| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs120744 | snp | A/G | 0.428484 | 0.175052 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234646 | GTGCTATCATTTAGG[A/G]CTCACCTCCTTTTCA | 7704 |
| rs238887 | snp | C/G | 0.495056 | 0.049474 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114127880 | ATGTGCTGAGCTTAG[C/G]TGCGCTGTCCAGGGC | 7704 |
| rs238888 | snp | C/T | 0.143959 | 0.226396 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114127759 | TGTGCTAACAGTGGA[C/T]GGAAGATTCAGGCTT | 7704 |
| rs238889 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114127272 | AACCCTTGATCTGCA[A/G]TGGAAGAGAAGAGAC | 7704 |
| rs238890 | snp | C/T | 0.492871 | 0.0592773 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124852 | TCCTCCACAGCACCC[C/T]CGTGCTGCACTCCAC | 7704 |
| rs238891 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124683 | TGAAGCTCAGGTTTC[A/G]GGGATATGGCCAAGA | 7704 |
| rs238892 | snp | G/T | 0.497803 | 0.033074 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124570 | TGTTTTGTTTTTGTT[G/T]TTTTTTTTTTTTGGT | 7704 |
| rs238893 | snp | G/T | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124557 | TTTTTTTTTTTTTTT[G/T]GTTTTTTTTTTTGTT | 7704 |
| rs238894 | snp | C/G | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124531 | ttgttttgtttttgC[C/G]TCTTCCCCCATCCCC | 7704 |
| rs238895 | snp | C/G | 0.48666 | 0.0805725 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114124390 | TGCTAAGAGAGAATA[C/G]AGGGTGGGAGAAGCA | 7704 |
| rs238896 | snp | C/T | 0.485324 | 0.0843964 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114123783 | CCTATTTTAAGGCCA[C/T]TGTCAAGAAGAGTGA | 7704 |
| rs238897 | snp | C/T | 0.49931 | 0.0185575 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114123652 | CAATTTCAAATACCA[C/T]GTGTAAACTGAGACA | 7704 |
| rs238898 | snp | C/G | 0.162909 | 0.23434 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114123322 | CACTGGTCTCCTTCT[C/G]GGGGAGCCAATGAGA | 7704 |
| rs238899 | snp | A/G | 0.498568 | 0.0267188 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114119995 | CTGCAATCTTTCTCC[A/G]AGAAATCCCTTCTCT | 7704 |
| rs238900 | snp | A/C | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114118976 | cacctggccCCCTCT[A/C]AATTCTTTGTAACAA | 7704 |
| rs238901 | snp | C/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114118952 | GTAACAAAAGTCAAC[C/T]TGAAATGTCAACCTG | 7704 |
| rs238902 | snp | C/T | 0.497959 | 0.0318836 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114118294 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATAA | 7704 |
| rs238903 | snp | A/T | 0.485799 | 0.0830599 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114118065 | ACCTGGGGTCCTGTG[A/T]TTAAGTCAGTTGTGC | 7704 |
| rs238904 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114117564 | AAACCTCAGGAGTCT[C/T]AACCAACTCCTTCCT | 7704 |
| rs238905 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116996 | CTAGTCAATTGCTGC[G/T]TCACCTCCATTTCCT | 7704 |
| rs238906 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116933 | TATTCTACTATAAAG[G/T]GCTGCTATGTCTCAG | 7704 |
| rs238907 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116893 | CCCCTACCAGCTTAT[G/T]AGATTCTTGGGGACG | 7704 |
| rs238908 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116846 | ACTTCTGTATCTCca[G/T]tgtctgggatacagt | 7704 |
| rs238909 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116838 | ATCTCcagtgtctgg[G/T]atacagtaggactca | 7704 |
| rs238910 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114116157 | GCTGTCCATTAAGCA[C/T]ACTTAAACACATGTA | 7704 |
| rs238911 | snp | C/T | 0.483636 | 0.0889627 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114115440 | ACACCTGCCGATGTG[C/T]TAAGAGTCCTCTTGA | 7704 |
| rs238912 | snp | A/G | 0.487113 | 0.0792303 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114113876 | TAAATGAATATAAAA[A/G]TAAAAGAATGAATTC | 7704 |
| rs238913 | snp | C/T | 0.498182 | 0.0300969 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114113767 | TGAAAAAGCCTCCAC[C/T]AGCTTCATTTAGGAA | 7704 |
| rs238914 | snp | G/T | 0.498109 | 0.0306926 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114113387 | AAAATTCCAACCAGT[G/T]TCCTCAACCTAATTT | 7704 |
| rs238915 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114111002 | GTTTTCCCCCCAACA[C/T]GCACAACAGGTTCCA | 7704 |
| rs238916 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114108906 | GCCCATCAACACTGA[A/G]GCCAGCCTGTCCCAA | 7704 |
| rs238917 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114108345 | TTTAGAAAGGAAAAA[G/T]ACCTGAAAAGGGATT | 7704 |
| rs238918 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114108216 | TGTGCACCCTCTTTT[A/G]TCCGGGCCTGGGGTC | 7704 |
| rs238919 | snp | A/C | 0.152667 | 0.230274 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114107992 | aataatgataataat[A/C]atcataataaAGGTG | 7704 |
| rs238920 | snp | C/T | 0.250168 | 0.25 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114107777 | CAGCCCAGCTTTGTT[C/T]CTCTTTGAAAATTAT | 7704 |
| rs238921 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114107461 | AGAACCCCTTGGCAG[A/G]GTTGTTGGATTTGTT | 7704 |
| rs238922 | snp | C/T | 0.250168 | 0.25 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114107306 | GTCTAAAAAGTTCTT[C/T]TCTGGATATCATCAG | 7704 |
| rs238923 | snp | C/T | 0.148661 | 0.22854 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114106805 | GGAATGAAAAAGAGC[C/T]AGATTTCTTTTCCAT | 7704 |
| rs238924 | snp | C/T | 0.498852 | 0.0239341 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114104724 | CAGAAGCTACAATGA[C/T]GTTTCCTATTTCGCA | 7704 |
| rs238925 | snp | G/T | 0.45889 | 0.13735 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114104625 | TGAAGGGATGGACCT[G/T]CAGGAAGCTGAGAGA | 7704 |
| rs238926 | snp | C/T | 0.495291 | 0.0482933 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114104488 | TGCTTGGGGGTACTT[C/T]CCTTTCCCTTCCTGC | 7704 |
| rs238927 | snp | C/T | 0.140581 | 0.224783 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114104204 | AGAGAAGAACATGGT[C/T]AGGTCCCAGTTTTCT | 7704 |
| rs238928 | snp | G/T | 0.495252 | 0.0484902 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114102462 | CACTGCTGTGATGAA[G/T]GAGAAGAGTGATGAT | 7704 |
| rs238929 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114101717 | TAGCCAGGAGATCTA[C/T]GTGTATTTTTTCATT | 7704 |
| rs238930 | snp | C/T | 0.445724 | 0.155538 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114101626 | CTGAATCTCAAAATG[C/T]TTATGGGGCTAAGGA | 7704 |
| rs238931 | snp | C/T | 0.498503 | 0.0273153 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114098839 | TCCCCCATTTCCTTT[C/T]CCCCTCACCAAGAAC | 7704 |
| rs238932 | snp | G/T | 0.424037 | 0.179474 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114096952 | TTCAATTATTTAGGG[G/T]GTGTGTGTGTGTGTG | 7704 |
| rs238933 | snp | A/T | 0.240765 | 0.249829 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114096560 | TGAGACAACGATGTT[A/T]AAAAAAACATAGGCA | 7704 |
| rs238934 | snp | C/G | 0.499776 | 0.0105807 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114096422 | GCCGTTGAGAGATGG[C/G]AGAATAGACCTCTGT | 7704 |
| rs238935 | snp | A/C | 0.496968 | 0.0388195 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114095703 | TAGGCCTGAGCCTCG[A/C]AGTTGTTTAAAAAGA | 7704 |
| rs238936 | snp | A/G | 0.165289 | 0.235211 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114095250 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 7704 |
| rs238937 | snp | A/C | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114094863 | GCCTTGGCCTTTGGA[A/C]ACTTGGAACTGATAG | 7704 |
| rs238938 | snp | G/T | 0 | 0 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114094793 | ACTCCAACCATGGAA[G/T]CCCCTTGGGCCAGGG | 7704 |
| rs238939 | snp | C/T | 0.3752 | 0.216391 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114094226 | CCGGGTTCACGCCAT[C/T]CTCCAGCCTCAGCCT | 7704 |
| rs238940 | snp | A/G | 0.347914 | 0.230028 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114092901 | ATAATGGAGACCAGA[A/G]GGGAACATGCCCAAA | 7704 |
| rs238941 | snp | C/T | 0.112983 | 0.209108 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114091844 | CCACTGCTTGACCGG[C/T]TTAGGAGAGGGGGAG | 7704 |
| rs364729 | snp | A/G | 0.483126 | 0.0902898 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114224721 | ttccagcaactcctc[A/G]atctccatcgtggat | 7704 |
| rs370238 | snp | A/G | 0.493568 | 0.0563433 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114231117 | TCCAGTATACTTCAC[A/G]TGTAAAAGATGCTTT | 7704 |
| rs370634 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114230987 | AAACCCAAAAACCTC[A/G]GCTAGGCTCTCATGT | 7704 |
| rs371267 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114232293 | TGCATTTGGGGGTAG[A/G]TGGGTAGCAAATAAA | 7704 |
| rs375328 | snp | C/T | 0.16976 | 0.236773 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234873 | TTTGCCCCCAGGTTG[C/T]TGCTGAAAAAGGTAG | 7704 |
| rs375620 | snp | A/T | 0.463559 | 0.129972 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114218713 | GCAGTCATGAGTTAC[A/T]GAACAAAAAAGAAAC | 7704 |
| rs376616 | snp | A/T | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114220354 | TGGGGGATGTGTGTG[A/T]GCAATGCATGCATGT | 7704 |
| rs377274 | snp | A/G | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114223539 | CAAATAAATACATTA[A/G]AAATAATCTATTAAT | 7704 |
| rs378331 | snp | G/T | 0.456332 | 0.141164 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114223218 | TATTCATTCATGTGG[G/T]ACTCAGTGCAGTGCT | 7704 |
| rs382312 | snp | C/T | 0.496778 | 0.0400063 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114233191 | AAGTTTTAATTCATT[C/T]TGGAATGTCTGGAAG | 7704 |
| rs383285 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114226890 | AGAGAGGAATATGAT[A/G]TGATAAAGAAAAATA | 7704 |
| rs386800 | snp | C/T | 0.304188 | 0.244057 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114211968 | GCCAGGAGGGCGAGT[C/T]CCCCTGCCCTCGCCC | 7704 |
| rs387301 | snp | A/G | 0.252421 | 0.249988 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114241291 | AGCATTAAAATCTAG[A/G]GTGTGTGAGTGTGAA | 7704 |
| rs387977 | snp | C/T | 0.483995 | 0.0880135 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234941 | CTTCGTGACCACACA[C/T]TCAAACCATCATATA | 7704 |
| rs388306 | snp | A/G | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114235035 | AAAGACATATCTGAA[A/G]GATTTGGGGGCTGGG | 7704 |
| rs389858 | snp | A/G | 0.321769 | 0.239477 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114222132 | TGTGAAGTTTTCAGT[A/G]CCTCAAGGATCAGCA | 7704 |
| rs390538 | snp | A/G | 0.417196 | 0.185864 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114223208 | TGTGGTACTCAGTGC[A/G]GTGCTACCCAGATGT | 7704 |
| rs394800 | snp | G/T | 0.482979 | 0.0906686 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114228080 | ccattggctccctgg[G/T]cagtctggcgaaacc | 7704 |
| rs397461 | snp | A/G | 0.278399 | 0.248382 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114216745 | CTTCTGAAAATGATA[A/G]GGAATAGGGGATCTT | 7704 |
| rs398055 | snp | A/G | 0.462363 | 0.131916 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114221819 | TTGTTTTCTGAAATT[A/G]CCTTTTAAGAGAAGA | 7704 |
| rs400920 | snp | A/C | 0.434831 | 0.168337 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114222153 | TTTGAACCCAGATGG[A/C]AGTTCTGTGAAGTTT | 7704 |
| rs401141 | snp | C/T | 0.482459 | 0.0919928 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234548 | GTACAGTAGTGCATC[C/T]CTAATGATCCTGAAA | 7704 |
| rs401479 | snp | G/T | 0.482384 | 0.0921818 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234664 | TAAATGATAGCACAG[G/T]GGAAGTCAAAATGGA | 7704 |
| rs402311 | snp | A/G | 0.482609 | 0.0916147 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114234905 | ACGCCTTTTCCTTTC[A/G]CCCATCTTCTCCTCC | 7704 |
| rs403104 | snp | C/T | 0.452473 | 0.146644 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114223661 | tagaaggcatgaaac[C/T]catgaagacatgggt | 7704 |
| rs404426 | snp | C/T | 0.325091 | 0.238456 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114221239 | CTGGAGAGAGTTTTC[C/T]TTCTATGAAGATCTT | 7704 |
| rs404509 | snp | C/T | 0.246485 | 0.249975 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114243655 | GGGGAAATGCTTACG[C/T]AATCGCTGTAGAGAA | 7704 |
| rs405388 | snp | C/T | 0.27893 | 0.24832 | intron-variant, utr-variant-3-prime | ZBTB16 | GRCh38.p7 | 11:114210549 | ATGGCCACACTAATC[C/T]GCTTCTTCCAAAATT | 7704 |
| rs405599 | snp | C/T | 0.189576 | 0.242588 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114242673 | TTGGGTCTACCTACA[C/T]GAGAATCCCTTGGGA | 7704 |
| rs410804 | snp | C/T | | | intron-variant | ZBTB16 | GRCh38.p7 | 11:114235713 | tctttcttttctttc[C/T]ttctttttctttctt | 7704 |
| rs415066 | snp | C/T | 0.47517 | 0.10862 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114238720 | GATCAGAGGGCTGCA[C/T]ATGCCAGGCAGGACA | 7704 |
| rs420234 | snp | A/G | 0.287867 | 0.247116 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114237244 | GAGATATCCACACGA[A/G]AAAACTTTATAATGT | 7704 |
| rs421535 | snp | C/T | 0.462582 | 0.131564 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114221119 | GAAGGGAAAAGGAAC[C/T]AGCACAGCCTTTGAA | 7704 |
| rs424337 | snp | C/G | 0.493837 | 0.055168 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114216855 | GACTAGACCCAGTCT[C/G]TTGATTCAAGGAATT | 7704 |
| rs424463 | snp | C/T | 0.342134 | 0.232404 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114239137 | ACTCTGCCCCCTTGG[C/T]CTTTCCAAGGCCCCT | 7704 |
| rs435562 | snp | C/G | 0.496874 | 0.0394129 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114233270 | GAGACTAATATCCTC[C/G]GCTGGTACCTCCCAC | 7704 |
| rs438490 | snp | A/G | 0.473634 | 0.111748 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114239531 | CAGTGAGTCTTCAAT[A/G]TCCCTCCCTGCTTGG | 7704 |
| rs441434 | snp | C/T | 0.306679 | 0.24349 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114221181 | ACTCAGTGATATTGC[C/T]GCTTGGCTCTTCCCT | 7704 |
| rs444146 | snp | C/T | 0.499997 | 0.00119808 | intron-variant, downstream-variant-500B | ZBTB16 | GRCh38.p7 | 11:114211225 | GAAATCAATCTGCAC[C/T]TTTAGGTCACTCACT | 7704 |
| rs444401 | snp | C/T | 0.0603597 | 0.1629 | intron-variant, downstream-variant-500B | ZBTB16 | GRCh38.p7 | 11:114211021 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 7704 |
| rs445785 | snp | A/G | 0.17332 | 0.23795 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114236722 | TTAGAAAATAAATAA[A/G]GGGTTGTAAGACAAT | 7704 |
| rs447174 | snp | G/T | 0.441977 | 0.16014 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114237818 | AAAAAAATGGAAAAG[G/T]GGGGGAGATGTGGAT | 7704 |
| rs454802 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114218382 | AAATGTAAAGCCCCA[A/G]TGGGGCAGGACCCAG | 7704 |
| rs471637 | snp | A/G | 0.187053 | 0.241946 | intron-variant | ZBTB16 | GRCh38.p7 | 11:114230302 | ATCAGGTGTAATCAG[A/G]CTGTGCGTACATTCT | 7704 |