| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs139771127 | snp | A/G | 0.000249898 | 0.0111753 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121198 | TTTATGGAAAATAGA[A/G]AAGAATAAAATTAGC | 55728 |
| rs139830934 | snp | C/T | 8.24804e-05 | 0.00642132 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122208 | TGAATCCCACTCCAG[C/T]GATGGCCAAATCTCT | 55728 |
| rs139833016 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072803 | CCATCTCGGCTCACT[C/G]CAATCTCTGCCTCCC | 55728 |
| rs139900341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153281 | AAATAATTAGGTAAT[A/G]TGTATCATACTTTAA | 55728 |
| rs139904538 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067971 | AGGCATGAGCCACTG[C/T]ACCTGGCCTGTTTTT | 55728 |
| rs139926187 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059120 | CCACCACGCCCGCCC[A/G/T]GCCGTTTTAAAACGC | 55728 |
| rs139937701 | in-del | -/ATTA | 0.463989 | 0.129263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151959 | GTGTGTTTTAAATTT[-/ATTA]ATTCATCTCATTAAT | 55728 |
| rs139969069 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176084 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 55728 |
| rs139970227 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103580 | TTCATGGAATGGAAG[A/T]CTTAAATACATTAAT | 55728 |
| rs139976418 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108872 | GCCAGGCTGGAGTGC[A/G]GTGGCGTGATCTTGG | 55728 |
| rs139977281 | snp | A/C/G | 0.00130091 | 0.025473 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123176 | AGATCTGAATCTGGC[A/C/G]AAAGTGATTCATGAG | 55728 |
| rs140004913 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137445 | TTTCCCAAAGTGGCT[C/T]TACCATTTTATATTT | 55728 |
| rs140033050 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149722 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55728 |
| rs140149317 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081570 | AGGATTGCTTGAACG[C/T]GGGAGCTGGAGGTTG | 55728 |
| rs140180468 | snp | C/G | 0.000183136 | 0.00956738 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120319 | AAATAATCAAGAAGA[C/G]TGTGATCTTGCAAAT | 55728 |
| rs140204091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062912 | CATGTTCTTTTATTA[A/C]ATTGTGATTGCTTGC | 55728 |
| rs140246892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150900 | TAAGGGACTTTTATT[A/G]ATTTTATAAGATATG | 55728 |
| rs140252040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113581 | GTTTAGATTTTTCCC[C/G]TTGTAAATGATGAAT | 55728 |
| rs140282363 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059995 | CCCAAAACCTTATTC[-/T]TTTTTTTTTTTCTTT | 55728 |
| rs140319093 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155256 | AATTAGCTGGGTGTG[A/G]TGGCGTGTGCCTGTA | 55728 |
| rs140321161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128404 | AGAAATATACTGCCA[C/T]TCCCATCTTTGTATC | 55728 |
| rs140325334 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061371 | TTTTATTTATTTATT[C/T]ATTTATTTTTGAGAT | 55728 |
| rs140340662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063433 | GGGTATCAACTAGAA[A/C]CTTGACCAAATCTAG | 55728 |
| rs140356088 | snp | A/G | 1.65194e-05 | 0.00287392 | synonymous-codon, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142699 | AAAAGAGACTGAAGA[A/G]ACACCAAGTGAACTG | 55728 |
| rs140389936 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127188 | GCCACTGTGCCTGAC[C/T]GGCTGCATCTTCTTC | 55728 |
| rs140390956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095853 | ACTTTAGTTTTTTCT[C/T]TGAGTGATATGGAGA | 55728 |
| rs140402064 | snp | C/T | 0.00031398 | 0.0125256 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117997 | GTATTGAGTTGTGTG[C/T]ATATTCTTGTGAGGA | 55728 |
| rs140408003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060547 | ACTGTGCCCGGCCGC[A/G]CATACTTTAAAAATT | 55728 |
| rs140435634 | in-del | -/A | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109089 | CGAAGTGCTGGGATT[-/A]CAGACATGAGCCACC | 55728 |
| rs140464370 | snp | G/T | 0.0883596 | 0.190715 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165464 | ATGTTGGCCAGGCTG[G/T]TCTTGAACTCCTGGC | 55728 |
| rs140476856 | snp | A/G/T | 3.30914e-05 | 0.00406753 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121739 | GAAATGAGAGCTGTC[A/G/T]CTCCTGAAAACCATG | 55728 |
| rs140487761 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138038 | GAGGGGGTTGTGAGA[A/G]TGGATGGAGATGAGG | 55728 |
| rs140521189 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178568 | GATTATTAACGTGGG[C/T]ATACTTTATCATTGT | 55728 |
| rs140532699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167130 | CCTGGTGTTTGTGGT[A/G]ATCTGATATTATCAG | 55728 |
| rs140532800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096284 | TGGGATAAATGGTGT[C/T]GGGGCTCTGAGGTCC | 55728 |
| rs140597170 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092771 | GTCTCAGCCTCCCAA[A/G]TAGCTGGGACTACTG | 55728 |
| rs140599106 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163541 | GAAAGGTTTTCCTCA[A/C/T]GAATACAGAGAAACA | 55728 |
| rs140689851 | snp | C/T | 4.95291e-05 | 0.00497615 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102613 | AGCAAGTGACTCCAT[C/T]GCAGGTTGTAGCAGT | 55728 |
| rs140697612 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120285 | TGGAGAGAGTATCAC[C/G]TAGTACTTGCTGTAG | 55728 |
| rs140738542 | in-del | -/AAA | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148958 | AAAATCGAAAAACAG[-/AAA]AATGAAATGGAAAGT | 55728 |
| rs140747474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148850 | ATTGTGTCTATATCA[C/T]ATTTTTTTATCAATT | 55728 |
| rs140757809 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075585 | GTATTTTTAGTAGAG[A/C]TGGGGTTTCACCATA | 55728 |
| rs140798023 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151280 | TTTTTGTAAGTAAAC[A/T]TTTTCTTTTTGAGAT | 55728 |
| rs140806567 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40185093 | GTTTTTCTCTATTTT[C/T]TTCAGGTCTCCCTTC | 55728 |
| rs140811782 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145595 | AGAAACTTTAAGAGC[C/T]GTTTAAATTATTATT | 55728 |
| rs140824406 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112901 | TATAGACAGGATTTC[A/C]CCATGGTGGCCAGGC | 55728 |
| rs140829882 | in-del | -/AACA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178158 | AGCGAGACTGGGTCC[-/AACA]AACAAACAAACAAAC | 55728 |
| rs140877901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183794 | AGAGGTGGTAAGTGA[A/G]TCAACAATGCCAGGC | 55728 |
| rs140886859 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182502 | GTCACCCAGGCTGGA[C/G]TGCAGTGGCGGGAAC | 55728 |
| rs140937699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160075 | TCCATCCGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 55728 |
| rs140952051 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064556 | GGGGTTACAGGCGTG[A/T]GCCACCGCGCCCGGC | 55728 |
| rs140955860 | in-del | -/TA/TATA | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080310 | AGATAGTGTGAGCTG[-/TA/TATA]TATATATATATATAT | 55728 |
| rs140977451 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171334 | GAAAGAGAGTGCCAT[C/G]TTGTTTTCTACTTAT | 55728 |
| rs140985560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101362 | ATGGGGTTTCGCCAC[A/G]TTGGCTAGGCTGGTC | 55728 |
| rs141088581 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106061 | ACAGTGCCTGGCACT[C/T]AATAGATGCTACAGA | 55728 |
| rs141109013 | snp | A/T | 9.98585e-05 | 0.00706536 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102424 | TCCCATTTTTTCTAC[A/T]CAAAATATGAATTTG | 55728 |
| rs141110607 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064331 | CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTTGAC | 55728 |
| rs141177881 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091416 | TAGGTGCTTTTATCA[G/T]GTTGAGAATATTTTT | 55728 |
| rs141184557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174461 | TGCAGCATTACTTAC[A/G]GTAGCCAGGATGTGG | 55728 |
| rs141190727 | snp | G/T | 0.000856221 | 0.0206731 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102922 | GCCTCCTCCGCCACC[G/T]CCACCGATGTGGAAT | 55728 |
| rs141289798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085687 | CTGAGCTCTGGAACG[C/T]TGTATTGTTTCCAAG | 55728 |
| rs141291206 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129924 | CAAGGTTTTAGTTCA[C/T]TGATGAAACCTCAGA | 55728 |
| rs141306546 | snp | C/T | 0.000149687 | 0.00864992 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120556 | TTCATCCGTACAAAG[C/T]GACAAAAAGTATAAT | 55728 |
| rs141322644 | in-del | -/AG | 0.0479149 | 0.147179 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171583 | TCTTAATTGGAGGTA[-/AG]TTCTTTACAGAAGTA | 55728 |
| rs141326820 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108329 | TTTACTCTTTTTTTT[G/T]TGAGACGAAGTCTTG | 55728 |
| rs141354134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083503 | ATATTTTCTAGCAGT[A/G]TCGGTGAAGTACCAA | 55728 |
| rs141386495 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148486 | AGGGAGAGGGGGAGG[G/T]GGAGGGGGAGAGGGA | 55728 |
| rs141390674 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084205 | ATCCACCTGCCTTGG[C/T]CTCTCAAAGTACTGG | 55728 |
| rs141421931 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124820 | AGAAAACTTTTGGTT[C/T]GAGAGCAACAGAGTG | 55728 |
| rs141423439 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125440 | CTTCTTGGTCCTTAG[A/G]ATGGGTGGCCAGAGC | 55728 |
| rs141489567 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115432 | GCCTGGGAGGTCGAG[C/G]CTGTGATGAACTGTG | 55728 |
| rs141533511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062458 | GCTTTCAGTCTTCCA[A/G]TGCATTTTTCCCACT | 55728 |
| rs141641298 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119307 | AGCACTCCTGAAGTT[-/A]AAAAAAAAGAGGAAA | 55728 |
| rs141648286 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129237 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTGAGACAG | 55728 |
| rs141669143 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122102 | GATGAAGAAGAATTT[A/G]TGAATGAAGATGAGA | 55728 |
| rs141673295 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139455 | TACATAGACATGCAG[C/T]TGGGTTTTTTGTATT | 55728 |
| rs141691386 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143389 | TGCAATCTCCGCTAA[C/T]TGCAGCCTTGACCTC | 55728 |
| rs141759420 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140071 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 55728 |
| rs141763440 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068072 | GTATTTCTCTGATTA[G/T]TGATAAGTATCTTTT | 55728 |
| rs141766114 | snp | A/C/T | 0.0107286 | 0.0724924 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145927 | CAGCACTTCGGAGGC[A/C/T]GAGGTGGGCGGATCA | 55728 |
| rs141776332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101853 | TATTACTGTTTTCCT[A/G]AAAGAATAGGATTGC | 55728 |
| rs141779954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072645 | CCTCCCTGTACCCCC[A/C]CAGGCCTCCCAAAGT | 55728 |
| rs141803000 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183058 | AAACCAACCATGTTA[C/T]CCTAAGACAATTCCT | 55728 |
| rs141823165 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180445 | GCAGATAGTTAGTCA[C/G]TCTCATACATCACTG | 55728 |
| rs141834087 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142199 | CTTCACTTCAGCCTC[C/T]GCACTTATTCTCTTA | 55728 |
| rs141852513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087685 | GCACCCCGCCCCCTC[C/T]GCCCAAAAAAAAGGA | 55728 |
| rs141961185 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092785 | AGTAGCTGGGACTAC[G/T]GGCGTGCACCACCAT | 55728 |
| rs142054417 | snp | C/G | 0.000446683 | 0.0149379 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102320 | AACTCTTCTCCTGAT[C/G]ACCAAGTATACTCAT | 55728 |
| rs142065316 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162081 | GCCTCCACCTTACTT[A/G]TGCCTCCGAAATCTC | 55728 |
| rs142118972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123760 | AAAGTGTTGGGATTA[C/T]AGGCATGAGCCACTG | 55728 |
| rs142137288 | snp | C/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056592 | CTTGCTCTCCAACGG[C/G]AGAGCGGGAGCGGGA | 55728 |
| rs142152862 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156477 | ATCATATGTATTTTT[A/G]TGAAGCTGCTTAATT | 55728 |
| rs142161101 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084576 | AAGTAGCTGGGATTA[C/T]AGGCATGCACCTCCA | 55728 |
| rs142162262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165858 | TATTCTTTCTGTCTT[A/C]CATTCTTATATTCCG | 55728 |
| rs142172693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095777 | AGTACAGGAGTTAGC[C/T]GTGCAGATATCTTGA | 55728 |
| rs142182181 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118228 | GTTCGAGACCAGCCT[G/T]ACCAACATGGAGAAA | 55728 |
| rs142192697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162756 | ATAGGAGATAGATAG[A/G]GGATTTATCAGGAGA | 55728 |
| rs142261044 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159065 | TTATTACATAGGTAG[C/T]GCTATCCCAATTTAA | 55728 |
| rs142302313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177952 | ATGAAATGAGAGCAA[A/C]AGAAAACAGAAAGAT | 55728 |
| rs142320352 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078384 | CTAGGTGATGCACCT[G/T]CCTCGGCCACCCAAA | 55728 |
| rs142325313 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078138 | TGTGTGTGTGTGTGT[-/TG]GTGTGTGTGTATGTG | 55728 |
| rs142355696 | snp | A/C/T | 0.000665633 | 0.0182313 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126306 | AATGTCAGAAGAAAT[A/C/T]GCCTTACAGGAAAAA | 55728 |
| rs142438093 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109363 | CCCAGTGTCCCCTTT[A/G]TAAAAGGGAATAATA | 55728 |
| rs142439900 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067478 | GACTATTGTGAATAA[C/T]GCTGTGATAAACATG | 55728 |
| rs142476320 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150623 | CTGCAGTGAACCGAG[A/C]TCATCCCACTGCACT | 55728 |
| rs142480188 | snp | C/T | 3.35621e-05 | 0.00409633 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120432 | AACAAAAAAGCAAAT[C/T]GACTTTGGAAAAGTT | 55728 |
| rs142480719 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115869 | ATTGTTACTCATATC[-/A]TCCTGTATTTGAGAG | 55728 |
| rs142481323 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055526 | GACAAAAACCACTTG[C/T]ACTTGCCCCAAATTT | 55728 |
| rs142493174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070502 | TGCCCAGACTAGAGT[A/G]CAGCAGCACATTCAT | 55728 |
| rs142505583 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107674 | CAGGTGTGAGCCACC[A/G]TGCGTGGCCTATAAC | 55728 |
| rs142511365 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126811 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGTAATCTT | 55728 |
| rs142559844 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138738 | ATTTATTGCTGGACT[C/G]CTAATTCTATTCCAT | 55728 |
| rs142566669 | in-del | -/TG/TGTG/TGTGTGTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078113 | TTGAATATTTCTAAA[-/TG/TGTG/TGTGTGTG]TGTGTGTGTGTGTGT | 55728 |
| rs142570098 | snp | C/T | 0.000148245 | 0.00860815 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102989 | CATGGCTTTGTAGCT[C/T]CTGTTGTAACCACAG | 55728 |
| rs142619918 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063984 | TTGGTGGGGCGGCAG[G/T]GGGGGGTCTCACTAT | 55728 |
| rs142620956 | snp | A/G/T | 0.00676944 | 0.0578265 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132127 | CTATGTTTTTTTCCT[A/G/T]TAAATAAGAATTGAT | 55728 |
| rs142624379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178803 | TGGGATAAGACATGC[G/T]TAGTGCAGCTGCTGT | 55728 |
| rs142631549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144469 | CACTGAAATTTACCT[A/G]AATTTTGGTGCATTC | 55728 |
| rs142662562 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169838 | GGCGTGGTGGCAGGC[A/G]TCTGTAATCTGAGCT | 55728 |
| rs142699854 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136062 | TACAGATAATATAGT[A/G]TCACCGTCAAGATAT | 55728 |
| rs142799232 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100620 | CAAGCGATCTACCTG[C/G]CTCAGCCTCCCAAAA | 55728 |
| rs142810144 | snp | A/G | 0.000609349 | 0.0174443 | utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097451 | GCCAACCACTACTCT[A/G]CCTTCCATGGGTGAG | 55728 |
| rs142875658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080703 | ATGGAATCTCGCCCG[G/T]CTGGAGTGCAGTGGC | 55728 |
| rs142895641 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081338 | GCTTTCATTTCTAAC[A/G]TTCTCTTTTAAAAAA | 55728 |
| rs142902061 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125955 | CTACATTAACACATA[C/T]TATTTCTTACTTGCG | 55728 |
| rs142906134 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059026 | AGGTTTCGCCATGTT[G/T]CCCAGGCTGGTCTCA | 55728 |
| rs142939671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078024 | ATTTGTATAGCTGAT[A/G]AGGTTCTTTTTAGAG | 55728 |
| rs142941513 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118614 | GCTATGAATTCTCCT[C/G/T]CCAGTTTTACTTGAC | 55728 |
| rs142957884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164096 | GTGGGAAGGAAAGGA[A/G]ACAAAATTCACGATG | 55728 |
| rs142959429 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145937 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCT | 55728 |
| rs142968103 | snp | A/T | 0.0127207 | 0.0787309 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120015 | TAGAGTTCACTGAAG[A/T]GAAGAATCTTGATGT | 55728 |
| rs142992636 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184782 | CCAACATGGAGAAAC[C/T]CCATCTCTACTGAAA | 55728 |
| rs142995005 | snp | C/G/T | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085168 | CACTTGCCTTGGCCT[C/G/T]CCAAAGTGCTGGGAT | 55728 |
| rs143000186 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152597 | TTTTAAAACATACAT[C/T]TTAAAACATTAATTT | 55728 |
| rs143021031 | snp | A/G | 0.000862283 | 0.020746 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102373 | TAGTTTTAATGACTC[A/G]AGTGAGTTTATAAAT | 55728 |
| rs143023608 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161513 | AAAACTTGACAATCA[A/C]ACGACAGTTGGCATT | 55728 |
| rs143053355 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143107 | CTTATGTGAATTACA[A/G]TTTATTCTGACAGTC | 55728 |
| rs143096533 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154503 | GCTACAGTTTTAAAG[C/T]TTAAAATGCTCTGAT | 55728 |
| rs143143789 | snp | A/C | 0.000398764 | 0.0141146 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122248 | CTGTCTGGAATTGGC[A/C]TTACCCCCTGAACTG | 55728 |
| rs143171986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117253 | TGACCCTTAACCTCT[C/T]TTTCATATTTTCTAT | 55728 |
| rs143205833 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161771 | ATGTCTACTTTTGAA[-/T]GTATTCAAAGCTCTA | 55728 |
| rs143236475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163222 | TGTTTACTATGAACT[A/G]GGCACCACTGGGTAC | 55728 |
| rs143302329 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098507 | AATTAAATGTTGATG[C/G]TTAGTATTGTTACTA | 55728 |
| rs143308208 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061916 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 55728 |
| rs143339561 | snp | A/G | 0.000248043 | 0.0111337 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121543 | GAATTTCCAAAAATC[A/G]TGTGATGGATCACAA | 55728 |
| rs143340580 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097260 | TGTGCAAGATATTTA[A/G]CCCTATTTTGTTTGA | 55728 |
| rs143356184 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139059 | GAGTATCTTTCAGTT[A/C]TTTAGGTCTTCTTTA | 55728 |
| rs143364287 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094375 | TTATTGGTGTTGTTG[A/T]GTTCTATATATTTGC | 55728 |
| rs143365308 | in-del | -/AATATTTCTGTA | 0.0659589 | 0.169201 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089908 | GGTCCATTGCGAGTT[-/AATATTTCTGTA]AATATTTCTGTAAAT | 55728 |
| rs143372677 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063031 | GTAATTTTGGGGTTT[A/G/T]TCTAATACAGAGAGG | 55728 |
| rs143407209 | in-del | -/T | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078880 | GGATACTGCATTTTG[-/T]TTTTTTTTAAGAAAA | 55728 |
| rs143430220 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168886 | CGCGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 55728 |
| rs143443165 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139085 | CTTTAATTTCCTTCA[A/G]CAATGCACTATAGTT | 55728 |
| rs143445275 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136689 | TACTGTGCCTGGCTG[A/C]ATTACCAATATACTA | 55728 |
| rs143461937 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066130 | GAGATGGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 55728 |
| rs143476284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179242 | GGGTGTGGTGGCTGA[C/T]GCCTGTAGTCCCAGC | 55728 |
| rs143484346 | snp | C/G/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080197 | GAAAAAAGGAAGATA[C/G/T]GTAAGATTAGATGAT | 55728 |
| rs143495091 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164985 | TAAGCTCTGGGCTAC[A/G]TTTTTCTTTTCATTG | 55728 |
| rs143510315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133480 | AGCAGGGATTACAGG[C/T]GCACACCACTACGCC | 55728 |
| rs143510359 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176490 | ACAAGGAGTGGAGAG[G/T]GTATAGTTTTGACAA | 55728 |
| rs143517897 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117799 | TATTGTTTTCCTAGA[C/T]ATATGTTCTGATTTT | 55728 |
| rs143573452 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182971 | CATGAGCCACCATGC[A/G]TGGCCCCATTTAATA | 55728 |
| rs143579068 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137692 | GGCTTGCTACCCAAG[G/T]TCACATGGGGAGCCA | 55728 |
| rs143617683 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125065 | CCTGAGTTCCTCCAC[A/T]TGCCTCTGTTGTCCA | 55728 |
| rs143682335 | snp | A/G | 6.62943e-05 | 0.00575698 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120702 | CTTCAGAGCCACTCA[A/G]TAGCTATAAATATGA | 55728 |
| rs143706188 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114173 | GCATGGATGTACAGT[G/T]TGTTTTGCTTTGTGT | 55728 |
| rs143742131 | snp | A/G | 8.25607e-05 | 0.00642445 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121842 | AGGAAGAACTTTTAT[A/G]TAGCAGTAAGCAGTC | 55728 |
| rs143769722 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155298 | TTGGGAGGCTGAGGC[A/G]GGAGAACCGCTTAAA | 55728 |
| rs143802649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074959 | CTGCAGTGAGCTGAG[C/T]TCTTGCCACTGCACT | 55728 |
| rs143842335 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114460 | TTGCGTATACTGCAT[A/G]TAAATGGAACATACA | 55728 |
| rs143873470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153585 | CCTGCAGATGTGTAT[C/G]ATTAACTCCTACCCA | 55728 |
| rs143880858 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081621 | ATTGCACTCCAGCCT[A/G]GGTGACAGTGTGAGA | 55728 |
| rs143945855 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079694 | ATAGCCCTTGCTGCT[G/T]GGGAGGTTGAGGCAG | 55728 |
| rs143965051 | snp | A/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095527 | TTAATTTAAATTTAA[A/T]TAGGAACATATGGCT | 55728 |
| rs143984503 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154033 | TAGATAAAAGGAACA[C/T]AAACCTAGATGTTGG | 55728 |
| rs144086517 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065147 | TGTGGGAAACAAATA[A/G]CTAGGTACAGGTGGA | 55728 |
| rs144099403 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077809 | TGGATATTGTTCCAC[C/T]GAGGTAAATTATTCA | 55728 |
| rs144101433 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148351 | AGGCACTGGGCAGGC[C/G]GAGGCAGGAGAATCA | 55728 |
| rs144133716 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099917 | GTCCCTGCCCACCCC[C/T]GCCACCTTTTTTTTT | 55728 |
| rs144165469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140351 | GAGAGTGTACACAAG[A/G]TGATTATGAGACCTT | 55728 |
| rs144166686 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095963 | GGGACAAAGTTGCAA[A/G]CAGGGAGAACAGGTA | 55728 |
| rs144196138 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170915 | TTTGATATGTTGGAA[A/G]GGGATTGAAACTAGG | 55728 |
| rs144255226 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145564 | AAAATCTAGAAAACA[A/G]TAAAGATTAGAAAAG | 55728 |
| rs144261324 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115050 | TTATTTGAACTCCAT[C/T]GTAAGTTTTCTAATG | 55728 |
| rs144271199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131676 | TTCAGCCTTTAATCC[A/G]TAAAGAAAGTCTGTG | 55728 |
| rs144277369 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085495 | GGGGTCTCACTCTGT[C/T]ACTGAGGCTGGAGTG | 55728 |
| rs144298108 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156100 | ACTATAATTGTTAAT[A/G]AAATAAGATATTCCT | 55728 |
| rs144367447 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054319 | GGTGCGGTGGCTCAC[A/G]CCTTTAATTCCAGCA | 55728 |
| rs144402424 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161935 | AGGAATCAGGAGGCC[A/C]CCATGGCACTGTTGC | 55728 |
| rs144402576 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088858 | TGAACATCTTTTTAT[G/T]TACTTATTTGCCACC | 55728 |
| rs144413421 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054278 | ATTCTTAAATGTCTT[C/G]TTTGAAATTTAAAGA | 55728 |
| rs144434956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164314 | AACTTCAGAGTTCAG[A/G]ATATTAGGATGTGGG | 55728 |
| rs144471030 | snp | C/T | 4.98591e-05 | 0.0049927 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121313 | CAAGAAGCAATTCCA[C/T]ATAGAGTAATGTATG | 55728 |
| rs144472877 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109649 | CTTGAACCTGGGAGG[C/T]GGAGGTTTCAGTGAG | 55728 |
| rs144476955 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116846 | TTTGCTGGATATGTA[C/T]ATTCTATACTGACAG | 55728 |
| rs144505923 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063666 | TAATTTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 55728 |
| rs144537201 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156924 | GGTCCTAAGCATTTT[A/G]AGTAGGGGATACTCA | 55728 |
| rs144538398 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099303 | GCCGGAGTGCAGTGG[C/T]GCCATCTTGGCTCAT | 55728 |
| rs144544954 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112611 | AGCTATTTTCTCTGA[A/G]TTTGCCAGATTTCTT | 55728 |
| rs144556959 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102151 | ATCTTCACAAAGTTT[C/T]GTTGCTTCTGAGAAC | 55728 |
| rs144580031 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111022 | CTTGTGCAATGGTGT[A/T]TTATAATGTTTTCTT | 55728 |
| rs144606888 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076274 | TGAGGTCAAGAGTTC[A/G]AGGCCAGCCTGGCCA | 55728 |
| rs144637334 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40185162 | ATTTGAAAAGTAATT[A/T]GTCTTCTGTAAGGGG | 55728 |
| rs144640309 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112978 | CAAAGTGTTGGGATT[A/G]CAGGCGTGAGCCACC | 55728 |
| rs144640453 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072011 | CTCCCGGGTTCAAGC[A/G]ATTCTCATGCGTCAG | 55728 |
| rs144683847 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148949 | AAAAATTGAAAAATC[A/G]AAAAACAGAAAAATG | 55728 |
| rs144686962 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182512 | CTGGAGTGCAGTGGC[A/G]GGAACACAGCTCACT | 55728 |
| rs144702681 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110211 | ACATTTTATTAATCT[A/G]TTCATCAGTTAATAG | 55728 |
| rs144704283 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181386 | TTTCGATACTAGCTC[A/T]TCTTGTAGATTAACA | 55728 |
| rs144711327 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081212 | AGTAGCATATAAAAA[A/G]TATATTAAAAAAATC | 55728 |
| rs144723329 | in-del | -/G | | | splice-acceptor-variant | N4BP2 | GRCh38.p7 | 4:40185098 | TCTCTATTTTTTTCA[-/G]GTCTCCCTTCCATTC | 55728 |
| rs144744607 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119613 | GGTGTCCTCTCCTGG[A/G]AACAAATTCAGAGCT | 55728 |
| rs144748140 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145713 | CTCAATAAATATTTG[A/G]TTATCTTCTGTATTC | 55728 |
| rs144762362 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073942 | GGATTACAGGCGCAT[A/G]CCACCACATCCAGCT | 55728 |
| rs144811641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184053 | AGGGGAAGCTGAGAA[C/G]CAGGAATCAGAAGAT | 55728 |
| rs144855617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059736 | ATCAACCTCATTGCC[C/T]TCGTCCTCATAGTAA | 55728 |
| rs144877735 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181806 | ATACAAAAATTAGCC[A/G]AGCATGGTGGCACAC | 55728 |
| rs144981511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091434 | TGAGAATATTTTTGT[A/T]CCTGTTTTTCTGGTA | 55728 |
| rs145031236 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134118 | CCAGCCCAGTCTGTA[C/T]TTAAGAATATTTATT | 55728 |
| rs145036976 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086361 | TTTTGTTTTTGAGAC[G/T]AAGTCTTACCCTGTC | 55728 |
| rs145037363 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087977 | TGCCCAGGATGGTCT[C/T]GAACTCCTGACCTCC | 55728 |
| rs145070998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130409 | ACTCCTTTTTAGTCA[C/T]ATTGTTACCTCTTGT | 55728 |
| rs145102170 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128779 | GTGATTCGGCTTCCC[A/G]AAGTGTTGGGATTAC | 55728 |
| rs145109257 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055797 | ACTAAACATTTCACA[C/T]CAGAACCCAGAACAA | 55728 |
| rs145109339 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095057 | CTGGGATTACAGTCG[C/T]GAGCCCCTGAGTCTG | 55728 |
| rs145170564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162472 | TCAAAAAAGAAGAAG[A/T]AGTAGAGCTGGAGGA | 55728 |
| rs145181681 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103977 | CTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 55728 |
| rs145211813 | snp | G/T | 3.30115e-05 | 0.00406259 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102266 | ATGCAGCTAACTGAA[G/T]ACCTGGATTCCTTAA | 55728 |
| rs145212646 | in-del | -/TTTA | 0.200801 | 0.245111 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061356 | ATATTTTTATTTCAT[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs145222954 | snp | C/G | 0.00676609 | 0.0577691 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158658 | AGCCAGGCATGGTGG[C/G]ATACACCTGTAATCC | 55728 |
| rs145299564 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150906 | ACTTTTATTAATTTT[A/G]TAAGATATGATGGTG | 55728 |
| rs145305469 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107354 | GTGCTGAGTTTGCAG[A/C]AGTGAGCCACTGCGC | 55728 |
| rs145313505 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138582 | AGTTAATTTTTGTAT[A/G]TGTAGTGAGATAGAA | 55728 |
| rs145354197 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073166 | GCTAGCCACCTTCTA[C/T]AAAGATAAGGTTTCT | 55728 |
| rs145365383 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148077 | GGCTGCAATCTCCGG[C/T]ACTTTGGGAGGCCAG | 55728 |
| rs145379837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150298 | ACTGACTACCATTTT[A/G]TAGGGATTTACAGGG | 55728 |
| rs145381729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078818 | CAGGGATAAGCCACC[A/T]ACACTTGGCCTCAGA | 55728 |
| rs145410522 | snp | A/G | 0.00034726 | 0.0131723 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126243 | TGAAATGCTACCTTT[A/G]TTGGATCATTGGAAT | 55728 |
| rs145418246 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111610 | AGGCATGAGCCACCG[C/T]GCCCGGCCTTGTTTT | 55728 |
| rs145418454 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070067 | TTTAAAAACTTTCAT[C/T]AGGAAAATAGAGATA | 55728 |
| rs145481437 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109162 | TGATTCTTGGGTTTG[C/T]CATCTTCAGACATTG | 55728 |
| rs145513497 | snp | A/C | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158378 | TTTATTTCTGTACCA[A/C]AACTTTTCTTCTGGT | 55728 |
| rs145552670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178669 | ACGAAATAAGTTGCC[C/G]AGGACAAAACAAAGT | 55728 |
| rs145636040 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162856 | GCCAGTAGCATGGCC[A/C]AGTACAAGTCTGAAG | 55728 |
| rs145644327 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091299 | ACTTCCAGCATTATT[C/T]TGAATAAAATTGGTG | 55728 |
| rs145666039 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167387 | ACCTAAACATACTCT[G/T]ACAGAATTCCTGAAT | 55728 |
| rs145671794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058418 | TATTTAAGTGCCGTG[A/C]TAGGATGGGGGGTAG | 55728 |
| rs145707091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163588 | TTCTTGTTCAGCAAG[A/T]CTTTGTGTCTGTATG | 55728 |
| rs145746829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174326 | AGGCTGCAGTGAGCC[A/G]TGATCATTTAAAGAA | 55728 |
| rs145789263 | snp | G/T | 1.75801e-05 | 0.00296475 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126135 | ATACTACTTTGTAGA[G/T]CCTTCCTTGGTTGGA | 55728 |
| rs145799674 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172734 | CTACTGTAGCCCTAG[C/T]AAACTAATACAGTGA | 55728 |
| rs145836978 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184639 | TTGTTGCCTTTCAGA[C/T]GTGAAAAATTTTTTT | 55728 |
| rs145837891 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112430 | GTCTTTTATGAAAAG[A/G]TAGTGGTACTAAATT | 55728 |
| rs145943433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123772 | TTATAGGCATGAGCC[A/G]CTGTGCCTGACCTGT | 55728 |
| rs145978476 | snp | A/G | 0.000840523 | 0.020483 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142809 | GCTACAGCAAGGCCA[A/G]AGAAGCTTATCGGAT | 55728 |
| rs145992470 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179957 | TTAGTAGAGACAGGG[C/T]TTCTCCATGTTGGTC | 55728 |
| rs145996426 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065992 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 55728 |
| rs146011194 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176044 | GCAGTGAGTTGAGAT[C/T]GGGCCACTGCAATCC | 55728 |
| rs146015825 | in-del | -/CAAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178176 | AAACAAACAAACAAA[-/CAAA]GAACCCAACAAAACA | 55728 |
| rs146016093 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103030 | GAGATCTGTCAACTA[C/T]ACATTTCCACCCTCA | 55728 |
| rs146054780 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176811 | GTTCATGCTGTTTGC[A/T]GCAGGGAGGAACCTG | 55728 |
| rs146070102 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118235 | ACCAGCCTGACCAAC[A/G]TGGAGAAACCCGTCT | 55728 |
| rs146100707 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084431 | AGATATGCCTGGTTT[C/G]AGATTTTTTTTTTTT | 55728 |
| rs146121108 | snp | A/G/T | 3.59384e-05 | 0.00423889 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126108 | TTTATTGTTGAGAGT[A/G/T]TGACAGTATTTATAC | 55728 |
| rs146167456 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123175 | TAGATCTGAATCTGG[C/T]GAAAGTGATTCATGA | 55728 |
| rs146197935 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159441 | TTGGGAATCTAGGAA[A/G]GTTCATCATTCTGCC | 55728 |
| rs146219712 | snp | A/G | 0.000312935 | 0.0125048 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102941 | CCGATGTGGAATCCA[A/G]TGATTCCTGCTTTTG | 55728 |
| rs146223449 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121900 | TCCTAAAGATATGAG[G/T]GAAACAGAAAAAAAC | 55728 |
| rs146237208 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143831 | TTCTTGAGATGGTGT[A/G]TTAGAGTTCTCTAGA | 55728 |
| rs146260613 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068277 | CGTAGGTTGCCTTAT[C/T]ATTCTGTTGATTGTT | 55728 |
| rs146274670 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180901 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 55728 |
| rs146317861 | in-del | -/C | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055559 | CTCTGTTTAAAGCAA[-/C]CTGCCATAACAACCA | 55728 |
| rs146358001 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160710 | AACTGGGAGAGTTGG[A/G/T]GAAACAAAAGATTCC | 55728 |
| rs146360547 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088250 | CTGCTGTAAACATTT[C/G]TTTACAGGTTTTTAG | 55728 |
| rs146379586 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084975 | TAGAATGCAGTGGTG[C/T]GATTTCAGCTCACTG | 55728 |
| rs146409608 | snp | C/T | 0.000331472 | 0.0128696 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121151 | AAAGAAGTAGGCATG[C/T]GCACCCAGACTGAAC | 55728 |
| rs146416125 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112807 | CTCCTGGGTTCAATC[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs146438206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154104 | AAATATTATATTAAG[C/T]GTAGGTACTTGGAAT | 55728 |
| rs146502340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064200 | GACCTGTGTATTCCA[G/T]GTACGAAAATGGTAA | 55728 |
| rs146518108 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169880 | TGAGGCAGAGAATTG[A/C]TTGAACCTGGGAGGC | 55728 |
| rs146520771 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061459 | AACCTCCGCCTCCTG[A/G]GTTCAAGTGATTCTT | 55728 |
| rs146521222 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099941 | TTTTTTTCTTCCATT[G/T]TTAGGTTTTCTGTCC | 55728 |
| rs146542945 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064432 | AGCGCGCACCACCAC[G/T]CCTGGCTAATTTTTG | 55728 |
| rs146579145 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168201 | TAATAGTAAATATAA[A/G]CAAGAGAGAAGGAAT | 55728 |
| rs146598670 | snp | A/G | 3.34554e-05 | 0.00408982 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120382 | TGGTGAAATAGTGGA[A/G]GAAAGAGCAACAGTA | 55728 |
| rs146640312 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117007 | TTGCTTTTAATATCA[C/T]CTCTTTGTCTTTGGT | 55728 |
| rs146655087 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150872 | TGGGGGAAATTTTGG[A/T]AACTAATGATATTAA | 55728 |
| rs146693102 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40185239 | GCTGTGTGGCCTTAT[A/G]TAAGTTGCTTAACCT | 55728 |
| rs146761792 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136892 | TGTGTTAATGTCCCA[C/T]ACAACTTATTTTCAT | 55728 |
| rs146763378 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066197 | GCCTCCCAGTGTGTT[A/G]GGATTACAGGTGTGA | 55728 |
| rs146767453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070687 | AACTTGTAGTCTCAA[C/G]TGATCCTCCTGCCTT | 55728 |
| rs146776150 | snp | A/C | 0.0109441 | 0.0731594 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166695 | ACTCCATCTAAAAAA[A/C]AAACAAACAAACAAA | 55728 |
| rs146779982 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096076 | TTTTGGATATGTTAA[G/T]TTTGAAATGTTTATT | 55728 |
| rs146874842 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184586 | ATCTCCAATTTTACC[-/A]TTCAGAGACAGTCAC | 55728 |
| rs146879196 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138802 | TTGTCTTGATTACTG[C/T]GGCTTCTTGATTACT | 55728 |
| rs146879967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153604 | AACTCCTACCCACCA[A/G]TTTCAGTGTAGCATA | 55728 |
| rs146894293 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066936 | TTGTAGATACCGCAT[A/G]TAAGTAGAAACATGC | 55728 |
| rs146908834 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178923 | GGTACTTCTATTTGA[C/T]TTGCAGTGTGACACT | 55728 |
| rs147013669 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152182 | GCAATCCAGCTGTGA[C/T]TAGTGGATTTGCTAA | 55728 |
| rs147031180 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155306 | CTGAGGCAGGAGAAC[C/T]GCTTAAACCTGGGAG | 55728 |
| rs147089669 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064906 | TCCTGTACTCAGGAG[G/T]ATTACAGGTATGCAC | 55728 |
| rs147089808 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105612 | TGGAGTGCAGTGGCA[C/T]GTTCATAGCTCAGTG | 55728 |
| rs147104369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173235 | ATTGCTCAGATCCTG[C/G]GTATGGACAAATTGG | 55728 |
| rs147105928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101891 | CATCATTCAGACTTT[G/T]TGCTACTACAGACTT | 55728 |
| rs147134727 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131218 | TCAGTACCAGAAAAA[A/G]CTGTACTTCTGAGCA | 55728 |
| rs147139946 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063343 | TTCCGTACTTATACT[C/G/T]TGTGCATACTGGCTT | 55728 |
| rs147150958 | snp | A/G | 0.208779 | 0.246578 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169127 | GTGGTTCTCGCCTGT[A/G]ATCCCAGCACTTTGG | 55728 |
| rs147152022 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126896 | CCAAGAATCAGGGAC[A/T]ACAGATGTGTGCCAC | 55728 |
| rs147167879 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165289 | TGACTTGCTCTATCA[C/T]CCAGGCTGGAGTACA | 55728 |
| rs147197612 | snp | A/G | 0.000198942 | 0.00997154 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120750 | ACAAAAACTCATTCA[A/G]CATTATGGGTGACTG | 55728 |
| rs147224002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114316 | CAGTGTTGTGTGATC[A/G]TCACCCCTATGTAAT | 55728 |
| rs147239392 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148526 | TTTTAGGTTCCACAT[A/G]TAAGTGAGATCATAC | 55728 |
| rs147242895 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078345 | GTTTCACCATGTTGG[C/T]CAGGCAGGTCTTGAA | 55728 |
| rs147349956 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094449 | TGTTGAAGTCTCCAC[C/T]TATAATTGTGAATTT | 55728 |
| rs147367726 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136324 | GGCTAATCTGCCTGG[A/T]ATAAAGGATTAGAAA | 55728 |
| rs147384270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131722 | TCAGTAGTTTTGCAA[C/T]AAGTTAACCATGCCT | 55728 |
| rs147472127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152675 | ATGGCAAACCCCAAA[A/T]TCCTCATGAAAACAA | 55728 |
| rs147488657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149351 | TGTTGTATGATTTCA[C/T]TTTTACCAAATGTTC | 55728 |
| rs147543806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | N4BP2 | GRCh38.p7 | 4:40098684 | GCTCAGAAATGACAG[C/T]ATATTGAGTTTTGTA | 55728 |
| rs147590566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123724 | TCCTGGCTTTAAGTG[A/G]TCCTCCTGCCTTGGC | 55728 |
| rs147606684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162715 | ATGTAGCTTATTGGT[A/G]TATGTATTAGGGTTC | 55728 |
| rs147623169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158958 | AGAGCTTTTATCCAG[A/T]ATTATAATTATTCTT | 55728 |
| rs147680514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073304 | ACCTCCAGTGGCAAT[A/G]AGTGCAGTCTTTCTT | 55728 |
| rs147688947 | snp | A/G | 1.66521e-05 | 0.00288544 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126271 | AATACTCAAACTAAA[A/G]AAGTATCACTCAGAG | 55728 |
| rs147697051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070110 | ATGATACATTGAAAC[C/T]ACAGGTACCCACCTG | 55728 |
| rs147710833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181581 | TCTCTCTTGTTCCTC[C/T]GAGCTCAACTCGCGG | 55728 |
| rs147713072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109348 | TTATACTTTCCAAGG[C/T]CCAGTGTCCCCTTTG | 55728 |
| rs147726803 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178681 | GCCCAGGACAAAACA[A/G]AGTTTTGGAAAGGTT | 55728 |
| rs147732271 | snp | A/C/T | 0.00993785 | 0.0698258 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105795 | GGCTCAAGCAGTCTT[A/C/T]CCACCTCAGCCTCCC | 55728 |
| rs147801678 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085587 | TAAGCTTCCAGAGTC[G/T]CTGGAATTACAGGCA | 55728 |
| rs147818251 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128287 | ATTCGTTTGACTGCA[C/T]AAAGGAGCACCTTTA | 55728 |
| rs147834470 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124776 | TATGCTCTCAAAGCA[C/T]TTCCTGTTGAGGTTT | 55728 |
| rs147908101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104781 | GAAATAACAGGAAGA[A/G]TGTTGAGACATAGAA | 55728 |
| rs147924721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101650 | GGATCATGTAAATAA[A/G]TTAGATTTACTAAGA | 55728 |
| rs147925491 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145921 | TAATCCCAGCACTTC[A/G]GAGGCCGAGGTGGGC | 55728 |
| rs147926795 | in-del | -/AGGGGAA | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063226 | CTTGAAGTAGCCTGT[-/AGGGGAA]AGGGGAAAAAGTTAT | 55728 |
| rs147988332 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139298 | GAAAAGGGTCTTGCT[A/G]TGTTGCCCAGACTGG | 55728 |
| rs147991850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067307 | AGTTAGTTAGCCTTG[A/G]CCTTCCAAAATGCTG | 55728 |
| rs148009547 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080198 | AAAAAAGGAAGATAC[A/G]TAAGATTAGATGATA | 55728 |
| rs148060267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182974 | GAGCCACCATGCGTG[G/T]CCCCATTTAATATTT | 55728 |
| rs148061796 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111122 | ATTTTTGAATATTAG[A/C]TATATGGAAAAGTTG | 55728 |
| rs148080024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159632 | TTCTACTTACGTCCT[A/G]TTGACCAGAACCTAG | 55728 |
| rs148081889 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087511 | TGAGATTACAGGCAT[G/T]TGCCACCAAACCCAG | 55728 |
| rs148109069 | in-del | -/TTAT | 0.204189 | 0.245767 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093588 | ATTTTTGTATTTGTA[-/TTAT]TTATTTATTTATTAT | 55728 |
| rs148132445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093756 | TCAGTGCGCGTGCCA[A/G]CGCTCCTGGCTAATT | 55728 |
| rs148185596 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065407 | ACAGGCATTGAAGCC[A/C]TGGGTTTGAATGGAC | 55728 |
| rs148188777 | in-del | -/AAAAGGAAAAAAC | 0.482831 | 0.0910472 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083126 | CGGTGCAGACATAGA[-/AAAAGGAAAAAAC]AAAAGGAAAAAAAGA | 55728 |
| rs148202030 | snp | C/G/T | 0.000881819 | 0.0209796 | missense, synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102442 | AAATATGAATTTGAA[C/G/T]GGTGAAAATTTAGAG | 55728 |
| rs148223077 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113416 | TTTAAAATGTTTTTG[C/T]CTTTGTTGTATGTAG | 55728 |
| rs148290470 | snp | A/C/G | 4.94176e-05 | 0.00497059 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103026 | ACTGGAGATCTGTCA[A/C/G]CTACACATTTCCACC | 55728 |
| rs148291751 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125307 | GAAGTTGAAATGTTA[C/T]ACATTAAATTCTGTT | 55728 |
| rs148292693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058217 | TTTTTCTTTCAAACA[C/T]CAGCTGTCTTTTGTA | 55728 |
| rs148306107 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163272 | TAATCATAACCACCC[A/G]CTGGGGTAGGTATTA | 55728 |
| rs148322475 | in-del | -/ATCCC | 0.0569829 | 0.158885 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071284 | ATTACTTCTTCCTCT[-/ATCCC]ATCCCCTATATTTAT | 55728 |
| rs148345484 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061941 | AAGTGCTGGGGTTAC[A/G]GGTGTGAACCACCAT | 55728 |
| rs148391550 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126717 | CTCAAGTGATCCTCC[C/T]ACCTCAGCCTCCTGA | 55728 |
| rs148430797 | snp | G/T | 0.000138773 | 0.00832871 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122082 | AGGATTATGTGAAAT[G/T]TTCAGATGAAGAAGA | 55728 |
| rs148443048 | snp | A/G | 0.00133757 | 0.0258263 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131845 | TTGTGCCACTAAACT[A/G]AAGGAGAAGCAGCTC | 55728 |
| rs148445684 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063677 | AGACGGAGTTTTGCT[A/C]TTGTTGCCCAGGCTG | 55728 |
| rs148459267 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169837 | GGGCGTGGTGGCAGG[C/T]GTCTGTAATCTGAGC | 55728 |
| rs148466917 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072495 | GTGATCCACCCACCT[C/T]GGCCTCCCAACGTGC | 55728 |
| rs148512410 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140723 | CTGGTTTTCCTAGGC[A/T]GAGGACCCTGCGGCC | 55728 |
| rs148517413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069392 | AGATTGCACCACTGC[A/G]CGAAAGAGTGAGACT | 55728 |
| rs148528443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181404 | TTGTAGATTAACATA[C/T]CAATTAGGATTAGAT | 55728 |
| rs148534038 | snp | C/T | 0.0018381 | 0.03026 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152758 | AAATGAATTTTAACT[C/T]CCCTGATTTCTGTTG | 55728 |
| rs148535315 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081327 | TTGAGTGTCTTGCTT[A/T]CATTTCTAACATTCT | 55728 |
| rs148579388 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184694 | GGCATGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 55728 |
| rs148598918 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161959 | CTGTTGCCACAGCTG[A/T]CTCTTAACCATTCTC | 55728 |
| rs148602767 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089210 | TCCCCCCCTCTTCAG[C/G]CCCTGTTGGGCTCCC | 55728 |
| rs148656158 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095660 | CAATGGATAGTTAGC[A/G]GGAAAGGGGAGATTG | 55728 |
| rs148673587 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108218 | GGATTACAGGTTTGA[A/G]CCACCATGCCCAGCC | 55728 |
| rs148716615 | in-del | -/AAAT | 0.0977824 | 0.198317 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118436 | AAACTCCATTTCAAA[-/AAAT]AAATAAATAAATAAG | 55728 |
| rs148723633 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177487 | TGCGCATGGTGGCAG[A/G]TGCCTGTAATCCCAG | 55728 |
| rs148742747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115171 | TACTTGAAGGTTTAG[C/G]TCATTTTCTAATATG | 55728 |
| rs148758133 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156392 | ATCAATGTTAATATT[A/G]TGCCTTATTTTGATA | 55728 |
| rs148824698 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179091 | AACGTTTTGGAGGCT[A/G]GGCGCAGCAGCTCAT | 55728 |
| rs148832572 | snp | A/T | 8.34383e-05 | 0.0064585 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120202 | ACAGGCAACAGACAA[A/T]AGTGAAAACGAGCAA | 55728 |
| rs148848810 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117464 | GCTAAAGCATAACAT[C/G]TGGCCTCCTGGCAGG | 55728 |
| rs148865166 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158523 | CTCTTAGAGGCCAGA[C/T]GCGGTGGCTTATGCT | 55728 |
| rs148902611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057949 | GGTTGTAATGTCTCC[A/G]TGGCACAGTTCTGGC | 55728 |
| rs148913952 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163003 | ATGGTGGCTGGTTTC[C/T]CCAGAACAGGTAATC | 55728 |
| rs148917117 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129130 | TCTCAGCTCACTGCA[A/C]CTTTGCCTTTTGGGC | 55728 |
| rs148960654 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126210 | AGGCAAAAAATTACT[A/G]AAGACTTTAACAGCA | 55728 |
| rs148966282 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134622 | GACTTCCAGCAGGTG[A/G]GTGATTTTAAGGCCT | 55728 |
| rs148982595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172892 | ATATTACTGTTTGTT[A/G]AATAAACAAAGGAAT | 55728 |
| rs148987998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074153 | TGGAGTGCAGTGGCA[C/G]GATCTTGGCTCACTG | 55728 |
| rs149004458 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112470 | TTTTTTTGTTTGTAC[A/C]TATGTTATATATATT | 55728 |
| rs149038233 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142980 | GAATGTAGTAGTTAT[A/G]TAAGTGACATAAATA | 55728 |
| rs149053384 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154343 | GTTTTATTATAAATA[A/G]TATTCAATTATGAAA | 55728 |
| rs149056042 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083052 | ATAGAGTAAACCTAC[C/T]CCGTATACTTCAGCC | 55728 |
| rs149109498 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087318 | TGTGTTAATGGTTAC[A/G]GAGAGGGGAGTTTCA | 55728 |
| rs149129443 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066274 | TTGATTATGTAGTTG[C/T]AATTAAATTTAGTTC | 55728 |
| rs149178963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096911 | ATGTTAAATTTATAA[G/T]GCCTATTGGACATCT | 55728 |
| rs149196937 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109351 | TACTTTCCAAGGCCC[A/T]GTGTCCCCTTTGTAA | 55728 |
| rs149199322 | snp | C/T | 0.000165374 | 0.00909173 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121500 | TGTTGGATTCTGAAA[C/T]TAAGTTATGTGAGGA | 55728 |
| rs149213317 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150619 | GAGGCTGCAGTGAAC[C/T]GAGATCATCCCACTG | 55728 |
| rs149248582 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107084 | AAAGAAAAAATTCAC[G/T]TAGTATTTGTTTGTG | 55728 |
| rs149302189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110874 | GGTTCTTTGTTTCTT[C/G]ATTAGTGAGTTGTTA | 55728 |
| rs149319628 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152148 | TTGTTAACAATTGAT[G/T]ATCTTTAATAGTAAG | 55728 |
| rs149354451 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080908 | CCTGATCTCGTGATC[C/T]GCCCACCTCAGCCTC | 55728 |
| rs149362796 | snp | A/G | 0.000248606 | 0.0111463 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120633 | ATTGTGTCCAGCAAC[A/G]AGGATCTCCACATGA | 55728 |
| rs149371359 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119090 | GTCCCAAAGCTTTGT[A/C]ATCTCTGACAAGTTA | 55728 |
| rs149427045 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059592 | TGGCCTCAAGTGATC[C/T]GCCCGCTTTGGCCTC | 55728 |
| rs149442844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164159 | AGATACAGGCTGGTA[A/G]GGAGTCAAGTGGAAT | 55728 |
| rs149445903 | snp | C/T | 0.000859518 | 0.0207128 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102307 | TTTTGAGAAATTGAA[C/T]TCTTCTCCTGATGAC | 55728 |
| rs149476119 | in-del | -/AT | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083296 | CTCAAAAGGTTAAAC[-/AT]ATAGAGTTACCGTAT | 55728 |
| rs149495871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136513 | CCTCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA | 55728 |
| rs149506250 | snp | C/T | 1.64846e-05 | 0.0028709 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142778 | GCTTTCCTTCACCAA[C/T]AGAAGAGGATGGAGT | 55728 |
| rs149511105 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148320 | GTCACGCATGGCGGC[A/G]CGCGCCTGCAATCGC | 55728 |
| rs149513721 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077617 | GGCCACCACACTCGA[C/T]TAATTTTTGTATTTT | 55728 |
| rs149517277 | in-del | -/T | 0.0551013 | 0.156571 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123392 | TAACAGATTACTGTC[-/T]TTTTTTTTTCTCTCT | 55728 |
| rs149527846 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186127 | TTGATGCAAAAGCCT[C/T]TGGAATCCCTTGTTT | 55728 |
| rs149580031 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155968 | ACACTTATGTTTGTA[A/G]TAATTTATTTAAAGA | 55728 |
| rs149585243 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084287 | AGGATTTGCTGAATG[A/T]TGAGGTGTGACGGAA | 55728 |
| rs149585792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061906 | CTGACCTCGGGTGAT[C/T]TGCCTGCCTCGGCCT | 55728 |
| rs149634623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088713 | CCTTGTTGGTCAGGC[C/T]GGTCTCGAATTCCTG | 55728 |
| rs149653081 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131198 | GGGGAAATTTCTCTC[A/G]GGTCTCAGTACCAGA | 55728 |
| rs149684420 | snp | C/T | 0.000262814 | 0.0114603 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119976 | AAAAAGAAGAAAATA[C/T]TTTATCTTTATCTTT | 55728 |
| rs149684694 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158298 | TATTAGAGTTAGTGG[G/T]TTAAATATTTTAAAA | 55728 |
| rs149702907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099264 | TTTTGTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 55728 |
| rs149733638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162833 | CTGCAAGCAGGAGAA[C/T]TAGGGAAGCCAGTAG | 55728 |
| rs149738462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091278 | TCTCTTATTTCATGA[G/T]CTAGAACTTCCAGCA | 55728 |
| rs149756315 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103959 | CTATTTTATATGCTA[A/G]TTCTTTTTTTTTTGA | 55728 |
| rs149770069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181323 | TCTGTTCGTTTCTTC[C/T]GGATAGCAATTCAGT | 55728 |
| rs149775033 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108566 | TGATTCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 55728 |
| rs149825543 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111990 | TAAAATTAGCACATC[A/G]TGATTTTCAAATTAT | 55728 |
| rs149827298 | snp | C/T | 0.000115309 | 0.00759218 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40124163 | TTTTGTGTTTAGGAG[C/T]GACAAAGACAAGAAG | 55728 |
| rs149878648 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082572 | TGTGGAAGAGTTAGT[G/T]CCTTGAGCCCAGGAC | 55728 |
| rs149881641 | snp | A/G | 1.65663e-05 | 0.002878 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121093 | AGTAGAACCACAAAC[A/G]TTAGCTGAATGTCAA | 55728 |
| rs149895073 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122405 | CTGAGATGGAGTCTC[C/G]CTCTGTTGCCCAGGC | 55728 |
| rs149916929 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065977 | AGATCTGTCGACAGG[C/T]TGGAGTGCAGTGGCG | 55728 |
| rs149948565 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128771 | GACCTCAAGTGATTC[A/G]GCTTCCCAAAGTGTT | 55728 |
| rs149966189 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166593 | ACTTGGGAGGTTGAG[A/G]CAGGAGAATCACTTG | 55728 |
| rs149970229 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068596 | CATTGTGTGGCCTTG[G/T]TACCCTTGTTGAAGA | 55728 |
| rs149985803 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145214 | TCTCCCACTCCAGTA[A/G]TTTTTTTGTTTGTTT | 55728 |
| rs150004769 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091603 | ATAGTATACAATCCT[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs150038668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078816 | TACAGGGATAAGCCA[A/C]CTACACTTGGCCTCA | 55728 |
| rs150087614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146700 | TGACTTACTCTCATA[A/G]CAAATTTCAAGTATA | 55728 |
| rs150138865 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080556 | TGGCCAGGCTGGTCT[C/T]GATCTCCTGATCTAG | 55728 |
| rs150139629 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151472 | AGATGGGGTTTTGCC[A/G]TGTTGCCCAGGCTGG | 55728 |
| rs150190493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118876 | TAAATAAAAACAGCA[C/T]TAACTGACAGACAGA | 55728 |
| rs150208905 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160107 | TTACAGGTGTGAACA[A/G]TCACACCCGGCCAGG | 55728 |
| rs150212042 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064839 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAACCTC | 55728 |
| rs150228309 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101451 | AGGCATGAGCAACCA[C/T]GCCAAAAAGTGTGCA | 55728 |
| rs150228636 | snp | C/T | 8.30544e-05 | 0.00644363 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120574 | CAAAAAGTATAATTA[C/T]CCTCAGTCACACAAA | 55728 |
| rs150277674 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106229 | ATAGACCTGCCTTAG[A/G]TCAGATTTTTTTTGG | 55728 |
| rs150295708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182025 | CCTGGAGGTTGCTTA[C/T]ACCCCATTACCCAGG | 55728 |
| rs150333192 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076949 | TCTCTTTCTGAGGAA[C/G]TTGTTTGCTGATCGT | 55728 |
| rs150344391 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185842 | TAATAATAATGAGAA[C/T]GCAGCAGGCTTAGTT | 55728 |
| rs150349696 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113756 | TGAGTTTTATTTATT[C/T]GTTTATTTATTTAAA | 55728 |
| rs150356537 | snp | C/G | 3.29837e-05 | 0.00406088 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142730 | TCTTTCCAGGACTTT[C/G]AGTACCCAGACTATG | 55728 |
| rs150368230 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061445 | TCCCAGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 55728 |
| rs150401910 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084217 | TGGCCTCTCAAAGTA[C/T]TGGGATTACAGGCGT | 55728 |
| rs150403405 | snp | C/T | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121758 | CTGAAAACCATGAAT[C/T]GATGACAAGTATATT | 55728 |
| rs150419698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096388 | AACCAAGGTGTAAAG[A/G]TTCCCAGGGGAGAAC | 55728 |
| rs150436804 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162759 | GAGATAGATAGGGGA[-/T]TTTATCAGGAGAATT | 55728 |
| rs150438676 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138481 | TGTGCTTCATTGCCA[A/C]ATCCAATGTCATGAA | 55728 |
| rs150489213 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168827 | CCTCCCTGGGTTCAA[A/G]TGATCTCCTGCCTCA | 55728 |
| rs150491844 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071623 | CCAGGCTGGAGTGCA[A/G]TGGTGCGATCTCGGC | 55728 |
| rs150539605 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139682 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTCTT | 55728 |
| rs150594921 | snp | A/G/T | 0.000197777 | 0.0099424 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144702 | TCTTTGAGAAAGTCA[A/G/T]TGCTTCGCTGCTGCC | 55728 |
| rs150596894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072782 | CCACGCTGGACTGCA[A/G]TGGTGCCATCTCGGC | 55728 |
| rs150605086 | snp | A/G | 0.00060952 | 0.0174467 | utr-variant-5-prime, synonymous-codon, intron-variant | N4BP2 | GRCh38.p7 | 4:40097505 | CTTCACCAGTATCTC[A/G]GAGATATTTTCTGAT | 55728 |
| rs150644562 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111669 | TGCCCAGGCTGGAGT[A/G]CAGTGGCCTGATCTT | 55728 |
| rs150663503 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153193 | GTTGCCAATAATCAT[C/T]TGATAAAACTTTCTA | 55728 |
| rs150665854 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059063 | TGAGCTCAAGCAATC[C/G]AACTGCCTCCGCCTC | 55728 |
| rs150681888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164098 | GGGAAGGAAAGGAGA[C/T]AAAATTCACGATGCT | 55728 |
| rs150728677 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162192 | TTCTTTTAAACTTTA[C/T]GGAAAGGCTCATTAG | 55728 |
| rs150733605 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065809 | AGGCTTTTTTGGCAG[A/T]GTTTGGGAGGTAAGA | 55728 |
| rs150758210 | snp | A/C | 0.000878917 | 0.0209448 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120891 | CCTTATCTACAGCAC[A/C]TGAGGCCTGTTGGGG | 55728 |
| rs150805266 | snp | G/T | 0.000874811 | 0.0208959 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106942 | AGTCATTCTTAGTAC[G/T]GATGATTATTTTTAT | 55728 |
| rs150820578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183100 | GGCTTTGCTTCCTCA[C/T]AGTCTTTGGAAACAC | 55728 |
| rs150856854 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078482 | AAGTTTCTTGACTTG[C/T]GTATGGTGGCATAGC | 55728 |
| rs150873742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115586 | TTATTTAGTTATTTT[C/G]TAGTTTGCATTATGA | 55728 |
| rs150891560 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130828 | TAGGAAGTTATTTTT[C/T]AGACATCAGCATTTT | 55728 |
| rs150895545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062683 | AGTTCCTTGTATTTC[C/T]CCCTGAAGGGGTCAG | 55728 |
| rs150921711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40185014 | TGGGATTTTACTGTA[C/T]AGATAGTTTAATTTT | 55728 |
| rs150926611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085198 | TTACAAGCGTGAGCT[A/G]CCACACCCGGCCAAT | 55728 |
| rs150926929 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158015 | TTAATAAATGATTGA[A/G]TTAACTGTGAGGCTT | 55728 |
| rs150950895 | in-del | -/TTAGTAGCGATGGGGTTTCACATATTGGTCAGGCTAG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074268 | CTAATTTTTGTATTT[lengthTooLong]TTAGTAGCGATGGGG | 55728 |
| rs150975696 | snp | A/G | 0.00512125 | 0.0503428 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117842 | TATCAATATTCCTTC[A/G]ACCCTTTTTTCCCCT | 55728 |
| rs150994154 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132466 | ATTTAACTTGTCTTT[C/T]CAAATGACTAACCAA | 55728 |
| rs151048810 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101188 | TTGAGAGGGAGTCTC[A/G]CTCTGTCACCAAGGC | 55728 |
| rs151090835 | in-del | -/TTGT | 0.0490535 | 0.14873 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163092 | CAGTTATCTGCCAAA[-/TTGT]TTGTTAGAACCAAGC | 55728 |
| rs151139696 | snp | C/T | 0.00264821 | 0.0362918 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121408 | TCTTTGTAAACTGTT[C/T]GGATCCTTTTCATTA | 55728 |
| rs151207412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095809 | GAAGAGTATATCAAG[G/T]GCTAGCAGAGAGATA | 55728 |
| rs151208058 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165873 | CCATTCTTATATTCC[A/G]TAGATACCCCAAAGC | 55728 |
| rs151260852 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137693 | GCTTGCTACCCAAGT[C/T]CACATGGGGAGCCAG | 55728 |
| rs151262830 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066371 | TTGCTCAGGCTGAAG[G/T]GCAGTGGCATGATCT | 55728 |
| rs151284530 | snp | A/G | 0.000132538 | 0.0081395 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121664 | AGCCATGGGATTGGT[A/G]TTAGTAACGCTGACT | 55728 |
| rs151312372 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071338 | CTAAAGGTGTGAGTA[A/G]ACTTAGGTTAAACAG | 55728 |
| rs151328250 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109422 | GTTAAATGAAGGTGA[A/G]AAGTGTTAACATTGG | 55728 |
| rs151328509 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181859 | GAGGCTGAGGCATGA[C/G]AATTGCTTGAACCCA | 55728 |
| rs151336992 | snp | A/G/T | 0.000100064 | 0.0070727 | missense, stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120212 | GACAAAAGTGAAAAC[A/G/T]AGCAAATAGAAATGG | 55728 |
| rs180676313 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154168 | ATTTTCATCTTTAAA[A/G]TAACTCTTTTCTCAT | 55728 |
| rs180681541 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172907 | AAATAAACAAAGGAA[C/T]GGTTACATTGAATCT | 55728 |
| rs180683249 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126838 | TCTTGGCTCACTGCA[A/G]CCTCCATCTTTCGGG | 55728 |
| rs180699746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181156 | GTCTGTCTCAAAAAA[A/G]AAAAAAATATATATA | 55728 |
| rs180714412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069160 | AAAAAATTCCCAGCC[A/G]GGCACAGTGACTCAT | 55728 |
| rs180714921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147332 | ACACAGACACAGCGA[C/T]CATCCGATTTCTCAA | 55728 |
| rs180725740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164222 | GTGAGCAGTGAAGGT[A/G]TAGTTGAGGAAAGAA | 55728 |
| rs180737631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114166 | AGTCAAGGCATGGAT[A/G]TACAGTTTGTTTTGC | 55728 |
| rs180744059 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101316 | CATGCGCCGCCACTA[C/T]GCCCAGCTAATTTTT | 55728 |
| rs180909428 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133428 | GCAGCCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 55728 |
| rs180911040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175895 | GGAGATCGAGACCAT[C/G]TTGGCTAACACGGTG | 55728 |
| rs180915533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167814 | CTATACGTGTTAAAT[A/G]AAGACTCTTAAGATA | 55728 |
| rs180992369 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184871 | TGAGGCGTAAGAATC[G/T]CTTGAACCTGGGAGG | 55728 |
| rs181108094 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065064 | TGAGCCACTGTGCCC[G/T]GCTGGGGTTAGAGGG | 55728 |
| rs181137329 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158171 | TTTTTAAATTGAAAA[G/T]GTTTTATAAATTTGC | 55728 |
| rs181141042 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111450 | CTCAGCCTCCCAAGT[A/G]GTTGGGACTACAGGT | 55728 |
| rs181145879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097128 | TAGCTCTGCTGTTAG[A/T]GTTGGTGGTACTTTC | 55728 |
| rs181148250 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140298 | CCTGGAAAACATGCT[G/T]TCATGGATAGATAGA | 55728 |
| rs181148272 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081145 | TATAATAATGATTTT[A/T]TCCTGATTATGGAAA | 55728 |
| rs181191956 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104881 | GCGATCTCGGCTCAC[G/T]GCAAGCTCCGCCTCC | 55728 |
| rs181209241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072676 | AATAGGACTACACTC[A/G]TGAGCTACCACTCCC | 55728 |
| rs181220421 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087457 | CAACCTCTACCTCCT[A/G]GATTCAAACAATTTT | 55728 |
| rs181243572 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119341 | ATTGACAAATTTAAT[C/T]GAGAAAAATTAACTA | 55728 |
| rs181283990 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173177 | ACCCCTTGTCCCCTT[A/G]GAGGGGCTAGTTTAG | 55728 |
| rs181304642 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091513 | ATACAATTCTTTCAC[A/G]CATTAAAATGGTGGA | 55728 |
| rs181310749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076711 | GCCAGGATGGTCTCA[A/G]TCTCCTGACCTTGTG | 55728 |
| rs181318279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059058 | ACCCCTGAGCTCAAG[C/G]AATCCAACTGCCTCC | 55728 |
| rs181344009 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155990 | ATTTAAAGAATGCCA[A/G]CAGTTTAGCACACTT | 55728 |
| rs181357527 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115035 | AAACAAGTCTCAGCT[G/T]TATTTGAACTCCATC | 55728 |
| rs181359103 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136873 | AAGATGTTTGAAGAT[G/T]GCTTGTGTTAATGTC | 55728 |
| rs181395569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069572 | TAAAAACTTGGCATT[G/T]TTGAATTACATGTTT | 55728 |
| rs181432109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145293 | CAGTGGTGCCATCTC[A/G]GTTCACTGCAACCTC | 55728 |
| rs181435095 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084264 | CTTATTTTGAATTTA[C/T]AACTGGCAGGATTTG | 55728 |
| rs181438492 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107394 | TTGGCTTAGTATTTT[G/T]TTTTTTTCGAGATGG | 55728 |
| rs181440754 | snp | A/C/G | 0.0245149 | 0.108383 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183397 | CTGGAGTGCAGTGGC[A/C/G]CGATCTCTGCTCACT | 55728 |
| rs181448773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149549 | CGCTTAATTGCATAT[C/T]TTAAAATGGTTAGTT | 55728 |
| rs181457400 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166830 | CATATTAATCACATC[A/G]GGGTAAATGGGATAT | 55728 |
| rs181467784 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180429 | TGTTGTGATAATGCA[A/C/G]GCAGATAGTTAGTCA | 55728 |
| rs181485255 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054339 | TAATTCCAGCACTTT[C/G]AGAGGCCGAGGTGGG | 55728 |
| rs181489921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119480 | CTAATTTCTCTTAAT[C/T]GGGCAAATAGCGTTG | 55728 |
| rs181503465 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40158923 | AGCACTCGTTACTGG[A/G]GTTACAGGGTAAATG | 55728 |
| rs181504074 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131720 | CATCAGTAGTTTTGC[A/C]ACAAGTTAACCATGC | 55728 |
| rs181509153 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087800 | CTCTGTTGCCCAGGC[C/T]GAATGGCTCGATCTC | 55728 |
| rs181514234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110423 | TATTGTCCGTTTTTT[G/T]GATTATTCCTATTCT | 55728 |
| rs181515476 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073895 | CTTCCCAGGTTTAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs181518139 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095692 | GGCAGAGGGAGCAGG[G/T]TATATGATTTTCAGT | 55728 |
| rs181524513 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063627 | TATTGATTTATTTAT[G/T]TTTAATTAAATTAAT | 55728 |
| rs181564801 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101689 | AAAATACTTAATATT[C/T]AAAAGTTTGCATGCA | 55728 |
| rs181576717 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125831 | GGCGGAGGTTGCAGT[G/T]AGCCGAGACTGCGCC | 55728 |
| rs181593900 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162808 | GGCTGAGAAGTTCAC[A/T]CCAGGCCATCTGCAA | 55728 |
| rs181639617 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176515 | TGACAAAAGTACTCC[C/T]GAGGTGATTCTGATA | 55728 |
| rs181642261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180662 | GCACTGTTGGTAATA[A/G]CAAAAAAGTGAAATA | 55728 |
| rs181650135 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079701 | TTGCTGCTTGGGAGG[C/T]TGAGGCAGGAGGATT | 55728 |
| rs181657131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163572 | CATAGGAAGAAATGC[A/T]TTCTTGTTCAGCAAG | 55728 |
| rs181675467 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105103 | CACCACGCCCAACAA[A/T]CCTGCGTTGTCTTGA | 55728 |
| rs181844206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092087 | GTTAAGGATTTTTGT[A/G]TCTGTAGTCATGAGG | 55728 |
| rs181854848 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077002 | GGTCCTGTAACTTCC[C/G]TATATATTACATATA | 55728 |
| rs181873021 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126426 | ATTTTCTAGTCTAGA[A/T]TCCATATTTAACCTG | 55728 |
| rs181876492 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146160 | AGAGCGAGACTCTTT[A/C]TCAAAAATAAATAAA | 55728 |
| rs181876721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071757 | TTTTAGTAGAGACGA[A/T]GTTTCGCCATATTGG | 55728 |
| rs181880044 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108008 | GGCTCACTGCAACCT[C/G]CGCCTCCCACGTTCA | 55728 |
| rs181997021 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176733 | GTCCCTGAGACAGCC[A/C]TGTGGGAGAGGGTCC | 55728 |
| rs182010001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100287 | TGTTTCCAGACTTAT[C/G]TTTCTTAAAACAGCA | 55728 |
| rs182080818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184052 | CAGGGGAAGCTGAGA[A/G]GCAGGAATCAGAAGA | 55728 |
| rs182092734 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068977 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 55728 |
| rs182101014 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085282 | CTCAGGCAATCTGCC[A/C]GCCTCAGCCTCCCAA | 55728 |
| rs182106358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070360 | ATATCTTCAGATCTC[G/T]CCAAGGAAAAGGAGG | 55728 |
| rs182120701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139242 | GGAATTATGTCCTTT[A/T]TAAAAGTTTATTTTT | 55728 |
| rs182130906 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116063 | TTTCTTTTGTCTTTA[A/G]TAGTGATTTTTGTTG | 55728 |
| rs182132068 | snp | G/T | 0.00075677 | 0.0194374 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103230 | CAAGGTATGAGGTTT[G/T]ATTGGGTTTTTAAAA | 55728 |
| rs182155037 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080557 | GGCCAGGCTGGTCTC[A/G]ATCTCCTGATCTAGT | 55728 |
| rs182269763 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156510 | AAATTGCCTCCCACC[C/T]CACTATCTAGCATAG | 55728 |
| rs182274291 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173814 | TCTCTGCGTTATCAC[G/T]TTCTCTTTCCTCTCT | 55728 |
| rs182291948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111240 | ACTAAGAAATTGGTT[C/T]ATTATTATTAACTAA | 55728 |
| rs182293405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113270 | AGTAGCTAAATTTCT[A/G]ATAGTTAATTGCTGG | 55728 |
| rs182303454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059304 | AAAATCATATTGTAA[A/G]TCTTGGGAAGAATCA | 55728 |
| rs182313001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152566 | TTTGATGGATAGATT[A/G]CAATGAGGCTATGTG | 55728 |
| rs182327663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150229 | AAATATACACTGCTA[C/T]GTACGAATCATTTTT | 55728 |
| rs182366922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092520 | AATTTCTGTCTTCTT[C/T]TTTCTTTGTCAGTCT | 55728 |
| rs182367558 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177716 | AGTATCAAATGCTCT[A/C]ATTTTCTAGTGTCAG | 55728 |
| rs182377033 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082999 | GCCACCGCACCCGGC[C/T]GGGCTGTATTCTTAC | 55728 |
| rs182380859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160493 | CTCCTAGTCAGCCAC[A/G]CTAACGTTAACTTTC | 55728 |
| rs182431087 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064093 | GAACCACTATGCCTG[A/G]CCTCATCCACTGTAA | 55728 |
| rs182460198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059921 | AAAGTTACCCGACTA[A/G]TGTGTGGGAGTGTTA | 55728 |
| rs182556936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132598 | GATCCTGAGTTGCCA[C/T]CGTGTTGTTTTAATT | 55728 |
| rs182572159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095900 | ATCAGACCCTTTTTA[C/T]ATCGTATAAAGCTCA | 55728 |
| rs182575488 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167044 | ATTATTCAGTGTACA[A/C]ATTATATGTATTTTA | 55728 |
| rs182591897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170973 | CATGTTTATGATTGA[A/G]AGATTTATTTACTTT | 55728 |
| rs182626928 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108113 | TTGTATTTTTAGTAG[A/C/T]GACGGGGTTTTGCCA | 55728 |
| rs182634181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105684 | CCTCCTGAGTAGCTA[C/T]GACTACAGGCATGGG | 55728 |
| rs182661087 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142060 | CCAGCTTCGGCTCGG[C/T]ATCAGAGGGAGACCG | 55728 |
| rs182665389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077954 | TGCAAGGATATGACA[C/T]GCAGATTCGTGAAGT | 55728 |
| rs182675575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060938 | TTGTATGAGCATATC[C/T]TTTGATCATGTATTA | 55728 |
| rs182697460 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108613 | GCCACTACGCCTGGC[A/G]ATTGGTTTACTTTTT | 55728 |
| rs182703040 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092757 | CAAACGATTCTCTTG[A/T]CTCAGCCTCCCAAGT | 55728 |
| rs182716667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111614 | ATGAGCCACCGCGCC[C/T]GGCCTTGTTTTGTAT | 55728 |
| rs182717075 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075639 | CTGACCTTATGATTC[A/G]CCTGCCTCGGCTTCC | 55728 |
| rs182723006 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055646 | TTCTGGGAAAAACCA[C/T]TGCAAGTGGAATGAA | 55728 |
| rs182732296 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151243 | AAGAGTGTGAGTTAT[C/G]ATTAGAGATTTAGTT | 55728 |
| rs182737900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106331 | CTTTGTGTTTAATTT[C/T]TTTTCTTTTTTGAGA | 55728 |
| rs182741981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168872 | TGGAATTACAAGTGC[A/G]CGCCACCACACCCGG | 55728 |
| rs182750472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090662 | TTACAGCCAGGCGTG[A/G]TGAGTCACGCCTGTA | 55728 |
| rs182750812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134195 | TTTAAAAGTAGTATT[A/C]CAATCCCTAATTTTC | 55728 |
| rs182774284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139479 | TTGTATTAATTTTGT[A/G]TCAGCATTAGGCTTT | 55728 |
| rs182794329 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174358 | TTAAAAATAGAATTA[A/C]TAGATGAGCCAGCAA | 55728 |
| rs182806911 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156836 | CATTTGTAGGTTAGC[A/G]ATACTCAACAAGTAA | 55728 |
| rs182899516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182059 | TAGCCACATGACTAC[A/G]TTCAGCTGAAAAGAA | 55728 |
| rs182900096 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121100 | CCACAAACGTTAGCT[A/G]AATGTCAAGAGCAAA | 55728 |
| rs182916125 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074967 | AGCTGAGCTCTTGCC[A/T]CTGCACTCCAGCCTG | 55728 |
| rs182920935 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089975 | TGAGACTTAGGTCAA[A/G]GTTTATTTTTTACTG | 55728 |
| rs182928426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109008 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 55728 |
| rs182943059 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093072 | CCTCAGTCTCCGGAG[C/T]AGCTAGGATTACAGG | 55728 |
| rs182951532 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147745 | GACGGGGTGGCTGCC[A/G]GGCGGAGGGGCTTCT | 55728 |
| rs182957793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165673 | TGTACGTGTGTGTGT[A/G]TATATGTATATATAA | 55728 |
| rs182961079 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129153 | TTTTGGGCTCAAGCC[A/G]TCCTCCCACTTCAGC | 55728 |
| rs183110386 | snp | A/C/G | 8.36903e-05 | 0.00646831 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118028 | TAGAAGCACTAGGTA[A/C/G]GTTAAAATGCCTTAT | 55728 |
| rs183138692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181852 | TACTATGGAGGCTGA[A/G]GCATGACAATTGCTT | 55728 |
| rs183218957 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055313 | TTTAAGGATGAACAT[A/G]AAGTCTGTGATTTAA | 55728 |
| rs183255501 | snp | C/T | 0.00109442 | 0.0233669 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121338 | TGTATGATAAAAGCA[C/T]GTTTGTTGAAGAAAG | 55728 |
| rs183310370 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066000 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCTC | 55728 |
| rs183321597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070172 | ATTTGTTTTATCTAC[A/G]TATATAAATTTCCTG | 55728 |
| rs183372626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165398 | GAACTACAGGTGTGC[A/G]GCACCATGTCTGGCG | 55728 |
| rs183377650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160911 | AGCAGACTTAAAGAC[C/T]AAGACACTCCATAAA | 55728 |
| rs183382158 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103472 | TTCAAAATTGTGAGC[C/T]ATTGATGTAGTAGTA | 55728 |
| rs183446012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128330 | ATACATCCAGTTAAG[A/G]CATAGGGATTGCTCT | 55728 |
| rs183476442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071918 | TTATTTTATTTTTTG[A/G]CTTTTTGGAGACAGA | 55728 |
| rs183483539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081421 | GAGGCCGAGGTGGGC[A/G]GATTACCTGAGGTCA | 55728 |
| rs183488444 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137997 | CCCAGACAGGTGTTT[G/T]TTATCTCTAGGAATT | 55728 |
| rs183503396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078438 | CACCGTGTCTAGCCC[A/G]ATATTCCTAAATATT | 55728 |
| rs183506290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160280 | CCCGCCCTATTTAAT[A/G]TAGGATATATGTACA | 55728 |
| rs183533683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173461 | CTCATTGCTATACTA[A/G]GAGGCAGCATTTGTA | 55728 |
| rs183542054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074550 | TATATTTGAGGGACT[A/G]AAAAAACACCTCATG | 55728 |
| rs183553717 | snp | A/C/G | 0.0004494 | 0.0149841 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120548 | GAAAAAACTTCATCC[A/C/G]TACAAAGCGACAAAA | 55728 |
| rs183561876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175582 | TCCCAGCACTTCGGG[A/C]GGCCGAGGTGGGCGG | 55728 |
| rs183589443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119085 | AAAAAGTCCCAAAGC[C/T]TTGTCATCTCTGACA | 55728 |
| rs183593409 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087307 | GGGAAGCTTCTTGTG[G/T]TAATGGTTACAGAGA | 55728 |
| rs183593537 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105460 | CTCCTGAGTAGCTGG[C/G]ATTACAGGTATCTGC | 55728 |
| rs183595246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066387 | GCAGTGGCATGATCT[C/T]GGCTCATTGCAGCCT | 55728 |
| rs183606393 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157784 | AAGGTAAAATAAGTT[C/T]ATGTAGAATGTATGT | 55728 |
| rs183621513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140127 | ACTTTACAGAATCTT[A/G]TCATCCTGCAATCCT | 55728 |
| rs183628329 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177944 | CTTTTGTTATGAAAT[G/T]AGAGCAACAGAAAAC | 55728 |
| rs183631014 | snp | A/G/T | 3.30492e-05 | 0.00406494 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142841 | GGGAAAAAAAATGTC[A/G/T]CCACCTTTTATGCCC | 55728 |
| rs183657095 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179955 | TTTTAGTAGAGACAG[G/T]GTTTCTCCATGTTGG | 55728 |
| rs183731508 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156288 | AATATTATAATTATG[A/C]TTAATGAAGGAGCAG | 55728 |
| rs183736038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115786 | GTGTTGATTTTTTAT[A/G]CATTTCATATTTGCT | 55728 |
| rs183799111 | snp | C/T | 0.000132341 | 0.00813344 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102595 | CAGTAGTTCTTTAAA[C/T]GTAGCAAGTGACTCC | 55728 |
| rs183845899 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098789 | AATTACAAGAAATCC[A/G/T]CATCATCCTATACCA | 55728 |
| rs183848132 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082442 | GCAAAAGAATCCAAA[C/G]AGACATTTATTCAAA | 55728 |
| rs183856772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067161 | CTCCCCAGACTCAAG[C/T]CATCCTCCCACCTCA | 55728 |
| rs183865095 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135635 | TGGCACCATCTCGGC[A/T]CACTGCAACCTCTGC | 55728 |
| rs183876153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112479 | TTGTACCTATGTTAT[A/G]TATATTTATTTCCTT | 55728 |
| rs183987007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061450 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 55728 |
| rs184007693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152015 | TTCTGCTACAGCTTT[G/T]ATTAGTTTTCAGGAT | 55728 |
| rs184018866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111950 | TTTATGTCCTCAAAG[A/G]GATATTTAGAAGTTG | 55728 |
| rs184073952 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40054992 | CTGACTTAAGATTTG[A/C]TGAATCCTTAACAGA | 55728 |
| rs184089006 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081955 | CCATCTCTACTAAAA[A/G]TACAAAATTAGCCGG | 55728 |
| rs184098800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062650 | TGACACTTGGCTGTC[A/G]GTGTGCTAGCCCTAT | 55728 |
| rs184140981 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093568 | TGTGCCACCTTGCGT[G/T]GCTAATTTTTGTATT | 55728 |
| rs184169137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134480 | AACGGCTGGCTGATT[C/G]TCTCAGCTAGCAGTA | 55728 |
| rs184189214 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169546 | ATTAGAAACTGAACT[A/G]AAATGATAAACTTTG | 55728 |
| rs184227180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098259 | CTTTGGAGTCAAGAA[A/G]CGTGGGTTGGATTTC | 55728 |
| rs184268344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095188 | TCCCAGGTTCAAGCA[A/G]TTCTGCTTCAGCCTC | 55728 |
| rs184274519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079209 | TTATAGGCATAAGCC[A/G]CTGTGCCTGTCCTGA | 55728 |
| rs184281400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063225 | AGCTTGAAGTAGCCT[A/G]TAGGGGAAAAAGTTA | 55728 |
| rs184287327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079012 | GCTGGAATGCAGTGG[C/T]GCGATCTCAAGCGAT | 55728 |
| rs184287900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130966 | CAGTTTAGAGCAGAT[C/T]CAAATATGAAATGTG | 55728 |
| rs184290848 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148951 | AAATTGAAAAATCGA[A/G]AAACAGAAAAATGAA | 55728 |
| rs184305800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109902 | CAGGGCTGTGCATTC[A/G]TTAATACACTCTATT | 55728 |
| rs184319541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129581 | CTGGTTGGCTTTGTC[C/G]CAAGGATACCCACCT | 55728 |
| rs184339749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166550 | CAAAATTAGCTTGGC[A/G]TAGTGATGCATGCCA | 55728 |
| rs184349989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144942 | ATGTTATTCATTCTT[C/T]AAGAGAACCTTCTTG | 55728 |
| rs184383378 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071630 | GGAGTGCAATGGTGC[A/G]ATCTCGGCTCACTGC | 55728 |
| rs184417824 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086460 | CTCCTGCCTCAGCCT[C/T]CCGAGTACCTGGGAT | 55728 |
| rs184426538 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148179 | GAGCACTGAGTGAAC[A/G]AGACTCCGTCTGCAA | 55728 |
| rs184427463 | snp | C/T | 8.28535e-05 | 0.00643583 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106897 | TTCATTTATCTTTCA[C/T]AGGACTTTGCAAGAG | 55728 |
| rs184440128 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109639 | AGGAGAATTGCTTGA[A/T]CCTGGGAGGCGGAGG | 55728 |
| rs184443620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076557 | GCAGTGGCGCCATCT[C/T]GGCTCACTGCAAGCT | 55728 |
| rs184473760 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182784 | CAGGTTCAAGCGATT[C/G]TCCTGTCTCAGCCTC | 55728 |
| rs184486511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162252 | TATGCCTGTAATCCC[A/T]ACACTTCTGGGGGCG | 55728 |
| rs184495374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136005 | CTTTAGATATTGGAA[C/T]GTGAGTGTGTCAGAC | 55728 |
| rs184512218 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171817 | TGTAGTCAAAGTTCC[A/T]AGAGTCCCAGAGCTG | 55728 |
| rs184523436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153321 | TTATTCTTTTGAAAG[A/G]AAATCAGTATTTGTG | 55728 |
| rs184526473 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058938 | CCATCCTCCCACCTC[A/G]TCCCCTAGAGTAGCT | 55728 |
| rs184546635 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132124 | ATACTATGTTTTTTT[C/T]CTATAAATAAGAATT | 55728 |
| rs184550947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110585 | CTCTGTCACTTAGAC[G/T]GGAGTGCAGTGGCAC | 55728 |
| rs184562397 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091446 | TGTTCCTGTTTTTCT[C/G]GTAGTTACCATGAAT | 55728 |
| rs184564387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183559 | GCCAGGATGGTCTCG[A/G]CCTTCTGACCTCGTG | 55728 |
| rs184574961 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149707 | AGACCATCCTGGCTA[A/G]CACAGTGAAACCCCG | 55728 |
| rs184579892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179013 | GTGGCAGAAAGCATA[A/C]GACCATTATAAGGAA | 55728 |
| rs184580787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166935 | GTTGACTGTAGTCAC[C/T]CTTTTATGCTATTAA | 55728 |
| rs184599008 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183146 | GCACAGATACAATCC[C/G]AAGTCCTGTTTCTCT | 55728 |
| rs184755064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166645 | GGTGAGCCGAGATCA[C/T]ACCATTGCACTCCAG | 55728 |
| rs184797722 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069035 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 55728 |
| rs184800753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106609 | GCTGGAGTACGGTGG[C/T]GCAATCTCAGCTCAC | 55728 |
| rs184805391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091084 | TTGCTAGTATGTATA[A/G]ATACAGTTTCTTTTA | 55728 |
| rs184818413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161952 | CATGGCACTGTTGCC[A/G]CAGCTGTCTCTTAAC | 55728 |
| rs184825201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123593 | TGGGCACATGATCCT[C/T]CTGCCTTAGCCTCCA | 55728 |
| rs184828828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143431 | TGAACCTCCCACATC[A/G]GCCTCCCAAATAGCT | 55728 |
| rs184828851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083379 | CACAGCAAACTCTTA[C/T]ACAAATGTTCATAGC | 55728 |
| rs185012950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067535 | TGTTATTAATTATTT[G/T]GGATATGTACCCTGA | 55728 |
| rs185040943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064267 | GCTAGCTTATAACAA[G/T]TACTTATTTATTGAT | 55728 |
| rs185069959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071422 | TAAGAGGCATATAAT[A/G]TCAGGTCCCACTATT | 55728 |
| rs185086142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101446 | ATTACAGGCATGAGC[A/G]ACCACGCCAAAAAGT | 55728 |
| rs185088241 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114514 | ATCTTTTCACTTAGC[A/T]TAATGTTTTTAAGGC | 55728 |
| rs185089538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162867 | GGCCAAGTACAAGTC[G/T]GAAGGCCACAGAGCC | 55728 |
| rs185091872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060396 | ATTACAGGTGCACAC[A/G]ATCACGCCCGGCTAA | 55728 |
| rs185100870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083927 | ACAGATGGTAGTGGT[A/G]AAGGTGATGATTTTA | 55728 |
| rs185108803 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154619 | GTGCTTTGAGACCTG[A/G]TTCATGCCCCCCAAA | 55728 |
| rs185109327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082891 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTTTT | 55728 |
| rs185112919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172924 | GTTACATTGAATCTA[C/T]GAACTTTTTTGCTTT | 55728 |
| rs185116960 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136775 | TTCCTTCTGATTATT[A/C]TTGATTTTTTTTTGA | 55728 |
| rs185141271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099868 | ATTTTTTTCATAGAA[A/G]TACTCCTTACGTTTG | 55728 |
| rs185156947 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069209 | TTGGGAGGCCGAGGC[A/G]GGCACATCACTTGAG | 55728 |
| rs185177813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175085 | GAGTGCAGTGGCACA[A/G]TGAGAACTCACTGCA | 55728 |
| rs185183941 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139703 | TCACTGTCTTGGCCA[A/G]GCTGGTCTTGAACTC | 55728 |
| rs185184948 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180575 | TACTTAATTACTCAT[G/T]CACAATTCATTCATG | 55728 |
| rs185220533 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141545 | GCGGCCGGGAAGAGG[C/T]GCTCCTCACTTCTTA | 55728 |
| rs185239386 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113039 | TCTTAACATTTTTTT[A/T]AAGAACATTCTGTCA | 55728 |
| rs185239525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105630 | TCATAGCTCAGTGTT[A/G]CCTTGAATTCCTGGG | 55728 |
| rs185241875 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176790 | ACTGAGGTGGAGCCT[C/T]GGGAAGTTCATGCTG | 55728 |
| rs185252428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079916 | GGTTAAAATTATATA[A/G]TAGAGGTAGAAGAAT | 55728 |
| rs185260874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103856 | GGCAGCTTTGTAATG[A/G]TTTCAGTGGCACTCC | 55728 |
| rs185261521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160299 | GATATATGTACAGAT[A/G]GTCTCCCACTTAGGA | 55728 |
| rs185270964 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145928 | AGCACTTCGGAGGCC[A/G]AGGTGGGCGGATCAC | 55728 |
| rs185289258 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088626 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55728 |
| rs185304457 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095778 | GTACAGGAGTTAGCC[A/G]TGCAGATATCTTGAG | 55728 |
| rs185306691 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157554 | GCTCTGACAATGTTT[C/T]AACTGCTCTCAATTT | 55728 |
| rs185320973 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111482 | CGTGCCACCACACCT[C/G]GCTAATTTTTGTATT | 55728 |
| rs185335800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097136 | CTGTTAGAGTTGGTG[A/G]TACTTTCTTAGAGCT | 55728 |
| rs185339197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081175 | AAAATGCATTTCTTA[C/T]GGATTATGTGGAAAA | 55728 |
| rs185347122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150649 | GCACTTCAACCTGGG[C/G]AACAGAGTGAGACTC | 55728 |
| rs185351208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167934 | GAAGTAAAAACATTC[A/T]AAAAGTTTTATCTTA | 55728 |
| rs185356389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133629 | GCGTGAGCCACCTCC[C/T]CTGGCCAATTTTTAA | 55728 |
| rs185360085 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176056 | GATCGGGCCACTGCA[A/C]TCCAGCCTGGGCGAC | 55728 |
| rs185370063 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118372 | GGTGAGCTGAGGTTG[C/T]GGTGAGCCGAGATTG | 55728 |
| rs185425874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153871 | GATTTCTTCTTGGTG[A/C]TTTCATGATGCACCA | 55728 |
| rs185545855 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172499 | ACTGGTGTCCTTATA[A/G]AAAGGAGGAATTTGG | 55728 |
| rs185556036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136535 | GGGATTACAGGCGCG[C/T]GTCACCACACCCAGC | 55728 |
| rs185600487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065866 | ATACATGCGCAGTTA[C/T]TGGGGAGTACAAGTA | 55728 |
| rs185688946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113943 | AAGCTAGAACAGACC[C/T]TAGGATTTGGCACAC | 55728 |
| rs185734902 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057395 | GATCTGTTCCCGCCG[C/G]GACCTGACCTTGCGC | 55728 |
| rs185778521 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156070 | AAGCAGTTCCTTTAA[A/G]CAACTTACTATGAAA | 55728 |
| rs185809477 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075990 | TACCACCAGGCCTAG[C/T]TAATTTTAAATTTTT | 55728 |
| rs185810823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173394 | TAGATGCTGTGGGAA[C/T]ACAACCCCTGTCCTC | 55728 |
| rs185825734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100515 | GCCTCCTATGTGGCT[A/G]GTACTATACGCACAT | 55728 |
| rs185860302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167086 | TTTAGGCTGCCTTCT[A/G]GTACCAAATGTTATA | 55728 |
| rs185936525 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132726 | TTAAATAGGTACTTT[C/T]TGAGAATCTTTTGAG | 55728 |
| rs185938830 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074943 | GCCTGGGAGGCAGAG[C/G]CTGCAGTGAGCTGAG | 55728 |
| rs185960286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077293 | GTTGGGACTACAGGT[A/G]TGTACCACCATGCCT | 55728 |
| rs185987329 | snp | C/G | 0.0825414 | 0.185628 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108438 | CTGCCTCAGCCTCCC[C/G]CTGAGTAGCTGGGAT | 55728 |
| rs186006441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150316 | GGGATTTACAGGGGA[C/G]AGAGGAACATGTTAA | 55728 |
| rs186022565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184437 | AGAGAATCACTGAAG[A/G]GAATAAACTATATGA | 55728 |
| rs186047109 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091759 | GACCACAGGTACGTA[C/T]CACTATGCTTGGCTA | 55728 |
| rs186052514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168901 | GGCTAATTTTTTGTA[C/T]TTTTAGTAGAGACGA | 55728 |
| rs186059134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076915 | GGAAAGACATTGATG[A/C]TACTGGTTTTTGGTA | 55728 |
| rs186067315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059216 | TATGCAAAGCAGCAA[C/G]CATTTATTAGTTAAT | 55728 |
| rs186068466 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111372 | GTCACCCAGGCTGGA[G/T]TACAATGGCGTGGTC | 55728 |
| rs186080778 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055162 | GTTTTTAGTCTCTTA[C/T]AATGGTTGTTTAGAG | 55728 |
| rs186088480 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125844 | GTGAGCCGAGACTGC[A/G]CCATTGCACTCCAGC | 55728 |
| rs186092478 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107580 | ATAGAGACGGGGTTT[C/T]CCCGTGTTGGCCAGG | 55728 |
| rs186106193 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088571 | AATATTGTGATCTCC[A/G]CTCACTGCAGCCTCC | 55728 |
| rs186110660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074158 | TGCAGTGGCACGATC[C/T]TGGCTCACTGCAACT | 55728 |
| rs186112993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181596 | CGAGCTCAACTCGCG[A/G]CTTTCATTTCACAGT | 55728 |
| rs186120586 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127108 | GTTGCCCAGGCTGGT[C/T]TCGAGTTCTGGGGTC | 55728 |
| rs186135337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092544 | TCAGTCTTGCTAGTC[G/T]TTCAGTTTTATAGAT | 55728 |
| rs186138822 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105216 | GGATATCTGAGAAAC[A/T]ATTTTGTTGTCCTGT | 55728 |
| rs186139158 | snp | C/G/T | 3.34394e-05 | 0.00408886 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120375 | CCTCACCTGGTGAAA[C/G/T]AGTGGAAGAAAGAGC | 55728 |
| rs186169736 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054515 | GAACTCGGGAGGCGT[C/T]AAGTTGAAGTGAGCT | 55728 |
| rs186170790 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184939 | CCAGCCTGGGCAACA[A/G]AGCAAGACTCTGTCT | 55728 |
| rs186214317 | snp | C/T | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158495 | TAACTGATATCAAAA[C/T]TAAGAATTATATCTC | 55728 |
| rs186216377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119427 | TATGGCTTTAAAAAA[C/T]CTTACCAAATGACAT | 55728 |
| rs186236218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164340 | GTGGGTATTTGTTCC[C/T]AAGGGAGTTTGATTT | 55728 |
| rs186315806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126443 | CCATATTTAACCTGA[A/T]TGAATTTAATGTTAA | 55728 |
| rs186325499 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108009 | GCTCACTGCAACCTC[C/T]GCCTCCCACGTTCAA | 55728 |
| rs186340653 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180891 | GCACGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 55728 |
| rs186350561 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146800 | TGTACCCTTTGACCA[A/G]CATTTCATTTCCTCC | 55728 |
| rs186352680 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163992 | TGACTTTTCTCCAGC[A/G]ATTCTCAGGAATCAG | 55728 |
| rs186357235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140303 | AAAACATGCTGTCAT[A/G]GATAGATAGATGCAG | 55728 |
| rs186498764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087686 | CACCCCGCCCCCTCC[A/G]CCCAAAAAAAAGGAA | 55728 |
| rs186672291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137647 | GAAGGAAGTTTATCA[C/T]ACTCACAGAGTTCTG | 55728 |
| rs186685952 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | N4BP2 | GRCh38.p7 | 4:40098685 | CTCAGAAATGACAGT[A/G]TATTGAGTTTTGTAA | 55728 |
| rs186699810 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104907 | CCTCCCAGGTTCACG[C/T]CATTCTCCTGCCTCG | 55728 |
| rs186707596 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082087 | ATTGCACTCTAGCTT[A/G]GGCAACGAGCGAAAC | 55728 |
| rs186711022 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40073469 | GTAAGAAGACATGTT[A/G]GATAACAAGAAGAGG | 55728 |
| rs186717817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066771 | ATCTTAACCACTTTT[A/G]AGAGTACAGAACAGT | 55728 |
| rs186743054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101791 | ATTTATGTATTTACT[C/T]AATTCAGCAAATAAT | 55728 |
| rs186752962 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069867 | GTTCAAAGCTGTAGT[A/G]TTGTACCACTGCACT | 55728 |
| rs186782966 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141168 | CCAGTAGGGGCAGCC[G/T]GGCAGAGGCGCCCCT | 55728 |
| rs186819577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085798 | TTTAAGTGCTGTTGA[C/T]AGGTCTAGAAAGACA | 55728 |
| rs186882220 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115389 | GTGGTCCCAGGTACT[C/T]GGATGCTGAGGTGGC | 55728 |
| rs186948765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139263 | GTTTATTTTTTGATA[C/T]TACTTTTAAATTAAA | 55728 |
| rs186953251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176565 | CAACTCCAGTTAAGA[A/C]ATGTAGGATTAAGGC | 55728 |
| rs186953586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117451 | AAACCTTTGAGGGGC[C/T]AAAGCATAACATCTG | 55728 |
| rs186957642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103314 | TTGCTTAGTAGAGAT[C/T]TTTAGTAACCCCTAA | 55728 |
| rs186960977 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084546 | GTTCAAGCAATCCTC[C/T]CGGCTCAGCCTGGCA | 55728 |
| rs186962174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173969 | TTATTTCTAATTATA[A/T]AAGTAATAATGCTTG | 55728 |
| rs186972228 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156605 | CTAAATCCTGTATGC[C/T]CGCAGTAAAGATAGT | 55728 |
| rs186981914 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135647 | GGCTCACTGCAACCT[C/G]TGCCTCCTGAGTTCA | 55728 |
| rs186994680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112600 | TCTGTAAACTCAGCT[A/G]TTTTCTCTGAATTTG | 55728 |
| rs186997656 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098807 | TCATCCTATACCATA[A/G]CAAAAAAACTTTTTT | 55728 |
| rs187021233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152648 | AATCTGTCTTACTAT[C/T]ACAGTTTTGAGATGG | 55728 |
| rs187029172 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171136 | TAGCCTATCTTGCTA[C/G]GTTGCATATTTAAAG | 55728 |
| rs187056527 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063668 | ATTTTTTTGAGACGG[A/G]GTTTTGCTCTTGTTG | 55728 |
| rs187062756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082560 | CCACTAGGATTATGT[A/G]GAAGAGTTAGTTCCT | 55728 |
| rs187067596 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067189 | TCAGCCTTCTGAGTA[C/G]CTGGAACCACAGGTG | 55728 |
| rs187069052 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156305 | TAATGAAGGAGCAGT[C/T]AGAAGTAGAGGTGTG | 55728 |
| rs187089184 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115864 | ATGCTTATTGTTACT[C/T]ATATCTCCTGTATTT | 55728 |
| rs187134414 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159476 | CCAAGATAATGGCCC[G/T]CATTTTCCTAGGCCA | 55728 |
| rs187206913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173700 | TGGACCAGTTAGTCA[C/T]AGTCAAAGTCAAACT | 55728 |
| rs187226408 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174601 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGGCCA | 55728 |
| rs187254867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138571 | AATCCATTTTGAGTT[A/T]ATTTTTGTATATGTA | 55728 |
| rs187294245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108636 | TACTTTTTATGGAAG[A/G]TAGTGTGAGAATAAA | 55728 |
| rs187295966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092772 | TCTCAGCCTCCCAAG[C/T]AGCTGGGACTACTGG | 55728 |
| rs187302097 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078327 | ATCTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 55728 |
| rs187318001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128424 | ATCTTTGTATCCTAA[C/T]GCAATCCAAGGAATA | 55728 |
| rs187319522 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147616 | CCCTCCCGGACGGGG[C/T]GGCTGGCCGGGCGGG | 55728 |
| rs187349952 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092214 | TCTGGAAGAGATTAT[A/G]TAGGATTAGTATTAT | 55728 |
| rs187354027 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061190 | TTATTATTATTTTGA[C/G]GTAGAGTCTTGCTGT | 55728 |
| rs187359399 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059753 | CGTCCTCATAGTAAT[G/T]AAGTGGCTTATGTGT | 55728 |
| rs187398270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075915 | TACTGCAGCCTTGGC[C/T]TCTCAGGCCCAAACA | 55728 |
| rs187403525 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056406 | TCCGGGCCTGTTGCA[A/G]TGTTCCCCAGCGCCA | 55728 |
| rs187496394 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151589 | TGTAAAACTTTTATG[C/T]GTAATATAACATATG | 55728 |
| rs187508593 | snp | C/T | 1.65392e-05 | 0.00287564 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121764 | ACCATGAATCGATGA[C/T]AAGTATATTTCCCAG | 55728 |
| rs187508709 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106571 | TTTATTTTTTTGAGA[C/T]ACAGTCTTGCTCTGT | 55728 |
| rs187513382 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090856 | GAGAATTGCTTGAAC[C/T]CAGGAGGTGGAGGTT | 55728 |
| rs187536789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143264 | TTTTTTGGGAAGTAA[A/G]ATTTCTACCTGGGCT | 55728 |
| rs187542730 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147926 | TCCCCACATTTCAGA[C/T]GATGGGCGGCCGGGC | 55728 |
| rs187547159 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166289 | AGCAGGCTATCTGGC[A/G]GGATAGGCCTGTGGG | 55728 |
| rs187548904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129478 | GCAATTCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 55728 |
| rs187571956 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182279 | TGCTTCGAACAGGAC[A/G]TGGGTGAAAGATCAG | 55728 |
| rs187614083 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077003 | GTCCTGTAACTTCCC[C/T]ATATATTACATATAG | 55728 |
| rs187701843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182834 | GGCACCTGTCACCAC[A/G]CCCAGCTAATGTTTG | 55728 |
| rs187748084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084906 | AGGTGTGAGCCACAG[C/T]GCCTGGCTTTTTTTT | 55728 |
| rs187765670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070259 | AAGTATCATATGATT[A/G]TATTATAAATGTATG | 55728 |
| rs187780289 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109690 | ACTACTGCACTCCAG[C/T]CTGGGTGACAGAGCA | 55728 |
| rs187799605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152041 | AGGATTTATATCCTT[G/T]ATTTTCACAAGGTCA | 55728 |
| rs187805468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160685 | GTTAGAAAACTCAGA[C/T]TGACTCCCTAACTGG | 55728 |
| rs187810353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143945 | TAGGCCAGCTGTAAG[A/C]TAGAGAACCAAAGAA | 55728 |
| rs187812564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162111 | CACTGGAGTGTATCT[A/G]ATTGGTAGAAACTAT | 55728 |
| rs187816981 | snp | A/T | 3.36276e-05 | 0.00410032 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112063 | TTAAAAAATGATTTT[A/T]AATTATGTTATGTTT | 55728 |
| rs187848647 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179597 | CATGGAAATTAAATA[A/G]TTTTCCTGAGGTTAC | 55728 |
| rs187849957 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055454 | ATATATTACTAGTTT[C/T]TTGAAAAAGCACTAC | 55728 |
| rs187876705 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090277 | AGTTCCTTTGTCTTA[C/T]CAATTTTAGAATAAT | 55728 |
| rs187903905 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070668 | GTTGCCCAGGCTGGT[A/C]TTAAACTTGTAGTCT | 55728 |
| rs187986129 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166565 | GTAGTGATGCATGCC[A/T]GTAATCCCAGCTACT | 55728 |
| rs188026227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094455 | AGTCTCCACCTATAA[C/T]TGTGAATTTGTCTAT | 55728 |
| rs188046958 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139553 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 55728 |
| rs188058623 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130051 | TGTGAAATATTTTAA[C/T]TTATTTTTTTTTGAG | 55728 |
| rs188074044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177771 | CTTTGGCTCTCTTTA[C/T]GGCTGCTCCCAGCTC | 55728 |
| rs188082175 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142073 | GGTATCAGAGGGAGA[C/T]CGTGGAAAGAGAGGG | 55728 |
| rs188087650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069066 | CAGATGTTGCAGTGA[A/G]CCGGGATCGCGCCAC | 55728 |
| rs188121817 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074980 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGTGA | 55728 |
| rs188155017 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105748 | TAGAGACAGAGTCTT[A/C]CCAGCTTGCCCAGGC | 55728 |
| rs188260991 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158170 | CTTTTTAAATTGAAA[A/G]TGTTTTATAAATTTG | 55728 |
| rs188269200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119121 | CAAATCTTTCTGTAC[C/T]TCAGCTCTTCATTTC | 55728 |
| rs188271227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140138 | TCTTATCATCCTGCA[A/G]TCCTTATTAATAAGA | 55728 |
| rs188289390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175716 | GGGAGGCTGAGGCAG[A/G]AAAATCGCTCTCAAA | 55728 |
| rs188289734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071509 | AAAGTTATGGTTTTC[C/T]TTTTGCTTCTAGCAA | 55728 |
| rs188311635 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165408 | TGTGCGGCACCATGT[C/T]TGGCGAATTTTTGTA | 55728 |
| rs188326522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181917 | TCATGCTACTGCACT[C/T]CAGCCTGTGCAACAG | 55728 |
| rs188336781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157108 | AGAGGACTAATGTGG[A/G]AACCCCAGAGGGTGT | 55728 |
| rs188338243 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104482 | TATTCTGCTGATACA[C/G]TTATAAGCATATTTT | 55728 |
| rs188406604 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111835 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 55728 |
| rs188416359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081519 | GGTGTGGTGCCGCAT[A/G]CCTGTAATCCCAGCT | 55728 |
| rs188443099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079137 | GTGCTGGCCAGGCTG[A/G]TCTTGAACTCCTGAC | 55728 |
| rs188454687 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062845 | TAGGAGAAAGCCCTC[A/G]GATACTTCAAGTCTG | 55728 |
| rs188489850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178522 | AACTAGTGGTACTTG[A/G]GCAGCATGTACCTTT | 55728 |
| rs188498141 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155207 | GACCAGCCTGGCCAA[C/T]ATGGTGAATCCCCGT | 55728 |
| rs188520895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136848 | GTAAGCCAGTTTTTC[A/C]TATTCTTGTAAGATG | 55728 |
| rs188535354 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173072 | CCTCTACCCCCAGCC[C/T]AGAATAAAAAAGGAT | 55728 |
| rs188554195 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058982 | AAAGCCACTACGCCC[A/G]GCTAATTTTTGTATT | 55728 |
| rs188588661 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118212 | TCACCTGAGGTCAGG[A/T]GTTCGAGACCAGCCT | 55728 |
| rs188630771 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061607 | TAACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC | 55728 |
| rs188661765 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093340 | GCTTAGATTATTCAT[C/T]TGAGACTTCTTTTCT | 55728 |
| rs188662512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066165 | CAATCCCTTGACCTT[A/G]TGATCCACCTGCCTC | 55728 |
| rs188694813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097830 | TTCTGTCTCTTTCAT[A/C]TTCACTCTAGAACAG | 55728 |
| rs188727498 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131224 | CCAGAAAAAGCTGTA[C/G]TTCTGAGCAACTGGT | 55728 |
| rs188735288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149138 | AGAAATAAAAACACA[A/G]TATGTCTTTACGGAA | 55728 |
| rs188770283 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166759 | ATTTTGTGGGTACAT[A/T]GTAGGTGTATACATT | 55728 |
| rs188829687 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134259 | TGAGAGTTTTGTGTT[A/G]AAATCTCCCAGATGC | 55728 |
| rs188837634 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161150 | AAAAAAATGAGAAGT[C/T]GAGAATTGAATTGGT | 55728 |
| rs188842234 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169807 | CCATCTCTGTTAAAA[A/G]TACAAAAATTAGCTG | 55728 |
| rs188935014 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109084 | CCTCCCGAAGTGCTG[A/G]GATTACAGACATGAG | 55728 |
| rs188951930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078683 | GGTGTGCACCATTAC[A/G]CCCAGCTTATTGTTT | 55728 |
| rs189004674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095244 | TGCCACCACGCCTGG[C/T]TAATTTTTGTATTTT | 55728 |
| rs189008573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079369 | TGATCCTCCTTCCTC[A/G]GCCTTCCAAAATGCT | 55728 |
| rs189018476 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063315 | GGTGGGAACTTTCCC[A/G]TAGTTGGGACCTTTC | 55728 |
| rs189038340 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184648 | TTCAGACGTGAAAAA[A/T]TTTTTTCATATTAAA | 55728 |
| rs189098726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106693 | AGCTGGGACTATAGG[C/T]GCATGCCACCGTACC | 55728 |
| rs189122657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076035 | CTCCCTATGTTGCCC[A/G]GGCTTGTATTGAACT | 55728 |
| rs189139618 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104018 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 55728 |
| rs189141724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118737 | AAATACTCTTTCAAG[A/C]TAGTGTTATAAAAAT | 55728 |
| rs189155936 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086968 | TGCCCAGGCTGGTTT[C/T]GAACTCCTGGACTCA | 55728 |
| rs189170631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171968 | TGGAGTGCAGTAGGC[A/G]CGATCTCAGCTCACT | 55728 |
| rs189174703 | snp | A/G | 1.66399e-05 | 0.00288438 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126269 | GGAATACTCAAACTA[A/G]AAAAGTATCACTCAG | 55728 |
| rs189176780 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146124 | GCCAAGATCACGCCA[C/T]TGCCCTCCAGCCTGG | 55728 |
| rs189193342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107992 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 55728 |
| rs189209801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163343 | TTCTTTCTATTACAG[C/G]TCTTTTTGTTCAGGC | 55728 |
| rs189211362 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071632 | AGTGCAATGGTGCGA[C/T]CTCGGCTCACTGCAA | 55728 |
| rs189245228 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091810 | GTTGAGGTCTCACTG[A/T]GTTGCCCAGGCTGGT | 55728 |
| rs189266220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059225 | CAGCAACCATTTATT[A/C]GTTAATGAATTTCAG | 55728 |
| rs189362228 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087420 | CTAGGCTGGAGAGCA[G/T]TGGCTTGATCTTGGC | 55728 |
| rs189372399 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114165 | TAGTCAAGGCATGGA[C/T]GTACAGTTTGTTTTG | 55728 |
| rs189383817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091465 | GTTACCATGAATGGT[G/T]TTGAATTTTGTCATT | 55728 |
| rs189388384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125083 | CCTCTGTTGTCCAGT[C/T]CACACTGGGACCAAG | 55728 |
| rs189388577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101187 | GTTGAGAGGGAGTCT[C/T]GCTCTGTCACCAAGG | 55728 |
| rs189392595 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083386 | AACTCTTATACAAAT[A/G]TTCATAGCAACATTA | 55728 |
| rs189397539 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091274 | TTTTTCTCTTATTTC[A/C]TGAGCTAGAACTTCC | 55728 |
| rs189418239 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125758 | CAGGCATGGTGGCGG[A/G]CGCCTGTAATCCCAG | 55728 |
| rs189420993 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166977 | TATTCATTCTAACTA[C/T]ACTTTTACATTTTGA | 55728 |
| rs189426845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183753 | TGTGGCTTAGGTAAG[A/G]CATTTATCTCACATA | 55728 |
| rs189430736 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149845 | AAGCTTGCAATGAGC[C/T]GAGATCGAGCCACTG | 55728 |
| rs189535218 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162259 | GTAATCCCAACACTT[C/T]TGGGGGCGAAGGCAG | 55728 |
| rs189592138 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176503 | AGTGTATAGTTTTGA[C/G]AAAAGTACTCCCGAG | 55728 |
| rs189635478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104933 | CCTCGGCCTCCGGAG[G/T]AGCGGGACTACAGCC | 55728 |
| rs189654057 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072051 | TAAGCTGGGACTACA[A/C]GCATTTGCCACTATG | 55728 |
| rs189660051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107160 | GCTAGAGTGCAGTGG[C/T]ATGATCTTGGCTCAC | 55728 |
| rs189662833 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140906 | AGCACAGGGTTGGGG[A/G]TAAGGTCATAGATCA | 55728 |
| rs189671367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076574 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAT | 55728 |
| rs189681719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145056 | TAATCTGCGAATCCT[C/T]TCTGTGACTTATAAA | 55728 |
| rs189704540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177040 | TGGCGGAATTAAGGA[A/G]GAGTCCTGCAACATC | 55728 |
| rs189719830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160428 | GTGATGGGCTAGTGA[C/T]ATGTGGTGCAATACT | 55728 |
| rs189817893 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180246 | ATATTCAATAGAAAA[A/G]AATGGGCACAAGATA | 55728 |
| rs189825667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096089 | AAGTTTGAAATGTTT[A/G]TTAGATATATTCAAG | 55728 |
| rs189850147 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139828 | TTTACATTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 55728 |
| rs189889616 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080918 | TGATCCGCCCACCTC[A/T]GCCTCCCAAAGTGCT | 55728 |
| rs189898354 | snp | A/C | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064617 | CTAAATAAAACACTT[A/C]TCTGCAAGATGCTTA | 55728 |
| rs189902879 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087789 | ATGGAGTGTCTCTCT[G/T]TTGCCCAGGCTGAAT | 55728 |
| rs189924306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183276 | AATCTACCAATCATT[G/T]CTATACAGTATTCTA | 55728 |
| rs189936107 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077643 | ATTTTTAGTAGAGGT[A/G]GGGTTTCACTATGTT | 55728 |
| rs189941883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114663 | ACCTACAGTTTTTTT[A/G]TTCCTTGACTTGTCT | 55728 |
| rs189942092 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101491 | CTGTATTATATTACA[A/G]TGTAATTGTCTCTAA | 55728 |
| rs189945328 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119479 | TCTAATTTCTCTTAA[C/T]CGGGCAAATAGCGTT | 55728 |
| rs189946091 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060807 | ACAGGGTCTCGCTGT[G/T]TTGCTTAGGCTGGTC | 55728 |
| rs189974138 | snp | A/G | 8.29057e-05 | 0.00643785 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120945 | CATTGGGTAGCTCCA[A/G]TCTAGGAAGTTCTGA | 55728 |
| rs190079460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092665 | TTTTTTTTTTTTGAG[A/G]CAGAGTCTTGCTCTG | 55728 |
| rs190110376 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153391 | TTATAATTTAGGTAC[A/G]TTTAAACTTTAGCAG | 55728 |
| rs190111371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150878 | AAATTTTGGAAACTA[A/G]TGATATTAAGGGACT | 55728 |
| rs190114758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180590 | GCACAATTCATTCAT[A/G]TACAATCAATTCAGT | 55728 |
| rs190117703 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168817 | GCAACCTCCACCTCC[C/T]TGGGTTCAAGTGATC | 55728 |
| rs190117839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133798 | AGGAGTAGTCAACAT[A/G]TACTTTTTTGTGTGT | 55728 |
| rs190144191 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082989 | ACAAGTGTGAGCCAC[C/T]GCACCCGGCCGGGCT | 55728 |
| rs190148787 | snp | A/G | 0.030278 | 0.119257 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186283 | AGAATCAACTGCTAT[A/G]AAAATCACTGGTTAT | 55728 |
| rs190170849 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113146 | CTATATTAATAGCCA[C/T]GTAGTTATTTGTATC | 55728 |
| rs190181488 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111499 | CTAATTTTTGTATTT[C/T]TAGTGGAGACGGGGT | 55728 |
| rs190186372 | snp | A/G | 0.000131804 | 0.00811695 | utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097370 | GAAAAATCTTGGGGG[A/G]AATCCTTTTCGGAAG | 55728 |
| rs190199514 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063769 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55728 |
| rs190202478 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081219 | TATAAAAAATATATT[A/T]AAAAAATCACCTATG | 55728 |
| rs190216054 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157580 | AATTTAAGAAAATGA[C/T]GAAATGTATAAAAAA | 55728 |
| rs190221856 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132376 | CCTAATATTATAAAA[A/C]TTTTTCTTTATTATT | 55728 |
| rs190236067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095807 | AGGAAGAGTATATCA[A/G]GGGCTAGCAGAGAGA | 55728 |
| rs190358114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165433 | TTTGTATTTATAGTA[A/G]AGATGGGGTTTTGCC | 55728 |
| rs190368591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128879 | AAACTCTAACACTTA[A/G]GCTTAAATGGTGTGA | 55728 |
| rs190372072 | snp | A/G | 0.264358 | 0.249587 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147629 | GGCGGCTGGCCGGGC[A/G]GGGGCTGACCCCCCA | 55728 |
| rs190392370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181985 | AAGAGAGTACTTCTT[C/T]CCATTAAAGACATTC | 55728 |
| rs190397876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068418 | ATGAAGCTTTCTCCC[C/T]GTTTTCTTCTACGAG | 55728 |
| rs190420087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136091 | ATGACTGAATAATGC[A/G]GGGATGAGAGGTAGG | 55728 |
| rs190433464 | snp | A/G | 0.000186515 | 0.00965519 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100001 | GTCTCTGCCAGGCTT[A/G]CCCCCTCCAATCCCT | 55728 |
| rs190437688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080181 | ATAAGGAGGCTCTCA[G/T]GAAAAAAGGAAGATA | 55728 |
| rs190468829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172502 | GGTGTCCTTATAAAA[A/G]GGAGGAATTTGGACA | 55728 |
| rs190472409 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175126 | CCTGGCCTCAAGCAA[C/T]CCTCCTGCCTCAGCC | 55728 |
| rs190476262 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139850 | TTTTTTTTGAGACAG[G/T]GTCTCACTGTGTTGC | 55728 |
| rs190477493 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136662 | CGAAGTGCTGGGATT[A/G]CAGGCGTGAGCTACT | 55728 |
| rs190478615 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111065 | TTACATTGTGTGTGT[A/G]TATATTTGTCCATTT | 55728 |
| rs190621931 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108996 | TAGTTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 55728 |
| rs190730578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153960 | AGGTTTTGACAAATC[C/T]TAAGTTATACTAAGT | 55728 |
| rs190807158 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169481 | TATAAAAGATTTAAA[A/C]ATAATTATTTGAAAT | 55728 |
| rs190869329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088579 | GATCTCCGCTCACTG[C/T]AGCCTCCGCCTCCCG | 55728 |
| rs190871545 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074195 | TCCTGGGTTCATGCA[A/G]CTCTTCTGCCTCAGC | 55728 |
| rs190882984 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089258 | GGCATGAGCCACCAT[A/G]CCTGGCATACTGTTG | 55728 |
| rs190883729 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40054929 | GGTGTTGTCTTTGTG[A/G]CTTGAAATATATTTT | 55728 |
| rs190889422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111447 | TGTCTCAGCCTCCCA[A/C]GTAGTTGGGACTACA | 55728 |
| rs190897204 | snp | A/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055300 | ATAGTGATTTTTTTT[A/T]AAGGATGAACATGAA | 55728 |
| rs190929051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150418 | ATGCCTGTAATTCCA[A/G]CACTTTGGAAGGCCG | 55728 |
| rs190978842 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069297 | TGCAAAAATTAGCTG[C/G]GCTTAGTTGTTCTTG | 55728 |
| rs191006869 | snp | A/C | 1.67494e-05 | 0.00289386 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120390 | TAGTGGAAGAAAGAG[A/C]AACAGTAACGAAAAA | 55728 |
| rs191007045 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105400 | GTGATCTCAGCTTAC[C/T]GCAACCTCCACCTCC | 55728 |
| rs191036844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138772 | TCTGTATGTCTGTCC[G/T]ATTGCCAGTACCACT | 55728 |
| rs191043032 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181030 | TGGCATGTGCCTGTA[A/G]TCCCAGCTACTCGGG | 55728 |
| rs191056653 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115946 | CTTATAATTCTGCCT[A/G]TGTTTGCTTTACATA | 55728 |
| rs191058532 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164069 | GGCGGATAGGTATGG[C/G]AAGGGTTCAGTGTGG | 55728 |
| rs191119601 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085092 | TAATTTTTATATTTT[C/T]AGTAGAGACGGGGCT | 55728 |
| rs191123644 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070342 | GATTATATAAGAAGA[C/T]GTATATCTTCAGATC | 55728 |
| rs191139061 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074960 | TGCAGTGAGCTGAGC[A/T]CTTGCCACTGCACTC | 55728 |
| rs191141599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127862 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 55728 |
| rs191155919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167407 | AATTCCTGAATCTCA[A/G]AGTTAAAGAGAAAAA | 55728 |
| rs191162258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165218 | GTGATTTTATTGTAA[A/G]CTAGCTCAAATCTTT | 55728 |
| rs191162571 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144409 | TTTTGGTTCAGAAAA[G/T]GTTAGAAAGAATGAC | 55728 |
| rs191163456 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105682 | GGCCTCCTGAGTAGC[C/T]ACGACTACAGGCATG | 55728 |
| rs191169741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133190 | AGTATATTTTCAACT[C/G]TGGTTAGTTTATTTC | 55728 |
| rs191220304 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177831 | CTCACATGCAGGGCT[C/T]TTTAGGGGACAGCAA | 55728 |
| rs191265484 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084241 | CAGGCGTGAGCCACC[A/G]CACCCAGCTTATTTT | 55728 |
| rs191288937 | snp | A/G | 0.000461878 | 0.0151897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112182 | GCTTTGGTTAGTACC[A/G]TAAGTTGTCATAAGT | 55728 |
| rs191380471 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108461 | GCTGGGATTACAGGC[A/G]CGTGCCACCATGCCT | 55728 |
| rs191408886 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181671 | GACAAAGAAGTCCGG[G/T]TGCGGTGGCTCACGC | 55728 |
| rs191419458 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147428 | CAATGAGCTGTTGGG[C/T]ACACCTCCCAGACGG | 55728 |
| rs191448605 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160738 | TCCAGATGAAAATAC[G/T]AAACACACACTAAAA | 55728 |
| rs191555005 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098713 | TAAGTTACTTTGACA[C/T]TTCCTAATTTTGATA | 55728 |
| rs191557220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082158 | GCGAGCGCCTGTAGT[C/T]CCAGCAAACTGGGAG | 55728 |
| rs191570192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066987 | GCTGTTTTTGGGGTG[A/G]CTGGCTTATTTCACT | 55728 |
| rs191700593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173446 | AAAGAAAATAGGATA[C/T]TCATTGCTATACTAG | 55728 |
| rs191706187 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156663 | ACCCATTTCTAAATC[C/T]TGTATGTCAAAGATA | 55728 |
| rs191706737 | snp | C/T | 0.021333 | 0.101051 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084695 | AGTGCAGTGGCATGA[C/T]CTTGGCTCACTGTAA | 55728 |
| rs191711708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109788 | TATATGTTAATAGGC[A/G]GAATTCATTTTAAAA | 55728 |
| rs191726640 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156231 | TTTCCTTACCTAGTT[A/T]TAAAAATCATCACTT | 55728 |
| rs191728437 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115482 | GCCTAGGCAACAGAG[C/T]GAGACTCTGTCTCCC | 55728 |
| rs191762653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094738 | TGTATTTTTAGTGGA[A/G]ATGGGGTTTCTCCAT | 55728 |
| rs191763231 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075397 | TTTACACAGCTTTTC[G/T]TTTATTTATTTATTT | 55728 |
| rs191764742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117568 | ATATGAGCTTATAAT[A/G]AAAAACATTTTTGAA | 55728 |
| rs191766827 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139368 | TTCCAAAGTGCTAGG[A/G]TTACAGGCTTGAGCC | 55728 |
| rs191773522 | snp | A/C | 0.0185938 | 0.0946107 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055559 | ACTCTGTTTAAAGCA[A/C]CTGCCATAACAACCA | 55728 |
| rs191774210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079173 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 55728 |
| rs191780370 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062886 | GCCTCCTCTTTGTGT[C/G]CTTAGCACTCCATGT | 55728 |
| rs191815500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135764 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 55728 |
| rs191819413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112999 | GTGAGCCACCATGTC[C/T]GGCCGAAAATTCTTT | 55728 |
| rs191822318 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098935 | TCTATGTTGCTGTAA[G/T]CTGTATTTTTAATGG | 55728 |
| rs191914980 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153264 | TTCTTTGATAATATG[C/G]AAAATAATTAGGTAA | 55728 |
| rs191925191 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171622 | GGATTAGTCAGGGTT[A/C]TCTAGAAGGACAGAA | 55728 |
| rs191934569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097861 | ACTGGCACTGTTGAC[A/G]CTTCAGGCTACATAA | 55728 |
| rs191943993 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066270 | ATTATTGATTATGTA[A/G]TTGTAATTAAATTTA | 55728 |
| rs191959586 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159643 | TCCTATTGACCAGAA[C/G]CTAGTCATGTCATAT | 55728 |
| rs191962433 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134424 | TGATTGGTCAGCCAG[A/G]GCCCTCATGTTAGGT | 55728 |
| rs191980738 | snp | A/G | 0.000681125 | 0.0184418 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102476 | TCTGGTTCTACTTTA[A/G]GTTTAAACCCATTAC | 55728 |
| rs192003532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173801 | CAGTATTTCCTTTTC[C/T]CTGCGTTATCACTTT | 55728 |
| rs192005368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070138 | CTGCTTGATTCAACA[A/G]TTGTTACCATTTTGC | 55728 |
| rs192010733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077123 | TAGTTGGTCGATATT[A/G]AATATTATGTAGAAT | 55728 |
| rs192011990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137667 | ACAGAGTTCTGGAAA[C/T]AGGAGGTATGGCTTG | 55728 |
| rs192037400 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108036 | TCAAGGGATTCTCAT[C/T]CTCAGCCTCCCAGCC | 55728 |
| rs192189597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152109 | ACTCCTTTGATGTTT[C/T]AAGAACTATCTATCA | 55728 |
| rs192230637 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071554 | GGTGGTACTTTGACA[A/T]CAGGTAAATTTTTTA | 55728 |
| rs192247487 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078335 | TAGAGACAGGGTTTC[A/T]CCATGTTGGCCAGGC | 55728 |
| rs192252933 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081949 | GAAACCCCATCTCTA[A/C]TAAAAATACAAAATT | 55728 |
| rs192275321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151742 | TCAGTTGAATTTTGA[A/G]CAACATATTGCTTGA | 55728 |
| rs192285933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111924 | CCCAGCCAACCCATA[C/G]TTACTTAATTTTTAT | 55728 |
| rs192291857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176662 | ATTGTGATACTCTTT[C/T]CTCACTGAGTTAATT | 55728 |
| rs192335864 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156469 | GTTTGAGCATCATAT[A/G]TATTTTTATGAAGCT | 55728 |
| rs192363358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059884 | AGGAGACAGAGACTG[A/G]GAAGTATTAAGAAAG | 55728 |
| rs192372728 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126788 | TTGGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG | 55728 |
| rs192397438 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092431 | AAACTTTTGTGTGTT[C/T]ATAGTTTACTTTATT | 55728 |
| rs192400326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161906 | GCTGCTACGTCTGCC[G/T]TAATTTAAAGGTGAG | 55728 |
| rs192413653 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123401 | TACTGTCTTTTTTTT[C/T]CTCTCTTTTCAGTAG | 55728 |
| rs192419597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143332 | TTTATTTATTTTTTT[A/T]AGATAAGGTCTTGCT | 55728 |
| rs192447705 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075928 | GCCTCTCAGGCCCAA[A/G]CAATCCTCCTACCTC | 55728 |
| rs192448340 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058427 | GCCGTGCTAGGATGG[C/G/T]GGGTAGGAGCGAGGG | 55728 |
| rs192451545 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant, synonymous-codon, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056417 | TGCAATGTTCCCCAG[C/T]GCCAAACAGCTCCCG | 55728 |
| rs192478559 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106604 | CCCAGGCTGGAGTAC[A/G]GTGGCGCAATCTCAG | 55728 |
| rs192481397 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090968 | AGTTTATAAGATCCT[A/G]TTGAGGTTAATAAGT | 55728 |
| rs192530776 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118871 | TTGAATAAATAAAAA[C/G/T]AGCATTAACTGACAG | 55728 |
| rs192532585 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104050 | AGCTCCGCCTCCCAG[A/C/G]TTCATGCCATTCCTG | 55728 |
| rs192546417 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087018 | CCTCCTAAAGTGCTG[A/G]CATTATAGGTGTAAG | 55728 |
| rs192576853 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106704 | TAGGCGCATGCCACC[A/G]TACCTGGCTAATTTT | 55728 |
| rs192579285 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135631 | GCAGTGGCACCATCT[C/T]GGCTCACTGCAACCT | 55728 |
| rs192597637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076373 | CCCAGCTATTCGGGA[A/G]GCTGAGGTAGGAAAA | 55728 |
| rs192629123 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170428 | GTTGAAGACCAGCCT[C/T]GGCAACATGACGATA | 55728 |
| rs192629941 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130205 | CAAAAATAAAATATA[G/T]TTTTAGTATAGATGG | 55728 |
| rs192651673 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157682 | GTTTGGTAATTTTTC[A/G]GTGTAGTAGTTAAAT | 55728 |
| rs192660962 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166619 | ACTTGAACCCAGGAG[A/G]CGGAGTTTGTGGTGA | 55728 |
| rs192666134 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166518 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 55728 |
| rs192672185 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182508 | CAGGCTGGAGTGCAG[G/T]GGCGGGAACACAGCT | 55728 |
| rs192674686 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139853 | TTTTTGAGACAGGGT[C/G]TCACTGTGTTGCTCA | 55728 |
| rs192680884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070906 | CTTCGCTCACTGCAA[C/T]CTCCTTCTCCTGAGT | 55728 |
| rs192705852 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103350 | TTTCTTTTTACTAAG[C/G]TTTCCTAACTTTGTG | 55728 |
| rs192711950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082596 | CCAGGACTTCGAGAC[C/T]AGCGTGTGCAACAGA | 55728 |
| rs192716427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105803 | CAGTCTTCCCACCTC[A/T]GCCTCCCAAAGTGCT | 55728 |
| rs192729099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142307 | CCCTCCTCTCTCTGG[C/T]GGTGGTGGCGACGGC | 55728 |
| rs192828996 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118289 | TGGCTGGTGGCGCAT[A/G]CCTGCAATCTCAGCT | 55728 |
| rs192839214 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086382 | TTACCCTGTCACCCA[G/T]GCTGGAGTGCAGTGG | 55728 |
| rs192851382 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157153 | GAGATATTAGACACT[C/T]AACAGTATTTTCAGT | 55728 |
| rs192869889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148838 | GAATAATATTCCATT[A/G]TGTCTATATCACATT | 55728 |
| rs192876213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183029 | CCAACATTTAGAAAA[G/T]AGAGGAATGTATAAA | 55728 |
| rs192888636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085900 | AGTGTGCTGCTCACA[C/G]CTGTAATCCCAGCAC | 55728 |
| rs192918156 | snp | A/G | 0.000416573 | 0.0144261 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121264 | AGATGGATTTAAGCC[A/G]AAAGTTTTCAATATT | 55728 |
| rs192919325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067385 | TAAGGCTGAATAATA[G/T]TCCATTGTATGTATG | 55728 |
| rs192925024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090539 | GTGATTTTAAGTGAA[A/G]CGACATGTATCAGGT | 55728 |
| rs192956339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061367 | TTCATTTTATTTATT[G/T]ATTTATTTATTTTTG | 55728 |
| rs193044190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103674 | GATTTGAAGGAAGAG[A/T]GTATAGGATGACAAC | 55728 |
| rs193051906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174989 | GTCACAGAAAGAAAA[A/G]TACTGCTTGGTCTCA | 55728 |
| rs193056212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139606 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCAGGTA | 55728 |
| rs193056419 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136094 | ACTGAATAATGCAGG[A/G]ATGAGAGGTAGGGTA | 55728 |
| rs193066666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172311 | ACCCAGATTGAGGGT[A/G]AGTCTGCCTTTCCCA | 55728 |
| rs193098243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109595 | TGGTGGTGCACACCT[A/G]TAGTCCCAGCTACTT | 55728 |
| rs193101397 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078833 | TACACTTGGCCTCAG[A/C]ATTAGTATCAATAGT | 55728 |
| rs193140836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175475 | TGAACCAGTCTGGAG[A/G]TCTGATGCAAAACAT | 55728 |
| rs193238724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178535 | TGGGCAGCATGTACC[A/T]TTCTGGTAGATTTCA | 55728 |
| rs193240857 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153680 | AAAATGATAGCATAA[A/G]TTATGAGCATAAAAC | 55728 |
| rs193255410 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093469 | TGGAGTGCAGTGGCT[C/T]GATCTTAGCTCACTG | 55728 |
| rs193265225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129540 | CCTTTTCTTGTTTTT[C/T]TGTAGATTGGGTAAT | 55728 |
| rs193272663 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062461 | TTCAGTCTTCCAATG[C/T]ATTTTTCCCACTGTA | 55728 |
| rs199515421 | snp | C/G/T | 0.000138389 | 0.00831737 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121958 | ATACATTCTCCTTCA[C/G/T]ATTTCTCTGATATTT | 55728 |
| rs199536066 | snp | A/C | 4.97591e-05 | 0.00498769 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154253 | AATAAACATCCTTGA[A/C]TTAGAAGTATGAAGG | 55728 |
| rs199547659 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102880 | TGTGAGTTACTGCCC[A/G]GTACTTGCTCCTCTC | 55728 |
| rs199557497 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134905 | TTCCTTCCTTCCTTT[C/T]TCTCTCTCTCTCTCT | 55728 |
| rs199559399 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084457 | TTTTTTTCCTCCGAG[A/G]TGGAGTCTTGGTTTT | 55728 |
| rs199582535 | in-del | -/AA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175339 | ATATGTGAAATATAG[-/AA]AAAAAAAAAAAAAAG | 55728 |
| rs199585855 | in-del | -/CTC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091963 | TCCAGCCTGGGTGAT[-/CTC]AGAGCAAGACCTTGT | 55728 |
| rs199590556 | snp | C/T | 4.96989e-05 | 0.00498467 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121092 | TAGTAGAACCACAAA[C/T]GTTAGCTGAATGTCA | 55728 |
| rs199593882 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143324 | TTTATTTATTTATTT[-/A]TTTTTTTAAGATAAG | 55728 |
| rs199604903 | snp | C/G | 0.000131632 | 0.00811164 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103259 | AAAATAGTATAATGT[C/G]TGAATTTGAACACAA | 55728 |
| rs199616721 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078149 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATTTATTA | 55728 |
| rs199620855 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179821 | CCAGGCTGGAGTGCA[A/G]TGGAGTGATCTTGGC | 55728 |
| rs199633376 | in-del | -/CCGAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125834 | GGAGGTTGCAGTGAG[-/CCGAGA]CTGCGCCATTGCACT | 55728 |
| rs199659511 | in-del | -/GTACCTG | 0.0562307 | 0.157967 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066445 | GCCTCAGTCTCCCAA[-/GTACCTG]GTACCTGGGACTACA | 55728 |
| rs199669109 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093599 | TGTATTATTTATTTA[-/T]TTATTATTATTATTT | 55728 |
| rs199713269 | in-del | -/TT | 0.0376037 | 0.131863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136217 | CAGCTTAAAGGTCTA[-/TT]GTCTGTGTTTGATGT | 55728 |
| rs199759531 | snp | A/G | 1.66751e-05 | 0.00288744 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120216 | AAAGTGAAAACGAGC[A/G]AATAGAAATGGTGGC | 55728 |
| rs199759657 | snp | A/T | 0.00199798 | 0.0315436 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120778 | CTGGCCTTCATCTGA[A/T]TCTTTAGCTCAGAGG | 55728 |
| rs199766834 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066111 | AATTTTTGTATTTTT[A/T]GTAGAGATGGGGTTT | 55728 |
| rs199810627 | in-del | -/AAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125905 | AAAAAAAAAAAAAAA[-/AAT]TATACACAGATCATT | 55728 |
| rs199830420 | in-del | -/GT | 0.0166325 | 0.0896639 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073556 | CTAGACAGACAGTAA[-/GT]GTTATTAAAGTTGTA | 55728 |
| rs199834535 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066317 | TCTATTTGTGATTTT[-/C]CCCTTTTTTTTTTTT | 55728 |
| rs199851218 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078700 | CCAGCTTATTGTTTT[G/T]TATTTTTTTGTTGAG | 55728 |
| rs199881701 | in-del | -/C | 0.223819 | 0.248625 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141494 | TCAGACGATGGGCGG[-/C]CGGGCAGAGGCGCTC | 55728 |
| rs199889967 | snp | C/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142764 | ACTACAGAGCAGAGG[C/T]TTTCCTTCACCAACA | 55728 |
| rs199929808 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088503 | AATATCTCATTATAG[-/T]TTTTTTTTTTTTTTG | 55728 |
| rs199933639 | in-del | -/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182401 | TAGATCCTTGTATTT[-/G]GTATAAATCCTTCCA | 55728 |
| rs199960541 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172672 | TTTAGCCTCCAGAAC[-/T]ATGAGATGATAAATT | 55728 |
| rs199964037 | snp | A/G/T | 0.00117968 | 0.0242583 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144619 | GTCCCTTGGTGATAT[A/G/T]TTTATGATTTAGGGT | 55728 |
| rs199987279 | snp | A/C | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102682 | CGTTGAGGCTCAATT[A/C]TCTGAAGCTCCTGTA | 55728 |
| rs199990567 | in-del | -/A/T/TA | 0.0232847 | 0.105357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073612 | TTTTTTTTTTTTTTT[-/A/T/TA]AAATTGAGTCTTGCT | 55728 |
| rs200031954 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184036 | CAGCCACTCATAGCT[A/G]CAGGGGAAGCTGAGA | 55728 |
| rs200041215 | snp | A/G | 0.000280841 | 0.0118466 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117994 | AACGTATTGAGTTGT[A/G]TGCATATTCTTGTGA | 55728 |
| rs200089607 | in-del | -/T | 0.0244538 | 0.107838 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060778 | GGCTCATTTTTAAAA[-/T]TTTTTTTGTAGAGAC | 55728 |
| rs200117837 | in-del | -/TCACTAGAGGC | 0.0505996 | 0.150943 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100442 | GCGCAGTAATCACTT[-/TCACTAGAGGC]TCACTAGAGGCTCAC | 55728 |
| rs200150921 | in-del | -/AAAAAAAAAAA | 0.464096 | 0.129085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155398 | CAAGACTCCGTCTCC[-/AAAAAAAAAAA]AGAAAAAAAAGAGAA | 55728 |
| rs200168505 | in-del | -/T | 0.493201 | 0.0579089 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066321 | ATTTGTGATTTTCCC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs200173902 | in-del | -/TCC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134895 | CCTTCCTCCCTTCCT[-/TCC]TTCCTTTCTCTCTCT | 55728 |
| rs200206717 | snp | C/G | 0.00199798 | 0.0315436 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121995 | TTGTATCTAGTACTT[C/G]AAATCTTGAATTAAA | 55728 |
| rs200208751 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140591 | ATTCTCTTTTTTTTT[-/A]AAATTAATTTATTTT | 55728 |
| rs200232013 | snp | G/T | 1.67753e-05 | 0.00289609 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120457 | AAAGTTCCCAAGACA[G/T]GAGCTATCAAATTTT | 55728 |
| rs200245752 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168592 | TGAAATTTATGGATT[C/T]TACACCTTTTTCAGA | 55728 |
| rs200252706 | snp | A/G | 0.000428322 | 0.014628 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103085 | AAAGTATGGAGAAAT[A/G]AAGATGGAACAAGTG | 55728 |
| rs200261641 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145479 | TCCACCTGCCTTGGC[C/T]TCCCAAAGTGAGCTA | 55728 |
| rs200290686 | in-del | -/AT | 0.0236746 | 0.106192 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170170 | CATGGAAATAAAAAC[-/AT]AAATTTCAAGATATA | 55728 |
| rs200304108 | snp | A/T | 4.99388e-05 | 0.00499669 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120281 | TCTATGGAGAGAGTA[A/T]CACCTAGTACTTGCT | 55728 |
| rs200319185 | in-del | -/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155823 | TAAAACCCCAAAACA[-/T]TTTTTTTTATATATC | 55728 |
| rs200320565 | in-del | -/TAATC | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100421 | CACTCAGTCGCCCAG[-/TAATC]GCTGGAGCGCAGTAA | 55728 |
| rs200362502 | in-del | -/AT/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128845 | TCTTTAAAAAAAAAA[-/AT/T]TAAATAAATAAAATA | 55728 |
| rs200373501 | in-del | -/CTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134900 | TCCCTTCCTTCCTTC[-/CTTT]CTTTCTCTCTCTCTC | 55728 |
| rs200450710 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178438 | AAACAAAAAAAAAAA[-/G]AAAAGAAAAACCTTC | 55728 |
| rs200467257 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134392 | GGGGCTGGGTGTGTC[C/T]TTCTGGGGATGGTCA | 55728 |
| rs200488634 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176804 | CGGGAAGTTCATGCT[-/G]GTTTGCAGCAGGGAG | 55728 |
| rs200488651 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081823 | GCTACTAAAAAATAC[A/C]AAAATAAGGTTGGGT | 55728 |
| rs200501367 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114927 | CTACTGTGTTAGCAG[-/T]TAAGTTCCCTCCTGC | 55728 |
| rs200552392 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182352 | GGTCAGGCTGAGAAG[A/T]TTCCTTTTGTCCTGT | 55728 |
| rs200601407 | snp | C/T | 0.00299557 | 0.0385851 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152721 | TAGCTAAGGTTTACG[C/T]TTTCTATTGAGAATG | 55728 |
| rs200612633 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127659 | TCTATCTCTGAGAAA[-/AT]ATATATATATATTTT | 55728 |
| rs200624267 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132923 | TGGTGTTGGTCTGTG[-/A]TTTTTTTTTTTCTGT | 55728 |
| rs200624860 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099682 | ATTGTTCATTCATTG[-/A]AAAAAAATTTTTTTA | 55728 |
| rs200630328 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099593 | TTGCATTTTTCCTAA[-/TT]TTTGTGTTTTTTTAA | 55728 |
| rs200639433 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150186 | TTAAAAAAGAGAGAC[-/AT]ATCTGGACCTTATGT | 55728 |
| rs200660990 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084826 | CTCCATATTGGTCAG[A/G]CTCATCTTGAACTCC | 55728 |
| rs200698088 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104410 | TAAACTTATTTTTAG[G/T]TTTTTTTTTTTGATA | 55728 |
| rs200766960 | snp | C/T | 1.70717e-05 | 0.00292157 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103191 | TTCTCAGAGGTCTTC[C/T]GGGATCTGGAAAATC | 55728 |
| rs200769028 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121734 | AGGCGGAAATGAGAG[C/T]TGTCACTCCTGAAAA | 55728 |
| rs200771934 | snp | C/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177005 | TTTCGTGGCTGTGGG[C/G/T]CGGATAAGAACCCCC | 55728 |
| rs200776584 | snp | A/C | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097471 | CCATGGGTGAGACAA[A/C]AGTTGATCAGGAAGA | 55728 |
| rs200778952 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134907 | CCTTCCTTCCTTTCT[C/T]TCTCTCTCTCTCTCT | 55728 |
| rs200786412 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140591 | TTCTCTTTTTTTTTA[-/T]AAATTAATTTATTTT | 55728 |
| rs200799800 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136392 | TCTATCTATCTATCT[A/T]TCTTTTTTTTGAGAC | 55728 |
| rs200815306 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121606 | AGAAATTATTAGCCA[A/G]AGAGGAACTTTAGAG | 55728 |
| rs200840604 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077141 | ATTATGTAGAATATA[-/TG]TATGTGTGTGTGTGT | 55728 |
| rs200845582 | in-del | -/A | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069275 | AAACTCCGTTTCTAC[-/A]AAAAAATGCAAAAAT | 55728 |
| rs200869312 | in-del | -/AAAC | 0.0397318 | 0.13523 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166696 | CTCCATCTAAAAAAA[-/AAAC]AAACAAACAAAAAGA | 55728 |
| rs200879802 | snp | G/T | 6.6517e-05 | 0.00576663 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102463 | AAATTTAGAGAATTC[G/T]GGTTCTACTTTAAGT | 55728 |
| rs200882600 | snp | A/C/T | 0.000157866 | 0.00888311 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117846 | AATATTCCTTCAACC[A/C/T]TTTTTTCCCCTGGAA | 55728 |
| rs200896183 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149902 | ACTCCATCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 55728 |
| rs200903507 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103963 | TTTATATGCTAGTTC[-/T]TTTTTTTTTGAGACG | 55728 |
| rs200908656 | snp | A/C | 1.67441e-05 | 0.0028934 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126173 | GGCTTGATAATCCTG[A/C]ACAAAAATCATCTCA | 55728 |
| rs200928243 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103633 | GGATTATAGAGTGTT[A/G]TTAAATAATGCTTTT | 55728 |
| rs200956579 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176296 | AGGTTCTAAAAAGAA[-/AT]AGTTACAAACATATA | 55728 |
| rs200976475 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169982 | AAAAAAAAAAAAAAG[A/T]AAAATAACCATAAAA | 55728 |
| rs201046626 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184037 | AGCCACTCATAGCTG[A/C]AGGGGAAGCTGAGAA | 55728 |
| rs201066226 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184983 | AATAAATAAATAAAT[-/A]AAATAAAAAATAAAT | 55728 |
| rs201074418 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099737 | AATCTGTATAAGGAC[-/T]TTTTTTTAATGTGAT | 55728 |
| rs201085128 | snp | C/T | 1.70316e-05 | 0.00291813 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131787 | TGAACATGATTTTTA[C/T]GTTTTTGTTTTAGAA | 55728 |
| rs201103053 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081819 | CATCGCTACTAAAAA[A/T]TACAAAAATAAGGTT | 55728 |
| rs201104252 | snp | C/T | 0.00200783 | 0.0316209 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102879 | ATGTGAGTTACTGCC[C/T]GGTACTTGCTCCTCT | 55728 |
| rs201108407 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067600 | TTAATTTTTTGAGGA[G/T]CTGCCATACCCTTTG | 55728 |
| rs201123235 | in-del | -/CGCAGTGGTT/TGGTT | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100428 | TCGCCCAGGCTGGAG[-/CGCAGTGGTT/TGGTT]CGCAGTAATCACTTT | 55728 |
| rs201127938 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120095 | GATTTAAACAAAAGA[A/G]GAAAAGAAATAAGTG | 55728 |
| rs201141215 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123653 | ACCACACCTAGGTAA[-/T]TTTTTTTTTTTTGTA | 55728 |
| rs201171424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063664 | ATTAATTTTTTTGAG[A/G]CGGAGTTTTGCTCTT | 55728 |
| rs201182690 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062540 | GTGACTTTTCATGGC[C/T]TTTAGGATAACTTCT | 55728 |
| rs201204950 | snp | C/T | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142820 | GCCAAAGAAGCTTAT[C/T]GGATAGGGAAAAAAA | 55728 |
| rs201226692 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178426 | GCCCCGCCACCAAAA[A/C]AAAAAAAAAAAGAAA | 55728 |
| rs201228144 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055756 | AACCAGAAAGCAAAG[-/GT]GAAAAATTTGCGTAC | 55728 |
| rs201245314 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071881 | CAAATTTCTTTTTTT[-/A]AAAAAACATTTTTAT | 55728 |
| rs201247824 | in-del | -/G | 0.0267878 | 0.112589 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108631 | TGGTTTACTTTTTAT[-/G]GAAGATAGTGTGAGA | 55728 |
| rs201262159 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071796 | GTCTTGAACTCCTGA[C/G]CTCAGGTGATCCTCC | 55728 |
| rs201270289 | snp | A/G | 1.75449e-05 | 0.00296178 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119975 | GAAAAAGAAGAAAAT[A/G]TTTTATCTTTATCTT | 55728 |
| rs201293201 | in-del | -/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156876 | CATGTTCTAAAATAT[-/C]CCCCCCAAACCCCAG | 55728 |
| rs201314266 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122261 | GCATTACCCCCTGAA[C/G]TGGCTTTTCAACTTA | 55728 |
| rs201349417 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143521 | GTCCAGGCTGGTCGT[A/G]AACTCCTGAGCTCAA | 55728 |
| rs201362758 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093415 | AGCCATGTTCTACAA[-/T]TTTTTTTTTGAGACA | 55728 |
| rs201364379 | in-del | -/A | 0.0839998 | 0.186933 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128835 | CAATGGATTTTCTTT[-/A]AAAAAAAAAATAAAT | 55728 |
| rs201385898 | snp | A/G | 0.000105235 | 0.00725304 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122308 | TGTTGGTATTGATTC[A/G]GGTAAGGAAAAAGTA | 55728 |
| rs201398612 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134956 | ATTTTATTTTATTTT[A/T]TATTATTATACTTTA | 55728 |
| rs201450244 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078112 | TGTTGAATATTTCTA[A/T]ATGTGTGTGTGTGTG | 55728 |
| rs201450840 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062486 | ACTGTAGCTAGAGTA[-/A]TCTGTCTAACACATT | 55728 |
| rs201454734 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155399 | AAGACTCCGTCTCCA[A/G]AAAAAAAAAAGAAAA | 55728 |
| rs201459157 | snp | C/T | 0.000131774 | 0.00811601 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102915 | TGCTGTTGCCTCCTC[C/T]GCCACCTCCACCGAT | 55728 |
| rs201460114 | snp | A/C/G | 5.022e-05 | 0.00501078 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120155 | ATTCTGGAAACTCCA[A/C/G]ACATGTATTTTTCTG | 55728 |
| rs201494276 | snp | C/T | 0.000693172 | 0.0186039 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152938 | ATTAATAATGGCAAC[C/T]GCCCATATAGATCTT | 55728 |
| rs201518664 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138008 | GTTTGTTATCTCTAG[C/G]AATTAGCTAAACCTG | 55728 |
| rs201569852 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175328 | AAGCCTGGTATATAT[A/G]TGAAATATAGAAAAA | 55728 |
| rs201590183 | snp | A/G | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120837 | GTTTAAGTGAGCCCA[A/G]CCTAGAAATTGGAAC | 55728 |
| rs201695131 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087267 | CCCTTCCCCTCCTTT[-/A]AAAAAAAAATTTTTT | 55728 |
| rs201776803 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157073 | CAGTAGTCTCTTACC[A/G]TTATCTCCCAGATGG | 55728 |
| rs201788833 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125078 | ACATGCCTCTGTTGT[A/C]CAGTCCACACTGGGA | 55728 |
| rs201789405 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081820 | ATCGCTACTAAAAAA[A/T]ACAAAAATAAGGTTG | 55728 |
| rs201796788 | in-del | -/A | 0.00676609 | 0.0577691 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185612 | AAACTTATTATTTGG[-/A]AAAAAACATTTTAAT | 55728 |
| rs201805188 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128276 | AACACTTTCTTATTC[A/G]TTTGACTGCACAAAG | 55728 |
| rs201855506 | snp | A/G | 0.00177424 | 0.0297316 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120090 | ATGCAGATTTAAACA[A/G]AAGAAGAAAAGAAAT | 55728 |
| rs201879087 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180241 | AACAATATTCAATAG[-/A]AAAAAAATGGGCACA | 55728 |
| rs201895626 | snp | C/T | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102380 | AATGACTCAAGTGAG[C/T]TTATAAATCCTGATT | 55728 |
| rs201906638 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090381 | GAAGAATTGACATAT[G/T]TACTGTGTTGTCTTC | 55728 |
| rs201952832 | snp | A/G | 0.000363715 | 0.0134806 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144623 | CTTGGTGATATGTTT[A/G]TGATTTAGGGTACTC | 55728 |
| rs201955533 | snp | C/T | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119989 | TATTTTATCTTTATC[C/T]TTGAAGCATCTAGAG | 55728 |
| rs201983746 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130171 | GCTGGGACCAGAAGC[A/G]CACATCACCACACCT | 55728 |
| rs201984458 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099888 | CTTACGTTTGCTTTC[-/T]TTTTTTTTCCCCCGT | 55728 |
| rs201989788 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145475 | GCAATCCACCTGCCT[C/T]GGCTTCCCAAAGTGA | 55728 |
| rs201989934 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178427 | CCCCGCCACCAAAAC[A/C]AAAAAAAAAAGAAAA | 55728 |
| rs202029831 | snp | A/G | 0.000313095 | 0.012508 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102668 | TTAGAATCTGAGTGC[A/G]TTGAGGCTCAATTCT | 55728 |
| rs202073676 | snp | G/T | 0.000247523 | 0.0111221 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113534 | GAGGCTACCTAACAT[G/T]CTTTTTATGTAACGA | 55728 |
| rs202087382 | in-del | -/T | 0.456803 | 0.140473 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088502 | TTTTTTTTTTTTTTT[-/T]GCAATGGGGTTTCGC | 55728 |
| rs202095933 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175192 | GCCTGGCTAAGTTTG[-/T]TTTTTTTTATGGTAA | 55728 |
| rs202101051 | snp | A/G | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144709 | GAAAGTCAATGCTTC[A/G]CTGCTGCCACAGAAT | 55728 |
| rs202128375 | snp | A/G | 0.000171098 | 0.00924769 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118044 | GTTAAAATGCCTTAT[A/G]TACAAAATTCAATTT | 55728 |
| rs202143891 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168591 | ATGAAATTTATGGAT[A/T]TTACACCTTTTTCAG | 55728 |
| rs202162739 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076507 | ATCTTTTTTTTTTTT[-/T]GAGACTGAGTCTTGC | 55728 |
| rs202172201 | in-del | -/T | 0.0916144 | 0.193427 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108320 | TAGATTGGTTTACTC[-/T]TTTTTTTTTTGAGAC | 55728 |
| rs202214906 | in-del | -/ATCTATCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136344 | AGGATTAGAAATTGA[-/ATCTATCT]ATCTATCTATCTATC | 55728 |
| rs267600151 | snp | C/T | | | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097362 | AGGAGAAGGAAAAAT[C/T]TTGGGGGAAATCCTT | 55728 |
| rs267600152 | snp | C/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126169 | ACTGGGCTTGATAAT[C/T]CTGAACAAAAATCAT | 55728 |
| rs367548025 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109213 | TTTGAACTAAAGATT[-/T]AAGAATTCAGGAATC | 55728 |
| rs367567454 | in-del | -/AACA | 0.0537404 | 0.154862 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178159 | AGCGAGACTGGGTCC[-/AACA]AACAAACAAACAAAG | 55728 |
| rs367574172 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093547 | GAGTAGCTGGGATTA[C/T]AGGTGTGTGCCACCT | 55728 |
| rs367578674 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150691 | GAAAAAAAAAAAAGA[A/G]GAAGTCTAGGATAAA | 55728 |
| rs367587078 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161189 | TGGCCTGATAATGCC[A/G]CCACTAGCTGCCTGA | 55728 |
| rs367603325 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107401 | AGTATTTTTTTTTTT[-/T]CGAGATGGAGTCTCA | 55728 |
| rs367603550 | snp | C/T | 1.75767e-05 | 0.00296446 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144581 | TTAACTTCCTCATCA[C/T]CCAAGTAGCAAACAG | 55728 |
| rs367612096 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177354 | GGCACGGTGGTTCAC[A/G]CCTGTAATACCAGCA | 55728 |
| rs367624616 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153403 | TACGTTTAAACTTTA[A/G]CAGAAATGTTCAGTT | 55728 |
| rs367672168 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149765 | AGCTGGGCATGGTGG[C/G]GGGCACCTGTAGTCC | 55728 |
| rs367688963 | snp | C/T | 4.94262e-05 | 0.00497098 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123160 | ATTGTGTGGTTCATA[C/T]AGATCTGAATCTGGC | 55728 |
| rs367690369 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157316 | ACTTTATGGCCTTTA[A/C]ATATAGGACATATTA | 55728 |
| rs367745461 | snp | C/T | 3.30732e-05 | 0.00406638 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121508 | TCTGAAACTAAGTTA[C/T]GTGAGGATACAGAGT | 55728 |
| rs367761431 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081207 | GCGAAAGTAGCATAT[-/A]AAAAATATATTAAAA | 55728 |
| rs367784842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110622 | GGCTCATTGCAACCT[C/T]CGCCTCCTGGGTTCA | 55728 |
| rs367787012 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093871 | TCCCAAAGTGCTGCA[A/G]TTACAGGTGTGAGCC | 55728 |
| rs367802115 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059918 | CTGAAAGTTACCCGA[C/T]TAGTGTGTGGGAGTG | 55728 |
| rs367809875 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064600 | TATTGAGCTCTTGTT[G/T]GCTAAATAAAACACT | 55728 |
| rs367835465 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110781 | AACCTCAGGTGATCC[A/G]CCCGCCTCAGTATCC | 55728 |
| rs367851027 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088969 | TGTGTGTGTTTTTTT[A/G]AAACAGAGTCTCTGT | 55728 |
| rs367855551 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110474 | TCACTGTGGTTTCAA[-/T]TTGCTTTTCTCTGAT | 55728 |
| rs367960439 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132634 | AGTGTTATGTTAGGT[A/G]TATCAGGAATGCTCT | 55728 |
| rs367982161 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113523 | GGTAAAACTTGGAGG[C/T]TACCTAACATGCTTT | 55728 |
| rs368006880 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067418 | CACATTTTTTTTTTT[-/TT]ATCCATTCACTTGTT | 55728 |
| rs368039220 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144155 | GAGGAGAACATCTGC[C/T]TGTTTGTCTTAGCCA | 55728 |
| rs368059826 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072644 | CCCTCCCTGTACCCC[C/G]CCAGGCCTCCCAAAG | 55728 |
| rs368085049 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064292 | ATTGATTGATTTATT[G/T]GAGACAGAGTCTCGC | 55728 |
| rs368087542 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114939 | CAGTTAAGTTCCCTC[C/G]TGCAATCTTAGTATG | 55728 |
| rs368093271 | snp | C/G | 0.0726307 | 0.176182 | upstream-variant-2KB, intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056860 | GCGGCAGTGTCTCCC[C/G]GCCGGGCGCGCTCGC | 55728 |
| rs368095557 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081970 | ATACAAAATTAGCCG[A/G]GTGTGGTGGCGCATG | 55728 |
| rs368100620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173141 | GGACATCTCTTGCGC[A/C]TCAGGCCAACTTCCC | 55728 |
| rs368125145 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121629 | CTTTAGAGAATTCTA[A/G]TTCTCCTGTGCCAGA | 55728 |
| rs368147776 | snp | A/C/T | 9.90204e-05 | 0.00703572 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102616 | AAGTGACTCCATCGC[A/C/T]GGTTGTAGCAGTCTC | 55728 |
| rs368159426 | in-del | -/AAAGTTGT/AAGTTGT/GTTGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090952 | AAAAAAAAAAAAAAA[-/AAAGTTGT/AAGTTGT/GTTGT]AGTTTATAAGATCCT | 55728 |
| rs368160998 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112522 | GCAGAATCAAAATTT[-/TT]GTTGGTCCTTTGTTT | 55728 |
| rs368169013 | snp | A/G | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106940 | GGAGTCATTCTTAGT[A/G]CTGATGATTATTTTT | 55728 |
| rs368174698 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144604 | GCAAACAGCAAAACT[A/G]TCCCTTGGTGATATG | 55728 |
| rs368188685 | snp | A/G | 5.01735e-05 | 0.00500842 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144653 | CTTCATGAGCAGAAG[A/G]TGAAAGAAGCCAATC | 55728 |
| rs368227812 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060405 | GCACACGATCACGCC[C/T]GGCTAATGTTTTTAT | 55728 |
| rs368249606 | in-del | -/ATTTCTGTAAAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089923 | AATATTTCTGTAAAT[-/ATTTCTGTAAAT]TTCCAAGAATACTAA | 55728 |
| rs368254564 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117173 | ATTGCTTCCGTCCCA[C/T]GCATTCTCTTCTCTT | 55728 |
| rs368259572 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182637 | TTTTTTTGTAGAGAC[A/G]AGGTTTCGCCATGTT | 55728 |
| rs368264111 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152376 | AATTAACAGGGTTGT[C/T]GTGAAGATTCTTAGT | 55728 |
| rs368269005 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165394 | GCTAGAACTACAGGT[A/G]TGCGGCACCATGTCT | 55728 |
| rs368270057 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102694 | ATTCTCTGAAGCTCC[C/T]GTAGATTTGGATGCC | 55728 |
| rs368279259 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084048 | CACTGCAACCTCCCC[C/T]TCCTGGGTTCTCCTG | 55728 |
| rs368282071 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134958 | TTTATTTTATTTTTT[A/T]TTATTATACTTTAAG | 55728 |
| rs368282873 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157916 | TGAAGAGCCGTTTAT[A/G]ACTTCATATTATATG | 55728 |
| rs368297424 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103038 | TCAACTACACATTTC[C/G]ACCCTCAGTTATTTC | 55728 |
| rs368321382 | in-del | -/TCTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135574 | TTTCTTTCTTTCTTT[-/TCTTT]CTTTCACAGAGTTTG | 55728 |
| rs368324890 | snp | A/G | 1.66779e-05 | 0.00288768 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40118024 | AGGATAGAAGCACTA[A/G]GTAGGTTAAAATGCC | 55728 |
| rs368330806 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145222 | TCCAGTAGTTTTTTT[-/G]TTTGTTTGTTTCTTT | 55728 |
| rs368338623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147831 | GCAGCCAGGCAGAGA[C/T]GCTCCTCACCTCCCA | 55728 |
| rs368348059 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113692 | AATTGAGTTAATTTA[C/T]GGTAAAAATTCCCCT | 55728 |
| rs368479461 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134972 | TATTATTATACTTTA[A/T]GTTTTAGGGTACATG | 55728 |
| rs368489718 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064502 | CTGGTCTCAAACTCC[C/T]GACCTTGTGATCCGC | 55728 |
| rs368499176 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140930 | TAGATCAACAGGATC[A/C]CAAGGCAGAAGAATT | 55728 |
| rs368570150 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104865 | GCTAGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 55728 |
| rs368580480 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088543 | TTCGCTCTTGTTGCC[C/T]GGGCTGGAGGGCAAT | 55728 |
| rs368582110 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068357 | TTGCTTTTGTTGCCT[A/G]TGCCTTTGGTGTCGT | 55728 |
| rs368585792 | snp | A/C | 0.000164761 | 0.00907487 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124244 | AATGTCTTAATGTTG[A/C]AATTTGGTGTGTGTG | 55728 |
| rs368604800 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149545 | AAACCGCTTAATTGC[A/T]TATTTTAAAATGGTT | 55728 |
| rs368624382 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120227 | GAGCAAATAGAAATG[C/G]TGGCTGTAAAAGGGT | 55728 |
| rs368656540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083258 | AAATTGGTGCAGCTG[C/T]TTTGGAAAACCGTTT | 55728 |
| rs368683631 | snp | A/G | 3.3162e-05 | 0.00407184 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120925 | AAGCTCTCAAAAACT[A/G]AAGACATTGGGTAGC | 55728 |
| rs368693476 | snp | A/C/G | 8.4314e-05 | 0.00649236 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137113 | TTTTTTTTCTACAAG[A/C/G]GTAGATAATTGCATA | 55728 |
| rs368709827 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121672 | GATTGGTATTAGTAA[C/T]GCTGACTCACAGTCT | 55728 |
| rs368732246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139096 | TTCAACAATGCACTA[C/T]AGTTTTCAGAGTATA | 55728 |
| rs368740595 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116248 | CACCTTGACTTTTAA[C/T]TGATAAACTTAGTTC | 55728 |
| rs368755016 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099173 | AGGTGTGCTGACTTG[C/T]AATTCCACCAGGCTT | 55728 |
| rs368769586 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169963 | GCAAGACTCAATCTC[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs368811045 | snp | A/G | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117903 | AGCAAAGAAAAAATA[A/G]CAAGAATGTTGGAAC | 55728 |
| rs368811566 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179786 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 55728 |
| rs368814959 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099844 | TTTTCTGGTTTTACT[G/T]TCATGTAGATTTTTT | 55728 |
| rs368849494 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102831 | TCAACTTCAAGCCAC[A/G]CAAACATCCTGAACT | 55728 |
| rs368851799 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107538 | ACAGGTGCATGCCAC[C/T]GCACCTGGCTAATTT | 55728 |
| rs368854449 | snp | A/T | 0.000117405 | 0.00766087 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120459 | AGTTCCCAAGACATG[A/T]GCTATCAAATTTTGT | 55728 |
| rs368859809 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107962 | AGTATCTCGCTCTGT[C/T]GCCCTGGCTGCAGTG | 55728 |
| rs368861094 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086896 | GGGACCACAGGTGAA[C/G]AGCACCATGCCTAAG | 55728 |
| rs368872863 | in-del | -/T/TT/TTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062078 | TTATTTTTTGGTTAC[-/T/TT/TTTT]TTTTTTTTTTTTTTT | 55728 |
| rs368875426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068431 | CCCGTTTTCTTCTAC[G/T]AGTTTTAAGTTTAAG | 55728 |
| rs368890558 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110749 | CACTGTGTTGGCCAG[-/G]ATGGTCTCGAACTCC | 55728 |
| rs368891245 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095659 | GCAATGGATAGTTAG[C/T]AGGAAAGGGGAGATT | 55728 |
| rs368910949 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134002 | TTGTAGAGATGGAGT[G/T]TCACCATGTTGCCCA | 55728 |
| rs368996033 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061659 | CTTGAGCCACTGTGT[C/T]TGGCGTATTTTATTT | 55728 |
| rs369013847 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166726 | AAGATAATTAATAGA[A/T]GCACTTTTTATTTTA | 55728 |
| rs369122694 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132846 | CAGATTTTTTTTTTT[C/T]CCTTTAATGCAGGTA | 55728 |
| rs369147671 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058535 | GAAAAAAGACTAACC[G/T]GTAAAACAATAAAGA | 55728 |
| rs369157007 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091180 | TTGGGATTTTCTGTA[A/G]TACATAGATAACCAT | 55728 |
| rs369190670 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186061 | CCAGGATGTGTTTCC[C/T]AGGTATAATTTCCAT | 55728 |
| rs369230455 | snp | C/T | 3.31148e-05 | 0.00406894 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113422 | ATGTTTTTGTCTTTG[C/T]TGTATGTAGTCTCAG | 55728 |
| rs369335729 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183618 | CGGGATTACAGGCGT[A/G]AGCCACTGCGACCGG | 55728 |
| rs369401023 | snp | G/T | 1.65507e-05 | 0.00287664 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154184 | TAACTCTTTTCTCAT[G/T]TCTGCAGGTTCTCTG | 55728 |
| rs369441898 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080174 | TGTATTAATAAGGAG[G/T]CTCTCATGAAAAAAG | 55728 |
| rs369443725 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121751 | GTCACTCCTGAAAAC[C/T]ATGAATCGATGACAA | 55728 |
| rs369448718 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105098 | TGAGCCACCACGCCC[A/G]ACAATCCTGCGTTGT | 55728 |
| rs369471394 | snp | C/G | 6.66267e-05 | 0.00577139 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126372 | ACTGTCTCTGATTCT[C/G]GTTTATTGTGTATGT | 55728 |
| rs369480878 | in-del | -/C | 0.460925 | 0.134204 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141223 | CTGGCGGGGGGCTGA[-/C]CCCCCCACCTCCCTC | 55728 |
| rs369485576 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062270 | TTTTTAATAGAGATG[G/T]GGTTTCACCGTGTTA | 55728 |
| rs369489376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100507 | CTACCTCAGCCTCCT[A/G]TGTGGCTGGTACTAT | 55728 |
| rs369508844 | in-del | -/TCTCT | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087784 | TTGAGATGGAGTGTC[-/TCTCT]GTTGCCCAGGCTGAA | 55728 |
| rs369509981 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105948 | AGAAGAGGATAAACA[-/TA]GGAATTGGGATCAAA | 55728 |
| rs369512401 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127822 | CCTGCCACCGCGCCC[A/G]GCTAATTTTTTGTAT | 55728 |
| rs369537901 | in-del | -/AATT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151962 | TGTTTTAAATTTATT[-/AATT]CATCTCATTAATAGT | 55728 |
| rs369585589 | snp | A/C | 1.66732e-05 | 0.00288727 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113399 | TTCTTGGAAATACCT[A/C]TTTTAAAATGTTTTT | 55728 |
| rs369646225 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161141 | GAGTAGGCAAAAAAA[-/A]TGAGAAGTCGAGAAT | 55728 |
| rs369647704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057205 | CCTCCGATCTGACCC[A/G]CGGGCCCGGCTGCCC | 55728 |
| rs369674933 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095145 | CTGGAGTGTAATGGC[A/G/T]CTATCTTGGCTCACT | 55728 |
| rs369730527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066089 | GCACACGCCACCACA[C/T]CCAGCTAATTTTTGT | 55728 |
| rs369766350 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184279 | TATGGCTGCACGGGC[C/T]AGAATGGAGAAACAG | 55728 |
| rs369782902 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124572 | GGCTGGTCTTGAACT[C/G]CTGACCTCAGGTGAT | 55728 |
| rs369800267 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070386 | GGAGGACATTCTCCC[C/T]ATATAGCCATAAAAC | 55728 |
| rs369801080 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155169 | GGCCGAGGTAGGTGG[A/G]TCGCCTGAGGTCAGA | 55728 |
| rs369808325 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144903 | TGCAGGCTGAGAATA[C/T]CTGTGTAACATCTGT | 55728 |
| rs369816628 | snp | A/G | 0.000280382 | 0.0118369 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136893 | GTGTTAATGTCCCAC[A/G]CAACTTATTTTCATT | 55728 |
| rs369883648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150630 | GAACCGAGATCATCC[C/T]ACTGCACTTCAACCT | 55728 |
| rs369897613 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174149 | TGGGAGGCTGAGGCG[A/G]GAGGATTGCTTGAGT | 55728 |
| rs369903625 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117832 | AAAACTTAATTATCA[A/G]TATTCCTTCAACCCT | 55728 |
| rs369917683 | in-del | -/CAAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178173 | CAACAAACAAACAAA[-/CAAA]GAACCCAACAAAACA | 55728 |
| rs369925627 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141796 | ACTCCAGCCTGGGCA[A/C]CATTGAGCACTGAGT | 55728 |
| rs369944820 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079444 | TTTTTTTTTTGAAGT[A/G]TTTATTGGTATATCT | 55728 |
| rs369959075 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171205 | TCGCAAGTTCTTCCA[A/C]CGTGAAGTGCCAGGG | 55728 |
| rs369960538 | snp | C/G | 3.31356e-05 | 0.00407022 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120687 | CACAGTGTGATGATG[C/G]TTCAGAGCCACTCAA | 55728 |
| rs369971165 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176066 | CTGCAATCCAGCCTG[A/G]GCGACAGAGCGAGAC | 55728 |
| rs369976271 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155347 | CAGTGACCCGAGATC[A/G]AGATCACACCACTGC | 55728 |
| rs369995999 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145460 | AACTCCTGGCCTCAA[A/G]CAATCCACCTGCCTT | 55728 |
| rs370022409 | snp | A/G | 3.29815e-05 | 0.00406075 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131938 | AGTGCTAGAAGGATT[A/G]TCTGTAGTTTCTACT | 55728 |
| rs370033782 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122213 | CCCACTCCAGCGATG[A/G]CCAAATCTCTGACCA | 55728 |
| rs370045457 | snp | C/T | 0.000133036 | 0.00815478 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102461 | GAAAATTTAGAGAAT[C/T]CTGGTTCTACTTTAA | 55728 |
| rs370046293 | snp | A/G | 1.64738e-05 | 0.00286995 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097443 | CGTGAGGAGCCAACC[A/G]CTACTCTACCTTCCA | 55728 |
| rs370062711 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087276 | TCCTTTAAAAAAAAA[-/A]TTTTTTTTAAAGGAG | 55728 |
| rs370069831 | snp | A/G | 1.68035e-05 | 0.00289853 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142869 | CCCAGCAGGTAAAGT[A/G]GAAAACTGATTATAT | 55728 |
| rs370097794 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071222 | GACCTGTTAGGTCTG[C/T]TGAGACGATTACATT | 55728 |
| rs370100487 | in-del | -/AAA/AAAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082275 | GCGAGACCCTGTCTC[-/AAA/AAAA]AAAAAAAAAAAAAAA | 55728 |
| rs370103174 | snp | C/T | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120981 | TGCTCAGTGAAATGA[C/T]CTGTGAGAGTCAGAC | 55728 |
| rs370120761 | in-del | -/T/TT | 0.462909 | 0.131034 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086131 | AACATGCCCGGCTAA[-/T/TT]TTTTTTTTTTTTTTT | 55728 |
| rs370161911 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179759 | AGTGGTAAAGCCTTT[-/C]TTTTTTTTTTTTTTT | 55728 |
| rs370193502 | snp | A/C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170489 | CCGGGTGTGGTGGTG[A/C/T]GTGCCTTTAGTCCCA | 55728 |
| rs370202129 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140665 | AGGGTCACAGGACAA[C/T]AGTGGAGGGAAGGTC | 55728 |
| rs370221262 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165397 | AGAACTACAGGTGTG[C/T]GGCACCATGTCTGGC | 55728 |
| rs370277608 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147453 | AGACGGGGTGGTGGC[C/T]GGGCAGAGGGGCTCC | 55728 |
| rs370295972 | in-del | -/TTACTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124025 | TCTAACTTTATTGTT[-/TTACTT]AGATTGAGTAAGAAT | 55728 |
| rs370304512 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092008 | AAAAAAAAAAAAAAA[A/T]TATATATATATATAT | 55728 |
| rs370309556 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155960 | TATTATTCACACTTA[C/T]GTTTGTAATAATTTA | 55728 |
| rs370317759 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171143 | TCTTGCTAGGTTGCA[C/T]ATTTAAAGGACTGGG | 55728 |
| rs370395613 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071774 | TTTCGCCATATTGGC[C/T]AGGCTGGTCTTGAAC | 55728 |
| rs370434708 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142106 | AGGGAGACCGTGGGG[A/G]GAGGGAGAGGGAGAC | 55728 |
| rs370444277 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077515 | CTAGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 55728 |
| rs370487835 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184716 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGTG | 55728 |
| rs370504732 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064446 | CGCCTGGCTAATTTT[C/T]GTATTTTTAGTAGAG | 55728 |
| rs370506590 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104211 | CCCGCCCCGGCCTCC[C/T]AAAGTGCTGGGATTA | 55728 |
| rs370542521 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140885 | GACACAGCACATGTT[G/T]CAGAGAGCACAGGGT | 55728 |
| rs370559845 | snp | C/T | 1.67103e-05 | 0.00289048 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120366 | ATGAAAAATCCTCAC[C/T]TGGTGAAATAGTGGA | 55728 |
| rs370573887 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169017 | AGGCTTGAGCCACTG[C/T]GCCTGGCCAAATATA | 55728 |
| rs370590934 | snp | A/T | 3.76011e-05 | 0.00433579 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119910 | AGACTTTCTCATGAT[A/T]CTCTTTAAAATAATC | 55728 |
| rs370593222 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121214 | AAGAATAAAATTAGC[A/G]TTTCAGATTCTATCA | 55728 |
| rs370608148 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165333 | AGGCCAGTGCAACCT[C/T]TGCTTCCCGGGCTCA | 55728 |
| rs370621616 | in-del | -/TTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146870 | TTCTATGTGTTTGGC[-/TTTT]TTTTTTTTTTTTTTT | 55728 |
| rs370631106 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154871 | TGGAAAGAAAGTTGG[A/G]TCTGAGATTATATTG | 55728 |
| rs370691315 | snp | C/T | 3.5692e-05 | 0.0042243 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122332 | AAAAGTAAATGACCA[C/T]GTGTGTGTCTTTGTG | 55728 |
| rs370708452 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092686 | TCTTGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 55728 |
| rs370712267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183422 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTTACG | 55728 |
| rs370735441 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099896 | TTGCTTTCTTTTTTT[-/T]CCCCCGTCCCTGCCC | 55728 |
| rs370758562 | in-del | -/CATGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165175 | TCCTGTCCTTAGAGT[-/CATGT]TAATAGTTTTAGGTC | 55728 |
| rs370767903 | in-del | -/GA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168282 | CTATCAACAGACAGA[-/GA]CTATCAGAATGGATT | 55728 |
| rs370787737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123937 | AGAAATTTTTTTTTT[A/T]AAATGCAGTATTTTT | 55728 |
| rs370813320 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088369 | TGCAGAATATTTTTC[A/G]GAGTGACTGTACCAT | 55728 |
| rs370874694 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135894 | TTCAAAAAATATTCG[-/TA]TATGGTCAGTTCCTC | 55728 |
| rs370910934 | snp | C/G | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117987 | AAAATTGAACGTATT[C/G]AGTTGTGTGCATATT | 55728 |
| rs370951763 | in-del | -/AAAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081003 | CATTATTTGGACACT[-/AAAA]AAAACTGCCTATATG | 55728 |
| rs370954418 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134964 | TTATTTTTTATTATT[A/T]TACTTTAAGTTTTAG | 55728 |
| rs370963126 | in-del | -/TATTTATT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101164 | CATTATTTATTTATT[-/TATTTATT]GTTGAGAGGGAGTCT | 55728 |
| rs370997420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067872 | TTTAGTAGAGATGGC[A/G]TTTTACCATGTTGGC | 55728 |
| rs371004957 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184371 | TGCCTTTTTTTTTTT[A/T]AATAAAAAATTCCCA | 55728 |
| rs371006257 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096862 | AGACTGGGAAAAGCA[C/G]GTTTGAAGGGGGTGA | 55728 |
| rs371015942 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169547 | TTAGAAACTGAACTG[A/G]AATGATAAACTTTGT | 55728 |
| rs371016021 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180437 | TAATGCAGGCAGATA[A/G]TTAGTCACTCTCATA | 55728 |
| rs371025593 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148405 | AGATGGCAGCAGTAC[A/C]GTCCAGCTTCGGCTC | 55728 |
| rs371060554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118810 | TCTGACAATTTGCAA[C/T]CCAAGGTAGCACTGA | 55728 |
| rs371072001 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134395 | GCTGGGTGTGTCCTT[C/T]TGGGGATGGTCAGTG | 55728 |
| rs371082098 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098949 | ATCTGTATTTTTAAT[C/G]GGTTTCTAATCTACT | 55728 |
| rs371098265 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077471 | TTTTTTTTTTTTTTT[G/T]GAGACTGAGTCTCGC | 55728 |
| rs371124253 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147074 | CCTTCCGCAGTGTTT[A/G]TGTCCCTGGGTACTT | 55728 |
| rs371147926 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142780 | TTTCCTTCACCAACA[A/G]AAGAGGATGGAGTGC | 55728 |
| rs371161111 | snp | A/G | 6.63559e-05 | 0.00575965 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102375 | GTTTTAATGACTCAA[A/G]TGAGTTTATAAATCC | 55728 |
| rs371219724 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088440 | TGAAGTCTTGCCATC[A/G]TTTGGTGTTGTACCT | 55728 |
| rs371228841 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056580 | GGCCGGGCAGGGCTT[A/C/G]CTCTCCAACGGGAGA | 55728 |
| rs371243897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131681 | CCTTTAATCCGTAAA[A/G]AAAGTCTGTGATTGC | 55728 |
| rs371251788 | snp | A/G | 0.000247457 | 0.0111206 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112192 | GTACCATAAGTTGTC[A/G]TAAGTTTATAACAGT | 55728 |
| rs371256921 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093275 | TATTTTCTTCTTTCT[G/T]CTGGGTTTGAGTTTA | 55728 |
| rs371264057 | snp | C/T | 1.67534e-05 | 0.0028942 | utr-variant-5-prime, synonymous-codon, intron-variant | N4BP2 | GRCh38.p7 | 4:40097565 | TTCTGAATGTGATTT[C/T]AAAGGTGAGAAAAAG | 55728 |
| rs371309025 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102851 | CATCCTGAACTGCCA[A/G]CTAAGGGGAAGGATG | 55728 |
| rs371314742 | snp | C/G/T | 8.27758e-05 | 0.00643288 | synonymous-codon, missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121600 | TTTGAAAGAAATTAT[C/G/T]AGCCAAAGAGGAACT | 55728 |
| rs371352230 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138949 | TTTAGGATTAGTTTG[-/TG]AATTTCTGCAAAGAA | 55728 |
| rs371408357 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181552 | CAATGTCATCTTCAG[G/T]GACTTGGCTTTCTTC | 55728 |
| rs371424781 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072136 | CTGGAGTGCGGTGGC[A/C]CAATCTCAGCTCACT | 55728 |
| rs371448304 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123077 | TATGTTTTCTGCAAA[C/T]ATATAATGAGTAATG | 55728 |
| rs371451226 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063252 | GTTATTGGTTCATAT[A/G]ACCATATAATAGGCA | 55728 |
| rs371451369 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136391 | ATCTATCTATCTATC[-/T]ATCTTTTTTTTGAGA | 55728 |
| rs371455749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116479 | TAAATTTTTTTCTTC[C/T]CTACTAATTTGGAAA | 55728 |
| rs371470314 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101406 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 55728 |
| rs371494007 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125906 | AAAAAAAAAAAAAAA[-/AT]TATACACAGATCATT | 55728 |
| rs371522855 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117678 | CTTTGTTTGAACTTA[A/T]GTGTATAATTTAAGA | 55728 |
| rs371525126 | in-del | -/CAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143674 | AGCAGAGAAGAGTAT[-/CAA]ACTGCTATAGGCCTG | 55728 |
| rs371556264 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141142 | GGCCGGGCAGAGGGG[C/T]TCCTCACCTCCCAGT | 55728 |
| rs371573437 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089061 | CTGCAAAGGATCCTT[C/T]CACCTTAGGCTCCTG | 55728 |
| rs371596305 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144044 | TGACTGCAGCCCCCA[A/G]TCCAGGGTCAAAGGC | 55728 |
| rs371601006 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183193 | GTATCATGAGCATCT[C/T]CTTATGTGGTCACAT | 55728 |
| rs371609952 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172828 | CCCAACAATGTGTTT[G/T]ATAATATCTTAAAAT | 55728 |
| rs371611507 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148426 | GCTTCGGCTCGGCAT[C/G]AGAGGGAGACCGTGG | 55728 |
| rs371611684 | in-del | -/TGTAT | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175512 | TGTAGGTAATAATAA[-/TGTAT]TGTATTCAAAAGAAA | 55728 |
| rs371620855 | in-del | -/CTGGC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085614 | GGCACGCCACCATGC[-/CTGGC]TAATTTTTAAATTTT | 55728 |
| rs371623688 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160043 | CAGGCTGGTCTCGAA[C/T]TCCTGATCTTAGGTG | 55728 |
| rs371627623 | snp | C/T | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40124185 | GACAAGAAGAGGTGT[C/T]TTGTGGCAAGTTTAT | 55728 |
| rs371648076 | snp | C/T | 3.32823e-05 | 0.00407922 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106884 | TAATGAAAATTATTT[C/T]ATTTATCTTTCACAG | 55728 |
| rs371694925 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084322 | TAGGCAAAAATGACT[C/T]AGTTTTTGGCTTCAA | 55728 |
| rs371726719 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108337 | TTTTTTTTTGAGACG[A/G]AGTCTTGCTTTGTTG | 55728 |
| rs371728484 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090465 | TTTCTTAGATTTATA[C/T]CTATGTGCTGAAATA | 55728 |
| rs371733301 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104311 | ATTAGCCTTCTAACA[G/T]TATCAGTTGGGTCTC | 55728 |
| rs371741472 | snp | G/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120270 | ACACAGATAGTTCTA[G/T]GGAGAGAGTATCACC | 55728 |
| rs371788329 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067370 | CCTTTTTTTTTTTTT[A/T]AAGGCTGAATAATAT | 55728 |
| rs371822717 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161624 | AAAAAAGAGATACAT[A/G]CTGAAATATGTACGT | 55728 |
| rs371824710 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132860 | TTCCTTTAATGCAGG[C/T]AGGAATTGATTTACT | 55728 |
| rs371828039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105465 | GAGTAGCTGGGATTA[C/T]AGGTATCTGCTGCCA | 55728 |
| rs371842728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104874 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAAGCTC | 55728 |
| rs371844703 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093565 | GTGTGTGCCACCTTG[C/G/T]GTGGCTAATTTTTGT | 55728 |
| rs371854244 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182687 | ATATATATATACATA[C/G/T]GTATAGAGAGACAGA | 55728 |
| rs371882082 | snp | A/G | 1.65004e-05 | 0.00287227 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112200 | AGTTGTCATAAGTTT[A/G]TAACAGTTTGTATGC | 55728 |
| rs371883574 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157586 | AGAAAATGACGAAAT[A/G]TATAAAAAAGACAAA | 55728 |
| rs371950665 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173893 | TTTTTTCTTTTTCCT[G/T]AACTGATGGCAAGAA | 55728 |
| rs371973548 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060006 | ATTCTTTTTTTTTTT[C/T]CTTTTTTTAAAGAGA | 55728 |
| rs372028208 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082900 | AGAGACGGGGTTTCA[C/T]CGTTTTAGCCAGGAT | 55728 |
| rs372072917 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186138 | GCCTCTGGAATCCCT[C/T]GTTTTTGGAGTCTGT | 55728 |
| rs372084170 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095381 | CCATAACGCCCAGCC[A/C]GCTATATCTTTTTGA | 55728 |
| rs372086892 | snp | A/C | 1.65452e-05 | 0.00287616 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126195 | ATCATCTCAGAGAAC[A/C]GGCAAAAAATTACTG | 55728 |
| rs372103367 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147849 | TCCTCACCTCCCAGA[C/T]GGGGTCGCGGCCAGG | 55728 |
| rs372118771 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184271 | CTTCCCTGTATGGCT[G/T]CACGGGCTAGAATGG | 55728 |
| rs372162338 | snp | C/G/T | 6.6302e-05 | 0.00575731 | missense, synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121403 | AACATTCTTTGTAAA[C/G/T]TGTTTGGATCCTTTT | 55728 |
| rs372174493 | snp | A/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185812 | AATGCACAGCTACAA[A/T]AATTTAGGTAATAAT | 55728 |
| rs372215847 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134973 | ATTATTATACTTTAA[G/T]TTTTAGGGTACATGT | 55728 |
| rs372242478 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124038 | TTTTACTTAGATTGA[C/G]TAAGAATGGTTTACA | 55728 |
| rs372274767 | snp | A/G | 1.66529e-05 | 0.00288551 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120263 | AAAACTGACACAGAT[A/G]GTTCTATGGAGAGAG | 55728 |
| rs372281148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083611 | ATACAATTCTCTTCA[C/T]ATAAATGCCTAGAAT | 55728 |
| rs372292780 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169772 | GTGTTCGAGACCAGC[A/G]TGACCAACATGGTGA | 55728 |
| rs372364982 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183044 | TAGAGGAATGTATAA[A/C]ACCAACCATGTTACC | 55728 |
| rs372393716 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160739 | CCAGATGAAAATACT[A/G]AACACACACTAAAAA | 55728 |
| rs372414469 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138453 | CTAGTTTGTCTACTT[C/T]TGCTATGTTGCCTGT | 55728 |
| rs372417591 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064564 | AGGCGTGAGCCACCG[C/T]GCCCGGCAATAACAA | 55728 |
| rs372431179 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099190 | ATTCCACCAGGCTTG[C/T]ATAAGTGTAGTGGTT | 55728 |
| rs372451748 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166461 | TTGGGAGGCTGAGGC[G/T]GGTGGATCACCTGAG | 55728 |
| rs372465653 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066398 | ATCTCGGCTCATTGC[A/C]GCCTCTGCCTCCCAG | 55728 |
| rs372473996 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141889 | TTAGGAGCTGGAGAC[C/G]AGCCCGGCCAACACA | 55728 |
| rs372502515 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060530 | GATTACAGGCATGAG[C/G]CACTGTGCCCGGCCG | 55728 |
| rs372503128 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170522 | CGCCACCACAGTCCC[A/G]CTCTACTTGTGGGGT | 55728 |
| rs372570271 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059963 | GGTAGGTTTCAGTCA[A/G]ACTTAGATCTTTGTG | 55728 |
| rs372581481 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079542 | TTGCCATAACACTAT[C/T]AGAGATCATGTTTGT | 55728 |
| rs372598217 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173863 | TTTTACCTCCCTTTT[-/T]CTTTTCTCATTTCTT | 55728 |
| rs372747686 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175303 | GCTAGGATTATAGGC[A/G]TGAGCCACCAAGCCT | 55728 |
| rs372754910 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102777 | GTGGGGATCAGAAAT[C/G]TACTCGGGTCTCTGA | 55728 |
| rs372771526 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062094 | TTTTTTTTTTTTTTT[C/T]TTGAGACGGAGTCTC | 55728 |
| rs372781523 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064577 | CGCGCCCGGCAATAA[C/G]AAGTATTTATTGAGC | 55728 |
| rs372787225 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123927 | CTTCATAACAAGAAA[A/T]TTTTTTTTTTAAATG | 55728 |
| rs372792952 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106983 | AGTACCAGTTTGATG[C/T]AAAGTACTTAGGAGA | 55728 |
| rs372828534 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085385 | TCAGTGAATACTTTG[A/G]TGTGGGTCTACAGTC | 55728 |
| rs372841993 | snp | A/G | 0.00113754 | 0.0238218 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122350 | GTGTGTCTTTGTGTG[A/G]CTAGACTACAGAGGG | 55728 |
| rs372862196 | snp | A/C | 1.65809e-05 | 0.00287926 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113417 | TTAAAATGTTTTTGT[A/C]TTTGTTGTATGTAGT | 55728 |
| rs372864311 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126970 | CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 55728 |
| rs372870291 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183990 | CAAGCAAGACTTTCC[C/G]GAACATTTCGTTGAT | 55728 |
| rs372886539 | in-del | -/TTAGTAGCGATGGGGTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074305 | TATTGGTCAGGCTAG[-/TTAGTAGCGATGGGGTT]TCTCTTAACCCTTGA | 55728 |
| rs372890613 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110548 | TGTATATCTTCTCTG[A/G]AGAAATGTCTATTCA | 55728 |
| rs372892819 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088585 | CGCTCACTGCAGCCT[C/T]CGCCTCCCGGGTTCA | 55728 |
| rs372953198 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134256 | TTCTGAGAGTTTTGT[A/G]TTAAAATCTCCCAGA | 55728 |
| rs373009294 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092009 | AAAAAAAAAAAAAAT[A/T]ATATATATATATATA | 55728 |
| rs373033269 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163039 | GAGCAAAACAGAAAC[A/T]GCAGTACCTTTTATG | 55728 |
| rs373048358 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40154102 | GTAAATATTATATTA[A/G]GCGTAGGTACTTGGA | 55728 |
| rs373060453 | in-del | -/GTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112048 | ATACTTAGTATTGTT[-/GTT]TAAAAAATGATTTTT | 55728 |
| rs373170902 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114419 | GGCAACCACTAATGT[A/G]TGTTCTGTATTTATG | 55728 |
| rs373180693 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081985 | GGTGTGGTGGCGCAT[G/T]CCTGTAATCCCAGCT | 55728 |
| rs373204382 | snp | A/G | 6.62778e-05 | 0.00575626 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120656 | CCACATGAAAGTGTA[A/G]AGGATGGCAGAAAGT | 55728 |
| rs373251697 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097585 | GTGAGAAAAAGTTTA[C/G]TTTGAACCCTGTCCA | 55728 |
| rs373277932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127754 | CATGCTCCGTCTCCC[A/G]GGTTCATGCCATTCT | 55728 |
| rs373290951 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145510 | CTGCTCCTAGCCTGA[A/C/T]CCCAGTTGTTTTTAA | 55728 |
| rs373302246 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074072 | ACTGGGATTACAGGC[A/G]TGAGCCACCGAGCCC | 55728 |
| rs373316620 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40054938 | TTTGTGGCTTGAAAT[A/G]TATTTTCCAATGTTA | 55728 |
| rs373325205 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129312 | GCTCACTGCAACCTC[C/T]ACTTCCCAGGTTCAA | 55728 |
| rs373331111 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096952 | GTTCAGTACGCATTC[C/T]AATTATATTTATGAA | 55728 |
| rs373333208 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124595 | CAGGTGATCTGCCCA[C/T]CTTGGCCTCCCAAAG | 55728 |
| rs373336029 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154186 | ACTCTTTTCTCATTT[C/T]TGCAGGTTCTCTGAA | 55728 |
| rs373337322 | snp | A/T | 0.000252189 | 0.0112263 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122020 | ATTAAATGAAGAAAT[A/T]TATTTTACTGATTCT | 55728 |
| rs373347038 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098894 | AATTTTGTTATTATG[C/T]GTTTTTAACTTAACA | 55728 |
| rs373376107 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135892 | ATTTCAAAAAATATT[C/T]GTATATGGTCAGTTC | 55728 |
| rs373381293 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162463 | GACTCTGTCTCAAAA[-/AAG]AAGAAGAAGTAGAGC | 55728 |
| rs373390043 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117667 | GAATTTTTTTTCTTT[-/G]TTTGAACTTAAGTGT | 55728 |
| rs373397743 | snp | C/G | 3.45764e-05 | 0.00415776 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122294 | GAATTATTTGGTCCT[C/G]TTGGTATTGATTCAG | 55728 |
| rs373405991 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082397 | TCCTGGGTTCAGCTT[A/C]ATAATAGAAACAACC | 55728 |
| rs373411920 | snp | A/G | 0.000116074 | 0.00761731 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120759 | CATTCAACATTATGG[A/G]TGACTGGCCTTCATC | 55728 |
| rs373414880 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114485 | ATACAATATGTGGCT[-/G]GTTTGTGTCTGGCAT | 55728 |
| rs373433932 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168568 | AATATAAGGATAACA[A/T]CATAAAAATGAAATT | 55728 |
| rs373453667 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081165 | GATTATGGAAAAAAT[A/G]CATTTCTTACGGATT | 55728 |
| rs373454489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174204 | CAAAATAGCAAGACA[C/G]TGTCTCTACAAAAAA | 55728 |
| rs373495561 | snp | C/T | 7.12352e-05 | 0.00596762 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122329 | GGAAAAAGTAAATGA[C/T]CATGTGTGTGTCTTT | 55728 |
| rs373513853 | snp | C/T | 0.000116182 | 0.00762085 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154261 | TCCTTGAATTAGAAG[C/T]ATGAAGGTTTGTAGG | 55728 |
| rs373537954 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099944 | TTTTCTTCCATTTTT[A/C]GGTTTTCTGTCCTTT | 55728 |
| rs373542581 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101469 | CAAAAAGTGTGCATT[A/T]TTTAATCTGTATTAT | 55728 |
| rs373552331 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178134 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCGAG | 55728 |
| rs373564617 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071022 | TGGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 55728 |
| rs373577242 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078159 | TGTGTATGTGTGTAT[G/T]TATTATTATTATTTT | 55728 |
| rs373585446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128501 | CTTCAATTAATATAT[A/G]TATTAATTTGAGGCA | 55728 |
| rs373618991 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160615 | ACAGTGAGTTTATTA[C/T]ATAAGTGACCCCATT | 55728 |
| rs373636197 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110823 | GATCATAGGTGTGAG[A/G]TACCGTGCCCAGCCT | 55728 |
| rs373642980 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115707 | TTCAACTTAACTACA[G/T]TAGGTCAGGTTGTGT | 55728 |
| rs373653964 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077049 | TTGTTTCTTTTTTGA[G/T]GGTCTTAAGGAGCTA | 55728 |
| rs373660938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148580 | CTTATTTCACTTAGT[A/G]TAATGCCCTCCAGCC | 55728 |
| rs373665207 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135311 | GCATAGTATTCCATG[A/G]TGTATATGTGCCACA | 55728 |
| rs373679092 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177348 | GGGCCCGGCACGGTG[A/G]TTCACGCCTGTAATA | 55728 |
| rs373732410 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099823 | ACATTAAGTTTTTAG[C/T]TGATCTTTTCTGGTT | 55728 |
| rs373741257 | snp | A/T | 1.65e-05 | 0.00287224 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112197 | ATAAGTTGTCATAAG[A/T]TTATAACAGTTTGTA | 55728 |
| rs373776151 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170171 | ATGGAAATAAAAACA[-/TA]AATTTCAAGATATAT | 55728 |
| rs373789805 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076758 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 55728 |
| rs373822937 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119532 | AAATGAAGCTTCCTC[A/G]GTATCAGACCTATTT | 55728 |
| rs373832759 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169858 | TAATCTGAGCTACTC[A/G]GGAGGCTGAGGCAGA | 55728 |
| rs373836099 | snp | C/T | 0.000173943 | 0.00932424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142642 | TTTTTTAACTTTCTG[C/T]GTGTGTTACTTATTG | 55728 |
| rs373839929 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132848 | GATTTTTTTTTTTTC[C/T]TTTAATGCAGGTAGG | 55728 |
| rs373840538 | snp | A/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123137 | ACAAGGGTCTCTAAC[A/T]GTTGAAGATTGTGTG | 55728 |
| rs373871430 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056742 | TCCACCTGGGCGACG[C/T]GGCAGCCATTGCCGG | 55728 |
| rs373872290 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178709 | GTTTGAACAGACTCC[A/G]TCTGCACAGTTTCCT | 55728 |
| rs373912661 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151129 | CTCTTACTTGAGGCA[C/T]GTGAATCAACTAGAG | 55728 |
| rs373941724 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140779 | ACTTGAGATTAGGGA[G/T]TGGTGATGACTCTTA | 55728 |
| rs373973789 | snp | A/T | 1.70203e-05 | 0.00291716 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121936 | AGTCACAGAGACTGG[A/T]GACAACATACATTCT | 55728 |
| rs373975176 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096223 | TGTAAAACATATGCT[A/G]TGTAAGAAAACAATA | 55728 |
| rs374008198 | in-del | -/AAAT | 0.116488 | 0.211364 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184958 | AGACTCTGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 55728 |
| rs374043860 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116838 | AAGATACTTTTGCTG[G/T]ATATGTATATTCTAT | 55728 |
| rs374077704 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118598 | GTGAGTCCGTGATTA[C/T]GCTATGAATTCTCCT | 55728 |
| rs374084866 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119071 | TATTTCCTGGGTTCA[A/G]AAAGTCCCAAAGCTT | 55728 |
| rs374108710 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160426 | GGTGATGGGCTAGTG[-/TG]ATATGTGGTGCAATA | 55728 |
| rs374225332 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180529 | TACTCTGAAACCTGC[A/G]AAGTCACTTCCTGTC | 55728 |
| rs374255637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068699 | AAGCCCTACCATACT[A/G]TGTTGATTACTGTAG | 55728 |
| rs374275374 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40185114 | GTCTCCCTTCCATTC[A/G]ACGTGTGCCTCTTGT | 55728 |
| rs374281963 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152339 | ATGATTCAGAACAAA[A/G]CTTGATGGCTTTAGA | 55728 |
| rs374283929 | snp | A/G | 0.000115315 | 0.00759236 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097458 | ACTACTCTACCTTCC[A/G]TGGGTGAGACAAAAG | 55728 |
| rs374287540 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169104 | AAAATAAAAAAGGGC[C/G]GGGCGTGGTGGTTCT | 55728 |
| rs374303570 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164335 | AGGATGTGGGTATTT[G/T]TTCCTAAGGGAGTTT | 55728 |
| rs374339859 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115390 | TGGTCCCAGGTACTC[A/G]GATGCTGAGGTGGCA | 55728 |
| rs374390792 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165799 | GAACTTATAGGAAAC[A/G]TTTGTGTTTTATATA | 55728 |
| rs374441813 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121353 | CGTTTGTTGAAGAAA[A/G]TGAGCTTACCAGTGC | 55728 |
| rs374444087 | snp | C/T | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102411 | CAAGTAATATGACTC[C/T]CATTTTTTCTACACA | 55728 |
| rs374456006 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131963 | TCTACTCTGATGTCA[C/T]TGAAAGCATATGCCA | 55728 |
| rs374488519 | in-del | -/CAAAAGGAAAAAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083138 | AGAAAAAGGAAAAAA[-/CAAAAGGAAAAAA]AGAAAAACAAACCCA | 55728 |
| rs374519077 | in-del | -/TTTTTTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145214 | CTCCCACTCCAGTAG[-/TTTTTTTT]TTTTTTTGTTTGTTT | 55728 |
| rs374532558 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110554 | TCTTCTCTGGAGAAA[C/T]GTCTATTCATATTTG | 55728 |
| rs374576486 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138859 | GGGAAGTGTGAGTTT[-/T]CCAACTATGTTCTAT | 55728 |
| rs374610792 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113031 | TCTTCCTTTCTTAAC[A/G]TTTTTTTAAAGAACA | 55728 |
| rs374622396 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141077 | AACCGCCATTGTCAT[C/G]ATGGCCCGTTCTCAA | 55728 |
| rs374666747 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174672 | GGCGGTGTAGTGGTG[C/T]GCACCTGTCATCCCA | 55728 |
| rs374695987 | snp | A/G | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121611 | TTATTAGCCAAAGAG[A/G]AACTTTAGAGAATTC | 55728 |
| rs374731036 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084614 | CAAATTTTGTGTGTG[-/TA]TATATATATATATAT | 55728 |
| rs374826242 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110756 | TTGGCCAGGATGGTC[G/T]CGAACTCCTAACCTC | 55728 |
| rs374829365 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064825 | CCCAGGCTGGAGTGC[A/C]GTGGTGTGATCTCGG | 55728 |
| rs374833696 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157296 | GTATTTCCATACTAT[C/T]TGCAACTTTATGGCC | 55728 |
| rs374840395 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172074 | ACCACACCTGGCTAA[C/T]TTTTTGTATTTTTAG | 55728 |
| rs374845650 | in-del | -/TTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159891 | TGTTGTTTTTTTTTT[-/TTT]GAGATGGATTCTCAC | 55728 |
| rs374855885 | snp | A/C/G | 6.6031e-05 | 0.00574558 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102614 | GCAAGTGACTCCATC[A/C/G]CAGGTTGTAGCAGTC | 55728 |
| rs374862729 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121008 | AGACTTGTCTAAGTA[A/C]AAAGAGTCATGGGCA | 55728 |
| rs374877710 | snp | C/T | 3.31879e-05 | 0.00407343 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120598 | ACACAAATTAGTTAA[C/T]AGTGTATCTGTGAAT | 55728 |
| rs374882770 | in-del | -/TGTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106302 | ATATTACAATATGTT[-/TGTT]CTTTTATTTATCTCT | 55728 |
| rs374883055 | snp | A/T | 4.94254e-05 | 0.00497094 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124229 | CATGTTTTTATTTCT[A/T]ATGTCTTAATGTTGA | 55728 |
| rs374892340 | snp | A/G | 0.000412565 | 0.0143566 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112217 | AACAGTTTGTATGCA[A/G]TTATTGGGGAACATT | 55728 |
| rs374893535 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060007 | TTCTTTTTTTTTTTT[C/T]TTTTTTTAAAGAGAC | 55728 |
| rs374962141 | snp | A/G | 1.66092e-05 | 0.00288172 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40118015 | ATTCTTGTGAGGATA[A/G]AAGCACTAGGTAGGT | 55728 |
| rs375092217 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060047 | CTATGTTGCTCAGGC[C/T]GCTCTCGAACTCCTG | 55728 |
| rs375145171 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113634 | ATTTCTATTGCTTAC[A/G]GCTTTTTGTCCAGTT | 55728 |
| rs375166755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133047 | TGTGGAAAGTTTAAA[G/T]AACTTAGTACCTTGA | 55728 |
| rs375186742 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063339 | ACCTTTCCGTACTTA[C/T]ACTCTGTGCATACTG | 55728 |
| rs375199579 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118907 | GTAAAGAAGAAACCA[C/G]AGGTCTGAATTATCC | 55728 |
| rs375223959 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149204 | GTGGTAACCTAAAAG[G/T]TCATTAACTGATGAA | 55728 |
| rs375260877 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069496 | TTTCTTTTTTCTTCT[C/T]GACATGTAAGGACAG | 55728 |
| rs375265000 | snp | A/G | 6.62899e-05 | 0.00575678 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121657 | AGAGTTTAGCCATGG[A/G]ATTGGTATTAGTAAC | 55728 |
| rs375278533 | in-del | -/T | 0.00454233 | 0.0474398 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127672 | AAATATATATATATA[-/T]TTTTTTGAGATGGAG | 55728 |
| rs375290380 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110954 | TACTTGTTGTGGTAC[A/C/G]TCATTAATTTCCTGT | 55728 |
| rs375334692 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170060 | GAAAAGATAAAAAAA[A/T]CTCTGAAAAAAGAGA | 55728 |
| rs375343163 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106913 | AGGACTTTGCAAGAG[A/G]ATAATCCAAGTGGAG | 55728 |
| rs375423661 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178640 | AACAAGGACAATATC[C/T]AGCTCTCTAGATAAC | 55728 |
| rs375431818 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070441 | CAGTAATTCCCTAGT[A/G]TTATACTACTTTTTG | 55728 |
| rs375454351 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159409 | TAAAAATTCCAGGAC[C/T]GCTTTACTTGACGCT | 55728 |
| rs375480847 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125879 | GCGACAGAGCAAGAC[G/T]CCGTCTCAAAAAAAA | 55728 |
| rs375515808 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119276 | TAGGAAGGCATCCTG[C/T]GAGAGTTGGGACTTC | 55728 |
| rs375544445 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085224 | CCAATTTATATTTTT[A/G]GTAGAGATGGGGTTT | 55728 |
| rs375547982 | snp | G/T | 0.00147123 | 0.0270823 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121757 | CCTGAAAACCATGAA[G/T]CGATGACAAGTATAT | 55728 |
| rs375576195 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101685 | ACATAAAATACTTAA[C/T]ATTTAAAAGTTTGCA | 55728 |
| rs375580627 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081507 | AAAAATTAATGGGGT[A/G]TGGTGCCGCATGCCT | 55728 |
| rs375582091 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056404 | ATTCCGGGCCTGTTG[C/T]AATGTTCCCCAGCGC | 55728 |
| rs375584603 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111413 | GCAACCTCCGCATAC[C/T]GGGTTCAAGTGATTC | 55728 |
| rs375586647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128676 | GGGATTACAGGCATG[C/T]GCCACCATACCCAGC | 55728 |
| rs375604805 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111747 | CAGCCTCCTGAGTAG[C/T]TGGGACTACAGGTGG | 55728 |
| rs375610531 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092746 | CCTACTGGGTTCAAA[C/T]GATTCTCTTGTCTCA | 55728 |
| rs375673740 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104321 | TAACATTATCAGTTG[A/G]GTCTCTATTTGATCC | 55728 |
| rs375678722 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063630 | TGATTTATTTATTTT[A/T]AATTAAATTAATTAA | 55728 |
| rs375689379 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056590 | GGCTTGCTCTCCAAC[C/G]GGAGAGCGGGAGCGG | 55728 |
| rs375734255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063562 | GAGTAGGGGAGAGGA[C/T]GGAGTTCTGGGCAGA | 55728 |
| rs375781383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060582 | GAGGCTTTAATAAAT[C/T]TATGTGGCTAAGTAG | 55728 |
| rs375789160 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141933 | TCCACCAAAAAAATA[C/G]GAAAACCAGTCAGGC | 55728 |
| rs375797305 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125907 | AAAAAAAAAAAAAAA[-/T]TATACACAGATCATT | 55728 |
| rs375800358 | in-del | -/TTTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134932 | CTCTCTTTCTTTCTT[-/TTTTA]TTTTATTTTATTTTA | 55728 |
| rs375804850 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125153 | GGTCCAGACCTGTGC[G/T]CATGTCATAGCCTCA | 55728 |
| rs375807953 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154167 | AATTTTCATCTTTAA[A/G]ATAACTCTTTTCTCA | 55728 |
| rs375815794 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102943 | GATGTGGAATCCAAT[A/G]ATTCCTGCTTTTGAC | 55728 |
| rs375832960 | snp | A/C | 1.66796e-05 | 0.00288782 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121224 | TTAGCATTTCAGATT[A/C]TATCAAAGTATTAAC | 55728 |
| rs375884572 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074464 | TCCGCCTGCCTCGGC[A/C]TCCCAAAGTGCTGGG | 55728 |
| rs375894342 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150689 | GGGAAAAAAAAAAAA[A/G]AGGAAGTCTAGGATA | 55728 |
| rs375900852 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140796 | GGTGATGACTCTTAA[C/G]GAGCATGCTGCCTTC | 55728 |
| rs375922646 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145454 | GTCTTGAACTCCTGG[C/T]CTCAAGCAATCCACC | 55728 |
| rs375938671 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112715 | CACCTTTTTTTTTTT[-/G]TTGTTGAGATGGAGT | 55728 |
| rs375950840 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104663 | GACAAGTTTGAAGAA[-/C]TAGGTTTCAGGGGCC | 55728 |
| rs375961483 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148145 | GATCACGCCACTGCA[C/T]TCCAGCCTGGGCACC | 55728 |
| rs375969356 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067910 | GTCTTGAACCCCTGA[C/T]CTCAGGTAATCCACC | 55728 |
| rs375972615 | snp | C/T | 0.000117342 | 0.00765881 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120399 | AAAGAGCAACAGTAA[C/T]GAAAAAAGCCTTTGG | 55728 |
| rs376075466 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108072 | AGTTGGGACTATAGG[A/G/T]GTGTGATACCATGCC | 55728 |
| rs376121939 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112685 | CTCTTCTTGCCCTTC[C/T]TGCTCTTTTTTGCTC | 55728 |
| rs376132796 | snp | C/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055700 | GGAGGAAGTAAAAAA[C/G]AGGCAAAACCACCAC | 55728 |
| rs376135572 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168812 | TTACTGCAACCTCCA[A/C]CTCCCTGGGTTCAAG | 55728 |
| rs376163835 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089201 | TTAAGGGATTCCCCC[C/G]CTCTTCAGCCCCTGT | 55728 |
| rs376166256 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147237 | TTGGGGGTAAGGTCA[C/T]AGATCAACAGGATCC | 55728 |
| rs376186187 | in-del | AGG/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171584 | TCTTAATTGGAGGTA[AGG/T]TCTTTACAGAAGTAA | 55728 |
| rs376195405 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103092 | GGAGAAATAAAGATG[C/G]AACAAGTGCTTATCA | 55728 |
| rs376210179 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135703 | AAGTAGTTGGGATTA[C/T]AGGCGCCCGCCACCA | 55728 |
| rs376274494 | snp | A/G | 1.82667e-05 | 0.00302209 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122358 | TTGTGTGACTAGACT[A/G]CAGAGGGTTCTATTT | 55728 |
| rs376287139 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134967 | TTTTTTATTATTATA[C/T]TTTAAGTTTTAGGGT | 55728 |
| rs376307079 | snp | A/G | 3.41268e-05 | 0.00413064 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121941 | CAGAGACTGGAGACA[A/G]CATACATTCTCCTTC | 55728 |
| rs376323905 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090897 | AAGATCACGCCATTG[A/C]ACTCCAGCCTGGGTG | 55728 |
| rs376374761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127945 | GGATTACAGGCGTGA[A/G]CCGCCATTCCTGGCC | 55728 |
| rs376384794 | snp | A/G | 1.64787e-05 | 0.00287038 | utr-variant-5-prime, missense, intron-variant | N4BP2 | GRCh38.p7 | 4:40097506 | TTCACCAGTATCTCA[A/G]AGATATTTTCTGATC | 55728 |
| rs376394474 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097357 | TGCCAAGGAGAAGGA[A/G]AAATCTTGGGGGAAA | 55728 |
| rs376417954 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088937 | CCAATTGTTTGGTTT[A/T]TATTTTTTGTTTTTT | 55728 |
| rs376429460 | snp | C/G | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126229 | ACTTTAACAGCATCT[C/G]AAATGCTACCTTTAT | 55728 |
| rs376447442 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167727 | GATGATGAGTGAACA[A/G]TAAGCCTTGTAATAT | 55728 |
| rs376468550 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111889 | CCAAAGTGCTGGGAT[G/T]ATGGGCATGAGCCAC | 55728 |
| rs376471009 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106585 | ATACAGTCTTGCTCT[A/G]TCTCCCAGGCTGGAG | 55728 |
| rs376471730 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066235 | TGCCCGGCCCATTTT[C/T]TTCAGGGGACCCAGA | 55728 |
| rs376472660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161637 | ATGCTGAAATATGTA[C/T]GTAAAATGATACGAT | 55728 |
| rs376536492 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079150 | TGGTCTTGAACTCCT[C/G]ACCTCAAGTGATCCT | 55728 |
| rs376544109 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131794 | GATTTTTATGTTTTT[A/G]TTTTAGAAAAGGGAG | 55728 |
| rs376553645 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071726 | CTCTCGCCACCACGC[C/G]CAGCTAATTATGTAT | 55728 |
| rs376571491 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117709 | AATCCTTAATAAAAT[C/G]AAAATTAGAATCAAA | 55728 |
| rs376572810 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144563 | CTTTTATTTGGGGCA[C/G]TATTAACTTCCTCAT | 55728 |
| rs376579921 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130699 | TAGAGATAGGGTCTT[-/G]GCTGTGTTGCCAGGT | 55728 |
| rs376580028 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163291 | GGGTAGGTATTATTG[-/C]CCACATGGCCGACAT | 55728 |
| rs376586958 | snp | A/G | 8.30475e-05 | 0.00644336 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40136968 | AGAACACACAGTGCA[A/G]TTTCTTAACTGTGTT | 55728 |
| rs376601198 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073011 | CAGGTGTGAGCCACC[A/G]CACCTGGCCAGGTCA | 55728 |
| rs376644836 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122438 | GAGTGCAGTGCCTCA[A/G]TCTTGGCTCACTGCA | 55728 |
| rs376653655 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104449 | GTGTCTGGGTTTCTC[G/T]GCTAGTAAATTTCCA | 55728 |
| rs376657571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125526 | CCAGTGTCCTGTATA[C/T]ATGTCACTATGTTTT | 55728 |
| rs376658244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084951 | GGAGTCTCGCTGTGT[C/T]GCCCAGGCTAGAATG | 55728 |
| rs376659929 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078031 | TAGCTGATAAGGTTC[A/T]TTTTAGAGAAAATAC | 55728 |
| rs376671875 | snp | A/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156534 | AGCATAGTTTAAGCA[A/T]CACATAATTTTGAAA | 55728 |
| rs376672770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141191 | GCGCCCCTCACCTCC[C/T]GGAGGGGGCGGCTGG | 55728 |
| rs376673021 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40154100 | TAGTAAATATTATAT[G/T]AAGCGTAGGTACTTG | 55728 |
| rs376683746 | in-del | -/AATT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116940 | GTCAGCTGTCATTCT[-/AATT]GTTTCTTTGTAGATA | 55728 |
| rs376691776 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150819 | TATTTCAATCTTGAT[G/T]CCAACAAATTACTGT | 55728 |
| rs376737148 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110160 | GTGTTTCATTCCTTT[A/T]TATGGATGAGTAAGA | 55728 |
| rs376739841 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164879 | TTATTTAAACAATTA[A/C]AGGCAACTCTGCTGA | 55728 |
| rs376745415 | snp | C/T | 0.000446646 | 0.0149373 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154189 | CTTTTCTCATTTCTG[C/T]AGGTTCTCTGAAATT | 55728 |
| rs376745820 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095438 | TGCCTTTCTTTGTCT[A/G]TGATAATTTTCTTTG | 55728 |
| rs376759041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058005 | CTACTCGACATCTTT[G/T]AGCCAATCAGCAAGG | 55728 |
| rs376765249 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065558 | AACCAGTAAATGCTG[A/C]TTGGGATGGGAGGGT | 55728 |
| rs376829059 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165097 | TACCTTATTAATTTT[-/AT]GTTACCTTCATAGAA | 55728 |
| rs376876308 | snp | C/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055165 | TTTAGTCTCTTATAA[C/T]GGTTGTTTAGAGGCA | 55728 |
| rs376882257 | snp | C/T | 0.00464035 | 0.0479441 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100027 | TCCCTCTTTGTTTTT[C/T]TTCTTAAGGGAACTT | 55728 |
| rs376890743 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181314 | CCCCAACTTTCTGTT[C/T]GTTTCTTCCGGATAG | 55728 |
| rs376893983 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166925 | CTAAATGATTGTTGA[C/T]TGTAGTCACCCTTTT | 55728 |
| rs376911909 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169883 | GGCAGAGAATTGCTT[C/G]AACCTGGGAGGCAGA | 55728 |
| rs376931333 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162805 | GAGGCTGAGAAGTTC[-/C]ACACCAGGCCATCTG | 55728 |
| rs376941283 | in-del | -/TGTA | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154472 | ATTGATTACAAAATA[-/TGTA]AGAAAATTATCAGCT | 55728 |
| rs376968913 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118802 | CATGGCCTTCTGACA[A/G]TTTGCAATCCAAGGT | 55728 |
| rs376969234 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169762 | CTGAGGTCAGGTGTT[C/T]GAGACCAGCGTGACC | 55728 |
| rs376990556 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186161 | GAGTCTGTCTGGAAG[G/T]TTGAATTGGCATTGG | 55728 |
| rs377000222 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059086 | TCCGCCTCCCAAAGT[C/G]CTGGGATTACAGGAG | 55728 |
| rs377008109 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101450 | CAGGCATGAGCAACC[A/G]CGCCAAAAAGTGTGC | 55728 |
| rs377010577 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115573 | CTTTATTTTTGTCTT[A/G]TTTAGTTATTTTCTA | 55728 |
| rs377016028 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141782 | GATCACGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 55728 |
| rs377171419 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102830 | TTCAACTTCAAGCCA[C/T]ACAAACATCCTGAAC | 55728 |
| rs377183488 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144776 | CTAGAACATTTGATG[A/G]GAGTTTTAGAGAAGA | 55728 |
| rs377188372 | snp | C/G | 0.000296912 | 0.0121806 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112159 | CATGGGAAATGAAAC[C/G]ATATGTTGCTTTGGT | 55728 |
| rs377202507 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104828 | TTTTTTTTTGGAGAC[A/G]GAGTCTTGCTCTGTC | 55728 |
| rs377207378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111343 | GGGGTTTTTTTGAGA[C/T]GGAGTCTTACTCTGT | 55728 |
| rs377207956 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129864 | AAATATAACTTTAGA[C/T]ATAATATATGAATAG | 55728 |
| rs377215062 | snp | C/T | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054383 | GTCAGGAGTTAGAGG[C/T]CAGCCTGGACAACAC | 55728 |
| rs377220524 | snp | A/G | 1.89453e-05 | 0.00307771 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119881 | TAAATCATAGTATTG[A/G]TGGCAGCATTAAGAG | 55728 |
| rs377239058 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083854 | TTTAATAAAGCTGGT[A/G]TAAGTAGAAATTTGG | 55728 |
| rs377276400 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108849 | TGGAGACAGAGTCCT[G/T]CTCTGTTGCCAGGCT | 55728 |
| rs377278240 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171275 | AAAACTAGCCAGGAA[A/G]CCAGGAGACGAGCTC | 55728 |
| rs377312791 | in-del | -/TC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179758 | GAGTGGTAAAGCCTT[-/TC]TTTTTTTTTTTTTTT | 55728 |
| rs377329606 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151628 | AGTGCCCAAAATTAT[A/G]GGTATATAGTGCAAA | 55728 |
| rs377340025 | snp | A/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113507 | CCAAAGGAACTTGCA[A/T]GGTAAAACTTGGAGG | 55728 |
| rs377383640 | snp | C/T | 3.48171e-05 | 0.00417221 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122301 | TTGGTCCTGTTGGTA[C/T]TGATTCAGGTAAGGA | 55728 |
| rs377395360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080691 | TTATTTGTTGAGATG[A/G]AATCTCGCCCGGCTG | 55728 |
| rs377411067 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176350 | TGTTGTTGGACATTC[A/G]TGCTGATCAAAATCT | 55728 |
| rs377444914 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058414 | TTATTATTTAAGTGC[C/T]GTGCTAGGATGGGGG | 55728 |
| rs377531975 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155278 | GTGCCTGTAATCCCA[A/G]CTACTTGGGAGGCTG | 55728 |
| rs377571002 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171852 | ATGTGGAGTCTGATG[C/T]TCGAGGGCAGGAAGC | 55728 |
| rs377583496 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071762 | GTAGAGACGAAGTTT[C/T]GCCATATTGGCCAGG | 55728 |
| rs377609065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135030 | GTATACATGTGACAT[A/G]CTGGTGTGCTGCACC | 55728 |
| rs377612297 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096436 | AGAAGAGTGAGGAGA[C/T]TTAAGTGTGGCTAAG | 55728 |
| rs377625019 | snp | A/C | 0.000123199 | 0.00784758 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119970 | TCTCTGAAAAAGAAG[A/C]AAATATTTTATCTTT | 55728 |
| rs377653995 | snp | A/G | 1.78299e-05 | 0.00298574 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122331 | AAAAAGTAAATGACC[A/G]TGTGTGTGTCTTTGT | 55728 |
| rs377677877 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150433 | GCACTTTGGAAGGCC[A/G]AGGCAGTCAGATCAC | 55728 |
| rs377678648 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168016 | ATATTCTTACATAAT[A/G]GTAATAAAATATGTG | 55728 |
| rs377681051 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093233 | ACAGGCATGAGCCAC[C/T]ATGCCTGGCCCCGGC | 55728 |
| rs377685682 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184009 | CATTTCGTTGATGAG[A/G]ACTGGGTCACACAGC | 55728 |
| rs377710600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135818 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGT | 55728 |
| rs377711369 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148421 | GTCCAGCTTCGGCTC[C/G]GCATCAGAGGGAGAC | 55728 |
| rs377715346 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181488 | AGTTGGTTTTTCCCT[A/G]CTGTGCAAATGAAAC | 55728 |
| rs377754093 | in-del | -/CTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146869 | TTTCTATGTGTTTGG[-/CTT]TTTTTTTTTTTTTTT | 55728 |
| rs386399876 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134393 | GGCTGGGTGTGTCCT[-/T]TCTGGGGATGGTCAG | 55728 |
| rs386399877 | in-del | -/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134394 | GCTGGGTGTGTCCTT[-/T]CTGGGGATGGTCAGT | 55728 |
| rs386673771 | multinucleotide-polymorphism | AG/CA | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056037 | GCCGATGGGGCTGGG[AG/CA]GCCTCCCTCCACCCC | 55728 |
| rs386673772 | in-del | AGTT/TGGCTAACC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109511 | TCACCTGAGGTCAGG[AGTT/TGGCTAACC]TGAGACCACCCTGGC | 55728 |
| rs386673773 | multinucleotide-polymorphism | GC/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137692 | GGCTTGCTACCCAAG[GC/TT]CACATGGGGAGCCAG | 55728 |
| rs386673774 | multinucleotide-polymorphism | GCT/TCC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138099 | GAAGGCTGCAAAAAT[GCT/TCC]AGTGGCAGAATACAG | 55728 |
| rs386673775 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142560 | TCTATTTCCTGAGGA[AAA/GAG]AGATGAAAATATACG | 55728 |
| rs386673776 | multinucleotide-polymorphism | CAT/GAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150184 | TTTTTAAAAAAGAGA[CAT/GAC]ATCTGGACCTTATGT | 55728 |
| rs386673777 | multinucleotide-polymorphism | CA/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164098 | GGGAAGGAAAGGAGA[CA/TG]AAATTCACGATGCTG | 55728 |
| rs397809924 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146870 | TTCTATGTGTTTGGC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs397878196 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067056 | ATGACCTAATTTCCT[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs397938446 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071839 | CAAAGTGCTGGGATT[-/T]ATAGGTGTGAGCCAC | 55728 |
| rs397952773 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065946 | AGCATTTTTTTTTTT[-/T]CTTGAGATGGAGTCT | 55728 |
| rs397976537 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104821 | CTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTTG | 55728 |
| rs397993060 | in-del | -/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107941 | CTTTTTTTTTTTTTT[-/T]GACACAGTATCTCGC | 55728 |
| rs397993061 | in-del | -/A | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178437 | AAAACAAAAAAAAAA[-/A]GAAAAGAAAAACCTT | 55728 |
| rs398063477 | in-del | -/GT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131582 | ATTGTGTGTGTGTGT[-/GT]ATATTTATAAGCAAC | 55728 |
| rs527238973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088717 | GTTGGTCAGGCCGGT[C/G]TCGAATTCCTGACCT | 55728 |
| rs527239458 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096962 | CATTCTAATTATATT[A/T]ATGAAGACTTTCGTG | 55728 |
| rs527281525 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153073 | AAATAGTTAACTAAA[C/T]TTAATCATCTGATTT | 55728 |
| rs527296138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096159 | TATGAGTCCCTGCCC[G/T]TGTGGAGCTTACACT | 55728 |
| rs527300673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104001 | GCTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCG | 55728 |
| rs527318166 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140590 | TATTCTCTTTTTTTT[A/T]AAAATTAATTTATTT | 55728 |
| rs527319327 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147559 | CCCCCACCTCCCTCC[C/T]GGACATGGCGGCTGG | 55728 |
| rs527322885 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055227 | TTATCTCTTGAGATT[C/T]TGGGTTATTACAATT | 55728 |
| rs527325471 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112519 | TTGGCAGAATCAAAA[-/TT]TTTGTTGGTCCTTTG | 55728 |
| rs527331250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054473 | GCAATTCCAGCTATT[C/T]GGGGGGCTGAGGCAC | 55728 |
| rs527348473 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147204 | GTGGACACAGCACAT[A/G]TTTCAGAGAGCACAG | 55728 |
| rs527385727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152988 | TATAGATTTCTGTTA[C/T]TGATAATAGCAATAG | 55728 |
| rs527422872 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061579 | CATGTTGGCCAGGCT[-/G]GTCTCAAACTCCTAA | 55728 |
| rs527431859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103372 | AACTTTGTGTAGCTA[A/G]TAACACTGTTTTCTG | 55728 |
| rs527468025 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109650 | TTGAACCTGGGAGGC[A/G]GAGGTTTCAGTGAGT | 55728 |
| rs527473299 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142560 | TCTATTTCCTGAGGA[A/G]AGAGATGAAAATATA | 55728 |
| rs527487299 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108909 | GCAATGTCTGCCTCC[C/T]GGGTTTAAGCGATTC | 55728 |
| rs527508643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109085 | CTCCCGAAGTGCTGG[A/G]ATTACAGACATGAGC | 55728 |
| rs527528524 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160342 | TTTTTCGATTTTGTG[A/T]TGGTGTGAATGCCGT | 55728 |
| rs527542810 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060755 | GTATAGGCACATACC[G/T]CTGTGCCTGGCTCAT | 55728 |
| rs527567182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160001 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 55728 |
| rs527572476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066597 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACCGTG | 55728 |
| rs527573523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167371 | ATGAGAAAAGGCATA[C/G]ACCTAAACATACTCT | 55728 |
| rs527583767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074460 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 55728 |
| rs527597022 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062638 | TTGGATCCTTATTGA[C/T]ACTTGGCTGTCAGTG | 55728 |
| rs527605802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166781 | GTATACATTTATGGG[A/G]TACATGAGATATTTT | 55728 |
| rs527611950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175456 | AAGTAGCAGACACCT[A/G]GGATGAACCAGTCTG | 55728 |
| rs527686141 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082149 | GGTGTGGTAGCGAGC[A/G/T]CCTGTAGTCCCAGCA | 55728 |
| rs527707745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111408 | TCACTGCAACCTCCG[C/T]ATACCGGGTTCAAGT | 55728 |
| rs527711599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062958 | CCACATAGCGGTAAA[G/T]GGACTGTCTTAAAAA | 55728 |
| rs527725507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090533 | GAAACTGTGATTTTA[A/G]GTGAAACGACATGTA | 55728 |
| rs527725604 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124641 | CATGAGCCACTGCGC[C/T]CAGCCAGTTCTTTAA | 55728 |
| rs527726411 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154630 | CCTGATTCATGCCCC[C/G]CAAAGGGTGGTATTA | 55728 |
| rs527762935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161684 | AAGATGGAGCAAGTG[A/G]CTGTGGGTACTTAGG | 55728 |
| rs527772396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069074 | GCAGTGAGCCGGGAT[C/T]GCGCCACTGCACTCC | 55728 |
| rs527792841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076203 | TTTTTTGGCCAGGTG[C/T]GGTGGCTCCTGCCTG | 55728 |
| rs527838817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177020 | ACGGATAAGAACCCC[C/T]TCTTTGGCGGAATTA | 55728 |
| rs527854828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083558 | TGGAAAACATGCCAA[A/G]CGAAAGGAGCCAGTC | 55728 |
| rs527862647 | snp | A/T | 0.00126236 | 0.0250916 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118435 | AAAACTCCATTTCAA[A/T]AAATAAATAAATAAA | 55728 |
| rs527876232 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127060 | CACCATGCCCACGAA[A/T]TTTTGAATTTATTAT | 55728 |
| rs527913230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134843 | AAATTTCTTTCCCTT[G/T]TGCTTTCTTGCTTCT | 55728 |
| rs527924810 | in-del | -/TTAT | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137516 | CACTGACATATATTA[-/TTAT]TTAACACCCGTCTTT | 55728 |
| rs527934909 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175958 | AGCCGGGCGCGGTGG[C/T]GGGCGCCTGTAGTCC | 55728 |
| rs528051650 | snp | A/C | 3.31939e-05 | 0.0040738 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120885 | AAATATCCTTATCTA[A/C]AGCACATGAGGCCTG | 55728 |
| rs528139848 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058110 | AACCTAGCCTCTCAG[-/AA]AAAACAATGACTGAT | 55728 |
| rs528146188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136511 | TGCCTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55728 |
| rs528148047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127747 | CTCGCTGCATGCTCC[A/G]TCTCCCGGGTTCATG | 55728 |
| rs528152079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077265 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGAGTAGTT | 55728 |
| rs528209241 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085144 | TCTTGAACTTCTGAC[C/G]TTGTGATCCACTTGC | 55728 |
| rs528229656 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091889 | TCTGGGATTATAAGT[G/T]TGAACTACTATGCCC | 55728 |
| rs528249802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141558 | GGCGCTCCTCACTTC[G/T]TAGATGGGATGGCAG | 55728 |
| rs528282220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142456 | TCAACATCTCCCGAG[A/T]GTGGTTAAAGAAAGG | 55728 |
| rs528306915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098879 | AGATTTGAGTGGTGG[A/G]ATTTTGTTATTATGC | 55728 |
| rs528385465 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056053 | AGCCTCCCTCCACCC[A/C]GTGGCAGTCGCCTAC | 55728 |
| rs528390299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148234 | CTGGCAGATCACTCG[C/T]GGTTAGGAGCTGGAG | 55728 |
| rs528398724 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063535 | CTGTTAGCAAAAAGC[A/T]GAGCAGACCTTGAGT | 55728 |
| rs528411497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098088 | AGAGTTTTTAAAAAC[G/T]TTGTTTTACTCCTGT | 55728 |
| rs528444577 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105348 | TTTTTTTTTTTGACA[A/G]AGTCTGACTCTGTCA | 55728 |
| rs528498867 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127903 | CCTGACCTTGTGATC[-/CA]CCTGCCTCGGCCTCC | 55728 |
| rs528508728 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166282 | ACTGAACAGCAGGCT[A/C]TCTGGCGGGATAGGC | 55728 |
| rs528542066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143827 | TTCCTTCTTGAGATG[G/T]TGTATTAGAGTTCTC | 55728 |
| rs528562789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150654 | TCAACCTGGGCAACA[A/G]AGTGAGACTCTGTCT | 55728 |
| rs528563739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092933 | ACAGGCATGAGCCAC[C/T]GTGCCCGGCCTGCTC | 55728 |
| rs528567991 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086741 | ATATTATATAGATTT[-/AA]AAAAATTATTTATTT | 55728 |
| rs528603824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057887 | TTTGTAACTAGGATC[C/T]GATATTTGTGGCACG | 55728 |
| rs528661390 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106306 | TTACAATATGTTCTT[G/T]TATTTATCTCTTTGT | 55728 |
| rs528687221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113194 | ACTGGAAAACTGGCT[A/G]TCCTGGCATATATCT | 55728 |
| rs528739659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138098 | TGAAGGCTGCAAAAA[C/T]TCCAGTGGCAGAATA | 55728 |
| rs528762098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070796 | TGAGTTGTTCCAAAA[A/C]TGTTTTTGATTGCTG | 55728 |
| rs528767094 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163892 | GATTATAGAATTTGC[A/G/T]AAATCTTTCCCGGCT | 55728 |
| rs528773899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064314 | GAGTCTCGCTCTGTT[G/T]TCCAGGCTGGAGTGC | 55728 |
| rs528779896 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156375 | GTTTACTTGTTTACT[A/G]TATCAATGTTAATAT | 55728 |
| rs528798743 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076730 | CCTGACCTTGTGGTC[C/T]GCCCGCCTTGGGCTC | 55728 |
| rs528804657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163317 | GACATTGTTGTCTTA[C/T]CCAACAGTTATTCTT | 55728 |
| rs528822021 | snp | C/T | 0.000132385 | 0.00813479 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121722 | GAAACTCAGAGCAGG[C/T]GGAAATGAGAGCTGT | 55728 |
| rs528859285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101974 | TTATATTCTGTTCAA[A/T]GCAAAATCCAATATA | 55728 |
| rs528874136 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134362 | CTCAGAGTTGTGCTT[C/T]CCCAGGCAAAGGAGG | 55728 |
| rs528876677 | snp | G/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131831 | ATGTTTGAAAAAGAT[G/T]GTGCCACTAAACTAA | 55728 |
| rs528884592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108116 | TATTTTTAGTAGCGA[C/T]GGGGTTTTGCCACAT | 55728 |
| rs528911843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059715 | TACATCAAGCCATGT[A/G]TCATTATCAACCTCA | 55728 |
| rs528942278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158861 | GTCCAAAGCAGAATT[C/T]ACTCATTTTGCAAGG | 55728 |
| rs528949649 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159311 | CTTCTTCCTTTATAC[A/G]AAAGCTGGTACTTTG | 55728 |
| rs528974049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066034 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs528983653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065742 | TAGACAGTTCTTCCA[A/T]TGCAGGGATTTGAAT | 55728 |
| rs529008529 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150671 | GTGAGACTCTGTCTC[-/AG]GGGGAAAAAAAAAAA | 55728 |
| rs529009510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165704 | ATGCAAACCCACACA[C/T]AGAGTGAATAGAATA | 55728 |
| rs529027534 | in-del | -/TTTTTT | 0.00349039 | 0.0416295 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104808 | AGAACCTGCGTTGTC[-/TTTTTT]TTTTTTTTGGAGACA | 55728 |
| rs529035608 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099580 | TAATAGGAATAAAAT[G/T]GCATTTTTCCTAATT | 55728 |
| rs529054965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114401 | TAGTTCCCCCCTCCT[C/T]TTGGCAACCACTAAT | 55728 |
| rs529064356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072286 | GAGTCTCACTTTGTC[A/G]CCAGGCTGGAGTTCA | 55728 |
| rs529067006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123265 | TCCATTTTGAACCTT[C/T]GAATTTCAGTGAAAT | 55728 |
| rs529074515 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104262 | GGCTTGCTAGTTCTT[-/C]TTTTTTTTTTTTTCC | 55728 |
| rs529105105 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157492 | TATAATATTGAGATC[A/G]GTTATTTCTGAGCTG | 55728 |
| rs529129295 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075941 | AAACAATCCTCCTAC[C/T]TCAGTCTCCTGAGCA | 55728 |
| rs529172663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173171 | CCTTGAACCCCTTGT[A/C]CCCTTAGAGGGGCTA | 55728 |
| rs529178475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079849 | CTCTGCTTACCATGT[C/T]GGAATATTATGATGA | 55728 |
| rs529226066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086586 | CAAGTAATCCACCCG[C/T]CTTGGCCTCCCAAAG | 55728 |
| rs529239050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167428 | AAGAGAAAAATATAT[A/G]AGATTCCAGACAGAA | 55728 |
| rs529239567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180736 | ATGGACTATTATGTT[A/G]CTATTAAAGGGTGAG | 55728 |
| rs529283611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074500 | AGGTGTGAGCCACCA[C/T]GCCTGGCCTACACAG | 55728 |
| rs529323547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125661 | GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTCA | 55728 |
| rs529343681 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096504 | TGGGCCATTTTAAGG[G/T]CTCTGGCTTTTGTCC | 55728 |
| rs529348793 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059443 | TGTCGCCCAGGCTGG[A/T]GTGCAGTGGCGCTAT | 55728 |
| rs529362523 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125125 | CACCTTGAAGATTCT[C/T]AGGATCCACTTTGGT | 55728 |
| rs529367327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082047 | AATCTGGGAGGCAGA[A/G]GTTGCAGTGAGCCAA | 55728 |
| rs529389613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099918 | TCCCTGCCCACCCCC[A/G]CCACCTTTTTTTTTC | 55728 |
| rs529405099 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066170 | CCTTGACCTTGTGAT[A/C]CACCTGCCTCAGCCT | 55728 |
| rs529427322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125221 | GATGGTGTGCAAATG[C/G]CAGTGTCTATTGTTT | 55728 |
| rs529466309 | in-del | -/TTAT | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086748 | ATAGATTTAAAAAAA[-/TTAT]TTATTTATACTTTTG | 55728 |
| rs529488022 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127425 | TTGCCATGTTGCCCA[A/G]GCTGGTCTTACACTC | 55728 |
| rs529515260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139681 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTCT | 55728 |
| rs529542161 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182961 | GGATTACAGACATGA[A/G]CCACCATGCGTGGCC | 55728 |
| rs529560731 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145277 | TGCCCAGGCTGGAGT[C/G]CAGTGGTGCCATCTC | 55728 |
| rs529577866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060437 | TTGAGTAGTGATGGG[G/T]TTACACCTTGTTGGT | 55728 |
| rs529625843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184157 | TTAGCAAGGAAGAAG[A/G]CATGACTATCGGGCA | 55728 |
| rs529639904 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102601 | TTCTTTAAATGTAGC[A/G]AGTGACTCCATCGCA | 55728 |
| rs529662208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094668 | TCAAGCAATTCTGCC[C/T]TAGCCTCTCGAGTAG | 55728 |
| rs529719427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183458 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC | 55728 |
| rs529735646 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062182 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs529750610 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055894 | AGCGGTCGCAAGAGG[G/T]AAGAGCACGTCTTTG | 55728 |
| rs529759640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141244 | CACCTCCCTCCTGGA[C/T]GGGGCGGCTGGCCTG | 55728 |
| rs529782219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089835 | TTCCCACAAGGAGAG[A/T]TTTTCCCCTTTTTTC | 55728 |
| rs529804393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104023 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 55728 |
| rs529813682 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147615 | TCCCTCCCGGACGGG[C/G]CGGCTGGCCGGGCGG | 55728 |
| rs529870898 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060493 | CAGGTGATCCACCCA[C/T]CTTGCCCTCCCAAAG | 55728 |
| rs529878118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062033 | TTTTTGGTTTTATTT[A/G]TTTATTTATTTTTGT | 55728 |
| rs529929840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068370 | CTATGCCTTTGGTGT[C/T]GTCTTCAAGAAATCA | 55728 |
| rs529959902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067637 | AGCTGAGCCATTGTA[C/T]GTTCCTACCAGTAGT | 55728 |
| rs530015239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160361 | TGTGAATGCCGTATG[C/T]GTTTAGTAGAAACCA | 55728 |
| rs530023475 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090021 | TTCCAGTATCATTTG[C/T]TGAAAAGGTGGTCTT | 55728 |
| rs530055932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118284 | TAGCCTGGCTGGTGG[C/T]GCATGCCTGCAATCT | 55728 |
| rs530083020 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090000 | TTACTGATTGATGTC[C/T]ACTTGTTCCAGTATC | 55728 |
| rs530085080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148829 | TTTATTGTTGAATAA[C/T]ATTCCATTGTGTCTA | 55728 |
| rs530088457 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant, missense | N4BP2, LOC344967 | GRCh38.p7 | 4:40056970 | GCGGACCTGCGGCGC[C/G]GCGTTGTGCGTTCGA | 55728 |
| rs530113430 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155584 | AAACCTGTGTAAAGG[A/G]GGTTATAATGTGGTA | 55728 |
| rs530146404 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156225 | TTTATATTTCCTTAC[C/G]TAGTTTTAAAAATCA | 55728 |
| rs530163972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064187 | GCCCTGTACTATGGA[A/C]CTGTGTATTCCAGGT | 55728 |
| rs530178205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111862 | CTCAAGTGGTCTGCC[C/T]GCTTTGGCTTCCCAA | 55728 |
| rs530185916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163189 | CAAAGGATTTGTGTA[C/T]GTATTTGGAAGCCAT | 55728 |
| rs530245067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127647 | CTATTAAAGATGTCT[A/G]TCTCTGAGAAAATAT | 55728 |
| rs530247308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119230 | GCATCATCTAACACA[C/T]AGAAAACTCAGCGTT | 55728 |
| rs530270243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170180 | AAAACATAAATTTCA[A/G]GATATATACCCTTAA | 55728 |
| rs530340586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083606 | AGATTATACAATTCT[C/T]TTCATATAAATGCCT | 55728 |
| rs530353402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077028 | ATATAGAGAGATTTT[G/T]TTTGTTTGTTTCTTT | 55728 |
| rs530362163 | in-del | -/AAGAA | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170017 | ATAGAGGAGGAAATT[-/AAGAA]AAGACTCATATTAAT | 55728 |
| rs530389923 | in-del | -/AAC | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109513 | CCTGAGGTCAGGAGT[-/AAC]TTGAGACCACCCTGG | 55728 |
| rs530406361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177967 | CAGAAAACAGAAAGA[C/T]GAGGCATTTAACTTA | 55728 |
| rs530416852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076307 | ATGGTGAAACTCTGT[C/G]TCTACTAAAAGTACA | 55728 |
| rs530421441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084231 | ACTGGGATTACAGGC[C/G]TGAGCCACCGCACCC | 55728 |
| rs530443375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177338 | ACTTCTTCCTGGGCC[C/T]GGCACGGTGGTTCAC | 55728 |
| rs530498456 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122663 | GGACTTTAAAAAATA[C/G]AATAGGAAGAAATAG | 55728 |
| rs530498504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113329 | TAACACACTCATCAA[A/G]ATTAGATAATCTTTA | 55728 |
| rs530510840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171911 | GGAGACTAAGCCAGT[C/T]TAGTCTTTTTCTGAG | 55728 |
| rs530546096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180012 | CAGGTGATCCGCCCA[C/T]CTCGGCCTCCCAAAC | 55728 |
| rs530560837 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082140 | AATAAATTGGGTGTG[A/G]TAGCGAGCGCCTGTA | 55728 |
| rs530582424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179165 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55728 |
| rs530586467 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163903 | TTGCGAAATCTTTCC[C/T]GGCTATTAATAGCAG | 55728 |
| rs530590124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085128 | GTGTTGGCCAGGCTG[A/G]TCTTGAACTTCTGAC | 55728 |
| rs530609418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128342 | AAGGCATAGGGATTG[C/T]TCTACCTTCATATTT | 55728 |
| rs530610448 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180357 | GCAAGACACCACTTT[C/T]CAACTAGAAAACTAA | 55728 |
| rs530640677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085722 | GAGATGTGAAAATCT[C/T]GAGAGTGGCAGTGTC | 55728 |
| rs530690203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142556 | AGAATCTATTTCCTG[A/C]GGAGAGAGATGAAAA | 55728 |
| rs530720544 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137097 | GGTATGGAGTTACTA[A/T]TTTTTTTTCTACAAG | 55728 |
| rs530725627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142138 | ATAGGGAGAGGGGGA[C/G]GGGGAGGGAGAGGGA | 55728 |
| rs530725687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149241 | AACAAAATGTGGTAA[A/G]TCTATACAATGAAAT | 55728 |
| rs530770177 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130221 | TTTTAGTATAGATGG[G/T]GTTTTGCCATGTTGC | 55728 |
| rs530779442 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108382 | CAGTGGCGTGATCTC[G/T]GCTCAGTGCAACCTC | 55728 |
| rs530809061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091960 | GCACTCCAGCCTGGG[A/T]GATAGAGCAAGACCT | 55728 |
| rs530897087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086878 | TCAGCCTCCTGAGTA[G/T]CTGGGACCACAGGTG | 55728 |
| rs530932443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131195 | CATGGGGAAATTTCT[C/G]TCAGGTCTCAGTACC | 55728 |
| rs530957465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093598 | TTGTATTATTTATTT[A/G]TTTATTATTATTATT | 55728 |
| rs530979585 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105480 | CAGGTATCTGCTGCC[A/G]CCCCCAGCTAATTTT | 55728 |
| rs531038407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151418 | CTGGGACTACAGGTG[C/T]GCCTCGCCATGCCCT | 55728 |
| rs531053726 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146169 | CTCTTTCTCAAAAAT[-/A]AATAAATAAATAAAT | 55728 |
| rs531069282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057960 | CTCCATGGCACAGTT[C/T]TGGCTTGAAGGCAGG | 55728 |
| rs531071619 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134145 | TATTCTCTGCTGAGT[G/T]TGCAGAGTTCTAAAT | 55728 |
| rs531101257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101309 | TTACAGGCATGCGCC[A/G]CCACTATGCCCAGCT | 55728 |
| rs531128843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064928 | GGTATGCACCACCAC[A/G]CTCGCTAAGTTTTGT | 55728 |
| rs531129011 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070831 | TGTTTTTTTTTCTTC[-/T]TTTTTTTTTTTGAGA | 55728 |
| rs531133349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104104 | ACTACAGGCGCCCAC[C/T]ACCACGCCCAGCTAC | 55728 |
| rs531141327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107518 | CTTCCTGAGTAGCTG[A/G]GATTACAGGTGCATG | 55728 |
| rs531179386 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058770 | ATCACTAGTTGCATG[G/T]TTTTTTTTTAGTATT | 55728 |
| rs531190076 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068171 | AAATTGGGTTATTTG[G/T]ATTTTGTTTGTTGAG | 55728 |
| rs531210877 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131235 | TGTACTTCTGAGCAA[C/G]TGGTTTGTTTTTATT | 55728 |
| rs531213075 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157808 | TGTATGTTCATGGTG[C/T]TTATTTTTAAAATGT | 55728 |
| rs531289554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095553 | TGGCTGGTGGCTGCC[A/G]TATTGACAATGCAGT | 55728 |
| rs531342876 | snp | A/T | 0.000445137 | 0.0149121 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102633 | GTTGTAGCAGTCTCA[A/T]TCAAAAACAGAAAGA | 55728 |
| rs531392350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060499 | ATCCACCCACCTTGC[C/T]CTCCCAAAGTGCTGG | 55728 |
| rs531406506 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153831 | TTGCATGGCCAGATT[A/T]ATCAGACTTACCTGA | 55728 |
| rs531419686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152321 | TCATTTAGTGGCAGA[A/G]CTATGATTCAGAACA | 55728 |
| rs531424502 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124806 | TTGCTCTGCATGAAA[G/T]AAAACTTTTGGTTTG | 55728 |
| rs531437863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073822 | TTTGAGGTGGAGTTT[C/T]ATTCTTGTTGCCCAG | 55728 |
| rs531461052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124348 | TTTATTTATTTATTT[A/T]TTTATTTTTTTATTT | 55728 |
| rs531477066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109016 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGATG | 55728 |
| rs531530348 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074038 | CTCAGGTGATCCGCC[C/G/T]GCCTCAGCCTCCCAA | 55728 |
| rs531541457 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138382 | TCCTTTCCATAGGTT[A/G]CCTTTCACTCTGTTG | 55728 |
| rs531552005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161052 | AGAAGAGACCAAAAA[A/C]TCAATCAATCAATCC | 55728 |
| rs531553999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169522 | CCTCCTAAATAATCA[C/T]TGGATCAAATTAGAA | 55728 |
| rs531573044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066121 | TTTTTAGTAGAGATG[A/G]GGTTTCACCGTGTTG | 55728 |
| rs531628588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073107 | ATTATTGGTTAAAAA[A/T]TGGTAATTAGTTTTG | 55728 |
| rs531629766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174659 | AATGCAAAAATTAGG[C/T]GGTGTAGTGGTGCGC | 55728 |
| rs531635675 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065594 | GTATTGGGTCAAGGA[A/G]TCAACAGAAAAAAGT | 55728 |
| rs531692735 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168165 | AAAGAAAAGGAAAAA[-/AG]AAAATTAATGAGGTA | 55728 |
| rs531706391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075459 | GCTGGAGTGCAGTGG[A/C]GCGATCTTAGCTCAC | 55728 |
| rs531719392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110780 | TAACCTCAGGTGATC[C/T]GCCCGCCTCAGTATC | 55728 |
| rs531722639 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170848 | AGACAGTGCAATTGT[A/G]TTTCACATATCCTCA | 55728 |
| rs531739179 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111396 | CGTGGTCTCAGCTCA[C/G]TGCAACCTCCGCATA | 55728 |
| rs531742272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176254 | GCAATGATTTTGCAA[G/T]ATAAAAAAGTTAAAC | 55728 |
| rs531756483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175857 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 55728 |
| rs531776590 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063006 | GAGTGTATTGAAAGA[A/G]AATGAAATAGTAATT | 55728 |
| rs531811028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133858 | TTGCCCAGGCTGGAG[A/T]GCAGTGGCACGATCT | 55728 |
| rs531823884 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141085 | TTGTCATCATGGCCC[A/G]TTCTCAATGAGCTGC | 55728 |
| rs531841926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074618 | TTTCAAAAGAGCTTT[C/T]GTGGTATAAGACATG | 55728 |
| rs531858551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140364 | AGATGATTATGAGAC[C/T]TTATGGGCCAAATTG | 55728 |
| rs531867994 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093067 | TCCTGCCTCAGTCTC[C/T]GGAGCAGCTAGGATT | 55728 |
| rs531978127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178394 | TGTAGGAAAACCTCC[A/G]GCAAGACTACTCCCC | 55728 |
| rs532012139 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127673 | AATATATATATATAT[A/T]TTTTTGAGATGGAGT | 55728 |
| rs532014417 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184962 | CTCTGTCTCAAAAAA[A/T]AAATAAATAAATAAA | 55728 |
| rs532025317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088657 | AGGCATGCACCACTA[C/T]GCCTGGCTAATTTTG | 55728 |
| rs532058692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091137 | CCCTTGTTAAACTCA[C/T]TTTCTTGTTGGAGAT | 55728 |
| rs532163957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098002 | TCTCCATGTATTGTC[A/G]TTTGTCCCCTGGGAG | 55728 |
| rs532181813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135795 | TGATCTTGAACTCCT[A/G]ACCTCAGGTGATCCA | 55728 |
| rs532210482 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085556 | CCAACTCCTAGAGTC[A/G]AGTGATCCTCCTGCC | 55728 |
| rs532213971 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104688 | GGGGCCTTTAGAATC[A/C]GAGGCAGCTACAGTG | 55728 |
| rs532222629 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056018 | CAGACCGCACGCTGG[C/T]AGGGCCGATGGGGCT | 55728 |
| rs532236982 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062934 | ATTGCTTGCTTATTT[A/G]TCATCTCACCACATA | 55728 |
| rs532248077 | in-del | -/T | 0.232943 | 0.249417 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129236 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTGAGACAG | 55728 |
| rs532253098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148136 | GCGAGCCGAGATCAC[A/G]CCACTGCATTCCAGC | 55728 |
| rs532254257 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141649 | CCCAGATGATGGGCG[A/G]CCAGGCAGAGACGCT | 55728 |
| rs532268462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184278 | GTATGGCTGCACGGG[C/T]TAGAATGGAGAAACA | 55728 |
| rs532269239 | in-del | -/TATGTT | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114951 | CTCCTGCAATCTTAG[-/TATGTT]TATATTATCTTCCTT | 55728 |
| rs532284569 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154477 | TTACAAAATATGTAA[G/T]AAAATTATCAGCTAC | 55728 |
| rs532295849 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083270 | CTGCTTTGGAAAACC[G/T]TTTGGCAGTTCCTCA | 55728 |
| rs532297869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062271 | TTTTAATAGAGATGG[A/G]GTTTCACCGTGTTAG | 55728 |
| rs532395898 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055481 | CTACAACGTTCTCAT[C/T]GTGAATAAGTGTTCC | 55728 |
| rs532410670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099536 | ATTACAGGCGTGAGC[C/T]ACTGCACCCGGCCCA | 55728 |
| rs532450989 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142055 | ACAGTCCAGCTTCGG[C/T]TCGGTATCAGAGGGA | 55728 |
| rs532454153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153865 | ATCAGAGATTTCTTC[C/T]TGGTGCTTTCATGAT | 55728 |
| rs532460537 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117655 | CTTCAAATACTAGAA[-/T]TTTTTTTCTTTGTTT | 55728 |
| rs532482883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149448 | TGAGCAGTGACTGCT[A/G]TGAGGCACAGAATTT | 55728 |
| rs532516216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106241 | TAGGTCAGATTTTTT[C/T]TGGAATTAAACTTCT | 55728 |
| rs532516587 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156276 | TAGACTTATTTCAAT[A/G]TTATAATTATGATTA | 55728 |
| rs532529622 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171584 | TCTTAATTGGAGGTA[G/T]TCTTTACAGAAGTAA | 55728 |
| rs532597051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057724 | CTCAATAGAGTGAGT[C/T]ATCTTAGCGGGGGCA | 55728 |
| rs532605008 | in-del | -/TGAGATCATAGGTG | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110805 | AGTATCCCAAAGTGC[-/TGAGATCATAGGTG]TGAGGTACCGTGCCC | 55728 |
| rs532626090 | in-del | -/TATA | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168548 | AAATCAGAAGATTGT[-/TATA]TATAAATATAAGGAT | 55728 |
| rs532628651 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165358 | GGCTCAAGCAATCCT[C/T]GTGCCTCAGTCTCCT | 55728 |
| rs532691418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070050 | CTTGAAGCATGGTAC[A/G]TTTTAAAAACTTTCA | 55728 |
| rs532806653 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079547 | ATAACACTATTAGAG[A/T]TCATGTTTGTTCATT | 55728 |
| rs532836777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077907 | CATTTCCTAAAATTG[A/G]AATGATACAGAGAAG | 55728 |
| rs532845802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171058 | GTATATTTTATTTAG[A/G]GATGCCCAGTTTAAT | 55728 |
| rs532852174 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136424 | AAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55728 |
| rs532885143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170394 | GAGACTGACGCAGGC[A/T]GATCACTTGAGTTTA | 55728 |
| rs532943682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107604 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTTAG | 55728 |
| rs532981291 | snp | C/T | 3.44869e-05 | 0.00415238 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121953 | ACAACATACATTCTC[C/T]TTCACATTTCTCTGA | 55728 |
| rs532992006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137876 | CCCCTGGTTGTCTGA[C/T]ACTCGGGGGCAGGTG | 55728 |
| rs532997546 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110917 | AACTTTGAAAACTTC[C/T]AAATAAATTACTTGT | 55728 |
| rs532997606 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077130 | TCGATATTGAATATT[A/T]TGTAGAATATATATG | 55728 |
| rs533007632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122782 | CCTTTTAAAATCCTT[C/T]GGTGCTACTCCAGAT | 55728 |
| rs533012383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129092 | AGTCTGGCTTTGTTA[C/G]AGGCTGGAGTGCGGT | 55728 |
| rs533026761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137142 | TATAAAAATATAATT[C/G]GTTCATTGAGTATAA | 55728 |
| rs533028321 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161394 | TTAAATAAGTTGAAG[A/G]TAAAATAAAACCACA | 55728 |
| rs533037464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072188 | CAAGTGATTCTTGTG[C/T]GTCAGCCTCCTGAGT | 55728 |
| rs533064880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079530 | CAGTATTGACCATTG[C/T]CATAACACTATTAGA | 55728 |
| rs533068094 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173026 | CTGTTGACAGTTTGC[C/T]CCCCTAACTTCCCCT | 55728 |
| rs533123939 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081277 | AGTCTAATTTAAGTC[A/C]GTCCCTTTTGTGTGT | 55728 |
| rs533126790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078844 | TCAGAATTAGTATCA[A/G]TAGTAAAGTTTGGGA | 55728 |
| rs533231002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088040 | TGGGATTACAGACCG[G/T]AGCCACCACGCCCGG | 55728 |
| rs533232862 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080784 | TGCCTCAGCCTCCCA[C/T]GTAGCTGGGACTACA | 55728 |
| rs533245420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085772 | TTCTTGGGGGAGAGA[C/T]TGATCAGCTGTTTAA | 55728 |
| rs533273708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145802 | ATTGTCTAGTGGGGT[A/G]TACCATCTAGTAGGA | 55728 |
| rs533306280 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095213 | AGCCTCCTGAGTAGC[A/T]GGGATTACAGGCCCA | 55728 |
| rs533315287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174759 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGT | 55728 |
| rs533325165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129329 | CTTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs533327218 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097008 | AAATGTATTGAAATA[A/G]TGTATTCATTGTTCT | 55728 |
| rs533327925 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079689 | TGCCCATAGCCCTTG[C/T]TGCTTGGGAGGTTGA | 55728 |
| rs533360183 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124993 | TCTCTTAGATAGTGT[G/T]GTCTTCAGTGACTGT | 55728 |
| rs533378807 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166025 | TTCTGGGCCTTTTGC[A/G]TATAAATCTCTCATC | 55728 |
| rs533398537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132119 | TCTATATACTATGTT[A/T]TTTTCCTATAAATAA | 55728 |
| rs533406924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059641 | AGACATGAGCCACCC[C/T]GCCTGGCCTTAGATT | 55728 |
| rs533408995 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127710 | CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGTGCGA | 55728 |
| rs533436097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139601 | AGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 55728 |
| rs533441853 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101934 | AAAATATTAATTTTT[A/T]AAAAATAACATGAAT | 55728 |
| rs533462980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150929 | TGATGGTGCCATTGT[A/G]GTTATGCTTTTTAAA | 55728 |
| rs533521896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094578 | ATTTATTTTTGAGAT[C/G]GAGTTTCGCTCTTGT | 55728 |
| rs533536528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133359 | CCTTTTTTTTGAAAC[A/G]GAGTCTCACTTTGTC | 55728 |
| rs533646661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139281 | CTTTTAAATTAAAAA[A/G]AGAAAAGGGTCTTGC | 55728 |
| rs533654890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146094 | CTTGAACCCTGGAGG[C/T]GGAGGTTGCAGTGAG | 55728 |
| rs533722235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081453 | GAGTTCAAGACCAAT[C/T]TGACCAACATGGTAA | 55728 |
| rs533763285 | snp | C/G/T | 8.28815e-05 | 0.00643698 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102360 | CACAAGATGTTAATA[C/G/T]TTTTAATGACTCAAG | 55728 |
| rs533783154 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138856 | ATTGGGAAGTGTGAG[-/T]TTTCCAACTATGTTC | 55728 |
| rs533844435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066172 | TTGACCTTGTGATCC[A/G]CCTGCCTCAGCCTCC | 55728 |
| rs533904341 | snp | C/T | 4.94262e-05 | 0.00497098 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097380 | GGGGGAAATCCTTTT[C/T]GGAAGACTGCAAACC | 55728 |
| rs533978486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094969 | TTTTAGTAGAGACAG[A/G]ATTTTGCCATTTTGG | 55728 |
| rs534001818 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084075 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55728 |
| rs534013784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153962 | GTTTTGACAAATCTT[A/G]AGTTATACTAAGTCA | 55728 |
| rs534030862 | in-del | -/AACAA | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178182 | ACAAACAAAGAACCC[-/AACAA]AACAAAACAAAACAA | 55728 |
| rs534061023 | in-del | -/CC | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057648 | TGTCCCTCAATGGGA[-/CC]CCCTTCTAGAGCCCC | 55728 |
| rs534069334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059851 | ACAACTCTGAGATTT[A/G]CACTATTCTTACAGG | 55728 |
| rs534087139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160546 | AGGCTAAGCTATGAT[A/G]TTCAGTAGCTTAGGG | 55728 |
| rs534184680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104198 | ACCTCGTGATCCACC[C/T]GCCCCGGCCTCCCAA | 55728 |
| rs534205164 | in-del | -/TAT | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153304 | TACTTTAAGATTTGC[-/TAT]TATTCTTTTGAAAGG | 55728 |
| rs534223633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096581 | CACCATGTGGTTTAA[C/T]TGAGTCACGCTGGCT | 55728 |
| rs534260307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175946 | ATACAAAAAATTAGC[A/C]GGGCGCGGTGGCGGG | 55728 |
| rs534277019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147407 | ATTGTCATCATGGCA[C/T]GTTCTCAATGAGCTG | 55728 |
| rs534288724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063248 | AAAAGTTATTGGTTC[A/G]TATGACCATATAATA | 55728 |
| rs534293207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062375 | ATCCTCGCTGCTGCC[C/T]TCCTACTCCATGGTT | 55728 |
| rs534298267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104993 | ATTTTTAGTAGAGAT[C/G]GGGTTTCACCGTGTT | 55728 |
| rs534335639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111509 | TATTTTTAGTGGAGA[C/T]GGGGTTTCAATATGT | 55728 |
| rs534372866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119454 | ACATTTCAAATGAAA[A/G]CTCTTTTTTTCTAAT | 55728 |
| rs534392630 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116401 | ATAGAAAATGATGTA[G/T]TTGGATTTTTTTCCT | 55728 |
| rs534451521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076663 | CTGGCTAATTTTTTG[C/T]ATTTTTAGTAGAGAC | 55728 |
| rs534454841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169708 | GGTGGCTCTCGCTTG[G/T]AATCCCAGCACTTTG | 55728 |
| rs534458627 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150930 | GATGGTGCCATTGTA[C/G]TTATGCTTTTTAAAG | 55728 |
| rs534471304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074747 | CATGGTGCCTCACGC[A/C]TGTAATCCCAGCACT | 55728 |
| rs534522356 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140663 | GCAGGGTCACAGGAC[A/G]ATAGTGGAGGGAAGG | 55728 |
| rs534531144 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170148 | CAATAATTGTGTCTA[C/T]AATTTTCATGGAAAT | 55728 |
| rs534542884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167052 | GTGTACACATTATAT[A/G]TATTTTAATATGTTT | 55728 |
| rs534560999 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155129 | TGGTGTGGTGGCCCA[C/T]GCCTGTAATCCCAGC | 55728 |
| rs534574193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162779 | TCAGGAGAATTGGCT[C/T]CTGTAATTTTGGAGG | 55728 |
| rs534602690 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182640 | TTTTGTAGAGACGAG[A/G]TTTCGCCATGTTGCC | 55728 |
| rs534615567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141347 | GGGCGGCTTCCGGGC[A/G]GAGGGTCTCCTCACT | 55728 |
| rs534638078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090094 | AGGCACACTTATGTT[A/G]CTGGGTTTTCTCTCT | 55728 |
| rs534646983 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183603 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 55728 |
| rs534686637 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149903 | CTCCATCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs534687969 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135244 | GAGAATGATGATTTC[A/C]AATTTCATCCATGTC | 55728 |
| rs534697231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106811 | AATGATAGTACTTGA[A/G]TAATTTATTTTGTTT | 55728 |
| rs534702185 | snp | C/G | 8.28658e-05 | 0.00643631 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121377 | CCAGTGCAGATGAAT[C/G]TGAAAATCTTAACAT | 55728 |
| rs534712565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170490 | CGGGTGTGGTGGTGC[A/G]TGCCTTTAGTCCCAT | 55728 |
| rs534721841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128558 | TTTTTTTTTGAGTCT[C/T]GTTCTGTCACCCAGG | 55728 |
| rs534803415 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127214 | TCTTCTTCTTTTTTT[C/G]TTTTTTTTAATTTTA | 55728 |
| rs534843349 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135283 | GGACATGAACTCATC[A/C]TTTTTGATGGCTGCA | 55728 |
| rs534845173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126792 | AGATGGAGTCTCGCT[C/G]TGTTGCCCAGGCTGG | 55728 |
| rs534852530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099730 | TTCCCAGCAATCTGT[A/G]TAAGGACTTTTTTTA | 55728 |
| rs534854574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116153 | GTTACTTCTTTTTTC[A/G]TACTTTTACTTTGAA | 55728 |
| rs534885144 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141692 | GACGGGGTGGCGGCC[A/G]GGCAGAGGCTGCAAT | 55728 |
| rs534890224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099070 | TCTTTTGGCTTTTTT[A/T]TCTTAGTTCCAAAAT | 55728 |
| rs534892079 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091085 | TGCTAGTATGTATAA[A/G]TACAGTTTCTTTTAT | 55728 |
| rs534904448 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151780 | GATGTGGATTAGAGA[C/G/T]GGAGATCATAGACAA | 55728 |
| rs534985048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148980 | AAATGGAAAGTAATC[A/G]GTATTGTTAAGGATG | 55728 |
| rs535085495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101858 | CTGTTTTCCTGAAAG[A/G]ATAGGATTGCATGTC | 55728 |
| rs535109382 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064040 | TGAGCTCAAGTGATC[C/T]TCCTGCTTCAGCCTC | 55728 |
| rs535134157 | in-del | -/CTC | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135670 | TGAGTTCAGGCAATT[-/CTC]CTGTCTCAGCCTCCC | 55728 |
| rs535148095 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071014 | ATTTTTAGTGGAGAC[A/G]GGGTTTCACCATGTT | 55728 |
| rs535177477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144116 | TAAAAGCTGAAGAAT[G/T]TGGAGTCTGAATTCC | 55728 |
| rs535226329 | snp | C/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055365 | AATACAAAATTCATA[C/T]AAAAGGAAAAATTCC | 55728 |
| rs535236667 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107649 | TTGGCCTCCCAAAGT[A/G]CTGAGATTACAGGTG | 55728 |
| rs535281235 | in-del | -/TTTT | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088947 | GGTTTTTATTTTTTG[-/TTTT]TTTTGTGTGTGTTTT | 55728 |
| rs535325800 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056709 | CCGGCGGGCTTGGGG[G/T]GGGGCGGTGGGCGGC | 55728 |
| rs535331050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063704 | GCTGGAGTGCAATGG[C/T]GTGATCTCGGCTTAC | 55728 |
| rs535342835 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056263 | TCAGGGCTCGTCCCA[G/T]CTCTGCTTTCCTTTC | 55728 |
| rs535363762 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155931 | TTAGAAATGGTTAGT[A/G]ACTGGTATTGAAGTA | 55728 |
| rs535382240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064578 | GCGCCCGGCAATAAC[A/G]AGTATTTATTGAGCT | 55728 |
| rs535411062 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067250 | ACATGAGGTTTTGCC[A/G]TGTTGCCCGGGCTGA | 55728 |
| rs535499640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117191 | ATTCTCTTCTCTTTC[C/T]GGGACTTAGATTAGA | 55728 |
| rs535500963 | snp | A/G | | | intron-variant, utr-variant-5-prime | N4BP2 | GRCh38.p7 | 4:40098692 | ATGACAGTATATTGA[A/G]TTTTGTAAGTTACTT | 55728 |
| rs535508973 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131125 | TGCCCATTGAGGAGA[A/G]TATGTTTTGAGGACG | 55728 |
| rs535550720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066215 | ATTACAGGTGTGAGC[C/T]ACCGTGCCCGGCCCA | 55728 |
| rs535565098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073341 | TCTCTTTTGTCACTT[C/T]CTTTTTGGAATATCA | 55728 |
| rs535566626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166871 | AAGCATTTATCCTTT[A/G]TGTTACAAACAATTC | 55728 |
| rs535584668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100799 | TAATGTACTTTTTAA[C/G]TTCATTTCTTCATCT | 55728 |
| rs535604295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065121 | ACAGAGCTGTGAAAT[C/G]GGCTACCTTGTGTGG | 55728 |
| rs535617970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174207 | AATAGCAAGACACTG[C/T]CTCTACAAAAAATAA | 55728 |
| rs535627928 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072643 | TCCCTCCCTGTACCC[C/G]CCCAGGCCTCCCAAA | 55728 |
| rs535652827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173533 | TTCATTTTGACTGGG[C/G]CAGCCAAGTAAGGCT | 55728 |
| rs535654722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181592 | CCTCCGAGCTCAACT[C/T]GCGGCTTTCATTTCA | 55728 |
| rs535745256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071741 | CCAGCTAATTATGTA[G/T]TTTTAGTAGAGACGA | 55728 |
| rs535759278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071159 | CATCCACCTCCTTCT[C/G]TACTCTGCCTCTCCT | 55728 |
| rs535759370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079014 | TGGAATGCAGTGGCG[C/T]GATCTCAAGCGATTC | 55728 |
| rs535783193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181024 | GCATGGTGGCATGTG[C/T]CTGTAGTCCCAGCTA | 55728 |
| rs535810802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151864 | ATCTTGGAGATATGA[C/T]ACTTGAAAAACCATT | 55728 |
| rs535836946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118109 | TTGTGGAATCATTGC[C/T]GATAAACTTTAAAAA | 55728 |
| rs535848857 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105044 | CCTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC | 55728 |
| rs535872749 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125914 | AAAAAAAATTATACA[A/C]AGATCATTACTCTTT | 55728 |
| rs535877416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181595 | CCGAGCTCAACTCGC[A/G]GCTTTCATTTCACAG | 55728 |
| rs535932183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133445 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCT | 55728 |
| rs535933477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159113 | ACTTAGAGAAGTTAA[C/T]TGGTTTGCTGTTTAA | 55728 |
| rs535951654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082455 | AACAGACATTTATTC[A/T]AAAAAGTATATAAAT | 55728 |
| rs535967686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140633 | TCTTGGGTGTTTCTC[A/G]CAGAGGGGGATTTGG | 55728 |
| rs536008452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088913 | TTTTTCTCCTTTTTT[A/G]CTGATTTTCCAATTG | 55728 |
| rs536025696 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090898 | AGATCACGCCATTGC[A/G]CTCCAGCCTGGGTGA | 55728 |
| rs536048359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124526 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 55728 |
| rs536075435 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171413 | TGTGTGGTGATTCCC[A/G/T]TGCAACATGGCCAGA | 55728 |
| rs536082278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131464 | TATATATATGCCTCT[A/G]TATCTTCATCCTTTT | 55728 |
| rs536162574 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058027 | TCAGCAAGGGCTGCT[A/T]GCCTGGAGACTGGTT | 55728 |
| rs536176011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060728 | TTGCAACAGCCTCCC[A/G]AGTAGCTGGGAGTAT | 55728 |
| rs536192190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087116 | GTAAATTGTGTTTTG[C/T]GGCTATTGGGTTCAA | 55728 |
| rs536204704 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169212 | ACGTAGAGAAACCCC[A/G/T]CCTTTACTAAAAATA | 55728 |
| rs536208619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167950 | AAAAGTTTTATCTTA[C/T]TGGGTGGAGGGAAAG | 55728 |
| rs536217931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176534 | GTGATTCTGATAAGC[A/C]TGCCTCCCTCTCCCC | 55728 |
| rs536254167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175966 | GCGGTGGCGGGCGCC[C/T]GTAGTCCCAGCTACT | 55728 |
| rs536298722 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141764 | GAGGTTGTAGCGAGC[C/T]GAGATCACGCCACTG | 55728 |
| rs536334131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148269 | GCCTGGCCAATACAG[C/T]GAAACCCTGTCTCCA | 55728 |
| rs536360881 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154767 | TTTGCCATATCCTAC[A/C]GGAAGGAAGACATGC | 55728 |
| rs536367916 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174210 | AGCAAGACACTGTCT[-/C]TACAAAAAATAAAAA | 55728 |
| rs536370891 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147775 | TCACTTCTCAGATGG[A/G]GCGGCTGCTGGGCGG | 55728 |
| rs536401066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154080 | AATAAGGGTCAATAC[G/T]TTGGTAGTAAATATT | 55728 |
| rs536404791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088436 | TCTTTGAAGTCTTGC[C/T]ATCATTTGGTGTTGT | 55728 |
| rs536434706 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072940 | TTGGCCAGGCTGGTC[C/T]CAAACTCCTGACCTC | 55728 |
| rs536488823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147330 | CTACACAGACACAGC[A/G]ACCATCCGATTTCTC | 55728 |
| rs536490325 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168560 | TTGTTATAAATATAA[-/G]GATAACATCATAAAA | 55728 |
| rs536535961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161188 | TTGGCCTGATAATGC[C/T]GCCACTAGCTGCCTG | 55728 |
| rs536537164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146250 | CTAAAATCCCTACAT[A/G]ATATCTCTTGCTTAC | 55728 |
| rs536570192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169018 | GGCTTGAGCCACTGC[A/G]CCTGGCCAAATATAT | 55728 |
| rs536610985 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147763 | CGGAGGGGCTTCTCA[C/T]TTCTCAGATGGGGCG | 55728 |
| rs536632100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099169 | AATGAGGTGTGCTGA[C/T]TTGTAATTCCACCAG | 55728 |
| rs536651741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098234 | GAATAGTATAATTTC[A/G]AAACATTGACTTTGG | 55728 |
| rs536668299 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105722 | CACCCGGCTCATTTT[A/T]AAATTTTTTGTAGAG | 55728 |
| rs536679394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064420 | GCTGGGACTGTAAGC[A/G]CGCACCACCACGCCT | 55728 |
| rs536684676 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056761 | AGCCATTGCCGGCGC[C/T]TCGAGACCCCTCCCC | 55728 |
| rs536691593 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083705 | GAATGGTTACTAATG[C/G]GTGGTGGGGTTTCTT | 55728 |
| rs536705466 | snp | A/T | 1.64974e-05 | 0.00287201 | splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40112174 | CATATGTTGCTTTGG[A/T]TAGTACCATAAGTTG | 55728 |
| rs536707657 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056149 | CGAGAAGGCGGGTTC[C/T]CGTGCCCGCCGCAGC | 55728 |
| rs536735413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141364 | AGGGTCTCCTCACTT[C/T]TCAGACGGGGCAGCC | 55728 |
| rs536775531 | snp | A/G | 3.29484e-05 | 0.00405871 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097462 | CTCTACCTTCCATGG[A/G]TGAGACAAAAGTTGA | 55728 |
| rs536817908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170546 | GTGGGGTGCTGAGAC[A/G]GGAGGATAGCTTGAA | 55728 |
| rs536824001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069441 | CTTTCATTTTTTTCC[C/T]TTCCTTTCATTTTAA | 55728 |
| rs536828570 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106382 | AGTGCAGTGGTGCAA[A/C]CTTGGCTCACTGTAA | 55728 |
| rs536833490 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137747 | GAGTAGGGGGGAAAT[G/T]TGGGCAAAAGCCTGT | 55728 |
| rs536844356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140576 | ATTATTTTTGCACTT[A/G]TTCTCTTTTTTTTTA | 55728 |
| rs536854339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169776 | TCGAGACCAGCGTGA[C/G]CAACATGGTGAAACC | 55728 |
| rs536854416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178665 | GATAACGAAATAAGT[C/T]GCCCAGGACAAAACA | 55728 |
| rs536867863 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184192 | GTCATCTATGTTAAA[C/T]GTGGGACTTACTGTG | 55728 |
| rs536978905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160690 | AAAACTCAGACTGAC[C/T]CCCTAACTGGGAGAG | 55728 |
| rs536992297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177650 | AAGAAAAAAAATAAA[A/G]ACTTCTACCTCAACT | 55728 |
| rs537003875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149091 | AATTAACCGTATGAC[C/T]CAGTAATTCTGCCCC | 55728 |
| rs537004977 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156419 | GATAAATCAAATAGT[A/G]TATCTTAATCATTGT | 55728 |
| rs537019698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079939 | AGAAGAATTTGAAAA[A/G]TGCATATATTCATGG | 55728 |
| rs537042329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113877 | GACCACAGGTGTGAG[C/T]CACCATGCCCAGCCT | 55728 |
| rs537042367 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158245 | TTTAATAAAATACTT[G/T]AGCCACAGTCCAGTG | 55728 |
| rs537051046 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092721 | CAATCTCAGCTCACT[A/G]CAGCCTCCACCTACT | 55728 |
| rs537054784 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159854 | TGAGTGTTAGGAATC[-/A]AAAAAAAGGAAATCA | 55728 |
| rs537055781 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127057 | AGCCACCATGCCCAC[A/G]AATTTTTGAATTTAT | 55728 |
| rs537101805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077554 | TGCCTCCCGGATTCA[A/G]GCGATTCTCCTGCCT | 55728 |
| rs537140011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163424 | GGTGAATTTTGATTG[A/G]TGGAAAAGCCAATCA | 55728 |
| rs537160269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128695 | ACCATACCCAGCTAA[C/T]TTTTGTAATTTTAGT | 55728 |
| rs537192412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085929 | ACTTTGGGAGGCTGA[C/G]GCAGGAGGAATATTT | 55728 |
| rs537194719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078528 | ATCCTTTTTTTTTTT[A/T]TACTTTTTTTCTTTG | 55728 |
| rs537205300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085283 | TCAGGCAATCTGCCC[A/G]CCTCAGCCTCCCAAA | 55728 |
| rs537206523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093018 | GCGCAGTTTCAGTTC[A/G]CTGCAACCTCTGCCT | 55728 |
| rs537252261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100517 | CTCCTATGTGGCTGG[C/T]ACTATACGCACATGC | 55728 |
| rs537277263 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127819 | GTGCCTGCCACCGCG[A/C]CCGGCTAATTTTTTG | 55728 |
| rs537304843 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066639 | TCTGTTTTTGAGTCT[A/G]TCTCTCTTGAGTGAA | 55728 |
| rs537315427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127241 | TTTATTTGTTTGAAA[C/T]AGGGTCTTGCTCTGT | 55728 |
| rs537327242 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085547 | GTGCAGCCTCCAACT[C/T]CTAGAGTCAAGTGAT | 55728 |
| rs537356538 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077137 | TGAATATTATGTAGA[-/AT]ATATATGTGTGTGTG | 55728 |
| rs537389948 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40185203 | GAAGTAAATTGATTC[A/C]GGGAGTCCCCTTACT | 55728 |
| rs537391307 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099878 | TAGAAATACTCCTTA[C/T]GTTTGCTTTCTTTTT | 55728 |
| rs537412986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071829 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTATAGG | 55728 |
| rs537461333 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133026 | GCCCGCCATTTTTCC[C/T]TCTGCTGTGGAAAGT | 55728 |
| rs537483945 | in-del | -/GACA | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118882 | AAAACAGCATTAACT[-/GACA]GACAGAGTAAAGAAG | 55728 |
| rs537492812 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064503 | TGGTCTCAAACTCCC[A/G]ACCTTGTGATCCGCC | 55728 |
| rs537492852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139150 | TTTATTTCTAAATAC[A/G]GTATTTTATTCTTTT | 55728 |
| rs537529786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145348 | CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55728 |
| rs537571832 | snp | C/T | 1.74665e-05 | 0.00295515 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144847 | GAATATATGTCTTTG[C/T]TTATATTGGTATAGC | 55728 |
| rs537620594 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064563 | CAGGCGTGAGCCACC[A/G]CGCCCGGCAATAACA | 55728 |
| rs537620907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179754 | TTTAGAGTGGTAAAG[C/T]CTTTCTTTTTTTTTT | 55728 |
| rs537626249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108233 | GCCACCATGCCCAGC[C/T]TGGTTACTGCTTTCT | 55728 |
| rs537705975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114536 | TTTTAAGGCTCATCC[A/G]TGTTGTAGCATGTGT | 55728 |
| rs537709500 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095753 | GACACTTGAACAAAA[A/C]TTTGAAGGAGTACAG | 55728 |
| rs537714472 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061583 | TTGGCCAGGCTGGTC[-/T]CAAACTCCTAACCTC | 55728 |
| rs537725943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143134 | AGTCCATATTTCTGG[C/T]AGCAGAATATTAATA | 55728 |
| rs537758780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072364 | AATTCTCCTGCCTCA[G/T]CCTCCTGAGTAGCTG | 55728 |
| rs537768407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057366 | CCCTCTCGACCCCCC[A/G]AGGTTTCCTCCCAGA | 55728 |
| rs537781362 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157206 | GTGAGAAATGGAAGT[G/T]TTTTTTTTTTTACGT | 55728 |
| rs537857851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094844 | GGTGTGAGCCACCGC[A/G]AGTGCAGTGGCGTGA | 55728 |
| rs537946269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160527 | AGCACATTTAAGGTA[A/G]GCTAGGCTAAGCTAT | 55728 |
| rs537947065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067740 | GTCTCACTCCGTCAC[C/G]CAGGGTGGAGTACAG | 55728 |
| rs537963769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059771 | GTGGCTTATGTGTAT[A/G]TACACACACATGCAC | 55728 |
| rs537969806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093922 | GTACTTTTAGTAGAG[A/T]TGGGGTTTTACCATA | 55728 |
| rs537979204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167597 | GCAGAAAGGATTCCA[A/G]GAATCTATCATCTGC | 55728 |
| rs537994101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181219 | CTAAAATAGTCATTG[A/G]TGGCTCTAGCCTGTC | 55728 |
| rs538017088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166943 | TAGTCACCCTTTTAT[A/G]CTATTAAATACTAGA | 55728 |
| rs538026244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074039 | TCAGGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 55728 |
| rs538064849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107690 | TGCGTGGCCTATAAC[G/T]GTATAGTATATATAA | 55728 |
| rs538127521 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116841 | ATACTTTTGCTGGAT[A/G]TGTATATTCTATACT | 55728 |
| rs538137052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065848 | ACCGGGGGCATGGAT[A/G]TGATACATGCGCAGT | 55728 |
| rs538160569 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139792 | CACTGCGCCAGGCCT[A/T]GCATTAGGCTTTTTT | 55728 |
| rs538170372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165166 | TTTCTTGGTTCCTGT[C/T]CTTAGAGTCATGTTA | 55728 |
| rs538181344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174325 | GAGGCTGCAGTGAGC[C/T]GTGATCATTTAAAGA | 55728 |
| rs538190225 | in-del | -/TG | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138947 | ATTTTAGGATTAGTT[-/TG]TGAATTTCTGCAAAG | 55728 |
| rs538196965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182203 | TGTTTTACCTTGCAT[A/G]CAGTAAAGGCTTTTC | 55728 |
| rs538201839 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170823 | GAGTTAATATGTCAT[A/G]GGCCATTTAAGACAG | 55728 |
| rs538287913 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173827 | ACTTTCTCTTTCCTC[C/T]CTCTGCTCCCCTGTC | 55728 |
| rs538301486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109445 | AACATTGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 55728 |
| rs538303664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090789 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCATG | 55728 |
| rs538366896 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061019 | GGGGTGTTGCCATAT[G/T]GCCCAGGCTGGCCTC | 55728 |
| rs538426089 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185631 | AAACATTTTAATAGA[A/G]ATTTTACTTTTTAAA | 55728 |
| rs538428023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183530 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTAGC | 55728 |
| rs538481452 | snp | G/T | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054646 | CAATGAGAACGAGCA[G/T]GATAACCAAAACCTT | 55728 |
| rs538502426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145941 | CCGAGGTGGGCGGAT[C/T]ACCTGAGGTCTGGAG | 55728 |
| rs538506430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124609 | ACCTTGGCCTCCCAA[A/T]GTCCTGGGGTTACAG | 55728 |
| rs538510432 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40073474 | AAGACATGTTGGATA[A/G]CAAGAAGAGGTGTAG | 55728 |
| rs538537739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131675 | TTTCAGCCTTTAATC[C/T]GTAAAGAAAGTCTGT | 55728 |
| rs538584981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096372 | GTGGTTCAGTAGAGG[G/T]AACCAAGGTGTAAAG | 55728 |
| rs538595796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161257 | CTCATCTTGGAGAAT[C/T]AGATCTGATCAAGGC | 55728 |
| rs538625500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178750 | GAAATGTGTAGGGAA[C/T]GAACTTCCTTTCAAT | 55728 |
| rs538633927 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109221 | TAAAGATTAAGAATT[C/G]AGGAATCTGAAAATG | 55728 |
| rs538655167 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150759 | CCAGGGGAGGGGAAA[C/T]CTTGTTACTTAAGAA | 55728 |
| rs538656376 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061933 | GCCTCCCAAAGTGCT[-/G]GGGTTACAGGTGTGA | 55728 |
| rs538692675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136068 | TAATATAGTATCACC[A/G]TCAAGATATGACTGA | 55728 |
| rs538729356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142154 | GGGGAGGGAGAGGGA[A/G]AGGGAGAGGGCAGCG | 55728 |
| rs538732187 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137580 | TGTGTTAAGAATACC[A/G]AGAATTTGTTTTAAT | 55728 |
| rs538752420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141859 | GGGAGGCCGAGGCTG[A/G]CGGATCACTCGCGGT | 55728 |
| rs538782098 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172784 | AGCAGTGTGTTTGAA[C/T]CTGTGAATGACCATT | 55728 |
| rs538831828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105536 | CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTTT | 55728 |
| rs538842628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098332 | TGTTAGGTAGAAATA[C/T]AACAGTATGTGCTTC | 55728 |
| rs538845150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097169 | ATAAAGATGTCATTC[C/T]GATTTTAGAAATGGA | 55728 |
| rs538883460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141333 | TCACTTGTCAGACGG[A/G]GCGGCTTCCGGGCGG | 55728 |
| rs538894054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138846 | AAGTTTTGAAATTGG[A/G]AAGTGTGAGTTTTCC | 55728 |
| rs538898188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077733 | TGCTAGGATTATAGG[C/T]GTGAGCCACCGCACT | 55728 |
| rs538919249 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147655 | CCCCACCTCCCTCCC[A/G]GACGGGGCGGCTGGC | 55728 |
| rs538919461 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140734 | AGGCAGAGGACCCTG[C/G]GGCCTTCCGCAGTGT | 55728 |
| rs538945110 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154932 | TTTCAGAGAAAAAGA[A/G]ATGGTTAAATATCTT | 55728 |
| rs538953725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147381 | CCCCTTTTCTATTCC[A/G]CAAAACCGCCATTGT | 55728 |
| rs539008897 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186260 | TGTGGTTCAGTGATT[C/G]TCCCCTGAGAATCAA | 55728 |
| rs539074169 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058198 | GTTTTTATTACTTCC[A/G]GTGTTTTTCTTTCAA | 55728 |
| rs539128496 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169659 | TCAGTGCTCATCTTT[-/A]AAAAAAAAAAACAAA | 55728 |
| rs539132087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117759 | AATAAAGCAGCTTTG[A/G]TATTCGTATCTATTA | 55728 |
| rs539134248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057485 | CCTGAGCACATAGTC[C/G]TAGCAGAGCCGTTTA | 55728 |
| rs539148246 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064497 | TCAGGCTGGTCTCAA[A/C]CTCCCGACCTTGTGA | 55728 |
| rs539148979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065063 | GTGAGCCACTGTGCC[C/T]GGCTGGGGTTAGAGG | 55728 |
| rs539159987 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056706 | CAGCCGGCGGGCTTG[C/G]GGGGGGGCGGTGGGC | 55728 |
| rs539162437 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090888 | CAGTGAGCCAAGATC[A/C]CGCCATTGCACTCCA | 55728 |
| rs539169797 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098998 | TTTAATTATATCTAC[A/G]TTTTTCGTGAATAAT | 55728 |
| rs539179895 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155636 | GACAATGGCTTAAAT[G/T]TGCCTTTGGAGATGG | 55728 |
| rs539232028 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087675 | CACTCCACGTGCACC[C/T]CGCCCCCTCCGCCCA | 55728 |
| rs539262754 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056191 | TAGTCAGGCAATGCC[C/G]AGGCCGGTCGCTCGC | 55728 |
| rs539328128 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158106 | GTATATCAGAAAAAT[A/G]TTTTTATTTGTACTG | 55728 |
| rs539329194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063218 | GAAATACAGCTTGAA[A/G]TAGCCTGTAGGGGAA | 55728 |
| rs539360159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127863 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 55728 |
| rs539394451 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077495 | GTCTCGCTCTGTCAC[A/C]CAGGCTAGAGTGCAG | 55728 |
| rs539404459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100591 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 55728 |
| rs539419202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073283 | CTTTTTCAGAGTGCA[A/G]TAGTCACCTCCAGTG | 55728 |
| rs539484513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124385 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTAGAGTG | 55728 |
| rs539500547 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105576 | TTTTTAAGAGACAGG[A/G]TCTTGCTTTGTCACC | 55728 |
| rs539546782 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174172 | GCTTGAGTCTAGGAG[C/T]TCGAGACCAGCCTGG | 55728 |
| rs539563599 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074100 | CCTGCTTGTTTTTGC[-/T]TTTTTTTTGAGATGG | 55728 |
| rs539586567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070974 | GGATTACAGGTGTCC[A/G]CCACCATGCCTGGCT | 55728 |
| rs539641555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112904 | AGACAGGATTTCACC[A/G]TGGTGGCCAGGCTGG | 55728 |
| rs539657247 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180523 | AAAATCTACTCTGAA[A/C]CCTGCAAAGTCACTT | 55728 |
| rs539660705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086070 | CCTGCTGGATTCGAG[C/T]GATCCTCCTGCCTCA | 55728 |
| rs539710788 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058803 | TTTTAAATCTAAATA[C/G]TGTTACATAGTTGCA | 55728 |
| rs539725760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078341 | CAGGGTTTCACCATG[G/T]TGGCCAGGCAGGTCT | 55728 |
| rs539753317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179348 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 55728 |
| rs539802483 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158359 | GGGAAAGTGTCATGA[A/G]AATTTTATTTCTGTA | 55728 |
| rs539827407 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088946 | GGTTTTTATTTTTTG[-/T]TTTTTTTTGTGTGTG | 55728 |
| rs539834338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116435 | ATGCCTTATTTAAAA[A/T]TTTTAAAATTGTTTC | 55728 |
| rs539835236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114743 | TATCTCCTCTTTTCT[A/T]CTTTTCTAGGTTTAT | 55728 |
| rs539873517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124705 | TAAAACTTAAAGGGG[A/G]AAAAAGCCCCTATAA | 55728 |
| rs539874226 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123699 | TATGTTGCCCAGGTT[G/T]GTTTTGAATTCCTGG | 55728 |
| rs539891404 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062481 | TTCCCACTGTAGCTA[C/G]AGTAATCTGTCTAAC | 55728 |
| rs539913067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085217 | CACCCGGCCAATTTA[C/T]ATTTTTAGTAGAGAT | 55728 |
| rs539915066 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119177 | TCATAAAAATCTTAT[A/C]AGGATTATGAATTAG | 55728 |
| rs540001151 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063985 | TGGTGGGGCGGCAGG[A/G]GGGGGTCTCACTATG | 55728 |
| rs540051104 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117572 | GAGCTTATAATAAAA[A/G]ACATTTTTGAAAAAG | 55728 |
| rs540067800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129383 | AGGTGTCTGCTACCA[C/T]GCCCTGCTAATTTTT | 55728 |
| rs540067857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138320 | AGTGTTCTTTATATA[C/T]TCTAGATACAAGTCC | 55728 |
| rs540113585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137956 | ATAGTTTCTGGACTG[G/T]TTGGTTTCCAAATGA | 55728 |
| rs540130773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143963 | GAGAACCAAAGAATT[C/T]GATAGCATAGCTTAA | 55728 |
| rs540152994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093207 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 55728 |
| rs540173418 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151241 | TGAAGAGTGTGAGTT[A/G]TGATTAGAGATTTAG | 55728 |
| rs540183553 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060802 | TAGAGACAGGGTCTC[A/G]CTGTGTTGCTTAGGC | 55728 |
| rs540212581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183143 | AATGCACAGATACAA[C/T]CCCAAGTCCTGTTTC | 55728 |
| rs540246990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182610 | GCACGCCACCATGCC[A/G]GGCTAAAATTTTTTT | 55728 |
| rs540248201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081062 | CAGTGAAAAAAAGGG[A/T]ATGGAAGGGATATAT | 55728 |
| rs540252124 | in-del | -/GAGGTTGCGGTGAGCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118349 | TGAACCCTGGAGGCA[-/GAGGTTGCGGTGAGCT]GAGGTTGCGGTGAGC | 55728 |
| rs540285527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123945 | TTTTTTTTAAATGCA[G/T]TATTTTTACCATTCT | 55728 |
| rs540332853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054243 | TGGGATTACAGGCGT[A/G]AGCCACTGTGCCAGG | 55728 |
| rs540343663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140189 | TGCTCCCTTTTTTCT[G/T]TGAATGTTTCATTGT | 55728 |
| rs540371196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173742 | GCAGAGAGCCTGGGC[C/T]GAACTCTTGTTAAAT | 55728 |
| rs540380195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152688 | AAATCCTCATGAAAA[C/T]AATTTCATGTGCTTG | 55728 |
| rs540414402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181170 | AGAAAAAAATATATA[C/T]ACATTGGCCAAATCT | 55728 |
| rs540456155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086463 | CTGCCTCAGCCTCCC[A/G]AGTACCTGGGATTAC | 55728 |
| rs540522191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160147 | TCGGGGAGGATTGCT[A/G]TATATGATCCTGTTC | 55728 |
| rs540523850 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169306 | AGAATTGCTTGAACC[C/T]AGCGGGTGGAGGTTG | 55728 |
| rs540557465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093349 | ATTCATTTGAGACTT[A/C]TTTTCTAATGTATGC | 55728 |
| rs540560854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159517 | CTACATCTCTAACTG[A/T]CACATCTGTATTCTG | 55728 |
| rs540582320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089127 | GGCTGATTGTTTTCT[A/T]TTTTTTCATAGAGAC | 55728 |
| rs540612208 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066361 | TCTCACTTTGTTGCT[C/T]AGGCTGAAGTGCAGT | 55728 |
| rs540641379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104505 | CATATTTTTCAGTAG[A/G]CATGTAGGCTTTTCT | 55728 |
| rs540771824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145890 | AGTTGTGGCCGGGTG[C/T]GGTGGCTCATGCCTG | 55728 |
| rs540778296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061947 | TGGGGTTACAGGTGT[A/G]AACCACCATGCCTGG | 55728 |
| rs540790078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060894 | ATGGGCCCGAGCCAT[C/T]ACGCCTGGCCTGTTT | 55728 |
| rs540805933 | snp | A/G | 0.000115305 | 0.00759205 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103033 | ATCTGTCAACTACAC[A/G]TTTCCACCCTCAGTT | 55728 |
| rs540819078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095237 | AGGCCCATGCCACCA[C/T]GCCTGGCTAATTTTT | 55728 |
| rs540822982 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081478 | TGGTAAAACCCTGTC[G/T]CTACTAAATATACAA | 55728 |
| rs540842792 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109511 | TCACCTGAGGTCAGG[A/T]GTTTGAGACCACCCT | 55728 |
| rs540844773 | snp | C/T | 1.65798e-05 | 0.00287917 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102564 | TGGAAAGTAACTACC[C/T]GGAAGATTCTCTTCT | 55728 |
| rs540860273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110515 | GTGGAACATCTTTTT[G/T]TGTGTTTTTTGGCCA | 55728 |
| rs540870470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168569 | ATATAAGGATAACAT[C/T]ATAAAAATGAAATTT | 55728 |
| rs540881717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108728 | TGTAACTGTCTATTC[A/G]GTGAAGATAGTTTTA | 55728 |
| rs540898961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118254 | AGAAACCCGTCTCCA[C/G]TAAAAGTACAAAATT | 55728 |
| rs540902144 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110299 | CACATGTCTATGTCT[A/G]ACCTTTTTAGGAACT | 55728 |
| rs540911823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075183 | TTATTAGTTGTAGAT[A/G]TAAACACATATAGAT | 55728 |
| rs540975332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074461 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 55728 |
| rs540994308 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055885 | TCATACTACAGCGGT[C/T]GCAAGAGGGAAGAGC | 55728 |
| rs541021246 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163271 | ATAATCATAACCACC[C/T]GCTGGGGTAGGTATT | 55728 |
| rs541039140 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138088 | TCTAGTGTCATGAAG[C/G]CTGCAAAAATTCCAG | 55728 |
| rs541068954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162479 | AGAAGAAGAAGTAGA[A/G]CTGGAGGATGAGTAT | 55728 |
| rs541089911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127976 | AAAACAAAATATTTT[A/G]GAGAAAAATTTTAGA | 55728 |
| rs541100719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062696 | TCTCCCTGAAGGGGT[C/G]AGAGTTCTTAAATCT | 55728 |
| rs541128665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127546 | GCTTTTAATATTTAC[C/G]TCTATTTTTTTATTT | 55728 |
| rs541133911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119686 | ATGTACTATTCAATT[A/T]AAAAAAAAGTTTGAG | 55728 |
| rs541153356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153695 | GTTATGAGCATAAAA[C/T]AGGTGACATCAGGGT | 55728 |
| rs541154925 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100256 | CAGACCAGAGCTGTT[A/G]CCTACTCTGCTGTGC | 55728 |
| rs541162069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068836 | CTTTAAAAAATTCCC[A/G]GGCTGGGCACAGTGG | 55728 |
| rs541163800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161347 | AGGATGCAATTACCA[A/G]GATAGACTGGGAAAC | 55728 |
| rs541216115 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156521 | CACCCCACTATCTAG[C/T]ATAGTTTAAGCAACA | 55728 |
| rs541239613 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101310 | TACAGGCATGCGCCG[C/T]CACTATGCCCAGCTA | 55728 |
| rs541239965 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129228 | TAGTTTTTATTTTGT[G/T]TTGTTTTGTTTTTTT | 55728 |
| rs541283496 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075759 | GTATTCCAAAGGATG[-/A]GTTCTGCCATAATTT | 55728 |
| rs541289022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083594 | AGGCCATGTTTTAGA[C/T]TATACAATTCTCTTC | 55728 |
| rs541301610 | snp | A/G | 1.67335e-05 | 0.00289248 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126174 | GCTTGATAATCCTGA[A/G]CAAAAATCATCTCAG | 55728 |
| rs541332629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133743 | AAAATTTGGAAAGAT[A/C]TGAAATCTCAGCCAC | 55728 |
| rs541362906 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127626 | TAATAAGAAATGTCT[A/G]TCTTACTATTAAAGA | 55728 |
| rs541374693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141496 | AGACGATGGGCGGCC[A/G]GGCAGAGGCGCTCCT | 55728 |
| rs541376248 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154318 | TCAGTCAATTCTACC[C/T]TAAAGATGTGTTTTA | 55728 |
| rs541378515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163015 | TTCTCCAGAACAGGT[A/G]ATCCAAGTGAGCAAA | 55728 |
| rs541381980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078637 | CTCAACTGATCCTCT[C/T]ACCTTAGCTTCCCAA | 55728 |
| rs541405103 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069895 | ACTCCAGCCTGGGTG[A/G]CAGAGTGAGACCCTG | 55728 |
| rs541409108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112301 | GTAAATGAGCTTTCA[C/T]TGGTGTTCAGCAAAA | 55728 |
| rs541410107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070381 | GAAAAGGAGGACATT[C/T]TCCCTATATAGCCAT | 55728 |
| rs541419167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170855 | GCAATTGTATTTCAC[A/G]TATCCTCATTTTGCT | 55728 |
| rs541442031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171844 | GCTGATGGATGTGGA[A/G]TCTGATGTTCGAGGG | 55728 |
| rs541550434 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066528 | TTACACTATGTTGGC[C/T]AGGCTGGTCTTGAAC | 55728 |
| rs541622229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142483 | AAGGGTAACCTTAGC[A/G]GCATAAAAAAGTTAA | 55728 |
| rs541655217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091912 | CTATGCCCCGCCAAA[A/G]TTCAACAATATATAA | 55728 |
| rs541661245 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095081 | GAGTCTGGCCAGGGT[A/T]ACTATATCTTTTTTT | 55728 |
| rs541662832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184799 | CATCTCTACTGAAAA[C/T]ACAAAAATTATCTGG | 55728 |
| rs541691293 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057640 | CTGCAACTTTGTCCC[A/T]CAATGGGACCCTTCT | 55728 |
| rs541720225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149216 | AAGTTCATTAACTGA[C/T]GAATAGAGAAACAAA | 55728 |
| rs541816304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094337 | TGGGTGGAGTGTTCT[G/T]TAAGTGTTGATTAGA | 55728 |
| rs541838921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101769 | CCTAATATGTCCAAT[G/T]ACAGATATTTATGTA | 55728 |
| rs541856483 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179164 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55728 |
| rs541877494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101192 | GAGGGAGTCTCGCTC[A/T]GTCACCAAGGCTGGA | 55728 |
| rs541894478 | snp | A/C/T | 3.29779e-05 | 0.00406055 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137015 | TAAAAACAGTTGTAG[A/C/T]CCAAGAGTTTGTTCA | 55728 |
| rs541894766 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128853 | AAAAAAAATAAATAA[A/T]TAAAATAAGGAAACT | 55728 |
| rs541929993 | in-del | -/TTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146888 | TTTTTTTTTTTTTTT[-/TTT]CCCCAGGTAATGTTT | 55728 |
| rs541933109 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143350 | ATAAGGTCTTGCTCT[C/G]TTGCCCAGGCTGGAG | 55728 |
| rs541952575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059309 | CATATTGTAAGTCTT[C/G]GGAAGAATCAGTTGT | 55728 |
| rs541965251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065968 | ATGGAGTCTAGATCT[G/T]TCGACAGGCTGGAGT | 55728 |
| rs541985508 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158422 | AGCAAATAAGAGTCT[A/G]CTTTTGAACCAGATA | 55728 |
| rs541994915 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092185 | TAAAATGGATTGGAA[A/G]TGCTTTCTTATTTTC | 55728 |
| rs542008932 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062235 | AGGTGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 55728 |
| rs542018027 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162496 | TGGAGGATGAGTATC[A/G]AATGCTCATATTTGC | 55728 |
| rs542062657 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099300 | CAGGCCGGAGTGCAG[A/T]GGCGCCATCTTGGCT | 55728 |
| rs542062729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106603 | TCCCAGGCTGGAGTA[C/G]GGTGGCGCAATCTCA | 55728 |
| rs542099407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105935 | GGAAAGCTACAAAGA[G/T]AAGAGGATAAACAGG | 55728 |
| rs542103145 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056910 | CAGCTGCTTGCTAGC[C/T]TTGCGCGGCGCGGGA | 55728 |
| rs542165282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079283 | AGGTTTTGTATTTTT[G/T]GTTTATTTATTTATT | 55728 |
| rs542172889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124096 | GAAAAATAATATAAC[C/G]TTGTATCCTTGTTTA | 55728 |
| rs542252297 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065299 | TAAGCTGGACCTCTC[A/G]GGTTTGAAGTGCCCA | 55728 |
| rs542253579 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109587 | ACCGGGCATGGTGGT[G/T]CACACCTATAGTCCC | 55728 |
| rs542258285 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149804 | TGGGAGGCTGAGGCA[C/G]GAGAATGGTGTGAAC | 55728 |
| rs542316533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058704 | TTCCTTCATTAAAGT[A/G]TATTAAAGTAGGCAT | 55728 |
| rs542322279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124759 | CTGTGGAACACCTAG[C/G]GTATGCTCTCAAAGC | 55728 |
| rs542341981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151305 | TGAGATGGGAGTCTG[A/G]CTCTGTTGCCCAGGC | 55728 |
| rs542369913 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131209 | TCTCAGGTCTCAGTA[C/T]CAGAAAAAGCTGTAC | 55728 |
| rs542376990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150735 | TTCAATAAATTGTAA[A/G]GAAAAACACCAGGGG | 55728 |
| rs542377993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065451 | ATCGAACAAAAGATT[A/C]GGAACAGAACCTTAG | 55728 |
| rs542384509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114623 | TCATTTAGGATTTTT[G/T]CATCTTTATAAATAA | 55728 |
| rs542402265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107454 | AGTGGTGCAATCTGG[G/T]TTCACTGCAACCTCT | 55728 |
| rs542407533 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157686 | GGTAATTTTTCGGTG[C/T]AGTAGTTAAATATTG | 55728 |
| rs542410820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164393 | GTAGTCGGAGTGGAG[A/G]AGGTCACAGAATTGA | 55728 |
| rs542439073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114152 | TGAATAAAAATGTTA[A/G]TCAAGGCATGGATGT | 55728 |
| rs542478659 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087815 | TGAATGGCTCGATCT[C/T]GGCTTACTGCAACCT | 55728 |
| rs542500026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130991 | AATGTGAGTAATAAT[A/G]TAATTCTTATACAGT | 55728 |
| rs542505225 | snp | A/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131887 | TCCAGCCATTAACCA[A/T]AATTTTCTGGTGGAC | 55728 |
| rs542507499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122563 | TATTTTGATTGTAAA[A/G]TTATATTCTATGTTA | 55728 |
| rs542547032 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095039 | TGCCCATTGTCCAAC[A/G]TGCTGGGATTACAGT | 55728 |
| rs542639903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109004 | GTATTTTTAGTAGAG[A/G]CAGGGTTTCACCATG | 55728 |
| rs542677255 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082871 | ATGCCCGGCTAATTT[C/T]TTGTATTTTTAGTAG | 55728 |
| rs542678908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116719 | TCTGGGAATTGCCTT[C/G]TGCCTGATGTTCATC | 55728 |
| rs542707974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183190 | CTTGTATCATGAGCA[A/T]CTCCTTATGTGGTCA | 55728 |
| rs542742706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133806 | TCAACATATACTTTT[G/T]TGTGTGTGTGTGTTT | 55728 |
| rs542774239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147463 | GTGGCCGGGCAGAGG[G/T]GCTCCTCACTTCCCA | 55728 |
| rs542783514 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162820 | CACACCAGGCCATCT[C/G]CAAGCAGGAGAACTA | 55728 |
| rs542790060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073697 | CTGCTAGGCTCAAGC[A/G]ATTCTCTCACCTCAG | 55728 |
| rs542807018 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075363 | CATTTAACAACATGT[C/T]TCAGAGGTCTATCCA | 55728 |
| rs542828310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080587 | TGACCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 55728 |
| rs542846870 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107772 | TTTATTTCATAGGGT[A/G]GTTATAAGGATTCAA | 55728 |
| rs542878261 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178514 | AGAATTGTAACTAGT[-/G]GTACTTGGGCAGCAT | 55728 |
| rs542909506 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146979 | GATTTGGCAGGGTCA[C/T]AGGACAATAGTGGAG | 55728 |
| rs542911357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153561 | AAATATCTGTTGATG[C/G]ATAGATTTCCTGCAG | 55728 |
| rs542939732 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107389 | TAAATTGGCTTAGTA[-/T]TTTTTTTTTTTTCGA | 55728 |
| rs542948208 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152807 | ACGGTGGGAAGCCCT[A/G]TTTGTCTGTGATTAC | 55728 |
| rs542949413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054304 | AAAGAGACACGGCCC[A/G]GTGCGGTGGCTCACG | 55728 |
| rs543034034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | N4BP2 | GRCh38.p7 | 4:40098686 | TCAGAAATGACAGTA[C/T]ATTGAGTTTTGTAAG | 55728 |
| rs543081070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097956 | TAGATGCCAATAGCT[C/T]CTTACCACCCAGTTG | 55728 |
| rs543088698 | snp | C/T | 3.31055e-05 | 0.00406837 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126253 | CCTTTATTGGATCAT[C/T]GGAATACTCAAACTA | 55728 |
| rs543201076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088597 | CCTCCGCCTCCCGGG[C/T]TCAAGTGATTCTCCT | 55728 |
| rs543209397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109659 | GGAGGCGGAGGTTTC[A/G]GTGAGTCAGGATCCC | 55728 |
| rs543219272 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154410 | GTTTGATTTTTTACT[A/G]AATCAAATGCAAATG | 55728 |
| rs543247459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104574 | TATTATAGATGTTAC[G/T]GTCAGTCATGGCAGT | 55728 |
| rs543257901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161472 | GTTGCAATTTGTGGA[A/C]CTTTTTTGGGTACTG | 55728 |
| rs543258381 | in-del | -/CTGT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058221 | TCTTTCAAACACCAG[-/CTGT]CTTTTGTAACTCGTT | 55728 |
| rs543286535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111288 | GATTTTAATTTTTCT[A/G]CTCAAGGTCTTTCTC | 55728 |
| rs543295097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174339 | CCGTGATCATTTAAA[G/T]AAATTAAAAATAGAA | 55728 |
| rs543299137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068988 | AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAATCC | 55728 |
| rs543343941 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097216 | GTGTTTTTAATTGCT[G/T]TCTATTTTAGGTCTT | 55728 |
| rs543360471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068385 | CGTCTTCAAGAAATC[A/G]TTGCCAAATCCGATG | 55728 |
| rs543371297 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135730 | ACCATGCCCGGCTAA[C/T]TTATTTTTGTATTTT | 55728 |
| rs543398982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148655 | ATTTTTAATTAAATT[C/T]TTATTTTTATTTAAA | 55728 |
| rs543401900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141922 | GAAACCCCGTCTCCA[C/T]CAAAAAAATAGGAAA | 55728 |
| rs543425610 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, missense | N4BP2, LOC344967 | GRCh38.p7 | 4:40057000 | ACGACGCGGCACCGG[C/T]TTCGACGCCCTCTGC | 55728 |
| rs543434189 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094292 | ATGTGTTCTGTTAAT[A/G]CTTGAAAAGAGTGTG | 55728 |
| rs543444278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113004 | CCACCATGTCCGGCC[A/G]AAAATTCTTTATCTT | 55728 |
| rs543456247 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099809 | TTTTCATTGTATAGA[-/C]ATTAAGTTTTTAGTT | 55728 |
| rs543459121 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134270 | TGTTAAAATCTCCCA[C/G]ATGCCAGAGGTTGAT | 55728 |
| rs543461738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105086 | GGATTACAGGCGTGA[A/G]CCACCACGCCCAACA | 55728 |
| rs543538514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148506 | GGGGAGAGGGAGTTC[A/G]GCTTTTTTAGGTTCC | 55728 |
| rs543578950 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084850 | GAACTCCCGACCTCA[A/G]GTGATCTGCCCACCT | 55728 |
| rs543594808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163214 | AGCCATTATGTTTAC[C/T]ATGAACTAGGCACCA | 55728 |
| rs543622868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115891 | ATTTGAGAGATGAAT[A/G]TTGAAATCTCCCTTT | 55728 |
| rs543625821 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152569 | GATGGATAGATTACA[A/G]TGAGGCTATGTGTTT | 55728 |
| rs543671804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077036 | AGATTTTTTTTGTTT[A/G]TTTCTTTTTTGATGG | 55728 |
| rs543707811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069469 | TAAACTCACTTACAG[C/T]GTGGTTGAATTTTTC | 55728 |
| rs543729517 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074051 | CCCGCCTCAGCCTCC[C/T]AAAGTACTGGGATTA | 55728 |
| rs543737205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091556 | TTGAATATGGAACTA[A/G]CCTTGCCTTCCTGGA | 55728 |
| rs543751070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126816 | AGGCTGGAGTACAGT[A/G]GTGTAATCTTGGCTC | 55728 |
| rs543768281 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156764 | GAAATGCTTCAAAAT[C/T]TGAAATTTTTCGAGC | 55728 |
| rs543775317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164561 | CCATTCTTCACATGG[A/G]TAGGATCTGACTCAA | 55728 |
| rs543777496 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173667 | GGCTGACAGTCAGTG[C/G]ATATACACCAGTGCA | 55728 |
| rs543789690 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061901 | AACTCCTGACCTCGG[A/G]TGATCTGCCTGCCTC | 55728 |
| rs543872672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181119 | CTCGCCATTGCACTC[C/T]AGCCTGGGTGACAGA | 55728 |
| rs543875986 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091690 | GGCTCACTGAAGCCT[C/T]GACCACCTGGGCCTA | 55728 |
| rs543916653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130593 | TCATCTGAGCTCACT[C/G]TAGCCTTGACCTCCT | 55728 |
| rs543960302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144184 | CAGCCTCCAGCTGCC[C/T]ACATGGTTGGTGCCT | 55728 |
| rs544010059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089376 | CTTTTCATCCTTTTA[A/G]CCAGGTCTTTCATCA | 55728 |
| rs544011714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084952 | GAGTCTCGCTGTGTC[A/G]CCCAGGCTAGAATGC | 55728 |
| rs544076514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136326 | CTAATCTGCCTGGTA[C/T]AAAGGATTAGAAATT | 55728 |
| rs544083586 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123893 | TCTTAATTTATTTAA[A/C]AATTTTTTTCAGACC | 55728 |
| rs544095979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150607 | ACCCAGGAGTCAGAG[C/G]CTGCAGTGAACCGAG | 55728 |
| rs544102971 | in-del | -/T | 0.288906 | 0.246954 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065935 | AGATCCAGTAAAGCA[-/T]TTTTTTTTTTTCTTG | 55728 |
| rs544167001 | in-del | -/GATA | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140303 | AAACATGCTGTCATG[-/GATA]GATAGATAGATGCAG | 55728 |
| rs544211822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079392 | AAAATGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 55728 |
| rs544213369 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098432 | TTATTAATAACTTGT[C/G]ATACATTGTTTAGAA | 55728 |
| rs544244103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087215 | ACCCCTTCCTCCTTG[C/T]CCCTTTCTTTCTTCC | 55728 |
| rs544274112 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122666 | CTTTAAAAAATACAA[A/T]AGGAAGAAATAGAGA | 55728 |
| rs544297901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145094 | TTTCAGGAATATTAC[A/G]TATCTTTGTCCAATA | 55728 |
| rs544301427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060193 | TCCAGAAATTATTTT[A/G]TTAGAACTGTACATC | 55728 |
| rs544390171 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119425 | AGTATGGCTTTAAAA[A/G]ATCTTACCAAATGAC | 55728 |
| rs544453976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100211 | GTGTCATAGCCAGCA[C/G]TAGAGATTTAAATGT | 55728 |
| rs544539423 | in-del | -/TTT | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101888 | CTCCATCATTCAGAC[-/TTT]TTGCTACTACAGACT | 55728 |
| rs544575261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146607 | TGTACACATTGTAAA[G/T]TGATTACCACAATGA | 55728 |
| rs544612007 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172923 | GGTTACATTGAATCT[A/G]CGAACTTTTTTGCTT | 55728 |
| rs544648706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175278 | CATATGTGCGTCAGC[C/T]TCCCAAAGTGCTAGG | 55728 |
| rs544676339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103978 | TTTTTTTTTTGAGAC[C/G]GAGTCTTGCTCTGTT | 55728 |
| rs544678111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109616 | CCAGCTACTTGAGAG[A/G]CTGAGGCAGGAGAAT | 55728 |
| rs544748229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151423 | ACTACAGGTGCGCCT[C/T]GCCATGCCCTGCTAA | 55728 |
| rs544802223 | in-del | -/TGCC | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084421 | GGTCACTTTTAGATA[-/TGCC]TGGTTTGAGATTTTT | 55728 |
| rs544807707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138616 | CAAGTTGATTCTTTC[A/G]CATGTGGATATTCAG | 55728 |
| rs544825690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108057 | CCTCCCAGCCTGAGT[A/G]GTTGGGACTATAGGT | 55728 |
| rs544844818 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090307 | TTTATCTATATCTAT[-/A]AAAAAAATCTTGCTT | 55728 |
| rs544930277 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134350 | GAGGTGAAATAGCTC[A/G]GAGTTGTGCTTCCCC | 55728 |
| rs544931056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088570 | CAATATTGTGATCTC[C/T]GCTCACTGCAGCCTC | 55728 |
| rs544933250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123926 | TCTTCATAACAAGAA[A/T]TTTTTTTTTTTAAAT | 55728 |
| rs544986501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061913 | CGGGTGATCTGCCTG[C/T]CTCGGCCTCCCAAAG | 55728 |
| rs544997933 | in-del | -/GGC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113802 | TTGCCATGTTACCCA[-/GGC]TGGTCTTGAACTCCT | 55728 |
| rs545012705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169564 | ATGATAAACTTTGTA[A/G]AGAAAAAAAGGGAAA | 55728 |
| rs545019211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182573 | CTCCCACCTCAGTGC[A/C]CAAGAAGCTGAGACT | 55728 |
| rs545064763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068239 | TTATCAGATGTATGG[G/T]TTGCAAATATTTTCT | 55728 |
| rs545067092 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135469 | GTATATACCCAGTAA[C/T]GGGATGGCTGGGTCA | 55728 |
| rs545068693 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072771 | CTCTCTGTTGCCCAC[A/G]CTGGACTGCAATGGT | 55728 |
| rs545085397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076130 | CATGCCTGCCCCTGA[C/T]AGATATATTTAAAGA | 55728 |
| rs545098970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126004 | TTACAATTTCAGAGT[G/T]GTGTTATATTTACAA | 55728 |
| rs545100010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061139 | TCTTAAAACTTTATG[C/T]AAGCCCCAGATTTAA | 55728 |
| rs545103560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134757 | AGTTGCACATGGCTT[C/G]CTTTCAAGGGTTGTC | 55728 |
| rs545157289 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160309 | CAGATGGTCTCCCAC[G/T]TAGGATGGTTTGACG | 55728 |
| rs545163269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067214 | CAGGTGTGCACCACC[A/C]CACCTAGATAATTTT | 55728 |
| rs545166180 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129295 | GCAGTGGCACAGTCT[C/T]GGCTCACTGCAACCT | 55728 |
| rs545195855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167242 | TTGTATATAATGGGA[A/G]TTCCAGAGTGAAATA | 55728 |
| rs545197135 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154577 | ATTTAGTAATGTCCT[A/G]AAAGTCTTTTGTGAG | 55728 |
| rs545221178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176903 | GAGACTCTGGCCTTT[C/T]GGGGGATCCCTGTTT | 55728 |
| rs545275215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141092 | CATGGCCCGTTCTCA[A/G]TGAGCTGCCGGGCAC | 55728 |
| rs545342557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076858 | ACCTTTTTCTTATCA[C/T]AGTAGTATTTTGAAA | 55728 |
| rs545365929 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093004 | GCTGGAATGCAATGG[C/T]GCAGTTTCAGTTCAC | 55728 |
| rs545366336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174751 | GGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 55728 |
| rs545382002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085056 | TAGCTGGGATTACAG[A/G]TGCCCACTACCACGC | 55728 |
| rs545395886 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147524 | CCTCCCGGACGGGGC[G/T]GCTGGCCGGGCAGAG | 55728 |
| rs545403709 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071686 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 55728 |
| rs545412000 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40158774 | TGAGACCATCTCAAA[A/T]AAAAAAAGAATCTCT | 55728 |
| rs545467944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179078 | TAGTAGATATTAAAA[C/T]GTTTTGGAGGCTGGG | 55728 |
| rs545494521 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056871 | TCCCCGCCGGGCGCG[C/G]TCGCCGTGTCTCCCC | 55728 |
| rs545505321 | in-del | -/TCT | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139709 | TCTTGGCCAAGCTGG[-/TCT]TGAACTCCTGACCTT | 55728 |
| rs545557890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064042 | AGCTCAAGTGATCCT[C/T]CTGCTTCAGCCTCCC | 55728 |
| rs545585608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097740 | GTTGGTATTTGGGAT[A/G]TGAAGAATAAAACAT | 55728 |
| rs545591740 | in-del | -/TTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135571 | GTCTTTCTTTCTTTC[-/TTTT]CTTTCTTTCACAGAG | 55728 |
| rs545607335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090385 | AATTGACATATTTAC[C/T]GTGTTGTCTTCCCAT | 55728 |
| rs545644612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104423 | AGTTTTTTTTTTTTG[A/G]TATCTTTTCTGTGTC | 55728 |
| rs545663216 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147832 | CAGCCAGGCAGAGAC[A/G]CTCCTCACCTCCCAG | 55728 |
| rs545668373 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063477 | GAAGTACTATGCTTA[C/G]TTCATTCTAGGTTGT | 55728 |
| rs545710396 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080025 | CATTGTTCATTTGAG[C/T]CAGTCCATTCACATT | 55728 |
| rs545785643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091693 | TCACTGAAGCCTCGA[A/C]CACCTGGGCCTAAGT | 55728 |
| rs545807182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107438 | GCCCAGGCTGTAGTA[C/T]AGTGGTGCAATCTGG | 55728 |
| rs545844341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106694 | GCTGGGACTATAGGC[A/G]CATGCCACCGTACCT | 55728 |
| rs545844705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113887 | GTGAGCCACCATGCC[A/C]AGCCTGTACTTTATT | 55728 |
| rs545893247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142401 | TTCCAACTCGGAGTT[C/T]AGTATCCCTAATTGT | 55728 |
| rs545900247 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149155 | ATGTCTTTACGGAAA[C/G/T]TTGCATATGAATGTC | 55728 |
| rs545941276 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156032 | AGAACAGTTCTATAC[A/C]TTAAAAATAAACATT | 55728 |
| rs545962097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065303 | CTGGACCTCTCAGGT[C/T]TGAAGTGCCCATGGA | 55728 |
| rs546054097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172578 | AAGACACCACACAGG[A/C]AAGGAGAGAGGCCTG | 55728 |
| rs546056700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105101 | GCCACCACGCCCAAC[A/C]ATCCTGCGTTGTCTT | 55728 |
| rs546094847 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095749 | ATGTGACACTTGAAC[-/AA]AAATTTGAAGGAGTA | 55728 |
| rs546103573 | in-del | -/AACA | 0.142225 | 0.225576 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178162 | AGACTGGGTCCAACA[-/AACA]AACAAACAAACAAAG | 55728 |
| rs546116403 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069512 | GACATGTAAGGACAG[A/C]TAACCTATACATAAC | 55728 |
| rs546140330 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061551 | TGTATTTTTAGTAGA[C/G]ATGGGGTCTCACCAT | 55728 |
| rs546185404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128183 | ATTCCAGGTCAAAAG[A/G]GAAAACATCTTAGAG | 55728 |
| rs546186633 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058674 | TGGGCTTAAGTTATG[G/T]TAGAGGCATGTTTTT | 55728 |
| rs546300716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057733 | GTGAGTCATCTTAGC[A/G]GGGGCACAGTTTATC | 55728 |
| rs546317110 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157360 | TTGACTTTAAATCCT[C/T]TTGAGTAGTATATTT | 55728 |
| rs546328727 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164947 | TTGCTGAGCTGTAGA[G/T]TAAGAAGAGCTCACT | 55728 |
| rs546330262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071477 | CTAATGTGGTGAGAA[C/G]CTGATCATTTCATTA | 55728 |
| rs546362600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065662 | CTGAAACCGTATAGG[A/G]AATAATAGGAGTTTT | 55728 |
| rs546368908 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061183 | TTATTATTATTATTA[-/TT]TTTTGAGGTAGAGTC | 55728 |
| rs546404307 | snp | C/T | 1.65748e-05 | 0.00287874 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121633 | AGAGAATTCTAATTC[C/T]CCTGTGCCAGAGTTT | 55728 |
| rs546424232 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072210 | CTCCTGAGTAAGCTG[A/T]GACTACAGGCGTGTG | 55728 |
| rs546427258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129639 | TAATTTTTTTCTTTC[C/T]TTTTTTTCTCGAATA | 55728 |
| rs546441378 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184795 | ACCCCATCTCTACTG[-/A]AAACACAAAAATTAT | 55728 |
| rs546465878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129104 | TTACAGGCTGGAGTG[C/T]GGTGGCACCATCTCA | 55728 |
| rs546502658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137174 | AATTTAATGATTATT[C/T]CTCACCATTTTGACT | 55728 |
| rs546523535 | snp | C/T | 3.39864e-05 | 0.00412214 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136941 | TACTTAAATTTTCTA[C/T]AGCTATTCATTAGAA | 55728 |
| rs546551009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150937 | CCATTGTAGTTATGC[A/T]TTTTAAAGGAGTCCT | 55728 |
| rs546551599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073902 | GGTTTAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 55728 |
| rs546609315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108106 | CTAATTTTTGTATTT[G/T]TAGTAGCGACGGGGT | 55728 |
| rs546613316 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081301 | TGTGTGTCTGGGTAG[A/C]TTATATTTAGTTGAG | 55728 |
| rs546648221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107626 | TGACCTTAGGTGGTC[C/T]GCCTGCCTTGGCCTC | 55728 |
| rs546649097 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166161 | ATGCCAATATTGGAA[C/T]CTTTTTCTTTGTTAG | 55728 |
| rs546691587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174781 | CACTCCAGTCTGGGC[A/G]ACAGAGTGAGATGCT | 55728 |
| rs546755427 | in-del | -/ATAAC | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126062 | GTCTCTGAGGTAAAT[-/ATAAC]AGAGTGAATAATGTT | 55728 |
| rs546778337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181544 | TATGGCAGCAATGTC[A/G]TCTTCAGGGACTTGG | 55728 |
| rs546812728 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117306 | AAACCAGACAAGATC[A/G]AGGTAGGTAAATATG | 55728 |
| rs546826003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180205 | TATCTTTCATATACA[A/G]ACAACTTTTCTAAAC | 55728 |
| rs546838143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078896 | TTTTTTTTAAGAAAA[C/T]CTGTAATAAAATTGT | 55728 |
| rs546875946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087572 | GTTTTGCCATGTTGC[A/G]TAGGCTGGTCTTGAA | 55728 |
| rs546925161 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138261 | CTGTTCATATCCTTT[C/G]TCTATTTTTAAATTG | 55728 |
| rs546931296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059673 | AACACTTTTTTGATA[C/T]CTACCTTGCCTGATA | 55728 |
| rs546955530 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103602 | TACATTAATTTTACT[A/G]GTAGTTGGAAATTCA | 55728 |
| rs546963102 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164908 | GATCTCTTTGCTGAG[A/T]CTCTGAAGACTCTGG | 55728 |
| rs547021989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174202 | GGCAAAATAGCAAGA[C/T]ACTGTCTCTACAAAA | 55728 |
| rs547050110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124420 | GGTGCCATTTTGCCT[C/T]ACTGCAACCTCTGCC | 55728 |
| rs547086144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088743 | GACCTCAGTTGATCT[C/G]CCCGCCTTGGCCTCC | 55728 |
| rs547088184 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073937 | AGCTGGGATTACAGG[C/T]GCATGCCACCACATC | 55728 |
| rs547130249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131362 | TTGTGGCATGCATTT[A/T]TATACTAATACTGCT | 55728 |
| rs547147747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096173 | CTTGTGGAGCTTACA[C/T]TTTATTGGAATATGG | 55728 |
| rs547181766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103376 | TTGTGTAGCTAATAA[C/T]ACTGTTTTCTGTGGA | 55728 |
| rs547211588 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147207 | GACACAGCACATGTT[G/T]CAGAGAGCACAGGGT | 55728 |
| rs547235905 | snp | A/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157889 | AAACAAGGCTAGAAC[A/T]CATCTACATCCTGAA | 55728 |
| rs547243857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093750 | GTTTCTTCAGTGCGC[A/G]TGCCAGCGCTCCTGG | 55728 |
| rs547348452 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117326 | AGGTAAATATGAAAG[C/T]CAGATTTGCCCAACT | 55728 |
| rs547352243 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155391 | GACAGAGCAAGACTC[C/T]GTCTCCAAAAAAAAA | 55728 |
| rs547359515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060640 | CAGGGTCTCCCTCTG[C/T]TGTCCAGGTTGGAGT | 55728 |
| rs547378226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117055 | CTATGTTTCTAGTTA[C/T]GGATTTCTTATTTTT | 55728 |
| rs547379439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097029 | TCATTGTTCTGAAAT[A/G]CATATTGTTAACATC | 55728 |
| rs547389338 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154659 | TAAAAGAGGAAAAAG[A/G]ACATAGTAGTGGTAG | 55728 |
| rs547413039 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104791 | GAAGAGTGTTGAGAC[A/T]TAGAACCTGCGTTGT | 55728 |
| rs547419510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066617 | GAGCCACCGTGCCTA[G/T]CCCTGGTCTGTTTTT | 55728 |
| rs547448961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148235 | TGGCAGATCACTCGC[A/G]GTTAGGAGCTGGAGA | 55728 |
| rs547521996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054474 | CAATTCCAGCTATTC[C/G]GGGGGCTGAGGCACG | 55728 |
| rs547535384 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113862 | CTCCCAAAGTGCTGG[A/G]ACCACAGGTGTGAGC | 55728 |
| rs547540176 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061272 | CCTCCCAGGTTCAAG[A/C]GATTCTCCTGCCTCA | 55728 |
| rs547575243 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108971 | ACAGGCATATGCCAC[C/T]ATGCCCAGCTAGTTT | 55728 |
| rs547580695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110926 | AACTTCCAAATAAAT[G/T]ACTTGTAAGACTTAC | 55728 |
| rs547589478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152996 | TCTGTTATTGATAAT[A/G]GCAATAGCCCTAATA | 55728 |
| rs547592736 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159429 | TACTTGACGCTTTTG[A/G]GAATCTAGGAAAGTT | 55728 |
| rs547620632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062420 | CCTGGGTTGTTGCAC[A/G]AGCCTCCTAACAGCT | 55728 |
| rs547631550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068447 | AGTTTTAAGTTTAAG[A/G]TCTTAGATTTAGGTC | 55728 |
| rs547634768 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131724 | AGTAGTTTTGCAACA[A/G]GTTAACCATGCCTTT | 55728 |
| rs547636069 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184887 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55728 |
| rs547688545 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096570 | AAGGCATGATCCACC[A/G]TGTGGTTTAATTGAG | 55728 |
| rs547693174 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116958 | TGTTTCTTTGTAGAT[-/A]ACTAGTTTTAAAATG | 55728 |
| rs547708025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167379 | AGGCATACACCTAAA[C/T]ATACTCTGACAGAAT | 55728 |
| rs547716729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118476 | TTTTGTTATTTTTAA[A/G]GATTTACTTATAGTC | 55728 |
| rs547740437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070831 | GTGTTTTTTTTTCTT[A/C]TTTTTTTTTTTGAGA | 55728 |
| rs547760483 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142562 | TATTTCCTGAGGAGA[A/G]AGATGAAAATATACG | 55728 |
| rs547801101 | in-del | -/GGT | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054356 | AGGCCGAGGTGGGAG[-/GGT]GATCACCTGAGGTCA | 55728 |
| rs547802735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070098 | TAGAAAAGTAGTATG[A/C]TACATTGAAACCACA | 55728 |
| rs547806136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105439 | ATGAGATTCTCCAGC[C/T]TCGGTCTCCTGAGTA | 55728 |
| rs547806939 | in-del | -/CT | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150662 | GGCAACAGAGTGAGA[-/CT]CTGTCTCAGGGGGAA | 55728 |
| rs547816161 | in-del | -/GAATGTTCTGGAATTA | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149479 | CTTTGTGAAATGATG[-/GAATGTTCTGGAATTA]GTGGTGGTGGTTGCA | 55728 |
| rs547836420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179134 | AGCAGTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 55728 |
| rs547872409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119141 | CTCTTCATTTCTAAA[A/G]TGCCAGTAATAACAC | 55728 |
| rs547909103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161730 | TAAGTTGGTAAATGG[A/G]AAAGATAGATGTTTA | 55728 |
| rs547911292 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076369 | TGGTCCCAGCTATTC[A/G]GGAGGCTGAGGTAGG | 55728 |
| rs547915070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069083 | CGGGATCGCGCCACT[C/G]CACTCCACTGAGTGA | 55728 |
| rs547947859 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059856 | TCTGAGATTTGCACT[A/G]TTCTTACAGGGGAGG | 55728 |
| rs547968711 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093624 | TTATTTATTTATTTA[C/T]TTACTTTTGGAGACA | 55728 |
| rs547978617 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063395 | GTTTCTTCACATGGT[A/G]AACCTGTTTCATGGC | 55728 |
| rs548007760 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40185117 | TCCCTTCCATTCGAC[A/G]TGTGCCTCTTGTTGT | 55728 |
| rs548012950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085101 | TATTTTTAGTAGAGA[C/T]GGGGCTTCACTGTGT | 55728 |
| rs548034737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075712 | ACACATCTTATTTCT[A/G]TATTCCACCAACTTT | 55728 |
| rs548069928 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060638 | GACAGGGTCTCCCTC[C/T]GTTGTCCAGGTTGGA | 55728 |
| rs548140566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129184 | CTCCCAAGTAGCTGG[A/G]ACTACAGGTGTGAGT | 55728 |
| rs548141111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082990 | CAAGTGTGAGCCACC[A/G]CACCCGGCCGGGCTG | 55728 |
| rs548153932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090671 | GGCGTGGTGAGTCAC[A/G]CCTGTAATCCCAGTA | 55728 |
| rs548184379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093523 | GTGATTCTCCTGCCT[C/G]AGCCTCCTGAGTAGC | 55728 |
| rs548197632 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056565 | GGAAGCAGCCGAACC[A/G]GCCGGGCAGGGCTTG | 55728 |
| rs548213869 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090085 | AAATCAGTCAGGCAC[A/G]CTTATGTTGCTGGGT | 55728 |
| rs548222299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141760 | GGTGGAGGTTGTAGC[A/G]AGCCGAGATCACGCC | 55728 |
| rs548231985 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183503 | ACCGTGCCCAGCTAA[-/TT]TTTTTGTATTTTTAG | 55728 |
| rs548245434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092940 | TGAGCCACCGTGCCC[A/G]GCCTGCTCTTTTTTT | 55728 |
| rs548250510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138065 | GAGGGGGCAGGAGGA[A/G]CAGCCTCTCTAGTGT | 55728 |
| rs548285042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086726 | GGATTCTAATTATAT[A/G]TATTATATAGATTTA | 55728 |
| rs548291814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128328 | TAATACATCCAGTTA[A/C]GGCATAGGGATTGCT | 55728 |
| rs548367933 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173246 | CCTGGGTATGGACAA[A/G]TTGGCCACCCAAAAT | 55728 |
| rs548392159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144427 | TAGAAAGAATGACTC[A/G]GTAGTTTAAGGACTA | 55728 |
| rs548465284 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142123 | AGGGAGAGGGAGACC[A/G]TAGGGAGAGGGGGAG | 55728 |
| rs548541939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152231 | AATCTATAAACTAGT[A/T]GCTATCATTATCCCT | 55728 |
| rs548559414 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079025 | GGCGCGATCTCAAGC[A/G/T]ATTCTCCAACCTCAG | 55728 |
| rs548571259 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113225 | AATGTATGTATTATA[G/T]AAATAAATGCTCTTA | 55728 |
| rs548572132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085902 | TGTGCTGCTCACACC[C/T]GTAATCCCAGCACTT | 55728 |
| rs548580201 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086534 | GTAGAGATGAGGTTT[C/T]ACCGTGTTGGTCAGG | 55728 |
| rs548595033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180812 | GAAAACAAAACAAAA[A/G]TAAGTTGTAAAACAA | 55728 |
| rs548630181 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180428 | GTGTTGTGATAATGC[A/G/T]GGCAGATAGTTAGTC | 55728 |
| rs548661731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137367 | GAATAGCAGTAATGT[A/G]ATGGGTCTTGAATAT | 55728 |
| rs548720681 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138759 | TCTATTCCATTGATC[C/T]GTATGTCTGTCCTAT | 55728 |
| rs548739210 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116168 | ATACTTTTACTTTGA[A/G]TATTTTTATGTTCGA | 55728 |
| rs548739271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145333 | GGTTCAAGCCATTCT[C/T]GTGCCTCAGCCTCCC | 55728 |
| rs548750287 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170121 | TTTAAAAATTAAAAT[A/G]TACATTTAACTCAAT | 55728 |
| rs548803255 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156908 | AATCCAAAACACTTC[C/T]GGTCCTAAGCATTTT | 55728 |
| rs548841707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161625 | AAAAAGAGATACATG[C/G]TGAAATATGTACGTA | 55728 |
| rs548843088 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180612 | CAATTCAGTTCACAA[C/T]TACAAAACGTGTTAC | 55728 |
| rs548847041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158862 | TCCAAAGCAGAATTC[A/T]CTCATTTTGCAAGGA | 55728 |
| rs548871333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112725 | TTTTTGTTGTTGAGA[C/T]GGAGTTTTGCTCTTG | 55728 |
| rs548883906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165708 | AAACCCACACATAGA[G/T]TGAATAGAATAGATT | 55728 |
| rs548888682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129688 | GTTGCCCAGGCTGGT[C/G]TCGAACTCCTGGCTT | 55728 |
| rs548918812 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077694 | TCTGACCTCAAGTGA[G/T]CCGTCCACTTCAGCC | 55728 |
| rs548925778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067729 | TTTGAGACAGAGTCT[C/T]ACTCCGTCACCCAGG | 55728 |
| rs548929929 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159892 | TGTTGTTTTTTTTTT[A/G]AGATGGATTCTCACT | 55728 |
| rs548941513 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156378 | TACTTGTTTACTATA[C/T]CAATGTTAATATTAT | 55728 |
| rs548981063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066747 | GGAAAAAAGTACAAC[A/G]TATTTACTATCTTAA | 55728 |
| rs549031621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101985 | TCAATGCAAAATCCA[A/G]TATAATTTTAGCTGG | 55728 |
| rs549041485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079863 | TTGGAATATTATGAT[A/G]ATAATCAGTGAGCAA | 55728 |
| rs549086518 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079737 | AGCATGGGCAGTTGA[C/G]GCTGTGGTGAGCTGA | 55728 |
| rs549093585 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074034 | CAACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC | 55728 |
| rs549126651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167467 | TTTGCAATGGGAAAA[G/T]AATTGGACTGGTATC | 55728 |
| rs549156477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072924 | ACGGGGTCTCACCAT[A/G]TTGGCCAGGCTGGTC | 55728 |
| rs549160391 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065760 | CAGGGATTTGAATTT[G/T]TTAGCATTTTTAAGG | 55728 |
| rs549187358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182072 | ACATTCAGCTGAAAA[A/G]AAGATTGGGAAAAAT | 55728 |
| rs549217590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173837 | TCCTCTCTCTGCTCC[C/T]CTGTCCTCTCCTTTT | 55728 |
| rs549219831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072324 | GATCTTGGCTCACTG[A/C]AACCTTCGACTCCCT | 55728 |
| rs549253114 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147354 | ATTTCTCAATCTTTT[-/C]CCCCACCTTTTCCCC | 55728 |
| rs549267675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132152 | ATTGATTTACAAATT[A/G]GGCACAGTAAAAAAT | 55728 |
| rs549297716 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070999 | CTGGCTAATTTTTGT[A/G]TTTTTAGTGGAGACG | 55728 |
| rs549302575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081367 | AACTACAGTGAAGGC[C/T]GGGCGAGGTGGCTCA | 55728 |
| rs549316698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088141 | TTTTTATTGCTGACT[A/G]GTATTTCATGGAATG | 55728 |
| rs549326580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126544 | CTATAAGCCATCCAT[G/T]TTAAGTTTGTGTTGT | 55728 |
| rs549363847 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105590 | GGTCTTGCTTTGTCA[C/T]CCAGGCTGGAGTGCA | 55728 |
| rs549371570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090540 | TGATTTTAAGTGAAA[C/T]GACATGTATCAGGTC | 55728 |
| rs549374334 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134526 | TGGTAAGAAGGGTAG[A/G]TGAGCTCAGTTACTA | 55728 |
| rs549432058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089927 | TTTCTGTAAATATTT[C/G]TGTAAATTTCCAAGA | 55728 |
| rs549463517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130196 | ACACCTGGCCAAAAA[C/T]AAAATATATTTTTAG | 55728 |
| rs549480264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125667 | AAGGCGGGCGGATCA[C/T]CTGAGGTCAGGAGTT | 55728 |
| rs549480777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133104 | GAGAGAATCTTGGTT[C/T]ATTGGTCAAAGTCTA | 55728 |
| rs549516733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083028 | ACACTGACTGTATAG[A/C]AAGAGGAGATAGAGT | 55728 |
| rs549523247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125208 | GAGGTGCCCAAAGGA[C/T]GGTGTGCAAATGCCA | 55728 |
| rs549528843 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101637 | AAATTCATAGCGTGG[A/G]TCATGTAAATAAGTT | 55728 |
| rs549545988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182686 | AATATATATATACAT[A/G]TGTATAGAGAGACAG | 55728 |
| rs549572016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183460 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55728 |
| rs549643065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141286 | CCCCCACCTCCTTCC[G/T]GGACGGGGTGGCTGC | 55728 |
| rs549666399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095389 | CCCAGCCCGCTATAT[A/C]TTTTTGATGGCCTGA | 55728 |
| rs549707561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134909 | TTCCTTCCTTTCTCT[A/C]TCTCTCTCTCTCTTT | 55728 |
| rs549720261 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142141 | GGGAGAGGGGGAGGG[A/G]GAGGGAGAGGGAGAG | 55728 |
| rs549793134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054583 | CAACTCTAGTCACCG[C/T]CCCCCCGCCGCCCCA | 55728 |
| rs549898509 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141629 | GGCAGAGGGGCTCCT[C/T]ACGTCCCAGATGATG | 55728 |
| rs549903526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099408 | CCACTGTGCCTGGCT[A/G]ATTTTTTTTTTTGTA | 55728 |
| rs549922297 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055436 | TTCTTGAGTTCTCTC[A/C]TTATATATTACTAGT | 55728 |
| rs549953117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153830 | ATTGCATGGCCAGAT[A/T]AATCAGACTTACCTG | 55728 |
| rs549968551 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054335 | CTTTAATTCCAGCAC[-/T]TTTGAGAGGCCGAGG | 55728 |
| rs549971935 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147628 | GGGCGGCTGGCCGGG[C/T]GGGGGCTGACCCCCC | 55728 |
| rs549981451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104035 | TCTCGGCTCACTGCA[A/G]GCTCCGCCTCCCAGG | 55728 |
| rs549985698 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184119 | GGAACAGAACATTTT[A/G]TCCATCTCAAAATAG | 55728 |
| rs550010916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119874 | GCTTCTTTAAATCAT[A/G]GTATTGATGGCAGCA | 55728 |
| rs550016013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104885 | TCTCGGCTCACTGCA[A/G]GCTCCGCCTCCCAGG | 55728 |
| rs550021267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110695 | GGTGCAAGCCACTAC[A/G]CCCGGCTAATTTTTG | 55728 |
| rs550044523 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056152 | GAAGGCGGGTTCCCG[C/T]GCCCGCCGCAGCGGC | 55728 |
| rs550047600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119243 | CATAGAAAACTCAGC[A/G]TTAGGTATGATTTCA | 55728 |
| rs550077011 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154812 | CTGCTTTGTATATGA[C/T]CTTGATCTTTTACCT | 55728 |
| rs550086644 | in-del | -/T | 0.0185685 | 0.0945488 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142622 | GGTGTAAGGCATGAG[-/T]TTTTTTTTTTAACTT | 55728 |
| rs550092882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160934 | TCCATAAACCTAACA[C/T]CCCACAGAGCTTTAT | 55728 |
| rs550102464 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148339 | GCCTGCAATCGCAGG[C/T]ACTGGGCAGGCGGAG | 55728 |
| rs550112665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064931 | ATGCACCACCACACT[C/T]GCTAAGTTTTGTATT | 55728 |
| rs550129390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161111 | ACAGAATAACAGCCC[A/G]AAGTCATAACACCTA | 55728 |
| rs550145488 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173938 | TTTGAAGTTTTACTC[-/AT]AAACTTTTCTGGGCT | 55728 |
| rs550203722 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065991 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 55728 |
| rs550221765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105478 | TACAGGTATCTGCTG[C/T]CACCCCCAGCTAATT | 55728 |
| rs550316210 | in-del | -/TGT | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138393 | GGTTGCCTTTCACTC[-/TGT]TGTTTCTGTTGTGAC | 55728 |
| rs550319030 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162663 | ATTTCAGGAGCACTG[C/G]TTTTACTCAATGGCA | 55728 |
| rs550350519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069949 | ACACAACCCCCAAAA[A/G]CTCTTTCTTTGCTTT | 55728 |
| rs550350581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063138 | AAAAAATCCTTTGAT[A/G]TCTAATTTTTATCAA | 55728 |
| rs550352188 | snp | C/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054784 | TATAAATATTCACAA[C/G]CGAAGGCTGATACTG | 55728 |
| rs550405694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170235 | ACTTACTATGTACAC[C/T]GGTCATCCCAACTTA | 55728 |
| rs550411811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069204 | GCCCTTTGGGAGGCC[A/G]AGGCGGGCACATCAC | 55728 |
| rs550470554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127098 | GTTTTGCCATGTTGC[C/G]CAGGCTGGTCTCGAG | 55728 |
| rs550484029 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180032 | GCCTCCCAAACTGCT[C/G]GGATTACAGGCATGA | 55728 |
| rs550489593 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083308 | AAACATAGAGTTACC[A/G]TATGAACTAGCAATT | 55728 |
| rs550541720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169690 | AAAAAGGAAGCTGGG[C/T]GTGGTGGCTCTCGCT | 55728 |
| rs550616965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136060 | TCTACAGATAATATA[A/G]TATCACCGTCAAGAT | 55728 |
| rs550644115 | snp | C/T | 1.65905e-05 | 0.0028801 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113414 | ATTTTAAAATGTTTT[C/T]GTCTTTGTTGTATGT | 55728 |
| rs550681135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112846 | AAACTGGGATTACAG[A/G]TGCCCGCCACCACGC | 55728 |
| rs550681990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070949 | CTTGCCTCAGCCTCC[A/T]AAATAGCTGGGATTA | 55728 |
| rs550743594 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078045 | CTTTTTAGAGAAAAT[A/C]CTTAAAAAAATGCAG | 55728 |
| rs550916541 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147085 | GTTTGTGTCCCTGGG[C/T]ACTTGAGATTAGGGA | 55728 |
| rs550918542 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139821 | TTTTTTTTTTACATT[A/T]TTTTTTCTTTTTTTT | 55728 |
| rs550980581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174077 | CAAACAACTGGATAG[C/T]TATTGTCAAAAAGAC | 55728 |
| rs550993233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123499 | TTATATCTTTTTTCT[A/G]TTTTAGAGACAGTGT | 55728 |
| rs551053655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146031 | GCCAGGCATGGTGGC[A/G]TGCACCTGTAATCCC | 55728 |
| rs551073876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109074 | CCTATCTCAGCCTCC[C/T]GAAGTGCTGGGATTA | 55728 |
| rs551145145 | snp | A/G | 0.000263757 | 0.0114808 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144747 | ACCTCCATGGGCTGC[A/G]TGTGGATGAAGCTCT | 55728 |
| rs551152110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144489 | TTGGTGCATTCTTAT[A/G]TATTAAACTCATTGC | 55728 |
| rs551157056 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127908 | CCTTGTGATCCACCT[-/G]CCTCGGCCTCCCAGA | 55728 |
| rs551173618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176822 | TTGCAGCAGGGAGGA[A/G]CCTGGCCCCTCCTCT | 55728 |
| rs551212067 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062165 | CTTGCTGCAATCTCC[A/G]CCTCCTGGGTTCAAG | 55728 |
| rs551216626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152374 | TTAATTAACAGGGTT[A/G]TTGTGAAGATTCTTA | 55728 |
| rs551259402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159667 | GTCATATCTAGCTGC[A/G]AGGGAGGCTGGGAAA | 55728 |
| rs551283310 | in-del | -/T | 0.320911 | 0.239733 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104813 | TGCGTTGTCTTTTTT[-/T]TTTTTTTTGGAGACA | 55728 |
| rs551287494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143885 | AAAGATAATTTATTA[A/G]GGGGAATTGGCTCTC | 55728 |
| rs551317921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062338 | CTCTCTTTAATATCT[C/G]TTGAATCTGTTCCTT | 55728 |
| rs551325910 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149491 | ATGGAATGTTCTGGA[A/C]TTAGTGGTGGTGGTT | 55728 |
| rs551333525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096122 | GAGAAAACAAGTAGA[C/T]TGCCTGTAGTTCTAT | 55728 |
| rs551343508 | in-del | -/T | 0.0252325 | 0.109451 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157206 | TGAGAAATGGAAGTG[-/T]TTTTTTTTTTTACGT | 55728 |
| rs551370956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161085 | ACAAGTTAAAATCAC[C/T]ACTGGCCCTCACAGA | 55728 |
| rs551371701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088246 | AAAGCTGCTGTAAAC[A/G]TTTGTTTACAGGTTT | 55728 |
| rs551377283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061488 | TTCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT | 55728 |
| rs551404310 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079548 | TAACACTATTAGAGA[A/T]CATGTTTGTTCATTC | 55728 |
| rs551474143 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104146 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 55728 |
| rs551487087 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108373 | GCTGGAGCGCAGTGG[C/T]GTGATCTCGGCTCAG | 55728 |
| rs551540526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060507 | ACCTTGCCCTCCCAA[A/G]GTGCTGGGATTACAG | 55728 |
| rs551554046 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101417 | CACCCGCCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 55728 |
| rs551563934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158915 | ATATTTAGAGCACTC[A/G]TTACTGGGGTTACAG | 55728 |
| rs551600940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133868 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCATTG | 55728 |
| rs551613555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067772 | GGCATGATGTTGGCT[C/G]ACTGTAACCTCTGCG | 55728 |
| rs551618533 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106023 | GTCTTTTTTTGTTCA[C/T]TGATGTATGCTCAGT | 55728 |
| rs551675638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140562 | AAGTTATTCTGGAAA[G/T]TATTTTTGCACTTAT | 55728 |
| rs551691314 | snp | C/G/T | 0.00358923 | 0.042236 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163792 | GAGACAATAAGCTGC[C/G/T]TTTGTTTGGGTTTTG | 55728 |
| rs551705820 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165712 | CCACACATAGAGTGA[A/G]TAGAATAGATTCTGG | 55728 |
| rs551745460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077145 | ATGTAGAATATATAT[A/G]TGTGTGTGTGTGTGT | 55728 |
| rs551757624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084315 | GAAAGAATAGGCAAA[A/G]ATGACTTAGTTTTTG | 55728 |
| rs551770506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068419 | TGAAGCTTTCTCCCC[A/G]TTTTCTTCTACGAGT | 55728 |
| rs551818650 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080887 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 55728 |
| rs551844891 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153664 | TTTGGCTACATTATC[A/G]AAAATGATAGCATAA | 55728 |
| rs551865428 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109795 | TAATAGGCGGAATTC[A/G]TTTTAAAACTGCTTT | 55728 |
| rs551877418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075545 | TGGGACTACAGGTGC[A/G]TGCCACCATGCCTGG | 55728 |
| rs551905182 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117921 | AGAATGTTGGAACAT[C/T]ATCAACGTTTTGTTT | 55728 |
| rs551905482 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127734 | GGTGCGATCTTGGCT[C/T]GCTGCATGCTCCGTC | 55728 |
| rs551936924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176362 | TTCATGCTGATCAAA[A/G]TCTTCACTAAGAATA | 55728 |
| rs551937574 | snp | C/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102912 | CATTGCTGTTGCCTC[C/G]TCCGCCACCTCCACC | 55728 |
| rs551938259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177536 | CAGGAGAATTGCTTA[A/G]ACCCCGGAGGCAGAG | 55728 |
| rs551945132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184307 | CAGGCCCTCAAAATG[C/G]AGCACTGGACTTCAC | 55728 |
| rs551965798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090067 | CTTTTGCACCATAGT[A/C]AAAAATCAGTCAGGC | 55728 |
| rs551971486 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071042 | TTGGCCAGGCTGGTG[-/T]TTTTTTTTTTAAATG | 55728 |
| rs551992659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082946 | ACCTCGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 55728 |
| rs552007121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082201 | GAATTGCTTGAACCC[A/G]AGAGGTGGAGGCTGC | 55728 |
| rs552033176 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056037 | GCCGATGGGGCTGGG[A/C]AGCCTCCCTCCACCC | 55728 |
| rs552066449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088670 | TACGCCTGGCTAATT[C/T]TGTATTTTTACTAGA | 55728 |
| rs552068320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081451 | AGGAGTTCAAGACCA[A/G]TCTGACCAACATGGT | 55728 |
| rs552069635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132316 | AGAAAATCTTTACCA[C/T]TATTGTTTCTGAGTT | 55728 |
| rs552094095 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055499 | GAATAAGTGTTCCAG[G/T]TAGACCTAAACGACA | 55728 |
| rs552101389 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131523 | TGACAGTATGTGTAT[-/A]ATATATTTACATACA | 55728 |
| rs552106210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136717 | CTATCTTTTGGCATT[A/C]ATTTTTTGAAAATTA | 55728 |
| rs552135633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170462 | TGTCTCTACAAAAAA[A/T]ACAAAAATTAGCCGG | 55728 |
| rs552162951 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062643 | TCCTTATTGACACTT[A/G]GCTGTCAGTGTGCTA | 55728 |
| rs552172272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178495 | CAGATATGAAAGAGA[C/T]TGAAGAATTGTAACT | 55728 |
| rs552192917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127700 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55728 |
| rs552214375 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147672 | ACGGGGCGGCTGGCC[A/G]GGTGGGGGCTGACCC | 55728 |
| rs552215868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169703 | GGTGTGGTGGCTCTC[A/G]CTTGTAATCCCAGCA | 55728 |
| rs552240861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143789 | CAGCATTATCAAAGG[A/G]TACACAAATAATAAA | 55728 |
| rs552270674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180917 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 55728 |
| rs552281324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135809 | TGACCTCAGGTGATC[C/T]ACCTGCCTCGGCCTC | 55728 |
| rs552293373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150969 | ATCTTTTATGAGGTA[C/T]GTACTGAAATATTTG | 55728 |
| rs552302199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100388 | TTTTTGGTTTCCTTT[G/T]TTTTTTGAGATAGGG | 55728 |
| rs552305359 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183550 | ACCATGTTAGCCAGG[A/T]TGGTCTCGACCTTCT | 55728 |
| rs552343383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106249 | ATTTTTTTTGGAATT[A/G]AACTTCTGCTTAGAG | 55728 |
| rs552352333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141687 | TCCCAGACGGGGTGG[C/T]GGCCGGGCAGAGGCT | 55728 |
| rs552380293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105542 | GTTGGCCAGGCTGGT[C/G]TCAAACTTTTTTTTT | 55728 |
| rs552437834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148187 | AGTGAACGAGACTCC[A/G]TCTGCAATCCCGGCA | 55728 |
| rs552449647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064288 | ATTTATTGATTGATT[G/T]ATTTGAGACAGAGTC | 55728 |
| rs552490075 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141335 | ACTTGTCAGACGGGG[C/T]GGCTTCCGGGCGGAG | 55728 |
| rs552511015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070712 | TGCCTTGGCCTCGCA[A/T]AGTGCTGGGATTACA | 55728 |
| rs552547496 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060846 | GTGGGCTCAAGCAGT[A/C]TTCTCACTTCAACCT | 55728 |
| rs552551541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092399 | TTGAGACATTGGTCC[A/G]TTTCATATAAATTGT | 55728 |
| rs552592331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099617 | TTTTTAATAAAGAGG[A/C]ATGTTGAACATTTTT | 55728 |
| rs552599907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090574 | GAACAACATACTTTC[A/G]TTCAACGTCATTCTG | 55728 |
| rs552605363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085207 | TGAGCTACCACACCC[A/G]GCCAATTTATATTTT | 55728 |
| rs552619940 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090627 | AATTGGTTATGTATT[A/G]TCTTGCTTAAAGTTG | 55728 |
| rs552628176 | snp | C/T | 1.65457e-05 | 0.00287621 | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142692 | AGAAATTAAAAGAGA[C/T]TGAAGAAACACCAAG | 55728 |
| rs552641458 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171078 | CCCAGTTTAATGATT[C/G/T]TATCAGTTATATTGG | 55728 |
| rs552651813 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055229 | ATCTCTTGAGATTCT[A/G]GGTTATTACAATTTT | 55728 |
| rs552665105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149473 | GAATTTCTTTGTGAA[A/G]TGATGGAATGTTCTG | 55728 |
| rs552678210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093208 | CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 55728 |
| rs552687943 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157040 | GTATGGAAGGTTTCA[A/G]TAATAATTATATTCA | 55728 |
| rs552745969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057178 | CCTGAATGTGGGGCC[C/T]GGCGCGGGCCGCCTC | 55728 |
| rs552763131 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156065 | AAATAAAGCAGTTCC[G/T]TTAAACAACTTACTA | 55728 |
| rs552839128 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173452 | AATAGGATACTCATT[G/T]CTATACTAGGAGGCA | 55728 |
| rs552850059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064518 | GACCTTGTGATCCGC[C/T]TGCCTCGGCCTCCCA | 55728 |
| rs552861666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070061 | GTACATTTTAAAAAC[G/T]TTCATTAGGAAAATA | 55728 |
| rs552890018 | in-del | -/AACA | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179369 | GTGAGACTCCATCTC[-/AACA]AACAAACAAACAAAC | 55728 |
| rs552952733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162723 | TATTGGTGTATGTAT[A/T]AGGGTTCTCCAGAAT | 55728 |
| rs553000018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099936 | ACCTTTTTTTTTCTT[A/C]CATTTTTAGGTTTTC | 55728 |
| rs553032405 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100592 | GCCCAGGCTGGTCTC[C/G]AACTCCTGGGCTCAA | 55728 |
| rs553033421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133484 | GGGATTACAGGCGCA[C/T]ACCACTACGCCTGGC | 55728 |
| rs553081740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149851 | GCAATGAGCCGAGAT[C/T]GAGCCACTGCACTCC | 55728 |
| rs553088429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072539 | GTGAGCCACCGCGCT[C/T]GGCCCACCTGGCTAA | 55728 |
| rs553111451 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075817 | TTATAACAGATAGAT[A/T]CATATTTCTTTTTTT | 55728 |
| rs553134386 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127671 | AAAATATATATATAT[-/A]TTTTTTTGAGATGGA | 55728 |
| rs553158011 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079211 | ATAGGCATAAGCCAC[A/T]GTGCCTGTCCTGATA | 55728 |
| rs553174823 | in-del | -/AGACCGG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088034 | AAGTGCTGGGATTAC[-/AGACCGG]AGCCACCACGCCCGG | 55728 |
| rs553176293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180933 | GAGGCGGGTGGATCA[G/T]GAGGTCGGGAGTCCG | 55728 |
| rs553219327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180551 | CTTCCTGTCATTATT[C/T]CACAGGAATACTTAA | 55728 |
| rs553223138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086138 | CCCGGCTAATTTTTT[A/T]TTTTTTTTTGCTAAT | 55728 |
| rs553262504 | snp | A/G | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158524 | TCTTAGAGGCCAGAC[A/G]CGGTGGCTTATGCTT | 55728 |
| rs553262979 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182723 | GTTCTGTTGCCCAGA[C/G/T]TGGAGTGCAGTGGCT | 55728 |
| rs553263920 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078088 | TGAATTGGATTTTAA[A/G]GCTTCTGATGTTGAA | 55728 |
| rs553281829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112279 | ATCTCAGAACCTTGG[A/G]TAGTCTGTAAATGAG | 55728 |
| rs553290151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066174 | GACCTTGTGATCCAC[C/T]TGCCTCAGCCTCCCA | 55728 |
| rs553311094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125422 | TTTGCCAAAGTAATC[A/G]ATCTTCTTGGTCCTT | 55728 |
| rs553347422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166096 | CATTTGTTTTATCTA[C/T]ACAATAAGACAATGG | 55728 |
| rs553349136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153353 | ATTTTGGATGGAATT[A/G]GGTGGCTTCTATTGA | 55728 |
| rs553349571 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167280 | AAAGCCAGATTTAAT[-/A]GAAGTAAATTTCCTG | 55728 |
| rs553409608 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092043 | ATATATATATATATA[G/T]ATAGCTGAATTTTAT | 55728 |
| rs553490647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122427 | TGCCCAGGCTGGAGT[A/G]CAGTGCCTCAATCTT | 55728 |
| rs553497109 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068908 | TGGATCACTTGAGGT[C/T]AGGGGTTCAAGACCA | 55728 |
| rs553501464 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110704 | ACTACGCCCGGCTAA[-/T]TTTTTGTATTTTTAG | 55728 |
| rs553561983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172631 | CCTCAGAAGGCACTA[A/G]CCCTGCTGACACTTC | 55728 |
| rs553631252 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074126 | GATGGAGTGTTGCTC[-/TA]TTGCTCAGGCTGGAG | 55728 |
| rs553667094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087809 | CCAGGCTGAATGGCT[C/G]GATCTCGGCTTACTG | 55728 |
| rs553692805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138406 | TCTGTTGTTTCTGTT[A/G]TGACACTGAAGCCTT | 55728 |
| rs553700997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129415 | TATTTTTAGAAGAGA[C/T]GGGGTTTCACCATGT | 55728 |
| rs553723003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175947 | TACAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGC | 55728 |
| rs553728293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094987 | TTTGCCATTTTGGCC[A/G]GGTTGGTCTCAAACT | 55728 |
| rs553738134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137660 | CATACTCACAGAGTT[C/G]TGGAAACAGGAGGTA | 55728 |
| rs553766988 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151837 | TTCTTTTAAAATTCC[A/T]GGCTGAATATCATCT | 55728 |
| rs553859112 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181734 | AGGCAGATCACCTGA[A/G]GTCAGGAGTTCAAGA | 55728 |
| rs553874838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081087 | ATATATAGCTTGCAA[A/T]CTGGAGGAAGTACAG | 55728 |
| rs553887897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154030 | CCGTAGATAAAAGGA[A/G]CACAAACCTAGATGT | 55728 |
| rs553895986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054827 | GAAGATTGCTTTGTT[C/T]TTCATTCCAGTCTCA | 55728 |
| rs553909529 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181718 | TTTGGGAGGCTAAGG[A/C]AGGCAGATCACCTGA | 55728 |
| rs553961716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160561 | GTTCAGTAGCTTAGG[A/G]GTATTGGATGCATTT | 55728 |
| rs553962292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075016 | TGTAAAGAAAAAAAA[A/G]AAAGTAAATAAATAA | 55728 |
| rs553970776 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128662 | CTTCCCAAGTAGCTG[A/G]GATTACAGGCATGCG | 55728 |
| rs553999843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160183 | TCAAGTAGGAAAAAA[C/T]TAAATGACACGGACT | 55728 |
| rs554038677 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140122 | ATTTTACTTTACAGA[A/G]TCTTATCATCCTGCA | 55728 |
| rs554095164 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104863 | AGGCTAGAGTGCAGT[A/G]GTGCGATCTCGGCTC | 55728 |
| rs554109059 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141351 | GGCTTCCGGGCGGAG[A/G]GTCTCCTCACTTCTC | 55728 |
| rs554119118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090240 | CTGCTTTGTTCTTTT[A/T]CAAAGCTATTTTACC | 55728 |
| rs554152643 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109514 | CCTGAGGTCAGGAGT[C/T]TGAGACCACCCTGGC | 55728 |
| rs554154439 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126770 | GGTATTTTTATTTTA[-/T]TTTTGGAGATGGAGT | 55728 |
| rs554156499 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151823 | GCAAGAGCAACATAT[G/T]CTTTTAAAATTCCAG | 55728 |
| rs554167780 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122185 | TGGGGAAGATAAAAC[C/T]GAGATATTGAATCCC | 55728 |
| rs554204199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067039 | CTTCCATGTTGCAGC[A/G]TATGACCTAATTTCC | 55728 |
| rs554228663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063746 | CCTCCCGTGTTCAAG[C/T]GATTCTCCTGTCTCA | 55728 |
| rs554252441 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097393 | TTCGGAAGACTGCAA[A/G]CCCTAAGGAAGTTGT | 55728 |
| rs554264670 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096596 | TTGAGTCACGCTGGC[A/T]TTGGTGCTAAATAGA | 55728 |
| rs554280078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069412 | AGAGTGAGACTGTTT[A/T]AAAAAAAAATTCCCT | 55728 |
| rs554282680 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179321 | CTTGCAGTGAGCCAA[G/T]ATCGAGCCACTGCAC | 55728 |
| rs554283910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162792 | CTCCTGTAATTTTGG[A/C]GGCTGAGAAGTTCAC | 55728 |
| rs554284951 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078699 | CCCAGCTTATTGTTT[C/T]GTATTTTTTTGTTGA | 55728 |
| rs554292234 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146666 | TTACCATTTTGTGTG[C/T]GGGGGATGAGAACAC | 55728 |
| rs554299570 | in-del | -/AAAT | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146164 | GAGACTCTTTCTCAA[-/AAAT]AAATAAATAAATAAA | 55728 |
| rs554303220 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061581 | TGTTGGCCAGGCTGG[A/T]CTCAAACTCCTAACC | 55728 |
| rs554314556 | snp | A/T | 0.000363805 | 0.0134822 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112096 | CAGCAAAAGAAGCAT[A/T]TGAGAAGAAGATATC | 55728 |
| rs554332665 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174250 | GATGTGGTAGTGCAT[A/G]CCTGTAGTCCCAGCT | 55728 |
| rs554339312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076691 | GACAGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 55728 |
| rs554341303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068884 | AGCACTTTGGGAGAC[C/T]GAGGCAGGTGGATCA | 55728 |
| rs554351857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076014 | AATTTTTCACAGAGA[C/T]GTGTTCTCCCTATGT | 55728 |
| rs554372281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177621 | ACTCTGTCTCAAAAA[A/G]TAAAATAAATAAGAA | 55728 |
| rs554408678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184517 | AGAGTTAATCCTTAC[C/T]GATCATTAAAAATCT | 55728 |
| rs554409019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176792 | TGAGGTGGAGCCTCG[A/G]GAAGTTCATGCTGTT | 55728 |
| rs554445754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183616 | GCCGGGATTACAGGC[A/G]TGAGCCACTGCGACC | 55728 |
| rs554476091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083852 | ATTTTAATAAAGCTG[C/G]TATAAGTAGAAATTT | 55728 |
| rs554484967 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059133 | CCGGCCGTTTTAAAA[C/T]GCTGATTATTTTCCT | 55728 |
| rs554536691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074931 | AGAATTGCTTGAGCC[C/T]GGGAGGCAGAGGCTG | 55728 |
| rs554558257 | snp | C/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055193 | GCAGAGTTAATGTTA[C/G]CTTCTCAGCAACAGC | 55728 |
| rs554585455 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155936 | AATGGTTAGTGACTG[A/G]TATTGAAGTATTATT | 55728 |
| rs554622508 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155158 | GCACTTTGGGAGGCC[A/G]AGGTAGGTGGATCGC | 55728 |
| rs554637718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128616 | CACTGCAACCTCCAC[C/T]TCCTGGGTTCGAGTG | 55728 |
| rs554674815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127998 | AATTTTAGAAACTTA[C/T]GAGTTTGAATTAAAA | 55728 |
| rs554726379 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171559 | TAACCCCCAGTACTC[C/T]TGAATGTGATCTTAA | 55728 |
| rs554733018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085264 | GACCAGGCTGGTCTT[A/G]ACCTCAGGCAATCTG | 55728 |
| rs554740499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169731 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 55728 |
| rs554790390 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171689 | AAGGAGTATTGACTC[-/AT]ATGATCACAAGGTGA | 55728 |
| rs554811697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099155 | CTGAATTGCCTACCA[A/G]TGAGGTGTGCTGACT | 55728 |
| rs554820141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083133 | GACATAGAAAAAGGA[A/G]AAAACAAAAGGAAAA | 55728 |
| rs554835231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143004 | ATAAATAAGGTATCC[C/T]AAGAAATGTATGGTT | 55728 |
| rs554886273 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146530 | TGGTAGTTATTACTC[-/T]TTATTTTTTTGACAA | 55728 |
| rs554902120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126798 | AGTCTCGCTCTGTTG[C/T]CCAGGCTGGAGTACA | 55728 |
| rs554902199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135288 | TGAACTCATCATTTT[C/T]GATGGCTGCATAGTA | 55728 |
| rs554931559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163669 | AAGGCCCAAGCCAAT[A/G]TGCTAAGGATGGTGA | 55728 |
| rs554938940 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134509 | TAGGTTCAGCTTCAT[A/C]CTGGTAAGAAGGGTA | 55728 |
| rs554993712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172354 | AAATTTTAATTTCCT[C/T]TGGCAACATCCTCAC | 55728 |
| rs555007664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078483 | AGTTTCTTGACTTGC[A/G]TATGGTGGCATAGCA | 55728 |
| rs555010347 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056710 | CGGCGGGCTTGGGGG[A/G]GGGCGGTGGGCGGCG | 55728 |
| rs555029664 | snp | G/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055426 | AAAATTTATCTTCTT[G/T]AGTTCTCTCCTTATA | 55728 |
| rs555041189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087139 | GGGTTCAATGTTCTA[C/T]AGATATGGAGTCAAG | 55728 |
| rs555088061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151026 | AAAATGAGTTAAACA[C/G]TCCTTTCTAAGGCGT | 55728 |
| rs555091874 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059204 | CATGTTTTTTGATAT[A/G]CAAAGCAGCAACCAT | 55728 |
| rs555110914 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105947 | GAGAAGAGGATAAAC[-/AT]AGGAATTGGGATCAA | 55728 |
| rs555113738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136114 | GAGGTAGGGTAGTGC[A/T]TAAGTTTTTCTTTTC | 55728 |
| rs555154308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142207 | CAGCCTCTGCACTTA[C/T]TCTCTTAAATTATCA | 55728 |
| rs555187156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091512 | GATACAATTCTTTCA[C/T]GCATTAAAATGGTGG | 55728 |
| rs555216998 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135179 | GTTCAATTCCCACCT[A/G]TGAGTGAGAATATAC | 55728 |
| rs555236855 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185496 | CAAGAATTAGAGAAC[A/G]AAAACAATTTTATTT | 55728 |
| rs555261702 | snp | C/G/T | 0.000230923 | 0.0107433 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122207 | TTGAATCCCACTCCA[C/G/T]CGATGGCCAAATCTC | 55728 |
| rs555287937 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162936 | TCTCAAAATCCAAGG[A/G]GAGAGGACCCCATGT | 55728 |
| rs555290542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157111 | GGACTAATGTGGAAA[C/T]CCCAGAGGGTGTCCA | 55728 |
| rs555295024 | in-del | -/TG/TGTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077143 | TATGTAGAATATATA[-/TG/TGTG]TGTGTGTGTGTGTGT | 55728 |
| rs555302159 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166637 | GAGTTTGTGGTGAGC[C/T]GAGATCACACCATTG | 55728 |
| rs555318050 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149065 | CTAGTTCTTTGAAAG[G/T]TTAAACATATAATTA | 55728 |
| rs555335332 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127222 | TTTTTTTCTTTTTTT[A/T]AATTTTATTTGTTTG | 55728 |
| rs555351565 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102624 | CCATCGCAGGTTGTA[A/G]CAGTCTCAATCAAAA | 55728 |
| rs555368277 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159839 | ATGCATTGATGACTT[C/T]TGAGTGTTAGGAATC | 55728 |
| rs555383301 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086342 | AAAAATTATTTATTT[A/T]TTTTTTTGTTTTTGA | 55728 |
| rs555400907 | in-del | -/ATCT | 0.407158 | 0.194426 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136344 | AGGATTAGAAATTGA[-/ATCT]ATCTATCTATCTATC | 55728 |
| rs555455521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093294 | GGTTTGAGTTTATTT[A/G]CCCTTCGTTTTCTGG | 55728 |
| rs555457361 | snp | C/T | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121263 | TAGATGGATTTAAGC[C/T]GAAAGTTTTCAATAT | 55728 |
| rs555467916 | snp | A/G | 1.65176e-05 | 0.00287376 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102152 | TCTTCACAAAGTTTC[A/G]TTGCTTCTGAGAACC | 55728 |
| rs555468965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066251 | TTCAGGGGACCCAGA[A/G]TTAATTATTGATTAT | 55728 |
| rs555491085 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075541 | TAGCTGGGACTACAG[A/G]TGCATGCCACCATGC | 55728 |
| rs555492680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060054 | GCTCAGGCTGCTCTC[A/G]AACTCCTGAGCTCAA | 55728 |
| rs555510636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100814 | CTTCATTTCTTCATC[C/T]GTTTGCTAGGAATAA | 55728 |
| rs555530971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065970 | GGAGTCTAGATCTGT[C/T]GACAGGCTGGAGTGC | 55728 |
| rs555533003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073351 | CACTTTCTTTTTGGA[A/G]TATCATATATATTAT | 55728 |
| rs555598251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173566 | TGATGATGAACATCA[G/T]ATGGAGGTGAAGGGA | 55728 |
| rs555598630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181593 | CTCCGAGCTCAACTC[A/G]CGGCTTTCATTTCAC | 55728 |
| rs555625656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159151 | GGTATAACTTGAACC[A/G]CATTCTCTGACTCCT | 55728 |
| rs555658192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065222 | TCATAGAAGTCCTTG[A/G]GTGCTTTATCACAGA | 55728 |
| rs555658591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112984 | GTTGGGATTACAGGC[A/G]TGAGCCACCATGTCC | 55728 |
| rs555661010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064606 | GCTCTTGTTTGCTAA[A/G]TAAAACACTTATCTG | 55728 |
| rs555690985 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064675 | CAAAGGTGCTAAGAT[A/G]GATGTCTAGGGTGCA | 55728 |
| rs555701184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118176 | GTAATCCCAGCAGTT[G/T]GGGAGGCCGAGGCAG | 55728 |
| rs555739089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160078 | ATCCGCCTCAGCCTC[C/G]CAAAGTGCTGGGATT | 55728 |
| rs555752027 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080303 | TGATTGGGAGATAGT[A/G]TGAGCTGTATATATA | 55728 |
| rs555752435 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066728 | TCATAGTTTTTTTAG[C/T]TGGGGAAAAAAGTAC | 55728 |
| rs555767104 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152646 | CAAATCTGTCTTACT[A/G]TTACAGTTTTGAGAT | 55728 |
| rs555780088 | in-del | -/TATAT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096095 | GAAATGTTTATTAGA[-/TATAT]TCAAGCAGAGAAAAC | 55728 |
| rs555803812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151963 | GTTTTAAATTTATTA[A/C]TTCATCTCATTAATA | 55728 |
| rs555919786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088953 | TATTTTTTGTTTTTT[G/T]TGTGTGTGTTTTTTT | 55728 |
| rs555922356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116078 | GTAGTGATTTTTGTT[A/G]TAAAGTGTAATTTGT | 55728 |
| rs555931667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080902 | CGATCTCCTGATCTC[A/G]TGATCCGCCCACCTC | 55728 |
| rs555953783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074217 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55728 |
| rs555959173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124561 | CATATTGGTCAGGCT[A/G]GTCTTGAACTCCTGA | 55728 |
| rs556023085 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094735 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCTC | 55728 |
| rs556039308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132618 | TTGTTTTAATTATTG[C/T]AGTGTTATGTTAGGT | 55728 |
| rs556054258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095055 | TGCTGGGATTACAGT[C/T]GCGAGCCCCTGAGTC | 55728 |
| rs556063230 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085603 | CTGGAATTACAGGCA[C/T]GCCACCATGCCTGGC | 55728 |
| rs556075434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098026 | CTGGGAGGCAAAATT[A/G]TACCTCGTTGAGAAC | 55728 |
| rs556094081 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123777 | GGCATGAGCCACTGT[G/T]CCTGACCTGTTTTTT | 55728 |
| rs556177727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169112 | AAAGGGCCGGGCGTG[A/G]TGGTTCTCGCCTGTA | 55728 |
| rs556191779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082475 | AGTATATAAATGCCA[A/G]TAAGAACATGTAAAG | 55728 |
| rs556214773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167962 | TTATTGGGTGGAGGG[A/G]AAGCATCAAGGAATA | 55728 |
| rs556216003 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082795 | AAGCTCTGCCGCCCG[A/G]GTTCACGCCATTCTC | 55728 |
| rs556232118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141772 | AGCGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55728 |
| rs556268991 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148305 | AAAATAAGAAAACCA[A/G]TCACGCATGGCGGCG | 55728 |
| rs556294519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140664 | CAGGGTCACAGGACA[A/G]TAGTGGAGGGAAGGT | 55728 |
| rs556305650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147777 | ACTTCTCAGATGGGG[C/T]GGCTGCTGGGCGGAG | 55728 |
| rs556352405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183723 | AGAAGACAGTCAAGT[A/G]TTAGAGTAATGAACT | 55728 |
| rs556387616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175300 | AGTGCTAGGATTATA[A/G]GCATGAGCCACCAAG | 55728 |
| rs556459001 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179152 | GGCGGGCAGATCACA[A/G]GGTCAGGAGATCGAG | 55728 |
| rs556474437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135335 | TGCCACATTTTCTTA[A/G]TCCAGTCTATCATTG | 55728 |
| rs556496871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083981 | ATTCATTCATTCAGA[C/T]GGGGTCTCACTCTGT | 55728 |
| rs556497979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149283 | ATGTAGAGAAATGGC[A/G]GACCTTGTAAACATT | 55728 |
| rs556528379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146379 | TCTCACAGTACTCCT[A/G]CCTCTCACAGTGTTT | 55728 |
| rs556545026 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181322 | TTCTGTTCGTTTCTT[C/G]CGGATAGCAATTCAG | 55728 |
| rs556553821 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184634 | ATTATTTGTTGCCTT[C/T]CAGACGTGAAAAATT | 55728 |
| rs556602778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110207 | TATCACATTTTATTA[A/G]TCTATTCATCAGTTA | 55728 |
| rs556636096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090808 | TGTGGTGGCATGTGC[C/T]TGTAAACCCAGCTAC | 55728 |
| rs556649299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149720 | TAACACAGTGAAACC[C/T]CGTCTCTACTAAAAA | 55728 |
| rs556668182 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063989 | GGGGCGGCAGGGGGG[G/T]GTCTCACTATGTTGC | 55728 |
| rs556670724 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055682 | ACCGCAAAGGGAGGG[A/G]ACGGAGGAAGTAAAA | 55728 |
| rs556684628 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171065 | TTATTTAGGGATGCC[A/C]AGTTTAATGATTGTA | 55728 |
| rs556708092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097643 | CCATGATTAATAGTA[A/G]TATAGAAAAATGTCT | 55728 |
| rs556724379 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061273 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs556729582 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063394 | TGTTTCTTCACATGG[G/T]AAACCTGTTTCATGG | 55728 |
| rs556730784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106420 | CCCCTGGGTTCAAGT[A/G]ATCCTCTCAACTTAG | 55728 |
| rs556740531 | in-del | -/TTT | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159881 | TCACAGTTGTTGTTG[-/TTT]TTTTTTTTTTGAGAT | 55728 |
| rs556766442 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104324 | CATTATCAGTTGGGT[A/C]TCTATTTGATCCTGG | 55728 |
| rs556798904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169829 | AATTAGCTGGGCGTG[G/T]TGGCAGGCGTCTGTA | 55728 |
| rs556809699 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145899 | CGGGTGCGGTGGCTC[A/C]TGCCTGTAATCCCAG | 55728 |
| rs556862566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161238 | TTCTCAGAGAGAATG[C/G]ACCCTCATCTTGGAG | 55728 |
| rs556878176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077428 | GCTGGGATTACAGGC[A/G]TGAACCACTGTGTCT | 55728 |
| rs556922284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061789 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55728 |
| rs556922531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068586 | CTCCTTTTCCCATTG[C/T]GTGGCCTTGGTACCC | 55728 |
| rs556930261 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056796 | GGCCGCCCACCCGCC[A/C]TCTCGCGGCGGGCTT | 55728 |
| rs556934820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084542 | CCAGGTTCAAGCAAT[C/T]CTCCCGGCTCAGCCT | 55728 |
| rs556967044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099196 | CCAGGCTTGCATAAG[G/T]GTAGTGGTTTCACTT | 55728 |
| rs557029442 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112334 | AGGAAATTAGGCCAT[G/T]TAGCTGAGTTTTTCC | 55728 |
| rs557079758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071862 | TGAGCCACTGCCCCC[A/G]GCCTCAAATTTCTTT | 55728 |
| rs557096869 | snp | C/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186095 | AAGGGAAAGTTAAGA[C/G]AGGCCTTTTAAGAGG | 55728 |
| rs557107710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085987 | TGTTTTTTTTTGAGA[C/T]GGAGTTTTGCTTTTG | 55728 |
| rs557141145 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154968 | TGTTGCTGCCTTATC[A/G]AAATGCTTCTAGAAC | 55728 |
| rs557170799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085362 | TTAGATACACAAAGT[A/G]GAGATGTTCAGTGAA | 55728 |
| rs557177453 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093441 | AGACAGAGTCTTGCC[-/G]TGTCACCCAGGCTGG | 55728 |
| rs557183288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092521 | ATTTCTGTCTTCTTT[C/T]TTCTTTGTCAGTCTT | 55728 |
| rs557205869 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105550 | GGCTGGTCTCAAACT[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs557232724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111615 | TGAGCCACCGCGCCC[A/G]GCCTTGTTTTGTATT | 55728 |
| rs557271470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119500 | AAATAGCGTTGGTTG[A/G]CCCTTTGTGACTTTG | 55728 |
| rs557308911 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157208 | GAGAAATGGAAGTGT[C/T]TTTTTTTTTACGTTT | 55728 |
| rs557382687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099911 | TCCCCCGTCCCTGCC[C/T]ACCCCCGCCACCTTT | 55728 |
| rs557391156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071383 | CTCATTTAGTAATGC[C/T]GTGTACTTCCTACTG | 55728 |
| rs557405435 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137620 | TAAGACGTGCAGACA[C/T]GGAAGTGTCGTGAAG | 55728 |
| rs557413993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164209 | TGGAATAGTGGAGGT[A/G]AGCAGTGAAGGTATA | 55728 |
| rs557447882 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093125 | ATTTTTGTATTTTTA[G/T]TAGAGAAAGGGTTTC | 55728 |
| rs557452990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172524 | ATTTGGACACAGAGA[C/T]AGCCACAGAGGGAAG | 55728 |
| rs557485042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128718 | ATTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 55728 |
| rs557494333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144877 | CTTGCAAATTCAGGA[C/G]AGTCTGAATATGCAG | 55728 |
| rs557509422 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078529 | TCCTTTTTTTTTTTT[A/T]ACTTTTTTTCTTTGA | 55728 |
| rs557540644 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174896 | GATATTATTCAGCCT[-/A]AAAAAAAAAAAAAGG | 55728 |
| rs557546185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137528 | TTATTATTTAACACC[C/T]GTCTTTTTATTATAA | 55728 |
| rs557556469 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162768 | TAGGGGATTTATCAG[C/G]AGAATTGGCTCCTGT | 55728 |
| rs557568252 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179766 | AAGCCTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 55728 |
| rs557585517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171592 | GGAGGTATTCTTTAC[A/G]GAAGTAATCTAGTTG | 55728 |
| rs557655706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093980 | GCTCAGAGTGGTCTG[C/T]CCACCTCAGCCTCCC | 55728 |
| rs557670247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151187 | TTAGCAGGTGATAAT[C/T]GTATAAATGACTGAC | 55728 |
| rs557683893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054613 | AAAAAAAAAAGAAAT[G/T]TAAAGGGACATGAAC | 55728 |
| rs557692811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101584 | TACAAAATATTTCTG[A/T]TATGCAGTACATGCT | 55728 |
| rs557757475 | in-del | -/TTATTTAT | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101151 | TATCAAAAGTGTGCA[-/TTATTTAT]TTATTTATTTATTGT | 55728 |
| rs557809041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094887 | GCACCTCTGTCTCCT[A/G]GGTTCAAGCGATTCT | 55728 |
| rs557826234 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087731 | AATAATTCAATATAG[A/C]CTTTTAGGACTGGCT | 55728 |
| rs557861058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087236 | TCTTTCTTCCTCTTA[C/T]GTTTCTTTCCTTTTC | 55728 |
| rs557875858 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185396 | AAAGAAAAAAATTTA[A/G]AGTTAAAAGAAAACT | 55728 |
| rs557876501 | snp | A/G | 0.00111562 | 0.0235916 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120332 | GACTGTGATCTTGCA[A/G]ATAGTGGACCACTTC | 55728 |
| rs557917051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160133 | CCAGGGAATTTTATT[C/T]GGGGAGGATTGCTGT | 55728 |
| rs557920586 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074126 | GATGGAGTGTTGCTC[C/T]ATTGCTCAGGCTGGA | 55728 |
| rs557923125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060206 | TTATTAGAACTGTAC[A/T]TCTAGATTGTGGTTA | 55728 |
| rs557954181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159461 | ATCATTCTGCCATAC[C/T]CAAGATAATGGCCCT | 55728 |
| rs557995697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100989 | TTTCACCCAATCGAC[C/G]TCCTTCTAGGGAGAG | 55728 |
| rs558002052 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059207 | GTTTTTTGATATGCA[A/T]AGCAGCAACCATTTA | 55728 |
| rs558008821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152656 | TTACTATTACAGTTT[A/T]GAGATGGCAAACCCC | 55728 |
| rs558073077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066308 | TCTCAGGATTTCTAT[C/T]TGTGATTTTCCCTTT | 55728 |
| rs558075641 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132115 | ACCCTCTATATACTA[C/T]GTTTTTTTCCTATAA | 55728 |
| rs558088989 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091357 | TGTTAGGAGGAAAGC[A/G/T]TTTAGTATTTCATTA | 55728 |
| rs558098192 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147387 | TTCTATTCCACAAAA[C/T]CGCCATTGTCATCAT | 55728 |
| rs558100178 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074276 | TTGTATTTTTAGTAG[C/T]GATGGGGTTTCACAT | 55728 |
| rs558113323 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065855 | GCATGGATATGATAC[A/T]TGCGCAGTTACTGGG | 55728 |
| rs558150507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094119 | TTTCGAGACTTCATC[A/G]TTGACCCATGGATTA | 55728 |
| rs558159394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103643 | GTGTTGTTAAATAAT[A/G]CTTTTAGAAATGTGT | 55728 |
| rs558179766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124616 | CCTCCCAAAGTCCTG[C/G]GGTTACAGGCATGAG | 55728 |
| rs558233427 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109499 | TAGGCAGATGGATCA[A/C]CTGAGGTCAGGAGTT | 55728 |
| rs558328313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083070 | GTATACTTCAGCCCA[C/T]GCCCTGTGCCTGTTC | 55728 |
| rs558333816 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074043 | GTGATCCGCCCGCCT[C/T]AGCCTCCCAAAGTAC | 55728 |
| rs558351317 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148941 | AAGAAAAAAAAAATT[A/G]AAAAATCGAAAAACA | 55728 |
| rs558391068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175088 | TGCAGTGGCACAATG[A/C]GAACTCACTGCAGCC | 55728 |
| rs558401904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068241 | ATCAGATGTATGGTT[A/T]GCAAATATTTTCTCT | 55728 |
| rs558404574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089057 | CCAGCTGCAAAGGAT[C/G]CTTCCACCTTAGGCT | 55728 |
| rs558428960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108684 | AATCTGTGGGGACAT[C/T]ATAGGTAAAAATTTA | 55728 |
| rs558448392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062670 | GCTAGCCCTATTAAG[C/T]TCCTTGTATTTCTCC | 55728 |
| rs558455424 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179140 | TTGGGAGGCCGAGGC[-/G]GGCAGATCACAAGGT | 55728 |
| rs558471141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075120 | TGTGTGGTACTATGC[A/G]TAGTACCATTTTGGC | 55728 |
| rs558486468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125760 | GGCATGGTGGCGGGC[A/G]CCTGTAATCCCAGCT | 55728 |
| rs558497947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176046 | AGTGAGTTGAGATCG[C/G]GCCACTGCAATCCAG | 55728 |
| rs558545040 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061611 | CTCAGGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 55728 |
| rs558559949 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150877 | GAAATTTTGGAAACT[A/G]ATGATATTAAGGGAC | 55728 |
| rs558616654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136082 | CGTCAAGATATGACT[G/T]AATAATGCAGGGATG | 55728 |
| rs558637431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126778 | TATTTTATTTTTGGA[A/G]ATGGAGTCTCGCTCT | 55728 |
| rs558638339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169153 | TTTGGGAGGCCAAGG[C/T]GGGGGGATCATCTGA | 55728 |
| rs558653304 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135521 | TCCCTGAGGAATCGC[C/T]ACACTGACTTCCACA | 55728 |
| rs558653692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075971 | AGCTGGGACTACAGG[C/G]ATGTACCACCAGGCC | 55728 |
| rs558674827 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058565 | AATAAAGCAGTTGAA[A/G]TCAGCACGCAGTACG | 55728 |
| rs558690984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141861 | GAGGCCGAGGCTGGC[A/G]GATCACTCGCGGTTA | 55728 |
| rs558708313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176724 | AAAGCAGATGTCCCT[C/G]AGACAGCCATGTGGG | 55728 |
| rs558745291 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183535 | TAGAGACGGGGTTTC[A/G]CCATGTTAGCCAGGA | 55728 |
| rs558775387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168528 | CAAACAATATCATAA[A/C]GATATAAATCAGAAG | 55728 |
| rs558827251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104446 | TCTGTGTCTGGGTTT[C/T]TCTGCTAGTAAATTT | 55728 |
| rs558863912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127899 | ATCTCCTGACCTTGT[A/G]ATCCACCTGCCTCGG | 55728 |
| rs558874941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099004 | TATATCTACGTTTTT[C/T]GTGAATAATTAATAT | 55728 |
| rs558898768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170831 | ATGTCATGGGCCATT[C/T]AAGACAGTGCAATTG | 55728 |
| rs558909345 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115753 | CTGACATTTATAAGA[-/T]TTTTTTGGCCTAGTT | 55728 |
| rs558916423 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140742 | GACCCTGCGGCCTTC[C/T]GCAGTGTTTGTGTCC | 55728 |
| rs558937222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178757 | GTAGGGAACGAACTT[C/T]CTTTCAATATGAGCA | 55728 |
| rs558945340 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182645 | TAGAGACGAGGTTTC[G/T]CCATGTTGCCCAGGC | 55728 |
| rs558953198 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170328 | GTCTAATAAGAGCAC[A/G]TGCAGGATGGCCGGG | 55728 |
| rs558967121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085059 | CTGGGATTACAGGTG[C/G]CCACTACCACGCCCA | 55728 |
| rs559002660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084834 | TGGTCAGGCTCATCT[C/T]GAACTCCCGACCTCA | 55728 |
| rs559030941 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143311 | ATAAGGAACTTGCTT[C/T]ATTTATTTATTTATT | 55728 |
| rs559041767 | snp | A/C | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055663 | GCAAGTGGAATGAAA[A/C]GTAACCGCAAAGGGA | 55728 |
| rs559134881 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098356 | GTGCTTCATAGGACT[A/T]TTTTTTGGTGAGGAT | 55728 |
| rs559152265 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116547 | TGGCTTTCCTCCTCA[C/T]GCATACGAAGACTTT | 55728 |
| rs559207052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083709 | GGTTACTAATGGGTG[A/G]TGGGGTTTCTTCTTG | 55728 |
| rs559212739 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | N4BP2, LOC344967 | GRCh38.p7 | 4:40056223 | TCGCCGTCCCTCCCA[A/T]CTTGCAGCCTGGACC | 55728 |
| rs559214806 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084088 | CCTGAGTAGCTGGGA[C/T]TACAGGCATGCGCCA | 55728 |
| rs559252757 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089144 | TTTTTCATAGAGACA[G/T]GGTCTCACTATTTTG | 55728 |
| rs559267212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149164 | CGGAAACTTGCATAT[C/G]AATGTCTGCAACAGC | 55728 |
| rs559358872 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108304 | TAACCACTGGTTTTC[C/T]TTAGATTGGTTTACT | 55728 |
| rs559403303 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136504 | ATTCTCGTGCCTCTC[A/G]GCCTCCCGAGTAGCT | 55728 |
| rs559404569 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100446 | AGTAATCACTTTCAC[-/T]TAGAGGCTCACTGTA | 55728 |
| rs559421169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063508 | GATATGCTCACTTAC[A/G]TGGCCAGGGATCTGT | 55728 |
| rs559432832 | in-del | -/A | 0.103438 | 0.202533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169964 | GCAAGACTCAATCTC[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs559569139 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127704 | CTCGCTCTGTCGCCC[A/C]GGCTGGAGTGCAGTG | 55728 |
| rs559649738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113159 | CATGTAGTTATTTGT[A/G]TCCTTTTGCTGTTAC | 55728 |
| rs559690292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064856 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 55728 |
| rs559701249 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111790 | CCAAATAATTTTTGT[A/G]TTTTTAGTAGAGATG | 55728 |
| rs559712133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151590 | GTAAAACTTTTATGC[A/G]TAATATAACATATGT | 55728 |
| rs559728717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092926 | TGGGATTACAGGCAT[A/G]AGCCACCGTGCCCGG | 55728 |
| rs559745966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158844 | TGGAACTTTATATTC[A/G]AGTCCAAAGCAGAAT | 55728 |
| rs559768049 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147501 | GGCCGGGCAGAGGCG[-/C]CCCCCCACCTCCCGG | 55728 |
| rs559796735 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095182 | TCTGCCTCCCAGGTT[C/T]AAGCAATTCTGCTTC | 55728 |
| rs559854216 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101828 | TTGATGATAGTTTAT[G/T]AGCTTGGTTTATTAC | 55728 |
| rs559890358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130882 | TATATCACAATGTTT[A/G]AGAATATTTATTATC | 55728 |
| rs559922326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057783 | AAATAGTTTTTTTTT[C/T]CCCTCCGAAAGAGAG | 55728 |
| rs559967396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070727 | AAGTGCTGGGATTAC[A/T]GGCATGTGACCTGAT | 55728 |
| rs559979081 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156859 | ACAAGTAAATATAAT[A/G]CACATGTTCTAAAAT | 55728 |
| rs559986224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115369 | GGGTATGGTGGCGTT[C/T]GCCTGTGGTCCCAGG | 55728 |
| rs559996465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173794 | GGCAAACCAGTATTT[C/G]CTTTTCTCTGCGTTA | 55728 |
| rs560001258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171090 | ATTGTATCAGTTATA[C/T]TGGAGTTTGGTCAAG | 55728 |
| rs560016307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163891 | AGATTATAGAATTTG[C/T]GAAATCTTTCCCGGC | 55728 |
| rs560022512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123997 | CTGTAGTCATACTTC[A/G]TAATTTTTATTATCT | 55728 |
| rs560092926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074493 | GGACAACAGGTGTGA[A/G]CCACCACGCCTGGCC | 55728 |
| rs560111046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176121 | AGAGAAAGAAAAAAA[A/T]CAAATTTTGATGATT | 55728 |
| rs560124640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166616 | ATCACTTGAACCCAG[A/G]AGACGGAGTTTGTGG | 55728 |
| rs560145079 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086538 | AGATGAGGTTTCACC[C/G]TGTTGGTCAGGCTGG | 55728 |
| rs560156463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082009 | CCCAGCTATTCGGGA[A/G]GCTGAGACAGGAGAC | 55728 |
| rs560159492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174448 | ACTCCATGTTCATTG[C/T]AGCATTACTTACAGT | 55728 |
| rs560263498 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122963 | AAGACAGTAACATAG[C/T]ATATAACATAAATAG | 55728 |
| rs560266961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082787 | CTGACTGCAAGCTCT[C/G]CCGCCCGGGTTCACG | 55728 |
| rs560272817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054254 | GCGTGAGCCACTGTG[C/T]CAGGCCCTATTCTTA | 55728 |
| rs560320563 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065031 | CCTCAGCCTCCCAAA[A/G]TGTTGGGATTACAAG | 55728 |
| rs560334579 | snp | C/T | 3.32071e-05 | 0.00407461 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152751 | GTAAGATAAATGAAT[C/T]TTAACTCCCCTGATT | 55728 |
| rs560340394 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087277 | CCTTTAAAAAAAAAA[A/T]TTTTTTTAAAGGAGG | 55728 |
| rs560377327 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061009 | AAATTGAGACGGGGT[A/G]TTGCCATATTGCCCA | 55728 |
| rs560401296 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088087 | CTGAGCATAATACTC[C/T]GGAATTTCATCCAGG | 55728 |
| rs560408740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106116 | GATAATTAAAAATTT[A/G]TTAATCTTCTAACCA | 55728 |
| rs560483968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125574 | AAAAGAGTGGGAAGC[A/C]TTGAGTCAGTTTAAA | 55728 |
| rs560492017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133014 | AATAAACTGGCAGCC[C/T]GCCATTTTTCCCTCT | 55728 |
| rs560502377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139677 | TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACT | 55728 |
| rs560577958 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147855 | CCTCCCAGACGGGGT[C/G]GCGGCCAGGCAGAGG | 55728 |
| rs560578686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097905 | GTGGCTCTCCTATGC[A/G]TTGTAGGTTTAGCAG | 55728 |
| rs560590007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088586 | GCTCACTGCAGCCTC[C/T]GCCTCCCGGGTTCAA | 55728 |
| rs560633262 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096577 | GATCCACCATGTGGT[-/TTAA]TTGAGTCACGCTGGC | 55728 |
| rs560634374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104508 | ATTTTTCAGTAGACA[G/T]GTAGGCTTTTCTAAC | 55728 |
| rs560720869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146920 | TTTATTTTTATTTTT[A/T]TATTTTTTTTATTGA | 55728 |
| rs560746086 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055886 | CATACTACAGCGGTC[C/G]CAAGAGGGAAGAGCA | 55728 |
| rs560755009 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173260 | AATTGGCCACCCAAA[A/G]TTGCAAAAGGTAGCT | 55728 |
| rs560758490 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068339 | TGTCCATTTTGTCTA[A/T]TTTTGCTTTTGTTGC | 55728 |
| rs560815458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075307 | TTATACAGAAATACA[C/T]TTGGAATTAAAGGTA | 55728 |
| rs560855938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062718 | CTTAAATCTGCACTT[C/G]AGTTCAGAAGCTTCT | 55728 |
| rs560857587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138859 | GGGAAGTGTGAGTTT[C/T]CCAACTATGTTCTAT | 55728 |
| rs560873155 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, frameshift-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056702 | GGACAGCCGGCGGGC[-/T]TTGGGGGGGGGCGGT | 55728 |
| rs560887506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147977 | AGATGGGATGGCAGC[C/T]GGGAAGAGGCGCTCC | 55728 |
| rs560920687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141532 | CCTAGATGGGATGGC[A/G]GCCGGGAAGAGGCGC | 55728 |
| rs560922153 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147601 | CTGACCCCCCCACCT[C/T]CCTCCCGGACGGGGC | 55728 |
| rs560929149 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156198 | TGCAGCTGCATACTC[A/G]CTTTCTGTGTTTTTA | 55728 |
| rs560931534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163519 | AATTCTGCTAGATTG[A/G]TTCTGGGAAAGGTTT | 55728 |
| rs560962845 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076978 | GTGTTTGGGAACATG[C/T]TATGTTTGGGTCCTG | 55728 |
| rs560975255 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080781 | TGCTGCCTCAGCCTC[C/T]CACGTAGCTGGGACT | 55728 |
| rs560990401 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067544 | TTATTTTGGATATGT[A/G]CCCTGAAGTGGAATT | 55728 |
| rs561046120 | snp | A/G | 1.66471e-05 | 0.00288501 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120544 | AACTGAAAAAACTTC[A/G]TCCGTACAAAGCGAC | 55728 |
| rs561056987 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153734 | TAAAAGGAGTAGTTA[A/G]ACCAGAACATTATGT | 55728 |
| rs561087725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112327 | CAAAATGAGGAAATT[A/G]GGCCATTTAGCTGAG | 55728 |
| rs561116359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064172 | TTGTGGTAAAGAGAT[C/G]CCCTGTACTATGGAC | 55728 |
| rs561116703 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127593 | GAAATCTTATTTAAA[C/G]ATAATTATATATATT | 55728 |
| rs561135446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061954 | ACAGGTGTGAACCAC[C/T]ATGCCTGGCCATTAG | 55728 |
| rs561145138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163181 | TACAATGTCAAAGGA[C/T]TTGTGTATGTATTTG | 55728 |
| rs561153794 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127085 | TATTATAGAGACAGT[G/T]TTGCCATGTTGCCCA | 55728 |
| rs561183951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170901 | TATTTTGGTTCCTCT[G/T]TGATATGTTGGAAAG | 55728 |
| rs561203298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168585 | ATAAAAATGAAATTT[A/G]TGGATTTTACACCTT | 55728 |
| rs561207880 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107928 | GTTTCCTATGTATCT[-/T]TTTTTTTTTTTTTGA | 55728 |
| rs561231138 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118268 | ACTAAAAGTACAAAA[G/T]TAGCCTGGCTGGTGG | 55728 |
| rs561271088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070449 | CCCTAGTATTATACT[A/G]CTTTTTGATTTTTTT | 55728 |
| rs561296433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105441 | GAGATTCTCCAGCCT[C/T]GGTCTCCTGAGTAGC | 55728 |
| rs561329249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071588 | TTTATTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 55728 |
| rs561330497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069729 | TGTGGGCAGCAAAGC[A/G]AGACCCTGTCTCTAC | 55728 |
| rs561337173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063607 | ACTTTAATTCTTTAT[C/T]GTTTTATTGATTTAT | 55728 |
| rs561376532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090998 | TGAGGACTTAGTGTA[G/T]TTCTCTGTTTTTTTT | 55728 |
| rs561378069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171854 | GTGGAGTCTGATGTT[C/T]GAGGGCAGGAAGCAT | 55728 |
| rs561394868 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134591 | TTTGCCTCAAACAAC[A/G]TCAGGGCTGGAGACT | 55728 |
| rs561409753 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104294 | TTTTCCAAATTTTAA[C/T]CATTAGCCTTCTAAC | 55728 |
| rs561434408 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111856 | CCTGGCCTCAAGTGG[C/T]CTGCCCGCTTTGGCT | 55728 |
| rs561468563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141894 | AGCTGGAGACCAGCC[C/T]GGCCAACACAGCGAA | 55728 |
| rs561492945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076230 | CCTGTAATCCCAGTA[C/T]TTAGAGACACTGAGG | 55728 |
| rs561529547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170130 | TAAAATATACATTTA[A/G]CTCAATAATTGTGTC | 55728 |
| rs561550759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150037 | CTGCCACCTGTGGTA[A/G]TCTGTAGTTACTGTC | 55728 |
| rs561552125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135929 | ATCTGGCCAATGGAA[A/G]AGGTGAGAGACATAA | 55728 |
| rs561583938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083598 | CATGTTTTAGATTAT[A/G]CAATTCTCTTCATAT | 55728 |
| rs561640492 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134354 | TGAAATAGCTCAGAG[C/T]TGTGCTTCCCCAGGC | 55728 |
| rs561671454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134887 | TCTTTCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 55728 |
| rs561673065 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107875 | GTAAATCTAATTTTC[A/T]GCTTGGGTCTCAGAA | 55728 |
| rs561690326 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149236 | AGAGAAACAAAATGT[C/G]GTAAATCTATACAAT | 55728 |
| rs561717933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074362 | TCCCAAAGTGCTGGA[A/G]TTACAGGCGTGAGCC | 55728 |
| rs561720176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163923 | ATTAATAGCAGAGCC[A/G]GGTTTCAGACTGAGA | 55728 |
| rs561773954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094352 | GTAAGTGTTGATTAG[A/G]TCCTTAATTATTGGT | 55728 |
| rs561836613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085122 | TTCACTGTGTTGGCC[A/G]GGCTGGTCTTGAACT | 55728 |
| rs561858082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105966 | AATTGGGATCAAATG[A/C]GCATTCACTAGAATG | 55728 |
| rs561862121 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, splice-donor-variant, missense, upstream-variant-2KB, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056960 | GGAAAGGGCTGCGGA[C/G]CTGCGGCGCCGCGTT | 55728 |
| rs561871026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101267 | GTTCAAGAGATTCTC[C/T]CACCTCAGGCTCCTG | 55728 |
| rs561891990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091946 | CAGTTATATCCACTG[C/T]ACTCCAGCCTGGGTG | 55728 |
| rs561895511 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129161 | TCAAGCCATCCTCCC[A/T]CTTCAGCCTCCCAAG | 55728 |
| rs561945866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065524 | CATGACAGAGACCAA[A/G]AAGGGCCAGACAGAA | 55728 |
| rs561994948 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069545 | TTGAAATATGGAGTG[C/T]GCCCTGCTTTATAAA | 55728 |
| rs561996207 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179787 | TTTTTTTTTTGAGAC[A/C/G]GAGTTTCACTCTTGT | 55728 |
| rs562008364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064918 | GAGGATTACAGGTAT[A/G]CACCACCACACTCGC | 55728 |
| rs562028299 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127365 | TGGAACCACAGGCAT[G/T]TGCCACCATGCCTGG | 55728 |
| rs562064551 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099496 | CTCAGGTGATCCACA[C/T]GCCTCAGCCTCCCAA | 55728 |
| rs562089647 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096390 | CCAAGGTGTAAAGGT[C/T]CCCAGGGGAGAACAT | 55728 |
| rs562203999 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164524 | GGGTGAAATAAAAAT[G/T]TTTTCTTTATTTGCG | 55728 |
| rs562205901 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151369 | CTCCACCTCCCAGGT[A/G]CAACCCATCCTCCTA | 55728 |
| rs562221563 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060406 | CACACGATCACGCCC[A/G]GCTAATGTTTTTATT | 55728 |
| rs562290979 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158499 | TGATATCAAAATTAA[A/G]AATTATATCTCTTAG | 55728 |
| rs562343493 | in-del | -/AATAAATAAAT | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184983 | ATAAATAAATAAATA[-/AATAAATAAAT]AAATAAAAAATAAAT | 55728 |
| rs562350646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060463 | TTGGTCAGGCTGGTC[A/G]TGAACTCCTGACCTC | 55728 |
| rs562403903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122637 | TGCCTTATTTTTGAC[A/G]CATTTCTGGAGGACT | 55728 |
| rs562431789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124272 | GTGTTTGAATTTTAA[C/T]TCATTCTAAATTACT | 55728 |
| rs562444160 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182959 | TGGGATTACAGACAT[G/T]AGCCACCATGCGTGG | 55728 |
| rs562483185 | snp | C/T | 8.23879e-05 | 0.00641772 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152841 | GAGAGGAAACCACAG[C/T]CAGGGAGGAGTTGCT | 55728 |
| rs562493362 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060966 | TTAGCTGCTTTTCTT[G/T]TCTTTTCTTCTTCTT | 55728 |
| rs562522211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068396 | AATCATTGCCAAATC[C/T]GATGTCATGAAGCTT | 55728 |
| rs562525874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167133 | GGTGTTTGTGGTGAT[C/T]TGATATTATCAGGAA | 55728 |
| rs562539629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166665 | TTGCACTCCAGCCTG[A/G]GCAACAACAGTGAAA | 55728 |
| rs562542577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169508 | AAATTTGAGACTGCC[C/T]TCCTAAATAATCATT | 55728 |
| rs562582132 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091909 | CTACTATGCCCCGCC[A/G]AAATTCAACAATATA | 55728 |
| rs562582929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174600 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 55728 |
| rs562610452 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162804 | GGAGGCTGAGAAGTT[-/C]CACACCAGGCCATCT | 55728 |
| rs562615251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176196 | TGTGATCATATTTTA[C/T]AAATATGTATCTTTG | 55728 |
| rs562648570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073714 | TTCTCTCACCTCAGC[C/G]TCCCGAGTAGCTGGG | 55728 |
| rs562708913 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096322 | GTAACATTTGAATAA[-/T]GATAAGAAGGTGATA | 55728 |
| rs562711079 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141069 | CTCCACAAAACCGCC[A/G]TTGTCATCATGGCCC | 55728 |
| rs562711884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073040 | CAATTTCTTTACCAA[A/C]TTTTCACCTAATGAT | 55728 |
| rs562712180 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165459 | TTGCCATGTTGGCCA[A/G]GCTGGTCTTGAACTC | 55728 |
| rs562715818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076042 | TGTTGCCCGGGCTTG[C/T]ATTGAACTCCTGCGC | 55728 |
| rs562740007 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160939 | AAACCTAACACCCCA[A/C]AGAGCTTTATCCTCA | 55728 |
| rs562745926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147514 | GCGCCCCCCACCTCC[C/T]GGACGGGGCGGCTGG | 55728 |
| rs562746898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173920 | AGAAATAGAAAGTAC[A/G]GATTTGAAGTTTTAC | 55728 |
| rs562754867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087924 | ATTTTTAGTAGAGGC[A/G]GGGTTTTGCCATGTT | 55728 |
| rs562793169 | snp | C/G | 1.64928e-05 | 0.00287161 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131942 | CTAGAAGGATTGTCT[C/G]TAGTTTCTACTCTGA | 55728 |
| rs562885606 | in-del | -/CCTTTC | 0.188946 | 0.24243 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134900 | CTCCCTTCCTTCCTT[-/CCTTTC]TCTCTCTCTCTCTCT | 55728 |
| rs562885793 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147064 | GACCCTGCGGCCTTC[C/T]GCAGTGTTTGTGTCC | 55728 |
| rs562894169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175414 | GTGGGAGGTAGGAAG[C/T]AGGGAGATAGAGGAT | 55728 |
| rs562909332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133119 | TATTGGTCAAAGTCT[A/T]TTTTATGCTGTCTTA | 55728 |
| rs563006992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090567 | GGTCCTTGAACAACA[C/T]ACTTTCGTTCAACGT | 55728 |
| rs563007666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183225 | ATCTTCCCAAATACT[A/G]TTTTCAAATGACCGT | 55728 |
| rs563021895 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056054 | GCCTCCCTCCACCCC[A/G]TGGCAGTCGCCTACC | 55728 |
| rs563029838 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133808 | AACATATACTTTTTT[G/T]TGTGTGTGTGTTTGT | 55728 |
| rs563102664 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114088 | ATATCTCACTCCATG[C/T]CTGCCTCCCACTATG | 55728 |
| rs563150624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081974 | AAAATTAGCCGGGTG[C/T]GGTGGCGCATGCCTG | 55728 |
| rs563198831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098781 | CAATGAGGAATTACA[A/G]GAAATCCACATCATC | 55728 |
| rs563208755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062251 | GCCCGGCTAATTTTT[C/T]GTATTTTTAATAGAG | 55728 |
| rs563209040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069032 | GGCTGAGGCAGGAGA[A/G]TCGCTTGAACCTGGG | 55728 |
| rs563238094 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079571 | GTTCATTCTATTACT[A/G]TTTGTAGATTTCATG | 55728 |
| rs563259702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135768 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGAT | 55728 |
| rs563274978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142026 | AGGTTGCAGTGAGCC[A/G]AGATGGCAGCAGGAC | 55728 |
| rs563384317 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138657 | CCATTTGTTACAAAG[A/G]CTATTCTTTCCCCAT | 55728 |
| rs563414038 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141647 | GTCCCAGATGATGGG[C/T]GGCCAGGCAGAGACG | 55728 |
| rs563417661 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073018 | GAGCCACCGCACCTG[G/T]CCAGGTCAATTTCTT | 55728 |
| rs563420979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097991 | AATAAAAAATGTCTC[C/T]ATGTATTGTCATTTG | 55728 |
| rs563450195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110699 | CAAGCCACTACGCCC[A/G]GCTAATTTTTGTATT | 55728 |
| rs563450389 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148131 | TTGTAGCGAGCCGAG[A/T]TCACGCCACTGCATT | 55728 |
| rs563485131 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075963 | TCCTGAGCAGCTGGG[A/C]CTACAGGCATGTACC | 55728 |
| rs563490959 | snp | C/T | 1.66095e-05 | 0.00288175 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120577 | AAAGTATAATTACCC[C/T]CAGTCACACAAATTA | 55728 |
| rs563509453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150074 | CACCAGGTGGCAGTA[C/T]TGTTGAATAGAAATG | 55728 |
| rs563520712 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154471 | TATTGATTACAAAAT[A/G]TGTAAGAAAATTATC | 55728 |
| rs563522858 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104016 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 55728 |
| rs563536989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104661 | TGAGACAAGTTTGAA[A/G]AATAGGTTTCAGGGG | 55728 |
| rs563561956 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094301 | GTTAATACTTGAAAA[G/T]AGTGTGTATTTTGCT | 55728 |
| rs563573940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106641 | GCAACCTCTGCCTCC[C/T]GGGTTCTAGCAATTC | 55728 |
| rs563589576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119063 | TTGAGCTATATTTCC[C/T]GGGTTCAAAAAGTCC | 55728 |
| rs563591091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085037 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55728 |
| rs563611132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107443 | GGCTGTAGTACAGTG[C/G]TGCAATCTGGGTTCA | 55728 |
| rs563646531 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126417 | TTTCAAAGTATTTTC[C/T]AGTCTAGAATCCATA | 55728 |
| rs563664127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057721 | ATCCTCAATAGAGTG[A/G]GTCATCTTAGCGGGG | 55728 |
| rs563678204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064831 | CTGGAGTGCAGTGGT[A/G]TGATCTCGGCTCACT | 55728 |
| rs563737890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064221 | AAAATGGTAAGTCCA[A/G]CATTTTAAAGAAGTT | 55728 |
| rs563764756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164598 | CCCATGTTGAAGAAA[G/T]AATTATAAGGATTAA | 55728 |
| rs563765078 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156255 | ATCACTTTTCGGCAC[G/T]TCAGCTAGACTTATT | 55728 |
| rs563803365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173019 | CGCCTTGCTGTTGAC[A/G]GTTTGCTCCCCTAAC | 55728 |
| rs563806489 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129461 | CAAACTCCTGAGCTC[A/C]AGCAATTCACCTGCC | 55728 |
| rs563818505 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129423 | GAAGAGATGGGGTTT[C/T]ACCATGTTGGCCAGG | 55728 |
| rs563821857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128115 | ACTTGCAGTAGATTT[C/T]GTTTGGATTTCGTCT | 55728 |
| rs563836410 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185656 | TTTAAAAGGTTTATG[C/T]GGTTTTTAAAAAAAG | 55728 |
| rs563856952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136391 | ATCTATCTATCTATC[A/T]ATCTTTTTTTTGAGA | 55728 |
| rs563869561 | in-del | -/AACA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103993 | GAGTCTTGCTCTGTT[-/AACA]GCCCAGGCTGGAGTG | 55728 |
| rs563901191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137864 | GCATAGGGACTTCCC[C/T]TGGTTGTCTGATACT | 55728 |
| rs563908729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171028 | GTTTTAATATTTCAG[C/G]AAAAGCAGATTGGTG | 55728 |
| rs563935611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170340 | CACATGCAGGATGGC[C/T]GGGTGTGGTGGCTCA | 55728 |
| rs563942411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144291 | CACCCAGAAACAATG[C/T]TTCACCAGCCATCTA | 55728 |
| rs563942421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137117 | TTTTCTACAAGGGTA[A/G]ATAATTGCATATAAA | 55728 |
| rs563952463 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156729 | AGGTTGAGTATCCCT[A/C]ATGAGAAAATTCAAA | 55728 |
| rs563962063 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40158791 | AAAAAAGAATCTCTT[A/C]GAGACTCAAGTAATG | 55728 |
| rs563997449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079399 | TGGGATTACAGGTGT[A/G]AGCCACTGTGCCCAC | 55728 |
| rs564006297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073634 | AGTCTTGCTGTATCA[C/T]CTAAGCTGAAGTACA | 55728 |
| rs564011896 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133820 | TTTGTGTGTGTGTGT[G/T]TGTGTGAGACAGGAT | 55728 |
| rs564027278 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114194 | TGCTTTGTGTTCTAT[A/G]CTTCCATAGAGATAG | 55728 |
| rs564052455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129615 | CCTTCACATGCAGCC[C/T]GAGAAAGATAATTTT | 55728 |
| rs564077898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143519 | TTGTCCAGGCTGGTC[A/G]TGAACTCCTGAGCTC | 55728 |
| rs564107275 | in-del | -/ATG | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101944 | TTTTTTAAAAATAAC[-/ATG]AATATTGTACATTTA | 55728 |
| rs564107423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072691 | GTGAGCTACCACTCC[C/T]GGCCCCAGATAAATT | 55728 |
| rs564126858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081243 | ACCTATGATTCTATT[A/T]TCCAGAGATTTCTTT | 55728 |
| rs564189878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088012 | ATCCGCCTTCCTTGG[C/T]CTCCCAAAGTGCTGG | 55728 |
| rs564199939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087430 | GAGCAGTGGCTTGAT[C/T]TTGGCTCACTGCAAC | 55728 |
| rs564224785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100213 | GTCATAGCCAGCAGT[A/T]GAGATTTAAATGTTG | 55728 |
| rs564260036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086413 | CATGATGTTGGCTCA[C/T]TGCAACCTCCTCCTC | 55728 |
| rs564271200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129077 | TTTTTTTTGAGACAC[A/C]GTCTGGCTTTGTTAC | 55728 |
| rs564288229 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132091 | CGAATATAGCTAAAC[A/C]CTCTATATACCCTCT | 55728 |
| rs564319422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085733 | ATCTCGAGAGTGGCA[A/G]TGTCCTCTGGAGAAG | 55728 |
| rs564321490 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093331 | ATGGTGGGGGCTTAG[A/G]TTATTCATTTGAGAC | 55728 |
| rs564333492 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092832 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTAT | 55728 |
| rs564344792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180111 | AACTTAAAAACTTGG[A/G]CATGGCAAAAGACAC | 55728 |
| rs564360648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059598 | CAAGTGATCCGCCCG[C/T]TTTGGCCTCCCAAAG | 55728 |
| rs564360809 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179585 | GAAACTGAGGCACAT[A/G]GAAATTAAATAATTT | 55728 |
| rs564427205 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124800 | GAGGTTTTGCTCTGC[A/G]TGAAAGAAAACTTTT | 55728 |
| rs564440921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092895 | GTGATCCACCCACCT[C/T]AGCCTCCCAAAGTGC | 55728 |
| rs564445311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094469 | ATTGTGAATTTGTCT[A/G]TTTCTCCTTTCAGTT | 55728 |
| rs564474551 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139561 | CAGTGGCGCGATCTC[C/G]GCTCACTGCAACCTG | 55728 |
| rs564580044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103993 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55728 |
| rs564595381 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066152 | GCCAGGATGGTGTCA[A/G]TCCCTTGACCTTGTG | 55728 |
| rs564616582 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085275 | TCTTGACCTCAGGCA[A/G]TCTGCCCGCCTCAGC | 55728 |
| rs564618307 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138852 | TGAAATTGGGAAGTG[G/T]GAGTTTTCCAACTAT | 55728 |
| rs564642350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145758 | AAGGTGGTGAAAAAG[A/G]CACACAATCCTTGTC | 55728 |
| rs564680033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059887 | AGACAGAGACTGAGA[A/G]GTATTAAGAAAGTTG | 55728 |
| rs564680540 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089052 | ACCTCCCAGCTGCAA[A/T]GGATCCTTCCACCTT | 55728 |
| rs564750182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147140 | GCTGCCTTCAAGCAT[C/T]TGTTTAACAAAGCAC | 55728 |
| rs564750300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108068 | GAGTAGTTGGGACTA[C/T]AGGTGTGTGATACCA | 55728 |
| rs564760390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096132 | GTAGACTGCCTGTAG[C/T]TCTATTCCAGGTATG | 55728 |
| rs564785386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107587 | CGGGGTTTCCCCGTG[C/T]TGGCCAGGCTGGTCT | 55728 |
| rs564799117 | in-del | -/AA | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118414 | TCCACCCTGGGCAAC[-/AA]GAGCAAAACTCCATT | 55728 |
| rs564836983 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072117 | TCTCCTTCTGTCACC[A/C]AAGCTGGAGTGCGGT | 55728 |
| rs564839318 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114877 | TTTATTAAGACTATT[A/G]AAGCAATTATAGTAG | 55728 |
| rs564895586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054343 | TCCAGCACTTTGAGA[A/G]GCCGAGGTGGGAGGA | 55728 |
| rs564923839 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160833 | GCAAAAGGTGCCTCT[G/T]CTCCTGACTCATGTT | 55728 |
| rs564926259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162285 | GGCAGGCAGATCACT[G/T]GAGGTCAGGAGTTCA | 55728 |
| rs564939018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066507 | TATTTTTTATTAGAG[A/G]TGAGGTTACACTATG | 55728 |
| rs564990653 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172445 | AACCACCACACAAGT[G/T]AAAATGGGGGTAATT | 55728 |
| rs565004575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061164 | ATTTAAGGTTATTAG[A/T]GTCTTTATTATTATT | 55728 |
| rs565007268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073888 | ACCTCTGCTTCCCAG[G/T]TTTAAGCGATTCTCC | 55728 |
| rs565032312 | snp | C/G | | | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057138 | TGAAGCAGCGGCGGG[C/G]GGCGCGGCGAATGAA | 55728 |
| rs565035534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174758 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 55728 |
| rs565037912 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145021 | TCCTGTGCTGTATTT[A/G]TTAACGGGAGGGCAT | 55728 |
| rs565086451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119614 | GTGTCCTCTCCTGGG[A/G]ACAAATTCAGAGCTT | 55728 |
| rs565100170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074370 | TGCTGGAATTACAGG[C/T]GTGAGCCACCGTGTC | 55728 |
| rs565103781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167302 | AATTTCCTGAGCTGA[A/G]TAAAGCCTTATATTT | 55728 |
| rs565109295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134782 | GTTGTCTTTAATAAA[C/T]TGAAGAATAGCAAAA | 55728 |
| rs565129201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069548 | AAATATGGAGTGTGC[C/T]CTGCTTTATAAAAAC | 55728 |
| rs565148480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133962 | AGACACGTGCCACCA[C/T]GCCTGGCTAGTTTTT | 55728 |
| rs565148583 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141433 | CCGGGTAGAGGCGCT[C/T]CTCACATCCCAGACG | 55728 |
| rs565150133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175430 | AGGGAGATAGAGGAT[C/G]GGGGGATACAAAGTA | 55728 |
| rs565177610 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141852 | GCACCTCGGGAGGCC[A/G]AGGCTGGCGGATCAC | 55728 |
| rs565177684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125506 | GCTACAACTTCCTCT[A/C]TTTACCAGTGTCCTG | 55728 |
| rs565205741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132859 | TTTCCTTTAATGCAG[A/G]TAGGAATTGATTTAC | 55728 |
| rs565232978 | in-del | -/GC | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109512 | ACCTGAGGTCAGGAG[-/GC]TTTGAGACCACCCTG | 55728 |
| rs565237905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111407 | CTCACTGCAACCTCC[A/G]CATACCGGGTTCAAG | 55728 |
| rs565241837 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170022 | GGAGGAAATTAAGAA[A/G]AGACTCATATTAATG | 55728 |
| rs565280875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062945 | ATTTGTCATCTCACC[A/G]CATAGCGGTAAATGG | 55728 |
| rs565282573 | in-del | -/TTT | 0.389527 | 0.207442 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146870 | TTCTATGTGTTTGGC[-/TTT]TTTTTTTTTTTTTTT | 55728 |
| rs565293349 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069068 | GATGTTGCAGTGAGC[C/G/T]GGGATCGCGCCACTG | 55728 |
| rs565338399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175408 | GGCAGGGTGGGAGGT[A/G]GGAAGTAGGGAGATA | 55728 |
| rs565348205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169579 | AAGAAAAAAAGGGAA[A/G]CTCGACATAACCAAA | 55728 |
| rs565375162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119102 | TGTCATCTCTGACAA[A/G]TTACAAATCTTTCTG | 55728 |
| rs565382205 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176487 | CATACAAGGAGTGGA[C/G]AGTGTATAGTTTTGA | 55728 |
| rs565384279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090456 | TGTACTTGTTTTCTT[A/G]GATTTATACCTATGT | 55728 |
| rs565384429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077262 | GCCTCCTGGGTTCAA[A/G]CAATTCTCCTGAGTA | 55728 |
| rs565385060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176920 | GGGGATCCCTGTTTT[C/G]CCCCGCTTTTTTCCC | 55728 |
| rs565413147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127019 | CTGCCTTAGCCTCCT[A/G]AAGTGCTGGGATTAC | 55728 |
| rs565423088 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080395 | TGCTCTGTTGCCAGG[C/G]TGGAGTGCAGTGGCA | 55728 |
| rs565491743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184419 | AGTGAAACCAAATAC[A/G]TTAGAGAATCACTGA | 55728 |
| rs565509524 | snp | A/G | 0.000167445 | 0.00914848 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120140 | ATTCAAAGTGCTTTA[A/G]TTCTGGAAACTCCAC | 55728 |
| rs565521469 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181369 | CCTTCTTCTCAAAAC[A/G]TTTTCGATACTAGCT | 55728 |
| rs565523984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082988 | TACAAGTGTGAGCCA[C/T]CGCACCCGGCCGGGC | 55728 |
| rs565532856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089409 | CAAAAGTTTTGATTT[A/G]ATGAACTATAATTTA | 55728 |
| rs565534785 | in-del | -/TTG | 0.000893609 | 0.0211189 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112043 | TCATAATACTTAGTA[-/TTG]TTGTTTAAAAAATGA | 55728 |
| rs565560685 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110476 | ACTGTGGTTTCAATT[C/T]GCTTTTCTCTGATGG | 55728 |
| rs565568198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083072 | ATACTTCAGCCCACG[C/T]CCTGTGCCTGTTCTG | 55728 |
| rs565581300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170476 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGCGT | 55728 |
| rs565593921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096932 | TTGGACATCTGAGTA[A/T]AGGTGTTCAGTACGC | 55728 |
| rs565656471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063236 | GCCTGTAGGGGAAAA[A/G]GTTATTGGTTCATAT | 55728 |
| rs565717595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069387 | AGCCAAGATTGCACC[A/G]CTGCACGAAAGAGTG | 55728 |
| rs565719320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128554 | GTTTTTTTTTTTTGA[C/G]TCTCGTTCTGTCACC | 55728 |
| rs565756033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136747 | AGCTTTTGAGAACCT[A/G]TTATTTGATAGTTTC | 55728 |
| rs565759476 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141691 | AGACGGGGTGGCGGC[C/T]GGGCAGAGGCTGCAA | 55728 |
| rs565769322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090659 | AGTTTACAGCCAGGC[A/G]TGGTGAGTCACGCCT | 55728 |
| rs565784210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177541 | GAATTGCTTAAACCC[C/T]GGAGGCAGAGATTGC | 55728 |
| rs565796105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148224 | GAGGCCGAGGCTGGC[A/G]GATCACTCGCGGTTA | 55728 |
| rs565817106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127204 | GGCTGCATCTTCTTC[C/T]TCTTTTTTTCTTTTT | 55728 |
| rs565830651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098046 | TCGTTGAGAACCACT[C/T]TCCTAGAATGTAAGC | 55728 |
| rs565892443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106260 | AATTAAACTTCTGCT[C/T]AGAGTATTTTTAGTA | 55728 |
| rs565902236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134443 | CTCATGTTAGGTGGC[C/T]GATTGCCTCCATTTG | 55728 |
| rs565939423 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141343 | GACGGGGCGGCTTCC[A/G]GGCGGAGGGTCTCCT | 55728 |
| rs565948342 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184913 | GTGAGCCGACATTGC[A/G]CCACTGCACTCCAGC | 55728 |
| rs566034409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092417 | TCATATAAATTGTCA[A/G]ACTTTTGTGTGTTCA | 55728 |
| rs566072737 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061203 | GAGGTAGAGTCTTGC[C/T]GTGTTGCCCAGGCTG | 55728 |
| rs566137569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149541 | CTAAAAACCGCTTAA[C/T]TGCATATTTTAAAAT | 55728 |
| rs566163665 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103713 | AGAGAACTTCAAGTT[C/T]TCAGGGACTTTTCTG | 55728 |
| rs566164887 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186292 | TGCTATAAAAATCAC[C/T]GGTTATTATGTAAAA | 55728 |
| rs566180092 | in-del | -/GTCAT | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165173 | GTTCCTGTCCTTAGA[-/GTCAT]GTTAATAGTTTTAGG | 55728 |
| rs566185161 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077448 | CCACTGTGTCTGGCC[A/T]GAATATCTTTTTTTT | 55728 |
| rs566186103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150458 | GATCACTTGAGGTCA[C/G]GAGTTTGAGACCAGC | 55728 |
| rs566194309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058295 | AGGAAATGTAAACAT[C/G]GTGTGTTCTGTGTTT | 55728 |
| rs566257380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142184 | GTGTAACCTTGGTAA[C/G]TTCACTTCAGCCTCT | 55728 |
| rs566275855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111997 | AGCACATCATGATTT[C/T]CAAATTATGAAAAGA | 55728 |
| rs566276813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057184 | TGTGGGGCCCGGCGC[A/G]GGCCGCCTCCGATCT | 55728 |
| rs566305702 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156345 | GGGCAGAAGTCAAAT[G/T]AAAAAAGCTATATTG | 55728 |
| rs566325249 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157078 | GTCTCTTACCATTAT[C/G]TCCCAGATGGAAAAA | 55728 |
| rs566339817 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144715 | CAATGCTTCGCTGCT[A/G]CCACAGAATGTTTTA | 55728 |
| rs566344401 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155795 | TTCCAAAAGAGCAGA[C/T]ATTTCAATGAAAATA | 55728 |
| rs566371792 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128447 | AAGGAATAACCTCTT[C/G/T]AGTAGATCTTAAAAT | 55728 |
| rs566385744 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087831 | GGCTTACTGCAACCT[A/C]TGTCTCCTGGGTTCT | 55728 |
| rs566473263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059002 | ATTTTTGTATTTTTT[A/G]TAGAGAGGAGGTTTC | 55728 |
| rs566493561 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150881 | TTTTGGAAACTAATG[A/C]TATTAAGGGACTTTT | 55728 |
| rs566560217 | snp | C/T | 1.80331e-05 | 0.00300271 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122025 | ATGAAGAAATTTATT[C/T]TACTGATTCTCTTGA | 55728 |
| rs566566292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164978 | GTCTTCTTAAGCTCT[A/G]GGCTACGTTTTTCTT | 55728 |
| rs566567336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073903 | GTTTAAGCGATTCTC[C/T]TGCCTCAGCCTCCCA | 55728 |
| rs566581405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073306 | CTCCAGTGGCAATAA[G/T]TGCAGTCTTTCTTGT | 55728 |
| rs566582127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164084 | GAAGGGTTCAGTGTG[A/G]GAAGGAAAGGAGACA | 55728 |
| rs566625264 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172230 | AACAATCTAGTCTTT[A/T]CATGTTCTTCTGCCT | 55728 |
| rs566642226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080815 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 55728 |
| rs566646773 | in-del | -/CATA | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059698 | CTGATAATGAGTAAG[-/CATA]CATCAAGCCATGTAT | 55728 |
| rs566654733 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072270 | TTTTTTTTTTGATAT[A/G]GAGTCTCACTTTGTC | 55728 |
| rs566713353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071096 | CGTTGCATTTGGGTT[A/G]TAATCTTGAGTCTTT | 55728 |
| rs566724462 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086751 | GATTTAAAAAAATTA[C/T]TTATTTATACTTTTG | 55728 |
| rs566728420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108504 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 55728 |
| rs566767907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171349 | CTTGTTTTCTACTTA[C/T]TGCTGTTGAGCCTGG | 55728 |
| rs566777939 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085857 | TTTTATTTTCTAGTT[G/T]TTGGTATAAAGAAAT | 55728 |
| rs566781282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180338 | TCTCAATAATAATTA[A/T]TCAGCAAGACACCAC | 55728 |
| rs566805344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180979 | AGATGGTGAAACCTC[A/C]TCTCTACTAAAAATA | 55728 |
| rs566839091 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166170 | TTGGAATCTTTTTCT[C/T]TGTTAGTAGGCAGGA | 55728 |
| rs566888059 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125881 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 55728 |
| rs566905845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159066 | TATTACATAGGTAGT[A/G]CTATCCCAATTTAAT | 55728 |
| rs566913894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138827 | ATTACTGTGGCTTTG[C/T]AGTAAGTTTTGAAAT | 55728 |
| rs566927254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133421 | GCTCACTGCAGCCTC[C/T]GCCTCCCGGGTTCAA | 55728 |
| rs566928876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174846 | CAGCAGTTTGGGAGG[A/G]AAAAAAGAAAAACTG | 55728 |
| rs566965294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084053 | CAACCTCCCCCTCCT[A/G]GGTTCTCCTGCCTCA | 55728 |
| rs566966470 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116292 | TTGGTTATTCATATA[A/T]TTGATCTTGTTTCTT | 55728 |
| rs566977106 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118107 | GCTTGTGGAATCATT[A/G]CTGATAAACTTTAAA | 55728 |
| rs567012497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138425 | CACTGAAGCCTTTTA[A/C]ATTTGATGTAGTCTA | 55728 |
| rs567019695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124493 | CTGGGACTACAGGTG[C/T]GCACCACCACACCTG | 55728 |
| rs567024675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096196 | GAATATGGGTGGTAA[A/G]TACAATACGTATGTA | 55728 |
| rs567045193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087085 | ATTTCTAGTATAATT[C/T]CATGTGCACTTGAAA | 55728 |
| rs567054420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131380 | TACTAATACTGCTAG[A/C]CTTAGCTTATATTTT | 55728 |
| rs567081936 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170127 | AATTAAAATATACAT[A/T]TAACTCAATAATTGT | 55728 |
| rs567082208 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103455 | AAAAAATTAAAGACA[A/G]TTTCAAAATTGTGAG | 55728 |
| rs567082663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087646 | TGGGATTACAGGCAC[G/T]AGCCACCTTCCCCCA | 55728 |
| rs567110644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145245 | GTTTCTTTTTCTGAG[A/G]CATAATCTCACTCTG | 55728 |
| rs567151811 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063789 | GCTGGGATTACAGGT[A/G]TGCATCACCACACCT | 55728 |
| rs567170795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141226 | GCGGGGGGCTGACCC[A/C]CCCACCTCCCTCCTG | 55728 |
| rs567178976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089743 | CACCCAGCCACGATC[A/G]GTTTTTCCTTTTATG | 55728 |
| rs567192021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101973 | TTTATATTCTGTTCA[A/G]TGCAAAATCCAATAT | 55728 |
| rs567220144 | snp | C/G | | | splice-acceptor-variant | N4BP2 | GRCh38.p7 | 4:40136943 | CTTAAATTTTCTACA[C/G]CTATTCATTAGAACA | 55728 |
| rs567231840 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079766 | GAGATCATGCCACTG[A/C]AGCTCAGCCTGGGTG | 55728 |
| rs567265626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181172 | AAAAAAATATATATA[C/T]ATTGGCCAAATCTTT | 55728 |
| rs567280460 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082454 | AAACAGACATTTATT[A/C]AAAAAAGTATATAAA | 55728 |
| rs567302092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148753 | CCTTGGCCTTCCAAA[A/G]TGCTGAGATTGCAGA | 55728 |
| rs567320673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183434 | TCCGCCTCCCGGGTT[C/T]ACGCCATTCTCCTGC | 55728 |
| rs567327596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139965 | CCACCACACCTGGCT[A/T]ATTTTTGTATTTTTT | 55728 |
| rs567350165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061286 | GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC | 55728 |
| rs567350982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182865 | CATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55728 |
| rs567353761 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135210 | GGTGTTTGGTTTTTT[A/G]TTCTTGCGATAGTTT | 55728 |
| rs567397287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140598 | TTTTTTTTAAAATTA[A/G]TTTATTTTTTATTGA | 55728 |
| rs567441448 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159963 | TAGCTGTGATTACAG[G/T]CACCCACCACCATGC | 55728 |
| rs567446180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109686 | TCCCACTACTGCACT[C/T]CAGCCTGGGTGACAG | 55728 |
| rs567457187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054479 | CCAGCTATTCGGGGG[A/G]CTGAGGCACGAGAAT | 55728 |
| rs567521197 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107217 | GATCCTCCCACCTTA[A/G]CCTCCCAAGTAGCTG | 55728 |
| rs567523357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160359 | GGTGTGAATGCCGTA[C/T]GCGTTTAGTAGAAAC | 55728 |
| rs567554584 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056080 | CTACCCCTTTGTCTC[C/T]CCGTGGGGCTCCGAG | 55728 |
| rs567558864 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108456 | GAGTAGCTGGGATTA[C/T]AGGCACGTGCCACCA | 55728 |
| rs567617639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063071 | TTATATTTGATAGAT[A/G]AAAGTTTTCTAAGCC | 55728 |
| rs567628844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098162 | AGTAAATATCTATTA[A/G]GCAACTAGGTAATTA | 55728 |
| rs567651282 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149547 | CCGCTTAATTGCATA[-/T]TTTTAAAATGGTTAG | 55728 |
| rs567687262 | in-del | -/T | 0.499692 | 0.0124024 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104411 | AAACTTATTTTTAGT[-/T]TTTTTTTTTTGATAT | 55728 |
| rs567736864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176187 | TTAAATAGTTGTGAT[C/T]ATATTTTATAAATAT | 55728 |
| rs567755100 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087993 | GAACTCCTGACCTCC[A/G]GTGATCCGCCTTCCT | 55728 |
| rs567755787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070894 | CAGTGGCGTGATCTT[C/T]GCTCACTGCAACCTC | 55728 |
| rs567789081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171155 | GCATATTTAAAGGAC[C/T]GGGCTTCCACTTTTC | 55728 |
| rs567806295 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150233 | ATACACTGCTACGTA[C/T]GAATCATTTTTGCCT | 55728 |
| rs567827728 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179151 | AGGCGGGCAGATCAC[A/C]AGGTCAGGAGATCGA | 55728 |
| rs567827792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077422 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAACCACT | 55728 |
| rs567835645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069157 | ACAAAAAAATTCCCA[A/G]CCGGGCACAGTGACT | 55728 |
| rs567882704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083000 | CCACCGCACCCGGCC[A/G]GGCTGTATTCTTACA | 55728 |
| rs567914564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075837 | TTTCTTTTTTTGTTT[A/G]TTTGTTTGAGACAGG | 55728 |
| rs567915290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112803 | CTGCCTCCTGGGTTC[A/G]ATCGATTCTCCTGCC | 55728 |
| rs567936047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071013 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 55728 |
| rs567956781 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107149 | GTGTTGCACAGGCTA[C/G]AGTGCAGTGGCATGA | 55728 |
| rs567967109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176518 | CAAAAGTACTCCCGA[G/T]GTGATTCTGATAAGC | 55728 |
| rs568077612 | snp | C/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122214 | CCACTCCAGCGATGG[C/G]CAAATCTCTGACCAT | 55728 |
| rs568082065 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099561 | GCCCATGTTTTAAGA[-/T]TTTTAATAGGAATAA | 55728 |
| rs568098650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077989 | CATATTTTTAGCTTC[A/G]GTATAAAAACTGTAC | 55728 |
| rs568172058 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131039 | ATTTGTGAAAAACTG[-/A]AAAAAAAAAATTGTG | 55728 |
| rs568228686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127815 | ACAGGTGCCTGCCAC[C/T]GCGCCCGGCTAATTT | 55728 |
| rs568351993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091341 | CTTGCCTTTTTCCTG[A/C]TGTTAGGAGGAAAGC | 55728 |
| rs568352976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092461 | TAGCCTTTTGATATC[C/T]GCAAGGTCTATAGTA | 55728 |
| rs568368430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129221 | GCCCTGCTAGTTTTT[A/G]TTTTGTTTTGTTTTG | 55728 |
| rs568385829 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135289 | GAACTCATCATTTTT[G/T]ATGGCTGCATAGTAT | 55728 |
| rs568388528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079088 | CACCACACTCGGCTA[A/G]TTTTTGTATTTTTGG | 55728 |
| rs568410787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129781 | CTCAGCCAGATAATT[A/T]CCTGATGCTGTCCTC | 55728 |
| rs568412083 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148350 | CAGGCACTGGGCAGG[A/C]GGAGGCAGGAGAATC | 55728 |
| rs568451056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085924 | CCAGCACTTTGGGAG[A/G]CTGAGGCAGGAGGAA | 55728 |
| rs568466169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086865 | TGATCCTCCCATCTC[A/G]GCCTCCTGAGTAGCT | 55728 |
| rs568503793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137402 | ATGTGGGCAGAAATA[C/T]TTAGCCTTTTGGGAA | 55728 |
| rs568515030 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056887 | TCGCCGTGTCTCCCC[C/G/T]GCGGCCGCAGCTGCT | 55728 |
| rs568515429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172450 | CCACACAAGTTAAAA[C/T]GGGGGTAATTTGGGT | 55728 |
| rs568526995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177542 | AATTGCTTAAACCCC[A/G]GAGGCAGAGATTGCA | 55728 |
| rs568543203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068036 | TGTAAGGTGATATCT[A/G]TCTCATTGTGGTTTT | 55728 |
| rs568563627 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103949 | TTCACCTAATCTATT[G/T]TATATGCTAGTTCTT | 55728 |
| rs568563842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151671 | AGTTCGTAAAAAGGT[C/T]TTACACTATATACCT | 55728 |
| rs568614568 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124958 | CCTGCCAACTTGAAA[A/G]TATTTGATTCCAGAT | 55728 |
| rs568627459 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057287 | CGAGGCCGGGCGAAG[A/G]CGGGGGCCGCGGCCG | 55728 |
| rs568648605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143856 | TCTAGAGAGACAGAC[C/T]AGTAGGATATATGAA | 55728 |
| rs568663491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115570 | ATACTTTATTTTTGT[A/C]TTATTTAGTTATTTT | 55728 |
| rs568672610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106363 | AGGGTCTTATTCTGA[C/T]TCCAGTGCAGTGGTG | 55728 |
| rs568675654 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057412 | ACCTGACCTTGCGCC[C/G]CTCCAGGCGCCTTAG | 55728 |
| rs568695984 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156910 | TCCAAAACACTTCTG[C/G]TCCTAAGCATTTTGA | 55728 |
| rs568700622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151039 | CAGTCCTTTCTAAGG[C/T]GTTAAACAGCAAGAA | 55728 |
| rs568723820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149668 | GGGAGGCCGAGGCTG[A/G]CGGATCACGAGGTCA | 55728 |
| rs568734875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106821 | CTTGAATAATTTATT[G/T]TGTTTATGACTTTGG | 55728 |
| rs568782888 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095688 | TTGGGGCAGAGGGAG[A/C]AGGGTATATGATTTT | 55728 |
| rs568838169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123435 | AAGTATTTCCAGACA[A/G]CCAAATTATATAATT | 55728 |
| rs568873651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101452 | GGCATGAGCAACCAC[A/G]CCAAAAAGTGTGCAT | 55728 |
| rs568897689 | in-del | -/TATG | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059384 | AGATTGAGCATTTTT[-/TATG]TATGTATGTATGTAT | 55728 |
| rs568907955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094843 | AGGTGTGAGCCACCG[C/T]GAGTGCAGTGGCGTG | 55728 |
| rs568912536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107678 | TGTGAGCCACCGTGC[A/G]TGGCCTATAACTGTA | 55728 |
| rs568951507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067735 | ACAGAGTCTCACTCC[A/G]TCACCCAGGGTGGAG | 55728 |
| rs568984187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167518 | TACCTGTTAAGAGAA[A/C]AGGAAAGTAACCAAG | 55728 |
| rs569020883 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175836 | AAAAAAAGGCCTGTA[A/T]TCCCAGCACTTTGGG | 55728 |
| rs569031760 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158900 | ACATTTATCTAACAA[A/T]TATTTAGAGCACTCG | 55728 |
| rs569042457 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083512 | AGCAGTATCGGTGAA[G/T]TACCAATACAGGCTA | 55728 |
| rs569053071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066112 | ATTTTTGTATTTTTA[G/T]TAGAGATGGGGTTTC | 55728 |
| rs569068539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165777 | TCAGAAGTCAGTATT[C/T]CTCAAAGAACTTATA | 55728 |
| rs569125197 | snp | C/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072362 | GCAATTCTCCTGCCT[C/G]AGCCTCCTGAGTAGC | 55728 |
| rs569135796 | snp | A/C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086332 | AAAAAATTTAAAAAA[A/C/T]TATTTATTTATTTTT | 55728 |
| rs569147382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175032 | ATTTTGTTTTGTTTT[A/G]TTTTTTCAAAGACAG | 55728 |
| rs569182965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173223 | CCACCTCAGCAAATT[A/G]CTCAGATCCTGGGTA | 55728 |
| rs569184604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109746 | GTGTTAGCATGGTTC[A/G]GCATGCCCTTATAAC | 55728 |
| rs569210661 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143196 | TTGTGCCTTCTGTCA[A/T]GTTTGAATTTTTGGT | 55728 |
| rs569224297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153231 | TTTAAAGTTCTAAAA[A/G]AAAGTAAATATATTT | 55728 |
| rs569242476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109423 | TTAAATGAAGGTGAA[A/G]AGTGTTAACATTGGC | 55728 |
| rs569261971 | in-del | -/T | 0.0785177 | 0.181917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084914 | GCCACAGCGCCTGGC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs569278874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118763 | AAAATTATTAACAGT[A/T]CACTTTTACCAAGTA | 55728 |
| rs569333198 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140420 | ATAATATGCAAGGCA[C/G]TGTGAGTCATTATGG | 55728 |
| rs569344652 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112420 | GTTTTTTGGGGTCTT[C/T]TATGAAAAGGTAGTG | 55728 |
| rs569400589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117238 | TGGCTCTGGCTCCTA[G/T]GACCCTTAACCTCTC | 55728 |
| rs569434880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132156 | ATTTACAAATTAGGC[A/G]CAGTAAAAAATTAAC | 55728 |
| rs569511174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182188 | TAACACAACTAACAG[C/T]GTTTTACCTTGCATA | 55728 |
| rs569532675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088163 | CATGGAATGGATGTA[C/T]CATAGTTTTTTTAAC | 55728 |
| rs569536101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076542 | TCACCCAGGCTGGGC[A/G]CAGTGGCGCCATCTC | 55728 |
| rs569549342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088979 | TTTTTGAAACAGAGT[C/T]TCTGTCTGTCACCTA | 55728 |
| rs569565519 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159682 | GAGGGAGGCTGGGAA[A/C]TTTTCTATTTCAGAC | 55728 |
| rs569574412 | in-del | -/TCT | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127196 | GCCTGACCGGCTGCA[-/TCT]TCTTCTTCTTTTTTT | 55728 |
| rs569589240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177389 | GGGAGGCCGAAGCAG[G/T]TGGATCACCTGAGGT | 55728 |
| rs569597532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083642 | AGGTAAACCTATAGA[A/G]ACAAAAGTAGATTCG | 55728 |
| rs569613074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096366 | AGAAAAGTGGTTCAG[C/T]AGAGGGAACCAAGGT | 55728 |
| rs569625865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179767 | AGCCTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTG | 55728 |
| rs569629983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184239 | CAAAAATGGTTTTCA[A/G]ATTAAGTTCTCAGAA | 55728 |
| rs569639018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126631 | TTTTCTTGATACATC[A/G]TCTTGGCTCTGTTGC | 55728 |
| rs569640410 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108374 | CTGGAGCGCAGTGGC[A/G]TGATCTCGGCTCAGT | 55728 |
| rs569656122 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172330 | CTGCCTTTCCCAGTG[C/T]ACTGACTCAAATTTT | 55728 |
| rs569692542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083049 | GAGATAGAGTAAACC[C/T]ACCCCGTATACTTCA | 55728 |
| rs569728359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142142 | GGAGAGGGGGAGGGG[A/G]AGGGAGAGGGAGAGG | 55728 |
| rs569744950 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146271 | TCTTGCTTACCTCTC[C/T]AGTCTCACCCTGTGT | 55728 |
| rs569745883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176628 | CACGAGAACAGTAAC[C/T]GTAACAAATGCCTGA | 55728 |
| rs569757866 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074234 | TAGCTGGGATTACAG[A/G]TGTGTGCCACCATGC | 55728 |
| rs569811613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153846 | AATCAGACTTACCTG[A/G]TATATCAGAGATTTC | 55728 |
| rs569915336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147338 | ACACAGCGACCATCC[A/G]ATTTCTCAATCTTTT | 55728 |
| rs569948478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103559 | AGAGATATAATTGAT[C/G]TTGATTTCATGGAAT | 55728 |
| rs569978803 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075007 | TGAGACTCTGTAAAG[-/A]AAAAAAAAAAAAGTA | 55728 |
| rs569989799 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185323 | ATAGTGGTTTTTGCT[G/T]TTTTATGGTTTTCTT | 55728 |
| rs570002523 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40097626 | AGACTTTGTGTACTA[C/T]GCCATGATTAATAGT | 55728 |
| rs570006388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111461 | AAGTAGTTGGGACTA[C/G]AGGTGCGTGCCACCA | 55728 |
| rs570014524 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066480 | TGTGCCACCACACAC[A/G]GCTAATTTTTGTATT | 55728 |
| rs570048691 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087489 | GTTTCTCAGCCTCTG[A/G]AGTAGCTGAGATTAC | 55728 |
| rs570058116 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083882 | TGGGAGCTCCCACAC[G/T]TAAAACCAATCCACG | 55728 |
| rs570085137 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, synonymous-codon, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056684 | ACGAAGCAGAGGTCG[A/T]GGCGGACAGCCGGCG | 55728 |
| rs570100131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091379 | ATTTCATTACAAATA[C/T]AATGTCAGCTGTAGG | 55728 |
| rs570109538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058115 | TAGCCTCTCAGAAAA[C/G]AATGACTGATTTGCA | 55728 |
| rs570119711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057476 | GGCCACCTTCCTGAG[C/T]ACATAGTCCTAGCAG | 55728 |
| rs570121642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065046 | GTGTTGGGATTACAA[A/G]CGTGAGCCACTGTGC | 55728 |
| rs570128717 | in-del | -/T | 0.32955 | 0.237006 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073597 | ATTTTACACATAAGA[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs570150344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098300 | ACTTAATCTCCCTGA[A/G]TCTCAGTTTTCTAAT | 55728 |
| rs570177860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164050 | TTCAGCAGAGGTAGT[A/G]ATTGGCGGATAGGTA | 55728 |
| rs570182122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064464 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 55728 |
| rs570225918 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056176 | CAGCGGCCACGGCCC[A/T]AGTCAGGCAATGCCG | 55728 |
| rs570256580 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154841 | CTTTTGTTCTGTTCT[G/T]CTGTGTGCATTTTAT | 55728 |
| rs570265443 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063711 | TGCAATGGTGTGATC[G/T]CGGCTTACTACAACC | 55728 |
| rs570293495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161943 | GGAGGCCCCCATGGC[A/C]CTGTTGCCACAGCTG | 55728 |
| rs570351682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150314 | TAGGGATTTACAGGG[A/G]ACAGAGGAACATGTT | 55728 |
| rs570366449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169697 | AAGCTGGGTGTGGTG[G/T]CTCTCGCTTGTAATC | 55728 |
| rs570385832 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152346 | AGAACAAAGCTTGAT[G/T]GCTTTAGAATATTTA | 55728 |
| rs570403433 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151320 | GCTCTGTTGCCCAGG[C/T]TGGCAGTTGGTTGTG | 55728 |
| rs570416401 | snp | C/T | 1.65803e-05 | 0.00287922 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107059 | TTCTGGGTAACGTTA[C/T]GAGTAATACAAAGAA | 55728 |
| rs570451935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136576 | GTTTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT | 55728 |
| rs570454496 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127859 | GTAGAGACGGGGTTT[C/T]ACCGTGTTAGCCAGG | 55728 |
| rs570521113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106421 | CCCTGGGTTCAAGTG[A/G]TCCTCTCAACTTAGC | 55728 |
| rs570540385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070973 | GGGATTACAGGTGTC[C/T]GCCACCATGCCTGGC | 55728 |
| rs570556083 | snp | C/T | 0.000135023 | 0.00821544 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121920 | CAGAAAAAAACCTAG[C/T]AGTCACAGAGACTGG | 55728 |
| rs570604611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078250 | TCAAGAGATTCTCAT[A/G]CTTCAGTGTCCTGAG | 55728 |
| rs570632139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179247 | TGGTGGCTGACGCCT[A/G]TAGTCCCAGCTACTT | 55728 |
| rs570673174 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186248 | GCTATGCTTAGCTGT[A/G]GTTCAGTGATTCTCC | 55728 |
| rs570781861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092222 | AGATTATGTAGGATT[A/G]GTATTATTTTTTCCT | 55728 |
| rs570783743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084732 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs570791463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124368 | TTTTTTTATTTAGAG[A/G]TGGAGTCTTGCTCTG | 55728 |
| rs570800982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072406 | ACGTGCCACCATGCC[C/T]AGCTAATTTTTGTAT | 55728 |
| rs570807386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173658 | CTGAAAACAGGCTGA[C/T]AGTCAGTGGATATAC | 55728 |
| rs570827033 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060896 | GGGCCCGAGCCATCA[A/C/T]GCCTGGCCTGTTTTT | 55728 |
| rs570874521 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180922 | TTTGGGAGGCTGAGG[A/C/T]GGGTGGATCATGAGG | 55728 |
| rs570899903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165261 | GATAAAAATCAATCT[A/G]TACTTTTTTTTTTGA | 55728 |
| rs570915854 | snp | A/C | 3.31884e-05 | 0.00407346 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120826 | GCCAAAGACTGGTTT[A/C]AGTGAGCCCAACCTA | 55728 |
| rs570935213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139824 | TTTTTTTACATTTTT[C/T]TTTCTTTTTTTTTTT | 55728 |
| rs570958929 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058573 | AGTTGAAATCAGCAC[A/G]CAGTACGTACGAATG | 55728 |
| rs571042912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138116 | CAGTGGCAGAATACA[A/G]AAAATAAAAGACATG | 55728 |
| rs571059338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093627 | TTTATTTATTTATTT[A/G]CTTTTGGAGACAGAG | 55728 |
| rs571073262 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145762 | TGGTGAAAAAGACAC[A/G]CAATCCTTGTCTTTA | 55728 |
| rs571075152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100529 | TGGTACTATACGCAC[A/G]TGCTACCACACTGGT | 55728 |
| rs571077694 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143535 | TGAACTCCTGAGCTC[A/G]AGCAATCCTCCCATC | 55728 |
| rs571077985 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083112 | GCGGGGTTGGGGGGC[A/G]GTGCAGACATAGAAA | 55728 |
| rs571078762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137630 | AGACATGGAAGTGTC[A/G]TGAAGGAAGTTTATC | 55728 |
| rs571103935 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101361 | GATGGGGTTTCGCCA[C/T]GTTGGCTAGGCTGGT | 55728 |
| rs571110575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182239 | GATACAAGAACATGC[G/T]CAGAGACAGGAAAAG | 55728 |
| rs571157848 | snp | C/T | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054276 | CTATTCTTAAATGTC[C/T]TCTTTGAAATTTAAA | 55728 |
| rs571236709 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115641 | GTTATGTCGTACTGT[G/T]TTTTTAAATTTCTGA | 55728 |
| rs571261509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094918 | CCTGCCTTAGCCTCT[C/T]GAGTAGCCGGGACTA | 55728 |
| rs571304754 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055510 | CCAGTTAGACCTAAA[C/G]GACAAAAACCACTTG | 55728 |
| rs571317569 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054625 | AATTTAAAGGGACAT[A/G]AACTTCAATGAGAAC | 55728 |
| rs571319342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062365 | CCTTTTCCCTATCCT[A/C]GCTGCTGCCCTCCTA | 55728 |
| rs571352506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145542 | TTGAATTTTGGAAAT[C/T]TTGTAGAAAATCTAG | 55728 |
| rs571355066 | in-del | -/TTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062026 | TATTTATTTTTTGGT[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs571412333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160537 | AGGTAGGCTAGGCTA[A/C]GCTATGATGTTCAGT | 55728 |
| rs571417149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152434 | ACTTGACTCCTTTTG[C/T]ATAGTAATTGTTAGG | 55728 |
| rs571456036 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106729 | AATTTTTGTATGTTT[A/G]GTAGAGATGGGATTT | 55728 |
| rs571475160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059797 | TGCACACCAGGTGCT[A/G]TTTTAAGCACTTTGC | 55728 |
| rs571500209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138504 | GTCATGAACTTTCCT[C/T]CTGTATTTTCTGTAG | 55728 |
| rs571531170 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158916 | TATTTAGAGCACTCG[C/T]TACTGGGGTTACAGG | 55728 |
| rs571536880 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117727 | AATTAGAATCAAATT[G/T]TATATATTGTGGTCA | 55728 |
| rs571549719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167651 | AAAGAGGACTGTAAC[C/T]AAATAACAAATTAAT | 55728 |
| rs571552173 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143733 | ATAGCTTCTGGGGTA[A/G]GTAACTACAAAATGT | 55728 |
| rs571566881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165950 | GATGTCTCTACCACT[C/G]CTGGGCCTTATCTAT | 55728 |
| rs571579649 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139453 | AATACATAGACATGC[A/T]GTTGGGTTTTTTGTA | 55728 |
| rs571580303 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184015 | GTTGATGAGGACTGG[A/G]TCACACAGCCACTCA | 55728 |
| rs571608959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109590 | GGGCATGGTGGTGCA[C/T]ACCTATAGTCCCAGC | 55728 |
| rs571610798 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149107 | CAGTAATTCTGCCCC[-/T]AACTATGTACCCAAG | 55728 |
| rs571611820 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147675 | GGGCGGCTGGCCGGG[C/T]GGGGGCTGACCCCCC | 55728 |
| rs571625031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104190 | ATTTCCTGACCTCGT[A/G]ATCCACCCGCCCCGG | 55728 |
| rs571625314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068426 | TTCTCCCCGTTTTCT[C/T]CTACGAGTTTTAAGT | 55728 |
| rs571655212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133348 | AATTTCTTTCTCCTT[C/T]TTTTTGAAACAGAGT | 55728 |
| rs571661103 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070081 | TTAGGAAAATAGAGA[C/T]ATAGAAAAGTAGTAT | 55728 |
| rs571668747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162517 | TCATATTTGCTACAC[C/T]GATGATACTTGTCCA | 55728 |
| rs571679836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104480 | CATATTCTGCTGATA[C/T]ACTTATAAGCATATT | 55728 |
| rs571682702 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118381 | AGGTTGCGGTGAGCC[A/G]AGATTGCGCCATTGC | 55728 |
| rs571718074 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165096 | GTACCTTATTAATTT[-/TA]TGTTACCTTCATAGA | 55728 |
| rs571719064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111125 | TTTGAATATTAGATA[C/T]ATGGAAAAGTTGCAG | 55728 |
| rs571729832 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137529 | TATTATTTAACACCC[A/G]TCTTTTTATTATAAC | 55728 |
| rs571750053 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108120 | TTAGTAGCGACGGGG[-/T]TTTTGCCACATTGGC | 55728 |
| rs571763640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110840 | ACCGTGCCCAGCCTC[C/T]TTTGCCCATTTTTAA | 55728 |
| rs571793867 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171399 | TCCCAGGGTAATGCT[A/G]TGTGGTGATTCCCGT | 55728 |
| rs571798992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067787 | CACTGTAACCTCTGC[A/G]TCCCAGGTTCAAGTG | 55728 |
| rs571800449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109890 | GAACTTAATATTCAG[C/G]GCTGTGCATTCGTTA | 55728 |
| rs571819670 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125818 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55728 |
| rs571825065 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092886 | TGACCTCAGGTGATC[C/T]ACCCACCTCAGCCTC | 55728 |
| rs571854151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074744 | GGGCATGGTGCCTCA[C/T]GCCTGTAATCCCAGC | 55728 |
| rs571862757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175119 | TAGAATTCCTGGCCT[C/T]AAGCAATCCTCCTGC | 55728 |
| rs571890516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175908 | ATCTTGGCTAACACG[A/G]TGAAACCCCGTCTCT | 55728 |
| rs571891311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125339 | TTGTGAACTTCCTAG[A/G]ATGTTCAGTTCCTTA | 55728 |
| rs571921621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182758 | CTCAGCTCAATGGAA[A/C]CTCTGCCTCCCAGGT | 55728 |
| rs571939214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075135 | ATAGTACCATTTTGG[C/T]GTATATATCATGATC | 55728 |
| rs571991747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081452 | GGAGTTCAAGACCAA[C/T]CTGACCAACATGGTA | 55728 |
| rs571999513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068820 | TCTCATAATTTTTAT[C/T]CTTTAAAAAATTCCC | 55728 |
| rs572000552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082590 | TTGAGCCCAGGACTT[C/T]GAGACCAGCGTGTGC | 55728 |
| rs572012753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081969 | AATACAAAATTAGCC[A/G]GGTGTGGTGGCGCAT | 55728 |
| rs572081811 | in-del | -/GGCCTCCGAGTGCCTGGCG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057310 | CGCGGCCGCTTCCTT[-/GGCCTCCGAGTGCCTGGCG]GGCCTCCAGGCCCCA | 55728 |
| rs572099654 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067395 | TAATATTCCATTGTA[C/T]GTATGTACCACATTT | 55728 |
| rs572102749 | snp | A/T | 3.3325e-05 | 0.00408184 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154283 | GTTTGTAGGTTAAAA[A/T]TACTTTTATTTGCAG | 55728 |
| rs572121160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068257 | GCAAATATTTTCTCT[C/T]ATTCCGTAGGTTGCC | 55728 |
| rs572141084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161321 | GAGGACACAGGAATA[C/T]GTGAGACATCAGGAT | 55728 |
| rs572165349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127465 | AGTGATCCTCCTGCC[G/T]CAGCTTCCCAAAGTG | 55728 |
| rs572192776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118251 | TGGAGAAACCCGTCT[A/C]CACTAAAAGTACAAA | 55728 |
| rs572250951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168551 | ATCAGAAGATTGTTA[C/T]AAATATAAGGATAAC | 55728 |
| rs572323153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126850 | GCAACCTCCATCTTT[C/T]GGGTTCAAACGATTC | 55728 |
| rs572327996 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149915 | AAGAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 55728 |
| rs572385581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128770 | TGACCTCAAGTGATT[C/T]GGCTTCCCAAAGTGT | 55728 |
| rs572387544 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095595 | GAGAGAGCTATGATA[A/C]AAATTTAATTAAAAG | 55728 |
| rs572398047 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091251 | ATCTATATGCGTTTT[A/C]TTTTCTTTTTTTCTC | 55728 |
| rs572438817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104964 | ACTGCCACCGCGCCT[G/T]GTTAATTTTTTGTAT | 55728 |
| rs572468433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179925 | ATGCGCCACCACGCC[C/T]GGCTACTTTTGTATT | 55728 |
| rs572532450 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180268 | CACAAGATATAAATA[A/T]GCCATTTTAGAGGAG | 55728 |
| rs572559551 | in-del | -/CTTTT | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060958 | ATCATGTATTAGCTG[-/CTTTT]CTTTTCTTTTCTTCT | 55728 |
| rs572563544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084842 | CTCATCTTGAACTCC[C/T]GACCTCAGGTGATCT | 55728 |
| rs572577913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084214 | CCTTGGCCTCTCAAA[A/G]TACTGGGATTACAGG | 55728 |
| rs572584969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141872 | TGGCGGATCACTCGC[A/G]GTTAGGAGCTGGAGA | 55728 |
| rs572596689 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185427 | TAGTAATGTGAATAC[C/T]CTTTCAAAGTATTTT | 55728 |
| rs572641382 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059551 | GATGGGTTTTTGTCA[C/T]GTTGGTGAGGCTGGT | 55728 |
| rs572678151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090508 | ACATAACATCATCAA[C/T]AGGTTCTCGGAAACT | 55728 |
| rs572679194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057605 | GTCTTTGGCCCTCGT[C/T]CCGCCTCCCCTGCCC | 55728 |
| rs572714649 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085586 | CTAAGCTTCCAGAGT[A/C]GCTGGAATTACAGGC | 55728 |
| rs572733773 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156552 | CATAATTTTGAAAGA[A/T]AAGTTTGTAATCCCT | 55728 |
| rs572741950 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056901 | CCGCGGCCGCAGCTG[C/T]TTGCTAGCCTTGCGC | 55728 |
| rs572742285 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144393 | TTCCCACTTTTACGA[C/T]TTTTGGTTCAGAAAA | 55728 |
| rs572750403 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056251 | ACCCCGCGCGCGTCA[G/T]GGCTCGTCCCAGCTC | 55728 |
| rs572769160 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119481 | TAATTTCTCTTAATC[A/G]GGCAAATAGCGTTGG | 55728 |
| rs572779602 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088715 | TTGTTGGTCAGGCCG[C/G]TCTCGAATTCCTGAC | 55728 |
| rs572782889 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155055 | CATGTAATTTTAAAA[C/T]TGCAGTAGGTTAAAA | 55728 |
| rs572806808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143346 | TAAGATAAGGTCTTG[C/G]TCTGTTGCCCAGGCT | 55728 |
| rs572851244 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146839 | TGGCCCCTGGCAACT[-/A]ACCATTCTATTATGT | 55728 |
| rs572854586 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128846 | TCTTTAAAAAAAAAA[A/T]AAATAAATAAAATAA | 55728 |
| rs572875569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101754 | ACTTTTATAAATAAG[A/C]CTAATATGTCCAATT | 55728 |
| rs572893305 | snp | G/T | 0.000329777 | 0.0128367 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137011 | CCTGTAAAAACAGTT[G/T]TAGCCCAAGAGTTTG | 55728 |
| rs573005849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112956 | TAATCCACCAACCTC[A/G]GCCTCTCAAAGTGTT | 55728 |
| rs573024074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149205 | TGGTAACCTAAAAGT[C/T]CATTAACTGATGAAT | 55728 |
| rs573047742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099276 | AGACGGAGTTTCGCT[C/T]TTGCTGCCCAGGCCG | 55728 |
| rs573060218 | snp | C/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120933 | AAAAACTAAAGACAT[C/T]GGGTAGCTCCAATCT | 55728 |
| rs573061065 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163581 | AAATGCATTCTTGTT[A/C]AGCAAGACTTTGTGT | 55728 |
| rs573084491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105894 | TATATACATGTTTAA[C/T]GGTAAAAAAGGAAGT | 55728 |
| rs573104464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112286 | AACCTTGGATAGTCT[A/G]TAAATGAGCTTTCAT | 55728 |
| rs573131595 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072001 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 55728 |
| rs573194079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079282 | AAGGTTTTGTATTTT[C/T]TGTTTATTTATTTAT | 55728 |
| rs573208859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058700 | TTTTTTCCTTCATTA[A/T]AGTATATTAAAGTAG | 55728 |
| rs573225101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180558 | TCATTATTCCACAGG[A/T]ATACTTAATTACTCA | 55728 |
| rs573240051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065910 | TTTGCACATAGTTTC[C/T]GGACCTATAAAGATC | 55728 |
| rs573259496 | in-del | -/GT | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165662 | TACATCTCTATGTAC[-/GT]GTGTGTGTGTGTATA | 55728 |
| rs573295482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165363 | AAGCAATCCTCGTGC[C/T]TCAGTCTCCTGAGTA | 55728 |
| rs573305036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125423 | TTGCCAAAGTAATCG[A/G]TCTTCTTGGTCCTTA | 55728 |
| rs573334430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114770 | TTATCTAAGTTTGAA[C/T]GTTAGAATTTACTTT | 55728 |
| rs573342877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114030 | CACTGGAAGGTAGTA[C/T]GGATATAGAGATGGA | 55728 |
| rs573343255 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133537 | GACAAGGTTTCACTA[C/T]GTTGGCCAGGCTGGT | 55728 |
| rs573379740 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122453 | ATCTTGGCTCACTGC[A/C]ACCTCTGCCTCCCAG | 55728 |
| rs573404091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164384 | GAGATGATGGTAGTC[A/G]GAGTGGAGAAGGTCA | 55728 |
| rs573412192 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078743 | ATGTTTCCCTGGCTG[G/T]TCTTAGACTCCTGGG | 55728 |
| rs573441035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172761 | GTGAGGTTGGATCAG[C/T]TCAACTCAGCAGTGT | 55728 |
| rs573441490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124737 | GTATATTGAACTTTC[A/G]TGAGTGCTGTGGAAC | 55728 |
| rs573508777 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113297 | CTGGGTTAAAGTGAT[C/T]GTATATTTTGCCATT | 55728 |
| rs573536340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129446 | TGGCCAGGCTGGTCT[C/G]AAACTCCTGAGCTCA | 55728 |
| rs573544893 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117434 | ATGTTTTCATTAAGA[A/C]CAAACCTTTGAGGGG | 55728 |
| rs573558305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116499 | TAATTTGGAAATTGT[G/T]CAGACTTTAAATCTA | 55728 |
| rs573596316 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110168 | TTCCTTTATATGGAT[A/G]AGTAAGATTCCACTG | 55728 |
| rs573598082 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162985 | CTTGAGTGTCCTTAC[A/C]ACATGGTGGCTGGTT | 55728 |
| rs573598488 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140593 | TCTCTTTTTTTTTAA[A/G]ATTAATTTATTTTTT | 55728 |
| rs573656871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088403 | ACATTCCCATCAGCA[A/G]CCATAAGTGATGTTG | 55728 |
| rs573659108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176142 | TTTGATGATTTTCCT[A/C]TCCAGCCTCTCTGCT | 55728 |
| rs573692053 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082704 | CCACAGGCTGTATTC[-/T]TTTTTTTTTTTTTTG | 55728 |
| rs573705168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074176 | GCTCACTGCAACTTC[C/T]GTCTCCTGGGTTCAT | 55728 |
| rs573711432 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150158 | AAGGAGTGTTAAAAT[C/T]GGAGATGAATTTTTT | 55728 |
| rs573716449 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099853 | TTACTGTCATGTAGA[-/T]TTTTTTTCATAGAAA | 55728 |
| rs573755192 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129177 | CTTCAGCCTCCCAAG[A/T]AGCTGGGACTACAGG | 55728 |
| rs573765275 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175277 | CCATATGTGCGTCAG[C/T]TTCCCAAAGTGCTAG | 55728 |
| rs573769449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073682 | CACTTCAGCCTCAAA[C/G]TGCTAGGCTCAAGCG | 55728 |
| rs573779966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081105 | GGAGGAAGTACAGAG[G/T]GAAGTCCATGATTCA | 55728 |
| rs573796517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139359 | GCCTCAGCCTTCCAA[A/C]GTGCTAGGGTTACAG | 55728 |
| rs573809495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138755 | TAATTCTATTCCATT[A/G]ATCTGTATGTCTGTC | 55728 |
| rs573833525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145635 | GAGAAGAAAACTCTT[A/C]AAGTATATAGAAGTG | 55728 |
| rs573841316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181755 | GAGTTCAAGACCAGC[C/T]TGGCCAACATGGTGA | 55728 |
| rs573849938 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106796 | TCAAGTGATCCACAA[A/C]ATGATAGTACTTGAA | 55728 |
| rs573860093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075648 | TGATTCGCCTGCCTC[A/G]GCTTCCCAAAGTGCT | 55728 |
| rs573871425 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110109 | GGCTTCTTTCACTTA[C/G]TATAATGTTTTCAAG | 55728 |
| rs573874922 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072163 | CACTGCAATCTCCGC[C/T]TTCCGGGTTCAAGTG | 55728 |
| rs573887639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147444 | ACACCTCCCAGACGG[G/T]GTGGTGGCCGGGCAG | 55728 |
| rs573890463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094325 | TTTTGCTGTTGTTGG[A/G]TGGAGTGTTCTGTAA | 55728 |
| rs573924872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153548 | AAAGTCAAAGATGAA[A/G]TATCTGTTGATGGAT | 55728 |
| rs573934997 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075085 | GTTAGCCATCCATAA[A/G]TATTTGTGCACCTGT | 55728 |
| rs573943742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082861 | ACCTGCCAGCATGCC[C/T]GGCTAATTTTTTGTA | 55728 |
| rs573968225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141356 | CCGGGCGGAGGGTCT[C/T]CTCACTTCTCAGACG | 55728 |
| rs573997094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133799 | GGAGTAGTCAACATA[C/T]ACTTTTTTGTGTGTG | 55728 |
| rs574002241 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127361 | TAGGTGGAACCACAG[A/G]CATGTGCCACCATGC | 55728 |
| rs574013266 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103466 | GACAATTTCAAAATT[A/G]TGAGCTATTGATGTA | 55728 |
| rs574128506 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054839 | GTTCTTCATTCCAGT[C/T]TCACTTTCAGAACTT | 55728 |
| rs574208773 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066033 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs574210703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069430 | AAAAAAATTCCCTTT[C/T]ATTTTTTTCCCTTCC | 55728 |
| rs574223726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096620 | AAATAGACTGAAGCG[A/G]CAAGGGTGGAAACCA | 55728 |
| rs574229267 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060900 | CCGAGCCATCACGCC[G/T]GGCCTGTTTTTCTAA | 55728 |
| rs574239973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110143 | CATCCATGTTGTAGC[A/G]TGTGTTTCATTCCTT | 55728 |
| rs574242380 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149586 | AATTTTATCTCAATT[-/A]AAAAAAATTGTAAGA | 55728 |
| rs574260500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103813 | GGCTGTGAGTGCCTT[A/C]ATCTGGGAGACAGGA | 55728 |
| rs574284452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160233 | GCAGGAAGTACATTA[A/G]TCAAAACATGTTTTT | 55728 |
| rs574302424 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109574 | AATACAAAAATTAAC[A/C]GGGCATGGTGGTGCA | 55728 |
| rs574364901 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141906 | GCCCGGCCAACACAG[C/T]GAAACCCCGTCTCCA | 55728 |
| rs574376179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177631 | AAAAAATAAAATAAA[C/T]AAGAAGAAAAAAAAT | 55728 |
| rs574380211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076015 | ATTTTTCACAGAGAT[A/G]TGTTCTCCCTATGTT | 55728 |
| rs574390594 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056321 | TGTTTGTTTTGTTTT[C/T]TGGGGCTCGGGAGAG | 55728 |
| rs574393807 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075355 | GGCTTTAACATTTAA[A/C]AACATGTCTCAGAGG | 55728 |
| rs574403916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067146 | CACTGCAGCCTTGAC[C/T]TCCCCAGACTCAAGC | 55728 |
| rs574414753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176810 | AGTTCATGCTGTTTG[C/T]AGCAGGGAGGAACCT | 55728 |
| rs574436986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105080 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCACGC | 55728 |
| rs574491553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062818 | TTCAGGTCTCAGCCT[A/G]GGTGGTAGCTCTAGG | 55728 |
| rs574492764 | snp | C/T | 0.00016536 | 0.00909136 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121518 | AGTTATGTGAGGATA[C/T]AGAGTTTGAGAATTT | 55728 |
| rs574511744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148491 | GAGGGGGAGGGGGAG[A/G]GGGAGAGGGAGTTCG | 55728 |
| rs574563536 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085629 | TGGCTAATTTTTAAA[-/T]TTTTTTGTAGAGGGA | 55728 |
| rs574594636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169763 | TGAGGTCAGGTGTTC[A/G]AGACCAGCGTGACCA | 55728 |
| rs574596169 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154346 | TTATTATAAATAATA[C/T]TCAATTATGAAACAA | 55728 |
| rs574661643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169396 | AAAAAAAAAAAAACC[G/T]TAAAAATAGAGATTT | 55728 |
| rs574668293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128034 | ACTCTTCCTTTTCAA[A/G]TAGAAGCTTCACTTT | 55728 |
| rs574743997 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149738 | CTCTACTAAAAATAC[-/A]AAAAAAAAATTAGCT | 55728 |
| rs574777686 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159883 | CACAGTTGTTGTTGT[A/T]TTTTTTTTGAGATGG | 55728 |
| rs574780102 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179160 | GATCACAAGGTCAGG[A/G]GATCGAGACCATCCT | 55728 |
| rs574805041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151705 | ATTTTGTGCACTGTG[A/T]ATACCTTTGTGAAGC | 55728 |
| rs574853075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175524 | TAATGTATTGTATTC[A/G]AAAGAAAAACAACTG | 55728 |
| rs574859508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077776 | CTTTTTTGATTGTTA[C/T]AGAGATCTGTTATTT | 55728 |
| rs574866634 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078489 | TTGACTTGCGTATGG[G/T]GGCATAGCAAACTTG | 55728 |
| rs574914300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071288 | ACTTCTTCCTCTATC[C/T]CCTATATTTATTTCC | 55728 |
| rs574946840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070475 | TTTTTTTGAGACAGG[G/T]TCTTGCTCTGTTGCC | 55728 |
| rs574971264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171502 | TGTGGCTGGGTGTTA[C/T]GGCTTGAATTATGTT | 55728 |
| rs574986102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142226 | CTTAAATTATCATCT[A/G]TAGTTTCAAAACTCA | 55728 |
| rs575009621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179752 | ATTTTAGAGTGGTAA[A/G]GCCTTTCTTTTTTTT | 55728 |
| rs575022867 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185618 | ATTATTTGGAAAAAA[A/C]CATTTTAATAGAAAT | 55728 |
| rs575030867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084843 | TCATCTTGAACTCCC[A/G]ACCTCAGGTGATCTG | 55728 |
| rs575040327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178893 | TTGCTTAAACCTGGC[C/T]GAGTTTTTGCAGCTG | 55728 |
| rs575083445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144169 | CCTGTTTGTCTTAGC[C/T]AGCCTCCAGCTGCCC | 55728 |
| rs575100288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168774 | TTGTTGCCCAAGCTG[G/T]AGTGCAATGGTGCAG | 55728 |
| rs575122658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150586 | TGAGGCAGAAGAATC[A/G]CTTGAACCCAGGAGT | 55728 |
| rs575128539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181084 | GAACCTGGGAGGCAG[A/G]GGTTGCAGTAATCTG | 55728 |
| rs575157766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150044 | CTGTGGTAGTCTGTA[A/G]TTACTGTCAGTCACC | 55728 |
| rs575346481 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078626 | GATTTCCTTGGCTCA[A/G]CTGATCCTCTCACCT | 55728 |
| rs575349433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087174 | ATTTATTGCACAGAT[A/C]AAATCTTCTGTGTTC | 55728 |
| rs575403441 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057650 | GTCCCTCAATGGGAC[C/T]CTTCTAGAGCCCCTC | 55728 |
| rs575410298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093890 | CAGGTGTGAGCCACC[A/G]CGCCCAGCTAATTTT | 55728 |
| rs575421401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093300 | AGTTTATTTGCCCTT[C/T]GTTTTCTGGGTTCTT | 55728 |
| rs575463444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100850 | CTCATGGTAGTATTT[A/G]AGGATTCAGTGAGGT | 55728 |
| rs575509170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174300 | GAGAATCACTTGAGC[C/T]TAGGAGATGGAGGCT | 55728 |
| rs575565140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065148 | GTGGGAAACAAATAA[C/T]TAGGTACAGGTGGAT | 55728 |
| rs575565524 | in-del | -/A | 0.00567442 | 0.0529623 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107073 | ATGAGTAATACAAAG[-/A]AAAAATTCACTTAGT | 55728 |
| rs575693201 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159238 | AGTCTACTGTTCTCT[C/G]CAGAGAGTTGTGGCT | 55728 |
| rs575715170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108039 | AGGGATTCTCATCCT[C/T]AGCCTCCCAGCCTGA | 55728 |
| rs575715326 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155682 | TACATAATTTTAACA[A/G]ATAGTTTTGTTGCTT | 55728 |
| rs575750101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071229 | TAGGTCTGTTGAGAC[A/G]ATTACATTTTGTATT | 55728 |
| rs575783909 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137629 | CAGACATGGAAGTGT[C/T]GTGAAGGAAGTTTAT | 55728 |
| rs575916413 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080325 | GTATATATATATATA[C/T]ACACACACACATATA | 55728 |
| rs575925586 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122886 | ACATATTTAGACTCA[-/T]GGAAAGGAATAACTT | 55728 |
| rs575929200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088520 | TTTTTTTTTTTTTGC[A/G]ATGGGGTTTCGCTCT | 55728 |
| rs575941799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095825 | GCTAGCAGAGAGATA[C/T]GTCATTGTAAGAACT | 55728 |
| rs575945675 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124046 | AGATTGAGTAAGAAT[A/G]GTTTACAGTTATACA | 55728 |
| rs576015623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074985 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 55728 |
| rs576023386 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093673 | CCAGGCTGGAGTGCA[A/G]TGGCACTGTCTTGGC | 55728 |
| rs576031614 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162837 | AAGCAGGAGAACTAG[A/G]GAAGCCAGTAGCATG | 55728 |
| rs576050110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123810 | TTAAGAAAATAATTA[G/T]AAACAGTGAGTTTTT | 55728 |
| rs576081708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082522 | GTCCTTAGGAAAATG[C/G]AAATCAAAACCACAG | 55728 |
| rs576089399 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152443 | TTTTGTATAGTAATT[-/G]GTTAGGTATCATTAA | 55728 |
| rs576097860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125969 | ACTATTTCTTACTTG[C/T]GATGACGTGAAGATG | 55728 |
| rs576112871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074265 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGCGATG | 55728 |
| rs576116867 | in-del | -/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185417 | AAGAAAACTTAGTAA[-/T]TGTGAATACCCTTTC | 55728 |
| rs576152216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068235 | CAACTTATCAGATGT[A/G]TGGTTTGCAAATATT | 55728 |
| rs576153779 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155545 | TTGTTTGGTTAGCTA[A/G]TAAATTCTGTTAGTA | 55728 |
| rs576162863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067206 | TGGAACCACAGGTGT[A/G]CACCACCACACCTAG | 55728 |
| rs576165498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125471 | AGACTGTAGCTGTTA[C/T]GGTTGCTCACTTCCA | 55728 |
| rs576200589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132769 | ATTTTGATCTTTAGT[C/T]TATTAATATATTTCA | 55728 |
| rs576218792 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175999 | GGAGGCTGAGCCAGG[A/T]GAATGGCGTGAACCC | 55728 |
| rs576219002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167231 | AGAGATCTAATTTGT[A/G]TATAATGGGAGTTCC | 55728 |
| rs576223749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081629 | CCAGCCTGGGTGACA[A/G]TGTGAGACTGTCTCA | 55728 |
| rs576229384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141379 | CTCAGACGGGGCAGC[C/T]GGGCAGAGACGCTCC | 55728 |
| rs576231572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182305 | ATCAGGCTAGAAAGA[C/G]AGGCAGATGCCACGT | 55728 |
| rs576269027 | snp | C/T | 1.6604e-05 | 0.00288127 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102511 | ACATTCAGTTTTGAA[C/T]GAGTCCAAGTGTTTT | 55728 |
| rs576300717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147518 | CCCCCACCTCCCGGA[C/T]GGGGCGGCTGGCCGG | 55728 |
| rs576334930 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110748 | TCACTGTGTTGGCCA[-/G]GATGGTCTCGAACTC | 55728 |
| rs576343927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127322 | TCCTGGGTTTAAGTG[A/T]GCCTCCTGTCTTAGA | 55728 |
| rs576356833 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140077 | GATTACAGGCGTGAG[A/C]CACCATGCCCAGCCT | 55728 |
| rs576382328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135380 | TGGTTCCAAGTCTTT[A/G]CTATTGTGAATAGTG | 55728 |
| rs576398436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091674 | ATAGTGGTGTGATCA[C/T]GGCTCACTGAAGCCT | 55728 |
| rs576457732 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061787 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAT | 55728 |
| rs576474734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176861 | AGAACCTGGGATTCA[A/T]ACTGCGTGCGGGAAG | 55728 |
| rs576484652 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127189 | CCACTGTGCCTGACC[A/G]GCTGCATCTTCTTCT | 55728 |
| rs576515393 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067408 | TATGTATGTACCACA[-/TT]TTTTTTTTTATCCAT | 55728 |
| rs576529251 | in-del | -/GCCTG | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085612 | CAGGCACGCCACCAT[-/GCCTG]GCTAATTTTTAAATT | 55728 |
| rs576539556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084046 | CTCACTGCAACCTCC[A/C]CCTCCTGGGTTCTCC | 55728 |
| rs576568188 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055686 | CAAAGGGAGGGGACG[A/G]AGGAAGTAAAAAACA | 55728 |
| rs576606050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083465 | GCATATGTACATAAA[A/C]TGTGTTATATCCGTA | 55728 |
| rs576610619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064039 | CTGAGCTCAAGTGAT[C/T]CTCCTGCTTCAGCCT | 55728 |
| rs576619426 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090372 | CAATTTGGGGAAGAA[C/T]TGACATATTTACTGT | 55728 |
| rs576620225 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111918 | ACCATGCCCAGCCAA[C/T]CCATACTTACTTAAT | 55728 |
| rs576624094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154105 | AATATTATATTAAGC[A/G]TAGGTACTTGGAATT | 55728 |
| rs576647305 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055141 | TCTAAAGTGGCATAT[A/G]TTACAGTTTTTAGTC | 55728 |
| rs576655413 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104326 | TTATCAGTTGGGTCT[C/G]TATTTGATCCTGGGT | 55728 |
| rs576656518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096871 | AAAGCAGGTTTGAAG[C/G]GGGTGATGAGGAGCT | 55728 |
| rs576697456 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151567 | ATGAGCCACTGTCCC[C/T]GGCCAATGTAAAACT | 55728 |
| rs576703649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170771 | GATCATTTCCTGTTC[A/G]ATAGCTCTATCAGGT | 55728 |
| rs576738050 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185664 | GTTTATGTGGTTTTT[A/T]AAAAAAGCAAAAAAC | 55728 |
| rs576782296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062572 | AACTTCTTTTTTTTT[C/T]TTTTTTGAGACTTCT | 55728 |
| rs576795699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107422 | TGGAGTCTCACTTTG[C/T]GCCCAGGCTGTAGTA | 55728 |
| rs576821149 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088696 | CTAGAAACGGGGTTT[A/C]TCCTTGTTGGTCAGG | 55728 |
| rs576858984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099216 | TGGTTTCACTTCAGC[C/T]TTTTCAACATTGTGT | 55728 |
| rs576939225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105100 | AGCCACCACGCCCAA[C/T]AATCCTGCGTTGTCT | 55728 |
| rs576968035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113085 | TTTAAATATTACTGT[A/G]TAGTATTTTCATCTT | 55728 |
| rs576999856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119286 | TCCTGCGAGAGTTGG[A/G]ACTTCGAGCACTCCT | 55728 |
| rs577006121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149049 | ACTGTGAAAAATTTC[A/G]CTAGTTCTTTGAAAG | 55728 |
| rs577025804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069497 | TTCTTTTTTCTTCTC[A/G]ACATGTAAGGACAGA | 55728 |
| rs577119377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111652 | GCAGAGTCTTACTCT[C/G]TTGCCCAGGCTGGAG | 55728 |
| rs577127780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085038 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55728 |
| rs577225008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071905 | TTTTTATTTTATTTT[A/G]TTTTATTTTTTGACT | 55728 |
| rs577257113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119531 | TAAATGAAGCTTCCT[C/G]GGTATCAGACCTATT | 55728 |
| rs577313366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122378 | GGGTTCTATTTTGTA[C/T]TTTTTTTTTTTCTGA | 55728 |
| rs577321876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180489 | GAGTGGATTTGGCAA[A/T]ATCTACTACAATAAA | 55728 |
| rs577349148 | snp | A/G | 0.000198857 | 0.00996939 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121623 | GAGGAACTTTAGAGA[A/G]TTCTAATTCTCCTGT | 55728 |
| rs577359671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065254 | TTGGAACTTGATCTT[A/G]AAAGCTATAGAGAGT | 55728 |
| rs577398373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078561 | TCAGGGTCTCGCTTT[A/G]TCGCCCAGGCTGGAG | 55728 |
| rs577431396 | in-del | -/TGTT | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106298 | TTGAATATTACAATA[-/TGTT]TGTTCTTTTATTTAT | 55728 |
| rs577466866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171684 | TTTATAAGGAGTATT[A/G]ACTCATATGATCACA | 55728 |
| rs577539864 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168353 | ACTTAGAGTGATAAA[G/T]AAGTATTTAAAGCAA | 55728 |
| rs577547712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124638 | AGGCATGAGCCACTG[C/T]GCCCAGCCAGTTCTT | 55728 |
| rs577548412 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107920 | TTGCAGTTGTTTCCT[A/G]TGTATCTTTTTTTTT | 55728 |
| rs577573188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182606 | AGGTGCACGCCACCA[G/T]GCCGGGCTAAAATTT | 55728 |
| rs577591748 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123938 | GAAATTTTTTTTTTT[A/T]AATGCAGTATTTTTA | 55728 |
| rs577622596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130688 | AACAATTTTATGTAG[A/C]GATAGGGTCTTGCTG | 55728 |
| rs577627639 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081773 | CTGAGGTCAGGAGTT[A/T]GAGACCAGCCTGGCC | 55728 |
| rs577627726 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116580 | AACATTTTAATTCTG[A/G]CACTTGCCTCCCTCT | 55728 |
| rs577648536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173718 | TCAAAGTCAAACTGT[G/T]TTCTCACTGCAGAGA | 55728 |
| rs577658008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181623 | CAGTTCAAGGTGGCT[G/T]CTCAAACTTAAGTAA | 55728 |
| rs577685660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181164 | CAAAAAAGAAAAAAA[A/T]ATATATACATTGGCC | 55728 |
| rs577735869 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094075 | GGTATATTTTCATTG[G/T]CATTCAATTTATTAT | 55728 |
| rs577747680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081034 | TTTAGATCTTTTTAC[A/G]TACAAATAGACACAG | 55728 |
| rs577776607 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099889 | CTTACGTTTGCTTTC[-/T]TTTTTTTCCCCCGTC | 55728 |
| rs577801437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060877 | CCCAAGTTGCTGGGA[A/T]TATGGGCCCGAGCCA | 55728 |
| rs577801911 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144879 | TGCAAATTCAGGAGA[C/G]TCTGAATATGCAGGC | 55728 |
| rs577804535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080507 | ACGCCCAGCTAATTT[A/T]TTGTATTTTAGTAAA | 55728 |
| rs577863990 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153743 | TAGTTAGACCAGAAC[A/G]TTATGTTGAGATTAA | 55728 |
| rs577891132 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101070 | AATCTTCAAGTCCCA[G/T]TTCACATATCACCTT | 55728 |
| rs577925794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096506 | GGCCATTTTAAGGGC[C/T]CTGGCTTTTGTCCTG | 55728 |
| rs577934842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166587 | CCAGCTACTTGGGAG[A/G]TTGAGGCAGGAGAAT | 55728 |
| rs577951009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128176 | TTAAAGAATTCCAGG[C/T]CAAAAGGGAAAACAT | 55728 |
| rs577980090 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059209 | TTTTTGATATGCAAA[G/T]CAGCAACCATTTATT | 55728 |
| rs577999024 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135520 | ATCCCTGAGGAATCG[C/T]CACACTGACTTCCAC | 55728 |
| rs578033631 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095907 | CCTTTTTACATCGTA[G/T]AAAGCTCAGTCTGGC | 55728 |
| rs578051670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074722 | TTCTTAAAGGCCAGT[A/C]TTGGCTGGGCATGGT | 55728 |
| rs578065965 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089843 | GGAGAGATTTTCCCC[-/T]TTTTTTCCTGAAAAT | 55728 |
| rs578066242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132881 | TTGATTTACTAATTC[A/T]TTGGTATTTTTACAA | 55728 |
| rs578115751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117339 | AGCCAGATTTGCCCA[A/G]CTGGCAAATGCATAT | 55728 |
| rs578145235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067027 | GTCCTCAAGATTCTT[C/T]CATGTTGCAGCATAT | 55728 |
| rs578213370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073627 | TAAATTGAGTCTTGC[C/T]GTATCACCTAAGCTG | 55728 |
| rs578227961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116375 | GCCTTTTCTGTGATT[A/G]TTCTTCTATTATAGA | 55728 |
| rs745311381 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126460 | GAATTTAATGTTAAA[A/G]TTGAAAAATATTTTA | 55728 |
| rs745315295 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108992 | CAGCTAGTTTTTGTA[A/T]TTTTAGTAGAGACAG | 55728 |
| rs745334946 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165562 | TTTTAAGAGAAAAAG[A/G]AGCAAGGTGCAAAAG | 55728 |
| rs745341415 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40141943 | AATAGGAAAACCAGT[-/C]CAGGCGTGGTGGCGC | 55728 |
| rs745356918 | snp | A/C | 3.31208e-05 | 0.00406931 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121605 | AAGAAATTATTAGCC[A/C]AAGAGGAACTTTAGA | 55728 |
| rs745401665 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151149 | ATCAACTAGAGAATA[G/T]TTTCAGAGCAATAAG | 55728 |
| rs745424930 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153655 | AAGATGTTATTTGGC[G/T]ACATTATCGAAAATG | 55728 |
| rs745449274 | snp | A/G | 1.79971e-05 | 0.0029997 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126106 | CATTTATTGTTGAGA[A/G]TATGACAGTATTTAT | 55728 |
| rs745466526 | in-del | -/AAAAACCAAAAA | 1.65839e-05 | 0.00287953 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120748 | GACAAAAACTCATTC[-/AAAAACCAAAAA]AACATTATGGGTGAC | 55728 |
| rs745475231 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058124 | AGAAAACAATGACTG[A/G]TTTGCAGCTGTATTA | 55728 |
| rs745488679 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095728 | AATCAATAGAGAAAT[A/C]ATTGAATGTGACACT | 55728 |
| rs745516458 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077744 | TAGGCGTGAGCCACC[A/G]CACTCAGCCAGAATA | 55728 |
| rs745522135 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133956 | GACTATAGACACGTG[C/T]CACCACGCCTGGCTA | 55728 |
| rs745535340 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154610 | GTATTTAAAGTGCTT[C/T]GAGACCTGATTCATG | 55728 |
| rs745585197 | snp | A/G | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121475 | GATATTATTTGGGCC[A/G]CAAGCCTTTTGTTGG | 55728 |
| rs745623755 | snp | A/G | 1.69663e-05 | 0.00291253 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122272 | TGAACTGGCTTTTCA[A/G]CTTAATGAATTATTT | 55728 |
| rs745631974 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104878 | GGTGCGATCTCGGCT[C/T]ACTGCAAGCTCCGCC | 55728 |
| rs745667862 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107045 | AACAGATAATCAGAT[C/T]CTGGGTAACGTTATG | 55728 |
| rs745716236 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182817 | AAGTAGCTGGGATTA[-/C]AGGCACCTGTCACCA | 55728 |
| rs745718400 | in-del | -/A | | | splice-acceptor-variant | N4BP2 | GRCh38.p7 | 4:40113429 | GTCTTTGTTGTATGT[-/A]AGTCTCAGAAACACA | 55728 |
| rs745721341 | snp | A/G | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102253 | TTCATTTTTGGACAT[A/G]CAGCTAACTGAAGAC | 55728 |
| rs745754782 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058973 | CTAGAGGCGAAAGCC[A/C]CTACGCCCGGCTAAT | 55728 |
| rs745765232 | snp | C/T | 1.66466e-05 | 0.00288496 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120295 | ATCACCTAGTACTTG[C/T]TGTAGTGAAAATAAT | 55728 |
| rs745771425 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085566 | GAGTCAAGTGATCCT[C/T]CTGCCTAAGCTTCCA | 55728 |
| rs745804294 | snp | A/T | 1.66275e-05 | 0.00288331 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106886 | ATGAAAATTATTTCA[A/T]TTATCTTTCACAGGA | 55728 |
| rs745806233 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060962 | TGTATTAGCTGCTTT[G/T]CTTTTCTTTTCTTCT | 55728 |
| rs745826189 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180659 | ATAGCACTGTTGGTA[A/G]TAGCAAAAAAGTGAA | 55728 |
| rs745864934 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132945 | TTTTTCTGTTCCTGG[A/G]CTATTTTTGTCAGAT | 55728 |
| rs745871037 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142729 | GTCTTTCCAGGACTT[C/T]GAGTACCCAGACTAT | 55728 |
| rs745872290 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088245 | TAAAGCTGCTGTAAA[C/T]ATTTGTTTACAGGTT | 55728 |
| rs745902465 | snp | A/G | 8.31317e-05 | 0.00644662 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121889 | AAAGCTACTACTCCT[A/G]AAGATATGAGTGAAA | 55728 |
| rs745905397 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105444 | ATTCTCCAGCCTCGG[C/T]CTCCTGAGTAGCTGG | 55728 |
| rs745927340 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103012 | AACCACAGCTGCACA[C/G]TGGAGATCTGTCAAC | 55728 |
| rs746008741 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128007 | AACTTATGAGTTTGA[A/G]TTAAAAAAATTACTC | 55728 |
| rs746018308 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145146 | ATATTTCTTGGATTT[C/T]AATTTTTCAGTAGAT | 55728 |
| rs746036223 | snp | C/T | 1.65531e-05 | 0.00287686 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154178 | TTAAAATAACTCTTT[C/T]CTCATTTCTGCAGGT | 55728 |
| rs746046604 | snp | A/G/T | 0.000100022 | 0.00707122 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121254 | CAGGAAGATTAGATG[A/G/T]ATTTAAGCCGAAAGT | 55728 |
| rs746070276 | in-del | -/AAAAAAAAAAA | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155399 | AAGACTCCGTCTCCA[-/AAAAAAAAAAA]GAAAAAAAAGAGAAA | 55728 |
| rs746076947 | snp | C/T | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112127 | TCCTATAATTATAGA[C/T]AATACAAACCTACAG | 55728 |
| rs746102532 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169567 | ATAAACTTTGTAAAG[A/G]AAAAAAGGGAAACTC | 55728 |
| rs746106756 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184585 | TATCTCCAATTTTAC[C/T]ATTCAGAGACAGTCA | 55728 |
| rs746130072 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147389 | ctattccacaaaacc[A/G]ccattgtcatcatgg | 55728 |
| rs746157362 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131908 | TCTGGTGGACATTTT[C/G]AAGGACCACAAGTGA | 55728 |
| rs746162688 | in-del | -/TC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183820 | CAGGCTTCTGCTGTG[-/TC]TCTCTGCAGTTTTTT | 55728 |
| rs746217206 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174329 | CTGCAGTGAGCCGTG[A/G]TCATTTAAAGAAATT | 55728 |
| rs746217423 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113477 | CGGGAACCAGACACA[C/T]GGTGGAAGTTTAAAC | 55728 |
| rs746239195 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142224 | CTCTTAAATTATCAT[C/T]TGTAGTTTCAAAACT | 55728 |
| rs746243449 | snp | C/G | 1.6546e-05 | 0.00287624 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144772 | AGCTCTAGAACATTT[C/G]ATGAGAGTTTTAGAG | 55728 |
| rs746249977 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170877 | CATTTTGCTCAATGA[C/T]GTATTTTCTATTTTG | 55728 |
| rs746269672 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118698 | CCACTCAAATCACTT[C/G]TTAATTTCCTTAAGT | 55728 |
| rs746272468 | snp | C/T | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102540 | TTATAAAGGATAACA[C/T]ATTGGCTTTGGAAAG | 55728 |
| rs746358055 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103671 | TGTGATTTGAAGGAA[A/G]AGAGTATAGGATGAC | 55728 |
| rs746402300 | snp | C/G | 1.64925e-05 | 0.00287158 | utr-variant-5-prime, missense, intron-variant | N4BP2 | GRCh38.p7 | 4:40097536 | CTGGATCCTGATGTA[C/G]TGTATTTGATGCTTT | 55728 |
| rs746430629 | snp | A/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144697 | AGAGATCTTTGAGAA[A/T]GTCAATGCTTCGCTG | 55728 |
| rs746466881 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143759 | AATGTTGAAGGTGAA[C/T]GCCAAGATGAGACCC | 55728 |
| rs746468914 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123354 | TTGAATTTTGACTTT[A/G]AGAGAGAATGAACTT | 55728 |
| rs746476620 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178970 | GTCTTTGTGGTTGCC[A/G]ATTTTTCATTTTTAT | 55728 |
| rs746488067 | snp | A/G | 3.30087e-05 | 0.00406242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126084 | AGTGAATAATGTTTA[A/G]TTTATACATTTATTG | 55728 |
| rs746498835 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075816 | GTTATAACAGATAGA[G/T]ACATATTTCTTTTTT | 55728 |
| rs746509205 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069536 | ACATAACCTTTGAAA[C/T]ATGGAGTGTGCCCTG | 55728 |
| rs746510287 | snp | A/C | 1.66446e-05 | 0.00288479 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121290 | ATATTAACACAAAAT[A/C]AGACGTTCAAGAAGC | 55728 |
| rs746522648 | snp | A/C/G | 3.31919e-05 | 0.0040737 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102531 | CCAAGTGTTTTATAA[A/C/G]GGATAACACATTGGC | 55728 |
| rs746556820 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125160 | ACCTGTGCTCATGTC[A/G]TAGCCTCAAGAGCTA | 55728 |
| rs746575092 | in-del | -/ATGAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151193 | GTGATAATCGTATAA[-/ATGAC]ATGACTGACCTAAGT | 55728 |
| rs746591107 | snp | C/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055122 | TTACTAGGGTTCTTT[C/G]ATTTCTAAAGTGGCA | 55728 |
| rs746592433 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163971 | CCTGGTCTTTTATCA[A/G]TTAAGTGACTTTTCT | 55728 |
| rs746594751 | snp | A/C | 1.66048e-05 | 0.00288134 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144663 | AGAAGATGAAAGAAG[A/C]CAATCACCTTGCTGC | 55728 |
| rs746617881 | snp | A/G | 1.65658e-05 | 0.00287795 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120665 | AGTGTAGAGGATGGC[A/G]GAAAGTCACAGTGTG | 55728 |
| rs746624523 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070769 | TGCTACTTATACTAT[A/G]TTCAGATTTCCTGAG | 55728 |
| rs746636783 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100782 | TGTGACTTGGGTCAA[A/G]TTAATGTACTTTTTA | 55728 |
| rs746656587 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104275 | TTTTTTTTTTTTTTT[-/C]CCTTTTTCCAAATTT | 55728 |
| rs746669638 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108591 | AGTGCTGGGATTACA[C/G]GCATGAGCCACTACG | 55728 |
| rs746682333 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152007 | TTTTGTTATTCTGCT[A/G]CAGCTTTTATTAGTT | 55728 |
| rs746687887 | snp | A/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113461 | ATATAAAGTCCTTTT[A/T]CGGGAACCAGACACA | 55728 |
| rs746714430 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056314 | GACCTTGTGTTTGTT[G/T]TGTTTTTTGGGGCTC | 55728 |
| rs746715802 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113984 | TGCTACTGGGAGGGG[C/T]GAATTGTCGTAGCTG | 55728 |
| rs746733649 | snp | A/T | 1.65965e-05 | 0.00288062 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123245 | TATAAAGAGCTCCTT[A/T]TTTGTCCATTTTGAA | 55728 |
| rs746781370 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129425 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 55728 |
| rs746792341 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170719 | TGTTGACTACCTTTT[C/T]TCAGCTGTATCTTTT | 55728 |
| rs746794287 | snp | A/G | 1.73637e-05 | 0.00294644 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137130 | TAGATAATTGCATAT[A/G]AAAATATAATTGGTT | 55728 |
| rs746797710 | snp | A/C/T | 6.6125e-05 | 0.00574969 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103120 | TCAAGTACAAGAAAC[A/C/T]CCAGTTTCTCAGGTT | 55728 |
| rs746804404 | snp | A/G | 1.66477e-05 | 0.00288506 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120287 | GAGAGAGTATCACCT[A/G]GTACTTGCTGTAGTG | 55728 |
| rs746838842 | snp | A/G | 1.67882e-05 | 0.00289721 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106863 | GAGAAAATTTAGAAG[A/G]AAAGGTAATGAAAAT | 55728 |
| rs746849215 | snp | A/G | 0.00017943 | 0.0094701 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097591 | AAAAGTTTAGTTTGA[A/G]CCCTGTCCATCTTAT | 55728 |
| rs746856101 | in-del | -/GT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077142 | TTATGTAGAATATAT[-/GT]ATGTGTGTGTGTGTG | 55728 |
| rs746885176 | snp | A/G | 1.65575e-05 | 0.00287724 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121455 | TATATGAGAGGTGCA[A/G]TAAAGATATTATTTG | 55728 |
| rs746907415 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082240 | GAGATGGCGCCACTG[C/T]ACTCCAGCCTGGGCG | 55728 |
| rs746919428 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100202 | TTGTTGAAAGTGTCA[C/T]AGCCAGCAGTAGAGA | 55728 |
| rs746925388 | snp | C/G | 5.02382e-05 | 0.00501164 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120088 | TAATGCAGATTTAAA[C/G]AAAAGAAGAAAAGAA | 55728 |
| rs746934179 | snp | A/C | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055803 | CATTTCACATCAGAA[A/C]CCAGAACAAATAAAC | 55728 |
| rs746936326 | snp | A/C | 1.66907e-05 | 0.00288879 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120199 | ACTACAGGCAACAGA[A/C]AAAAGTGAAAACGAG | 55728 |
| rs746961919 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084098 | TGGGATTACAGGCAT[G/T]CGCCACCACTCCCAA | 55728 |
| rs746984452 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077913 | TAAAATTGGAATGAT[-/A]ACAGAGAAGATGAGC | 55728 |
| rs746999365 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177953 | TGAAATGAGAGCAAC[A/G]GAAAACAGAAAGATG | 55728 |
| rs747011101 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083690 | GAGAGGGAGGAATGG[A/G]AATGGTTACTAATGG | 55728 |
| rs747027921 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068048 | TCTATCTCATTGTGG[A/T]TTTAATTTGTATTTC | 55728 |
| rs747046684 | snp | A/G | 5.34707e-05 | 0.00517035 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118062 | CAAAATTCAATTTGA[A/G]ATATAATTTTTAAAA | 55728 |
| rs747052585 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118590 | AGAGTTTTGTGAGTC[C/T]GTGATTATGCTATGA | 55728 |
| rs747081148 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160291 | TAATATAGGATATAT[A/G]TACAGATGGTCTCCC | 55728 |
| rs747106589 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086274 | CCAGGAGTTTGAGAC[A/C]AGCCTGGACAACATT | 55728 |
| rs747106713 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103507 | AGAGCTAATTTGAGT[A/G]GGAGAAAGATGAGTT | 55728 |
| rs747175265 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145596 | GAAACTTTAAGAGCC[A/G]TTTAAATTATTATTT | 55728 |
| rs747196174 | snp | A/C | 4.97203e-05 | 0.00498575 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121075 | ACCAACTGTTTCTGG[A/C]GTAGTAGAACCACAA | 55728 |
| rs747203550 | snp | C/T | 3.3168e-05 | 0.00407221 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120932 | CAAAAACTAAAGACA[C/T]TGGGTAGCTCCAATC | 55728 |
| rs747209713 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168798 | GGTGCAGTCTTGGCT[A/T]ACTGCAACCTCCACC | 55728 |
| rs747239831 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126843 | GCTCACTGCAACCTC[C/T]ATCTTTCGGGTTCAA | 55728 |
| rs747242166 | in-del | -/CAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125886 | AGCAAGACTCCGTCT[-/CAA]AAAAAAAAAAAAAAA | 55728 |
| rs747257070 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073146 | TGTTCCTTATACATT[G/T]AGTAGCTAGCCACCT | 55728 |
| rs747258669 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117981 | CCAGAGAAAATTGAA[C/T]GTATTGAGTTGTGTG | 55728 |
| rs747259299 | snp | C/T | 0.000115337 | 0.00759312 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152857 | CAGGGAGGAGTTGCT[C/T]GCATCAAACCAGCTG | 55728 |
| rs747294580 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088818 | TTAGAGTTTTAATTC[A/G]CACTTACTTAATGGT | 55728 |
| rs747297691 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162058 | TGAGCCGTACCAGTG[A/G]ATAGATGGCCTCCAC | 55728 |
| rs747304347 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094941 | CGGGACTACAGGTTA[C/G]TTCTTTTTGTATTTT | 55728 |
| rs747337964 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153283 | ATAATTAGGTAATAT[G/T]TATCATACTTTAAGA | 55728 |
| rs747345914 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065396 | ACTGGAGTCACACAG[C/G]CATTGAAGCCATGGG | 55728 |
| rs747353676 | snp | G/T | 1.66208e-05 | 0.00288273 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120565 | ACAAAGCGACAAAAA[G/T]TATAATTACCCTCAG | 55728 |
| rs747364259 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186202 | TCTAAATATGATCCT[A/G]TGTAAGCTGAGTAAT | 55728 |
| rs747365503 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095413 | GGCCTGATCCTTTAT[C/T]ATTACACAGTGCCTT | 55728 |
| rs747384116 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133698 | GGACCCCATTCCCAA[C/G]ATACCTCATTATGTA | 55728 |
| rs747395304 | snp | A/T | 1.73255e-05 | 0.0029432 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142887 | AAACTGATTATATAT[A/T]TTTTGTCAGTTATAA | 55728 |
| rs747453798 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172608 | GGAACAGCTGCCTCC[C/T]TTGCAGCCCTCAGAA | 55728 |
| rs747474458 | snp | C/T | 1.65436e-05 | 0.00287602 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121753 | CACTCCTGAAAACCA[C/T]GAATCGATGACAAGT | 55728 |
| rs747551757 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098471 | ACAGAAGGGAGTTTA[C/T]ATAAGTTGGCTAGAT | 55728 |
| rs747582718 | snp | C/T | 3.30415e-05 | 0.00406444 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121861 | CAGTAAGCAGTCCTT[C/T]CCAGGTATTCTAAAA | 55728 |
| rs747621702 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157337 | GGACATATTATATAG[C/T]AGAAATTTTGACTTT | 55728 |
| rs747625690 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137766 | GCAAAAGCCTGTATT[C/T]TGGTTTCTATGGGAA | 55728 |
| rs747626790 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100429 | TCGCCCAGGCTGGAG[C/T]GCAGTAATCACTTTC | 55728 |
| rs747632475 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081147 | TAATAATGATTTTTT[C/G]CTGATTATGGAAAAA | 55728 |
| rs747632901 | snp | A/G | 1.67964e-05 | 0.00289792 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144649 | TACTCTTCATGAGCA[A/G]AAGATGAAAGAAGCC | 55728 |
| rs747663183 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123111 | ACATTTTCTTCCCTC[C/T]CCCTTCCCCCACAAG | 55728 |
| rs747664097 | snp | A/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120740 | AAAAATATTGACAAA[A/T]ACTCATTCAACATTA | 55728 |
| rs747689257 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112184 | TTTGGTTAGTACCAT[A/G]AGTTGTCATAAGTTT | 55728 |
| rs747707819 | snp | G/T | 1.6625e-05 | 0.00288309 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102405 | CTGATTCAAGTAATA[G/T]GACTCCCATTTTTTC | 55728 |
| rs747713223 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139012 | AATATGTAGACCAAT[A/T]AACAATATTAAGTCT | 55728 |
| rs747714502 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157484 | TAGACATGTATAATA[C/T]TGAGATCGGTTATTT | 55728 |
| rs747751904 | snp | G/T | | | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121445 | CTGAAAGACTTATAT[G/T]AGAGGTGCAATAAAG | 55728 |
| rs747766045 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121839 | GCCAGGAAGAACTTT[C/T]ATATAGCAGTAAGCA | 55728 |
| rs747771049 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127385 | ACCATGCCTGGCTAC[A/T]TTTATTTTTTGTAGA | 55728 |
| rs747814919 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129079 | TTTTTTGAGACACAG[C/T]CTGGCTTTGTTACAG | 55728 |
| rs747820488 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178774 | TTTCAATATGAGCAC[A/G]CATTTGCCTTCCATG | 55728 |
| rs747834309 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122771 | GTACGGATGAACCTT[C/T]TAAAATCCTTTGGTG | 55728 |
| rs747848577 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162823 | ACCAGGCCATCTGCA[A/G]GCAGGAGAACTAGGG | 55728 |
| rs747854473 | snp | A/C | 1.66374e-05 | 0.00288417 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120552 | AAACTTCATCCGTAC[A/C]AAGCGACAAAAAGTA | 55728 |
| rs747862512 | snp | A/C | 1.67083e-05 | 0.00289031 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142864 | TTATGCCCAGCAGGT[A/C]AAGTGGAAAACTGAT | 55728 |
| rs747880625 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069413 | GAGTGAGACTGTTTT[A/T]AAAAAAAATTCCCTT | 55728 |
| rs747891816 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127821 | GCCTGCCACCGCGCC[C/G]GGCTAATTTTTTGTA | 55728 |
| rs747904738 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058319 | TGTGTTTTGATAAAC[A/G]TGGTTCCATCTGCCT | 55728 |
| rs747946850 | snp | A/G | 8.34341e-05 | 0.00645834 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120046 | AACCAAAGAAACAAT[A/G]TTACCTGAGAATGTT | 55728 |
| rs747971536 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082097 | AGCTTGGGCAACGAG[C/T]GAAACTCCATCTCAA | 55728 |
| rs747981970 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074749 | TGGTGCCTCACGCCT[A/G]TAATCCCAGCACTTT | 55728 |
| rs747988836 | snp | C/T | 9.93641e-05 | 0.00704785 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123239 | TCTTTTTATAAAGAG[C/T]TCCTTTTTTGTCCAT | 55728 |
| rs747997505 | snp | A/C/G | 5.01847e-05 | 0.00500902 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120170 | CACATGTATTTTTCT[A/C/G]ACTCTGAAAGCAAAC | 55728 |
| rs748050254 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080154 | TACAAGGTTGTTTAA[A/G]CTAATGTATTAATAA | 55728 |
| rs748071836 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121102 | ACAAACGTTAGCTGA[A/G]TGTCAAGAGCAAATG | 55728 |
| rs748076904 | snp | C/T | 1.65441e-05 | 0.00287607 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154196 | CATTTCTGCAGGTTC[C/T]CTGAAATTAAACCAG | 55728 |
| rs748110264 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156328 | GAGGTGTGGTATTCC[A/G]TGGGCAGAAGTCAAA | 55728 |
| rs748112633 | snp | A/G/T | 9.8841e-05 | 0.00702935 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097429 | CCAGTGTTGCTAGTC[A/G/T]TGAGGAGCCAACCAC | 55728 |
| rs748197458 | snp | C/T | 3.31257e-05 | 0.00406962 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152761 | TGAATTTTAACTCCC[C/T]TGATTTCTGTTGTAA | 55728 |
| rs748213384 | snp | A/G | 1.67214e-05 | 0.00289144 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117876 | ATTTTCAGGCGTAAC[A/G]TTCATGGGGTAAGCA | 55728 |
| rs748214472 | in-del | -/AGCT | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057797 | TTCCCTCCGAAAGAG[-/AGCT]AGAGTAATAGAATGT | 55728 |
| rs748214742 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133493 | GGCGCACACCACTAC[G/T]CCTGGCTAATTTTTG | 55728 |
| rs748215519 | snp | C/T | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120924 | CAAGCTCTCAAAAAC[C/T]AAAGACATTGGGTAG | 55728 |
| rs748260075 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063635 | TATTTATTTTTAATT[A/T]AATTAATTAATTAAT | 55728 |
| rs748268660 | snp | A/G | 3.30028e-05 | 0.00406205 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117963 | ATTATGAGTTCTTCG[A/G]TTCCAGAGAAAATTG | 55728 |
| rs748282972 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159164 | CCACATTCTCTGACT[A/C]CTAATATGGAGCAGC | 55728 |
| rs748306834 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100459 | CACTAGAGGCTCACT[G/T]TAGCCTCGACCTCAT | 55728 |
| rs748319724 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162891 | CAGAGCCAGGGAAGC[C/T]GATGGTATCTTTCAG | 55728 |
| rs748377130 | snp | A/G | 1.65897e-05 | 0.00288003 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120808 | GGAACACAGATCAAG[A/G]ATGCCAAAGACTGGT | 55728 |
| rs748393801 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079900 | ATTAGATTTTACATC[A/T]GGTTAAAATTATATA | 55728 |
| rs748402614 | snp | A/G/T | 8.31987e-05 | 0.00644928 | missense, stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102131 | GATACCAAGATAGAA[A/G/T]AATCATCTTCACAAA | 55728 |
| rs748407660 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165341 | GCAACCTCTGCTTCC[C/T]GGGCTCAAGCAATCC | 55728 |
| rs748411132 | in-del | -/TTTTATTTTATTTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134936 | TTTCTTTCTTTTTTA[-/TTTTATTTTATTTTA]TTTTATTTTATTTTA | 55728 |
| rs748432614 | snp | A/C/G | 1.64735e-05 | 0.00286993 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124142 | TTTGCCAATCTCTTG[A/C/G]CTGGCTTTTGTGTTT | 55728 |
| rs748438146 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136067 | ATAATATAGTATCAC[C/T]GTCAAGATATGACTG | 55728 |
| rs748451260 | in-del | -/CTA | 1.65999e-05 | 0.00288091 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120882 | ATGAAATATCCTTAT[-/CTA]CAGCACATGAGGCCT | 55728 |
| rs748456941 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102881 | GTGAGTTACTGCCCG[C/G]TACTTGCTCCTCTCC | 55728 |
| rs748494225 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088059 | CACCACGCCCGGCTA[A/C]GACTGGCTTTTACTG | 55728 |
| rs748533205 | snp | A/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054647 | AATGAGAACGAGCAT[A/G]ATAACCAAAACCTTT | 55728 |
| rs748534332 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091119 | TTTATCTTGTATCTT[A/G]CACCCTTGTTAAACT | 55728 |
| rs748538737 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184809 | GAAAACACAAAAATT[A/G]TCTGGGCGTGGTGGC | 55728 |
| rs748590826 | in-del | -/G | 1.65577e-05 | 0.00287725 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131832 | TGTTTGAAAAAGATT[-/G]TGCCACTAAACTAAA | 55728 |
| rs748621477 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152849 | ACCACAGCCAGGGAG[G/T]AGTTGCTCGCATCAA | 55728 |
| rs748622286 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093838 | CTCCTGACCTCAGGC[A/G]ATCCACCCACCTCGG | 55728 |
| rs748623848 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149113 | TTCTGCCCCTAACTA[C/T]GTACCCAAGAGAAAT | 55728 |
| rs748665473 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150795 | TCAATCAAATAGAAT[A/G]TATAGACTTATTTCA | 55728 |
| rs748675972 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111467 | TTGGGACTACAGGTG[C/T]GTGCCACCACACCTG | 55728 |
| rs748706503 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154936 | AGAGAAAAAGAAATG[G/T]TTAAATATCTTCCAG | 55728 |
| rs748711667 | snp | C/T | 6.58924e-05 | 0.0057395 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102807 | ATGTGTTTCTACCTT[C/T]CGAAGGGTTCAACTT | 55728 |
| rs748721208 | snp | G/T | 2.87691e-05 | 0.00379259 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126359 | TAAATATTAAGCTAC[G/T]GTCTCTGATTCTGGT | 55728 |
| rs748731332 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072730 | TTATTTTTGTGGGAC[-/T]TTTTTTTTTTTTTGG | 55728 |
| rs748771622 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127130 | TCTGGGGTCAGTGAT[A/T]CACCTGCCTTGCCCT | 55728 |
| rs748785574 | snp | A/G | 6.714e-05 | 0.00579357 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120413 | ACGAAAAAAGCCTTT[A/G]GGAAACAAAAAAGCA | 55728 |
| rs748794269 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135940 | GGAAGAGGTGAGAGA[C/T]ATAAATAGTGTGAAA | 55728 |
| rs748825641 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097116 | TTGACTACTTTTTAG[C/T]TCTGCTGTTAGAGTT | 55728 |
| rs748839067 | snp | C/T | 3.32105e-05 | 0.00407482 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107066 | TAACGTTATGAGTAA[C/T]ACAAAGAAAAAATTC | 55728 |
| rs748893657 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122971 | AACATAGCATATAAC[-/AT]AAATAGAAATACTCT | 55728 |
| rs748903374 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079871 | TTATGATGATAATCA[G/T]TGAGCAAGTATTGAT | 55728 |
| rs748942859 | snp | A/C | 3.33e-05 | 0.00408031 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120308 | TGCTGTAGTGAAAAT[A/C]ATCAAGAAGACTGTG | 55728 |
| rs748959807 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40154065 | TTGGATATTGACTTA[-/AT]ATAAGGGTCAATACT | 55728 |
| rs748962363 | in-del | -/ACGTTATGAGTAAT | 1.656e-05 | 0.00287745 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107053 | ATCAGATTCTGGGTA[-/ACGTTATGAGTAAT]ACAAAGAAAAAATTC | 55728 |
| rs748975448 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121727 | TCAGAGCAGGCGGAA[A/G]TGAGAGCTGTCACTC | 55728 |
| rs748989613 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176689 | AATTATTCAAGCTCC[C/G]TGTGCTAGAATTCAC | 55728 |
| rs749001613 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081757 | GAGACGGGTGGATTA[C/T]CTGAGGTCAGGAGTT | 55728 |
| rs749006510 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125100 | ACACTGGGACCAAGG[C/G]AAGGAGTTTCACCTT | 55728 |
| rs749045255 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145434 | TTACCATGTTGGCCA[A/G]GCTGGTCTTGAACTC | 55728 |
| rs749058383 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078080 | TACCTTTTTGAATTG[G/T]ATTTTAAAGCTTCTG | 55728 |
| rs749068187 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071370 | TTTGGAAGAGTATCT[C/G]ATTTAGTAATGCTGT | 55728 |
| rs749072655 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180879 | ACTGTAGGCCAGGCA[C/T]GGTGGCTCACACCTG | 55728 |
| rs749080566 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110972 | ATTAATTTCCTGTAT[A/G]GTCTAATTCCTTTGG | 55728 |
| rs749114534 | snp | C/T | 3.30442e-05 | 0.0040646 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142840 | AGGGAAAAAAAATGT[C/T]GCCACCTTTTATGCC | 55728 |
| rs749115601 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152879 | AACCAGCTGTCATTA[A/G]GTACCTCATAAGCCA | 55728 |
| rs749159677 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165872 | TCCATTCTTATATTC[C/T]GTAGATACCCCAAAG | 55728 |
| rs749163834 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181702 | CTGTTAGTCCCAGCA[C/G]TTTGGGAGGCTAAGG | 55728 |
| rs749169862 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163701 | TGTAGAGAAGAAAAA[-/C]CCTCTGTTCTTGATG | 55728 |
| rs749177686 | snp | C/T | 3.46428e-05 | 0.00416176 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122296 | ATTATTTGGTCCTGT[C/T]GGTATTGATTCAGGT | 55728 |
| rs749199515 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057334 | GTGCCTGGCGGGCCT[C/T]CAGGCCCCAGACACA | 55728 |
| rs749207386 | in-del | -/AA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109819 | CTGCTTTGTTAAGAC[-/AA]AATTCATGTGCCATA | 55728 |
| rs749209325 | snp | C/T | 1.65203e-05 | 0.002874 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102284 | CTGGATTCCTTAATA[C/T]AGAATGCTTTTGAGA | 55728 |
| rs749223108 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072999 | GTGTTGGGATTACAG[A/G]TGTGAGCCACCGCAC | 55728 |
| rs749231306 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110415 | ACACTTGTTATTGTC[C/T]GTTTTTTTGATTATT | 55728 |
| rs749249177 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166756 | AAAATTTTGTGGGTA[C/T]ATTGTAGGTGTATAC | 55728 |
| rs749287457 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058277 | AACTAAAAGACGCGC[C/T]TTAGGAAATGTAAAC | 55728 |
| rs749304241 | snp | C/T | 1.66059e-05 | 0.00288144 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123079 | TGTTTTCTGCAAATA[C/T]ATAATGAGTAATGAT | 55728 |
| rs749307220 | in-del | -/A | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079987 | TGTTTTGAGGATGGG[-/A]GGGGGGGATATATTT | 55728 |
| rs749324357 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148475 | ACTGTGGGGAGAGGG[A/G]GAGGGGGAGGGGGAG | 55728 |
| rs749330979 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151676 | GTAAAAAGGTTTTAC[A/T]CTATATACCTAGAAT | 55728 |
| rs749348467 | snp | A/G | 0.000132701 | 0.00814449 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122146 | AATTCTAATGGCAGG[A/G]AGTAGTTTATCAGCT | 55728 |
| rs749380044 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064722 | AATCATGCTTTGAGA[C/T]AGTGGGAAACTTTCC | 55728 |
| rs749384999 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162717 | GTAGCTTATTGGTGT[A/G]TGTATTAGGGTTCTC | 55728 |
| rs749385417 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061229 | GGCTGGAGTGCAGTG[A/G]CATAATCTTGGCTCA | 55728 |
| rs749415290 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131630 | AAAATGAGATATAAA[C/T]AAATAGTGCAAGAGT | 55728 |
| rs749416043 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076213 | AGGTGCGGTGGCTCC[G/T]GCCTGTAATCCCAGT | 55728 |
| rs749421803 | in-del | -/C | 1.65806e-05 | 0.00287924 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121155 | AAGTAGGCATGTGCA[-/C]CCAGACTGAACCACA | 55728 |
| rs749436804 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114064 | GGTAGCAAATATCCA[G/T]CTGTCCAGATATCTC | 55728 |
| rs749446441 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137002 | GAAGGGGACCCTGTA[A/G]AAACAGTTGTAGCCC | 55728 |
| rs749498973 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061821 | AGGCACCTGCCACCA[C/T]GCTTGGCTAATTTTA | 55728 |
| rs749522234 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157802 | GTAGAATGTATGTTC[A/G]TGGTGCTTATTTTTA | 55728 |
| rs749523920 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172307 | GCCTACCCAGATTGA[A/G]GGTGAGTCTGCCTTT | 55728 |
| rs749531149 | snp | C/T | 3.43265e-05 | 0.00414271 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137125 | AAGGGTAGATAATTG[C/T]ATATAAAAATATAAT | 55728 |
| rs749543853 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084615 | CAAATTTTGTGTGTG[-/TA]TATATATATATATAA | 55728 |
| rs749544300 | snp | A/G | 4.95258e-05 | 0.00497599 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103109 | ACAAGTGCTTATCAA[A/G]TACAAGAAACCCCAG | 55728 |
| rs749545039 | snp | A/G | 1.64741e-05 | 0.00286998 | utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097433 | TGTTGCTAGTCGTGA[A/G]GAGCCAACCACTACT | 55728 |
| rs749577478 | snp | C/T | 1.76905e-05 | 0.00297404 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121990 | TAACTTTGTATCTAG[C/T]ACTTCAAATCTTGAA | 55728 |
| rs749582480 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177551 | AACCCCGGAGGCAGA[A/G]ATTGCAGTGAGCTGA | 55728 |
| rs749615344 | snp | A/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117934 | ATTATCAACGTTTTG[A/T]TTCAGTGCCAATAAT | 55728 |
| rs749629431 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161482 | GTGGACCTTTTTTGG[G/T]TACTGGTTCAGCAGA | 55728 |
| rs749666343 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102791 | TCTACTCGGGTCTCT[C/G]ATGTGTTTCTACCTT | 55728 |
| rs749669817 | snp | C/T | 3.29636e-05 | 0.00405964 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102667 | TTTAGAATCTGAGTG[C/T]GTTGAGGCTCAATTC | 55728 |
| rs749672204 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162677 | GGTTTTACTCAATGG[C/T]AAATAATACACATTA | 55728 |
| rs749679470 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105782 | TCTCAAACTCCTGGG[C/T]TCAAGCAGTCTTCCC | 55728 |
| rs749682385 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094141 | CATGGATTATTTAGA[-/T]GTATATTGCTTGGAA | 55728 |
| rs749729734 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089244 | GTGCTAGGTTTACAG[A/G]CATGAGCCACCATGC | 55728 |
| rs749750843 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072770 | TCTCTCTGTTGCCCA[C/T]GCTGGACTGCAATGG | 55728 |
| rs749754675 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171553 | AAGTCCTAACCCCCA[A/G]TACTCCTGAATGTGA | 55728 |
| rs749755513 | snp | A/G | 3.32906e-05 | 0.00407973 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144785 | TTGATGAGAGTTTTA[A/G]AGAAGAAGACTGAAG | 55728 |
| rs749756991 | in-del | -/T | 0.000100138 | 0.00707523 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137098 | GTATGGAGTTACTAA[-/T]TTTTTTTCTACAAGG | 55728 |
| rs749757133 | snp | C/G | 1.65897e-05 | 0.00288003 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120788 | TCTGATTCTTTAGCT[C/G]AGAGGGAACACAGAT | 55728 |
| rs749787563 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107313 | ACTCCTGGGCTCAAG[C/T]AATCTGCCTCTCTTA | 55728 |
| rs749818029 | snp | A/G/T | 6.72104e-05 | 0.00579666 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117871 | CTGGAATTTTCAGGC[A/G/T]TAACATTCATGGGGT | 55728 |
| rs749859519 | in-del | -/AA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125888 | CAAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 55728 |
| rs749871559 | snp | G/T | 1.68741e-05 | 0.00290461 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126286 | AAAGTATCACTCAGA[G/T]AAATAATGTCAGAAG | 55728 |
| rs749874685 | snp | C/G | 3.58051e-05 | 0.00423099 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126114 | GTTGAGAGTATGACA[C/G]TATTTATACTACTTT | 55728 |
| rs749878345 | snp | A/G | 1.66225e-05 | 0.00288287 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152741 | TATTGAGAATGTAAG[A/G]TAAATGAATTTTAAC | 55728 |
| rs749888663 | snp | A/G | 6.6335e-05 | 0.00575874 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40118012 | CATATTCTTGTGAGG[A/G]TAGAAGCACTAGGTA | 55728 |
| rs749890403 | snp | A/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102754 | AGGGCTTGATTTACC[A/T]GGTACAGGTGGGGAT | 55728 |
| rs749925175 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181444 | TGTGACAGAAAACCC[A/C]CAAGCAATGGTGGGC | 55728 |
| rs749943323 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149622 | AAAAGAGGCCAGGCT[C/T]AGTGGCTCATGCCTG | 55728 |
| rs749998886 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081177 | AATGCATTTCTTACG[A/G]ATTATGTGGAAAATG | 55728 |
| rs750002270 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137168 | TATAATAATTTAATG[A/G]TTATTTCTCACCATT | 55728 |
| rs750015376 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102857 | GAACTGCCAACTAAG[A/G]GGAAGGATGTGAGTT | 55728 |
| rs750019918 | in-del | -/T | 1.64855e-05 | 0.00287097 | splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40152904 | AGCCATAGCTTCAGG[-/T]TGAGTGTAGATTTCT | 55728 |
| rs750026087 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167965 | TTGGGTGGAGGGAAA[A/G]CATCAAGGAATAGAG | 55728 |
| rs750029871 | snp | C/T | 1.74778e-05 | 0.00295611 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144848 | AATATATGTCTTTGC[C/T]TATATTGGTATAGCT | 55728 |
| rs750045082 | in-del | -/AC | 3.57079e-05 | 0.00422524 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126312 | AGAAGAAATTGCCTT[-/AC]AGGAAAAACATAATT | 55728 |
| rs750045375 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168460 | CAAGCTATTAATGAA[C/T]TAAACAGGGAGAAGA | 55728 |
| rs750074278 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111405 | AGCTCACTGCAACCT[C/T]CGCATACCGGGTTCA | 55728 |
| rs750081509 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059550 | GGATGGGTTTTTGTC[A/C]TGTTGGTGAGGCTGG | 55728 |
| rs750102047 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152828 | CTGTGATTACGGGGA[A/G]AGGAAACCACAGCCA | 55728 |
| rs750125465 | snp | C/G | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117924 | ATGTTGGAACATTAT[C/G]AACGTTTTGTTTCAG | 55728 |
| rs750134614 | snp | A/T | 1.67536e-05 | 0.00289423 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097298 | CTTAAATGTCAAACA[A/T]CTTAACTAAGAAAAG | 55728 |
| rs750175430 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093532 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAT | 55728 |
| rs750176343 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173586 | AGGTGAAGGGAAATA[C/T]GCTCTGTGCAAGGTT | 55728 |
| rs750212828 | snp | C/T | 1.67083e-05 | 0.00289031 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120506 | GATAAGACTATTGGT[C/T]AGAGGACAAAAAGGA | 55728 |
| rs750223683 | snp | A/G | 1.6525e-05 | 0.00287441 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142829 | GCTTATCGGATAGGG[A/G]AAAAAAATGTCGCCA | 55728 |
| rs750230875 | snp | A/C | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112158 | GCATGGGAAATGAAA[A/C]CATATGTTGCTTTGG | 55728 |
| rs750266278 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160066 | CTTAGGTGATCCATC[C/T]GCCTCAGCCTCCCAA | 55728 |
| rs750283956 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065584 | AGGGTGGATTGTATT[G/T]GGTCAAGGAGTCAAC | 55728 |
| rs750292214 | snp | C/T | 8.23716e-05 | 0.00641709 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103064 | ATTTCTCACACTTCC[C/T]CAACAAAAGTATGGA | 55728 |
| rs750319125 | snp | A/G | 1.65496e-05 | 0.00287655 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121699 | GTCTACTTGTGATGC[A/G]GAAAGAGGAAACTCA | 55728 |
| rs750326569 | snp | A/T | 1.70507e-05 | 0.00291977 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131786 | TTGAACATGATTTTT[A/T]TGTTTTTGTTTTAGA | 55728 |
| rs750326620 | snp | A/T | 0.000148455 | 0.00861425 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123109 | TTACATTTTCTTCCC[A/T]CCCCCTTCCCCCACA | 55728 |
| rs750353967 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160914 | AGACTTAAAGACTAA[G/T]ACACTCCATAAACCT | 55728 |
| rs750372495 | snp | A/G | 1.67559e-05 | 0.00289442 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120397 | AGAAAGAGCAACAGT[A/G]ACGAAAAAAGCCTTT | 55728 |
| rs750374247 | snp | C/G | 3.306e-05 | 0.00406558 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121793 | AGTGCTGCTGTGGGT[C/G]TAAAGAATAATAATG | 55728 |
| rs750415285 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087495 | CAGCCTCTGGAGTAG[C/G]TGAGATTACAGGCAT | 55728 |
| rs750430489 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104486 | CTGCTGATACACTTA[C/T]AAGCATATTTTTCAG | 55728 |
| rs750433176 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178411 | CAAGACTACTCCCCC[A/G]CCCCGCCACCAAAAC | 55728 |
| rs750481558 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069050 | GCTTGAACCTGGGAG[A/G]CAGATGTTGCAGTGA | 55728 |
| rs750614915 | snp | A/C | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102592 | TCTCAGTAGTTCTTT[A/C]AATGTAGCAAGTGAC | 55728 |
| rs750624275 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124227 | CACATGTTTTTATTT[C/T]TAATGTCTTAATGTT | 55728 |
| rs750670032 | in-del | -/GT | 3.30486e-05 | 0.00406487 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102152 | TCTTCACAAAGTTTC[-/GT]TGCTTCTGAGAACCA | 55728 |
| rs750710828 | snp | A/G | 1.66454e-05 | 0.00288486 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154280 | AAGGTTTGTAGGTTA[A/G]AATTACTTTTATTTG | 55728 |
| rs750731116 | snp | A/T | 3.57839e-05 | 0.00422974 | utr-variant-5-prime, missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102081 | GTTGTACAGTTGAAA[A/T]TGCTATGGATTGTCT | 55728 |
| rs750738234 | snp | C/T | 1.65842e-05 | 0.00287955 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120768 | TTATGGGTGACTGGC[C/T]TTCATCTGATTCTTT | 55728 |
| rs750755112 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113111 | ATCTTGTGGTTATGC[C/T]TTCACTTATTTAGTC | 55728 |
| rs750823127 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137391 | TGAATATAAACATGT[A/G]GGCAGAAATATTTAG | 55728 |
| rs750837199 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106381 | CAGTGCAGTGGTGCA[A/G]CCTTGGCTCACTGTA | 55728 |
| rs750839766 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156846 | TTAGCGATACTCAAC[A/C]AGTAAATATAATGCA | 55728 |
| rs750841894 | snp | C/T | 1.65938e-05 | 0.00288039 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120890 | TCCTTATCTACAGCA[C/T]ATGAGGCCTGTTGGG | 55728 |
| rs750845299 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098188 | AATTATAATTATGCA[A/G]ATAAGAGCTGATTAA | 55728 |
| rs750851980 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074371 | GCTGGAATTACAGGC[A/G]TGAGCCACCGTGTCT | 55728 |
| rs750867354 | in-del | -/ATTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151958 | GTGTGTTTTAAATTT[-/ATTA]ATTAATTCATCTCAT | 55728 |
| rs750868486 | snp | A/G | 3.29723e-05 | 0.00406018 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102193 | AGCAGAAAGTAAAAT[A/G]ATGGAAAAACGTCCT | 55728 |
| rs750897821 | snp | C/T | 1.67981e-05 | 0.00289806 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122124 | AAGATGAGAAGGAAA[C/T]GAAGGAAATTCTAAT | 55728 |
| rs750936098 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059138 | CGTTTTAAAACGCTG[-/ATT]ATTTTCCTTTTAAAA | 55728 |
| rs750940388 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099412 | TGTGCCTGGCTAATT[C/T]TTTTTTTTGTATTTT | 55728 |
| rs750941706 | snp | A/C | 1.66222e-05 | 0.00288285 | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142680 | TCTTATAGCCAAAGA[A/C]ATTAAAAGAGACTGA | 55728 |
| rs750957566 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083038 | TATAGAAAGAGGAGA[C/T]AGAGTAAACCTACCC | 55728 |
| rs750991227 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059738 | CAACCTCATTGCCCT[C/T]GTCCTCATAGTAATG | 55728 |
| rs750999047 | in-del | -/TTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061360 | TTTTATTTCATTTTA[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs751005133 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067734 | GACAGAGTCTCACTC[C/T]GTCACCCAGGGTGGA | 55728 |
| rs751046831 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107225 | CACCTTAGCCTCCCA[A/C]GTAGCTGGGACCACA | 55728 |
| rs751050426 | snp | G/T | 3.48365e-05 | 0.00417337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144844 | ATAGAATATATGTCT[G/T]TGCTTATATTGGTAT | 55728 |
| rs751077190 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085327 | AGGCCTGAGTCACTG[C/T]GCCCAGCCTGAGATG | 55728 |
| rs751077254 | snp | C/T | 6.58935e-05 | 0.00573955 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102808 | TGTGTTTCTACCTTC[C/T]GAAGGGTTCAACTTC | 55728 |
| rs751080511 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136854 | CAGTTTTTCATATTC[C/T]TGTAAGATGTTTGAA | 55728 |
| rs751109222 | snp | A/G | 0.00063058 | 0.0177452 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120871 | TGACAAAATGAATGA[A/G]ATATCCTTATCTACA | 55728 |
| rs751127053 | in-del | -/CT | 1.65589e-05 | 0.00287736 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154172 | TCATCTTTAAAATAA[-/CT]CTTTTCTCATTTCTG | 55728 |
| rs751159518 | in-del | -/AG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107788 | GTTATAAGGATTCAA[-/AG]AGTTAATTTTTGTAA | 55728 |
| rs751160423 | snp | A/G | 1.65064e-05 | 0.00287279 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117914 | AATAACAAGAATGTT[A/G]GAACATTATCAACGT | 55728 |
| rs751181806 | snp | A/G/T | 3.51842e-05 | 0.00419417 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122065 | AAATGAAAATTTTCC[A/G/T]AAGGATTATGTGAAA | 55728 |
| rs751187193 | snp | A/T | 1.97307e-05 | 0.00314085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102049 | TCTATATTTTTGTTG[A/T]TGTTATTATTCTTGT | 55728 |
| rs751191220 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176321 | ACATATAATAATAAC[-/AT]AATTTATTTTCCTGT | 55728 |
| rs751242026 | snp | C/G/T | 1.6582e-05 | 0.00287936 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126261 | GGATCATTGGAATAC[C/G/T]CAAACTAAAAAAGTA | 55728 |
| rs751290123 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166388 | TACTATTAGAAAGTC[A/G/T]TTAAAAAATAGAGAT | 55728 |
| rs751308674 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131299 | GCTTTGGCCACTAAG[A/G]GTCTCAGAACTAAAT | 55728 |
| rs751311509 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134202 | GTAGTATTCCAATCC[C/G]TAATTTTCTTATTTA | 55728 |
| rs751320395 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185802 | TGATTAAAAAAATGC[A/G]CAGCTACAATAATTT | 55728 |
| rs751340569 | snp | C/G | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121678 | TATTAGTAACGCTGA[C/G]TCACAGTCTACTTGT | 55728 |
| rs751364412 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172083 | GGCTAATTTTTTGTA[C/T]TTTTAGTAGAGATGG | 55728 |
| rs751394409 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115185 | GGTCATTTTCTAATA[C/T]GACATTTGATGTTAA | 55728 |
| rs751415669 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077563 | GATTCAAGCGATTCT[C/T]CTGCCTCAGCCATCT | 55728 |
| rs751426363 | in-del | -/A | 1.64874e-05 | 0.00287113 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102643 | CTCAATCAAAAACAG[-/A]AAAGAACTTTTAGAA | 55728 |
| rs751427492 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116670 | CTAGTTATTGCTTTC[C/T]GCTTCATTTTTTTCT | 55728 |
| rs751471993 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147337 | GACACAGCGACCATC[C/T]GATTTCTCAATCTTT | 55728 |
| rs751476299 | snp | C/T | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152822 | ATTTGTCTGTGATTA[C/T]GGGGAGAGGAAACCA | 55728 |
| rs751493365 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063069 | CATTATATTTGATAG[A/G]TGAAAGTTTTCTAAG | 55728 |
| rs751498300 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173456 | GGATACTCATTGCTA[C/T]ACTAGGAGGCAGCAT | 55728 |
| rs751514495 | snp | A/G | 1.67022e-05 | 0.00288978 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126274 | ACTCAAACTAAAAAA[A/G]TATCACTCAGAGAAA | 55728 |
| rs751516776 | snp | A/G | 1.65405e-05 | 0.00287576 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121564 | TGGATCACAAATTGG[A/G]CCTTTTTCTCTGGGG | 55728 |
| rs751533860 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137139 | GCATATAAAAATATA[A/T]TTGGTTCATTGAGTA | 55728 |
| rs751553704 | snp | C/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185986 | TACCCAGAAACCTCA[C/G]TTTTTTATTTTTGAG | 55728 |
| rs751559251 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101497 | TATATTACAGTGTAA[C/T]TGTCTCTAATATAAT | 55728 |
| rs751587796 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064378 | CTCTTGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs751605770 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081445 | GAGGTCAGGAGTTCA[A/T]GACCAATCTGACCAA | 55728 |
| rs751644370 | snp | A/G | 1.6676e-05 | 0.00288751 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121212 | AAAAGAATAAAATTA[A/G]CATTTCAGATTCTAT | 55728 |
| rs751661474 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175339 | ATATGTGAAATATAG[A/G]AAAAAAAAAAAAAAA | 55728 |
| rs751670149 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138306 | ATTGTTGAGTTGTAA[A/G]TGTTCTTTATATATT | 55728 |
| rs751675757 | snp | C/T | 3.29484e-05 | 0.00405871 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124214 | ATGCAAGGTAAAGCA[C/T]ATGTTTTTATTTCTA | 55728 |
| rs751731675 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131619 | ATACTTTGCAAAAAA[-/TG]AGATATAAATAAATA | 55728 |
| rs751751376 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177251 | TTCTTTGGGAGATAA[A/C]AGGTGATCTGGTACC | 55728 |
| rs751760503 | in-del | -/C | 1.88902e-05 | 0.00307323 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119902 | GCATTAAGAGACTTT[-/C]TCATGATACTCTTTA | 55728 |
| rs751780095 | snp | A/G | 3.62319e-05 | 0.00425613 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122353 | TGTCTTTGTGTGACT[A/G]GACTACAGAGGGTTC | 55728 |
| rs751792551 | snp | C/T | 1.73658e-05 | 0.00294662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144618 | TGTCCCTTGGTGATA[C/T]GTTTATGATTTAGGG | 55728 |
| rs751800641 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105092 | CAGGCGTGAGCCACC[A/G]CGCCCAACAATCCTG | 55728 |
| rs751813831 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162124 | CTAATTGGTAGAAAC[C/T]ATTGTATTCTAATAT | 55728 |
| rs751814431 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109764 | ATGCCCTTATAACAG[C/G]AACAATAATATATGT | 55728 |
| rs751850326 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103059 | CAGTTATTTCTCACA[A/C]TTCCCCAACAAAAGT | 55728 |
| rs751857788 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057850 | GTGTTGGCTTCAAAG[A/G]CTCTTCCTTTCGGCG | 55728 |
| rs751890155 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106828 | AATTTATTTTGTTTA[C/T]GACTTTGGAAAAATT | 55728 |
| rs751897603 | snp | C/T | | | upstream-variant-2KB, intron-variant, synonymous-codon, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056597 | TCTCCAACGGGAGAG[C/T]GGGAGCGGGAGAGGT | 55728 |
| rs751920111 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128483 | TGTCCTGTCAAATAG[A/C]CTCTTCAATTAATAT | 55728 |
| rs751924396 | snp | A/G | 8.32674e-05 | 0.00645188 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137096 | AGGTATGGAGTTACT[A/G]ATTTTTTTTCTACAA | 55728 |
| rs751967879 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065183 | TGGAAGAAGAGGAGG[-/C]CCAAAGGTAGATAAG | 55728 |
| rs751972749 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154437 | AATGTTACCTGTTAA[A/C]GATATTACAGAGAAA | 55728 |
| rs751975046 | snp | C/T | 3.41052e-05 | 0.00412934 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103190 | CTTCTCAGAGGTCTT[C/T]CGGGATCTGGAAAAT | 55728 |
| rs752025623 | snp | A/C | 1.6755e-05 | 0.00289435 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120129 | TGAATCCTAGCATTC[A/C]AAGTGCTTTAATTCT | 55728 |
| rs752055018 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155555 | AGCTAATAAATTCTG[C/T]TAGTATGCAAGTTAA | 55728 |
| rs752068236 | snp | A/G | 1.70153e-05 | 0.00291674 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136940 | CTACTTAAATTTTCT[A/G]CAGCTATTCATTAGA | 55728 |
| rs752076684 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098052 | AGAACCACTCTCCTA[C/G]AATGTAAGCTCCATA | 55728 |
| rs752086286 | in-del | -/TTAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101154 | AAAAGTGTGCATTAT[-/TTAT]TTATTTATTTATTTA | 55728 |
| rs752087472 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096781 | ATGTGGGATGAGAGG[A/G]GTCAAGGATTATTCC | 55728 |
| rs752092694 | snp | C/G | 1.64768e-05 | 0.00287021 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097479 | GAGACAAAAGTTGAT[C/G]AGGAAGAACTCTTCA | 55728 |
| rs752112169 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156692 | TAGTTTGGAGATTAT[A/G]AAAATTTTCATGTAT | 55728 |
| rs752129710 | in-del | -/ACAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178175 | CAAACAAACAAACAA[-/ACAC]AGAACCCAACAAAAC | 55728 |
| rs752145081 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114860 | ATAGCAACGTTTCCA[A/T]ATTTATTAAGACTAT | 55728 |
| rs752147972 | snp | A/G | 1.65701e-05 | 0.00287833 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120658 | ACATGAAAGTGTAGA[A/G]GATGGCAGAAAGTCA | 55728 |
| rs752201004 | snp | A/C | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113442 | TGTAGTCTCAGAAAC[A/C]CAAATATAAAGTCCT | 55728 |
| rs752214136 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171989 | TCAGCTCACTGCAAC[A/C]TCCACCTCCTGGGTT | 55728 |
| rs752237593 | snp | A/C | 1.8025e-05 | 0.00300203 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122031 | AAATTTATTTTACTG[A/C]TTCTCTTGAAATAAA | 55728 |
| rs752272580 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101305 | GGGATTACAGGCATG[C/T]GCCGCCACTATGCCC | 55728 |
| rs752289474 | snp | C/T | 1.65767e-05 | 0.00287891 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120732 | ATGCTTATAAAAATA[C/T]TGACAAAAACTCATT | 55728 |
| rs752341604 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059671 | GAACACTTTTTTGAT[-/A]ACCTACCTTGCCTGA | 55728 |
| rs752345680 | snp | G/T | 1.74455e-05 | 0.00295338 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136909 | CAACTTATTTTCATT[G/T]ATTGACATTATGTTT | 55728 |
| rs752394779 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143339 | ATTTTTTTAAGATAA[C/G]GTCTTGCTCTGTTGC | 55728 |
| rs752396183 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086917 | CATGCCTAAGTTTTT[A/G]AAAGATTTTTTGTAG | 55728 |
| rs752426641 | snp | C/G | 1.64792e-05 | 0.00287042 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097366 | GAAGGAAAAATCTTG[C/G]GGGAAATCCTTTTCG | 55728 |
| rs752427915 | snp | G/T | 1.73228e-05 | 0.00294297 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126145 | GTAGATCCTTCCTTG[G/T]TTGGACATACTGGGC | 55728 |
| rs752440915 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159672 | ATCTAGCTGCGAGGG[A/G]GGCTGGGAAATTTTC | 55728 |
| rs752477190 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151398 | TACCTCAGCTTCCCA[A/C]GTAGCTGGGACTACA | 55728 |
| rs752477260 | snp | G/T | 1.65392e-05 | 0.00287564 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121551 | AAAAATCGTGTGATG[G/T]ATCACAAATTGGGCC | 55728 |
| rs752486578 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116986 | ATGATTTTTTAAAAT[C/T]TCTGGTTGCTTTTAA | 55728 |
| rs752499623 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183870 | TCAGGGCTGCTGCAA[A/C]CTTCAAGGCATCTAA | 55728 |
| rs752526829 | snp | C/T | 1.65729e-05 | 0.00287857 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121419 | TGTTTGGATCCTTTT[C/T]ATTAGAAGCCCTGAA | 55728 |
| rs752581678 | in-del | -/C | 1.66807e-05 | 0.00288792 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120347 | AATAGTGGACCACTT[-/C]AAAATGAAAAATCCT | 55728 |
| rs752590500 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144740 | GTTTTAGACCTCCAT[A/G]GGCTGCATGTGGATG | 55728 |
| rs752591653 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170642 | AGACCCTGTCCCCCA[A/G]AAGAAAAAGCACATG | 55728 |
| rs752608621 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170190 | TTTCAAGATATATAC[C/T]CTTAATCATTCAGTT | 55728 |
| rs752617024 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130429 | TTACCTCTTGTGGTT[C/G]CTCTTTTATTGCTGT | 55728 |
| rs752632971 | in-del | -/T | 5.21082e-05 | 0.00510406 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103206 | GGGATCTGGAAAATC[-/T]TTTTTTGGCAAGGTA | 55728 |
| rs752675302 | snp | C/T | 1.65427e-05 | 0.00287595 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154216 | AATTAAACCAGGGTG[C/T]TTGAAAGTCATGCTA | 55728 |
| rs752751758 | snp | A/T | 0.000148671 | 0.00862051 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112110 | TTTGAGAAGAAGATA[A/T]CTCCTATAATTATAG | 55728 |
| rs752756658 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102236 | GAAGATTCAAAAATG[C/G]ATTCATTTTTGGACA | 55728 |
| rs752761215 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134643 | TTTAAGGCCTAGAAA[C/G]GATGTGGATAATTGT | 55728 |
| rs752817547 | snp | A/G | 4.97574e-05 | 0.00498761 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121033 | TGGGCAACACACATC[A/G]TTGCCTCTTACTTTT | 55728 |
| rs752818218 | snp | A/G | | | intron-variant, utr-variant-5-prime | N4BP2 | GRCh38.p7 | 4:40098616 | TCGTGTGGTCTGCGA[A/G]CATATCTTGTCCAGT | 55728 |
| rs752820414 | snp | A/G | 3.30077e-05 | 0.00406236 | synonymous-codon, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142714 | AACACCAAGTGAACT[A/G]TCTTTCCAGGACTTT | 55728 |
| rs752870677 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079725 | GAGGATTGCTTAAGC[A/G]TGGGCAGTTGAGGCT | 55728 |
| rs752873217 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070591 | AGTGGCTGGGGGCTA[C/T]AGGCACATACCACCA | 55728 |
| rs752879446 | snp | G/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102340 | AGTATACTCATTTTT[G/T]CCTTCACAAGATGTT | 55728 |
| rs752951711 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136562 | CAGCTAATTTTTGGG[C/T]TTTTTGTAGAGACGG | 55728 |
| rs752979464 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094552 | TATATCTTTTTTATT[G/T]TTATTTATTTATTTA | 55728 |
| rs752982475 | snp | A/T | 1.67206e-05 | 0.00289137 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120499 | GCCAGTTGATAAGAC[A/T]ATTGGTCAGAGGACA | 55728 |
| rs752989763 | snp | C/T | 3.30077e-05 | 0.00406236 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106972 | TATAAATGGACAGTA[C/T]CAGTTTGATGTAAAG | 55728 |
| rs753008897 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065835 | TAAGAAGTGGTTGAC[C/T]GGGGGCATGGATATG | 55728 |
| rs753028032 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179922 | GGCATGCGCCACCAC[A/G]CCCGGCTACTTTTGT | 55728 |
| rs753072349 | snp | C/T | 1.65754e-05 | 0.00287879 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154247 | AAGTAAAATAAACAT[C/T]CTTGAATTAGAAGTA | 55728 |
| rs753077715 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131851 | CACTAAACTAAAGGA[A/G]AAGCAGCTCTTTAAG | 55728 |
| rs753088903 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080888 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT | 55728 |
| rs753120031 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165410 | TGCGGCACCATGTCT[A/G]GCGAATTTTTGTATT | 55728 |
| rs753137884 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125975 | TCTTACTTGCGATGA[C/T]GTGAAGATGTATTTT | 55728 |
| rs753149523 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078852 | AGTATCAATAGTAAA[G/T]TTTGGGATTTTTAGG | 55728 |
| rs753158765 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177559 | AGGCAGAGATTGCAG[C/T]GAGCTGAGATCAAGC | 55728 |
| rs753198717 | snp | A/T | 3.31818e-05 | 0.00407306 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154149 | ATTCCTTAGCTAATT[A/T]GAAATTTTCATCTTT | 55728 |
| rs753210039 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166276 | TAAGAAACTGAACAG[C/T]AGGCTATCTGGCGGG | 55728 |
| rs753212502 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056261 | CGTCAGGGCTCGTCC[C/G]AGCTCTGCTTTCCTT | 55728 |
| rs753226562 | snp | C/T | 0.000169451 | 0.00920309 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118038 | AGGTAGGTTAAAATG[C/T]CTTATGTACAAAATT | 55728 |
| rs753252607 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153000 | TTATTGATAATAGCA[A/G]TAGCCCTAATATAGC | 55728 |
| rs753259182 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095144 | GCTGGAGTGTAATGG[A/C]GCTATCTTGGCTCAC | 55728 |
| rs753274513 | snp | A/G | 3.30491e-05 | 0.00406491 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121803 | TGGGTCTAAAGAATA[A/G]TAATGACATACTTCC | 55728 |
| rs753308407 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057716 | AATTCATCCTCAATA[C/G]AGTGAGTCATCTTAG | 55728 |
| rs753329630 | snp | C/T | 1.66477e-05 | 0.00288506 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120547 | TGAAAAAACTTCATC[C/T]GTACAAAGCGACAAA | 55728 |
| rs753384608 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114031 | ACTGGAAGGTAGTAC[A/G]GATATAGAGATGGAA | 55728 |
| rs753407910 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113615 | TTGATTAGATTGTAA[C/T]TTAATTTCTATTGCT | 55728 |
| rs753430123 | snp | A/G | 1.67877e-05 | 0.00289716 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121910 | ATGAGTGAAACAGAA[A/G]AAAACCTAGTAGTCA | 55728 |
| rs753439784 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156952 | TCACTCAACCTGTAT[A/C]TTTGTGCTAATACAT | 55728 |
| rs753440864 | snp | C/T | | | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057188 | GGGCCCGGCGCGGGC[C/T]GCCTCCGATCTGACC | 55728 |
| rs753451892 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061197 | TATTTTGAGGTAGAG[G/T]CTTGCTGTGTTGCCC | 55728 |
| rs753457342 | snp | A/C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170284 | ATATTTAAAGATTAC[A/C/G]AATAAAAAAGAAAAT | 55728 |
| rs753463560 | in-del | -/T | 1.67677e-05 | 0.00289544 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120474 | AGCTATCAAATTTTG[-/T]TGGTGACTGGCCAGT | 55728 |
| rs753465263 | snp | G/T | 1.65773e-05 | 0.00287895 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097329 | GGAAACATTTTAGTT[G/T]TGGAAGTCAGAATGC | 55728 |
| rs753466292 | snp | C/T | 0.000230601 | 0.0107353 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119953 | AGACGATGAAGATAT[C/T]ATCTCTGAAAAAGAA | 55728 |
| rs753471184 | in-del | -/CTTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075391 | CCAGTTTTTACACAG[-/CTTTT]CTTTTATTTATTTAT | 55728 |
| rs753491174 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099767 | TAAGTACCTATCCAT[C/T]TTGATCTTTAATTTA | 55728 |
| rs753495487 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098409 | GGTAAAGTCTTCAGT[A/G]TGGTAGGTTATTAAT | 55728 |
| rs753500044 | snp | C/T | 1.65198e-05 | 0.00287395 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152940 | TAATAATGGCAACTG[C/T]CCATATAGATCTTTA | 55728 |
| rs753506533 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067056 | ATGACCTAATTTCCT[-/TT]TTTTTTTTTTTTTTT | 55728 |
| rs753538105 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177129 | CAGAACTTTCCTCCA[A/G]TGACCAACCTGGAGG | 55728 |
| rs753544189 | snp | G/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144714 | TCAATGCTTCGCTGC[G/T]GCCACAGAATGTTTT | 55728 |
| rs753548048 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139741 | TGTGATCCACCCACC[G/T]TGACTTCCCAAAGTG | 55728 |
| rs753558067 | in-del | -/GTACCTTCTCAGAGAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133076 | GAAGGTTCTGGGCTT[-/GTACCTTCTCAGAGAGA]GAATCTTGGTTTATT | 55728 |
| rs753560148 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102878 | GATGTGAGTTACTGC[C/T]CGGTACTTGCTCCTC | 55728 |
| rs753564949 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067289 | TCCTGGGCTCAAGTG[A/T]TCAGTTAGTTAGCCT | 55728 |
| rs753568389 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182714 | CAGAGTCTTGTTCTG[G/T]TGCCCAGACTGGAGT | 55728 |
| rs753620949 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119471 | TCTTTTTTTCTAATT[C/T]CTCTTAATCGGGCAA | 55728 |
| rs753626290 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162014 | AAGTGTTGTAGAAAT[A/G]GTCTCCATCATTTGC | 55728 |
| rs753628749 | snp | A/G | 3.4174e-05 | 0.0041335 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103192 | TCTCAGAGGTCTTCC[A/G]GGATCTGGAAAATCT | 55728 |
| rs753631420 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161001 | CCTCCTTCCCACCCC[C/T]AGAAGGACTGCAAGG | 55728 |
| rs753662912 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123194 | AGTGATTCATGAGAA[A/G]TGGAAAGAATCTGTA | 55728 |
| rs753692443 | snp | A/C | 0.000116245 | 0.00762293 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102492 | GTTTAAACCCATTAC[A/C]TTCACATTCAGTTTT | 55728 |
| rs753717660 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104557 | AACATAAAACAATTT[A/G]ATATTATAGATGTTA | 55728 |
| rs753783609 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074569 | AAACACCTCATGAGA[A/T]GGAAAATATAATCAC | 55728 |
| rs753802319 | in-del | -/GAAGGAAAT | 1.69308e-05 | 0.00290949 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122116 | TATGAATGAAGATGA[-/GAAGGAAAT]GAAGGAAATTCTAAT | 55728 |
| rs753811778 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165066 | GCAGTGGGTTACATA[A/G]GAATTTATTTTTAAA | 55728 |
| rs753839813 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180145 | AAATAAAATAAAGAC[-/A]AATGACTGAGAGATA | 55728 |
| rs753841057 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182682 | ATTTAATATATATAT[A/G]CATATGTATAGAGAG | 55728 |
| rs753855635 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108339 | TTTTTTTGAGACGAA[A/G]TCTTGCTTTGTTGCC | 55728 |
| rs753882734 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090324 | AAAAAATCTTGCTTG[G/T]GTTCTGGTAGGCATT | 55728 |
| rs753891725 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093712 | ACCTCTGCTTCCTGG[G/T]TTCAAACGATTCTCC | 55728 |
| rs753904562 | snp | G/T | 1.8788e-05 | 0.0030649 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103258 | AAAAATAGTATAATG[G/T]CTGAATTTGAACACA | 55728 |
| rs753906998 | in-del | -/C | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058979 | GCGAAAGCCACTACG[-/C]CCGGCTAATTTTTGT | 55728 |
| rs753936409 | snp | C/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185955 | CTTTCTTTTTGAGCA[C/G]AGACACTGAATTAAT | 55728 |
| rs753984150 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077755 | CACCGCACTCAGCCA[G/T]AATATCTTTTTTGAT | 55728 |
| rs754000323 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094281 | TCTATCTTGGTATGT[A/G]TTCTGTTAATACTTG | 55728 |
| rs754008713 | snp | A/G | 1.73649e-05 | 0.00294655 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102097 | TGCTATGGATTGTCT[A/G]TTAGAATTATCTGCC | 55728 |
| rs754009597 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152697 | TGAAAACAATTTCAT[G/T]TGCTTGAGTAGCTAA | 55728 |
| rs754030229 | snp | A/G | 3.30147e-05 | 0.00406279 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106958 | GATGATTATTTTTAT[A/G]TAAATGGACAGTACC | 55728 |
| rs754036777 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095058 | TGGGATTACAGTCGC[A/G]AGCCCCTGAGTCTGG | 55728 |
| rs754041315 | in-del | -/CCTTTC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134899 | CTCCCTTCCTTCCTT[-/CCTTTC]CCTTTCTCTCTCTCT | 55728 |
| rs754109904 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40154143 | AGGTATATTCCTTAG[C/G]TAATTTGAAATTTTC | 55728 |
| rs754138547 | snp | A/C | 1.66471e-05 | 0.00288501 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120277 | TAGTTCTATGGAGAG[A/C]GTATCACCTAGTACT | 55728 |
| rs754190234 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077195 | TGAGAGAGTCTTGCT[C/T]TGTTGCCCATGCTGG | 55728 |
| rs754202067 | snp | A/G | 1.65842e-05 | 0.00287955 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121021 | TAAAAAGAGTCATGG[A/G]CAACACACATCGTTG | 55728 |
| rs754215218 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177467 | CTAAAAATACAAAAA[G/T]TAGCTGCGCATGGTG | 55728 |
| rs754219362 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108919 | CCTCCCGGGTTTAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs754230653 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152838 | GGGGAGAGGAAACCA[C/T]AGCCAGGGAGGAGTT | 55728 |
| rs754246441 | snp | A/G | 3.29712e-05 | 0.00406011 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142789 | CCAACAGAAGAGGAT[A/G]GAGTGCTACAGCAAG | 55728 |
| rs754252457 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133976 | ACGCCTGGCTAGTTT[C/T]TGTATATTTTTTGTA | 55728 |
| rs754255206 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083080 | GCCCACGCCCTGTGC[C/T]TGTTCTGTATTATGA | 55728 |
| rs754268777 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102204 | AAATAATGGAAAAAC[C/G]TCCTGAAGAAGAGAG | 55728 |
| rs754272549 | snp | C/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142845 | AAAAAAATGTCGCCA[C/T]CTTTTATGCCCAGCA | 55728 |
| rs754304565 | snp | A/C/G | 3.30799e-05 | 0.00406682 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122235 | CTCTGACCATAGACT[A/C/G]TCTGGAATTGGCATT | 55728 |
| rs754309532 | snp | G/T | 3.30038e-05 | 0.00406212 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106979 | GGACAGTACCAGTTT[G/T]ATGTAAAGTACTTAG | 55728 |
| rs754344999 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084353 | CAAGTAGAAATTGCC[A/G]TTAGCTGAGATTGCA | 55728 |
| rs754345123 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069208 | TTTGGGAGGCCGAGG[C/T]GGGCACATCACTTGA | 55728 |
| rs754357575 | snp | C/T | 1.65872e-05 | 0.00287981 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120907 | TGAGGCCTGTTGGGG[C/T]ACAAGCTCTCAAAAA | 55728 |
| rs754358381 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124639 | GGCATGAGCCACTGC[A/G]CCCAGCCAGTTCTTT | 55728 |
| rs754432787 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070343 | ATTATATAAGAAGAC[A/G]TATATCTTCAGATCT | 55728 |
| rs754438067 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104261 | CTGGCTTGCTAGTTC[-/T]TTTTTTTTTTTTTTC | 55728 |
| rs754481648 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171450 | TTTCAGTGTTGTCTG[-/AT]GACACTTAGGTTCAG | 55728 |
| rs754509140 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061300 | TCAGCCTCCCGAGTA[G/T]CTGGGATTACAGGTG | 55728 |
| rs754511706 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098449 | TACATTGTTTAGAAG[A/T]ATGTAGACAGAAGGG | 55728 |
| rs754516348 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057328 | CTCCGAGTGCCTGGC[A/G]GGCCTCCAGGCCCCA | 55728 |
| rs754522599 | snp | A/G | 1.65192e-05 | 0.00287391 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097338 | TTAGTTTTGGAAGTC[A/G]GAATGCCAAGGAGAA | 55728 |
| rs754532528 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116883 | TCTGTTGTTGAAGAT[-/A]ACACTTCACTCCCTT | 55728 |
| rs754532952 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156311 | AGGAGCAGTCAGAAG[C/T]AGAGGTGTGGTATTC | 55728 |
| rs754545903 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159638 | TTACGTCCTATTGAC[C/T]AGAACCTAGTCATGT | 55728 |
| rs754565388 | in-del | -/AGAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162746 | TCCAGAATGAATAGG[-/AGAT]AGATAGGGGATTTAT | 55728 |
| rs754582458 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114819 | ATGTTTTCTTTGTGA[A/G]AATGTTTAGTTGGAA | 55728 |
| rs754583432 | snp | A/G | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121731 | AGCAGGCGGAAATGA[A/G]AGCTGTCACTCCTGA | 55728 |
| rs754620983 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157219 | GTGTTTTTTTTTTTA[C/T]GTTTATTGGCTCTTC | 55728 |
| rs754663519 | snp | A/G | 1.65291e-05 | 0.00287476 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131842 | AGATTGTGCCACTAA[A/G]CTAAAGGAGAAGCAG | 55728 |
| rs754664344 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102962 | CCTGCTTTTGACCTC[C/T]TCCAAGGAAACCATG | 55728 |
| rs754670424 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099892 | ACGTTTGCTTTCTTT[C/T]TTTTCCCCCGTCCCT | 55728 |
| rs754679511 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087674 | CCACTCCACGTGCAC[C/T]CCGCCCCCTCCGCCC | 55728 |
| rs754688132 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081807 | GTGGTGAAACCCCAT[C/T]GCTACTAAAAAATAC | 55728 |
| rs754692963 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138803 | TGTCTTGATTACTGC[A/G]GCTTCTTGATTACTG | 55728 |
| rs754709444 | snp | A/C | 1.6522e-05 | 0.00287414 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121811 | AAGAATAATAATGAC[A/C]TACTTCCTAACAGCC | 55728 |
| rs754738533 | in-del | -/C | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102889 | TGCCCGGTACTTGCT[-/C]CCTCTCCCATTGCTG | 55728 |
| rs754746552 | snp | G/T | 1.66054e-05 | 0.00288139 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102499 | CCCATTACCTTCACA[G/T]TCAGTTTTGAACGAG | 55728 |
| rs754747385 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054594 | ACCGCCCCCCCGCCG[-/C]CCCAAAAAAAAAAGA | 55728 |
| rs754792865 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162034 | CCATCATTTGCCTTT[G/T]GAACAGAATGAGCCG | 55728 |
| rs754818550 | snp | A/C | 3.31395e-05 | 0.00407046 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120655 | TCCACATGAAAGTGT[A/C]GAGGATGGCAGAAAG | 55728 |
| rs754842774 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150122 | GTGGCTCTGACCTGC[A/G]TTGCCTTTTGACATA | 55728 |
| rs754846467 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127763 | TCTCCCGGGTTCATG[C/G]CATTCTCCTGCTTCA | 55728 |
| rs754854976 | snp | A/C | 1.64982e-05 | 0.00287208 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112180 | TTGCTTTGGTTAGTA[A/C]CATAAGTTGTCATAA | 55728 |
| rs754865711 | snp | C/T | 1.73102e-05 | 0.0029419 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144624 | TTGGTGATATGTTTA[C/T]GATTTAGGGTACTCT | 55728 |
| rs754867680 | in-del | -/CA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137651 | GAAGTTTATCATACT[-/CA]CAGAGTTCTGGAAAC | 55728 |
| rs754877442 | in-del | -/CAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168271 | GCCCAATTTTCCTAT[-/CAA]CAGACAGAGACTATC | 55728 |
| rs754895375 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182736 | GACTGGAGTGCAGTG[C/G]CTGGATCTCAGCTCA | 55728 |
| rs754912576 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123195 | GTGATTCATGAGAAA[C/T]GGAAAGAATCTGTAA | 55728 |
| rs754926859 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074619 | TTCAAAAGAGCTTTC[A/G]TGGTATAAGACATGT | 55728 |
| rs754931761 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128773 | CCTCAAGTGATTCGG[C/T]TTCCCAAAGTGTTGG | 55728 |
| rs754976468 | snp | G/T | 9.92539e-05 | 0.00704394 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113424 | GTTTTTGTCTTTGTT[G/T]TATGTAGTCTCAGAA | 55728 |
| rs754991307 | snp | C/T | 3.35182e-05 | 0.00409365 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102121 | ATCTGCCACTGATAC[C/T]AAGATAGAAGAATCA | 55728 |
| rs754998827 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093719 | CTTCCTGGGTTCAAA[C/T]GATTCTCCTGCTTCT | 55728 |
| rs755005879 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168968 | TGACTTCAGGTGATC[C/T]GCCCACCTCTGCCTC | 55728 |
| rs755023152 | snp | C/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056206 | GAGGCCGGTCGCTCG[C/G]CTCGCCGTCCCTCCC | 55728 |
| rs755072348 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165148 | ATATAGTTGTCTCTT[A/G]TATTTCTTGGTTCCT | 55728 |
| rs755090772 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095062 | ATTACAGTCGCGAGC[C/T]CCTGAGTCTGGCCAG | 55728 |
| rs755121234 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077877 | TTTATTTATAAAATG[A/G]TATGGAGTGCAGCAC | 55728 |
| rs755142099 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172425 | TCAAGTTGACACTCA[A/G]TATTAACCACCACAC | 55728 |
| rs755170263 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169465 | AATGAAATTAGAAAT[A/G]TATAAAAGATTTAAA | 55728 |
| rs755193754 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173606 | TGTGCAAGGTTAACA[C/G]TGTATTCCCAAACAC | 55728 |
| rs755196258 | snp | A/G | 1.66468e-05 | 0.00288498 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120280 | TTCTATGGAGAGAGT[A/G]TCACCTAGTACTTGC | 55728 |
| rs755202049 | snp | C/T | 1.65179e-05 | 0.00287379 | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142701 | AAGAGACTGAAGAAA[C/T]ACCAAGTGAACTGTC | 55728 |
| rs755221402 | snp | A/G | 1.73117e-05 | 0.00294203 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137126 | AGGGTAGATAATTGC[A/G]TATAAAAATATAATT | 55728 |
| rs755234261 | snp | A/G | 3.3042e-05 | 0.00406447 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122158 | AGGAAGTAGTTTATC[A/G]GCTGGAGTTAGTGGG | 55728 |
| rs755241266 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124006 | TACTTCATAATTTTT[A/G]TTATCTAACTTTATT | 55728 |
| rs755277777 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117031 | CTTTGGTGAATGACA[A/G]TTTCAGTACTATGTT | 55728 |
| rs755296198 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125964 | CACATACTATTTCTT[A/G]CTTGCGATGACGTGA | 55728 |
| rs755339834 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102800 | GTCTCTGATGTGTTT[C/T]TACCTTCCGAAGGGT | 55728 |
| rs755356759 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078710 | GTTTTGTATTTTTTT[A/G]TTGAGACAGGTTTTA | 55728 |
| rs755398579 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152952 | CTGCCCATATAGATC[C/T]TTATCAGATATTTCT | 55728 |
| rs755400795 | in-del | -/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079423 | GCCCACCCTGGATGG[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs755414093 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120909 | AGGCCTGTTGGGGCA[C/T]AAGCTCTCAAAAACT | 55728 |
| rs755428438 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179883 | CATTCTCCTGCCTCT[A/G]CCTCCCGAGTAGCTG | 55728 |
| rs755464295 | snp | C/G | 1.64844e-05 | 0.00287087 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102228 | AAGAGAGTGAAGATT[C/G]AAAAATGGATTCATT | 55728 |
| rs755502527 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175048 | TTTTTTCAAAGACAG[C/T]CTCATTCTGTTGCCC | 55728 |
| rs755539557 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088588 | TCACTGCAGCCTCCG[C/T]CTCCCGGGTTCAAGT | 55728 |
| rs755540758 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070484 | GACAGGGTCTTGCTC[A/T]GTTGCCCAGACTAGA | 55728 |
| rs755541983 | snp | C/T | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121031 | CATGGGCAACACACA[C/T]CGTTGCCTCTTACTT | 55728 |
| rs755548103 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077241 | TCTCAGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 55728 |
| rs755567628 | snp | C/T | 6.60022e-05 | 0.00574428 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117961 | TAATTATGAGTTCTT[C/T]GGTTCCAGAGAAAAT | 55728 |
| rs755580939 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072911 | ATTTTTAGCAGAGAC[A/G]GGGTCTCACCATGTT | 55728 |
| rs755611223 | in-del | -/A | 1.84366e-05 | 0.00303611 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103241 | TTTGATTGGGTTTTT[-/A]AAAAAATAGTATAAT | 55728 |
| rs755666224 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102866 | ACTAAGGGGAAGGAT[A/G]TGAGTTACTGCCCGG | 55728 |
| rs755673315 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182351 | GGGTCAGGCTGAGAA[C/G]TTTCCTTTTGTCCTG | 55728 |
| rs755682841 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182609 | TGCACGCCACCATGC[C/T]GGGCTAAAATTTTTT | 55728 |
| rs755732809 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168780 | CCCAAGCTGGAGTGC[A/C]ATGGTGCAGTCTTGG | 55728 |
| rs755792095 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113566 | AGACAGACAAGGTCC[A/G]TTTAGATTTTTCCCC | 55728 |
| rs755796394 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064665 | CAAGTAAATACAAAG[C/G]TGCTAAGATAGATGT | 55728 |
| rs755813614 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110040 | CTGTGTTTTGTCCCT[A/G]TAGATAATTTGCCTA | 55728 |
| rs755820826 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156103 | ATAATTGTTAATGAA[A/G]TAAGATATTCCTATG | 55728 |
| rs755825858 | snp | A/C/G | 3.2961e-05 | 0.00405951 | missense, synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152829 | TGTGATTACGGGGAG[A/C/G]GGAAACCACAGCCAG | 55728 |
| rs755829882 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096896 | GGAGCTGTTTTGGAC[A/G]TGTTAAATTTATAAT | 55728 |
| rs755839499 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101595 | TCTGATATGCAGTAC[A/G]TGCTCAAATATTCTT | 55728 |
| rs755840973 | snp | A/G | 1.70551e-05 | 0.00292015 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126294 | ACTCAGAGAAATAAT[A/G]TCAGAAGAAATTGCC | 55728 |
| rs755866206 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060263 | TCATTTATTTTTTTT[C/G]AGATGGAGTCTCACT | 55728 |
| rs755873254 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113235 | TTATATAAATAAATG[A/C]TCTTATATAAGTATT | 55728 |
| rs755901784 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102762 | ATTTACCAGGTACAG[C/G]TGGGGATCAGAAATC | 55728 |
| rs755928272 | snp | A/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142837 | GATAGGGAAAAAAAA[A/T]GTCGCCACCTTTTAT | 55728 |
| rs755937987 | snp | C/G | 1.65274e-05 | 0.00287462 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121798 | TGCTGTGGGTCTAAA[C/G]AATAATAATGACATA | 55728 |
| rs755941754 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137371 | AGCAGTAATGTGATG[A/G]GTCTTGAATATAAAC | 55728 |
| rs755950401 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090510 | ATAACATCATCAATA[A/G]GTTCTCGGAAACTGT | 55728 |
| rs756001144 | snp | A/G | 4.94572e-05 | 0.00497254 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103094 | AGAAATAAAGATGGA[A/G]CAAGTGCTTATCAAG | 55728 |
| rs756009390 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145250 | TTTTTCTGAGACATA[A/C]TCTCACTCTGTTGCC | 55728 |
| rs756021587 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120420 | AAGCCTTTGGGAAAC[-/A]AAAAAGCAAATCGAC | 55728 |
| rs756061031 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107054 | TCAGATTCTGGGTAA[C/T]GTTATGAGTAATACA | 55728 |
| rs756087834 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087552 | GTATTTTTAGTAGAG[A/G]CTGGGTTTTGCCATG | 55728 |
| rs756139528 | snp | C/T | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40136977 | AGTGCAATTTCTTAA[C/T]TGTGTTCTTGAAGGG | 55728 |
| rs756150865 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069064 | GGCAGATGTTGCAGT[G/T]AGCCGGGATCGCGCC | 55728 |
| rs756172575 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181668 | AAGGACAAAGAAGTC[C/T]GGGTGCGGTGGCTCA | 55728 |
| rs756231868 | snp | C/G | 6.66045e-05 | 0.00577043 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120267 | CTGACACAGATAGTT[C/G]TATGGAGAGAGTATC | 55728 |
| rs756246298 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163516 | AAGAATTCTGCTAGA[C/T]TGGTTCTGGGAAAGG | 55728 |
| rs756248450 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150301 | GACTACCATTTTATA[A/G]GGATTTACAGGGGAC | 55728 |
| rs756260890 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090847 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 55728 |
| rs756284877 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184633 | AATTATTTGTTGCCT[C/T]TCAGACGTGAAAAAT | 55728 |
| rs756308904 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131503 | AATGTGTTGGATATG[C/T]ATGTGTGACAGTATG | 55728 |
| rs756330399 | snp | A/T | 3.32978e-05 | 0.00408017 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154281 | AGGTTTGTAGGTTAA[A/T]ATTACTTTTATTTGC | 55728 |
| rs756399782 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148317 | CCAGTCACGCATGGC[A/G]GCGCGCGCCTGCAAT | 55728 |
| rs756414846 | in-del | -/TTTAAGATA | 1.64982e-05 | 0.00287208 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131861 | AAGGAGAAGCAGCTC[-/TTTAAGATA]TTTCCAGCCATTAAC | 55728 |
| rs756449662 | snp | A/G | 3.51056e-05 | 0.00418946 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144852 | TATGTCTTTGCTTAT[A/G]TTGGTATAGCTTGCA | 55728 |
| rs756461877 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074468 | CCTGCCTCGGCCTCC[C/G]AAAGTGCTGGGACAA | 55728 |
| rs756481554 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171238 | TGCTGTCACTTTCAT[C/T]GTTTGTCCATCCCTT | 55728 |
| rs756495675 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098226 | GGCTAGCAGAATAGT[A/C]TAATTTCAAAACATT | 55728 |
| rs756503424 | in-del | -/TT | 1.65562e-05 | 0.00287712 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154175 | TCTTTAAAATAACTC[-/TT]TTCTCATTTCTGCAG | 55728 |
| rs756527174 | snp | A/G | 1.64953e-05 | 0.00287182 | utr-variant-5-prime, synonymous-codon, intron-variant | N4BP2 | GRCh38.p7 | 4:40097538 | GGATCCTGATGTAGT[A/G]TATTTGATGCTTTCT | 55728 |
| rs756530795 | snp | C/T | 1.71787e-05 | 0.00293071 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117855 | TCAACCCTTTTTTCC[C/T]CTGGAATTTTCAGGC | 55728 |
| rs756535897 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138458 | TTGTCTACTTTTGCT[A/G]TGTTGCCTGTGCTTC | 55728 |
| rs756564031 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067804 | CCCAGGTTCAAGTGA[C/T]TCTCCTGTCTCAGCC | 55728 |
| rs756598448 | snp | A/T | 3.68963e-05 | 0.00429497 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103242 | TTTGATTGGGTTTTT[A/T]AAAAATAGTATAATG | 55728 |
| rs756607551 | in-del | -/GAAGTGTCAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105905 | TTAACGGTAAAAAAG[-/GAAGTGTCAGA]GAAGGGAAAGCTACA | 55728 |
| rs756609440 | snp | A/T | 3.33317e-05 | 0.00408224 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122134 | GGAAATGAAGGAAAT[A/T]CTAATGGCAGGAAGT | 55728 |
| rs756651870 | snp | A/T | 1.75579e-05 | 0.00296288 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102090 | TTGAAAATGCTATGG[A/T]TTGTCTATTAGAATT | 55728 |
| rs756662869 | snp | C/T | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122223 | CGATGGCCAAATCTC[C/T]GACCATAGACTGTCT | 55728 |
| rs756686883 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178413 | AGACTACTCCCCCGC[A/C]CCGCCACCAAAACAA | 55728 |
| rs756692751 | snp | C/T | 1.65869e-05 | 0.00287979 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120771 | TGGGTGACTGGCCTT[C/T]ATCTGATTCTTTAGC | 55728 |
| rs756711852 | snp | A/G | 1.80605e-05 | 0.00300498 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126092 | ATGTTTAATTTATAC[A/G]TTTATTGTTGAGAGT | 55728 |
| rs756719866 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085456 | GTTGATAGGATTTAT[A/T]TTTTATTCTTTTTCT | 55728 |
| rs756722574 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180488 | GGAGTGGATTTGGCA[A/T]TATCTACTACAATAA | 55728 |
| rs756723738 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162275 | TGGGGGCGAAGGCAG[A/G]CAGATCACTTGAGGT | 55728 |
| rs756744704 | snp | A/G | 1.74522e-05 | 0.00295394 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144846 | AGAATATATGTCTTT[A/G]CTTATATTGGTATAG | 55728 |
| rs756768164 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070772 | TACTTATACTATATT[C/G]AGATTTCCTGAGTTG | 55728 |
| rs756778764 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177766 | TAAGGCTTTGGCTCT[A/C]TTTACGGCTGCTCCC | 55728 |
| rs756794041 | snp | A/G | 3.30066e-05 | 0.00406229 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117919 | CAAGAATGTTGGAAC[A/G]TTATCAACGTTTTGT | 55728 |
| rs756794236 | in-del | -/GT | 1.65636e-05 | 0.00287776 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120675 | TGGCAGAAAGTCACA[-/GT]GTGTGATGATGCTTC | 55728 |
| rs756800607 | in-del | -/CA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125886 | AGCAAGACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 55728 |
| rs756811562 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087287 | AAAAATTTTTTTTAA[A/G]GGAGGGGAAGCTTCT | 55728 |
| rs756815035 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165465 | TGTTGGCCAGGCTGG[C/T]CTTGAACTCCTGGCC | 55728 |
| rs756841870 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096311 | GTCCTGAGAAGGTAA[C/T]ATTTGAATAATGATA | 55728 |
| rs756847373 | in-del | -/AT | 3.56544e-05 | 0.00422208 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122331 | AAAAAGTAAATGACC[-/AT]GTGTGTGTCTTTGTG | 55728 |
| rs756852007 | snp | A/C | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144757 | GCTGCATGTGGATGA[A/C]GCTCTAGAACATTTG | 55728 |
| rs756855720 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056362 | TAGAAACAGCTGTGG[C/T]TTACCGCGCCGCTTA | 55728 |
| rs756889610 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181409 | GATTAACATATCAAT[C/T]AGGATTAGATTAAAT | 55728 |
| rs756889944 | in-del | -/AAAAGGAAAAAAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083125 | CGGTGCAGACATAGA[-/AAAAGGAAAAAAC]AAAAGGAAAAAACAA | 55728 |
| rs756894036 | snp | A/G | 5.65403e-05 | 0.00531667 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126357 | TATAAATATTAAGCT[A/G]CTGTCTCTGATTCTG | 55728 |
| rs756920196 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072505 | CACCTCGGCCTCCCA[A/G]CGTGCTGGGATTACA | 55728 |
| rs756971265 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166416 | GATAATTGGCTGGGC[A/G]AGGTGGCTTATGTCT | 55728 |
| rs756976222 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109784 | ATAATATATGTTAAT[A/C]GGCGGAATTCATTTT | 55728 |
| rs756982706 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115345 | CTACAAAAAATAAAA[A/G]AATTAGCTGGGTATG | 55728 |
| rs757024838 | snp | C/T | 1.7318e-05 | 0.00294256 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117850 | TTCCTTCAACCCTTT[C/T]TTCCCCTGGAATTTT | 55728 |
| rs757075778 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077610 | AGGCACCGGCCACCA[C/T]ACTCGACTAATTTTT | 55728 |
| rs757089118 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102717 | TGGATGCCAGTGAAC[C/T]TCAGGCTTGTTTAAA | 55728 |
| rs757114100 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100212 | TGTCATAGCCAGCAG[G/T]AGAGATTTAAATGTT | 55728 |
| rs757118577 | snp | A/T | 1.64966e-05 | 0.00287194 | missense, splice-acceptor-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142722 | GTGAACTGTCTTTCC[A/T]GGACTTTGAGTACCC | 55728 |
| rs757126045 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173488 | TGTAGTACACACTAC[A/G]TGAGAGGTATGAGGG | 55728 |
| rs757127752 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123471 | TGGAGCTCATTGTAA[-/T]TGTTGATTTTTTTTA | 55728 |
| rs757129530 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116734 | CTGCCTGATGTTCAT[C/T]TTTGAGAATTTTCTT | 55728 |
| rs757144948 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161633 | ATACATGCTGAAATA[C/T]GTACGTAAAATGATA | 55728 |
| rs757157992 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40158883 | TTTGCAAGGACTTAA[A/T]AACATTTATCTAACA | 55728 |
| rs757165702 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063301 | CCATGAAGAGCTAGG[A/G]TGGGAACTTTCCCAT | 55728 |
| rs757168780 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159868 | TCAAAAAAAGGAAAT[C/T]ACAGTTGTTGTTGTT | 55728 |
| rs757187243 | snp | A/G | 0.000116528 | 0.00763219 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120288 | AGAGAGTATCACCTA[A/G]TACTTGCTGTAGTGA | 55728 |
| rs757232361 | snp | A/G | 4.96602e-05 | 0.00498274 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121688 | GCTGACTCACAGTCT[A/G]CTTGTGATGCAGAAA | 55728 |
| rs757248030 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143796 | ATCAAAGGATACACA[A/G]ATAATAAACCAGTGA | 55728 |
| rs757310290 | snp | A/G | 1.70093e-05 | 0.00291622 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119994 | TATCTTTATCTTTGA[A/G]GCATCTAGAGTTCAC | 55728 |
| rs757327503 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119807 | TTTATAATTTTAATG[C/T]AATTTATTTATAAAA | 55728 |
| rs757351099 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067481 | TATTGTGAATAACGC[A/T]GTGATAAACATGCAT | 55728 |
| rs757358489 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117336 | GAAAGCCAGATTTGC[C/T]CAACTGGCAAATGCA | 55728 |
| rs757361745 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071519 | TTTTCTTTTTGCTTC[G/T]AGCAAGTAGTAATCT | 55728 |
| rs757412449 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177353 | CGGCACGGTGGTTCA[C/T]GCCTGTAATACCAGC | 55728 |
| rs757425944 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105099 | GAGCCACCACGCCCA[A/G]CAATCCTGCGTTGTC | 55728 |
| rs757427468 | snp | A/G | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102465 | ATTTAGAGAATTCTG[A/G]TTCTACTTTAAGTTT | 55728 |
| rs757456238 | snp | A/G | 6.63427e-05 | 0.00575907 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102368 | GTTAATAGTTTTAAT[A/G]ACTCAAGTGAGTTTA | 55728 |
| rs757478152 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182833 | AGGCACCTGTCACCA[C/T]GCCCAGCTAATGTTT | 55728 |
| rs757495288 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114534 | GTTTTTAAGGCTCAT[-/C]CATGTTGTAGCATGT | 55728 |
| rs757500073 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162173 | ATCAAAGATCTGGGA[A/G]ATGTTCTTTTAAACT | 55728 |
| rs757547611 | snp | C/G | 3.29533e-05 | 0.00405901 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123182 | GAATCTGGCGAAAGT[C/G]ATTCATGAGAAATGG | 55728 |
| rs757547917 | in-del | -/TATCTATA/TATG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136390 | ATCTATCTATCTATC[-/TATCTATA/TATG]TATCTTTTTTTTGAG | 55728 |
| rs757551743 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170582 | GAGGTTGAGGCTGCA[C/G]TGAGCTGAGTGGTGC | 55728 |
| rs757563218 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074123 | TGAGATGGAGTGTTG[C/T]TCTATTGCTCAGGCT | 55728 |
| rs757568152 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088888 | CTGTATCTCCTCTTT[C/T]GTGTAGTGTTTTTTC | 55728 |
| rs757575381 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057950 | GTTGTAATGTCTCCA[A/T]GGCACAGTTCTGGCT | 55728 |
| rs757600421 | snp | C/T | 1.64784e-05 | 0.00287035 | utr-variant-5-prime, missense, intron-variant | N4BP2 | GRCh38.p7 | 4:40097510 | CCAGTATCTCAGAGA[C/T]ATTTTCTGATCTGGA | 55728 |
| rs757607452 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096791 | AGAGGAGTCAAGGAT[C/T]ATTCCAAGATTTTGG | 55728 |
| rs757649922 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111269 | AAACTCAAGACTATA[A/G]TTTGATTTTAATTTT | 55728 |
| rs757679481 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169721 | GTAATCCCAGCACTT[-/G]TGGGAGGCCGAGGTG | 55728 |
| rs757692226 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155683 | ACATAATTTTAACAA[A/G]TAGTTTTGTTGCTTT | 55728 |
| rs757700792 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103005 | CTGTTGTAACCACAG[C/G]TGCACACTGGAGATC | 55728 |
| rs757715442 | snp | A/G | 4.9689e-05 | 0.00498418 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120669 | TAGAGGATGGCAGAA[A/G]GTCACAGTGTGATGA | 55728 |
| rs757754891 | snp | C/T | 1.6708e-05 | 0.00289028 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137098 | GTATGGAGTTACTAA[C/T]TTTTTTTCTACAAGG | 55728 |
| rs757784184 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137165 | GAGTATAATAATTTA[A/G]TGATTATTTCTCACC | 55728 |
| rs757820188 | in-del | -/A | 1.6503e-05 | 0.0028725 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152926 | TAGATTTCTGTTATT[-/A]ATAATGGCAACTGCC | 55728 |
| rs757831372 | snp | A/G | 4.94262e-05 | 0.00497098 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097381 | GGGGAAATCCTTTTC[A/G]GAAGACTGCAAACCC | 55728 |
| rs757889668 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083477 | AAAATGTGTTATATC[C/T]GTACCATGCAATATT | 55728 |
| rs757904907 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144741 | TTTTAGACCTCCATG[A/G]GCTGCATGTGGATGA | 55728 |
| rs757914325 | in-del | -/AAAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184962 | TCTGTCTCAAAAAAT[-/AAAT]AAATAAATAAATAAA | 55728 |
| rs757955634 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113450 | CAGAAACACAAATAT[A/G]AAGTCCTTTTTCGGG | 55728 |
| rs757961710 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134077 | GCCTCCCAAAGTTCT[C/G]GGATTACAGGTGTGA | 55728 |
| rs757969108 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139079 | GGTCTTCTTTAATTT[C/T]CTTCAACAATGCACT | 55728 |
| rs757971026 | snp | C/T | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158734 | GGCGAGATTGTGCCA[C/T]TGAGCTCCAGCCTGG | 55728 |
| rs757973616 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161647 | TGTACGTAAAATGAT[-/A]ACGATGTTAGCAATT | 55728 |
| rs757977759 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069439 | CCCTTTCATTTTTTT[C/T]CCTTCCTTTCATTTT | 55728 |
| rs758003977 | in-del | -/TAAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116938 | AGTCAGCTGTCATTC[-/TAAT]TAATTGTTTCTTTGT | 55728 |
| rs758010674 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058176 | CCAACATCAGCCTTT[C/T]CACTCCGTTTTTATT | 55728 |
| rs758011614 | snp | C/T | 1.65803e-05 | 0.00287922 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120733 | TGCTTATAAAAATAT[C/T]GACAAAAACTCATTC | 55728 |
| rs758076382 | snp | G/T | 1.6476e-05 | 0.00287014 | utr-variant-5-prime, missense, intron-variant | N4BP2 | GRCh38.p7 | 4:40097492 | ATCAGGAAGAACTCT[G/T]CACCAGTATCTCAGA | 55728 |
| rs758185459 | snp | A/G | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120660 | ATGAAAGTGTAGAGG[A/G]TGGCAGAAAGTCACA | 55728 |
| rs758188625 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151434 | GCCTCGCCATGCCCT[C/G]CTAATTTTTGTATTT | 55728 |
| rs758210452 | snp | C/T | 1.75551e-05 | 0.00296264 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117844 | TCAATATTCCTTCAA[C/T]CCTTTTTTCCCCTGG | 55728 |
| rs758215157 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184122 | ACAGAACATTTTGTC[C/G]ATCTCAAAATAGAGG | 55728 |
| rs758232347 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074957 | GGCTGCAGTGAGCTG[A/T]GCTCTTGCCACTGCA | 55728 |
| rs758241974 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084096 | GCTGGGATTACAGGC[A/T]TGCGCCACCACTCCC | 55728 |
| rs758246553 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113883 | AGGTGTGAGCCACCA[C/T]GCCCAGCCTGTACTT | 55728 |
| rs758248067 | snp | C/T | 3.30797e-05 | 0.00406679 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121560 | GTGATGGATCACAAA[C/T]TGGGCCTTTTTCTCT | 55728 |
| rs758251695 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124250 | TTAATGTTGAAATTT[A/G]GTGTGTGTGTTTGAA | 55728 |
| rs758261597 | in-del | -/TTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067055 | TATGACCTAATTTCC[-/TTT]TTTTTTTTTTTTTTT | 55728 |
| rs758273128 | snp | C/G | 3.32049e-05 | 0.00407448 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102514 | TTCAGTTTTGAACGA[C/G]TCCAAGTGTTTTATA | 55728 |
| rs758287546 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185975 | ACTGAATTAATTACC[C/T]AGAAACCTCACTTTT | 55728 |
| rs758309406 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170695 | CATTTTTGTGTTCTA[A/G]TTGGAAATTGTTGAC | 55728 |
| rs758310967 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172047 | CAGTAGCTGGGATTA[C/T]AGGCATGCGCCACCA | 55728 |
| rs758318336 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075962 | CTCCTGAGCAGCTGG[A/G]ACTACAGGCATGTAC | 55728 |
| rs758319053 | snp | A/G | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121427 | TCCTTTTCATTAGAA[A/G]CCCTGAAAGACTTAT | 55728 |
| rs758397642 | snp | C/T | 1.73063e-05 | 0.00294157 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126146 | TAGATCCTTCCTTGG[C/T]TGGACATACTGGGCT | 55728 |
| rs758417611 | snp | A/G | 4.94303e-05 | 0.00497119 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152851 | CACAGCCAGGGAGGA[A/G]TTGCTCGCATCAAAC | 55728 |
| rs758427626 | snp | G/T | 1.65789e-05 | 0.0028791 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121057 | TACTTTTACCAATAG[G/T]GCACCAACTGTTTCT | 55728 |
| rs758435033 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078963 | ATTTTCATTTTTTTA[G/T]TTGTTTAGAGTGGAG | 55728 |
| rs758435800 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170387 | ACTTTGGGAGACTGA[C/T]GCAGGCAGATCACTT | 55728 |
| rs758442543 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168643 | AAAAAATAGGAGACC[A/G]CAGAAATCAATTGAC | 55728 |
| rs758450238 | in-del | -/AAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137246 | TATCTGTGCACTCAA[-/AAT]AATGAATTTATAGCT | 55728 |
| rs758453994 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157369 | AATCCTCTTGAGTAG[C/T]ATATTTTGAGAAGAA | 55728 |
| rs758483385 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134672 | GTTGGTAGCATCCAG[C/T]CCCTAATACTGATAT | 55728 |
| rs758501469 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175111 | CTGCAGCCTAGAATT[C/T]CTGGCCTCAAGCAAT | 55728 |
| rs758510033 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173701 | GGACCAGTTAGTCAC[A/G]GTCAAAGTCAAACTG | 55728 |
| rs758557271 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064855 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 55728 |
| rs758584675 | snp | G/T | 1.79371e-05 | 0.0029947 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122338 | AAATGACCATGTGTG[G/T]GTCTTTGTGTGACTA | 55728 |
| rs758588043 | snp | A/C | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106973 | ATAAATGGACAGTAC[A/C]AGTTTGATGTAAAGT | 55728 |
| rs758600350 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160185 | AAGTAGGAAAAAACT[A/G]AATGACACGGACTAG | 55728 |
| rs758645676 | snp | C/T | 1.66599e-05 | 0.00288611 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122252 | CTGGAATTGGCATTA[C/T]CCCCTGAACTGGCTT | 55728 |
| rs758692153 | snp | A/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142812 | ACAGCAAGGCCAAAG[A/T]AGCTTATCGGATAGG | 55728 |
| rs758696131 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103486 | CTATTGATGTAGTAG[C/T]AGAAGAGAGCTAATT | 55728 |
| rs758708120 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119508 | TTGGTTGGCCCTTTG[A/T]GACTTTGTAAATGAA | 55728 |
| rs758717307 | snp | C/T | 1.73495e-05 | 0.00294524 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136920 | CATTTATTGACATTA[C/T]GTTTCTACTTAAATT | 55728 |
| rs758725333 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070708 | CTCCTGCCTTGGCCT[C/T]GCAAAGTGCTGGGAT | 55728 |
| rs758733003 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066826 | GCAGTTTTTTTCATC[C/T]TGCCAAACTGAAACT | 55728 |
| rs758757611 | snp | A/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102237 | AAGATTCAAAAATGG[A/T]TTCATTTTTGGACAT | 55728 |
| rs758758884 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165412 | CGGCACCATGTCTGG[C/T]GAATTTTTGTATTTA | 55728 |
| rs758766225 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108512 | GTAGAGACGGGATTT[C/T]ACCATGTTGGCCAGG | 55728 |
| rs758804353 | snp | A/G | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126183 | TCCTGAACAAAAATC[A/G]TCTCAGAGAACAGGC | 55728 |
| rs758846964 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166320 | GTCAGAGGTAGGAGA[A/C]TTAGATTTTGCCTTC | 55728 |
| rs758859814 | snp | A/G | 1.65135e-05 | 0.00287341 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121840 | CCAGGAAGAACTTTT[A/G]TATAGCAGTAAGCAG | 55728 |
| rs758868444 | snp | G/T | 0.000116672 | 0.00763689 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121201 | ATGGAAAATAGAAAA[G/T]AATAAAATTAGCATT | 55728 |
| rs758882371 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079024 | TGGCGCGATCTCAAG[C/T]GATTCTCCAACCTCA | 55728 |
| rs758906041 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178969 | TGTCTTTGTGGTTGC[C/T]GATTTTTCATTTTTA | 55728 |
| rs758922100 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136219 | CTTAAAGGTCTATTG[-/TT]TCTGTGTTTGATGTT | 55728 |
| rs758927992 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122476 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 55728 |
| rs758935265 | snp | A/C | 1.65833e-05 | 0.00287948 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154153 | CTTAGCTAATTTGAA[A/C]TTTTCATCTTTAAAA | 55728 |
| rs758961255 | snp | C/T | 3.5108e-05 | 0.0041896 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119974 | TGAAAAAGAAGAAAA[C/T]ATTTTATCTTTATCT | 55728 |
| rs758961365 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102895 | GGTACTTGCTCCTCT[C/T]CCATTGCTGTTGCCT | 55728 |
| rs758996376 | snp | A/G | 0.000181194 | 0.00951651 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40124180 | ACAAAGACAAGAAGA[A/G]GTGTCTTGTGGCAAG | 55728 |
| rs759018447 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152355 | CTTGATGGCTTTAGA[A/C]TATTTAATTAACAGG | 55728 |
| rs759020036 | snp | C/T | 0.000165199 | 0.00908693 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131872 | GCTCTTTAAGATATT[C/T]CCAGCCATTAACCAA | 55728 |
| rs759106287 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132397 | CTTTATTATTTTAAA[C/T]GTCTACCTTTTTATG | 55728 |
| rs759112996 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077054 | TCTTTTTTGATGGTC[G/T]TAAGGAGCTAAATAT | 55728 |
| rs759128734 | snp | A/G | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121304 | TCAGACGTTCAAGAA[A/G]CAATTCCATATAGAG | 55728 |
| rs759136604 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137051 | ATGAGAATGTCACAT[C/G]TCATACTGGCCAGAA | 55728 |
| rs759170899 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063961 | TTTTATTTATTTATT[C/T]AGAGAGATTGGTGGG | 55728 |
| rs759180625 | snp | A/C | 1.76961e-05 | 0.00297452 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119962 | AGATATTATCTCTGA[A/C]AAAGAAGAAAATATT | 55728 |
| rs759207299 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171944 | GGAGTCTCACTCTGT[C/G]GCTCAGGCTGGAGTG | 55728 |
| rs759228344 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073218 | GTTACCTGGAATTAG[C/T]GTTCTACTTAAAGGC | 55728 |
| rs759232628 | snp | C/T | 1.65941e-05 | 0.00288041 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120825 | TGCCAAAGACTGGTT[C/T]AAGTGAGCCCAACCT | 55728 |
| rs759240989 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178059 | TAGCTACTCAGGAGG[C/G]TGAGGCAGGAGAATC | 55728 |
| rs759247281 | snp | C/T | 1.65518e-05 | 0.00287674 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154227 | GGTGCTTGAAAGTCA[C/T]GCTAAAGTAAAATAA | 55728 |
| rs759249996 | snp | C/T | 1.67593e-05 | 0.00289471 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120109 | AAGAAAAGAAATAAG[C/T]GATATGAATCCTAGC | 55728 |
| rs759258295 | in-del | -/AAAAAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177994 | CTTAAGCAACCAGAA[-/AAAAAC]AAAAACAAAAAAACA | 55728 |
| rs759269842 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082379 | TATTCAATAATCTAA[C/T]AATCCTGGGTTCAGC | 55728 |
| rs759273629 | in-del | -/AA | 1.85451e-05 | 0.00304503 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119935 | ATAATCTTACAGCCC[-/AA]GAGACGATGAAGATA | 55728 |
| rs759295201 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172832 | ACAATGTGTTTTATA[A/G]TATCTTAAAATCTCC | 55728 |
| rs759297825 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123840 | TCACTCCCAGAATTA[A/C]AGACTTCAATGCTGA | 55728 |
| rs759301843 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118259 | CCCGTCTCCACTAAA[A/G]GTACAAAATTAGCCT | 55728 |
| rs759306649 | snp | C/T | 4.95397e-05 | 0.00497668 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113547 | ATGCTTTTTATGTAA[C/T]GACAGACAGACAAGG | 55728 |
| rs759328813 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163218 | ATTATGTTTACTATG[A/T]ACTAGGCACCACTGG | 55728 |
| rs759445983 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106678 | CTCAGCCTCCCTAGT[A/G]GCTGGGACTATAGGC | 55728 |
| rs759477379 | snp | C/G | 3.31516e-05 | 0.0040712 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103144 | TCAGGTTGTAAGAAA[C/G]AAGACATCTTACGTT | 55728 |
| rs759492789 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151141 | GCATGTGAATCAACT[A/G]GAGAATATTTTCAGA | 55728 |
| rs759507487 | snp | C/G | 1.64751e-05 | 0.00287007 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097466 | ACCTTCCATGGGTGA[C/G]ACAAAAGTTGATCAG | 55728 |
| rs759522963 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166208 | AGCTACAAATACCCC[C/T]ACAGTAATAAGTTTT | 55728 |
| rs759525219 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170078 | CTGAAAAAAGAGAAA[C/T]GTCTTATGAATTTGA | 55728 |
| rs759574606 | in-del | -/CT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164909 | ATCTCTTTGCTGAGA[-/CT]CTGAAGACTCTGGTG | 55728 |
| rs759583901 | snp | G/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055359 | CCTCTAAATACAAAA[G/T]TCATACAAAAGGAAA | 55728 |
| rs759587739 | snp | G/T | 3.31549e-05 | 0.0040714 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120716 | AATAGCTATAAATAT[G/T]ATGCTTATAAAAATA | 55728 |
| rs759596910 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182145 | CTGTTGCTAAGGAAA[C/T]GGATTTTGGGGGATA | 55728 |
| rs759606684 | snp | A/G | 0.000496829 | 0.0157533 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121673 | ATTGGTATTAGTAAC[A/G]CTGACTCACAGTCTA | 55728 |
| rs759621778 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138195 | GATGACTATTGATGT[C/T]GAGCATCTTTTTATG | 55728 |
| rs759622537 | in-del | -/TTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104410 | TAAACTTATTTTTAG[-/TTT]TTTTTTTTTGATATC | 55728 |
| rs759626671 | snp | G/T | 1.67691e-05 | 0.00289556 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120470 | CATGAGCTATCAAAT[G/T]TTGTTGGTGACTGGC | 55728 |
| rs759633476 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102836 | TTCAAGCCACACAAA[C/T]ATCCTGAACTGCCAA | 55728 |
| rs759689994 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142793 | CAGAAGAGGATGGAG[C/T]GCTACAGCAAGGCCA | 55728 |
| rs759714018 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127836 | CGGCTAATTTTTTGT[A/G]TTTTTTAGTAGAGAC | 55728 |
| rs759725171 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073226 | GAATTAGTGTTCTAC[C/T]TAAAGGCAGAATAGA | 55728 |
| rs759732772 | snp | A/G | 3.34381e-05 | 0.00408876 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120371 | AAATCCTCACCTGGT[A/G]AAATAGTGGAAGAAA | 55728 |
| rs759738369 | in-del | -/GCC | 1.65496e-05 | 0.00287655 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121471 | AAAGATATTATTTGG[-/GCC]GCCACAAGCCTTTTG | 55728 |
| rs759777969 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100933 | TTCCCTTCGAAAATA[A/G]AATTAATATTTCTTA | 55728 |
| rs759866611 | snp | A/G | 3.32215e-05 | 0.00407549 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121172 | CAGACTGAACCACAG[A/G]ATTTTGCTCTTTTAT | 55728 |
| rs759933283 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054596 | GCCCCCCCGCCGCCC[-/A]CAAAAAAAAAAGAAA | 55728 |
| rs759963425 | snp | A/C | 0.000258685 | 0.01137 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112040 | AAAATCATAATACTT[A/C]GTATTGTTTAAAAAA | 55728 |
| rs759971747 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124147 | CAATCTCTTGCCTGG[C/T]TTTTGTGTTTAGGAG | 55728 |
| rs759976491 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145743 | CTAGGCATCAAGGAT[A/G]AGGTGGTGAAAAAGA | 55728 |
| rs759994214 | snp | A/G | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102286 | GGATTCCTTAATACA[A/G]AATGCTTTTGAGAAA | 55728 |
| rs760029381 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084496 | ACTGGAGTGCAGTGG[C/T]ACAATCTCAGCTCAC | 55728 |
| rs760081076 | snp | A/G | 1.77436e-05 | 0.0029785 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119943 | ACAGCCCAAGAGACG[A/G]TGAAGATATTATCTC | 55728 |
| rs760097700 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123152 | AGTTGAAGATTGTGT[A/G]GTTCATATAGATCTG | 55728 |
| rs760101042 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166776 | TAGGTGTATACATTT[A/G]TGGGGTACATGAGAT | 55728 |
| rs760104347 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125780 | TAATCCCAGCTACTT[C/T]GGAGGCTGAGGCAGG | 55728 |
| rs760105079 | in-del | -/TTAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136385 | TATCTATCTATCTAT[-/TTAT]CTATCTATCTTTTTT | 55728 |
| rs760124947 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138157 | AAATGGTGTCTTATT[A/G]TGGTTTTGATTTGCA | 55728 |
| rs760159056 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149626 | GAGGCCAGGCTCAGT[A/G]GCTCATGCCTGTAAT | 55728 |
| rs760190242 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106411 | AACCTAAACCCCCTG[A/G]GTTCAAGTGATCCTC | 55728 |
| rs760260911 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129909 | AGATGATTAAGGTTA[C/T]AAGGTTTTAGTTCAT | 55728 |
| rs760265241 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123136 | CACAAGGGTCTCTAA[C/G]AGTTGAAGATTGTGT | 55728 |
| rs760272884 | in-del | -/ATT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145602 | TTAAGAGCCGTTTAA[-/ATT]ATTATTTAATCCAGA | 55728 |
| rs760280092 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089821 | TCTCTCTTTTTTAGT[A/T]CCCACAAGGAGAGAT | 55728 |
| rs760286640 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116016 | TTTTATATCACCCTA[A/G]TTAATTGAACCTTTT | 55728 |
| rs760302867 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128627 | CCACCTCCTGGGTTC[A/G]AGTGATTCTCCTGCC | 55728 |
| rs760314191 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075741 | TTTTTTTATTACTGC[A/G]TAGTATTCCAAAGGA | 55728 |
| rs760315776 | snp | C/T | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121143 | ACCCTGGAAAAGAAG[C/T]AGGCATGTGCACCCA | 55728 |
| rs760317072 | snp | A/G | 1.65844e-05 | 0.00287957 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121017 | TAAGTAAAAAGAGTC[A/G]TGGGCAACACACATC | 55728 |
| rs760356984 | snp | A/G | 1.79987e-05 | 0.00299984 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122016 | TTGAATTAAATGAAG[A/G]AATTTATTTTACTGA | 55728 |
| rs760365110 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097009 | AATGTATTGAAATAG[C/T]GTATTCATTGTTCTG | 55728 |
| rs760381306 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123043 | ACAAGTTAGTTTTGT[A/G]ATGCATAAGGTGGTT | 55728 |
| rs760381526 | in-del | -/GAA | 1.72753e-05 | 0.00293894 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122090 | GTGAAATTTTCAGAT[-/GAA]GAAGAATTTATGAAT | 55728 |
| rs760398013 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40097909 | CTCTCCTATGCATTG[C/T]AGGTTTAGCAGCGTC | 55728 |
| rs760411951 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081240 | ATCACCTATGATTCT[A/G]TTATCCAGAGATTTC | 55728 |
| rs760416978 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143419 | CCCAGGCTCAGGTGA[A/T]CCTCCCACATCAGCC | 55728 |
| rs760419937 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168267 | ATGAGCCCAATTTTC[A/C]TATCAACAGACAGAG | 55728 |
| rs760432969 | snp | C/G | 0.000149225 | 0.00863657 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120617 | GTATCTGTGAATACA[C/G]ATTGTGTCCAGCAAC | 55728 |
| rs760434163 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170079 | TGAAAAAAGAGAAAC[A/G]TCTTATGAATTTGAG | 55728 |
| rs760454468 | snp | A/C | 1.65111e-05 | 0.0028732 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152937 | TATTAATAATGGCAA[A/C]TGCCCATATAGATCT | 55728 |
| rs760505020 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174780 | GCACTCCAGTCTGGG[C/T]GACAGAGTGAGATGC | 55728 |
| rs760542562 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104523 | TGTAGGCTTTTCTAA[C/T]TGACTTAATAACAAC | 55728 |
| rs760566283 | in-del | -/TTTC | 1.65194e-05 | 0.00287392 | frameshift-variant, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142699 | AAAGAGACTGAAGAA[-/TTTC]ACACCAAGTGAACTG | 55728 |
| rs760605506 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138071 | GCAGGAGGAGCAGCC[C/T]CTCTAGTGTCATGAA | 55728 |
| rs760659415 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179555 | GGCTATTATTATCCC[C/T]ATTTAACAGTTGAGG | 55728 |
| rs760689647 | in-del | -/CT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145630 | CCAGAGAGAAGAAAA[-/CT]CTTCAAGTATATAGA | 55728 |
| rs760694175 | snp | A/G | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121339 | GTATGATAAAAGCAC[A/G]TTTGTTGAAGAAAGT | 55728 |
| rs760715266 | snp | A/T | | | intron-variant, splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40080481 | GTCTGGGACTACAGG[A/T]ACGTGCCACCACGCC | 55728 |
| rs760722924 | snp | A/C | 1.67111e-05 | 0.00289055 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121898 | ACTCCTAAAGATATG[A/C]GTGAAACAGAAAAAA | 55728 |
| rs760748420 | snp | C/G/T | 6.93764e-05 | 0.00588934 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126144 | TGTAGATCCTTCCTT[C/G/T]GTTGGACATACTGGG | 55728 |
| rs760823375 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108724 | CTAGTGTAACTGTCT[A/G]TTCAGTGAAGATAGT | 55728 |
| rs760848063 | snp | A/G | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117885 | CGTAACATTCATGGG[A/G]TAAGCAAAGAAAAAA | 55728 |
| rs760857636 | in-del | -/TTTTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175017 | CACTTGCATGTAAAA[-/TTTTG]TTTTGTTTTGTTTTG | 55728 |
| rs760890188 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152793 | AGAATTTAAGCAGAA[C/T]GGTGGGAAGCCCTAT | 55728 |
| rs760890747 | in-del | -/TATG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059388 | TGAGCATTTTTTATG[-/TATG]TATGTATGTATGTAT | 55728 |
| rs760890885 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102690 | CTCAATTCTCTGAAG[A/C]TCCTGTAGATTTGGA | 55728 |
| rs760897139 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109140 | TATGATAAGTGTACT[A/G]TAAAGGTGATTCTTG | 55728 |
| rs760947228 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176936 | CCCCGCTTTTTTCCC[C/T]TTTCACCCAATAAAA | 55728 |
| rs760968356 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060947 | CATATCCTTTGATCA[C/T]GTATTAGCTGCTTTT | 55728 |
| rs760974059 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166108 | CTACACAATAAGACA[A/G]TGGAAGGTGGGGGTG | 55728 |
| rs760978448 | in-del | -/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056176 | CAGCGGCCACGGCCC[-/T]AGTCAGGCAATGCCG | 55728 |
| rs761011893 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057506 | GAGCCGTTTATTTAC[C/T]CAGTTCAAGTCCAGA | 55728 |
| rs761022102 | snp | A/T | 1.65419e-05 | 0.00287588 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126248 | TGCTACCTTTATTGG[A/T]TCATTGGAATACTCA | 55728 |
| rs761054532 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062332 | ATCCTCCTCTCTTTA[A/G]TATCTCTTGAATCTG | 55728 |
| rs761060363 | snp | A/G | 5.27245e-05 | 0.00513415 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122312 | GGTATTGATTCAGGT[A/G]AGGAAAAAGTAAATG | 55728 |
| rs761079616 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166778 | GGTGTATACATTTAT[-/G]GGGTACATGAGATAT | 55728 |
| rs761089436 | snp | A/G | 0.000417498 | 0.0144421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112068 | AAATGATTTTTAATT[A/G]TGTTATGTTTTTCAG | 55728 |
| rs761106816 | in-del | -/TTCCCTTTTC | 1.74528e-05 | 0.00295399 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097581 | AAGGTGAGAAAAAGT[-/TTCCCTTTTC]TTAGTTTGAACCCTG | 55728 |
| rs761142558 | snp | C/T | 0.000115749 | 0.00760666 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102308 | TTTGAGAAATTGAAC[C/T]CTTCTCCTGATGACC | 55728 |
| rs761156447 | snp | A/T | 4.98484e-05 | 0.00499216 | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142681 | CTTATAGCCAAAGAA[A/T]TTAAAAGAGACTGAA | 55728 |
| rs761157783 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160851 | CCTGACTCATGTTAA[A/G]TTTTAGTTTTCAGTT | 55728 |
| rs761179421 | snp | C/G | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158409 | TTACGTTTTCTGTAG[C/G]AAATAAGAGTCTACT | 55728 |
| rs761219195 | snp | A/G | 3.33433e-05 | 0.00408296 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120338 | GATCTTGCAAATAGT[A/G]GACCACTTCAAAATG | 55728 |
| rs761237481 | snp | A/C/G | 3.29643e-05 | 0.00405971 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152823 | TTTGTCTGTGATTAC[A/C/G]GGGAGAGGAAACCAC | 55728 |
| rs761250021 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100712 | TGTGTTATAACAGAA[C/T]GAGCTCAGCATTGGA | 55728 |
| rs761250134 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083042 | GAAAGAGGAGATAGA[A/G]TAAACCTACCCCGTA | 55728 |
| rs761269517 | snp | A/G | 5.03647e-05 | 0.00501795 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142664 | TACTTATTGTTTAAT[A/G]TCTTATAGCCAAAGA | 55728 |
| rs761285432 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069012 | GTAATCCTAGCTCCT[C/T]GGGAGGCTGAGGCAG | 55728 |
| rs761289335 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176805 | CGGGAAGTTCATGCT[C/G]TTTGCAGCAGGGAGG | 55728 |
| rs761308264 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162979 | AGGCTGCTTGAGTGT[A/C]CTTACAACATGGTGG | 55728 |
| rs761309944 | snp | A/G | 1.65329e-05 | 0.0028751 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102305 | GCTTTTGAGAAATTG[A/G]ACTCTTCTCCTGATG | 55728 |
| rs761314919 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142773 | CAGAGGCTTTCCTTC[A/G]CCAACAGAAGAGGAT | 55728 |
| rs761346105 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065467 | GGAACAGAACCTTAG[C/T]GAGCAATGACACTGA | 55728 |
| rs761382385 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149305 | GTAAACATTATTCTT[G/T]GTGAAAGATGAAGGC | 55728 |
| rs761416919 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182372 | TTTTGTCCTGTAGGC[A/G]GTAGGGAGCCAAATA | 55728 |
| rs761419530 | snp | A/T | 0.000173419 | 0.00931017 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102054 | ATTTTTGTTGTTGTT[A/T]TTATTCTTGTTGTTG | 55728 |
| rs761438302 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088272 | GGTTTTTAGATGAAT[A/G]TAATTTTTCAGTCCT | 55728 |
| rs761461376 | snp | C/G | 6.59826e-05 | 0.00574343 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122209 | GAATCCCACTCCAGC[C/G]ATGGCCAAATCTCTG | 55728 |
| rs761470953 | snp | A/T | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102178 | GAACCAAGTAGGTGC[A/T]GCAGAAAGTAAAATA | 55728 |
| rs761490438 | snp | G/T | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106933 | TCCAAGTGGAGTCAT[G/T]CTTAGTACTGATGAT | 55728 |
| rs761503186 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102930 | CGCCACCTCCACCGA[C/T]GTGGAATCCAATGAT | 55728 |
| rs761514316 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096652 | GAGATAGGAGACTTA[C/T]AGTAATTCAGGCAAG | 55728 |
| rs761553127 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110815 | AGTGCTGAGATCATA[A/G]GTGTGAGGTACCGTG | 55728 |
| rs761568358 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134291 | AGAGGTTGATGCTAG[C/T]ATATGGCCACTCCTG | 55728 |
| rs761615843 | snp | C/T | 3.31978e-05 | 0.00407404 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120882 | ATGAAATATCCTTAT[C/T]TACAGCACATGAGGC | 55728 |
| rs761618654 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131934 | AGTGAGTGCTAGAAG[A/G]ATTGTCTGTAGTTTC | 55728 |
| rs761625079 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095010 | CTCAAACTCCTCACC[C/T]TAAGTGATCCTCCTG | 55728 |
| rs761648047 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079368 | ATGATCCTCCTTCCT[C/T]GGCCTTCCAAAATGC | 55728 |
| rs761658582 | in-del | -/TCTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089810 | TGAAGATTTTCTCTC[-/TCTT]TTTTAGTTCCCACAA | 55728 |
| rs761716849 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078439 | ACCGTGTCTAGCCCA[A/G]TATTCCTAAATATTT | 55728 |
| rs761728695 | snp | A/G | 1.68128e-05 | 0.00289933 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126283 | AAAAAAGTATCACTC[A/G]GAGAAATAATGTCAG | 55728 |
| rs761767824 | snp | A/C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174750 | GGGGTTGCAGTGAGC[A/C/T]GAGATCGCGCCACTG | 55728 |
| rs761771423 | in-del | -/TGAT | 1.69602e-05 | 0.00291201 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142875 | GGTAAAGTGGAAAAC[-/TGAT]TGATTATATATTTTT | 55728 |
| rs761781833 | snp | A/C | 1.71302e-05 | 0.00292657 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131780 | TTCATCTTGAACATG[A/C]TTTTTATGTTTTTGT | 55728 |
| rs761797001 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152887 | GTCATTAAGTACCTC[A/G]TAAGCCATAGCTTCA | 55728 |
| rs761811079 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102853 | TCCTGAACTGCCAAC[C/T]AAGGGGAAGGATGTG | 55728 |
| rs761820429 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178158 | GAGCGAGACTGGGTC[A/C]AACAAACAAACAAAC | 55728 |
| rs761840471 | snp | A/C | 3.29582e-05 | 0.00405931 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102678 | AGTGCGTTGAGGCTC[A/C]ATTCTCTGAAGCTCC | 55728 |
| rs761844515 | in-del | -/TTG | 4.0899e-05 | 0.00452193 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102043 | TCTCTGTCTATATTT[-/TTG]TTGTTGTTATTATTC | 55728 |
| rs761846240 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082976 | AAGTGCTGGGATTAC[A/G]AGTGTGAGCCACCGC | 55728 |
| rs761848034 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122863 | ACTAATAGAAATGAA[A/T]AAAGTAAACATATTT | 55728 |
| rs761849121 | snp | C/T | 1.85782e-05 | 0.00304775 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119932 | AAAATAATCTTACAG[C/T]CCAAGAGACGATGAA | 55728 |
| rs761849439 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138366 | ATTTGCAGATATTCT[A/G]TCCTTTCCATAGGTT | 55728 |
| rs761859049 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136347 | ATTAGAAATTGAATC[A/T]ATCTATCTATCTATC | 55728 |
| rs761859071 | in-del | -/TTAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101151 | TATCAAAAGTGTGCA[-/TTAT]TTATTTATTTATTTA | 55728 |
| rs761893586 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062429 | TTGCACGAGCCTCCT[A/G]ACAGCTCATCCCTGC | 55728 |
| rs761915553 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084007 | TCTGTCACCCAGGCT[G/T]GAGTTGCAGTGGTGT | 55728 |
| rs761923039 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060604 | GCTAAGTAGCTAGAT[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs761930055 | snp | C/T | 4.94425e-05 | 0.0049718 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144708 | AGAAAGTCAATGCTT[C/T]GCTGCTGCCACAGAA | 55728 |
| rs761935067 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142586 | ATATACGACAGCCCA[C/G]TTTTCATGTGCGTTT | 55728 |
| rs761942022 | snp | C/G | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102575 | TACCCGGAAGATTCT[C/G]TTCTCAGTAGTTCTT | 55728 |
| rs761974212 | snp | A/C | 1.65732e-05 | 0.00287859 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120700 | TGCTTCAGAGCCACT[A/C]AATAGCTATAAATAT | 55728 |
| rs761976419 | snp | C/T | 1.65748e-05 | 0.00287874 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113418 | TAAAATGTTTTTGTC[C/T]TTGTTGTATGTAGTC | 55728 |
| rs761982669 | snp | C/T | 1.65844e-05 | 0.00287957 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121345 | TAAAAGCACGTTTGT[C/T]GAAGAAAGTGAGCTT | 55728 |
| rs762006338 | snp | C/T | 7.10505e-05 | 0.00595988 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126126 | ACAGTATTTATACTA[C/T]TTTGTAGATCCTTCC | 55728 |
| rs762009916 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106134 | AATCTTCTAACCATT[A/C]TAAAGATTTTATAGT | 55728 |
| rs762014206 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073938 | GCTGGGATTACAGGC[A/G]CATGCCACCACATCC | 55728 |
| rs762017217 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068899 | CGAGGCAGGTGGATC[A/G]CTTGAGGTCAGGGGT | 55728 |
| rs762067118 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168307 | ATGGATTAAAAACAA[A/G]CCCAGTGAATATGTT | 55728 |
| rs762073694 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178172 | CCAACAAACAAACAA[A/G]CAAAGAACCCAACAA | 55728 |
| rs762095218 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089563 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55728 |
| rs762133769 | snp | A/G | 1.68417e-05 | 0.00290182 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144804 | AGAAGACTGAAGGTA[A/G]GACTGTGGTAATCAC | 55728 |
| rs762155324 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163302 | ATTGCCCACATGGCC[A/G]ACATTGTTGTCTTAC | 55728 |
| rs762161491 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179454 | GTAGCTAATGTTTAT[A/T]GAAATCTTCTGTGTT | 55728 |
| rs762174139 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124216 | GCAAGGTAAAGCACA[C/T]GTTTTTATTTCTAAT | 55728 |
| rs762187126 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075665 | CTTCCCAAAGTGCTG[C/G]GGTTACAGGCATGAG | 55728 |
| rs762195517 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131684 | TTAATCCGTAAAGAA[A/G]GTCTGTGATTGCTTT | 55728 |
| rs762209389 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059398 | TTTATGTATGTATGT[A/T]TGTATGTATTTTGAG | 55728 |
| rs762217210 | snp | G/T | 1.66554e-05 | 0.00288573 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120325 | TCAAGAAGACTGTGA[G/T]CTTGCAAATAGTGGA | 55728 |
| rs762218694 | in-del | -/AGAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175337 | ATATATGTGAAATAT[-/AGAA]AAAAAAAAAAAAAAG | 55728 |
| rs762228532 | in-del | -/GTC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115631 | TAACTCTTGGGTTAT[-/GTC]GTACTGTGTTTTTAA | 55728 |
| rs762247024 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171434 | CATGGCCAGAGAAGC[A/G]TTTCAGTGTTGTCTG | 55728 |
| rs762296019 | snp | C/T | 3.33072e-05 | 0.00408075 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120256 | GTATAGTAAAACTGA[C/T]ACAGATAGTTCTATG | 55728 |
| rs762311337 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169846 | GGCAGGCGTCTGTAA[C/T]CTGAGCTACTCGGGA | 55728 |
| rs762312751 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112876 | CCCAGCTAATTGTTT[A/G]TATTTTTAGTATAGA | 55728 |
| rs762338016 | in-del | -/TTGTATGCAAAC | 1.65e-05 | 0.00287224 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112197 | TAAGTTGTCATAAGT[-/TTGTATGCAAAC]TTATAACAGTTTGTA | 55728 |
| rs762345856 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083576 | AAAGGAGCCAGTCAC[A/G]AAAGGCCATGTTTTA | 55728 |
| rs762353276 | snp | A/G | 4.2996e-05 | 0.00463639 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102024 | AAAATTATTAAATCT[A/G]TTTTCTCTGTCTATA | 55728 |
| rs762353692 | snp | C/T | 1.6537e-05 | 0.00287545 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121516 | TAAGTTATGTGAGGA[C/T]ACAGAGTTTGAGAAT | 55728 |
| rs762365266 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159272 | CAGTATATGTCTTTG[A/T]AAACCTACCATTTAT | 55728 |
| rs762370797 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098090 | AGTTTTTAAAAACTT[C/T]GTTTTACTCCTGTAT | 55728 |
| rs762417107 | in-del | -/TTG | | | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40185126 | TTCGACGTGTGCCTC[-/TTG]TTGTCCTGTAATGAA | 55728 |
| rs762443043 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174419 | TGAAATTACCACCTC[A/C]TGAAGATATCTGGAC | 55728 |
| rs762482045 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065417 | AAGCCATGGGTTTGA[A/G]TGGACCTAGAAGAGG | 55728 |
| rs762496832 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078303 | CCACCATGGCCGGCT[A/G]CTTTTTGTATCTTTA | 55728 |
| rs762533151 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160659 | CATCTTTATTTCACA[A/T]GCATTTCTTAGTTAG | 55728 |
| rs762540782 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103044 | ACACATTTCCACCCT[C/T]AGTTATTTCTCACAC | 55728 |
| rs762560702 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102159 | AAAGTTTCGTTGCTT[C/T]TGAGAACCAAGTAGG | 55728 |
| rs762572098 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079128 | GGTTTTACCGTGCTG[G/T]CCAGGCTGGTCTTGA | 55728 |
| rs762594799 | snp | A/G | 1.67114e-05 | 0.00289057 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103166 | TCTTACGTTGGACTA[A/G]TTCTTGTTCTTCTCA | 55728 |
| rs762609443 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087530 | ACCAAACCCAGCTAA[-/T]TTTTTTGTATTTTTA | 55728 |
| rs762656935 | snp | A/G | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137080 | AAGTCTAAAGAGAAA[A/G]AGGTATGGAGTTACT | 55728 |
| rs762676633 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069910 | GCAGAGTGAGACCCT[A/G]TCTCTTAAAAAAACA | 55728 |
| rs762710326 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109036 | TGGCCAGGATGGTCT[C/T]GATCTCTTAACTTTG | 55728 |
| rs762720479 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152577 | GATTACAATGAGGCT[A/G]TGTGTTTTAAAACAT | 55728 |
| rs762734239 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088712 | TCCTTGTTGGTCAGG[C/T]CGGTCTCGAATTCCT | 55728 |
| rs762739748 | snp | C/G | 1.80143e-05 | 0.00300114 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122036 | TATTTTACTGATTCT[C/G]TTGAAATAAAGAGAA | 55728 |
| rs762768866 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055574 | ACTGCCATAACAACC[A/G]ACAATGTATCTTCGA | 55728 |
| rs762785614 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102698 | TCTGAAGCTCCTGTA[A/G]ATTTGGATGCCAGTG | 55728 |
| rs762816469 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164518 | AAGTCTGGGTGAAAT[A/C]AAAATGTTTTCTTTA | 55728 |
| rs762825863 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185602 | TTGAGAACTTAAACT[C/T]ATTATTTGGAAAAAA | 55728 |
| rs762863021 | snp | A/G | 3.44204e-05 | 0.00414838 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144836 | AGTTTTCAATAGAAT[A/G]TATGTCTTTGCTTAT | 55728 |
| rs762880262 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105691 | AGTAGCTACGACTAC[A/G]GGCATGGGCCCACCA | 55728 |
| rs762893577 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093246 | ACCATGCCTGGCCCC[A/G]GCCTACTCTTTATTA | 55728 |
| rs762903186 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112736 | GAGATGGAGTTTTGC[C/T]CTTGTTGCCCACGCT | 55728 |
| rs762913806 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073597 | TATTTTACACATAAG[-/A]TTTTTTTTTTTTTTT | 55728 |
| rs762921932 | snp | A/G | 3.32e-05 | 0.00407417 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120844 | TGAGCCCAACCTAGA[A/G]ATTGGAACAAATGAC | 55728 |
| rs762923423 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155507 | GAGCCAACTTTCTCA[A/G]AGGAAGCTGTCATTA | 55728 |
| rs762924357 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146831 | TCTCTATTCTGGCCC[C/T]TGGCAACTACCATTC | 55728 |
| rs762951724 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108820 | CTGTATTTTCCTCAG[-/T]TTTTTTTTTTTTTTG | 55728 |
| rs762961695 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153712 | GGTGACATCAGGGTT[A/C]TTTTTATAAAAGGAG | 55728 |
| rs762982855 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094803 | GTGATCTGCCCACCT[C/T]GACCTCCCAAAACGC | 55728 |
| rs762993457 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40097997 | AAATGTCTCCATGTA[A/T]TGTCATTTGTCCCCT | 55728 |
| rs763020485 | in-del | -/T | 5.2627e-05 | 0.0051294 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117846 | ATATTCCTTCAACCC[-/T]TTTTTTCCCCTGGAA | 55728 |
| rs763026448 | snp | A/C | 1.67178e-05 | 0.00289113 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120500 | CCAGTTGATAAGACT[A/C]TTGGTCAGAGGACAA | 55728 |
| rs763050336 | snp | C/G | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120950 | GGTAGCTCCAATCTA[C/G]GAAGTTCTGAAATGC | 55728 |
| rs763101697 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058987 | CACTACGCCCGGCTA[A/T]TTTTTGTATTTTTTG | 55728 |
| rs763103103 | snp | C/T | 1.66682e-05 | 0.00288684 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121894 | TACTACTCCTAAAGA[C/T]ATGAGTGAAACAGAA | 55728 |
| rs763107252 | in-del | -/TCTGA | 3.30164e-05 | 0.00406289 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102158 | CAAAGTTTCGTTGCT[-/TCTGA]GAACCAAGTAGGTGC | 55728 |
| rs763147025 | snp | A/G | 3.30349e-05 | 0.00406403 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112116 | AAGAAGATATCTCCT[A/G]TAATTATAGATAATA | 55728 |
| rs763248223 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138149 | TAATACAGAAATGGT[A/G]TCTTATTGTGGTTTT | 55728 |
| rs763250420 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072157 | TCAGCTCACTGCAAT[C/T]TCCGCCTTCCGGGTT | 55728 |
| rs763269260 | snp | A/T | 1.67556e-05 | 0.0028944 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120125 | GATATGAATCCTAGC[A/T]TTCAAAGTGCTTTAA | 55728 |
| rs763278593 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177150 | AACCTGGAGGGGGTC[G/T]TGCCTAGCTAAAGCT | 55728 |
| rs763300825 | snp | G/T | 1.65919e-05 | 0.00288022 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120600 | ACAAATTAGTTAACA[G/T]TGTATCTGTGAATAC | 55728 |
| rs763319774 | snp | C/T | 1.75502e-05 | 0.00296223 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144594 | CACCCAAGTAGCAAA[C/T]AGCAAAACTGTCCCT | 55728 |
| rs763343288 | snp | A/G | 1.65381e-05 | 0.00287555 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121496 | CTTTTGTTGGATTCT[A/G]AAACTAAGTTATGTG | 55728 |
| rs763400520 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088229 | TTTTGGTTATTATGA[A/G]TAAAGCTGCTGTAAA | 55728 |
| rs763409628 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175808 | GAGACTCGTCTCAAG[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs763415346 | snp | C/T | 1.65822e-05 | 0.00287938 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154250 | TAAAATAAACATCCT[C/T]GAATTAGAAGTATGA | 55728 |
| rs763425200 | snp | C/G | 1.6615e-05 | 0.00288223 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121317 | AAGCAATTCCATATA[C/G]AGTAATGTATGATAA | 55728 |
| rs763462736 | in-del | -/GGGAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148466 | GAGAGGGAGACTGTG[-/GGGAGA]GGGAGAGGGGGAGGG | 55728 |
| rs763469183 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149230 | ATGAATAGAGAAACA[A/C]AATGTGGTAAATCTA | 55728 |
| rs763487068 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168035 | ATAAAATATGTGTTT[C/G]ATGATGTGTATTAAA | 55728 |
| rs763488143 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073692 | TCAAACTGCTAGGCT[C/T]AAGCGATTCTCTCAC | 55728 |
| rs763510266 | snp | A/C/T | 3.32625e-05 | 0.00407803 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102462 | AAAATTTAGAGAATT[A/C/T]TGGTTCTACTTTAAG | 55728 |
| rs763523292 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159652 | CCAGAACCTAGTCAT[A/G]TCATATCTAGCTGCG | 55728 |
| rs763593035 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101466 | CGCCAAAAAGTGTGC[A/G]TTATTTAATCTGTAT | 55728 |
| rs763644663 | snp | A/G | 8.28919e-05 | 0.00643732 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120738 | ATAAAAATATTGACA[A/G]AAACTCATTCAACAT | 55728 |
| rs763658239 | snp | A/C | 1.73453e-05 | 0.00294489 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144842 | CAATAGAATATATGT[A/C]TTTGCTTATATTGGT | 55728 |
| rs763697820 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120857 | GAAATTGGAACAAAT[A/G]ACAAAATGAATGAAA | 55728 |
| rs763701290 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088961 | TTTTTTTTGTGTGTG[-/T]TTTTTTTGAAACAGA | 55728 |
| rs763729712 | snp | G/T | 1.6806e-05 | 0.00289875 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103177 | ACTAGTTCTTGTTCT[G/T]CTCAGAGGTCTTCCG | 55728 |
| rs763781079 | snp | G/T | 1.99177e-05 | 0.0031557 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102047 | TGTCTATATTTTTGT[G/T]GTTGTTATTATTCTT | 55728 |
| rs763806044 | snp | A/T | 0.000124132 | 0.00787723 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122059 | AAAGAGAAATGAAAA[A/T]TTTCCAAAGGATTAT | 55728 |
| rs763807539 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066318 | TCTATTTGTGATTTT[-/C]CCTTTTTTTTTTTTT | 55728 |
| rs763829983 | snp | C/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055653 | AAAAACCACTGCAAG[C/T]GGAATGAAAAGTAAC | 55728 |
| rs763842625 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087167 | AAGTTATATTTATTG[C/T]ACAGATCAAATCTTC | 55728 |
| rs763863305 | in-del | -/TAAAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127589 | GAAGGAAATCTTATT[-/TAAAGA]TAATTATATATATTA | 55728 |
| rs763888303 | snp | A/C/T | 4.97321e-05 | 0.00498638 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126188 | AACAAAAATCATCTC[A/C/T]GAGAACAGGCAAAAA | 55728 |
| rs763921375 | snp | A/G | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117909 | GAAAAAATAACAAGA[A/G]TGTTGGAACATTATC | 55728 |
| rs763929397 | in-del | -/A | 0.5 | 0 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142829 | GCTTATCGGATAGGG[-/A]AAAAAAATGTCGCCA | 55728 |
| rs763969547 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102847 | CAAACATCCTGAACT[A/G]CCAACTAAGGGGAAG | 55728 |
| rs763974608 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134151 | CTGCTGAGTGTGCAG[A/T]GTTCTAAATATGTCA | 55728 |
| rs763974891 | snp | G/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102701 | GAAGCTCCTGTAGAT[G/T]TGGATGCCAGTGAAC | 55728 |
| rs763993371 | snp | C/T | 1.7081e-05 | 0.00292237 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126156 | CTTGGTTGGACATAC[C/T]GGGCTTGATAATCCT | 55728 |
| rs764012483 | snp | C/T | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121675 | TGGTATTAGTAACGC[C/T]GACTCACAGTCTACT | 55728 |
| rs764031078 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094927 | GCCTCTCGAGTAGCC[A/G]GGACTACAGGTTAGT | 55728 |
| rs764043060 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132599 | ATCCTGAGTTGCCAC[C/T]GTGTTGTTTTAATTA | 55728 |
| rs764044577 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152819 | CCTATTTGTCTGTGA[C/T]TACGGGGAGAGGAAA | 55728 |
| rs764056874 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116595 | ACACTTGCCTCCCTC[C/T]CAATTTACATGCTCT | 55728 |
| rs764074053 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172056 | GGATTATAGGCATGC[A/G]CCACCACACCTGGCT | 55728 |
| rs764091667 | in-del | -/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058057 | TAACTCAGTAAAGGT[-/G]GCCATTGGTTGAGCT | 55728 |
| rs764098144 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062954 | CTCACCACATAGCGG[C/T]AAATGGACTGTCTTA | 55728 |
| rs764099396 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115622 | TTCATTCTTTAACTC[-/TT]GGGTTATGTCGTACT | 55728 |
| rs764142907 | snp | C/T | 1.66776e-05 | 0.00288765 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121210 | AGAAAAGAATAAAAT[C/T]AGCATTTCAGATTCT | 55728 |
| rs764149004 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173379 | TGATCCCTGGCAAGT[G/T]AGATGCTGTGGGAAT | 55728 |
| rs764159894 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156803 | GATGCTCAAAGGAAA[C/T]ACTCACAGAGCATTT | 55728 |
| rs764166223 | in-del | -/GAAGGAAAT | 1.69308e-05 | 0.00290949 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122115 | TATGAATGAAGATGA[-/GAAGGAAAT]GAAGGAAATGAAGGA | 55728 |
| rs764171516 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138215 | ATCTTTTTATGTGCT[A/G]TTTGTCATTTGTACA | 55728 |
| rs764215779 | in-del | -/CT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170446 | CAACATGACGATACC[-/CT]GTCTCTACAAAAAAT | 55728 |
| rs764216909 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081425 | CCGAGGTGGGCGGAT[A/T]ACCTGAGGTCAGGAG | 55728 |
| rs764278701 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073761 | ACCACACCCAGCTAA[G/T]TTTTGTATTTTTTGG | 55728 |
| rs764286200 | snp | C/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120603 | AATTAGTTAACAGTG[C/T]ATCTGTGAATACAGA | 55728 |
| rs764306875 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067470 | CACCTCTTGACTATT[A/G]TGAATAACGCTGTGA | 55728 |
| rs764320774 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131183 | TTTATGAGGACCCAT[-/G]GGGAAATTTCTCTCA | 55728 |
| rs764352980 | in-del | -/TGTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131568 | ATGTATACATGTGAT[-/TGTG]TGTGTGTGTGTGTGT | 55728 |
| rs764361125 | snp | A/G | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112126 | CTCCTATAATTATAG[A/G]TAATACAAACCTACA | 55728 |
| rs764367432 | in-del | -/AGCTCC | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158737 | GAGATTGTGCCACTG[-/AGCTCC]AGCCTGGGCAACAGA | 55728 |
| rs764374020 | snp | A/G | | | upstream-variant-2KB, intron-variant, synonymous-codon, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056546 | ACTTGGGGGGTGGGC[A/G]ACCGGAAGCAGCCGA | 55728 |
| rs764384056 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182282 | TTCGAACAGGACATG[C/G]GTGAAAGATCAGGCT | 55728 |
| rs764391384 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177244 | AACTAGGTTCTTTGG[C/G]AGATAACAGGTGATC | 55728 |
| rs764398729 | snp | C/G | 1.67598e-05 | 0.00289476 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120128 | ATGAATCCTAGCATT[C/G]AAAGTGCTTTAATTC | 55728 |
| rs764423216 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088238 | TTATGAATAAAGCTG[C/T]TGTAAACATTTGTTT | 55728 |
| rs764435263 | snp | C/T | 3.32751e-05 | 0.00407878 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137094 | AAAGGTATGGAGTTA[C/T]TAATTTTTTTTCTAC | 55728 |
| rs764436167 | snp | A/G | 3.48699e-05 | 0.00417537 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144611 | GCAAAACTGTCCCTT[A/G]GTGATATGTTTATGA | 55728 |
| rs764449105 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181375 | TCTCAAAACATTTTC[A/G]ATACTAGCTCATCTT | 55728 |
| rs764453866 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103055 | CCCTCAGTTATTTCT[C/T]ACACTTCCCCAACAA | 55728 |
| rs764465385 | snp | G/T | 1.71278e-05 | 0.00292637 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136934 | ATGTTTCTACTTAAA[G/T]TTTCTACAGCTATTC | 55728 |
| rs764468526 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166375 | AAACTATATATATTA[C/T]TATTAGAAAGTCATT | 55728 |
| rs764481185 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178157 | AGAGCGAGACTGGGT[C/T]CAACAAACAAACAAA | 55728 |
| rs764532962 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096779 | GGATGTGGGATGAGA[A/G]GAGTCAAGGATTATT | 55728 |
| rs764558092 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168105 | TTTTGAAATTATAAG[A/G]GGAAACAAAGGAATA | 55728 |
| rs764604869 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086595 | CACCCGCCTTGGCCT[C/G]CCAAAGTGCAATTGC | 55728 |
| rs764621895 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057808 | AGAGAGCTAGAGTAA[C/T]AGAATGTAGATGACA | 55728 |
| rs764639205 | snp | A/G | 1.66101e-05 | 0.0028818 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121319 | GCAATTCCATATAGA[A/G]TAATGTATGATAAAA | 55728 |
| rs764646070 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155554 | TAGCTAATAAATTCT[G/T]TTAGTATGCAAGTTA | 55728 |
| rs764663160 | in-del | -/CT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115637 | TTGGGTTATGTCGTA[-/CT]GTGTTTTTAAATTTC | 55728 |
| rs764686885 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112773 | CAGTGGCGTGATCTC[A/G]GCTTACTGCAACCTC | 55728 |
| rs764695385 | snp | A/T | 1.65872e-05 | 0.00287981 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154252 | AAATAAACATCCTTG[A/T]ATTAGAAGTATGAAG | 55728 |
| rs764721205 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132400 | TATTATTTTAAATGT[A/C]TACCTTTTTATGTAT | 55728 |
| rs764722749 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062844 | CTAGGAGAAAGCCCT[C/T]GGATACTTCAAGTCT | 55728 |
| rs764728799 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099902 | TCTTTTTTTTCCCCC[A/G]TCCCTGCCCACCCCC | 55728 |
| rs764783940 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102972 | ACCTCTTCCAAGGAA[A/G]CCATGGCTTTGTAGC | 55728 |
| rs764793858 | snp | A/G | 3.37758e-05 | 0.00410935 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121921 | AGAAAAAAACCTAGT[A/G]GTCACAGAGACTGGA | 55728 |
| rs764797732 | in-del | -/A | 1.67609e-05 | 0.00289486 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126173 | GGCTTGATAATCCTG[-/A]ACAAAAATCATCTCA | 55728 |
| rs764811735 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116361 | TTTTTGTTTATCTCG[C/T]CTTTTCTGTGATTGT | 55728 |
| rs764815407 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088492 | GATAGGTAAGTAATA[C/T]CTCATTATAGTTTTT | 55728 |
| rs764837469 | snp | C/T | 0.00184681 | 0.0303314 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097342 | TTTTGGAAGTCAGAA[C/T]GCCAAGGAGAAGGAA | 55728 |
| rs764844925 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060079 | GCTCAAGCAGTCCTC[C/T]TGCCTCAGCCTCTCA | 55728 |
| rs764847469 | in-del | -/GA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175338 | TATATGTGAAATATA[-/GA]AAAAAAAAAAAAAAA | 55728 |
| rs764848877 | snp | C/T | 1.80442e-05 | 0.00300363 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122028 | AAGAAATTTATTTTA[C/T]TGATTCTCTTGAAAT | 55728 |
| rs764849166 | in-del | -/TT | 1.72427e-05 | 0.00293616 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144838 | TTTCAATAGAATATA[-/TT]TGTCTTTGCTTATAT | 55728 |
| rs764854819 | snp | A/G | 3.35317e-05 | 0.00409448 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120113 | AAAGAAATAAGTGAT[A/G]TGAATCCTAGCATTC | 55728 |
| rs764872142 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124238 | ATTTCTAATGTCTTA[A/G]TGTTGAAATTTGGTG | 55728 |
| rs764942342 | snp | A/C/T | 0.00013742 | 0.00828811 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144834 | CAAGTTTTCAATAGA[A/C/T]TATATGTCTTTGCTT | 55728 |
| rs764955465 | snp | A/G | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158557 | AATCCCAGCACTTTA[A/G]GAGGCTGAGACGGGC | 55728 |
| rs764957502 | snp | G/T | 3.49742e-05 | 0.00418161 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136903 | CCCACACAACTTATT[G/T]TCATTTATTGACATT | 55728 |
| rs764958182 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063966 | TTTATTTATTTAGAG[A/T]GATTGGTGGGGCGGC | 55728 |
| rs764963069 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068882 | TCAGCACTTTGGGAG[A/C]CCGAGGCAGGTGGAT | 55728 |
| rs764966322 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100964 | ACATGACATACAGGA[C/G]TCCTCCCAATTTCAC | 55728 |
| rs764968877 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172903 | TGTTAAATAAACAAA[A/G/T]GAATGGTTACATTGA | 55728 |
| rs764979203 | snp | C/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103037 | GTCAACTACACATTT[C/G]CACCCTCAGTTATTT | 55728 |
| rs764985883 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185843 | AATAATAATGAGAAC[A/G]CAGCAGGCTTAGTTT | 55728 |
| rs765039548 | snp | G/T | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102604 | TTTAAATGTAGCAAG[G/T]GACTCCATCGCAGGT | 55728 |
| rs765045025 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159626 | GGACACTTCTACTTA[C/T]GTCCTATTGACCAGA | 55728 |
| rs765075054 | snp | A/C | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120727 | ATATGATGCTTATAA[A/C]AATATTGACAAAAAC | 55728 |
| rs765091985 | snp | A/G | 6.61365e-05 | 0.00575012 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117893 | TCATGGGGTAAGCAA[A/G]GAAAAAATAACAAGA | 55728 |
| rs765096016 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163253 | TTTGCAAATGTACCT[A/G]GTATAATCATAACCA | 55728 |
| rs765109427 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144728 | CTGCCACAGAATGTT[C/T]TAGACCTCCATGGGC | 55728 |
| rs765128213 | snp | A/T | 1.78851e-05 | 0.00299036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117824 | GATTTTTAAAAACTT[A/T]ATTATCAATATTCCT | 55728 |
| rs765158812 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142808 | TGCTACAGCAAGGCC[A/G]AAGAAGCTTATCGGA | 55728 |
| rs765170417 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170093 | CGTCTTATGAATTTG[-/A]GGGTAAAAAGCTTTT | 55728 |
| rs765183575 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151310 | TGGGAGTCTGGCTCT[G/T]TTGCCCAGGCTGGCA | 55728 |
| rs765187348 | snp | G/T | 1.67663e-05 | 0.00289532 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120475 | GCTATCAAATTTTGT[G/T]GGTGACTGGCCAGTT | 55728 |
| rs765206169 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183830 | CTGTGTCTCTCTGCA[G/T]TTTTTTGGGTTTCTT | 55728 |
| rs765266860 | in-del | -/TCTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062731 | TTGAGTTCAGAAGCT[-/TCTA]TCTGTCTGGAATACC | 55728 |
| rs765295021 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095094 | GTTACTATATCTTTT[G/T]TTTTTTGAGATGGAG | 55728 |
| rs765304007 | snp | A/G/T | 5.35521e-05 | 0.00517433 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122333 | AAAGTAAATGACCAT[A/G/T]TGTGTGTCTTTGTGT | 55728 |
| rs765308394 | in-del | -/TTG | 1.88044e-05 | 0.00306624 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102061 | TTGTTGTTATTATTC[-/TTG]TTGTTGTACAGTTGA | 55728 |
| rs765317650 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167957 | TTATCTTATTGGGTG[G/T]AGGGAAAGCATCAAG | 55728 |
| rs765355231 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110965 | GTACATCATTAATTT[C/T]CTGTATGGTCTAATT | 55728 |
| rs765362016 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057714 | GAAATTCATCCTCAA[C/T]AGAGTGAGTCATCTT | 55728 |
| rs765366087 | snp | A/G | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106968 | TTTATATAAATGGAC[A/G]GTACCAGTTTGATGT | 55728 |
| rs765372011 | snp | A/G | 1.65416e-05 | 0.00287586 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154211 | TCTGAAATTAAACCA[A/G]GGTGCTTGAAAGTCA | 55728 |
| rs765412225 | snp | A/G | 1.75668e-05 | 0.00296363 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144586 | TTCCTCATCACCCAA[A/G]TAGCAAACAGCAAAA | 55728 |
| rs765420597 | snp | C/T | 1.65381e-05 | 0.00287555 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112097 | AGCAAAAGAAGCATT[C/T]GAGAAGAAGATATCT | 55728 |
| rs765465516 | in-del | -/CTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146869 | TTTCTATGTGTTTGG[-/CTTT]TTTTTTTTTTTTTTT | 55728 |
| rs765467144 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178735 | TTCCTTGAGACATGC[A/G]AAATGTGTAGGGAAC | 55728 |
| rs765479012 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143901 | GGGGAATTGGCTCTC[A/T]CAGTCATAGAGGTGG | 55728 |
| rs765514742 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156282 | TATTTCAATATTATA[A/G]TTATGATTAATGAAG | 55728 |
| rs765519955 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134606 | ATCAGGGCTGGAGAC[C/T]GACTTCCAGCAGGTG | 55728 |
| rs765532957 | snp | C/T | 1.66266e-05 | 0.00288323 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121177 | TGAACCACAGGATTT[C/T]GCTCTTTTATGGAAA | 55728 |
| rs765578454 | snp | A/C | 3.31851e-05 | 0.00407326 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154145 | GTATATTCCTTAGCT[A/C]ATTTGAAATTTTCAT | 55728 |
| rs765582847 | snp | A/G | 1.65562e-05 | 0.00287712 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154234 | GAAAGTCATGCTAAA[A/G]TAAAATAAACATCCT | 55728 |
| rs765588041 | snp | A/G | 1.7688e-05 | 0.00297383 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119963 | GATATTATCTCTGAA[A/G]AAGAAGAAAATATTT | 55728 |
| rs765591027 | snp | A/G | 0.000181364 | 0.00952098 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152794 | GAATTTAAGCAGAAC[A/G]GTGGGAAGCCCTATT | 55728 |
| rs765594689 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078771 | GGGGTCAAGCAGTTC[A/G]CCCACTGTGGCCTCC | 55728 |
| rs765702648 | snp | A/G | 3.42677e-05 | 0.00413916 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144829 | AATCACAAGTTTTCA[A/G]TAGAATATATGTCTT | 55728 |
| rs765712060 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109575 | ATACAAAAATTAACC[C/G]GGCATGGTGGTGCAC | 55728 |
| rs765712814 | snp | C/T | 3.31702e-05 | 0.00407235 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121032 | ATGGGCAACACACAT[C/T]GTTGCCTCTTACTTT | 55728 |
| rs765740049 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123157 | AAGATTGTGTGGTTC[A/G]TATAGATCTGAATCT | 55728 |
| rs765750256 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109287 | TGGTGATGAAGATCA[C/T]CCTTGGATTCACCAG | 55728 |
| rs765758291 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070537 | TACTGCAGCCTTGAC[C/G]TCCCAGGCTCAAGCC | 55728 |
| rs765785899 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182560 | GGCTCAAGCGATCCT[-/C]CCACCTCAGTGCCCA | 55728 |
| rs765812575 | in-del | -/AGTTGTATGGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088314 | GAAGTGCAATTGCTG[-/AGTTGTATGGT]AGTTGTATGGTAGTT | 55728 |
| rs765833633 | snp | A/G | 1.65537e-05 | 0.0028769 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102324 | CTTCTCCTGATGACC[A/G]AGTATACTCATTTTT | 55728 |
| rs765839960 | snp | C/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056220 | GCCTCGCCGTCCCTC[C/T]CAACTTGCAGCCTGG | 55728 |
| rs765840471 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166215 | AATACCCCCACAGTA[A/G]TAAGTTTTTTCCCTG | 55728 |
| rs765848402 | snp | A/G | 9.97042e-05 | 0.0070599 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131818 | AAGGGAGACCCTTAT[A/G]TTTGAAAAAGATTGT | 55728 |
| rs765862403 | snp | C/T | 4.94833e-05 | 0.00497385 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131953 | GTCTGTAGTTTCTAC[C/T]CTGATGTCACTGAAA | 55728 |
| rs765882835 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151021 | GCTGAAAAATGAGTT[A/C]AACAGTCCTTTCTAA | 55728 |
| rs765892275 | snp | A/G | 1.66438e-05 | 0.00288472 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102443 | AATATGAATTTGAAC[A/G]GTGAAAATTTAGAGA | 55728 |
| rs765904431 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113582 | TTTAGATTTTTCCCC[G/T]TGTAAATGATGAATG | 55728 |
| rs765920849 | snp | G/T | 4.96282e-05 | 0.00498113 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154213 | TGAAATTAAACCAGG[G/T]TGCTTGAAAGTCATG | 55728 |
| rs765922927 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182671 | CAGGCTGGTCCATTT[A/G]ATATATATATACATA | 55728 |
| rs765926405 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143794 | TTATCAAAGGATACA[C/T]AAATAATAAACCAGT | 55728 |
| rs765927906 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075811 | AGGATGTTATAACAG[A/G]TAGATACATATTTCT | 55728 |
| rs765938507 | snp | A/G | 1.6631e-05 | 0.00288362 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40118018 | CTTGTGAGGATAGAA[A/G]CACTAGGTAGGTTAA | 55728 |
| rs765981852 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121802 | GTGGGTCTAAAGAAT[A/G]ATAATGACATACTTC | 55728 |
| rs765981959 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184845 | TTTGTAATCCCAGCT[G/T]CTCGGGAGGCTGAGG | 55728 |
| rs766010604 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130098 | TTGCCCATGCTGGAA[C/T]GTGCAGTGGCGCAAT | 55728 |
| rs766010766 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183772 | TTATCTCACATAATA[A/C]AAAGTAAGAGGTGGT | 55728 |
| rs766012345 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102942 | CGATGTGGAATCCAA[C/T]GATTCCTGCTTTTGA | 55728 |
| rs766045773 | snp | A/T | 0.000165736 | 0.00910167 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121149 | GAAAAGAAGTAGGCA[A/T]GTGCACCCAGACTGA | 55728 |
| rs766052742 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092284 | ATTTGGCCCTGGAAA[-/T]TTTTTTTTTTTGAGT | 55728 |
| rs766096752 | snp | C/T | 3.54925e-05 | 0.00421248 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119952 | GAGACGATGAAGATA[C/T]TATCTCTGAAAAAGA | 55728 |
| rs766106209 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184888 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55728 |
| rs766107123 | in-del | -/TAAAA | 1.6571e-05 | 0.0028784 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154164 | TGAAATTTTCATCTT[-/TAAAA]TAACTCTTTTCTCAT | 55728 |
| rs766113753 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168269 | GAGCCCAATTTTCCT[A/G/T]TCAACAGACAGAGAC | 55728 |
| rs766123778 | snp | C/T | 3.31499e-05 | 0.0040711 | stop-gained, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120632 | GATTGTGTCCAGCAA[C/T]GAGGATCTCCACATG | 55728 |
| rs766142577 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081314 | AGATTATATTTAGTT[A/G]AGTGTCTTGCTTTCA | 55728 |
| rs766176518 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102870 | AGGGGAAGGATGTGA[A/G]TTACTGCCCGGTACT | 55728 |
| rs766179532 | snp | A/T | 1.65701e-05 | 0.00287833 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113420 | AAATGTTTTTGTCTT[A/T]GTTGTATGTAGTCTC | 55728 |
| rs766185721 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161000 | CCCTCCTTCCCACCC[C/G]CAGAAGGACTGCAAG | 55728 |
| rs766194318 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107095 | TCACTTAGTATTTGT[C/T]TGTGTGTTTGTTTTT | 55728 |
| rs766206709 | snp | C/G | 1.67262e-05 | 0.00289185 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121901 | CCTAAAGATATGAGT[C/G]AAACAGAAAAAAACC | 55728 |
| rs766220064 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177097 | GCAGTGGAAAGCTAG[A/C]CTGCTTCTCTGTCTT | 55728 |
| rs766263137 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139633 | GGTAGCTGGGATTAC[A/G]GGTGCCTGCCACCAC | 55728 |
| rs766267254 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067255 | AGGTTTTGCCATGTT[G/T]CCCGGGCTGATCTTG | 55728 |
| rs766273543 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162004 | GGCACCAGAAAAGTG[A/T]TGTAGAAATAGTCTC | 55728 |
| rs766274512 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119291 | CGAGAGTTGGGACTT[C/T]GAGCACTCCTGAAGT | 55728 |
| rs766333547 | snp | A/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121658 | GAGTTTAGCCATGGG[A/G]TTGGTATTAGTAACG | 55728 |
| rs766350568 | snp | A/C | 1.66004e-05 | 0.00288096 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097325 | AAAGGGAAACATTTT[A/C]GTTTTGGAAGTCAGA | 55728 |
| rs766382735 | snp | A/G | 1.86911e-05 | 0.00305699 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103252 | TTTTTAAAAAATAGT[A/G]TAATGTCTGAATTTG | 55728 |
| rs766442080 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106540 | GAGGCTGATTTTTAC[C/T]CTTTTATTTTATTTA | 55728 |
| rs766470593 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166169 | ATTGGAATCTTTTTC[G/T]TTGTTAGTAGGCAGG | 55728 |
| rs766482154 | snp | A/G | 1.64743e-05 | 0.00287 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097460 | TACTCTACCTTCCAT[A/G]GGTGAGACAAAAGTT | 55728 |
| rs766519415 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109224 | AGATTAAGAATTCAG[A/G]AATCTGAAAATGCCA | 55728 |
| rs766519754 | snp | A/C | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057538 | ACACAGCCACTCACA[A/C]GTTCGGATTTTGGAG | 55728 |
| rs766531098 | snp | A/G | 1.6651e-05 | 0.00288535 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120269 | GACACAGATAGTTCT[A/G]TGGAGAGAGTATCAC | 55728 |
| rs766549036 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168978 | TGATCCGCCCACCTC[C/T]GCCTCCCAAAGTGCT | 55728 |
| rs766578610 | in-del | -/TA | 1.65419e-05 | 0.00287588 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102312 | GAAATTGAACTCTTC[-/TA]TCCTGATGACCAAGT | 55728 |
| rs766582547 | snp | A/G | 1.66932e-05 | 0.002889 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120356 | CCACTTCAAAATGAA[A/G]AATCCTCACCTGGTG | 55728 |
| rs766583022 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102692 | CAATTCTCTGAAGCT[C/T]CTGTAGATTTGGATG | 55728 |
| rs766602352 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104134 | CTTTTTTGTATTTTT[-/A]GTAGAGACGGGGTTT | 55728 |
| rs766625153 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125866 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 55728 |
| rs766631772 | in-del | -/G | 1.6513e-05 | 0.00287336 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117989 | AATTGAACGTATTGA[-/G]TTGTGTGCATATTCT | 55728 |
| rs766658577 | in-del | -/AC | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154660 | AAAAGAGGAAAAAGG[-/AC]ATAGTAGTGGTAGTA | 55728 |
| rs766658779 | snp | A/G | 1.65866e-05 | 0.00287976 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121019 | AGTAAAAAGAGTCAT[A/G]GGCAACACACATCGT | 55728 |
| rs766669111 | snp | A/G | | | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158492 | TTTTAACTGATATCA[A/G]AATTAAGAATTATAT | 55728 |
| rs766675506 | snp | C/T | 1.6546e-05 | 0.00287624 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102315 | AATTGAACTCTTCTC[C/T]TGATGACCAAGTATA | 55728 |
| rs766685074 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062360 | CTGTTCCTTTTCCCT[A/G]TCCTCGCTGCTGCCC | 55728 |
| rs766688847 | snp | C/T | 1.65386e-05 | 0.00287559 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121544 | AATTTCCAAAAATCG[C/T]GTGATGGATCACAAA | 55728 |
| rs766731618 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150503 | GAAACCACGTCTCCA[C/G]TAATAATATACAAAA | 55728 |
| rs766759135 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142821 | CCAAAGAAGCTTATC[A/G]GATAGGGAAAAAAAA | 55728 |
| rs766774181 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066318 | CTATTTGTGATTTTC[-/C]CCTTTTTTTTTTTTT | 55728 |
| rs766775578 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178515 | GAATTGTAACTAGTG[A/G]TACTTGGGCAGCATG | 55728 |
| rs766784804 | in-del | -/AGAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064671 | AATACAAAGGTGCTA[-/AGAT]AGATGTCTAGGGTGC | 55728 |
| rs766840592 | snp | A/G | 1.65255e-05 | 0.00287445 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122232 | AATCTCTGACCATAG[A/G]CTGTCTGGAATTGGC | 55728 |
| rs766845027 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099737 | CAATCTGTATAAGGA[C/T]TTTTTTTAATGTGAT | 55728 |
| rs766848366 | snp | A/T | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142787 | CACCAACAGAAGAGG[A/T]TGGAGTGCTACAGCA | 55728 |
| rs766873572 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126383 | TTCTGGTTTATTGTG[-/TA]TGTTTACTTTGTGAT | 55728 |
| rs766890412 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133616 | GCTGGGATTACAGGC[A/G]TGAGCCACCTCCCCT | 55728 |
| rs766929787 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104365 | TCTAGTCTTAATGAA[C/T]ATGCATAGATAACTG | 55728 |
| rs766959829 | snp | C/T | 0.000115374 | 0.0075943 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102203 | AAAATAATGGAAAAA[C/T]GTCCTGAAGAAGAGA | 55728 |
| rs766962073 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144533 | TTAGGTTTATTATTC[C/T]CTTTTTCCCCCTTCC | 55728 |
| rs766988216 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063164 | ATCAATTTGGTTTCT[C/G]TATTTTATTAGTTAG | 55728 |
| rs767003249 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152925 | GTAGATTTCTGTTAT[C/T]AATAATGGCAACTGC | 55728 |
| rs767015013 | snp | C/T | 1.65811e-05 | 0.00287929 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120982 | GCTCAGTGAAATGAC[C/T]TGTGAGAGTCAGACT | 55728 |
| rs767016407 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161604 | TTAAAAGGATCTCTA[C/T]TTTTAAAAAAGAGAT | 55728 |
| rs767020858 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084299 | ATGATGAGGTGTGAC[A/G]GAAAGAATAGGCAAA | 55728 |
| rs767025941 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127496 | CTGGGATTATCAACA[C/T]GAACCACCATGCCCA | 55728 |
| rs767032765 | snp | A/G | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112086 | TTATGTTTTTCAGCA[A/G]AAGAAGCATTTGAGA | 55728 |
| rs767067923 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138650 | TCTTGTACCATTTGT[C/T]ACAAAGACTATTCTT | 55728 |
| rs767077231 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178998 | TATTGATAGCAGCAG[A/G]TGGCAGAAAGCATAA | 55728 |
| rs767091978 | snp | C/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102182 | CAAGTAGGTGCAGCA[C/G]AAAGTAAAATAATGG | 55728 |
| rs767123574 | snp | G/T | 3.37109e-05 | 0.0041054 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126284 | AAAAAGTATCACTCA[G/T]AGAAATAATGTCAGA | 55728 |
| rs767151593 | snp | A/C | 1.65282e-05 | 0.00287469 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117998 | TATTGAGTTGTGTGC[A/C]TATTCTTGTGAGGAT | 55728 |
| rs767157091 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066143 | ACCGTGTTGGCCAGG[A/T]TGGTGTCAATCCCTT | 55728 |
| rs767180458 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182436 | TGTAAGCTAATTGCT[C/T]GTCTGAGTTCATTTT | 55728 |
| rs767185339 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078556 | TTGAGTCAGGGTCTC[A/G]CTTTATCGCCCAGGC | 55728 |
| rs767187834 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074082 | CAGGCGTGAGCCACC[A/G]AGCCCTGCTTGTTTT | 55728 |
| rs767192476 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112748 | TGCTCTTGTTGCCCA[C/T]GCTGGAGGGCAGTGG | 55728 |
| rs767230180 | in-del | -/TC | 1.65386e-05 | 0.00287559 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121493 | AGCCTTTTGTTGGAT[-/TC]TGAAACTAAGTTATG | 55728 |
| rs767264584 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168342 | ACAAGAAACACACTT[A/C]GAGTGATAAAGAAGT | 55728 |
| rs767302466 | snp | C/G | 1.67142e-05 | 0.00289081 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120503 | GTTGATAAGACTATT[C/G]GTCAGAGGACAAAAA | 55728 |
| rs767305307 | in-del | -/A | 1.66918e-05 | 0.00288888 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120056 | ACAATGTTACCTGAG[-/A]ATGTTGCATATCTCT | 55728 |
| rs767311574 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096128 | ACAAGTAGACTGCCT[A/G]TAGTTCTATTCCAGG | 55728 |
| rs767320465 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173524 | AGGAAGAAGTTCATT[C/T]TGACTGGGGCAGCCA | 55728 |
| rs767336597 | snp | C/T | 1.70813e-05 | 0.00292239 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131783 | ATCTTGAACATGATT[C/T]TTATGTTTTTGTTTT | 55728 |
| rs767347661 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183524 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACCAT | 55728 |
| rs767372994 | snp | A/G | 1.67514e-05 | 0.00289403 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097297 | ACTTAAATGTCAAAC[A/G]TCTTAACTAAGAAAA | 55728 |
| rs767399524 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079405 | TACAGGTGTGAGCCA[C/T]TGTGCCCACCCTGGA | 55728 |
| rs767410530 | snp | A/G | 1.65548e-05 | 0.002877 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121694 | TCACAGTCTACTTGT[A/G]ATGCAGAAAGAGGAA | 55728 |
| rs767415561 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164016 | GAATCAGAGAGGAGA[A/G]ACAGAGACATCAGTT | 55728 |
| rs767469126 | in-del | -/TAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136383 | ATCTATCTATCTATC[-/TAT]CTATCTATCTTTTTT | 55728 |
| rs767501974 | snp | A/G | 1.67469e-05 | 0.00289364 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120145 | AAGTGCTTTAATTCT[A/G]GAAACTCCACACATG | 55728 |
| rs767536196 | snp | A/G | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102916 | GCTGTTGCCTCCTCC[A/G]CCACCTCCACCGATG | 55728 |
| rs767562219 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102854 | CCTGAACTGCCAACT[A/G]AGGGGAAGGATGTGA | 55728 |
| rs767564455 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065572 | GCTTGGGATGGGAGG[C/G]TGGATTGTATTGGGT | 55728 |
| rs767575082 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148215 | GCACCTCGGGAGGCC[A/G]AGGCTGGCAGATCAC | 55728 |
| rs767578071 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142598 | CCAGTTTTCATGTGC[A/G]TTTTGTGAAGGTGTA | 55728 |
| rs767594815 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166219 | CCCCACAGTAATAAG[-/T]TTTTTTCCCTGTTTC | 55728 |
| rs767607084 | in-del | -/AG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105740 | ATTTTTTGTAGAGAC[-/AG]AGTCTTACCAGCTTG | 55728 |
| rs767613731 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102932 | CCACCTCCACCGATG[C/T]GGAATCCAATGATTC | 55728 |
| rs767654565 | snp | A/C | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121351 | CACGTTTGTTGAAGA[A/C]AGTGAGCTTACCAGT | 55728 |
| rs767656438 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176525 | ACTCCCGAGGTGATT[C/T]TGATAAGCATGCCTC | 55728 |
| rs767659539 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108099 | TGCCTGGCTAATTTT[C/T]GTATTTTTAGTAGCG | 55728 |
| rs767664495 | snp | G/T | 1.76924e-05 | 0.0029742 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126130 | TATTTATACTACTTT[G/T]TAGATCCTTCCTTGG | 55728 |
| rs767665900 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124299 | TACTTCCACAAAATA[C/T]GGTACCCACAAATTT | 55728 |
| rs767683928 | snp | C/T | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102591 | TTCTCAGTAGTTCTT[C/T]AAATGTAGCAAGTGA | 55728 |
| rs767688361 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151471 | GAGATGGGGTTTTGC[C/T]GTGTTGCCCAGGCTG | 55728 |
| rs767693833 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068992 | GGGCATGGTGGCGGG[A/C]GCCTGTAATCCTAGC | 55728 |
| rs767714319 | snp | C/G | 8.25226e-05 | 0.00642296 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106967 | TTTTATATAAATGGA[C/G]AGTACCAGTTTGATG | 55728 |
| rs767723269 | snp | A/T | 9.9005e-05 | 0.0070351 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113532 | TGGAGGCTACCTAAC[A/T]TGCTTTTTATGTAAC | 55728 |
| rs767731934 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178251 | TCTAAAAACAATCTT[C/T]ACCTTTCTCTCAACT | 55728 |
| rs767786012 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169872 | CGGGAGGCTGAGGCA[G/T]AGAATTGCTTGAACC | 55728 |
| rs767803072 | snp | C/T | 3.34141e-05 | 0.00408729 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142670 | TTGTTTAATATCTTA[C/T]AGCCAAAGAAATTAA | 55728 |
| rs767803337 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131929 | CCACAAGTGAGTGCT[A/G]GAAGGATTGTCTGTA | 55728 |
| rs767816124 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124218 | AAGGTAAAGCACATG[C/T]TTTTATTTCTAATGT | 55728 |
| rs767830295 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103339 | CCCTAAAATGTTTTC[C/T]TTTTACTAAGGTTTC | 55728 |
| rs767842404 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075718 | CTTATTTCTATATTC[C/T]ACCAACTTTTTTTTA | 55728 |
| rs767879006 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155859 | TGCATGCTTTTAAAA[C/T]AAGGAGGCTTATCAT | 55728 |
| rs767893774 | snp | C/T | 1.83788e-05 | 0.00303135 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102068 | TATTATTCTTGTTGT[C/T]GTACAGTTGAAAATG | 55728 |
| rs767900570 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059179 | TTCATCATGATTAGC[C/T]ATGATTATGCATGTT | 55728 |
| rs767942281 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081568 | GGAGGATTGCTTGAA[C/T]GCGGGAGCTGGAGGT | 55728 |
| rs767986148 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104411 | AAACTTATTTTTAGT[-/TT]TTTTTTTTTGATATC | 55728 |
| rs768013652 | snp | C/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142760 | GATGACTACAGAGCA[C/G]AGGCTTTCCTTCACC | 55728 |
| rs768014631 | in-del | -/ATAAAGA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074648 | GTTGACTGAGGAAGC[-/ATAAAGA]ACTGAATTGTGGTGT | 55728 |
| rs768036606 | snp | A/G | 1.68471e-05 | 0.00290228 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137112 | ATTTTTTTTCTACAA[A/G]GGTAGATAATTGCAT | 55728 |
| rs768056174 | snp | C/T | 1.66543e-05 | 0.00288563 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120258 | ATAGTAAAACTGACA[C/T]AGATAGTTCTATGGA | 55728 |
| rs768057276 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138393 | GGTTGCCTTTCACTC[C/T]GTTGTTTCTGTTGTG | 55728 |
| rs768104097 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127131 | CTGGGGTCAGTGATT[C/T]ACCTGCCTTGCCCTC | 55728 |
| rs768137050 | snp | C/T | | | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057157 | GCGGCGAATGAACCC[C/T]CAAGCCCTGAATGTG | 55728 |
| rs768138358 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137618 | GGTAAGACGTGCAGA[C/T]ATGGAAGTGTCGTGA | 55728 |
| rs768186964 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097125 | TTTTAGCTCTGCTGT[G/T]AGAGTTGGTGGTACT | 55728 |
| rs768187979 | snp | A/G | 3.32452e-05 | 0.00407695 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107071 | TTATGAGTAATACAA[A/G]GAAAAAATTCACTTA | 55728 |
| rs768189944 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102170 | GCTTCTGAGAACCAA[A/G]TAGGTGCAGCAGAAA | 55728 |
| rs768197023 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136006 | TTTAGATATTGGAAC[A/G]TGAGTGTGTCAGACA | 55728 |
| rs768238569 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161489 | TTTTTTGGGTACTGG[G/T]TCAGCAGAAAAACTT | 55728 |
| rs768242793 | snp | A/G | 3.35616e-05 | 0.0040963 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120425 | TTTGGGAAACAAAAA[A/G]GCAAATCGACTTTGG | 55728 |
| rs768284565 | snp | A/G | 1.73378e-05 | 0.00294425 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122297 | TTATTTGGTCCTGTT[A/G]GTATTGATTCAGGTA | 55728 |
| rs768284814 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119132 | GTACTTCAGCTCTTC[A/G]TTTCTAAAATGCCAG | 55728 |
| rs768297801 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178112 | TTGCAGTGAGCCGAG[A/G]TCATGCCACTGCACT | 55728 |
| rs768335909 | snp | A/T | 1.69671e-05 | 0.00291261 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142654 | CTGTGTGTGTTACTT[A/T]TTGTTTAATATCTTA | 55728 |
| rs768340863 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181776 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 55728 |
| rs768345203 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177735 | TTCTAGTGTCAGATC[C/T]CTCATTTGTAGAGTG | 55728 |
| rs768347815 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081004 | CATTATTTGGACACT[A/G]AAACTGCCTATATGT | 55728 |
| rs768349447 | snp | A/G | 1.65364e-05 | 0.0028754 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106912 | CAGGACTTTGCAAGA[A/G]GATAATCCAAGTGGA | 55728 |
| rs768352447 | snp | C/T | 6.66034e-05 | 0.00577038 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120310 | CTGTAGTGAAAATAA[C/T]CAAGAAGACTGTGAT | 55728 |
| rs768356378 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164741 | ACAGTTCTTTGCAGC[A/G]GGACCTCACTGTTTT | 55728 |
| rs768377829 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152880 | ACCAGCTGTCATTAA[A/G]TACCTCATAAGCCAT | 55728 |
| rs768416261 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110499 | TCTGATGGCTAATGA[C/T]GTGGAACATCTTTTT | 55728 |
| rs768425485 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181528 | GTGCTCCAAGGCTGG[-/T]TATGGCAGCAATGTC | 55728 |
| rs768435539 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066519 | GAGATGAGGTTACAC[C/T]ATGTTGGCCAGGCTG | 55728 |
| rs768505730 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095874 | GATATGGAGAACATA[C/T]AGGGGTTTAGATCAG | 55728 |
| rs768525755 | snp | A/G | 3.30535e-05 | 0.00406518 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102297 | TACAGAATGCTTTTG[A/G]GAAATTGAACTCTTC | 55728 |
| rs768564395 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058286 | ACGCGCTTTAGGAAA[G/T]GTAAACATCGTGTGT | 55728 |
| rs768574309 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165958 | TACCACTGCTGGGCC[A/T]TATCTATCTCCCTTC | 55728 |
| rs768590203 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114202 | GTTCTATACTTCCAT[A/G]GAGATAGCCCTAACT | 55728 |
| rs768592357 | snp | A/C/T | 9.39389e-05 | 0.00685286 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119911 | GACTTTCTCATGATA[A/C/T]TCTTTAAAATAATCT | 55728 |
| rs768606965 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079956 | GCATATATTCATGGT[A/G]TTGTTAATAATTATT | 55728 |
| rs768624274 | snp | G/T | 3.30398e-05 | 0.00406434 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123102 | GTAATGATTACATTT[G/T]CTTCCCTCCCCCTTC | 55728 |
| rs768630811 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105725 | CGGCTCATTTTTAAA[-/T]TTTTTTGTAGAGACA | 55728 |
| rs768636433 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108185 | GTGGTCTGCCTAACT[C/T]GGCCTCTGAAAGTCC | 55728 |
| rs768656449 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162726 | TGGTGTATGTATTAG[C/G]GTTCTCCAGAATGAA | 55728 |
| rs768664312 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153735 | AAAAGGAGTAGTTAG[A/T]CCAGAACATTATGTT | 55728 |
| rs768675325 | snp | C/T | 4.9552e-05 | 0.0049773 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117991 | TTGAACGTATTGAGT[C/T]GTGTGCATATTCTTG | 55728 |
| rs768701076 | snp | A/G | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120971 | TCTGAAATGCTGCTC[A/G]GTGAAATGACCTGTG | 55728 |
| rs768718613 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081157 | TTTTCCTGATTATGG[-/A]AAAAAATGCATTTCT | 55728 |
| rs768746356 | snp | A/C | 1.65877e-05 | 0.00287986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120799 | AGCTCAGAGGGAACA[A/C]AGATCAAGAATGCCA | 55728 |
| rs768749612 | in-del | -/TTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130890 | AATGTTTAAGAATAT[-/TTA]TTATCATCTTAGGTT | 55728 |
| rs768752101 | snp | C/T | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121098 | AACCACAAACGTTAG[C/T]TGAATGTCAAGAGCA | 55728 |
| rs768804456 | in-del | -/TTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062025 | TATTTATTTTTTGGT[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs768806070 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113527 | AAACTTGGAGGCTAC[C/T]TAACATGCTTTTTAT | 55728 |
| rs768829950 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131638 | ATATAAATAAATAGT[A/G]CAAGAGTACTCGTAT | 55728 |
| rs768854497 | snp | C/T | 1.77451e-05 | 0.00297863 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121994 | TTTGTATCTAGTACT[C/T]CAAATCTTGAATTAA | 55728 |
| rs768871212 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082599 | GGACTTCGAGACCAG[C/T]GTGTGCAACAGAGTG | 55728 |
| rs768907861 | snp | A/G | 1.65699e-05 | 0.00287831 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120694 | TGATGATGCTTCAGA[A/G]CCACTCAATAGCTAT | 55728 |
| rs768917524 | snp | C/G | 1.66974e-05 | 0.00288936 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144790 | GAGAGTTTTAGAGAA[C/G]AAGACTGAAGGTAGG | 55728 |
| rs768919570 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115532 | ATGTATTATTTTAGC[G/T]GCTCTCAGAATTTTA | 55728 |
| rs768929391 | in-del | -/G | 3.31912e-05 | 0.00407363 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120832 | GACTGGTTTAAGTGA[-/G]CCCAACCTAGAAATT | 55728 |
| rs768930827 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100298 | TTATCTTTCTTAAAA[C/G]AGCAAGACAAAACAC | 55728 |
| rs768944042 | snp | C/G | 1.65206e-05 | 0.00287403 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103112 | AGTGCTTATCAAGTA[C/G]AAGAAACCCCAGTTT | 55728 |
| rs768975099 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105881 | AAGATAGCTGAGATA[C/T]ATACATGTTTAACGG | 55728 |
| rs768988160 | snp | G/T | 1.75637e-05 | 0.00296337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097583 | AGGTGAGAAAAAGTT[G/T]AGTTTGAACCCTGTC | 55728 |
| rs768989380 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088054 | GGAGCCACCACGCCC[-/G]GCTACGACTGGCTTT | 55728 |
| rs769041030 | in-del | -/TTATG | 8.37949e-05 | 0.00647228 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112066 | AAAAATGATTTTTAA[-/TTATG]TTATGTTTTTCAGCA | 55728 |
| rs769065056 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089352 | ATTTTCTCATAGTCT[A/G]TAGCTTGTCTTTTCA | 55728 |
| rs769077907 | snp | A/T | 1.65751e-05 | 0.00287876 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121627 | AACTTTAGAGAATTC[A/T]AATTCTCCTGTGCCA | 55728 |
| rs769093389 | snp | A/C | 1.65192e-05 | 0.00287391 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126214 | AAAAAATTACTGAAG[A/C]CTTTAACAGCATCTG | 55728 |
| rs769099514 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067823 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGAGACTA | 55728 |
| rs769103263 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184713 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 55728 |
| rs769108970 | in-del | -/TCTG | 2.13295e-05 | 0.00326562 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102030 | ATTAAATCTGTTTTC[-/TCTG]TCTATATTTTTGTTG | 55728 |
| rs769143539 | snp | A/G/T | 3.3155e-05 | 0.00407144 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102565 | GGAAAGTAACTACCC[A/G/T]GAAGATTCTCTTCTC | 55728 |
| rs769146729 | snp | C/T | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120326 | CAAGAAGACTGTGAT[C/T]TTGCAAATAGTGGAC | 55728 |
| rs769178346 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183063 | AACCATGTTACCCTA[A/C]GACAATTCCTGTTAG | 55728 |
| rs769209263 | snp | C/T | 4.98948e-05 | 0.00499449 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103156 | AAAGAAGACATCTTA[C/T]GTTGGACTAGTTCTT | 55728 |
| rs769224269 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150532 | AAATATTAGCTGGGC[A/T]TGATGTCTCAGGCCT | 55728 |
| rs769224321 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128206 | TCTTAGAGGTTATTT[A/G]GTCTAATTCTCAAGG | 55728 |
| rs769256700 | snp | A/G | 1.78899e-05 | 0.00299076 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126116 | TGAGAGTATGACAGT[A/G]TTTATACTACTTTGT | 55728 |
| rs769268712 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154679 | AGTAGTGGTAGTAAA[G/T]AAAAAAAGGAGATCT | 55728 |
| rs769304855 | snp | A/T | | | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121888 | AAAAGCTACTACTCC[A/T]AAAGATATGAGTGAA | 55728 |
| rs769314888 | snp | C/T | 1.66457e-05 | 0.00288489 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120301 | TAGTACTTGCTGTAG[C/T]GAAAATAATCAAGAA | 55728 |
| rs769316064 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129421 | TAGAAGAGATGGGGT[G/T]TCACCATGTTGGCCA | 55728 |
| rs769346251 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079108 | TGTATTTTTGGTAGA[A/G]ATGGGGTTTTACCGT | 55728 |
| rs769378230 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133961 | TAGACACGTGCCACC[A/G]CGCCTGGCTAGTTTT | 55728 |
| rs769381685 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054590 | AGTCACCGCCCCCCC[-/G]CCGCCCCAAAAAAAA | 55728 |
| rs769395224 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174359 | TAAAAATAGAATTAC[C/T]AGATGAGCCAGCAAT | 55728 |
| rs769410135 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110267 | GCTATTAAGAACAGT[A/G]CTGCTATAAACAAAC | 55728 |
| rs769410343 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094764 | TCCATGTTGGTCAGG[C/G]TGGTCTCAAACTCCT | 55728 |
| rs769410583 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149630 | CCAGGCTCAGTGGCT[C/T]ATGCCTGTAATCCCA | 55728 |
| rs769420745 | snp | G/T | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121489 | CACAAGCCTTTTGTT[G/T]GATTCTGAAACTAAG | 55728 |
| rs769440498 | snp | A/T | 6.60164e-05 | 0.0057449 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102264 | ACATGCAGCTAACTG[A/T]AGACCTGGATTCCTT | 55728 |
| rs769458729 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143999 | GGAGTGTAGCGCAGT[C/T]GAAGTTCAAAGCCTC | 55728 |
| rs769466121 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135928 | TATCTGGCCAATGGA[A/G]GAGGTGAGAGACATA | 55728 |
| rs769469538 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109678 | GTCAGGATCCCACTA[-/C]CTGCACTCCAGCCTG | 55728 |
| rs769476717 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177836 | ATGCAGGGCTCTTTA[C/G]GGGACAGCAACTTTA | 55728 |
| rs769485475 | snp | C/T | 1.65836e-05 | 0.0028795 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120942 | AGACATTGGGTAGCT[C/T]CAATCTAGGAAGTTC | 55728 |
| rs769498079 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095736 | GAGAAATCATTGAAT[G/T]TGACACTTGAACAAA | 55728 |
| rs769499859 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152457 | TTGTTAGGTATCATT[-/A]ATGGTATTATTGCCA | 55728 |
| rs769510141 | snp | G/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102651 | AAAAACAGAAAGAAC[G/T]TTTAGAATCTGAGTG | 55728 |
| rs769520294 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175952 | AAAATTAGCCGGGCG[C/T]GGTGGCGGGCGCCTG | 55728 |
| rs769566537 | in-del | -/TGTGTC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163592 | TGTTCAGCAAGACTT[-/TGTGTC]TGTATGTGATGTCTG | 55728 |
| rs769575542 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164439 | TCATCCACTTTGTGT[A/G]CATATTACCTAGAAA | 55728 |
| rs769615765 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123855 | AAGACTTCAATGCTG[A/T]TTGGTTAAATTTCAA | 55728 |
| rs769632872 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055418 | TTCATCAGAAAATTT[A/G]TCTTCTTGAGTTCTC | 55728 |
| rs769642740 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069783 | ACAAAAAATAAGCCA[G/T]GTGGAATGGTGCATG | 55728 |
| rs769649608 | in-del | -/GTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103479 | TTGTGAGCTATTGAT[-/GTA]GTAGTAGAAGAGAGC | 55728 |
| rs769665179 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060999 | TTTAAAATTTAAATT[A/G]AGACGGGGTGTTGCC | 55728 |
| rs769665850 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152457 | TTGTTAGGTATCATT[A/C]ATGGTATTATTGCCA | 55728 |
| rs769701613 | snp | C/T | 3.31609e-05 | 0.00407177 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106895 | ATTTCATTTATCTTT[C/T]ACAGGACTTTGCAAG | 55728 |
| rs769728738 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179184 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGACT | 55728 |
| rs769734290 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071207 | CTTCCCTGTGGTATT[C/G]ACCTGTTAGGTCTGT | 55728 |
| rs769737203 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132952 | GTTCCTGGGCTATTT[A/T]TGTCAGATTTTGGTT | 55728 |
| rs769764235 | in-del | -/GG | 1.64972e-05 | 0.00287199 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113501 | TTAAACCAAAGGAAC[-/GG]TTGCAAGGTAAAACT | 55728 |
| rs769774788 | snp | C/T | 1.75007e-05 | 0.00295805 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121973 | CATTTCTCTGATATT[C/T]TTAACTTTGTATCTA | 55728 |
| rs769814968 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165753 | ACTCAGTTTCAAAGG[A/T]TGTCATGTTCAGAAG | 55728 |
| rs769828568 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122198 | ACCGAGATATTGAAT[C/T]CCACTCCAGCGATGG | 55728 |
| rs769837740 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102927 | CTCCGCCACCTCCAC[C/T]GATGTGGAATCCAAT | 55728 |
| rs769850368 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112381 | AAATTCTGAAATTCA[A/G]TTTTTGAACTCTAAG | 55728 |
| rs769876320 | snp | A/G | 1.66626e-05 | 0.00288635 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121892 | GCTACTACTCCTAAA[A/G]ATATGAGTGAAACAG | 55728 |
| rs769933356 | in-del | -/TA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084616 | AATTTTGTGTGTGTA[-/TA]TATATATATATATAA | 55728 |
| rs769955147 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084806 | TTTTGGTAGAGACAG[A/G]GTTTCTCCATATTGG | 55728 |
| rs769968272 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160436 | CTAGTGATATGTGGT[A/G]CAATACTCGCCTGTG | 55728 |
| rs769968496 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169582 | AAAAAAAGGGAAACT[C/T]GACATAACCAAACCT | 55728 |
| rs769990530 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129230 | GTTTTTATTTTGTTT[C/T]GTTTTGTTTTTTTTG | 55728 |
| rs770001758 | snp | G/T | 1.64735e-05 | 0.00286993 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124148 | AATCTCTTGCCTGGC[G/T]TTTGTGTTTAGGAGC | 55728 |
| rs770015989 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065214 | GGATCACGTCATAGA[A/T]GTCCTTGAGTGCTTT | 55728 |
| rs770034944 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075437 | GGAGTCTCACTCTGT[C/T]GCCTAGGCTGGAGTG | 55728 |
| rs770036287 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40097933 | CAGCGTCCCTGGCCT[A/G]TACACGCTAGATGCC | 55728 |
| rs770077114 | snp | A/G | 3.35109e-05 | 0.00409321 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120016 | AGAGTTCACTGAAGA[A/G]AAGAATCTTGATGTA | 55728 |
| rs770086988 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113985 | GCTACTGGGAGGGGC[A/G]AATTGTCGTAGCTGC | 55728 |
| rs770107061 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156607 | AAATCCTGTATGCCC[A/G]CAGTAAAGATAGTTT | 55728 |
| rs770115501 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103023 | CACACTGGAGATCTG[C/T]CAACTACACATTTCC | 55728 |
| rs770120336 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118748 | CAAGCTAGTGTTATA[A/C]AAATTATTAACAGTA | 55728 |
| rs770128214 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060513 | CCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA | 55728 |
| rs770145680 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105800 | AAGCAGTCTTCCCAC[C/T]TCAGCCTCCCAAAGT | 55728 |
| rs770146839 | snp | A/G | 4.986e-05 | 0.00499274 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121312 | TCAAGAAGCAATTCC[A/G]TATAGAGTAATGTAT | 55728 |
| rs770160096 | snp | A/T | 1.65509e-05 | 0.00287666 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144773 | GCTCTAGAACATTTG[A/T]TGAGAGTTTTAGAGA | 55728 |
| rs770184106 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144698 | GAGATCTTTGAGAAA[A/G]TCAATGCTTCGCTGC | 55728 |
| rs770195156 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176238 | AATGATTTTTCATCT[G/T]GCAATGATTTTGCAA | 55728 |
| rs770196505 | snp | C/T | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120690 | AGTGTGATGATGCTT[C/T]AGAGCCACTCAATAG | 55728 |
| rs770207495 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115020 | TTAGCCTTTTCAGAT[A/C]AACAAGTCTCAGCTT | 55728 |
| rs770209119 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105653 | TTCCTGGGTTCAAGC[A/T]ATCCTCCTGCCTTGG | 55728 |
| rs770242423 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142304 | TGGCCCTCCTCTCTC[C/T]GGCGGTGGTGGCGAC | 55728 |
| rs770254468 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103728 | TTCAGGGACTTTTCT[A/G]TTCCAAAATAGAGTA | 55728 |
| rs770291423 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160518 | ACTTTCCTAAGCACA[C/T]TTAAGGTAGGCTAGG | 55728 |
| rs770310034 | snp | A/G | 1.65905e-05 | 0.0028801 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102541 | TATAAAGGATAACAC[A/G]TTGGCTTTGGAAAGT | 55728 |
| rs770342383 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088053 | CGGAGCCACCACGCC[C/T]GGCTACGACTGGCTT | 55728 |
| rs770349548 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182226 | GGCTTTTCAGGCTGA[C/T]ACAAGAACATGCGCA | 55728 |
| rs770359408 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175254 | CCAGGCAGGTTTGGA[A/T]CTCCTGGCCATATGT | 55728 |
| rs770364088 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149220 | TCATTAACTGATGAA[C/T]AGAGAAACAAAATGT | 55728 |
| rs770377016 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072442 | GTAGAGATGGGGTTT[C/T]GCCATGTTTGCCAGG | 55728 |
| rs770386769 | in-del | -/TTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061357 | ATATTTTTATTTCAT[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs770401729 | in-del | -/AACT | 1.65773e-05 | 0.00287895 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121063 | TACCAATAGTGCACC[-/AACT]GTTTCTGGAGTAGTA | 55728 |
| rs770416440 | snp | G/T | 3.34622e-05 | 0.00409023 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113384 | AACAATAATTTTAAT[G/T]TCTTGGAAATACCTA | 55728 |
| rs770438200 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145884 | AATACAAGTTGTGGC[C/T]GGGTGCGGTGGCTCA | 55728 |
| rs770469647 | snp | A/G | 1.64936e-05 | 0.00287168 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113485 | AGACACATGGTGGAA[A/G]TTTAAACCAAAGGAA | 55728 |
| rs770478620 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073127 | AATTAGTTTTGGGTT[C/T]TGTTGTTCCTTATAC | 55728 |
| rs770495007 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094523 | CTTTTTAGTGCATAT[A/G]CATTTAGGGTTGCTA | 55728 |
| rs770529831 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132183 | TAACAACTATAACTA[A/C]CAATAAAATAGAACA | 55728 |
| rs770534887 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107751 | TGTTACATAGTAAGA[A/G]GTGAGTTTATTTCAT | 55728 |
| rs770550499 | snp | C/T | 1.66435e-05 | 0.0028847 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102436 | TACACAAAATATGAA[C/T]TTGAACGGTGAAAAT | 55728 |
| rs770555848 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172478 | GGTGGACCCTAATCC[A/G]ATGTGACTGGTGTCC | 55728 |
| rs770561773 | snp | A/T | 1.66181e-05 | 0.00288249 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123253 | GCTCCTTTTTTGTCC[A/T]TTTTGAACCTTTGAA | 55728 |
| rs770613049 | snp | C/T | 3.3284e-05 | 0.00407932 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121294 | TAACACAAAATCAGA[C/T]GTTCAAGAAGCAATT | 55728 |
| rs770630073 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157496 | ATATTGAGATCGGTT[A/G]TTTCTGAGCTGGAAA | 55728 |
| rs770639357 | snp | C/T | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113462 | TATAAAGTCCTTTTT[C/T]GGGAACCAGACACAT | 55728 |
| rs770639936 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100824 | TCATCTGTTTGCTAG[A/G]AATAATATACCTCAT | 55728 |
| rs770648289 | snp | A/T | 0.000296927 | 0.0121809 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122176 | TGGAGTTAGTGGGGA[A/T]GATAAAACCGAGATA | 55728 |
| rs770703832 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111389 | CAATGGCGTGGTCTC[-/A]AGCTCACTGCAACCT | 55728 |
| rs770707667 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103031 | AGATCTGTCAACTAC[A/G]CATTTCCACCCTCAG | 55728 |
| rs770713949 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139584 | GCAACCTGTGCCCTC[C/T]GAGTTCAAGTGATTC | 55728 |
| rs770716402 | in-del | -/AA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117676 | TCTTTGTTTGAACTT[-/AA]AAGTGTATAATTTAA | 55728 |
| rs770744536 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178018 | AACAAAAAAACAGTA[A/T]GTAGAAAGTAAGGTG | 55728 |
| rs770784103 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061785 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 55728 |
| rs770789492 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068158 | TTTGCCCACTTTTAA[A/G]TTGGGTTATTTGGAT | 55728 |
| rs770798546 | snp | C/T | 1.76163e-05 | 0.0029678 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142632 | CATGAGTTTTTTTTT[C/T]AACTTTCTGTGTGTG | 55728 |
| rs770804719 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129552 | TTTCTGTAGATTGGG[C/T]AATATAATAGAAGCT | 55728 |
| rs770868673 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083724 | GTGGGGTTTCTTCTT[C/G]AGTTAATAGAAATGT | 55728 |
| rs770869481 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137030 | CCCAAGAGTTTGTTC[A/G]CCAAAATGAGAATGT | 55728 |
| rs770880542 | snp | C/G | 1.80282e-05 | 0.0030023 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097593 | AAGTTTAGTTTGAAC[C/G]CTGTCCATCTTATAA | 55728 |
| rs770898023 | in-del | -/CT | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055545 | TGCCCCAAATTTACA[-/CT]CTGTTTAAAGCAACT | 55728 |
| rs770913684 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40163053 | CTGCAGTACCTTTTA[C/T]GACTTAGTATTGGAA | 55728 |
| rs770930282 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181019 | GCCGGGCATGGTGGC[A/G]TGTGCCTGTAGTCCC | 55728 |
| rs770932652 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131888 | CCAGCCATTAACCAA[A/G]ATTTTCTGGTGGACA | 55728 |
| rs770950555 | in-del | -/TAGAG | 1.66192e-05 | 0.00288259 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121315 | AGAAGCAATTCCATA[-/TAGAG]TAATGTATGATAAAA | 55728 |
| rs771005362 | in-del | -/CT | 1.69226e-05 | 0.00290878 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137117 | TTTCTACAAGGGTAG[-/CT]ATAATTGCATATAAA | 55728 |
| rs771026196 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102918 | TGTTGCCTCCTCCGC[C/T]ACCTCCACCGATGTG | 55728 |
| rs771028610 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076495 | AAACCCAAAAATATC[-/T]TTTTTTTTTTTTGAG | 55728 |
| rs771059815 | snp | A/C | 1.65414e-05 | 0.00287583 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121756 | TCCTGAAAACCATGA[A/C]TCGATGACAAGTATA | 55728 |
| rs771074541 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084630 | TATATATATATATAT[-/A]ATTTTTTTTTTTTTT | 55728 |
| rs771085143 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126989 | GTCTCAAACTCCTGA[C/T]CTCAAGTGAGCCACC | 55728 |
| rs771107724 | snp | A/T | 0.000115337 | 0.00759312 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152865 | AGTTGCTCGCATCAA[A/T]CCAGCTGTCATTAAG | 55728 |
| rs771123973 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164768 | TTTTGTTTGAAGTTG[-/C]TTCTTGCCTATTTAT | 55728 |
| rs771155348 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077976 | TCGTGAAGTGTTCCA[C/T]ATTTTTAGCTTCAGT | 55728 |
| rs771157300 | snp | C/T | 1.73706e-05 | 0.00294703 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142891 | TGATTATATATTTTT[C/T]GTCAGTTATAATAAC | 55728 |
| rs771162779 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110827 | ATAGGTGTGAGGTAC[C/T]GTGCCCAGCCTCCTT | 55728 |
| rs771173348 | snp | A/G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127865 | ACGGGGTTTCACCGT[A/G/T]TTAGCCAGGATGGTC | 55728 |
| rs771203311 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40087983 | GGATGGTCTCGAACT[C/G]CTGACCTCCGGTGAT | 55728 |
| rs771324922 | snp | C/G/T | 3.3144e-05 | 0.00407076 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121878 | CAGGTATTCTAAAAG[C/G/T]TACTACTCCTAAAGA | 55728 |
| rs771328421 | snp | A/C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063934 | ACAGGTGTGAGCCAC[A/C/T]GTGCTGGCCAATTTT | 55728 |
| rs771335743 | snp | A/G | 4.97096e-05 | 0.00498521 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144666 | AGATGAAAGAAGCCA[A/G]TCACCTTGCTGCCAT | 55728 |
| rs771337196 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091725 | ATCCTTTCACCTCAC[C/G]CTGCCCACCAGTACC | 55728 |
| rs771354224 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067821 | CTCCTGTCTCAGCCT[C/T]CCGAGTAGCTGAGAC | 55728 |
| rs771356590 | in-del | -/AAC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132476 | TCTTTCCAAATGACT[-/AAC]CAAATGAATGGATCA | 55728 |
| rs771438104 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172653 | TGACACTTCGATTTT[G/T]GAATTTAGCCTCCAG | 55728 |
| rs771442589 | snp | A/T | 1.65004e-05 | 0.00287227 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112202 | TTGTCATAAGTTTAT[A/T]ACAGTTTGTATGCAA | 55728 |
| rs771443624 | snp | C/T | 6.59457e-05 | 0.00574182 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123118 | CTTCCCTCCCCCTTC[C/T]CCCACAAGGGTCTCT | 55728 |
| rs771496518 | snp | A/G | 1.65594e-05 | 0.0028774 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121114 | TGAATGTCAAGAGCA[A/G]ATGCCTAAGAGAGAC | 55728 |
| rs771499301 | snp | C/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102166 | CGTTGCTTCTGAGAA[C/G]CAAGTAGGTGCAGCA | 55728 |
| rs771502503 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142440 | AATTTTAGAGAACTC[-/T]TCAACATCTCCCGAG | 55728 |
| rs771531127 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171630 | CAGGGTTCTCTAGAA[A/G]GACAGAACTAATAGG | 55728 |
| rs771539987 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151020 | GCTGAAAAATGAGTT[-/A]AAACAGTCCTTTCTA | 55728 |
| rs771602072 | snp | A/G | 1.66161e-05 | 0.00288232 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120567 | AAAGCGACAAAAAGT[A/G]TAATTACCCTCAGTC | 55728 |
| rs771627750 | snp | G/T | 1.65737e-05 | 0.00287864 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123240 | CTTTTTATAAAGAGC[G/T]CCTTTTTTGTCCATT | 55728 |
| rs771654972 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066932 | CTACTTGTAGATACC[A/G]CATATAAGTAGAAAC | 55728 |
| rs771674263 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150949 | TGCTTTTTAAAGGAG[C/T]CCTTATCTTTTATGA | 55728 |
| rs771689281 | snp | C/T | 5.05804e-05 | 0.00502868 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112059 | TTGTTTAAAAAATGA[C/T]TTTTAATTATGTTAT | 55728 |
| rs771742233 | in-del | -/GGAA | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096818 | TTGGCCCAAGTCATT[-/GGAA]GGATATAGTTGCACT | 55728 |
| rs771751278 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067986 | CACCTGGCCTGTTTT[C/T]TAACTCATTTGTTGA | 55728 |
| rs771763819 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069203 | AGCCCTTTGGGAGGC[C/T]GAGGCGGGCACATCA | 55728 |
| rs771770309 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169297 | TGAGGCACGAGAATT[A/G]CTTGAACCCAGCGGG | 55728 |
| rs771771916 | snp | A/T | 0.000148794 | 0.00862407 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102306 | CTTTTGAGAAATTGA[A/T]CTCTTCTCCTGATGA | 55728 |
| rs771822894 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111859 | GGCCTCAAGTGGTCT[G/T]CCCGCTTTGGCTTCC | 55728 |
| rs771837868 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077138 | AATATTATGTAGAAT[-/AT]ATATATGTGTGTGTG | 55728 |
| rs771857958 | snp | A/T | 1.66765e-05 | 0.00288756 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121895 | ACTACTCCTAAAGAT[A/T]TGAGTGAAACAGAAA | 55728 |
| rs771882180 | in-del | -/TTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124333 | TTTGCAAATAAAAGT[-/TTTA]TTTATTTATTTATTT | 55728 |
| rs771905339 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081203 | AAATGCGAAAGTAGC[A/G]TATAAAAAATATATT | 55728 |
| rs771957270 | in-del | -/CAC | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055727 | CACCACTACCATCAC[-/CAC]CACCACCACCACCAA | 55728 |
| rs771998522 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155191 | GAGGTCAGAAGTTCA[A/G]GACCAGCCTGGCCAA | 55728 |
| rs772000831 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098546 | TAGTATAAGGTAAAA[C/T]TATTCTGGATTTGGG | 55728 |
| rs772001426 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063647 | ATTAAATTAATTAAT[G/T]AATTAATTTTTTTGA | 55728 |
| rs772024668 | snp | A/G | 0.000198508 | 0.00996065 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154200 | TCTGCAGGTTCTCTG[A/G]AATTAAACCAGGGTG | 55728 |
| rs772027051 | snp | A/C/G | 3.29458e-05 | 0.00405857 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103029 | GGAGATCTGTCAACT[A/C/G]CACATTTCCACCCTC | 55728 |
| rs772101502 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084100 | GGATTACAGGCATGC[A/G]CCACCACTCCCAACT | 55728 |
| rs772113068 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152036 | TTTTCAGGATTTATA[G/T]CCTTGATTTTCACAA | 55728 |
| rs772122848 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179907 | GTAGCTGGAATTACA[C/G]GCATGCGCCACCACG | 55728 |
| rs772135137 | snp | C/G | 1.84766e-05 | 0.0030394 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119941 | TTACAGCCCAAGAGA[C/G]GATGAAGATATTATC | 55728 |
| rs772151059 | snp | C/T | 1.65414e-05 | 0.00287583 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152766 | TTTAACTCCCCTGAT[C/T]TCTGTTGTAACAGAA | 55728 |
| rs772160856 | snp | C/T | 1.69072e-05 | 0.00290746 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144810 | CTGAAGGTAGGACTG[C/T]GGTAATCACAAGTTT | 55728 |
| rs772172669 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117966 | ATGAGTTCTTCGGTT[C/T]CAGAGAAAATTGAAC | 55728 |
| rs772190334 | snp | A/G | 1.66918e-05 | 0.00288888 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120056 | ACAATGTTACCTGAG[A/G]ATGTTGCATATCTCT | 55728 |
| rs772221695 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144203 | TGGTTGGTGCCTGCC[C/T]GCATGGAGGGGAGGT | 55728 |
| rs772224954 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102679 | GTGCGTTGAGGCTCA[A/G]TTCTCTGAAGCTCCT | 55728 |
| rs772260317 | in-del | -/AAGG | | | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113495 | TGGAAGTTTAAACCA[-/AAGG]AACTTGCAAGGTAAA | 55728 |
| rs772281095 | snp | A/G | 3.31813e-05 | 0.00407302 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120811 | ACACAGATCAAGAAT[A/G]CCAAAGACTGGTTTA | 55728 |
| rs772290643 | snp | A/G | 1.65252e-05 | 0.00287443 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126237 | AGCATCTGAAATGCT[A/G]CCTTTATTGGATCAT | 55728 |
| rs772309400 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125473 | ACTGTAGCTGTTATG[G/T]TTGCTCACTTCCAGC | 55728 |
| rs772323971 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145440 | TGTTGGCCAGGCTGG[C/T]CTTGAACTCCTGGCC | 55728 |
| rs772335456 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101743 | CAGGCTTTAGGACTT[A/T]TATAAATAAGCCTAA | 55728 |
| rs772343261 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086228 | CAGACCAACCTGGAT[A/T]ACAGGTGTGAACCAT | 55728 |
| rs772403013 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091150 | CACTTTCTTGTTGGA[G/T]ATTTTATAGATTATT | 55728 |
| rs772404476 | in-del | -/T | 0.0185685 | 0.0945488 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142623 | GGTGTAAGGCATGAG[-/T]TTTTTTTTTAACTTT | 55728 |
| rs772456939 | snp | C/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120852 | ACCTAGAAATTGGAA[C/G]AAATGACAAAATGAA | 55728 |
| rs772481752 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151792 | AGATGGAGATCATAG[A/G]CAAGGAATTAGAAAT | 55728 |
| rs772482332 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142774 | AGAGGCTTTCCTTCA[C/T]CAACAGAAGAGGATG | 55728 |
| rs772495487 | snp | A/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054836 | TTTGTTCTTCATTCC[A/G]GTCTCACTTTCAGAA | 55728 |
| rs772496937 | snp | C/T | 1.66571e-05 | 0.00288587 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120327 | AAGAAGACTGTGATC[C/T]TGCAAATAGTGGACC | 55728 |
| rs772503512 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172590 | AGGCAAGGAGAGAGG[C/T]CTGGAACAGCTGCCT | 55728 |
| rs772512614 | snp | A/G | 1.67804e-05 | 0.00289653 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120444 | AATCGACTTTGGAAA[A/G]GTTCCCAAGACATGA | 55728 |
| rs772569368 | in-del | -/A | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, frameshift-variant, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097469 | TTCCATGGGTGAGAC[-/A]AAAGTTGATCAGGAA | 55728 |
| rs772577746 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132084 | GAAACCACGAATATA[C/G]CTAAACCCTCTATAT | 55728 |
| rs772578361 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077955 | GCAAGGATATGACAC[A/G]CAGATTCGTGAAGTG | 55728 |
| rs772590049 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171456 | TGTTGTCTGATGACA[C/T]TTAGGTTCAGCTTTG | 55728 |
| rs772597247 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068016 | ATAGTGGCCATCTCA[A/G]TAGGTGTAAGGTGAT | 55728 |
| rs772597947 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091064 | TTCAGTGTCCATGTG[-/T]TTTTTTGCTAGTATG | 55728 |
| rs772636527 | in-del | -/AC/ATAC | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080325 | TATATATATATATAT[-/AC/ATAC]ACACACACACATATA | 55728 |
| rs772643416 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062319 | TCCTGACTTCGTGAT[C/T]CTCCTCTCTTTAATA | 55728 |
| rs772643620 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072806 | TCTCGGCTCACTGCA[A/C]TCTCTGCCTCCCAGG | 55728 |
| rs772658845 | snp | C/G | 1.66502e-05 | 0.00288527 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121284 | TTTTCAATATTAACA[C/G]AAAATCAGACGTTCA | 55728 |
| rs772662031 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161649 | GTACGTAAAATGATA[C/T]GATGTTAGCAATTCA | 55728 |
| rs772667512 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186107 | AGACAGGCCTTTTAA[A/G]AGGTTTGATGCAAAA | 55728 |
| rs772671628 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104807 | AGAACCTGCGTTGTC[-/T]TTTTTTTTTTTTTTG | 55728 |
| rs772690042 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084631 | ATATATATATATATA[-/AT]TTTTTTTTTTTTTTT | 55728 |
| rs772691274 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089720 | GGGATTACAGGCATG[A/G]GCCACTGCACCCAGC | 55728 |
| rs772694103 | snp | G/T | 1.65765e-05 | 0.00287888 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121636 | GAATTCTAATTCTCC[G/T]GTGCCAGAGTTTAGC | 55728 |
| rs772699868 | snp | C/T | 2.98191e-05 | 0.00386118 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126363 | TATTAAGCTACTGTC[C/T]CTGATTCTGGTTTAT | 55728 |
| rs772700177 | snp | C/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056151 | AGAAGGCGGGTTCCC[C/G]TGCCCGCCGCAGCGG | 55728 |
| rs772712717 | snp | A/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121137 | AGAGAGACCCTGGAA[A/G]AGAAGTAGGCATGTG | 55728 |
| rs772726351 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115744 | TATGATTCACTGACA[C/T]TTATAAGATTTTTTT | 55728 |
| rs772749147 | snp | C/T | 1.65485e-05 | 0.00287645 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121742 | ATGAGAGCTGTCACT[C/T]CTGAAAACCATGAAT | 55728 |
| rs772749628 | snp | C/T | 3.30077e-05 | 0.00406236 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152931 | TTCTGTTATTAATAA[C/T]GGCAACTGCCCATAT | 55728 |
| rs772757020 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088381 | TTCAGAGTGACTGTA[C/T]CATTTTACATTCCCA | 55728 |
| rs772763086 | snp | A/C | 1.65833e-05 | 0.00287948 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121013 | TGTCTAAGTAAAAAG[A/C]GTCATGGGCAACACA | 55728 |
| rs772874900 | snp | C/G | 1.64822e-05 | 0.00287068 | splice-acceptor-variant | N4BP2 | GRCh38.p7 | 4:40123126 | CCCCTTCCCCCACAA[C/G]GGTCTCTAACAGTTG | 55728 |
| rs772887130 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075728 | TATTCCACCAACTTT[G/T]TTTTATTACTGCATA | 55728 |
| rs772893604 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079537 | GACCATTGCCATAAC[A/G]CTATTAGAGATCATG | 55728 |
| rs772972801 | snp | A/G | 4.96266e-05 | 0.00498105 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154207 | GTTCTCTGAAATTAA[A/G]CCAGGGTGCTTGAAA | 55728 |
| rs772988131 | snp | C/T | 3.33762e-05 | 0.00408497 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121896 | CTACTCCTAAAGATA[C/T]GAGTGAAACAGAAAA | 55728 |
| rs772993146 | snp | C/T | 1.67105e-05 | 0.0028905 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120070 | GAATGTTGCATATCT[C/T]TCTAATGCAGATTTA | 55728 |
| rs773027915 | snp | C/T | 1.6492e-05 | 0.00287154 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131940 | TGCTAGAAGGATTGT[C/T]TGTAGTTTCTACTCT | 55728 |
| rs773041168 | snp | A/G | 1.7959e-05 | 0.00299652 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122010 | CAAATCTTGAATTAA[A/G]TGAAGAAATTTATTT | 55728 |
| rs773041524 | snp | C/T | 1.65817e-05 | 0.00287933 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120613 | CAGTGTATCTGTGAA[C/T]ACAGATTGTGTCCAG | 55728 |
| rs773047065 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127460 | GCTCAAGTGATCCTC[C/T]TGCCTCAGCTTCCCA | 55728 |
| rs773075183 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082050 | CTGGGAGGCAGAGGT[G/T]GCAGTGAGCCAAGGT | 55728 |
| rs773129195 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177038 | TTTGGCGGAATTAAG[A/G]AAGAGTCCTGCAACA | 55728 |
| rs773171396 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073598 | ATTTTACACATAAGA[-/T]TTTTTTTTTTTTTTA | 55728 |
| rs773176767 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136514 | CTCTCAGCCTCCCGA[C/G]TAGCTGGGATTACAG | 55728 |
| rs773181844 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119280 | AAGGCATCCTGCGAG[A/C]GTTGGGACTTCGAGC | 55728 |
| rs773217096 | snp | C/T | 3.3012e-05 | 0.00406262 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117976 | CGGTTCCAGAGAAAA[C/T]TGAACGTATTGAGTT | 55728 |
| rs773223924 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179919 | ACAGGCATGCGCCAC[C/T]ACGCCCGGCTACTTT | 55728 |
| rs773229185 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102680 | TGCGTTGAGGCTCAA[C/T]TCTCTGAAGCTCCTG | 55728 |
| rs773236074 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152040 | CAGGATTTATATCCT[A/T]GATTTTCACAAGGTC | 55728 |
| rs773247183 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067152 | AGCCTTGACCTCCCC[A/G]GACTCAAGCCATCCT | 55728 |
| rs773256332 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102938 | CCACCGATGTGGAAT[C/G]CAATGATTCCTGCTT | 55728 |
| rs773286931 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159379 | TATTTCTTTCTTCCT[A/G]TAAAATCCCAGGGAT | 55728 |
| rs773310496 | snp | A/C | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152785 | GTTGTAACAGAATTT[A/C]AGCAGAACGGTGGGA | 55728 |
| rs773342440 | in-del | -/C | 1.7561e-05 | 0.00296314 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117844 | TCAATATTCCTTCAA[-/C]CCTTTTTTCCCCTGG | 55728 |
| rs773346400 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102809 | GTGTTTCTACCTTCC[A/G]AAGGGTTCAACTTCA | 55728 |
| rs773350211 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084152 | GACGGGGTTTCGGCA[C/T]GTTGCCCAGGCTGGT | 55728 |
| rs773360240 | in-del | -/ATCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136347 | TTAGAAATTGAATCT[-/ATCT]ATCTATCTATCTATC | 55728 |
| rs773392848 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179552 | AGAGGCTATTATTAT[A/C]CCCATTTAACAGTTG | 55728 |
| rs773393390 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117882 | AGGCGTAACATTCAT[A/G]GGGTAAGCAAAGAAA | 55728 |
| rs773440090 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070094 | GATATAGAAAAGTAG[G/T]ATGATACATTGAAAC | 55728 |
| rs773475964 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132098 | AGCTAAACCCTCTAT[A/G]TACCCTCTATATACT | 55728 |
| rs773477837 | snp | A/G | 1.65762e-05 | 0.00287886 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121649 | CCTGTGCCAGAGTTT[A/G]GCCATGGGATTGGTA | 55728 |
| rs773488495 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171573 | CCTGAATGTGATCTT[A/G]ATTGGAGGTATTCTT | 55728 |
| rs773490525 | snp | A/G | 3.51198e-05 | 0.0041903 | splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40122310 | TTGGTATTGATTCAG[A/G]TAAGGAAAAAGTAAA | 55728 |
| rs773526923 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086232 | CCAACCTGGATTACA[G/T]GTGTGAACCATCATG | 55728 |
| rs773541922 | in-del | -/TGT | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078986 | AGTGGAGTCTCACTC[-/TGT]TGTTGCCCAGGCTGG | 55728 |
| rs773550647 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076782 | TGTGAGCCACCACAC[C/G]CGGCCCAAAAATATC | 55728 |
| rs773562794 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129830 | AGAAATATACTTTGT[A/G]TATATTTTTTAAAGC | 55728 |
| rs773568783 | snp | C/G/T | 3.30263e-05 | 0.00406353 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106941 | GAGTCATTCTTAGTA[C/G/T]TGATGATTATTTTTA | 55728 |
| rs773614160 | snp | A/G | 5.17299e-05 | 0.0050855 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142885 | GAAAACTGATTATAT[A/G]TTTTTTGTCAGTTAT | 55728 |
| rs773638727 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062323 | GACTTCGTGATCCTC[C/T]TCTCTTTAATATCTC | 55728 |
| rs773657561 | snp | A/G | 8.38835e-05 | 0.0064757 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120456 | AAAAGTTCCCAAGAC[A/G]TGAGCTATCAAATTT | 55728 |
| rs773663568 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184848 | GTAATCCCAGCTGCT[C/T]GGGAGGCTGAGGCGT | 55728 |
| rs773674233 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065623 | GTTGAAACAACAAAT[A/G]TAAACTACTTTCATT | 55728 |
| rs773681513 | in-del | -/G | 1.65679e-05 | 0.00287814 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121145 | CCTGGAAAAGAAGTA[-/G]GCATGTGCACCCAGA | 55728 |
| rs773734836 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063739 | ACCTCCACCTCCCGT[A/G]TTCAAGCGATTCTCC | 55728 |
| rs773739559 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114406 | CCCCCCTCCTCTTGG[C/T]AACCACTAATGTGTG | 55728 |
| rs773743772 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119138 | CAGCTCTTCATTTCT[A/G]AAATGCCAGTAATAA | 55728 |
| rs773765037 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172603 | GGCCTGGAACAGCTG[C/T]CTCCCTTGCAGCCCT | 55728 |
| rs773770541 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160822 | GAGGCACTTTTGCAA[A/G]AGGTGCCTCTGCTCC | 55728 |
| rs773789504 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161346 | CAGGATGCAATTACC[A/G]GGATAGACTGGGAAA | 55728 |
| rs773799961 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174681 | GTGGTGCGCACCTGT[C/T]ATCCCAGTTACTCGG | 55728 |
| rs773806098 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102177 | AGAACCAAGTAGGTG[C/T]AGCAGAAAGTAAAAT | 55728 |
| rs773806250 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107072 | TATGAGTAATACAAA[A/G]AAAAAATTCACTTAG | 55728 |
| rs773831222 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115771 | TTTTGGCCTAGTTAA[A/G]TGTTGATTTTTTATA | 55728 |
| rs773857635 | snp | A/G | 1.65285e-05 | 0.00287471 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102301 | GAATGCTTTTGAGAA[A/G]TTGAACTCTTCTCCT | 55728 |
| rs773880322 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088471 | GTTTTTTATTTTAGT[C/G]AATTTGATAGGTAAG | 55728 |
| rs773890434 | snp | A/T | 1.65441e-05 | 0.00287607 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121752 | TCACTCCTGAAAACC[A/T]TGAATCGATGACAAG | 55728 |
| rs773900705 | in-del | -/TC | 0.000259887 | 0.0113963 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126361 | AATATTAAGCTACTG[-/TC]TCTGATTCTGGTTTA | 55728 |
| rs773907812 | snp | A/G | 1.73504e-05 | 0.00294532 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122298 | TATTTGGTCCTGTTG[A/G]TATTGATTCAGGTAA | 55728 |
| rs773919322 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100609 | ACTCCTGGGCTCAAG[A/C]GATCTACCTGCCTCA | 55728 |
| rs773920972 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068635 | TCACATATGTGAGTA[C/T]TTATTTCTGGGCTTT | 55728 |
| rs773963871 | snp | C/T | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40106932 | ATCCAAGTGGAGTCA[C/T]TCTTAGTACTGATGA | 55728 |
| rs773984554 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065455 | AACAAAAGATTAGGA[A/G]CAGAACCTTAGCGAG | 55728 |
| rs774019699 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094995 | TTTGGCCAGGTTGGT[C/T]TCAAACTCCTCACCT | 55728 |
| rs774029246 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109718 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAGTG | 55728 |
| rs774051705 | snp | A/T | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120980 | CTGCTCAGTGAAATG[A/T]CCTGTGAGAGTCAGA | 55728 |
| rs774053126 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105911 | GTAAAAAAGGAAGTG[A/T]CAGAGAAGGGAAAGC | 55728 |
| rs774058160 | snp | C/G | 0.000329663 | 0.0128344 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142762 | TGACTACAGAGCAGA[C/G]GCTTTCCTTCACCAA | 55728 |
| rs774091353 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176052 | TTGAGATCGGGCCAC[G/T]GCAATCCAGCCTGGG | 55728 |
| rs774130829 | snp | C/T | 5.15362e-05 | 0.00507597 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131776 | ACATTTCATCTTGAA[C/T]ATGATTTTTATGTTT | 55728 |
| rs774169404 | snp | A/G | 1.654e-05 | 0.00287571 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121760 | GAAAACCATGAATCG[A/G]TGACAAGTATATTTC | 55728 |
| rs774173060 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152883 | AGCTGTCATTAAGTA[C/T]CTCATAAGCCATAGC | 55728 |
| rs774179577 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078255 | AGATTCTCATGCTTC[A/T]GTGTCCTGAGTAGCC | 55728 |
| rs774203980 | in-del | -/CAC | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055725 | CACCACCACTACCAT[-/CAC]CACCACCACCACCAA | 55728 |
| rs774228013 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166018 | TGAATAGTTCTGGGC[A/C]TTTTGCATATAAATC | 55728 |
| rs774240913 | snp | A/C/T | 4.95073e-05 | 0.0049751 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113531 | TTGGAGGCTACCTAA[A/C/T]ATGCTTTTTATGTAA | 55728 |
| rs774272435 | snp | G/T | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102928 | TCCGCCACCTCCACC[G/T]ATGTGGAATCCAATG | 55728 |
| rs774317795 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153765 | TGAGATTAATTATCT[A/G]TTTTAGAGACTAGTC | 55728 |
| rs774321266 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134189 | CAAATCTTTAAAAGT[A/G]GTATTCCAATCCCTA | 55728 |
| rs774336579 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108366 | TGCCCAGGCTGGAGC[G/T]CAGTGGCGTGATCTC | 55728 |
| rs774357548 | in-del | -/TAA | 1.70612e-05 | 0.00292067 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137123 | CAAGGGTAGATAATT[-/TAA]GCATATAAAAATATA | 55728 |
| rs774383958 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100379 | TTGTTTTTTTTTTTG[A/G]TTTCCTTTTTTTTTT | 55728 |
| rs774407566 | snp | C/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154989 | CTTCTAGAACTGTCT[C/G]TATAAGTCGTATTTC | 55728 |
| rs774441643 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158146 | TGTAATTTTGCTGTT[A/G]ACTCTGTACTTTTTA | 55728 |
| rs774452673 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178147 | CCTGGGTGACAGAGC[A/G]AGACTGGGTCCAACA | 55728 |
| rs774474618 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106084 | GCTACAGAAAGGGAC[-/AT]ATATTTTCAGAAAAG | 55728 |
| rs774496170 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173584 | GAGGTGAAGGGAAAT[-/A]ACGCTCTGTGCAAGG | 55728 |
| rs774513533 | snp | A/G | 6.63042e-05 | 0.0057574 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121628 | ACTTTAGAGAATTCT[A/G]ATTCTCCTGTGCCAG | 55728 |
| rs774527244 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076336 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGCACACC | 55728 |
| rs774561879 | snp | A/C | 1.67522e-05 | 0.0028941 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117874 | GAATTTTCAGGCGTA[A/C]CATTCATGGGGTAAG | 55728 |
| rs774588120 | snp | C/G | 3.31378e-05 | 0.00407036 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120696 | ATGATGCTTCAGAGC[C/G]ACTCAATAGCTATAA | 55728 |
| rs774588262 | in-del | -/T | 1.65507e-05 | 0.00287664 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121467 | GCAATAAAGATATTA[-/T]TTGGGCCACAAGCCT | 55728 |
| rs774618938 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144115 | CTAAAAGCTGAAGAA[C/T]GTGGAGTCTGAATTC | 55728 |
| rs774622392 | snp | C/T | 1.7879e-05 | 0.00298985 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126117 | GAGAGTATGACAGTA[C/T]TTATACTACTTTGTA | 55728 |
| rs774648313 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059355 | AGAAGTAGTTTATGT[A/T]AGGAATTTAAGAAGA | 55728 |
| rs774701876 | snp | C/T | 1.77928e-05 | 0.00298263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097587 | GAGAAAAAGTTTAGT[C/T]TGAACCCTGTCCATC | 55728 |
| rs774708718 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40089559 | CTCTTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAT | 55728 |
| rs774709074 | snp | C/G | 1.66535e-05 | 0.00288556 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120246 | CTGTAAAAGGGTATA[C/G]TAAAACTGACACAGA | 55728 |
| rs774730516 | snp | C/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144704 | TTTGAGAAAGTCAAT[C/G]CTTCGCTGCTGCCAC | 55728 |
| rs774768819 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060801 | GTAGAGACAGGGTCT[C/T]GCTGTGTTGCTTAGG | 55728 |
| rs774802298 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086270 | AAGTCCAGGAGTTTG[A/C]GACCAGCCTGGACAA | 55728 |
| rs774841184 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132520 | TTATATAAAACATAA[-/C]CAGTAATTCTACATC | 55728 |
| rs774848756 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088608 | CGGGTTCAAGTGATT[-/C]TCCTGCCTCAGCCTC | 55728 |
| rs774875834 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128290 | CGTTTGACTGCACAA[A/G]GGAGCACCTTTATAT | 55728 |
| rs774911357 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132412 | TGTCTACCTTTTTAT[A/G]TATGTGGTATGAGGT | 55728 |
| rs774919355 | snp | A/G | 1.66496e-05 | 0.00288522 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103157 | AAGAAGACATCTTAC[A/G]TTGGACTAGTTCTTG | 55728 |
| rs774921595 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184753 | CAAAGATCAGGAGTT[C/G]GAGACTAGCCTGGCC | 55728 |
| rs774922984 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088057 | GCCACCACGCCCGGC[C/T]ACGACTGGCTTTTAC | 55728 |
| rs774970925 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076490 | CAAAAAAAACCCAAA[A/C]ATATCTTTTTTTTTT | 55728 |
| rs775037405 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073613 | TTTTTTTTTTTTTTT[-/A]AATTGAGTCTTGCTG | 55728 |
| rs775045891 | snp | A/G | 3.31499e-05 | 0.0040711 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106896 | TTTCATTTATCTTTC[A/G]CAGGACTTTGCAAGA | 55728 |
| rs775068239 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114294 | CAACCTAATTTTAGT[A/G]TATTCACAGTGTTGT | 55728 |
| rs775079839 | snp | A/C | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117900 | GTAAGCAAAGAAAAA[A/C]TAACAAGAATGTTGG | 55728 |
| rs775105818 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091846 | ACTCCTGGGCTCAAG[C/T]GATCCTCCCAACTCA | 55728 |
| rs775127459 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078298 | ATGTGCCACCATGGC[C/T]GGCTACTTTTTGTAT | 55728 |
| rs775134660 | snp | A/G | 0.000557673 | 0.0166891 | utr-variant-5-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40100101 | TTCATGGATTATCTC[A/G]TTTAATCCTCACAGC | 55728 |
| rs775139666 | snp | A/G/T | 0.000136521 | 0.00826108 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142650 | CTTTCTGTGTGTGTT[A/G/T]CTTATTGTTTAATAT | 55728 |
| rs775155463 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108023 | CCGCCTCCCACGTTC[A/G]AGGGATTCTCATCCT | 55728 |
| rs775176427 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122205 | TATTGAATCCCACTC[C/T]AGCGATGGCCAAATC | 55728 |
| rs775199836 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174377 | ATGAGCCAGCAATCC[C/T]TCTTCTAGGCATATA | 55728 |
| rs775256999 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065264 | ATCTTGAAAGCTATA[A/G]AGAGTCATTGAAGGA | 55728 |
| rs775258608 | snp | G/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152799 | TAAGCAGAACGGTGG[G/T]AAGCCCTATTTGTCT | 55728 |
| rs775264200 | snp | A/T | 1.65146e-05 | 0.0028735 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102154 | TTCACAAAGTTTCGT[A/T]GCTTCTGAGAACCAA | 55728 |
| rs775282949 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137073 | TGGCCAGAAGTCTAA[A/G]GAGAAAAAGGTATGG | 55728 |
| rs775340759 | snp | A/G | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055565 | TTTAAAGCAACTGCC[A/G]TAACAACCAACAATG | 55728 |
| rs775390669 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164488 | AGAGAGGAAGATTGA[A/G]AGCCAGTCTGCTGGA | 55728 |
| rs775405222 | snp | C/T | 1.75693e-05 | 0.00296384 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144587 | TCCTCATCACCCAAG[C/T]AGCAAACAGCAAAAC | 55728 |
| rs775412937 | snp | A/T | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117984 | GAGAAAATTGAACGT[A/T]TTGAGTTGTGTGCAT | 55728 |
| rs775412960 | in-del | -/T | 1.65121e-05 | 0.00287329 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121836 | ACAGCCAGGAAGAAC[-/T]TTTATATAGCAGTAA | 55728 |
| rs775415328 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174354 | AAATTAAAAATAGAA[-/T]TTACTAGATGAGCCA | 55728 |
| rs775482260 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40152474 | TGGTATTATTGCCAT[C/T]ATCATTATTTCAGGG | 55728 |
| rs775502269 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167970 | TGGAGGGAAAGCATC[A/C]AGGAATAGAGTAACT | 55728 |
| rs775527951 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114026 | AGAGCACTGGAAGGT[A/G]GTACGGATATAGAGA | 55728 |
| rs775544093 | in-del | -/AA | 1.65285e-05 | 0.00287471 | frameshift-variant, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142698 | TAAAAGAGACTGAAG[-/AA]ACACCAAGTGAACTG | 55728 |
| rs775552857 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165790 | TTCCTCAAAGAACTT[A/G]TAGGAAACATTTGTG | 55728 |
| rs775564551 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156633 | AGTTTGGGGATTTTA[A/G]AAGTTTTCTCTATTA | 55728 |
| rs775599816 | in-del | -/TTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105491 | GCCACCCCCAGCTAA[-/TTT]TTTTTATATTTTTAG | 55728 |
| rs775612013 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094769 | GTTGGTCAGGCTGGT[C/G]TCAAACTCCTGACTT | 55728 |
| rs775637544 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075451 | TCGCCTAGGCTGGAG[G/T]GCAGTGGCGCGATCT | 55728 |
| rs775641372 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40097938 | TCCCTGGCCTGTACA[A/C]GCTAGATGCCAATAG | 55728 |
| rs775694988 | snp | C/G | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120692 | TGTGATGATGCTTCA[C/G]AGCCACTCAATAGCT | 55728 |
| rs775710593 | snp | A/T | 3.33378e-05 | 0.00408262 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121893 | CTACTACTCCTAAAG[A/T]TATGAGTGAAACAGA | 55728 |
| rs775733230 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098895 | ATTTTGTTATTATGC[A/G]TTTTTAACTTAACAT | 55728 |
| rs775765132 | snp | C/T | 1.65389e-05 | 0.00287562 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121495 | CCTTTTGTTGGATTC[C/T]GAAACTAAGTTATGT | 55728 |
| rs775801331 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084943 | TTTGAGATGGAGTCT[C/T]GCTGTGTCGCCCAGG | 55728 |
| rs775824309 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088094 | TAATACTCTGGAATT[C/T]CATCCAGGTTGTTGT | 55728 |
| rs775836757 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127132 | TGGGGTCAGTGATTC[A/T]CCTGCCTTGCCCTCC | 55728 |
| rs775882266 | snp | C/G | 3.35368e-05 | 0.00409479 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120120 | TAAGTGATATGAATC[C/G]TAGCATTCAAAGTGC | 55728 |
| rs775939075 | in-del | -/G | 1.64754e-05 | 0.00287009 | utr-variant-5-prime, frameshift-variant, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097472 | ATGGGTGAGACAAAA[-/G]GTTGATCAGGAAGAA | 55728 |
| rs775943482 | snp | C/G | 1.65875e-05 | 0.00287984 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102550 | TAACACATTGGCTTT[C/G]GAAAGTAACTACCCG | 55728 |
| rs775950879 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40164107 | AGGAGACAAAATTCA[C/G]GATGCTGTATGTGTA | 55728 |
| rs776020351 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092588 | CAGCAATTTATTTCA[C/T]TGAATTTTCTCATTA | 55728 |
| rs776027103 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145936 | GGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC | 55728 |
| rs776030440 | snp | A/T | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113502 | TTAAACCAAAGGAAC[A/T]TGCAAGGTAAAACTT | 55728 |
| rs776059448 | snp | A/G | 1.66779e-05 | 0.00288768 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120209 | ACAGACAAAAGTGAA[A/G]ACGAGCAAATAGAAA | 55728 |
| rs776061587 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184924 | TTGCGCCACTGCACT[A/C]CAGCCTGGGCAACAG | 55728 |
| rs776062358 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151089 | GAAACATATACATTA[C/T]TTCATGCAACAAACA | 55728 |
| rs776068961 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112688 | TTCTTGCCCTTCTTG[C/T]TCTTTTTTGCTCACC | 55728 |
| rs776088466 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138520 | CTGTATTTTCTGTAG[A/G]AGTCTTATAGTTTCA | 55728 |
| rs776094431 | snp | C/G | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144700 | GATCTTTGAGAAAGT[C/G]AATGCTTCGCTGCTG | 55728 |
| rs776109347 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40149259 | TATACAATGAAATTT[A/C]ATTTAGCCATGTAGA | 55728 |
| rs776130147 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128127 | TTTCGTTTGGATTTC[A/G]TCTTACTCTTTTCTG | 55728 |
| rs776150901 | snp | A/G | 3.35025e-05 | 0.00409269 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120092 | GCAGATTTAAACAAA[A/G]GAAGAAAAGAAATAA | 55728 |
| rs776206426 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172605 | CCTGGAACAGCTGCC[-/T]CCCTTGCAGCCCTCA | 55728 |
| rs776209450 | in-del | -/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156727 | TAGGTTGAGTATCCC[-/T]TAATGAGAAAATTCA | 55728 |
| rs776223451 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138144 | ATGGTTAATACAGAA[A/G]TGGTGTCTTATTGTG | 55728 |
| rs776225513 | snp | C/T | 1.65748e-05 | 0.00287874 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120715 | CAATAGCTATAAATA[C/T]GATGCTTATAAAAAT | 55728 |
| rs776245462 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132354 | TTATTTAGGGAGTCT[G/T]TTATGTCCTAATATT | 55728 |
| rs776261334 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103032 | GATCTGTCAACTACA[C/T]ATTTCCACCCTCAGT | 55728 |
| rs776274935 | snp | A/G | 0.000131994 | 0.00812277 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131959 | AGTTTCTACTCTGAT[A/G]TCACTGAAAGCATAT | 55728 |
| rs776300347 | snp | A/G | 1.66405e-05 | 0.00288443 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121295 | AACACAAAATCAGAC[A/G]TTCAAGAAGCAATTC | 55728 |
| rs776308167 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094598 | TTCGCTCTTGTTGCC[C/T]AGGCTGGAGTGCAAT | 55728 |
| rs776321965 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086457 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTACCTGG | 55728 |
| rs776322423 | snp | A/C | 1.65897e-05 | 0.00288003 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102539 | TTTATAAAGGATAAC[A/C]CATTGGCTTTGGAAA | 55728 |
| rs776326262 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137038 | TTTGTTCACCAAAAT[A/G]AGAATGTCACATCTC | 55728 |
| rs776331236 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40133887 | CTTGGCTCATTGCAG[C/T]CTTGACCTCCTAAGC | 55728 |
| rs776397281 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078000 | CTTCAGTATAAAAAC[C/T]GTACAGATATTTGTA | 55728 |
| rs776401987 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103121 | CAAGTACAAGAAACC[C/T]CAGTTTCTCAGGTTG | 55728 |
| rs776423803 | snp | C/T | 3.29935e-05 | 0.00406149 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122179 | AGTTAGTGGGGAAGA[C/T]AAAACCGAGATATTG | 55728 |
| rs776424828 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179087 | TTAAAACGTTTTGGA[A/G]GCTGGGCGCAGCAGC | 55728 |
| rs776427485 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40171942 | ATGGAGTCTCACTCT[G/T]TCGCTCAGGCTGGAG | 55728 |
| rs776455447 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069717 | GTTGGAGACCAGTGT[G/T]GGCAGCAAAGCGAGA | 55728 |
| rs776459334 | snp | C/T | 1.80153e-05 | 0.00300122 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122021 | TTAAATGAAGAAATT[C/T]ATTTTACTGATTCTC | 55728 |
| rs776465677 | snp | G/T | 7.57877e-05 | 0.00615533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097612 | TCCATCTTATAAGAA[G/T]ACTTTGTGTACTATG | 55728 |
| rs776505840 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140072 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 55728 |
| rs776509596 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125727 | CCCCGTCTCTACTAA[A/C]AATACAAAAACTAGC | 55728 |
| rs776522186 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102921 | TGCCTCCTCCGCCAC[C/T]TCCACCGATGTGGAA | 55728 |
| rs776541096 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40178034 | GTAGAAAGTAAGGTG[C/T]CTGTAATCCTAGCTA | 55728 |
| rs776549399 | snp | C/G | 1.65913e-05 | 0.00288017 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120813 | ACAGATCAAGAATGC[C/G]AAAGACTGGTTTAAG | 55728 |
| rs776551945 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101040 | TTTTCTCTTGTGTCT[A/G]GCAAGTTACTTTTTA | 55728 |
| rs776565868 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068303 | TTGTTTCCTTTGTGA[C/T]ACAGAATTCTTTAAG | 55728 |
| rs776571475 | in-del | -/AAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125887 | GCAAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55728 |
| rs776590778 | snp | A/T | 3.31016e-05 | 0.00406813 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121464 | GGTGCAATAAAGATA[A/T]TATTTGGGCCACAAG | 55728 |
| rs776634240 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082793 | GCAAGCTCTGCCGCC[C/T]GGGTTCACGCCATTC | 55728 |
| rs776678092 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123778 | GCATGAGCCACTGTG[C/T]CTGACCTGTTTTTTT | 55728 |
| rs776686493 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40106653 | TCCTGGGTTCTAGCA[A/G]TTCTCATGCCTCAGC | 55728 |
| rs776716331 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40167661 | GTAACTAAATAACAA[A/G]TTAATGAGAATAGAG | 55728 |
| rs776726830 | snp | A/G | 0.000134463 | 0.00819837 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126373 | CTGTCTCTGATTCTG[A/G]TTTATTGTGTATGTT | 55728 |
| rs776737308 | snp | A/G | 1.74242e-05 | 0.00295157 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142641 | TTTTTTTAACTTTCT[A/G]TGTGTGTTACTTATT | 55728 |
| rs776739262 | in-del | -/AA | 1.65292e-05 | 0.00287477 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142829 | GCTTATCGGATAGGG[-/AA]AAAAAATGTCGCCAC | 55728 |
| rs776743763 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129566 | GTAATATAATAGAAG[C/G]TGGTTGGCTTTGTCC | 55728 |
| rs776745551 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088954 | ATTTTTTGTTTTTTT[-/TG]TGTGTGTTTTTTTGA | 55728 |
| rs776776355 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107780 | ATAGGGTGGTTATAA[G/T]GATTCAAAGAGTTAA | 55728 |
| rs776787653 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152867 | TTGCTCGCATCAAAC[C/T]AGCTGTCATTAAGTA | 55728 |
| rs776791968 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40068312 | TTGTGACACAGAATT[A/C]TTTAAGTTTGATGTC | 55728 |
| rs776797030 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126998 | TCCTGACCTCAAGTG[A/G]GCCACCTGCCTTAGC | 55728 |
| rs776797500 | in-del | -/TCA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073183 | AAGATAAGGTTTCTC[-/TCA]TCAACTAAGGCTATT | 55728 |
| rs776801788 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102835 | CTTCAAGCCACACAA[A/G]CATCCTGAACTGCCA | 55728 |
| rs776810079 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110828 | TAGGTGTGAGGTACC[A/G]TGCCCAGCCTCCTTT | 55728 |
| rs776840179 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071710 | TAGCTGGGACTACAG[G/T]CTCTCGCCACCACGC | 55728 |
| rs776843476 | snp | C/T | 1.65018e-05 | 0.00287239 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144681 | ATCACCTTGCTGCCA[C/T]AGAGATCTTTGAGAA | 55728 |
| rs776892030 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062699 | CCCTGAAGGGGTCAG[-/A]GTTCTTAAATCTGCA | 55728 |
| rs776897400 | snp | A/G | 1.67702e-05 | 0.00289566 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120463 | CCCAAGACATGAGCT[A/G]TCAAATTTTGTTGGT | 55728 |
| rs776904639 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096205 | TGGTAAATACAATAC[A/G]TATGTAAAACATATG | 55728 |
| rs776906676 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078114 | TGAATATTTCTAAAT[-/AT]GTGTGTGTGTGTGTG | 55728 |
| rs776931909 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073216 | TTGTTACCTGGAATT[A/G]GTGTTCTACTTAAAG | 55728 |
| rs776940551 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114907 | GTCTCTTACTATTTA[C/T]ACATCTACTGTGTTA | 55728 |
| rs776947742 | in-del | -/AAAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184959 | AGACTCTGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 55728 |
| rs776979917 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123147 | CTAACAGTTGAAGAT[G/T]GTGTGGTTCATATAG | 55728 |
| rs776994907 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144538 | TTTATTATTCCCTTT[C/T]TCCCCCTTCCTTTTA | 55728 |
| rs776995930 | snp | C/T | 6.6189e-05 | 0.0057524 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102316 | ATTGAACTCTTCTCC[C/T]GATGACCAAGTATAC | 55728 |
| rs777023638 | in-del | -/TA | 3.3493e-05 | 0.00409211 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112067 | AAAATGATTTTTAAT[-/TA]TGTTATGTTTTTCAG | 55728 |
| rs777055533 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103537 | TCAGCTTTGATCACA[G/T]AGTTAAAGAGATATA | 55728 |
| rs777057195 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100826 | ATCTGTTTGCTAGGA[A/G]TAATATACCTCATGG | 55728 |
| rs777077442 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112216 | TAACAGTTTGTATGC[A/G]ATTATTGGGGAACAT | 55728 |
| rs777089448 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172731 | TTGCTACTGTAGCCC[C/T]AGCAAACTAATACAG | 55728 |
| rs777097021 | snp | C/G | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113456 | CACAAATATAAAGTC[C/G]TTTTTCGGGAACCAG | 55728 |
| rs777145206 | snp | A/G/T | 6.61605e-05 | 0.00575116 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121759 | TGAAAACCATGAATC[A/G/T]ATGACAAGTATATTT | 55728 |
| rs777152198 | snp | C/T | 1.66021e-05 | 0.0028811 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102516 | CAGTTTTGAACGAGT[C/T]CAAGTGTTTTATAAA | 55728 |
| rs777161752 | in-del | -/TGTCTA | 2.12529e-05 | 0.00325975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40102032 | TAAATCTGTTTTCTC[-/TGTCTA]TATTTTTGTTGTTGT | 55728 |
| rs777177230 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159534 | ACATCTGTATTCTGC[G/T]GGAGGAAAGACAAAG | 55728 |
| rs777198096 | snp | A/G | 1.75554e-05 | 0.00296267 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142895 | TATATATTTTTTGTC[A/G]GTTATAATAACTAAA | 55728 |
| rs777200794 | snp | A/C | 1.65756e-05 | 0.00287881 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123242 | TTTTATAAAGAGCTC[A/C]TTTTTTGTCCATTTT | 55728 |
| rs777202912 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144743 | TTAGACCTCCATGGG[C/T]TGCATGTGGATGAAG | 55728 |
| rs777270104 | in-del | -/A | 1.84366e-05 | 0.00303611 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103242 | TTTGATTGGGTTTTT[-/A]AAAAATAGTATAATG | 55728 |
| rs777273929 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104187 | TCGATTTCCTGACCT[C/T]GTGATCCACCCGCCC | 55728 |
| rs777306397 | snp | C/G | 3.31082e-05 | 0.00406854 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112089 | TGTTTTTCAGCAAAA[C/G]AAGCATTTGAGAAGA | 55728 |
| rs777323830 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070716 | TTGGCCTCGCAAAGT[C/G]CTGGGATTACAGGCA | 55728 |
| rs777327778 | snp | A/G | 8.24355e-05 | 0.00641957 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124257 | TGAAATTTGGTGTGT[A/G]TGTTTGAATTTTAAC | 55728 |
| rs777330216 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108574 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55728 |
| rs777337093 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083505 | ATTTTCTAGCAGTAT[C/T]GGTGAAGTACCAATA | 55728 |
| rs777385620 | snp | A/G | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121562 | GATGGATCACAAATT[A/G]GGCCTTTTTCTCTGG | 55728 |
| rs777421299 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094369 | CCTTAATTATTGGTG[-/T]TGTTGAGTTCTATAT | 55728 |
| rs777432141 | snp | A/G | 1.66576e-05 | 0.00288592 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144658 | TGAGCAGAAGATGAA[A/G]GAAGCCAATCACCTT | 55728 |
| rs777432914 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131101 | AGCTTGTTTGTACAC[A/T]GTAGTTTCTGCCCAT | 55728 |
| rs777440987 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40143476 | GTGCCACCAGGCCCA[C/G]CTAATTTTTGTATGG | 55728 |
| rs777448781 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060400 | CAGGTGCACACGATC[A/C]CGCCCGGCTAATGTT | 55728 |
| rs777468510 | snp | A/G | 1.73498e-05 | 0.00294527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137128 | GGTAGATAATTGCAT[A/G]TAAAAATATAATTGG | 55728 |
| rs777476470 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084097 | CTGGGATTACAGGCA[C/T]GCGCCACCACTCCCA | 55728 |
| rs777484255 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184431 | TACATTAGAGAATCA[C/T]TGAAGAGAATAAACT | 55728 |
| rs777489005 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061526 | TGCACCACCACGCCC[A/G]GCTAAGTTTTGTATT | 55728 |
| rs777508074 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132361 | GGGAGTCTGTTATGT[A/C]CTAATATTATAAAAA | 55728 |
| rs777528806 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124939 | AGCCTGCTTTTTGGT[A/G]CATCCTGCCAACTTG | 55728 |
| rs777534913 | snp | A/G | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120662 | GAAAGTGTAGAGGAT[A/G]GCAGAAAGTCACAGT | 55728 |
| rs777552679 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157402 | GCTATACTGCTCTTC[C/T]GGATGGTTTCCATCC | 55728 |
| rs777558182 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40113923 | GAATCATATGTTAAT[A/G]TCTAAAGCTAGAACA | 55728 |
| rs777558513 | in-del | -/AAAA | 1.6792e-05 | 0.00289754 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120420 | AAGCCTTTGGGAAAC[-/AAAA]AAGCAAATCGACTTT | 55728 |
| rs777569362 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169466 | ATGAAATTAGAAATA[C/T]ATAAAAGATTTAAAA | 55728 |
| rs777577360 | snp | C/G | 1.67209e-05 | 0.00289139 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120174 | TGTATTTTTCTGACT[C/G]TGAAAGCAAACTACA | 55728 |
| rs777595782 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060272 | TTTTTTGAGATGGAG[A/T]CTCACTGTGTTGCCC | 55728 |
| rs777596604 | snp | G/T | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40054986 | ATTGTTCTGACTTAA[G/T]ATTTGATGAATCCTT | 55728 |
| rs777635359 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060603 | GGCTAAGTAGCTAGA[-/TT]TTTTTTTTTTTTTTT | 55728 |
| rs777649946 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098574 | GGGAAGTTTTGGTAA[A/T]GTGTTATAAACTTCC | 55728 |
| rs777656934 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173716 | AGTCAAAGTCAAACT[A/G]TGTTCTCACTGCAGA | 55728 |
| rs777660679 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140438 | TGAGTCATTATGGTA[A/G]TAGGGGGTGATAAGA | 55728 |
| rs777720092 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118389 | GTGAGCCGAGATTGC[A/G]CCATTGCATTCCACC | 55728 |
| rs777737816 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099955 | TTTTAGGTTTTCTGT[C/T]CTTTGTAGTATTGCT | 55728 |
| rs777739130 | snp | G/T | 0.000115918 | 0.0076122 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121451 | GACTTATATGAGAGG[G/T]GCAATAAAGATATTA | 55728 |
| rs777746612 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160191 | GAAAAAACTAAATGA[C/T]ACGGACTAGCTTAAT | 55728 |
| rs777752823 | snp | A/T | 1.65751e-05 | 0.00287876 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154159 | TAATTTGAAATTTTC[A/T]TCTTTAAAATAACTC | 55728 |
| rs777849324 | snp | C/T | 3.31483e-05 | 0.004071 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121070 | AGTGCACCAACTGTT[C/T]CTGGAGTAGTAGAAC | 55728 |
| rs777857273 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168679 | TGCTTTAATAAATAT[A/G]TATAGAATTATACAT | 55728 |
| rs777886940 | snp | A/G | 3.31658e-05 | 0.00407208 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120931 | TCAAAAACTAAAGAC[A/G]TTGGGTAGCTCCAAT | 55728 |
| rs777889955 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066153 | CCAGGATGGTGTCAA[A/T]CCCTTGACCTTGTGA | 55728 |
| rs777891186 | snp | G/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152856 | CCAGGGAGGAGTTGC[G/T]CGCATCAAACCAGCT | 55728 |
| rs777895696 | snp | A/G | 7.0189e-05 | 0.00592364 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118056 | TATGTACAAAATTCA[A/G]TTTGAAATATAATTT | 55728 |
| rs777898057 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114750 | TCTTTTCTTCTTTTC[C/T]AGGTTTATCTAAGTT | 55728 |
| rs777916100 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169671 | TTTAAAAAAAAAAAC[-/A]AAAAAAAAGGAAGCT | 55728 |
| rs777946275 | snp | A/C/G | 0.000287723 | 0.011991 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126367 | AAGCTACTGTCTCTG[A/C/G]TTCTGGTTTATTGTG | 55728 |
| rs777953166 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40145446 | CCAGGCTGGTCTTGA[A/G]CTCCTGGCCTCAAGC | 55728 |
| rs777988372 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094323 | TATTTTGCTGTTGTT[C/G]GGTGGAGTGTTCTGT | 55728 |
| rs778034531 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161124 | CCGAAGTCATAACAC[C/T]TAGAGTAGGCAAAAA | 55728 |
| rs778070236 | snp | A/C/T | 3.29453e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103000 | AGCTCCTGTTGTAAC[A/C/T]ACAGCTGCACACTGG | 55728 |
| rs778124926 | snp | A/G | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102247 | AATGGATTCATTTTT[A/G]GACATGCAGCTAACT | 55728 |
| rs778137408 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153217 | CTTTCTATCATAAAT[G/T]TAAAGTTCTAAAAGA | 55728 |
| rs778162443 | snp | A/C | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131884 | ATTTCCAGCCATTAA[A/C]CAAAATTTTCTGGTG | 55728 |
| rs778170857 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124623 | AAGTCCTGGGGTTAC[A/G]GGCATGAGCCACTGC | 55728 |
| rs778188759 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077962 | TATGACACGCAGATT[C/T]GTGAAGTGTTCCATA | 55728 |
| rs778216034 | snp | G/T | 4.94271e-05 | 0.00497102 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097379 | TGGGGGAAATCCTTT[G/T]CGGAAGACTGCAAAC | 55728 |
| rs778229446 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102914 | TTGCTGTTGCCTCCT[A/C]CGCCACCTCCACCGA | 55728 |
| rs778259477 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056310 | GGCCGACCTTGTGTT[C/T]GTTTTGTTTTTTGGG | 55728 |
| rs778277698 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40095295 | ATTGTTGGCCAGGCC[C/T]GTCTCAAACTCCTGA | 55728 |
| rs778278392 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078993 | GTCTCACTCTGTTGC[C/T]CAGGCTGGAATGCAG | 55728 |
| rs778278406 | in-del | -/G | 1.64844e-05 | 0.00287087 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137022 | AGTTGTAGCCCAAGA[-/G]TTTGTTCACCAAAAT | 55728 |
| rs778297722 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066697 | GTCTCAGTTTTTTTC[-/T]TTGTAGTTAAGCTAC | 55728 |
| rs778329440 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186136 | AAGCCTCTGGAATCC[C/T]TTGTTTTTGGAGTCT | 55728 |
| rs778337183 | snp | A/G | 3.41956e-05 | 0.00413481 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121945 | GACTGGAGACAACAT[A/G]CATTCTCCTTCACAT | 55728 |
| rs778351595 | snp | A/G | 1.6631e-05 | 0.00288362 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120557 | TCATCCGTACAAAGC[A/G]ACAAAAAGTATAATT | 55728 |
| rs778386053 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082705 | CCACAGGCTGTATTC[-/T]TTTTTTTTTTTTTGA | 55728 |
| rs778450632 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083366 | ATGAAAACATGTCCA[C/T]AGCAAACTCTTATAC | 55728 |
| rs778472001 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098455 | GTTTAGAAGTATGTA[C/G]ACAGAAGGGAGTTTA | 55728 |
| rs778489795 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122481 | CAGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 55728 |
| rs778500923 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156323 | AAGTAGAGGTGTGGT[A/G]TTCCGTGGGCAGAAG | 55728 |
| rs778501074 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40170388 | CTTTGGGAGACTGAC[A/G]CAGGCAGATCACTTG | 55728 |
| rs778510036 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40114561 | ATGTGTCACTACTTC[C/G]TTTTCATTTCCTTTT | 55728 |
| rs778523686 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177809 | CTTCCATCTTCTCTG[C/T]AGTCATCTCACATGC | 55728 |
| rs778524931 | snp | A/G | 3.36366e-05 | 0.00410088 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144648 | GTACTCTTCATGAGC[A/G]GAAGATGAAAGAAGC | 55728 |
| rs778588966 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157273 | TGTGCAGTTTCTTCA[A/G]TTGGTTAGTATTTCC | 55728 |
| rs778598272 | snp | A/G | 1.6782e-05 | 0.00289668 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120426 | TTGGGAAACAAAAAA[A/G]CAAATCGACTTTGGA | 55728 |
| rs778612517 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182774 | CTCTGCCTCCCAGGT[C/T]CAAGCGATTCTCCTG | 55728 |
| rs778631226 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157144 | TGGACCAGGGAGATA[C/T]TAGACACTTAACAGT | 55728 |
| rs778632619 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081871 | TAATCCCAGCACTTT[A/G]AGAGGCCAAGGTGGG | 55728 |
| rs778661243 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074711 | CGTTTCTCTGCTTCT[A/T]AAAGGCCAGTCTTGG | 55728 |
| rs778672897 | in-del | -/TC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181142 | GTGACAGAGCGAGAG[-/TC]TGTCTCAAAAAAGAA | 55728 |
| rs778680680 | snp | A/C | 1.65211e-05 | 0.00287407 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121814 | AATAATAATGACATA[A/C]TTCCTAACAGCCAGG | 55728 |
| rs778695341 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127787 | TGCTTCAGCCTCCTG[A/T]GTATCTGGAACTACA | 55728 |
| rs778703109 | in-del | -/TACT | 0.00034531 | 0.0131353 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112035 | TTTTGAAAATCATAA[-/TACT]TAGTATTGTTTAAAA | 55728 |
| rs778706737 | snp | A/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080152 | TATACAAGGTTGTTT[A/T]AACTAATGTATTAAT | 55728 |
| rs778712732 | snp | C/T | | | | | GRCh38.p7 | 4:40181805 | AATACAAAAATTAGC[C/T]GAGCATGGTGGCACA | 55728 |
| rs778725813 | snp | C/T | | | | | GRCh38.p7 | 4:40067839 | GAGTAGCTGAGACTA[C/T]AGGCTAATTCTTGTA | 55728 |
| rs778751260 | snp | C/G | | | | | GRCh38.p7 | 4:40059811 | TGTTTTAAGCACTTT[C/G]CATATGTGATTGTAT | 55728 |
| rs778754407 | in-del | -/ATG | 3.31488e-05 | 0.00407103 | | | GRCh38.p7 | 4:40120714 | TCAATAGCTATAAAT[-/ATG]ATGCTTATAAAAATA | 55728 |
| rs778755388 | snp | A/G | 8.35624e-05 | 0.0064633 | | | GRCh38.p7 | 4:40097309 | AACATCTTAACTAAG[A/G]AAAGGGAAACATTTT | 55728 |
| rs778811868 | snp | A/G | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102387 | CAAGTGAGTTTATAA[A/G]TCCTGATTCAAGTAA | 55728 |
| rs778848479 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088779 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCACC | 55728 |
| rs778863068 | snp | A/G | 1.6607e-05 | 0.00288153 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102503 | TTACCTTCACATTCA[A/G]TTTTGAACGAGTCCA | 55728 |
| rs778896976 | snp | A/T | 0.000165325 | 0.00909038 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113426 | TTTTGTCTTTGTTGT[A/T]TGTAGTCTCAGAAAC | 55728 |
| rs778907960 | snp | C/G | 3.31802e-05 | 0.00407296 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120801 | CTCAGAGGGAACACA[C/G]ATCAAGAATGCCAAA | 55728 |
| rs778921890 | snp | C/T | 1.67309e-05 | 0.00289226 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120022 | CACTGAAGAGAAGAA[C/T]CTTGATGTAACCAAA | 55728 |
| rs778940693 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165230 | AAGCTAGCTCAAATC[-/T]TTTTTTTGGAAATAG | 55728 |
| rs778941844 | snp | G/T | 3.29772e-05 | 0.00406048 | splice-donor-variant | N4BP2 | GRCh38.p7 | 4:40123214 | AAGAATCTGTAATGG[G/T]TGGTAGGCTTCTTTT | 55728 |
| rs778996888 | snp | A/G | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122246 | GACTGTCTGGAATTG[A/G]CATTACCCCCTGAAC | 55728 |
| rs779006380 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137709 | CACATGGGGAGCCAG[C/G]AGGATTGGTCAGGAG | 55728 |
| rs779035122 | snp | C/T | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120913 | CTGTTGGGGCACAAG[C/T]TCTCAAAAACTAAAG | 55728 |
| rs779040064 | in-del | -/ACCCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173622 | TGTATTCCCAAACAC[-/ACCCT]TCCTTGTAAAGTGAG | 55728 |
| rs779046931 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078648 | CTCTCACCTTAGCTT[C/T]CCAAGTAGCTGGGAC | 55728 |
| rs779085734 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40159081 | GCTATCCCAATTTAA[C/T]GAATAAAGCCACATA | 55728 |
| rs779095793 | snp | A/G | 1.66807e-05 | 0.00288792 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102127 | CACTGATACCAAGAT[A/G]GAAGAATCATCTTCA | 55728 |
| rs779097836 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094457 | TCTCCACCTATAATT[G/T]TGAATTTGTCTATTT | 55728 |
| rs779108947 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102802 | CTCTGATGTGTTTCT[A/G]CCTTCCGAAGGGTTC | 55728 |
| rs779134474 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40115560 | TTAATATATAATACT[G/T]TATTTTTGTCTTATT | 55728 |
| rs779146770 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102235 | TGAAGATTCAAAAAT[G/T]GATTCATTTTTGGAC | 55728 |
| rs779168914 | in-del | -/ATGTGTGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078112 | GTTGAATATTTCTAA[-/ATGTGTGT]ATGTGTGTGTGTGTG | 55728 |
| rs779172242 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40160116 | TGAACAATCACACCC[A/G]GCCAGGGAATTTTAT | 55728 |
| rs779214852 | snp | C/T | 1.65157e-05 | 0.0028736 | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142703 | GAGACTGAAGAAACA[C/T]CAAGTGAACTGTCTT | 55728 |
| rs779222898 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064797 | GGGGTAGAGATGGAG[G/T]CTTGCTCTGTTGCCC | 55728 |
| rs779233211 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101659 | AAATAAGTTAGATTT[A/G]CTAAGAGAATACATA | 55728 |
| rs779240747 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117182 | GTCCCATGCATTCTC[C/T]TCTCTTTCCGGGACT | 55728 |
| rs779253277 | snp | A/G | 1.68074e-05 | 0.00289887 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106853 | AAAATTAGGAGAGAA[A/G]ATTTAGAAGAAAAGG | 55728 |
| rs779282215 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150714 | GGATAAATGATCCAA[-/T]TTTTTTTCAATAAAT | 55728 |
| rs779341474 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124779 | GCTCTCAAAGCATTT[C/T]CTGTTGAGGTTTTGC | 55728 |
| rs779351999 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108452 | CCCTGAGTAGCTGGG[A/T]TTACAGGCACGTGCC | 55728 |
| rs779372401 | snp | A/G | 4.95045e-05 | 0.00497492 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117962 | AATTATGAGTTCTTC[A/G]GTTCCAGAGAAAATT | 55728 |
| rs779373163 | snp | A/G | 1.65474e-05 | 0.00287636 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121723 | AAACTCAGAGCAGGC[A/G]GAAATGAGAGCTGTC | 55728 |
| rs779386060 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40069393 | GATTGCACCACTGCA[C/T]GAAAGAGTGAGACTG | 55728 |
| rs779455018 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151717 | GTGAATACCTTTGTG[A/C]AGCTAGCACTCAGTT | 55728 |
| rs779480447 | snp | C/T | 1.66485e-05 | 0.00288513 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120307 | TTGCTGTAGTGAAAA[C/T]AATCAAGAAGACTGT | 55728 |
| rs779482086 | snp | A/G | 0.000428682 | 0.0146341 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142731 | CTTTCCAGGACTTTG[A/G]GTACCCAGACTATGA | 55728 |
| rs779503174 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074366 | AAAGTGCTGGAATTA[C/T]AGGCGTGAGCCACCG | 55728 |
| rs779505195 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058256 | TAACTCTCATCCTTT[A/G]ATTTTAACTAAAAGA | 55728 |
| rs779525210 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153854 | TTACCTGATATATCA[C/G]AGATTTCTTCTTGGT | 55728 |
| rs779541045 | snp | A/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156120 | AAGATATTCCTATGT[A/G]TACATTAGTATGATT | 55728 |
| rs779572056 | in-del | -/A | 5.18578e-05 | 0.00509178 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131758 | AGTGTTTCTAGTATT[-/A]ACACATTTCATCTTG | 55728 |
| rs779578725 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40127129 | TTCTGGGGTCAGTGA[A/T]TCACCTGCCTTGCCC | 55728 |
| rs779596275 | snp | A/G | 1.71402e-05 | 0.00292742 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126297 | CAGAGAAATAATGTC[A/G]GAAGAAATTGCCTTA | 55728 |
| rs779603330 | snp | A/G | 1.67654e-05 | 0.00289524 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120400 | AAGAGCAACAGTAAC[A/G]AAAAAAGCCTTTGGG | 55728 |
| rs779626482 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111462 | AGTAGTTGGGACTAC[A/G]GGTGCGTGCCACCAC | 55728 |
| rs779628918 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137457 | GCTCTACCATTTTAT[A/G]TTTCCACTAGAACAG | 55728 |
| rs779638658 | snp | A/C | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154765 | ATTTTGCCATATCCT[A/C]CAGGAAGGAAGACAT | 55728 |
| rs779728590 | snp | A/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054305 | AAGAGACACGGCCCG[A/G]TGCGGTGGCTCACGC | 55728 |
| rs779787449 | snp | A/T | 3.29946e-05 | 0.00406155 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40112160 | ATGGGAAATGAAACC[A/T]TATGTTGCTTTGGTT | 55728 |
| rs779811831 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126483 | ATATTTTAAGTATAA[C/T]TTGAAGCTGGAGGTT | 55728 |
| rs779826311 | in-del | -/AAGTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40130817 | TTGAAACTGTATAGG[-/AAGTT]ATTTTTCAGACATCA | 55728 |
| rs779849459 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075034 | AGTAAATAAATAAAA[A/C]ATAGGCCAATCTTGC | 55728 |
| rs779882526 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085682 | TAGGACTGAGCTCTG[G/T]AACGCTGTATTGTTT | 55728 |
| rs779898301 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40098403 | GTTTTTGGTAAAGTC[G/T]TCAGTATGGTAGGTT | 55728 |
| rs779899694 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110272 | TAAGAACAGTGCTGC[G/T]ATAAACAAACACACA | 55728 |
| rs779899936 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071274 | CATGGTGTAGTATTA[C/G]TTCTTCCTCTATCCC | 55728 |
| rs779900539 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080943 | AGTGCTGGGATTACA[C/G]GCATGAGCCACTGCG | 55728 |
| rs779926948 | snp | A/G | 1.66048e-05 | 0.00288134 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123076 | GTATGTTTTCTGCAA[A/G]TATATAATGAGTAAT | 55728 |
| rs779934153 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088000 | TGACCTCCGGTGATC[C/T]GCCTTCCTTGGCCTC | 55728 |
| rs779935424 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40108018 | AACCTCCGCCTCCCA[C/T]GTTCAAGGGATTCTC | 55728 |
| rs779939040 | in-del | -/TATGTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077142 | ATTATGTAGAATATA[-/TATGTG]TGTGTGTGTGTGTGT | 55728 |
| rs779946801 | snp | C/T | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120546 | CTGAAAAAACTTCAT[C/T]CGTACAAAGCGACAA | 55728 |
| rs779978973 | snp | A/G | | | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054299 | AATTTAAAGAGACAC[A/G]GCCCGGTGCGGTGGC | 55728 |
| rs779985824 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072953 | TCTCAAACTCCTGAC[A/C]TCAAGTAATCCACCC | 55728 |
| rs780013232 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40064431 | AAGCGCGCACCACCA[C/T]GCCTGGCTAATTTTT | 55728 |
| rs780037551 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180785 | CTTCTTGTCCTTGCT[A/G]TATTGATTGGTGAAA | 55728 |
| rs780041249 | snp | C/T | 1.76674e-05 | 0.0029721 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121987 | TTTTAACTTTGTATC[C/T]AGTACTTCAAATCTT | 55728 |
| rs780051010 | snp | A/G | 1.69163e-05 | 0.00290824 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137116 | TTTTTCTACAAGGGT[A/G]GATAATTGCATATAA | 55728 |
| rs780051814 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40123188 | GGCGAAAGTGATTCA[C/T]GAGAAATGGAAAGAA | 55728 |
| rs780059160 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061060 | GCTCAAGCAATCCTC[C/T]CACCTTGGCCTCCTA | 55728 |
| rs780059870 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110129 | ATGTTTTCAAGCTTC[A/G]TCCATGTTGTAGCAT | 55728 |
| rs780072946 | snp | G/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142839 | TAGGGAAAAAAAATG[G/T]CGCCACCTTTTATGC | 55728 |
| rs780145206 | snp | C/T | 4.95037e-05 | 0.00497488 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103103 | GATGGAACAAGTGCT[C/T]ATCAAGTACAAGAAA | 55728 |
| rs780167016 | snp | A/G | 3.32806e-05 | 0.00407912 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122137 | AATGAAGGAAATTCT[A/G]ATGGCAGGAAGTAGT | 55728 |
| rs780194131 | snp | A/G | 1.65149e-05 | 0.00287353 | utr-variant-5-prime, missense, intron-variant | N4BP2 | GRCh38.p7 | 4:40097547 | TGTAGTGTATTTGAT[A/G]CTTTCTGAATGTGAT | 55728 |
| rs780217114 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123306 | ATATTAAGGAGTTCT[A/G]TTGAATTTTGGCTTT | 55728 |
| rs780222340 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40176349 | CTGTTGTTGGACATT[A/C]ATGCTGATCAAAATC | 55728 |
| rs780239412 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40162536 | GATACTTGTCCAACC[A/G]GGTATAGAAATAAAA | 55728 |
| rs780286893 | snp | C/T | 0.000280554 | 0.0118405 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40136997 | TTCTTGAAGGGGACC[C/T]TGTAAAAACAGTTGT | 55728 |
| rs780291219 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151646 | TATATAGTGCAAAAA[A/C]TTTGTAAAAAGTTCG | 55728 |
| rs780306291 | in-del | -/TATG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059385 | AGATTGAGCATTTTT[-/TATG]TATGTATGTATGTAT | 55728 |
| rs780345488 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077696 | TGACCTCAAGTGATC[C/T]GTCCACTTCAGCCTC | 55728 |
| rs780360384 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074990 | CCAGCCTGGGCGACA[C/G]AGTGAGACTCTGTAA | 55728 |
| rs780381234 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131582 | ATTGTGTGTGTGTGT[A/G]TATATTTATAAGCAA | 55728 |
| rs780396042 | snp | A/C | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120786 | CATCTGATTCTTTAG[A/C]TCAGAGGGAACACAG | 55728 |
| rs780397372 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120226 | CGAGCAAATAGAAAT[A/G]GTGGCTGTAAAAGGG | 55728 |
| rs780405758 | snp | C/G | 1.67332e-05 | 0.00289246 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120160 | GGAAACTCCACACAT[C/G]TATTTTTCTGACTCT | 55728 |
| rs780417256 | snp | A/G | 1.65891e-05 | 0.00287998 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120894 | TATCTACAGCACATG[A/G]GGCCTGTTGGGGCAC | 55728 |
| rs780422665 | snp | A/G | 1.74781e-05 | 0.00295614 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102093 | AAAATGCTATGGATT[A/G]TCTATTAGAATTATC | 55728 |
| rs780443712 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174480 | GCCAGGATGTGGAAA[C/T]AACCTAAGTGTGTGT | 55728 |
| rs780446855 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40119887 | ATAGTATTGATGGCA[G/T]CATTAAGAGACTTTC | 55728 |
| rs780468314 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138591 | TTGTATATGTAGTGA[C/G]ATAGAAGTTCAAGTT | 55728 |
| rs780476202 | snp | A/G | 8.2498e-05 | 0.00642201 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117928 | TGGAACATTATCAAC[A/G]TTTTGTTTCAGTGCC | 55728 |
| rs780509049 | snp | A/C | 1.65504e-05 | 0.00287662 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126194 | AATCATCTCAGAGAA[A/C]AGGCAAAAAATTACT | 55728 |
| rs780550224 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067808 | GGTTCAAGTGATTCT[C/G]CTGTCTCAGCCTCCC | 55728 |
| rs780553006 | snp | A/G | 3.32851e-05 | 0.00407939 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152731 | TTACGTTTTCTATTG[A/G]GAATGTAAGATAAAT | 55728 |
| rs780561212 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081628 | TCCAGCCTGGGTGAC[A/G]GTGTGAGACTGTCTC | 55728 |
| rs780572335 | in-del | -/TTCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40138309 | GTTGAGTTGTAAGTG[-/TTCT]TTATATATTCTAGAT | 55728 |
| rs780573571 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102664 | ACTTTTAGAATCTGA[A/G]TGCGTTGAGGCTCAA | 55728 |
| rs780575054 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107190 | CTGCAGCCTTGACTT[C/G]TGGGTTCAGGTGATC | 55728 |
| rs780602532 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40181418 | ATCAATTAGGATTAG[A/G]TTAAATTGTATGTGA | 55728 |
| rs780606080 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148505 | GGGGGAGAGGGAGTT[C/T]GGCTTTTTTAGGTTC | 55728 |
| rs780609812 | snp | G/T | 3.31033e-05 | 0.00406823 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121465 | GTGCAATAAAGATAT[G/T]ATTTGGGCCACAAGC | 55728 |
| rs780626048 | snp | A/G | 3.33145e-05 | 0.00408119 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126180 | TAATCCTGAACAAAA[A/G]TCATCTCAGAGAACA | 55728 |
| rs780650775 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40070932 | TGAGTTCATGCAGTT[C/G]TCTTGCCTCAGCCTC | 55728 |
| rs780682370 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166549 | ACAAAATTAGCTTGG[C/T]GTAGTGATGCATGCC | 55728 |
| rs780686709 | in-del | -/GAGTAGCTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077579 | CTGCCTCAGCCATCT[-/GAGTAGCTG]GAATTACAGGCACCG | 55728 |
| rs780691061 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40180536 | AAACCTGCAAAGTCA[C/T]TTCCTGTCATTATTC | 55728 |
| rs780714529 | snp | C/T | 1.6628e-05 | 0.00288335 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144783 | ATTTGATGAGAGTTT[C/T]AGAGAAGAAGACTGA | 55728 |
| rs780737754 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058003 | TTCTACTCGACATCT[C/T]TGAGCCAATCAGCAA | 55728 |
| rs780760113 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095653 | ATAAGGGCAATGGAT[A/G]GTTAGCAGGAAAGGG | 55728 |
| rs780763224 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072508 | CTCGGCCTCCCAACG[G/T]GCTGGGATTACAGGC | 55728 |
| rs780773660 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150457 | AGATCACTTGAGGTC[A/G]GGAGTTTGAGACCAG | 55728 |
| rs780789058 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40165468 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 55728 |
| rs780803720 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40153506 | TTTTCATTAAGTGAT[A/C]ATTATTTAATAACAG | 55728 |
| rs780806546 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102631 | AGGTTGTAGCAGTCT[C/T]AATCAAAAACAGAAA | 55728 |
| rs780859612 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102753 | CAGGGCTTGATTTAC[C/T]AGGTACAGGTGGGGA | 55728 |
| rs780885965 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154572 | ATGACATTTAGTAAT[G/T]TCCTAAAAGTCTTTT | 55728 |
| rs780894779 | snp | C/T | 3.33545e-05 | 0.00408364 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122253 | TGGAATTGGCATTAC[C/T]CCCTGAACTGGCTTT | 55728 |
| rs780895840 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40172160 | CTCAAGTGATCTGCC[C/G]ACCTCGGCCTCCCAA | 55728 |
| rs780929416 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101589 | AATATTTCTGATATG[C/T]AGTACATGCTCAAAT | 55728 |
| rs780955525 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40110068 | CTATTCCAGACATTT[C/T]CTACAACATGTGGAC | 55728 |
| rs780966012 | snp | G/T | 1.72704e-05 | 0.00293852 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117852 | CCTTCAACCCTTTTT[G/T]CCCCTGGAATTTTCA | 55728 |
| rs780971143 | snp | G/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157512 | TTTCTGAGCTGGAAA[G/T]TGGAAACTTTGGAAA | 55728 |
| rs781010726 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107515 | CAGCTTCCTGAGTAG[C/T]TGGGATTACAGGTGC | 55728 |
| rs781042138 | in-del | -/ACTTCCCCAACAAAAGTA | 1.64741e-05 | 0.00286998 | cds-indel, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103058 | TCAGTTATTTCTCAC[-/ACTTCCCCAACAAAAGTA]TGGAGAAATAAAGAT | 55728 |
| rs781043758 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111382 | CTGGAGTACAATGGC[G/T]TGGTCTCAGCTCACT | 55728 |
| rs781072377 | snp | G/T | 0.000197925 | 0.00994602 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142724 | GAACTGTCTTTCCAG[G/T]ACTTTGAGTACCCAG | 55728 |
| rs781074719 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117511 | GTGTGAAAGTACTCC[A/G]AGTTGAAGGCCTCAG | 55728 |
| rs781101144 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067516 | AAGTATCTCTTGGAG[A/G]TCCTGTTATTAATTA | 55728 |
| rs781117188 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132883 | GATTTACTAATTCAT[G/T]GGTATTTTTACAATA | 55728 |
| rs781119986 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105131 | TGAAGAGAATGGTCT[A/C]GTATTCAAACCAAAG | 55728 |
| rs781140846 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080625 | CAGGCGTGAACCACC[A/G]TGCCTGGCCTATATA | 55728 |
| rs781149055 | snp | G/T | 1.6646e-05 | 0.00288491 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120294 | TATCACCTAGTACTT[G/T]CTGTAGTGAAAATAA | 55728 |
| rs781236761 | snp | A/G | 1.88482e-05 | 0.00306981 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119907 | AAGAGACTTTCTCAT[A/G]ATACTCTTTAAAATA | 55728 |
| rs781239737 | snp | G/T | 4.98037e-05 | 0.00498993 | utr-variant-3-prime, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40154263 | CTTGAATTAGAAGTA[G/T]GAAGGTTTGTAGGTT | 55728 |
| rs781242946 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074358 | GACCTCCCAAAGTGC[C/T]GGAATTACAGGCGTG | 55728 |
| rs781282057 | snp | A/G | 6.75276e-05 | 0.00581027 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120001 | ATCTTTGAAGCATCT[A/G]GAGTTCACTGAAGAG | 55728 |
| rs781291914 | snp | A/G | 3.37314e-05 | 0.00410665 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40136946 | AAATTTTCTACAGCT[A/G]TTCATTAGAACACAC | 55728 |
| rs781322046 | snp | C/T | 0.000115385 | 0.00759468 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131894 | ATTAACCAAAATTTT[C/T]TGGTGGACATTTTCA | 55728 |
| rs781332398 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103010 | GTAACCACAGCTGCA[C/G]ACTGGAGATCTGTCA | 55728 |
| rs781334065 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125237 | CAGTGTCTATTGTTT[C/G]TTCACTCTCTAGGAC | 55728 |
| rs781350146 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177432 | ATTAGCTTGGCCAAC[A/G]TGGTGAAACCCCGTT | 55728 |
| rs781400221 | snp | A/T | 3.31142e-05 | 0.00406891 | intron-variant | N4BP2 | GRCh38.p7 | 4:40154173 | CATCTTTAAAATAAC[A/T]CTTTTCTCATTTCTG | 55728 |
| rs781499225 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40088947 | GGTTTTTATTTTTTG[G/T]TTTTTTTGTGTGTGT | 55728 |
| rs781528686 | in-del | -/GT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131160 | TCACAGCATCACACA[-/GT]GTCACTTTTATGAGG | 55728 |
| rs781531986 | snp | A/G | 1.66724e-05 | 0.0028872 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121242 | TCAAAGTATTAACAG[A/G]AAGATTAGATGGATT | 55728 |
| rs781534622 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40129056 | CTTGTTTTTCTTTTT[A/C]TTTTCTTTTTTTTGA | 55728 |
| rs781541627 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103069 | TCACACTTCCCCAAC[A/G]AAAGTATGGAGAAAT | 55728 |
| rs781541760 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120429 | GGAAACAAAAAAGCA[A/G]ATCGACTTTGGAAAA | 55728 |
| rs781548933 | in-del | -/A | 1.66014e-05 | 0.00288104 | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120858 | AAATTGGAACAAATG[-/A]CAAAATGAATGAAAT | 55728 |
| rs781591328 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074975 | TCTTGCCACTGCACT[C/G]CAGCCTGGGCGACAG | 55728 |
| rs781606373 | in-del | -/AC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135553 | TGGTTGAACTAGTTT[-/AC]AGTCTTTCTTTCTTT | 55728 |
| rs781634282 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137211 | GAAATTTAACCACCA[A/G]TGGCATATTTGGCTT | 55728 |
| rs781639372 | snp | A/G | 8.28288e-05 | 0.00643487 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120676 | TGGCAGAAAGTCACA[A/G]TGTGATGATGCTTCA | 55728 |
| rs781655183 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142173 | GAGAGGGCAGCGTGT[A/C]ACCTTGGTAACTTCA | 55728 |
| rs781659109 | snp | A/G | 0.000148494 | 0.00861539 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144758 | CTGCATGTGGATGAA[A/G]CTCTAGAACATTTGA | 55728 |
| rs781659200 | snp | A/G | 8.23716e-05 | 0.00641709 | utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097400 | GACTGCAAACCCTAA[A/G]GAAGTTGTCGTATCC | 55728 |
| rs781687735 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066224 | GTGAGCCACCGTGCC[C/T]GGCCCATTTTTTTCA | 55728 |
| rs781688663 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096852 | GAGATGGGAAAGACT[A/G]GGAAAAGCAGGTTTG | 55728 |
| rs781694984 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40118660 | AGTATTTCCCTTATC[G/T]TCTCGCTGTTATTAT | 55728 |
| rs781709605 | in-del | -/GAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150675 | ACTCTGTCTCAGGGG[-/GAA]GAAAAAAAAAAAAGA | 55728 |
| rs781730465 | snp | A/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40113463 | ATAAAGTCCTTTTTC[A/G]GGAACCAGACACATG | 55728 |
| rs781743001 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40103567 | AATTGATCTTGATTT[C/T]ATGGAATGGAAGACT | 55728 |
| rs796078351 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168737 | TTTTTTCTTCTTTTT[G/T]TTTTGAGATGGAGTT | 55728 |
| rs796117214 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139537 | CACTCTGTCGCCCAG[A/G]CTGGAGTGCAGTGGC | 55728 |
| rs796139999 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40060620 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCCC | 55728 |
| rs796151619 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146922 | TATTTTTATTTTTTT[A/T]TTTTTTTTATTGATC | 55728 |
| rs796160784 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104420 | TTTAGTTTTTTTTTT[-/TT]GATATCTTTTCTGTG | 55728 |
| rs796165040 | in-del | -/AGGGAG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40142125 | GGAGAGGGAGACCAT[-/AGGGAG]AGGGGGAGGGGGAGG | 55728 |
| rs796231498 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081846 | GGTTGGGTGCTGTGG[C/T]TCACGCCTGTAATCC | 55728 |
| rs796274584 | snp | C/G | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155314 | GGAGAACCGCTTAAA[C/G]CTGGGAGGTGGAGGT | 55728 |
| rs796306822 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132116 | CCTCTATATACTATG[-/T]TTTTTTTCCTATAAA | 55728 |
| rs796309485 | in-del | -/AT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40128845 | TTCTTTAAAAAAAAA[-/AT]AAATAAATAAAATAA | 55728 |
| rs796363763 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40059759 | CATAGTAATGAAGTG[G/T]CTTATGTGTATGTAC | 55728 |
| rs796382273 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072264 | TTTTTTTTTTTTTTT[-/T]GATATGGAGTCTCAC | 55728 |
| rs796388604 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066320 | ATTTGTGATTTTCCC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs796407235 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40085501 | TCACTCTGTCACTGA[G/T]GCTGGAGTGCAGTGG | 55728 |
| rs796437551 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123652 | ACCACACCTAGGTAA[-/T]TTTTTTTTTTTTTGT | 55728 |
| rs796452679 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184883 | ATCGCTTGAACCTGG[A/G]AGGCGGAGGTTGCAG | 55728 |
| rs796476598 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091847 | CTCCTGGGCTCAAGC[A/G]ATCCTCCCAACTCAG | 55728 |
| rs796481624 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132934 | TGTGATTTTTTTTTT[-/T]CTGTTCCTGGGCTAT | 55728 |
| rs796493476 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40074479 | CTCCCAAAGTGCTGG[C/G]ACAACAGGTGTGAGC | 55728 |
| rs796502421 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084434 | TATGCCTGGTTTGAG[A/T]TTTTTTTTTTTTTTC | 55728 |
| rs796545652 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137206 | GACTGGAAATTTAAC[C/T]ACCAATGGCATATTT | 55728 |
| rs796575357 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131293 | CCCTTTGCTTTGGCC[A/G]CTAAGAGTCTCAGAA | 55728 |
| rs796580215 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139815 | GCTTTTTTTTTTTTT[-/T]ACATTTTTTTTTCTT | 55728 |
| rs796654443 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40168526 | ACCAAACAATATCAT[A/G]AAGATATAAATCAGA | 55728 |
| rs796720608 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142718 | CCAAGTGAACTGTCT[G/T]TCCAGGACTTTGAGT | 55728 |
| rs796724190 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146908 | CCAGGTAATGTTTTT[A/T]TTTTTATTTTTTTAT | 55728 |
| rs796728524 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131038 | ATTTGTGAAAAACTG[-/A]AAAAAAAAAAATTGT | 55728 |
| rs796751364 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40151612 | AACATATGTAAAGAA[C/T]AGTGCCCAAAATTAT | 55728 |
| rs796764172 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40094531 | TGCATATACATTTAG[C/G]GTTGCTATATCTTTT | 55728 |
| rs796764490 | snp | A/G | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152875 | ATCAAACCAGCTGTC[A/G]TTAAGTACCTCATAA | 55728 |
| rs796768120 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084282 | CTGGCAGGATTTGCT[G/T]AATGATGAGGTGTGA | 55728 |
| rs796840394 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123937 | AGAAATTTTTTTTTT[-/T]AAATGCAGTATTTTT | 55728 |
| rs796845437 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40099762 | TGTGATAAGTACCTA[A/T]CCATTTTGATCTTTA | 55728 |
| rs796883834 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140053 | CACCTTGGCCTCCCA[A/C]AGTGCTGGGATTACA | 55728 |
| rs796887630 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40182878 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55728 |
| rs796931343 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080384 | AGGTGGAGTCTTGCT[-/CT]GTTGCCAGGCTGGAG | 55728 |
| rs796931608 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40062644 | CCTTATTGACACTTG[A/G]CTGTCAGTGTGCTAG | 55728 |
| rs796964450 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40109717 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGT | 55728 |
| rs796980872 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146914 | AATGTTTTTATTTTT[A/T]TTTTTTTATTTTTTT | 55728 |
| rs796983442 | in-del | AAA/GTTGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090950 | AAAAAAAAAAAAAAA[AAA/GTTGT]GTTTATAAGATCCTA | 55728 |
| rs796985688 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40116649 | TGTTTATTTTCACTT[A/G]TTCATCTAGTTATTG | 55728 |