/G]CATTTGTTTGTGTCC | 115426 |
rs531429889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505797 | ATTTTAGTAGATGAG[A/G]AAACTGATGCACAAA | 115426 |
rs531470781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462429 | TATTGCTAGACTAAG[A/G]GTATAGCTCAGTCAC | 115426 |
rs531500679 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500206 | CTCCTGGGCTGAAGG[C/G]ATCCTCCTGCCTCAG | 115426 |
rs531522850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457839 | TTGAACCAGCCTTGC[A/G]TCCCAGGGATGAAGC | 115426 |
rs531542758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462808 | TGTAGTCCCAGCTAC[A/G]TGGGTGGCTGAGGCA | 115426 |
rs531576477 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495954 | GAGTTGATGGCTGTG[G/T]TTTTTTCTACCTCTC | 115426 |
rs531578868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489189 | ATATTAACCTTTAGG[A/G]TTGGCTTTTTCCACT | 115426 |
rs531644308 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428011 | TGATGCCAGAAAGAT[C/T]GTACTTTCAAGTGGC | 115426 |
rs531708039 | snp | A/G | 3.65017e-05 | 0.00427194 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499913 | CCCAGTGGAACCACA[A/G]AAAGGCCAATTTCAG | 115426 |
rs531727877 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456166 | TTTAGAATGTTTCTA[C/G]AGAGCTGGCTACATG | 115426 |
rs531729048 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425896 | TAACCTGTGTATATA[A/T]ACATCTATGAATATT | 115426 |
rs531767477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446876 | AACAAATAATACTTA[C/T]AAGTTTTATTTTTGG | 115426 |
rs531825553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414658 | GCTCCAATCCTGTGG[G/T]TTTAAATAAGTGTAG | 115426 |
rs531841078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430097 | CCCATTACAACCTCC[A/C]CCTCCTGGGTTCAAG | 115426 |
rs531853941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429639 | CCCGGGCTATACTCT[A/G]AGTTTTAATGAGTCT | 115426 |
rs531859429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483497 | TGCAGAATCATGACA[A/G]GAAAAAGTCTGGACA | 115426 |
rs531865515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499395 | CGCTAACTTTAGGAG[A/G]TGAGAAGTTTGACCC | 115426 |
rs531866854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488487 | CTATCAGACGTAGCC[A/C]CCCCACTGCTTCTTA | 115426 |
rs531885372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441100 | AATGCAAATTCTTGG[C/T]CTGTGCAGTGGCTCA | 115426 |
rs531937429 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502732 | TAACTCAAAATACCT[A/G]TATTAGATATACCCG | 115426 |
rs531963333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473238 | GAGACAATTTGAACA[C/T]TGATAAGAAAAATAA | 115426 |
rs531980373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477942 | GCCAGTGGTTACTTA[A/G]CATTCATAGCTCTAT | 115426 |
rs531983632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490453 | GCCAACATGATGAAA[C/T]TCCGTCTCTACTAAA | 115426 |
rs532018177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483019 | GACACCAAAGTCTGT[C/G]GATGCTCAAATTGCA | 115426 |
rs532019940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451509 | TTTGAGACGGAGTCT[C/T]GCTGTCGCCCAGGTT | 115426 |
rs532133894 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428014 | TGCCAGAAAGATCGT[A/G]CTTTCAAGTGGCTGT | 115426 |
rs532183283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481892 | ATCAATGGTACTTAA[A/C]TTACATAAACAGTTG | 115426 |
rs532184223 | snp | C/T | 0.0134861 | 0.0810011 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413375 | GTCCGGTGGGCGCGC[C/T]CGCCCGCCTGCCGCT | 115426 |
rs532195350 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437223 | CAGTAGTAATAAGCA[G/T]ATTTTTTATTTTATT | 115426 |
rs532196316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418452 | TTGTTCTACTTGACA[A/G]ATGTGAATACCTGTA | 115426 |
rs532198120 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413005 | GCGTGCCCAGTGGCC[A/C]GGTGCAGGCGGTGGG | 115426 |
rs532210431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472038 | AAGTGTATCTTAAAT[A/G]CAGTGAACATTGACA | 115426 |
rs532222336 | in-del | -/T | 0.0248432 | 0.108648 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455474 | GACATGCACTTATCC[-/T]TTTTTATGGCTGCAT | 115426 |
rs532247319 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471568 | AGGGAAGCCAGTTGC[A/G]TGTGATGAGGCTATC | 115426 |
rs532281082 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454911 | ATGTAGATTGCTGGA[A/C]CTCATTTCCAGAGTT | 115426 |
rs532285977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476814 | TGGCCAGGTTGGTCT[C/T]GAACTCCTGAGCTCG | 115426 |
rs532311143 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434974 | TAGCTGAGAATATAG[C/G]CATATGTATTACCAT | 115426 |
rs532331310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466821 | TGTACTTGATGTTCC[C/G]TCCTACACAGATACT | 115426 |
rs532345251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432921 | TCTCCGTTCACTGCA[A/C]CCTCCACCTCCCGGG | 115426 |
rs532345282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438752 | ACGTATCTAATAGAT[A/T]ACTAGACCAGATTAT | 115426 |
rs532372661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503056 | CTGAAGTACAGTAGC[A/G]TGATCTCAGCTCACT | 115426 |
rs532398451 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464204 | AGTGGGGTTGAGAAT[A/C]TTTTCGTATTTTTAT | 115426 |
rs532425412 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425704 | GGAAGCAGAGGTTAC[A/G/T]GGGAGCCGAGATCGC | 115426 |
rs532425934 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434353 | TTTTAGCTCTCGATT[A/T]TCTCTGGTTCTTAAG | 115426 |
rs532434939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470233 | AAAAATTTAGCCATA[C/T]GTGGTAGTGCACACC | 115426 |
rs532453998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438347 | TCTATGAAGTTAGTA[A/G]TTGTATTAGATGACC | 115426 |
rs532477357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439604 | AAGTTTTTTTTCTGG[A/G]TTGCTGTTCTATGTC | 115426 |
rs532517265 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448338 | ATACTTCATTACTTA[C/T]CTGTGAATACTATTT | 115426 |
rs532547687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470849 | TATTAGTCTAATCCA[A/G]AATAAGGCAATTGTG | 115426 |
rs532582505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475970 | GCTTCTGAATACTAG[A/G]TTTTATTCCTTCTGT | 115426 |
rs532622214 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475598 | AAGGAAGTATAAAAC[C/T]GTAGACCATACAAAT | 115426 |
rs532675582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433440 | TTTTTTTTATTGTGC[A/G]TAATTCTCTCATTTT | 115426 |
rs532686129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443847 | ACTCATCTGGCAAAC[A/G]TCTTAAAATATGTTG | 115426 |
rs532707567 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428256 | ATTAGACAATACAAA[C/G]AGCACGATCACTGTC | 115426 |
rs532708990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491614 | AAGTTTGGGATAAAG[C/G]TCTTCCACCTGATCT | 115426 |
rs532716278 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500421 | TATCCTAAATTTTAG[C/G]GGAAATTAGATGCTG | 115426 |
rs532724773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496605 | CATTAGCACAGGCAT[A/T]TGGATGCTTCAGGCT | 115426 |
rs532744468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459647 | GCACTCCAGCCTGGC[C/T]GACAGAGTAAGACTC | 115426 |
rs532792073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421494 | CAATCTTGGCTCGCT[A/G]TGACCTCTGCCTCCC | 115426 |
rs532846025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463010 | GAGTGGGCCAGGTGC[C/T]GTGGCTCACGCCTGT | 115426 |
rs532884195 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426965 | TGTTGGCTAGGCTGG[C/T]CTTGAACTCCTGACC | 115426 |
rs532896218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431680 | ATGTGTTGATGTTCA[A/G]GCAATGGCAGTATTT | 115426 |
rs532913986 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480151 | CTTTGTCTTCCTCAA[A/G]GCATACCATTTCTTT | 115426 |
rs532942891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443345 | GAAACTCAGTGAAGT[A/G]TAGATGTTTTCTTAT | 115426 |
rs533011225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416827 | CCACCGCGCCCGGCC[G/T]AAATCTTTTGAGAAT | 115426 |
rs533014577 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414206 | ATTCGAAGGGTTTCC[A/G]GAACTTCTGGTCCCT | 115426 |
rs533021876 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411669 | ACAGGCCTGAGCCAC[A/T]GCGCCCGGCCTTTCT | 115426 |
rs533045558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432163 | TGTTTGTCCTACCCA[A/G]CATGGTTGGCTCTTA | 115426 |
rs533073482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421775 | CTTCTCTCTGTGTCT[C/G]CCTAAGAGGTAAACT | 115426 |
rs533104344 | snp | G/T | 0.0198623 | 0.0976557 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468738 | CAGCAGTCTTAGAAG[G/T]CATACACTGGATTTT | 115426 |
rs533107789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448911 | TTGGATTTTCAATTG[C/T]GTAGCATTTGTGTTT | 115426 |
rs533128505 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412194 | ACATACATAATAAAT[A/G]AAATAAAATAAACCC | 115426 |
rs533206592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480260 | CCACTTCTAGTCACT[C/G]TTGTCACATATAACC | 115426 |
rs533219339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483966 | AGTGCTGGGATTACA[G/T]GCGTGAGCCACTGCA | 115426 |
rs533247688 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505282 | AATATATATATATGC[-/GT]GTGTGTGTGTGTGTA | 115426 |
rs533295335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453123 | AGAATATATATAATC[C/T]ACTATATAATTCTCT | 115426 |
rs533330737 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507335 | CCTGTCACCTGGGTT[C/T]GCGCCATTCTCCCAC | 115426 |
rs533371201 | snp | C/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507440 | AAAGACGGGGTTTCA[C/T]CGTGTTAGCCAGGTT | 115426 |
rs533382914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446982 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 115426 |
rs533414607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473775 | ATAGATAATACAAAA[A/G]TCAGATGGCATAACT | 115426 |
rs533419654 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420707 | GTGAGACACCGTCTC[A/C]AAAAAAAAAAAAAAG | 115426 |
rs533487123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495112 | AAGTTGTCAAATCTG[A/G]AAATTATTTTTCCCT | 115426 |
rs533500842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451706 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTTTCT | 115426 |
rs533503257 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492776 | CTGAATCAGATAGAG[-/AC]AATAATATCCATATA | 115426 |
rs533523028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431169 | TCTTGGCCTATTCAA[A/G]TTTTGCTTGACTTAG | 115426 |
rs533525054 | snp | A/G | 1.65214e-05 | 0.0028741 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460755 | TGAAGACAATCTCAA[A/G]GACCAAAAAAGAACT | 115426 |
rs533547257 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480860 | ACAAAGTATCTCATA[A/T]TTGGATTGACTTGTG | 115426 |
rs533561283 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504854 | GGTAAATGCATGTTT[C/T]AATTAGATAGTGATA | 115426 |
rs533576563 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506671 | TCTTCTTCCATTACA[A/G]TGTGTGTTTTGCAAG | 115426 |
rs533584914 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466983 | TTTTTCTGAATTCTT[A/T]ATTTTATTTATTATC | 115426 |
rs533585812 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484047 | TTAGTTGTCTCCTAT[A/G]CATTTACCTTCTTAT | 115426 |
rs533593312 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456559 | CCATTTGTCAATTTT[C/G]GCTTCTGTTGCCGTT | 115426 |
rs533621550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472193 | GCCTTCTATCAGATT[A/G]GATTTTAGTCTCCAG | 115426 |
rs533629088 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435121 | GCCTCAGCCTCCCGA[C/G]TAGCTAGCATTAGAG | 115426 |
rs533654028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442799 | CCTGGCATGGCACGA[A/G]CTTCATGATGATATG | 115426 |
rs533688861 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484474 | CCTCCTGGATGCAGT[A/G]CCATAATCACAGTCC | 115426 |
rs533710734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488113 | CTGGGTGTGGTGGCA[C/T]GTGCCTGTAGTCCCG | 115426 |
rs533718027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442422 | ATAAATTTTCAATCA[G/T]TTCAAAAGTTCTCTA | 115426 |
rs533727003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447747 | ACACAAGAGAAAGCA[A/G]CAAAATTTTGGAAGG | 115426 |
rs533742437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424081 | TTCATGCTTCCTTAT[C/T]TGACATCTTTCTGGA | 115426 |
rs533744830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451444 | GATTCCTTCTATCTT[G/T]TTTCTTACCTAGTTT | 115426 |
rs533870358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429412 | TCTGAGGTTTTGTGG[G/T]TTTTTTGTTTCTGTT | 115426 |
rs533882563 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420378 | TTGTTTTAATGGCTA[A/G]CAGTGTTCTCTGTAG | 115426 |
rs533889028 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482415 | TTAAACTTGAATCAT[A/G]TGGCAAATTCTCATT | 115426 |
rs533894589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471755 | CAGTTTGCAGTAAGA[G/T]CTGAAGGGGCTAGAG | 115426 |
rs533905967 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492118 | GATAATATAATGTTT[C/T]TGTTGATGTAATGAT | 115426 |
rs533980838 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446033 | GTCTCACTCCCGTCA[C/G]CCAGGCAGGAATGCA | 115426 |
rs534000357 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479803 | TTCTTTTGTTCTTTC[A/C]CATACTCTACCTCAA | 115426 |
rs534007635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454275 | ATAGAACATCTTTTG[A/T]GTGAAGACACCAGGA | 115426 |
rs534019900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413948 | CTGGGTGCCCAGGTC[C/T]CTCGCTTCCCGCGCT | 115426 |
rs534044316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428711 | TGTGCCACCATACCC[A/G]GCTAATTTTCAATTT | 115426 |
rs534062272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498219 | ACACCTCTTCTATCT[A/G]CATGCCTTAACACTG | 115426 |
rs534070018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491372 | ATGAATTAATTATAC[A/G]TAAAATGCTTCTCCT | 115426 |
rs534071359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419522 | CTTTAGAAAGATAAC[A/G]TATTTGACTTAATGT | 115426 |
rs534079585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493821 | AAGAAAATCTTCTCT[G/T]ACAGGACCGAGGTGA | 115426 |
rs534087606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487746 | ACCTCAGATGATCTG[C/T]GCACCTTGGCTTCCC | 115426 |
rs534090042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424635 | GATCTTAAGTTAGTG[C/T]GGTGTATTTGTTGAA | 115426 |
rs534098925 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476254 | TTATTGTATATGTAT[A/G]TACCATATTGTCTTT | 115426 |
rs534133039 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453431 | GAGAAAGGAATATTA[C/T]CTGAAATAGAACAGG | 115426 |
rs534147189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439199 | TTGTTTTTTGTTTGT[G/T]TCTTTGAGACAGCCC | 115426 |
rs534194466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449850 | ATATTTCCCATGTGT[C/T]GTCACAGTTGGTTGT | 115426 |
rs534205089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454772 | TCCCTTAGTTTCTAC[C/G]TTTTTAATGCTGCCT | 115426 |
rs534247932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487224 | AGATGGAGTCTCGCT[A/G]TATCACCTGGGCTGG | 115426 |
rs534255687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459753 | CCAAGGCAGGGGGTT[G/T]CTTGAGGCCAGGAGT | 115426 |
rs534256167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450410 | ATTTGACACATTCTT[C/T]TGTTATGTGTTAGTT | 115426 |
rs534284161 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417254 | CTTCTTTCAACTCAG[G/T]AAAATTTCAAGAGTG | 115426 |
rs534329704 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473904 | CCATACTTTGGGAAT[C/G]CAAATATCAAAAATC | 115426 |
rs534397665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480423 | GTTCTGAACAAACCT[C/G]TTGAAGGAGTGAATC | 115426 |
rs534434649 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411419 | GTCTCACTCTATCGC[C/T]CAGGCTGTAGTGCAG | 115426 |
rs534434760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485615 | GCCTTTCCACCCCCG[C/T]CCCCCGCCCCAAATT | 115426 |
rs534482475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503734 | TGTTCATACTTTGGA[A/G]TACTGTGCAAAACAG | 115426 |
rs534483743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497657 | TATAACTTGATTTTT[A/G]TATATCTTTTTGAAT | 115426 |
rs534516365 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481581 | CTAGGAAGGCTAATA[G/T]TCTGTTACTAGCTTT | 115426 |
rs534524612 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413141 | TAAGGCGGAGCCCGG[A/C]GTGGATCTCGCGAGA | 115426 |
rs534554628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444159 | CTTGAATTAAGTGTC[A/G]TGTCAGTCTTGAGTA | 115426 |
rs534583397 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428836 | TTACAGTGTGAGCCA[G/T]CACACCCAGCCCTGC | 115426 |
rs534602501 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446183 | TTTTTATACAGTCTT[C/G]CTCTGTCACCAGGCT | 115426 |
rs534620127 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469974 | TGGTATATCACAAAC[A/T]AGAATGCTAAAAACT | 115426 |
rs534621000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443425 | AGAGAGCTAGTAAGT[A/G]GCAGGCAGATTCCAA | 115426 |
rs534668317 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411933 | GGCCGGGCGCGGTGG[C/G]TCACGCCTGTAATCC | 115426 |
rs534692901 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457748 | GAAGGCCTTTTCTGC[A/G]TCTGTTAAGATAATC | 115426 |
rs534732844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416944 | TGTGGGGCATGAACT[A/G]TAGTTGAAGAAAAAA | 115426 |
rs534740910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462794 | TAGTGGCACGTGCCT[A/G]TAGTCCCAGCTACAT | 115426 |
rs534788380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428427 | TAACTTTCTTATTAA[C/T]ATTAACCTTTAACAA | 115426 |
rs534791690 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431448 | TCTGTCTCTACAAGA[A/C/T]GTAACATTAGCTAGG | 115426 |
rs534792922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459308 | GTTCTTATAAGTACT[A/G]CAAAATGGCAGAACT | 115426 |
rs534800724 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466143 | TGGTGGCTTGTGCCT[A/G]TAATCCTAGCACTTT | 115426 |
rs534803483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465315 | CTCAGTGTCCTTCAC[A/G]GATTTATGCTAGTTT | 115426 |
rs534811170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473907 | TACTTTGGGAATGCA[A/G]ATATCAAAAATCAAC | 115426 |
rs534845126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464598 | GTACAGTGTGAGTGA[A/G]GTAAGGGTCTAATTT | 115426 |
rs534886911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470394 | CCCAACTTAAAATAT[A/C]TTTTTCATGAAGATA | 115426 |
rs534890210 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433511 | TGGACTGTGTAAGTT[A/G]TCTTTAGGATTATGA | 115426 |
rs534900858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448108 | CAAAGCCTACAATCT[A/G]GACAAAGCAAGGTGT | 115426 |
rs534914857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452803 | GTGCTTCTGGGACAT[C/T]TCAGTTTGGGGTGTA | 115426 |
rs534937262 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416533 | TTGGTGGATCTCTAA[A/G]TCTTTTTTTTTTTTT | 115426 |
rs534960814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438533 | TCTCCTAGAGTGATA[A/T]GCATTATTTGGCAAA | 115426 |
rs534988896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431818 | CTTCATTTGTGCCGC[C/G]TCGTGTTCCTTAGTA | 115426 |
rs534990045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502168 | GTGTATATATATTTA[G/T]GTCCAAACTCCTTCC | 115426 |
rs535022509 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460104 | AAGAATAGTTTTGCT[C/T]TGGGAAGTCAAATCA | 115426 |
rs535037705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435471 | GATAGTTCACATACA[G/T]TTTACCTGTTTAAAG | 115426 |
rs535059104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488827 | GTTTTGTTTTGTTTT[G/T]TTTGAGATAGAGTCT | 115426 |
rs535083434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474529 | CAGCCAACATGGTGA[A/T]ACCCTGTCTCTACTA | 115426 |
rs535100192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437256 | TATTATTTTTTAGAC[A/G]GAGTCTCGTTCTGTT | 115426 |
rs535103344 | snp | G/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451856 | TGGCACGATCTGGGC[G/T]CACTGCAGTCTCTGC | 115426 |
rs535111781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420496 | TCACGAGGTCAGGAG[A/G]TCAAGACCATCCTGG | 115426 |
rs535163217 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507009 | AATTTTATATTCACT[A/G]TATTCCCTAAAGTAT | 115426 |
rs535170997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425707 | AGCAGAGGTTACGGG[A/G]AGCCGAGATCGCGCC | 115426 |
rs535179457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490308 | CATAGCACGGACTCA[A/G]ATGTTAGTTATATTC | 115426 |
rs535197342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494543 | ATGACATCTCAGCTC[C/T]CGTGGGTACAGAAAA | 115426 |
rs535211297 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412094 | GGGAGGCGGAGCTTG[C/T]AGTGAGCCGAGATCG | 115426 |
rs535216387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453418 | TCACTTTACAGCTGA[A/G]AAAGGAATATTATCT | 115426 |
rs535230085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442623 | AGCTGGGACCACAGG[C/T]GCACACCACTGTGAC | 115426 |
rs535264783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421866 | CAGTATGTTTTGTCT[G/T]TATTTGAATTTTATA | 115426 |
rs535291408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447412 | AAAAATTGCTGTTTT[A/G]TAGTATGATGGAAAT | 115426 |
rs535326926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496703 | TTTTAAACTTTAAGG[A/G]TTCTCTATTGTCTGG | 115426 |
rs535340135 | in-del | -/T | 0.277334 | 0.248501 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423635 | TTGAGTCATTAGTGA[-/T]TTTTTTTTTTTTTTT | 115426 |
rs535392570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414989 | ATTTGCTTTGCTGTG[C/T]CTCAAGTGGCTGATA | 115426 |
rs535498548 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483075 | TCACACCTGTAATCT[C/G]AGCACTTTGGAAGGC | 115426 |
rs535534294 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502334 | TACATACATACTGTT[A/G]CTCTGACTGGAATTC | 115426 |
rs535534875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482748 | ACTACAGGCGCCTGC[C/T]ACCACGCCTGGCTAA | 115426 |
rs535569114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487649 | TGGGATTACAGGCGT[C/G]AGCCACCACACCTGG | 115426 |
rs535574006 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465578 | AATCTGTTGTCATAA[A/G]TTTTTTTGGTACCTA | 115426 |
rs535585188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419316 | AACCCATAACCCTTA[A/C]CAAAATATGGGTGGG | 115426 |
rs535615864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505874 | AAACTAAAGCCATGA[C/T]TGTAGTCTTTTCCAT | 115426 |
rs535626214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500137 | CACACCTGGCTAATT[A/T]TTGTATCTTTTGTAA | 115426 |
rs535637027 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469440 | GGAGAATCACCTGAA[C/T]CTGGGAGACAGAGGT | 115426 |
rs535780284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478046 | GACTCTGTGTTCATT[A/C]AAAAATGCAAATCTG | 115426 |
rs535823427 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417172 | CCTCTCAGCCACTTC[C/T]ACTTGGCATTTGCTT | 115426 |
rs535826536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434447 | TTTCTCTATTAGGTG[C/G]GCTTTTTTTGAGATG | 115426 |
rs535835094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466306 | ACTTTGGGAGGCTGA[C/G]GCGGACGGATCACCT | 115426 |
rs535843849 | snp | A/C/G | 0.000100756 | 0.00709712 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481622 | TGTGAAAATGCCTTC[A/C/G]TTCTTTTTTTTCTTT | 115426 |
rs535874137 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445979 | CTTCCCCCCCCGCCA[C/G]CCTTTTTTTTTTTTT | 115426 |
rs535895994 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471696 | AACTACCCAGCTAAG[C/G]TACTCCCAGATTCCT | 115426 |
rs535931915 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476842 | TCGTGATCCGCCCAA[C/G]CCAGCCTCCTAAAGT | 115426 |
rs535951246 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413545 | TGCACCATTGAGGAC[A/G]TGTCTCGCAAAGCCA | 115426 |
rs535992998 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425754 | GGGTGAGTGAGACTT[C/T]GTCTCAAAGTAAATA | 115426 |
rs536013334 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493253 | CAGCGAGCCGAGATC[A/G]TGCCACCGCACTCCA | 115426 |
rs536041548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461611 | TCCTGCCCTCAAGTG[A/G]TGTACCCGCCTCTGC | 115426 |
rs536052802 | snp | C/G/T | 5.07756e-05 | 0.00503837 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460563 | GCCATATGGTTTTCT[C/G/T]TCTCCTCAGATACCC | 115426 |
rs536084386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467724 | TTTACTAGTCACTTG[G/T]GAGTGCCATTTAACT | 115426 |
rs536150633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472370 | AAAATAAGGAACAGT[A/G]TAACATGCTTACAAG | 115426 |
rs536156025 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447044 | CAGGTGCCTGCTACC[A/G]CACCCGGCTAATTTT | 115426 |
rs536190392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435306 | GCCGGCTAATTTTTT[C/T]GTAGAGATGTGGTCT | 115426 |
rs536199596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441221 | CAGTCTCTACAAAAA[A/G]AACTCAGCCACCTAT | 115426 |
rs536209642 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428899 | CCGAGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 115426 |
rs536212804 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469345 | CAACATAGTGAAACC[C/G]CGTCTCTACTGAAAA | 115426 |
rs536217691 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504302 | AGTGCTGGGATTACA[G/T]GCGTGAGCCACCGCG | 115426 |
rs536223111 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444325 | GCTCCTGAGTGGATG[A/G]TAATCAAAAGGAGGA | 115426 |
rs536254121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503937 | AAACTAATGTGTATG[A/G]AATGGGATTTCTTTA | 115426 |
rs536261351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433765 | AAATCAGAAAGAATA[C/G]TTTTGATCTAATCTT | 115426 |
rs536323073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458783 | GTATGTTTATTGCAG[C/T]ACTGTTCACAACAGC | 115426 |
rs536329051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421986 | TTAACATACCGCGGT[A/T]TATTTAATCCATAAT | 115426 |
rs536371821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496864 | GCTTTAGTTTTCCAA[C/T]GTTCTCCCTTCCCCC | 115426 |
rs536391142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427906 | ATTGAATCACACTGG[G/T]TCTAGATTGGGAACT | 115426 |
rs536394059 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422459 | TTTAATATTTGCATA[C/G]AAAAAACTGTAGAAA | 115426 |
rs536417071 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418797 | TTCCTAGGGCTGTTG[A/T]ACTAATGTACCAAAA | 115426 |
rs536418778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424447 | TCTGATTTCATCCAC[C/G]TTTTAAATACCAATA | 115426 |
rs536449931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450585 | AGCCTGATACACTCA[A/C]AATTTGTTACCAGCT | 115426 |
rs536457223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455380 | ACCTATGAGTGAGAG[C/T]ATGCGGTGTTTGGTT | 115426 |
rs536471206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449817 | TATCTTGAATGCTCT[A/C]ATCTGCCCTAGCAGA | 115426 |
rs536525982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480904 | TTGCTCTAAAAGCTA[C/T]GTAGAATAGATAATT | 115426 |
rs536531181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424027 | AAACACATTCTATAC[C/T]GGTATTCCCTTTAAA | 115426 |
rs536536324 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492549 | CAATAACACTTTAAG[A/G]CCATGAGATGTTTAT | 115426 |
rs536575793 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498894 | CATGTGTAGGGGCTG[A/T]ACTATGGGCAAGTGT | 115426 |
rs536580371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454657 | TGAGCTTACATAGTC[C/T]TTGTTTGATTTGGAA | 115426 |
rs536614572 | snp | A/G | 0.00017773 | 0.00942516 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422660 | TGTCACCCAGGCTGT[A/G]GTGCAGTGACGTGAA | 115426 |
rs536661219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459284 | ACTATCGGAATATGC[C/T]AGGTTCATGTTCTTA | 115426 |
rs536685719 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411222 | TCATCTCATTTACAT[A/T]TGTAATAAATACTCA | 115426 |
rs536690217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485456 | TAGAAAGTGGGGAAG[A/G]TTTAGGAAAAACAGA | 115426 |
rs536696388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464489 | ATGCTTGTACTTTCT[A/G]TGTCTTTCTTAAAGA | 115426 |
rs536729745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485021 | TGGTCTCAAACTCCC[A/G]ACCTCAGGTGATCCA | 115426 |
rs536738661 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420427 | TAAGAATTTATGGCC[A/G]GGTGCGGTGCTCACG | 115426 |
rs536741378 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497578 | AGAGTTGGGTTAAGG[G/T]TTTTTTTTTTAAAAT | 115426 |
rs536743676 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495876 | GAAACTTACCCTAGC[C/T]CTTTAAGATAAAATA | 115426 |
rs536756223 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415796 | CCAGAACTGCAAGTA[C/G]TTGAATTTAACAAGA | 115426 |
rs536767536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489774 | ATATGTGGTCTTCAG[A/G]TATTTACTTGCTTTC | 115426 |
rs536779386 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503186 | TTTTTTTCTAGAGAC[C/G]GTTTTGGCCATGTTG | 115426 |
rs536803561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432565 | TCTCAGAGCCTTTGT[C/T]TCCGTATTTTGTAAA | 115426 |
rs536840674 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419112 | CTCTCTAAAGACCCT[A/G]TCTCAAAATGAAGTC | 115426 |
rs536880108 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413039 | AGTAACGGCTTTTGG[C/T]AGCCCCGCCCCTCCG | 115426 |
rs536921874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486692 | GATTTAAAATGAGAG[A/G]GCAAAAGATAGAACT | 115426 |
rs536942365 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412637 | GGTTTCCGCGCGAAA[A/G]TAGCATTGCGGCCAG | 115426 |
rs536958922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486207 | GTGATAGATAGGATG[A/G]GTTTGAAGGAGCAAA | 115426 |
rs536975649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437368 | CTCATGAGTACCTGG[G/T]ATGACAGGTGCCTGC | 115426 |
rs536982832 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494267 | CAAAGCTAAAAGTGA[C/G/T]AAACTCCTTTTTAGA | 115426 |
rs537045301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448085 | CTGTGGACCAGGCGT[A/G]AAGCCTACAAAGCCT | 115426 |
rs537055162 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466722 | TATGCATATCAAGTT[A/G]TAAGTCACTGGTCAC | 115426 |
rs537068823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436228 | AGGATATCTGGAAAT[G/T]AATCAAAAGTAGATC | 115426 |
rs537073432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468323 | ATTGAATCACTTAAA[A/G]TAGTACATGGAAAGC | 115426 |
rs537106150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452710 | CTTCTAAGAGCATGA[A/G]GGGTTTTTCTCAGAG | 115426 |
rs537110681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473444 | AATTGTGCCAAGTAA[A/G]TGAGATGAGAAAGGA | 115426 |
rs537148320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416319 | GTGATGCGCCCACCT[C/T]GGCTTCCCAAAGTGC | 115426 |
rs537154508 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430701 | CCTACAATCCAAAGC[C/G]CACTGACATTATTCA | 115426 |
rs537160382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421528 | TTCAAGCAAATCTCC[C/T]GCCTTAGTCTCCTGA | 115426 |
rs537178641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441807 | CTAAAATTATATTTC[A/C]TTCAAGCTAAATGAT | 115426 |
rs537189838 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468866 | CTGTAAACCAGCCTT[A/G]ACTCAGCATAGATGC | 115426 |
rs537230254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470331 | TGAGCTGAGATCGTG[C/G]CTAGGTGACAGAGCA | 115426 |
rs537232164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463706 | GAACCCCTGAGCTCA[C/G]GCTATCTGCCTGCCT | 115426 |
rs537255045 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465277 | TGTATTAATGCGTGA[A/G]ATTTACATGTTAATT | 115426 |
rs537260031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457601 | GTTTTCCAAGGGAAT[G/T]CTTCCAGTTTTTGCC | 115426 |
rs537268298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437901 | ACAGGTGTGAGCCAC[C/T]GCACCCGGCTAGTTT | 115426 |
rs537274634 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422167 | TGGTTCCATTGGTCT[G/T]TTTGTCTATCTGTGT | 115426 |
rs537319125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462693 | GGAGACCAAGGTGGG[C/T]GGATCATGAGGTCAG | 115426 |
rs537353130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480380 | AACATTTATCCCCAG[C/T]ACGAAAATAGTGCCT | 115426 |
rs537372066 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501415 | TTTTCTGTTTTCTTT[C/G]TCTCCAAAGTGTTGA | 115426 |
rs537377988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443390 | TAACTGAGGTTTAAA[G/T]AAGTAACTTGCTCAG | 115426 |
rs537382427 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431598 | AAAAAAAAATTCTTA[-/C]GTCCAGTTGTAAATC | 115426 |
rs537419966 | in-del | -/CATA | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412184 | ATACATACATACATA[-/CATA]ATAAATAAAATAAAA | 115426 |
rs537433967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452709 | ACTTCTAAGAGCATG[A/C]AGGGTTTTTCTCAGA | 115426 |
rs537452113 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506140 | GATTCTGCAGACTCT[A/G]CTTGACCTTTTCTTC | 115426 |
rs537471734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442534 | CCCTGATTGAAATGC[A/G]GTGGCACAAACATGG | 115426 |
rs537475793 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440385 | CAAGGATTAATTATA[C/T]AATTAGCCAAGGGTC | 115426 |
rs537483303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461473 | TGCCTCTTGGGTTCA[C/T]GCAGTTCTCCTGCCT | 115426 |
rs537534846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500085 | TCAAGCGATCCACCT[A/G]CCTCAACCTCTGAAG | 115426 |
rs537572916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505282 | AAATATATATATATG[C/T]GTGTGTGTGTGTGTA | 115426 |
rs537582086 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498663 | CTTTTTTCCCCTTTG[C/T]CCATGCTCAGCTGTT | 115426 |
rs537586484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435634 | TATTTAGAGACAGAG[A/T]CTTGCTCTGTCACCC | 115426 |
rs537626785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458038 | AAATGAGTTAGGGAG[C/G]AGTCCCTCTTTTCCT | 115426 |
rs537638129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447049 | GCCTGCTACCACACC[C/T]GGCTAATTTTTTTGT | 115426 |
rs537650276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451760 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTGTTT | 115426 |
rs537685148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483778 | CACCACAACCTCTAC[C/G]TCCCGGGTTCAAGCA | 115426 |
rs537719559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426423 | GGAGCACATTGGAAT[A/C]TAGTAATAAAATTCT | 115426 |
rs537741414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502068 | ACAAGTTTCATGCCC[A/G]TTCTCTTCAGATAAG | 115426 |
rs537783051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431317 | TTTAGTAGGATAATC[C/G]TTTTTTTTGGCCAGG | 115426 |
rs537797341 | snp | C/T | 0.000103295 | 0.00718588 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494007 | GTAAATTGTAACTTA[C/T]GTTGCAGAGGAGAAT | 115426 |
rs537832867 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469516 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAATTAAA | 115426 |
rs537875502 | in-del | -/T | 0.435247 | 0.167879 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446160 | CCTCACCTGGATAAT[-/T]TTTTTTTTTTTTATA | 115426 |
rs537885179 | snp | A/G | 1.71053e-05 | 0.00292444 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413489 | CCTCTCTAGGCGCCA[A/G]GATGTGGATACAGGT | 115426 |
rs537894396 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480936 | TGAAATAGAAAGTAT[-/G]GGCAAAGAAATTTAA | 115426 |
rs537914627 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467604 | AGAATAGTTTTTTTT[G/T]TTTTTTTTTTTTTGG | 115426 |
rs537923588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424685 | TTAGCTTTTACCTCA[C/T]GTCCTCTTTTTGTTC | 115426 |
rs537949004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418756 | TGCCAACTGAACTTT[A/G]TAAAGAAACAAAATG | 115426 |
rs537951640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472744 | TGCAAAAAATTTAAA[G/T]TGTTTTCAGTAATTG | 115426 |
rs537974830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499733 | TTCAGTTTGGGGAAC[A/G]TGTAGTCTTCCCCTC | 115426 |
rs538000840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435176 | TTTTTGTATTTTTAC[G/T]AGATATGGGGTTTCA | 115426 |
rs538015393 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421459 | GCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGCG | 115426 |
rs538021956 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501074 | TAAGCAGTTCAGCAC[A/G]ATTTTCAAAACCTAC | 115426 |
rs538051888 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449326 | CCCAATGTTAATTTC[A/T]CACCTGAGCTTACCA | 115426 |
rs538068736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440491 | TACATATAATTGATA[A/G]TAGCCAACTTTTCTA | 115426 |
rs538116857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488753 | GTGATCTGCCCACCT[C/T]GGCTTCCCAAAGTGC | 115426 |
rs538120287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483274 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 115426 |
rs538153590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494499 | CAAAAGAGCCACCGT[G/T]TGCTGATCTTTATTC | 115426 |
rs538156074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488173 | GCTTGAGCTCAGGAG[A/G]TCGAGGCTGTAGTGA | 115426 |
rs538159789 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487350 | CCTGCCATCACACCT[A/G]GCTAATTTTTGTATT | 115426 |
rs538162243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413821 | CGCCGAATGGTGGGG[A/G]GTGGGTCCCTGCCAG | 115426 |
rs538166257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477450 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGCTG | 115426 |
rs538178864 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482692 | AGCTCTGCCTCGTGG[G/T]TTCACGCCATTCTCC | 115426 |
rs538186690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445891 | AATATTGAAAATAAC[A/C]TGGTGATAATGGTAT | 115426 |
rs538187536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451203 | TTGTCTTTAGGAAAT[A/G]TATCATTTGGGCTGT | 115426 |
rs538222218 | in-del | -/TT | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442665 | TGATTTTTTTTTTTT[-/TT]GGGGGGGTAGAGATG | 115426 |
rs538223393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503336 | ATAAATATGAAATAT[A/G]CTCCCTTACTACCTA | 115426 |
rs538225263 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445458 | TAGAGATGGGATCTC[A/C]CCATGTTGGCCAGGC | 115426 |
rs538272248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444648 | CTCTTGTTGCTTAGG[C/G]TGGAGTACAATGGCA | 115426 |
rs538278607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482281 | TACATCACAGAATTG[A/G]GCATTAGCTATGCAT | 115426 |
rs538296151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470541 | AGATTCCCGATGGAA[C/T]ATCGAAATATGGGAC | 115426 |
rs538314790 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426945 | GTAGAGACAAGATTT[C/T]ACCATGTTGGCTAGG | 115426 |
rs538315589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487268 | GATCTCAGCTCCCTG[C/T]AACCTCTGCCTTTGG | 115426 |
rs538330907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475835 | GATCAAATCTGGGAA[A/G]CTGGGATATTCATCA | 115426 |
rs538366383 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497902 | ACTGTCCTTACAGCA[A/C]AGCAGAATATTCAGA | 115426 |
rs538373415 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456165 | TTTTAGAATGTTTCT[A/G]GAGAGCTGGCTACAT | 115426 |
rs538400325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491933 | AGACAAGGTCTCGCT[A/T]TGTCACCCAGGCTGG | 115426 |
rs538419676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429202 | TGGTACAATGAGAGA[A/G]CAATTTTCAGAGTTG | 115426 |
rs538432203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460196 | TATAACAGTAATACG[A/T]GACTGAATAGATACA | 115426 |
rs538514833 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470667 | GACAACAATAATGCA[A/G]AAGATGGGGTTGGTA | 115426 |
rs538550404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504276 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 115426 |
rs538555844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471096 | ATGACAACAGCAAAG[A/G]CTTTTCAAATCCCCT | 115426 |
rs538626397 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458631 | TGTTGGTGGGAGTGT[A/T]AATTAGTTCAACCAT | 115426 |
rs538641983 | snp | A/C | 1.66211e-05 | 0.00288275 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421174 | AGACTTACTGTTGTG[A/C]GAATACAAATAAATT | 115426 |
rs538751347 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412510 | TTCTCCAAGGCCGGA[A/G]GGCCGGCTGGGAGCG | 115426 |
rs538756775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444187 | GTACAGGAGGGAACT[A/G]GAATGAGTTGTTTAA | 115426 |
rs538767985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469589 | TTAGGAAACCAGAAG[A/T]TAAGTCAATAAAAAC | 115426 |
rs538790236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423502 | TACTTTAAGCAAATA[C/T]GGTTTGTCAGGATGT | 115426 |
rs538815829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480444 | GGAGTGAATCAATCC[C/T]AGAGATGACTTTAGG | 115426 |
rs538850657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454019 | TAAAAAAATACTAAT[A/T]GACATTTACTTTACC | 115426 |
rs538858795 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497718 | CACATCATAGTAATA[C/G]ATTTTCATTCTTTGT | 115426 |
rs538867212 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469495 | TGCACTTCAGCCTGG[C/T]GACAGAGCGAGACTC | 115426 |
rs538897938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465367 | CTTTTTCTTTCTTAC[G/T]GTAGAGTTTTGTGTC | 115426 |
rs538900085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428783 | TGAACTCCTGGGTTC[A/G]AACAGTCCTCCTGCC | 115426 |
rs538912881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453519 | AATTAGAAAAGCATT[A/G]AAAGATCTAGTTTAA | 115426 |
rs538954642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503800 | TGAGACACGTTGCCC[A/G]TGATTTTTTTATTTT | 115426 |
rs538963304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422500 | AGCTCTACAAATCTG[A/G]TGGGATTCTATGGAG | 115426 |
rs538990956 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470719 | CATCATTGGGGAAGT[A/G]GTGAAAGTAAAATTT | 115426 |
rs538997597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427813 | GAAACTAGATACCAC[C/T]ACTACATATGGAGAG | 115426 |
rs539004809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496782 | TTATATTTCTGGATT[G/T]CTTTCTACATTATTC | 115426 |
rs539030390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502576 | TATAGGCATGAGTCA[C/G]TTTGCTCTGTTTCAT | 115426 |
rs539055243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447488 | GTTCCTGAAGGAGAA[C/T]AGCAGTATACAAGGA | 115426 |
rs539055817 | in-del | -/CT | 0.021333 | 0.101051 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429156 | GGCAACAGAGCAAGA[-/CT]CTGTCTCAGGAAAAA | 115426 |
rs539057041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463584 | CAAGCAGTTCTCCTG[C/T]CGCAGCCACCGGAGT | 115426 |
rs539074161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415694 | TACCCGCCCCCCATA[C/T]TCCATTCGTATGTTA | 115426 |
rs539093723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469908 | GATACAAGTTCAGGT[C/T]AAAGAAGTTCTGTAA | 115426 |
rs539127470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496401 | TTTTGGTACAACTAG[C/G]TTCTCCCAAGAGTAA | 115426 |
rs539136194 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420972 | GATATAATTCAGCTG[C/G]TAGTTCGCCCAGACC | 115426 |
rs539143642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475039 | AAACATACCTTATTT[C/G]TTGATAGAAAGGTTT | 115426 |
rs539148376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420573 | AGCCGGGCATGATGA[C/T]GGGCACCTGTAGTCC | 115426 |
rs539199783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437302 | CAGTGGCACGATCTC[A/G]GCTCGCTGCAACCTC | 115426 |
rs539219928 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482819 | GCCAGGATGGTCTCG[A/T]TCTCCTAACCTCGTG | 115426 |
rs539261113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486227 | GAAGGAGCAAAACTA[C/G]AGGCAGTAAAAAAAG | 115426 |
rs539262762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417403 | ATGCTTCTGACTCAC[A/G]GATGTTTGTGATTTC | 115426 |
rs539262953 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412035 | CGGGCGCCTGTAGTC[A/C]CAGCTACCCCAGGGA | 115426 |
rs539265186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436917 | ACGATAGCTGAACTT[C/T]CTTTGAAAAATGAAA | 115426 |
rs539311846 | in-del | -/TGTC | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502884 | GTGTTTATAATACTT[-/TGTC]TGTAATATATTTGAC | 115426 |
rs539330844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421980 | ATTTTATTAACATAC[C/T]GCGGTATATTTAATC | 115426 |
rs539336688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491007 | CATGAAGCCAGTGAT[C/G]TTTGTTCTGTCTGGG | 115426 |
rs539373112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497510 | CAGATGCATAAAGCA[A/G]ACTCTTAACTTCAGC | 115426 |
rs539393196 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506811 | TGCTGCATTAGTGTA[A/G]TGTGGTGTGGTTTTG | 115426 |
rs539400537 | in-del | -/AGAG | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420721 | CAAAAAAAAAAAAAA[-/AGAG]AGAGAGAGAATGTAT | 115426 |
rs539433163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452698 | ATAACTCTTACACTT[A/C]TAAGAGCATGAAGGG | 115426 |
rs539443469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452277 | TATCTTTTCATCAGG[A/G]TTTTATTTATGTCCA | 115426 |
rs539491462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478971 | CTGCTTCTCTAAAAT[A/G]CGCTCTTTCACCTGC | 115426 |
rs539493906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472887 | AAAAAAGACACATAA[C/T]TTTTTTAAAAAGTAA | 115426 |
rs539527262 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444603 | TAGGGCCTAAGAATC[C/T]GCTTTTTTTTTGGTT | 115426 |
rs539530090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426383 | GGCAAGTAAATCTTA[C/G]ATTAAGGTTCCCTTT | 115426 |
rs539553884 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488876 | ACAGGGCAGTGATGC[A/G/T]ATTTCGGCTCACTGC | 115426 |
rs539568892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483212 | CGCCTATAATACCAG[C/G]TACTCAGGAGGCTGA | 115426 |
rs539582624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446535 | ATTCGTCTGCCTCAG[C/T]CCCGGTCTACATACT | 115426 |
rs539613475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494730 | TAAGGGTATTTTGTC[A/G]ATTGAGTAAAAGTGA | 115426 |
rs539634932 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442980 | CTTTTCCTTTATTGC[G/T]TTATTTAACTTAGTG | 115426 |
rs539665703 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431890 | TTAGTATCAACTATA[C/T]GCTGCATTCTCTGCT | 115426 |
rs539686564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462227 | TTTGTGCTCCACAGT[A/G]TTGTTGAATAATTGC | 115426 |
rs539693235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474574 | AGCCGGGTATGGTGG[C/T]GCAGGCCTGTAATCC | 115426 |
rs539731986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479805 | CTTTTGTTCTTTCAC[A/G]TACTCTACCTCAATA | 115426 |
rs539732291 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446159 | ACCTCACCTGGATAA[-/T]TTTTTTTTTTTTTAT | 115426 |
rs539751129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448008 | AAACAGGAAAGAAGA[C/T]ATGCTCTCCAGGAAA | 115426 |
rs539768216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479430 | CTCTTGTTGGGTTCC[C/T]GTCACCTACCAGATT | 115426 |
rs539793912 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426921 | GCCCAGCTAATTTTT[A/G]TACTTTCAGTAGAGA | 115426 |
rs539803262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505358 | TAGAGTGTAGTGGTG[C/T]GATCTGGGCTCACTG | 115426 |
rs539804359 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441774 | TTATAGACATAAATT[A/T]TTGGAACTAATTCTT | 115426 |
rs539817588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492876 | AGTAGATACTTTATA[C/T]TACTTTTAGATTTTT | 115426 |
rs539854445 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476609 | TGTTTTTTGTTTTTT[C/G]TTTTGAGACAGTTTT | 115426 |
rs539863012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441229 | ACAAAAAAAACTCAG[C/T]CACCTATGGTGGTGT | 115426 |
rs539894681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459993 | CCAAAACAAAACTTG[A/G]GTTAAAAAAATGTAG | 115426 |
rs539955473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414404 | TCTCGCCTTCTAATA[C/T]TCATGTCGTTCACGC | 115426 |
rs539959956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465576 | AAAATCTGTTGTCAT[A/T]AATTTTTTTGGTACC | 115426 |
rs539972471 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453675 | TGGGATTGGCCAAGG[C/T]GGGCAGATCACGGGG | 115426 |
rs539989290 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479254 | TCTAGCTTTCCTTCC[A/G]CTGTATCTGCTTATG | 115426 |
rs539995199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431298 | TAGTAGGGTACTTAC[C/T]ATATTTAGTAGGATA | 115426 |
rs540000862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477221 | CCTGGGTGACAGAGT[A/G]AGACTCCATCTCAAA | 115426 |
rs540009496 | in-del | -/TG | 0.0189856 | 0.0955633 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478036 | TCTGATAATAGACTC[-/TG]TGTTCATTCAAAAAT | 115426 |
rs540011020 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414620 | TAAAAAGTTGGCATC[C/G]TGAGTTGATAGACCA | 115426 |
rs540012124 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433493 | ACTTTACTGTTTTCT[C/G]GTTGGACTGTGTAAG | 115426 |
rs540058408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445629 | GTGGCACAACCACAG[C/T]TCACTGCAACCTTGA | 115426 |
rs540135614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482425 | ATCATGTGGCAAATT[C/G]TCATTGAATGTCGTG | 115426 |
rs540145571 | snp | A/G | 2.94781e-05 | 0.00383903 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413640 | CTTCTACCGGGGCAA[A/G]CAGGTGAGGCGCGCC | 115426 |
rs540175057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430346 | ATGTGAATGAATGCA[A/G]CTCTTAAGTGTAGAA | 115426 |
rs540197286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487029 | TGTGTCTTTTTAGCA[C/T]AGTTTTTGTTGAAGT | 115426 |
rs540206438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450189 | AACCAATCAATGTTC[A/G]TAGTTCCTTAATTAT | 115426 |
rs540223037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438267 | GAAGTAGCCAGTAAA[C/G]TAGCATTGGCCATTT | 115426 |
rs540229239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444397 | GTGTTGCAAGATCAC[A/T]TAGTACTTAGAAAAA | 115426 |
rs540258689 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500489 | GCCAGTTAACTCTTT[G/T]GTTTCATAGTTCTGC | 115426 |
rs540275739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449328 | CAATGTTAATTTCAC[A/G]CCTGAGCTTACCATT | 115426 |
rs540298500 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412684 | CGAAGCAGGAGGGCC[A/C]CCGGGGCCTTTCCCG | 115426 |
rs540317375 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423675 | TCTCGGCCGGGCGTG[C/G]TGGCTCACACCTGTA | 115426 |
rs540326833 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458128 | ATTCAGCTGTGAATC[C/T]GTCTAGTCCTAGGCT | 115426 |
rs540338984 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476645 | TGTTGCCCAGGCTGG[A/T]GTGCAGTGGCGCAAT | 115426 |
rs540357787 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449915 | AGGAGATGACTCTTA[C/G]AGAGCTTGTGTCTGG | 115426 |
rs540362550 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471644 | TGCACCCCTGACCAA[C/T]GGCTTAACTGCAATC | 115426 |
rs540370780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486264 | TTGTGAGCATTCATG[A/G]CTCAAACTACGATTG | 115426 |
rs540373808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498494 | AGGACATTTATCCTA[G/T]AGGGCACAGGGGGTG | 115426 |
rs540379668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423041 | AATTCTTATCAGTTG[C/T]GATAAATGGGCACCT | 115426 |
rs540487751 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445013 | ATTTGGGTTGAGGCC[A/G]GTCATGGTGGCTCAC | 115426 |
rs540516826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471400 | TCCTGCTTACTAATA[C/G]TCACCCTCATGTGGT | 115426 |
rs540520681 | snp | C/G | 0.0134861 | 0.0810011 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413371 | GTCGGTCCGGTGGGC[C/G]CGCTCGCCCGCCTGC | 115426 |
rs540558959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438712 | TAAAATGGAGCTGTT[G/T]AAAAGCTGTTTTTTA | 115426 |
rs540576872 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430286 | AACTGCTGGGATTAC[A/G]GGCGTGAGCCCCTGT | 115426 |
rs540589002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481048 | TCTCATTCTGTAGAC[A/G]TATACCTTGCTTTTT | 115426 |
rs540632852 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436710 | ATGGATAGGACCTAC[C/G]CTTCAGTTTGGTGTA | 115426 |
rs540689057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448887 | GAGCCTTTTGTGTTT[A/C]GCCAGTGTTTGGATT | 115426 |
rs540695574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431665 | GAGCTGATATGTTCT[A/G]TGTGTTGATGTTCAA | 115426 |
rs540711499 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412130 | CTGCACTCCAGCCTG[A/G]GCGACAGAGAGAGAT | 115426 |
rs540723468 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507301 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA | 115426 |
rs540748218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479950 | CGTTCTCCCATAGCA[A/G]CAGAATGAGCTTAAA | 115426 |
rs540751629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485937 | GAGGCAGGAATGAAG[A/G]TATGAGGGGAAAAGC | 115426 |
rs540782142 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428589 | ACGATCTCATTCTGT[C/T]ACTTGGCTGGAGTGC | 115426 |
rs540799558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422092 | ATATGTTCAAGAATT[A/T]CTACCTAGGAATAGA | 115426 |
rs540809832 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414134 | GGGCATTGAGCTCTC[A/T]AGAATAAGAACCCTA | 115426 |
rs540834382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496926 | ATTTCTAGTTGTTTT[C/T]TATTATACGTGGCAC | 115426 |
rs540846616 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416229 | CCACCACTCCCGGCA[A/G]ATTTTTTGTATTTTA | 115426 |
rs540868065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465077 | CTTCTTCTTGTCCTT[A/G]TTCACCAGTTGGGCC | 115426 |
rs540903828 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421701 | GAATTACCGGGGTGA[A/G]CCACCTCGCCCAGCC | 115426 |
rs540947191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475911 | ATCTATTCTTTTAGC[A/G]ATTTTGAAACATACA | 115426 |
rs540954038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428021 | AAGATCGTACTTTCA[A/G]GTGGCTGTCATCCTG | 115426 |
rs540973380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502724 | GCTACCTGTAACTCA[A/G]AATACCTGTATTAGA | 115426 |
rs540975277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427556 | GCTGGCTGTGGTGGC[A/G]TACGACTAATCCCAG | 115426 |
rs540982210 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432137 | AATGTATAACATGCT[C/G]CATCTCTGATTGTTT | 115426 |
rs541008124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457721 | TTTAGCATGAAGGGG[C/T]TGAATTTTGTAGAAG | 115426 |
rs541027498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461619 | TCAAGTGATGTACCC[A/G]CCTCTGCCTCCCAAA | 115426 |
rs541051370 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437451 | TTGGTCAGGCTGGTC[C/T]TGAACTCTGGACCTC | 115426 |
rs541065929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469719 | ACATATACACACATA[C/T]ATGTGCATATATACG | 115426 |
rs541083566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462329 | TCCTGAGATTTAAAA[A/G]AAAAAAAAAAATGAT | 115426 |
rs541104972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474644 | ACAGGAGGTGGAGAC[C/T]ACAGTGAGCCAAGAT | 115426 |
rs541146748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461887 | TATCAGTAATTACAT[A/T]AACATCCTTGTATAT | 115426 |
rs541185532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479579 | ACCAAGCTAATAGTT[C/T]TGAATTTATGTCTTC | 115426 |
rs541200905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453785 | TGGCAGGTACTTGTA[C/G]TCCCAGCTACTTGGG | 115426 |
rs541270205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458979 | GGAACAGAAAACCAA[A/G]CACCACATGTTCTCA | 115426 |
rs541301848 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463771 | CCACCGTGTCTGGAG[A/G]AAAAAAATTTTTTTT | 115426 |
rs541325093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484442 | TCCTGTCTCTTCCCT[C/T]CTCCCTCCTCCCCCC | 115426 |
rs541332357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436018 | AAAAAATTGTAGTAC[A/G]AAAGTTACTGTTGGG | 115426 |
rs541340600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463432 | AGAAACGTTAGGAAC[A/G]CAATAGCTAAAAAGG | 115426 |
rs541361696 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483941 | TGATCTGCCTGTCTC[A/C]GCCTCCCAAAGTGCT | 115426 |
rs541364817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415336 | CTACTTGGGTTTCTT[C/T]AGCCCAGTGATAAAC | 115426 |
rs541388581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495832 | AAGGTATCTGTGAGC[A/T]TTAAAGCATTCCATT | 115426 |
rs541415818 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480436 | CTGTTGAAGGAGTGA[A/G]TCAATCCCAGAGATG | 115426 |
rs541420140 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432402 | ACTTATTTCTAAGTT[C/T]CTCACTTACCTTTGA | 115426 |
rs541432951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446155 | ACGTCACCTCACCTG[C/G]ATAATTTTTTTTTTT | 115426 |
rs541530075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451120 | CTTTATCCTACTCAC[A/G]GTAGTTTCAGACTAA | 115426 |
rs541552846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414149 | AAGAATAAGAACCCT[A/G]ACTCTGCTTCCTGAC | 115426 |
rs541556071 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458969 | AACTAACACAGGAAC[A/G]GAAAACCAAACACCA | 115426 |
rs541559736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431081 | CATATTAATCATACA[C/G]GCCTAAGTATTTTTC | 115426 |
rs541566703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419743 | TTTGGGATTTATTTA[C/T]TTATTTGTTTATTTT | 115426 |
rs541585877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501030 | GAAAGTTTTTGTTAC[A/G]GTTCAAAGTTACCTA | 115426 |
rs541585911 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425509 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 115426 |
rs541642507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442753 | ACCTCGGCCTCCTAA[A/G]GTCCTGGAAGTACAG | 115426 |
rs541653702 | in-del | -/ATATA | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504426 | ATATGTTCATATAAC[-/ATATA]ATAAATCAGGGTAAT | 115426 |
rs541682792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435872 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 115426 |
rs541689029 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477468 | GAGGCAGAGGCTGCA[A/G]TGAGCCAAGATCACG | 115426 |
rs541717362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447215 | CTTTTAACCTAATTA[C/T]GTTGTTTCTACTATT | 115426 |
rs541740422 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473141 | GAATATCTTGTCATG[C/G]AAATAAGGAGTCCCA | 115426 |
rs541750053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421307 | ATTGATATGAAATAC[A/G]TAGACAAATGTACAA | 115426 |
rs541767986 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477695 | TTGCTCCTGTCGTGT[A/T]TGTGGTGGGAAACAT | 115426 |
rs541779098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478532 | CTATTTTTCTCCTAT[A/G]GCGTGGTGATAACTA | 115426 |
rs541816767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451516 | CGGAGTCTCGCTGTC[A/G]CCCAGGTTGGAGTGC | 115426 |
rs541839374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414550 | TTACAATCTATATCC[C/T]TAGCCACTCAGACCC | 115426 |
rs541878969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440230 | CATTAGTGTTTTTAA[C/T]AATATCTGTGGCATA | 115426 |
rs541889800 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489629 | GTGTGTGTTGATATC[-/TTA]TTGTTGGACGTGATT | 115426 |
rs541901579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471881 | AGTAGGACCAGGAGA[A/G]TAGAGACAAAGGAAA | 115426 |
rs541902483 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483400 | TGCACATCCTCCTTT[A/G]TATGTTAAATCACCT | 115426 |
rs541906609 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488328 | GAAGGGGATCCTGTG[C/G]CCTCTACCCAGTTTC | 115426 |
rs541936510 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477106 | GGTGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 115426 |
rs541965915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436453 | TAAATGCTGTGTCAA[A/G]ACAGGTAAATAAGTA | 115426 |
rs541982684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487901 | TTATTTTTTAAAATT[A/G]AACTTACTATTTTGA | 115426 |
rs542023700 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506261 | GAGGGTGGAAGAAAT[A/G]GTGGACTGTATCTCT | 115426 |
rs542029724 | snp | A/G | 3.30284e-05 | 0.00406363 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500677 | AACCAGAAGCTGTGG[A/G]ATGAAGTGCTTTCAC | 115426 |
rs542030370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493357 | TAGTACTTATTTATT[C/G]TCAATGCCAGAATTT | 115426 |
rs542049890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473597 | GACCTATGAAATTAT[C/G]TTACCAAGAAAATGA | 115426 |
rs542098590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429990 | AATATTAGATATTTG[G/T]ACAGGGGAAACTTTT | 115426 |
rs542123591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460214 | CTGAATAGATACATA[A/G]CATATAGTTTATTCT | 115426 |
rs542163147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429567 | AACTCCTGACCTCAG[C/G]TGCTCCACCTGCCTC | 115426 |
rs542165268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504887 | AATTCAAATATGTGT[C/T]ATTTGAGATATTCTA | 115426 |
rs542207942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453820 | TGAGGCAGGAGAATC[G/T]CTTGGACCCAGGAGG | 115426 |
rs542222912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498364 | GACCAAGGGTTGTGC[C/T]TGGGAAAAGTTGGAC | 115426 |
rs542243524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459876 | TACTCAGGCAGCTCA[C/G]GCTCGGGGATTTCTT | 115426 |
rs542274686 | snp | C/T | 0.000179324 | 0.0094673 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422681 | GTGACGTGAACACGG[C/T]TCGCTGTAGCCTTGA | 115426 |
rs542281441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464903 | TCATCTTTTCTCTTT[C/G]TGGTATATAGGAATA | 115426 |
rs542318181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463937 | ACCTGTATCCTGGCA[C/G]TTGTGTGCATTAGTT | 115426 |
rs542326686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476687 | GCAACCTCTGCCTCC[C/T]GGGTTCAGGTGATTC | 115426 |
rs542375876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419109 | TACCTCTCTAAAGAC[C/G]CTATCTCAAAATGAA | 115426 |
rs542378959 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445566 | ACGCCTAGCCTCTTT[A/C]TTTATTTTTGAGACA | 115426 |
rs542404802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433281 | CAGCCACTGGAATTG[A/T]CTACCTCCATTTTGT | 115426 |
rs542421017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493069 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGAG | 115426 |
rs542427605 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413292 | GTTCCGGTCGTCTCT[C/G]CTCAAGTCGGCTAGT | 115426 |
rs542453637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455538 | TAATCCAGTCTATCA[C/T]TGATGGACATTTGGG | 115426 |
rs542487263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460980 | TGGCTTAGATCTTCA[A/G]CTTTAAGGTTGGAGA | 115426 |
rs542503984 | snp | C/G/T | 0.000212414 | 0.0103039 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486943 | AAGTCATTATACAAC[C/G/T]TTACTCATTAGTACC | 115426 |
rs542529981 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435975 | GAGGGTTTAGATTCT[C/G]ACAGTAAACTATTGT | 115426 |
rs542539803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418305 | GCAATATTCCCATCC[C/G]TATCCTTATCAGGGC | 115426 |
rs542544219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466763 | CCATGCTGGCCTCCT[C/T]GTGTTGCTTGATCAC | 115426 |
rs542557699 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499277 | AAAGAAGGTAGCCAT[G/T]GAAACATAAGGATGA | 115426 |
rs542582027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492011 | GTGCTGGGATTACAG[G/T]CATGAATCATTGCGC | 115426 |
rs542609051 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448760 | TCTTGAGTAACAGGA[G/T]TTAAGAATGTGGTAG | 115426 |
rs542649157 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419790 | CTGTTGCCCAGACTT[C/G]AGTGCAATAGCATGA | 115426 |
rs542654345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459531 | AAAATTAACCAGGAG[C/T]GGTGGCACATGCCTG | 115426 |
rs542710874 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476926 | AACCTCACACTTGAT[G/T]ATTCTTTTTGGTTCC | 115426 |
rs542771248 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487694 | TTTAGTAGAGCTGGG[A/G]TTTCGCCATGTTGGC | 115426 |
rs542808142 | in-del | -/AAGAG | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462012 | TAAAAAAAAAAAAAT[-/AAGAG]AAACAGCTAAACGAA | 115426 |
rs542899724 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412804 | TTAGGCCGCACCCAC[C/G]CGCGCCCCCTTTCCA | 115426 |
rs542912976 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449439 | ATCATGGTCTAAGGG[C/G]TTTTACTGCCTAGTT | 115426 |
rs542913888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417734 | TATGTTACTGTGGAT[G/T]TAACTTATAGGGTCT | 115426 |
rs542986649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423607 | AAAATGTTTTCTGCA[C/T]TTAAATACAAATTTG | 115426 |
rs543014525 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439209 | TTTGTTTCTTTGAGA[C/T]AGCCCTGCTCTATGG | 115426 |
rs543051568 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414369 | TGAAAAGGAGTGTAA[C/G]ACTGTTTGCTTTTCT | 115426 |
rs543089622 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416770 | CTGACCTCGTGATCC[G/T]CCCGCCTCGGCCTCC | 115426 |
rs543128843 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444605 | GGCCTAAGAATCCGC[-/T]TTTTTTTTTGGTTTA | 115426 |
rs543133246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485330 | TTTGCATCTTTTTTC[A/G]TATACCTGTCTGTCA | 115426 |
rs543152868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421614 | TAGAAACAGGGTTTC[A/G]CCATGTAGGCCAGGC | 115426 |
rs543160719 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490234 | GTAAAAAGAAGAAAT[A/G]GTATTTTATGTGGAG | 115426 |
rs543171483 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490094 | AAATAAACCAACTAG[A/T]AATGTAGTCTCTTTA | 115426 |
rs543186501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442164 | GAGACAAGGTTTCAC[C/T]ATGTTGTCCAGGCTG | 115426 |
rs543208934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421436 | TTTGTTTTTGATAAC[A/G]GAGGCTTGCTCTGTC | 115426 |
rs543228957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502901 | TCTGTAATATATTTG[A/G]CTTTAATGATCCATG | 115426 |
rs543232074 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431982 | ACCTCAGTTTATTCT[C/G]CCAAGTATGATGGAC | 115426 |
rs543232119 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426848 | CTGCCTCCTGGGTTC[A/C]AGCGATTCTACTGCT | 115426 |
rs543253727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495959 | GATGGCTGTGTTTTT[C/T]TCTACCTCTCAGAAT | 115426 |
rs543287412 | snp | A/C | 3.29886e-05 | 0.00406118 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475473 | CCTGGAGCCCATCCC[A/C]TTTCATTTGCAGATG | 115426 |
rs543297519 | snp | A/C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464435 | TTAATTTTAATGCAG[A/C/T]TGAGGTTATCAAAGT | 115426 |
rs543298962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457844 | CCAGCCTTGCATCCC[A/G]GGGATGAAGCCGATT | 115426 |
rs543310711 | in-del | -/CT | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424849 | TTGTAAAATCTCCCC[-/CT]GTTAGGATTCATTTG | 115426 |
rs543317210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462909 | GCTACAGAGCGAGAC[C/T]CTGTCTAAAAAAAAA | 115426 |
rs543353225 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412099 | GCGGAGCTTGCAGTG[A/G]GCCGAGATCGCGCCA | 115426 |
rs543373379 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442673 | TTTTTTTTTGGGGGG[A/G]TAGAGATGGGGTCTC | 115426 |
rs543406953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425480 | AGGATAGAGGCCGGG[C/T]GCAGTGGCTCATGCC | 115426 |
rs543439737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456364 | TGTTCATATCCTTTG[C/T]CCACTTTTTGATGGG | 115426 |
rs543443555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474003 | GCATGTGAATTTATA[G/T]ATTAGAGACTTTTCA | 115426 |
rs543455895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500398 | AGCCAAATAGCAGGA[A/G]ATAACAGTATCCTAA | 115426 |
rs543507399 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447553 | AGATTAATACAGCTG[A/G]AGTGTAGAAAGCATA | 115426 |
rs543511641 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473060 | GTACCTAACTATGGT[C/G]TCGAAATACCTTTCC | 115426 |
rs543512020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467291 | GACAGTTCTTTTTGT[G/T]GCTACATCCCCTTCA | 115426 |
rs543522245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473679 | TCTTCTGTAAAGAGC[C/T]GGATAGTAAATAGTT | 115426 |
rs543542755 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416612 | CTGTGGCGCGATCTC[A/C]GCTCACTGCAAGCTC | 115426 |
rs543567321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496531 | GTTCTTCTTTGACCA[C/T]GCATTAATGCATTAT | 115426 |
rs543592403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505624 | TTTTGAAGACTCACC[A/G]TATGTGTTAAGTGGT | 115426 |
rs543608722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483904 | ATGTTGGTCAGGCTG[A/G]TCTCGAACTCCCAAC | 115426 |
rs543670012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463274 | CAACAAGAGTGAAAC[C/T]TCGTCTCAATAAAAA | 115426 |
rs543691376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414678 | AATAAGTGTAGCTCT[C/T]TGATTTGGTAGAAGT | 115426 |
rs543697236 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507430 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCGTGT | 115426 |
rs543786719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462259 | ACTGAGACCATCTAG[C/T]CTGCAAAGCCAAAAC | 115426 |
rs543796523 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424128 | ATTAGGCAGGAGAAC[-/AA]AATAAAGTGTAAATA | 115426 |
rs543806352 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420272 | ATGTTGGTCAGCCTG[G/T]TCTCAAACTCCTGAC | 115426 |
rs543844305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456019 | TGTAAAATTGAAGAA[A/C]CTTATAAAGCTTTAG | 115426 |
rs543856021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455465 | CCTACAAAGGACATG[C/T]ACTTATCCTTTTTTA | 115426 |
rs544015387 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424124 | TGCAATTAGGCAGGA[C/G]AACAAAATAAAGTGT | 115426 |
rs544026013 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502092 | AGATAAGCCAGGAAC[A/G]CATTTATTAAGCCAG | 115426 |
rs544068104 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456923 | CTGTAGCCTTGTATA[C/G]TTTGAAGTCAGGTAG | 115426 |
rs544078410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420612 | TCAGGGAGGCTGAGG[C/T]AGGAGAATGGTGTGA | 115426 |
rs544081359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440880 | TCCTTCTGAGGGAGC[C/T]CCCTTCCCTCTCCCT | 115426 |
rs544101002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451585 | GGGGTTCACACCATT[C/G]TCCTGCCTCAGCCTC | 115426 |
rs544122460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494883 | TAGAATCTCTGTTTT[G/T]ATGTGTTCTATATTG | 115426 |
rs544136960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425871 | GCAAGGAAATAATAC[A/G]TATTTGTACTAACCT | 115426 |
rs544142488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446080 | TCACTGCTGCCTTGA[C/T]TTCCCTGGCTCAGGT | 115426 |
rs544144621 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482488 | GGATTTATCCTCCTG[A/G]ACAAATGCTAAGACA | 115426 |
rs544154916 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477550 | TGCTGTTTCCATGGG[C/G]TTTTCTTTATGAGAT | 115426 |
rs544184190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487782 | GCTGGGATTATAGGC[A/G]TGAGCCACGGTGCCC | 115426 |
rs544185859 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499389 | TCCTGCCGCTAACTT[C/T]AGGAGATGAGAAGTT | 115426 |
rs544200707 | snp | A/G | 0.000216255 | 0.0103962 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413684 | GCGAGGCTGGGGGCC[A/G]GAACAGCTGGGCTCC | 115426 |
rs544250795 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450842 | GCCCTGGGTTCAGCC[A/G]TGTCTAGGAATCCCA | 115426 |
rs544273383 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439323 | CTGAGACACAGATGT[G/T]CACCACCACGCCCGG | 115426 |
rs544299262 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413234 | GCGCAGACATGGCCT[C/G]TTCCTATCTTTGAGG | 115426 |
rs544311706 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412730 | CAGGCCGCGTGGCGG[A/G]AGCTTTCCTGTTGAG | 115426 |
rs544317307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487373 | TTTGTATTTTTATGT[A/T]TTTATTTTTTGAGGC | 115426 |
rs544325781 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469720 | CATATACACACATAT[A/G]TGTGCATATATACGT | 115426 |
rs544354337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429455 | AGTCTTGCACTGTCA[G/T]GCAGGCTGGAGTATA | 115426 |
rs544356911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481625 | GAAAATGCCTTCGTT[C/G]TTTTTTTTCTTTTAA | 115426 |
rs544364922 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447696 | AAATAATAAATCCAT[A/T]AACCCCCGAGGACAA | 115426 |
rs544419255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429057 | GTAATCCCAGCTACT[C/G]AGGAGGCTGAAGCAG | 115426 |
rs544419381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434618 | TAATTCTTGTATTTT[C/T]AGTAGAGATGGGGTT | 115426 |
rs544445592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499097 | AGATTTTTCAGATGT[C/G]CCTGTTGAGAGCATT | 115426 |
rs544482225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504404 | TTGGGATACATGTGA[A/G]ATTTTGATATGTTCA | 115426 |
rs544494918 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479309 | TCTAAACCTAAGGGT[C/G]AGTTCTCATTCCTTA | 115426 |
rs544511696 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474522 | ACGAGCCCAGCCAAC[A/G]TGGTGAAACCCTGTC | 115426 |
rs544528086 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413965 | TCGCTTCCCGCGCTC[C/G]GCGGGGCCTGGGGCC | 115426 |
rs544599295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438796 | GAAGCTTCATTAAAA[C/G]AGAATTCGTTGCTGA | 115426 |
rs544609009 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447911 | GTAGTTTGGAGGAAG[A/G]CATGTGGAATAGAAC | 115426 |
rs544616949 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424941 | TATATAGGGCACATA[C/T]TATCAGTATTCTATT | 115426 |
rs544655076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470916 | AAATGGCAGAAACAA[A/G]CACAACTGTATCAGC | 115426 |
rs544657153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476605 | TGTTTGTTTTTTGTT[C/T]TTTGTTTTGAGACAG | 115426 |
rs544678426 | in-del | -/GTTTCTA | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439852 | TGAATGAAAACTCTT[-/GTTTCTA]GTGGTATTTTGAACA | 115426 |
rs544679699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450015 | TTGTTTTTTGACTGT[A/T]TTAACTCAGCCATGG | 115426 |
rs544692961 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427618 | TGAACCCAGGAGGTG[G/T]AGGTTTCAGTGAGCT | 115426 |
rs544695795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476007 | GTATCTTTGCACCCT[A/G]TAGCCAACCCTTCTT | 115426 |
rs544699506 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436270 | TACTTTTCTGGTACT[C/T]ATTGTGGTTGTGGCT | 115426 |
rs544746234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423763 | AGCCTGGCCAAGATG[C/G]TGAAACCCCGTCTCC | 115426 |
rs544765594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463458 | AAAGGAACCAGTGTG[A/G]CTTATGGATAGAATT | 115426 |
rs544780551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492239 | TTAGCTTACATTTGT[C/T]TTATTATGCTCTCTT | 115426 |
rs544792779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498554 | GGCTTTATAAGAGTG[A/G]TCTGCCTTCTCCCTT | 115426 |
rs544852408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465627 | ATCTGTTACGATGTT[C/T]TTTATTTCTGAATTT | 115426 |
rs544883413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471807 | TGGTCGGTTAAAGCT[C/G]CATTCCAGGACTAAA | 115426 |
rs544896105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491417 | CACCAGTAGTAGATG[C/T]GTGTTACACTAGCAG | 115426 |
rs544930125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504133 | TTGGTTCACTCCATT[C/G]TCCTGCCTCAGCCTC | 115426 |
rs544930797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497710 | CAAAGCAGCACATCA[C/T]AGTAATAGATTTTCA | 115426 |
rs544942581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428059 | TAATGACTGTTTAGA[A/G]TGATGATGGTAAGCC | 115426 |
rs544968492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485966 | GCCGTCATCCATTGA[A/T]GTAGAAATGGATAGC | 115426 |
rs544978089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452860 | AGGCGAGAGTGGAGC[G/T]TTAGAGTTGTCACTG | 115426 |
rs544986941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464718 | ATATCAAGAATCTTA[C/T]ATTTGGTGAATCCTT | 115426 |
rs545004945 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422752 | GTGCTGGGATACAGG[C/T]GTGAGCCACCATGCC | 115426 |
rs545029272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484482 | ATGCAGTGCCATAAT[C/T]ACAGTCCCCTCCTGG | 115426 |
rs545035190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432674 | TACTTCTCCCACGAG[G/T]TATGCCATCTATTAG | 115426 |
rs545038019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463786 | AAAAAAAATTTTTTT[C/T]TTTAATGATTAGAAA | 115426 |
rs545038739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452528 | AATATGATATGGATT[C/G]AAAGGTGTGATCCTA | 115426 |
rs545049310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421598 | ATTTTTGTATTTTTA[A/G]TAGAAACAGGGTTTC | 115426 |
rs545049402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447792 | ACATTGCCTAGTTTA[G/T]CAGGCCAGAGAAAAC | 115426 |
rs545093413 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470567 | GGGACAGAATTAAGA[A/G]CAGGGAAAGGGTAAA | 115426 |
rs545158733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474761 | TACAAATCCACACCC[A/G]TAGTAGGAAACTTTG | 115426 |
rs545208914 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465349 | AAAATAATTTGGAAT[C/G]TTCTTTTTCTTTCTT | 115426 |
rs545265896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443479 | TACCATACTACCTCT[C/G]ATTTTAAGAGAAGCA | 115426 |
rs545273921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453836 | CTTGGACCCAGGAGG[C/T]GGAGGTTACACTGAG | 115426 |
rs545282997 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441965 | GAAATACTATGTAAT[A/G]GTTGACTGTTCCGAG | 115426 |
rs545301579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459030 | AATGAGAACCCATGG[A/G]CGCAGGGAGGGGAAC | 115426 |
rs545326393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422160 | CTATACTTGGTTCCA[C/T]TGGTCTGTTTGTCTA | 115426 |
rs545346074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442814 | ACTTCATGATGATAT[A/G]GTCTAGGCTTTAATT | 115426 |
rs545347238 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505691 | TCCAGATTTTTTTTC[C/T]CCCTCTAGGGCTCTG | 115426 |
rs545381988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436048 | GACAGATTTAGTATA[G/T]TAAACACACTAAATG | 115426 |
rs545394374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415979 | GCTGACCTACTGAAG[C/T]AGAATCTGTATTTTA | 115426 |
rs545395563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441560 | TTGATAAATTCCTTT[A/T]GACCCAGCCTTATCC | 115426 |
rs545424888 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478375 | ATGGTCCTCTACCCC[-/T]AACCATGTTAGATAT | 115426 |
rs545437194 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466002 | TTTGTTCACTTACTA[C/G]TGTAATATAATATTT | 115426 |
rs545484144 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478466 | GGATTACTGTATTTA[A/G]TCCTGTGACGTTGAT | 115426 |
rs545494685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414589 | TTTCTTTGTCTTCAT[A/G]TTGTTGTTAATACAC | 115426 |
rs545495277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462844 | ATCACTTGAACCCAC[A/G]AGGCAGAGGTTGCAG | 115426 |
rs545511224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489579 | TCACCAGCATTCGCT[A/G]TTGTTGCTGTTTTTT | 115426 |
rs545549141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446811 | AATGGCGCCACTGCA[A/C]TCCAGCCTGGGTGAC | 115426 |
rs545549953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495912 | AATATCTCAATAGGT[A/G]TTCTGTAAGACGTAA | 115426 |
rs545556998 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467172 | TTGTAGACTCTAAGG[A/G]AGAACCCATTTTCTT | 115426 |
rs545566804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420738 | AGAGAGAGAGAATGT[A/G]TTGGGGTCCAGAGAA | 115426 |
rs545583500 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443163 | ATGAAGCTACCTTTG[C/G]CTAGGCAAGTTGCAG | 115426 |
rs545593769 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445258 | AACTATTTGACCTGT[A/G]TTATTTATGTATTGA | 115426 |
rs545621193 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438165 | CTCTTAGAAGAGATT[G/T]CTGTATAACACAGAA | 115426 |
rs545630941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426025 | GGATGGATTTGCTTT[A/C]AAAGGAGGGCCAGTT | 115426 |
rs545706466 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462423 | TGATTCTATTGCTAG[A/T]CTAAGGGTATAGCTC | 115426 |
rs545712636 | in-del | -/ACA | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470653 | GAAAAAAAATGCGTG[-/ACA]ACAATAATGCAGAAG | 115426 |
rs545713925 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411445 | TGCAGTGGCGTGATC[G/T]CAGCTCACTGCAGCC | 115426 |
rs545727872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416712 | GCCCGGCTGATTTTT[C/T]GTATTTTTAGTAGAG | 115426 |
rs545776837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479225 | CCTCTCCTATTCATA[C/G]TTCAGCACTCCAGTC | 115426 |
rs545777284 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473185 | GTTCTCGTCAGAAGG[A/T]TTTGGGAGTCAACTG | 115426 |
rs545824934 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506309 | AATCCTCTTTCCCAC[A/G]TAGCCATCATCTTGT | 115426 |
rs545881815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483870 | AATTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC | 115426 |
rs545890432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451930 | GTTTTTTAAGTAACA[A/G]TGTTAGTTTGGTTTA | 115426 |
rs545910500 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454278 | GAACATCTTTTGAGT[G/T]AAGACACCAGGATTG | 115426 |
rs545917931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477503 | TGCACTCCAGCCTGG[A/G]TAACAAGAGCAAAAC | 115426 |
rs545925131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467206 | TTTACCATGTTTCAG[A/G]CGCCTCCCACATGCC | 115426 |
rs545951690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420241 | TTTGTATTTCTAGTA[C/G]AGACGGGGTTTCACC | 115426 |
rs545967950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472433 | AGGAGAGCCAAGGAT[A/T]TTAAGTCAAGCCAAA | 115426 |
rs545985759 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507157 | CATCTCTATTGAAAC[A/T]TTTTTTTTACTTTGT | 115426 |
rs545989233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495146 | ATAATCGATAATTTT[A/G]CTTGAAAGGAACTTC | 115426 |
rs545996147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494241 | GGTGGCTTGTCTACT[A/G]CTCCATTGGTCAAAG | 115426 |
rs546060287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451545 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAGGCT | 115426 |
rs546098101 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462439 | CTAAGGGTATAGCTC[A/C]GTCACAGACTTCTAA | 115426 |
rs546137266 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502527 | ACCTGGGCTCAGGCA[A/G]TCCTCCCGCTTCAGC | 115426 |
rs546150267 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500076 | CTCCTGGGCTCAAGC[A/G]ATCCACCTACCTCAA | 115426 |
rs546151146 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450252 | AGGATCAAAAACAAA[C/G]CCCACCCATTACATT | 115426 |
rs546162294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481265 | CCAATTTAGATGGGG[A/G]GTTGTATCTGTTACA | 115426 |
rs546190212 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425752 | CTGGGTGAGTGAGAC[G/T]TCGTCTCAAAGTAAA | 115426 |
rs546192153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429591 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGAATTAC | 115426 |
rs546192744 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474086 | AGGTAAATATAACTT[C/T]GGAGGACATGAAGTT | 115426 |
rs546233597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435365 | TCCTGGGCTCAAGTG[A/G]TCCTCCCACCTCAGC | 115426 |
rs546242131 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412940 | ACGAGGCCTCAAAAC[G/T]GCAACCGATGTGGTA | 115426 |
rs546263143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466795 | CAAACATGCTCCTGC[C/T]TTGGGGCCTTTGTAC | 115426 |
rs546301631 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472006 | TAACTTACATACAGT[A/T]ATATGTACTTACCCT | 115426 |
rs546321920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449558 | GATTCTTTTTAGAGT[G/T]TGCAGAAAAGAGTTA | 115426 |
rs546347788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440812 | CACATTGTCTAGGAA[A/G]TTTTCAAAATAATCG | 115426 |
rs546406437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503738 | CATACTTTGGAATAC[A/T]GTGCAAAACAGCTTT | 115426 |
rs546409845 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450980 | ATACTTAAATATACC[A/G]TGGGTGAATATTGAT | 115426 |
rs546438140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471514 | TTAAAAAGATACCAG[C/G]TTCCATTTTGGGTGC | 115426 |
rs546472366 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456124 | ACATGGTTTTACTTT[A/C]TGATGAAATTTCTTG | 115426 |
rs546529770 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421336 | AAGATGTATATGTAC[A/G]GTTTAAAGAGCAATA | 115426 |
rs546535693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461091 | AACAAAACAATATAT[A/G]AAAGCATTTTAATAA | 115426 |
rs546537115 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470649 | CATAGAAAAAAAATG[C/G]GTGACAACAATAATG | 115426 |
rs546596752 | snp | A/T | | | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421083 | AGGGTAGGACCTTCC[A/T]ATCAGCCATCTACAT | 115426 |
rs546599362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444622 | TTTTTTTTGGTTTAG[A/G]CTGAGTCTTGCTCTT | 115426 |
rs546616867 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481498 | ATATTTTGAAAAGTT[C/T]AGTATTTTAATGCCA | 115426 |
rs546654063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437263 | TTTTAGACAGAGTCT[C/T]GTTCTGTTGCTCAGT | 115426 |
rs546655909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443297 | AAGCAGTATACAGAT[A/G]CTTTACCTGGATTAT | 115426 |
rs546668701 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469094 | AAGTTATCAGAGAAA[C/G]TTTCAAGTAACTGTG | 115426 |
rs546732206 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481867 | TTAAACAGTATCATT[A/G]TTTGTTAATATCAAT | 115426 |
rs546734125 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423447 | TATTTGCTGATTTAA[C/G]TTGCTTTTAAAAAAT | 115426 |
rs546737653 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411891 | CCTTCTTGAGAAGAC[A/G]TATTTTCATTTAAAA | 115426 |
rs546756029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417324 | TTGTAAATACTGCAT[C/T]TCCATCTTCGAGTAT | 115426 |
rs546763020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428730 | AATTTTCAATTTTTC[A/G]TAGAGACAGAGTTTC | 115426 |
rs546774885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433658 | AAAGTCTAGTGTATA[C/T]GTCAGTAAGGCGTAA | 115426 |
rs546779627 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411629 | AAGTGATCCGCCCAC[C/T]TCGGCCTCCCAAAGC | 115426 |
rs546788615 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426641 | TGGATATCTAGCATA[C/T]GTTTGTAATCGGTAT | 115426 |
rs546816264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474556 | ACTAAAAATACAAAA[A/G]TTAGCCGGGTATGGT | 115426 |
rs546818983 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459213 | CAAGAACTTAAATTT[A/T]AAAAAAAGAAAGAAA | 115426 |
rs546873182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471070 | AGGTGGATGGTTGGG[A/C]TTGTAAGAAGATGAC | 115426 |
rs546874081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464065 | ACAGTTCTGCAACAG[C/T]ATGAGAGTTCCTGTT | 115426 |
rs546880238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458607 | GAAGAAATAGGAACG[C/G]TTTTATACTGTTGGT | 115426 |
rs546880728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439007 | AATTCTAAAATATAA[C/G]TGAAATAATTTGTTT | 115426 |
rs546902355 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428221 | GTTCTTGATGTTTAA[C/G]CTTTTTGATTATGAA | 115426 |
rs546908754 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497504 | ATTGAACAGATGCAT[A/G]AAGCAAACTCTTAAC | 115426 |
rs546934309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469867 | TTTGAAAATATAGTA[A/G]CCCAAAATTTCCAAA | 115426 |
rs546939762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420836 | ATTTTAAGTTTGGCT[A/G]GGACATTTGAGCAAC | 115426 |
rs546950041 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426888 | TGAGTAGTTGGGATT[A/T]CAGGCACCCGCCACC | 115426 |
rs546962048 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433519 | GTAAGTTATCTTTAG[A/G]ATTATGAAGAAATTA | 115426 |
rs546987498 | in-del | -/GA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424386 | GTCACAATTAAGAGA[-/GA]ATTTTTAGCACTGAA | 115426 |
rs546997881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502543 | TCCTCCCGCTTCAGC[C/T]TCCTAAGTAGCTGGG | 115426 |
rs546998544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470183 | TTCAAGACCAGCCTG[A/G]CCAACATGGCAAAAC | 115426 |
rs547009018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501870 | TTAGTGATAACTGAG[G/T]TGAGTTTCCACTGTA | 115426 |
rs547013096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426263 | AACTCTATTTGACAT[C/G]TCTTCTATTTCCTAT | 115426 |
rs547014558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432903 | TGGAGTGCACTGGCA[C/T]GATCTCCGTTCACTG | 115426 |
rs547046659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501238 | GGGCTTTGTGTTAAG[C/G]TGTGTTTTGCAAACA | 115426 |
rs547061835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489281 | ACTAGTCCATGGTGT[A/G]GATGTACCACAGTTC | 115426 |
rs547096654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495487 | GACCCATAGTATACT[C/T]TTTGCCCAGTAGTGT | 115426 |
rs547154482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490921 | CTATAGGATTAGGAA[A/G]AGGAAACCTGAATAA | 115426 |
rs547177436 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422456 | GCTTTTAATATTTGC[A/T]TACAAAAAACTGTAG | 115426 |
rs547228369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421879 | CTGTATTTGAATTTT[A/G]TATAATGGAATTCTA | 115426 |
rs547254203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448463 | TTCTAGAGCCAGGTG[A/T]TCAGTTTGAAAAACG | 115426 |
rs547271407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502963 | GAAATGTGACATTCA[A/G]TTTTTAAATTTGAAA | 115426 |
rs547310762 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485785 | CCTGGGCAACATGGT[A/G]AGACCCCTGTCTCTA | 115426 |
rs547353167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496045 | TCTTTGACCACAGCT[A/G]TATAAGTTATTTTTT | 115426 |
rs547360148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496710 | CTTTAAGGATTCTCT[A/G]TTGTCTGGAATGTGG | 115426 |
rs547393015 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452245 | TTACAAATAGTGCAG[C/G]TATAAATAGCCTTGT | 115426 |
rs547413182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415638 | CACGTAGTGAAAAAT[G/T]TCATAAATTGTAGAC | 115426 |
rs547445248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457264 | ATTTTATTCTCTTTG[A/T]AGCAATTGTGAATGG | 115426 |
rs547461823 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462968 | TAAGAGTGGGAACAC[A/C/G]CTGGCTTTAGAAGTG | 115426 |
rs547489560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468682 | GAATACTGGACTTCT[C/G]CTGGACAAGAGGCTG | 115426 |
rs547490034 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419461 | AATTATCCCTTCTTG[-/T]TTTTTTTTTCTGCTT | 115426 |
rs547506014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431233 | TAAGAGCATTTCTGT[C/T]CCCACCCAGTTTATG | 115426 |
rs547506461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462565 | TTGGAAGTAGAAAGC[A/G]TGTGTACACAGTAGG | 115426 |
rs547513589 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501607 | ATTTATATTGGAATC[A/G]TTACTTCCTTTGTCT | 115426 |
rs547527922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451400 | ATCTCCAAAACAAAA[G/T]ATACTAAGAGAAATT | 115426 |
rs547577858 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506653 | ATATACTTTTTTAAC[A/G]TCTCTTCTTCCATTA | 115426 |
rs547585264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485358 | TCACGTATTTATTTT[C/G]TAAACTCTGAAAGCC | 115426 |
rs547615987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505903 | ATAGTGCAGATTCAA[A/G]CCTTTATGTTTGTTC | 115426 |
rs547621316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484898 | TCCTGGTTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 115426 |
rs547637413 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479193 | TCAAGAGCTATCTCT[A/G]CTAATTGTTTCCATT | 115426 |
rs547647721 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416167 | CTCCCGGGTTCAAGC[A/G]ATTCCCCTGCCGCAG | 115426 |
rs547659077 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475110 | TTTTAATTGACAGAG[-/T]TGCCATTTTATCTAG | 115426 |
rs547672462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430734 | CTAGCCATCTTGTTT[A/C]CCCTGCCTTGCCTTT | 115426 |
rs547679192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479311 | TAAACCTAAGGGTCA[A/G]TTCTCATTCCTTACT | 115426 |
rs547714175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489726 | TTTCTAATTGGGTTT[C/T]TGTTTTTTTTTTTTT | 115426 |
rs547719931 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431696 | GCAATGGCAGTATTT[A/T]GAGGTTGATTTAGGT | 115426 |
rs547734610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414823 | CTTTTTTTTCCCCTT[G/T]CCTTCTCTCTTTAAA | 115426 |
rs547738433 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429710 | CATTTGTGTGTACTA[C/T]ATGCTTGCTGGGTTG | 115426 |
rs547777060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488611 | GGAGTGCAATGGCGC[C/T]ATCTCAGTTCACTGC | 115426 |
rs547792705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440423 | TTAAACTGTCTGACT[C/G]AAGAGCCCAAGAGTT | 115426 |
rs547796105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446957 | GCAGTAGCACAATCT[C/T]GGCTCACTGCAAGCT | 115426 |
rs547813169 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451640 | CGCCCGCCACCACTC[C/G]CGGCTAATTTTTAGT | 115426 |
rs547822750 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429370 | AAACAGCTAATGTTT[A/G]CCAGCAGTATGGTAA | 115426 |
rs547825624 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456470 | GCAAAAATGTTCTCT[C/G]GTTCTGTAGGTTGCC | 115426 |
rs547852297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446481 | AAGCAGGGTTTCGCC[A/G]TGTTGCCCAGGCTGG | 115426 |
rs547852587 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445754 | CTTTTTGTAGAGACA[G/T]GGTCTCCCTATGTTG | 115426 |
rs547884462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467189 | GAACCCATTTTCTTG[C/G]CTTTACCATGTTTCA | 115426 |
rs547889231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420335 | ACTGAGATTACAGGC[A/G]TGAGCCACCGCGCCC | 115426 |
rs547915247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494318 | TAAAGTTATGTTTGG[A/G]AGCCACATTTATGTA | 115426 |
rs547931799 | in-del | -/AAATG | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506514 | ATTGAATAACTAGTT[-/AAATG]AAATTTTAGCTACAC | 115426 |
rs548082564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441757 | TTTTCCATTTTATTT[C/T]CTTATAGACATAAAT | 115426 |
rs548105626 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456296 | GACCAGTGATGATGA[C/G]CTTTTTTTCATATGT | 115426 |
rs548136389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429133 | TCGCACCACTGCACT[A/C]CAGCCTGGGCAACAG | 115426 |
rs548138239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423198 | AGATTAAGAAGAGAT[G/T]AGAACCATGTTTCCA | 115426 |
rs548138688 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439308 | TCCTGTCTCAGCCTC[C/G]TGAGACACAGATGTG | 115426 |
rs548216905 | in-del | -/C | 0.0321975 | 0.122728 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461390 | TCCTCCTTCTCTCCT[-/C]CCCCCCGCCCCTTGT | 115426 |
rs548275769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498628 | GCTTCCCTGCCCTGC[C/T]ACCACCTTTAGTGCT | 115426 |
rs548298108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476873 | GCTGGTATTACAGGC[A/G]TGAGCCACCACGCCC | 115426 |
rs548364680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425072 | AAACTACTCCCACAC[C/G]TCCTTCCTGTCTTTC | 115426 |
rs548412900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471032 | AAAGACTCCTTAAAT[A/G]TAAAATCACAGAAGT | 115426 |
rs548426283 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499987 | TTTGTTGTTGTTGTT[G/T]TTGAGACGGGGTCTC | 115426 |
rs548429365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433546 | ATTAATGGAACAGAT[C/T]AGTCATATTAGCTTA | 115426 |
rs548460330 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413403 | GCTGAGGGCCCGAGC[C/T]GCAGGGAAAGCGGCG | 115426 |
rs548483442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472599 | GAAATAAAGAGTTGC[A/G]CTAAACATTTAAAAT | 115426 |
rs548517936 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423867 | GGAGAATTGCTTGAA[C/G]TTGGAGGGCAGAGGT | 115426 |
rs548545761 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450321 | CCCCCCCCCCATTTA[A/T]TTAAATAAACTGTGT | 115426 |
rs548556153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455186 | GGTGCATGTGCACAA[C/T]GAGCTCGTTTGTTAC | 115426 |
rs548579366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418530 | TTACTGATCTAGTAG[A/G]TTAAAAGTTTTAAAT | 115426 |
rs548649628 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492600 | GAAAAACAAAGTATA[A/C]ATAATTGACTTCTAT | 115426 |
rs548670118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417274 | TTTCAAGAGTGGTCT[G/T]ACAAAAAATCCTAAC | 115426 |
rs548711909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490728 | TTAAAACATTTGTGG[A/G]GATAAGTACTGATGA | 115426 |
rs548718220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490283 | GAGATAATTTATGTG[C/G]CCCTTTGCACATAGC | 115426 |
rs548769971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482175 | TAATGTCTGTTGATT[A/G]TAAGTGAACCTAACA | 115426 |
rs548786061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422297 | ATTTTGGTCAGGCTG[G/T]TCTCGAACTCCTGAC | 115426 |
rs548813249 | snp | C/T | 0.435263 | 0.167862 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487182 | TTTTATTTTTTTTTC[C/T]TTTTTTTTTTTTTTT | 115426 |
rs548818423 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480993 | CTTTGTTAGAGTATT[C/G]CCAGAGTTTCCTTTG | 115426 |
rs548824584 | snp | A/C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488920 | CAGGTTCAAGTGATT[A/C/G]TCCTGGTGCAGCTTT | 115426 |
rs548863442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476191 | TCTCCAGTTTCATCC[A/G]TGTTGTAAATGAAAG | 115426 |
rs548871955 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412364 | TTCTTCGGAGGCGCG[C/T]AGCTCTGCATTATTT | 115426 |
rs548888942 | snp | A/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411534 | AGGCAACTGCCACCA[A/T]GCTCAGCTAGTTTTT | 115426 |
rs548901105 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444518 | CATTTTCACCCATGT[A/G]AGGTGTTTAAGAAAC | 115426 |
rs548904507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438927 | TATAGATTTATGATG[C/T]TTCTTCTTAGGTAGA | 115426 |
rs548919010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460101 | AACAAGAATAGTTTT[C/G]CTCTGGGAAGTCAAA | 115426 |
rs549002592 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493530 | TATTTAAATCCATAA[C/G]ACCTTACCTTGTTTG | 115426 |
rs549038695 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477932 | AAATGTTATGGCCAG[A/T]GGTTACTTAGCATTC | 115426 |
rs549043920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448586 | TAAGTATATGTGAAC[A/G]CTTAATGCAGTGCTG | 115426 |
rs549054576 | snp | A/C | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439044 | TTATCTCCACTATTC[A/C]TTCAAAAATTACAGA | 115426 |
rs549059636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504970 | ATTGCTCTTGTCTGT[A/G]ATAGCTTATATGTTT | 115426 |
rs549082076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458413 | TCTGGCTGGCAGTCT[A/G]TTTTGCTGATCTTTT | 115426 |
rs549123767 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445634 | ACAACCACAGCTCAC[C/T]GCAACCTTGACCTCC | 115426 |
rs549156514 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470376 | AAAAAAAAAAAAAAA[A/T]TTCCCAACTTAAAAT | 115426 |
rs549159950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433009 | CCACGCCTGGCTAAT[C/T]TTTGTATTTTTAGTA | 115426 |
rs549205436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444574 | CCCTGCTTCCTCATT[A/G]TGTGGGCCTTGGGTA | 115426 |
rs549207864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463502 | GGGAGATGGGGTCTC[A/G]CTCTGTTGCCCAGGC | 115426 |
rs549253965 | in-del | -/TTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465625 | TAATCTGTTACGATG[-/TTT]TTTATTTCTGAATTT | 115426 |
rs549255525 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416077 | TTTGTTGTTGTTTTT[G/T]TTTTTTTTTTAAGCC | 115426 |
rs549255911 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475735 | TTGCTATTATTTTAT[C/T]TTAAAAATATTTATG | 115426 |
rs549324298 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431179 | TTCAAATTTTGCTTG[A/T]CTTAGTATGTCTATC | 115426 |
rs549345484 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486126 | TTGATACTGTGTGAC[C/T]ACTTAATATATTTTA | 115426 |
rs549378971 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506553 | CCTCCCAAATATTAG[C/T]TGTGCCTGGTTCTTG | 115426 |
rs549443186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437574 | CAAGTGAGTCGATAG[A/G]ATGTGGTTGTCATAT | 115426 |
rs549452398 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485138 | ATTTAGTTTAATACT[C/G]TCTGTGTTCTCTTAT | 115426 |
rs549494749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457372 | ATATCCTGAGACTTT[A/G]CTGAAGTTGCTTATC | 115426 |
rs549527162 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484582 | TGATTTTTGTGTTTT[G/T]TTTTTTTTTTGTAGA | 115426 |
rs549536907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500818 | CTTCATCCTTCTACC[C/T]GGTTTTCTAATCCAG | 115426 |
rs549545199 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461998 | ACAATTTTTGTTTTT[A/T]AAAAAAAAAAAATAA | 115426 |
rs549550981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452581 | CTAGTCTGAGAAAGG[C/T]AGATTTTAACTAAGG | 115426 |
rs549576905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502514 | ACTGATCTCAAACAC[C/G]TGGGCTCAGGCAATC | 115426 |
rs549617340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432257 | ATTTCATTGCTACCA[C/T]GTTCATTACATACAG | 115426 |
rs549619228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427075 | TTTTATATTTGCATT[A/G]GGTTTTTTGTATTTC | 115426 |
rs549644962 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488617 | CAATGGCGCCATCTC[A/C]GTTCACTGCAAGCAG | 115426 |
rs549654759 | in-del | -/TC | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416869 | CCTATTTTAAAGGAT[-/TC]TCTCTCGTCATTCTT | 115426 |
rs549681640 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462771 | AAAATACAAAAATTA[G/T]CTGGGTGTAGTGGCA | 115426 |
rs549713837 | in-del | -/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411386 | CATCTTTTTTTTCTC[-/T]TTTTTTTTTGAGATG | 115426 |
rs549722375 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413828 | TGGTGGGGAGTGGGT[C/T]CCTGCCAGCCCCAAC | 115426 |
rs549728817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487980 | ATCCAGTGGCTCATG[A/C]CTGTAATCCCAGCAC | 115426 |
rs549731271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431749 | TTAGATGTTAAGGTA[C/G]CCAGCTATTAGATCT | 115426 |
rs549738136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501217 | AATCACAGTTAATTA[A/G]TGTGTGGGCTTTGTG | 115426 |
rs549829611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456650 | AGGTTTTATTCTAGG[G/T]TTTTTATGGTTTTAG | 115426 |
rs549843171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468651 | TATGGCCTGCTTTCA[C/G]CTTTGGGCTTTGGTT | 115426 |
rs549850193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420445 | TGCGGTGCTCACGCT[A/G]TAATCCCAGCACTTT | 115426 |
rs549854331 | in-del | -/CTG | | | cds-indel, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506896 | TCTCTACTAGTCGAA[-/CTG]CTTTTAGTGTCTCAC | 115426 |
rs549881660 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436125 | TTATGCTACCAAATT[C/G]TTAACAAGTACGAGT | 115426 |
rs549881948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468191 | GAATTGATTATATGC[A/C]TGTTTTTATTATGAT | 115426 |
rs549916074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415577 | TCCTGTAAAATACCA[C/T]GTCCTCATTGGAAAA | 115426 |
rs549960316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505286 | ATATATATATGCGTG[C/T]GTGTGTGTGTATATA | 115426 |
rs549973942 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483994 | GCACCCGGCTTCATC[A/G]TCATTTTCTGTTTCT | 115426 |
rs550029786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420747 | GAATGTATTGGGGTC[C/T]AGAGAAGACACTGAC | 115426 |
rs550038099 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424397 | GAGAGAATTTTTAGC[A/C]CTGAAAGCCAACTTG | 115426 |
rs550070594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462453 | CAGTCACAGACTTCT[A/G]AACAACTTGAAACCC | 115426 |
rs550097236 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495308 | GATAGTGAAAATGAA[A/T]TATCAACTGAAAACA | 115426 |
rs550102040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435643 | ACAGAGTCTTGCTCT[A/G]TCACCCAGGCTGGAG | 115426 |
rs550104894 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414275 | GGAGGTTAGAGACCT[A/G]GGCATGAAGAAACTG | 115426 |
rs550107164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419900 | ATGTACAATCACACC[C/T]GGCTACGTTTTTTTA | 115426 |
rs550166425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425004 | TAACATTAACACTGA[A/T]GTGAACCTTAATCAT | 115426 |
rs550187284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451369 | TATGTGACACATTAC[A/G]TAGTTCTGTAGTTAA | 115426 |
rs550197020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456178 | CTAGAGAGCTGGCTA[C/T]ATGTAAAAACTAGAA | 115426 |
rs550198124 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434475 | ATGGTCTCTCTCTGT[C/T]GCCCAAGTTGGAGTG | 115426 |
rs550198322 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478013 | TTTTTAATCCCTTCC[A/G]TTTCTTCTCTGATAA | 115426 |
rs550254169 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476378 | AGTTTTTAATAATGA[G/T]ATTTATTTTTACACG | 115426 |
rs550263445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476815 | GGCCAGGTTGGTCTC[A/G]AACTCCTGAGCTCGT | 115426 |
rs550285034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496566 | AAAATGTAGTGATCT[C/G]AAGCAGCCAGAAGTC | 115426 |
rs550302141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439605 | AGTTTTTTTTCTGGA[C/T]TGCTGTTCTATGTCA | 115426 |
rs550311723 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481105 | ATACAAGTTACAGTA[C/G]GGTAATCAATTACAA | 115426 |
rs550316048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445241 | TTTCCTTATCTGTCA[A/G]TAACTATTTGACCTG | 115426 |
rs550342754 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462395 | ATTTCAGAACTTCTT[A/G]CAAACAAAAGTGTGA | 115426 |
rs550354473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472761 | GTTTTCAGTAATTGA[C/T]AGCTGGCAACAATGT | 115426 |
rs550381456 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496742 | AAGTAGACCTGGGAA[C/G]GTCATTTGTACCTTG | 115426 |
rs550401270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466835 | CCTCCTACACAGATA[C/G]TCATTTGACTTACTC | 115426 |
rs550407765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446912 | TTTTTGTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 115426 |
rs550432818 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419737 | AAACATTTTGGGATT[G/T]ATTTATTTATTTGTT | 115426 |
rs550439900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466292 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 115426 |
rs550445955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482701 | TCGTGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 115426 |
rs550478002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499462 | ATTTACTGTGATCCA[A/G]TCCATCTGCTTTCTA | 115426 |
rs550479102 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471586 | TGATGAGGCTATCCA[C/G]GCAGCTTTTTTATTT | 115426 |
rs550483511 | snp | C/T | 8.61571e-05 | 0.00656286 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486807 | TTTTGAGACTCTCTT[C/T]AATTGTTTTATAGGT | 115426 |
rs550484196 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459231 | AAAAAGAAAGAAAGA[A/G]ACTGGAATCTTTCCT | 115426 |
rs550554879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433463 | CTCATTTTCAAGTTT[G/T]GTTTTCTTTTTAATA | 115426 |
rs550558506 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439045 | TATCTCCACTATTCC[G/T]TCAAAAATTACAGAT | 115426 |
rs550565055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432934 | CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 115426 |
rs550623449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444656 | GCTTAGGCTGGAGTA[A/C]AATGGCATAATCTCA | 115426 |
rs550628368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438369 | TAGATGACCTGTAAT[A/G]ACAGCATGTCATTTT | 115426 |
rs550630940 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425959 | TTACTTTTCATCTTT[G/T]GCCAGAGTTTAGAAG | 115426 |
rs550674666 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440938 | GATTCTAATCATTCC[C/T]TGTGATTCTATTTCA | 115426 |
rs550679172 | snp | C/G | 0.0134861 | 0.0810011 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413377 | CCGGTGGGCGCGCTC[C/G]CCCGCCTGCCGCTGA | 115426 |
rs550680211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481343 | GAACTTCAAATTTCT[A/G]TTCTCAGGGTTAGTG | 115426 |
rs550698332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418472 | GAATACCTGTAGTGT[C/T]TGAGATTGTGCTTGT | 115426 |
rs550719727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487152 | ATTATAAGGAAAACA[C/T]ATTCTCTATAGAGCT | 115426 |
rs550749022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455130 | TAGGAGCAGCAGCTT[G/T]TTTGTTTGTTTGTTT | 115426 |
rs550776094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498797 | CAGAGCATGGTTTGA[A/G]TTCATCTCCCATCAT | 115426 |
rs550791281 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423695 | TCACACCTGTAATCC[C/T]AACACTTTGGGAGGC | 115426 |
rs550812249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454612 | TAATATCTATTTAAT[C/G]GAAATGAGTTAGGTA | 115426 |
rs550859122 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420485 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCAA | 115426 |
rs550864781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477347 | CTGACCAACATGGAG[A/T]AACCCCATCTCTACT | 115426 |
rs550890384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428653 | CTTCTGGGCTTAAGC[A/G]ATCCTGCTGCCTCAG | 115426 |
rs550910219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423121 | ATTACTCAAGATTAT[C/T]CAAATGGAGATAATT | 115426 |
rs550927377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434367 | TATCTCTGGTTCTTA[A/G]GTGGTTTATTTTTTA | 115426 |
rs550970135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497548 | TTTTAAGGCTTATTT[C/T]GAGTTCCTAGGGGCA | 115426 |
rs550991564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464218 | TCTTTTCGTATTTTT[A/G]TTGACAAGTTGGATA | 115426 |
rs550993722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465164 | CCAAGAGAAAACATA[G/T]AAAATTTCATCAATA | 115426 |
rs551053129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485012 | TGGTCAGGCTGGTCT[C/T]AAACTCCCGACCTCA | 115426 |
rs551072546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470255 | GTGCACACCTGTAAC[C/G]CCAGCTATTTGTGAG | 115426 |
rs551100620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496166 | TCTATTTTTTTTAAC[A/T]TGAGCCTGCATAAAA | 115426 |
rs551133463 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412213 | TAAAATAAACCCACT[C/G]ACCCCCACCCCGACT | 115426 |
rs551139611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437783 | CCACCACACCTGGCT[A/G]ATGTTTGTATTTTTA | 115426 |
rs551152544 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477513 | CCTGGGTAACAAGAG[C/T]AAAACTCCATTTCAA | 115426 |
rs551263870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443878 | TCTTTGCTCCCAGCA[G/T]TCTTTAAGATTTCTG | 115426 |
rs551411950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452104 | TTTTTAAGTTCATAT[A/G]TCCTGGAGATCACTT | 115426 |
rs551444988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452704 | CTTACACTTCTAAGA[C/G]CATGAAGGGTTTTTC | 115426 |
rs551445792 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460326 | GCAAGCCATGAAGAG[A/G]TCCACATCTCCAAGG | 115426 |
rs551475549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451707 | CGATCTCCTGACCTC[G/T]TGATCCGCCTTTCTC | 115426 |
rs551482844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426992 | GACCTCAGGTGATCA[A/C]CTGCCTCGGCCTCCC | 115426 |
rs551522300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474969 | AAAGTATATAAAAAT[A/G]TATTGCTTACATAAA | 115426 |
rs551537356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446984 | AGCTCCGCCTCCCGG[A/G]TTCACGCCATTCTCT | 115426 |
rs551552767 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475105 | CTTTCATTTTAATTG[A/T]CAGAGTGCCATTTTA | 115426 |
rs551562627 | snp | C/G/T | 0.000185822 | 0.00963724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468656 | CCTGCTTTCACCTTT[C/G/T]GGCTTTGGTTGAATA | 115426 |
rs551610226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483698 | TTATCTTTTTTGTTT[A/G]TTTGTTTGGAGACAG | 115426 |
rs551618593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489374 | AAGCTACAGTAAATA[C/T]TTGTGAACAGGTTTT | 115426 |
rs551652433 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446195 | CTTGCTCTGTCACCA[C/G]GCTGAAGTGCAGTGG | 115426 |
rs551656071 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443389 | ATAACTGAGGTTTAA[A/G]GAAGTAACTTGCTCA | 115426 |
rs551669674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473785 | CAAAAATCAGATGGC[A/G]TAACTAAGTTCTAAT | 115426 |
rs551674558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426416 | CCATTTAGGAGCACA[C/T]TGGAATCTAGTAATA | 115426 |
rs551684345 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485415 | AGGTTGTTTTCCTGA[A/G]CATCTAGTGAGATGG | 115426 |
rs551748449 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506765 | CAAGTTGACTACTAA[C/T]GACTAATGAGAACAA | 115426 |
rs551757584 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435564 | AAATCTCATACTGAT[A/T]ATCAGTCACTCCCCA | 115426 |
rs551823332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435139 | GCTAGCATTAGAGGC[A/G]CGCACCACCACGCCT | 115426 |
rs551874855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430209 | GAGACAGGGTTTCGC[A/C]ATGTTTGCCGGGCTG | 115426 |
rs551879557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489134 | CCTGTAATTTTCTCA[C/G]TTCAAGAATTTTTAT | 115426 |
rs551881581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436491 | TTAAGTTCTTGAGAT[C/T]TGTTGTGGAAAGGGG | 115426 |
rs551973491 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507336 | CTGTCACCTGGGTTC[A/G]CGCCATTCTCCCACC | 115426 |
rs551975239 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452623 | CATTAAACAGTCATT[A/C]ACAGGTTATCGTAAA | 115426 |
rs551989797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469313 | TCATGAGGTCAGGAG[A/G]TCAAGACTATCCTGG | 115426 |
rs552004539 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412748 | CTTTCCTGTTGAGCG[C/T]GGTGGAGCGCACACA | 115426 |
rs552013660 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429087 | GGAGAATTGCTTGTA[A/C]CTGGGAGGCAGAGGT | 115426 |
rs552041619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456236 | CGCCATTCTAACTGG[C/T]GTGATATGGTATCTC | 115426 |
rs552054543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488702 | AGATGGGGTTTCTCC[A/G]TATTGGCCAGGCTAG | 115426 |
rs552067988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428098 | TTAGCTGAGCATGTG[A/G]CACTGTTAAACTTCT | 115426 |
rs552114550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418688 | TCTGGGAAAGTGATA[A/G]TTGTGGCCTGAAAGG | 115426 |
rs552120397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493092 | CACTTGAGACCGGGA[C/G]TTGGAGACCAACATG | 115426 |
rs552129411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505750 | CCAGAAGATTAGGCT[A/C]GTGGCAACCATATGT | 115426 |
rs552159240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499325 | TTCAAATCTAACTCT[G/T]AGCTGGTGGAGGATT | 115426 |
rs552167592 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423953 | CAGTATCAAAAAAAA[A/T]AAATAAATAAATAAA | 115426 |
rs552189418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461393 | TCCTTCTCTCCTCCC[C/T]CCCGCCCCTTGTTCT | 115426 |
rs552208073 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424641 | AAGTTAGTGTGGTGT[A/G]TTTGTTGAAATTAAT | 115426 |
rs552216263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425156 | GAAGTTAATGTACTT[C/T]ACTGCCTTGAGGGCA | 115426 |
rs552300821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472710 | AGCTATATTATAACT[A/G]AAACGTAGAAGGGAA | 115426 |
rs552315289 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472293 | GGGTTTAGGAAATTT[A/G]TCTTATGAAAATAAG | 115426 |
rs552333440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440484 | GACATGGTACATATA[A/G]TTGATAATAGCCAAC | 115426 |
rs552362925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425561 | GGAGTTTGAGATCAG[C/G]CTGGTGAACATGGTG | 115426 |
rs552407090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494496 | TTACAAAAGAGCCAC[C/G]GTGTGCTGATCTTTA | 115426 |
rs552412642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466267 | TTATGGCCAGGTGTG[C/G]TGGCTCACGCCTGTA | 115426 |
rs552416431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429169 | GACTCTGTCTCAGGA[A/G]AAAAAAAAAAAGGAA | 115426 |
rs552433251 | snp | A/G | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500563 | CTAGATGACTGTCCA[A/G]GTGCCTCCAAAGTGT | 115426 |
rs552439611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413773 | GCTGCGGGTGGGCAG[C/T]CCCCGCGAGGCGCGG | 115426 |
rs552511957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487226 | ATGGAGTCTCGCTAT[A/G]TCACCTGGGCTGGAG | 115426 |
rs552523982 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475807 | TTTTGATACAGGCAT[A/G]CAGTGTGTAAATGAT | 115426 |
rs552533726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445856 | GGCATTAGCCACTGG[C/T]CCTAGCTCTTTCTTC | 115426 |
rs552584702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482679 | TCAGCTCACTGCAAG[C/G]TCTGCCTCGTGGGTT | 115426 |
rs552622923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487579 | ACCACGATGGCCAGG[C/G]TGGTCTCGAACTCCT | 115426 |
rs552631579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460431 | CAACATGAAGTAATA[A/C]CACCTGCTATTTAAG | 115426 |
rs552631711 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455287 | ATGCTATCCCTCCCC[A/C/G]CTCTCTCCACCCCAC | 115426 |
rs552640595 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475234 | CTATGGACTTTTCCT[A/C/G]CTATTGAAAACAATA | 115426 |
rs552694764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460194 | ATTATAACAGTAATA[C/T]GTGACTGAATAGATA | 115426 |
rs552738619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422741 | GGCCTCCCAAAGTGC[C/T]GGGATACAGGCGTGA | 115426 |
rs552756274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477427 | GCTACTCGAGAAGCT[G/T]AGGCGGGAGAATCGC | 115426 |
rs552841438 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411960 | ATCCCAGCACTTTGG[A/T]AGGCCGAGGCGGGTG | 115426 |
rs552883388 | snp | A/C/T | 3.66718e-05 | 0.00428192 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413450 | CGGCGCCCAGAGCTC[A/C/T]GGGGGAGACAAAGGG | 115426 |
rs552883815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470032 | TTTTCATTAGAAGCA[A/G]TTTAAGCTAGGAGAC | 115426 |
rs552913970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432661 | CTGATATTTAACTTA[C/T]TTCTCCCACGAGGTA | 115426 |
rs552918006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455615 | CTTGAGGAGCAGCAG[C/G]TCTTAATTTTATAGA | 115426 |
rs553027781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470531 | GGGAGGAATGAGATT[C/T]CCGATGGAACATCGA | 115426 |
rs553092983 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431832 | CCTCGTGTTCCTTAG[C/T]AAGGTTGATGATATA | 115426 |
rs553115073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479984 | GCCTGAATTAGATCA[C/T]TCATCTGTTTGAAAC | 115426 |
rs553167042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459338 | TTGATGAACTTGTAC[A/G]AAGATCAGAAAGAGG | 115426 |
rs553189144 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469498 | ACTTCAGCCTGGCGA[C/T]AGAGCGAGACTCTGT | 115426 |
rs553253897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458197 | ACTTGTTATTGGTCT[A/G]TTTAGGGATTCGACT | 115426 |
rs553256712 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485639 | CCAAATTATTGTGCA[A/C]GCTTGAATTCAGTTT | 115426 |
rs553312479 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498742 | TGCATTAATCCCTTC[A/C]CTGCCTGTATACCCT | 115426 |
rs553317872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453444 | TATCTGAAATAGAAC[A/T]GGTTTCTGTCTTACA | 115426 |
rs553364555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420526 | GCAAACACGGTGAAA[C/T]CCCGTCTCTACTAAA | 115426 |
rs553396793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431476 | AGGTGTGGTGGCATA[C/T]ACCTGTAGTCCTAGC | 115426 |
rs553414312 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469347 | ACATAGTGAAACCCC[A/G]TCTCTACTGAAAATA | 115426 |
rs553420269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502189 | AACTCCTTCCAAAGG[A/C]CCTGTGATCAGCAGC | 115426 |
rs553468332 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469062 | GGGAATAGACCCATA[C/G]GTGATCTTGATAATT | 115426 |
rs553492491 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411424 | ACTCTATCGCCCAGG[A/C]TGTAGTGCAGTGGCG | 115426 |
rs553501331 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457393 | GTTGCTTATCACCTT[A/G]AGGAGATTTTGGGCT | 115426 |
rs553526013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436878 | TGATGGAATTAAATG[C/T]TTCAATGCTGGCAAC | 115426 |
rs553532921 | in-del | -/TTG | 4.44346e-05 | 0.00471331 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499972 | AATAATAACATACTT[-/TTG]TTGTTGTTGTTGTTG | 115426 |
rs553535618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485190 | ATTTTGGTTGAACCA[G/T]TATTCAGAGTTTAGG | 115426 |
rs553555310 | snp | A/G | | | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6465762 | CAAAGGAAGAAGCAA[A/G]TAGAGGACATGATTT | 115426 |
rs553556111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448138 | TCCAGATTGGAATTT[G/T]ACAGAGGCTCTAGAA | 115426 |
rs553565392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416969 | AAAAAAGTTGCCTCT[C/T]CCACTTGGTTTTCAC | 115426 |
rs553575751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451520 | GTCTCGCTGTCGCCC[A/T]GGTTGGAGTGCAGTG | 115426 |
rs553585650 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434759 | TAGGTATTTTGATAT[A/G]TATTTTAACAGTATT | 115426 |
rs553588253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456276 | TTGATGTGCGTTTCT[C/G]TAATGACCAGTGATG | 115426 |
rs553591265 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479831 | CAATAGATTTTGACA[G/T]TTCTTAATATTTCTC | 115426 |
rs553627731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416574 | TTGAGACGGAGTCTC[C/G]TTCTGTCGCCCAGGC | 115426 |
rs553628001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488396 | TATCAGAACCAGGAT[A/G]TTGACACTATACAGT | 115426 |
rs553646045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444890 | TACAGGCATGAGCCA[C/T]CAAGTCCAGCCTAGG | 115426 |
rs553680246 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415006 | TCAAGTGGCTGATAC[A/C/G]GTTTCCTTTTGATCA | 115426 |
rs553695714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473614 | TACCAAGAAAATGAA[C/G]CTAAATCTGATTGAG | 115426 |
rs553722360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436483 | AGAATGTTTTAAGTT[C/T]TTGAGATTTGTTGTG | 115426 |
rs553730685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492919 | AAATTTCTTCTTAAT[A/G]GGAGGCTATTATTTT | 115426 |
rs553743059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504897 | TGTGTCATTTGAGAT[A/G]TTCTATCATGTTTGG | 115426 |
rs553751710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488856 | CTCACTCTGTCTTCC[A/T]GGCTACAGGGCAGTG | 115426 |
rs553798790 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506405 | TAGTTTTAATGAGTA[A/G]AAAGTCAAAGCCTCA | 115426 |
rs553816644 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477130 | CCCAGCTATTCCGGA[C/G]GCTGAGGCAGGAGAA | 115426 |
rs553928912 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507112 | TTATCAGTTTTAAAG[G/T]ATCCTATATTTCTGG | 115426 |
rs553960314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473935 | AACACTGTGAGAAAC[A/G]CTATAGGACAAATGG | 115426 |
rs553963674 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500233 | TCAGCCTCCTAAAGT[A/G]CTGGGATTACAGGCA | 115426 |
rs553988594 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449893 | GCATGCCCTGTGTGA[-/CT]CTACTAGGAGATGAC | 115426 |
rs554053623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447129 | CTCCTGACCTCATGA[A/T]CTGCCCGCTTCTGCC | 115426 |
rs554132690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430004 | GGACAGGGGAAACTT[C/T]TTGTCTAAATGTGGC | 115426 |
rs554154461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484036 | ACTTTAAAATTTTAG[A/T]TGTCTCCTATGCATT | 115426 |
rs554239472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465497 | ATCAGAGGACTATTC[A/G]TGTTTTCTATTTCTT | 115426 |
rs554254647 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422941 | TTTGGCTTTTGTAAC[C/G]AGCAACCTTTTCAAA | 115426 |
rs554256217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450967 | GAACTAGGAAATAAT[A/G]CTTAAATATACCATG | 115426 |
rs554265852 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420012 | CCTTGACTTCCCAAA[A/G]TGTTGGGATTACAGA | 115426 |
rs554305101 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453503 | GAATTTACAACTGTG[A/G]AATTAGAAAAGCATT | 115426 |
rs554340990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433794 | TTATTAACCACTTTA[A/C]ACATGAGTAGCTGCA | 115426 |
rs554345886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430320 | TGGCCCTTAATGTGG[C/G]TATATCTTTGATGTG | 115426 |
rs554364014 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487319 | TCAGCCTCCCAAGTA[G/T]GTGAGATTTCAGGCG | 115426 |
rs554400256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471257 | AAGCTTCAAGACCTG[C/T]GTAGTATCAGTGGCT | 115426 |
rs554409613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435732 | CTACCTCAGCCTCCT[C/G]AGTAGCTGGGGGCTA | 115426 |
rs554418432 | snp | A/C | 0.000189333 | 0.00972783 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413605 | GCGCTGTTCGACGTG[A/C]GGCCCGAATGCCAGC | 115426 |
rs554444303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467754 | TTTAACTTAAATACT[C/G]TGCTTGAGCCTTTTT | 115426 |
rs554526954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492772 | AGTACTGAATCAGAT[A/G]GAGACAATAATATCC | 115426 |
rs554558871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434500 | GGAGTGCTGAATGGC[A/G]CAATCTCGCCTCACT | 115426 |
rs554604315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429273 | TGTGTATCTCTTGAG[C/T]AAATGTATTTCATGT | 115426 |
rs554616330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428935 | TTGGGAGGTGGAGGA[C/T]AAGTGGATCACTTGA | 115426 |
rs554620781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417503 | CTTTCATTAAATGTG[C/G]AAGAACTTCGGTACT | 115426 |
rs554637403 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504303 | GTGCTGGGATTACAG[C/G]CGTGAGCCACCGCGC | 115426 |
rs554664307 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471172 | TTCACAAACTCATGG[A/G]CAGCATCTACAATGA | 115426 |
rs554696099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454238 | AAGCTAAATTGGGAA[A/T]CTAAACCTAGGCAGA | 115426 |
rs554701681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419396 | TTGATAATTGCAGAT[C/T]GATAGAATTAGAGAA | 115426 |
rs554714896 | in-del | -/GGC | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484360 | GATTATAGGCTTAGT[-/GGC]GGCGGCGGTGGTGGC | 115426 |
rs554724574 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497588 | TAAGGTTTTTTTTTT[A/T]AAAATGTAAGTGTAT | 115426 |
rs554732215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487685 | TTTTGTATTTTTAGT[A/G]GAGCTGGGGTTTCGC | 115426 |
rs554759493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459292 | AATATGCCAGGTTCA[C/T]GTTCTTATAAGTACT | 115426 |
rs554768943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493269 | TGCCACCGCACTCCA[C/G]CCTGGGTGACAGAGC | 115426 |
rs554779953 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455813 | ACATGGTGAGACCCT[C/G]TCTCCACAAAAAGTT | 115426 |
rs554789155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444701 | CCCCCTCCAGGGTTC[A/G]AGTGATGTCTCCTGC | 115426 |
rs554795399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444310 | GTCTATGACTTGTAG[A/G]CTCCTGAGTGGATGG | 115426 |
rs554838127 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451307 | TTTCGTTCATTATGC[-/T]TTTGGTTTTTAGGGA | 115426 |
rs554922377 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453830 | GAATCGCTTGGACCC[A/G]GGAGGCGGAGGTTAC | 115426 |
rs554939032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424045 | TATTCCCTTTAAAGA[C/T]GAGCTAGACAAGGAA | 115426 |
rs554962517 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417119 | GCCCTTCACTGGCAT[C/G]CCTAGTCAGTAGTTG | 115426 |
rs554993167 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495783 | CCAGAAGTGAGTTGA[A/C]AGTGCCAGTTAGTGG | 115426 |
rs555002342 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412643 | CGCGCGAAAGTAGCA[C/T]TGCGGCCAGGCGGGA | 115426 |
rs555013083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479784 | CTAAACTTCATCCCA[A/G]TTCTTCTTTTGTTCT | 115426 |
rs555025636 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411371 | CTCTTCTGTGTTGGG[C/T]CATCTTTTTTTTCTC | 115426 |
rs555050269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458825 | ACCAACCCAAATGCC[C/T]GTCGATGATAGACTG | 115426 |
rs555092079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485119 | TTTCTGTGGAAGATG[A/T]AACATTTAGTTTAAT | 115426 |
rs555103589 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473414 | AACTAGTTTAGTGAG[G/T]TCATTTCTCTGTAAA | 115426 |
rs555120192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464500 | TTCTATGTCTTTCTT[A/G]AAGATACTCTTGTAT | 115426 |
rs555139185 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503193 | CTAGAGACGGTTTTG[G/T]CCATGTTGGCCAGGT | 115426 |
rs555175991 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502642 | ACTCTGCTGTAGGAA[C/G/T]GTAAGTTCCAGGAGA | 115426 |
rs555190519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452752 | CCAGCAGATTATGGG[A/G]TAGGGGGATTCCATT | 115426 |
rs555211366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416367 | GCTACCGTGCCCAGC[C/T]TTGACTCCACATTTG | 115426 |
rs555223782 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413047 | CTTTTGGTAGCCCCG[C/T]CCCTCCGACCCGCCC | 115426 |
rs555229387 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463080 | TGAGGTCAGGAGATC[A/G]AGACCAGTCTGACCA | 115426 |
rs555251387 | in-del | -/AAAA | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423944 | GTGAGACTCAGTATC[-/AAAA]AAAAAAAATAAATAA | 115426 |
rs555275869 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416037 | GGTGAAGTTGGAGAA[A/G]GCAGTGTTAATTGAC | 115426 |
rs555284786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432568 | CAGAGCCTTTGTTTC[C/T]GTATTTTGTAAAATA | 115426 |
rs555298824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468880 | TGACTCAGCATAGAT[C/G]CTGATTAAATGTTAA | 115426 |
rs555309527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462270 | CTAGCCTGCAAAGCC[A/G]AAACTACTTACTTTC | 115426 |
rs555323057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497094 | AGAATCATAGAATCT[G/T]AACCATCAGGTAAGG | 115426 |
rs555351269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480905 | TGCTCTAAAAGCTAC[A/G]TAGAATAGATAATTG | 115426 |
rs555351302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486750 | GGTACCAAGAATATA[C/T]ATGAAAGCATTTTGT | 115426 |
rs555408952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475201 | TTCTCATATTACACT[A/G]TGAATGTTAACTAAT | 115426 |
rs555435841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468361 | TGCAGGTAGGGTGGG[A/G]CAGCTGGCAGTAGAT | 115426 |
rs555458595 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461359 | TCTCTCTCTCCCCCC[A/C]CTCCTCCTCTCCCCC | 115426 |
rs555484564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436791 | GTCAGTTAGAATGAA[C/T]GTTAAGTAAAGGGGA | 115426 |
rs555511323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500990 | AGTTTGTGAAACATC[A/G]TCATTTTAATCTAAA | 115426 |
rs555522467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447566 | TGGAGTGTAGAAAGC[A/C]TATAGTGAGTAAGAA | 115426 |
rs555528928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489802 | TTCATGGATTGTTAC[A/G]AAGATGAATCAATAT | 115426 |
rs555559021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463720 | AGGCTATCTGCCTGC[C/G]TCAGTCTCCCAAAGT | 115426 |
rs555565556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489437 | AATGCCCCAGAAGTG[C/T]AATTCCTGGGTCATA | 115426 |
rs555609974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432075 | TGTCAGTGATTAGTA[A/T]GGGAGAAATGAGCCT | 115426 |
rs555741646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449421 | TCAAAATGATAGACC[A/G]GCATCATGGTCTAAG | 115426 |
rs555757075 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455704 | AAAGTGAAGAACCTG[A/G]CTCAGCATGATTGCT | 115426 |
rs555760420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425207 | TTAAAATTACTCAAC[A/C]TGGGAGGTGTATTTA | 115426 |
rs555774721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451114 | GATTTGCTTTATCCT[A/G]CTCACGGTAGTTTCA | 115426 |
rs555790663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456946 | TCAGGTAGCATGATG[A/C]CACCAGCTTTGTTCT | 115426 |
rs555793699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431319 | TAGTAGGATAATCCT[A/T]TTTTTTGGCCAGGCA | 115426 |
rs555804525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436351 | ATTATCTGAGTATTT[A/G]GATCTGAGATTGGCC | 115426 |
rs555808118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431056 | TTACCATGGCAGGAT[C/T]TTCTGTGTTCATATT | 115426 |
rs555826371 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506961 | TGTGCTGACCTTTGA[C/G]AGGATTTGAAATTGC | 115426 |
rs555844362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482877 | GGCATGAGCCACTGC[A/G]CCCGGCCTGGCTTTA | 115426 |
rs555862182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473480 | AGAATGGGAATATCA[A/C]CATTTTCTAATCCCC | 115426 |
rs555863329 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506141 | ATTCTGCAGACTCTA[C/T]TTGACCTTTTCTTCC | 115426 |
rs555891873 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432164 | GTTTGTCCTACCCAG[C/T]ATGGTTGGCTCTTAG | 115426 |
rs555909674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473088 | TCCCACTGAAAGAAA[C/G]TCCTGGCTGGGGGCA | 115426 |
rs555923162 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421277 | ATCATAACTTTTAAA[-/AGT]AGTCTTTTAAAAATT | 115426 |
rs555960313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452391 | AGAGGGGAAAATACC[A/G]CTTTGTATTTGTCAG | 115426 |
rs555980075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456055 | GGTCAGGTTAGGTTT[A/G]TAATACTTACTATTA | 115426 |
rs555983480 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447050 | CCTGCTACCACACCC[G/T]GCTAATTTTTTTGTA | 115426 |
rs555997536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451767 | TGAGCCACCGCGCCC[C/G]GCCTGTTTGTTGTTG | 115426 |
rs556019008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424704 | CTCTTTTTGTTCCAG[A/G]ATCCCACTAGGATAC | 115426 |
rs556019762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457605 | TCCAAGGGAATTCTT[C/T]CAGTTTTTGCCCATT | 115426 |
rs556020288 | snp | C/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461268 | GAATGCAAAATGTCA[C/G/T]CTGAATCAAATCCTT | 115426 |
rs556046129 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469831 | GGAATTCCTAAAGAA[G/T]AGAGTAGAGTGAAAA | 115426 |
rs556072232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435853 | ACCTCAAGTGATCCA[C/T]CCACCTTGGCCTCCC | 115426 |
rs556079465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420103 | CCTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCG | 115426 |
rs556094453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478475 | TATTTAATCCTGTGA[C/T]GTTGATACATTGAAG | 115426 |
rs556129155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426477 | AATAAATTTAGAGCT[G/T]TTTAATCTTAGTTGA | 115426 |
rs556158643 | snp | C/T | 6.7314e-05 | 0.00580108 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413521 | CGCACCATTGATGGC[C/T]CCAAGACGTGCACCA | 115426 |
rs556185709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500108 | CTCTGAAGTAGCCCA[C/T]GGCTGTACACCACCA | 115426 |
rs556218596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461577 | GGGGTTTCACCATGT[G/T]GGCCAGGCTGGTCTC | 115426 |
rs556250200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477051 | CAGTCTGGCCAACCT[A/G]GTGAAACCCTGTCTC | 115426 |
rs556256974 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493341 | GGTAAATTTGCTTTT[G/T]TAGTACTTATTTATT | 115426 |
rs556266266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440156 | AGAGACCCTGAAGCT[A/G]TTGTTGAAGAGTCAG | 115426 |
rs556286757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482291 | AATTGGGCATTAGCT[A/G]TGCATTTTCATCACT | 115426 |
rs556294397 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479095 | GAATCTCTTGAATTT[A/T]CAAAATACACACAAA | 115426 |
rs556312176 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467699 | TCTTTCAAAGATTTG[A/T]ATTTGCTTGTTTACT | 115426 |
rs556332001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445519 | ACCTGCCTCGGCCTC[A/C]CAAAGTTCTGGAATT | 115426 |
rs556346788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429522 | TTAGTAGAGATGGGG[A/G]TTTTAGCCATGTTGG | 115426 |
rs556401793 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483781 | CACAACCTCTACCTC[C/T]CGGGTTCAAGCAATT | 115426 |
rs556433601 | in-del | -/A | 0.115788 | 0.21092 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503408 | TTTTCCTTCTAGCTT[-/A]AAAAAAAAAAACCAG | 115426 |
rs556437543 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438333 | CACTGCAAAGAGAAT[A/C]TATGAAGTTAGTAAT | 115426 |
rs556493141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471121 | TCCCCTTAAATGTCC[C/T]GGTAATATAGAGCAA | 115426 |
rs556542971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483359 | AAAATCCTTTATACA[A/G]TGGTGCAGTATTTTC | 115426 |
rs556578365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444868 | CGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 115426 |
rs556583936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445921 | TAAAACTTTTTGCTT[C/T]TCATTTACTAATTAA | 115426 |
rs556597066 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418676 | ATTGATTATGTTTCT[G/T]GGAAAGTGATAGTTG | 115426 |
rs556629166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470577 | TAAGAGCAGGGAAAG[G/T]GTAAATGTATGAGTA | 115426 |
rs556650078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418757 | GCCAACTGAACTTTA[C/T]AAAGAAACAAAATGG | 115426 |
rs556669856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475860 | TCATCACCTCAAACA[G/T]TCTATCATTTTTTGT | 115426 |
rs556675102 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453703 | GGGTCAGGAGATTGA[A/G]ACCATCCTGGCTAAC | 115426 |
rs556681975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503909 | AACTTTTCCTACCCA[A/G]TACTCTGATTTAAAA | 115426 |
rs556714206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450048 | ATAGCTTCATGCTAT[A/G]ATGTGTAGAGGAGTC | 115426 |
rs556722972 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486901 | TTATTCTCTTGTACT[A/G]GCTGGTGGATTTGCG | 115426 |
rs556741330 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431679 | TATGTGTTGATGTTC[A/G]AGCAATGGCAGTATT | 115426 |
rs556760162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491947 | TATGTCACCCAGGCT[G/T]GTCTTGAACTCCTGG | 115426 |
rs556769597 | snp | A/C | | | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475433 | CAAGATAATATCTGT[A/C]GATGAAATCTTCAAG | 115426 |
rs556788931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504406 | GGGATACATGTGAAA[C/T]TTTGATATGTTCATA | 115426 |
rs556834871 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422414 | TCTCCTATCTCCCCA[A/G]TTTCTTTCCTCTTTC | 115426 |
rs556834976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418291 | TTTAAATCAAGGAAG[C/T]AATATTCCCATCCCT | 115426 |
rs556844372 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477453 | ATCGCTTGAACCCGG[C/G]AGGCAGAGGCTGCAG | 115426 |
rs556870793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464807 | CACTTTCATAATACA[A/G]CAGAGCACATGATCC | 115426 |
rs556889608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466714 | ATACTTAATATGCAT[A/G]TCAAGTTGTAAGTCA | 115426 |
rs556915994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497711 | AAAGCAGCACATCAT[A/T]GTAATAGATTTTCAT | 115426 |
rs556937353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498357 | GCCCTGGGACCAAGG[G/T]TTGTGCTTGGGAAAA | 115426 |
rs556952884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503381 | TTATCTTTATGACTA[C/G]GAAAAAAACTAGTTT | 115426 |
rs556972400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452884 | GTCACTGTATATTTT[A/G]AAATATGTGTAGCTG | 115426 |
rs556989687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428529 | TGGAACCATATTGCT[C/T]TTGCTTTTTTTTTTT | 115426 |
rs556990623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465388 | GTTTTGTGTCCTTGT[C/G]TTGAATGTTTGGTAG | 115426 |
rs557038339 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466810 | CTTGGGGCCTTTGTA[C/T]TTGATGTTCCCTCCT | 115426 |
rs557038781 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419192 | GGACGCAACTTAGCT[C/T]GTAACAGTAGGTTTT | 115426 |
rs557071599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421982 | TTTATTAACATACCG[C/T]GGTATATTTAATCCA | 115426 |
rs557073347 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444812 | TTCACCATGTTGGCC[A/G]GGCTGGTCTTGAACC | 115426 |
rs557074519 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423988 | CTCTTGATAAGAGGA[A/C]TAGACAGAATAGGTT | 115426 |
rs557082146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427854 | ATTGTACAGAGGCTG[C/G]GTCCATCCATTCACA | 115426 |
rs557099315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475326 | CCAAACTGGCTTTTA[A/T]TTATTATTTGTATAT | 115426 |
rs557110734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458677 | CTCAAGGACCTAGAA[C/G]CAGAAATACCATTTG | 115426 |
rs557181243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449191 | GTGCAGTTAGCTGAT[A/C]GTCTTCAACTACAGC | 115426 |
rs557195182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448650 | AGTGAACTGTATTTG[A/G]TGGATGTTAAGAGTA | 115426 |
rs557274156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486160 | AGTTGAAAGTCAAAA[A/G]CAGAATTATTTTTAA | 115426 |
rs557387794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416734 | TTAGTAGAGACGGGG[G/T]TTCACCGTGGTCTCG | 115426 |
rs557405961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489978 | TGCATTCTTCTTTAG[A/C]ATCCATATTTTGAAG | 115426 |
rs557442716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496416 | GTTCTCCCAAGAGTA[A/G]GGTCTTCTAACATCT | 115426 |
rs557444093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463225 | GGCGCAGATTGCCGT[G/T]AGCTGAGGTCATGCC | 115426 |
rs557463850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415066 | CATTTTATTTTCTAG[C/G]TGGGGACAAATAGTA | 115426 |
rs557482025 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416311 | GACCTCAGGTGATGC[A/G]CCCACCTCGGCTTCC | 115426 |
rs557513658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438069 | AGGACTCAAAATGTA[A/C]AACTACAGTGAAGAG | 115426 |
rs557525913 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439672 | CCTAATCAGTACTCA[-/G]GGAGAACTTTGACAG | 115426 |
rs557527779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447178 | ACAGGCATGAGCCAC[C/T]GCGCCCAGCCAGCAC | 115426 |
rs557546024 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435140 | CTAGCATTAGAGGCG[C/T]GCACCACCACGCCTG | 115426 |
rs557578838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420469 | GCACTTTGGGAGGTC[A/G]AGGTGGGTGGATCAC | 115426 |
rs557600837 | snp | C/G | 0.000131813 | 0.00811721 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421036 | AGGCTAAACCCTGTT[C/G]TAATAGTCCACCTAA | 115426 |
rs557610688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483877 | TATTTTTAGTAGAGA[C/T]AGGGTTTCTCCATGT | 115426 |
rs557617459 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490046 | TTATATAGTTTATTA[C/T]AGTCAGCTCTTGGAA | 115426 |
rs557642340 | in-del | -/GTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442481 | TGTTTTGTTTTGTTT[-/GTTT]TGTTTTGTTTTTGAG | 115426 |
rs557691524 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463598 | GCCGCAGCCACCGGA[A/G]TAGCTGGAACTACAG | 115426 |
rs557705209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479431 | TCTTGTTGGGTTCCC[A/G]TCACCTACCAGATTT | 115426 |
rs557719546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442698 | GGTCTCACTTTGTTG[C/T]CCAGGCTGGTCTCGA | 115426 |
rs557735579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484100 | TTTTAAGAGACAGGG[G/T]CTTGCTCTATCACCC | 115426 |
rs557740065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443022 | AGGTCTCGGGTTATA[A/C]CTTTTAGCTGATTTC | 115426 |
rs557782550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447521 | AAGAAGCAGAAAATA[C/T]GGGGCTACCTGAGAG | 115426 |
rs557820639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472908 | TAAAAAGTAAATATC[C/G]TTTAGCCCTGAATTT | 115426 |
rs557848286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430365 | TTAAGTGTAGAATTA[C/T]GTGGTTGGCTTAAAC | 115426 |
rs557893264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505425 | CTCAGCCTGTGGAGT[A/G]GCTGGGAGTACAAGC | 115426 |
rs557905386 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473489 | ATATCAACATTTTCT[A/C]ATCCCCAAAGAATTA | 115426 |
rs557906802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488937 | CCTGGTGCAGCTTTC[C/T]GAGTAGCTGGGACTA | 115426 |
rs557908765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495632 | CAAAGTAACCTGGCC[A/G]TCTTTTATCAGGGCA | 115426 |
rs557926015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420591 | GCACCTGTAGTCCCA[A/G]CTACTTCAGGGAGGC | 115426 |
rs557936920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469638 | TACAAGAGTGTTAGA[C/T]ACATAGGACTTGATG | 115426 |
rs557945823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494806 | CCCTTAATTTCTGAT[G/T]ACTGTGTGATGTAAA | 115426 |
rs557970071 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438003 | GAATATTGTCCTCCA[G/T]CTCTCATGCCTTAAA | 115426 |
rs558003302 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423635 | TGAGTCATTAGTGAT[-/TT]TTTTTTTTTTTTTTT | 115426 |
rs558110621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451158 | TTCATATTGCAAACA[A/G]TAGGACTACTGAAAA | 115426 |
rs558114968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473988 | AGGAGGAAAGAGATG[C/G]CATGTGAATTTATAG | 115426 |
rs558146869 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461262 | AATTCAGAATGCAAA[A/G]TGTCACCTGAATCAA | 115426 |
rs558162248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436188 | CCACAAAACAGTATA[A/G]CAACACTTCAGTATT | 115426 |
rs558166741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455446 | TTCCAGCTTCATCCC[A/T]GTCCCTACAAAGGAC | 115426 |
rs558218594 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424739 | CTGTGTGTAGTTTTT[A/C]AATCTCCTTTGACAT | 115426 |
rs558237727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441243 | GCCACCTATGGTGGT[A/G]TGCACCTGTAGTCCC | 115426 |
rs558247475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446538 | CGTCTGCCTCAGCCC[C/T]GGTCTACATACTCTT | 115426 |
rs558293724 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477507 | CTCCAGCCTGGGTAA[A/C]AAGAGCAAAACTCCA | 115426 |
rs558299145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440822 | AGGAAGTTTTCAAAA[G/T]AATCGGTGCATGAGA | 115426 |
rs558334995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429432 | TTGTTTCTGTTTCTT[C/T]TAGACAGAGTCTTGC | 115426 |
rs558370804 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457172 | TTTGTTTGTGTCCTC[A/T]TTTTTTTCGTTGAGC | 115426 |
rs558426824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456852 | AGTTGAAGATGTGTG[A/G]CGTTATTTCTGAGAC | 115426 |
rs558441689 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468255 | TTGATAAGCCTTTAA[C/G]AAAAATGGTACATAA | 115426 |
rs558449077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455911 | ATTGCTTGAGCCTGG[G/T]AGGCCAAGGCTGCAG | 115426 |
rs558498104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446061 | GCAGTGGCATGATCT[C/T]GGCTCACTGCTGCCT | 115426 |
rs558528396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429880 | TTTCTGCAAAACAAA[C/T]GGTACCTAGCATATA | 115426 |
rs558533076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451041 | TTACAACTTAACCTC[G/T]GTGGTTTTATGTTTA | 115426 |
rs558563829 | snp | C/T | 0.124837 | 0.216412 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493296 | GAGCAAGACTCTGTT[C/T]AAAAAAAAAAAGTTA | 115426 |
rs558599600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492882 | TACTTTATACTACTT[C/T]TAGATTTTTCAAATT | 115426 |
rs558600638 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467596 | ATTCCGAGAGAATAG[-/T]TTTTTTTTTTTTTTT | 115426 |
rs558601460 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499720 | TTATGTAAAGTTTTT[C/T]AGTTTGGGGAACGTG | 115426 |
rs558617387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487747 | CCTCAGATGATCTGC[A/G]CACCTTGGCTTCCCA | 115426 |
rs558626718 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495155 | AATTTTGCTTGAAAG[A/G]AACTTCCTTCATAAC | 115426 |
rs558638483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499047 | AAAATAATTCTTTTT[A/G]ATATAAAAATAACTT | 115426 |
rs558639767 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413146 | CGGAGCCCGGCGTGG[A/G]TCTCGCGAGATCCGG | 115426 |
rs558644952 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414814 | AGGAGAGAGCTTTTT[C/T]TTCCCCTTTCCTTCT | 115426 |
rs558653257 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423432 | ATAGAATTATGGCTG[G/T]ATTTGCTGATTTAAC | 115426 |
rs558661254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417604 | GGAACTTGTTATTGC[C/G]GTAGATAAATGGTCA | 115426 |
rs558682318 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483230 | CTCAGGAGGCTGAGG[C/T]AGGGGAATTGCTTGA | 115426 |
rs558686773 | snp | A/G | 1.87848e-05 | 0.00306465 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486772 | GCATTTTGTAAATGT[A/G]TCTTAACTGTTCAGA | 115426 |
rs558707396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434553 | AAGTGATTCTCCTGC[C/G]TCAGCCTCCCAAGTA | 115426 |
rs558768734 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439958 | GTAAAAGAAAAAAGG[A/G]AGAAAACATCAAATT | 115426 |
rs558768829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497801 | CATAATCTTGTTACT[C/G]TATTAAATTTATAGC | 115426 |
rs558801042 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470797 | CTAAAAATAAAGGAT[A/T]TTTAACAAATTAACA | 115426 |
rs558801623 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452393 | AGGGGAAAATACCAC[G/T]TTGTATTTGTCAGCA | 115426 |
rs558808080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413951 | GGTGCCCAGGTCCCT[A/C]GCTTCCCGCGCTCGG | 115426 |
rs558813915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503954 | ATGGGATTTCTTTAT[A/G]TAACTTTGCTCTTCT | 115426 |
rs558835198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471772 | TGAAGGGGCTAGAGT[A/G]CTCTTTAAACTCTTT | 115426 |
rs558855135 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501795 | CTTATAGGAAATTAA[G/T]ATACAGGAAGCAGTT | 115426 |
rs558895959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474476 | TTTGGGAGGCCGAGG[C/T]GGGCAGGTCACCTGA | 115426 |
rs558913764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496603 | GTCATTAGCACAGGC[A/G]TTTGGATGCTTCAGG | 115426 |
rs558925842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419546 | TTAATGTGTTTTTTA[A/C]AAAAGTGAAACACTG | 115426 |
rs558933215 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412687 | AGCAGGAGGGCCCCC[A/G]GGGCCTTTCCCGGGC | 115426 |
rs558950880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502410 | ATAGATTCCTCAGAG[A/G]GATCTTCCCAAACTA | 115426 |
rs558963443 | in-del | -/TTTGATGTGAATGAA | 0.0142736 | 0.0832652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430327 | TAATGTGGCTATATC[-/TTTGATGTGAATGAA]TGCAGCTCTTAAGTG | 115426 |
rs558988126 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501928 | GGAAAAAGCCACCTG[A/T]GTGGTGTGAAAGTTG | 115426 |
rs558999405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449330 | ATGTTAATTTCACAC[C/T]TGAGCTTACCATTAG | 115426 |
rs558999753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449248 | AAGCAAAGCTATGCT[C/T]TTTCTTGGCCTCCCT | 115426 |
rs559050120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474704 | AGCGAGACTCCATCT[C/T]AATAAATAATACAAA | 115426 |
rs559081095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454782 | TCTACCTTTTTAATG[A/C]TGCCTCACTCTAGGA | 115426 |
rs559095194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454302 | AGGATTGATACAAGG[A/G]TCCAAAACCTTGTCA | 115426 |
rs559105696 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438447 | AAATAGGCTTTAAGT[A/G]CTTATAGGTTACCAT | 115426 |
rs559119342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417138 | AGTCAGTAGTTGCTT[A/G]GGAATGACTTCCCAC | 115426 |
rs559125843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422115 | GGAATAGAAGTGCTA[A/G]TTGTTCACCCACAGG | 115426 |
rs559125902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459497 | AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAT | 115426 |
rs559173740 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469733 | ATATGTGCATATATA[C/T]GTGTATATATATACA | 115426 |
rs559176971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496928 | TTCTAGTTGTTTTCT[A/G]TTATACGTGGCACAG | 115426 |
rs559191015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471414 | ACTCACCCTCATGTG[C/G]TTTTCAGCCATACTT | 115426 |
rs559193406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421717 | CCACCTCGCCCAGCC[C/T]TAAATACCTGTTTAA | 115426 |
rs559263116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485939 | GGCAGGAATGAAGAT[A/G]TGAGGGGAAAAGCCG | 115426 |
rs559284336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476897 | CACGCCCGGCCTCAG[G/T]CATTTATTCTTAAAA | 115426 |
rs559301896 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483965 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACTGC | 115426 |
rs559318429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476577 | GTCTTTTAATTCATG[A/T]TGGGGCTTTTTTTGT | 115426 |
rs559396283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456989 | TAGTCTTGGCTATAC[A/G]GGCTCTTTTTTAGTT | 115426 |
rs559446544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437453 | GGTCAGGCTGGTCTT[C/G]AACTCTGGACCTCAG | 115426 |
rs559522976 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479589 | TAGTTCTGAATTTAT[A/G]TCTTCATATCTAATT | 115426 |
rs559534807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448465 | CTAGAGCCAGGTGAT[C/T]AGTTTGAAAAACGTC | 115426 |
rs559551038 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490232 | CTGTAAAAAGAAGAA[A/G]TAGTATTTTATGTGG | 115426 |
rs559553939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453819 | CTGAGGCAGGAGAAT[C/T]GCTTGGACCCAGGAG | 115426 |
rs559558799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467375 | AATCTTCCCATTTCA[A/G]GGTTTTTTATATGCA | 115426 |
rs559597634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453080 | TTACCTTTTACAGAC[C/T]TAACTATGTATGTGT | 115426 |
rs559614133 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493610 | ATTTGGAGATGTTGA[A/G]AAGTATAATTTAAAG | 115426 |
rs559652147 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496047 | TTTGACCACAGCTAT[A/G]TAAGTTATTTTTTAA | 115426 |
rs559663748 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452074 | GAAACTACACATACC[A/G/T]TTTGCACCTTATTTT | 115426 |
rs559698103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458311 | TTCTCTGATGGTAGT[A/T]TGTATTTCTGTGGGA | 115426 |
rs559710185 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500228 | CTGCCTCAGCCTCCT[A/G]AAGTGCTGGGATTAC | 115426 |
rs559716434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489089 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCTCC | 115426 |
rs559741763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446701 | TATAGGAAAATTTGC[G/T]TGGTGTGGTGGTGCA | 115426 |
rs559743311 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464524 | CTTGTATTACCTTCT[A/G]AAAGCTTTGTGGTTT | 115426 |
rs559745915 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502533 | GCTCAGGCAATCCTC[A/C]CGCTTCAGCCTCCTA | 115426 |
rs559747690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441032 | CACTGCCTTAGTTCA[G/T]TGATTCTCAAAATAA | 115426 |
rs559752776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495088 | TCAAATTTGCAAAAG[G/T]ACTCTTTCAAGTTGT | 115426 |
rs559759858 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424615 | CACCTAGTTTTCCCT[C/G]TTAAGATCTTAAGTT | 115426 |
rs559771205 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487933 | ATAGTTGTAGATTCA[C/T]GTGTAGCATTAGAAA | 115426 |
rs559782645 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504966 | GGTCATTGCTCTTGT[C/G]TGTAATAGCTTATAT | 115426 |
rs559786534 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427757 | GTTTGATAACTGAGC[A/G]ATATTTAACCAGTTT | 115426 |
rs559795504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420700 | CGACAGAGTGAGACA[C/T]CGTCTCAAAAAAAAA | 115426 |
rs559802744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446237 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 115426 |
rs559805008 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470108 | GGGCGTGGTGGCTCA[C/T]GCCTATATAATCGCA | 115426 |
rs559807234 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462134 | CAAGCTTATAGCCCA[C/G]TAGCTGCCTATTTTT | 115426 |
rs559832547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415943 | AGCTTTACCTGAAAT[A/C]CTCACGCCAGACCTA | 115426 |
rs559849958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425983 | TTAGAAGCTGCTGCT[C/T]TTGAATTGATTGTTT | 115426 |
rs559858046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420344 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCCATTT | 115426 |
rs559858463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472641 | TAGAAACAGAACTAA[C/G]TGAACATAAAGGAGA | 115426 |
rs559901428 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467027 | TAGTTTCCTATTGCT[-/G]GCTACAACAAATTAC | 115426 |
rs560018193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442773 | TGGAAGTACAGGCCT[G/T]AGCCACTGTGCCTGG | 115426 |
rs560036688 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439687 | GGGAGAACTTTGACA[G/T]CAGAATTATTAAATT | 115426 |
rs560055068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421606 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTA | 115426 |
rs560064970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468457 | AATCAAAGAGAACCA[A/G]CTGCGGGTATGTCTC | 115426 |
rs560067102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431082 | ATATTAATCATACAG[G/T]CCTAAGTATTTTTCC | 115426 |
rs560076244 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442908 | ATGTACTGTCGGTCA[A/G]TCTTACAGTTCAGTT | 115426 |
rs560080359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442408 | AGAATAATCAATCCA[C/T]AAATTTTCAATCAGT | 115426 |
rs560087425 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499381 | GTAAAAGCTCCTGCC[C/G]CTAACTTTAGGAGAT | 115426 |
rs560107264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499298 | ATAAGGATGATAGAT[A/G]GAATGTATTACTTCA | 115426 |
rs560122844 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506269 | AAGAAATGGTGGACT[C/G]TATCTCTCACGTTCT | 115426 |
rs560143787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504472 | TCACTATAAACATCT[G/T]TTATGCTGGGAACAT | 115426 |
rs560157156 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495681 | GCTGAGTGGCAGATA[C/G]ATTAATGGAGGAGCT | 115426 |
rs560174858 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503269 | CCAGAGTACTGGGAT[C/T]ACATGTGTGAACCAC | 115426 |
rs560180591 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504194 | CCACGCCCAGATAAT[A/T]TTTTGTATTTTTAGT | 115426 |
rs560191094 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477755 | ATGTAATGTGGCTTA[C/T]CATATTTACTGTCTG | 115426 |
rs560259761 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485501 | GTTGATGAGGTGGGG[A/G]GATCAAATGGTACCT | 115426 |
rs560306561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468002 | AGTCTTTTTTTCTTA[C/T]TTGAAATTACATAAT | 115426 |
rs560315812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424872 | ATTCATTTGTTTTCC[G/T]TATTTGTCTGGGTTT | 115426 |
rs560323746 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448244 | TAAATTAATGATAGG[C/T]ACATAGTAACAACCA | 115426 |
rs560325656 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429162 | AGAGCAAGACTCTGT[C/T]TCAGGAAAAAAAAAA | 115426 |
rs560326045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419149 | TGAGGTACTGGGGGT[C/T]AGGACTTTAACAAAA | 115426 |
rs560335759 | snp | A/T | 0.000173753 | 0.00931913 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434208 | AGGACTTTATTCATA[A/T]TTTCATTTGTAGAAA | 115426 |
rs560346585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435944 | TAGGATGGAAGTGGT[A/T]TTAAGAACTTGTCTT | 115426 |
rs560377935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424238 | AAGTGGCTATCTTCA[A/G]AGTTAACATTGAGCT | 115426 |
rs560430263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471496 | CCACTTCAAGATGAG[G/T]TTTTAAAAAGATACC | 115426 |
rs560459569 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430409 | TTTAGTTCAACTCCT[A/C]TCCTCCCCATATTAA | 115426 |
rs560493305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466212 | TCGAGACCAGCCTGG[C/T]CAGCAGGGTGAAACC | 115426 |
rs560520799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413732 | GAGGGCTCTGTGCGC[C/G]GCGCGCGCAGGGCTC | 115426 |
rs560522525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440271 | TTTTAGAGAATGTTG[C/T]CTTATGTGCCGGACT | 115426 |
rs560542970 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486427 | ACTAGGTAGGCAACA[C/G]GGCCACTATCCAAGA | 115426 |
rs560572598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434846 | TGTATGTTTTGGGGG[A/G]TGGGGACCGGGTCCC | 115426 |
rs560577276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493079 | AAGGCGGGTGGATCA[C/T]TTGAGACCGGGAGTT | 115426 |
rs560582348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439487 | TCGATTGTCAGCCTT[A/C]AGGCCTACGTTAAGC | 115426 |
rs560601138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455565 | TGGGTTGGTTCCAAG[A/T]CTTTGCTATTGTGAA | 115426 |
rs560620628 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450026 | CTGTATTAACTCAGC[C/G]ATGGGTATAGCTTCA | 115426 |
rs560683705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464946 | GATCTTGGACTCAGT[A/G]GCTTTACTAGATTTA | 115426 |
rs560683826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477175 | GAGGCAGGGGCTGCA[A/G]TGAGCTAAGATTGGC | 115426 |
rs560689002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454450 | TCATGGACTTAAGGC[A/G]TAGAATGAGTTCCAA | 115426 |
rs560709677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417794 | CTTACGACATTTTTT[C/T]CTGTCAAATCAAATT | 115426 |
rs560735794 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415527 | AGCCAGCCTGTAGCA[C/G]GTAACTACTGGAATG | 115426 |
rs560770876 | snp | A/G/T | 0.000165649 | 0.0090994 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481778 | CAGGGTAAAGAAGAA[A/G/T]TTCCCCTTTTCTTCC | 115426 |
rs560776423 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419095 | TGTTTTAACTTAATT[A/G]CCTCTCTAAAGACCC | 115426 |
rs560777753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497777 | ACGATACAAAATTCT[A/G]TTAATTAGCATAATC | 115426 |
rs560806499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460395 | AACTACCCTGTAGGT[A/G]TCGCAGTACAGGTGA | 115426 |
rs560809068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486993 | ATAGAATAGCTTTGC[C/G]TAGGATACATCAAAT | 115426 |
rs560809287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481242 | TTTTTCTCTGGGAAT[C/T]CTAATAACCAATTTA | 115426 |
rs560911177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476688 | CAACCTCTGCCTCCC[A/G]GGTTCAGGTGATTCT | 115426 |
rs561032235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449497 | TGTTACCTTCATCTT[A/G]TCGTCTGTTTCCCAG | 115426 |
rs561050073 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502109 | ATTTATTAAGCCAGA[A/T]AAAAACAGGTGTTAG | 115426 |
rs561052262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447943 | AAAAACAAGAGGATT[A/G]GTTAATTTGTATTAA | 115426 |
rs561052975 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412903 | CTAAGCCTGAGGAGG[A/C]ACCCGCCCCCTCAGC | 115426 |
rs561066072 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447703 | AAATCCATAAACCCC[C/T]GAGGACAAAAAAAGG | 115426 |
rs561118810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464030 | CTTGAGTAGATAGAA[A/C]CAAGTGTCTGTACCA | 115426 |
rs561150084 | snp | C/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413324 | GGGCGCGCGCGCTGA[C/G]AGTCGTCGCCGCCTG | 115426 |
rs561154906 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476930 | TCACACTTGATTATT[A/C]TTTTTGGTTCCTTTC | 115426 |
rs561160580 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444597 | CTTGGGTAGGGCCTA[A/C]GAATCCGCTTTTTTT | 115426 |
rs561187373 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428068 | TTTAGAATGATGATG[A/G]TAAGCCTTTACAGTT | 115426 |
rs561228778 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453004 | GTTTTTTCTTCCCCC[G/T]AGCAATTGACTTACT | 115426 |
rs561229109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450138 | GTGTAACAACAAATG[C/T]CACATAAAATTCCCA | 115426 |
rs561241226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454983 | CCAGATGATGTTGAT[A/G]CTGCTGATCTTGGGA | 115426 |
rs561251154 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416772 | GACCTCGTGATCCGC[C/G]CGCCTCGGCCTCCCA | 115426 |
rs561261777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418315 | CATCCCTATCCTTAT[C/G]AGGGCTTACTTGCTT | 115426 |
rs561262529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443674 | CTCTGTGGGGGAGAA[C/T]ACATACTTTTTAGTA | 115426 |
rs561281972 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423266 | ACCTATGAGGAGTAG[A/G]TCATTATAATGTTAC | 115426 |
rs561283208 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411525 | TGGGACTACAGGCAA[C/G]TGCCACCATGCTCAG | 115426 |
rs561287224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485921 | TGACACTTGTTTCAG[G/T]GAGGCAGGAATGAAG | 115426 |
rs561288502 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412126 | GCCACTGCACTCCAG[C/G]CTGGGCGACAGAGAG | 115426 |
rs561293333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469833 | AATTCCTAAAGAAGA[C/G]AGTAGAGTGAAAACA | 115426 |
rs561326941 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473765 | GAAACCAGCCATAGA[C/T]AATACAAAAATCAGA | 115426 |
rs561333751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470143 | TTTGGAAGGCCAAGG[C/T]GGGCAGATCACTTGA | 115426 |
rs561335245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426126 | CTTCTCAATACTCCA[C/G]TATTCCTTCCTCTTC | 115426 |
rs561394435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431186 | TTTGCTTGACTTAGT[A/T]TGTCTATCCAATGTG | 115426 |
rs561427178 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506609 | TGACACTTGAGATCC[G/T]TGGAATGAACACAGC | 115426 |
rs561443392 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428124 | CTTCTTACATGTTTT[C/G]TTATGCTCATTGTAT | 115426 |
rs561454971 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420617 | GAGGCTGAGGCAGGA[A/G]AATGGTGTGAACCCG | 115426 |
rs561497819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502905 | TAATATATTTGACTT[C/T]AATGATCCATGTTCA | 115426 |
rs561525569 | snp | C/T | 0.000330685 | 0.0128543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497166 | CTTGAAGAAAAATTA[C/T]ATGGTATAAAGACTT | 115426 |
rs561534743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421636 | AGGCCAGGCTAGTCT[C/G]GAACTCCTGACCTCA | 115426 |
rs561535225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474058 | AGGTAGACAAGTGAC[A/G]TGAAAAAAATTAAGG | 115426 |
rs561557801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427515 | AACATGGTGAAACTC[C/T]GTCTCTACTGAAAAT | 115426 |
rs561576355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436961 | TAGTAACAGGTAAAT[A/G]TCACCTCTTTAAAAA | 115426 |
rs561619383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502298 | TTAAACATGCTCGAC[A/G]TCTTGATACCCCTGG | 115426 |
rs561641491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437664 | GCACTGTGGCCCAGG[C/T]TGGAGTGCAGTGGTG | 115426 |
rs561704199 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475062 | AAAGGTTTAATATTG[-/CA]CAGATTTAACAGGAA | 115426 |
rs561727183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442729 | ACTCCAGGCTCAAGC[A/C]ATCCTTTCACCTCGG | 115426 |
rs561807884 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461130 | GCTATGAGGATCTGT[A/G]TTGATGTAATAGCAG | 115426 |
rs561836835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442249 | GATTACAGGTGTGAG[C/T]CACCACCTCCAGTCA | 115426 |
rs561861191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484651 | CCCTGGGGTCAATTT[C/T]TCCTGCCTTAGTTTC | 115426 |
rs561861268 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463042 | ATCCCAGCACTTTGG[A/G]AGGCCAGGGTGGGTG | 115426 |
rs561889043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452593 | AGGTAGATTTTAACT[A/G]AGGATATAGAGTTAC | 115426 |
rs561898151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489663 | GTTTGCTTATTTGCC[A/G]TCTGTATAGCCTCTT | 115426 |
rs561906801 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478701 | CTGAGTCAGAAATAA[C/G]TGATGTCACAAGTGG | 115426 |
rs561908665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416087 | TTTTTGTTTTTTTTT[A/T]AAGCCGGAGTCTTGC | 115426 |
rs561921694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422856 | GCTTTGTTTTTGATG[C/T]AATTATTATATATGG | 115426 |
rs561939392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419907 | ATCACACCCGGCTAC[A/G]TTTTTTTATTTATTT | 115426 |
rs561958619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463277 | CAAGAGTGAAACTTC[A/G]TCTCAATAAAAAAAA | 115426 |
rs561969655 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483927 | CTCCCAACCTCGGGT[A/G]ATCTGCCTGTCTCAG | 115426 |
rs561995050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457888 | ATAAGCTTTTTGATA[C/T]ATGCTGCTGGATTCG | 115426 |
rs562002307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489053 | GACCTCAAGTGACCC[A/G]CCTACCTCAGCCTCC | 115426 |
rs562006447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483561 | TCCCAAATATTTTTT[A/G]CTCTCTCGACTTGGC | 115426 |
rs562010033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493727 | CAAGAGAAAATGTCA[A/G]CTCATAACATCCTAA | 115426 |
rs562021366 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430219 | TTCGCCATGTTTGCC[A/G]GGCTGGTCTTGAACT | 115426 |
rs562047956 | snp | A/G | 2.68402e-05 | 0.00366325 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499949 | AGGTAATGATTGCAA[A/G]ATATAAATAATAATA | 115426 |
rs562076714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425482 | GATAGAGGCCGGGCG[C/T]AGTGGCTCATGCCTG | 115426 |
rs562083489 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461241 | GAATTTAAACTTAAT[A/G]AAGAGAATTCAGAAT | 115426 |
rs562103158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420282 | GCCTGGTCTCAAACT[C/T]CTGACCTCGTCATCT | 115426 |
rs562145228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494271 | GCTAAAAGTGACAAA[C/T]TCCTTTTTAGAGTAA | 115426 |
rs562157455 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435994 | GTAAACTATTGTCTT[C/T]ATCCATTTAAAAAAT | 115426 |
rs562167440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478837 | AAAGGATATATCTTC[C/T]TCCTTTTACCTCCTA | 115426 |
rs562172405 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495229 | TTGGACAATCTGATA[A/G]GTACCGCTACAATCT | 115426 |
rs562172699 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478471 | ACTGTATTTAATCCT[C/G]TGACGTTGATACATT | 115426 |
rs562178697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445706 | GGGATCACAGGTGCA[C/T]GCCACCATAACTGGC | 115426 |
rs562184100 | snp | C/T | 1.66294e-05 | 0.00288347 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500571 | CTGTCCAAGTGCCTC[C/T]AAAGTGTACAAAGCA | 115426 |
rs562211369 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454440 | GTCGATTTCTTCATG[A/G]ACTTAAGGCATAGAA | 115426 |
rs562218268 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478829 | AAAGGGGGAAAGGAT[A/G]TATCTTCTTCCTTTT | 115426 |
rs562272251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420631 | AGAATGGTGTGAACC[C/T]GGGAGGAGGCGCTTG | 115426 |
rs562313871 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467349 | TGTGATTATATTGGA[A/T]CTGCGTGGATAATCT | 115426 |
rs562363224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482515 | GACATTGGGCAGAGG[A/C]AGTGCCAGCTAATCC | 115426 |
rs562371860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451629 | GGGACTACAGGCGCC[C/T]GCCACCACTCCCGGC | 115426 |
rs562483940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413699 | GGAACAGCTGGGCTC[A/C]TCTGGACGCACCGGT | 115426 |
rs562528141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428682 | AGCTTCCTGAGTAAC[C/T]GGGACTACAGGTCTG | 115426 |
rs562592924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433484 | CTTTTTAATACTTTA[C/T]TGTTTTCTGGTTGGA | 115426 |
rs562598186 | snp | C/G | 0.0134861 | 0.0810011 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413381 | TGGGCGCGCTCGCCC[C/G]CCTGCCGCTGAGGGC | 115426 |
rs562601596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435053 | CACTCTGTCACTCAG[C/G]CTGGGAGTACAGTGA | 115426 |
rs562610435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455483 | TTATCCTTTTTTATG[A/G]CTGCATAATATTCCA | 115426 |
rs562630929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6419014 | CATTGTCTTCCGGCT[A/G]CATCTTTCCAAATGT | 115426 |
rs562718174 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505007 | TTATAGCGCAAACTG[G/T]AGTGTTTTCATTAAT | 115426 |
rs562749675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435458 | AGCTTTTTATTGAGA[C/T]AGTTCACATACAGTT | 115426 |
rs562784126 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425851 | TTTAGAGCCTTCAAC[A/G]GACAGCAAGGAAATA | 115426 |
rs562840056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471454 | GGCTCTTTGTGACCA[A/G]TAGAATATGGTGTAA | 115426 |
rs562840122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465198 | ACAATGTTTGATATA[A/G]GAATTTTGTAGATAT | 115426 |
rs562846353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477565 | CTTTTCTTTATGAGA[C/T]TCATAGATATAAAAA | 115426 |
rs562907528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455176 | TAAGTTCTAGGGTGC[A/G]TGTGCACAACGAGCT | 115426 |
rs562943721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490697 | CATGTTTTTGAATAT[A/G]CTTACTGGTCAAACG | 115426 |
rs562950208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505533 | AATGCCTGACCTAAG[A/G]TGATCCACCTGCCTC | 115426 |
rs562979487 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427832 | ACATATGGAGAGCCT[A/G]TGAAAGATTGTACAG | 115426 |
rs562989407 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472385 | ATAACATGCTTACAA[-/G]GAAAACATTCCAGAA | 115426 |
rs563011896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498567 | TGGTCTGCCTTCTCC[C/G]TTTCTCACTTTTCCT | 115426 |
rs563016875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496625 | TGCTTCAGGCTTATT[A/G]AAATTTATCTTTTTA | 115426 |
rs563020502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460053 | CCAGTCCCCTACTTT[C/G]CCAGCTAGCAATGAA | 115426 |
rs563067692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487158 | AGGAAAACACATTCT[C/G]TATAGAGCTTTTATT | 115426 |
rs563068269 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460337 | AGAGATCCACATCTC[C/G]AAGGCCTAGTGGGAA | 115426 |
rs563071939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493032 | CCAGGGCGCAGTGGG[C/T]CATGCCTGTAATCCC | 115426 |
rs563075233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470092 | AAAAACATTCCCAGC[C/T]GGGCGTGGTGGCTCA | 115426 |
rs563106881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459063 | AACACAGAGGGGCCT[G/T]TCGGAGGGTAGGGGG | 115426 |
rs563171879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497101 | TAGAATCTTAACCAT[C/T]AGGTAAGGTATAATT | 115426 |
rs563207083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466042 | TGAAGTTATGCTGAT[G/T]TAGATATTTGTAAGT | 115426 |
rs563209920 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502861 | CATAATTGCCATATT[G/T]TAAAAATGTGTTTAT | 115426 |
rs563230085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463789 | AAAAATTTTTTTTTT[A/T]AATGATTAGAAATCT | 115426 |
rs563271933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417205 | TAGTATTCCCTTGCA[A/T]CATTGTTGCAGTTCC | 115426 |
rs563300059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421831 | TTTTTATTTTTGCTA[C/G]TTACGTATATTTCTC | 115426 |
rs563367898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427639 | TCAGTGAGCTTAGAC[C/T]GCGCCACTGCACTCC | 115426 |
rs563377975 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458386 | GTTCTTCTCTCTTTT[A/C]TTCTATGTTAGTCTG | 115426 |
rs563406571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502444 | TTTCTAAAATGGCAA[C/G]TCTTTAAAATTTAGT | 115426 |
rs563415875 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473535 | ATTAGTAGCTGCCGT[A/C]AGGAGAGGAAAAGAG | 115426 |
rs563427251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463499 | TTTGGGAGATGGGGT[C/T]TCGCTCTGTTGCCCA | 115426 |
rs563448956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452110 | AGTTCATATATCCTG[C/G]AGATCACTTCCTAGT | 115426 |
rs563450791 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457833 | CATATGTTGAACCAG[C/G]CTTGCATCCCAGGGA | 115426 |
rs563498813 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426736 | TGCTACTTTTGAAAT[G/T]ATTTGCTTTATTTTT | 115426 |
rs563518365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480679 | GTTATAAAGATGAGC[C/T]CATCAGATAAAATAC | 115426 |
rs563544105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474788 | TTTGAAGAAGTATAT[A/G]CAAACAAATATGAAT | 115426 |
rs563567683 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490987 | CTTGAATTTGGTATA[A/C]ATTTCATGAAGCCAG | 115426 |
rs563581429 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453863 | TGAGCTGAGATCATG[C/G]CATTGTACTCCAACC | 115426 |
rs563594730 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436499 | TTGAGATTTGTTGTG[C/G]AAAGGGGAGAAACAA | 115426 |
rs563690676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416058 | GTTAATTGACTCCAC[C/T]TTTTTTGTTGTTGTT | 115426 |
rs563722094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436603 | TGGCACAACATAGAC[A/G]TAGAATAAGGAACTT | 115426 |
rs563723743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430671 | CAGCCAGGTACCAAA[C/G]AACTAGAGGCCACCC | 115426 |
rs563724277 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484498 | ACAGTCCCCTCCTGG[A/G]CTCAAGCTGTCCTTT | 115426 |
rs563776033 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487419 | TCACCTAGACTGGAG[G/T]TCAGTGGCTCAGTCT | 115426 |
rs563792180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443166 | AAGCTACCTTTGGCT[A/G]GGCAAGTTGCAGTCT | 115426 |
rs563803593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415499 | GTGGTCTCTGGAGCT[C/G]CACAGATGAGGTAGC | 115426 |
rs563867225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480084 | TATCTACTCTCTAAC[C/T]TCGGTTGCTTATCAC | 115426 |
rs563910156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457107 | TTTGGGCAGTATGGG[C/T]ATTTTCACAATACTG | 115426 |
rs563964439 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461636 | CTCTGCCTCCCAAAG[C/T]GTTGGGATTACAGGT | 115426 |
rs563970891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442123 | GTGCCTGGCACCACG[C/T]CTGGCTAGTTTTGGT | 115426 |
rs563974617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505777 | ATGTAATCTCTAACT[C/G]CACCATTTTAGTAGA | 115426 |
rs563990797 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439234 | CTATGGCTTGGGCTG[C/G]AGTGCCGTGGTGTGA | 115426 |
rs563999663 | in-del | -/CGCGAGG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413777 | CGGGTGGGCAGCCCC[-/CGCGAGG]CGCGGGGTGCGGGGC | 115426 |
rs564004835 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411471 | CAGCCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 115426 |
rs564034501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442838 | TTTAATTTTTAGGCC[A/G]TAGTTACCACACTAC | 115426 |
rs564072299 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479506 | ATCCACTTCTTTTCT[A/G]TGCTAGGGAACTATG | 115426 |
rs564080849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462854 | CCCACGAGGCAGAGG[A/T]TGCAGTAAGCCGAGA | 115426 |
rs564148438 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431887 | ATTTTAGTATCAACT[A/G]TATGCTGCATTCTCT | 115426 |
rs564166283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441565 | AAATTCCTTTTGACC[C/G]AGCCTTATCCATTAC | 115426 |
rs564185907 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480354 | TACTATGTACAAACA[-/T]TTTTATCACAAACAT | 115426 |
rs564210853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478739 | GTATCTGTGAAAAAT[A/G]GATTGTTCCTTTGAT | 115426 |
rs564216906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499366 | GTTGCTTTAGGTCTT[A/G]TAAAAGCTCCTGCCG | 115426 |
rs564224523 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428614 | GAGTGCAGTGGCATG[A/T]TCATAGCTTACTGCA | 115426 |
rs564256281 | in-del | -/AG | 0.00159617 | 0.0282053 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412136 | TCCAGCCTGGGCGAC[-/AG]AGAGAGATTCCGTCT | 115426 |
rs564266814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472443 | AGGATTTTAAGTCAA[A/G]CCAAACTAGCCTTTA | 115426 |
rs564299638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420739 | GAGAGAGAGAATGTA[C/T]TGGGGTCCAGAGAAG | 115426 |
rs564310850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495199 | AATGTACATGTTAAG[A/G]TTCCTTTCACACTTT | 115426 |
rs564313963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426053 | GTTTATGTATCTGCA[C/T]ATCTGAGATTAATCA | 115426 |
rs564329182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424307 | GAAAAAAATTTGCAA[G/T]AACAAAAGGTAGAAT | 115426 |
rs564334003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414617 | CACTAAAAAGTTGGC[A/G]TCCTGAGTTGATAGA | 115426 |
rs564346547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414241 | CTCGCCGCCTTTCCT[A/T]GGTTTGGAATGTCTC | 115426 |
rs564379571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501194 | CACATAATTTTAAAG[A/T]AAAAAGGAATCACAG | 115426 |
rs564389222 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437094 | GTTTCATTCTTTGTG[A/G]TCATTAGAAAAATGA | 115426 |
rs564392133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494242 | GTGGCTTGTCTACTA[A/C]TCCATTGGTCAAAGC | 115426 |
rs564407937 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506391 | GTTCCTGTAACAACT[A/G]GTTTTAATGAGTAAA | 115426 |
rs564408735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419860 | ATCTCCCACCTCAGC[C/G]TCCTGAGTAGCTGGG | 115426 |
rs564434278 | snp | C/T | 0.000928419 | 0.0215255 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468523 | GTAGTTGTGTTTTGC[C/T]CCTAGGGAATCTGCT | 115426 |
rs564451699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466802 | GCTCCTGCCTTGGGG[C/G]CTTTGTACTTGATGT | 115426 |
rs564477719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461096 | AACAATATATAAAAG[C/G]ATTTTAATAACTATA | 115426 |
rs564485989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424965 | TTCTATTTGCTAAGT[A/T]TAACTTAGGTTTTAC | 115426 |
rs564525414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435383 | CTCCCACCTCAGCCT[C/T]CCTGAGTGCTGGGAT | 115426 |
rs564540612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483001 | GTTCCAAGATCCCCT[A/G]TAGACACCAAAGTCT | 115426 |
rs564547913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430089 | AATATTGGCCCATTA[C/T]AACCTCCACCTCCTG | 115426 |
rs564564899 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419639 | TCTTGAAGTTGATTC[A/G]AGCACTGATTAAACA | 115426 |
rs564566718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504996 | TGTTTTATATATTAT[A/G]GCGCAAACTGGAGTG | 115426 |
rs564682024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483463 | ATGCTATGTAAATAG[C/T]TGTTAACACTGTATT | 115426 |
rs564707335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451576 | CCGCCCCCCGGGGTT[A/C]ACACCATTCTCCTGC | 115426 |
rs564743112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477235 | TGAGACTCCATCTCA[A/T]AAAAAAAGACTGGGT | 115426 |
rs564764060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450201 | TTCATAGTTCCTTAA[C/T]TATCTATTTAAAAAT | 115426 |
rs564766951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456320 | CATATGTTTGTTGGC[C/T]GCATAAATGTCTCCT | 115426 |
rs564802253 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459144 | ATGGGTGCAGCAAAC[C/T]ACCGTGGCACCTGTA | 115426 |
rs564848793 | in-del | -/TAA | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440227 | TTTCATTAGTGTTTT[-/TAA]TAATATCTGTGGCAT | 115426 |
rs564871012 | snp | C/G | 0.0134861 | 0.0810011 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413373 | CGGTCCGGTGGGCGC[C/G]CTCGCCCGCCTGCCG | 115426 |
rs564872805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487354 | CCATCACACCTGGCT[A/C]ATTTTTGTATTTTTA | 115426 |
rs564883121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418434 | TGTGAAATTCTTGAT[C/G]CCTTGTTCTACTTGA | 115426 |
rs564923789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492160 | TGAGTTAATGGTACA[A/G]AATTTTAGCCATGTT | 115426 |
rs564958771 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451421 | AAGAGAAATTGAGCT[G/T]CCATCCTGATTCCTT | 115426 |
rs564960924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423686 | CGTGGTGGCTCACAC[C/T]TGTAATCCCAACACT | 115426 |
rs565007912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493242 | GGCAGAGGCTACAGC[A/G]AGCCGAGATCGTGCC | 115426 |
rs565039750 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450310 | TCTTCCCCTTCCCCC[C/G]CCCCCATTTATTTAA | 115426 |
rs565044613 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467178 | ACTCTAAGGGAGAAC[C/T]CATTTTCTTGCCTTT | 115426 |
rs565055625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445060 | CTTTGGGAGACCAAG[A/G]TGGGAGGATCATTTG | 115426 |
rs565056338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434908 | TGATCCTGGCTCGCT[A/G]CAATCTCCGCCTCCT | 115426 |
rs565103489 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498910 | ACTATGGGCAAGTGT[C/T]TGACCACCCAGGCAG | 115426 |
rs565105439 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470113 | TGGTGGCTCACGCCT[A/G]TATAATCGCAGCATT | 115426 |
rs565109417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459639 | ACACCACTGCACTCC[A/T]GCCTGGCTGACAGAG | 115426 |
rs565144993 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472195 | CTTCTATCAGATTAG[A/G]TTTTAGTCTCCAGAA | 115426 |
rs565242278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475947 | TGTTAACTGTAGTCC[C/T]CCATCGTGCTTCTGA | 115426 |
rs565254033 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438739 | TTTATAGTAATCTAC[A/G]TATCTAATAGATTAC | 115426 |
rs565271684 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412151 | AGAGAGAGATTCCGT[C/T]TCTAAATACATACAT | 115426 |
rs565281418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475578 | CTGGTCAGTGAATAA[C/T]TTGGAAGGAAGTATA | 115426 |
rs565321072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421490 | CACGCAATCTTGGCT[C/T]GCTATGACCTCTGCC | 115426 |
rs565323484 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418260 | CTAGAGGATGTTCCT[-/T]TTTTTTTTTTTTTTT | 115426 |
rs565345696 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415462 | CGCTGACAAGTAGCT[A/G]TGGCAATGAGTGTTA | 115426 |
rs565364326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496049 | TGACCACAGCTATAT[A/C]AGTTATTTTTTAAAA | 115426 |
rs565382542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420871 | AATGTAGTAAGATAC[A/G]TTTTAGAGAAGCATT | 115426 |
rs565416956 | snp | A/C | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420301 | ACCTCGTCATCTGCT[A/C]TTTTCGGCCTCCCAA | 115426 |
rs565500904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504094 | GCAGTGGCGTGATCT[C/G]AGCTCACTGCAAGCT | 115426 |
rs565527606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489731 | AATTGGGTTTTTGTT[C/T]TTTTTTTTTTTTTTT | 115426 |
rs565572223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442915 | GTCGGTCAGTCTTAC[A/G]GTTCAGTTAAAAAGG | 115426 |
rs565587893 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422987 | AGAAATAATCGAATG[A/G]CAGTTTTGCTTTATC | 115426 |
rs565588236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432910 | CACTGGCACGATCTC[C/T]GTTCACTGCAACCTC | 115426 |
rs565593389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426374 | ATACAAATTGGCAAG[C/T]AAATCTTACATTAAG | 115426 |
rs565610846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416173 | GGTTCAAGCGATTCC[C/G]CTGCCGCAGTCTCCC | 115426 |
rs565610927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428786 | ACTCCTGGGTTCAAA[C/T]AGTCCTCCTGCCACT | 115426 |
rs565639028 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418156 | TGGGTTTTTTTGTGG[A/G]GGTGTTGGAGAATGT | 115426 |
rs565656152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431249 | CCCACCCAGTTTATG[C/T]GCATTTCTGTGAGTG | 115426 |
rs565697345 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489361 | GCTATTACAGATAAA[C/G]CTACAGTAAATATTT | 115426 |
rs565701948 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506768 | GTTGACTACTAATGA[C/G]TAATGAGAACAATAA | 115426 |
rs565713294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478912 | AACTATTTCCTCTGA[C/T]GTCTCATATTTTCCT | 115426 |
rs565719957 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489021 | CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 115426 |
rs565743017 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411161 | TGTGGTTTTTGCCAC[C/T]GAAAGAAATGGCAAA | 115426 |
rs565749420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483671 | TTTATATTTTAAAAA[C/T]GCGCCCTACTTTTAT | 115426 |
rs565753751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478142 | GTTGCTTCTCCAGCA[A/G]TATCTCTTACCACTT | 115426 |
rs565765111 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465659 | GTTTGTGACTTTTTG[A/T]CCATTCTCATCAGAG | 115426 |
rs565786302 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425753 | TGGGTGAGTGAGACT[A/T]CGTCTCAAAGTAAAT | 115426 |
rs565792816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483205 | TGGCAAGCGCCTATA[A/G]TACCAGCTACTCAGG | 115426 |
rs565834818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447993 | CCTACCTAGTGTTTA[A/T]AACAGGAAAGAAGAC | 115426 |
rs565862224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474562 | AATACAAAAATTAGC[C/T]GGGTATGGTGGCGCA | 115426 |
rs565900770 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446974 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 115426 |
rs565927100 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460832 | TTAATTAACTGAATT[C/G]ATCAAGGAATGTATT | 115426 |
rs565965648 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445650 | GCAACCTTGACCTCC[C/T]GGGTTCAAGTGATCC | 115426 |
rs565968543 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485585 | TTCTTGTTGGCTTCT[A/C/G]AAAGCTTCTAAAGTG | 115426 |
rs565976464 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447477 | GAGATATTTTAGTTC[C/G]TGAAGGAGAACAGCA | 115426 |
rs565995499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488676 | CCGGTTAATTTTTGT[C/G]TTTTTACTAGAGATG | 115426 |
rs566018178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451662 | ATTTTTAGTTCAGAC[A/G]GGGTTTCACCATGTT | 115426 |
rs566056050 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481970 | ATAACTGATTTCTCA[A/G]CGTTTGTTTTGCGTC | 115426 |
rs566107932 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425884 | ACATATTTGTACTAA[C/T]CTGTGTATATATACA | 115426 |
rs566113771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441225 | CTCTACAAAAAAAAC[C/T]CAGCCACCTATGGTG | 115426 |
rs566145378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473772 | GCCATAGATAATACA[A/C]AAATCAGATGGCATA | 115426 |
rs566162359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446502 | CCCAGGCTGGTCTCA[A/G]ACTCCTGGGCTGAAG | 115426 |
rs566176526 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451414 | ATATACTAAGAGAAA[G/T]TGAGCTTCCATCCTG | 115426 |
rs566189488 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437659 | GTCTTGCACTGTGGC[C/G]CAGGCTGGAGTGCAG | 115426 |
rs566190681 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506657 | ACTTTTTTAACGTCT[C/T]TTCTTCCATTACAAT | 115426 |
rs566230797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445789 | GACTGATCTCAAACT[C/T]CTGGGCTCAAGCAGT | 115426 |
rs566233113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439917 | TTAAGGTAATAGAGG[C/T]AATTATAAATCATTA | 115426 |
rs566237844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462119 | TAAAGCGAGGATAGG[C/G]AAGCTTATAGCCCAC | 115426 |
rs566238215 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418033 | GTTTTATACTGTTAG[-/T]TTTTTTTTAATTATC | 115426 |
rs566265830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468237 | TTGTGCATAAAGAGT[A/G]TCTTGATAAGCCTTT | 115426 |
rs566304965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456225 | TTTTTAATGATCGCC[A/G]TTCTAACTGGCGTGA | 115426 |
rs566305511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436684 | AGTTGCTTTTGAAGT[A/T]AGACTATCCAATGGA | 115426 |
rs566332903 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470659 | AAATGCGTGACAACA[A/G]TAATGCAGAAGATGG | 115426 |
rs566350738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505906 | GTGCAGATTCAAGCC[G/T]TTATGTTTGTTCATT | 115426 |
rs566362772 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415059 | TTTGATGCATTTTAT[C/T]TTCTAGCTGGGGACA | 115426 |
rs566368834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436145 | CAAGTACGAGTTAGA[A/T]ATCCTAGAACGCTTA | 115426 |
rs566435413 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420269 | ACCATGTTGGTCAGC[C/G]TGGTCTCAAACTCCT | 115426 |
rs566435755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434508 | GAATGGCACAATCTC[A/G]CCTCACTGCAACCTC | 115426 |
rs566463481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472174 | CCCAGACCACCACTG[A/G]TTGGCCTTCTATCAG | 115426 |
rs566493525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435118 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTAGCATTA | 115426 |
rs566538475 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424589 | AGTAGAGAGAGTTCC[C/T]ATATATCCCACACCT | 115426 |
rs566544322 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488365 | TGGTGACATCTTGCA[A/G]AACTATATAGTACAA | 115426 |
rs566548863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504315 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTCTAAA | 115426 |
rs566579244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428709 | TCTGTGCCACCATAC[A/C]CAGCTAATTTTCAAT | 115426 |
rs566611138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477399 | GGCGTGGTGGCACAT[G/T]CCTGTAATCCCAGCT | 115426 |
rs566628361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503671 | TTTTAAGCTCCTAAA[A/G]ACAAATATTCAAGTT | 115426 |
rs566641251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455835 | CAAAAAGTTTTAAAA[C/G]TAGCCAGGCATAGTG | 115426 |
rs566677740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467527 | TTTGCTGTTGTGTGC[C/T]AGGCCTTGTTCTAGG | 115426 |
rs566689086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445348 | GACCCACTGCAACCT[C/G]CACCTCCCAGGTTCA | 115426 |
rs566704100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454737 | GGCCACTCTTAGTTG[C/G]GTAACGGTTCAAGAT | 115426 |
rs566713920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425092 | TCCTGTCTTTCCATA[C/G]TGTACTGTTGGAGAG | 115426 |
rs566738089 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499992 | TGTTGTTGTTGTTGA[G/T]ACGGGGTCTCACTCT | 115426 |
rs566741473 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494346 | GTACATAAATGAAAC[A/G]TAAGGTAACTTAATC | 115426 |
rs566775170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505161 | AGTGGTGATTATGTG[C/G]CCTAACTTCAGAACT | 115426 |
rs566775177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499659 | AAATTGGGATTTTAA[C/T]AGTTGTCTGTGCTTT | 115426 |
rs566782498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491853 | GATCATTGACTAGAA[C/G]ATGCAACAAATTTAG | 115426 |
rs566824099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460111 | GTTTTGCTCTGGGAA[G/T]TCAAATCATGAGTGT | 115426 |
rs566865176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486757 | AGAATATATATGAAA[A/G]CATTTTGTAAATGTA | 115426 |
rs566885260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459750 | AGTCCAAGGCAGGGG[G/T]TTGCTTGAGGCCAGG | 115426 |
rs566900427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480748 | TGATTTCCCAACTAG[A/G]AAGGACTTTACTTCA | 115426 |
rs566928150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476885 | GGCATGAGCCACCAC[A/G]CCCGGCCTCAGGCAT | 115426 |
rs566937583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480403 | TAGTGCCTTGCACAT[A/G]GGAGGTTCTGAACAA | 115426 |
rs566939661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486044 | TGAAGGAGAAGCTGC[A/C]CATAAGGCTAGGAAA | 115426 |
rs566976636 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485614 | TGCCTTTCCACCCCC[G/T]CCCCCCGCCCCAAAT | 115426 |
rs567019988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459303 | TTCATGTTCTTATAA[A/G]TACTGCAAAATGGCA | 115426 |
rs567026816 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413092 | CATTTTCGTTCCCTC[C/G]GGTCTGTAACCCTCT | 115426 |
rs567064255 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413425 | AAAGCGGCGCGGGCC[A/G]GGCGGGGCGCGGCGC | 115426 |
rs567064841 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444911 | CCAGCCTAGGAATCT[A/G]CTTTTCAAAGAGGTA | 115426 |
rs567077276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469307 | GGTGGATCATGAGGT[C/T]AGGAGATCAAGACTA | 115426 |
rs567084576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482208 | TGACATTCACTTGTT[A/G]GAATGAAATATATTT | 115426 |
rs567091763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449848 | CAATATTTCCCATGT[G/T]TTGTCACAGTTGGTT | 115426 |
rs567119708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481563 | CTTAAAACTTGCTCT[A/T]ACCTAGGAAGGCTAA | 115426 |
rs567127105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418592 | CTTCTCAAATATGAT[A/G]TTACTGTGTTAGAGT | 115426 |
rs567160363 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411922 | TAAACCCACTTGGCC[A/G]GGCGCGGTGGCTCAC | 115426 |
rs567163122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503200 | CGGTTTTGGCCATGT[G/T]GGCCAGGTTGGTCTA | 115426 |
rs567192422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455219 | ATGCATACATGTGCC[A/G]TGTTGGTGTGCTGCA | 115426 |
rs567223935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416920 | AGGTGGTCTTAAAAT[A/C]GATAACAATGTGGGG | 115426 |
rs567231332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475223 | TTAACTAATCACTAT[A/G]GACTTTTCCTACTAT | 115426 |
rs567235000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449017 | ATAGCCAATTTTGTC[C/T]TTACCTTTACCAGCA | 115426 |
rs567266167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417290 | ACAAAAAATCCTAAC[C/G]ATTTTTGCTTCTTAA | 115426 |
rs567306686 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469286 | GCACTTTGGGAGGCC[A/C/G/T]AGGCAGGTGGATCAT | 115426 |
rs567309873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469465 | AGAGGTTGCAGTGAG[C/T]CAAGATTGCGCCACT | 115426 |
rs567329928 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470561 | AAATATGGGACAGAA[C/T]TAAGAGCAGGGAAAG | 115426 |
rs567331984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453906 | TAAGACTCCGTCTCA[A/G]AAAAAGAAAAAAAGT | 115426 |
rs567344894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448607 | TGCAGTGCTGTGTGT[A/T]AGTAATTATAAGAGG | 115426 |
rs567347396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468934 | GTAGGAAGGTTGAAC[A/T]TTCCTTTATATAAGA | 115426 |
rs567349990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470387 | AAAATTTCCCAACTT[A/G]AAATATCTTTTTCAT | 115426 |
rs567367933 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444320 | TGTAGGCTCCTGAGT[A/G]GATGGTAATCAAAAG | 115426 |
rs567410681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442889 | TTAAAACCAAGGATT[C/T]AACATGTACTGTCGG | 115426 |
rs567422801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442566 | TCACTGCAGCCTCGA[A/C]TTTCTGGGCTGAAGT | 115426 |
rs567426398 | in-del | -/TTTCTCAGAGCC | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432548 | CCTAGAGGAAGTTAA[-/TTTCTCAGAGCC]TTTGTTTCCGTATTT | 115426 |
rs567441934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438477 | TCCCATTGCATTTAT[A/G]GCTTTATGGTATTTC | 115426 |
rs567478885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438942 | TTTCTTCTTAGGTAG[A/G]GGAGTTTCAAACACC | 115426 |
rs567488106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475760 | TTTATGGATATATAA[C/T]AGTTGTAGATATTTA | 115426 |
rs567514774 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424306 | GGAAAAAAATTTGCA[A/G]TAACAAAAGGTAGAA | 115426 |
rs567552030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426099 | GGTCAACTTAAATTT[C/T]TGTTTAGCAAACTTC | 115426 |
rs567567564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444069 | GTGATCTTTTTTCTA[A/G]GAGTTCCAAAAATGT | 115426 |
rs567574976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471184 | TGGACAGCATCTACA[A/G]TGAAACAGGGTGGTA | 115426 |
rs567578091 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437239 | ATTTTTTATTTTATT[A/C]TTATTATTTTTTAGA | 115426 |
rs567668176 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463139 | ATACAAAATTAGCTG[C/G]GTGCGGTGTTGCATG | 115426 |
rs567677666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431432 | GGGCAACATAGCAAA[C/T]TCTGTCTCTACAAGA | 115426 |
rs567698469 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415542 | GGTAACTACTGGAAT[A/G]GCATCACAGAGAGTC | 115426 |
rs567705829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458420 | GGCAGTCTATTTTGC[C/T]GATCTTTTCAAAAAA | 115426 |
rs567712303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473880 | GAATGACAGAAAAAA[C/T]TGTTTAACCCATACT | 115426 |
rs567737839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436861 | CCCTAAATAATTTTA[C/T]GTGATGGAATTAAAT | 115426 |
rs567746533 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507003 | ATCCTAAATTTTATA[C/T]TCACTATATTCCCTA | 115426 |
rs567766621 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430691 | AGAGGCCACCCCTAC[A/T]ATCCAAAGCCCACTG | 115426 |
rs567794129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496672 | ACATTCTCATACACC[A/T]CTTATTCTTAATATC | 115426 |
rs567827922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430268 | ATCCACCCTGGCCCC[A/C]TAAACTGCTGGGATT | 115426 |
rs567832501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416403 | CAAAATGGAGACCTG[A/C]AATTCAGGGCTATAA | 115426 |
rs567879390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489822 | TGAATCAATATGAGT[A/C]GTTATGGAGAGAGAA | 115426 |
rs567901872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432268 | ACCATGTTCATTACA[A/T]ACAGTGCCTTTGGTC | 115426 |
rs567906543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421561 | AGCTGGGATTACAGA[C/T]GTGCACCACCACGCC | 115426 |
rs567910535 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427082 | TTTGCATTGGGTTTT[C/T]TGTATTTCCCATAGT | 115426 |
rs567928325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502534 | CTCAGGCAATCCTCC[A/C]GCTTCAGCCTCCTAA | 115426 |
rs567959843 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429860 | TACCTGCAGAGCTGG[A/C]GTGTTTTCTGCAAAA | 115426 |
rs567963413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502095 | TAAGCCAGGAACACA[C/T]TTATTAAGCCAGAAA | 115426 |
rs567988964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447069 | AATTTTTTTGTATTT[G/T]TAGTAGAGATGGGGT | 115426 |
rs568059494 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439841 | GAGACTATACTTGAA[C/T]GAAAACTCTTGTTTC | 115426 |
rs568077178 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436136 | AATTCTTAACAAGTA[C/G/T]GAGTTAGAAATCCTA | 115426 |
rs568078529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462039 | TAAACGAATATTTGT[C/G]TCAAGTTCTGATTAA | 115426 |
rs568115050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500831 | CCCGGTTTTCTAATC[C/T]AGTGCCACTACCTTT | 115426 |
rs568138081 | snp | A/G | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500605 | GATTCAGCAGAAGCA[A/G]TTGAGGCTTTTCAAC | 115426 |
rs568148515 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487991 | CATGCCTGTAATCCC[A/C]GCACTTTGAGAGGCT | 115426 |
rs568186839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487616 | AGGTGATCCTCCCGC[C/T]TTGGCCTCCCAAAGT | 115426 |
rs568188565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461595 | CCAGGCTGGTCTCGA[C/G]TCCTGCCCTCAAGTG | 115426 |
rs568194706 | in-del | -/C/CC | 0.00281531 | 0.037413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499822 | GTACTCTCCCTCCTC[-/C/CC]CCCCCCCATCAGTAT | 115426 |
rs568208403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468209 | TTTTTATTATGATCA[A/G]TGGCATTTAGTTTTG | 115426 |
rs568226527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420758 | GGTCCAGAGAAGACA[C/G]TGACATCAGAGGCCA | 115426 |
rs568243989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479400 | TACCTACTTCACTGG[C/G]CTTTCCTTCTTAGTC | 115426 |
rs568257721 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425541 | GGGTGGATCACTACA[G/T]GTCAGGAGTTTGAGA | 115426 |
rs568271475 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495356 | CAGAGAGACTTTAAC[A/G]TCTGGTCAGTTTATA | 115426 |
rs568294436 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429550 | TGGCCAGACTGGTCT[C/G/T]GAACTCCTGACCTCA | 115426 |
rs568296185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483996 | ACCCGGCTTCATCAT[A/C]ATTTTCTGTTTCTCA | 115426 |
rs568305910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457180 | TGTCCTCTTTTTTTT[C/T]GTTGAGCAGTGGTTT | 115426 |
rs568314696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483783 | CAACCTCTACCTCCC[A/G]GGTTCAAGCAATTCT | 115426 |
rs568332990 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489257 | GTTCATTTCTTTTTA[C/T]TGATGAGTACTAGTC | 115426 |
rs568352788 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414348 | CCAAGAGTTTTATTC[C/G]CGAAGTGAAAAGGAG | 115426 |
rs568357381 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505295 | TGCGTGTGTGTGTGT[A/G]TATATATATATATAT | 115426 |
rs568387285 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453216 | CTGTCTCCATATAAA[C/T]ATAACTGTATATACA | 115426 |
rs568409657 | in-del | -/C | 0.0475154 | 0.146629 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461390 | CCTCCTTCTCTCCTC[-/C]CCCCCCGCCCCTTGT | 115426 |
rs568426318 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429824 | TAGTGGGTGATAGAT[-/G]GAAGAACTTGAACCT | 115426 |
rs568431767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445950 | AATAAAGACAGGTTG[C/T]TTTGGTAAATACTCT | 115426 |
rs568450775 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447928 | ATGTGGAATAGAACT[-/A]AAAACAAGAGGATTG | 115426 |
rs568496113 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471654 | ACCAATGGCTTAACT[G/T]CAATCTCATGAAAGA | 115426 |
rs568505036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419311 | ATTTCAACCCATAAC[C/G]CTTACCAAAATATGG | 115426 |
rs568546623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473224 | CACTGGTCAAAGATG[A/G]GACAATTTGAACATT | 115426 |
rs568549720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493246 | GAGGCTACAGCGAGC[C/T]GAGATCGTGCCACCG | 115426 |
rs568659816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472765 | TCAGTAATTGACAGC[C/T]GGCAACAATGTCTTG | 115426 |
rs568699880 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478027 | CGTTTCTTCTCTGAT[A/C]ATAGACTCTGTGTTC | 115426 |
rs568854811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476827 | CTCGAACTCCTGAGC[C/T]CGTGATCCGCCCAAC | 115426 |
rs568863529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444660 | AGGCTGGAGTACAAT[A/G]GCATAATCTCAGCTC | 115426 |
rs568869273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439625 | GTTCTATGTCACTTA[C/T]CTGTCCTTAACCTTG | 115426 |
rs568891600 | snp | C/G | 1.65696e-05 | 0.00287828 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481959 | TAAAATTTAACATAA[C/G]TGATTTCTCAACGTT | 115426 |
rs568897982 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433740 | TTAGTCAATAGATTT[A/C]AGATAGCACAAATCA | 115426 |
rs568912855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455343 | CCTTCCTGTGTCCAA[A/G]TGTTGTCATTGTTCA | 115426 |
rs568931564 | in-del | -/GAT | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480623 | TTTTCTCATCAGAGA[-/GAT]AATACTTGCTTTAAA | 115426 |
rs568934430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418793 | TAATTTCCTAGGGCT[A/G]TTGTACTAATGTACC | 115426 |
rs568957700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428324 | ACTCCCAGGAACTTA[A/C]CAGGTGCCTCCTCCT | 115426 |
rs568972066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427858 | TACAGAGGCTGGGTC[C/T]ATCCATTCACATTAT | 115426 |
rs568972109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432976 | CTCCTGAATAGCTGG[A/G]ATTACAAGCATGCTC | 115426 |
rs568972936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460211 | TGACTGAATAGATAC[A/G]TAACATATAGTTTAT | 115426 |
rs568988501 | snp | C/T | 1.71546e-05 | 0.00292865 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460550 | TTGGTAATCATAAGC[C/T]ATATGGTTTTCTCTC | 115426 |
rs569007485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424009 | AGAATAGGTTAATAT[G/T]TTAAACACATTCTAT | 115426 |
rs569075755 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449783 | ATGTGCTAGGCAGTA[C/G]CTGTTATCAGCCCCT | 115426 |
rs569076845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499542 | ACTTTCCTTAAACTT[A/T]AAGGAAATCTAATCA | 115426 |
rs569106513 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497838 | TCCTCATGGGAAGTA[C/T]TGTAATAGGAATTAA | 115426 |
rs569112113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459278 | ATGGAGACTATCGGA[A/G]TATGCCAGGTTCATG | 115426 |
rs569123100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429665 | AGTCTTAACATTGAA[C/T]GTATATACTTAGTAA | 115426 |
rs569135320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429246 | CTCAGCTTAACTCCC[A/C]CATTTTTTACCTGTG | 115426 |
rs569165275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464459 | TCAAAGTTCAAGAAA[C/G]TTTTTTTTTCCTTTA | 115426 |
rs569192890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504287 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 115426 |
rs569198620 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434444 | CTTTTTCTCTATTAG[A/G]TGGGCTTTTTTTGAG | 115426 |
rs569253881 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454147 | TTAGGAATATAGTCC[A/T]AAAGATTTGGTAACT | 115426 |
rs569301672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416870 | CTATTTTAAAGGATT[A/C]TCTCTCGTCATTCTT | 115426 |
rs569303287 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411213 | ACCTAAATATCATCT[C/T]ATTTACATATGTAAT | 115426 |
rs569313885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416230 | CACCACTCCCGGCAA[A/T]TTTTTTGTATTTTAG | 115426 |
rs569347540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490258 | TGTGGAGAAGATGAT[A/T]ACATTAACTGAGATA | 115426 |
rs569351845 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481412 | GCTTTGAGTTTTGAA[C/G]TGAATTTGAGGATTT | 115426 |
rs569356957 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438379 | GTAATGACAGCATGT[C/G]ATTTTTACCTCTAAG | 115426 |
rs569386701 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489762 | ACCATTCATCAGATA[C/T]GTGGTCTTCAGGTAT | 115426 |
rs569415192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417442 | CGCTTCCTTTTTTCC[A/C]TACTTAGAGCTTAAT | 115426 |
rs569418918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470279 | TTGTGAGACTGAAGC[A/G]GGAGAACTGCTTGAT | 115426 |
rs569423907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496174 | TTTTAACTTGAGCCT[G/T]CATAAAAAGAATTAA | 115426 |
rs569424403 | snp | G/T | 7.35254e-05 | 0.00606278 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486789 | CTTAACTGTTCAGAG[G/T]TATTTTGAGACTCTC | 115426 |
rs569432727 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440109 | GGGCCCTAAACATCT[A/C]AATTCACAAAACTGA | 115426 |
rs569463884 | snp | C/G | 0.0236746 | 0.106192 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413029 | CGGTGGGGCAAGTAA[C/G]GGCTTTTGGTAGCCC | 115426 |
rs569469711 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501043 | ACAGTTCAAAGTTAC[C/G]TAACCGCATAAGTCT | 115426 |
rs569476361 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412616 | GACGGGAAACCCTCG[C/G]AAGTGGGTTTCCGCG | 115426 |
rs569476884 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470120 | TCACGCCTATATAAT[C/G]GCAGCATTTTGGAAG | 115426 |
rs569506730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423130 | GATTATTCAAATGGA[G/T]ATAATTTTAGATATA | 115426 |
rs569542545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486182 | TATTTTTAAAAGAAT[C/T]ATCCAGTTTGTGATA | 115426 |
rs569550125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485438 | TGAGATGGATTTGCT[A/G]TTTAGAAAGTGGGGA | 115426 |
rs569578256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459675 | CTCCATCTCACAAAA[C/T]AAAACAAAAAACTTG | 115426 |
rs569621525 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465600 | TGGTACCTACATCTT[C/T]TTAATGTGTTAATCT | 115426 |
rs569627144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479842 | GACAGTTCTTAATAT[C/T]TCTCCATTCTCACCT | 115426 |
rs569638967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453322 | GGTTAATGGAGGTGG[C/T]TCTTTTGCCACTGAA | 115426 |
rs569640840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448083 | AGCTGTGGACCAGGC[A/G]TAAAGCCTACAAAGC | 115426 |
rs569670065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485020 | CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC | 115426 |
rs569697384 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473809 | TTCTAATAAAACTTT[A/C]TTTTTAAAGTTTTTT | 115426 |
rs569703513 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467964 | AAGCTTTATTTGAAG[G/T]TGTTCCTTAGACACC | 115426 |
rs569720799 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6475210 | TACACTATGAATGTT[A/C]ACTAATCACTATGGA | 115426 |
rs569809209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480343 | CTTTCCTTCACTACT[A/G]TGTACAAACATTTTT | 115426 |
rs569847828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443365 | TGTTTTCTTATGTGT[A/G]AAGTGGGAATAACTG | 115426 |
rs569850113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469955 | ATATAAAGAAAATGC[A/G]CAGTGGTATATCACA | 115426 |
rs569885134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475124 | AGTGCCATTTTATCT[A/G]GTCTTTAAATTTACA | 115426 |
rs569922437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469322 | CAGGAGATCAAGACT[A/G]TCCTGGCCAACATAG | 115426 |
rs569927990 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421833 | TTATTTTTGCTACTT[-/AA]ACGTATATTTCTCTA | 115426 |
rs569942449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443039 | TTTTAGCTGATTTCT[A/G]TAAGAATAAAAGTAA | 115426 |
rs569966747 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465104 | GGCCCTGAATTACAT[G/T]GTTGAAAATAAGTAG | 115426 |
rs569975162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448561 | TGCCAGACTGTCCTA[A/C]GGGTTGTTATAAGTA | 115426 |
rs569986412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442516 | CAGGGTCTTGTTCCA[G/T]CACCCTGATTGAAAT | 115426 |
rs570031841 | in-del | -/TTTGTTT | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507545 | GCACTCGGCCCTCAG[-/TTTGTTT]TTTGTTTTTTGTTTT | 115426 |
rs570048331 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447350 | ATTTGTGGGCCTGGT[C/G]TCTCCCAAACACTCT | 115426 |
rs570091553 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479062 | TGCCATTACTAGATC[A/C]TTCTCATTAGCATTC | 115426 |
rs570102082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436222 | ATTTCCAGGATATCT[A/G]GAAATGAATCAAAAG | 115426 |
rs570110657 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497442 | GGAACTACTGTGGGT[-/G]GGCTCGAGGAAACAG | 115426 |
rs570133552 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427000 | GTGATCACCTGCCTC[G/T]GCCTCCCAAAGTGCT | 115426 |
rs570134878 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481357 | TATTCTCAGGGTTAG[A/T]GATAAGTTTAGAGTT | 115426 |
rs570169772 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435598 | CCACTTCCCCAAGAT[A/T]ATAGGATTTATTTAT | 115426 |
rs570170081 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456756 | TTCTACATGTGGCTA[G/T]CCAGTTTTCCCAACA | 115426 |
rs570187044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457577 | AGAGGCCATCCCTGT[C/T]TTGTGCCAGTTTTCC | 115426 |
rs570232330 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507382 | GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCC | 115426 |
rs570232804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435164 | ACGCCTGGCTAATTT[C/T]TGTATTTTTACTAGA | 115426 |
rs570248566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462666 | GCTCATGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 115426 |
rs570273243 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411410 | TGAGATGGAGTCTCA[C/T]TCTATCGCCCAGGCT | 115426 |
rs570277074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426420 | TTAGGAGCACATTGG[A/C]ATCTAGTAATAAAAT | 115426 |
rs570310902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431684 | GTTGATGTTCAAGCA[A/G]TGGCAGTATTTTGAG | 115426 |
rs570385210 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461415 | CCTTGTTCTGTCACC[C/T]AGGCTGGAGTGCAGC | 115426 |
rs570385929 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436760 | GTACCTTAGCATATA[A/T]TTGGCAACTTTTTTT | 115426 |
rs570397841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451461 | TTCTTACCTAGTTTT[G/T]TTTTGTTTTTTTTTT | 115426 |
rs570427876 | in-del | -/AA | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501035 | TTTTTGTTACAGTTC[-/AA]AGTTACCTAACCGCA | 115426 |
rs570433714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467600 | CGAGAGAATAGTTTT[G/T]TTTTTTTTTTTTTTT | 115426 |
rs570454931 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464743 | ATCCTTTTGACTTCT[C/G]TATTCTGTACCATGG | 115426 |
rs570457720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456237 | GCCATTCTAACTGGC[A/G]TGATATGGTATCTCA | 115426 |
rs570473530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441085 | GCACCACGTGTTAGA[A/G]ATGCAAATTCTTGGC | 115426 |
rs570474699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500078 | CCTGGGCTCAAGCGA[G/T]CCACCTACCTCAACC | 115426 |
rs570475751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504862 | CATGTTTTAATTAGA[C/T]AGTGATAATAATTCA | 115426 |
rs570513318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505277 | CTGCTAAATATATAT[A/G]TATGCGTGTGTGTGT | 115426 |
rs570516737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418723 | TAGTTTTCTTGTTTC[A/G]CTGTATCATAGTGAA | 115426 |
rs570591199 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442803 | GCATGGCACGAACTT[C/T]ATGATGATATGGTCT | 115426 |
rs570620533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483762 | TGGCACGATCTTGGC[G/T]CACCACAACCTCTAC | 115426 |
rs570623645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498710 | GTTGATTTTGTGTGC[A/G]TAGTGGATGGTATGG | 115426 |
rs570664918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500775 | AATAATTGTCTCATG[A/G]AGTCTGTTTTTCACA | 115426 |
rs570692116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420073 | ACCTTTTTTTTTTTC[A/T]TTTTTGACAGTCTCC | 115426 |
rs570696503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488732 | GTCTGGAACTCCTGG[C/G]CTCAGGTGATCTGCC | 115426 |
rs570727125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450426 | TGTTATGTGTTAGTT[C/T]CCTGAGAAGCTAATA | 115426 |
rs570754213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482269 | AACAAAGGAACATAC[A/G]TCACAGAATTGGGCA | 115426 |
rs570840015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413774 | CTGCGGGTGGGCAGC[C/T]CCCGCGAGGCGCGGG | 115426 |
rs570871320 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489148 | ACTTCAAGAATTTTT[A/G]TAAATGGAAGTATGT | 115426 |
rs570895039 | snp | A/G | 0.000799201 | 0.019974 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423968 | TAAATAAATAAATAA[A/G]GGAACTCTTGATAAG | 115426 |
rs570908282 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507094 | ACACTTGTCTGGCTT[A/G]TGTTATCAGTTTTAA | 115426 |
rs570942607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455311 | ACCCCACAACAGGCC[C/T]GGGTGTGCGATGTTC | 115426 |
rs570950035 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453674 | ATGGGATTGGCCAAG[A/G]CGGGCAGATCACGGG | 115426 |
rs570963727 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480780 | AGTATTTAGTGCCTT[C/G]TCAAACATAATTTGC | 115426 |
rs571021333 | in-del | -/AT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456306 | GATGAGCTTTTTTTC[-/AT]ATGTTTGTTGGCCGC | 115426 |
rs571036958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472297 | TTAGGAAATTTATCT[C/T]ATGAAAATAAGCGAA | 115426 |
rs571063946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445435 | TTCGGCTAATTTTGT[A/G]CTTTTAGTAGAGATG | 115426 |
rs571072696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477428 | CTACTCGAGAAGCTG[A/T]GGCGGGAGAATCGCT | 115426 |
rs571119372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445858 | CATTAGCCACTGGTC[C/G]TAGCTCTTTCTTCTA | 115426 |
rs571157663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498288 | GTGAGGAATAAGATC[A/G]TGCAAATAGACAGAG | 115426 |
rs571168397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450902 | GCACATAGTCTGTGC[C/T]GCTTACTGATATGTG | 115426 |
rs571219494 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412504 | CCCGACTTCTCCAAG[A/G]CCGGAGGGCCGGCTG | 115426 |
rs571224749 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412460 | AACGGAAATGTCCGG[A/T]GTTAGAGAGCGGCCT | 115426 |
rs571238143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481279 | GAGTTGTATCTGTTA[C/T]ACAGTTGAATGTTCT | 115426 |
rs571297236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438581 | CTGCAAACCTCTTGA[A/G]TGTAGCAGTGTAGTT | 115426 |
rs571297568 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491893 | TTTTCCATAGGAAAA[A/G]TATTTTATTTTTATT | 115426 |
rs571300358 | in-del | -/A/AG | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488087 | CCTACCAAAAAAACA[-/A/AG]GAGAAATTAGCTGGG | 115426 |
rs571317691 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494008 | TAAATTGTAACTTAC[A/G/T]TTGCAGAGGAGAATT | 115426 |
rs571324847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491414 | ACCCACCAGTAGTAG[A/G]TGTGTGTTACACTAG | 115426 |
rs571336419 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423471 | AAAAAATTATGGCTG[C/G]TTATTAAAAATATAT | 115426 |
rs571387019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466276 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 115426 |
rs571437892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503787 | TATGTAATGACCTTG[A/G]GACACGTTGCCCATG | 115426 |
rs571468184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504268 | CTGACCTTGTGATCC[A/G]CCTGCCTCGGCCTCC | 115426 |
rs571512741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434348 | GGTCCTTTTAGCTCT[C/T]GATTATCTCTGGTTC | 115426 |
rs571517506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463580 | GATTCAAGCAGTTCT[C/T]CTGCCGCAGCCACCG | 115426 |
rs571523329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423820 | TGCGATGGCAGGTGC[C/T]TGTAATCCCAGCTAC | 115426 |
rs571533801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427753 | CTCTGTTTGATAACT[C/G]AGCAATATTTAACCA | 115426 |
rs571554582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469881 | AGCCCAAAATTTCCA[A/G]AACTGATTAAAGATA | 115426 |
rs571581791 | in-del | -/GAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462488 | ATGGATGCAAATCAT[-/GAA]GAAGGAGAAAGCCCC | 115426 |
rs571584704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439035 | TTTCCTAATTTATCT[C/G]CACTATTCCTTCAAA | 115426 |
rs571594726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453452 | ATAGAACAGGTTTCT[A/G]TCTTACATGGACTTA | 115426 |
rs571597794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432418 | CTCACTTACCTTTGA[A/G]GTTCCTGTATACCTG | 115426 |
rs571607475 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460457 | TTAAGGACACTTCAA[C/T]CTATTTTACTCTTTC | 115426 |
rs571654897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458617 | GAACGCTTTTATACT[G/T]TTGGTGGGAGTGTAA | 115426 |
rs571738484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486089 | ATATTTAGAGAGGGT[A/G]ATAAATCATGTTGAC | 115426 |
rs571754080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469536 | AAAAAATTAAAAAAC[A/T]TAAAAAAATAACAAA | 115426 |
rs571765938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420530 | ACACGGTGAAACCCC[G/T]TCTCTACTAAAAATA | 115426 |
rs571773746 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415242 | GACTTTCAGTAAACT[A/G]GGAAGCTCATTCCAG | 115426 |
rs571775106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490975 | GTTTCCTGAATTCTT[C/G]AATTTGGTATAAATT | 115426 |
rs571812435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475017 | ACCAAAGGACAAAAC[A/G]AACAGAAAACATACC | 115426 |
rs571839375 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436798 | AGAATGAATGTTAAG[C/T]AAAGGGGAATCTAAA | 115426 |
rs571851317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417388 | ATGGACCTAAGTTAC[A/G]TGCTTCTGACTCACA | 115426 |
rs571851696 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417344 | TCTTCGAGTATGGCA[C/G]TTCTCAAACATTTGC | 115426 |
rs571870638 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446172 | AATTTTTTTTTTTTT[-/T]ATACAGTCTTGCTCT | 115426 |
rs571874411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490360 | AGGCCAGTCACAGTG[C/G]CTCATGCCTGTAATC | 115426 |
rs571898587 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438753 | CGTATCTAATAGATT[A/G]CTAGACCAGATTATC | 115426 |
rs571914214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416972 | AAAGTTGCCTCTCCC[A/T]CTTGGTTTTCACACA | 115426 |
rs571922066 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462424 | GATTCTATTGCTAGA[C/G]TAAGGGTATAGCTCA | 115426 |
rs571935695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464092 | TGTTGTTAGTTTTCT[C/T]ATCCATGCTTAGTTT | 115426 |
rs571938793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421945 | CTGTGTTTTATTCCT[G/T]TTCACTATTATGTCA | 115426 |
rs571974158 | in-del | -/TTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416063 | TTGACTCCACTTTTT[-/TTG]TTGTTGTTTTTGTTT | 115426 |
rs571975010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483846 | AGGCATGCACCACCA[C/T]GCCTGACTAATTTTG | 115426 |
rs571981545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496715 | AGGATTCTCTATTGT[A/C]TGGAATGTGGAAAGT | 115426 |
rs572004667 | snp | G/T | 0.311369 | 0.242351 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442666 | GATTTTTTTTTTTTT[G/T]GGGGGGGTAGAGATG | 115426 |
rs572016832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442090 | ATGCCTTAGCCTGTC[A/G]AGTAGCTGAGATTAC | 115426 |
rs572031510 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465979 | TTCAAAAACATTTTT[A/T]AAAATAATTTGTTCA | 115426 |
rs572057493 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502469 | TTTAGTTTAAAAAGT[C/G]CAAACAGATGGGGTT | 115426 |
rs572061432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479216 | TTTCCATTTCCTCTC[A/C]TATTCATACTTCAGC | 115426 |
rs572097192 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507135 | ATTTCTGGAGTTTTT[C/T]ATTGTGCATCTCTAT | 115426 |
rs572109414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488398 | TCAGAACCAGGATAT[C/T]GACACTATACAGTCA | 115426 |
rs572154048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451537 | GTTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 115426 |
rs572218605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456784 | ACACCATTTATTAAA[C/T]AGGGAATCCTTTCCC | 115426 |
rs572247579 | in-del | -/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506697 | GCAAGGACAGGTTCA[-/T]TTTTTTTAGCCCACT | 115426 |
rs572260999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473627 | AACCTAAATCTGATT[G/T]AGACTGAGTCTTTAG | 115426 |
rs572335480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425348 | GTGTTTTGTTTTTCT[C/T]AAGCATTATCTTACT | 115426 |
rs572359556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424891 | TTGTCTGGGTTTGTT[C/T]TGGGGAGGAAGACCG | 115426 |
rs572383686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467197 | TTTCTTGCCTTTACC[A/G]TGTTTCAGACGCCTC | 115426 |
rs572428892 | snp | A/C/G | 0.00019207 | 0.00979808 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499826 | CTCTCCCTCCTCCCC[A/C/G]CCCATCAGTATCCAG | 115426 |
rs572437268 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435364 | CTCCTGGGCTCAAGT[G/T]ATCCTCCCACCTCAG | 115426 |
rs572580233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440281 | TGTTGTCTTATGTGC[C/T]GGACTCTGAGCATAA | 115426 |
rs572631906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456288 | TCTCTAATGACCAGT[A/G]ATGATGAGCTTTTTT | 115426 |
rs572635767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493493 | ATTGATAAGTTTTAA[C/T]ATTGAATTGAATAAA | 115426 |
rs572637963 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494236 | AATAAGGTGGCTTGT[C/G]TACTACTCCATTGGT | 115426 |
rs572640582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465506 | CTATTCATGTTTTCT[A/G]TTTCTTGAACTAAAA | 115426 |
rs572641619 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430326 | TTAATGTGGCTATAT[A/C/G]TTTGATGTGAATGAA | 115426 |
rs572663605 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505311 | TATATATATATATAT[A/T]TTTTGACGGAATCTC | 115426 |
rs572670227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435742 | CTCCTGAGTAGCTGG[A/G]GGCTACAGGTGCTTG | 115426 |
rs572700233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461633 | CGCCTCTGCCTCCCA[A/G]AGTGTTGGGATTACA | 115426 |
rs572710422 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455019 | CTTTGAGAACCACTG[C/G]TGTAGTAGCCTGGCC | 115426 |
rs572718904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430036 | TTTCTTTTTTTGAAA[A/T]GGAGTTTTACTCTTT | 115426 |
rs572723682 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477180 | AGGGGCTGCAGTGAG[C/G]TAAGATTGGCACCAT | 115426 |
rs572790110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492143 | AATGATTAAAGTACA[A/G]ATGAGTTAATGGTAC | 115426 |
rs572809719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461089 | TGAACAAAACAATAT[A/G]TAAAAGCATTTTAAT | 115426 |
rs572856226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428582 | TTTTTGAACGATCTC[A/G]TTCTGTCACTTGGCT | 115426 |
rs572875165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443690 | ACATACTTTTTAGTA[C/T]TAAAAGGGTTGCTTA | 115426 |
rs572888129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428937 | GGGAGGTGGAGGACA[A/G]GTGGATCACTTGAGG | 115426 |
rs572905368 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422725 | AGTGATCTTCCTGCT[C/T]GGCCTCCCAAAGTGC | 115426 |
rs572923096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450978 | TAATACTTAAATATA[C/T]CATGGGTGAATATTG | 115426 |
rs572936242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413923 | TTTGGTAGGACAGCG[A/G]CCGTAGGCACTGGGT | 115426 |
rs572955054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422697 | TCGCTGTAGCCTTGA[C/G]CTGCTGGGGTCAAGT | 115426 |
rs572955210 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447410 | TGAAAAATTGCTGTT[A/C/T]TATAGTATGATGGAA | 115426 |
rs572979744 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487700 | AGAGCTGGGGTTTCG[C/G]CATGTTGGCCAGGTT | 115426 |
rs572988308 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503968 | TATAACTTTGCTCTT[C/G]TCAGGTAGTTAAAAA | 115426 |
rs573040314 | snp | C/T | 0.000111499 | 0.00746572 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413625 | CGAATGCCAGCGCCT[C/T]TTCTACCGGGGCAAG | 115426 |
rs573055449 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486998 | ATAGCTTTGCCTAGG[A/T]TACATCAAATACTGT | 115426 |
rs573056744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487333 | ATGTGAGATTTCAGG[C/T]GCCTGCCATCACACC | 115426 |
rs573141929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455419 | TTGCGATAGTTTGCT[A/G]AGAATGATGGTTTCC | 115426 |
rs573176889 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412651 | AGTAGCATTGCGGCC[A/G]GGCGGGAAACGTGTT | 115426 |
rs573179835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438685 | ATTCTGGGGTATGCA[A/G]TGTTTGTCAGTTAAA | 115426 |
rs573191898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424066 | AGACAAGGAAGCCAA[C/T]TCATGCTTCCTTATT | 115426 |
rs573202820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412128 | CACTGCACTCCAGCC[C/T]GGGCGACAGAGAGAG | 115426 |
rs573235986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417512 | AATGTGGAAGAACTT[C/T]GGTACTTTTCAAGTA | 115426 |
rs573238643 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428902 | AGTGTGGTGGCTCAT[-/G]CCTGTAATCCCAGCA | 115426 |
rs573242002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448774 | AGTTAAGAATGTGGT[A/G]GGTTGTGGCAGTAGA | 115426 |
rs573244898 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474164 | CTATGTCTTCTGTCA[-/T]TGGTGGTCACAACGG | 115426 |
rs573274779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454266 | AGACTGAAAATAGAA[C/G]ATCTTTTGAGTGAAG | 115426 |
rs573297972 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421848 | TACGTATATTTCTCT[A/T]GGCAGTATGTTTTGT | 115426 |
rs573363089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471351 | TTGAAAATAGCAGCT[A/G]TGGTAGCCATCTTTT | 115426 |
rs573371710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470758 | TTATATCAGGTTTGC[A/G]CAGTCCAATCTCTAA | 115426 |
rs573375781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467064 | CATAGTAGCTTAAAC[A/T]ATAAAGCATAGTACA | 115426 |
rs573525307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437387 | ACAGGTGCCTGCCAC[C/T]ACGCCTGGCTAACTT | 115426 |
rs573533126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421639 | CCAGGCTAGTCTCGA[A/G]CTCCTGACCTCAGGT | 115426 |
rs573567998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474604 | CCAGCTACTTGGAAG[A/G]CTGAGGCAGGAGAAT | 115426 |
rs573617159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434984 | TATAGGCATATGTAT[C/T]ACCATGTTTGGCTAG | 115426 |
rs573655691 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411406 | TTTTTGAGATGGAGT[A/C]TCACTCTATCGCCCA | 115426 |
rs573659584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436984 | TTTAAAAAGAGGAAA[G/T]GACTATATAAAATAT | 115426 |
rs573685952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462764 | TCTACTAAAAATACA[A/G]AAATTAGCTGGGTGT | 115426 |
rs573690494 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422437 | CCTCTTTCAGGGTCT[C/T]TTGGCTTTTAATATT | 115426 |
rs573698069 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462325 | TGACTCCTGAGATTT[A/T]AAAAAAAAAAAAAAA | 115426 |
rs573715739 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444826 | CAGGCTGGTCTTGAA[A/C]CCTGACCTTAGGTGA | 115426 |
rs573756743 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443138 | AATATGTCTGTATCT[C/G]ATCTTAAGAATGAAG | 115426 |
rs573822595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442730 | CTCCAGGCTCAAGCA[A/G]TCCTTTCACCTCGGC | 115426 |
rs573834577 | snp | A/T | 0.000638366 | 0.0178543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468390 | ATTAGTGCTTTTAGC[A/T]AAAACAACTAAATAG | 115426 |
rs573843178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458828 | AACCCAAATGCCCGT[C/T]GATGATAGACTGGAT | 115426 |
rs573885470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479542 | TCCCTAGATGATCTC[A/G]TCCAATTATGAGATG | 115426 |
rs573966131 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456973 | TTCTTTTTGCTTAGG[A/T]TAGTCTTGGCTATAC | 115426 |
rs573999720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489071 | TACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 115426 |
rs574022660 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463417 | ATTAAAGTTTTTACT[A/T]GAAACGTTAGGAACA | 115426 |
rs574045296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446133 | AAGTAACTAGGACTA[C/T]AGGCATACGTCACCT | 115426 |
rs574055799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436412 | GTTGAAGTTGGTGTA[C/T]TAATAGTAAGTGGTC | 115426 |
rs574086480 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495389 | TTAAGTTGTGAATAC[A/G]CCTTGTGATTGTAAA | 115426 |
rs574158758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501016 | CTAAAAATCACCACG[A/G]AAGTTTTTGTTACAG | 115426 |
rs574173502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490101 | CCAACTAGAAATGTA[G/T]TCTCTTTAACATTTG | 115426 |
rs574177404 | in-del | -/GA | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439822 | AAACCCTGGTTACTG[-/GA]GAGAGACTATACTTG | 115426 |
rs574184843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430537 | CCTAGAGATAGTAAA[C/G]AGCTGATCAGTGAGC | 115426 |
rs574203639 | snp | C/G/T | 6.61141e-05 | 0.00574922 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506192 | TGATCTGCCTGCTTT[C/G/T]ACTGTGTTGTTCATG | 115426 |
rs574208994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424719 | AATCCCACTAGGATA[C/T]TATACTGTGTGTAGT | 115426 |
rs574218644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489439 | TGCCCCAGAAGTGCA[A/G]TTCCTGGGTCATATG | 115426 |
rs574235147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492456 | TAAAGATTAAGTTTC[A/G]TAATACCTTGTTTAA | 115426 |
rs574235223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415322 | TAGTGGGTAATTCAC[C/T]ACTTGGGTTTCTTCA | 115426 |
rs574236406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447576 | AAAGCATATAGTGAG[A/T]AAGAAGAAATGAAAC | 115426 |
rs574267585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467991 | CACCTCATCACAGTC[C/T]TTTTTTCTTACTTGA | 115426 |
rs574273316 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504800 | AAGCGGGATAGTTGC[A/G]GAACCTTCTAGTTAA | 115426 |
rs574278929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457706 | AGTTTATTGAGAGTT[G/T]TTAGCATGAAGGGGT | 115426 |
rs574296734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420632 | GAATGGTGTGAACCC[A/G]GGAGGAGGCGCTTGC | 115426 |
rs574334646 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495606 | AAACTTTAAGAAACT[A/G]AAGAGGGCAGCAAAG | 115426 |
rs574338958 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414538 | TCCACAAGTCTCTTA[A/C]AATCTATATCCCTAG | 115426 |
rs574344097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421299 | TTTTAAAAATTGATA[C/T]GAAATACGTAGACAA | 115426 |
rs574344269 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463691 | GTCCAGGCTGGTTTC[A/G]AACCCCTGAGCTCAG | 115426 |
rs574365397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456265 | TCAGTGTGGTTTTGA[C/T]GTGCGTTTCTCTAAT | 115426 |
rs574401719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426522 | TATTTACTTTTTGGG[A/G]GATGAACCTTAGTAA | 115426 |
rs574423752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414107 | TCTTCGGCTCTCAAA[A/C]AGGGGAAACTCGGGC | 115426 |
rs574500108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456067 | TTTGTAATACTTACT[A/G]TTAGGAAATATACGT | 115426 |
rs574502106 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420320 | TCGGCCTCCCAAAGT[A/G]CTGAGATTACAGGCG | 115426 |
rs574513921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488191 | GAGGCTGTAGTGAGC[C/T]ATGATCATGCCAGCG | 115426 |
rs574542739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435856 | TCAAGTGATCCACCC[A/C]CCTTGGCCTCCCAAA | 115426 |
rs574552273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487832 | TTGGTCATTCTTCTT[A/T]AAGTTTTCTCTTTTA | 115426 |
rs574556038 | snp | C/T | 6.73117e-05 | 0.00580098 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413522 | GCACCATTGATGGCT[C/T]CAAGACGTGCACCAT | 115426 |
rs574587472 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477543 | AAAAAAATGCTGTTT[C/T]CATGGGCTTTTCTTT | 115426 |
rs574601302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487292 | CCTTTGGGTTCAAGT[C/G]ATTTTCCTGCCTCAG | 115426 |
rs574682570 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449824 | AATGCTCTAATCTGC[C/T]CTAGCAGACAATATT | 115426 |
rs574717762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425513 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGGAGGG | 115426 |
rs574738960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440200 | GGAAGTAGTGGTCTT[C/G]AAGGGCAGTCATTTC | 115426 |
rs574756673 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469749 | GTGTATATATATACA[A/C/T]GTATATATACACACG | 115426 |
rs574766524 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427621 | ACCCAGGAGGTGGAG[A/G]TTTCAGTGAGCTTAG | 115426 |
rs574772513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504883 | TAATAATTCAAATAT[G/T]TGTCATTTGAGATAT | 115426 |
rs574792274 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498502 | ATCCTAGAGGGCACA[-/G]GGGGGTGTCTCTCTG | 115426 |
rs574808726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504426 | ATATGTTCATATAAC[A/G]TATAATAAATCAGGG | 115426 |
rs574811109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476641 | CTCTTGTTGCCCAGG[C/G]TGGAGTGCAGTGGCG | 115426 |
rs574811669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477101 | AGCTGGGTGTGGTGG[C/G]AGGCGCCTGTAATCC | 115426 |
rs574813275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439337 | TGCACCACCACGCCC[A/G]GCTAATTTTTGTGTT | 115426 |
rs574826546 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452086 | ACCGTTTGCACCTTA[-/T]TTTTTTTAAGTTCAT | 115426 |
rs574935255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460372 | GAGACAGTTCATGCT[A/G]ATATAGAAACTACCC | 115426 |
rs574943018 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422768 | GTGAGCCACCATGCC[C/T]GGCTAACTTAGATCT | 115426 |
rs574967432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445552 | AGAGGTGAGCCACCA[C/T]GCCTAGCCTCTTTAT | 115426 |
rs575020572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435294 | CCACCACACCTGGCC[A/G]GCTAATTTTTTTGTA | 115426 |
rs575081540 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413283 | CTCAGAGTGGTTCCG[A/G]TCGTCTCTCCTCAAG | 115426 |
rs575110369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467128 | TTTCACTAGGCAAAA[A/G]TCATTGTTAGCAGGG | 115426 |
rs575119935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459500 | ATGGCAAAACCCCGT[C/T]TCTACTAAAAATTCA | 115426 |
rs575181817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491481 | TGAGAGAAGTTGGTA[A/G]CATTTGAGGCTATGG | 115426 |
rs575194221 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453598 | CGTTGTGAAACAACA[C/G]GAGTGTATAAATACC | 115426 |
rs575249640 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489819 | AGATGAATCAATATG[A/G]GTAGTTATGGAGAGA | 115426 |
rs575291058 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467195 | ATTTTCTTGCCTTTA[A/C]CATGTTTCAGACGCC | 115426 |
rs575300396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438655 | ATGAGATGAAAGAAA[A/C]CTGCCTCTGGAATTA | 115426 |
rs575336770 | snp | C/T | 0.00158657 | 0.0281206 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481634 | TTCGTTCTTTTTTTT[C/T]TTTTAAAGGTATTGT | 115426 |
rs575347643 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498587 | TCACTTTTCCTCACC[C/G]CTTTTCTCTCTTCCC | 115426 |
rs575411503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417702 | CCTGTCATAGCAAGC[A/T]TGAGGAAAGGTGGTT | 115426 |
rs575415900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501836 | CTAATTATTCTCTGA[C/T]TGGGAAAGATAGGGC | 115426 |
rs575426893 | in-del | -/ACAT | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469714 | TACATACATATACAC[-/ACAT]ATATGTGCATATATA | 115426 |
rs575444968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423538 | CAGTTCATTATTATA[A/G]AATGTTTCAATATAA | 115426 |
rs575462620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422894 | CTAAAATAGTAATCT[G/T]TTTGCTGATATAGAG | 115426 |
rs575465964 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470881 | CTAAAAGAAGCAGAT[A/G]AAGTAGAAAACATAC | 115426 |
rs575493616 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478858 | TTACCTCCTACTACT[A/T]CCTCATATGATCACA | 115426 |
rs575500136 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436199 | TATAACAACACTTCA[C/G]TATTCAGATTTCCAG | 115426 |
rs575500686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498360 | CTGGGACCAAGGGTT[C/G]TGCTTGGGAAAAGTT | 115426 |
rs575571662 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474517 | TCGAGACGAGCCCAG[C/G]CAACATGGTGAAACC | 115426 |
rs575609693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450787 | GTGACATAATAGTTT[C/T]TGAATGTTTCTTTGT | 115426 |
rs575611790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458777 | GCACATGTATGTTTA[C/T]TGCAGCACTGTTCAC | 115426 |
rs575642602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421983 | TTATTAACATACCGC[A/G]GTATATTTAATCCAT | 115426 |
rs575686109 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411488 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCG | 115426 |
rs575695834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415790 | CTCACCCCAGAACTG[C/T]AAGTAGTTGAATTTA | 115426 |
rs575712978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438077 | AAATGTAAAACTACA[A/G]TGAAGAGTAGCCAAA | 115426 |
rs575740879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489397 | CAGGTTTTTTGTAAA[C/T]GTAAGTCTTTATTTC | 115426 |
rs575754457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485304 | TTGTGTATTTCTAAT[A/T]GCCTTATTTTTTTGC | 115426 |
rs575754466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490459 | ATGATGAAACTCCGT[C/T]TCTACTAAAAGTACA | 115426 |
rs575807177 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503803 | ACACGTTGCCCATGA[-/T]TTTTTTTATTTTTTA | 115426 |
rs575831693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458304 | TGTAGTATTCTCTGA[G/T]GGTAGTTTGTATTTC | 115426 |
rs575867058 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436049 | ACAGATTTAGTATAT[G/T]AAACACACTAAATGA | 115426 |
rs575868870 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461275 | AAATGTCACCTGAAT[C/G]AAATCCTTCAGATAT | 115426 |
rs575868904 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431969 | CGACAGAGTAGTAAC[C/G]TCAGTTTATTCTCCC | 115426 |
rs575901820 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424903 | GTTTTGGGGAGGAAG[A/G]CCGCAGAGGTATTTT | 115426 |
rs575904587 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438438 | ACTTTAACTAAATAG[A/G]CTTTAAGTGCTTATA | 115426 |
rs575913230 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442721 | GGTCTCGAACTCCAG[C/G]CTCAAGCAATCCTTT | 115426 |
rs575949738 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507240 | CTCAGTTTTTGTTTG[G/T]TTGGTTGGTTTTTTG | 115426 |
rs575975917 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412097 | AGGCGGAGCTTGCAG[A/T]GAGCCGAGATCGCGC | 115426 |
rs575991114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479439 | GGTTCCCGTCACCTA[C/T]CAGATTTCAGAGCAC | 115426 |
rs576016121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485804 | CCCCTGTCTCTACCC[A/C]AAAAAAAAAAAAAAA | 115426 |
rs576062216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479269 | ACTGTATCTGCTTAT[A/G]TCAGGTTCACAGACA | 115426 |
rs576098902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483878 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 115426 |
rs576112301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502289 | CTGTTTTATTTAAAC[A/G]TGCTCGACGTCTTGA | 115426 |
rs576129376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447179 | CAGGCATGAGCCACC[A/G]CGCCCAGCCAGCACA | 115426 |
rs576140800 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463228 | GCAGATTGCCGTGAG[C/G]TGAGGTCATGCCATT | 115426 |
rs576185068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447546 | TGAGAGTAGATTAAT[A/G]CAGCTGGAGTGTAGA | 115426 |
rs576207475 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498469 | ATTTAGGTATAGGAG[A/G]CCCTGGAAAAGGACA | 115426 |
rs576208449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462857 | ACGAGGCAGAGGTTG[C/T]AGTAAGCCGAGATCA | 115426 |
rs576247268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452353 | ATAGACAGTGTTTCT[G/T]GTAATTAACAGATGC | 115426 |
rs576252202 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461334 | CTTTCTGTCTCTCTC[C/T]CTCCCTCCCTCTCTC | 115426 |
rs576267328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501828 | TAATCAGCCTAATTA[A/T]TCTCTGATTGGGAAA | 115426 |
rs576309205 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502761 | CGTATTATAGGAACT[A/G]TGGAAGTACCAGGTT | 115426 |
rs576312818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494867 | TGCGTATCAATTTAC[A/G]TAGAATCTCTGTTTT | 115426 |
rs576362893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474592 | AGGCCTGTAATCCCA[A/G]CTACTTGGAAGGCTG | 115426 |
rs576365141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469158 | GAGAATTGGAATTCA[C/G]AAAATAATTATATGG | 115426 |
rs576404056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467899 | GAATTTTTTCTATCT[G/T]CAAGGTGTGGTTTAT | 115426 |
rs576468492 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431992 | ATTCTCCCAAGTATG[A/G]TGGACCTTAACATTG | 115426 |
rs576489577 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478162 | TCTTACCACTTTCCT[C/T]TTTCATTTCCCCAAA | 115426 |
rs576500198 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477440 | CTGAGGCGGGAGAAT[C/T]GCTTGAACCCGGGAG | 115426 |
rs576539655 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453768 | AAACCAACCAGGAGT[A/G]GTGGCAGGTACTTGT | 115426 |
rs576545384 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457718 | GTTTTTAGCATGAAG[A/G]GGTTGAATTTTGTAG | 115426 |
rs576580442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456900 | GGTCTACATGTCTGT[A/T]TTGGTTACTGTAGCC | 115426 |
rs576582868 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423521 | TTGTCAGGATGTGGG[G/T]ACAGTTCATTATTAT | 115426 |
rs576608396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435820 | CACTATGTTGGCCAC[A/G]GTGGTCTCGAACTCC | 115426 |
rs576627401 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420254 | TAGAGACGGGGTTTC[A/G]CCATGTTGGTCAGCC | 115426 |
rs576660665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477526 | AGCAAAACTCCATTT[A/C]AAAAAAAATGCTGTT | 115426 |
rs576811031 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424659 | TGTTGAAATTAATGA[C/G]CCATATTTTCTTAGC | 115426 |
rs576830584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430982 | TTCCTCTTTTGTCTG[C/T]TATTTTGCTACTCCT | 115426 |
rs576833044 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413209 | GCTCTATAAGTAAAC[A/G]CTCTGCGCGGCGCAG | 115426 |
rs576836878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456327 | TTGTTGGCCGCATAA[A/G]TGTCTCCTTTTGAGA | 115426 |
rs576850418 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499726 | AAAGTTTTTCAGTTT[C/G]GGGAACGTGTAGTCT | 115426 |
rs576892903 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412688 | GCAGGAGGGCCCCCG[A/G]GGCCTTTCCCGGGCG | 115426 |
rs576894551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429445 | TTTTAGACAGAGTCT[C/T]GCACTGTCATGCAGG | 115426 |
rs576894927 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418215 | CTCCTTGAGTTTTTT[G/T]GGGTTTTTTTCCCTC | 115426 |
rs576933886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491925 | TTTAATAGAGACAAG[G/T]TCTCGCTATGTCACC | 115426 |
rs576941450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440827 | GTTTTCAAAATAATC[A/G]GTGCATGAGACCTCT | 115426 |
rs576945629 | in-del | -/TGTG | 0.0829062 | 0.185956 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469721 | ATATACACACATATA[-/TGTG]CATATATACGTGTAT | 115426 |
rs576952899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418927 | CCTTTACACTTTGCC[A/G]GAAATTTTCTTTCTT | 115426 |
rs576958177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478302 | TGGTTAACTTCAAGA[C/T]GATACTAATCCTTCA | 115426 |
rs576985195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456013 | AAAATATGTAAAATT[A/G]AAGAACCTTATAAAG | 115426 |
rs577036989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482823 | GGATGGTCTCGATCT[C/T]CTAACCTCGTGATCC | 115426 |
rs577051414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446069 | ATGATCTCGGCTCAC[G/T]GCTGCCTTGACTTCC | 115426 |
rs577079812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487756 | ATCTGCGCACCTTGG[C/T]TTCCCAAACTGCTGG | 115426 |
rs577102195 | in-del | -/AAAAAAAAAAAA | 0.151668 | 0.229849 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485804 | CCCCTGTCTCTACCC[-/AAAAAAAAAAAA]AAAAAAAAAAAAACA | 115426 |
rs577120327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439989 | TTCTTGTTTCATTTT[A/G]GTAAGTGTGTACTGT | 115426 |
rs577148033 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471906 | AGGAAAAAGGAGTCC[A/G/T]GTTAGAAATAGGGGA | 115426 |
rs577177059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413964 | CTCGCTTCCCGCGCT[C/G]GGCGGGGCCTGGGGC | 115426 |
rs577184659 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474023 | GAGACTTTTCAAACA[C/T]AGGCAAAACTGTTTT | 115426 |
rs577250508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449943 | TGGTTTCCTCTGGTC[A/G]CCTCATGTGCCTTTT | 115426 |
rs577273210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475295 | AATTTATAAATAGAC[A/G]GATTTCAGTGAGATT | 115426 |
rs577278054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486330 | TTAGGAGGTAAAATC[A/G]GCAATCCTTGTAACC | 115426 |
rs577287650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501301 | CTTCAAATATGAACT[A/G]TCTCTTCATTCTTTC | 115426 |
rs577306494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476580 | TTTTAATTCATGATG[A/G]GGCTTTTTTTGTTTG | 115426 |
rs577321115 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421320 | ACGTAGACAAATGTA[C/G]AAGATGTATATGTAC | 115426 |
rs577350137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466658 | TTAAGAAATTTCTAT[A/G]GTGATATACTTCTTA | 115426 |
rs577386930 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432209 | CTAAACTGTTCATTC[C/T]TGTGTAATATTAAAC | 115426 |
rs577395343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417615 | TTGCGGTAGATAAAT[A/G]GTCACTATTGTAGGA | 115426 |
rs577398472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429055 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAAGC | 115426 |
rs577500941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497697 | TGTAATAGATTTTCA[A/G]AGCAGCACATCATAG | 115426 |
rs577538490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497085 | AATATGGAAAGAATC[A/G]TAGAATCTTAACCAT | 115426 |
rs577547806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463779 | TCTGGAGAAAAAAAA[A/T]TTTTTTTTTTAATGA | 115426 |
rs577569109 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476153 | GTCCTTCTGTACTTG[A/G]CTTCTTTCACTTAAC | 115426 |
rs577569502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471434 | CAGCCATACTTCACT[A/G]GGGTGGCTCTTTGTG | 115426 |
rs577571474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476951 | GGTTCCTTTCTTTTC[A/G]TTAGAAAAGCTGTAT | 115426 |
rs577634430 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441864 | ATTTCTCCACTATAC[A/C]GTCTTTACCCATATT | 115426 |
rs577636879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457817 | TATGTTTATTGATTT[A/G]CATATGTTGAACCAG | 115426 |
rs577671167 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416503 | GGATTGGGTCTTTTT[A/C]AGGAAGAGATTATGT | 115426 |
rs577676061 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444697 | ACCTCCCCCTCCAGG[A/G]TTCAAGTGATGTCTC | 115426 |
rs577680298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443446 | CAGATTCCAAAAAGC[A/G]CATGCTTGCAACTAC | 115426 |
rs577707596 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489875 | GACAAATAGAAAAGC[C/G]TGCTGGCTTTCTGAA | 115426 |
rs577749707 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457912 | GGATTCGGTTTGCCC[A/G]TATTTTATTGAGGAT | 115426 |
rs577807513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480428 | GAACAAACCTGTTGA[A/G]GGAGTGAATCAATCC | 115426 |
rs577811720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474735 | CAAACAAATAAATAA[A/G]TGGAGAAATGTACAA | 115426 |
rs577814206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422814 | GTTCTTTCTTTACAT[A/G]TTTAATATTTTGCTT | 115426 |
rs577819387 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422150 | TGCCAAACTACTATA[C/G]TTGGTTCCATTGGTC | 115426 |
rs577824924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437455 | TCAGGCTGGTCTTGA[A/G]CTCTGGACCTCAGGT | 115426 |
rs577891507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503308 | GCCTTAACTTTTTCT[A/G]TTAATATAAAAAATA | 115426 |
rs577963917 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452844 | TGAATCTGAAAAGTT[A/T]AGGCGAGAGTGGAGC | 115426 |
rs577973569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463204 | GAGAATCACTTGAAC[C/G]TGGGAGGCGCAGATT | 115426 |
rs578002397 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426710 | GACTAAACTGAAAAC[A/C]ATTTAGAAGCTGCTA | 115426 |
rs578006428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489537 | GTTCCTATCGGCAGT[A/G]TATGAGTGATCCAGT | 115426 |
rs578067013 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424123 | ATGCAATTAGGCAGG[-/AGA]ACAAAATAAAGTGTA | 115426 |
rs578088149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443160 | AGAATGAAGCTACCT[C/T]TGGCTAGGCAAGTTG | 115426 |
rs578101721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421354 | TTAAAGAGCAATAAA[A/G]GAAATACTTGTGTAA | 115426 |
rs578104290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448631 | TAAGAGGAGGATGGA[A/G]GCAAGTGAACTGTAT | 115426 |
rs578113103 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411443 | AGTGCAGTGGCGTGA[G/T]CTCAGCTCACTGCAG | 115426 |
rs578135354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502190 | ACTCCTTCCAAAGGC[A/C]CTGTGATCAGCAGCC | 115426 |
rs578166803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485262 | TATAAATTGAATATA[A/C]TACTATAAATATAGT | 115426 |
rs578202755 | in-del | -/TTTA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425288 | GCCTTTAGAAACTCG[-/TTTA]TTTGATGGCTATGTC | 115426 |
rs745313542 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504309 | GGATTACAGGCGTGA[A/G]CCACCGCGCCCGGCC | 115426 |
rs745322843 | snp | C/G | 1.73153e-05 | 0.00294233 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504676 | GACAACTGAGTGCTT[C/G]CACAATGTCTGTAAA | 115426 |
rs745342236 | snp | A/G | 1.76883e-05 | 0.00297386 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434219 | CATATTTTCATTTGT[A/G]GAAACCAAAGCCTTC | 115426 |
rs745345064 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476646 | GTTGCCCAGGCTGGA[G/T]TGCAGTGGCGCAATC | 115426 |
rs745387272 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505319 | TATATATTTTTTGAC[A/G]GAATCTCACTCTGTC | 115426 |
rs745419468 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484507 | TCCTGGGCTCAAGCT[A/G]TCCTTTACTCTGAGC | 115426 |
rs745442641 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433755 | AAGATAGCACAAATC[A/G]GAAAGAATAGTTTTG | 115426 |
rs745444623 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444239 | ACCTGTCTGCTCTAT[C/T]GCTTCTTGGTTGTTA | 115426 |
rs745459637 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443578 | ATTTCTGTTTATCTC[G/T]CTAGTCAGAATGCTT | 115426 |
rs745480386 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425302 | GTTTATTTGATGGCT[A/T]TGTCCCTTTGACATA | 115426 |
rs745487619 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434734 | GTGAGCCACTGCGCC[C/T]GGCCTCTATTAGGTA | 115426 |
rs745539350 | in-del | -/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460307 | TTACTTGCCTGACAA[-/CC]CCTGCAAGCCATGAA | 115426 |
rs745553878 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461311 | CATTTCTTTCTTTTC[-/T]TTTTTTTCTTTCTGT | 115426 |
rs745571210 | snp | A/T | 1.74705e-05 | 0.00295549 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497153 | ACTCGATTGTGTACT[A/T]GAAGAAAAATTACAT | 115426 |
rs745604969 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494307 | GTAATTTGAAATAAA[C/G]TTATGTTTGGGAGCC | 115426 |
rs745633105 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459744 | TTTGGGAGTCCAAGG[A/C]AGGGGGTTGCTTGAG | 115426 |
rs745638905 | snp | A/G | 5.96973e-05 | 0.00546307 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499805 | GAAGCTTAAATCTGC[A/G]TTGTACTCTCCCTCC | 115426 |
rs745692350 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450726 | TTGTTACTTTGATGC[G/T]TATATTGTCTCATCT | 115426 |
rs745707880 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472494 | TTGTCATTAACTTCC[A/G]AAACTGGGGGAATAT | 115426 |
rs745714336 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449352 | TACCATTAGACTGGC[C/G]AAGATGTTGTCAGAG | 115426 |
rs745738921 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430761 | CTTTCCCATGGAAAA[C/T]ACAATAAAGGCTCTG | 115426 |
rs745777042 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419213 | AGTAGGTTTTACATT[C/T]CTTTTGTTAAATTTA | 115426 |
rs745799221 | in-del | -/CTTCTATTGAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440614 | AAAGCACACACGCAA[-/CTTCTATTGAG]CTAAACCGTAGGTAT | 115426 |
rs745801510 | snp | C/G | | | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421110 | ACATCAGCTCGTGCC[C/G]GTCTTATTGATCCTG | 115426 |
rs745830188 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420807 | TTTAAAATCTCTAAA[C/G]TGTAGTGCTATGGAT | 115426 |
rs745840976 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451204 | TGTCTTTAGGAAATA[G/T]ATCATTTGGGCTGTC | 115426 |
rs745919224 | snp | A/G | 1.65416e-05 | 0.00287586 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482139 | GAAAGGGGAGAATTG[A/G]CTATCAGATTATAGC | 115426 |
rs745949113 | snp | A/C | 3.29576e-05 | 0.00405928 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460672 | TGTTGGTGATGTGGT[A/C]ATGGTTAATTATAAT | 115426 |
rs745962029 | snp | C/T | 1.66829e-05 | 0.00288811 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486826 | TGTTTTATAGGTGAG[C/T]GAAGCAGGTGTTCAC | 115426 |
rs745967335 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479930 | CTTTGCTTCCATGTA[C/T]TATCCGTTCTCCCAT | 115426 |
rs745999744 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438241 | TGAAGATGGAGAATG[A/G]TCTGCCTTGAGAAGT | 115426 |
rs746006995 | in-del | -/TAAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6475679 | TTTTTCCTAAATGAT[-/TAAG]TGTTATTTTTGAAGA | 115426 |
rs746013012 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446270 | ATTCTCATACCTCAG[A/C]CTCCCAGGTAGATGG | 115426 |
rs746016208 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470167 | CACTTGAGGTCAGGA[A/C]TTCAAGACCAGCCTG | 115426 |
rs746023677 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495010 | TCTAGCAAGAAAGCA[-/G]TCCTTCAAGAAGAGT | 115426 |
rs746046053 | snp | C/T | 1.72555e-05 | 0.00293725 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413484 | CGGTTCCTCTCTAGG[C/T]GCCAAGATGTGGATA | 115426 |
rs746066035 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436765 | TTAGCATATATTTGG[C/T]AACTTTTTTTGTCAG | 115426 |
rs746083147 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469962 | AAAATGCACAGTGGT[-/A]ATATCACAAACAAGA | 115426 |
rs746088219 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437630 | TTATTTTATTTATTT[A/G]TTTTTGAGACAGAGT | 115426 |
rs746105180 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413754 | GCAGGGCTCACCTGG[C/G]TCCGCTGCGGGTGGG | 115426 |
rs746164838 | snp | A/G | 1.65192e-05 | 0.00287391 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506187 | GACGATGATCTGCCT[A/G]CTTTCACTGTGTTGT | 115426 |
rs746181764 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504415 | TGAAATTTTGATATG[-/T]TTCATATAACATATA | 115426 |
rs746232707 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462013 | AAAAAAAAAAAAATA[-/A]GAGAAACAGCTAAAC | 115426 |
rs746235082 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502335 | ACATACATACTGTTA[C/T]TCTGACTGGAATTCT | 115426 |
rs746244269 | snp | C/G | 3.55916e-05 | 0.00421836 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477571 | TTTATGAGATTCATA[C/G]ATATAAAAAATGTTT | 115426 |
rs746249399 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474487 | GAGGCGGGCAGGTCA[C/T]CTGAGGTCAGGAGTT | 115426 |
rs746266828 | snp | A/G | 1.78436e-05 | 0.00298688 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499904 | AAGAAGCAGCCCAGT[A/G]GAACCACAAAAAGGC | 115426 |
rs746267850 | in-del | -/ATC | 8.27493e-05 | 0.00643178 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482141 | AGGGGAGAATTGGCT[-/ATC]ATCAGATTATAGCAA | 115426 |
rs746282129 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427218 | TAAATATTTTTTTTT[-/A]ATACATGTAGAGCTT | 115426 |
rs746312647 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453458 | CAGGTTTCTGTCTTA[C/T]ATGGACTTAAGAATA | 115426 |
rs746382414 | snp | A/C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422761 | TACAGGCGTGAGCCA[A/C/G]CATGCCCGGCTAACT | 115426 |
rs746388398 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455415 | GTACTTGCGATAGTT[A/T]GCTGAGAATGATGGT | 115426 |
rs746414268 | in-del | -/A | 1.73225e-05 | 0.00294295 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433874 | TTTGAAGCAGTAGAC[-/A]AAAATTAAGCTTCAT | 115426 |
rs746437870 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418999 | TTTCCTGTGTCTTCA[C/T]ATTGTCTTCCGGCTG | 115426 |
rs746457158 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502846 | TTTCCAGCATCTCCA[C/T]ATAATTGCCATATTT | 115426 |
rs746515183 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503155 | ACCCGCCACCACGCC[C/T]GGCTAATTTCTTGTA | 115426 |
rs746518896 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450662 | GATACTTTTAAGTAT[C/T]ATTATGAACTTCCAG | 115426 |
rs746519393 | snp | G/T | 3.03578e-05 | 0.00389589 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504568 | CTGCTAACTTTTCTT[G/T]CCTTATCCTTGGATA | 115426 |
rs746528411 | snp | A/G | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434044 | ATGGCAGTTCTTGTA[A/G]AAGGACTAATGGAAA | 115426 |
rs746552088 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442067 | GCCTCCTGGGTTCAA[C/T]AATTCTCATGCCTTA | 115426 |
rs746571657 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503538 | CTGTAAATAAACATT[A/G]GCATCAGGAAGGTAT | 115426 |
rs746572255 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451178 | ACTACTGAAAAGTTA[C/T]GTGTTTTTTTTGTCT | 115426 |
rs746603918 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465900 | TCTAGTTATCAAATT[C/T]TATTTTCATGTTGTC | 115426 |
rs746605286 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432762 | ATCTTGTGTTGATTT[C/T]ATTTTTTCCTTTTTA | 115426 |
rs746611824 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413025 | CAGGCGGTGGGGCAA[A/G]TAACGGCTTTTGGTA | 115426 |
rs746625230 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443433 | AGTAAGTAGCAGGCA[C/G]ATTCCAAAAAGCGCA | 115426 |
rs746679081 | snp | A/G | 1.83165e-05 | 0.00302621 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493781 | AGAATTGATGAAATT[A/G]TACTTGGGTTTAGCT | 115426 |
rs746692099 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433561 | TAGTCATATTAGCTT[A/G]AAGTCCTGGCTTTTC | 115426 |
rs746703037 | snp | A/C | 0.0136055 | 0.0813489 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504651 | GTCAGGAGCTAGTTT[A/C]CCAGCCTGTGACAAC | 115426 |
rs746723302 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491825 | GCTACTGCCTGCCAG[A/G]CACAATTTAATGGAT | 115426 |
rs746741417 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504151 | CTGCCTCAGCCTCCC[C/T]AGCAGCTGGGACTAC | 115426 |
rs746768889 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469416 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 115426 |
rs746772215 | snp | C/G | 5.14443e-05 | 0.00507144 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413577 | GATTGAGGAGCTGCG[C/G]GAGCGGGTGTGGGCG | 115426 |
rs746822818 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496900 | ACGTTATTTAAAGAA[A/G]AATTCCATGTATTTC | 115426 |
rs746830580 | snp | C/T | 1.65745e-05 | 0.00287871 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477768 | TATCATATTTACTGT[C/T]TGAATCCACCTTTGG | 115426 |
rs746830713 | snp | C/G | 3.31279e-05 | 0.00406975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498011 | GCACTGAAATATTGT[C/G]ATTTAGGTGGTGAAA | 115426 |
rs746847882 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458994 | ACACCACATGTTCTC[A/C]CTCATAAGTGGAAGT | 115426 |
rs746851409 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470097 | CATTCCCAGCTGGGC[A/G]TGGTGGCTCACGCCT | 115426 |
rs746861590 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467247 | ACCTGCTTTCTCCAC[C/T]TTCAAAGCCAACGAT | 115426 |
rs746888624 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418279 | TTTTTTTTTTTTTTT[-/A]AATCAAGGAAGCAAT | 115426 |
rs746890852 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459662 | TGACAGAGTAAGACT[C/T]CATCTCACAAAACAA | 115426 |
rs746899236 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449953 | TGGTCACCTCATGTG[C/T]CTTTTCCCTTTGCTG | 115426 |
rs746908788 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461998 | ACAATTTTTGTTTTT[-/A]AAAAAAAAAAAATAA | 115426 |
rs746911686 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502192 | TCCTTCCAAAGGCCC[C/T]GTGATCAGCAGCCCT | 115426 |
rs746912528 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428002 | AGCTTTTTATGATGC[C/T]AGAAAGATCGTACTT | 115426 |
rs746940519 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469630 | GAAACATGTACAAGA[A/G/T]TGTTAGACACATAGG | 115426 |
rs746973271 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498456 | AGGGATTCATAAAAT[A/T]TAGGTATAGGAGGCC | 115426 |
rs746988049 | snp | A/G | 1.68812e-05 | 0.00290522 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481610 | TTAATATGGTATTGT[A/G]AAAATGCCTTCGTTC | 115426 |
rs746990899 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447396 | TACTTGCTCCTCAGT[G/T]AAAAATTGCTGTTTT | 115426 |
rs746991121 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417956 | GTTCTTTCAATTTCC[A/G]GCAGTTTTATCACTT | 115426 |
rs747057715 | snp | C/T | 3.37092e-05 | 0.0041053 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421108 | CTACATCAGCTCGTG[C/T]CCGTCTTATTGATCC | 115426 |
rs747059626 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502149 | ACTTTAAATAAATAC[A/G]TATGTGTATATATAT | 115426 |
rs747119200 | snp | C/G | 1.83159e-05 | 0.00302615 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500501 | TTTTGTTTCATAGTT[C/G]TGCTTAGAACCACTT | 115426 |
rs747121284 | snp | C/T | 1.65119e-05 | 0.00287327 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481982 | TCAACGTTTGTTTTG[C/T]GTCTTGTAGGGAATG | 115426 |
rs747136763 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432166 | TTGTCCTACCCAGCA[-/T]GGTTGGCTCTTAGGT | 115426 |
rs747137057 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455202 | GAGCTCGTTTGTTAC[A/G]TATGCATACATGTGC | 115426 |
rs747138418 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478636 | GGTTTTTTCTTTTTA[A/C]ACTATGTGCCATATT | 115426 |
rs747152388 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453368 | TGTTATTTAAAAACA[C/T]ACAGAATGATGATAA | 115426 |
rs747194084 | in-del | -/T | 1.66707e-05 | 0.00288705 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420896 | AGCATTTCACTATTC[-/T]TTCTTTATTTTCTAG | 115426 |
rs747199808 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437948 | CCTAGTACAAACCAG[A/G]TGATGCTGCTGTTGT | 115426 |
rs747204061 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445824 | CCCCCTTGGCCTCCC[A/T]AAGTGCTGGGCTTAC | 115426 |
rs747211232 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422644 | AGACAGGGTCTGGCT[C/T]TGTCACCCAGGCTGT | 115426 |
rs747217480 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488435 | ACATTTATATTACCA[C/G]AGTTTCCATTATTGT | 115426 |
rs747222669 | in-del | -/AA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439950 | TGGTTAATGTAAAAG[-/AA]AAAAGGGAGAAAACA | 115426 |
rs747239490 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435933 | TTTTAAACTGTTAGG[A/G]TGGAAGTGGTATTAA | 115426 |
rs747272483 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506701 | GGACAGGTTCATTTT[A/T]TTTAGCCCACTTTGT | 115426 |
rs747303878 | snp | A/G | 1.70889e-05 | 0.00292304 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460553 | GTAATCATAAGCCAT[A/G]TGGTTTTCTCTCTCC | 115426 |
rs747351571 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482782 | CTTGTATTTGTAGTA[G/T]AGACGAGGTTTCACC | 115426 |
rs747365028 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481918 | AGTTGGGTTCCTAGT[A/C]ACATCTCAGAATTAA | 115426 |
rs747374567 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448347 | TACTTATCTGTGAAT[A/G]CTATTTAGTTAACAT | 115426 |
rs747383315 | snp | C/T | 3.31087e-05 | 0.00406857 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493864 | CACTGGAAGCGGTGG[C/T]AAAAATCTTGCTGGT | 115426 |
rs747393456 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472154 | CTACCATCTGTAGCA[C/T]TGGTCCCAGACCACC | 115426 |
rs747394395 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445012 | AATTTGGGTTGAGGC[C/T]GGTCATGGTGGCTCA | 115426 |
rs747438994 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439332 | AGATGTGCACCACCA[C/G]GCCCGGCTAATTTTT | 115426 |
rs747446375 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473083 | ACCTTTCCCACTGAA[A/G]GAAACTCCTGGCTGG | 115426 |
rs747472385 | snp | A/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420977 | AATTCAGCTGCTAGT[A/T]CGCCCAGACCCTGAT | 115426 |
rs747473207 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415432 | TGGTACCAGCTGTGT[G/T]TTCACTTTCTTATGC | 115426 |
rs747484441 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430950 | ATTCAGATGCTCCCA[C/T]ATAGGCAAATTCTGT | 115426 |
rs747513162 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476595 | GGCTTTTTTTGTTTG[-/T]TTTTTTGTTTTTTGT | 115426 |
rs747519261 | in-del | -/AG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469450 | CTGAACCTGGGAGAC[-/AG]AGGTTGCAGTGAGCC | 115426 |
rs747567068 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440262 | CTTATGATATTTTAG[A/G]GAATGTTGTCTTATG | 115426 |
rs747570069 | in-del | -/AACAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424124 | GCAATTAGGCAGGAG[-/AACAA]AACAAAATAAAGTGT | 115426 |
rs747579691 | snp | C/G | 3.50797e-05 | 0.00418791 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499824 | TACTCTCCCTCCTCC[C/G]CCCCCATCAGTATCC | 115426 |
rs747582960 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501268 | AAGCCCTTCTTATCA[A/G]ATCCCTAAAGTTGGA | 115426 |
rs747614857 | snp | C/G | 1.69464e-05 | 0.00291083 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481593 | ATATTCTGTTACTAG[C/G]TTTAATATGGTATTG | 115426 |
rs747629767 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448951 | ATCTTTAAACATCGC[A/G]GAACAAGCAGTATCA | 115426 |
rs747658140 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449858 | CATGTGTTGTCACAG[C/T]TGGTTGTTGGAGGCA | 115426 |
rs747663342 | snp | C/G/T | 8.68446e-05 | 0.00658906 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433867 | TTAAGGTTTTTGAAG[C/G/T]AGTAGACAAAATTAA | 115426 |
rs747664297 | in-del | -/A | 1.77979e-05 | 0.00298306 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500530 | TGTAAGTCTGCTGAT[-/A]ACATTTTTAAAATAA | 115426 |
rs747681197 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477728 | ACCCAACATGCAGCT[C/T]CTGTGTGATGAATGT | 115426 |
rs747714806 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440716 | TTTATCCTGCTTTTG[C/T]ATATAAAAAGCATCT | 115426 |
rs747717067 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447222 | CCTAATTATGTTGTT[G/T]CTACTATTAGCAAAA | 115426 |
rs747728298 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417207 | GTATTCCCTTGCATC[A/G]TTGTTGCAGTTCCTC | 115426 |
rs747737737 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474516 | TTCGAGACGAGCCCA[A/G]CCAACATGGTGAAAC | 115426 |
rs747751105 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434008 | CTGATGGACAGTCAC[A/G]TGGCAAAACTCCACT | 115426 |
rs747752006 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429122 | GTGAGCCAACATCGC[A/T]CCACTGCACTCCAGC | 115426 |
rs747779712 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417852 | TATTTACTCCTGACC[A/G]TCATTTAGTAGAAAC | 115426 |
rs747789910 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501670 | AATGAAGCTTACATG[-/T]TTAGAGGACAGGGGA | 115426 |
rs747795444 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450583 | TCAGCCTGATACACT[C/G]AAAATTTGTTACCAG | 115426 |
rs747812447 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501489 | GCAACACAAAAACTC[-/T]TACAGAGTTTCCTTT | 115426 |
rs747813155 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431821 | CATTTGTGCCGCCTC[G/T]TGTTCCTTAGTAAGG | 115426 |
rs747866837 | in-del | -/C | 3.56875e-05 | 0.00422404 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486949 | TTATACAACCTTACT[-/C]ATTAGTACCTGCCTT | 115426 |
rs747896957 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506077 | GGTTTTCTCCTGCCC[C/T]GCTTGCCGGCATGAT | 115426 |
rs747910206 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416636 | CAAGCTCCGCCTTCC[A/G]GGTTCACGCCATTCT | 115426 |
rs747910811 | snp | C/T | 1.74251e-05 | 0.00295165 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413478 | GGGGACCGGTTCCTC[C/T]CTAGGCGCCAAGATG | 115426 |
rs747927494 | snp | C/T | 1.73667e-05 | 0.0029467 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497168 | TGAAGAAAAATTACA[C/T]GGTATAAAGACTTCT | 115426 |
rs747929365 | in-del | -/CTCTGT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486638 | GAGCAAAAGATAGAA[-/CTCTGT]GAGACTCACTTCTTG | 115426 |
rs747980432 | in-del | -/TTTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484785 | GTATTCACTTCTTTC[-/TTTTT]TTTTTTTTTTTTTTT | 115426 |
rs747990125 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506623 | CTTGGAATGAACACA[G/T]CTTCTAAAGTGTGCA | 115426 |
rs748000928 | in-del | -/CTTCCT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415289 | AGGATAACCGTTGTA[-/CTTCCT]CTTCCAGGGTCCTAG | 115426 |
rs748021186 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469342 | GGCCAACATAGTGAA[A/G]CCCCGTCTCTACTGA | 115426 |
rs748023467 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457122 | CATTTTCACAATACT[C/G]ATTCTTCTATCCATG | 115426 |
rs748034941 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436272 | CTTTTCTGGTACTTA[C/T]TGTGGTTGTGGCTAA | 115426 |
rs748058524 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488205 | CCATGATCATGCCAG[C/T]GCAGCACTCCAGCCT | 115426 |
rs748081827 | snp | C/T | 1.68408e-05 | 0.00290175 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413553 | TGAGGACGTGTCTCG[C/T]AAAGCCACGATTGAG | 115426 |
rs748135432 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427133 | TATAAAAACTTTTAA[A/G]TTGATTATAAGTCAC | 115426 |
rs748147649 | in-del | -/TTGTTTGTTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449985 | TTTTGCTTTTCATTG[-/TTGTTTGTTTT]TTGTTTGTTTTTTGA | 115426 |
rs748234698 | snp | A/G | 1.67329e-05 | 0.00289243 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475392 | CCTTTTTTAAACAGG[A/G]GTTCTGAAGGAACAT | 115426 |
rs748262518 | snp | C/T | 2.00174e-05 | 0.00316359 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499813 | AATCTGCATTGTACT[C/T]TCCCTCCTCCCCCCC | 115426 |
rs748274089 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420932 | AAATGGATATACCTT[A/G]TTTGATTATGATGTT | 115426 |
rs748285115 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439288 | CTCCCGGGTTCAAAC[G/T]ATTCTCCTGTCTCAG | 115426 |
rs748300596 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462568 | GAAGTAGAAAGCATG[C/T]GTACACAGTAGGATA | 115426 |
rs748333015 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452365 | TCTGGTAATTAACAG[A/G]TGCCCCTCTAAGAGG | 115426 |
rs748344564 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421835 | TATTTTTGCTACTTA[C/T]GTATATTTCTCTAGG | 115426 |
rs748354495 | in-del | -/TTCCTC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430967 | TAGGCAAATTCTGTT[-/TTCCTC]TTTTGTCTGCTATTT | 115426 |
rs748374349 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421274 | AATATCATAACTTTT[A/G]AAAGTAGTCTTTTAA | 115426 |
rs748386086 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444403 | CAAGATCACTTAGTA[C/G]TTAGAAAAAGAACTT | 115426 |
rs748386201 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453099 | CTATGTATGTGTATG[A/C]GTACAGATAGAATAT | 115426 |
rs748387462 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489314 | TTAATCATTTACTCA[A/T]GGAAGAACAGCTGGG | 115426 |
rs748421705 | snp | C/T | 1.71888e-05 | 0.00293157 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499851 | ATCCAGCAGGTTACC[C/T]TTCAGATAAAGAAGG | 115426 |
rs748483188 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493024 | TATGAAAGCCAGGGC[A/G]CAGTGGGTCATGCCT | 115426 |
rs748508734 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466790 | TCACGCAAACATGCT[C/G]CTGCCTTGGGGCCTT | 115426 |
rs748512596 | snp | A/G | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486857 | AGACCCCATGTTGGT[A/G]GAATTCATGGTCGAA | 115426 |
rs748529349 | snp | A/G | 7.83853e-05 | 0.00625991 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486977 | CTTGACCATTTGTAA[A/G]ATAGAATAGCTTTGC | 115426 |
rs748535828 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504542 | GATGAATTTTATTAG[C/T]ATATTATGAACTGCT | 115426 |
rs748536233 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480803 | TAATTTGCTCAAGAT[C/G]AGGGACTGAATTATT | 115426 |
rs748541040 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471529 | CTTCCATTTTGGGTG[C/T]GCCCTCTTGGATCAC | 115426 |
rs748555308 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448276 | AAAGAGCAACCAAAT[A/G]CTCAAAGGAAAACAC | 115426 |
rs748560776 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460884 | CCTTAGTAAAAAAAG[A/G]TGGAGTCTATAAAAG | 115426 |
rs748589716 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481880 | TTATTTGTTAATATC[A/G]ATGGTACTTAAATTA | 115426 |
rs748593328 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447372 | AAACACTCTATATTT[C/T]GAACATGGTACTTGC | 115426 |
rs748632031 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423781 | AAACCCCGTCTCCAC[C/T]AAAAATACAAAAAAT | 115426 |
rs748660998 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438665 | AGAAACCTGCCTCTG[A/G]AATTATTCTGGGGTA | 115426 |
rs748662269 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473148 | TTGTCATGCAAATAA[A/G]GAGTCCCACAAAGTC | 115426 |
rs748664052 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461992 | ACCCTGACAATTTTT[-/G]TTTTTAAAAAAAAAA | 115426 |
rs748684618 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414707 | GTAGCCTACAGTTGC[A/G]AACTACTTAAAAGGA | 115426 |
rs748685619 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443067 | TAAGCTAGAAAACAC[C/T]TAGTAGTTTGAACAA | 115426 |
rs748731264 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468345 | ATGGAAAGCACCTGT[A/T]TGCAGGTAGGGTGGG | 115426 |
rs748757857 | snp | C/G/T | 0.00034653 | 0.013159 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481985 | ACGTTTGTTTTGCGT[C/G/T]TTGTAGGGAATGGCT | 115426 |
rs748759950 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506529 | AAATGAAATTTTAGC[C/T]ACACACTGCCTCCCA | 115426 |
rs748776720 | snp | C/G | 1.78912e-05 | 0.00299086 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413464 | CAGGGGGAGACAAAG[C/G]GGACCGGTTCCTCTC | 115426 |
rs748792538 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457049 | ATTCTGTGAAGAAAG[A/T]CATTGTCAGTTTGAT | 115426 |
rs748813384 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495470 | GAAAGGCACTTTGCT[C/T]TGACCCATAGTATAC | 115426 |
rs748816687 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435670 | GGAGTTCAGTGGTGC[C/G]ATCTTGGCTCACTGC | 115426 |
rs748818004 | snp | A/G | 1.74233e-05 | 0.0029515 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497160 | TGTGTACTTGAAGAA[A/G]AATTACATGGTATAA | 115426 |
rs748832208 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416605 | GGGAGTGCTGTGGCG[C/G]GATCTCCGCTCACTG | 115426 |
rs748861596 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425797 | AAAAATCAAGATCTC[A/G]GCTCTAGGTATGCTT | 115426 |
rs748888067 | snp | A/G | 4.37235e-05 | 0.00467545 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421147 | GAATATATAAGGTAT[A/G]TTGTTTTCTTCAGAC | 115426 |
rs748896970 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449181 | GCTGCAAGTAGTGCA[A/G]TTAGCTGATCGTCTT | 115426 |
rs748912678 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427072 | TTGTTTTATATTTGC[A/G]TTGGGTTTTTTGTAT | 115426 |
rs748926161 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458556 | TGAATGTGTTTGCTC[G/T]TGCTTCTCTAGTTCT | 115426 |
rs748950062 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449702 | ATAGTTCTCTGTGCC[C/T]AAACTGTTTTTGCAA | 115426 |
rs748952874 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413456 | CCAGAGCTCAGGGGG[A/G]GACAAAGGGGACCGG | 115426 |
rs748966033 | snp | C/T | 6.68975e-05 | 0.0057831 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421104 | CCATCTACATCAGCT[C/T]GTGCCCGTCTTATTG | 115426 |
rs749012294 | in-del | -/AAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466553 | TCAAAAAAAAAAGGA[-/AAA]AAAAAAAAAAAAAAA | 115426 |
rs749027671 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451385 | TAGTTCTGTAGTTAA[A/G]TCTCCAAAACAAAAT | 115426 |
rs749033730 | snp | A/T | 6.62109e-05 | 0.00575335 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481965 | TTAACATAACTGATT[A/T]CTCAACGTTTGTTTT | 115426 |
rs749047434 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433335 | TATTTTATCTTTGTT[C/T]TTTGAGGTGGTAGAT | 115426 |
rs749049543 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487540 | CCTGGCTAATTCTTG[C/T]ATTTTTAGTAGAAAT | 115426 |
rs749051797 | snp | G/T | 6.95193e-05 | 0.00589532 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460530 | GCATAAAACTTTAGT[G/T]GTCTTTGGTAATCAT | 115426 |
rs749069263 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506954 | TGAGGGCTGTGCTGA[C/G]CTTTGAGAGGATTTG | 115426 |
rs749083566 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443605 | GCTTTCACAGAACAG[A/G]TACTATAAACCAGAG | 115426 |
rs749094481 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462235 | CCACAGTATTGTTGA[A/G]TAATTGCAACTGAGA | 115426 |
rs749103471 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489167 | ATGGAAGTATGTAGC[A/G]TATTATATATTAACC | 115426 |
rs749106924 | snp | A/G | 1.65501e-05 | 0.00287659 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434144 | TGTTGCTGCTGATGA[A/G]GACGTTATTTACCAT | 115426 |
rs749136043 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431112 | CTCTGAACTGCCTTT[A/G]AAATCCAGGCTTTAT | 115426 |
rs749136406 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452364 | TTCTGGTAATTAACA[C/G]ATGCCCCTCTAAGAG | 115426 |
rs749206534 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444316 | GACTTGTAGGCTCCT[A/G]AGTGGATGGTAATCA | 115426 |
rs749231354 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421714 | GAGCCACCTCGCCCA[A/G]CCTTAAATACCTGTT | 115426 |
rs749261877 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434934 | CTCCTGGGCTCAAGC[A/G]ATCTTCCCACCTTAG | 115426 |
rs749281952 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505665 | ATAAAATTCATTTCT[A/C]AGCAAGGGAATCCAG | 115426 |
rs749288613 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506063 | TCCTTTAAGGCACAG[A/G]TTTTCTCCTGCCCTG | 115426 |
rs749355841 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423546 | TATTATAAAATGTTT[C/T]AATATAATTCATTGT | 115426 |
rs749369934 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492455 | CTAAAGATTAAGTTT[C/T]GTAATACCTTGTTTA | 115426 |
rs749380931 | snp | G/T | 1.77776e-05 | 0.00298136 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413592 | CGAGCGGGTGTGGGC[G/T]CTGTTCGACGTGCGG | 115426 |
rs749400159 | snp | C/G | 0.000185787 | 0.00963634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468579 | GTTCAGAGCAGCTAG[C/G]AGTAGGATGGAAAAA | 115426 |
rs749420174 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471347 | TAATTTGAAAATAGC[A/G]GCTATGGTAGCCATC | 115426 |
rs749427937 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437681 | GGAGTGCAGTGGTGC[A/G]ATCTCAGGTCACTGC | 115426 |
rs749447182 | in-del | -/ATATT | 0.000676556 | 0.0183799 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504543 | ATGAATTTTATTAGC[-/ATATT]ATGAACTGCTAACTT | 115426 |
rs749447195 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414615 | TACACTAAAAAGTTG[G/T]CATCCTGAGTTGATA | 115426 |
rs749463387 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474184 | GGTCACAACGGATGT[A/G]CATGTTGATAATTGG | 115426 |
rs749480983 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438567 | GTGCACAATTGTGTC[A/T]GCAAACCTCTTGAGT | 115426 |
rs749483905 | snp | A/C/G | 0.000236394 | 0.0108696 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413670 | CCGCCGCGCCCCTAG[A/C/G]GAGGCTGGGGGCCGG | 115426 |
rs749490438 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430075 | AAGTGCAATGGCACA[A/G]TATTGGCCCATTACA | 115426 |
rs749498581 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472781 | GGCAACAATGTCTTG[C/T]GTGTAATGTGGGATA | 115426 |
rs749567384 | snp | C/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498055 | TTTCATCAAGCCATG[C/G]ATTCTTGGTTTGGCG | 115426 |
rs749606036 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503075 | TCTCAGCTCACTGCA[A/G]CCTCCACCTCCTGGG | 115426 |
rs749607636 | snp | A/T | 1.73144e-05 | 0.00294226 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500544 | ATACATTTTTAAAAT[A/T]AATCTAGATGACTGT | 115426 |
rs749615770 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411261 | TTTAATTAAAATAGG[C/G]GTAGACAAGTGAATT | 115426 |
rs749620191 | snp | A/G | 0.000179678 | 0.00947665 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422684 | ACGTGAACACGGCTC[A/G]CTGTAGCCTTGACCT | 115426 |
rs749627759 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491654 | CAAGAATGTGAGCAT[C/G]CAGCTTGTTGTCTTA | 115426 |
rs749654621 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464761 | TTCTGTACCATGGGT[C/G]TGTTTTTTGTGTATC | 115426 |
rs749658164 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465712 | TTACAAAGAACTAAC[C/G]TTCAGCTTTGATCCT | 115426 |
rs749698854 | in-del | -/TTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468099 | TTTCAGTCTAGTTTC[-/TTTT]TTATTAGTACATAAA | 115426 |
rs749705479 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454295 | AGACACCAGGATTGA[A/T]ACAAGGATCCAAAAC | 115426 |
rs749734909 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432539 | TAGCTTTAACCTAGA[A/G]GAAGTTAATTTCTCA | 115426 |
rs749786274 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423935 | GGGCGACACAGTGAG[A/T]CTCAGTATCAAAAAA | 115426 |
rs749791452 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490683 | TATTTTCTTGTTTCC[A/G]TGTTTTTGAATATAC | 115426 |
rs749792858 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428716 | ACCATACCCAGCTAA[-/T]TTTTCAATTTTTCGT | 115426 |
rs749797863 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447266 | GTCATACTTTATTAT[A/G]TATTTGATTAAGACC | 115426 |
rs749811443 | snp | C/T | 0.000315157 | 0.0125491 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486835 | GGTGAGCGAAGCAGG[C/T]GTTCACAGACCCCAT | 115426 |
rs749817655 | in-del | -/T | 7.75825e-05 | 0.00622778 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499971 | ATAATAATAACATAC[-/T]TTTGTTGTTGTTGTT | 115426 |
rs749834405 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458911 | GATGAGTTCCTGTCC[A/T]TTGCAGGGACATAGA | 115426 |
rs749839342 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424905 | TTTGGGGAGGAAGAC[C/T]GCAGAGGTATTTTCA | 115426 |
rs749869662 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482027 | TACGAGAGAATGTAC[C/T]ATTGTCCCTTCTAAT | 115426 |
rs749873850 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436037 | GTTACTGTTGGGACA[C/G]ATTTAGTATATTAAA | 115426 |
rs749886947 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431452 | TCTCTACAAGAAGTA[A/G]CATTAGCTAGGTGTG | 115426 |
rs749905824 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501775 | TTAGGTCACACTCAT[G/T]TTCACTTATAGGAAA | 115426 |
rs749911749 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488965 | CTACAGGCATGCATC[A/G]CCATTGACTAATTTT | 115426 |
rs749969067 | snp | A/G | 1.64931e-05 | 0.00287163 | intron-variant | UHRF2 | GRCh38.p7 | 9:6506029 | GTTTTTGTTTTTACC[A/G]TAGGATTGCCTACAG | 115426 |
rs749979045 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477717 | GGGAAACATGAACCC[A/G]ACATGCAGCTTCTGT | 115426 |
rs749993111 | in-del | -/TAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473686 | TAAAGAGCCGGATAG[-/TAAA]TAGTTTAACATGGGG | 115426 |
rs749999664 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454134 | TACGTTTTACGGGTT[A/G]GGAATATAGTCCAAA | 115426 |
rs750002457 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416166 | CCTCCCGGGTTCAAG[C/G]GATTCCCCTGCCGCA | 115426 |
rs750013112 | snp | A/G | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460607 | CTAGAAATGAATGTC[A/G]AGGATCTTAGACCAC | 115426 |
rs750030048 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468264 | CTTTAACAAAAATGG[A/T]ACATAAGTGAAAAAG | 115426 |
rs750031343 | snp | A/G/T | 4.94868e-05 | 0.00497407 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460738 | TGCAGAAATTACCAC[A/G/T]TTGAAGACAATCTCA | 115426 |
rs750051796 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411480 | CCTCCCGGGTTCAAG[C/G]AATTCTCCTGCCTCA | 115426 |
rs750086912 | in-del | -/ATATAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469701 | TATACACGTATATAC[-/ATATAT]ATACATATACACACA | 115426 |
rs750092977 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422355 | AAAGTGCTGGGATTA[C/T]AGTTCTGAGTACTGT | 115426 |
rs750125114 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506136 | ATGAGATTCTGCAGA[C/G]TCTACTTGACCTTTT | 115426 |
rs750145049 | in-del | -/A | 5.32983e-05 | 0.00516201 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477576 | GAGATTCATAGATAT[-/A]AAAAATGTTTTAAGA | 115426 |
rs750161544 | snp | A/C | 4.99538e-05 | 0.00499744 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420899 | ATTTCACTATTCTTT[A/C]TTTATTTTCTAGTTG | 115426 |
rs750168737 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506386 | AGGTAGTTCCTGTAA[C/G]AACTAGTTTTAATGA | 115426 |
rs750225316 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499575 | ACTCCTGAAGACTTA[C/T]CTTTCTTAGATCTGA | 115426 |
rs750244058 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423149 | ATTTTAGATATATGG[A/G]AAAATGCCAACAGAT | 115426 |
rs750246217 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444278 | TTTACCAAAGACTTA[A/G]AGTATTTCCTCTAAC | 115426 |
rs750258458 | in-del | -/GTTTTGTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442467 | GTTTTGTTTTGTTTT[-/GTTTTGTTT]TGTTTGTTTTGTTTT | 115426 |
rs750275855 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462029 | GAGAAACAGCTAAAC[A/G]AATATTTGTGTCAAG | 115426 |
rs750281096 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471826 | TCCAGGACTAAAGCT[C/G]TATATTGAGAAGAAA | 115426 |
rs750282520 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448746 | GGAAAGTTTTCGCCT[C/T]TTGAGTAACAGGAGT | 115426 |
rs750285525 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415097 | CATGAATTCCTAGGA[C/T]ACTGGTGATTTCAGC | 115426 |
rs750292681 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419506 | AAACCTACTGATAAT[-/G]CTTTAGAAAGATAAC | 115426 |
rs750293258 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498297 | AGATCATGCAAATAG[-/A]ACAGAGGAAAAGAAG | 115426 |
rs750298708 | in-del | -/TC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452197 | GTTATCTTAAGGGTT[-/TC]TGTTATGGACGTTTG | 115426 |
rs750338343 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472551 | TCTTCAGGAGAACTA[C/G]GTTCAGACAATCAAG | 115426 |
rs750340298 | snp | G/T | 1.6591e-05 | 0.00288015 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481951 | GCTTTCATTAAAATT[G/T]AACATAACTGATTTC | 115426 |
rs750347385 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479790 | TTCATCCCAATTCTT[-/C]TTTTGTTCTTTCACA | 115426 |
rs750408381 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496340 | CTAATTTTAAACTGA[C/T]TCTAAAATTGTTATT | 115426 |
rs750413798 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430583 | AAAAACATGTAATCC[C/G]GAGTCCATGCACTTA | 115426 |
rs750419536 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501015 | TCTAAAAATCACCAC[A/G]AAAGTTTTTGTTACA | 115426 |
rs750458552 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433079 | CTCAAGTGATCTGCC[C/T]CTGCCTTGGCCTTCC | 115426 |
rs750466142 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476292 | TTGATGCGTTTCTTG[C/G]TGTTTCTTCTGTTAT | 115426 |
rs750475658 | snp | A/C/G | 7.28616e-05 | 0.00603541 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500743 | AAATAATAACATTCT[A/C/G]ATATTAACAAATGAT | 115426 |
rs750489914 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492520 | AGGTGAAAGTAAATT[G/T]AAGGGTTTTGGACCA | 115426 |
rs750492759 | snp | G/T | 1.6495e-05 | 0.0028718 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433955 | TGTCGGCCTTGGTGC[G/T]TGGTTTGAAGCACAC | 115426 |
rs750501161 | snp | C/T | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500606 | ATTCAGCAGAAGCAA[C/T]TGAGGCTTTTCAACT | 115426 |
rs750530608 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458412 | GTCTGGCTGGCAGTC[A/T]ATTTTGCTGATCTTT | 115426 |
rs750536802 | snp | A/T | 1.65111e-05 | 0.0028732 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434092 | AAGAGAACACAAATA[A/T]ATTGGACAGTGTACC | 115426 |
rs750550060 | snp | C/G | | | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504661 | AGTTTACCAGCCTGT[C/G]ACAACTGAGTGCTTC | 115426 |
rs750565516 | snp | G/T | 7.09685e-05 | 0.00595644 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486944 | AGTCATTATACAACC[G/T]TACTCATTAGTACCT | 115426 |
rs750573947 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414539 | CCACAAGTCTCTTAC[A/T]ATCTATATCCCTAGC | 115426 |
rs750601378 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493778 | ATAAGAATTGATGAA[A/G]TTATACTTGGGTTTA | 115426 |
rs750668481 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447880 | TTGGGGAAGGCTCAG[G/T]CCTTGAATTCACTAG | 115426 |
rs750694650 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425655 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 115426 |
rs750710031 | in-del | -/GTG | | | cds-indel, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506813 | CTGCATTAGTGTAAT[-/GTG]GTGTGGTTTTGCACT | 115426 |
rs750724918 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417769 | CCGTGATATGCTTAG[A/G]CATGGTGCTCTTACG | 115426 |
rs750730067 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450827 | TAACAGAATGTTCCA[A/G]CCCTGGGTTCAGCCA | 115426 |
rs750785957 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498202 | TGTGTTCATAAAAAT[A/G]TACACCTCTTCTATC | 115426 |
rs750786149 | snp | C/T | 4.9525e-05 | 0.00497595 | synonymous-codon, nc-transcript-variant, intron-variant | UHRF2 | GRCh38.p7 | 9:6497345 | AGAAGGCAACAGATA[C/T]GATGGCATTTATAAG | 115426 |
rs750804667 | snp | C/T | 5.01911e-05 | 0.0050093 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497982 | AATAAGTCTAAATTT[C/T]AAATCTCAAACTGGC | 115426 |
rs750807944 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450498 | CTTGAGAGACAGTGT[G/T]TGTTTACCTATGGCA | 115426 |
rs750831747 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485721 | ATAATCCCAACACTA[C/T]TGGGGGCTGAGGCTG | 115426 |
rs750843849 | in-del | -/TC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428398 | TCTATGGTAATCATT[-/TC]TTTGTTCTTTACTAA | 115426 |
rs750858559 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460430 | CCAACATGAAGTAAT[A/T]ACACCTGCTATTTAA | 115426 |
rs750903366 | snp | G/T | 1.72829e-05 | 0.00293959 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477828 | GATTATCAGGTTTTT[G/T]TTGTTGTTGTTCTTG | 115426 |
rs750909382 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450891 | TGGTATTTAGAGCAC[A/G]TAGTCTGTGCTGCTT | 115426 |
rs750921117 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418467 | AATGTGAATACCTGT[A/G]GTGTTTGAGATTGTG | 115426 |
rs750924892 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441700 | GAATCTGAGCATTCA[G/T]TCTTATTTTAGTATG | 115426 |
rs750972394 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419975 | ACTGGTCTGGAGCTC[C/T]TGGGCTCAAGTGATC | 115426 |
rs750989228 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442938 | TAAAAAGGTAAGTGT[A/G]AGGAAACTATTCTTG | 115426 |
rs751026108 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460876 | CACGTGTACCTTAGT[A/G]AAAAAAGATGGAGTC | 115426 |
rs751046655 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499466 | ACTGTGATCCAATCC[A/G]TCTGCTTTCTATCTG | 115426 |
rs751075675 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471792 | TTAAACTCTTTAAAT[G/T]GGTCGGTTAAAGCTC | 115426 |
rs751086251 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473398 | ATACTACTGGGTCAC[C/T]AACTAGTTTAGTGAG | 115426 |
rs751116262 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487077 | TTAGAAAGTAAATCA[C/T]TTGACAGTGTTTATT | 115426 |
rs751126676 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461926 | GTGCATTTCTTTTCT[G/T]TAGAATAAATTGTTA | 115426 |
rs751140872 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451150 | ACAATACTTTCATAT[C/T]GCAAACAATAGGACT | 115426 |
rs751155835 | in-del | -/CCCT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445981 | CCCCCCCCGCCACCC[-/CCCT]TTTTTTTTTTTTTTT | 115426 |
rs751194381 | in-del | -/TG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434783 | CAGTATTTTGGAAAC[-/TG]TATTTTATAATATGT | 115426 |
rs751221575 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482014 | CTTGTGTTGGTCGTA[C/T]GAGAGAATGTACTAT | 115426 |
rs751230287 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444139 | GGGAGAGAGAGTAGA[C/T]TTTTCTTGAATTAAG | 115426 |
rs751241985 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430443 | TTTAAAAATAATTGT[A/G]TATTTTATGATGTTT | 115426 |
rs751292697 | snp | C/T | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421079 | TCCGAGGGTAGGACC[C/T]TCCAATCAGCCATCT | 115426 |
rs751364340 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455733 | CTTATGCCTGTAATC[C/G]AAGCACTTTGGGAGG | 115426 |
rs751374827 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492430 | AGAATTCCTTCTCAT[A/G]GAATACATACTAAAG | 115426 |
rs751394715 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470975 | CAAGACAATGATCAA[C/G]AAACTAGATTAAAAT | 115426 |
rs751410168 | snp | A/C | 4.02099e-05 | 0.00448367 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413659 | GTGAGGCGCGCCCGC[A/C]GCGCCCCTAGCGAGG | 115426 |
rs751416548 | snp | A/T | 5.16658e-05 | 0.00508234 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475350 | TGTATATACCTTAGA[A/T]TTTGCTGGCAGAAGT | 115426 |
rs751425324 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447824 | GAAACCTATGTACGA[C/G]AAGCCAACAAACAAA | 115426 |
rs751427855 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480475 | ATGGTATAATTAGAA[A/G]AGTGTTTTGTATTAC | 115426 |
rs751428789 | snp | A/G | 0.000117709 | 0.00767078 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420882 | ATACATTTTAGAGAA[A/G]CATTTCACTATTCTT | 115426 |
rs751440988 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469775 | ACACGTATATATGTG[-/T]GTATATATATGTATA | 115426 |
rs751471968 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422671 | CTGTAGTGCAGTGAC[A/G]TGAACACGGCTCGCT | 115426 |
rs751504250 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414467 | GCATACTTGAAGGCT[A/G]TCTGTGGGCATCTCT | 115426 |
rs751515813 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437480 | TCAGGTGATCCACCT[A/G]CCTCAACCTCCCAAA | 115426 |
rs751542014 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418193 | GATGGTGTGAATGCA[G/T]TGTTTGCTCCTTGAG | 115426 |
rs751571809 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438207 | GGATAACCTAAACTT[C/G]CTACCAGTCAAATAT | 115426 |
rs751577229 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485421 | TTTTCCTGAGCATCT[A/G]GTGAGATGGATTTGC | 115426 |
rs751594354 | snp | C/T | 1.99031e-05 | 0.00315454 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499801 | CTGTGAAGCTTAAAT[C/T]TGCATTGTACTCTCC | 115426 |
rs751623894 | snp | C/T | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477659 | CCTGTGTGGTGGAGA[C/T]CCAGAAAAGAAATGT | 115426 |
rs751628170 | in-del | -/TG | 1.65842e-05 | 0.00287955 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498008 | CTGGCACTGAAATAT[-/TG]TGATTTAGGTGGTGA | 115426 |
rs751634299 | in-del | -/TTTGTTTTGTTTTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442464 | AAGGTTTTGTTTTGT[-/TTTGTTTTGTTTTG]TTTGTTTTGTTTTGT | 115426 |
rs751678275 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464297 | AATTAAATAATGTGT[C/G]TGATTCATTTTTAGG | 115426 |
rs751777723 | snp | C/G | 1.65438e-05 | 0.00287605 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500597 | AAGCATCAGATTCAG[C/G]AGAAGCAATTGAGGC | 115426 |
rs751781201 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442596 | TGATCCTCCTGCCTC[C/T]GCCTCTCATGTAGCT | 115426 |
rs751802241 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426751 | GATTTGCTTTATTTT[C/T]ATTTTATTTTATTTT | 115426 |
rs751819229 | in-del | -/AGTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494741 | TGTCGATTGAGTAAA[-/AGTG]AGTGTTTTTCACTTT | 115426 |
rs751826136 | in-del | -/T | 1.65567e-05 | 0.00287716 | frameshift-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481666 | TTCTTGTAAAACTGA[-/T]TTCCAGTGAAGTTGT | 115426 |
rs751850386 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436297 | GGCTAAGCGGCCAAC[A/G]CTGCTTACTTGACAT | 115426 |
rs751851075 | snp | C/T | 3.32254e-05 | 0.00407573 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6460585 | CAGATACCCAGAAAG[C/T]GGTACTCTAGAAATG | 115426 |
rs751863747 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469007 | CATTCTGCCAAAAGA[C/T]GGTGCCACATAATCA | 115426 |
rs751892336 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491232 | AGCCAGAGTCTGTTT[C/G]GTTTTGTGTCCTGGC | 115426 |
rs751907562 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant | UHRF2 | GRCh38.p7 | 9:6506009 | ATGCTCAGATTAAAT[C/T]GGATGTTTTTGTTTT | 115426 |
rs751926078 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446685 | GGTGAAACCCCGTCT[A/C]TATAGGAAAATTTGC | 115426 |
rs751967166 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417715 | GCATGAGGAAAGGTG[C/G]TTATATGTTACTGTG | 115426 |
rs752001077 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500338 | GCAAAGGATTTGGCT[-/G]GGGGGGGCATGGTAG | 115426 |
rs752008331 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465968 | CAAGTTTGGGATTCA[A/G]AAACATTTTTTAAAA | 115426 |
rs752010270 | in-del | -/AT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481018 | CCTTTGCTTGGTGAC[-/AT]AAGAATAGCCTCCTC | 115426 |
rs752014795 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458271 | TATACATTTCTTCTA[A/G]ATTTTCTAGTTTATT | 115426 |
rs752076076 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449619 | TGGTCAGCTTATATG[C/G]GTTGGCCCTGGCCTG | 115426 |
rs752121188 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450419 | ATTCTTCTGTTATGT[A/G]TTAGTTTCCTGAGAA | 115426 |
rs752129940 | snp | C/G | 3.25675e-05 | 0.00403518 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413643 | CTACCGGGGCAAGCA[C/G]GTGAGGCGCGCCCGC | 115426 |
rs752132514 | in-del | -/CCA/CG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445977 | TCTTCCCCCCCCGCC[-/CCA/CG]ACCCTTTTTTTTTTT | 115426 |
rs752200279 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469811 | GTATATATATATTTA[C/T]ATTTGGAATTCCTAA | 115426 |
rs752212468 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420702 | ACAGAGTGAGACACC[A/G]TCTCAAAAAAAAAAA | 115426 |
rs752212658 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418159 | GTTTTTTTGTGGGGG[A/T]GTTGGAGAATGTCAA | 115426 |
rs752250723 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480315 | TCTGAAATTCTTTCC[A/G]TATATGTTCTGGCTT | 115426 |
rs752252710 | snp | A/T | 2.06345e-05 | 0.00321198 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499785 | TCTAAACCCCCCTTC[A/T]CTGTGAAGCTTAAAT | 115426 |
rs752253442 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459479 | TTCGAGACCAGCCTG[A/G]CCAACATGGCAAAAC | 115426 |
rs752310291 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469285 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 115426 |
rs752314304 | snp | C/G | 1.69683e-05 | 0.00291271 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420862 | GCAACTAAAAATGTA[C/G]TAAGATACATTTTAG | 115426 |
rs752324063 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429728 | GCTTGCTGGGTTGGC[A/G]CGTTACATGAATTTT | 115426 |
rs752327635 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427209 | TGCCACTTGGTAAAT[-/A]TTTTTTTTTATACAT | 115426 |
rs752347210 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503224 | TGGTCTAGCACTCCT[A/G]ACCTCAAATGATCCA | 115426 |
rs752375668 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428474 | AACTTATTTATGCAA[C/T]CCTAATCCCTAATTT | 115426 |
rs752380376 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438005 | ATATTGTCCTCCAGC[C/T]CTCATGCCTTAAAAA | 115426 |
rs752405660 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437718 | CACTTCCTGGTTTCA[A/G]GTAATTCTCGTGCCT | 115426 |
rs752417450 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421814 | TTTTATACTCTTTTT[-/G]TTTTTTATTTTTGCT | 115426 |
rs752423118 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432061 | AATGTCTTTAAATTT[C/G]TCAGTGATTAGTATG | 115426 |
rs752471637 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422582 | TTTTAATTCATGAAC[A/C]TTAAAAGACTTGACT | 115426 |
rs752482108 | snp | C/T | 1.70324e-05 | 0.00291821 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486811 | GAGACTCTCTTTAAT[C/T]GTTTTATAGGTGAGC | 115426 |
rs752498789 | snp | A/G | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460760 | ACAATCTCAAGGACC[A/G]AAAAAGAACTTCGTG | 115426 |
rs752498848 | snp | A/G | 1.76052e-05 | 0.00296686 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486941 | GTAAGTCATTATACA[A/G]CCTTACTCATTAGTA | 115426 |
rs752516776 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490253 | TTTTATGTGGAGAAG[A/C]TGATTACATTAACTG | 115426 |
rs752530883 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464279 | GTGACTTTTTTTGTT[A/G/T]TTAATTAAATAATGT | 115426 |
rs752536234 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412833 | CAGGATTATACAAGT[C/G]CACGCCAGGGTTTCT | 115426 |
rs752555248 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451418 | ACTAAGAGAAATTGA[A/G]CTTCCATCCTGATTC | 115426 |
rs752586598 | snp | A/G | 0.000142664 | 0.00844461 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468418 | TAGCCCGATCAAATA[A/G]TCATCTCTTTGAATG | 115426 |
rs752588951 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453885 | ACTCCAACCTGGGCA[A/G]CAGAGTAAGACTCCG | 115426 |
rs752619256 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423335 | TTGCTTTATAAATTG[A/T]GTTTAATACTGATAC | 115426 |
rs752640250 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454655 | CCTGAGCTTACATAG[C/T]CCTTGTTTGATTTGG | 115426 |
rs752642270 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445773 | CTCCCTATGTTGCCT[A/T]GACTGATCTCAAACT | 115426 |
rs752763116 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472954 | GCATGAACTCATGAG[A/G]TGTTTTGTGTTTGAG | 115426 |
rs752773877 | in-del | -/ATTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445272 | GTTATTTATGTATTG[-/ATTG]ATTGATTGATTGATG | 115426 |
rs752779636 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449457 | TTACTGCCTAGTTCT[A/C]CTTTCTTTCCCTGTC | 115426 |
rs752801243 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483527 | AGATTCAGTACAGAC[A/G]CAGCCGTCTGTTTAT | 115426 |
rs752804604 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426697 | ATACTGACTTGTTGA[C/G]TAAACTGAAAACCAT | 115426 |
rs752819917 | snp | A/G | 5.41565e-05 | 0.0052034 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493973 | TTTGAACATTGAATA[A/G]AAGTTTCATTATAGG | 115426 |
rs752868979 | in-del | -/GAG | 1.68145e-05 | 0.00289948 | cds-indel, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413539 | AAGACGTGCACCATT[-/GAG]GACGTGTCTCGCAAA | 115426 |
rs752875334 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497628 | AATAAAGCCATTTAA[C/G]TAACTGGCTGTTGTA | 115426 |
rs752899893 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478918 | TTCCTCTGACGTCTC[A/G]TATTTTCCTTCTTTC | 115426 |
rs752904663 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473924 | TATCAAAAATCAACA[C/T]TGTGAGAAACACTAT | 115426 |
rs752942422 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431645 | AAAGAATGCCCTACC[A/T]TTGTGAGCTGATATG | 115426 |
rs752963156 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417641 | TAGGAAGACTGGAGG[A/G]GTACCTATGAATTAG | 115426 |
rs752989529 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500207 | TCCTGGGCTGAAGGG[A/G]TCCTCCTGCCTCAGC | 115426 |
rs753024588 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502070 | AAGTTTCATGCCCAT[A/T]CTCTTCAGATAAGCC | 115426 |
rs753032950 | snp | A/G | 3.39859e-05 | 0.00412211 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504646 | TTGCTGTCAGGAGCT[A/G]GTTTACCAGCCTGTG | 115426 |
rs753057697 | snp | A/G | 1.71281e-05 | 0.00292639 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434194 | TGCTCAAGCTATTGA[A/G]GACTTTATTCATATT | 115426 |
rs753116597 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414680 | TAAGTGTAGCTCTTT[G/T]ATTTGGTAGAAGTAG | 115426 |
rs753118708 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435738 | CAGCCTCCTGAGTAG[C/G]TGGGGGCTACAGGTG | 115426 |
rs753132041 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444687 | GCTCACTGCAACCTC[C/G]CCCTCCAGGGTTCAA | 115426 |
rs753132306 | in-del | -/TG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441732 | TAGGTGGTTTGTGGC[-/TG]CGGTTTTTTTTTTCC | 115426 |
rs753134061 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506107 | TCTTGGCCAGAATTA[C/T]ATCATGATTCCCAAT | 115426 |
rs753154354 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485999 | GTTTGGGTAATATTG[A/G]GTAGTTTTGGCTCAG | 115426 |
rs753172068 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487401 | GGCGGAGTTTTACTC[-/TT]GTCACCTAGACTGGA | 115426 |
rs753206431 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468790 | CCACAGAATATGTAG[G/T]TCTTTTAGTTTGAAA | 115426 |
rs753254353 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448941 | TATTACGGAAATCTT[C/T]AAACATCGCAGAACA | 115426 |
rs753255860 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460745 | ATTACCACATTGAAG[A/G]CAATCTCAAGGACCA | 115426 |
rs753272224 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417928 | CTGGTCCCTCAAACC[C/T]AAGTGGAAAAATGTT | 115426 |
rs753280879 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426655 | ATGTTTGTAATCGGT[A/G]TTCTGCCTTCACAGA | 115426 |
rs753293087 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505998 | TTACATGCTTTATGC[C/T]CAGATTAAATTGGAT | 115426 |
rs753334011 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423225 | TCCAAAGAAAGTACC[A/G]GGCTTGGATGGCTGA | 115426 |
rs753335136 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478875 | CTCATATGATCACAC[C/T]CTGAATTTTACCATC | 115426 |
rs753349329 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437520 | TTACAGGTATGAGTC[A/T]CTGCACCTGGCCAGA | 115426 |
rs753404381 | snp | G/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507502 | GCCTCGGCCTCCCAA[G/T]GTGCTGGGATTATAG | 115426 |
rs753453186 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411626 | CTCAAGTGATCCGCC[C/T]ACCTCGGCCTCCCAA | 115426 |
rs753459104 | snp | A/G | 1.68151e-05 | 0.00289953 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413540 | AGACGTGCACCATTG[A/G]GGACGTGTCTCGCAA | 115426 |
rs753469018 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445972 | AATACTCTTCCCCCC[-/A]CCGCCACCCTTTTTT | 115426 |
rs753475746 | snp | C/T | 2.44681e-05 | 0.00349764 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413631 | CCAGCGCCTCTTCTA[C/T]CGGGGCAAGCAGGTG | 115426 |
rs753479663 | in-del | -/AT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480268 | AGTCACTCTTGTCAC[-/AT]ATAACCCTGATGTAT | 115426 |
rs753483250 | snp | C/T | 1.66807e-05 | 0.00288792 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497993 | ATTTTAAATCTCAAA[C/T]TGGCACTGAAATATT | 115426 |
rs753542937 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412628 | TCGGAAGTGGGTTTC[C/T]GCGCGAAAGTAGCAT | 115426 |
rs753579779 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466850 | CTCATTTGACTTACT[C/G]TGTCTCTTATTTCAG | 115426 |
rs753580013 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489698 | GTATAGCACTTCAGG[-/T]TTTTTTGGCCATTTT | 115426 |
rs753597436 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454696 | GCTAGCTCCTTCTAA[C/T]TTCAGGCCCACTTTG | 115426 |
rs753613885 | snp | C/T | 3.515e-05 | 0.00419211 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499966 | TATAAATAATAATAA[C/T]ATACTTTTGTTGTTG | 115426 |
rs753614155 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447815 | AGAAAACTGAAACCT[-/A]ATGTACGAGAAGCCA | 115426 |
rs753632026 | snp | C/T | 6.62372e-05 | 0.0057545 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500588 | AAGTGTACAAAGCAT[C/T]AGATTCAGCAGAAGC | 115426 |
rs753648664 | snp | C/T | 0.000291163 | 0.0120622 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422599 | TAAAAGACTTGACTT[C/T]TCCATTAACTTAGAT | 115426 |
rs753652078 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490131 | GTTTTTAGTGTCTGA[C/G]CAATTGTATTTGATC | 115426 |
rs753668193 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486804 | GTATTTTGAGACTCT[A/C]TTTAATTGTTTTATA | 115426 |
rs753669590 | snp | G/T | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482069 | CATTCCTGGTATTCC[G/T]GTTGGATCAACTTGG | 115426 |
rs753699024 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431483 | GTGGCATATACCTGT[A/C]GTCCTAGCTGCTCAG | 115426 |
rs753700722 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440021 | CAGTTGTATATCTTC[C/T]TCAATGTTCTGTATT | 115426 |
rs753731637 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444981 | ACAGGCTACATAGTT[G/T]AGGCACTAGATTTAG | 115426 |
rs753759384 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460635 | CACGAGCTAGAACCA[G/T]TTTGAAATGGAATGA | 115426 |
rs753787687 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464151 | TGGGTATGTAATAGT[A/G]TTTCATTTTGGCTTT | 115426 |
rs753789721 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453071 | TTTCATGACTTACCT[C/T]TTACAGACTTAACTA | 115426 |
rs753816521 | in-del | -/T | 1.69143e-05 | 0.00290807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481601 | TTACTAGCTTTAATA[-/T]GGTATTGTGAAAATG | 115426 |
rs753841160 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453827 | GGAGAATCGCTTGGA[C/T]CCAGGAGGCGGAGGT | 115426 |
rs753882536 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494069 | AATTCCAGTGCCTGA[C/T]TATGTAATTGTTTTT | 115426 |
rs753931819 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444568 | CTCTCTCCCTGCTTC[C/T]TCATTGTGTGGGCCT | 115426 |
rs753932533 | in-del | -/AG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442502 | TTTTGTTTTTGAGAC[-/AG]GGTCTTGTTCCATCA | 115426 |
rs753935379 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494873 | TCAATTTACATAGAA[A/T]CTCTGTTTTTATGTG | 115426 |
rs753949505 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471971 | TTCCATGCTGTCTTT[G/T]TAAAATTGTTTTTGA | 115426 |
rs753963942 | snp | C/G | 1.80253e-05 | 0.00300206 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486954 | CAACCTTACTCATTA[C/G]TACCTGCCTTGACCA | 115426 |
rs753967714 | snp | A/C/T | 6.82983e-05 | 0.00584338 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475369 | GCTGGCAGAAGTTAA[A/C/T]CTTTCTTCCTTTTTT | 115426 |
rs753985347 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462800 | CACGTGCCTGTAGTC[C/T]CAGCTACATGGGTGG | 115426 |
rs754017266 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415214 | ATTGGGTTAAATTCA[A/G]GGCAACAAAGTAGAC | 115426 |
rs754026769 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448842 | CTTTTAAAGTTTGTA[C/T]ACATAAGGAAAAACT | 115426 |
rs754035207 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482507 | AATGCTAAGACATTG[C/G]GCAGAGGAAGTGCCA | 115426 |
rs754049459 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416005 | TTTTAACAAGATCTC[C/T]AGGTGATCTGTATGT | 115426 |
rs754073469 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449379 | AGAGTTGAACAGCAC[C/T]CAGGCTTTTCCTGCC | 115426 |
rs754079931 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439278 | CAACTTCTGTCTCCC[A/G]GGTTCAAACGATTCT | 115426 |
rs754103557 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426460 | GTTGCTGTTCATACA[A/G]TAATAAATTTAGAGC | 115426 |
rs754146105 | snp | A/G | 3.6848e-05 | 0.00429216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498186 | TTGTCTAGGCTGCCT[A/G]TGTGTTCATAAAAAT | 115426 |
rs754171599 | snp | C/G | 1.76076e-05 | 0.00296707 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477846 | GTTGTTGTTCTTGCT[C/G]TGTAAACATGAAATA | 115426 |
rs754212788 | snp | G/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481668 | TCTTGTAAAACTGAT[G/T]CCAGTGAAGTTGTAA | 115426 |
rs754215460 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443147 | GTATCTGATCTTAAG[A/C]ATGAAGCTACCTTTG | 115426 |
rs754259394 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433981 | CACACATACATAGTG[C/T]TACTAGAGCTTCTGA | 115426 |
rs754286228 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460043 | ATCACCCTCCCCAGT[C/G]CCCTACTTTCCCAGC | 115426 |
rs754286305 | in-del | -/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485788 | GGCAACATGGTGAGA[-/CC]CCCCTGTCTCTACCC | 115426 |
rs754299745 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476358 | TTTGTTAGCCACCCA[A/T]GTTTAGTTTTTAATA | 115426 |
rs754302595 | snp | A/G | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434097 | AACACAAATAAATTG[A/G]ACAGTGTACCCTCTA | 115426 |
rs754315203 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435981 | TTAGATTCTGACAGT[-/A]AACTATTGTCTTTAT | 115426 |
rs754321507 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466497 | GTGAGCAGAGATCAC[A/G]CCACTGTACTCCAGC | 115426 |
rs754350931 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477419 | TAATCCCAGCTACTC[A/G]AGAAGCTGAGGCGGG | 115426 |
rs754374053 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483575 | TACTCTCTCGACTTG[G/T]CAGATGTGGAACCTG | 115426 |
rs754385360 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412679 | GTTCGCGAAGCAGGA[C/G]GGCCCCCGGGGCCTT | 115426 |
rs754391454 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501542 | AAGGAAGAATTTTTT[-/A]AATATGATTTTTAAA | 115426 |
rs754398540 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504804 | GGGATAGTTGCGGAA[A/C]CTTCTAGTTAAGAAG | 115426 |
rs754422447 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434608 | CACGCCTGATTAATT[C/G]TTGTATTTTTAGTAG | 115426 |
rs754432262 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445711 | CACAGGTGCATGCCA[A/C]CATAACTGGCTAATT | 115426 |
rs754445595 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479515 | TTTTCTATGCTAGGG[A/T]ACTATGCTTGTTCCC | 115426 |
rs754454228 | snp | C/G | 1.68153e-05 | 0.00289955 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413541 | GACGTGCACCATTGA[C/G]GACGTGTCTCGCAAA | 115426 |
rs754462364 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489709 | TCAGGTTTTTTGGCC[A/G]TTTTCTAATTGGGTT | 115426 |
rs754462716 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458624 | TTTATACTGTTGGTG[C/G]GAGTGTAAATTAGTT | 115426 |
rs754485260 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436587 | ATAATATTATGCAGA[A/G]TGGCACAACATAGAC | 115426 |
rs754491954 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466980 | GACTTTTTCTGAATT[A/C]TTTATTTTATTTATT | 115426 |
rs754497098 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435766 | GTGCTTGGTACCACA[C/G]CAGGCTAATTCTTCT | 115426 |
rs754625836 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417843 | AACAGTTTGTATTTA[C/T]TCCTGACCGTCATTT | 115426 |
rs754679883 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447142 | GATCTGCCCGCTTCT[G/T]CCTCCCAAAGTGCTG | 115426 |
rs754682951 | snp | A/G | 1.77134e-05 | 0.00297597 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477854 | TCTTGCTGTGTAAAC[A/G]TGAAATATGTATTTG | 115426 |
rs754689565 | in-del | -/TTAAGGCA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454442 | GATTTCTTCATGGAC[-/TTAAGGCA]TTAAGGCATAGAATG | 115426 |
rs754727035 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498273 | GGTGGACTATAAGGG[G/T]TGAGGAATAAGATCA | 115426 |
rs754735284 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480946 | GTATGGGCAAAGAAA[-/T]TTTAAGATTAATTGG | 115426 |
rs754735681 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501987 | ACAGATTCTGACCTT[C/T]CTAGGTCATATTATT | 115426 |
rs754756698 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440101 | ATTTTTAAGGGCCCT[A/C]AACATCTAAATTCAC | 115426 |
rs754773732 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421760 | GTCCCTATCAGAACA[C/G]TTCTCTCTGTGTCTC | 115426 |
rs754790284 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463373 | GCTATCCCAACAGTA[C/G]AATAAAATGTAAAGT | 115426 |
rs754843733 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453087 | TTACAGACTTAACTA[A/T]GTATGTGTATGAGTA | 115426 |
rs754887595 | snp | C/T | 1.73453e-05 | 0.00294489 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486805 | TATTTTGAGACTCTC[C/T]TTAATTGTTTTATAG | 115426 |
rs754896865 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453841 | ACCCAGGAGGCGGAG[A/G]TTACACTGAGCTGAG | 115426 |
rs754919979 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436139 | TCTTAACAAGTACGA[A/G]TTAGAAATCCTAGAA | 115426 |
rs754959579 | snp | A/C | 8.24192e-05 | 0.00641894 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506161 | CCTTTTCTTCCCTGG[A/C]TACAGCAAAGGACGA | 115426 |
rs754974097 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506581 | TTGTAATTTGATTTT[A/G]CAGAAAAGGAAATGA | 115426 |
rs755020059 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482520 | TGGGCAGAGGAAGTG[C/T]CAGCTAATCCAAGAA | 115426 |
rs755032882 | snp | C/T | 1.77713e-05 | 0.00298083 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413469 | GGAGACAAAGGGGAC[C/T]GGTTCCTCTCTAGGC | 115426 |
rs755037535 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481816 | AAGTTATAATATATA[A/G]TGTTTTAATACCAAT | 115426 |
rs755063954 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456575 | GCTTCTGTTGCCGTT[A/G]CTTTTGGTGTTTTGG | 115426 |
rs755076483 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491041 | ATGGATGTAATACTC[-/T]TGCGTACCTGCTGAT | 115426 |
rs755127842 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439283 | TCTGTCTCCCGGGTT[C/G]AAACGATTCTCCTGT | 115426 |
rs755205130 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476241 | GCAGAATAATATTTT[A/T]TTGTATATGTATATA | 115426 |
rs755217962 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472780 | TGGCAACAATGTCTT[A/G]CGTGTAATGTGGGAT | 115426 |
rs755266770 | snp | C/G | 1.65534e-05 | 0.00287688 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481669 | CTTGTAAAACTGATT[C/G]CAGTGAAGTTGTAAA | 115426 |
rs755268155 | snp | A/G | 1.66288e-05 | 0.00288343 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420903 | CACTATTCTTTCTTT[A/G]TTTTCTAGTTGGAAA | 115426 |
rs755268867 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433992 | AGTGTTACTAGAGCT[G/T]CTGATGGACAGTCAC | 115426 |
rs755314009 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466684 | TCTTATTGAACATGG[C/G]TTCTTACAGAATATA | 115426 |
rs755330443 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443917 | CTCAGTCTGTGGTAC[A/T]TGATTTTGAGTAGCC | 115426 |
rs755331434 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465738 | ATCCTCTCTATTGTA[C/T]TGAAGGTGCAAAGGA | 115426 |
rs755342737 | in-del | -/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412960 | CGATGTGGTAGCCGC[-/G]GCAATCTTCCGAAAC | 115426 |
rs755349968 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443201 | CTGTGGGCAAATGAT[C/T]GCCAGGAGCCTTTTC | 115426 |
rs755356776 | snp | C/T | 1.65138e-05 | 0.00287343 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434099 | CACAAATAAATTGGA[C/T]AGTGTACCCTCTACG | 115426 |
rs755357824 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476377 | TAGTTTTTAATAATG[A/T]GATTTATTTTTACAC | 115426 |
rs755385885 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434670 | TCTCAAACACCTGAC[C/T]TCAAGTGATCTGCCC | 115426 |
rs755405002 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433305 | ATTTTGTGTCTTACG[A/C]CCTGTTCATTTTTAT | 115426 |
rs755504645 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456077 | TTACTATTAGGAAAT[A/G]TACGTACAGCCAAGT | 115426 |
rs755516617 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505335 | GAATCTCACTCTGTC[A/G]TTCAGGGTAGAGTGT | 115426 |
rs755529534 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477719 | GAAACATGAACCCAA[C/T]ATGCAGCTTCTGTGT | 115426 |
rs755560189 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453047 | AGAATTTAAAAATGT[A/G]TGCTTCATTTTCATG | 115426 |
rs755580443 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468290 | AAAAGTGGCTTTGGC[C/G]TTGAATTTGTGACAT | 115426 |
rs755600666 | snp | A/G | 3.65377e-05 | 0.00427405 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486956 | ACCTTACTCATTAGT[A/G]CCTGCCTTGACCATT | 115426 |
rs755602612 | snp | C/T | 5.12545e-05 | 0.00506207 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504634 | TTTTATGTGCGTTTG[C/T]TGTCAGGAGCTAGTT | 115426 |
rs755624092 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478852 | TTCCTTTTACCTCCT[A/C]CTACTACCTCATATG | 115426 |
rs755692411 | snp | C/G | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506138 | GAGATTCTGCAGACT[C/G]TACTTGACCTTTTCT | 115426 |
rs755704532 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466056 | TTTAGATATTTGTAA[A/G]TAAAGTAGTATTTGA | 115426 |
rs755736154 | snp | A/G | 3.49889e-05 | 0.00418249 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497154 | CTCGATTGTGTACTT[A/G]AAGAAAAATTACATG | 115426 |
rs755808834 | snp | A/G | 8.24463e-05 | 0.00642 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421067 | AGTAAAGAAAGCTCC[A/G]AGGGTAGGACCTTCC | 115426 |
rs755812631 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416355 | TTACAGGCGTAAGCT[A/G]CCGTGCCCAGCCTTG | 115426 |
rs755826334 | snp | G/T | 1.65919e-05 | 0.00288022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497363 | TGGCATTTATAAGGT[G/T]CTCTATCTGGCATGA | 115426 |
rs755829520 | snp | A/G | 1.71894e-05 | 0.00293162 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499843 | CCATCAGTATCCAGC[A/G]GGTTACCCTTCAGAT | 115426 |
rs755844761 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438550 | CATTATTTGGCAAAC[C/T]TGTGCACAATTGTGT | 115426 |
rs755849035 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499724 | GTAAAGTTTTTCAGT[G/T]TGGGGAACGTGTAGT | 115426 |
rs755852124 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469101 | CAGAGAAACTTTCAA[C/G]TAACTGTGATTAATA | 115426 |
rs755854697 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507258 | GGTTGGTTTTTTGAG[A/G]TGGAGTCTTGCTCTG | 115426 |
rs755866461 | in-del | -/TTTA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466986 | TTCTGAATTCTTTAT[-/TTTA]TTTATTATCACCCCA | 115426 |
rs755867003 | snp | G/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411512 | CCTCCCGAGTAGCTG[G/T]GACTACAGGCAACTG | 115426 |
rs755871429 | snp | C/G | 1.68156e-05 | 0.00289957 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413526 | CATTGATGGCTCCAA[C/G]ACGTGCACCATTGAG | 115426 |
rs755885400 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456913 | GTTTTGGTTACTGTA[A/G]CCTTGTATAGTTTGA | 115426 |
rs755899891 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487998 | GTAATCCCAGCACTT[C/T]GAGAGGCTGAAGTGG | 115426 |
rs755901040 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430057 | TTTACTCTTTTTGCC[C/G]TGAAGTGCAATGGCA | 115426 |
rs755934739 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471834 | TAAAGCTCTATATTG[A/G]GAAGAAACTGGTGGG | 115426 |
rs755983315 | snp | A/T | 1.65666e-05 | 0.00287802 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481955 | TCATTAAAATTTAAC[A/T]TAACTGATTTCTCAA | 115426 |
rs755989720 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462126 | AGGATAGGCAAGCTT[A/G]TAGCCCACTAGCTGC | 115426 |
rs756029278 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487444 | CAGTCTCGGCTTACT[C/G]CAATCTCCTCCTCCC | 115426 |
rs756029326 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454486 | TATCTTTGATTCAGT[A/G]TCAAGTACCTTCTCT | 115426 |
rs756060262 | snp | C/G | 2.44645e-05 | 0.00349738 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499946 | GGTAGGTAATGATTG[C/G]AAAATATAAATAATA | 115426 |
rs756065325 | snp | C/G | | | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421048 | GTTCTAATAGTCCAC[C/G]TAAAGTAAAGAAAGC | 115426 |
rs756083463 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488975 | GCATCGCCATTGACT[A/G]ATTTTTGTATTTTTA | 115426 |
rs756110169 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459926 | TACAGTGAGCTATTA[-/T]CGTGTCACTGTACTG | 115426 |
rs756110491 | snp | A/C | 0.000315465 | 0.0125552 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486832 | ATAGGTGAGCGAAGC[A/C]GGTGTTCACAGACCC | 115426 |
rs756144819 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482044 | TTGTCCCTTCTAATC[A/G]TTATGGACCCATTCC | 115426 |
rs756159853 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454824 | ATATCATAAATACTA[A/C]TTCCTGTATTTCTAT | 115426 |
rs756189181 | snp | C/G | 1.78931e-05 | 0.00299102 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434224 | TTTCATTTGTAGAAA[C/G]CAAAGCCTTCTATTT | 115426 |
rs756191330 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463173 | GTAATCCCAGCTACT[C/T]GAAAGGCTGAGGCAG | 115426 |
rs756210992 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455928 | GGCCAAGGCTGCAGC[A/G]GGCATGATCACACCA | 115426 |
rs756254693 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433080 | TCAAGTGATCTGCCC[C/T]TGCCTTGGCCTTCCA | 115426 |
rs756262986 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424849 | TTGTAAAATCTCCCC[C/T]TGTTAGGATTCATTT | 115426 |
rs756281976 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415142 | TGAAGGATGTTCTTG[G/T]GCAACACTCCTAAAA | 115426 |
rs756341299 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481370 | AGTGATAAGTTTAGA[A/G]TTCATGGTATCATTT | 115426 |
rs756345699 | in-del | -/GAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492193 | CTTGATTTGCTGCTT[-/GAA]GAATAATCAGAAATG | 115426 |
rs756402340 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414598 | CTTCATGTTGTTGTT[A/C]ATACACTAAAAAGTT | 115426 |
rs756407299 | snp | C/G | 8.23947e-05 | 0.00641799 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477708 | GTATGTGGTGGGAAA[C/G]ATGAACCCAACATGC | 115426 |
rs756413528 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503050 | CCCAGGCTGAAGTAC[A/G]GTAGCATGATCTCAG | 115426 |
rs756428542 | snp | A/G | 0.000185753 | 0.00963545 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468516 | TAGCTTTGTAGTTGT[A/G]TTTTGCCCCTAGGGA | 115426 |
rs756450824 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471100 | CAACAGCAAAGACTT[G/T]TCAAATCCCCTTAAA | 115426 |
rs756451030 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474504 | TGAGGTCAGGAGTTC[A/G]AGACGAGCCCAGCCA | 115426 |
rs756470414 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428412 | TTCTTTGTTCTTTAC[C/T]AACTTTCTTATTAAT | 115426 |
rs756474284 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429044 | GTGGTGGATACCTGT[A/T]ATCCCAGCTACTCAG | 115426 |
rs756477596 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450550 | ATAATACTTTTCTGT[A/G]GTAAGATTCAGGTGT | 115426 |
rs756495099 | snp | C/T | 6.92521e-05 | 0.00588398 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477832 | ATCAGGTTTTTGTTG[C/T]TGTTGTTCTTGCTGT | 115426 |
rs756497866 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485905 | GAAGTTCACAAAGAA[A/G]TGACACTTGTTTCAG | 115426 |
rs756532786 | in-del | -/AAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457392 | GTTGCTTATCACCTT[-/AAG]AAGGAGATTTTGGGC | 115426 |
rs756557839 | in-del | -/TATTAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428421 | CTTTACTAACTTTCT[-/TATTAA]TATTAACCTTTAACA | 115426 |
rs756575731 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412479 | AGAGAGCGGCCTTTC[A/G]GGCAGCTGCCCCGAC | 115426 |
rs756583276 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502914 | TGACTTTAATGATCC[A/G]TGTTCATAAATCAGT | 115426 |
rs756617514 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433970 | TTGGTTTGAAGCACA[C/T]ATACATAGTGTTACT | 115426 |
rs756630362 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443101 | AGTGTCTATGTAAAG[A/C]AGGAAAATTCTTATG | 115426 |
rs756636282 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503863 | ACATTTAGGGGGACA[G/T]TGACTTTTTAACATC | 115426 |
rs756639873 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465623 | GTTAATCTGTTACGA[A/T]GTTTTTTATTTCTGA | 115426 |
rs756688430 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461973 | TGCCGAGGGTTTTAG[A/G]ATAACCCTGACAATT | 115426 |
rs756689599 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466217 | CCAGCCTGGCCAGCA[-/G]GGGTGAAACCTCATC | 115426 |
rs756709532 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445976 | ACTCTTCCCCCCCCG[C/G]CACCCTTTTTTTTTT | 115426 |
rs756743544 | snp | C/T | 1.74842e-05 | 0.00295665 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434214 | TTATTCATATTTTCA[C/T]TTGTAGAAACCAAAG | 115426 |
rs756754852 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452096 | CCTTATTTTTTTTAA[A/G]TTCATATATCCTGGA | 115426 |
rs756757398 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505988 | TGCTGAGTACTTACA[C/T]GCTTTATGCTCAGAT | 115426 |
rs756763305 | snp | C/T | 4.97104e-05 | 0.00498525 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481949 | GGGCTTTCATTAAAA[C/T]TTAACATAACTGATT | 115426 |
rs756785057 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452012 | CCATATACCCATATC[G/T]AGTGTATATATGTGT | 115426 |
rs756785124 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443477 | TCTACCATACTACCT[C/G]TCATTTTAAGAGAAG | 115426 |
rs756840275 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444168 | AGTGTCATGTCAGTC[G/T]TGAGTACAGGAGGGA | 115426 |
rs756851982 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476513 | CATTTAACGGATTTT[G/T]CTTACTTGATATCAA | 115426 |
rs756945974 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475352 | TATATACCTTAGATT[C/T]TGCTGGCAGAAGTTA | 115426 |
rs756952176 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470154 | AAGGCGGGCAGATCA[C/G]TTGAGGTCAGGAATT | 115426 |
rs756979489 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477554 | GTTTCCATGGGCTTT[C/T]CTTTATGAGATTCAT | 115426 |
rs756983372 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492012 | TGCTGGGATTACAGG[C/T]ATGAATCATTGCGCC | 115426 |
rs756984671 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447130 | TCCTGACCTCATGAT[C/G]TGCCCGCTTCTGCCT | 115426 |
rs756985196 | snp | C/T | 1.69706e-05 | 0.0029129 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413665 | CGCGCCCGCCGCGCC[C/T]CTAGCGAGGCTGGGG | 115426 |
rs757017031 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466813 | GGGGCCTTTGTACTT[G/T]ATGTTCCCTCCTACA | 115426 |
rs757073174 | snp | C/T | 1.6806e-05 | 0.00289875 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420883 | TACATTTTAGAGAAG[C/T]ATTTCACTATTCTTT | 115426 |
rs757102851 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447852 | AAAGCAAGCAAATTG[A/G]TGTTGGAGAACCTTG | 115426 |
rs757121815 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451159 | TCATATTGCAAACAA[C/T]AGGACTACTGAAAAG | 115426 |
rs757177538 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498470 | TTTAGGTATAGGAGG[A/C]CCTGGAAAAGGACAT | 115426 |
rs757200420 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438208 | GATAACCTAAACTTC[C/G]TACCAGTCAAATATC | 115426 |
rs757212066 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499490 | CTATCTGTTGTGCTC[C/T]ATGATTGGTTCTCAT | 115426 |
rs757227129 | snp | A/C/G | 1.99595e-05 | 0.00315901 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499803 | GTGAAGCTTAAATCT[A/C/G]CATTGTACTCTCCCT | 115426 |
rs757234325 | snp | G/T | 1.8272e-05 | 0.00302253 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500508 | TCATAGTTCTGCTTA[G/T]AACCACTTGTAAGTC | 115426 |
rs757276347 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461054 | AGAAATTCTTACTTC[A/C]TCATAGGATTCTTAT | 115426 |
rs757283646 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464311 | TCTGATTCATTTTTA[A/G]GAGTTCTAATTACGG | 115426 |
rs757324685 | snp | C/G | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481706 | TGAAAGACTCAAGAT[C/G]AGTAAAAAGAAAGCA | 115426 |
rs757340283 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465541 | ATTTTCTAGGAATTT[A/C]TCTATTGCATCTAAA | 115426 |
rs757344846 | snp | C/G | 0.000178047 | 0.00943354 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422670 | GCTGTAGTGCAGTGA[C/G]GTGAACACGGCTCGC | 115426 |
rs757396304 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441547 | TGAGAACAAATCATT[C/G]ATAAATTCCTTTTGA | 115426 |
rs757396966 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432383 | CCTTTTTATATTTTC[A/G]GTAACTTATTTCTAA | 115426 |
rs757423306 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424603 | CCATATATCCCACAC[C/T]TAGTTTTCCCTCTTA | 115426 |
rs757436284 | snp | C/G | 1.65086e-05 | 0.00287298 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482121 | TTTAACTTGGGCTTA[C/G]TTGAAAGGGGAGAAT | 115426 |
rs757484402 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454740 | CACTCTTAGTTGGGT[A/C]ACGGTTCAAGATTTC | 115426 |
rs757492629 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498348 | TGTCAGACTGCCCTG[A/G]GACCAAGGGTTGTGC | 115426 |
rs757520078 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446802 | GTGAGCTGAAATGGC[A/G]CCACTGCACTCCAGC | 115426 |
rs757529046 | snp | C/T | 1.68627e-05 | 0.00290363 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486816 | TCTCTTTAATTGTTT[C/T]ATAGGTGAGCGAAGC | 115426 |
rs757598170 | snp | A/G | 0.000140164 | 0.00837033 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497148 | TAATGACTCGATTGT[A/G]TACTTGAAGAAAAAT | 115426 |
rs757612913 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426836 | TCACTGCAACCTCTG[C/T]CTCCTGGGTTCAAGC | 115426 |
rs757612976 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436335 | GGTAATAGTACCAAC[A/G]ATTATCTGAGTATTT | 115426 |
rs757642159 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440273 | TTAGAGAATGTTGTC[G/T]TATGTGCCGGACTCT | 115426 |
rs757662789 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417694 | TTAAAAAGCCTGTCA[C/T]AGCAAGCATGAGGAA | 115426 |
rs757663957 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427588 | TACTTGGGAGGCTGA[A/G]ACGGGAGAATCACTT | 115426 |
rs757681113 | in-del | -/TTC | 0.000132703 | 0.00814456 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481787 | GAAGAAATTCCCCTT[-/TTC]TTCCTAATAGCAAGT | 115426 |
rs757685255 | snp | C/G | 1.65081e-05 | 0.00287293 | synonymous-codon, nc-transcript-variant, intron-variant | UHRF2 | GRCh38.p7 | 9:6497279 | AGCTGGTAAGCCAGT[C/G]AGAGTGATACGCAGT | 115426 |
rs757699477 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483752 | TGGAGTGCAATGGCA[C/T]GATCTTGGCTCACCA | 115426 |
rs757753676 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428746 | TAGAGACAGAGTTTC[A/C]CTATGTTGTCCAGGC | 115426 |
rs757775191 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477683 | GAAATGTCATTCTTG[C/T]TCCTGTCGTGTATGT | 115426 |
rs757777332 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498314 | CAGAGGAAAAGAAGA[A/G]AAAAGGTAGTATCCT | 115426 |
rs757805640 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470859 | ATCCAAAATAAGGCA[A/G]TTGTGACTAAAAGAA | 115426 |
rs757810824 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474328 | AGTAAACTTTTGATT[A/C]AGAATGCATTACTAG | 115426 |
rs757817085 | in-del | -/TTTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455134 | GCAGCAGCTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 115426 |
rs757837077 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500375 | GATCTTTTGTTTAAT[A/G]GTGTCAGAGCCAAAT | 115426 |
rs757867429 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450604 | TTGTTACCAGCTTGT[A/G]TTGTAATTCCCTAGA | 115426 |
rs757874186 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459592 | GAGAATCACTTGAAC[A/C]CAGGAGGTGGAAGTG | 115426 |
rs757875958 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471637 | ATGAGACTGCACCCC[G/T]GACCAATGGCTTAAC | 115426 |
rs757909807 | snp | A/G | 1.69666e-05 | 0.00291256 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421111 | CATCAGCTCGTGCCC[A/G]TCTTATTGATCCTGG | 115426 |
rs757914653 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463739 | GTCTCCCAAAGTGGT[A/G]GGATTATAGGTATGA | 115426 |
rs757916712 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427861 | AGAGGCTGGGTCCAT[A/C]CATTCACATTATATG | 115426 |
rs757917146 | snp | C/T | 1.75207e-05 | 0.00295973 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460798 | TTTCCTGGGGTAAGA[C/T]TGTCTTCACTGGTGC | 115426 |
rs757961302 | snp | C/G | 3.30371e-05 | 0.00406417 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481700 | GGCTGGTGAAAGACT[C/G]AAGATGAGTAAAAAG | 115426 |
rs757968926 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437418 | TTGTATCTTTAGTAG[A/C]TACGGGGTTTCACCG | 115426 |
rs757987892 | snp | C/T | 3.12769e-05 | 0.00395442 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504564 | TGAACTGCTAACTTT[C/T]CTTTCCTTATCCTTG | 115426 |
rs758051034 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434106 | AAATTGGACAGTGTA[C/T]CCTCTACGTCTAATT | 115426 |
rs758053610 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499457 | CCACAATTTACTGTG[A/G]TCCAATCCATCTGCT | 115426 |
rs758096222 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453902 | AGAGTAAGACTCCGT[C/G]TCAAAAAAAGAAAAA | 115426 |
rs758119466 | snp | A/G | 1.6582e-05 | 0.00287936 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460766 | TCAAGGACCAAAAAA[A/G]AACTTCGTGTGAAAA | 115426 |
rs758122195 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486002 | TGGGTAATATTGAGT[A/G]GTTTTGGCTCAGGCA | 115426 |
rs758153587 | snp | A/C/G | 3.37976e-05 | 0.0041107 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413562 | GTCTCGCAAAGCCAC[A/C/G]ATTGAGGAGCTGCGC | 115426 |
rs758172422 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437760 | GAAGCTAGGATTATA[A/G]GCATGCACCACCACA | 115426 |
rs758187133 | snp | C/G | 0.00546995 | 0.0520101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422601 | AAAGACTTGACTTCT[C/G]CATTAACTTAGATCT | 115426 |
rs758219497 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479646 | CAGTTGGTTAGTTGA[C/T]TGGGACCACAAAATT | 115426 |
rs758222351 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491086 | TTTAGCCTAGTAACT[G/T]AAGAATTAATCAAAT | 115426 |
rs758292044 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445794 | ATCTCAAACTCCTGG[A/G]CTCAAGCAGTCCTTC | 115426 |
rs758299322 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463597 | GCCGCAGCCACCGGA[-/GT]GTAGCTGGAACTACA | 115426 |
rs758345105 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436651 | CTTATTAAATTTTAC[A/G]GTTTTAGGGGCTCTT | 115426 |
rs758345211 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446962 | AGCACAATCTCGGCT[C/T]ACTGCAAGCTCCGCC | 115426 |
rs758399793 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412878 | TTTTGAGACCAAAGA[A/G]CCATATCCGCTAAGC | 115426 |
rs758405553 | snp | A/C | 4.75138e-05 | 0.00487388 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413652 | CAAGCAGGTGAGGCG[A/C]GCCCGCCGCGCCCCT | 115426 |
rs758419192 | snp | A/G | 1.66103e-05 | 0.00288182 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498002 | CTCAAACTGGCACTG[A/G]AATATTGTGATTTAG | 115426 |
rs758422422 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472969 | ATGTTTTGTGTTTGA[A/G]TGTGTATATTAATGT | 115426 |
rs758473938 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474044 | AAACTGTTTTAGGGA[C/G]GTAGACAAGTGACAT | 115426 |
rs758484430 | snp | G/T | 1.67508e-05 | 0.00289398 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475533 | TGGTCTTAGACTACA[G/T]GTGTTGTACATGATT | 115426 |
rs758485403 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449517 | CTGTTTCCCAGAGTA[C/T]CCAACGGACAAAATG | 115426 |
rs758486614 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420943 | CCTTATTTGATTATG[A/G]TGTTGGACTGAATGA | 115426 |
rs758494558 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476369 | CCCAAGTTTAGTTTT[G/T]AATAATGAGATTTAT | 115426 |
rs758508112 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463446 | CACAATAGCTAAAAA[G/T]GAACCAGTGTGGCTT | 115426 |
rs758516830 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426885 | TCTTGAGTAGTTGGG[A/G]TTACAGGCACCCGCC | 115426 |
rs758530388 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415918 | CTGGATTCTCAGGAC[C/T]AGCAGCATTAGCTTT | 115426 |
rs758533593 | in-del | -/GCGCGCCCGCC | 3.8359e-05 | 0.00437927 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413649 | GGGCAAGCAGGTGAG[-/GCGCGCCCGCC]GCGCCCCTAGCGAGG | 115426 |
rs758540573 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440153 | AGTAGAGACCCTGAA[G/T]CTATTGTTGAAGAGT | 115426 |
rs758589495 | snp | A/T | 1.71876e-05 | 0.00293147 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499857 | CAGGTTACCCTTCAG[A/T]TAAAGAAGGGAAGAA | 115426 |
rs758608159 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417648 | ACTGGAGGAGTACCT[A/G]TGAATTAGCGAAGGA | 115426 |
rs758615370 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454914 | TAGATTGCTGGACCT[A/C]ATTTCCAGAGTTTCT | 115426 |
rs758620399 | in-del | -/T | 0.000101106 | 0.00710935 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481625 | AAAATGCCTTCGTTC[-/T]TTTTTTTTCTTTTAA | 115426 |
rs758621271 | snp | A/C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506127 | TGATTCCCAATGAGA[A/C/T]TCTGCAGACTCTACT | 115426 |
rs758630054 | snp | A/T | 3.82343e-05 | 0.00437215 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499969 | AAATAATAATAACAT[A/T]CTTTTGTTGTTGTTG | 115426 |
rs758704721 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453105 | ATGTGTATGAGTACA[G/T]ATAGAATATATATAA | 115426 |
rs758727403 | snp | C/T | 5.16667e-05 | 0.00508239 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434200 | AGCTATTGAGGACTT[C/T]ATTCATATTTTCATT | 115426 |
rs758731954 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435367 | CTGGGCTCAAGTGAT[C/T]CTCCCACCTCAGCCT | 115426 |
rs758737264 | snp | G/T | 0.000118954 | 0.0077112 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504647 | TGCTGTCAGGAGCTA[G/T]TTTACCAGCCTGTGA | 115426 |
rs758738978 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502657 | CGTAAGTTCCAGGAG[A/G]GCACAGACTGCCTTT | 115426 |
rs758759185 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478962 | GACATATTCCTGCTT[C/T]TCTAAAATACGCTCT | 115426 |
rs758778244 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434700 | CCCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 115426 |
rs758837581 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425715 | TTACGGGGAGCCGAG[A/G]TCGCGCCACTGCACT | 115426 |
rs758880245 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416092 | GTTTTTTTTTTAAGC[C/T]GGAGTCTTGCCCTGT | 115426 |
rs758887101 | snp | A/G | 3.25749e-05 | 0.00403564 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493984 | AATAAAAGTTTCATT[A/G]TAGGACTGTAAATTG | 115426 |
rs758896534 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448954 | TTTAAACATCGCAGA[A/T]CAAGCAGTATCATGA | 115426 |
rs758906167 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481900 | TACTTAAATTACATA[A/G]ACAGTTGGGTTCCTA | 115426 |
rs758910545 | snp | C/T | 0.000737735 | 0.0191917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468382 | GGCAGTAGATTAGTG[C/T]TTTTAGCTAAAACAA | 115426 |
rs758945415 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465620 | TGTGTTAATCTGTTA[C/T]GATGTTTTTTATTTC | 115426 |
rs758985672 | snp | A/G | 1.756e-05 | 0.00296306 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493805 | TTTAGCTTTCTTAAT[A/G]AAGAAAATCTTCTCT | 115426 |
rs759063188 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425787 | TTAAAAAAAAAAAAA[-/T]CAAGATCTCGGCTCT | 115426 |
rs759065282 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480173 | CATTTCTTTTTATGC[C/T]TCAGGACCTTTGCAC | 115426 |
rs759088775 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414782 | GAAATTTCATAGTAA[C/T]AAATTACACTTTGGG | 115426 |
rs759093837 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454599 | TCCCACACAGGATTA[A/G]TATCTATTTAATCGA | 115426 |
rs759113138 | snp | A/G | 0.000226321 | 0.0106353 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468766 | TTTAGGGTAACTGGT[A/G]TAATGGCTCCACAGA | 115426 |
rs759122737 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421835 | TATTTTTGCTACTTA[-/C]GTATATTTCTCTAGG | 115426 |
rs759148547 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455333 | GCGATGTTCCCCTTC[C/T]TGTGTCCAAGTGTTG | 115426 |
rs759173684 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421363 | AATAAAGGAAATACT[A/T]GTGTAATTGCACCAA | 115426 |
rs759209023 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447482 | ATTTTAGTTCCTGAA[G/T]GAGAACAGCAGTATA | 115426 |
rs759212327 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478899 | TACCATCGCTAATAA[C/T]TATTTCCTCTGACGT | 115426 |
rs759250285 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471239 | GGTGGGATAAACAGT[G/T]GAAAGCTTCAAGACC | 115426 |
rs759251743 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470657 | AAAAATGCGTGACAA[C/T]AATAATGCAGAAGAT | 115426 |
rs759261037 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474708 | AGACTCCATCTCAAT[A/C]AATAATACAAACAAA | 115426 |
rs759262802 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414131 | CTCGGGCATTGAGCT[C/T]TCAAGAATAAGAACC | 115426 |
rs759284039 | snp | A/G | 4.96718e-05 | 0.00498331 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500589 | AGTGTACAAAGCATC[A/G]GATTCAGCAGAAGCA | 115426 |
rs759285458 | snp | C/G | 1.73622e-05 | 0.00294632 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413690 | CTGGGGGCCGGAACA[C/G]CTGGGCTCCTCTGGA | 115426 |
rs759287483 | snp | G/T | 1.84361e-05 | 0.00303607 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498187 | TGTCTAGGCTGCCTG[G/T]GTGTTCATAAAAATA | 115426 |
rs759370400 | in-del | -/C | 0.000252827 | 0.0112405 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504575 | CTTTTCTTTCCTTAT[-/C]CTTGGATACTGTTCT | 115426 |
rs759377544 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502620 | CTGAAACAGTTTTTG[G/T]TTGTTTACTCTGCTG | 115426 |
rs759395285 | snp | A/G | 1.70825e-05 | 0.00292249 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433891 | AAATTAAGCTTCATT[A/G]ACTGATTTTAAACTT | 115426 |
rs759423382 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442107 | GTAGCTGAGATTACA[C/G]GTGCCTGGCACCACG | 115426 |
rs759425081 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432006 | GATGGACCTTAACAT[A/T]GATTATTTTCATTTT | 115426 |
rs759428005 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464196 | TGACTCCTAGTGGGG[C/T]TGAGAATCTTTTCGT | 115426 |
rs759443076 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490984 | ATTCTTGAATTTGGT[A/G]TAAATTTCATGAAGC | 115426 |
rs759447482 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500721 | ACCAGTATGTGAAGA[C/T]TTTTTTAAATAATAA | 115426 |
rs759457342 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465201 | ATGTTTGATATAGGA[A/G]TTTTGTAGATATGCT | 115426 |
rs759470877 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418003 | TTTTGGAAATATGCT[A/G]CTAGTTAATTTGCAT | 115426 |
rs759489195 | in-del | -/A | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411755 | TTATTAGTTTATTAC[-/A]AAAAAAATGGTACTG | 115426 |
rs759490163 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506988 | TTGCTTCATATTGTG[A/T]TCCTAAATTTTATAT | 115426 |
rs759495331 | in-del | -/TCT | 8.61705e-05 | 0.00656337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493813 | TCTTAATAAAGAAAA[-/TCT]TCTCTGACAGGACCG | 115426 |
rs759503909 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457832 | GCATATGTTGAACCA[G/T]CCTTGCATCCCAGGG | 115426 |
rs759520377 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480103 | GTTGCTTATCACTAA[C/T]CTGTTTACTTACTAA | 115426 |
rs759531788 | snp | A/G | 1.73243e-05 | 0.0029431 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486933 | ATGAAGTCGTAAGTC[A/G]TTATACAACCTTACT | 115426 |
rs759533017 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445367 | CTCCCAGGTTCAAGC[C/G]ATTCTCCTGCTTCAG | 115426 |
rs759548417 | in-del | -/TAATT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434324 | TTGGTGGTTGTACTC[-/TAATT]TAAAGGTCCTTTTAG | 115426 |
rs759557437 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458060 | TCTTTTCCTGTTGTT[C/T]GGAATAGTTTCAGAA | 115426 |
rs759570234 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494891 | CTGTTTTTATGTGTT[C/T]TATATTGTTTCTGAT | 115426 |
rs759570523 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465400 | TGTCTTGAATGTTTG[G/T]TAGAACTTCTCAATA | 115426 |
rs759610818 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449403 | TCCTGCCCCTTCCTT[C/T]TTTCAAAATGATAGA | 115426 |
rs759619457 | snp | C/T | 5.54677e-05 | 0.005266 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413440 | GGGCGGGGCGCGGCG[C/T]CCAGAGCTCAGGGGG | 115426 |
rs759651477 | snp | C/T | 8.23689e-05 | 0.00641698 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506089 | CCCTGCTTGCCGGCA[C/T]GATCTTGGCCAGAAT | 115426 |
rs759661330 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435334 | TCTCACTATATTGTC[A/C]AGGCTGGTGTTGAAC | 115426 |
rs759672070 | in-del | -/ATAC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469698 | TATATATACACGTAT[-/ATAC]ATACATATACACACA | 115426 |
rs759674278 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447983 | CACTTTTAACCCTAC[C/G]TAGTGTTTAAAACAG | 115426 |
rs759709984 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469542 | TTAAAAAACATAAAA[A/G]AATAACAAATAAGAC | 115426 |
rs759734575 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459085 | GGTAGGGGGCTAGGG[A/G]AAGGATAGCATTAGG | 115426 |
rs759739548 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426521 | TTATTTACTTTTTGG[A/G]GGATGAACCTTAGTA | 115426 |
rs759743016 | snp | C/T | 1.66813e-05 | 0.00288797 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475518 | ATGGATTTTTGTTTT[C/T]GGTCTTAGACTACAT | 115426 |
rs759766412 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468049 | ATTACCATTTAGTGT[-/C]CCCAGCTTTATTTGG | 115426 |
rs759794589 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427298 | CTTCTGACTGAAATA[C/T]TCTTTGAACATCATG | 115426 |
rs759801615 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426275 | CATCTCTTCTATTTC[C/T]TATTACTATGTGGTA | 115426 |
rs759807186 | snp | A/G | 2.54754e-05 | 0.0035689 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493968 | TAGAATTTGAACATT[A/G]AATAAAAGTTTCATT | 115426 |
rs759818044 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463029 | GCTCACGCCTGTAAT[-/C]CCAGCACTTTGGGAG | 115426 |
rs759820067 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446271 | TTCTCATACCTCAGC[C/T]TCCCAGGTAGATGGA | 115426 |
rs759839765 | snp | A/G | 1.66557e-05 | 0.00288575 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481796 | CCCCTTTTCTTCCTA[A/G]TAGCAAGTTATAATA | 115426 |
rs759873022 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451872 | CACTGCAGTCTCTGC[C/T]TCCCTGGGTTCAAGC | 115426 |
rs759876383 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421435 | GTTTGTTTTTGATAA[C/T]GGAGGCTTGCTCTGT | 115426 |
rs759902780 | snp | A/T | 6.7498e-05 | 0.005809 | splice-acceptor-variant | UHRF2 | GRCh38.p7 | 9:6497196 | TCTTTGTTGTTTTTT[A/T]GGGCATTGGCCCTAA | 115426 |
rs759908191 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501303 | TCAAATATGAACTAT[C/G]TCTTCATTCTTTCCT | 115426 |
rs759927480 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505583 | TAACAGGCATGAGCC[-/A]ACCATACCTGGCTGC | 115426 |
rs759945081 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489894 | TGGCTTTCTGAAAGG[C/T]GGATTTGGCAGTGCA | 115426 |
rs759987893 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453664 | CCATTAAAAAATGGG[A/G]TTGGCCAAGGCGGGC | 115426 |
rs759996345 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477431 | CTCGAGAAGCTGAGG[C/T]GGGAGAATCGCTTGA | 115426 |
rs760101684 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485880 | CTGCAATACCTTTTT[A/C]AGGGAGTTTGAAGTT | 115426 |
rs760142422 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479932 | TTGCTTCCATGTACT[A/G]TCCGTTCTCCCATAG | 115426 |
rs760146010 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435547 | AACAACCCCCCAAAA[A/G]GAAATCTCATACTGA | 115426 |
rs760174906 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417845 | CAGTTTGTATTTACT[C/G]CTGACCGTCATTTAG | 115426 |
rs760176184 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478730 | GGGTAATTGGTATCT[G/T]TGAAAAATAGATTGT | 115426 |
rs760188387 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480083 | TATCTACTCTCTAAC[-/G]TTCGGTTGCTTATCA | 115426 |
rs760229184 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440966 | TCATTCCCTGTGATT[C/T]CCTGTGATAATAATT | 115426 |
rs760243768 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464100 | GTTTTCTCATCCATG[C/G]TTAGTTTTTTCAGAC | 115426 |
rs760251233 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438908 | TATGAGGAATGATAG[C/T]CATTATAGATTTATG | 115426 |
rs760284224 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431919 | CTATGCAATATTTTT[A/C]TAGTAATATATGAAA | 115426 |
rs760293028 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465034 | AATTATTACATTTTT[C/G]TTTTGTCTTTTTCTT | 115426 |
rs760315601 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422396 | ACTGTTTTGATCTCC[C/G]TTTCTCCTATCTCCC | 115426 |
rs760366723 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423126 | TCAAGATTATTCAAA[C/T]GGAGATAATTTTAGA | 115426 |
rs760379843 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479386 | TAATCCCGATTTTCT[A/G]CCTACTTCACTGGCC | 115426 |
rs760386734 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412573 | CCGCGGCCTGAGGAT[A/G]GGCCTGGAGCTGCCG | 115426 |
rs760419713 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424180 | GCCTATGGATACCTG[A/G]GAGAGCTGAGAAAAT | 115426 |
rs760443942 | snp | A/G | 1.99918e-05 | 0.00316157 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460837 | TAACTGAATTGATCA[A/G]GGAATGTATTTTTAG | 115426 |
rs760458160 | snp | A/C | 1.70472e-05 | 0.00291947 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477614 | TGCTATAATTTTGTT[A/C]TTAATAGGGCGAAAT | 115426 |
rs760479236 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439864 | CTTGTTTCTAGTGGT[A/G]TTTTGAACAGAAAAG | 115426 |
rs760490900 | in-del | -/A | 1.72116e-05 | 0.00293351 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477605 | GACTAGACTTGCTAT[-/A]ATTTTGTTCTTAATA | 115426 |
rs760501803 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417383 | CATTGATGGACCTAA[A/G]TTACATGCTTCTGAC | 115426 |
rs760502455 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449315 | GGCAATTTCTGCCCA[A/G]TGTTAATTTCACACC | 115426 |
rs760538932 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486813 | GACTCTCTTTAATTG[-/T]TTTATAGGTGAGCGA | 115426 |
rs760551839 | snp | A/T | 1.66771e-05 | 0.00288761 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421178 | TTACTGTTGTGAGAA[A/T]ACAAATAAATTTATT | 115426 |
rs760560794 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472572 | GACAATCAAGATGAC[C/T]GAAGATAATTTGAAA | 115426 |
rs760564115 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432999 | GCATGCTCCACCACG[-/C]CTGGCTAATTTTTGT | 115426 |
rs760579366 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501862 | AGGGCTTGTTAGTGA[G/T]AACTGAGGTGAGTTT | 115426 |
rs760581436 | snp | C/T | 1.73201e-05 | 0.00294274 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433870 | AGGTTTTTGAAGCAG[C/T]AGACAAAATTAAGCT | 115426 |
rs760599817 | snp | A/G | 1.6591e-05 | 0.00288015 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500577 | AAGTGCCTCCAAAGT[A/G]TACAAAGCATCAGAT | 115426 |
rs760607957 | in-del | -/C | 0.000188164 | 0.00969777 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6492359 | ATACCGGGTGGAAGA[-/C]TGGTTTTGATCAGTT | 115426 |
rs760644823 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477396 | CCAGGCGTGGTGGCA[C/T]ATGCCTGTAATCCCA | 115426 |
rs760692234 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467463 | ACCTCTTTGGGGCCC[A/G]TTGTTCTGCCTGTCA | 115426 |
rs760700970 | snp | A/G | 1.65836e-05 | 0.0028795 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434151 | GCTGATGAAGACGTT[A/G]TTTACCATATCCAGT | 115426 |
rs760803463 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465210 | ATAGGAATTTTGTAG[A/G]TATGCTCTCCTAGAT | 115426 |
rs760821342 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456379 | CCCACTTTTTGATGG[C/G]GTGGTTTGTTTTTTT | 115426 |
rs760842671 | snp | A/G | 0.000281865 | 0.0118682 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498119 | TCCTTGGACCTCTGA[A/G]GGAATAGAACGGTCA | 115426 |
rs760857769 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435014 | GTTTTTTTTTTTTTT[A/G]ATTTTAGTTTTGAGA | 115426 |
rs760872284 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505891 | GTAGTCTTTTCCATA[A/G]TGCAGATTCAAGCCT | 115426 |
rs760883822 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434543 | TCCTGGGTTTAAGTG[A/G]TTCTCCTGCCTCAGC | 115426 |
rs760928029 | snp | C/G/T | 6.7861e-05 | 0.00582459 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460561 | AAGCCATATGGTTTT[C/G/T]TCTCTCCTCAGATAC | 115426 |
rs760932648 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435287 | GCGTAAGCCACCACA[A/C]CTGGCCGGCTAATTT | 115426 |
rs760946866 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453644 | GACTTTAAATTTAGG[-/T]TTGACCATTAAAAAA | 115426 |
rs760957476 | snp | C/T | 1.72299e-05 | 0.00293508 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504628 | ACAATCTTTTATGTG[C/T]GTTTGCTGTCAGGAG | 115426 |
rs760991663 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415381 | AATAGACCTTTGGTG[C/T]CAGCCATTAACTTGG | 115426 |
rs760997421 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494733 | GGGTATTTTGTCGAT[A/T]GAGTAAAAGTGAGTG | 115426 |
rs761007274 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471575 | CCAGTTGCATGTGAT[A/G]AGGCTATCCAGGCAG | 115426 |
rs761049693 | snp | A/G | 4.10754e-05 | 0.00453167 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504728 | CTTTCCCTGTTAGGT[A/G]TGAAGGCACACTAAT | 115426 |
rs761054069 | snp | A/T | 1.78896e-05 | 0.00299073 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498172 | AGGTTAGATTACATT[A/T]GTCTAGGCTGCCTGT | 115426 |
rs761080211 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499229 | CATGACTGTTATTAC[A/G]AAGCATGCTTCTCCC | 115426 |
rs761127431 | snp | A/C | 1.72701e-05 | 0.0029385 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413683 | AGCGAGGCTGGGGGC[A/C]GGAACAGCTGGGCTC | 115426 |
rs761134058 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420024 | AAAATGTTGGGATTA[C/T]AGATGTGAGGCCCGG | 115426 |
rs761185805 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451709 | ATCTCCTGACCTCGT[A/G]ATCCGCCTTTCTCGG | 115426 |
rs761211953 | snp | G/T | 1.66813e-05 | 0.00288797 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481636 | CGTTCTTTTTTTTCT[G/T]TTAAAGGTATTGTCC | 115426 |
rs761220910 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439070 | ACAGATACAAACACT[A/G]AGTTTATGAAAAACA | 115426 |
rs761315040 | in-del | -/T | 1.69539e-05 | 0.00291147 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475378 | GTTAACCTTTCTTCC[-/T]TTTTTTAAACAGGGG | 115426 |
rs761353386 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472508 | CAAAACTGGGGGAAT[A/G]TTGTTCTCATGAACC | 115426 |
rs761385259 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452677 | GCAACATAAGATAAA[C/T]TGGAGATAACTCTTA | 115426 |
rs761412581 | snp | C/T | 4.9953e-05 | 0.0049974 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500568 | TGACTGTCCAAGTGC[C/T]TCCAAAGTGTACAAA | 115426 |
rs761419059 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490080 | TTTGAAGGCTTTATA[A/T]ATAAACCAACTAGAA | 115426 |
rs761431087 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439782 | GCACATACAACTTGG[C/T]TGTGAGAACTACCTC | 115426 |
rs761434516 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482015 | TTGTGTTGGTCGTAC[A/G]AGAGAATGTACTATT | 115426 |
rs761444341 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501661 | CTTTGGCAAAATGAA[C/G]CTTACATGTTTAGAG | 115426 |
rs761472752 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477609 | AGACTTGCTATAATT[G/T]TGTTCTTAATAGGGC | 115426 |
rs761568259 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435172 | CTAATTTTTGTATTT[C/T]TACTAGATATGGGGT | 115426 |
rs761569011 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422261 | TAATTTTTATATTTC[C/T]AGTAGAGACGGGATT | 115426 |
rs761577448 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467217 | TCAGACGCCTCCCAC[A/G]TGCCTTAGCTTGTTA | 115426 |
rs761591483 | in-del | -/ATATACACACATATATGTGCATATATACGTGTATATATATACACGTAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469706 | CACGTATATACATAC[lengthTooLong]ATATACACACGTATA | 115426 |
rs761599432 | snp | A/G/T | 5.61565e-05 | 0.00529864 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486781 | AAATGTATCTTAACT[A/G/T]TTCAGAGGTATTTTG | 115426 |
rs761599771 | snp | A/G | 0.000115598 | 0.0076017 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460604 | ACTCTAGAAATGAAT[A/G]TCAAGGATCTTAGAC | 115426 |
rs761612617 | snp | A/G | 2.04652e-05 | 0.00319878 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493950 | ACTACTATAGACACT[A/G]TTTAGAATTTGAACA | 115426 |
rs761629472 | in-del | -/CTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479158 | CTACCCCGTTCTCTG[-/CTT]CTTTCATGCAAAGAT | 115426 |
rs761700892 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475484 | TCCCCTTTCATTTGC[A/G]GATGGAAAGTTTTTA | 115426 |
rs761705538 | snp | A/C | 1.73757e-05 | 0.00294747 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477597 | TGTTTTAAGACTAGA[A/C]TTGCTATAATTTTGT | 115426 |
rs761714461 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496147 | GTTAGTCATTTTCTT[G/T]ACGTCTATTTTTTTT | 115426 |
rs761736529 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441876 | TACAGTCTTTACCCA[C/T]ATTAATTTTTCATAG | 115426 |
rs761739669 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424339 | TGGGAATAAGTTAAG[A/T]CTTATGTAAATTAAA | 115426 |
rs761773550 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445397 | GCCTCCTGAGTAACG[C/G]ATTACAGGGGCATTC | 115426 |
rs761786211 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421057 | GTCCACCTAAAGTAA[A/G]GAAAGCTCCGAGGGT | 115426 |
rs761787084 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461513 | AAGTAGCTGGGACTA[C/T]AGGCGTATGACACCA | 115426 |
rs761809831 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476243 | AGAATAATATTTTAT[C/T]GTATATGTATATACC | 115426 |
rs761823113 | snp | A/G | 3.42977e-05 | 0.00414097 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498151 | GGAGATTATGTCTAC[A/G]TTTACAGGTTAGATT | 115426 |
rs761834007 | snp | C/T | 1.67267e-05 | 0.0028919 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481628 | AATGCCTTCGTTCTT[C/T]TTTTTCTTTTAAAGG | 115426 |
rs761896941 | snp | A/G | 1.71516e-05 | 0.0029284 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477821 | CTGGTATGATTATCA[A/G]GTTTTTGTTGTTGTT | 115426 |
rs761899928 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482182 | TGTTGATTGTAAGTG[A/G]ACCTAACACATGACA | 115426 |
rs761932195 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485169 | CTTTGCAATAGTTGT[A/G]TTATAATTTTGGTTG | 115426 |
rs761946534 | snp | C/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507497 | CGCCTGCCTCGGCCT[C/T]CCAAGGTGCTGGGAT | 115426 |
rs761967646 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450882 | AATTGGAAATGGTAT[G/T]TAGAGCACATAGTCT | 115426 |
rs762012359 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433947 | GCCAGAGATGTCGGC[C/T]TTGGTGCTTGGTTTG | 115426 |
rs762020507 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442625 | CTGGGACCACAGGTG[C/T]ACACCACTGTGACCA | 115426 |
rs762022570 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451673 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGCATGG | 115426 |
rs762049809 | in-del | -/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412265 | TTAAGAAGGCGGGGT[-/G]GGGGGGTGGGGGAAG | 115426 |
rs762087051 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466383 | TCTCTACTAAAAATA[C/T]AAAAATGTTAGCTGG | 115426 |
rs762087555 | snp | C/T | 5.0497e-05 | 0.00502453 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413520 | TCGCACCATTGATGG[C/T]TCCAAGACGTGCACC | 115426 |
rs762094857 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434460 | TGGGCTTTTTTTGAG[A/G]TGGTCTCTCTCTGTC | 115426 |
rs762102806 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483276 | GTTGCAGTGAGCCGA[A/G]ATTGTGCCACTGCAC | 115426 |
rs762106257 | in-del | -/TG | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506322 | ACATAGCCATCATCT[-/TG]TGTGTGTAGTAAGAG | 115426 |
rs762116865 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459697 | AAAAACTTGAGGCCT[A/G]ACATGGTGGCTCATG | 115426 |
rs762126086 | snp | C/T | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506129 | ATTCCCAATGAGATT[C/T]TGCAGACTCTACTTG | 115426 |
rs762134134 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480130 | CTAACCTTGGTCTCT[A/G]CCCACCTTTGTCTTC | 115426 |
rs762145614 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504456 | GTAATTGGAATGTTC[A/T]TCACTATAAACATCT | 115426 |
rs762164161 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477276 | ACATCTGTAATCCCA[G/T]CACTTTGGGAGGTTG | 115426 |
rs762201194 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468584 | GAGCAGCTAGGAGTA[-/G]GATGGAAAAAGTCAG | 115426 |
rs762257596 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460702 | TGTAGAAAGTCCTGG[A/G]CAAAGAGGATTCTGG | 115426 |
rs762261094 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421692 | AAAGTGCTGGAATTA[C/G]CGGGGTGAGCCACCT | 115426 |
rs762263064 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428303 | GTTATGAAATAGAAT[A/C]ACAATACTCCCAGGA | 115426 |
rs762264286 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470602 | TGAGTAAGTATAAAT[A/G]ATTTTTTTTAAATAG | 115426 |
rs762266674 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437881 | GCCTCCCAGAGTGCG[A/G]GATTACAGGTGTGAG | 115426 |
rs762274036 | snp | A/G | 9.16431e-05 | 0.00676854 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460815 | GTCTTCACTGGTGCC[A/G]TTTAATTAACTGAAT | 115426 |
rs762293034 | snp | A/C | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419666 | AACATAAAACTTGAG[A/C]AATTAAATCTAGTTT | 115426 |
rs762317410 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460282 | GTGGTTCTTGAATGC[A/G]GGCTGAACACTTACT | 115426 |
rs762318050 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429396 | GGTAATAAGACTGTA[C/G]TCTGAGGTTTTGTGG | 115426 |
rs762320655 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493630 | ATAATTTAAAGTGAA[A/G]GTGTTAGGTCAAGTT | 115426 |
rs762331981 | snp | C/G | 1.9907e-05 | 0.00315486 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413610 | GTTCGACGTGCGGCC[C/G]GAATGCCAGCGCCTC | 115426 |
rs762353213 | snp | A/G | 1.69441e-05 | 0.00291063 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420864 | AACTAAAAATGTAGT[A/G]AGATACATTTTAGAG | 115426 |
rs762391320 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418376 | AGAGTAAGCATGGTA[A/T]CTTGTGAGGTAGTAC | 115426 |
rs762395435 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452540 | ATTGAAAGGTGTGAT[-/C]CTAAAGATGGGGAAG | 115426 |
rs762422752 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443639 | TTCTTTTTCTTGTCC[A/G]TAAACACCTGTATGT | 115426 |
rs762431844 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485552 | GCCAAAACCTTTCCA[A/G]GTTCTGTTGCTGTCA | 115426 |
rs762438786 | snp | A/C | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475465 | TTGAGAGACCTGGAG[A/C]CCATCCCCTTTCATT | 115426 |
rs762452527 | snp | A/C | 1.67399e-05 | 0.00289304 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497970 | ACTAATGTGATGAAT[A/C]AGTCTAAATTTTAAA | 115426 |
rs762480956 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480994 | TTTGTTAGAGTATTC[C/G]CAGAGTTTCCTTTGC | 115426 |
rs762506171 | in-del | -/TC | 1.69908e-05 | 0.00291463 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460560 | TAAGCCATATGGTTT[-/TC]TCTCTCCTCAGATAC | 115426 |
rs762516595 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473363 | TGCTAAGTCAGCATT[C/T]TATCTTTGTTATATG | 115426 |
rs762541770 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447765 | AAATTTTGGAAGGCA[C/G]AACACTAATTAACAT | 115426 |
rs762547344 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424039 | TACCGGTATTCCCTT[A/T]AAAGACGAGCTAGAC | 115426 |
rs762596530 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448522 | TAACTTCTATGCTTC[A/C]TCTGTAAAATGGGGA | 115426 |
rs762633113 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444844 | TGACCTTAGGTGATT[C/G]ACCTGCCCCGGCCTC | 115426 |
rs762649547 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438883 | GCAGAGTTAAAAACA[A/G]TCTTTAGTCTATGAG | 115426 |
rs762658431 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461903 | AACATCCTTGTATAT[A/G]CATTTTTGTGCATTT | 115426 |
rs762667881 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434682 | ACCTCAAGTGATCTG[-/C]CCCCCCTTGGCCTCC | 115426 |
rs762712484 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411860 | TCTTGTTTTGTTTAC[A/G]TTTATATCCTCTCTC | 115426 |
rs762732211 | snp | A/G | 1.67464e-05 | 0.0028936 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481811 | ATAGCAAGTTATAAT[A/G]TATAATGTTTTAATA | 115426 |
rs762762358 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493812 | TTCTTAATAAAGAAA[A/C]TCTTCTCTGACAGGA | 115426 |
rs762774113 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503478 | CAGGGTATCCATTTG[A/T]TCATGTTTACATTAG | 115426 |
rs762777340 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465456 | TGTGGGAAAGTTCTT[C/T]TATGGTCAGTTCGGT | 115426 |
rs762836146 | snp | A/T | 0.000102281 | 0.00715052 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434188 | AGTAAGTGCTCAAGC[A/T]ATTGAGGACTTTATT | 115426 |
rs762836219 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424445 | ACTCTGATTTCATCC[A/G]CCTTTTAAATACCAA | 115426 |
rs762872526 | snp | C/G | 1.65332e-05 | 0.00287512 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506194 | ATCTGCCTGCTTTCA[C/G]TGTGTTGTTCATGGT | 115426 |
rs762891706 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425376 | ACTTTCTGGCACTAC[A/G]ACATGCTTCAGGTAC | 115426 |
rs762905135 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497602 | TTAAAATGTAAGTGT[A/G]TGTTCTCTATAATAA | 115426 |
rs762922541 | snp | C/T | 1.7249e-05 | 0.0029367 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475344 | ATTATTTGTATATAC[C/T]TTAGATTTTGCTGGC | 115426 |
rs762962243 | snp | A/G | 1.68114e-05 | 0.00289921 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497403 | TGTCATTCTTCCTGG[A/G]CTTTCAAGGCAGGGT | 115426 |
rs762967437 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483589 | GGCAGATGTGGAACC[C/T]GTGGGCCAACTGTAA | 115426 |
rs762999909 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428193 | ACTTCTTATTTCTTT[C/T]GTCCACAGTACAGTT | 115426 |
rs763012426 | snp | A/G | 3.38507e-05 | 0.0041139 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413503 | AAGATGTGGATACAG[A/G]TTCGCACCATTGATG | 115426 |
rs763019153 | snp | A/G | 4.97756e-05 | 0.00498852 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497228 | CTGTGATGCTCCATT[A/G]GATGATAAAATTGGA | 115426 |
rs763022748 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485336 | TCTTTTTTCGTATAC[C/T]TGTCTGTCACGTATT | 115426 |
rs763062946 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504258 | GTCGATCTCCTGACC[-/A]TTGTGATCCGCCTGC | 115426 |
rs763081266 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460451 | TGCTATTTAAGGACA[C/T]TTCAACCTATTTTAC | 115426 |
rs763099591 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459133 | ATGACAGGTTGATGG[A/G]TGCAGCAAACCACCG | 115426 |
rs763144494 | snp | A/T | 1.6604e-05 | 0.00288127 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477639 | CGAAATGACCCTGAA[A/T]GTGACCTGTGTGGTG | 115426 |
rs763152624 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459905 | TTGAGCCCAGGAGTT[G/T]GAGGCTACAGTGAGC | 115426 |
rs763163312 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411457 | ATCTCAGCTCACTGC[A/G]GCCTCCGCCTCCCGG | 115426 |
rs763167150 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482010 | ATGGCTTGTGTTGGT[C/T]GTACGAGAGAATGTA | 115426 |
rs763180514 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449897 | GCCCTGTGTGACTCT[A/G]CTAGGAGATGACTCT | 115426 |
rs763182069 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450840 | CAGCCCTGGGTTCAG[C/T]CATGTCTAGGAATCC | 115426 |
rs763187499 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478821 | GGTGAGAGAAAGGGG[A/G]AAAGGATATATCTTC | 115426 |
rs763214940 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474871 | TTATTTTTGCCTAGA[A/G]ATTATATTTATTGGA | 115426 |
rs763235186 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418144 | GGTATTTTGTTTTGG[A/G/T]TTTTTTTGTGGGGGT | 115426 |
rs763262758 | snp | C/T | 0.000100822 | 0.00709934 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460570 | GGTTTTCTCTCTCCT[C/T]AGATACCCAGAAAGC | 115426 |
rs763294131 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444700 | TCCCCCTCCAGGGTT[C/G]AAGTGATGTCTCCTG | 115426 |
rs763294176 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453686 | AAGGCGGGCAGATCA[C/T]GGGGTCAGGAGATTG | 115426 |
rs763299008 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502588 | TCAGTTTGCTCTGTT[G/T]CATCAGTTATTACTA | 115426 |
rs763300611 | in-del | -/TA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505297 | GTGTGTGTGTGTGTA[-/TA]TATATATATATATTT | 115426 |
rs763303233 | snp | A/G | 1.69461e-05 | 0.0029108 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477803 | AGTCCCAGAAGAGGA[A/G]TACTGGTATGATTAT | 115426 |
rs763324465 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487454 | TTACTGCAATCTCCT[C/T]CTCCCAGATTCAAGC | 115426 |
rs763344603 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445480 | TGGCCAGGCTGGTCT[A/G]GAACTCCTGACCTCA | 115426 |
rs763372123 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488938 | CTGGTGCAGCTTTCC[A/G]AGTAGCTGGGACTAC | 115426 |
rs763420161 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468801 | GTAGGTCTTTTAGTT[A/T]GAAAAGTGGATGGCT | 115426 |
rs763445750 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471745 | TAAGTACAAGCAGTT[C/T]GCAGTAAGATCTGAA | 115426 |
rs763452215 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436859 | TGCCCTAAATAATTT[C/T]ACGTGATGGAATTAA | 115426 |
rs763475523 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423052 | GTTGCGATAAATGGG[C/T]ACCTATACTGTTTTT | 115426 |
rs763495883 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419286 | ACATTCTCAAGTACC[A/G]TGGATTAGGATTTCA | 115426 |
rs763518914 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427521 | GTGAAACTCCGTCTC[C/T]ACTGAAAATAAAAAA | 115426 |
rs763523599 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471719 | AGATTCCTGACCCAC[A/C]CCCATATGAGTAAGT | 115426 |
rs763527572 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429848 | TGAACCTAGGTTTAC[C/T]TGCAGAGCTGGAGTG | 115426 |
rs763529975 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431482 | GGTGGCATATACCTG[C/T]AGTCCTAGCTGCTCA | 115426 |
rs763541376 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412412 | ACCCGCAATCCCTTA[A/G]GCCAAAGGCACCCCT | 115426 |
rs763567919 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496038 | CTTCAACTCTTTGAC[C/G]ACAGCTATATAAGTT | 115426 |
rs763568027 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460694 | AATTATAATGTAGAA[A/G]GTCCTGGACAAAGAG | 115426 |
rs763572232 | snp | A/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506104 | TGATCTTGGCCAGAA[A/T]TACATCATGATTCCC | 115426 |
rs763603330 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493647 | TGTTAGGTCAAGTTA[C/T]ATGACTTGAAAGTAT | 115426 |
rs763609365 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414886 | AGCCAGTTTTGTACT[A/G]ACTTCTTAGTGTTTG | 115426 |
rs763626885 | snp | A/C/G | 1.79416e-05 | 0.00299507 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486950 | TATACAACCTTACTC[A/C/G]TTAGTACCTGCCTTG | 115426 |
rs763653523 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473380 | ATCTTTGTTATATGA[A/G]CTATACTACTGGGTC | 115426 |
rs763713912 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438892 | AAAACAATCTTTAGT[C/G]TATGAGGAATGATAG | 115426 |
rs763719017 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493051 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG | 115426 |
rs763722511 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420377 | TTTGTTTTAATGGCT[A/G]GCAGTGTTCTCTGTA | 115426 |
rs763736897 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454706 | TCTAACTTCAGGCCC[A/C]CTTTGGTTTTGAGCA | 115426 |
rs763772784 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463057 | GAGGCCAGGGTGGGT[A/G]GATCACCTGAGGTCA | 115426 |
rs763815582 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466308 | TTTGGGAGGCTGAGG[C/T]GGACGGATCACCTGA | 115426 |
rs763827093 | snp | C/T | 3.85966e-05 | 0.00439281 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499925 | ACAAAAAGGCCAATT[C/T]CAGATGGTAGGTAAT | 115426 |
rs763845489 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482011 | TGGCTTGTGTTGGTC[A/G]TACGAGAGAATGTAC | 115426 |
rs763847747 | snp | C/G | 1.71622e-05 | 0.0029293 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493814 | CTTAATAAAGAAAAT[C/G]TTCTCTGACAGGACC | 115426 |
rs763861093 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434690 | TGATCTGCCCCCCTT[-/G]GGCCTCCCAAAGTGC | 115426 |
rs763882994 | in-del | -/ACGT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469762 | CACGTATATATACAC[-/ACGT]ATATATGTGTGTATA | 115426 |
rs763885603 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439591 | ATAGATATTTATAAG[-/T]TTTTTTTTCTGGATT | 115426 |
rs763909335 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422655 | GGCTCTGTCACCCAG[C/G]CTGTAGTGCAGTGAC | 115426 |
rs763910879 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459396 | ACTTGGGGCCGGGTG[C/T]GGTGGCTCATGCCTG | 115426 |
rs763958199 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481034 | TAAGAATAGCCTCCT[A/C]TCATTCTGTAGACGT | 115426 |
rs763972945 | in-del | -/TACATG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464974 | TTACTAATTTTAATT[-/TACATG]TAGATTGTTTCAAAA | 115426 |
rs763979048 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491870 | TGCAACAAATTTAGG[C/G]TGATTATTTTTCCAT | 115426 |
rs763999353 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441734 | AGGTGGTTTGTGGCC[A/G]GTTTTTTTTTTCCAT | 115426 |
rs764000722 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483129 | CCAGGAATTCAAAAC[C/T]AGCCTCGCCAACATG | 115426 |
rs764017880 | snp | A/T | 1.72383e-05 | 0.00293578 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475345 | TTATTTGTATATACC[A/T]TAGATTTTGCTGGCA | 115426 |
rs764028557 | snp | A/G | 1.68618e-05 | 0.00290356 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420878 | TAAGATACATTTTAG[A/G]GAAGCATTTCACTAT | 115426 |
rs764056663 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417670 | AGCGAAGGAGTGGAT[A/T]ATCTGGGTTTAAAAA | 115426 |
rs764059337 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480459 | CAGAGATGACTTTAG[G/T]ATGGTATAATTAGAA | 115426 |
rs764078860 | in-del | -/AT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505568 | TCCCAGAGTACTGGG[-/AT]AACAGGCATGAGCCA | 115426 |
rs764104761 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493365 | ATTTATTGTCAATGC[C/T]AGAATTTGAAATTTG | 115426 |
rs764125623 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447023 | CCTCCCAAGTAGCTG[C/G]GACCACAGGTGCCTG | 115426 |
rs764180504 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447786 | TAATTAACATTGCCT[A/G]GTTTAGCAGGCCAGA | 115426 |
rs764211600 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428194 | CTTCTTATTTCTTTT[C/G]TCCACAGTACAGTTC | 115426 |
rs764221151 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474092 | ATATAACTTCGGAGG[A/T]CATGAAGTTGTCATT | 115426 |
rs764222913 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485350 | CCTGTCTGTCACGTA[C/T]TTATTTTCTAAACTC | 115426 |
rs764277775 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442276 | GTCAGTCCTTCTAAG[A/G]CAAGCTTCCTGAACG | 115426 |
rs764297328 | in-del | -/TG | 6.00667e-05 | 0.00547994 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493949 | TACTACTATAGACAC[-/TG]TTTAGAATTTGAACA | 115426 |
rs764315287 | snp | A/C | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477644 | TGACCCTGAATGTGA[A/C]CTGTGTGGTGGAGAC | 115426 |
rs764341390 | in-del | -/TAAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416914 | CTATAGAGGTGGTCT[-/TAAAA]TAGATAACAATGTGG | 115426 |
rs764353010 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411963 | CCAGCACTTTGGAAG[C/G]CCGAGGCGGGTGGAT | 115426 |
rs764357608 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465860 | TTGTGAGTACCAAAA[A/G]GTACATATGCTTGAA | 115426 |
rs764409787 | snp | C/T | 5.138e-05 | 0.00506827 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477819 | TACTGGTATGATTAT[C/T]AGGTTTTTGTTGTTG | 115426 |
rs764411429 | snp | G/T | 0.000215959 | 0.0103891 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422622 | ACTTAGATCTTTTCT[G/T]TTTTTGAGACAGGGT | 115426 |
rs764449034 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468922 | ATCTCTCCAGCAGTA[A/G]GAAGGTTGAACTTTC | 115426 |
rs764449260 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506121 | ACATCATGATTCCCA[A/G]TGAGATTCTGCAGAC | 115426 |
rs764473571 | snp | A/G | 0.000117209 | 0.00765445 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6460573 | TTTCTCTCTCCTCAG[A/G]TACCCAGAAAGCGGT | 115426 |
rs764536570 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411459 | CTCAGCTCACTGCAG[C/G]CTCCGCCTCCCGGGT | 115426 |
rs764537225 | snp | A/C | 1.65386e-05 | 0.00287559 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497253 | ATTGGAGCAGAGTCT[A/C]GGAATTGGAGAGCTG | 115426 |
rs764565657 | snp | C/T | 1.68752e-05 | 0.00290471 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413511 | GATACAGGTTCGCAC[C/T]ATTGATGGCTCCAAG | 115426 |
rs764595158 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483694 | ACTTTTATCTTTTTT[A/G]TTTGTTTGTTTGGAG | 115426 |
rs764600053 | snp | A/C | 3.34163e-05 | 0.00408742 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494002 | GGACTGTAAATTGTA[A/C]CTTACGTTGCAGAGG | 115426 |
rs764631239 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424318 | GCAATAACAAAAGGT[A/G]GAATCTGGGAATAAG | 115426 |
rs764668067 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489814 | TACAAAGATGAATCA[A/G]TATGAGTAGTTATGG | 115426 |
rs764672361 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420307 | TCATCTGCTCTTTTC[A/G]GCCTCCCAAAGTACT | 115426 |
rs764683203 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458247 | GGAGGGTGTATGTGT[C/G]CAGGAATTTATACAT | 115426 |
rs764734580 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459176 | ACCTAAGTAACAAAC[C/G]TGCACTTTCTGCACA | 115426 |
rs764735070 | snp | C/T | 1.94945e-05 | 0.003122 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498203 | GTGTTCATAAAAATA[C/T]ACACCTCTTCTATCT | 115426 |
rs764758420 | snp | C/T | 2.96925e-05 | 0.00385297 | stop-gained, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413641 | TTCTACCGGGGCAAG[C/T]AGGTGAGGCGCGCCC | 115426 |
rs764769860 | snp | C/G | 8.90115e-05 | 0.00667067 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413694 | GGGCCGGAACAGCTG[C/G]GCTCCTCTGGACGCA | 115426 |
rs764775665 | in-del | -/TAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482584 | CAGGATTCTGAATAT[-/TAAA]TAAGAGGGGCCTTTT | 115426 |
rs764828911 | snp | A/G | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481694 | TGTAAAGGCTGGTGA[A/G]AGACTCAAGATGAGT | 115426 |
rs764845119 | in-del | -/TACTACATATATAGCATGAGAC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493566 | TTCTGTTGATTATTT[-/TACTACATATATAGCATGAGAC]TAACCATATTTGGAG | 115426 |
rs764859498 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428442 | TATTAACCTTTAACA[A/G]CCTATTAATAATCTT | 115426 |
rs764899403 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471643 | CTGCACCCCTGACCA[A/G]TGGCTTAACTGCAAT | 115426 |
rs764909982 | snp | C/G/T | 1.64822e-05 | 0.00287068 | synonymous-codon, missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460637 | CGAGCTAGAACCATT[C/G/T]TGAAATGGAATGAAC | 115426 |
rs764932990 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498276 | GGACTATAAGGGGTG[A/G]GGAATAAGATCATGC | 115426 |
rs764980382 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431626 | ATCTAGGTTTACTAT[A/T]TTCAAAGAATGCCCT | 115426 |
rs764997859 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437944 | GATACCTAGTACAAA[C/G]CAGATGATGCTGCTG | 115426 |
rs765031180 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432056 | GACTAAATGTCTTTA[A/T]ATTTGTCAGTGATTA | 115426 |
rs765032760 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471261 | TTCAAGACCTGTGTA[C/G]TATCAGTGGCTGTGC | 115426 |
rs765113484 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492017 | GGATTACAGGCATGA[A/G]TCATTGCGCCTGGCC | 115426 |
rs765137140 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478915 | TATTTCCTCTGACGT[C/G]TCATATTTTCCTTCT | 115426 |
rs765142039 | snp | A/G | 1.74683e-05 | 0.00295531 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486936 | AAGTCGTAAGTCATT[A/G]TACAACCTTACTCAT | 115426 |
rs765193716 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491014 | CCAGTGATCTTTGTT[C/T]TGTCTGGGTGAATGG | 115426 |
rs765206052 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465273 | CATTTGTATTAATGC[A/G]TGAAATTTACATGTT | 115426 |
rs765209338 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437699 | CTCAGGTCACTGCAA[C/T]CTCCACTTCCTGGTT | 115426 |
rs765241585 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503278 | TGGGATTACATGTGT[C/G]AACCACCATGCTTGG | 115426 |
rs765261837 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453865 | AGCTGAGATCATGCC[A/G]TTGTACTCCAACCTG | 115426 |
rs765264671 | snp | C/T | 9.22654e-05 | 0.00679148 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413442 | GCGGGGCGCGGCGCC[C/T]AGAGCTCAGGGGGAG | 115426 |
rs765287713 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423290 | ATGTTACCTAAGTTG[A/T]CCTACAACATAAAGA | 115426 |
rs765302056 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458070 | TTGTTTGGAATAGTT[A/T]CAGAAGAAATGGTAC | 115426 |
rs765376544 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426543 | ACCTTAGTAATTGTC[A/G]TAGGTATTTGAAATT | 115426 |
rs765411015 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473911 | TTGGGAATGCAAATA[C/T]CAAAAATCAACACTG | 115426 |
rs765413150 | in-del | -/CTGGGGCCCCCAGAGGGCGGGGA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6413973 | CGCGCTCGGCGGGGC[-/CTGGGGCCCCCAGAGGGCGGGGA]GGGCAGAGGGCTCTG | 115426 |
rs765427765 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483493 | TGTTTGCAGAATCAT[A/G]ACAAGAAAAAGTCTG | 115426 |
rs765445564 | snp | A/T | 2.60379e-05 | 0.00360809 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493970 | GAATTTGAACATTGA[A/T]TAAAAGTTTCATTAT | 115426 |
rs765469930 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428128 | TTACATGTTTTCTTA[C/T]GCTCATTGTATAATA | 115426 |
rs765489257 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417587 | GTGGAATAAAGTTGT[G/T]TGGAACTTGTTATTG | 115426 |
rs765491979 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440117 | AACATCTAAATTCAC[A/G]AAACTGACAGCAGTC | 115426 |
rs765504236 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448142 | GATTGGAATTTGACA[A/G]AGGCTCTAGAAGAAA | 115426 |
rs765527513 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444682 | TCTCAGCTCACTGCA[A/T]CCTCCCCCTCCAGGG | 115426 |
rs765542496 | snp | A/G | 0.000100673 | 0.0070941 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497201 | GTTGTTTTTTAGGGC[A/G]TTGGCCCTAAACTGT | 115426 |
rs765542504 | snp | G/T | 3.33968e-05 | 0.00408623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475520 | GGATTTTTGTTTTTG[G/T]TCTTAGACTACATGT | 115426 |
rs765558961 | snp | C/T | 1.69137e-05 | 0.00290802 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477619 | TAATTTTGTTCTTAA[C/T]AGGGCGAAATGACCC | 115426 |
rs765568763 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502007 | GTCATATTATTGTGA[C/T]CTTGCTGCTAGTGAT | 115426 |
rs765587538 | in-del | -/GTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442472 | GTTTTGTTTTGTTTT[-/GTTT]TGTTTGTTTTGTTTT | 115426 |
rs765588624 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444078 | TTTCTAAGAGTTCCA[A/G]AAATGTTTTTAATAG | 115426 |
rs765609642 | snp | C/G/T | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506086 | CTGCCCTGCTTGCCG[C/G/T]CATGATCTTGGCCAG | 115426 |
rs765637065 | snp | A/G/T | 3.30263e-05 | 0.00406353 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434101 | CAAATAAATTGGACA[A/G/T]TGTACCCTCTACGTC | 115426 |
rs765639599 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414577 | ACCCATCGTATTTTT[C/G]TTTGTCTTCATGTTG | 115426 |
rs765693613 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456672 | TGGTTTTAGGTCTTA[C/T]GTTTAAGTCTTTAAT | 115426 |
rs765724206 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411439 | CTGTAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 115426 |
rs765726205 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435344 | TTGTCCAGGCTGGTG[C/T]TGAACTCCTGGGCTC | 115426 |
rs765726737 | snp | A/G | 3.40959e-05 | 0.00412878 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434189 | GTAAGTGCTCAAGCT[A/G]TTGAGGACTTTATTC | 115426 |
rs765731531 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432652 | TCTGGCATACTGATA[C/T]TTAACTTACTTCTCC | 115426 |
rs765734977 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494941 | AACCAGCAGAGGAGA[C/T]AGGTCAGATTTGCTG | 115426 |
rs765760297 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477472 | CAGAGGCTGCAGTGA[A/G]CCAAGATCACGCCAT | 115426 |
rs765776780 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507001 | TGATCCTAAATTTTA[C/T]ATTCACTATATTCCC | 115426 |
rs765855311 | snp | A/G | 0.00557127 | 0.0524842 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486910 | TGTACTGGCTGGTGG[A/G]TTTGCGGATGAAGTC | 115426 |
rs765860381 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471079 | GTTGGGATTGTAAGA[A/G]GATGACAACAGCAAA | 115426 |
rs765876000 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468781 | GTAATGGCTCCACAG[A/C]ATATGTAGGTCTTTT | 115426 |
rs765913005 | in-del | -/GATA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415858 | TAGAAAATGAATGTT[-/GATA]GATAGTCTCCCACTA | 115426 |
rs765942410 | snp | A/G | 0.00129408 | 0.025404 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468368 | AGGGTGGGACAGCTG[A/G]CAGTAGATTAGTGCT | 115426 |
rs765970137 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487860 | TTAAAAAATAAAAAC[-/T]GGTTCCAGTGTTAAA | 115426 |
rs765995364 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479416 | CTTTCCTTCTTAGTC[C/T]CTTGTTGGGTTCCCG | 115426 |
rs766041295 | snp | A/G | 0.000100817 | 0.00709917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421191 | AATACAAATAAATTT[A/G]TTTTCTGTTCAGGAT | 115426 |
rs766047161 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439260 | TGTGATCTTGACTCA[A/C]TGCAACTTCTGTCTC | 115426 |
rs766052402 | snp | A/G | 1.66807e-05 | 0.00288792 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497992 | AATTTTAAATCTCAA[A/G]CTGGCACTGAAATAT | 115426 |
rs766085261 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439067 | ATTACAGATACAAAC[A/G]CTAAGTTTATGAAAA | 115426 |
rs766106678 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415981 | TGACCTACTGAAGCA[C/G]AATCTGTATTTTAAC | 115426 |
rs766113300 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446857 | CTCAAAAAATAAATA[A/C]ACAAACAAATAATAC | 115426 |
rs766121974 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449347 | GAGCTTACCATTAGA[C/G]TGGCCAAGATGTTGT | 115426 |
rs766139341 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416895 | ATTCTTTCACTCCTT[A/T]CCACTATAGAGGTGG | 115426 |
rs766144950 | snp | G/T | 2.28266e-05 | 0.00337828 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413627 | AATGCCAGCGCCTCT[G/T]CTACCGGGGCAAGCA | 115426 |
rs766197235 | snp | C/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412577 | GGCCTGAGGATAGGC[C/T]TGGAGCTGCCGCCTC | 115426 |
rs766211219 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472597 | TTGAAATAAAGAGTT[A/G]CGCTAAACATTTAAA | 115426 |
rs766214012 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496458 | TGATTTACTACTATT[A/G]GGTGAATGCATATAC | 115426 |
rs766214915 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482057 | TCATTATGGACCCAT[C/T]CCTGGTATTCCTGTT | 115426 |
rs766221468 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426054 | TTTATGTATCTGCAC[A/G]TCTGAGATTAATCAA | 115426 |
rs766244855 | snp | A/G | 1.65721e-05 | 0.0028785 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500582 | CCTCCAAAGTGTACA[A/G]AGCATCAGATTCAGC | 115426 |
rs766276571 | in-del | -/T | 3.66146e-05 | 0.00427855 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493785 | TTGATGAAATTATAC[-/T]TGGGTTTAGCTTTCT | 115426 |
rs766291641 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501907 | AGAGAAGCAATTACA[A/G]ATGGAGGAAAAAGCC | 115426 |
rs766302991 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462714 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 115426 |
rs766318402 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490107 | AGAAATGTAGTCTCT[C/T]TAACATTTGTTTTTA | 115426 |
rs766351225 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454651 | GAGTCCTGAGCTTAC[A/G]TAGTCCTTGTTTGAT | 115426 |
rs766396361 | snp | C/T | 1.68986e-05 | 0.00290672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434181 | TATGATGAGTAAGTG[C/T]TCAAGCTATTGAGGA | 115426 |
rs766400095 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498277 | GACTATAAGGGGTGA[G/T]GAATAAGATCATGCA | 115426 |
rs766409683 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463174 | TAATCCCAGCTACTC[C/G]AAAGGCTGAGGCAGG | 115426 |
rs766444828 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444564 | CCCTCTCTCTCCCTG[C/T]TTCCTCATTGTGTGG | 115426 |
rs766460589 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464124 | TTCAGACTTCAGTTT[C/G]CACTAATCAGGTGGG | 115426 |
rs766471275 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485741 | GGCTGAGGCTGGAGG[A/G]TTGCTTGAGCCCAGG | 115426 |
rs766476251 | in-del | -/TTG | 1.72314e-05 | 0.0029352 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477826 | ATGATTATCAGGTTT[-/TTG]TTGTTGTTGTTCTTG | 115426 |
rs766487133 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494817 | TGATTACTGTGTGAT[A/G]TAAAGAATATACCAG | 115426 |
rs766513151 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505948 | TCTCATTACCAGTTT[A/C]TGGTTCCTATTTAAA | 115426 |
rs766515862 | snp | A/G | 2.42034e-05 | 0.00347867 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493963 | CTGTTTAGAATTTGA[A/G]CATTGAATAAAAGTT | 115426 |
rs766529289 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434600 | CATATCACCACGCCT[C/G]ATTAATTCTTGTATT | 115426 |
rs766534211 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482451 | TCGTGGAACTCTAAG[A/C]TTGTTTCAGGTGTTG | 115426 |
rs766584258 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425690 | ATCACTTGAACCCAG[G/T]AAGCAGAGGTTACGG | 115426 |
rs766610687 | snp | A/G | 3.43318e-05 | 0.00414303 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504629 | CAATCTTTTATGTGC[A/G]TTTGCTGTCAGGAGC | 115426 |
rs766612231 | snp | C/G | 1.7009e-05 | 0.0029162 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493817 | AATAAAGAAAATCTT[C/G]TCTGACAGGACCGAG | 115426 |
rs766620784 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456557 | TCCCATTTGTCAATT[A/T]TGGCTTCTGTTGCCG | 115426 |
rs766630767 | snp | C/T | 1.72074e-05 | 0.00293316 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475353 | ATATACCTTAGATTT[C/T]GCTGGCAGAAGTTAA | 115426 |
rs766635844 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448796 | GGCAGTAGACAGACT[A/G]CTTGTCTTCATTGTA | 115426 |
rs766673548 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465216 | ATTTTGTAGATATGC[G/T]CTCCTAGATTTGGTT | 115426 |
rs766676197 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424624 | TTCCCTCTTAAGATC[C/T]TAAGTTAGTGTGGTG | 115426 |
rs766698661 | snp | A/T | 2.17901e-05 | 0.00330069 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504738 | TAGGTATGAAGGCAC[A/T]CTAATTTCTATACCT | 115426 |
rs766719994 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505678 | CTAAGCAAGGGAATC[C/T]AGATTTTTTTTCCCC | 115426 |
rs766739090 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429706 | GTTTCATTTGTGTGT[A/T]CTATATGCTTGCTGG | 115426 |
rs766754684 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420037 | TACAGATGTGAGGCC[C/T]GGAGCCCAGCCTCCC | 115426 |
rs766776622 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426207 | AGGTCTTTGCTTTTT[A/G]TTTTCAGTGTTAGTG | 115426 |
rs766805784 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421328 | AAATGTACAAGATGT[A/T]TATGTACAGTTTAAA | 115426 |
rs766810095 | snp | A/T | 3.30218e-05 | 0.00406323 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434094 | GAGAACACAAATAAA[A/T]TGGACAGTGTACCCT | 115426 |
rs766818792 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498184 | ATTTGTCTAGGCTGC[C/T]TGTGTGTTCATAAAA | 115426 |
rs766827480 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466467 | ATCACTTTAACTCAG[G/T]AGGCTGAGGTTGTAG | 115426 |
rs766868804 | snp | A/T | 0.000283425 | 0.0119009 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481639 | TCTTTTTTTTCTTTT[A/T]AAGGTATTGTCCTTC | 115426 |
rs766880480 | in-del | -/CTTA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414383 | AGACTGTTTGCTTTT[-/CTTA]CTTCTCGCCTTCTAA | 115426 |
rs766912071 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483541 | CACAGCCGTCTGTTT[A/G]TTTTTCCCAAATATT | 115426 |
rs766944767 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484363 | TTATAGGCTTAGTGG[C/T]GGCGGTGGTGGCAGG | 115426 |
rs766973822 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487934 | TAGTTGTAGATTCAC[A/G]TGTAGCATTAGAAAC | 115426 |
rs767028849 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477416 | CTGTAATCCCAGCTA[C/G]TCGAGAAGCTGAGGC | 115426 |
rs767081781 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501720 | AGTGTTTACTTGTAT[G/T]TTAGCCAAGACACCC | 115426 |
rs767124254 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490086 | GGCTTTATAAATAAA[C/T]CAACTAGAAATGTAG | 115426 |
rs767164630 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447865 | TGGTGTTGGAGAACC[C/T]TGGGGAAGGCTCAGG | 115426 |
rs767168775 | snp | A/T | 1.65157e-05 | 0.0028736 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475486 | CCCTTTCATTTGCAG[A/T]TGGAAAGTTTTTAAG | 115426 |
rs767181530 | snp | A/G | 4.94262e-05 | 0.00497098 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506134 | CAATGAGATTCTGCA[A/G]ACTCTACTTGACCTT | 115426 |
rs767186246 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482019 | GTTGGTCGTACGAGA[A/G]AATGTACTATTGTCC | 115426 |
rs767191598 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425544 | TGGATCACTACAGGT[C/T]AGGAGTTTGAGATCA | 115426 |
rs767202356 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444783 | AATTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 115426 |
rs767208864 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422309 | CTGGTCTCGAACTCC[G/T]GACCTCCTCATCTGC | 115426 |
rs767221536 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478825 | AGAGAAAGGGGGAAA[C/G]GATATATCTTCTTCC | 115426 |
rs767245708 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416155 | TACAACCTCTGCCTC[C/T]CGGGTTCAAGCGATT | 115426 |
rs767253340 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456314 | TTTTTTCATATGTTT[G/T]TTGGCCGCATAAATG | 115426 |
rs767271899 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415082 | TGGGGACAAATAGTA[C/G]ATGAATTCCTAGGAC | 115426 |
rs767276224 | snp | C/G | 3.30229e-05 | 0.0040633 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460606 | TCTAGAAATGAATGT[C/G]AAGGATCTTAGACCA | 115426 |
rs767292666 | snp | A/C | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460736 | GATGCAGAAATTACC[A/C]CATTGAAGACAATCT | 115426 |
rs767332959 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419471 | TTCTTGTTTTTTTTT[-/C]TGCTTGACTTAAAAA | 115426 |
rs767346440 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448647 | GCAAGTGAACTGTAT[C/T]TGGTGGATGTTAAGA | 115426 |
rs767368562 | in-del | -/T | 1.77525e-05 | 0.00297925 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477575 | TGAGATTCATAGATA[-/T]AAAAAATGTTTTAAG | 115426 |
rs767390545 | in-del | -/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495491 | ATAGTATACTCTTTG[-/CC]CCCAGTAGTGTATGG | 115426 |
rs767397842 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496229 | TATCTGCTTTCACCA[A/G]ATTGGGTATAGTTCT | 115426 |
rs767410621 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421064 | TAAAGTAAAGAAAGC[C/T]CCGAGGGTAGGACCT | 115426 |
rs767415762 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505245 | TTGAGTTAACTGTAT[C/G]TTTAATGTATTTAGT | 115426 |
rs767444746 | snp | G/T | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433950 | AGAGATGTCGGCCTT[G/T]GTGCTTGGTTTGAAG | 115426 |
rs767449863 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441994 | AGATCTAAGGTTTTT[A/C]TTGCTCTGTTGCCCA | 115426 |
rs767455863 | snp | G/T | 3.17385e-05 | 0.00398349 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421172 | TCAGACTTACTGTTG[G/T]GAGAATACAAATAAA | 115426 |
rs767486790 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481216 | CTGTATACTTGTTAT[A/G]TAAACTACCATTTTT | 115426 |
rs767504852 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415910 | TATGGTCCCTGGATT[C/T]TCAGGACCAGCAGCA | 115426 |
rs767522047 | snp | A/G/T | 4.09889e-05 | 0.00452693 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499929 | AAAGGCCAATTTCAG[A/G/T]TGGTAGGTAATGATT | 115426 |
rs767538119 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471808 | GGTCGGTTAAAGCTC[C/T]ATTCCAGGACTAAAG | 115426 |
rs767539755 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482268 | TAACAAAGGAACATA[A/C]ATCACAGAATTGGGC | 115426 |
rs767586036 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504582 | TTCCTTATCCTTGGA[A/T]ACTGTTCTAGAATTT | 115426 |
rs767591245 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472519 | GAATATTGTTCTCAT[A/G]AACCCTTCCTAAGGA | 115426 |
rs767639100 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493592 | TAGCATGAGACTAAC[C/T]ATATTTGGAGATGTT | 115426 |
rs767644618 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433058 | GTTGGCCAGGCTGGT[C/T]TTGACCTCAAGTGAT | 115426 |
rs767665776 | snp | C/T | 1.84113e-05 | 0.00303402 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504608 | AATTTTCTGAAAAAA[C/T]TGGAACAATCTTTTA | 115426 |
rs767677341 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503565 | GTATGGGATTTTAGG[A/T]TTGAGGTAAAATATG | 115426 |
rs767684232 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459714 | CATGGTGGCTCATGC[C/T]GGTAGTCCCAGTACT | 115426 |
rs767689926 | in-del | -/C | 8.41007e-05 | 0.00648408 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499821 | TGTACTCTCCCTCCT[-/C]CCCCCCCCATCAGTA | 115426 |
rs767696105 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434507 | TGAATGGCACAATCT[C/T]GCCTCACTGCAACCT | 115426 |
rs767717058 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466395 | ATATAAAAATGTTAG[C/T]TGGGCATGCTGGTGC | 115426 |
rs767720747 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470633 | TGAACTTTAAAATAT[A/G]CATAGAAAAAAAATG | 115426 |
rs767722417 | snp | C/T | 1.815e-05 | 0.00301242 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500741 | TTAAATAATAACATT[C/T]TGATATTAACAAATG | 115426 |
rs767727582 | in-del | -/AG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414108 | CTTCGGCTCTCAAAC[-/AG]GGGAAACTCGGGCAT | 115426 |
rs767750776 | snp | A/G | 4.95266e-05 | 0.00497603 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434089 | CCAAAGAGAACACAA[A/G]TAAATTGGACAGTGT | 115426 |
rs767770437 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467350 | GTGATTATATTGGAT[A/C]TGCGTGGATAATCTT | 115426 |
rs767792616 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467595 | ATTCCGAGAGAATAG[-/TT]TTTTTTTTTTTTTTT | 115426 |
rs767841748 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418444 | TTGATCCCTTGTTCT[A/C]CTTGACAAATGTGAA | 115426 |
rs767889227 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428379 | TGTAACTGCTACCCA[A/G]ACTTCTATGGTAATC | 115426 |
rs767912028 | snp | C/T | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant, intron-variant | UHRF2 | GRCh38.p7 | 9:6497289 | CCAGTCAGAGTGATA[C/T]GCAGTTTTAAAGGGA | 115426 |
rs768002063 | snp | C/G | 3.34975e-05 | 0.00409238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497974 | ATGTGATGAATAAGT[C/G]TAAATTTTAAATCTC | 115426 |
rs768016664 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490906 | TGTAGGCAAGTATAT[C/T]TATAGGATTAGGAAA | 115426 |
rs768018943 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468587 | CAGCTAGGAGTAGGA[C/T]GGAAAAAGTCAGCAG | 115426 |
rs768035793 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430159 | GGGATTACAGGTGCA[C/T]GCCACCATGCCCGGC | 115426 |
rs768081770 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429590 | CCTGCCTCGGCCTCC[C/T]GAAGTGCTGGAATTA | 115426 |
rs768092757 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486461 | GAAATAAGAGAGAAA[C/G]GGTATAGACTGCTGG | 115426 |
rs768116391 | snp | C/G | 1.75016e-05 | 0.00295813 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477592 | AAAAATGTTTTAAGA[C/G]TAGACTTGCTATAAT | 115426 |
rs768116578 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415861 | AAAATGAATGTTGAT[A/G]GATAGTCTCCCACTA | 115426 |
rs768131128 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450448 | AAGCTAATAATTAAA[A/G]TTTAATTTGATTTAA | 115426 |
rs768138622 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425870 | AGCAAGGAAATAATA[C/T]ATATTTGTACTAACC | 115426 |
rs768147008 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495929 | TCTGTAAGACGTAAT[A/G]GTAGCCCTAGAGTTG | 115426 |
rs768148902 | in-del | -/GCG | 0.000185856 | 0.00963813 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468459 | CAAAGAGAACCAACT[-/GCG]GCGGGTATGTCTCTG | 115426 |
rs768169713 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486804 | TATTTTGAGACTCTC[-/T]TTTAATTGTTTTATA | 115426 |
rs768176692 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457051 | TCTGTGAAGAAAGTC[A/G]TTGTCAGTTTGATGG | 115426 |
rs768184507 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450884 | TTGGAAATGGTATTT[A/G]GAGCACATAGTCTGT | 115426 |
rs768201837 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501503 | TCTACAGAGTTTCCT[C/T]TGTGAGAAATAGTCA | 115426 |
rs768225068 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495489 | CCCATAGTATACTCT[C/T]TGCCCAGTAGTGTAT | 115426 |
rs768245178 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417144 | TAGTTGCTTGGGAAT[G/T]ACTTCCCACTGCCCT | 115426 |
rs768256928 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449718 | AAACTGTTTTTGCAA[A/G]CAGTATGGTTTATGC | 115426 |
rs768273757 | snp | C/G | 2.48574e-05 | 0.00352535 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421160 | ATGTTGTTTTCTTCA[C/G]ACTTACTGTTGTGAG | 115426 |
rs768337927 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427429 | CAGTGGCTCACACCT[G/T]TAATCCCAGCACTTT | 115426 |
rs768363626 | snp | A/T | 1.73549e-05 | 0.0029457 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433864 | ACATTAAGGTTTTTG[A/T]AGCAGTAGACAAAAT | 115426 |
rs768380264 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476829 | CGAACTCCTGAGCTC[A/G]TGATCCGCCCAACCC | 115426 |
rs768429329 | snp | A/T | 1.68596e-05 | 0.00290336 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500555 | AAATAAATCTAGATG[A/T]CTGTCCAAGTGCCTC | 115426 |
rs768431987 | snp | A/G | 6.90072e-05 | 0.00587357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460544 | TTGTCTTTGGTAATC[A/G]TAAGCCATATGGTTT | 115426 |
rs768462707 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443671 | CTTCTCTGTGGGGGA[G/T]AACACATACTTTTTA | 115426 |
rs768477571 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506070 | AGGCACAGGTTTTCT[C/G]CTGCCCTGCTTGCCG | 115426 |
rs768486977 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439607 | TTTTTTTTCTGGATT[A/G]CTGTTCTATGTCACT | 115426 |
rs768517949 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434236 | AAACCAAAGCCTTCT[A/G]TTTCAAGATTATTTT | 115426 |
rs768543317 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452335 | GGGTCAGAAAGCAAA[A/T]GTATAGACAGTGTTT | 115426 |
rs768546529 | snp | C/T | 1.97775e-05 | 0.00314458 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504719 | CCTTCCTCACTTTCC[C/T]TGTTAGGTATGAAGG | 115426 |
rs768573546 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471424 | ATGTGGTTTTCAGCC[A/G]TACTTCACTAGGGTG | 115426 |
rs768577002 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477923 | AAGTGCTTAAAATGT[C/T]ATGGCCAGTGGTTAC | 115426 |
rs768603762 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443652 | CCATAAACACCTGTA[C/T]GTACTTCTCTGTGGG | 115426 |
rs768620448 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414661 | CCAATCCTGTGGTTT[G/T]AAATAAGTGTAGCTC | 115426 |
rs768631930 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468420 | GCCCGATCAAATAGT[A/C]ATCTCTTTGAATGCA | 115426 |
rs768638529 | snp | C/T | 1.85606e-05 | 0.0030463 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493939 | CATGAACAGGTACTA[C/T]TATAGACACTGTTTA | 115426 |
rs768645217 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429294 | TATTTCATGTCTGGA[C/T]CTCATTAGAAAATGG | 115426 |
rs768686833 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463856 | TGAAAGAACAAATGC[A/T]TTCTGCTGTTGATAG | 115426 |
rs768699780 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486395 | CTAAAATAACTCCTG[C/G]ATTTTTGACTTCACA | 115426 |
rs768726301 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473063 | CCTAACTATGGTCTC[A/G]AAATACCTTTCCCAC | 115426 |
rs768747782 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494516 | GCTGATCTTTATTCT[A/T]TAGAAATACTAATGA | 115426 |
rs768760089 | snp | A/C | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411157 | TAATTGTGGTTTTTG[A/C]CACCGAAAGAAATGG | 115426 |
rs768811320 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459946 | TCACTGTACTGCAGC[C/T]TAGGTGGCAGAGTGA | 115426 |
rs768864158 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454405 | TAGGCTAAGTGTTAG[A/C]TCTGTTGTGGCAAGA | 115426 |
rs768892063 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500061 | CACTGTAGCCTTGAC[C/G]TCCTGGGCTCAAGCG | 115426 |
rs768897429 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476235 | TTTATGGCAGAATAA[C/T]ATTTTATTGTATATG | 115426 |
rs768909977 | in-del | -/CT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485792 | AACATGGTGAGACCC[-/CT]GTCTCTACCCAAAAA | 115426 |
rs768937052 | snp | C/T | 1.98553e-05 | 0.00315075 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499806 | AAGCTTAAATCTGCA[C/T]TGTACTCTCCCTCCT | 115426 |
rs768942560 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491696 | TAGCAGCTTGGGAGA[A/G]GAATAGAGGTTGGGA | 115426 |
rs768953428 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487624 | CTCCCGCCTTGGCCT[A/C]CCAAAGTGTTGGGAT | 115426 |
rs769014806 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438773 | ACCAGATTATCAGTC[-/TT]TGAAATGAAGCTTCA | 115426 |
rs769015407 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460696 | TTATAATGTAGAAAG[C/T]CCTGGACAAAGAGGA | 115426 |
rs769029432 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421481 | GCAGTGGCGCACGCA[A/G]TCTTGGCTCGCTATG | 115426 |
rs769054578 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451467 | CCTAGTTTTTTTTTG[G/T]TTTTTTTTTTTGTTT | 115426 |
rs769093434 | snp | A/G | 1.65067e-05 | 0.00287282 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500637 | AACTCCTCAACAGCA[A/G]CATCTCATCAGAGAA | 115426 |
rs769125862 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423055 | GCGATAAATGGGCAC[C/G]TATACTGTTTTTCAA | 115426 |
rs769181645 | snp | A/G | 1.65323e-05 | 0.00287505 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506196 | CTGCCTGCTTTCACT[A/G]TGTTGTTCATGGTGG | 115426 |
rs769194486 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480086 | TCTACTCTCTAACTT[C/T]GGTTGCTTATCACTA | 115426 |
rs769214346 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436913 | AGATACGATAGCTGA[A/C]CTTTCTTTGAAAAAT | 115426 |
rs769216626 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447336 | ACATGTTTCCAGACA[A/T]TTGTGGGCCTGGTCT | 115426 |
rs769247326 | snp | A/G | 3.40119e-05 | 0.00412368 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493912 | ACCTTCAGCTGATCA[A/G]ACATTAACAAACATG | 115426 |
rs769255051 | snp | C/T | 3.30764e-05 | 0.00406659 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486850 | TGTTCACAGACCCCA[C/T]GTTGGTGGAATTCAT | 115426 |
rs769294878 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467018 | CATTTGTATTTAGTT[G/T]CCTATTGCTGCTACA | 115426 |
rs769303518 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494454 | AGTTACAAAAGTGAT[C/G]TTTTCTAACTAAATC | 115426 |
rs769322958 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434804 | TTATAATATGTAGTG[A/T]AATAGCATTAGAGTG | 115426 |
rs769378507 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425303 | TTTATTTGATGGCTA[G/T]GTCCCTTTGACATAC | 115426 |
rs769417012 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424032 | CATTCTATACCGGTA[A/T]TCCCTTTAAAGACGA | 115426 |
rs769460270 | snp | A/G | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475425 | AATGACTGCAAGATA[A/G]TATCTGTAGATGAAA | 115426 |
rs769478447 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480885 | CTTGTGGGCATAGTC[G/T]TCTTTGCTCTAAAAG | 115426 |
rs769493591 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451307 | TTTCGTTCATTATGC[G/T]TTTGGTTTTTAGGGA | 115426 |
rs769496560 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477572 | TTATGAGATTCATAG[A/G]TATAAAAAATGTTTT | 115426 |
rs769508899 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486248 | GTAAAAAAAGGATCT[A/G]TTGTGAGCATTCATG | 115426 |
rs769525344 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451280 | GGTGGTGTTAGGCTA[C/T]CAGTTGTGTAGTTTC | 115426 |
rs769544048 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414834 | CCTTTCCTTCTCTCT[C/T]TAAAATAATGTTATA | 115426 |
rs769595252 | snp | A/G | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481750 | CTAGTACTGAAAGCC[A/G]AAGAGACTGGGGCAG | 115426 |
rs769602205 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476040 | TCCCCTGTCCCACTT[A/C]CCTTCCCAGACTCTG | 115426 |
rs769624793 | snp | C/T | 1.89006e-05 | 0.00307407 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504704 | AAAGTAAGTAGAATT[C/T]CTTCCTCACTTTCCC | 115426 |
rs769668243 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422523 | CTATGGAGATTGCAT[C/G]TATAGATCAGCTTGG | 115426 |
rs769668264 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461255 | TGAAGAGAATTCAGA[A/G]TGCAAAATGTCACCT | 115426 |
rs769703237 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504135 | GGTTCACTCCATTCT[C/T]CTGCCTCAGCCTCCC | 115426 |
rs769704070 | snp | C/G/T | 7.06728e-05 | 0.00594409 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504585 | CTTATCCTTGGATAC[C/G/T]GTTCTAGAATTTTCT | 115426 |
rs769715938 | snp | C/T | | | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413859 | TGGAGGTGCGCCGCG[C/T]GGGGTCAGAAGTGAG | 115426 |
rs769724023 | snp | A/C | 1.74989e-05 | 0.00295789 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493806 | TTAGCTTTCTTAATA[A/C]AGAAAATCTTCTCTG | 115426 |
rs769756013 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423838 | TAATCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 115426 |
rs769782681 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488701 | GAGATGGGGTTTCTC[C/G]ATATTGGCCAGGCTA | 115426 |
rs769793335 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443577 | AATTTCTGTTTATCT[C/G]TCTAGTCAGAATGCT | 115426 |
rs769808981 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476655 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 115426 |
rs769821842 | snp | C/T | 6.59098e-05 | 0.00574026 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460681 | TGTGGTAATGGTTAA[C/T]TATAATGTAGAAAGT | 115426 |
rs769834849 | snp | A/T | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434115 | AGTGTACCCTCTACG[A/T]CTAATTCAGACTGTG | 115426 |
rs769843328 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490482 | AAAGTACAAAAATTA[-/C]CCAGGCGTGGTGATG | 115426 |
rs769879997 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504313 | TACAGGCGTGAGCCA[A/C]CGCGCCCGGCCTCTA | 115426 |
rs769923396 | snp | C/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412300 | GTTAGGTAGTGCTGC[C/G]TTGGGCCCACTTCTG | 115426 |
rs769936929 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469597 | CCAGAAGATAAGTCA[A/G]TAAAAACTACCCATA | 115426 |
rs769953708 | snp | G/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506095 | TTGCCGGCATGATCT[G/T]GGCCAGAATTACATC | 115426 |
rs769985304 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497561 | TTCGAGTTCCTAGGG[A/G]CAGAGTTGGGTTAAG | 115426 |
rs769988587 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437650 | TGAGACAGAGTCTTG[C/T]ACTGTGGCCCAGGCT | 115426 |
rs769999814 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479243 | CAGCACTCCAGTCTA[C/G]CTTTCCTTCCACTGT | 115426 |
rs770002087 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463732 | TGCCTCAGTCTCCCA[A/T]AGTGGTAGGATTATA | 115426 |
rs770021941 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485196 | GTTGAACCAGTATTC[A/G]GAGTTTAGGTTATTA | 115426 |
rs770037983 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498605 | TTTCTCTCTTCCCCC[A/G]CAAAGCTGCTTCCCT | 115426 |
rs770054900 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462325 | TGACTCCTGAGATTT[-/A]AAAAAAAAAAAAAAA | 115426 |
rs770065064 | snp | A/G | 1.71555e-05 | 0.00292873 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413579 | TTGAGGAGCTGCGCG[A/G]GCGGGTGTGGGCGCT | 115426 |
rs770082449 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489915 | TGGCAGTGCATTTAC[A/C]TTAACATGGCAAAGT | 115426 |
rs770101116 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459804 | ATAGTAAGACCCTGC[A/T]TCTACAAAAGAAAAA | 115426 |
rs770104599 | snp | C/T | 1.81112e-05 | 0.0030092 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499909 | GCAGCCCAGTGGAAC[C/T]ACAAAAAGGCCAATT | 115426 |
rs770130505 | in-del | -/CT | 3.5412e-05 | 0.0042077 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486800 | AGAGGTATTTTGAGA[-/CT]CTCTTTAATTGTTTT | 115426 |
rs770132287 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470176 | TCAGGAATTCAAGAC[C/G]AGCCTGGCCAACATG | 115426 |
rs770223700 | in-del | -/AT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504426 | ATATGTTCATATAAC[-/AT]ATAATAAATCAGGGT | 115426 |
rs770233286 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491546 | TTGGAGAATGTTTGT[C/G]TTCATTGTGCTTTGG | 115426 |
rs770309675 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490524 | TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA | 115426 |
rs770325038 | in-del | -/T | 1.67998e-05 | 0.00289821 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433905 | TAACTGATTTTAAAC[-/T]TTTTTTAGGTAAATG | 115426 |
rs770327923 | snp | A/C/G | 3.55103e-05 | 0.00421356 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500532 | GTAAGTCTGCTGATA[A/C/G]ATTTTTAAAATAAAT | 115426 |
rs770344293 | snp | A/G | 0.000132433 | 0.00813627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482142 | AGGGGAGAATTGGCT[A/G]TCAGATTATAGCAAT | 115426 |
rs770347540 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454185 | GTATACACAGTGGCC[A/G]GAAGCTAAGTTGAGG | 115426 |
rs770399935 | in-del | -/TA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438334 | ACTGCAAAGAGAATC[-/TA]TGAAGTTAGTAATTG | 115426 |
rs770423536 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433732 | TTTTCATCTTAGTCA[A/G]TAGATTTAAGATAGC | 115426 |
rs770428190 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6475864 | CACCTCAAACATTCT[A/G]TCATTTTTTGTGTGT | 115426 |
rs770451310 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479226 | CTCTCCTATTCATAC[A/T]TCAGCACTCCAGTCT | 115426 |
rs770470964 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419150 | GAGGTACTGGGGGTT[A/G]GGACTTTAACAAAAA | 115426 |
rs770518551 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465130 | AGTAGTGATAACAGG[C/T]ATCTTTTTCCCCTGC | 115426 |
rs770530381 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503182 | TGTATTTTTTTCTAG[A/G]GACGGTTTTGGCCAT | 115426 |
rs770553014 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424222 | TTATGAGCAGTCACT[A/G]AAGTGGCTATCTTCA | 115426 |
rs770571572 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465902 | TAGTTATCAAATTCT[A/G]TTTTCATGTTGTCAT | 115426 |
rs770627482 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459179 | TAAGTAACAAACCTG[C/T]ACTTTCTGCACAGGT | 115426 |
rs770650329 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433425 | GGGTTCATTAGACTC[-/TT]TTTTTTATTGTGCAT | 115426 |
rs770652004 | snp | A/G | | | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497034 | TGATTTGTCTTCTCT[A/G]CTGGTGGGGGAAAGC | 115426 |
rs770653959 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469894 | CAAAACTGATTAAAG[A/G]TACAAGTTCAGGTCA | 115426 |
rs770662545 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467477 | CATTGTTCTGCCTGT[C/G]ATACCACTGGAATGT | 115426 |
rs770719133 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450031 | TTAACTCAGCCATGG[A/G]TATAGCTTCATGCTA | 115426 |
rs770798436 | snp | A/G | 1.6631e-05 | 0.00288362 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477776 | TTACTGTCTGAATCC[A/G]CCTTTGGATAAAGTC | 115426 |
rs770831281 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436712 | GGATAGGACCTACCC[C/T]TCAGTTTGGTGTATC | 115426 |
rs770858685 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469658 | AGGACTTGATGAAAG[-/GT]GTGTGTGTGTGTGTG | 115426 |
rs770869871 | in-del | -/CTTTT | 0.000224618 | 0.0105952 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504560 | ATTATGAACTGCTAA[-/CTTTT]CTTTCCTTATCCTTG | 115426 |
rs770873348 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453371 | TATTTAAAAACATAC[A/C]GAATGATGATAATGT | 115426 |
rs770915403 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450692 | GTGCCTTTTAACACC[C/T]ATTTTTAACCTATCC | 115426 |
rs770932132 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487049 | TTTGTTGAAGTAATC[A/C]GTTTTATACAAGTTA | 115426 |
rs770958099 | snp | A/C | 1.68744e-05 | 0.00290463 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481612 | AATATGGTATTGTGA[A/C]AATGCCTTCGTTCTT | 115426 |
rs770958469 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411262 | TTAATTAAAATAGGG[A/G]TAGACAAGTGAATTA | 115426 |
rs770985128 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422006 | TAATCCATAATTCAT[A/G]GATATCTGGGCTGTT | 115426 |
rs771064060 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490425 | TTGAGGTCAGGACTT[C/T]GAAACCAGCCTGGCC | 115426 |
rs771119811 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506727 | TTTGTGAACTCCATT[G/T]TGCTTTTTTCTGGTG | 115426 |
rs771157384 | snp | A/G | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475419 | ACATTAAATGACTGC[A/G]AGATAATATCTGTAG | 115426 |
rs771171154 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495830 | TGAAGGTATCTGTGA[A/G]CATTAAAGCATTCCA | 115426 |
rs771173598 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438846 | CTATTCTCTTGCATT[C/T]TCAACTTCTACTCCA | 115426 |
rs771189609 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488436 | CATTTATATTACCAC[A/T]GTTTCCATTATTGTG | 115426 |
rs771206114 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415532 | GCCTGTAGCAGGTAA[C/G]TACTGGAATGGCATC | 115426 |
rs771248536 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425353 | TTGTTTTTCTTAAGC[A/T]TTATCTTACTTTCTG | 115426 |
rs771253964 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446099 | CCTGGCTCAGGTGAT[C/T]CTCCTGCCTTAGCCT | 115426 |
rs771262502 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479084 | TTAGCATTCTAGAAT[A/C]TCTTGAATTTTCAAA | 115426 |
rs771286854 | snp | A/C | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506084 | TCCTGCCCTGCTTGC[A/C]GGCATGATCTTGGCC | 115426 |
rs771326770 | snp | C/T | 1.75007e-05 | 0.00295805 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499825 | ACTCTCCCTCCTCCC[C/T]CCCCATCAGTATCCA | 115426 |
rs771337779 | in-del | -/CCA | 2.20136e-05 | 0.00331758 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421148 | ATATATAAGGTATGT[-/CCA]TGTTTTCTTCAGACT | 115426 |
rs771351938 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439433 | TTTGGGATTACAGGC[A/G]TGAGCCTTCTTGAAT | 115426 |
rs771396475 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476884 | AGGCATGAGCCACCA[C/T]GCCCGGCCTCAGGCA | 115426 |
rs771403310 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430962 | CCACATAGGCAAATT[C/T]TGTTTTCCTCTTTTG | 115426 |
rs771416958 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501637 | TATAAATGTGATACA[C/T]TGAGTTATCTTTGGC | 115426 |
rs771422272 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462904 | CCTGGGCTACAGAGC[A/G]AGACTCTGTCTAAAA | 115426 |
rs771430754 | snp | C/T | 1.65858e-05 | 0.00287969 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481784 | AAAGAAGAAATTCCC[C/T]TTTTCTTCCTAATAG | 115426 |
rs771470484 | snp | A/C | 1.76468e-05 | 0.00297037 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499896 | GACAGTCAAAGAAGC[A/C]GCCCAGTGGAACCAC | 115426 |
rs771475813 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463585 | AAGCAGTTCTCCTGC[C/T]GCAGCCACCGGAGTA | 115426 |
rs771544815 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420984 | CTGCTAGTTCGCCCA[C/G]ACCCTGATCATCTTC | 115426 |
rs771556073 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442046 | TCTTGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 115426 |
rs771561424 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417231 | GTTCCTCTTGTTACC[C/T]GGAGTTTCTTCTTTC | 115426 |
rs771601389 | in-del | -/T | 1.72815e-05 | 0.00293946 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500720 | ACCAGTATGTGAAGA[-/T]TTTTTTTAAATAATA | 115426 |
rs771632174 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440724 | GCTTTTGTATATAAA[A/G]AGCATCTGCTTTCAG | 115426 |
rs771638109 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499168 | GTGAGCCCATCTGCT[A/G]TGATGAGTAATAGTC | 115426 |
rs771674521 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464921 | GTATATAGGAATACA[A/G]GTATCCTTTGATCTT | 115426 |
rs771679932 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457283 | AATTGTGAATGGGAG[G/T]TCACTCATGATTTGG | 115426 |
rs771690390 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502583 | ATGAGTCAGTTTGCT[C/G]TGTTTCATCAGTTAT | 115426 |
rs771707266 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464443 | AATGCAGTTGAGGTT[A/G]TCAAAGTTCAAGAAA | 115426 |
rs771736124 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434011 | ATGGACAGTCACGTG[A/G]CAAAACTCCACTGAA | 115426 |
rs771743649 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503088 | CAACCTCCACCTCCT[A/G]GGTTCAAGTGATTCT | 115426 |
rs771749326 | in-del | -/CTCA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502363 | TCTCTTTTCATGTGT[-/CTCA]CTCTTTCATATCCTT | 115426 |
rs771754443 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463932 | CCTATACCTGTATCC[C/T]GGCACTTGTGTGCAT | 115426 |
rs771754691 | snp | A/T | 4.94996e-05 | 0.00497467 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500656 | CTCATCAGAGAAGAT[A/T]GTCAAAACCAGAAGC | 115426 |
rs771781627 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431877 | TGCTGTTACCATTTT[A/G]GTATCAACTATATGC | 115426 |
rs771792787 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486766 | ATGAAAGCATTTTGT[-/A]AATGTATCTTAACTG | 115426 |
rs771806586 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468551 | GCTAATTCTGGATGC[A/G]GTGTAAAATCTAGTT | 115426 |
rs771819442 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506637 | AGCTTCTAAAGTGTG[C/T]ATATACTTTTTTAAC | 115426 |
rs771836526 | snp | C/T | 1.73942e-05 | 0.00294903 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413479 | GGGACCGGTTCCTCT[C/T]TAGGCGCCAAGATGT | 115426 |
rs771840252 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427165 | TAAAAATTGGGCGTT[A/G]TATTGCTTTTGTCTT | 115426 |
rs771857375 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429130 | ACATCGCACCACTGC[A/T]CTCCAGCCTGGGCAA | 115426 |
rs771860117 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457181 | GTCCTCTTTTTTTTC[A/G]TTGAGCAGTGGTTTG | 115426 |
rs771865613 | snp | C/T | 1.6531e-05 | 0.00287493 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486889 | TAATGATGGGGCTTA[C/T]TCTCTTGTACTGGCT | 115426 |
rs771875396 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435202 | TTTCACCATGTTGGC[C/T]AGGCTGGTCGCAAAC | 115426 |
rs771884569 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492832 | TGGAGAGCTTTTGGC[-/T]TTTTTTTTTTTTTTT | 115426 |
rs771917492 | snp | C/G | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477731 | CAACATGCAGCTTCT[C/G]TGTGATGAATGTAAT | 115426 |
rs771958797 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449263 | CTTTCTTGGCCTCCC[G/T]CAGCCAGTGACCAAG | 115426 |
rs771961865 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445211 | TTGTTTTCTCTTAAA[A/T]TTTTCAGCTTTTAAT | 115426 |
rs771980910 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487789 | TTATAGGCGTGAGCC[A/G]CGGTGCCCATCCTCT | 115426 |
rs772016752 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435901 | GGCCTGAGCCACCAC[A/G]ACCGGCCCAAAATAG | 115426 |
rs772039263 | snp | C/T | 1.65072e-05 | 0.00287286 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506180 | AGCAAAGGACGATGA[C/T]CTGCCTGCTTTCACT | 115426 |
rs772039436 | snp | C/T | 1.72961e-05 | 0.00294071 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497173 | AAAAATTACATGGTA[C/T]AAAGACTTCTTTGTT | 115426 |
rs772040923 | snp | A/G | 3.45997e-05 | 0.00415916 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477600 | TTTAAGACTAGACTT[A/G]CTATAATTTTGTTCT | 115426 |
rs772056381 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458965 | AGCAAACTAACACAG[A/G]AACAGAAAACCAAAC | 115426 |
rs772058717 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452404 | CCACTTTGTATTTGT[C/G]AGCAATATATGAGAG | 115426 |
rs772093190 | snp | A/C/G | 8.75218e-05 | 0.00661472 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499822 | TGTACTCTCCCTCCT[A/C/G]CCCCCCCATCAGTAT | 115426 |
rs772112948 | in-del | -/CAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447356 | GGGCCTGGTCTCTCC[-/CAAA]CACTCTATATTTTGA | 115426 |
rs772129340 | snp | A/C | 1.66441e-05 | 0.00288474 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497375 | GGTGCTCTATCTGGC[A/C]TGACATCTTGTTTGT | 115426 |
rs772164748 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436390 | ACTGAGGCTGGGGTA[C/G]AAAGGGGTTGAAGTT | 115426 |
rs772172853 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421278 | TCATAACTTTTAAAA[C/G]TAGTCTTTTAAAAAT | 115426 |
rs772174735 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430789 | CTGGGCCCTAATTTT[C/G]CCCTGTTCCCTCTGC | 115426 |
rs772184475 | in-del | -/TTTTTTTTC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445998 | TTTTTTTTTTTTTTT[-/TTTTTTTTC]TTCCTGTTTTTGAGA | 115426 |
rs772200757 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445509 | CAAGTGATCCACCTG[C/T]CTCGGCCTCCCAAAG | 115426 |
rs772226057 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421846 | CTTACGTATATTTCT[C/G]TAGGCAGTATGTTTT | 115426 |
rs772237467 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451692 | TAGCCAGCATGGTCT[C/T]GATCTCCTGACCTCG | 115426 |
rs772273519 | snp | C/T | 0.000188519 | 0.00970691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492253 | TCTTATTATGCTCTC[C/T]TACTTTCCATTACTT | 115426 |
rs772326930 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489403 | TTTTGTAAACGTAAG[C/T]CTTTATTTCTTTGGA | 115426 |
rs772345258 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505856 | CAATATCTGCCAGAG[A/T]TGAAACTAAAGCCAT | 115426 |
rs772346590 | in-del | -/TG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432356 | TACCCTCTGTCATTT[-/TG]TGGTTTGAAACCTTT | 115426 |
rs772368825 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480854 | TGCTCAACAAAGTAT[C/G]TCATAATTGGATTGA | 115426 |
rs772378693 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478212 | ATTAAATATCTTTCA[A/T]CTCCTTAAGTAAGCC | 115426 |
rs772396676 | snp | C/T | 1.65386e-05 | 0.00287559 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481971 | TAACTGATTTCTCAA[C/T]GTTTGTTTTGCGTCT | 115426 |
rs772426197 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451510 | TTGAGACGGAGTCTC[A/G]CTGTCGCCCAGGTTG | 115426 |
rs772435208 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421732 | TTAAATACCTGTTTA[A/C]AGCCTCGTGTGTGTC | 115426 |
rs772436084 | snp | C/T | 2.04255e-05 | 0.00319567 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413616 | CGTGCGGCCCGAATG[C/T]CAGCGCCTCTTCTAC | 115426 |
rs772462794 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423934 | TGGGCGACACAGTGA[C/G]ACTCAGTATCAAAAA | 115426 |
rs772489330 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444480 | TTTACATTTATGCTT[C/G]TCAAAGATGGTCAGA | 115426 |
rs772499598 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493037 | GCGCAGTGGGTCATG[C/T]CTGTAATCCCAGCAC | 115426 |
rs772500094 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448304 | CACAGTTGTGGAAGG[A/G]AGGAAATGTAATTAA | 115426 |
rs772524008 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414708 | TAGCCTACAGTTGCA[A/G]ACTACTTAAAAGGAA | 115426 |
rs772526068 | snp | A/T | 1.84371e-05 | 0.00303615 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460818 | TTCACTGGTGCCATT[A/T]AATTAACTGAATTGA | 115426 |
rs772537973 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440934 | TAATGATTCTAATCA[A/T]TCCCTGTGATTCTAT | 115426 |
rs772575549 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414096 | GCTCTTCCGCGTCTT[C/T]GGCTCTCAAACAGGG | 115426 |
rs772576492 | snp | A/G | 1.72397e-05 | 0.00293591 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498155 | ATTATGTCTACGTTT[A/G]CAGGTTAGATTACAT | 115426 |
rs772607705 | snp | A/G | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500661 | CAGAGAAGATTGTCA[A/G]AACCAGAAGCTGTGG | 115426 |
rs772660459 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464075 | AACAGTATGAGAGTT[C/T]CTGTTGTTAGTTTTC | 115426 |
rs772684718 | snp | A/C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455932 | AAGGCTGCAGCGGGC[A/C/G]TGATCACACCACTGC | 115426 |
rs772686187 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461530 | GGCGTATGACACCAC[A/G]CCCACCTAACTTTTA | 115426 |
rs772711746 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453756 | AAAAATACAAAAAAA[A/C]CAACCAGGAGTGGTG | 115426 |
rs772734010 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431880 | TGTTACCATTTTAGT[A/G]TCAACTATATGCTGC | 115426 |
rs772736860 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500157 | ATCTTTTGTAAAGAT[G/T]GGGTTTCTCCATGTT | 115426 |
rs772751373 | snp | G/T | 1.66026e-05 | 0.00288115 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500575 | CCAAGTGCCTCCAAA[G/T]TGTACAAAGCATCAG | 115426 |
rs772763589 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473155 | GCAAATAAGGAGTCC[A/C]ACAAAGTCTGCTAAG | 115426 |
rs772784717 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503143 | GGGATTGCAGGCACC[C/T]GCCACCACGCCCGGC | 115426 |
rs772793113 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490774 | AGTTAAGTCTGTTAC[A/G]TAATGTGAAGAAAAA | 115426 |
rs772809922 | in-del | -/TTTTTTAA | 1.72894e-05 | 0.00294013 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500722 | CCAGTATGTGAAGAT[-/TTTTTTAA]ATAATAACATTCTGA | 115426 |
rs772879120 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494626 | AATAAGTAACCCAGA[C/G]CACCAGATAGCAAAA | 115426 |
rs772902477 | in-del | -/T | 1.90134e-05 | 0.00308323 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486970 | TACCTGCCTTGACCA[-/T]TTGTAAAATAGAATA | 115426 |
rs772934073 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492557 | TTTAAGACCATGAGA[-/T]TGTTTATTTGTGGCT | 115426 |
rs772938052 | snp | A/G | 1.7232e-05 | 0.00293525 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477603 | AAGACTAGACTTGCT[A/G]TAATTTTGTTCTTAA | 115426 |
rs772942505 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454437 | TGTGTCGATTTCTTC[A/G]TGGACTTAAGGCATA | 115426 |
rs772960937 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432693 | GCCATCTATTAGACA[C/T]CTTAAGAGTGGTGTC | 115426 |
rs773023964 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415950 | CCTGAAATCCTCACG[C/T]CAGACCTACTGAAGC | 115426 |
rs773065319 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464892 | GAATTTTGCAGTCAT[C/T]TTTTCTCTTTCTGGT | 115426 |
rs773084881 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435904 | CTGAGCCACCACGAC[C/T]GGCCCAAAATAGGTT | 115426 |
rs773085782 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416776 | TCGTGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT | 115426 |
rs773108095 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495811 | TGGTGGCAGTAATTA[C/T]GACTGAAGGTATCTG | 115426 |
rs773109285 | snp | A/G | 1.72788e-05 | 0.00293923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497174 | AAAATTACATGGTAT[A/G]AAGACTTCTTTGTTG | 115426 |
rs773110725 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449304 | CTTCTGGATTTGGCA[A/G]TTTCTGCCCAATGTT | 115426 |
rs773132991 | snp | A/T | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477754 | AATGTAATGTGGCTT[A/T]TCATATTTACTGTCT | 115426 |
rs773182731 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482405 | ATTTGAAATATTAAA[C/T]TTGAATCATGTGGCA | 115426 |
rs773199052 | snp | G/T | 1.6651e-05 | 0.00288535 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497376 | GTGCTCTATCTGGCA[G/T]GACATCTTGTTTGTC | 115426 |
rs773200532 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427167 | AAAATTGGGCGTTGT[A/G]TTGCTTTTGTCTTGA | 115426 |
rs773224990 | snp | G/T | 1.7333e-05 | 0.00294384 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433869 | AAGGTTTTTGAAGCA[G/T]TAGACAAAATTAAGC | 115426 |
rs773232775 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439857 | GAAAACTCTTGTTTC[C/T]AGTGGTATTTTGAAC | 115426 |
rs773248858 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505884 | CATGACTGTAGTCTT[C/T]TCCATAGTGCAGATT | 115426 |
rs773260498 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462524 | ATAAACTGGCTATGT[C/T]AGGAGCCTTTTAACC | 115426 |
rs773269837 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478535 | TTTTTCTCCTATGGC[A/G]TGGTGATAACTACAA | 115426 |
rs773320888 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468552 | CTAATTCTGGATGCA[A/G]TGTAAAATCTAGTTC | 115426 |
rs773349517 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415348 | CTTCAGCCCAGTGAT[A/C]AACCAGTAGGGTAGA | 115426 |
rs773357224 | snp | C/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443862 | GTCTTAAAATATGTT[C/G/T]TCTTTGCTCCCAGCA | 115426 |
rs773391015 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477363 | AACCCCATCTCTACT[A/G]AAAAATAAAAAAATT | 115426 |
rs773422800 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487808 | TGCCCATCCTCTATA[G/T]AGCTTTTTTTGGTCA | 115426 |
rs773430619 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452751 | ACCAGCAGATTATGG[G/T]GTAGGGGGATTCCAT | 115426 |
rs773435699 | snp | C/T | 1.76129e-05 | 0.00296752 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504618 | AAAAATTGGAACAAT[C/T]TTTTATGTGCGTTTG | 115426 |
rs773435738 | in-del | -/TT | 0.000121727 | 0.00780057 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486805 | TATTTTGAGACTCTC[-/TT]TAATTGTTTTATAGG | 115426 |
rs773448058 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467353 | ATTATATTGGATCTG[C/T]GTGGATAATCTTCCC | 115426 |
rs773477622 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489480 | ATGTTTAGTTGTTTA[A/G]AGAAACTGCCAAACT | 115426 |
rs773494150 | in-del | -/TTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452982 | TATGTTCCTTTTCTG[-/TTTT]TTTGTTTTTTCTTCC | 115426 |
rs773547201 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444545 | AAACAGATTCCTGAG[C/G]GGACCCTCTCTCTCC | 115426 |
rs773550017 | in-del | -/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412908 | CCTGAGGAGGCACCC[-/G]CCCCCTCAGCTCTGA | 115426 |
rs773560511 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437902 | CAGGTGTGAGCCACC[A/G]CACCCGGCTAGTTTC | 115426 |
rs773561935 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461547 | CCACCTAACTTTTAT[A/G]TTTTTAGTAGAGATG | 115426 |
rs773581376 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421791 | CCTAAGAGGTAAACT[A/G]CTTATTCTTTTATAC | 115426 |
rs773602317 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435245 | GTGATCTGCCCGCCT[C/T]AGCCTTCCAAAGTGC | 115426 |
rs773673298 | snp | A/C | 1.77546e-05 | 0.00297943 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498169 | TACAGGTTAGATTAC[A/C]TTTGTCTAGGCTGCC | 115426 |
rs773686803 | in-del | -/ATTTGC | 5.01358e-05 | 0.00500653 | cds-indel, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486910 | TGTACTGGCTGGTGG[-/ATTTGC]GGATGAAGTCGTAAG | 115426 |
rs773690085 | snp | A/C | 1.86242e-05 | 0.00305152 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460820 | CACTGGTGCCATTTA[A/C]TTAACTGAATTGATC | 115426 |
rs773733313 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499159 | CAGAAGCATGTGAGC[C/G]CATCTGCTATGATGA | 115426 |
rs773751417 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414741 | TTTTCCTCCCCTTCA[C/T]AGGCTTAGTCTTCGA | 115426 |
rs773778406 | snp | C/G | 0.000557465 | 0.016686 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468688 | TGGACTTCTGCTGGA[C/G]AAGAGGCTGGAAATG | 115426 |
rs773780301 | snp | C/G | 2.17654e-05 | 0.00329882 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413622 | GCCCGAATGCCAGCG[C/G]CTCTTCTACCGGGGC | 115426 |
rs773786418 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500168 | AGATGGGGTTTCTCC[A/T]TGTTGCCCAAGCTGG | 115426 |
rs773793325 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462767 | ACTAAAAATACAAAA[A/G]TTAGCTGGGTGTAGT | 115426 |
rs773798433 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486513 | GAGCTGGAAGTTCCA[A/G]TAGACATAAGATGAT | 115426 |
rs773798793 | snp | G/T | 0.000270874 | 0.0116346 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413681 | CTAGCGAGGCTGGGG[G/T]CCGGAACAGCTGGGC | 115426 |
rs773806645 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474980 | AAATATATTGCTTAC[A/G]TAAAAGAAATGTTAA | 115426 |
rs773831685 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463077 | ACCTGAGGTCAGGAG[A/T]TCGAGACCAGTCTGA | 115426 |
rs773861307 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417178 | AGCCACTTCCACTTG[A/G]CATTTGCTTTCTAGT | 115426 |
rs773890123 | snp | A/G/T | 0.0001232 | 0.00784772 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421171 | TTCAGACTTACTGTT[A/G/T]TGAGAATACAAATAA | 115426 |
rs773894246 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415873 | GATAGATAGTCTCCC[A/G/T]CTAGTCTCTTACTAT | 115426 |
rs773903777 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425712 | AGGTTACGGGGAGCC[A/G]AGATCGCGCCACTGC | 115426 |
rs773937286 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501540 | TTAAGGAAGAATTTT[C/T]TAAATATGATTTTTA | 115426 |
rs773947393 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477575 | GAGATTCATAGATAT[-/A]AAAAAATGTTTTAAG | 115426 |
rs773958801 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434295 | AGGTTATGTTCATTT[A/G]TTACTTTTTGGTTTT | 115426 |
rs773971442 | in-del | -/GT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469659 | GACTTGATGAAAGGT[-/GT]GTGTGTGTGTGTGTG | 115426 |
rs773989336 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504455 | GGTAATTGGAATGTT[C/T]ATCACTATAAACATC | 115426 |
rs773989413 | snp | C/T | 2.03784e-05 | 0.00319199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504727 | ACTTTCCCTGTTAGG[C/T]ATGAAGGCACACTAA | 115426 |
rs773992677 | snp | C/G | 1.65614e-05 | 0.00287757 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482146 | GAGAATTGGCTATCA[C/G]ATTATAGCAATGTTA | 115426 |
rs773998150 | in-del | -/T | 1.72308e-05 | 0.00293515 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475350 | TGTATATACCTTAGA[-/T]TTTGCTGGCAGAAGT | 115426 |
rs774012877 | snp | A/C | 5.84482e-05 | 0.00540562 | stop-gained, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499926 | CAAAAAGGCCAATTT[A/C]AGATGGTAGGTAATG | 115426 |
rs774013317 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473395 | GCTATACTACTGGGT[A/C]ACCAACTAGTTTAGT | 115426 |
rs774053472 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483091 | AGCACTTTGGAAGGC[C/T]GCAGCAGCCAGATCG | 115426 |
rs774064210 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463753 | TAGGATTATAGGTAT[A/G]AGCCACCGTGTCTGG | 115426 |
rs774106907 | snp | A/G | 1.66999e-05 | 0.00288958 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500564 | TAGATGACTGTCCAA[A/G]TGCCTCCAAAGTGTA | 115426 |
rs774110409 | in-del | -/AA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417277 | CAAGAGTGGTCTGAC[-/AA]AAAATCCTAACCATT | 115426 |
rs774129374 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439654 | TGTTTTAGTAGAACT[C/T]AACCTAATCAGTACT | 115426 |
rs774192203 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467190 | AACCCATTTTCTTGC[C/G]TTTACCATGTTTCAG | 115426 |
rs774208556 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475478 | AGCCCATCCCCTTTC[A/G]TTTGCAGATGGAAAG | 115426 |
rs774229918 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444400 | TTGCAAGATCACTTA[A/G]TACTTAGAAAAAGAA | 115426 |
rs774265875 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425444 | ATTTCTCCAAGGTTC[C/G]CTGTTTCCTTTAATT | 115426 |
rs774267131 | snp | A/G | 1.6743e-05 | 0.0028933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497968 | CCACTAATGTGATGA[A/G]TAAGTCTAAATTTTA | 115426 |
rs774279643 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451419 | CTAAGAGAAATTGAG[C/G]TTCCATCCTGATTCC | 115426 |
rs774280327 | snp | A/G | 5.21209e-05 | 0.00510468 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497167 | TTGAAGAAAAATTAC[A/G]TGGTATAAAGACTTC | 115426 |
rs774292289 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421053 | AATAGTCCACCTAAA[A/G]TAAAGAAAGCTCCGA | 115426 |
rs774311913 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493412 | TATGGTGTAGATGTC[A/G]GTTGGAAATTTGGTT | 115426 |
rs774337693 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435153 | CGCGCACCACCACGC[C/G]TGGCTAATTTTTGTA | 115426 |
rs774356990 | snp | A/G | 3.4256e-05 | 0.00413845 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477820 | ACTGGTATGATTATC[A/G]GGTTTTTGTTGTTGT | 115426 |
rs774363664 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429350 | GAGGTAAAGTATGTA[A/G]TGGTAAACAGCTAAT | 115426 |
rs774365064 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494534 | GAAATACTAATGACA[A/T]CTCAGCTCCCGTGGG | 115426 |
rs774368383 | snp | A/G | 3.48547e-05 | 0.00417446 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477594 | AAATGTTTTAAGACT[A/G]GACTTGCTATAATTT | 115426 |
rs774375662 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483211 | GCGCCTATAATACCA[A/G]CTACTCAGGAGGCTG | 115426 |
rs774387194 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443825 | TTAGGCTAGGCTATA[A/G]TTAAAAACTCATCTG | 115426 |
rs774393426 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464398 | GTCTTTTTCTCCTTA[C/T]GATGTTTGAATAGTA | 115426 |
rs774464138 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443744 | TTTTAATACAGTGTC[A/T]AGGCTTTACCATGGG | 115426 |
rs774466070 | snp | A/C | 1.69766e-05 | 0.00291342 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504653 | CAGGAGCTAGTTTAC[A/C]AGCCTGTGACAACTG | 115426 |
rs774490524 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419785 | TCACTCTGTTGCCCA[G/T]ACTTGAGTGCAATAG | 115426 |
rs774490814 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421198 | ATAAATTTATTTTCT[A/G]TTCAGGATGTTTTGA | 115426 |
rs774557720 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466322 | GCGGACGGATCACCT[A/G]AAGTCAGGAGTTCTA | 115426 |
rs774591419 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438905 | GTCTATGAGGAATGA[C/T]AGCCATTATAGATTT | 115426 |
rs774596108 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431375 | CACTATGAGAGACCA[A/T]GGAAAGAGGATTGTT | 115426 |
rs774642773 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461475 | CCTCTTGGGTTCATG[C/T]AGTTCTCCTGCCTCA | 115426 |
rs774664727 | snp | C/G | 1.81214e-05 | 0.00301004 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460810 | AGATTGTCTTCACTG[C/G]TGCCATTTAATTAAC | 115426 |
rs774705643 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447344 | CCAGACATTTGTGGG[A/C]CTGGTCTCTCCCAAA | 115426 |
rs774722072 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463472 | GGCTTATGGATAGAA[-/T]TTTTTTTTTTTTTTG | 115426 |
rs774750401 | snp | A/G | 3.83061e-05 | 0.00437625 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413607 | GCTGTTCGACGTGCG[A/G]CCCGAATGCCAGCGC | 115426 |
rs774828974 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490733 | ACATTTGTGGAGATA[A/C]GTACTGATGAACTGC | 115426 |
rs774838855 | snp | C/T | 1.88078e-05 | 0.00306652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486774 | ATTTTGTAAATGTAT[C/T]TTAACTGTTCAGAGG | 115426 |
rs774840178 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461925 | TGTGCATTTCTTTTC[-/T]TTAGAATAAATTGTT | 115426 |
rs774848298 | snp | G/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460699 | TAATGTAGAAAGTCC[G/T]GGACAAAGAGGATTC | 115426 |
rs774849081 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6413957 | CAGGTCCCTCGCTTC[C/T]CGCGCTCGGCGGGGC | 115426 |
rs774860559 | snp | C/T | 1.68635e-05 | 0.0029037 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413513 | TACAGGTTCGCACCA[C/T]TGATGGCTCCAAGAC | 115426 |
rs774862885 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493318 | AAAAAGTTAAGGTGA[A/C]GTTTTTAGGTAAATT | 115426 |
rs774899938 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480907 | CTCTAAAAGCTACGT[A/G]GAATAGATAATTGTG | 115426 |
rs774900411 | snp | G/T | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412572 | CCCGCGGCCTGAGGA[G/T]AGGCCTGGAGCTGCC | 115426 |
rs774916846 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6489162 | TATAAATGGAAGTAT[C/G]TAGCATATTATATAT | 115426 |
rs774922911 | snp | C/G | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486854 | CACAGACCCCATGTT[C/G]GTGGAATTCATGGTC | 115426 |
rs774940111 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471480 | TGTAAGTGATGCTGT[A/G]CCACTTCAAGATGAG | 115426 |
rs774962235 | snp | A/G | 1.70075e-05 | 0.00291607 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493915 | TTCAGCTGATCAAAC[A/G]TTAACAAACATGAAC | 115426 |
rs774962357 | snp | C/T | 5.17621e-05 | 0.00508708 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475343 | TATTATTTGTATATA[C/T]CTTAGATTTTGCTGG | 115426 |
rs774969100 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421624 | GTTTCACCATGTAGG[C/T]CAGGCTAGTCTCGAA | 115426 |
rs774972230 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422519 | GATTCTATGGAGATT[A/G]CATCTATAGATCAGC | 115426 |
rs775052106 | snp | A/T | 3.29919e-05 | 0.00406138 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475436 | GATAATATCTGTAGA[A/T]GAAATCTTCAAGATT | 115426 |
rs775072746 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471649 | CCCTGACCAATGGCT[G/T]AACTGCAATCTCATG | 115426 |
rs775083742 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442148 | TTTGGTGTTTTTAAT[A/G]GAGACAAGGTTTCAC | 115426 |
rs775166544 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424036 | CTATACCGGTATTCC[C/T]TTTAAAGACGAGCTA | 115426 |
rs775210836 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447613 | TAAATAAAGATTTCC[A/G]GTTAAACATGGCAGG | 115426 |
rs775239198 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459275 | AAAATGGAGACTATC[A/G]GAATATGCCAGGTTC | 115426 |
rs775258457 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486273 | TTCATGACTCAAACT[A/G]CGATTGAACAGTGGA | 115426 |
rs775308396 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476085 | TCTATTCTCCACCTG[C/T]ACAAGATCAATTTTT | 115426 |
rs775317729 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438859 | TTTTCAACTTCTACT[C/G]CAGTCAGAGCAGAGT | 115426 |
rs775337707 | snp | C/T | | | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413804 | GGTGCGGGGCCCAGT[C/T]CCGCCGAATGGTGGG | 115426 |
rs775391239 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483043 | AATTGCACACAAGCT[C/G]AGGCTGGTGTGGTGG | 115426 |
rs775395864 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432862 | TTTTTTCTTTTTGAG[A/G]CAGAGTCTTGCTGTA | 115426 |
rs775407179 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470059 | AGACAGTGGAATGGC[A/T]TGTGAAAATACTAAT | 115426 |
rs775443766 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492101 | ACAGTTTTTTCCCTC[A/G]TGATAATATAATGTT | 115426 |
rs775459984 | snp | C/G | 5.70727e-05 | 0.00534164 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504705 | AAGTAAGTAGAATTC[C/G]TTCCTCACTTTCCCT | 115426 |
rs775467244 | snp | C/T | 1.65425e-05 | 0.00287593 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434141 | CTGTGTTGCTGCTGA[C/T]GAAGACGTTATTTAC | 115426 |
rs775483308 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480268 | AGTCACTCTTGTCAC[A/G]TATAACCCTGATGTA | 115426 |
rs775511359 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498629 | CTTCCCTGCCCTGCC[A/G]CCACCTTTAGTGCTT | 115426 |
rs775549503 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467689 | AAGTTGAATTCTTTC[-/A]AAAGATTTGAATTTG | 115426 |
rs775578535 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436809 | TAAGTAAAGGGGAAT[C/T]TAAATCCAACATGTG | 115426 |
rs775583957 | snp | A/G | 3.41676e-05 | 0.00413311 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413490 | CTCTCTAGGCGCCAA[A/G]ATGTGGATACAGGTT | 115426 |
rs775622145 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429228 | AGTTGGAGAACCTGT[A/G]TTCTCAGCTTAACTC | 115426 |
rs775624876 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477021 | GAATCACCTGAGGGG[-/T]CAGGAGTTTGAGACC | 115426 |
rs775653738 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449835 | CTGCCCTAGCAGACA[A/G]TATTTCCCATGTGTT | 115426 |
rs775719908 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423035 | CTTCCTAATTCTTAT[C/T]AGTTGCGATAAATGG | 115426 |
rs775720670 | snp | A/G | 1.67486e-05 | 0.00289379 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6497204 | GTTTTTTAGGGCATT[A/G]GCCCTAAACTGTGAT | 115426 |
rs775732937 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419157 | TGGGGGTTAGGACTT[C/T]AACAAAAAAATTTTG | 115426 |
rs775737937 | snp | C/T | 3.35509e-05 | 0.00409564 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497399 | TGTTTGTCATTCTTC[C/T]TGGGCTTTCAAGGCA | 115426 |
rs775755018 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490582 | GCGGTGAGCCAAGAT[C/T]ACATCACTGTACTCC | 115426 |
rs775767554 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459124 | CTAATGTAGATGACA[C/G]GTTGATGGGTGCAGC | 115426 |
rs775774653 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428088 | CCTTTACAGTTTAGC[G/T]GAGCATGTGGCACTG | 115426 |
rs775784018 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502505 | GTTGCCCAGACTGAT[A/C]TCAAACACCTGGGCT | 115426 |
rs775799825 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507120 | TTTAAAGGATCCTAT[A/G]TTTCTGGAGTTTTTC | 115426 |
rs775811835 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479316 | CTAAGGGTCAGTTCT[C/G]ATTCCTTACTCAACT | 115426 |
rs775872897 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422229 | TGGGATTACAGGCGC[G/T]TACCACCATGCCTGG | 115426 |
rs775887819 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460687 | AATGGTTAATTATAA[C/T]GTAGAAAGTCCTGGA | 115426 |
rs775889911 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436113 | GTATGGAAAATATTA[C/T]GCTACCAAATTCTTA | 115426 |
rs775894893 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453584 | TTTTCTGACCAAACC[A/G]TTGTGAAACAACACG | 115426 |
rs775907531 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490047 | TATATAGTTTATTAC[A/G]GTCAGCTCTTGGAAT | 115426 |
rs775943519 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431814 | AGTACTTCATTTGTG[C/T]CGCCTCGTGTTCCTT | 115426 |
rs775953881 | in-del | -/T | 1.74336e-05 | 0.00295237 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460524 | TACATTGCATAAAAC[-/T]TTAGTTGTCTTTGGT | 115426 |
rs775958090 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454237 | GAAGCTAAATTGGGA[A/G]TCTAAACCTAGGCAG | 115426 |
rs775963998 | snp | A/G | 1.82533e-05 | 0.00302098 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499912 | GCCCAGTGGAACCAC[A/G]AAAAGGCCAATTTCA | 115426 |
rs776003127 | snp | C/T | 1.84042e-05 | 0.00303344 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413447 | GCGCGGCGCCCAGAG[C/T]TCAGGGGGAGACAAA | 115426 |
rs776004957 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446432 | ACAGGCGTGAGCCAC[C/T]ATGCCTGGCCTAATT | 115426 |
rs776047160 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491901 | AGGAAAAATATTTTA[C/T]TTTTATTTTTTAATA | 115426 |
rs776057532 | snp | A/T | 1.82583e-05 | 0.0030214 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493785 | TTGATGAAATTATAC[A/T]TGGGTTTAGCTTTCT | 115426 |
rs776071665 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457533 | CCCTGGCCAGAACTT[C/G]CAACACTCTGTTGAA | 115426 |
rs776077883 | snp | C/G | 0.000440044 | 0.0148266 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468757 | ACACTGGATTTTAGG[C/G]TAACTGGTGTAATGG | 115426 |
rs776087014 | snp | A/T | 1.64735e-05 | 0.00286993 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504581 | TTTCCTTATCCTTGG[A/T]TACTGTTCTAGAATT | 115426 |
rs776124753 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446900 | TTTTTGGCATACTTT[C/T]TGTTTTGAGACAGAG | 115426 |
rs776178539 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417475 | GAGTGTCAGAGATAA[C/G]TTTCAATCTTCACTT | 115426 |
rs776206283 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421742 | GTTTAAAGCCTCGTG[C/T]GTGTCCCTATCAGAA | 115426 |
rs776216334 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502713 | AGCACATTGTAGCTA[C/T]CTGTAACTCAAAATA | 115426 |
rs776241859 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417531 | ACTTTTCAAGTAAAT[C/G]ATCTCAACACTTCAC | 115426 |
rs776256753 | in-del | -/CTTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492738 | GTGCACTGATAGTTA[-/CTTTT]CTTAATTTGTTTCAA | 115426 |
rs776261089 | snp | C/G | 0.000283166 | 0.0118955 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468374 | GGACAGCTGGCAGTA[C/G]ATTAGTGCTTTTAGC | 115426 |
rs776301039 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440396 | TATATAATTAGCCAA[-/G]GGTCACATCTATTAA | 115426 |
rs776343343 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473893 | AACTGTTTAACCCAT[A/G]CTTTGGGAATGCAAA | 115426 |
rs776347460 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454578 | GCCCCCATCACCTAC[A/G]TAAGATCCCACACAG | 115426 |
rs776364775 | snp | A/G | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475420 | CATTAAATGACTGCA[A/G]GATAATATCTGTAGA | 115426 |
rs776365897 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491001 | AAATTTCATGAAGCC[A/G]GTGATCTTTGTTCTG | 115426 |
rs776372117 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414126 | GGAAACTCGGGCATT[C/G]AGCTCTCAAGAATAA | 115426 |
rs776392276 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455288 | TGCTATCCCTCCCCC[A/C]TCTCTCCACCCCACA | 115426 |
rs776393696 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6497161 | GTGTACTTGAAGAAA[A/C]ATTACATGGTATAAA | 115426 |
rs776449584 | snp | C/G | 1.73234e-05 | 0.00294302 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413685 | CGAGGCTGGGGGCCG[C/G]AACAGCTGGGCTCCT | 115426 |
rs776478641 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450111 | ACAGACTTGGAAACA[C/G]TGACATACAAAGTGT | 115426 |
rs776498874 | snp | A/G | 1.67565e-05 | 0.00289447 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500706 | ACATCTTGTGGAAGG[A/G]CCAGTATGTGAAGAT | 115426 |
rs776525231 | in-del | -/T | 9.62634e-05 | 0.00693703 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504561 | TTATGAACTGCTAAC[-/T]TTTCTTTCCTTATCC | 115426 |
rs776529957 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450717 | CTATCCCAGTTGTTA[C/T]TTTGATGCTTATATT | 115426 |
rs776537872 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502326 | TGGGCCTTTACATAC[A/G]TACTGTTACTCTGAC | 115426 |
rs776571873 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502619 | TCTGAAACAGTTTTT[C/G]TTTGTTTACTCTGCT | 115426 |
rs776594394 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474698 | TGACAGAGCGAGACT[C/G]CATCTCAATAAATAA | 115426 |
rs776637964 | snp | C/T | 5.14973e-05 | 0.00507405 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433887 | GACAAAATTAAGCTT[C/T]ATTAACTGATTTTAA | 115426 |
rs776656325 | snp | A/G | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434061 | AGGACTAATGGAAAT[A/G]TAAAGCATAAATCCA | 115426 |
rs776660830 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488517 | AACCTCTGACAACCA[C/G]TAATCTTTTCTCTTT | 115426 |
rs776665800 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431955 | ATTTTGATTTGCTGC[G/T]ACAGAGTAGTAACCT | 115426 |
rs776668882 | snp | C/G | 1.69522e-05 | 0.00291132 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434183 | TGATGAGTAAGTGCT[C/G]AAGCTATTGAGGACT | 115426 |
rs776675636 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469516 | AGCGAGACTCTGTCT[C/G]AAAAAAAAAATTAAA | 115426 |
rs776679408 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412117 | CGAGATCGCGCCACT[A/G]CACTCCAGCCTGGGC | 115426 |
rs776709361 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445319 | CCCAGGCTGGAGTGC[A/C]GTGGTATCATGTTGA | 115426 |
rs776710039 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506740 | TTGTGCTTTTTTCTG[A/G]TGTTTTATGCAAGTT | 115426 |
rs776717062 | in-del | -/A | 1.74096e-05 | 0.00295034 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493809 | GCTTTCTTAATAAAG[-/A]AAATCTTCTCTGACA | 115426 |
rs776730956 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459066 | ACAGAGGGGCCTGTC[A/G]GAGGGTAGGGGGCTA | 115426 |
rs776732099 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411274 | GGGGTAGACAAGTGA[A/G]TTATATTTAGAGGTT | 115426 |
rs776732939 | in-del | -/TTTTG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451475 | TTTTTTGTTTTTTTT[-/TTTTG]TTTGTTTGTTTGTTT | 115426 |
rs776751438 | snp | G/T | 1.72791e-05 | 0.00293926 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413483 | CCGGTTCCTCTCTAG[G/T]CGCCAAGATGTGGAT | 115426 |
rs776756711 | snp | A/T | 1.69795e-05 | 0.00291367 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460560 | TAAGCCATATGGTTT[A/T]CTCTCTCCTCAGATA | 115426 |
rs776761468 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436738 | GTATCTTAGAGCACA[A/G]AACACAGTACCTTAG | 115426 |
rs776764861 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495891 | TCTTTAAGATAAAAT[A/G]GGTGTAATATCTCAA | 115426 |
rs776786308 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435309 | GGCTAATTTTTTTGT[A/G]GAGATGTGGTCTCAC | 115426 |
rs776866861 | snp | A/G | 2.19229e-05 | 0.00331073 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504741 | GTATGAAGGCACACT[A/G]ATTTCTATACCTGTT | 115426 |
rs776868654 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436841 | GAAAAGACTAAAATT[A/G]CCTGCCCTAAATAAT | 115426 |
rs776897448 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479171 | TGCTTCTTTCATGCA[A/G]AGATTCTCAAGAGCT | 115426 |
rs776954686 | snp | G/T | 2.53155e-05 | 0.00355768 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493967 | TTAGAATTTGAACAT[G/T]GAATAAAAGTTTCAT | 115426 |
rs776960027 | snp | A/G | 3.55657e-05 | 0.00421682 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499902 | CAAAGAAGCAGCCCA[A/G]TGGAACCACAAAAAG | 115426 |
rs776970608 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452583 | AGTCTGAGAAAGGTA[C/G]ATTTTAACTAAGGAT | 115426 |
rs776983436 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436047 | GGACAGATTTAGTAT[A/G]TTAAACACACTAAAT | 115426 |
rs777034276 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427237 | CATGTAGAGCTTTCT[A/G]TAGTTGAAATTGCTT | 115426 |
rs777037496 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463017 | CCAGGTGCCGTGGCT[C/G]ACGCCTGTAATCCCA | 115426 |
rs777054245 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422069 | TGAACCTTCTGTTAA[C/G]CTGGTGCATATGTTC | 115426 |
rs777081316 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439569 | GGTTCACATCATGTA[C/T]AAAGTAGATAGATAT | 115426 |
rs777082435 | snp | C/T | 1.66244e-05 | 0.00288304 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481793 | ATTCCCCTTTTCTTC[C/T]TAATAGCAAGTTATA | 115426 |
rs777141810 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453411 | GTAATTTTCACTTTA[C/T]AGCTGAGAAAGGAAT | 115426 |
rs777179392 | snp | G/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420990 | GTTCGCCCAGACCCT[G/T]ATCATCTTCCTGGCA | 115426 |
rs777179510 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487958 | TAGAAACAATACAGA[C/G]GGCCGAATCCAGTGG | 115426 |
rs777191148 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434043 | AATGGCAGTTCTTGT[A/G]AAAGGACTAATGGAA | 115426 |
rs777192114 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421427 | GTTTGTTTGTTTGTT[A/T]TTGATAACGGAGGCT | 115426 |
rs777226481 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414795 | AACAAATTACACTTT[-/G]GGAAGGAGAGAGCTT | 115426 |
rs777240754 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455408 | GTTTTTTGTACTTGC[A/G]ATAGTTTGCTGAGAA | 115426 |
rs777248602 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417277 | CAAGAGTGGTCTGAC[-/A]AAAAATCCTAACCAT | 115426 |
rs777260246 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504831 | GAAGCATTTAGTTAC[A/G]TCTTGGTGGTAAATG | 115426 |
rs777274679 | in-del | -/TAAT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450440 | TTCCTGAGAAGCTAA[-/TAAT]TAAAGTTTAATTTGA | 115426 |
rs777285552 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478680 | GTTTTTAAGTAAGAC[A/G]GACGACTGAGTCAGA | 115426 |
rs777330416 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443271 | CTCTTGTTAAAATAA[C/T]ACAGTGTGCCAAGCA | 115426 |
rs777357346 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418851 | AATTTACTGTCTCAC[A/G]GTTCTAGAGGTCTAG | 115426 |
rs777364903 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418142 | AAGGTATTTTGTTTT[G/T]GGTTTTTTTGTGGGG | 115426 |
rs777366517 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481441 | TTATAAGTTATCTAA[A/G]GGAATGACAAGGATA | 115426 |
rs777377904 | snp | A/G | 1.65173e-05 | 0.00287374 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481703 | TGGTGAAAGACTCAA[A/G]ATGAGTAAAAAGAAA | 115426 |
rs777418371 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467235 | CCTTAGCTTGTTACC[C/T]GCTTTCTCCACCTTC | 115426 |
rs777440361 | snp | C/G | 3.12466e-05 | 0.00395251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504565 | GAACTGCTAACTTTT[C/G]TTTCCTTATCCTTGG | 115426 |
rs777465154 | snp | C/G/T | 3.30241e-05 | 0.0040634 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434111 | GGACAGTGTACCCTC[C/G/T]ACGTCTAATTCAGAC | 115426 |
rs777470975 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442054 | CACTGCAACCTCTGC[C/T]TCCTGGGTTCAACAA | 115426 |
rs777499273 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479669 | ACAAAATTAGTCCAG[A/G]TGGAGTTCTTGATTT | 115426 |
rs777519365 | in-del | -/AAAC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490083 | GAAGGCTTTATAAAT[-/AAAC]CAACTAGAAATGTAG | 115426 |
rs777521385 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412922 | CGCCCCCTCAGCTCT[A/G]AAACGAGGCCTCAAA | 115426 |
rs777530001 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496891 | CCCCAACAAACGTTA[C/T]TTAAAGAAAAATTCC | 115426 |
rs777541002 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6475743 | ATTTTATTTTAAAAA[C/T]ATTTATGGATATATA | 115426 |
rs777577232 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484314 | CTCCTGGCCTAAAGC[A/T]GTACTCCAGCCTTGG | 115426 |
rs777591231 | snp | C/T | 3.37724e-05 | 0.00410914 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481607 | GCTTTAATATGGTAT[C/T]GTGAAAATGCCTTCG | 115426 |
rs777594324 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476422 | AATTATAGTGCTGAT[C/T]GAGCCTTGAATTTCT | 115426 |
rs777624018 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427972 | TTCGTTTTAATTTTG[G/T]TTTTTGTGTATGGAA | 115426 |
rs777653381 | snp | A/G | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411817 | AATATTTAAGTTACC[A/G]ATTTTGGCAAATGTG | 115426 |
rs777655517 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445818 | GTCCTTCCCCCTTGG[C/T]CTCCCAAAGTGCTGG | 115426 |
rs777669178 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440248 | TATCTGTGGCATAGC[C/T]TATGATATTTTAGAG | 115426 |
rs777678931 | snp | C/T | 3.93151e-05 | 0.00443351 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413656 | CAGGTGAGGCGCGCC[C/T]GCCGCGCCCCTAGCG | 115426 |
rs777691942 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469386 | AGCTGGGCGTGGTGG[C/T]AGGTGCCTGTAGTCC | 115426 |
rs777726531 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469562 | ACAAATAAGACACAG[C/G]AGAAGATAGGATTAG | 115426 |
rs777781103 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430824 | TGACCAAACCTAGTG[C/T]TTTCCTGTATTTCCC | 115426 |
rs777781205 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463447 | ACAATAGCTAAAAAG[G/T]AACCAGTGTGGCTTA | 115426 |
rs777825012 | snp | A/C/G | | | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6421030 | AGATTGAGGCTAAAC[A/C/G]CTGTTCTAATAGTCC | 115426 |
rs777834726 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453353 | ATATGCTTTTTACAG[C/T]GTTATTTAAAAACAT | 115426 |
rs777836173 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431662 | TGTGAGCTGATATGT[C/T]CTATGTGTTGATGTT | 115426 |
rs777864831 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426947 | AGAGACAAGATTTCA[C/T]CATGTTGGCTAGGCT | 115426 |
rs777874408 | snp | A/G | 2.00813e-05 | 0.00316864 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499797 | TTCTCTGTGAAGCTT[A/G]AATCTGCATTGTACT | 115426 |
rs777886413 | snp | A/C | 1.74546e-05 | 0.00295415 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499888 | GCCTAAAGGACAGTC[A/C]AAGAAGCAGCCCAGT | 115426 |
rs777939720 | in-del | -/T | 0.000101106 | 0.00710935 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481626 | AAAATGCCTTCGTTC[-/T]TTTTTTTCTTTTAAA | 115426 |
rs777959952 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425719 | GGGGAGCCGAGATCG[C/T]GCCACTGCACTCCAA | 115426 |
rs777974090 | snp | A/T | 1.69893e-05 | 0.00291451 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504650 | TGTCAGGAGCTAGTT[A/T]ACCAGCCTGTGACAA | 115426 |
rs777979832 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488252 | AGACCCTGTCTCCTT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 115426 |
rs777986291 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415387 | CCTTTGGTGCCAGCC[A/G]TTAACTTGGAAACAG | 115426 |
rs778027390 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422603 | AGACTTGACTTCTCC[A/T]TTAACTTAGATCTTT | 115426 |
rs778034163 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464291 | GTTGTTAATTAAATA[A/C]TGTGTCTGATTCATT | 115426 |
rs778035000 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502121 | AGAAAAAAACAGGTG[G/T]TAGCCAACAGTGACT | 115426 |
rs778066400 | snp | C/T | 1.65592e-05 | 0.00287738 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493858 | CACATACACTGGAAG[C/T]GGTGGTAAAAATCTT | 115426 |
rs778073066 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478972 | TGCTTCTCTAAAATA[C/T]GCTCTTTCACCTGCT | 115426 |
rs778104529 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490338 | CTCTGTAGCAGAATA[C/T]TAAATAAGGCCAGTC | 115426 |
rs778108985 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445006 | ATTTAGAATTTGGGT[C/T]GAGGCCGGTCATGGT | 115426 |
rs778172281 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481916 | ACAGTTGGGTTCCTA[A/G]TCACATCTCAGAATT | 115426 |
rs778202306 | in-del | -/CGCGCCCGC | 3.94034e-05 | 0.00443849 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413650 | GGCAAGCAGGTGAGG[-/CGCGCCCGC]CGCGCCCCTAGCGAG | 115426 |
rs778210292 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463318 | GTGGAAATTATGGAT[A/T]GGCAAATACCGGCTT | 115426 |
rs778212065 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6426691 | TATCACATACTGACT[C/T]GTTGACTAAACTGAA | 115426 |
rs778214788 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456789 | ATTTATTAAATAGGG[A/G]ATCCTTTCCCCATTT | 115426 |
rs778225234 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472137 | TCCCATTACAGTTAC[C/T]GCTACCATCTGTAGC | 115426 |
rs778262490 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6473046 | AGTAAGCTTTCCTAG[A/T]ACCTAACTATGGTCT | 115426 |
rs778292165 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474371 | CAGTAAGATTTAGGC[-/T]TCTTAAATCTGTAGC | 115426 |
rs778328119 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477720 | AAACATGAACCCAAC[A/C]TGCAGCTTCTGTGTG | 115426 |
rs778365910 | snp | C/T | 1.66604e-05 | 0.00288616 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475397 | TTTAAACAGGGGTTC[C/T]GAAGGAACATTAAAT | 115426 |
rs778410470 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416845 | ATCTTTTGAGAATCC[A/G]GAGCTTTTCCTATTT | 115426 |
rs778439262 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436617 | CATAGAATAAGGAAC[G/T]TTAAATAGTGAACTA | 115426 |
rs778446472 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474507 | GGTCAGGAGTTCGAG[A/G]CGAGCCCAGCCAACA | 115426 |
rs778452015 | snp | A/G | 1.6855e-05 | 0.00290297 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475541 | GACTACATGTGTTGT[A/G]CATGATTGAACTTTA | 115426 |
rs778453485 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444109 | TGTCAAATGTAATTA[-/T]TTCTAGGTTTTGATG | 115426 |
rs778467933 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449581 | AAGAGTTAACATCAG[A/G]TCTGAGACTGGTATC | 115426 |
rs778471689 | snp | A/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507530 | TAGGCATGAGCCACC[A/G]CACTCGGCCCTCAGT | 115426 |
rs778479331 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427452 | AGCACTTTGGGAGGT[C/T]GAGGCAGGCAGAGCA | 115426 |
rs778523861 | snp | A/G | 0.000104163 | 0.007216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433866 | ATTAAGGTTTTTGAA[A/G]CAGTAGACAAAATTA | 115426 |
rs778525877 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459425 | TGTAATCCCAGCACT[C/T]TGTGAGACTGAGGCG | 115426 |
rs778554950 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486486 | TGCTGGTAGTCCTCT[G/T]TTAGCTGAGTTGAGC | 115426 |
rs778568842 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434000 | TAGAGCTTCTGATGG[A/G]CAGTCACGTGGCAAA | 115426 |
rs778604186 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500425 | CTAAATTTTAGGGGA[A/G]ATTAGATGCTGTTTT | 115426 |
rs778611597 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436212 | CAGTATTCAGATTTC[C/T]AGGATATCTGGAAAT | 115426 |
rs778612659 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449743 | TTATGCTGAACACTT[C/G]CTTCTGGGAGTCTGG | 115426 |
rs778651069 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506598 | AGAAAAGGAAATGAC[A/G]CTTGAGATCCTTGGA | 115426 |
rs778665567 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448608 | CAGTGCTGTGTGTTA[-/TT]GTAATTATAAGAGGA | 115426 |
rs778701752 | snp | C/T | 5.18533e-05 | 0.00509156 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434203 | TATTGAGGACTTTAT[C/T]CATATTTTCATTTGT | 115426 |
rs778722851 | snp | C/T | 1.68221e-05 | 0.00290014 | | | GRCh38.p7 | 9:6413544 | GTGCACCATTGAGGA[C/T]GTGTCTCGCAAAGCC | 115426 |
rs778740324 | snp | G/T | | | | | GRCh38.p7 | 9:6478045 | AGACTCTGTGTTCAT[G/T]CAAAAATGCAAATCT | 115426 |
rs778740871 | snp | A/G | 1.66308e-05 | 0.00288359 | | | GRCh38.p7 | 9:6497372 | TAAGGTGCTCTATCT[A/G]GCATGACATCTTGTT | 115426 |
rs778772910 | in-del | -/CCTAGCACTTTGGGAGG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441126 | GCTCATACCTGTAAA[-/CCTAGCACTTTGGGAGG]CCAAGGCAGGTGGAT | 115426 |
rs778793337 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453091 | AGACTTAACTATGTA[C/T]GTGTATGAGTACAGA | 115426 |
rs778793812 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468440 | CTTTGAATGCACCAG[A/G]GAATCAAAGAGAACC | 115426 |
rs778908894 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500062 | ACTGTAGCCTTGACC[A/T]CCTGGGCTCAAGCGA | 115426 |
rs778914077 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438664 | AAGAAACCTGCCTCT[A/G]GAATTATTCTGGGGT | 115426 |
rs778930212 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506167 | CTTCCCTGGCTACAG[C/T]AAAGGACGATGATCT | 115426 |
rs778931152 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472080 | GCATGTCACCACTAA[G/T]CAAAACACAATGTTT | 115426 |
rs778935424 | snp | C/T | 0.000100617 | 0.00709213 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499811 | TAAATCTGCATTGTA[C/T]TCTCCCTCCTCCCCC | 115426 |
rs778965483 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430102 | TACAACCTCCACCTC[A/C]TGGGTTCAAGTGATT | 115426 |
rs778985014 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424759 | TCCTTTGACATTGAC[G/T]GTGACAATTTCTCAG | 115426 |
rs778989406 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445057 | GCACTTTGGGAGACC[A/G]AGGTGGGAGGATCAT | 115426 |
rs778990323 | snp | C/T | 1.66081e-05 | 0.00288163 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420908 | TTCTTTCTTTATTTT[C/T]TAGTTGGAAAATGGA | 115426 |
rs779027124 | snp | C/T | 1.6517e-05 | 0.00287372 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481757 | TGAAAGCCGAAGAGA[C/T]TGGGGCAGGGTAAAG | 115426 |
rs779034470 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445764 | AGACAGGGTCTCCCT[A/G]TGTTGCCTAGACTGA | 115426 |
rs779082210 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455099 | TTTCTTTGTCCCTCT[A/G]CTACCTAGCAATACA | 115426 |
rs779102603 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433386 | TTACTAACTAGTGAT[C/T]GAACTTCACCATTTT | 115426 |
rs779104540 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439287 | TCTCCCGGGTTCAAA[C/T]GATTCTCCTGTCTCA | 115426 |
rs779119086 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6468788 | TCCACAGAATATGTA[-/G]GGTCTTTTAGTTTGA | 115426 |
rs779138803 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494857 | AAGACTTTCATGCGT[A/G]TCAATTTACATAGAA | 115426 |
rs779157986 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430765 | CCCATGGAAAACACA[A/G]TAAAGGCTCTGGGCC | 115426 |
rs779165277 | in-del | -/A | 3.61056e-05 | 0.00424871 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413459 | AGCTCAGGGGGAGAC[-/A]AAAGGGGACCGGTTC | 115426 |
rs779173390 | snp | C/G | 0.000100481 | 0.00708733 | synonymous-codon, nc-transcript-variant, missense | UHRF2 | GRCh38.p7 | 9:6475391 | TCCTTTTTTAAACAG[C/G]GGTTCTGAAGGAACA | 115426 |
rs779177780 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472853 | AAGAACTGGGATTTT[C/T]CTGGTTGGGGGAAAA | 115426 |
rs779215602 | snp | A/C | 1.93295e-05 | 0.00310875 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500754 | TTCTGATATTAACAA[A/C]TGATAAATAATTGTC | 115426 |
rs779222732 | snp | G/T | 1.71894e-05 | 0.00293162 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499845 | ATCAGTATCCAGCAG[G/T]TTACCCTTCAGATAA | 115426 |
rs779300933 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492991 | AAAGGGAACTTAACT[A/G]TGCTGTTAGAATTTT | 115426 |
rs779330068 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442897 | AAGGATTTAACATGT[A/G]CTGTCGGTCAGTCTT | 115426 |
rs779343728 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434681 | TGACCTCAAGTGATC[C/T]GCCCCCCTTGGCCTC | 115426 |
rs779355207 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466774 | TCCTTGTGTTGCTTG[A/T]TCACGCAAACATGCT | 115426 |
rs779369213 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416582 | GAGTCTCGTTCTGTC[-/G]CCCAGGCGGGAGTGC | 115426 |
rs779402461 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500640 | TCCTCAACAGCAACA[C/T]CTCATCAGAGAAGAT | 115426 |
rs779409923 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506046 | AGGATTGCCTACAGC[A/G]CTCCTTTAAGGCACA | 115426 |
rs779444661 | in-del | -/TTG | 4.44346e-05 | 0.00471331 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499973 | AATAATAACATACTT[-/TTG]TTGTTGTTGTTGTTG | 115426 |
rs779488865 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6434904 | AATGTGATCCTGGCT[C/T]GCTGCAATCTCCGCC | 115426 |
rs779505660 | snp | C/G | 1.84452e-05 | 0.00303682 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486962 | CTCATTAGTACCTGC[C/G]TTGACCATTTGTAAA | 115426 |
rs779514105 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448263 | TAGTAACAACCAAAA[A/G]GAGCAACCAAATACT | 115426 |
rs779539765 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435592 | CCAGTCCCACTTCCC[C/G]AAGATAATAGGATTT | 115426 |
rs779541903 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425755 | GGTGAGTGAGACTTC[A/G]TCTCAAAGTAAATAA | 115426 |
rs779553769 | in-del | -/AA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466554 | CAAAAAAAAAAGGAA[-/AA]AAAAAAAAAAAAAAA | 115426 |
rs779574166 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6482894 | CCGGCCTGGCTTTAA[C/T]TTTTATATTGAATGG | 115426 |
rs779583279 | snp | G/T | 1.67441e-05 | 0.0028934 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493826 | AATCTTCTCTGACAG[G/T]ACCGAGGTGATGAGT | 115426 |
rs779608488 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458368 | TTTTATTGTGTCTAT[G/T]TGGTTCTTCTCTCTT | 115426 |
rs779625379 | snp | C/G | 1.66023e-05 | 0.00288113 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497366 | CATTTATAAGGTGCT[C/G]TATCTGGCATGACAT | 115426 |
rs779627563 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477575 | TGAGATTCATAGATA[C/T]AAAAAATGTTTTAAG | 115426 |
rs779632804 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483324 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 115426 |
rs779645439 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415019 | ACCGTTTCCTTTTGA[C/T]CACAAGTGAAAAAGC | 115426 |
rs779661387 | snp | A/G | 1.79774e-05 | 0.00299806 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413461 | GCTCAGGGGGAGACA[A/G]AGGGGACCGGTTCCT | 115426 |
rs779684981 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467683 | CTGACAGAAGTTGAA[C/T]TCTTTCAAAGATTTG | 115426 |
rs779704988 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474013 | TTATAGATTAGAGAC[-/TT]TTCAAACACAGGCAA | 115426 |
rs779710530 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505497 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGTTAG | 115426 |
rs779714101 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477710 | ATGTGGTGGGAAACA[C/T]GAACCCAACATGCAG | 115426 |
rs779723843 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430612 | TAACTACCTCCCTTA[C/T]CTAACTCTTAAACAC | 115426 |
rs779731307 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456945 | GTCAGGTAGCATGAT[A/G]CCACCAGCTTTGTTC | 115426 |
rs779763378 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494466 | GATCTTTTCTAACTA[A/T]ATCCCCTTAAGACAT | 115426 |
rs779763449 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506457 | ATGATTTATTTTGCA[A/G]CTACCTCAGGACAGA | 115426 |
rs779814877 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495428 | GGCAAAGGTACCTGT[A/G]TGTCTTACAAACATG | 115426 |
rs779827482 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451310 | CGTTCATTATGCTTT[C/T]GGTTTTTAGGGATTT | 115426 |
rs779834566 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451294 | ACCAGTTGTGTAGTT[A/T]CGTTCATTATGCTTT | 115426 |
rs779838389 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452251 | ATAGTGCAGCTATAA[A/G]TAGCCTTGTGTATCT | 115426 |
rs779867686 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496445 | CTAATAAGCTCATTG[A/T]TTTACTACTATTAGG | 115426 |
rs779896424 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466753 | TGTGCTTCGGCCATG[C/G]TGGCCTCCTTGTGTT | 115426 |
rs779931074 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462222 | CTATTTTTGTGCTCC[A/C]CAGTATTGTTGAATA | 115426 |
rs779962015 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506351 | GAGGCCCATTTCTCA[A/G]CTGTCTTTTAAATAT | 115426 |
rs779970923 | in-del | -/AAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423301 | GTTGACCTACAACAT[-/AAA]GAAGGAAAGCTTCCT | 115426 |
rs779979433 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414601 | CATGTTGTTGTTAAT[A/C]CACTAAAAAGTTGGC | 115426 |
rs780006632 | snp | A/C/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421050 | TCTAATAGTCCACCT[A/C/G]AAGTAAAGAAAGCTC | 115426 |
rs780016202 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440609 | AGCAAAAAGCACACA[C/G]GCAACTTCTATTGAG | 115426 |
rs780042443 | snp | C/T | 3.59842e-05 | 0.00424155 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486952 | TACAACCTTACTCAT[C/T]AGTACCTGCCTTGAC | 115426 |
rs780049072 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6447201 | GCCAGCACACGTACC[G/T]TTTAACCTAATTATG | 115426 |
rs780053155 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6455934 | GGCTGCAGCGGGCAT[A/G]ATCACACCACTGCAC | 115426 |
rs780082058 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6453061 | TATGCTTCATTTTCA[C/T]GACTTACCTTTTACA | 115426 |
rs780088914 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485136 | ACATTTAGTTTAATA[C/T]TCTCTGTGTTCTCTT | 115426 |
rs780127877 | snp | C/T | 1.73945e-05 | 0.00294906 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460526 | CATTGCATAAAACTT[C/T]AGTTGTCTTTGGTAA | 115426 |
rs780144388 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460625 | GATCTTAGACCACGA[G/T]CTAGAACCATTTTGA | 115426 |
rs780161843 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492280 | ACTTTTTCTTTATGG[A/C]ACTCCCATAATAACT | 115426 |
rs780206649 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459940 | ATCGTGTCACTGTAC[C/T]GCAGCCTAGGTGGCA | 115426 |
rs780239634 | snp | A/G | 1.75804e-05 | 0.00296478 | missense, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413590 | CGCGAGCGGGTGTGG[A/G]CGCTGTTCGACGTGC | 115426 |
rs780246502 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424871 | GATTCATTTGTTTTC[C/G]TTATTTGTCTGGGTT | 115426 |
rs780248232 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6448082 | AAGCTGTGGACCAGG[C/T]GTAAAGCCTACAAAG | 115426 |
rs780251688 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415187 | TATGCTAAAATAATT[A/T]TCACATATGGGATTG | 115426 |
rs780256304 | snp | A/G | 4.52049e-05 | 0.00475399 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413668 | GCCCGCCGCGCCCCT[A/G]GCGAGGCTGGGGGCC | 115426 |
rs780292440 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6481511 | TTTAGTATTTTAATG[C/T]CAGTTAAAGCTCTGT | 115426 |
rs780330568 | snp | C/T | 0.000179195 | 0.00946391 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422683 | GACGTGAACACGGCT[C/T]GCTGTAGCCTTGACC | 115426 |
rs780340094 | in-del | -/AAT | 2.89809e-05 | 0.00380652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499955 | TGATTGCAAAATATA[-/AAT]AATAATAACATACTT | 115426 |
rs780372226 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438557 | TGGCAAACCTGTGCA[C/G]AATTGTGTCTGCAAA | 115426 |
rs780389641 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6471129 | AATGTCCTGGTAATA[C/T]AGAGCAAAATATTAC | 115426 |
rs780393146 | in-del | -/A | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412463 | GAAATGTCCGGAGTT[-/A]AGAGAGCGGCCTTTC | 115426 |
rs780405087 | in-del | -/AATA | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411226 | CTCATTTACATATGT[-/AATA]AATACTCAATATTTG | 115426 |
rs780405490 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479387 | AATCCCGATTTTCTA[C/T]CTACTTCACTGGCCT | 115426 |
rs780449911 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457015 | TAGTTCCATATGAAA[C/T]TTAAAGTAGTTTTTT | 115426 |
rs780467919 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458768 | AAGACACATGCACAT[A/G]TATGTTTATTGCAGC | 115426 |
rs780470175 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443139 | ATATGTCTGTATCTG[A/G]TCTTAAGAATGAAGC | 115426 |
rs780499457 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503919 | ACCCAATACTCTGAT[G/T]TAAAACTAATGTGTA | 115426 |
rs780516452 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441921 | AATGTATTTATGGGG[A/C]AATTTGTCTGTTAAA | 115426 |
rs780545247 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484493 | TAATCACAGTCCCCT[C/T]CTGGGCTCAAGCTGT | 115426 |
rs780567212 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432520 | TCCTAACCTTACATT[C/T]CATTAGCTTTAACCT | 115426 |
rs780592908 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6465687 | GAGGTTTATCGGTTT[C/T]ATTAGACTTTTACAA | 115426 |
rs780594256 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452164 | GGAGCACAATATTCT[A/G]TTATGTACCTGTATT | 115426 |
rs780603676 | in-del | -/TCTT | 1.75102e-05 | 0.00295885 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486803 | GGTATTTTGAGACTC[-/TCTT]TAATTGTTTTATAGG | 115426 |
rs780605302 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6433971 | TGGTTTGAAGCACAC[A/G]TACATAGTGTTACTA | 115426 |
rs780613385 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480003 | TCTGTTTGAAACCCT[C/T]TGATGTCTTCCTATT | 115426 |
rs780626331 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443521 | AACTATTGTAAAACA[A/C]CATCTATCTATAGCA | 115426 |
rs780637762 | snp | A/G | 1.65941e-05 | 0.00288041 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486834 | AGGTGAGCGAAGCAG[A/G]TGTTCACAGACCCCA | 115426 |
rs780642907 | snp | C/G | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500617 | GCAATTGAGGCTTTT[C/G]AACTAACTCCTCAAC | 115426 |
rs780666449 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423852 | CCGGAGGCTGAGGCA[G/T]GAGAATTGCTTGAAC | 115426 |
rs780669925 | in-del | -/AAAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6459218 | ACTTAAATTTTAAAA[-/AAAG]AAAGAAAGAAACTGG | 115426 |
rs780674061 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477607 | CTAGACTTGCTATAA[G/T]TTTGTTCTTAATAGG | 115426 |
rs780717296 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6494274 | AAAAGTGACAAACTC[C/T]TTTTTAGAGTAAACT | 115426 |
rs780730696 | snp | A/G | 1.84198e-05 | 0.00303472 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500744 | AATAATAACATTCTG[A/G]TATTAACAAATGATA | 115426 |
rs780753060 | snp | C/T | 1.65699e-05 | 0.00287831 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6493876 | TGGTAAAAATCTTGC[C/T]GGTAACAAAAGAATT | 115426 |
rs780754978 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant | UHRF2 | GRCh38.p7 | 9:6506013 | TCAGATTAAATTGGA[C/T]GTTTTTGTTTTTACC | 115426 |
rs780761601 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433150 | GATCTTTTAAACAGC[A/G]TTTAAAAGGAGAGGA | 115426 |
rs780766866 | in-del | -/AAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466552 | CTCAAAAAAAAAAGG[-/AAAA]AAAAAAAAAAAAAAA | 115426 |
rs780783949 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413238 | AGACATGGCCTCTTC[C/T]TATCTTTGAGGCGGT | 115426 |
rs780799407 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504218 | TTTTAGTAGCGATGG[G/T]GTTTCACTGTGTTAG | 115426 |
rs780809352 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476633 | CAGTTTTGCTCTTGT[G/T]GCCCAGGCTGGAGTG | 115426 |
rs780816943 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420624 | AGGCAGGAGAATGGT[A/G]TGAACCCGGGAGGAG | 115426 |
rs780825490 | snp | A/T | 1.6507e-05 | 0.00287284 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6498044 | CTGGCCAGAGATTTC[A/T]TCAAGCCATGGATTC | 115426 |
rs780842802 | snp | G/T | 5.24719e-05 | 0.00512183 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497149 | AATGACTCGATTGTG[G/T]ACTTGAAGAAAAATT | 115426 |
rs780850175 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6438427 | CACATTTTTGTACTT[A/T]AACTAAATAGGCTTT | 115426 |
rs780878426 | snp | G/T | 8.70985e-05 | 0.00659861 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421146 | GGAATATATAAGGTA[G/T]GTTGTTTTCTTCAGA | 115426 |
rs780893468 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433743 | GTCAATAGATTTAAG[A/G]TAGCACAAATCAGAA | 115426 |
rs780902341 | snp | C/T | 1.7598e-05 | 0.00296626 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434218 | TCATATTTTCATTTG[C/T]AGAAACCAAAGCCTT | 115426 |
rs780914530 | snp | A/C | 1.67773e-05 | 0.00289626 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420884 | ACATTTTAGAGAAGC[A/C]TTTCACTATTCTTTC | 115426 |
rs780949110 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6472275 | GAAGTTAGACCCTTT[A/G]AAGGGTTTAGGAAAT | 115426 |
rs780965632 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492074 | ATATGGTTTGAGCTC[-/T]TTACAGTCTTGACAG | 115426 |
rs780990015 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414524 | AGTTTTTTTCCTATT[C/T]CACAAGTCTCTTACA | 115426 |
rs780993689 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437595 | GTTGTCATATAGTTA[C/T]GCTGTAAATCTGTTT | 115426 |
rs781018456 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498493 | AAGGACATTTATCCT[A/G]GAGGGCACAGGGGGT | 115426 |
rs781025723 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451236 | AGTGAACTTGGTGTG[C/G]TTTCACATAACTTGT | 115426 |
rs781051614 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6414843 | CTCTCTTTAAAATAA[A/T]GTTATAGCACCTTTG | 115426 |
rs781071777 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499555 | TTTAAGGAAATCTAA[C/T]CACAACTCCTGAAGA | 115426 |
rs781091175 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432388 | TTATATTTTCAGTAA[C/T]TTATTTCTAAGTTCC | 115426 |
rs781121818 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502826 | AGAGAGTACCTGTTA[C/T]AAAGTTTCCAGCATC | 115426 |
rs781137642 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429135 | GCACCACTGCACTCC[A/G]GCCTGGGCAACAGAG | 115426 |
rs781175483 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6491460 | GCAGGGATGTAAAGG[A/G]TGTTATGAGAGAAGT | 115426 |
rs781178513 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454098 | CTCAAAACCACCATA[C/T]GAGATACAGTTACCA | 115426 |
rs781190261 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487388 | ATTTATTTTTTGAGG[C/T]GGAGTTTTACTCTTG | 115426 |
rs781212053 | snp | A/G | 0.000117892 | 0.00767672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486817 | CTCTTTAATTGTTTT[A/G]TAGGTGAGCGAAGCA | 115426 |
rs781215624 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503793 | ATGACCTTGAGACAC[A/G]TTGCCCATGATTTTT | 115426 |
rs781220093 | snp | A/G | 3.3024e-05 | 0.00406336 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481714 | TCAAGATGAGTAAAA[A/G]GAAAGCAAAGATGCC | 115426 |
rs781261459 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446250 | CCGCCTCCCAGGTTC[A/G]AGCGATTCTCATACC | 115426 |
rs781309644 | snp | G/T | 1.81585e-05 | 0.00301313 | intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6500516 | CTGCTTAGAACCACT[G/T]GTAAGTCTGCTGATA | 115426 |
rs781312268 | snp | C/G | 0.000132175 | 0.00812833 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482133 | TTAGTTGAAAGGGGA[C/G]AATTGGCTATCAGAT | 115426 |
rs781313483 | snp | A/C/G | 4.95351e-05 | 0.00497649 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434114 | CAGTGTACCCTCTAC[A/C/G]TCTAATTCAGACTGT | 115426 |
rs781313503 | snp | G/T | 3.31746e-05 | 0.00407262 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481950 | GGCTTTCATTAAAAT[G/T]TAACATAACTGATTT | 115426 |
rs781326855 | snp | A/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413721 | CGCACCGGTCCGAGG[A/G]CTCTGTGCGCCGCGC | 115426 |
rs781332259 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6458397 | TTTTCTTCTATGTTA[C/G]TCTGGCTGGCAGTCT | 115426 |
rs781335701 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429915 | AACCATCAAATATTT[C/G]CTGTTGGTATTTTCT | 115426 |
rs781335992 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419191 | GGGACGCAACTTAGC[G/T]CGTAACAGTAGGTTT | 115426 |
rs781359862 | in-del | -/T | 0.000230282 | 0.0107279 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422620 | AACTTAGATCTTTTC[-/T]TTTTTTTGAGACAGG | 115426 |
rs781378230 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416896 | TTCTTTCACTCCTTA[A/C]CACTATAGAGGTGGT | 115426 |
rs781386342 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6500960 | TTTGAGGTACTGTTC[C/G]TCAGAAGAATTTTCA | 115426 |
rs781413548 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6490457 | ACATGATGAAACTCC[A/G]TCTCTACTAAAAGTA | 115426 |
rs781418928 | snp | A/G | 4.99671e-05 | 0.00499811 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460773 | CCAAAAAAGAACTTC[A/G]TGTGAAAATTTTCCT | 115426 |
rs781440660 | in-del | -/TT | 6.60589e-05 | 0.00574675 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482117 | TGTTTTAACTTGGGC[-/TT]TTAGTTGAAAGGGGA | 115426 |
rs781453907 | snp | G/T | 3.38868e-05 | 0.0041161 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475549 | GTGTTGTACATGATT[G/T]AACTTTATTTTTACT | 115426 |
rs781489797 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6470166 | TCACTTGAGGTCAGG[A/C]ATTCAAGACCAGCCT | 115426 |
rs781507233 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479149 | ACTGGCTGCCTACCC[C/T]GTTCTCTGCTTCTTT | 115426 |
rs781528397 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6418509 | CTTGGACCACCTGAG[C/T]TCAAATTACTGATCT | 115426 |
rs781550834 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427206 | TTATGCCACTTGGTA[A/G]ATATTTTTTTTTATA | 115426 |
rs781577231 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480527 | CGTATCAAGGTCTTT[C/T]GCTTCACCTGAAACT | 115426 |
rs781595972 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6477105 | GGGTGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 115426 |
rs781603178 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428757 | TTTCACTATGTTGTC[C/G]AGGCTGGTCTTGAAC | 115426 |
rs781612834 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488258 | CTGTCTCCTTAAAAA[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 115426 |
rs781635155 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417742 | TGTGGATGTAACTTA[G/T]AGGGTCTCATGCCGT | 115426 |
rs781639001 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463615 | AGCTGGAACTACAGG[C/T]GCATGCCACCATGCC | 115426 |
rs781677241 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464352 | ATTTCAGTTATATGT[C/G]GCAAAAATACTTTTT | 115426 |
rs781717816 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477689 | TCATTCTTGCTCCTG[C/T]CGTGTATGTGGTGGG | 115426 |
rs781722852 | snp | C/T | 0.000357846 | 0.0133714 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422678 | GCAGTGACGTGAACA[C/T]GGCTCGCTGTAGCCT | 115426 |
rs781762669 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6440417 | CATCTATTAAACTGT[C/G]TGACTCAAGAGCCCA | 115426 |
rs781775936 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441636 | AGTTGATATATGACA[A/G]TTTAACTAAATATAT | 115426 |
rs796162012 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6437110 | TCATTAGAAAAATGA[A/G]TTATAAAATATAATG | 115426 |
rs796292936 | in-del | -/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499822 | TGTACTCTCCCTCCT[-/CC]CCCCCCATCAGTATC | 115426 |
rs796319703 | in-del | -/ACAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439061 | TCAAAAATTACAGAT[-/ACAA]ACACTAAGTTTATGA | 115426 |
rs796358949 | multinucleotide-polymorphism | CTC/TTA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6493295 | GAGCAAGACTCTGTT[CTC/TTA]AAAAAAAAAGTTAAG | 115426 |
rs796359848 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432852 | CCATTTTTTTTTTTT[-/T]CTTTTTGAGACAGAG | 115426 |
rs796371616 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6439484 | TATTCGATTGTCAGC[C/T]TTAAGGCCTACGTTA | 115426 |
rs796381026 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476392 | AGATTTATTTTTACA[C/T]GAGTAAAGCCTTAGA | 115426 |
rs796407412 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450305 | AGATTTCTTCCCCTT[-/C]CCCCCCCCCCATTTA | 115426 |
rs796414445 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483032 | GTGGATGCTCAAATT[A/G]CACACAAGCTCAGGC | 115426 |
rs796428411 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442983 | TTCCTTTATTGCTTT[A/G]TTTAACTTAGTGGTC | 115426 |
rs796448488 | in-del | -/AC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469704 | TACACGTATATACAT[-/AC]ATATACACACATATA | 115426 |
rs796468919 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461389 | TCCTCCTTCTCTCCT[-/C]CCCCCCCGCCCCTTG | 115426 |
rs796577583 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478827 | AGAAAGGGGGAAAGG[A/G]TATATCTTCTTCCTT | 115426 |
rs796625198 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492100 | GACAGTTTTTTCCCT[C/T]GTGATAATATAATGT | 115426 |
rs796704189 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441389 | ACCCCTCCCAAAAAG[-/A]AAAAAAAAAAAAGCA | 115426 |
rs796744538 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428543 | TTTTGCTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 115426 |
rs796759537 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6479472 | CATCCACTCCCACCC[C/T]CAACCCTGCCAAAGC | 115426 |
rs796863719 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506369 | GTCTTTTAAATATCT[A/G]AAGGTAGTTCCTGTA | 115426 |
rs796887493 | in-del | -/AG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488087 | CCCTACCAAAAAAAC[-/AG]AGAAATTAGCTGGGT | 115426 |
rs796894503 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436754 | AACACAGTACCTTAG[C/T]ATATATTTGGCAACT | 115426 |
rs796945350 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499829 | TCCCTCCTCCCCCCC[-/C]ATCAGTATCCAGCAG | 115426 |
rs796964898 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6435013 | AGTTTTTTTTTTTTT[-/T]AATTTTAGTTTTGAG | 115426 |