| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs1995 | snp | C/T | 0.258565 | 0.249853 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158088 | TTTTCTGATATACTG[C/T]CTGAAAATTTTATAA | 55728 |
| rs793993 | snp | G/T | 0.288646 | 0.246995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111808 | gccaacatggtgaaa[G/T]cccatctctactaaa | 55728 |
| rs793994 | snp | A/G | 0.288646 | 0.246995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111432 | ttgggaggctgagac[A/G]gcagaatcacttgaa | 55728 |
| rs793995 | snp | A/T | 0.448963 | 0.151372 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111068 | AACAAATGGACAAAT[A/T]TACACACACACAATG | 55728 |
| rs793996 | snp | C/T | 0.184521 | 0.241273 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110992 | GGGATTTTCTTACCT[C/T]TCTTCCAAAGGAATT | 55728 |
| rs793997 | snp | A/T | 0.160609 | 0.233472 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127094 | agaccagcctgggca[A/T]catggcaaaactgtc | 55728 |
| rs793998 | snp | A/G | 0.290977 | 0.246619 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125495 | TAAATAGAGGAAGTT[A/G]TAGCCAGCTGGAAGT | 55728 |
| rs793999 | snp | A/C | 0.168135 | 0.236216 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097677 | TTCTATTTTATTCAT[A/C]ATTTATTAATCATCT | 55728 |
| rs794000 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104534 | CTAACTGACTTAATA[A/G]CAACAACAACATAAA | 55728 |
| rs794001 | snp | A/G | 0.306922 | 0.243434 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40119942 | TACAGCCCAAGAGAC[A/G]ATGAAGATATTATCT | 55728 |
| rs794002 | snp | C/T | 0.325563 | 0.238307 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142453 | TTCTTTAACCACTCT[C/T]GGGAGATGTTGAAGA | 55728 |
| rs794003 | snp | A/C | 0.324382 | 0.238678 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142179 | ctgaagtgaagttac[A/C]aaggttacacGCTGc | 55728 |
| rs794004 | snp | C/T | 0.290201 | 0.246747 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142129 | ctccccctccccctc[C/T]ccctatggtctccct | 55728 |
| rs794005 | snp | C/G | 0.255782 | 0.249933 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141324 | agccgccccgtctga[C/G]aagtgaggagcgtca | 55728 |
| rs794006 | snp | C/T | 0.292523 | 0.246357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141121 | ctgcccggccaccac[C/T]ccatctgggaggtgt | 55728 |
| rs794007 | snp | A/G | 0.299411 | 0.245069 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140915 | ggatcctgttgatct[A/G]tgaccttacccccaa | 55728 |
| rs794008 | snp | A/G | 0.289942 | 0.246789 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138718 | cagcaataaatcctt[A/G]taactatggtcaatt | 55728 |
| rs794009 | snp | A/C | 0.295854 | 0.245759 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138099 | gtattctgccactgg[A/C]atttttgcagccttc | 55728 |
| rs794010 | snp | C/T | 0.163892 | 0.234703 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137977 | acctgtctgggagca[C/T]gcctttcatttggaa | 55728 |
| rs794011 | snp | A/C | 0.161267 | 0.233723 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137794 | aacctgcttaccctg[A/C]cttacccattccttc | 55728 |
| rs794012 | snp | A/G | 0.161596 | 0.233848 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136531 | ggtgtggtgacgcgc[A/G]cctgtaatcccagct | 55728 |
| rs794018 | snp | A/G | 0.36606 | 0.221428 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167804 | GTCTTTATTTAACAC[A/G]TATAGTACACATTTT | 55728 |
| rs794019 | snp | C/G | 0.44546 | 0.155869 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161105 | TTATGACTTCGGGCT[C/G]TTATTCTGTGAGGGC | 55728 |
| rs794020 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160910 | TTATGGAGTGTCTTA[A/G]TCTTTAAGTCTGCTG | 55728 |
| rs794021 | snp | A/T | 0.411578 | 0.190768 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069721 | AGGGTCTCGCTTTGC[A/T]GCCCACACTGGTCTC | 55728 |
| rs794022 | snp | C/G | 0.193653 | 0.243567 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069248 | gtttcaccatgttgg[C/G]caggctggtcttgaa | 55728 |
| rs794023 | snp | C/T | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066414 | agagaattgcttgaa[C/T]ctgggaggcagaggc | 55728 |
| rs794024 | snp | C/T | 0.190519 | 0.242821 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066405 | cttgaacctgggagg[C/T]agaggctgcaatgag | 55728 |
| rs794025 | snp | A/G | 0.193653 | 0.243567 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066353 | tcagcctgagcaaca[A/G]agtgagacactgtct | 55728 |
| rs794026 | snp | A/G | 0.192715 | 0.243348 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065999 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 55728 |
| rs794027 | snp | A/G | 0.182614 | 0.240747 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064377 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAAGAGG | 55728 |
| rs794028 | snp | A/G | 0.19459 | 0.243782 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062060 | accaaaaaaTAAAGC[A/G]GTAAAAACAAAACAA | 55728 |
| rs794029 | snp | A/G | 0.192088 | 0.2432 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061521 | aaaacttagctgggc[A/G]tggtggtgcacatct | 55728 |
| rs794030 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060694 | gatcccttgagccca[A/G]gaattcaaggctaca | 55728 |
| rs794031 | snp | A/G | 0.247337 | 0.249986 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059591 | AGGCCAAAGCGGGCG[A/G]ATCACTTGAGGCCAG | 55728 |
| rs807787 | snp | C/T | 0.157311 | 0.232183 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150036 | ACAGTAACTACAGAC[C/T]ACCACAGGTGGCAGC | 55728 |
| rs809913 | snp | A/C | 0.497855 | 0.0326773 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111262 | aaatcaaactatagt[A/C]ttgagtttagttaat | 55728 |
| rs809914 | snp | A/G | 0.244776 | 0.249945 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160050 | gatggatcacctaag[A/G]tcaggaattcgagac | 55728 |
| rs809915 | snp | C/T | 0.192401 | 0.243274 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060338 | agaattgcttgaacc[C/T]gggaggcagaggttg | 55728 |
| rs813230 | snp | G/T | 0.425586 | 0.17796 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095995 | gaggttGGAATATGG[G/T]TGAAAGATGACAGGT | 55728 |
| rs813809 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174775 | ccactgcactccagt[C/T]tgggcgacagagtga | 55728 |
| rs813810 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175106 | actcactgcagccta[A/G]aattcctggcctcaa | 55728 |
| rs907356 | snp | C/T | 0.203882 | 0.245709 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057256 | GGCTGAGCGCCAGGG[C/T]CCGCCTCTCGCCGAC | 55728 |
| rs937967 | snp | A/C | 0.14665 | 0.227637 | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057142 | GGGGTTCATTCGCCG[A/C]GCCGCCCGCCGCTGC | 55728 |
| rs937968 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125051 | ATGTGGAGGAACTCA[A/G]GCACAAAAGGAGGAT | 55728 |
| rs971010 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091506 | ttttaatgcgtgaaa[A/G]aattgtatcaatcaa | 55728 |
| rs1004294 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061003 | aaatttaaattgaga[C/T]ggggtgttgccatat | 55728 |
| rs1008086 | snp | C/T | 0.152334 | 0.230133 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145137 | ACTTAATTGATATTT[C/T]TTGGATTTCAATTTT | 55728 |
| rs1087313 | snp | C/T | 0.191147 | 0.242974 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067817 | cagctactcgggagg[C/T]tgagacaggagaatc | 55728 |
| rs1091048 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088684 | tttgtatttttacta[A/G]aaacggggtttctcc | 55728 |
| rs1128372 | snp | C/T | 0.320763 | 0.239776 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117881 | CAGGCGTAACATTCA[C/T]GGGGTAAGCAAAGAA | 55728 |
| rs1128374 | snp | C/T | 3.30006e-05 | 0.00406192 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117927 | TTGGAACATTATCAA[C/T]GTTTTGTTTCAGTGC | 55728 |
| rs1396952 | snp | G/T | 0.318415 | 0.240457 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055239 | TCAAAAACAAAAAAT[G/T]GTAATAACCCAGAAT | 55728 |
| rs1397933 | snp | G/T | 0.263809 | 0.249618 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185917 | GTTTTCCTCTAATGA[G/T]CCTCAAGCATTTCCC | 55728 |
| rs1397934 | snp | A/G | 0.257454 | 0.249889 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185976 | CTGAATTAATTACCC[A/G]GAAACCTCACTTTTT | 55728 |
| rs1509813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057915 | GCATGGCGAGAATGT[C/G]TACAAACCTGTCCGT | 55728 |
| rs1533063 | snp | C/T | 0.288646 | 0.246995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114842 | GAAACGTTGCTATAA[C/T]GGAAAAATTCCAACT | 55728 |
| rs1533064 | snp | A/G | 0.449853 | 0.150196 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114747 | ttagataaacctaga[A/G]aagaagaaaagagga | 55728 |
| rs1553773 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060753 | gagccaggcacagcg[C/G]tatgtgcctatactc | 55728 |
| rs1623354 | snp | C/T | 0.2462 | 0.249971 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158391 | ACAGAAAACGTAAAC[C/T]AGAAGAAAAGTTTTG | 55728 |
| rs1623513 | snp | A/G | 0.0352966 | 0.128072 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158320 | TACAAAGTTAGACAT[A/G]AAAATATTTTAAAAT | 55728 |
| rs1624604 | snp | A/G | 0.192088 | 0.2432 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058977 | AAAAATTAGCCGGGC[A/G]TAGTGGCTTTCGCCT | 55728 |
| rs1625495 | snp | C/T | 0.191775 | 0.243125 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058855 | CCAGCCTTGGCGATA[C/T]GGCCAGACCTTGTCT | 55728 |
| rs1704153 | snp | C/T | 0.383824 | 0.211166 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098964 | GGGTTTCTAATCTAC[C/T]GAGTTGTGCTGTAGT | 55728 |
| rs1704154 | snp | C/T | 0.497881 | 0.0324789 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107130 | tttgagacagggtct[C/T]gctgtgttgcacagg | 55728 |
| rs1704155 | snp | A/G | 0.127599 | 0.217986 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056289 | AAGGTCGGCCTCGCG[A/G]GGTGAGGGGAGAAAG | 55728 |
| rs1704156 | snp | A/G | 0.204803 | 0.245881 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056079 | TCGGAGCCCCACGGG[A/G]AGACAAAGGGGTAGG | 55728 |
| rs1704157 | snp | A/G | 0.315758 | 0.241197 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055669 | GTCCCCTCCCTTTGC[A/G]GTTACTTTTCATTCC | 55728 |
| rs1704158 | snp | A/G | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071607 | tgcactccagcctgg[A/G]caacaagagcaaaac | 55728 |
| rs1704160 | snp | A/G | 0.215747 | 0.247642 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144072 | GGCTCAAGAGCCACC[A/G]AGAGGCAGCTGGTGC | 55728 |
| rs1706022 | snp | A/C | 0.154993 | 0.231244 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159579 | AACCATCTTTAAGAC[A/C]ACTTGGCACTTGCCT | 55728 |
| rs1706023 | snp | C/T | 0.388587 | 0.208071 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073122 | aggaacaacagaacc[C/T]aaaactaattaccat | 55728 |
| rs1706024 | snp | G/T | 0.335152 | 0.279336 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056443 | GTGTCGGGTTCTGCT[G/T]GGGGGGAAGGCGGGA | 55728 |
| rs1706025 | snp | C/T | 0.145305 | 0.227022 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056038 | GGGGTGGAGGGAGGC[C/T]GCCCAGCCCCATCGG | 55728 |
| rs1706026 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117398 | TTGAATTCAACCCAA[A/G]ACAGGAAAGTTGCAA | 55728 |
| rs1706027 | snp | A/G | 0.16976 | 0.236773 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079125 | agaccagcctggcca[A/G]cacggtaaaacccca | 55728 |
| rs1706028 | snp | C/G | 0.223522 | 0.248594 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099056 | AATATTTTTTTCTTT[C/G]TTTTGGCTTTTTTTT | 55728 |
| rs1706029 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126752 | aaataaaaaTACCCA[A/G]gcctggtagtccctg | 55728 |
| rs1706030 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40126749 | taaaaaTACCCAAGC[A/C]TGgtagtccctgtta | 55728 |
| rs1706032 | snp | A/G | 0.256061 | 0.249927 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148264 | acagggtttcgctgt[A/G]ttggccaggctgctc | 55728 |
| rs1706034 | snp | A/G | 0.450483 | 0.149354 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119277 | AGGAAGGCATCCTGC[A/G]AGAGTTGGGACTTCG | 55728 |
| rs1714383 | snp | A/G | 0.255503 | 0.249939 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150292 | AAATCCCTATAAAAT[A/G]GTAGTCAGTTCTAAA | 55728 |
| rs1714384 | snp | C/T | 0.155987 | 0.23165 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150287 | CCTATAAAATGGTAG[C/T]CAGTTCTAAAGGTTT | 55728 |
| rs1714385 | snp | C/G | 0.155987 | 0.23165 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148416 | cctctgatgccgagc[C/G]gaagctggactgtac | 55728 |
| rs1714386 | snp | C/T | 0.155987 | 0.23165 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148322 | ctgcgattgcaggcg[C/T]gcgccgccatgcgtg | 55728 |
| rs1714387 | snp | C/T | 0.163892 | 0.234703 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143865 | AAATTATCTTTCATA[C/T]ATCCTACTGGTCTGT | 55728 |
| rs1812396 | snp | C/T | 0.201727 | 0.245295 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109497 | cttaggcagatggat[C/T]acctgaagtcaagag | 55728 |
| rs1876874 | snp | G/T | 0.268724 | 0.249298 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117779 | CGTATCTATTAGAAA[G/T]ATATTATTGTTTTCC | 55728 |
| rs1985721 | snp | G/T | 0.427727 | 0.175821 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145222 | TCCAGTAGTTTTTTT[G/T]TTTGTTTGTTTCTTT | 55728 |
| rs1985722 | snp | G/T | 0.464309 | 0.12873 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145226 | GTAGTTTTTTTGTTT[G/T]TTTGTTTCTTTTTCT | 55728 |
| rs1996559 | snp | C/T | 0.255782 | 0.249933 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145748 | GTGTGTCTTTTTCAC[C/T]ACCTTATCCTTGATG | 55728 |
| rs2012638 | snp | A/C | 0.208779 | 0.246578 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109458 | cgcggtggctcatgc[A/C]tgtaattccagcact | 55728 |
| rs2055821 | snp | A/T | 0.201418 | 0.245234 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119170 | actctgctcataaaa[A/T]tcttataaggattat | 55728 |
| rs2136563 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117192 | ttctcttctctttcc[A/G]ggacttagattagat | 55728 |
| rs2136565 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146921 | TTAtttttatttttt[A/T]attttttttattgat | 55728 |
| rs2137103 | snp | C/T | 0.276534 | 0.248588 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180348 | AATTAATCAGCAAGA[C/T]ACCACTTTTCAACTA | 55728 |
| rs2252352 | snp | C/T | 0.26518 | 0.249539 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126470 | AAATTATACTTAAAA[C/T]ATTTTTCAATTTTAA | 55728 |
| rs2271395 | snp | C/T | 0.157647 | 0.232316 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137056 | TAGACTTCTGGCCAG[C/T]ATGAGATGTGACATT | 55728 |
| rs2381486 | snp | A/G | 0.226779 | 0.248919 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081571 | GGATTGCTTGAACGC[A/G]GGAGCTGGAGGTTGT | 55728 |
| rs2381488 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143254 | AACATTAATTTTTTT[G/T]GGGAAGTAAAATTTC | 55728 |
| rs2664187 | snp | A/C | 0.176618 | 0.238988 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142643 | ACAATAAGTAACACA[A/C]ACAGAAAGTTAAAAA | 55728 |
| rs2664188 | snp | C/T | 0.47852 | 0.101384 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079994 | TAAAAACAAATATAT[C/T]CCCCCCTCCCATCCT | 55728 |
| rs2664197 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067188 | acctgtggttccagc[A/T]actcagaaggctgag | 55728 |
| rs2664198 | snp | G/T | 0.234401 | 0.249513 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065545 | AAGCAGCATTTACTG[G/T]TTTTTTTCTGTCTGG | 55728 |
| rs2664199 | snp | A/G | 0.48995 | 0.0701706 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064872 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 55728 |
| rs2664200 | snp | C/T | 0.268452 | 0.249318 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114845 | TTGGAAACGTTGCTA[C/T]AACGGAAAAATTCCA | 55728 |
| rs2664203 | snp | A/T | 0.227074 | 0.248947 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111495 | CGTCTCCACTAAAAA[A/T]ACAAAAATTAGCCAG | 55728 |
| rs2664204 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125624 | tgctgggattacagg[C/T]gtgagccaccgcacc | 55728 |
| rs2664208 | snp | C/G | 0.264906 | 0.249555 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133405 | GAGGCTGCAGTGAGC[C/G]ACGATGGTGCCACTG | 55728 |
| rs2664209 | snp | A/G | 0.222035 | 0.248431 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131994 | TACATTATTTTTGTT[A/G]TCAGAAAAATAAACA | 55728 |
| rs2667715 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066593 | gtggctcacacctgt[A/G]atcccagcactttgg | 55728 |
| rs2667718 | snp | C/T | 0.226484 | 0.248892 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124911 | GCTGGGTTTTGTGGT[C/T]TAACAATACTGACAT | 55728 |
| rs2667719 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40107290 | tttgttgtccagcct[A/G]gtcttgaactcctgg | 55728 |
| rs2732058 | snp | A/G | 0.254664 | 0.249956 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112699 | AAAAAAAAAAAGGTG[A/G]GCAAAAAAGAGCAAG | 55728 |
| rs2732065 | snp | C/T | 0.234109 | 0.249494 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063332 | CACAGAGTATAAGTA[C/T]GGAAAGGTCCCAACT | 55728 |
| rs2732076 | snp | C/T | 0.267908 | 0.249358 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100524 | GTGGCTGGTACTATA[C/T]GCACATGCTACCACA | 55728 |
| rs2732083 | snp | A/G | 0.225005 | 0.248747 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082876 | CGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 55728 |
| rs3070962 | in-del | -/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057783 | AAATAGTTTTTTTTT[-/T]CCCTCCGAAAGAGAG | 55728 |
| rs3070964 | in-del | -/ATTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40061379 | tttatttatttattt[-/ATTT]ttgagatggagtctc | 55728 |
| rs3210732 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40137029 | GCCCAAGAGTTTGTT[A/C]ACCAAAATGAGAATG | 55728 |
| rs3733298 | snp | A/G | 0.264906 | 0.249555 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152974 | GATATTTCTGTGAGT[A/G]TAGATTTCTGTTATT | 55728 |
| rs3930932 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146958 | ctgccaaatccccct[C/T]tgcgagaaacaccca | 55728 |
| rs4277787 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147283 | tttcttagtacagaa[A/C]aaaatgaaaagtctc | 55728 |
| rs4397001 | snp | A/C | 0.289683 | 0.24683 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147406 | cattgtcatcatggc[A/C]cgttctcaatgagct | 55728 |
| rs4627877 | snp | G/T | 0.278399 | 0.248382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182999 | GAACTTACACAATTT[G/T]TATATTAAAAAATAT | 55728 |
| rs4974919 | snp | G/T | 0.481856 | 0.0935034 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075888 | ctggagtgcagtgct[G/T]tgattactgcctact | 55728 |
| rs4974920 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147987 | gcagccgggaagagg[C/T]gctcctcacttccca | 55728 |
| rs4974958 | snp | C/T | 0.480461 | 0.0968913 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064845 | TGTGATCTCGGCTCA[C/T]TGCAACCTCCGCCTC | 55728 |
| rs4974959 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40078113 | GTTGAATATTTCTAA[A/G]TGTGTGTGTGTGTGT | 55728 |
| rs4974960 | snp | A/G | 0.483345 | 0.0897213 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095037 | CCTGCCCATTGTCCA[A/G]CGTGCTGGGATTACA | 55728 |
| rs4974961 | snp | C/T | 0.483923 | 0.0882034 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095937 | ctggtatattgaaaa[C/T]agactatagggggac | 55728 |
| rs4974962 | snp | A/T | 0.463126 | 0.13068 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113619 | TTAGATTGTAACTTA[A/T]TTTCTATTGCTTACG | 55728 |
| rs4974963 | snp | A/G | 0.290201 | 0.246747 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136014 | TTGGAACGTGAGTGT[A/G]TCAGACATTTGTTGA | 55728 |
| rs4974966 | snp | A/G | 0.461259 | 0.133677 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141762 | tggaggttgtagcga[A/G]ccgagatcacgccac | 55728 |
| rs4974967 | snp | A/G | 0.248471 | 0.249995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168481 | AGGGAGAAGAACAGT[A/G]CCTATAAAAGACAAT | 55728 |
| rs4974968 | snp | C/T | 0.195526 | 0.243993 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171313 | AGGCTGCCAATACCA[C/T]TGGCAGAAAGAGAGT | 55728 |
| rs4974969 | snp | A/T | 0.264084 | 0.249603 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172117 | ttcatcatgttggcc[A/T]gactagtctcggtct | 55728 |
| rs6531755 | snp | G/T | 0.436692 | 0.166271 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079332 | gtgttgcccaggatg[G/T]tcttgaattcctgag | 55728 |
| rs6531758 | snp | A/G | 0.490943 | 0.0666801 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147536 | ggcggctggccgggc[A/G]gaggcgccccccacc | 55728 |
| rs6531759 | snp | A/G | 0.47023 | 0.118317 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161351 | tgcaattaccaggat[A/G]gactgggaaactgac | 55728 |
| rs6813471 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173730 | TGTGTTCTCACTGCA[C/G]AGAGCCTGGGCCGAA | 55728 |
| rs6816051 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111188 | ctcatttatccttca[C/T]gttaacatctaatat | 55728 |
| rs6821957 | snp | C/G | 0.248755 | 0.249997 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169604 | accaaacctacaaaa[C/G]ccagcaagagctgta | 55728 |
| rs6822789 | snp | C/T | 0.49607 | 0.0441545 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169289 | tgggtgtctgaggca[C/T]gagaattgcttgaac | 55728 |
| rs6824091 | snp | C/T | 0.482008 | 0.0931261 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076814 | TTTTTAGTGACATAC[C/T]TTTGGTATCTCATGA | 55728 |
| rs6824580 | snp | C/G | 0.440746 | 0.161604 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156942 | TAGGGGATACTCACT[C/G]AACCTGTATATTTGT | 55728 |
| rs6828069 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087673 | CCCACTCCACGTGCA[A/C]CCCGCCCCCTCCGCC | 55728 |
| rs6828497 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075367 | TAACAACATGTCTCA[C/G]AGGTCTATCCAGTTT | 55728 |
| rs6831249 | snp | A/G | 0.4973 | 0.0366419 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171913 | agactaagccagtct[A/G]gtctttttctgagat | 55728 |
| rs6833196 | snp | G/T | 0.461148 | 0.133852 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141465 | ggcggcggggcagag[G/T]cgctccccacatctc | 55728 |
| rs6834460 | snp | C/T | 0.461148 | 0.133852 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141370 | tcctcacttctcaga[C/T]ggggcagccgggcag | 55728 |
| rs6834469 | snp | C/T | 0.475081 | 0.108804 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141389 | gcagccgggcagaga[C/T]gctcctcacctccca | 55728 |
| rs6836716 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127661 | TATCTCTGAGAAAAT[A/G]TATATATATAttttt | 55728 |
| rs6837532 | snp | C/T | 0.177182 | 0.23916 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076734 | accttgtggtccgcc[C/T]gccttgggctcccaa | 55728 |
| rs6839826 | snp | C/G | 0.469937 | 0.118861 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159659 | ctagtcatgtcatat[C/G]tagctgcgagggagg | 55728 |
| rs6842435 | snp | C/T | 0.255224 | 0.249945 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155593 | TAAAGGAGGTTATAA[C/T]GTGGTAAGGTATAAT | 55728 |
| rs6842657 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165392 | tagctagaactacag[A/G]tgtgcggcaccatgt | 55728 |
| rs6847860 | snp | G/T | 0.377187 | 0.215229 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185988 | CCCAGAAACCTCACT[G/T]TTTTATTTTTGAGTA | 55728 |
| rs6849159 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108463 | tgggattacaggcac[A/G]tgccaccatgcctgg | 55728 |
| rs6850765 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40166248 | TCACATGAAGAATTT[C/T]TGAAGGATTCTGTAA | 55728 |
| rs6852446 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117375 | CCCTGGGATCCAGTC[A/C]CAAAGCCTTGAATTC | 55728 |
| rs6853146 | snp | A/T | 0.49614 | 0.0437598 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140591 | ATTCTCTTTTTTTTT[A/T]AAATTAAtttatttt | 55728 |
| rs6857384 | snp | C/T | 0.462691 | 0.131387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072060 | actacaagcatttgc[C/T]actatgcctggctaa | 55728 |
| rs7376373 | snp | C/T | 0.463881 | 0.12944 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147568 | ccctcccggacatgg[C/T]ggctggccgggtggg | 55728 |
| rs7656730 | snp | C/T | 0.040671 | 0.13668 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157997 | CCAATGATGAACTTA[C/T]TATTAATAAATGATT | 55728 |
| rs7657511 | snp | A/C | 0.449091 | 0.151204 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115633 | actcttgggttatgt[A/C]gtactgtgtttttaa | 55728 |
| rs7658672 | snp | A/G | 0.410568 | 0.191619 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073567 | GTAAGTGTTATTAAA[A/G]TTGTAGAGTATGAAT | 55728 |
| rs7661041 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082174 | ccagcaaactgggag[A/G]ctaaggcaggggaat | 55728 |
| rs7666837 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153637 | TATTTTATGCCATGT[A/G]ATAAGATGTTATTTG | 55728 |
| rs7668906 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146817 | atttcatttcctcct[C/T]tctattctggcccct | 55728 |
| rs7670176 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080719 | ctggagtgcagtggc[A/G]tgatcttggctcact | 55728 |
| rs7671140 | snp | C/T | 0.029116 | 0.117091 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080493 | aggtacgtgccacca[C/T]gcccagctaattttt | 55728 |
| rs7673397 | snp | A/G | 0.0661048 | 0.171561 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158213 | CTTATGAAGCCATTT[A/G]CAAATTACATACTTA | 55728 |
| rs7674515 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062943 | TTATTTGTCATCTCA[C/T]CACATAGCGGTAAAT | 55728 |
| rs7675163 | snp | A/G | 0.105569 | 0.204058 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175953 | aaattagccgggcgc[A/G]gtggcgggcgcctgt | 55728 |
| rs7675453 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078748 | tccctggctggtctt[A/G]gactcctggggtcaa | 55728 |
| rs7675671 | snp | C/T | 0.463774 | 0.129618 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078698 | gcccagcttattgtt[C/T]tgtatttttttgttg | 55728 |
| rs7675675 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078709 | tgttttgtatttttt[C/T]gttgagacaggtttt | 55728 |
| rs7675677 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078712 | tttgtatttttttgt[G/T]gagacaggttttata | 55728 |
| rs7676448 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079264 | GATGTGGTTTTCAGT[A/G]GGAAGGTTTTGTATT | 55728 |
| rs7681558 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079364 | tcaaatgatcctcct[G/T]cctcggccttccaaa | 55728 |
| rs7681564 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079374 | ctccttcctcggcct[C/T]ccaaaatgctgggat | 55728 |
| rs7681860 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081973 | caaaattagccgggt[A/G]tggtggcgcatgcct | 55728 |
| rs7682084 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082135 | aacaaaataaattgg[A/G]tgtggtagcgagcgc | 55728 |
| rs7682645 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082344 | CTAAATTTCCATTAT[A/G]TCAatctaaagaggt | 55728 |
| rs7683639 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082144 | aattgggtgtggtag[C/T]gagcgcctgtagtcc | 55728 |
| rs7683647 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082148 | gggtgtggtagcgag[C/T]gcctgtagtcccagc | 55728 |
| rs7684708 | snp | C/T | 0.0105029 | 0.0717016 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144830 | ATCACAAGTTTTCAA[C/T]AGAATATATGTCTTT | 55728 |
| rs7686083 | snp | C/T | 0.388587 | 0.208071 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077427 | tgctgggattacagg[C/T]gtgaaccactgtgtc | 55728 |
| rs7686896 | snp | A/G | 0.463343 | 0.130326 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116025 | ACCCTAATTAATTGA[A/G]CCTTTTATTATTTTC | 55728 |
| rs7689782 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171483 | TTTGGATCATCCCCT[A/G]TGATGTGGCTGGGtg | 55728 |
| rs7697025 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079122 | agatggggttttacc[C/G]tgctggccaggctgg | 55728 |
| rs7697684 | snp | A/C | 0.261056 | 0.249755 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054597 | GCCCCCCCGCCGCCC[A/C]AAAAAAAAAAGAAAT | 55728 |
| rs7698626 | snp | C/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079233 | gtccTGATAATGGTG[C/G]TTTTTTTGTATTGAT | 55728 |
| rs7699412 | snp | C/T | 0.449345 | 0.150869 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117592 | TTTTGAAAAAGGCAC[C/T]ATGAGTGAAAACACA | 55728 |
| rs7699729 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151573 | CACTGTCCCTGGCCA[A/G]TGTAAAACTTTTATG | 55728 |
| rs9884175 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182388 | GTAGGGAGCCAAATA[A/G]ATCCTTGTATTTGGT | 55728 |
| rs9990921 | snp | C/T | 0.0501905 | 0.150254 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158568 | tttaggaggctgaga[C/T]gggcaggttgcttga | 55728 |
| rs9991110 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148031 | ggcagaggggctcct[C/T]acatcccagacgggg | 55728 |
| rs9991922 | snp | C/T | 0.264358 | 0.249587 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154307 | TTTGCAGTAATTCAG[C/T]CAATTCTACCCTAAA | 55728 |
| rs9993439 | snp | C/T | 0.247905 | 0.249991 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158914 | AATATTTAGAGCACT[C/T]GTTACTGGGGTTACA | 55728 |
| rs9994005 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124580 | ttgaactcctgacct[C/T]aggtgatctgcccac | 55728 |
| rs9994542 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160882 | TTGGGGTGGAGGGAC[A/C]GATGACAAAGGACAG | 55728 |
| rs9995001 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107134 | agacagggtctcgct[G/T]tgttgcacaggctag | 55728 |
| rs9998630 | snp | A/G | 0.177182 | 0.23916 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156810 | aaaggaaatactcac[A/G]gagcattttacattt | 55728 |
| rs9998717 | snp | A/G | 0.494651 | 0.0514399 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156844 | GGTTAGCGATACTCA[A/G]CAAGTAAATATAATG | 55728 |
| rs10000000 | snp | A/T | 0.282105 | 0.24793 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087276 | tcctttAAAAAAAAA[A/T]TTTTTTTTAAAGGAG | 55728 |
| rs10001172 | snp | C/T | 0.0341408 | 0.126114 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156957 | CAACCTGTATATTTG[C/T]GCTAATACATGACTC | 55728 |
| rs10002778 | snp | A/G | 0.0422008 | 0.138995 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155221 | acatggtgaatcccc[A/G]tctctattaaaaata | 55728 |
| rs10005788 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148882 | atccatcgatggaca[A/G]ttaggttgtttcACC | 55728 |
| rs10006674 | snp | G/T | 0.26518 | 0.249539 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146066 | ACTTGGGAGGCTGAG[G/T]CAGGGAGAATTACTT | 55728 |
| rs10008408 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168885 | gcgcgccaccacacc[C/T]ggctaattttttgta | 55728 |
| rs10008656 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162613 | TTTAGAGGTATGCCA[A/G]GGAGTACCCCAAGTC | 55728 |
| rs10010148 | snp | C/T | 0.476314 | 0.106217 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150186 | TTTAAAAAAGAGAGA[C/T]ATCTGGACCTTATGT | 55728 |
| rs10011231 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071622 | cccaggctggagtgc[A/C]atggtgcgatctcgg | 55728 |
| rs10012659 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171809 | cttctgtctgtagtc[A/G]aagttccaagagtcc | 55728 |
| rs10014170 | snp | A/G | 0.0186939 | 0.0948552 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102431 | TTTTCTACACAAAAT[A/G]TGAATTTGAACGGTG | 55728 |
| rs10017194 | snp | A/C/G | 0.059584 | 0.16355 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170536 | cactctacttgtggg[A/C/G]tgctgagacaggagg | 55728 |
| rs10017867 | snp | G/T | 0.192715 | 0.243348 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070212 | aaagtaaACTAAGAG[G/T]GGCAAATAAGTTTTT | 55728 |
| rs10018901 | snp | A/G | 0.264632 | 0.249571 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125444 | TTGGTCCTTAGAATG[A/G]GTGGCCAGAGCAGAC | 55728 |
| rs10022294 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168790 | agtgcaatggtgcag[C/T]cttggcttactgcaa | 55728 |
| rs10023102 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40135005 | cacaatgtgcaggtt[A/G]gttacatatgtatac | 55728 |
| rs10026654 | snp | A/G | 0.182933 | 0.240836 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076145 | TAGATATATTTAAAG[A/G]TGATTGGTTACTTTA | 55728 |
| rs10029236 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106586 | tacagtcttgctctg[C/T]ctcccaggctggagt | 55728 |
| rs10029586 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137240 | TTATAATATCTGTGC[A/G]CTCAAAATAATGAAT | 55728 |
| rs10031722 | snp | C/G | 0.476487 | 0.105846 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150184 | TTTTTAAAAAAGAGA[C/G]ACATCTGGACCTTAT | 55728 |
| rs10032009 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137271 | TTATAGCTGATTTTT[C/T]CCTTCGTGTGCATGA | 55728 |
| rs10033188 | snp | A/G | 0.26818 | 0.249338 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108717 | TTCCTTGCTAGTGTA[A/G]CTGTCTATTCAGTGA | 55728 |
| rs10517537 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184189 | GTAGTCATCTATGTT[A/G]AACGTGGGACTTACT | 55728 |
| rs10646836 | in-del | -/ATC/ATCTATA/ATCTATC/ATCTATCTATCTATC/ATGT/TATA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136386 | ATCTATCTATCTATC[lengthTooLong]TATCTATCTATCTTT | 55728 |
| rs10666428 | in-del | -/TAC | 0.254385 | 0.249962 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168592 | GAAATTTATGGATTT[-/TAC]TACACCTTTTTCAGA | 55728 |
| rs10675156 | in-del | -/A/AA/AAA/AAAA/GAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150676 | CTCTGTCTCAGGGGG[-/A/AA/AAA/AAAA/GAA]AAAAAAAAAAAAGAG | 55728 |
| rs10714755 | in-del | -/T | 0.303187 | 0.244277 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132835 | TACTTTACTTTCAGA[-/T]TTTTTTTTTTTCCTT | 55728 |
| rs11097014 | snp | A/C | 0.249603 | 0.25 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058748 | TACACAGTAGAAGCT[A/C]AATATTATCACTAGT | 55728 |
| rs11097015 | snp | A/G | 0.279726 | 0.248226 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072022 | aagcgattctcatgc[A/G]tcagcctcctgagta | 55728 |
| rs11097016 | snp | C/T | 0.198634 | 0.244666 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135711 | gggattacaggcgcc[C/T]gccaccatgcccggc | 55728 |
| rs11290025 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107927 | TGTTTCCTATGTATC[-/T]TTTTTTTTTTTTTTG | 55728 |
| rs11302996 | in-del | -/T | 0.410737 | 0.191478 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060603 | GGCTAAGTAGCTAGA[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs11339497 | in-del | -/A | 0.390464 | 0.206809 | intron-variant | N4BP2 | GRCh38.p7 | 4:40176090 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs11356257 | in-del | -/A | 0.264358 | 0.249587 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178427 | CCCCGCCACCAAAAC[-/A]AAAAAAAAAAGAAAA | 55728 |
| rs11384930 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066336 | TTTTTTTTTTTTTTT[-/T]GAGACAGTGTCTCAC | 55728 |
| rs11387761 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066321 | TTTGTGATTTTCCCT[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs11423243 | in-del | -/T | 0.49995 | 0.00499176 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128539 | CTGTTTTTTTTTTTT[-/T]GAGTCTCGTTCTGTC | 55728 |
| rs11454392 | in-del | -/T/TT | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183353 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGCGTCTGGC | 55728 |
| rs11614296 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141679 | CCCGGCCGCCACCCC[A/G]TCTGGGAAGTGAGGA | 55728 |
| rs11721966 | snp | A/G | 0.243061 | 0.249904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136536 | ggattacaggcgcgc[A/G]tcaccacacccagct | 55728 |
| rs11722533 | snp | A/G | 0.20111 | 0.245173 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152613 | TTAAAACATTAATTT[A/G]GGGGCTTTTTGAGAT | 55728 |
| rs11723134 | snp | C/T | 0.171057 | 0.237209 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185488 | TTAAAAGACAAGAAT[C/T]AGAGAACAAAAACAA | 55728 |
| rs11724877 | snp | C/G | 0.24134 | 0.24985 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178820 | AGTGCAGCTGCTGTC[C/G]GAGAGCTCTGTCAGG | 55728 |
| rs11727866 | snp | C/T | 0.201727 | 0.245295 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103780 | ATATACACCTTTATC[C/T]CTTCTGTAGTTAAGG | 55728 |
| rs11729752 | snp | A/G | 0.222333 | 0.248464 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118373 | GTGAGCTGAGGTTGC[A/G]GTGAGCCGAGATTGC | 55728 |
| rs11730862 | snp | C/T | 0.47726 | 0.104176 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152097 | TAGGAGGCTCAGACT[C/T]CTTTGATGTTTTAAG | 55728 |
| rs11731404 | snp | C/T | 0.00938946 | 0.0678717 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082651 | aaacaaccaaaaaGC[C/T]TAAGCAAACAAACCA | 55728 |
| rs11731729 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173424 | CAAGGATTTACACAA[C/T]AGCAGGAAAGAAAAT | 55728 |
| rs11734859 | snp | A/C | 0.463881 | 0.12944 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145670 | GAAAGAATATTCTTT[A/C]TATAGAGGATGAATT | 55728 |
| rs11735047 | snp | C/T | 0.207864 | 0.246424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151635 | AAAATTATAGGTATA[C/T]AGTGCAAAAACTTTG | 55728 |
| rs11735928 | snp | C/T | 0.208474 | 0.246527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151789 | TAGAGATGGAGATCA[C/T]AGACAAGGAATTAGA | 55728 |
| rs11737087 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40057121 | AGCCGAAGCGGAGGG[C/T]CTGAAGCAGCGGCGG | 55728 |
| rs11929884 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054633 | GGGACATGAACTTCA[A/G]TGAGAACGAGCATGA | 55728 |
| rs11930588 | snp | C/T | 0.436976 | 0.165952 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179090 | AAACGTTTTGGAGGC[C/T]GGGCGCAGCAGCTCA | 55728 |
| rs11931647 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090525 | ggttctcggaaactg[A/T]gattttaagtgaaac | 55728 |
| rs11932747 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170854 | TGCAATTGTATTTCA[C/T]ATATCCTCATTTTGC | 55728 |
| rs11934650 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072160 | gctcactgcaatctc[C/T]gccttccgggttcaa | 55728 |
| rs11935984 | snp | G/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060881 | agttgctgggaatat[G/T]ggcccgagccatcac | 55728 |
| rs11945867 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073852 | ggctgtagtgcaatg[A/G]catgatctcagctca | 55728 |
| rs11946808 | snp | G/T | 0.330249 | 0.23677 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174937 | atttgctgccacgtg[G/T]gaacctgaaggacat | 55728 |
| rs11947064 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087038 | ataggtgtaagccat[C/T]gtgcctggTGTAATT | 55728 |
| rs12498783 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076607 | cattctcctgcctca[A/G]cctcccgagtagctg | 55728 |
| rs12499003 | snp | G/T | 0.454904 | 0.143228 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179527 | tcctcacaacagcca[G/T]aagaggtgtagaggc | 55728 |
| rs12501627 | snp | A/G | 0.187685 | 0.242109 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179349 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 55728 |
| rs12505176 | snp | C/T | 0.384209 | 0.210922 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080327 | ATATATATATATATA[C/T]ACACACACATATATA | 55728 |
| rs12505339 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066128 | tagagatggggtttc[A/C]ccgtgttggccagga | 55728 |
| rs12507226 | snp | C/T | 0.207864 | 0.246424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127218 | CTTCtttttttcttt[C/T]ttttaattttatttg | 55728 |
| rs12509177 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080346 | cacacatatatatgt[A/G]tatatataatttttt | 55728 |
| rs12510011 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080337 | atatacacacacaca[C/T]atatatgtatatata | 55728 |
| rs12511590 | snp | A/G | 0.413582 | 0.189052 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077143 | TTATGTAGAATATAT[A/G]TGTGTGTGTGTGTGT | 55728 |
| rs12512309 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076958 | GAGGAAGTTGTTTGC[G/T]GATCGTGTTTGGGAA | 55728 |
| rs12512577 | snp | A/G | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080344 | cacacacatatatat[A/G]tatatatataatttt | 55728 |
| rs12645398 | snp | G/T | 0.461259 | 0.133677 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163685 | TGCTAAGGATGGTGA[G/T]TGTAGAGAAGAAAAA | 55728 |
| rs12650412 | snp | G/T | 0.224412 | 0.248687 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134380 | CAGGCAAAGGAGGGG[G/T]CTGGGTGTGTCCTTC | 55728 |
| rs12650953 | snp | A/G | 0.323434 | 0.238972 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140074 | TGGGATTACAGGCGT[A/G]AGCCACCATGCCCAG | 55728 |
| rs12651527 | snp | C/G | 0.46137 | 0.133501 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163387 | gggctcagggaagat[C/G]aacccctctgtagct | 55728 |
| rs13102281 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147748 | ggggtggctgccggg[C/T]ggaggggcttctcac | 55728 |
| rs13102311 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147808 | gggctcctcacttct[C/T]agacggggcagccag | 55728 |
| rs13102494 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147861 | agacggggtcgcggc[C/T]aggcagaggcgctcc | 55728 |
| rs13102511 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147889 | tcctcacatcccaga[C/T]ggggcggcggggcag | 55728 |
| rs13103318 | snp | C/T | 0.207559 | 0.246371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141004 | cctactacacaaaca[C/T]ggcaaccatccgatt | 55728 |
| rs13105086 | snp | A/G | 0.221141 | 0.248329 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136495 | gttcaagcgattctc[A/G]tgcctctcagcctcc | 55728 |
| rs13106642 | snp | A/T | 0.215816 | 0.247652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127671 | AAAATATATATATAt[A/T]tttttttgagatgga | 55728 |
| rs13106923 | snp | G/T | 0.209084 | 0.246629 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114389 | aagcagttactctag[G/T]tcccccctcctcttg | 55728 |
| rs13107857 | snp | A/G | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064299 | GAtttatttgagaca[A/G]agtctcgctctgttg | 55728 |
| rs13108364 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166828 | tgcatattaatcaca[C/T]cggggtaaatgggat | 55728 |
| rs13110235 | snp | A/G | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082251 | actgcactccagcct[A/G]ggcgacagagcgaga | 55728 |
| rs13119145 | snp | A/T | 0.207253 | 0.246318 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134677 | TAGCATCCAGCCCCT[A/T]ATACTGATATCCTTT | 55728 |
| rs13120329 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40091917 | ccccgccAAAATTCA[A/C]CAATATATAAAAACA | 55728 |
| rs13121509 | snp | A/T | 0.242201 | 0.249878 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099689 | ATTCATTGAAAAAAA[A/T]TTTTTTTATACCATG | 55728 |
| rs13123459 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40169006 | gctgggattacaggc[G/T]tgagccactgcgcct | 55728 |
| rs13123712 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140362 | CAAGATGATTATGAG[A/G]CCTTATGGGCCAAAT | 55728 |
| rs13129420 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147862 | gacggggtcgcggcc[A/G]ggcagaggcgctcct | 55728 |
| rs13129437 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147881 | agaggcgctcctcac[A/C]tcccagacggggcgg | 55728 |
| rs13130198 | snp | A/G | 0.208474 | 0.246527 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155261 | gctgggtgtggtggc[A/G]tgtgcctgtaatccc | 55728 |
| rs13145671 | snp | A/G | | | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056766 | TTGCCGGCGCCTCGA[A/G]ACCCCTCCCCACCCG | 55728 |
| rs13146962 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140361 | ACAAGATGATTATGA[A/G]ACCTTATGGGCCAAA | 55728 |
| rs13152574 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40147870 | cgcggccaggcagag[A/G]cgctcctcacatccc | 55728 |
| rs16995560 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097831 | TCTGTCTCTTTCATC[C/T]TCACTCTAGAACAGA | 55728 |
| rs16995563 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119491 | TAATCGGGCAAATAG[C/T]GTTGGTTGGCCCTTT | 55728 |
| rs16995565 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125399 | GTGTGCCTTCACTGA[A/C/G]TTACAGGTTTGCCAA | 55728 |
| rs16995572 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181324 | CTGTTCGTTTCTTCC[A/G]GATAGCAATTCAGTG | 55728 |
| rs17439873 | snp | C/T | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070306 | ATTTAAAGATTTAGA[C/T]TGATATTTGCTCTTT | 55728 |
| rs17440042 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128973 | TAATATCTTGATGTA[A/G]TAGGTGAACAAATGA | 55728 |
| rs17511668 | snp | G/T | 0.320052 | 0.239985 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102147 | AATCATCTTCACAAA[G/T]TTTCGTTGCTTCTGA | 55728 |
| rs17511730 | snp | A/C | 0.208779 | 0.246578 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115087 | TAATTTCTGCTTCTC[A/C]TTATTCTACCTTTAT | 55728 |
| rs17619330 | snp | C/T | 0.444533 | 0.157025 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118800 | GTCATGGCCTTCTGA[C/T]AATTTGCAATCCAAG | 55728 |
| rs17619392 | snp | A/G | 0.463989 | 0.129263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126538 | ACTCAACTATAAGCC[A/G]TCCATGTTAAGTTTG | 55728 |
| rs28376837 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159933 | GGCTGGAGTGCAGTG[A/G]TGCAGTCTCCCAAGT | 55728 |
| rs28379929 | snp | A/G | 0.281841 | 0.247964 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066734 | TTTTTTTAGTTGGGG[A/G]AAAAAGTACAACGTA | 55728 |
| rs28409253 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132910 | AATAGTAATGAAATG[G/T]TGTTGGTCTGTGATT | 55728 |
| rs28416588 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082232 | AGTGAGCCGAGATGG[A/C]GCCACTGCACTCCAG | 55728 |
| rs28433068 | snp | C/G | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097133 | CTGCTGTTAGAGTTG[C/G]TGGTACTTTCTTAGA | 55728 |
| rs28446542 | snp | G/T | 0.264906 | 0.249555 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133520 | TTTGTATTTTTAGTA[G/T]AGACAAGGTTTCACT | 55728 |
| rs28447121 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140743 | ACCCTGCGGCCTTCC[C/G]CAGTGTTTGTGTCCC | 55728 |
| rs28463032 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160095 | AAAGTGCTGGGATTA[C/T]AGGTGTGAACAATCA | 55728 |
| rs28463489 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084568 | AGCCTGGCAAGTAGC[G/T]GGGATTACAGGCATG | 55728 |
| rs28492984 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057643 | CAACTTTGTCCCTCA[A/G]TGGGACCCTTCTAGA | 55728 |
| rs28494890 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057663 | ACCCTTCTAGAGCCC[C/T]TCTCTCATCGGGACT | 55728 |
| rs28505756 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132146 | ATAAGAATTGATTTA[A/C]AAATTAGGCACAGTA | 55728 |
| rs28512258 | snp | C/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40148470 | GGGAGACTGTGGGGA[C/G]AGGGAGAGGGGGAGG | 55728 |
| rs28513687 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168711 | CTTCAGAGAATAAAT[A/G]TGTATATTTCTTTTT | 55728 |
| rs28515039 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142538 | ACAAGGTAGACGCTG[A/G]GGAGAATCTATTTCC | 55728 |
| rs28519512 | snp | C/T | 0.40086 | 0.199352 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085132 | TGGCCAGGCTGGTCT[C/T]GAACTTCTGACCTTG | 55728 |
| rs28530746 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130109 | GGAATGTGCAGTGGC[A/G]CAATCTCCTGGGCTC | 55728 |
| rs28538731 | snp | C/T | 0.26518 | 0.249539 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144377 | TCGTGTTTAGTTAAG[C/T]TTCCCACTTTTACGA | 55728 |
| rs28609857 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165979 | ATCTCCCTTCCCATT[A/T]TCTTTCTGTTTTCTT | 55728 |
| rs28612311 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172934 | ATCTACGAACTTTTT[G/T]GCTTTTTTTTTGCAA | 55728 |
| rs28622271 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150483 | ACCAGCCTGGCCAAC[A/C]TGGTGAAACCACGTC | 55728 |
| rs28630396 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076637 | GGGACTACAGGCTCC[C/T]GCCACCACGCCTGGC | 55728 |
| rs28631830 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129637 | GATAATTTTTTTCTT[C/T]CTTTTTTTTCTCGAA | 55728 |
| rs28636058 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063272 | TATAATAGGCATTGT[A/G]TGAATAAGGATGGCC | 55728 |
| rs28663603 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40071527 | TTGCTTCTAGCAAGT[A/G]GTAATCTATAGGGTG | 55728 |
| rs28670524 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40063219 | AAATACAGCTTGAAG[A/T]AGCCTGTAGGGGAAA | 55728 |
| rs28677176 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148324 | CGCATGGCGGCGCGC[A/G]CCTGCAATCGCAGGC | 55728 |
| rs28691166 | snp | C/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136477 | GCAACCTCTGCCTTC[C/T]GGGTTCAAGCGATTC | 55728 |
| rs28701756 | snp | A/C | 0.0138799 | 0.0821421 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156573 | TGTAATCCCTCCTTT[A/C]TTTTTTTTGCCCATT | 55728 |
| rs28712195 | snp | A/C | 0.26518 | 0.249539 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132058 | TATTCCAAGACCCAC[A/C]GTGGGTGCATGAAAC | 55728 |
| rs28750463 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169197 | AAACTAGCCTGGCCA[A/T]CGTAGAGAAACCCCG | 55728 |
| rs28758772 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085723 | AGATGTGAAAATCTC[A/G]AGAGTGGCAGTGTCC | 55728 |
| rs28769356 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169624 | CAAGAGCTGTATGTA[A/G]AGTACATAAAGATTG | 55728 |
| rs28817648 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169619 | GCCAGCAAGAGCTGT[A/C]TGTAAAGTACATAAA | 55728 |
| rs28826871 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169147 | CAGCACTTTGGGAGG[C/T]CAAGGCGGGGGGATC | 55728 |
| rs28829300 | snp | C/T | 0.224116 | 0.248656 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093671 | GCCCAGGCTGGAGTG[C/T]AATGGCACTGTCTTG | 55728 |
| rs28848791 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40081822 | CGCTACTAAAAAATA[A/C]AAAAATAAGGTTGGG | 55728 |
| rs33917180 | in-del | -/C | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168651 | GGAGACCACAGAAAT[-/C]AATTGACCTACTTGC | 55728 |
| rs33948660 | in-del | -/TAC | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168593 | AAATTTATGGATTTT[-/TAC]ACACCTTTTTCAGAA | 55728 |
| rs33951887 | in-del | -/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132924 | GGTGTTGGTCTGTGA[-/T]TTTTTTTTTTCTGTT | 55728 |
| rs33960807 | in-del | -/TTTC | 0.0486741 | 0.148216 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168718 | GAATAAATATGTATA[-/TTTC]TTTTTTCTTCTTTTT | 55728 |
| rs33993973 | in-del | -/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146890 | TTTTTTTTTTTTTTT[-/T]CCCCAGGTAATGTTT | 55728 |
| rs34040953 | in-del | -/T | 0.370162 | 0.219229 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183337 | AAACTACTTTTTACA[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs34084471 | snp | C/T | 0.207864 | 0.246424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148591 | TAGTATAATGCCCTC[C/T]AGCCACATCTGTATT | 55728 |
| rs34085143 | snp | C/T | 0.209084 | 0.246629 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111574 | TCCGCCTGACTTGGC[C/T]TCCCAAAGTGCTGGG | 55728 |
| rs34087637 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132743 | AGAATCTTTTGAGAA[-/T]TCTAATATAGATTTT | 55728 |
| rs34089362 | in-del | -/A | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097339 | AGTTTTGGAAGTCAG[-/A]AATGCCAAGGAGAAG | 55728 |
| rs34105639 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40139923 | TCCCATCTCCCCCTC[A/C]TGAGTAGCTGGGACT | 55728 |
| rs34106957 | in-del | -/A | 0.474272 | 0.110462 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125887 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs34189324 | in-del | -/T | 0.260504 | 0.249779 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077456 | TCTGGCCAGAATATC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs34214762 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084630 | ATATATATATATATA[-/T]AATTTTTTTTTTTTT | 55728 |
| rs34245436 | in-del | -/T | 0.455621 | 0.142197 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091005 | TTTTTTTTTTTTTTT[-/T]GCAATTGTGAAGGGT | 55728 |
| rs34258238 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117334 | TGAAAGCCAGATTTG[-/C]CCCAACTGGCAAATG | 55728 |
| rs34266556 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40144390 | GTTTCCCACTTTTAC[-/G]GACTTTTGGTTCAGA | 55728 |
| rs34303447 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183136 | AGTCATAATGCACAG[-/T]ATACAATCCCAAGTC | 55728 |
| rs34314258 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105898 | TACATGTTTAACGGT[-/A]AAAAAGGAAGTGTCA | 55728 |
| rs34338879 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125127 | CCTTGAAGATTCTTA[A/G]GATCCACTTTGGTCC | 55728 |
| rs34354667 | snp | C/T | 0.202651 | 0.245475 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088490 | TTGATAGGTAAGTAA[C/T]ATCTCATTATAGTTT | 55728 |
| rs34356835 | in-del | -/T | 0.232943 | 0.249417 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156728 | TAGGTTGAGTATCCC[-/T]AATGAGAAAATTCAA | 55728 |
| rs34368881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103497 | GTAGTAGAAGAGAGC[C/T]AATTTGAGTGGGAGA | 55728 |
| rs34370849 | in-del | -/T | 0.286564 | 0.247312 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139802 | GGCCTAGCATTAGGC[-/T]TTTTTTTTTTTTTAC | 55728 |
| rs34381362 | in-del | -/A | 0.290977 | 0.246619 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081820 | TCGCTACTAAAAAAT[-/A]ACAAAAATAAGGTTG | 55728 |
| rs34417224 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140003 | TAGGGTTTTGGTTGC[A/C]TAGGCTGGTCTTGAA | 55728 |
| rs34471259 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40150341 | GTTAAACAACACCAT[-/G]GGGGATACAGTCAGC | 55728 |
| rs34544517 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094258 | TTTGGTTTTAGCTTA[A/G]GATATGATCTATCTT | 55728 |
| rs34683508 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40122582 | ATTCTATGTTAACTG[-/A]AAATGCAAAAGTAAT | 55728 |
| rs34692647 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065598 | TGGGTCAAGGAGTCA[A/T]CAGAAAAAAGTTGAA | 55728 |
| rs34758221 | in-del | -/T | 0.392325 | 0.205532 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105326 | AAAGTGTAGTTACAA[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs34762682 | in-del | -/T | 0.341909 | 0.232492 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057774 | TTTTGGTTAAAATAG[-/T]TTTTTTTTTCCCTCC | 55728 |
| rs34768159 | in-del | -/T | 0.451483 | 0.148002 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067075 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 55728 |
| rs34777132 | in-del | -/T | 0.231482 | 0.249313 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067357 | CTGTGCCTGGCCTCC[-/T]TTTTTTTTTTTTTAA | 55728 |
| rs34782994 | in-del | -/T | 0.499859 | 0.0083854 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105549 | AGGCTGGTCTCAAAC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs34784076 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080839 | TTTTTTTTTTTTTTT[-/T]GTATTATTAGTAGAG | 55728 |
| rs34819122 | in-del | -/T | 0.44858 | 0.151875 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092646 | CTATTTATTATTTCC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs34844530 | in-del | -/A | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079038 | CGATTCTCCAACCTC[-/A]AGCCTCCTGAGTAGT | 55728 |
| rs34888161 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112312 | TCATTGGTGTTCAGC[-/A]AAAATGAGGAAATTA | 55728 |
| rs34890927 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075491 | CAACCTCTGCCTCCC[-/A]AGTTAAAGTGATTCT | 55728 |
| rs34936281 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40179759 | GTGGTAAAGCCTTTC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs35049615 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084632 | ATATATATATATATA[A/T]TTTTTTTTTTTTTTT | 55728 |
| rs35118643 | in-del | -/T/TA | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055300 | TAGTGATTTTTTTTT[-/T/TA]AAGGATGAACATGAA | 55728 |
| rs35142277 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091602 | TATAGTATACAATCC[-/T]TTTTTTTTTTTTTTT | 55728 |
| rs35152952 | in-del | -/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079424 | TTTTTTTTTTTTTTT[-/T]GAAGTGTTTATTGGT | 55728 |
| rs35236806 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073598 | TTTTACACATAAGAT[-/T]TTTTTTTTTTTTTTA | 55728 |
| rs35263645 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40173889 | TCTTTTTTTCTTTTT[-/C]CCTGAACTGATGGCA | 55728 |
| rs35336260 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40112345 | CATTTAGCTGAGTTT[-/C]TTCCATAAAGTTAAA | 55728 |
| rs35397085 | in-del | -/CT | 0.285519 | 0.247464 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080382 | TGAGGTGGAGTCTTG[-/CT]CTGTTGCCAGGCTGG | 55728 |
| rs35421606 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40075494 | ACCTCTGCCTCCCAG[-/T]TAAAGTGATTCTTCT | 55728 |
| rs35483366 | in-del | -/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124121 | GTTTACTAATGCACT[-/C]CCCTGTTTGCCAATC | 55728 |
| rs35498360 | in-del | -/T | 0.359787 | 0.224604 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055291 | GTTTTTGTATAGTGA[-/T]TTTTTTTTTAAGGAT | 55728 |
| rs35510255 | in-del | -/TT/TTCTCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134906 | CCTTCCTTCCTTTCT[-/TT/TTCTCT]CTCTCTCTCTCTCTC | 55728 |
| rs35556710 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40104410 | TAAACTTATTTTTAG[-/T]TTTTTTTTTTTGATA | 55728 |
| rs35559698 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40177086 | TGCAGCAGACAGCAG[A/T]GGAAAGCTAGCCTGC | 55728 |
| rs35602950 | snp | G/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078933 | TGAAAAATGATATGG[G/T]GCTTTTTAATTTTTA | 55728 |
| rs35631478 | snp | A/G | 0.202959 | 0.245534 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098996 | TATTTAATTATATCT[A/G]CGTTTTTCGTGAATA | 55728 |
| rs35648874 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102500 | CATTACCTTCACATT[-/C]CAGTTTTGAACGAGT | 55728 |
| rs35730860 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40123267 | CATTTTGAACCTTTG[-/A]ATTTCAGTGAAATCT | 55728 |
| rs35762490 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40137373 | AGTAATGTGATGGGT[-/A]CTTGAATATAAACAT | 55728 |
| rs35764978 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40117341 | CAGATTTGCCCAACT[-/G]GGCAAATGCATATAT | 55728 |
| rs35797512 | in-del | -/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40161727 | CATAAGTTGGTAAAT[-/G]GGGAAAGATAGATGT | 55728 |
| rs35811935 | snp | C/T | 0.20111 | 0.245173 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093622 | TATTATTTATTTATT[C/T]ATTTACTTTTGGAGA | 55728 |
| rs35865799 | in-del | -/A | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174895 | GATATTATTCAGCCT[-/A]AAAAAAAAAAAAAAG | 55728 |
| rs35874092 | in-del | -/T | 0.255782 | 0.249933 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134392 | GGGCTGGGTGTGTCC[-/T]TTCTGGGGATGGTCA | 55728 |
| rs35923621 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090896 | CAAGATCACGCCATT[A/G]CACTCCAGCCTGGGT | 55728 |
| rs35952502 | snp | A/G | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071535 | AGCAAGTAGTAATCT[A/G]TAGGGTGGTACTTTG | 55728 |
| rs36010066 | in-del | -/T | 0.499918 | 0.00638925 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123927 | CTTCATAACAAGAAA[-/T]TTTTTTTTTTAAATG | 55728 |
| rs36030516 | snp | A/C/G/T | 0.0146728 | 0.0844358 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056707 | AGCCGGCGGGCTTGG[A/C/G/T]GGGGGGCGGTGGGCG | 55728 |
| rs36035941 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184611 | AGTCACTATTACTAT[C/T]GGGTCTAATTATTTG | 55728 |
| rs36211512 | in-del | -/ATGTGTGT | 0.0737376 | 0.17729 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078113 | GTTGAATATTTCTAA[-/ATGTGTGT]GTGTGTGTGTGTGTG | 55728 |
| rs55691639 | in-del | -/AA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125905 | AAAAAAAAAAAAAAA[-/AA]TTATACACAGATCAT | 55728 |
| rs55695600 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40105565 | TTTTTTTTTTTTTTT[-/T]AAGAGACAGGGTCTT | 55728 |
| rs55709780 | in-del | -/ATTTTATTTTATTTTA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134931 | CTCTCTTTCTTTCTT[-/ATTTTATTTTATTTTA]TTTTATTTTATTTTA | 55728 |
| rs55832101 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134919 | TCTCTCTCTCTCTCT[C/T]TCTTTCTTTCTTTTT | 55728 |
| rs55916486 | snp | A/C | 0.155987 | 0.23165 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154478 | TACAAAATATGTAAG[A/C]AAATTATCAGCTACA | 55728 |
| rs55956320 | snp | A/T | 0.463989 | 0.129263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148640 | TTCCCCTTTTAAAAA[A/T]TTTTTAATTAAATTT | 55728 |
| rs56042009 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065982 | TGTCGACAGGCTGGA[G/T]TGCAGTGGCGTGATC | 55728 |
| rs56047604 | snp | A/T | 0.257176 | 0.249897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162282 | GAAGGCAGGCAGATC[A/T]CTTGAGGTCAGGAGT | 55728 |
| rs56056321 | in-del | -/TT | 0.335615 | 0.234883 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104410 | TAAACTTATTTTTAG[-/TT]TTTTTTTTTTGATAT | 55728 |
| rs56204145 | snp | A/G | 0.344815 | 0.231323 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166848 | GTAAATGGGATATCC[A/G]TCCCCTCAAGCATTT | 55728 |
| rs56274935 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134929 | TCTCTCTCTTTCTTT[C/T]TTTTTTATTTTATTT | 55728 |
| rs56276709 | in-del | -/ATCATCTATCTATCTATCT/ATCTATCT | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136395 | TCTATCTATCTATCT[-/ATCATCTATCTATCTATCT/ATCTATCT]TTTTTTTGAGACAAA | 55728 |
| rs56365389 | snp | A/T | 0.463989 | 0.129263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153040 | AAACACTAATAGCGT[A/T]CTCAGAACAATCTGT | 55728 |
| rs56934412 | in-del | -/AATCA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100422 | ACTCAGTCGCCCAGG[-/AATCA]CTGGAGCGCAGTAAT | 55728 |
| rs57169655 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161807 | AAGGATTTTTAAAAA[A/G]TTGATGGAAGAGCTG | 55728 |
| rs57402597 | in-del | -/GTAGTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40090956 | AAAAAAAAAAAAGTT[-/GTAGTT]TATAAGATCCTATTG | 55728 |
| rs57650677 | in-del | -/G/GAGCGC | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100426 | AGTCGCCCAGGCTGG[-/G/GAGCGC]AGCGCAGTAATCACT | 55728 |
| rs57721440 | in-del | -/A/AAA | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150688 | GGGAAAAAAAAAAAA[-/A/AAA]GAGGAAGTCTAGGAT | 55728 |
| rs57741235 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175132 | CTCAAGCAATCCTCC[C/T]GCCTCAGCCTCCCTA | 55728 |
| rs57800229 | snp | A/G | 0.29175 | 0.246489 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093789 | TGTATTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 55728 |
| rs57995358 | snp | C/T | 0.232067 | 0.249356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072392 | CTGGGATTATAGGCA[C/T]GTGCCACCATGCCCA | 55728 |
| rs58127628 | in-del | -/AGAT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40140314 | CATGGATAGATAGAT[-/AGAT]GCAGCATATTATAAA | 55728 |
| rs58270483 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179763 | GTAAAGCCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 55728 |
| rs58452837 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40101660 | AATAAGTTAGATTTA[C/T]TAAGAGAATACATAA | 55728 |
| rs58496143 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086051 | GCTCACTGCAACCTC[C/T]CTGCCTGCTGGATTC | 55728 |
| rs58829649 | snp | A/G | 0.277867 | 0.248442 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181881 | TTGAACCCAGGTGGC[A/G]GAGGTTGCAGTGAGC | 55728 |
| rs58857905 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40083542 | ACAACATGGATGAAC[C/T]TGGAAAACATGCCAA | 55728 |
| rs58928456 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40175202 | AGTTTGTTTTTTTTA[C/T]GGTAAAGACAGGGTC | 55728 |
| rs59057325 | in-del | -/T/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40080824 | CCACGCCTGGCTAAT[-/T/TT]TTTTTTTTTTTTTTG | 55728 |
| rs59063094 | in-del | -/TA/TATA | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080326 | ATATATATATATATA[-/TA/TATA]CACACACACATATAT | 55728 |
| rs59070532 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144410 | TTTGGTTCAGAAAAT[A/G]TTAGAAAGAATGACT | 55728 |
| rs59181131 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40092661 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 55728 |
| rs59486363 | in-del | -/T | | | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40059165 | TTAAAATCTCCCTTT[-/T]CATCATGATTAGCCA | 55728 |
| rs59500808 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117090 | CTTGTTTGGCATTTG[C/T]TGGCTTCTGAAATTA | 55728 |
| rs59563580 | snp | C/T | 0.298651 | 0.24522 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175981 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGCCA | 55728 |
| rs59701323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094639 | CAGCTCAATGCAACC[G/T]CTGCCTCATGGGTTC | 55728 |
| rs59750839 | snp | C/T | 0.476574 | 0.105661 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080577 | CCTGATCTAGTGACC[C/T]GCCCGCCTCGGCCTC | 55728 |
| rs59835141 | snp | A/G/T | 0.0391387 | 0.134304 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100422 | CACTCAGTCGCCCAG[A/G/T]CTGGAGCGCAGTAAT | 55728 |
| rs59860358 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40076355 | GTGGTGCACACCTGT[A/G]GTCCCAGCTATTCGG | 55728 |
| rs59899449 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40086147 | TTTTTTTTTTTTTTT[-/T]GCTAATTTTTGTATT | 55728 |
| rs60101951 | in-del | -/T | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071837 | CCCAAAGTGCTGGGA[-/T]TTATAGGTGTGAGCC | 55728 |
| rs60235459 | snp | A/T | 0.264906 | 0.249555 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124352 | TTTATTTATTTATTT[A/T]TTTTTTTATTTAGAG | 55728 |
| rs60248775 | snp | C/T | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078607 | ATGGCTCAACTGCAG[C/T]CTTGATTTCCTTGGC | 55728 |
| rs60325663 | in-del | -/GGTTCGCAGT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100434 | AGGCTGGAGCGCAGT[-/GGTTCGCAGT]AATCACTTTCACTAG | 55728 |
| rs60430101 | in-del | -/GT/TGTG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131570 | GTATACATGTGATTG[-/GT/TGTG]TGTGTGTGTGTGTAT | 55728 |
| rs60554493 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077471 | TTTTTTTTTTTTTTT[-/T]GAGACTGAGTCTCGC | 55728 |
| rs60837662 | snp | C/T | 0.0494327 | 0.149241 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155605 | TAATGTGGTAAGGTA[C/T]AATTTTCCAATATGA | 55728 |
| rs60972080 | in-del | -/TAGTAGCGATGGGGTTTCACATATTGGTCAGGCTAGT/TTAGTAGCGATGGGGTTTCACATATTGGTCAGGCTAG | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074306 | ATTGGTCAGGCTAGT[lengthTooLong]CTCTTAACCCTTGAC | 55728 |
| rs61125129 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40065936 | AGCATTTTTTTTTTT[-/T]CTTGAGATGGAGTCT | 55728 |
| rs61255650 | in-del | -/ATCT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40136392 | TCTATCTATCTATCT[-/ATCT]TTTTTTTGAGACAAA | 55728 |
| rs61474507 | snp | G/T | 0.154993 | 0.231244 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154957 | TATCTTCCAGATGTT[G/T]CTGCCTTATCGAAAT | 55728 |
| rs61551143 | in-del | -/AGAGGCTCACT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40100458 | CACTAGAGGCTCACT[-/AGAGGCTCACT]GTAGCCTCGACCTCA | 55728 |
| rs61609256 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150252 | TCATTTTTGCCTCCA[A/T]ATCAAACTAGGAGCA | 55728 |
| rs61748746 | snp | A/G | 0.127114 | 0.217713 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102197 | GAAAGTAAAATAATG[A/G]AAAAACGTCCTGAAG | 55728 |
| rs61748747 | snp | C/T | 0.000616877 | 0.0175516 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120211 | AGACAAAAGTGAAAA[C/T]GAGCAAATAGAAATG | 55728 |
| rs61748748 | snp | A/T | 0.0409831 | 0.137157 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120693 | GTGATGATGCTTCAG[A/T]GCCACTCAATAGCTA | 55728 |
| rs61748749 | snp | G/T | 0.12736 | 0.217855 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122170 | ATCAGCTGGAGTTAG[G/T]GGGGAAGATAAAACC | 55728 |
| rs61753851 | snp | A/G | 0.0028979 | 0.0379546 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102366 | ATGTTAATAGTTTTA[A/G]TGACTCAAGTGAGTT | 55728 |
| rs62302099 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054594 | ACCGCCCCCCCGCCG[A/C]CCCAAAAAAAAAAGA | 55728 |
| rs62302100 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055158 | TACAGTTTTTAGTCT[A/C]TTATAATGGTTGTTT | 55728 |
| rs62302101 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067355 | TACTGTGCCTGGCCT[C/T]CTTTTTTTTTTTTTT | 55728 |
| rs62302102 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40072535 | AGGCGTGAGCCACCG[C/T]GCTCGGCCCACCTGG | 55728 |
| rs62302103 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072746 | TTTTTTTTTTTTTGG[G/T]ACAGAGCCTCTCTCT | 55728 |
| rs62302104 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40073615 | TTTTTTTTTTTTTAA[A/T]TTGAGTCTTGCTGTA | 55728 |
| rs62302105 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40077013 | TTCCCTATATATTAC[A/G]TATAGAGAGATTTTT | 55728 |
| rs62302133 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104823 | TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTTGCT | 55728 |
| rs62302134 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40131051 | CTGAAAAAAAAAAAT[A/T]GTGAATTCCAAGATT | 55728 |
| rs62302139 | snp | A/G | 0.493793 | 0.055364 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168821 | CCTCCACCTCCCTGG[A/G]TTCAAGTGATCTCCT | 55728 |
| rs62302140 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170712 | TGGAAATTGTTGACT[A/G]CCTTTTTTCAGCTGT | 55728 |
| rs62302151 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174297 | CAGGAGAATCACTTG[A/C]GCCTAGGAGATGGAG | 55728 |
| rs62621880 | snp | A/C | 0.00353041 | 0.0418658 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40103119 | ATCAAGTACAAGAAA[A/C]CCCAGTTTCTCAGGT | 55728 |
| rs63034660 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131049 | AACTGAAAAAAAAAA[A/T]TTGTGAATTCCAAGA | 55728 |
| rs66598411 | snp | A/G | 0.204189 | 0.245767 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107627 | GACCTTAGGTGGTCC[A/G]CCTGCCTTGGCCTCC | 55728 |
| rs66609025 | snp | G/T | 0.483418 | 0.0895317 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092438 | TGTGTGTTCATAGTT[G/T]ACTTTATTAGCCTTT | 55728 |
| rs66675307 | in-del | -/TT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40184370 | TGCCTTTTTTTTTTT[-/TT]AAATAAAAAATTCCC | 55728 |
| rs66840598 | snp | A/G | 0.444799 | 0.156695 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060097 | CCTCAGCCTCTCAAG[A/G]CGCTGAGATTACAGG | 55728 |
| rs67026895 | snp | A/G | 0.482831 | 0.0910472 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093325 | GTTCTTATGGTGGGG[A/G]CTTAGATTATTCATT | 55728 |
| rs67269894 | in-del | -/AT/T/TAA | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084632 | ATATATATATATATA[-/AT/T/TAA]TTTTTTTTTTTTTTT | 55728 |
| rs67496061 | snp | C/T | 0.209084 | 0.246629 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101688 | TAAAATACTTAATAT[C/T]TAAAAGTTTGCATGC | 55728 |
| rs67511607 | snp | C/T | 0.266 | 0.249487 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169704 | GTGTGGTGGCTCTCG[C/T]TTGTAATCCCAGCAC | 55728 |
| rs67534535 | snp | C/T | 0.461037 | 0.134028 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138457 | TTTGTCTACTTTTGC[C/T]ATGTTGCCTGTGCTT | 55728 |
| rs67569805 | snp | C/G | 0.213333 | 0.247296 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162909 | TGGTATCTTTCAGTT[C/G]AAGTGTGAAGTTCTC | 55728 |
| rs68040934 | snp | C/G | 0.202343 | 0.245416 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089670 | TTGAACTCTTGAGCT[C/G]AAGTGATCTGCATGC | 55728 |
| rs68050728 | in-del | -/T | 0.163236 | 0.234461 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128846 | TCTTTAAAAAAAAAA[-/T]AAATAAATAAAATAA | 55728 |
| rs71194968 | in-del | -/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062093 | CTTTTTTTTTTTTTT[-/T]CTTGAGACGGAGTCT | 55728 |
| rs71194969 | in-del | -/GTGT/GTGTGT | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40078148 | TGTGTGTGTGTGTGT[-/GTGT/GTGTGT]ATGTGTGTATTTATT | 55728 |
| rs71194970 | in-del | -/AGTTGTA | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090953 | AAAAAAAAAAAAAAA[-/AGTTGTA]GTTTATAAGATCCTA | 55728 |
| rs71194972 | in-del | -/TAC | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168595 | ATTTATGGATTTTAC[-/TAC]ACCTTTTTCAGAACT | 55728 |
| rs71594928 | multinucleotide-polymorphism | ACCTCT/GCCTTG | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40168973 | TCAGGTGATCCGCCC[ACCTCT/GCCTTG]GCCTCCCAAAGTGCT | 55728 |
| rs71608014 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112047 | TAATACTTAGTATTG[G/T]TTAAAAAATGATTTT | 55728 |
| rs71608015 | snp | A/G | 0.20111 | 0.245173 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124722 | AAAAGCCCCTATAAT[A/G]TATATTGAACTTTCA | 55728 |
| rs71608016 | snp | C/T | 0.200492 | 0.245049 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146119 | AGTGAGCCAAGATCA[C/T]GCCACTGCCCTCCAG | 55728 |
| rs71646919 | in-del | -/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079413 | GAGCCACTGTGCCCA[-/C]CCCTGGATGGTTTTT | 55728 |
| rs71646921 | in-del | -/TAAT | 0.20111 | 0.245173 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116939 | AGTCAGCTGTCATTC[-/TAAT]TGTTTCTTTGTAGAT | 55728 |
| rs71646923 | in-del | -/T/TT | 0.299158 | 0.245119 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184359 | GAAACTTCATCTGCC[-/T/TT]TTTTTTTTTTTAAAT | 55728 |
| rs71843378 | in-del | -/TT | 0.491368 | 0.0651254 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134905 | TCCTTCCTTCCTTTC[-/TT]TCTCTCTCTCTCTCT | 55728 |
| rs72280590 | in-del | -/TG | 0.162253 | 0.234095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131569 | ATGTATACATGTGAT[-/TG]TGTGTGTGTGTGTAT | 55728 |
| rs73140119 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056007 | TTCCCCGAGCTCAGA[C/T]CGCACGCTGGCAGGG | 55728 |
| rs73140122 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058304 | AAACATCGTGTGTTC[A/T]GTGTTTTGATAAACG | 55728 |
| rs73140131 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064775 | ATAAATATGGGTTGG[A/G]TGTGATGGGGTAGAG | 55728 |
| rs73140151 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088072 | TACGACTGGCTTTTA[C/G]TGAGCATAATACTCT | 55728 |
| rs73140157 | snp | A/C/G/T | 0.0107382 | 0.0726223 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089202 | TAAGGGATTCCCCCC[A/C/G/T]TCTTCAGCCCCTGTT | 55728 |
| rs73140158 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091356 | ATGTTAGGAGGAAAG[C/T]GTTTAGTATTTCATT | 55728 |
| rs73144041 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110239 | TAGACATTTGAGTTG[C/T]TTTCACTTTTTGGCT | 55728 |
| rs73144066 | snp | C/T | 0.222928 | 0.24853 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134880 | CTTTCTCTCTTTCTT[C/T]CTTCCTCCCTTCCTT | 55728 |
| rs73144073 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138987 | TAGAATTTTGATGGG[G/T]TTCGTGTTGAATATG | 55728 |
| rs73144078 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142597 | CCCAGTTTTCATGTG[C/T]GTTTTGTGAAGGTGT | 55728 |
| rs73144089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159546 | TGCTGGAGGAAAGAC[A/G]AAGAAAAAGGGAGCA | 55728 |
| rs73146058 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171728 | CAGTAGGCCATCTGC[A/T]GGCTGAGGAACAAGG | 55728 |
| rs73229742 | snp | A/C | 0.326506 | 0.238006 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058548 | CCTGTAAAACAATAA[A/C]GAATAAAGCAGTTGA | 55728 |
| rs73229745 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083829 | GAATTTTATGGTTTA[C/G]ATATTATATTTTAAT | 55728 |
| rs73229746 | snp | A/G | 0.4628 | 0.13121 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090364 | GTGTATATCAATTTG[A/G]GGAAGAATTGACATA | 55728 |
| rs73229748 | snp | A/G | 0.231775 | 0.249335 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099233 | TTTCAACATTGTGTG[A/G]TAGTGTTTTAAGATT | 55728 |
| rs73229750 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40109731 | TCAAAAAAAAAAAAA[A/G]TGTTAGCATGGTTCA | 55728 |
| rs73229752 | snp | C/G | 0.103082 | 0.202275 | intron-variant | N4BP2 | GRCh38.p7 | 4:40124011 | CATAATTTTTATTAT[C/G]TAACTTTATTGTTTT | 55728 |
| rs73229753 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125907 | AAAAAAAAAAAAAAA[A/T]TATACACAGATCATT | 55728 |
| rs73229754 | snp | A/G | 0.103438 | 0.202533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128309 | GCACCTTTATATTTG[A/G]CTGTAATACATCCAG | 55728 |
| rs73229756 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136751 | TTTGAGAACCTATTA[C/T]TTGATAGTTTCCTTC | 55728 |
| rs73229759 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150677 | CTCTGTCTCAGGGGG[A/G]AAAAAAAAAAAGAGG | 55728 |
| rs73229764 | snp | A/G | 0.425277 | 0.178263 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179685 | CATTATATTATTGCA[A/G]TGTAATTTTGAAAGA | 55728 |
| rs73229765 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183826 | TCTGCTGTGTCTCTC[C/T]GCAGTTTTTTGGGTT | 55728 |
| rs73808619 | snp | G/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058607 | GTTTGTGTACTTGTT[G/T]ACTTTAGTTAATTTG | 55728 |
| rs73808621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065652 | TTTTAAGAAACTGAA[A/G]CCGTATAGGAAATAA | 55728 |
| rs73808622 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079991 | TTGAGGATGGGAGGG[A/G]GGGATATATTTGTTT | 55728 |
| rs73808623 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100873 | AGTGAGGTGATGTGT[A/G]TAAAACTTCTAGCTC | 55728 |
| rs73808624 | snp | C/G/T | 1.80419e-05 | 0.00300344 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126099 | ATTTATACATTTATT[C/G/T]TTGAGAGTATGACAG | 55728 |
| rs73808625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126360 | AAATATTAAGCTACT[C/G]TCTCTGATTCTGGTT | 55728 |
| rs73808626 | snp | C/T | 0.0356815 | 0.128715 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156967 | ATTTGTGCTAATACA[C/T]GACTCATTAGAATGA | 55728 |
| rs73808629 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163301 | TATTGCCCACATGGC[C/T]GACATTGTTGTCTTA | 55728 |
| rs74389688 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181594 | TCCGAGCTCAACTCG[C/T]GGCTTTCATTTCACA | 55728 |
| rs74392454 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144936 | ATGTTTATGTTATTC[A/G]TTCTTCAAGAGAACC | 55728 |
| rs74406264 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084931 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 55728 |
| rs74424498 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180576 | ACTTAATTACTCATG[C/G]ACAATTCATTCATGT | 55728 |
| rs74459342 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178562 | TTCAATGATTATTAA[C/T]GTGGGCATACTTTAT | 55728 |
| rs74473678 | snp | A/C | 0.226188 | 0.248863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161429 | TGGAGGGAGAACTTA[A/C]CCATTGAAACAAAAG | 55728 |
| rs74726096 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171131 | ATATTTAGCCTATCT[C/T]GCTAGGTTGCATATT | 55728 |
| rs74740705 | snp | C/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110937 | AAATTACTTGTAAGA[C/T]TTACTTGTTGTGGTA | 55728 |
| rs74749842 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122943 | TGCAGTAGTCAAGAA[G/T]TGTGAAGACAGTAAC | 55728 |
| rs74762089 | snp | G/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40105344 | TTTTTTTTTTTTTTT[G/T]ACAGAGTCTGACTCT | 55728 |
| rs74778372 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078577 | TCGCCCAGGCTGGAG[A/T]ACAGTGGCATGCTTA | 55728 |
| rs74798061 | snp | A/G | 0.288646 | 0.246995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179813 | CTTGTTGCCCAGGCT[A/G]GAGTGCAGTGGAGTG | 55728 |
| rs74857814 | snp | A/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064075 | GGTGCTGGGACCACA[A/T]GTGAACCACTATGCC | 55728 |
| rs74860697 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132780 | TAGTTTATTAATATA[G/T]TTCATATCAATCACA | 55728 |
| rs74961130 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106374 | CTGACTCCAGTGCAG[C/T]GGTGCAACCTTGGCT | 55728 |
| rs74981500 | snp | C/T | 0.226188 | 0.248863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161244 | GAGAGAATGCACCCT[C/T]ATCTTGGAGAATTAG | 55728 |
| rs74983140 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151962 | TGTTTTAAATTTATT[A/T]ATTCATCTCATTAAT | 55728 |
| rs75033955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40172541 | GCCACAGAGGGAAGA[C/T]GATGTGAAGAGACAC | 55728 |
| rs75047034 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079425 | CCCACCCTGGATGGT[G/T]TTTTTTTTTTTTTGA | 55728 |
| rs75068895 | snp | A/C | 0.0494327 | 0.149241 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158347 | TGTAATTTCAGGGGG[A/C]AAGTGTCATGAAAAT | 55728 |
| rs75087390 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40082387 | AATCTAACAATCCTG[C/G]GTTCAGCTTAATAAT | 55728 |
| rs75145498 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40159861 | TTAGGAATCAAAAAA[A/G]GGAAATCACAGTTGT | 55728 |
| rs75189081 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092949 | GTGCCCGGCCTGCTC[C/T]TTTTTTTTTTAAAGA | 55728 |
| rs75199069 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134903 | CCTTCCTTCCTTCCT[C/T]TCTCTCTCTCTCTCT | 55728 |
| rs75254876 | snp | C/G | 0.0733688 | 0.176922 | upstream-variant-2KB, intron-variant, missense, nc-transcript-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056482 | GGGCTTGCTCCTCCA[C/G]GGACCCCCTGATAAG | 55728 |
| rs75295919 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125715 | ACATGGTGAAACCCC[C/T]GTCTCTACTAAAAAT | 55728 |
| rs75297598 | snp | C/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104262 | TGGCTTGCTAGTTCT[C/T]TTTTTTTTTTTTTCC | 55728 |
| rs75313591 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142399 | TCTTCCAACTCGGAG[C/T]TCAGTATCCCTAATT | 55728 |
| rs75338782 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40076055 | TGTATTGAACTCCTG[C/T]GCTTAAGCAATCCTC | 55728 |
| rs75342917 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181374 | TTCTCAAAACATTTT[C/T]GATACTAGCTCATCT | 55728 |
| rs75359059 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087810 | CAGGCTGAATGGCTC[A/G]ATCTCGGCTTACTGC | 55728 |
| rs75365336 | snp | G/T | 0.291493 | 0.246533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090731 | TGAGGTCAGGAGTTC[G/T]AGACCAGCCTGGTCA | 55728 |
| rs75406760 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153808 | CTCTCCGGATAGAGT[C/T]GAAAGCATTGCATGG | 55728 |
| rs75427827 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181615 | TCATTTCACAGTTCA[A/G]GGTGGCTGCTCAAAC | 55728 |
| rs75497114 | snp | A/G | 0.226188 | 0.248863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161147 | GGCAAAAAAATGAGA[A/G]GTCGAGAATTGAATT | 55728 |
| rs75549942 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113878 | ACCACAGGTGTGAGC[C/T]ACCATGCCCAGCCTG | 55728 |
| rs75565352 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123651 | CCACCACACCTAGGT[A/T]ATTTTTTTTTTTTTG | 55728 |
| rs75605287 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160528 | GCACATTTAAGGTAG[C/G]CTAGGCTAAGCTATG | 55728 |
| rs75618012 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088123 | GTATGCATCAGTAAT[A/G]TGTTTTTATTGCTGA | 55728 |
| rs75655978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163555 | ACGAATACAGAGAAA[C/T]ACATAGGAAGAAATG | 55728 |
| rs75659057 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | N4BP2 | GRCh38.p7 | 4:40185060 | TAATAATAAATCCAT[A/G]TCCCTTTAAAAATAA | 55728 |
| rs75841753 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143331 | ATTTATTTATTTTTT[A/T]AAGATAAGGTCTTGC | 55728 |
| rs75852437 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090952 | AAAAAAAAAAAAAAA[A/T]AGTTTATAAGATCCT | 55728 |
| rs75860795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086220 | TCGAATGCCAGACCA[A/G]CCTGGATTACAGGTG | 55728 |
| rs75895961 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40067036 | ATTCTTCCATGTTGC[A/G]GCATATGACCTAATT | 55728 |
| rs75924549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40080131 | CAGGTATGTATATGA[A/G]GATGCTATACAAGGT | 55728 |
| rs75980259 | snp | A/T | 0.0825414 | 0.185628 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128065 | GAATTTTATTTTTGG[A/T]CTTTATTTCAAAATA | 55728 |
| rs75982727 | snp | A/C | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169380 | GAGCAAGACTGTCTC[A/C]AAAAAAAAAAAAACC | 55728 |
| rs76010866 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144488 | TTTGGTGCATTCTTA[C/T]ATATTAAACTCATTG | 55728 |
| rs76038978 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40075973 | CTGGGACTACAGGCA[A/T]GTACCACCAGGCCTA | 55728 |
| rs76062443 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40132160 | ACAAATTAGGCACAG[C/T]AAAAAATTAACAACT | 55728 |
| rs76067319 | snp | C/T | 0.193028 | 0.243422 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134896 | CTTCCTCCCTTCCTT[C/T]CTTCCTTTCTCTCTC | 55728 |
| rs76068487 | snp | A/G | 0.129664 | 0.219133 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183662 | TTTTATAAGAGGTTG[A/G]TAGCTTCAACGTCAT | 55728 |
| rs76088122 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149150 | ACAATATGTCTTTAC[A/G]GAAACTTGCATATGA | 55728 |
| rs76097044 | snp | A/C | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169379 | AGAGCAAGACTGTCT[A/C]AAAAAAAAAAAAAAC | 55728 |
| rs76106753 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164019 | TCAGAGAGGAGAAAC[A/G]GAGACATCAGTTGGT | 55728 |
| rs76115153 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180732 | TACAATGGACTATTA[C/T]GTTGCTATTAAAGGG | 55728 |
| rs76121030 | snp | A/G/T | 0.00874735 | 0.0655527 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160356 | GATGGTGTGAATGCC[A/G/T]TATGCGTTTAGTAGA | 55728 |
| rs76144000 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122725 | ATACATAGTTTGAAC[A/G]TTTTCTCTGGTATTT | 55728 |
| rs76181460 | snp | G/T | 0.0425829 | 0.139564 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40157344 | TTATATAGCAGAAAT[G/T]TTGACTTTAAATCCT | 55728 |
| rs76213187 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092660 | CTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG | 55728 |
| rs76263584 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103790 | TTATCCCTTCTGTAG[A/T]TAAGGTAGGCTGTGA | 55728 |
| rs76282869 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107106 | TTGTTTGTGTGTTTG[C/T]TTTTGTTTTTTGAGA | 55728 |
| rs76283233 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103973 | AGTTCTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 55728 |
| rs76368711 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103539 | AGCTTTGATCACAGA[A/C/G]TTAAAGAGATATAAT | 55728 |
| rs76427752 | snp | A/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098822 | ACAAAAAAACTTTTT[A/T]GTTTTCCAGAATCTT | 55728 |
| rs76438214 | snp | C/G | 0.00253473 | 0.0355097 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102674 | TCTGAGTGCGTTGAG[C/G]CTCAATTCTCTGAAG | 55728 |
| rs76494472 | in-del | -/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40067370 | CCTTTTTTTTTTTTT[-/T]AAGGCTGAATAATAT | 55728 |
| rs76512387 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144391 | GTTTCCCACTTTTAC[G/T]ACTTTTGGTTCAGAA | 55728 |
| rs76661820 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166192 | TAGGCAGGAGGAAGG[A/T]AGCTACAAATACCCC | 55728 |
| rs76679913 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151079 | TTTGGGAAACGAAAC[A/C]TATACATTACTTCAT | 55728 |
| rs76681979 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112955 | TTAATCCACCAACCT[C/T]GGCCTCTCAAAGTGT | 55728 |
| rs76806492 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100394 | GTTTCCTTTTTTTTT[G/T]GAGATAGGGCCTCAC | 55728 |
| rs76923324 | snp | C/T | 0.208169 | 0.246476 | intron-variant | N4BP2 | GRCh38.p7 | 4:40147441 | ggtacacctcccaga[C/T]ggggtggtggccggg | 55728 |
| rs76942222 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | N4BP2 | GRCh38.p7 | 4:40069971 | CTTTGCTTTGTAGAG[A/G]TATTCTTTTAGTGGA | 55728 |
| rs76951270 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150244 | CGTACGAATCATTTT[G/T]GCCTCCAAATCAAAC | 55728 |
| rs76951861 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175810 | GACTCGTCTCAAGAA[A/G]AAAAAAAAAAAAAAA | 55728 |
| rs76983579 | snp | A/C | | | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102823 | CGAAGGGTTCAACTT[A/C]AAGCCACACAAACAT | 55728 |
| rs77126422 | snp | C/T | 0.133435 | 0.221162 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169702 | GGGTGTGGTGGCTCT[C/T]GCTTGTAATCCCAGC | 55728 |
| rs77135513 | snp | A/G | 0.224412 | 0.248687 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145692 | GGATGAATTAATAGT[A/G]TTTTACTCAATAAAT | 55728 |
| rs77196368 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150180 | GAATTTTTTAAAAAA[A/G]AGAGACATCTGGACC | 55728 |
| rs77202191 | snp | C/G | 0.0825414 | 0.185628 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097044 | ACATATTGTTAACAT[C/G]TTAATTTTTAACATG | 55728 |
| rs77218447 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118356 | TGGAGGCAGAGGTTG[C/T]GGTGAGCTGAGGTTG | 55728 |
| rs77222976 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183353 | TTTTTTTTTTTTTTT[G/T]GAGACGGCGTCTGGC | 55728 |
| rs77286832 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155396 | AGCAAGACTCCGTCT[A/C]CAAAAAAAAAAAAGA | 55728 |
| rs77388304 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083099 | TCTGTATTATGAAGC[A/G]GGGTTGGGGGGCGGT | 55728 |
| rs77403318 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183354 | TTTTTTTTTTTTTTT[G/T]AGACGGCGTCTGGCT | 55728 |
| rs77432881 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090359 | TAAACGTGTATATCA[A/G]TTTGGGGAAGAATTG | 55728 |
| rs77435078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162702 | ACATTATTATTTAAT[C/G]TAGCTTATTGGTGTA | 55728 |
| rs77609125 | snp | C/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126957 | AGAGACAGGGTTTCA[C/G]CATGTTGGCCAGGCT | 55728 |
| rs77636217 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059389 | TGAGCATTTTTTATG[G/T]ATGTATGTATGTATG | 55728 |
| rs77669134 | snp | A/G | 0.46875 | 0.121031 | intron-variant | N4BP2 | GRCh38.p7 | 4:40141330 | CCCGGCAGCCGCCCC[A/G]TCTGACAAGTGAGGA | 55728 |
| rs77696803 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | N4BP2 | GRCh38.p7 | 4:40061491 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55728 |
| rs77698991 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072692 | TGAGCTACCACTCCC[A/G]GCCCCAGATAAATTT | 55728 |
| rs77745514 | in-del | -/CTTTT | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40146869 | TTTCTATGTGTTTGG[-/CTTTT]TTTTTTTTTTTTTTT | 55728 |
| rs77771426 | snp | C/T | | | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155947 | ACTGGTATTGAAGTA[C/T]TATTCACACTTATGT | 55728 |
| rs77772797 | snp | G/T | 0.225597 | 0.248806 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162267 | AACACTTCTGGGGGC[G/T]AAGGCAGGCAGATCA | 55728 |
| rs77773664 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054610 | CCCAAAAAAAAAAGA[A/C]ATTTAAAGGGACATG | 55728 |
| rs77775967 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146487 | TTTCTTCAACACTCA[A/G]AAAAGTTTTTGAATA | 55728 |
| rs77798140 | snp | A/G | 1.66768e-05 | 0.00288758 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120214 | CAAAAGTGAAAACGA[A/G]CAAATAGAAATGGTG | 55728 |
| rs77801147 | snp | A/C | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149517 | TGGTTGCACAACATG[A/C]TGAATATGCTAAAAA | 55728 |
| rs77892092 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059431 | AGAGCCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 55728 |
| rs77932539 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104821 | TCTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTTG | 55728 |
| rs77940711 | snp | C/T | | | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078696 | ACGCCCAGCTTATTG[C/T]TTTGTATTTTTTTGT | 55728 |
| rs78041123 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143822 | AGTGATTCCTTCTTG[A/G]GATGGTGTATTAGAG | 55728 |
| rs78055245 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103972 | TAGTTCTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 55728 |
| rs78059303 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145026 | TGCTGTATTTATTAA[C/T]GGGAGGGCATGGTGT | 55728 |
| rs78123229 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107828 | GAATATTGTGTGGCA[C/T]ATTTAAGTTATCAGT | 55728 |
| rs78152193 | snp | A/G | 0.280785 | 0.248097 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156547 | CAACACATAATTTTG[A/G]AAGAAAAGTTTGTAA | 55728 |
| rs78199997 | snp | A/G | 0.0209961 | 0.100286 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106867 | AAATTTAGAAGAAAA[A/G]GTAATGAAAATTATT | 55728 |
| rs78202044 | snp | C/G | 0.145642 | 0.227177 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183498 | CCGCTACCGTGCCCA[C/G]CTAATTTTTTTGTAT | 55728 |
| rs78215389 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177820 | TCTGCAGTCATCTCA[C/T]ATGCAGGGCTCTTTA | 55728 |
| rs78227303 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059679 | TTTTTGATACCTACC[C/T]TGCCTGATAATGAGT | 55728 |
| rs78235595 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119824 | ATTTATTTATAAAAT[G/T]TTCAGAATAACTGTT | 55728 |
| rs78270713 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151660 | ACTTTGTAAAAAGTT[C/T]GTAAAAAGGTTTTAC | 55728 |
| rs78271664 | snp | A/C | 0.021333 | 0.101051 | intron-variant | N4BP2 | GRCh38.p7 | 4:40128964 | CCCTCCCTTTAATAT[A/C]TTGATGTAATAGGTG | 55728 |
| rs78304076 | snp | C/T | 0.226188 | 0.248863 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160145 | ATTCGGGGAGGATTG[C/T]TGTATATGATCCTGT | 55728 |
| rs78306755 | snp | G/T | 0.131038 | 0.219882 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169635 | TGTAAAGTACATAAA[G/T]ATTGGAAATTCAGTG | 55728 |
| rs78322700 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107940 | TCTTTTTTTTTTTTT[G/T]TGACACAGTATCTCG | 55728 |
| rs78340276 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132515 | CCCACTTATATAAAA[C/T]ATAACCAGTAATTCT | 55728 |
| rs78341554 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133353 | CTTTCTCCTTTTTTT[G/T]GAAACAGAGTCTCAC | 55728 |
| rs78353009 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077923 | AATGATACAGAGAAG[A/G]TGAGCATGGCCTCTG | 55728 |
| rs78417585 | snp | C/T | 0.0160856 | 0.0882273 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120833 | ACTGGTTTAAGTGAG[C/T]CCAACCTAGAAATTG | 55728 |
| rs78445388 | snp | C/T | 0.021333 | 0.101051 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060395 | GATTACAGGTGCACA[C/T]GATCACGCCCGGCTA | 55728 |
| rs78463015 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108132 | GGGGTTTTGCCACAT[C/T]GGCCAGGGCCAGGCT | 55728 |
| rs78495335 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062578 | TTTTTTTTTTTTTTT[G/T]GAGACTTCTGAACTT | 55728 |
| rs78618307 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077841 | ACTTAATTGTCCTTG[C/T]CATATACTACATATA | 55728 |
| rs78648205 | snp | A/G | 0.202035 | 0.245356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086963 | TATGGTGCCCAGGCT[A/G]GTTTCGAACTCCTGG | 55728 |
| rs78657092 | snp | G/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091622 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGGGTCT | 55728 |
| rs78660083 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123653 | ACCACACCTAGGTAA[A/T]TTTTTTTTTTTTGTA | 55728 |
| rs78697596 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108834 | AGTTTTTTTTTTTTT[G/T]GGAGACAGAGTCCTG | 55728 |
| rs78752104 | snp | C/T | 0.0217236 | 0.101931 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40154745 | TAAACACATAAAATG[C/T]TTTTATTTTGCCATA | 55728 |
| rs78767806 | snp | A/G | 0.0123447 | 0.0775884 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120757 | CTCATTCAACATTAT[A/G]GGTGACTGGCCTTCA | 55728 |
| rs78814335 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134562 | TGTGCTTGAGGTGTA[A/T]TCTTCTAGGGCTGTT | 55728 |
| rs78825220 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100395 | TTTCCTTTTTTTTTT[G/T]AGATAGGGCCTCACT | 55728 |
| rs78838308 | snp | C/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185329 | GTTTTTGCTGTTTTA[C/T]GGTTTTCTTGTGATA | 55728 |
| rs78842825 | in-del | -/G | 0.157311 | 0.232183 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173180 | CCTTGTCCCCTTAGA[-/G]GGGCTAGTTTAGGAA | 55728 |
| rs78847120 | snp | C/T | 0.078151 | 0.181571 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184839 | CACACATTTGTAATC[C/T]CAGCTGCTCGGGAGG | 55728 |
| rs78903112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181468 | GGTGGGCTGTGCAAG[A/G]TAGAAGTTGGTTTTT | 55728 |
| rs78932259 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113740 | ATCTTACTACCTTTT[C/T]TGAGTTTTATTTATT | 55728 |
| rs78951726 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167609 | CCAAGAATCTATCAT[C/T]TGCATATCCCCATCT | 55728 |
| rs78989823 | snp | A/G | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065563 | GTAAATGCTGCTTGG[A/G]ATGGGAGGGTGGATT | 55728 |
| rs79026130 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101793 | TTATGTATTTACTCA[A/G]TTCAGCAAATAATAT | 55728 |
| rs79029309 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131623 | TTTGCAAAAAATGAG[A/T]TATAAATAAATAGTG | 55728 |
| rs79112018 | snp | A/G | 0.114387 | 0.210022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177041 | GGCGGAATTAAGGAA[A/G]AGTCCTGCAACATCA | 55728 |
| rs79155494 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | N4BP2 | GRCh38.p7 | 4:40146900 | TTTTTTCCCCAGGTA[A/T]TGTTTTTATTTTTAT | 55728 |
| rs79158185 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152275 | AAAATAGGCACAAAA[A/G]AAGCTAAGTAACTTG | 55728 |
| rs79164134 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129677 | GGTCTTGCAGTGTTG[C/T]CCAGGCTGGTCTCGA | 55728 |
| rs79168257 | snp | A/G | 0.222035 | 0.248431 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163875 | GGAAACATGTTCAGA[A/G]AGATTATAGAATTTG | 55728 |
| rs79256619 | snp | A/G | 0.0726307 | 0.176182 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058305 | AACATCGTGTGTTCT[A/G]TGTTTTGATAAACGT | 55728 |
| rs79258688 | snp | A/C | 1.72499e-05 | 0.00293677 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117853 | CTTCAACCCTTTTTT[A/C]CCCTGGAATTTTCAG | 55728 |
| rs79304399 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143333 | TTATTTATTTTTTTA[A/G]GATAAGGTCTTGCTC | 55728 |
| rs79414412 | in-del | -/AAA | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40125904 | AAAAAAAAAAAAAAA[-/AAA]TTATACACAGATCAT | 55728 |
| rs79504371 | snp | G/T | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055764 | AGCAAAGGTGAAAAA[G/T]TTGCGTACCCTGAAA | 55728 |
| rs79554678 | snp | A/G | 0.103794 | 0.20279 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183170 | TTTCTCTTTTTGCAC[A/G]TAACCTTGTATCATG | 55728 |
| rs79598633 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140309 | TGCTGTCATGGATAG[A/T]TAGATGCAGCATATT | 55728 |
| rs79627850 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160836 | AAAGGTGCCTCTGCT[C/T]CTGACTCATGTTAAG | 55728 |
| rs79655861 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177895 | CCTGCATGGGTTCAC[C/T]CTGTCCTTTGAATAA | 55728 |
| rs79667551 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127198 | CTGACCGGCTGCATC[A/T]TCTTCTTCTTTTTTT | 55728 |
| rs79685915 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092647 | TATTTATTATTTCCT[C/T]TTTTTTTTTTTTTTG | 55728 |
| rs79705935 | snp | A/G | 0.224412 | 0.248687 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164539 | GTTTTCTTTATTTGC[A/G]TGGTCTCCATTCTTC | 55728 |
| rs79707154 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175231 | TCTCGGTGTGTTACC[C/T]ATGTTACCCAGGCAG | 55728 |
| rs79717465 | snp | C/T | 0.343477 | 0.231866 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080957 | AGGCATGAGCCACTG[C/T]GCCTGGCAAGAATTT | 55728 |
| rs79891809 | in-del | -/AA | 0.0854556 | 0.188216 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117677 | TCTTTGTTTGAACTT[-/AA]GTGTATAATTTAAGA | 55728 |
| rs79924329 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151207 | AAATGACTGACCTAA[A/G]TGATAAGGGGAGCCA | 55728 |
| rs80021489 | snp | C/T | 0.22263 | 0.248497 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163922 | TATTAATAGCAGAGC[C/T]GGGTTTCAGACTGAG | 55728 |
| rs80027990 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056008 | TCCCCGAGCTCAGAC[C/T]GCACGCTGGCAGGGC | 55728 |
| rs80051645 | snp | C/T | 0.108048 | 0.20579 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127063 | CATGCCCACGAATTT[C/T]TGAATTTATTATAGA | 55728 |
| rs80142817 | snp | G/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40183131 | TGTTGTAGTCATAAT[G/T]CACAGATACAATCCC | 55728 |
| rs80192073 | snp | G/T | 0.00354858 | 0.0419726 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121779 | CAAGTATATTTCCCA[G/T]TGCTGCTGTGGGTCT | 55728 |
| rs80290629 | snp | C/T | 0.278664 | 0.248351 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077936 | AGATGAGCATGGCCT[C/T]TGTGCAAGGATATGA | 55728 |
| rs80303631 | snp | G/T | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072743 | ACTTTTTTTTTTTTT[G/T]GGGACAGAGCCTCTC | 55728 |
| rs111233982 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40070925 | CTTCTCCTGAGTTCA[C/T]GCAGTTCTCTTGCCT | 55728 |
| rs111253385 | snp | A/G | 3.33206e-05 | 0.00408156 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121265 | GATGGATTTAAGCCG[A/G]AAGTTTTCAATATTA | 55728 |
| rs111267128 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090215 | CTTGAAATCAGGTTG[-/A]CGATTCCTCCTGCTT | 55728 |
| rs111375366 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178051 | TGTAATCCTAGCTAC[G/T]CAGGAGGCTGAGGCA | 55728 |
| rs111380328 | snp | A/G | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40167096 | CTTCTAGTACCAAAT[A/G]TTATAATCAGATAAT | 55728 |
| rs111393833 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120827 | CCAAAGACTGGTTTA[A/G]GTGAGCCCAACCTAG | 55728 |
| rs111405924 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40131919 | TTTTCAAGGACCACA[A/G]GTGAGTGCTAGAAGG | 55728 |
| rs111408942 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40084925 | TGGCTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT | 55728 |
| rs111418993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106610 | CTGGAGTACGGTGGC[G/T]CAATCTCAGCTCACT | 55728 |
| rs111469440 | snp | A/C | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40082923 | GCCAGGATGGTCTCG[A/C]TCTCCTGACCTCGTG | 55728 |
| rs111509170 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40174572 | CTTTGGGAGGCTGAG[A/G]TGGGTGGATCATTTG | 55728 |
| rs111531433 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | N4BP2 | GRCh38.p7 | 4:40145148 | ATTTCTTGGATTTCA[A/G]TTTTTCAGTAGATGC | 55728 |
| rs111565826 | in-del | -/A | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180444 | GGCAGATAGTTAGTC[-/A]CTCTCATACATCACT | 55728 |
| rs111590962 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130620 | TCCTGGGCTCAAGCC[A/G]TCCTCCCACCTCAGC | 55728 |
| rs111601413 | snp | A/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134931 | TCTCTCTTTCTTTCT[A/T]TTTTATTTTATTTTA | 55728 |
| rs111601923 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065314 | AGGTTTGAAGTGCCC[A/G]TGGAATATTCAAGTG | 55728 |
| rs111607362 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058907 | CTCACTGCAACGTCT[C/G]CCTCCTGGGCTCAAG | 55728 |
| rs111643092 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | N4BP2 | GRCh38.p7 | 4:40181777 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 55728 |
| rs111655327 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098913 | TTTAACTTAACATAA[A/G]CATTTGTCTATGTTG | 55728 |
| rs111681190 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142319 | TGGCGGTGGTGGCGA[A/C/T]GGCTGGAGTTGGGCT | 55728 |
| rs111702444 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093851 | GCGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 55728 |
| rs111791984 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088219 | TGTTTCCAGTTTTTG[A/G]TTATTATGAATAAAG | 55728 |
| rs111816118 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165845 | AGTTTTCCCTTCATA[-/T]TCTTTCTGTCTTCCA | 55728 |
| rs111824794 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156335 | GGTATTCCGTGGGCA[A/G]AAGTCAAATGAAAAA | 55728 |
| rs111825356 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40124182 | AAAGACAAGAAGAGG[C/T]GTCTTGTGGCAAGTT | 55728 |
| rs111862510 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165640 | TAGATAGATCCACTG[A/T]TATACTATACATCTC | 55728 |
| rs111864935 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153185 | ATGTGTTTGTTGCCA[A/G]TAATCATCTGATAAA | 55728 |
| rs111869045 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092835 | TTTTAGTAGAGACGG[C/G]GTTTCACCGTATTGG | 55728 |
| rs111870621 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171288 | AAACCAGGAGACGAG[C/T]TCTAGGAGAAGGCTG | 55728 |
| rs111889876 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080624 | ACAGGCGTGAACCAC[C/T]GTGCCTGGCCTATAT | 55728 |
| rs111911418 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102714 | ATTTGGATGCCAGTG[A/G]ACCTCAGGCTTGTTT | 55728 |
| rs111912668 | snp | A/C | | | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40056159 | GGTTCCCGTGCCCGC[A/C]GCAGCGGCCACGGCC | 55728 |
| rs111921109 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136379 | ATCTATCTATCTATC[-/T]ATCTATCTATCTATC | 55728 |
| rs111988883 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40093176 | CTTGAACTCCTGACC[C/T]CAGGTGATCCACCCG | 55728 |
| rs112073368 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133550 | TATGTTGGCCAGGCT[C/G]GTCTCGAACTCCTGA | 55728 |
| rs112076944 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137269 | ATTTATAGCTGATTT[C/T]TTCCTTCGTGTGCAT | 55728 |
| rs112088662 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072540 | TGAGCCACCGCGCTC[A/G]GCCCACCTGGCTAAT | 55728 |
| rs112112632 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062212 | GTCTCCTGAGTAGCC[A/G]GGACTACAGGTGCCC | 55728 |
| rs112118580 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132298 | GGAGATTGGTTACAG[A/G]ACAGAAAATCTTTAC | 55728 |
| rs112161576 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084453 | TTTTTTTTTTTCCTC[C/T]GAGATGGAGTCTTGG | 55728 |
| rs112236718 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072000 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 55728 |
| rs112239370 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178319 | ATAAATTGGAAAATA[A/T]TGATAAAGCAAGAGT | 55728 |
| rs112280934 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40095948 | AAAATAGACTATAGG[G/T]GGACAAAGTTGCAAA | 55728 |
| rs112288110 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083478 | AAATGTGTTATATCC[A/G]TACCATGCAATATTT | 55728 |
| rs112310717 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186141 | TCTGGAATCCCTTGT[G/T]TTTGGAGTCTGTCTG | 55728 |
| rs112330577 | snp | A/G | 0 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101591 | TATTTCTGATATGCA[A/G]TACATGCTCAAATAT | 55728 |
| rs112334631 | snp | A/G | 0.0520825 | 0.152737 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155432 | AAGAGAAAATATTTT[A/G]GTTATAATCATAAGA | 55728 |
| rs112337291 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111344 | GGGTTTTTTTGAGAC[A/G]GAGTCTTACTCTGTC | 55728 |
| rs112350263 | snp | C/T | 0.00953873 | 0.0683987 | downstream-variant-500B, intron-variant | N4BP2 | GRCh38.p7 | 4:40158609 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACT | 55728 |
| rs112411055 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089308 | TAGATTTTAGATATT[A/G]GTCCTTATCCTGAAT | 55728 |
| rs112423260 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40185307 | GTTGCTAATAATAGC[A/C]ATAGTGGTTTTTGCT | 55728 |
| rs112473157 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182754 | GGATCTCAGCTCAAT[A/G]GAACCTCTGCCTCCC | 55728 |
| rs112477521 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40073655 | CTGAAGTACAGTGGC[A/G]CAATCTTGACTCACT | 55728 |
| rs112481201 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098938 | ATGTTGCTGTAATCT[A/G]TATTTTTAATGGGTT | 55728 |
| rs112492474 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151248 | TGTGAGTTATGATTA[A/G]AGATTTAGTTGGGCT | 55728 |
| rs112510955 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125258 | TCTCTAGGACAGCAG[A/T]GGAATGTATCAGAAT | 55728 |
| rs112515359 | in-del | -/T | 0.44638 | 0.154709 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084434 | ATTTTTTTTTTTTTT[-/T]CCTCCGAGATGGAGT | 55728 |
| rs112584119 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40179453 | AGTAGCTAATGTTTA[C/T]TGAAATCTTCTGTGT | 55728 |
| rs112586567 | snp | C/T | 0.461259 | 0.133677 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142121 | AGAGGGAGAGGGAGA[C/T]CATAGGGAGAGGGGG | 55728 |
| rs112650568 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140581 | ATTCTCTTTTTTTTT[-/T]AAAATTAATTTATTT | 55728 |
| rs112665910 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098785 | GAGGAATTACAAGAA[A/T]TCCACATCATCCTAT | 55728 |
| rs112683436 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108950 | GCCTCCTGAGTAGCT[A/G]GGACTACAGGCATAT | 55728 |
| rs112702832 | snp | A/T | 0 | 0 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186051 | CTGAGATTGCCCAGG[A/T]TGTGTTTCCCAGGTA | 55728 |
| rs112725450 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126642 | CATCGTCTTGGCTCT[A/G]TTGCCCACACTAGAC | 55728 |
| rs112729754 | snp | C/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163304 | TGCCCACATGGCCGA[C/T]ATTGTTGTCTTACCC | 55728 |
| rs112768092 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117802 | TGTTTTCCTAGACAT[A/G]TGTTCTGATTTTTAA | 55728 |
| rs112784633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088358 | CTTTAAGAAACTGCA[A/G]AATATTTTTCAGAGT | 55728 |
| rs112818338 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084786 | ATGCCCAGCTAATTT[C/T]GTATTTTTGGTAGAG | 55728 |
| rs112826867 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089392 | CCAGGTCTTTCATCA[A/G]ACAAAAGTTTTGATT | 55728 |
| rs112837896 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104936 | CGGCCTCCGGAGTAG[C/T]GGGACTACAGCCACT | 55728 |
| rs112860135 | in-del | -/A | 0.478932 | 0.10045 | intron-variant | N4BP2 | GRCh38.p7 | 4:40175339 | ATATGTGAAATATAG[-/A]AAAAAAAAAAAAAAA | 55728 |
| rs112864446 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107500 | GTGATTCTTCTGCCT[C/T]AGCTTCCTGAGTAGC | 55728 |
| rs112867145 | snp | G/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173465 | TTGCTATACTAGGAG[G/T]CAGCATTTGTAGTAC | 55728 |
| rs112882098 | snp | A/G | 0.461037 | 0.134028 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129330 | TTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55728 |
| rs112936789 | snp | A/C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148316 | ACCAGTCACGCATGG[A/C/T]GGCGCGCGCCTGCAA | 55728 |
| rs112937281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162212 | AGGCTCATTAGAAGT[A/G]GAGCTGGGGCTGGGT | 55728 |
| rs112965192 | in-del | -/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100366 | AAAATTCTTATTTTG[-/T]TTTTTTTTTTTGGTT | 55728 |
| rs112979222 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184630 | TCTAATTATTTGTTG[C/T]CTTTCAGACGTGAAA | 55728 |
| rs113039135 | snp | A/G | 0.463881 | 0.12944 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149892 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAGAAAAA | 55728 |
| rs113051768 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40060439 | GAGTAGTGATGGGGT[G/T]ACACCTTGTTGGTCA | 55728 |
| rs113057026 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126489 | TAAGTATAATTTGAA[A/G]CTGGAGGTTTTTGCT | 55728 |
| rs113101288 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40081368 | ACTACAGTGAAGGCC[A/G]GGCGAGGTGGCTCAC | 55728 |
| rs113139921 | snp | A/G | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40124494 | TGGGACTACAGGTGC[A/G]CACCACCACACCTGG | 55728 |
| rs113170311 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090068 | TTTTGCACCATAGTC[A/C]AAAATCAGTCAGGCA | 55728 |
| rs113213099 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100774 | ACTATCTGTGTGACT[C/T]GGGTCAAGTTAATGT | 55728 |
| rs113248831 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087266 | CCCCTTCCCCTCCTT[A/T]AAAAAAAAAATTTTT | 55728 |
| rs113288359 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087374 | AATTAAAAAATTAGG[A/T]TTTTTTTGAGGCTAA | 55728 |
| rs113370066 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127244 | ATTTGTTTGAAACAG[G/T]GTCTTGCTCTGTTGC | 55728 |
| rs113404449 | snp | A/G | 0.0462244 | 0.144829 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40152845 | GGAAACCACAGCCAG[A/G]GAGGAGTTGCTCGCA | 55728 |
| rs113424716 | snp | A/G | 0.463126 | 0.13068 | intron-variant | N4BP2 | GRCh38.p7 | 4:40111409 | CACTGCAACCTCCGC[A/G]TACCGGGTTCAAGTG | 55728 |
| rs113429871 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40088593 | GCAGCCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 55728 |
| rs113582483 | snp | C/T | 0.000214977 | 0.0103654 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121542 | AGAATTTCCAAAAAT[C/T]GTGTGATGGATCACA | 55728 |
| rs113593567 | snp | A/G/T | 0.00345755 | 0.0414357 | intron-variant | N4BP2 | GRCh38.p7 | 4:40126382 | ATTCTGGTTTATTGT[A/G/T]TATGTTTACTTTGTG | 55728 |
| rs113638450 | in-del | -/A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169379 | GAGCAAGACTGTCTC[-/A/T]AAAAAAAAAAAAAAC | 55728 |
| rs113658531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40184817 | AAAAATTATCTGGGC[A/G]TGGTGGCACACATTT | 55728 |
| rs113670298 | in-del | -/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063990 | ATTGGTGGGGCGGCA[-/G]GGGGGGGTCTCACTA | 55728 |
| rs113673899 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152630 | GGGCTTTTTGAGATA[A/G]CAAATCTGTCTTACT | 55728 |
| rs113673974 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | N4BP2 | GRCh38.p7 | 4:40072594 | GGTTTCATCACGTTG[C/T]CCTGGCTGGTCTCCA | 55728 |
| rs113674388 | snp | A/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131650 | AGTGCAAGAGTACTC[A/G]TATTACTAATTTCAG | 55728 |
| rs113729532 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086025 | GGCTGGAGTGCAATG[A/G]CTCGATCTCAGCTCA | 55728 |
| rs113789305 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150954 | TTTAAAGGAGTCCTT[A/G]TCTTTTATGAGGTAT | 55728 |
| rs113812588 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116100 | GTAATTTGTCTAATA[G/T]TGATAGACCTACATC | 55728 |
| rs113858022 | snp | C/T | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40066321 | ATTTGTGATTTTCCC[C/T]TTTTTTTTTTTTTTT | 55728 |
| rs113878718 | snp | C/G | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180532 | TCTGAAACCTGCAAA[C/G]TCACTTCCTGTCATT | 55728 |
| rs113890645 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40079038 | GCGATTCTCCAACCT[A/C]AGCCTCCTGAGTAGT | 55728 |
| rs113893786 | snp | A/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40122520 | CTGGGATTATAGGCA[A/T]GTGCCACCGTACCTG | 55728 |
| rs113895552 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178887 | TTGTATTTGCTTAAA[C/G]CTGGCTGAGTTTTTG | 55728 |
| rs113911852 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083807 | AATTGTACACTTTTG[A/G]AATGGTGAATTTTAT | 55728 |
| rs113947548 | snp | C/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164056 | AGAGGTAGTGATTGG[C/T]GGATAGGTATGGGAA | 55728 |
| rs113964478 | snp | C/T | 0.5 | 0 | intron-variant | N4BP2 | GRCh38.p7 | 4:40162088 | CCTTACTTATGCCTC[C/T]GAAATCTCACTGGAG | 55728 |
| rs113970476 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102330 | CTGATGACCAAGTAT[A/G]CTCATTTTTGCCTTC | 55728 |
| rs113981519 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087660 | CGAGCCACCTTCCCC[C/T]ACTCCACGTGCACCC | 55728 |
| rs113997075 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40158795 | AAGAATCTCTTAGAG[A/G]CTCAAGTAATGCTTT | 55728 |
| rs114007703 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063180 | TATTTTATTAGTTAG[A/G]ACTTTTTGGTGTTCA | 55728 |
| rs114078166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115343 | CTCTACAAAAAATAA[A/G]AAAATTAGCTGGGTA | 55728 |
| rs114115109 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40093407 | CACTGCTTTAGCCAT[A/G]TTCTACAATTTTTTT | 55728 |
| rs114136661 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40132564 | TTTAAGGACTTTAAT[G/T]CCATTGAGCTATTTG | 55728 |
| rs114198420 | snp | A/T | 0.00546961 | 0.0520085 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121966 | TCCTTCACATTTCTC[A/T]GATATTTTTAACTTT | 55728 |
| rs114335460 | snp | C/T | 0.029116 | 0.117091 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180578 | TTAATTACTCATGCA[C/T]AATTCATTCATGTAC | 55728 |
| rs114359847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150049 | GTAGTCTGTAGTTAC[C/T]GTCAGTCACCACCAG | 55728 |
| rs114489806 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166718 | CAAACAAAAAGATAA[C/T]TAATAGATGCACTTT | 55728 |
| rs114491797 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | N4BP2 | GRCh38.p7 | 4:40148710 | GCTTAGACTGGTCTC[A/G]AACTTCTGGGCTCAA | 55728 |
| rs114497467 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | N4BP2 | GRCh38.p7 | 4:40112712 | GCTCACCTTTTTTTT[G/T]TTGTTGTTGAGATGG | 55728 |
| rs114508261 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40064086 | CACATGTGAACCACT[A/G]TGCCTGGCCTCATCC | 55728 |
| rs114584966 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | N4BP2 | GRCh38.p7 | 4:40138101 | AGGCTGCAAAAATTC[C/T]AGTGGCAGAATACAG | 55728 |
| rs114614724 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180621 | TCACAATTACAAAAC[A/G]TGTTACATCATTTTG | 55728 |
| rs114648308 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | N4BP2 | GRCh38.p7 | 4:40123453 | AAATTATATAATTAG[C/T]GATGGAGCTCATTGT | 55728 |
| rs114706962 | snp | C/T | 0.182614 | 0.240747 | intron-variant, upstream-variant-2KB | LOC344967, N4BP2 | GRCh38.p7 | 4:40054318 | CGGTGCGGTGGCTCA[C/T]GCCTTTAATTCCAGC | 55728 |
| rs114736092 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091060 | TTAATTTCAGTGTCC[A/G/T]TGTGTTTTTTGCTAG | 55728 |
| rs114747154 | snp | A/T | 0.046775 | 0.145601 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182648 | AGACGAGGTTTCGCC[A/T]TGTTGCCCAGGCTGG | 55728 |
| rs114764356 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171396 | GCTTCCCAGGGTAAT[G/T]CTGTGTGGTGATTCC | 55728 |
| rs114793990 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | N4BP2 | GRCh38.p7 | 4:40113880 | CACAGGTGTGAGCCA[A/C]CATGCCCAGCCTGTA | 55728 |
| rs114844057 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119617 | TCCTCTCCTGGGAAC[A/C]AATTCAGAGCTTTAA | 55728 |
| rs114844967 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131543 | ATTTACATACAGATG[C/G]CCACACATACATGTA | 55728 |
| rs114873693 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40170816 | AATGATTGAGTTAAT[A/G]TGTCATGGGCCATTT | 55728 |
| rs114875365 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086291 | GCCTGGACAACATTG[C/T]GAGACACTGTCTCTA | 55728 |
| rs114894646 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | N4BP2 | GRCh38.p7 | 4:40117309 | CCAGACAAGATCGAG[A/G]TAGGTAAATATGAAA | 55728 |
| rs114959768 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150081 | TGGCAGTATTGTTGA[A/C]TAGAAATGAATCCAG | 55728 |
| rs115033173 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40100498 | GTGATTCTCCTACCT[A/C]AGCCTCCTATGTGGC | 55728 |
| rs115150961 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40062535 | TTTTTGTGACTTTTC[A/T]TGGCCTTTAGGATAA | 55728 |
| rs115157705 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40074514 | ACGCCTGGCCTACAC[A/G]GGTTTCTAAGCTTTT | 55728 |
| rs115170344 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40095085 | CTGGCCAGGGTTACT[A/G]TATCTTTTTTTTTTT | 55728 |
| rs115184768 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134046 | CTCCTGAGCTCAAGG[G/T]ATTCTTCCCCTATTG | 55728 |
| rs115228265 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065251 | GAGTTGGAACTTGAT[C/G]TTGAAAGCTATAGAG | 55728 |
| rs115328697 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40108654 | GTGTGAGAATAAAAA[C/T]GACTCTCTAAACTGA | 55728 |
| rs115433915 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | N4BP2 | GRCh38.p7 | 4:40090658 | TAGTTTACAGCCAGG[C/T]GTGGTGAGTCACGCC | 55728 |
| rs115481055 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065885 | GGAGTACAAGTATCT[A/G]GTAGAGTATTTTGCA | 55728 |
| rs115494326 | snp | C/T | 0.039522 | 0.134904 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068496 | ACCTTTTGTATTCAA[C/T]GTAACATAAGATTCT | 55728 |
| rs115528806 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103307 | AAATGCTTTGCTTAG[C/T]AGAGATCTTTAGTAA | 55728 |
| rs115557822 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098097 | AAAAACTTTGTTTTA[C/T]TCCTGTATCTTCAGC | 55728 |
| rs115639326 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129669 | AGAGATGAGGTCTTG[C/T]AGTGTTGCCCAGGCT | 55728 |
| rs115674483 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071754 | TATTTTTAGTAGAGA[C/G]GAAGTTTCGCCATAT | 55728 |
| rs115699000 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161520 | GACAATCACACGACA[A/G]TTGGCATTGTGAACA | 55728 |
| rs115783549 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40057543 | GCCACTCACACGTTC[C/G]GATTTTGGAGACTGC | 55728 |
| rs115817789 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | N4BP2 | GRCh38.p7 | 4:40133141 | GCTGTCTTATCATTT[A/G]TTTTTTACTGATATC | 55728 |
| rs115840916 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | N4BP2 | GRCh38.p7 | 4:40107450 | GTACAGTGGTGCAAT[C/G]TGGGTTCACTGCAAC | 55728 |
| rs115886848 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104275 | CTTTTTTTTTTTTTT[C/T]CCTTTTTCCAAATTT | 55728 |
| rs115889698 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068551 | ACCCAGTTTTTCCTA[C/T]ATCATTTGTTGAAGA | 55728 |
| rs115905666 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164740 | AACAGTTCTTTGCAG[C/T]GGGACCTCACTGTTT | 55728 |
| rs116067347 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118664 | TTTCCCTTATCTTCT[C/T]GCTGTTATTATTTTG | 55728 |
| rs116068392 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165141 | TATCTGAATATAGTT[G/T]TCTCTTATATTTCTT | 55728 |
| rs116074479 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40092243 | ATTTTTTCCTAAAAA[A/T]GTTTGTTAGAATTTT | 55728 |
| rs116159629 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174526 | AAAAACTGCTGGCCA[G/T]GTGCGGTGGCTCACG | 55728 |
| rs116163253 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165349 | TGCTTCCCGGGCTCA[A/G]GCAATCCTCGTGCCT | 55728 |
| rs116185621 | snp | C/T | 0.029116 | 0.117091 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083014 | CGGGCTGTATTCTTA[C/T]ACTGACTGTATAGAA | 55728 |
| rs116242606 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065736 | AATTTTTAGACAGTT[A/C]TTCCAATGCAGGGAT | 55728 |
| rs116253456 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | N4BP2 | GRCh38.p7 | 4:40115610 | ATTATGATTAATTTC[A/G]TTCTTTAACTCTTGG | 55728 |
| rs116279458 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089502 | AGTGCACTAGTGCCA[C/T]CTTGGGTCACTACAG | 55728 |
| rs116290436 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160332 | GTTTGACGTATTTTT[C/T]GATTTTGTGATGGTG | 55728 |
| rs116297816 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | N4BP2 | GRCh38.p7 | 4:40165556 | CTCTACTTTTAAGAG[A/G]AAAAGAAGCAAGGTG | 55728 |
| rs116336507 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | N4BP2 | GRCh38.p7 | 4:40137822 | GTTTAGGATTGGCTA[A/G]TTTAAATAATTTCAG | 55728 |
| rs116394227 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | N4BP2 | GRCh38.p7 | 4:40171243 | TCACTTTCATCGTTT[G/T]TCCATCCCTTCTGCC | 55728 |
| rs116442243 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | N4BP2 | GRCh38.p7 | 4:40104801 | GAGACATAGAACCTG[A/C]GTTGTCTTTTTTTTT | 55728 |
| rs116466687 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | N4BP2 | GRCh38.p7 | 4:40103879 | GGCACTCCTTGAAGA[A/G]TATTGTTTTCATAGT | 55728 |
| rs116495703 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | N4BP2 | GRCh38.p7 | 4:40087406 | TCTCACTCTGTCACC[C/T]AGGCTGGAGAGCAGT | 55728 |
| rs116500149 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40149562 | ATTTTAAAATGGTTA[C/G]TTTTATGTTAATTTT | 55728 |
| rs116552493 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178393 | TTGTAGGAAAACCTC[C/T]GGCAAGACTACTCCC | 55728 |
| rs116556288 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127441 | GCTGGTCTTACACTC[A/C]TGGGCTCAAGTGATC | 55728 |
| rs116648948 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | N4BP2 | GRCh38.p7 | 4:40063080 | ATAGATGAAAGTTTT[C/T]TAAGCCAGAGAAGGC | 55728 |
| rs116655749 | snp | C/T | 0.324382 | 0.238678 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174147 | TTTGGGAGGCTGAGG[C/T]GGGAGGATTGCTTGA | 55728 |
| rs116663307 | snp | A/C/T | 0.0197687 | 0.0974348 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110784 | CTCAGGTGATCCGCC[A/C/T]GCCTCAGTATCCCAA | 55728 |
| rs116667081 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152652 | TGTCTTACTATTACA[A/G]TTTTGAGATGGCAAA | 55728 |
| rs116667537 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40097921 | TTGTAGGTTTAGCAG[C/T]GTCCCTGGCCTGTAC | 55728 |
| rs116702630 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | N4BP2 | GRCh38.p7 | 4:40177339 | CTTCTTCCTGGGCCC[A/G]GCACGGTGGTTCACG | 55728 |
| rs116705582 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116830 | ATTCTTGTAAGATAC[G/T]TTTGCTGGATATGTA | 55728 |
| rs116707122 | snp | A/G | 0.021333 | 0.101051 | intron-variant | N4BP2 | GRCh38.p7 | 4:40127111 | GCCCAGGCTGGTCTC[A/G]AGTTCTGGGGTCAGT | 55728 |
| rs116760802 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101083 | CAGTTCACATATCAC[C/T]TTATGTGAGATCTTT | 55728 |
| rs116762378 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160791 | GCTTAGGTCAGAAAT[C/T]TAAGTGAGAATATTA | 55728 |
| rs116776643 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101590 | ATATTTCTGATATGC[A/G]GTACATGCTCAAATA | 55728 |
| rs116804146 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183699 | TTTGTTATTTGTTAC[C/T]ATATCATTAGAAGAC | 55728 |
| rs116807441 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | N4BP2 | GRCh38.p7 | 4:40150575 | ACTCTGGAAACTGAG[A/G]CAGAAGAATCGCTTG | 55728 |
| rs116808913 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144145 | CCAAAGGCAGGAGGA[A/G]AACATCTGCCTGTTT | 55728 |
| rs116990509 | snp | G/T | 0.00025773 | 0.0113489 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40122285 | CAACTTAATGAATTA[G/T]TTGGTCCTGTTGGTA | 55728 |
| rs117274298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091221 | AATAGGGACACTTTT[A/G]TTTCTTCTTCCCTAA | 55728 |
| rs117853869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40086940 | TTTTGTAGAGATGGG[A/G]GTCTCACTATGGTGC | 55728 |
| rs117959423 | snp | A/T | 0.030665 | 0.119967 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143324 | TTTATTTATTTATTT[A/T]TTTTTTTAAGATAAG | 55728 |
| rs118012789 | snp | A/G | 0.000148575 | 0.00861774 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117982 | CAGAGAAAATTGAAC[A/G]TATTGAGTTGTGTGC | 55728 |
| rs137867135 | snp | A/C/T | 0.00133804 | 0.0258308 | intron-variant | N4BP2 | GRCh38.p7 | 4:40142668 | TATTGTTTAATATCT[A/C/T]ATAGCCAAAGAAATT | 55728 |
| rs137882519 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | N4BP2 | GRCh38.p7 | 4:40071692 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55728 |
| rs137904368 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110086 | ACAACATGTGGACTT[C/T]TGTGATTGGCTTCTT | 55728 |
| rs137922312 | in-del | -/TCTC | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40134904 | CTTCCTTCCTTCCTT[-/TCTC]TCTCTCTCTCTCTCT | 55728 |
| rs137933485 | in-del | -/CT | 0.0482946 | 0.147699 | intron-variant | N4BP2 | GRCh38.p7 | 4:40169372 | CAAAACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAA | 55728 |
| rs137933667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182238 | TGATACAAGAACATG[C/T]GCAGAGACAGGAAAA | 55728 |
| rs137953758 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | N4BP2 | GRCh38.p7 | 4:40136706 | TACCAATATACTATC[-/T]TTTTGGCATTCATTT | 55728 |
| rs138016525 | snp | C/T | 6.59435e-05 | 0.00574172 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40142758 | ATGATGACTACAGAG[C/T]AGAGGCTTTCCTTCA | 55728 |
| rs138053192 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40186034 | ATGAGAAGAGAAAGC[C/T]ACTGAGATTGCCCAG | 55728 |
| rs138065545 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40144052 | GCCCCCAGTCCAGGG[C/T]CAAAGGCTCAAGAGC | 55728 |
| rs138170975 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155965 | TTCACACTTATGTTT[G/T]TAATAATTTATTTAA | 55728 |
| rs138175148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40084229 | GTACTGGGATTACAG[A/G]CGTGAGCCACCGCAC | 55728 |
| rs138208702 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40155292 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAACCG | 55728 |
| rs138211226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40083824 | ATGGTGAATTTTATG[C/G]TTTACATATTATATT | 55728 |
| rs138224367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40096863 | GACTGGGAAAAGCAG[G/T]TTTGAAGGGGGTGAT | 55728 |
| rs138257938 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40114395 | TTACTCTAGTTCCCC[A/C/G]CTCCTCTTGGCAACC | 55728 |
| rs138260728 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40129879 | CATAATATATGAATA[G/T]AATAATTAATTTTAA | 55728 |
| rs138317254 | snp | C/T | 0.000296492 | 0.012172 | utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40097428 | TCCAGTGTTGCTAGT[C/T]GTGAGGAGCCAACCA | 55728 |
| rs138323392 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | N4BP2 | GRCh38.p7 | 4:40125515 | TCCTCTATTTACCAG[C/G/T]GTCCTGTATACATGT | 55728 |
| rs138323778 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40131139 | AATATGTTTTGAGGA[C/G]GATGTTCACAGCATC | 55728 |
| rs138329174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | N4BP2, LOC344967 | GRCh38.p7 | 4:40058696 | CATGTTTTTTCCTTC[A/G]TTAAAGTATATTAAA | 55728 |
| rs138331460 | snp | C/T | 0.000131809 | 0.00811708 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102716 | TTGGATGCCAGTGAA[C/T]CTCAGGCTTGTTTAA | 55728 |
| rs138365452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40106457 | AAGCAGCTGGGACTA[C/T]AGGTGCACACTACCA | 55728 |
| rs138365558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40178929 | TCTATTTGATTTGCA[A/G]TGTGACACTGCCCTT | 55728 |
| rs138391681 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40163847 | GATTTGATATACCCC[G/T]TTTTACAGACTAGGA | 55728 |
| rs138441778 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40161290 | TAGATCCAACAACCA[A/G]TTTACAGGGATTACA | 55728 |
| rs138467723 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40066450 | CAGTCTCCCAAGTAC[C/T]TGGGACTACAGGCAT | 55728 |
| rs138510176 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065079 | GGCTGGGGTTAGAGG[A/G]ACTTTCAGGCAGAGA | 55728 |
| rs138534358 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40173296 | CCCTAAATGCAGGAA[A/C]TCCCTGGAAAGCACC | 55728 |
| rs138551543 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40101899 | AGACTTTTTGCTACT[A/G]CAGACTTTGGTATGT | 55728 |
| rs138573117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40110416 | CACTTGTTATTGTCC[A/G]TTTTTTTGATTATTC | 55728 |
| rs138586271 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40143383 | TAGTGGTGCAATCTC[C/T]GCTAACTGCAGCCTT | 55728 |
| rs138605041 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40151858 | AATATCATCTTGGAG[A/G]TATGATACTTGAAAA | 55728 |
| rs138627960 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40135857 | CAGGCGTGAGCCACC[A/G]TGTCTGCCTAGTTAA | 55728 |
| rs138635283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40182603 | TACAGGTGCACGCCA[A/C]CATGCCGGGCTAAAA | 55728 |
| rs138688087 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | N4BP2 | GRCh38.p7 | 4:40174333 | AGTGAGCCGTGATCA[C/T]TTAAAGAAATTAAAA | 55728 |
| rs138704936 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180197 | ATTATTGATATCTTT[C/G]ATATACAAACAACTT | 55728 |
| rs138739590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40118997 | GAGAAAATTTATAAA[A/T]GCTTTTTTGATTGAG | 55728 |
| rs138784643 | snp | A/G | 3.31884e-05 | 0.00407346 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40120596 | TCACACAAATTAGTT[A/G]ACAGTGTATCTGTGA | 55728 |
| rs138796419 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40160267 | ATTGCTACATTAGCC[C/T]GCCCTATTTAATATA | 55728 |
| rs138817644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40134311 | GGCCACTCCTGTTCT[A/G]TGAGTACCTAGAGCA | 55728 |
| rs138832806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40091662 | CCAGGCTGGAGCATA[A/G]TGGTGTGATCATGGC | 55728 |
| rs138929353 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40077963 | ATGACACGCAGATTC[A/G]TGAAGTGTTCCATAT | 55728 |
| rs138937801 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164099 | GGAAGGAAAGGAGAC[A/G]AAATTCACGATGCTG | 55728 |
| rs138942561 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | N4BP2 | GRCh38.p7 | 4:40130510 | TTCTAGCATTTTCCC[A/G]GATTATTTTGTTTAT | 55728 |
| rs138945229 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094148 | TATTTAGATGTATAT[G/T]GCTTGGAAATTTTTA | 55728 |
| rs138982106 | snp | A/G | 0.000693676 | 0.0186107 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40126232 | TTAACAGCATCTGAA[A/G]TGCTACCTTTATTGG | 55728 |
| rs139003019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40152193 | GTGACTAGTGGATTT[C/G]CTAATAGCTATTACT | 55728 |
| rs139003131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40080800 | GTAGCTGGGACTACA[A/G]GCGCCTGCCACCACG | 55728 |
| rs139052225 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | N4BP2 | GRCh38.p7 | 4:40153663 | ATTTGGCTACATTAT[C/T]GAAAATGATAGCATA | 55728 |
| rs139089220 | snp | A/C | 0.000165714 | 0.00910107 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40121086 | CTGGAGTAGTAGAAC[A/C]ACAAACGTTAGCTGA | 55728 |
| rs139094515 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | N4BP2 | GRCh38.p7 | 4:40065879 | TACTGGGGAGTACAA[A/G]TATCTAGTAGAGTAT | 55728 |
| rs139188435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | N4BP2 | GRCh38.p7 | 4:40166260 | TTTCTGAAGGATTCT[C/G]TAAGAAACTGAACAG | 55728 |
| rs139202801 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40068591 | TTTCCCATTGTGTGG[C/T]CTTGGTACCCTTGTT | 55728 |
| rs139212731 | in-del | -/TG | | | intron-variant | N4BP2 | GRCh38.p7 | 4:40111056 | TTCAGATCATTACAT[-/TG]TGTGTGTGTATATTT | 55728 |
| rs139228666 | snp | C/G | 0.000435365 | 0.0147476 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40144795 | TTTTAGAGAAGAAGA[C/G]TGAAGGTAGGACTGT | 55728 |
| rs139262627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40183238 | CTATTTTCAAATGAC[C/T]GTGTGTAACATCCCA | 55728 |
| rs139267274 | snp | C/T | 0.000329402 | 0.0128294 | synonymous-codon, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40102976 | CTTCCAAGGAAACCA[C/T]GGCTTTGTAGCTCCT | 55728 |
| rs139286597 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | N4BP2 | GRCh38.p7 | 4:40098362 | CATAGGACTTTTTTT[A/T]GGTGAGGATTGAGTT | 55728 |
| rs139332057 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099347 | TCCCGAGTTAAAGTG[A/G]TTCTCCTGCCTCAGG | 55728 |
| rs139341486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | N4BP2 | GRCh38.p7 | 4:40078563 | AGGGTCTCGCTTTAT[C/T]GCCCAGGCTGGAGTA | 55728 |
| rs139358932 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139029 | ACAATATTAAGTCTT[C/T]CAATTCATGAAATGG | 55728 |
| rs139410404 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40140113 | TTTTATTTTATTTTA[C/T]TTTACAGAATCTTAT | 55728 |
| rs139425404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | N4BP2 | GRCh38.p7 | 4:40059781 | TGTATGTACACACAC[A/G]TGCACACCAGGTGCT | 55728 |
| rs139470519 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40100079 | CAGTTCTTGTGCACA[A/G]CACTTTTTCATGGAT | 55728 |
| rs139470812 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40158209 | TTTTCTTATGAAGCC[A/G]TTTGCAAATTACATA | 55728 |
| rs139475471 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | N4BP2 | GRCh38.p7 | 4:40164984 | TTAAGCTCTGGGCTA[C/T]GTTTTTCTTTTCATT | 55728 |
| rs139477290 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | N4BP2 | GRCh38.p7 | 4:40085454 | ATGTTGATAGGATTT[A/G]TTTTTTATTCTTTTT | 55728 |
| rs139493726 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | N4BP2, LOC344967 | GRCh38.p7 | 4:40055739 | TCACCACCACCACCA[A/C]CAACCAGAAAGCAAA | 55728 |
| rs139493820 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | N4BP2 | GRCh38.p7 | 4:40094631 | TGTGATCTCAGCTCA[A/G]TGCAACCTCTGCCTC | 55728 |
| rs139518808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | N4BP2 | GRCh38.p7 | 4:40099165 | TACCAATGAGGTGTG[C/T]TGACTTGTAATTCCA | 55728 |
| rs139552932 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | N4BP2 | GRCh38.p7 | 4:40139863 | AGGGTCTCACTGTGT[C/T]GCTCAGGCTGGAGTG | 55728 |
| rs139555443 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | N4BP2 | GRCh38.p7 | 4:40089976 | GAGACTTAGGTCAAG[G/T]TTTATTTTTTACTGA | 55728 |
| rs139623682 | snp | C/T | 1.64857e-05 | 0.00287099 | utr-variant-5-prime, synonymous-codon, intron-variant | N4BP2 | GRCh38.p7 | 4:40097529 | TTCTGATCTGGATCC[C/T]GATGTAGTGTATTTG | 55728 |
| rs139660897 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | N4BP2 | GRCh38.p7 | 4:40119845 | AATAACTGTTAAGTG[C/T]CCTGTCAATTAATGC | 55728 |
| rs139664437 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | LOC344967 | GRCh38.p7 | 4:40054221 | CTGCCTCAGCCTCCC[A/T]AAGTGCTGGGATTAC | 55728 |
| rs139672383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | N4BP2 | GRCh38.p7 | 4:40180923 | TTGGGAGGCTGAGGC[A/G]GGTGGATCATGAGGT | 55728 |
| rs139720518 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | N4BP2 | GRCh38.p7 | 4:40116752 | TGAGAATTTTCTTTA[C/T]AGTAAGGGTCTGCTT | 55728 |
| rs139756456 | snp | C/G | 0.0185938 | 0.0946107 | utr-variant-3-prime, intron-variant | N4BP2 | GRCh38.p7 | 4:40156868 | TATAATGCACATGTT[C/G]TAAAATATCCCCCCA | 55728 |
| rs139764100 | snp | C/T | 6.73605e-05 | 0.00580308 | missense, nc-transcript-variant | N4BP2 | GRCh38.p7 | 4:40117870 | CCTGGAATTTTCAGG[C/T]GTAACATTCATGGGG | 55728 |