| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs896621 | snp | C/G | 0.419936 | 0.183362 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200428 | TGTGGAAAACCCCCT[C/G]AGCCTGACAAGTTCT | 79931 |
| rs896623 | snp | C/T | 0.474 | 0.111014 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212944 | ACATCTGCCTGTCAC[C/T]CCATAAACATTCCTA | 79931 |
| rs921551 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189820 | GCAACAACAGAGCCC[A/G]GGTTTATAAGAAACA | 79931 |
| rs959268 | snp | A/C | 0.210909 | 0.246925 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153308 | TGGACATGAGCAAAA[A/C]TACAGCATTCTTGGC | 79931 |
| rs998327 | snp | C/T | 0.304937 | 0.243889 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162957 | CAAAAAGCACACTGT[C/T]TCATTGTTCCACATC | 79931 |
| rs1014556 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152543 | TACCAAACATATTAT[A/G]TACTAGCTAATTAAA | 79931 |
| rs1031413 | snp | A/G | 0.210301 | 0.246828 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174798 | AAATGTAATAAAAAC[A/G]CTTTTTACTTTATTT | 79931 |
| rs1397640 | snp | A/G | 0.498632 | 0.0261223 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177120 | CAGGATGCTTGAAAT[A/G]TATTTCTTGGATAAA | 79931 |
| rs1452498 | snp | A/C | 0.382279 | 0.212137 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220493 | AGGGCAAATACAAAA[A/C]AAAAGTAGTTAATTA | 79931 |
| rs1452500 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205237 | agtgaaggaggtgta[G/T]tatgggccatgtggc | 79931 |
| rs1470821 | snp | A/G | 0.370162 | 0.219229 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177796 | AGCATTCTGCAGAAA[A/G]AAACCCTATATTTAA | 79931 |
| rs1511093 | snp | C/T | 0.109814 | 0.206997 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133532 | ATACCTAGGGAGAGG[C/T]ATCATTAGTGGATTT | 79931 |
| rs1562988 | snp | C/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152527 | TGGGTCCAGAATTGT[C/T]TACCAAACATATTAT | 79931 |
| rs1597829 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208427 | gcccccacccaggaa[A/C]tgactcagcacaaga | 79931 |
| rs1858291 | snp | C/T | 0.41507 | 0.187755 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134801 | TGGCTGGAGGAGGGC[C/T]AGAGCAGAGTCCTCT | 79931 |
| rs1877167 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178380 | AGTGTTTGCCGGAGG[A/G]TCAGAGTCCTTTCAC | 79931 |
| rs2044970 | snp | C/T | 0.153665 | 0.230694 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227632 | GTATTTTCACATAGG[C/T]TGTGAATCTTTTATC | 79931 |
| rs2136941 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184524 | TCTCTCCATCTCTCA[A/G]CTCCGCATTTCTCTA | 79931 |
| rs2136942 | snp | A/C | 0.409552 | 0.192466 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184500 | TTCTCTACCCATATG[A/C]TTCATTCTCAGCTCA | 79931 |
| rs2136943 | snp | A/G | 0.420733 | 0.18262 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184485 | ATTCATTCTCAGCTC[A/G]CTCCAGACACAGAGG | 79931 |
| rs2136945 | snp | G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152880 | CCAACTCCTCCATTA[G/T]GCACCAGAAGCACAG | 79931 |
| rs2198315 | snp | A/T | 0.412249 | 0.190198 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173694 | tttcagtgagccaag[A/T]tctcaccattgcgct | 79931 |
| rs2198316 | snp | A/T | 0.0752113 | 0.178743 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173518 | GAGAAAATAATTTTT[A/T]AAAAAAAACTCAAAC | 79931 |
| rs2198317 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169362 | GACTCAATAAACAGA[A/T]GTCACTTACACCATT | 79931 |
| rs2218959 | snp | A/C | 0.411914 | 0.190483 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169145 | AGTTCTGCTTTCACT[A/C]TGAGTGACATGGGAA | 79931 |
| rs3028475 | in-del | -/GT/GTGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181656 | TGTGTGTGTGTGTGT[-/GT/GTGT]AAAACACAGAGGTAT | 79931 |
| rs3817171 | snp | C/T | 0.304188 | 0.244057 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142580 | CCATCAACGGATAGA[C/T]AGTGCTTAGGCACCA | 79931 |
| rs3899636 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207976 | tgaggtagtaaatac[G/T]tctcctgaaatctga | 79931 |
| rs4455437 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215608 | TCCTTCTATTTTTCC[A/G]TCTTTCTCCTGTTTC | 79931 |
| rs4513592 | snp | C/T | 0.499527 | 0.0153681 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222966 | GCCCACCACCACGCC[C/T]GCCTAATTTTTAGTA | 79931 |
| rs4833203 | snp | A/G | 0.498734 | 0.0251279 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195236 | CTTTGAGTAACCCCC[A/G]TACACCTTCAAAATC | 79931 |
| rs4833204 | snp | C/T | 0.499515 | 0.0155675 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224223 | CAAAAATTAGCTGAA[C/T]GTGGTGGTGGGCGCC | 79931 |
| rs4833205 | snp | C/T | 0.461481 | 0.133325 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224317 | GCAGTGAGCAGAGAT[C/T]GTGCTACTGCACTTT | 79931 |
| rs4833206 | snp | A/T | 0.289424 | 0.246872 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224369 | CTCTGTCTCAAAAAA[A/T]AAAAAGAAAAAAGAA | 79931 |
| rs4833706 | snp | A/G | 0.473359 | 0.112298 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143905 | CATGACAGCATATAC[A/G]TGTGGGCCATTCTAA | 79931 |
| rs4833708 | snp | C/T | 0.487113 | 0.0792303 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224208 | TCTCTACTAAAAGTA[C/T]AAAAATTAGCTGAAT | 79931 |
| rs6534254 | snp | A/C | 0.368324 | 0.220226 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164839 | TTAAGTCTGTCTTTT[A/C]TATAAATCAAGTCCA | 79931 |
| rs6534255 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208361 | agaccctgaactcaa[C/T]gtgtcggctggagcc | 79931 |
| rs6534256 | snp | A/C/G | 0.0995577 | 0.199816 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208386 | ggagccacccagatc[A/C/G]ataaactgattcatc | 79931 |
| rs6811411 | snp | C/T | 0.309154 | 0.242901 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197603 | tttaaattttttaGA[C/T]aaaaatGAAGAATCG | 79931 |
| rs6812399 | snp | A/G | 0.37138 | 0.218556 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201026 | CTGTGTGCTGGGGAA[A/G]AGAGTAGGAGTTGAA | 79931 |
| rs6812515 | snp | A/C | 0.337614 | 0.234145 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201300 | CAAGGACGTTCTATG[A/C]AAGATGGCGTGTGGT | 79931 |
| rs6814480 | snp | C/T | 0.307423 | 0.243316 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175085 | CAACTCTTATGAACA[C/T]GTTATTTATGGTACC | 79931 |
| rs6817294 | snp | A/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170497 | CCGTGTATTTTCTTT[A/T]TATTCATTTTATAGG | 79931 |
| rs6820363 | snp | C/G | 0.366266 | 0.221319 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161780 | TGAATAAAGTCACTA[C/G]GTTACTAGTTTAGAT | 79931 |
| rs6820783 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154743 | GAGATGATATTGTAG[A/G]AATTCTGATATATCA | 79931 |
| rs6821331 | snp | A/G | 0.366266 | 0.221319 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162273 | TTTGTTTATGTTTCA[A/G]CATTTTAGGGTTTGA | 79931 |
| rs6825601 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195843 | TAGTAAGAACAAGGA[C/T]CAGCAGGGAGTGAAG | 79931 |
| rs6833114 | snp | A/C | 0.318174 | 0.240525 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139453 | GCTTTACCTGCCCAC[A/C]AAGCAGGTCTGTCTT | 79931 |
| rs6834599 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157025 | AACGGTAGGTTTTCT[A/G]CAGGAAATCCCCCCG | 79931 |
| rs6835076 | snp | C/T | 0.289942 | 0.246789 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222193 | AATATTAGTGAATTT[C/T]TTCCCCTGCGAAGAG | 79931 |
| rs6835704 | snp | C/T | 0.469346 | 0.119947 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222509 | ACAAAGTAAGGATAA[C/T]ACTTCCCTTCTTCAA | 79931 |
| rs6835790 | snp | C/G | 0.304688 | 0.243945 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157361 | AGGACGTCCCCTAAG[C/G]AGAGGTTCTAGCTCC | 79931 |
| rs6836120 | snp | C/T | 0.469247 | 0.120128 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222699 | AGCCTGTAGAGAAAG[C/T]GATTTTTATGGGACA | 79931 |
| rs6837332 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152116 | GTATGTTAATTACAA[A/G]GCTGACATATTACAA | 79931 |
| rs6837539 | snp | A/C | 0.118933 | 0.212888 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145184 | AAGGTAATGTCAGTT[A/C]TTTTTAAAATATCAT | 79931 |
| rs6837596 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210270 | TTACATAGAGATAAA[A/G]TAAGTCCTTGTTTTC | 79931 |
| rs6838000 | snp | A/G | 0.216048 | 0.247684 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175587 | CAAAAGACAATCTGC[A/G]TCTCCCAGTTTTCTG | 79931 |
| rs6839386 | snp | A/C | 0.368529 | 0.220116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170297 | AGAGTATTACAATAC[A/C]TTTTTATTGAATGAG | 79931 |
| rs6839726 | snp | C/T | 0.326035 | 0.238157 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140288 | gcagtgagccaagat[C/T]gcaccactgcactac | 79931 |
| rs6840309 | snp | C/G | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170486 | CTGGCCTGTTTCCGT[C/G]TATTTTCTTTTTATT | 79931 |
| rs6842037 | snp | A/G | 0.499515 | 0.0155675 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223095 | CAGGCGCAAGCCACC[A/G]CGCCCAGCCAGGTGT | 79931 |
| rs6845343 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170795 | TGTTTTATGTAGCTA[A/G]TTCTTTCTTTGCTCG | 79931 |
| rs6845524 | snp | C/T | 0.466927 | 0.124269 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225359 | GATATTTAATCTTGG[C/T]CATGTTTTCAAATAT | 79931 |
| rs6846458 | snp | G/T | 0.351418 | 0.228505 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133715 | AAGATAGGTCTTTAG[G/T]TTCTTGAAGGGAAGG | 79931 |
| rs6846553 | snp | C/T | 0.471483 | 0.115954 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132068 | ACTTATTTAATTTAA[C/T]GAGGTATATACACCT | 79931 |
| rs6847595 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199523 | GGAGGAGGAAGTGAC[A/G]CCTGGGAACCATTGA | 79931 |
| rs6847834 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199652 | AAGAATAGTGTGTGC[A/G]CCAAGCTTCAACAGC | 79931 |
| rs6847971 | snp | A/G | 0.100944 | 0.200705 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199500 | TTATGAGCAGGGATC[A/G]ATGAATGGGAGGAGG | 79931 |
| rs6848563 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159093 | actaaaaatacaaaa[C/T]ttagccggacgtggt | 79931 |
| rs6851067 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204880 | CTAGGTGTTATTGGT[A/G]TATTTGCCAACCAAA | 79931 |
| rs6851990 | snp | C/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226174 | CAAAAAAGAGAGAAA[C/T]AGACAAAGGGGGACA | 79931 |
| rs6852366 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147450 | AGACATAAATTATAA[C/G]TTGAATGCAAAAAAG | 79931 |
| rs6855628 | snp | C/T | 0.422158 | 0.181278 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151050 | CATTATGTTTGGTAA[C/T]ATCATATGAAAGACA | 79931 |
| rs6856825 | snp | G/T | 0.303438 | 0.244222 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144402 | TAAAGCGTTTTTTTG[G/T]TTTTTTCTTTTCTTT | 79931 |
| rs7356195 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167335 | TAGAGACAATAAAGC[C/T]TGTAAGAATTCAGAG | 79931 |
| rs7436617 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121208125 | caatctcagatatgt[C/G]tttatcagcagcatg | 79931 |
| rs7661427 | snp | A/G | 0.479014 | 0.100263 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166986 | AGGTCTCTAAGGCTC[A/G]ATTTCCATTTTATAC | 79931 |
| rs7663440 | snp | G/T | 0.188082 | 0.242211 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216507 | ACATGGAATCTAAAA[G/T]AAAAAAATATGAAGG | 79931 |
| rs7680038 | snp | C/G | 0.397813 | 0.201621 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210147 | GAACTTTTGCTATCA[C/G]CTTTGCTCAAAAGGG | 79931 |
| rs7682759 | snp | A/T | 0.084728 | 0.187577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154266 | CACCCACTTGCTTTA[A/T]GTGGTTCTTCAAACT | 79931 |
| rs7684167 | snp | A/G | 0.409212 | 0.192748 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185887 | AGGTACTGACTTTTC[A/G]CAGAAATAATCACAT | 79931 |
| rs7684168 | snp | A/G | 0.388587 | 0.208071 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185889 | GTACTGACTTTTCAC[A/G]GAAATAATCACATGC | 79931 |
| rs7684215 | snp | C/T | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193048 | TATATATATGTAGAA[C/T]TACCCTATACATAAT | 79931 |
| rs7684241 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193086 | GATCATGATTTGATT[C/T]AGAATGTTTCGTATC | 79931 |
| rs7684464 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193225 | GTCATATGTAAGCTC[A/G]TTTTTATAAAAAATT | 79931 |
| rs7684586 | snp | A/G | 0.100231 | 0.200173 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193092 | GATTTGATTCAGAAT[A/G]TTTCGTATCATCTCT | 79931 |
| rs7687870 | snp | A/G | 0.215144 | 0.247558 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204345 | tcttatctacctatg[A/G]tctggaagctcccta | 79931 |
| rs7693320 | snp | A/G | 0.154993 | 0.231244 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212078 | TCCCAAACACTTTCT[A/G]GCATACAGTAATAGC | 79931 |
| rs9284633 | snp | A/G | 0.420255 | 0.183066 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180317 | aggcaggagaatggc[A/G]tgaactcaggaggcg | 79931 |
| rs9307490 | snp | G/T | 0.409552 | 0.192466 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178400 | CGGCAAACACTGGAA[G/T]TGCAAGCTAAAGTTG | 79931 |
| rs9685224 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208854 | gttatgctaatgaag[G/T]ctgtcagggtggaat | 79931 |
| rs9784553 | snp | A/G | 0.10237 | 0.201756 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179102 | TGGGCAAAGAAGCAA[A/G]GATTTCCAGAAAGAG | 79931 |
| rs9985644 | snp | A/G | 0.206336 | 0.246157 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218891 | TTTCTGAGAACCAAA[A/G]GATTTACAATTAAAA | 79931 |
| rs9985938 | snp | C/T | 0.195214 | 0.243923 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121218659 | ctctttcttttgaga[C/T]gatgtctcactatat | 79931 |
| rs9992473 | snp | G/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179709 | GTGAATGGTGCCACC[G/T]GAGTGGTGCAGCATG | 79931 |
| rs9992960 | snp | A/C | 0.420255 | 0.183066 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183336 | AGCTACTTGCCACCA[A/C]ATGGAAATAATATAT | 79931 |
| rs9992978 | snp | A/C | 0.084364 | 0.187256 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203813 | TGCTTCCTTCAGTTC[A/C]ACTCTACTCTGATAA | 79931 |
| rs9993163 | snp | C/T | 0.420255 | 0.183066 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183561 | CCACACAGCAGGAAG[C/T]GAGAGGCAGGCAAGT | 79931 |
| rs9995558 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150477 | GATATTGGACCCTCC[A/T]CCTCCACCTAGCCAA | 79931 |
| rs9998339 | snp | A/T | 0.420255 | 0.183066 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181163 | AGGAGGACCAAGAAG[A/T]CGAATGAACAGAATT | 79931 |
| rs10000692 | snp | C/T | 5.34383e-05 | 0.00516878 | missense | TNIP3 | GRCh38.p7 | 4:121157162 | TCTGCCTGTCGTCCT[C/T]TCTCTGCCTCTGATG | 79931 |
| rs10004021 | snp | G/T | 0.108755 | 0.206276 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158376 | AACTTTGTGTATTTG[G/T]GGCTTCTAGTGACAA | 79931 |
| rs10004221 | snp | G/T | 0.419616 | 0.183658 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202423 | tcaactcaagatgga[G/T]caaagacttaaatat | 79931 |
| rs10004623 | snp | A/G | 0.24134 | 0.24985 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219946 | CTTTACTAAATTAAC[A/G]TTAAATGTTAACCAG | 79931 |
| rs10007399 | snp | G/T | 0.418007 | 0.185132 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168520 | TTttttcttttcttt[G/T]ctttttttttttttt | 79931 |
| rs10009822 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200543 | ACCCCCGAGCACACA[C/T]ACCCTGACCAGTGGG | 79931 |
| rs10015340 | snp | A/G | 0.420096 | 0.183214 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175760 | CCACTTCTGTCCTGT[A/G]TAGAAATTTCTGCCC | 79931 |
| rs10017221 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199671 | AGCTTCAACAGCCTG[A/C]GAAGAATGGCCTGGA | 79931 |
| rs10021787 | snp | C/G | 0.0850919 | 0.187897 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148021 | GAAGGGAAACTACAT[C/G]CAGCCACATTGACAT | 79931 |
| rs10024729 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145669 | tattaaaaattgttt[A/T]aaaattaaaGTTGTT | 79931 |
| rs10030846 | snp | C/G | 0.126564 | 0.217402 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156689 | TGAAAAGCTACTGCA[C/G]AAATACAAGGTATTG | 79931 |
| rs10446733 | snp | A/T | 0.309648 | 0.24278 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178611 | CAGCAGTCAATAACT[A/T]CATGACACCAGGATG | 79931 |
| rs10454795 | snp | A/G | 0.308166 | 0.243139 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191709 | CTAATAATTTTCCCT[A/G]GTATCTCATTGTTAT | 79931 |
| rs10518383 | snp | C/G | 0.318174 | 0.240525 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138265 | CATCTGTCTAGCAAA[C/G]TCAACCTGGAATAGT | 79931 |
| rs10518384 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178365 | CTGAACAACGACAAA[C/G]TGAAAGGACTCTGAC | 79931 |
| rs10518385 | snp | C/T | 0.406814 | 0.194704 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221069 | GTTTACTGTTAGCAA[C/T]TCTCATGGCCTTTTG | 79931 |
| rs10531225 | in-del | -/AACA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200642 | AAGAGAACTGTTGCA[-/AACA]CTTAATGCCAAAGCT | 79931 |
| rs10561132 | in-del | -/ACACACAC | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132214 | TTTTTACCCCAGGAA[-/ACACACAC]ACACACACACACACA | 79931 |
| rs10672885 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160477 | TCTCAAAAAAAAAAA[-/AA]AGAAGGAATTACAAA | 79931 |
| rs11098601 | snp | A/T | 0.408188 | 0.193589 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131485 | AATTAATCAAATCCA[A/T]GGGAAGGAAAAACAC | 79931 |
| rs11098602 | snp | A/G | 0.408188 | 0.193589 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131486 | ATTAATCAAATCCAA[A/G]GGAAGGAAAAACACA | 79931 |
| rs11098604 | snp | A/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152604 | AAGAACTTACTCTGA[A/G]CAAAGTCCTGTTCTA | 79931 |
| rs11098605 | snp | G/T | 0.217851 | 0.247924 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152984 | GACATTATATATACA[G/T]TAGATAGTAATAAAT | 79931 |
| rs11281118 | in-del | -/AGAAAC | 0.444799 | 0.156695 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226168 | CAAGACAAAAAAGAG[-/AGAAAC]AGAAATAGACAAAGG | 79931 |
| rs11288825 | in-del | -/A | 0.289942 | 0.246789 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223618 | GAAACTAGAAAAGGT[-/A]AAAATGCCTCATTAT | 79931 |
| rs11302369 | snp | C/T | 0.39551 | 0.20329 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161847 | CTTTCTTTTCAGTTA[C/T]TTTTTTCAGGAGTGA | 79931 |
| rs11338982 | in-del | -/A | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136878 | AAAAAAAAAAAAAAA[-/A]GCTTAGGTTGGTACA | 79931 |
| rs11344644 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160184 | CACAGAATGAATTAG[-/A]AAAGGAATTACAGGC | 79931 |
| rs11399717 | in-del | -/T | 0.41141 | 0.19091 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161326 | TCCTGTTGCGATTTA[-/T]AAAAATACCTGATTC | 79931 |
| rs11729830 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140289 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTACA | 79931 |
| rs11730435 | snp | A/C | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183210 | ACTTAAGTGAAGTCA[A/C]ACTGAAACATCGGCA | 79931 |
| rs11737150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221894 | TCTACAGCTCAATCA[C/T]ATCAGAACACCTGCA | 79931 |
| rs11938699 | snp | C/T | 0.101658 | 0.201233 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175487 | CTGCTCCCTTGCCCA[C/T]CCCATTGACCCAAAT | 79931 |
| rs11947841 | snp | G/T | 0.368529 | 0.220116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173529 | TTTTTAAAAATTATT[G/T]TCTCTGGAAGGAAAT | 79931 |
| rs12507932 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212481 | CTTTGATGTTTATTA[C/G]TTTGAAGACATGTAA | 79931 |
| rs12511821 | snp | C/T | 0.293551 | 0.246177 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221206 | ATTTTTAGTATAAAA[C/T]CTTGGTTATGTTTTT | 79931 |
| rs12639692 | snp | C/T | 0.142609 | 0.225759 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227846 | CACATAGGTCACACA[C/T]TCATTTCTAGGAATG | 79931 |
| rs12640705 | snp | C/T | 0.134119 | 0.221521 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229515 | gagaattgcttgaac[C/T]tgggaggtggaggtt | 79931 |
| rs12648211 | snp | C/T | 0.1652 | 0.235179 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139259 | TCATATAGTTTAGTC[C/T]ACAGAGACAAGATTT | 79931 |
| rs12649636 | snp | G/T | 0.123452 | 0.215605 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220371 | CACATGTGTCTTCTG[G/T]CCCACAATAAATCCT | 79931 |
| rs13101385 | snp | C/T | 0.309401 | 0.24284 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194388 | GATTTGATCTTAAAA[C/T]TATCTTTTGCTCAAT | 79931 |
| rs13102428 | snp | C/T | 0.307919 | 0.243198 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170394 | AACACACAATGACCA[C/T]GGGGATACACAAAGT | 79931 |
| rs13103433 | snp | C/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131602 | AGGACTTTGTCTTCC[C/T]ttttttttttttttt | 79931 |
| rs13104663 | snp | A/G | 0.345704 | 0.230956 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215956 | TGAAAGATTGATAGA[A/G]TGTGGAAAGCGCCTA | 79931 |
| rs13104875 | snp | C/T | 0.411242 | 0.191052 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215966 | ATAGAGTGTGGAAAG[C/T]GCCTAAGTAAGGGAT | 79931 |
| rs13106084 | snp | A/G | 0.190833 | 0.242898 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182936 | AACTCTAATCTCATT[A/G]TGTTTTCATTAGTCC | 79931 |
| rs13106137 | snp | G/T | 0.309401 | 0.24284 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186229 | TGGTGACCAGACGTG[G/T]GGGGGTTTGGTCACA | 79931 |
| rs13107912 | snp | A/G | 0.370365 | 0.219117 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176254 | GCCATAAGGTGCAGC[A/G]GCTGAGCTGACAGGC | 79931 |
| rs13108214 | snp | A/G | 0.309401 | 0.24284 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204024 | taACTCTGCTATTTG[A/G]TTATTTTGCATTTAT | 79931 |
| rs13108739 | snp | C/G | 0.317451 | 0.240729 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140741 | TGTTATTGGTAAAGA[C/G]TGAAAAGTAAGCAAA | 79931 |
| rs13109100 | snp | C/G | 0.191775 | 0.243125 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204460 | tgtatacaatcaaac[C/G]gtgcgctgaccacct | 79931 |
| rs13110041 | snp | G/T | 0.239326 | 0.249772 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141186 | AAAAAGTAGAGGAGG[G/T]TAGGTGGAATACTGC | 79931 |
| rs13112211 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159284 | gaaaagaaaagaaaa[A/C]CCAGTAAGTCTCAGG | 79931 |
| rs13112459 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121159352 | CTTTTAACTTTTTTT[A/T]GTTATTTGGATTTTC | 79931 |
| rs13112923 | snp | C/G | 0.409212 | 0.192748 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217100 | TTTCACTTAAGTTTG[C/G]TGCAACTTAAGCACC | 79931 |
| rs13115256 | snp | A/G | 0.346368 | 0.23068 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205166 | gagatgggaattgca[A/G]ttttaaatggagtga | 79931 |
| rs13116723 | snp | G/T | 0.221737 | 0.248397 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205569 | ggaagcatatgtaaa[G/T]gtactgagacagttt | 79931 |
| rs13116936 | snp | G/T | 0.346147 | 0.230772 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205653 | gtagtgagggatgtg[G/T]aaagaaaaggtggga | 79931 |
| rs13118027 | snp | C/T | 0.369958 | 0.21934 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183950 | acagtgcacaatcaa[C/T]gtaatgtgcttgaaa | 79931 |
| rs13123960 | snp | A/C | 0.308166 | 0.243139 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173090 | GAACCCATATCAGAG[A/C]TCATTTAGTCTTCCT | 79931 |
| rs13124511 | snp | A/G | 0.368529 | 0.220116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173199 | CATTTACCAATGATG[A/G]AAAAGCATCGCAGGA | 79931 |
| rs13124522 | snp | A/G | 0.306927 | 0.243432 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173213 | GGAAAAGCATCGCAG[A/G]AGCCTAAGTCATTAG | 79931 |
| rs13125962 | snp | A/G | 0.318656 | 0.240388 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224605 | TTATTGTTTTCACCC[A/G]TATTTAGGCAGGTTT | 79931 |
| rs13126929 | snp | C/G | 0.315516 | 0.241263 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153961 | TGAACTAGTTAGCGA[C/G]CCATTCCTCCAAAAC | 79931 |
| rs13127072 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131201 | atatatatgtatata[C/T]atataaatgtataat | 79931 |
| rs13127436 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131194 | tatatatatatatat[A/G]tatatacatataaat | 79931 |
| rs13128962 | snp | C/T | 0.412082 | 0.190341 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169860 | CTCTGAAACAATGCT[C/T]CTATGCGATATAGCG | 79931 |
| rs13129000 | snp | C/T | 0.412082 | 0.190341 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169904 | TCTGTCTTGATTATA[C/T]ACTTTTAGTTTTTAG | 79931 |
| rs13129293 | snp | A/G | 0.309648 | 0.24278 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179008 | AGGGGGCTGAGTAAC[A/G]CCATGTGGGACTAGA | 79931 |
| rs13129450 | snp | G/T | 0.47802 | 0.102502 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170078 | AGTTCCTCTGTGAAG[G/T]CTCCCCTGGTCTTCC | 79931 |
| rs13133184 | snp | C/T | 0.31014 | 0.242659 | intron-variant | TNIP3 | GRCh38.p7 | 4:121216295 | CTTTTCTATTCTATA[C/T]AGCTCCATTCAGACA | 79931 |
| rs13133221 | snp | A/G | 0.303187 | 0.244277 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202648 | gtaaacagacaaccc[A/G]gagtgggagaaaatc | 79931 |
| rs13133584 | snp | A/T | 0.366473 | 0.221211 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161957 | TAAATAAAGGACTGG[A/T]TCCTCTATAATAATT | 79931 |
| rs13133740 | snp | A/G | 0.475437 | 0.108066 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195637 | GTTTGGAATAAAATT[A/G]TTTGTTGTTCTTCAT | 79931 |
| rs13135784 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149768 | gagactctgtctcaa[A/G]aacaaaaacaaaaaC | 79931 |
| rs13137539 | snp | A/C | 0.303688 | 0.244167 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150482 | TGGACCCTCCTCCTC[A/C]ACCTAGCCAACTATG | 79931 |
| rs13138203 | snp | A/T | 0.317692 | 0.240661 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141630 | ATTCGTATCTATGTG[A/T]CCTATGGATTCAGTG | 79931 |
| rs13139777 | snp | A/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159295 | aaaaACCAGTAAGTC[A/T]CAGGTATATCTTGAC | 79931 |
| rs13143534 | snp | C/T | 0.347253 | 0.230308 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205563 | ctgtagggaagcata[C/T]gtaaaggtactgaga | 79931 |
| rs13150702 | snp | A/C | 0.303688 | 0.244167 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151961 | CACGAGCTGAGTAGC[A/C]TTAGGTAATTGTTTT | 79931 |
| rs13151913 | snp | C/G | 0.409382 | 0.192607 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121182458 | CCTGGACACTTTAAA[C/G]TGGAAAGTGCCAGCA | 79931 |
| rs13152159 | snp | G/T | 0.409041 | 0.192888 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182581 | AAGTACATGACTGAC[G/T]GTAAATGACTTGGGG | 79931 |
| rs13152687 | snp | C/T | 0.307176 | 0.243374 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169748 | ACCTCTCTTTGATCC[C/T]CCAAACCTGGTTTTG | 79931 |
| rs17051294 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144209 | AGTTTTCGTTTTCTC[A/G]CAGCATATAGCAGAA | 79931 |
| rs17051295 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148471 | GTGTACCTTATATGC[A/G]AGTTCCGAAGATGTC | 79931 |
| rs17051296 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149231 | GTCCACTTGGCAATA[A/G]CGCGTGAGGTTAGGT | 79931 |
| rs17051297 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154378 | AAGCCTCCTTAGCCA[A/C]GTATGACTGAAAGCT | 79931 |
| rs17051298 | snp | C/T | 0.183739 | 0.241059 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121154584 | TTCACATTCGTAATG[C/T]TCCTTTTCCTTGTTC | 79931 |
| rs17051299 | snp | A/C | 0.0597298 | 0.162164 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157260 | TGAGGAGGTCGTTCA[A/C]AGACAGCTGCAGATA | 79931 |
| rs17051300 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157828 | GTCTTCACACACCTG[A/C]AAGCCGTTCGAGAAA | 79931 |
| rs17051301 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158562 | CTTAGCACCCTTCCC[A/G]TCATTTTCCAACAGT | 79931 |
| rs17051302 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162956 | AGATGTGGAACAATG[A/C]GACAGTGTGCTTTTT | 79931 |
| rs17051303 | snp | C/T | 0.046775 | 0.145601 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163202 | ACTAGGAATGGCATG[C/T]AAGTCACAAATGTAT | 79931 |
| rs17051304 | snp | A/G | 0.0460142 | 0.144533 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164240 | AAAACACACATCACC[A/G]TTAACTCATAATAGA | 79931 |
| rs17051305 | snp | C/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169629 | AATTGCCTTCCTTAC[C/T]CCAAAACAAATGTAT | 79931 |
| rs17051306 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174131 | TGCCAAGGGGTTGTC[C/T]AGATTAGCTTGGATA | 79931 |
| rs17051307 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175620 | ACTCTTTCTTTTGTG[A/G]AACATGGGACAAATT | 79931 |
| rs17051308 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184434 | CTGATTGGACCAAGA[A/G]TAAACAATTGATCCC | 79931 |
| rs17051309 | snp | A/C | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184988 | ACTAGTCTAAATGTT[A/C]AGCTCTTGAGGCAGC | 79931 |
| rs17051310 | snp | A/G | 0.16028 | 0.233346 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185138 | GATAAAACTCATCAC[A/G]ATCTACAAGTCCTCA | 79931 |
| rs17051311 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186716 | CTGAGGGTGTGGAAT[A/C]GTTACCAAACATTCT | 79931 |
| rs17051312 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186864 | AATAAATGAGAATTA[C/T]GTCACCTACTTGGGC | 79931 |
| rs17051313 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187750 | TTTGACCAAAGTCCA[A/T]GGATGGGATTCAATC | 79931 |
| rs17051314 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187831 | AAGATAGGGTCTCTA[A/G]CAAGTTCTGGACCTC | 79931 |
| rs17051315 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189831 | AACCTGGGCTCTGTT[A/G]TTGCCCTCAATCTGC | 79931 |
| rs17051316 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191394 | AAGAGAACAAAGTTA[A/T]CCTAGCTACACATGC | 79931 |
| rs17051317 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194231 | TCACAAAGCAGACTT[A/T]AAACTTTCAGTGGTA | 79931 |
| rs17051318 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195560 | ATCGAATTCAGATGG[C/G]AATTAACAAGGGTCA | 79931 |
| rs17051319 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197118 | CTATTTATCAGTGCA[A/G]TATAAAAGTTGTACT | 79931 |
| rs17051320 | snp | A/G | 0.308908 | 0.242961 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198126 | TTCTTAAGGACCTTG[A/G]CTAGGAGAAGTTTCA | 79931 |
| rs17051321 | snp | C/T | 0.309154 | 0.242901 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198294 | AAAGTAGCACATGAC[C/T]TTCATTGTAAAGAAT | 79931 |
| rs17368488 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159440 | TCTGTAAGATTTCTT[A/T]ATGCATGGAGGTTCT | 79931 |
| rs17434881 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185646 | TAATTATTAACTCAA[A/G]TCTAACCAATAAATT | 79931 |
| rs17435444 | snp | A/G | 0.112631 | 0.208878 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200339 | TATTTACAGTCCAAG[A/G]TTTCTCAAAAACTTT | 79931 |
| rs28380115 | snp | C/T | 0.127254 | 0.217792 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153018 | AAGGAAAAATTAAAC[C/T]GGGAAATACCAGTAG | 79931 |
| rs28432367 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131178 | CATTTCTTGTTATAT[A/G]TATATATATATATAT | 79931 |
| rs28452005 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176818 | AAGTATATATTAATC[C/T]CTGAACCAACCAAAG | 79931 |
| rs28452943 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213853 | TCAAAAAAAGGATGA[A/C]CCCAGGATCATACAT | 79931 |
| rs28465139 | snp | A/G | 0.127944 | 0.218179 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148478 | TTATATGCGAGTTCC[A/G]AAGATGTCAAGTGTT | 79931 |
| rs28513714 | snp | A/G | 0.369958 | 0.21934 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184549 | GAGAGAGTCCTGACA[A/G]TTTTCTGGTTTAGAA | 79931 |
| rs28525244 | snp | C/G | 0.109814 | 0.206997 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132799 | ATAAGCTCCCCACAA[C/G]TTTACACTGAGAAAT | 79931 |
| rs28530598 | snp | A/G | 0.370365 | 0.219117 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176383 | TTTTTTTTCTAGCAG[A/G]AAAAAATAGATCAAA | 79931 |
| rs28562240 | snp | A/T | 0.118933 | 0.212888 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146028 | TATACTCTTTTTTTT[A/T]ACCAAGAGTAATCAG | 79931 |
| rs28567402 | snp | C/G | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180731 | ACAGGAACCCCCACA[C/G]TGTTAAGTGATTGGT | 79931 |
| rs28572759 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214509 | TCAGAATTCTCCATG[C/T]AGAAGGAAATGGCTT | 79931 |
| rs28600934 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210859 | TAGGAGTTCAACATA[C/T]GAATTTAGGGGGACA | 79931 |
| rs28648448 | snp | C/T | 0.154993 | 0.231244 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211423 | ACAAGGGATGAAAAC[C/T]CAACTCACTGAGGAT | 79931 |
| rs28669888 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214140 | TATTCTCTTCCTGTC[A/C]TGTTGGCTCTCGCCT | 79931 |
| rs28707603 | snp | C/T | 0.101301 | 0.200969 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191099 | TTGTTTTTGTTGTTG[C/T]TGTTGTTATTTTAGT | 79931 |
| rs28733524 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121200756 | TTATTTTTGTTTTAA[A/T]TTCCTCAGAGAGCTT | 79931 |
| rs33953894 | in-del | -/AGAAAC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121226169 | AAGACAAAAAAGAGA[-/AGAAAC]GAAATAGACAAAGGG | 79931 |
| rs34017482 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205274 | GGAAAGAGCATTCCC[-/C]TGTAAAGGTAGCCAG | 79931 |
| rs34050109 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218155 | AACTAACCTACAAAA[-/A]TTTTTACATTACAGA | 79931 |
| rs34117851 | snp | A/G | 0.16911 | 0.236552 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191255 | TATGAACAAGGCTGA[A/G]CCCCTATATTTAGGT | 79931 |
| rs34136611 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141479 | CATTTTTCTTGTTTT[-/T]GCCATATCCACTTTC | 79931 |
| rs34141533 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177799 | ATATAGGGTTTTTTT[-/T]CTGCAGAATGCTATT | 79931 |
| rs34166132 | snp | A/G | 0.00190993 | 0.0308435 | missense | TNIP3 | GRCh38.p7 | 4:121147114 | GAGAGACTTAATCAA[A/G]AGAAAGAGGAGCTAC | 79931 |
| rs34236581 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131005 | GTATCCAGATACTGG[-/G]AATAATAATAATTTG | 79931 |
| rs34237623 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121211183 | GTCTTGGAAAGAGGG[-/G]TGATGTGTGATTTAA | 79931 |
| rs34262162 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121202583 | TTTAGTTTAATTAGA[C/T]CCCATTTGTCAATTT | 79931 |
| rs34263702 | in-del | -/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121227756 | CTGCCCACTTAATGG[-/G]AAAAGTTAGATCAGC | 79931 |
| rs34399214 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224382 | ATAAAAAGAAAAAAG[-/G]AAAAAAGAAAAAGAA | 79931 |
| rs34452968 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184104 | AAACAACTCACAAGG[-/G]AAAAATGCATTAATT | 79931 |
| rs34477589 | in-del | -/AAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213738 | CTCAAAAAAAAAAAA[-/AAA]AACAAAAAAAGACAT | 79931 |
| rs34511503 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168806 | CTTTTAATAACTTTT[-/T]CAAAATGAGGACTTT | 79931 |
| rs34534171 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182694 | CAGAGAACATAGATT[-/T]CTGTGAGTTGGCATG | 79931 |
| rs34556861 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174773 | TGCCTCACTCTCCCC[-/C]ACAAGTACAAAATAA | 79931 |
| rs34604982 | in-del | -/C | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132594 | CTCAGCCACGCTCCC[-/C]TCGTTGCCTGTTGTC | 79931 |
| rs34762847 | snp | A/T | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167494 | AAGAAACAGAACACA[A/T]CTGGGCAAGCCTAGT | 79931 |
| rs34781512 | in-del | -/C | | | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217552 | AAGCAAATGCCTTTC[-/C]TGGATGACTGGAGGA | 79931 |
| rs34833075 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121190238 | ATATCTTGGCCTTTT[-/T]GCCTGGCGTGTTTAC | 79931 |
| rs34891453 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121175303 | AATACCTTTGGCTTT[-/T]AAGTGTCCATTCAGT | 79931 |
| rs34899973 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183201 | AATTTACTAACTTAA[G/T]TGAAGTCAAACTGAA | 79931 |
| rs34903516 | in-del | -/T | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131484 | AATTAATCAAATCCA[-/T]AGGGAAGGAAAAACA | 79931 |
| rs34936208 | in-del | -/A/AA | 0.335788 | 0.23482 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176658 | TGATTAAAAAAAAAA[-/A/AA]CAGCTTTCAAAAAAA | 79931 |
| rs34984367 | snp | A/C | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183913 | ATTTCATTATATATT[A/C]CAATATAATAATAAT | 79931 |
| rs35009575 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121186070 | CCCTCAGGACCACAA[-/A]CCAAAGAGGGACGGG | 79931 |
| rs35035169 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189354 | GAAAAGGAAGAATTG[-/G]ACAGTAGATTCTTCT | 79931 |
| rs35066674 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121157825 | CTGTCTTCACACACC[-/C]TGCAAGCCGTTCGAG | 79931 |
| rs35185456 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176086 | TGGTGATATTTTGGG[-/G]AAATACAACCTGGCC | 79931 |
| rs35189859 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131046 | AAGTAGCATAATTTT[-/T]GGAAGCTGAAACTGG | 79931 |
| rs35204292 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121135785 | CAACAGATTAAAAGG[-/G]ACCGTTTTAATTAAA | 79931 |
| rs35283394 | snp | A/T | 0.209693 | 0.246729 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227075 | TAGGGTAACATTCAC[A/T]TAGTTAAATGTGTCA | 79931 |
| rs35305244 | in-del | -/A | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188310 | TTGACAATGAAACTT[-/A]AAAAAAAAAACTCTC | 79931 |
| rs35307961 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168536 | TTTTTTTTTTTTTTT[-/T]AAGAGACAGAGTTAT | 79931 |
| rs35389783 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121180985 | CTGCCCTTTGCCTGG[-/A]AAGTGTGAAGTGCAG | 79931 |
| rs35449703 | snp | G/T | 0.314057 | 0.241654 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217665 | ATATTACACAATTCT[G/T]CAAATATGTTGAAGA | 79931 |
| rs35519499 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179916 | GTAGAAAAGCACTCC[-/C]ATGTTTAGTAAGTAC | 79931 |
| rs35546916 | snp | A/G/T | 0.00281591 | 0.0374265 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121147136 | CAAAAAGGAACGATC[A/G/T]GATCGAGAGAGACTT | 79931 |
| rs35581258 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121205892 | GTTCTGCATGGCTGG[-/G]AAAGGCCTCAGAAAA | 79931 |
| rs35594626 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121144392 | AATGTTTTCTAAAGC[-/T]GTTTTTTTGTTTTTT | 79931 |
| rs35599975 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121182928 | TCTCCCAAACTCTAA[-/A]TCTCATTATGTTTTC | 79931 |
| rs35672087 | in-del | -/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161327 | CCTGTTGCGATTTAA[-/T]AAAATACCTGATTCT | 79931 |
| rs35684713 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121132763 | AGGATGGCAAAAAAA[-/A]AAAAAAAGTTATGTT | 79931 |
| rs35703511 | in-del | -/G | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131488 | TAATCAAATCCAAGG[-/G]AAGGAAAAACACAGA | 79931 |
| rs35815979 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195541 | ATTATAACATGTCAA[-/C]ACAATCGAATTCAGA | 79931 |
| rs35858395 | in-del | -/G | | | frameshift-variant | TNIP3 | GRCh38.p7 | 4:121141849 | TGCACAGCTCCAGGG[-/G]CCTGTTGGTACCCAT | 79931 |
| rs35965824 | in-del | -/C | 0.441817 | 0.227347 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194859 | AATAGAAAAAAAAAA[-/C]GTACACACACACACA | 79931 |
| rs35971082 | snp | C/G | 0.304438 | 0.244001 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155210 | CCTCGTGATCTGCCC[C/G]TCTCAGCCTCCCAAA | 79931 |
| rs36011009 | snp | A/G | 0.142012 | 0.225474 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202858 | ATCAGAGAAATGCAA[A/G]TCAAAACCACAATGA | 79931 |
| rs36026700 | in-del | -/TA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203919 | GTGTATATATATATA[-/TA]CTAATACACAAAATA | 79931 |
| rs36070539 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121178350 | CACAGCAGCTAAAAC[C/T]TGAACAACGACAAAG | 79931 |
| rs36087391 | snp | C/T | 0.307423 | 0.243316 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173339 | AACAAATTCCCACCA[C/T]GGCATGCCTAGAGAT | 79931 |
| rs41278073 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121164244 | CACACATCACCGTTA[A/G]CTCATAATAGAAAAT | 79931 |
| rs41413145 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197835 | GAGCCGTATAAGAAA[A/G]TCAAAGTCCTTATCA | 79931 |
| rs55763910 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213741 | CAAAAAAAAAAAAAA[A/C]AAAAAAAGACATTCT | 79931 |
| rs55838274 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121149319 | CACGGGACTAGCTGA[A/G]AAACCTGGTTTCAGT | 79931 |
| rs56067151 | snp | G/T | 0.461037 | 0.134028 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224840 | ATTTTTGAACACCTT[G/T]CTAAGTAAAGAGTTT | 79931 |
| rs56072275 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121179149 | TGATAGCACAGGAAA[C/T]TTCATGGTTTGTTAA | 79931 |
| rs56350847 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121213742 | AAAAAAAAAAAAAAC[A/C]AAAAAAGACATTCTT | 79931 |
| rs56735757 | in-del | -/TAGA/TAGATAGA | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203261 | AGATAGATAGATAGA[-/TAGA/TAGATAGA]AAGATACCATGAAAT | 79931 |
| rs56861192 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163841 | CCCACAGAACTGGAA[A/G]GCTGAAAGGAATTTA | 79931 |
| rs57087658 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197503 | GGCCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 79931 |
| rs57117360 | in-del | -/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181622 | GTAAGTTAATAAGAC[-/G]AGGTGTGTGTGTGTG | 79931 |
| rs57489234 | in-del | -/ACACAA/ACAT/CA | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132251 | CACACACACACACAC[-/ACACAA/ACAT/CA]ATATGCACTTTAAAT | 79931 |
| rs57518169 | in-del | -/CACACACACA | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132243 | ACACACACACACACA[-/CACACACACA]TATGCACTTTAAATC | 79931 |
| rs57634077 | snp | A/T | 0.133777 | 0.221342 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222191 | GAAATATTAGTGAAT[A/T]TCTTCCCCTGCGAAG | 79931 |
| rs58385037 | snp | A/G | 0.121022 | 0.21416 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223697 | AGAAGCCAGAGCTGT[A/G]TCCTTGAACACCTTT | 79931 |
| rs58534056 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203378 | CAAGAATGGAAAAAC[A/C]AACATCATATGTTCT | 79931 |
| rs58983477 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197483 | ATTGCAGTAAGCCGA[A/G]ATCAGGCCACTGCAC | 79931 |
| rs59245086 | snp | C/T | 0.498611 | 0.0263212 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184175 | TTTTTTTGCCTGACT[C/T]ATCATATCTCACCCC | 79931 |
| rs59255247 | in-del | -/GTGT/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181624 | AAGTTAATAAGACAG[-/GTGT/T]GTGTGTGTGTGTGTG | 79931 |
| rs59909239 | snp | C/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121161571 | TCAGGTAAGTTTCAT[C/G]GATATATTTTAGGTA | 79931 |
| rs60033855 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189875 | TCCCTGTTTATTTCC[G/T]CCCTGCTTTTGTGAT | 79931 |
| rs60358563 | snp | A/G | 0.193653 | 0.243567 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221875 | TTTTTGCCACCACAG[A/G]TTCTCTACAGCTCAA | 79931 |
| rs60529029 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181623 | GTAAGTTAATAAGAC[A/T]GGTGTGTGTGTGTGT | 79931 |
| rs60572544 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172979 | ACTTCATAACAGCCC[C/T]GTAAGAAGAGGCAGC | 79931 |
| rs60828360 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197217 | TGGATGTTCTTACAT[A/G/T]AATGCTCTCTTTAAG | 79931 |
| rs61313316 | in-del | -/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221768 | TAACTATTTTTTTTT[-/T]CCACTTCATATTTCT | 79931 |
| rs61344205 | in-del | -/GTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206549 | ATATTGTGTGTGTGT[-/GTGTGTGTGTGTGTGT]TTTATCTTTTCTTTT | 79931 |
| rs61650606 | in-del | -/AA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154982 | TTTTTTTTTTTTAAA[-/AA]GACGAATTCTCACAC | 79931 |
| rs62321465 | snp | G/T | 0.0200698 | 0.0981432 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137987 | CCTCACAAGACCATA[G/T]AAACAAGCAGTAGAA | 79931 |
| rs62321466 | snp | A/G | 0.0186211 | 0.0948911 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144201 | CAAGAACCAGTTTTC[A/G]TTTTCTCACAGCATA | 79931 |
| rs62321468 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167159 | TATGCATCACTCACC[A/C]TGTACTTGACATTGT | 79931 |
| rs62321499 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188029 | TCTTGATTTAAGGGG[G/T]CCTCTTGACTAAATT | 79931 |
| rs62321500 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192222 | AGTTTGCCAATCTCA[A/G]TCGACGCCTGAACTG | 79931 |
| rs62321501 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201944 | ATAGCCCATGCTCGT[A/G]GATGGGTAGAATCAA | 79931 |
| rs62321502 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203262 | AGATAGATAGATAGA[A/T]AGATACCATGAAATA | 79931 |
| rs62321503 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209049 | ATGTCTACTGGGTTC[A/T]GTATGGATATAAATA | 79931 |
| rs62321504 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121210163 | CTTTGCTCAAAAGGG[C/T]AGGTATGAGGTGCCC | 79931 |
| rs62321506 | snp | C/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220222 | AGGCAGTCAGTTAAT[C/T]AAAATATTAGTTAAA | 79931 |
| rs62321508 | snp | A/T | 0.495963 | 0.0447464 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226586 | CAAAGTTCTCAGCAT[A/T]TCACAGCAGGGAGTT | 79931 |
| rs62321509 | snp | A/G | 0.131723 | 0.220251 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228965 | TCAGATCTAACTAAT[A/G]TCTTTCTTTCCTGAA | 79931 |
| rs66460023 | in-del | -/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121194860 | ATAGAAAAAAAAAAG[-/C]TACACACACACACAG | 79931 |
| rs66462643 | in-del | -/GT | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131181 | TCTTGTTATATGTAT[-/GT]ATATATATATATGTA | 79931 |
| rs66470281 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139787 | ATCACCTCTGTTTTT[C/T]ATCTTCTCGTTTATT | 79931 |
| rs66605057 | multinucleotide-polymorphism | AG/TA | 0 | 0 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131486 | AATTAATCAAATCCA[AG/TA]GGAAGGAAAAACACA | 79931 |
| rs66732919 | in-del | -/A | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229609 | AAAAAAAAAAAAAAA[-/A]CAAATCACGCCTGTA | 79931 |
| rs66930642 | in-del | -/AGAT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203251 | ATAGATAGATAGATA[-/AGAT]GATAGATAGAAAGAT | 79931 |
| rs67417520 | in-del | -/CAAA | 0.433963 | 0.169285 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200640 | CAAAGAGAACTGTTG[-/CAAA]CACTTAATGCCAAAG | 79931 |
| rs67730856 | in-del | -/GT/TG | | | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165660 | TGTGTGTGTGTGTGT[-/GT/TG]TTACTTTCTTCTGGT | 79931 |
| rs70948380 | in-del | -/ATATATATGTATATATATATATATATATATATGTATATATATATAT | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131193 | TATATATATATATAT[lengthTooLong]GTATATACATATAAA | 79931 |
| rs70948381 | in-del | -/CACACACA | 0 | 0 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132245 | ACACACACACACACA[-/CACACACA]TATGCACTTTAAATC | 79931 |
| rs70948383 | in-del | -/GAT | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176555 | GATGATGATGATGAT[-/GAT]AGTGTTGTGTTGGTT | 79931 |
| rs70948384 | in-del | -/GTGTGT | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181651 | TGTGTGTGTGTGTGT[-/GTGTGT]AAAACACAGAGGTAT | 79931 |
| rs70948385 | in-del | -/A | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215889 | AAAAAAAAAAAAAAA[-/A]GAAATAACTGAACCA | 79931 |
| rs70948386 | in-del | -/CAGAAA | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226173 | CAAAAAAGAGAGAAA[-/CAGAAA]TAGACAAAGGGGGAC | 79931 |
| rs71304318 | in-del | -/TATATGTATATATATATA/TATATGTATATATATATATATATA | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131172 | TCTCACATTTCTTGT[lengthTooLong]TATATGTATATATAT | 79931 |
| rs71599110 | in-del | -/A | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145928 | TTGCGGTGAGCCGAG[-/A]ATCATGCCATTGCAC | 79931 |
| rs71599111 | in-del | -/A | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145963 | CCTGGGCAACAAGAG[-/A]CAAAACACCATCTCA | 79931 |
| rs71602310 | snp | A/C | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146007 | AGAGAGAGAGAATAT[A/C]CAATATATACTCTTT | 79931 |
| rs71602311 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205304 | GTGCAAAATCTCTAA[A/G]GCTAGAGCTTGTGTG | 79931 |
| rs71602312 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214450 | GCATTGCTGGCTGTG[A/G]AGAAGAGGCAAGAGA | 79931 |
| rs71629498 | snp | A/G | 0.24134 | 0.24985 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223189 | AGGTGTGCCAGCCTT[A/G]GCCCATCCTTAGCCT | 79931 |
| rs72030805 | in-del | -/TAAGTAATATTCA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163126 | AGTTTTTGAAATTCA[-/TAAGTAATATTCA]GTTATAGGTGGGGGA | 79931 |
| rs72685936 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155578 | GACAATCTAAAATTG[C/T]CATCCAGAAGTGCAG | 79931 |
| rs72685939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175684 | ATAGAAAGCATCCTA[C/T]TCAAAAGTGTGTCTT | 79931 |
| rs72685950 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121192019 | TTATAATAGAAATGC[A/G]TTACCTTTTTGTTTA | 79931 |
| rs72685957 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205026 | TGATTTTTCATTATG[G/T]GTGTCTTTTCCCTTT | 79931 |
| rs72685958 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214321 | TTACTATTAAAGAAC[C/G]TAACCCTATCTATTT | 79931 |
| rs72685960 | snp | C/G | 0.0225389 | 0.103983 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216932 | TTCTTCTAGGAAGAC[C/G]GCTCATGCCAGCTTT | 79931 |
| rs72913742 | snp | C/T | 0.167158 | 0.235875 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146978 | TAACAGAAGTCCAAA[C/T]GTCTTGAATTTTTTT | 79931 |
| rs72913746 | snp | A/T | 0.163564 | 0.234582 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160560 | ACTTCCTCTGTCAAG[A/T]AGAGTAAAGAGGTTC | 79931 |
| rs72913751 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177984 | AGAATTTACCCGGGG[A/G]AGAGAATCAAGTAAC | 79931 |
| rs72913757 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190786 | ATACTCCCCGAACAA[A/T]CTCTCAGAGAGTTTC | 79931 |
| rs72913772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223460 | CATGGTAAAGTAGCT[A/G]AAAGATGGTTTTAAA | 79931 |
| rs73843518 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199629 | TTCCTCTATTCTTCA[A/G]TGGAATTAAGAATAG | 79931 |
| rs73843557 | snp | A/T | 0.178465 | 0.239547 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226910 | AAAAATGTCCCCTGC[A/T]GAGGAACACACTAAA | 79931 |
| rs73847413 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | TNIP3 | GRCh38.p7 | 4:121140612 | AAGAATATTTCTCCA[A/G]TCCCCCAACCTGTAG | 79931 |
| rs74324096 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184724 | CTTGACTTTCATATT[G/T]ATATTGTTTCTTTCA | 79931 |
| rs74396543 | snp | C/G | 0.0556226 | 0.157218 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158672 | AGAAAATACCGAATA[C/G]AGAGAGGTATTTACC | 79931 |
| rs74415105 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174632 | GTTTTAATGACAAAC[A/G]TTTATTTTAAAAAGA | 79931 |
| rs74488613 | snp | C/T | 0.0883596 | 0.190715 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166228 | CCTTTGCCTCTTCTG[C/T]TATGCAGATAAACAA | 79931 |
| rs74496564 | snp | G/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206550 | ATATTGTGTGTGTGT[G/T]TTATCTTTTCTTTTC | 79931 |
| rs74507662 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141390 | TTCAATTGGAAAATG[G/T]CAAAATCTATTTTGC | 79931 |
| rs74571284 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121145581 | TCACCAATCTTAATA[C/T]AGTAGAATAAATAAA | 79931 |
| rs74618360 | snp | A/G | 0.0267878 | 0.112589 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217152 | CAGACTACATAGTAT[A/G]TCATGGGACTTACAG | 79931 |
| rs74770152 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150466 | ATTTAGGCTTTGATA[C/T]TGGACCCTCCTCCTC | 79931 |
| rs74812416 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172037 | CACACCTGGCCCCTA[C/T]TCCCCTACTTCTAGG | 79931 |
| rs74814323 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145980 | AAAACACCATCTCAT[A/T]AAAAAAAAAAGAGAG | 79931 |
| rs74820468 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163934 | TTGGTTAAAAATATA[A/G]AGCAAATCTTAGCTA | 79931 |
| rs74909505 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193059 | AGAACTACCCTATAC[A/G]TAATAACAACAGATC | 79931 |
| rs74973596 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167862 | CATATCCCTGGACTC[C/G]AGACTCCTGTATTAA | 79931 |
| rs75056710 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180780 | TTTTCAAACTCAACT[C/T]GGTCCTCACTACTAC | 79931 |
| rs75063796 | snp | G/T | 0.0356815 | 0.128715 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132351 | GCAATATGCTGAAGA[G/T]ATTTTCAGGGAGTCG | 79931 |
| rs75115139 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197556 | AAAAAAAAAGAACAC[C/G]TAAGTTCAAGCTAAA | 79931 |
| rs75171177 | snp | G/T | 0.0644147 | 0.167506 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154706 | ACCAAGAAAAGAAAA[G/T]AAAAGTCAGTACAAG | 79931 |
| rs75209858 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159264 | AGAAAAGAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 79931 |
| rs75235341 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136333 | TTCAGAAAATTTCAA[C/T]AAAGTGAGAGAGGTA | 79931 |
| rs75249037 | in-del | -/TT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121173517 | TGTTTGAGTTTTTTT[-/TT]AAAAATTATTTTCTC | 79931 |
| rs75382441 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154128 | CTCAGCCTTGGATTC[G/T]GCATTTAGCATGCTT | 79931 |
| rs75386686 | snp | G/T | 0.0544774 | 0.155791 | missense | TNIP3 | GRCh38.p7 | 4:121147161 | TTTTTGAAGTCTTCT[G/T]CGTATATTTGCACCT | 79931 |
| rs75434033 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138925 | TTTGAGGTTGTGACA[C/T]ATTTTCTTTCTTTTT | 79931 |
| rs75441220 | snp | G/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158455 | TCTTGAGACATCACT[G/T]GGGGCCATTTTTGCA | 79931 |
| rs75502622 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155290 | AGGATAAGCAAGTCC[C/T]TATATACTGTCACTA | 79931 |
| rs75517341 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165660 | AACTTTTTGCTAGTT[G/T]GTGTGTGTGTGTGTG | 79931 |
| rs75543335 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199393 | GGACATGAGGTCTAT[A/C]AGAAAACAATATTAC | 79931 |
| rs75715669 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179313 | TGTTTTAAAATTTCT[A/G]TGAGCCTTAATTCCT | 79931 |
| rs75823990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142198 | TTTTGAGTTATCTTT[A/T]TTGAGGGCCCTCAAT | 79931 |
| rs75941537 | snp | A/C | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176432 | CTTTGAAATTAGATA[A/C]TGAGATTCAAAGAGG | 79931 |
| rs76119939 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133193 | TGAAAGACAAAGTCA[A/G]ATAAGTTTACTCATG | 79931 |
| rs76147592 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220861 | TTGGCTGAGTAGGGG[A/T]TGAAAAAGAGCAATA | 79931 |
| rs76151677 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182199 | TTATATAAAGCACCA[C/T]AGACAAATACCCTGA | 79931 |
| rs76246873 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155318 | CTAGGTGATGGATAA[A/G]TGATTAAGAAAAATA | 79931 |
| rs76348865 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157606 | AAAGGGCAATGAGGG[A/G]CAGCAGGTTAAGTAG | 79931 |
| rs76390956 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205067 | GTAGTTCTTTGTCTA[G/T]TTAGCATTTTAACAG | 79931 |
| rs76602906 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180401 | CGAGACTCCGCCTCA[A/G]AAAAAAAAAATTATA | 79931 |
| rs76606514 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179364 | AAGACAGTCATATTT[A/C]AGTGTTGTTGTAGGT | 79931 |
| rs76621735 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157591 | CCTAGCCTGGTCTGG[A/G]AAGGGCAATGAGGGG | 79931 |
| rs76626011 | snp | C/T | 0.0444908 | 0.142359 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166196 | AATTCTATACCTTTG[C/T]TTCTTTCTTTACAAT | 79931 |
| rs76655812 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163274 | GTTCATATGTCTCAG[A/G]TTTCTATAAAATAAA | 79931 |
| rs76688189 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183084 | CACGGTGAGCCAGGT[G/T]CTTTCACGCATTTTC | 79931 |
| rs76779944 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145979 | CAAAACACCATCTCA[A/T]AAAAAAAAAAAGAGA | 79931 |
| rs76790569 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190756 | GGTAGAACCTTAACC[A/G]AAGTGTTGAGCTCAA | 79931 |
| rs76809568 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167888 | ATTAATTGCTTAATT[A/G]TCATCTCTGCTTGTA | 79931 |
| rs76831298 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196041 | GCATTAAACACCACA[C/T]GCTTGATTTTATTAA | 79931 |
| rs76868523 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174615 | AAACATTTGCTAAGT[C/T]GGTTTTAATGACAAA | 79931 |
| rs76888333 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194774 | CATAATAAACAAATA[A/G]GCTCTGTTGGAATCC | 79931 |
| rs76950261 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204608 | TATGATGGAATAGCA[A/C]GTTGTTTCTAATTAC | 79931 |
| rs76959364 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202871 | AAGTCAAAACCAAAA[A/T]GTAATACCACCTTAC | 79931 |
| rs76992857 | snp | A/G | 0.0252325 | 0.109451 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132287 | TACAATATCCCTGCA[A/G]CAAACACTGAGTTGC | 79931 |
| rs77017693 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180402 | GAGACTCCGCCTCAG[A/G]AAAAAAAAATTATAG | 79931 |
| rs77151732 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138411 | AAGGAACAGAAGCCA[C/G]AATTGAGGTTCATGC | 79931 |
| rs77161438 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181657 | TGTGTGTGTGTGTGT[A/G]AAACACAGAGGTATC | 79931 |
| rs77195037 | snp | A/G | 0.079617 | 0.182947 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176314 | GCTTTTCAGCCAGGT[A/G]TCCAAAGGTTTCCCA | 79931 |
| rs77267840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146645 | CACATATAAATGGCA[A/T]TTAGAAATACGTATG | 79931 |
| rs77311966 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205325 | AGCTTGTGTGGTTTT[C/T]CCAACATACAGCAAG | 79931 |
| rs77366509 | snp | A/C | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208461 | CAGCTTCAAATCTGT[A/C]TGATTTCATCTCCAA | 79931 |
| rs77437633 | snp | A/G | 0.0680777 | 0.171477 | intron-variant | TNIP3 | GRCh38.p7 | 4:121164048 | ACTCATCTCCTAGAA[A/G]TATGTTCTTACCTCT | 79931 |
| rs77461353 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141619 | TCAGTTAATTTATTC[G/T]TATCTATGTGTCCTA | 79931 |
| rs77526113 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179108 | AAGAAGCAAGGATTT[A/C]CAGAAAGAGTAAACA | 79931 |
| rs77652797 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223213 | TTAGCCTCCTGCTAA[C/T]TGTATCAGTTCCTCC | 79931 |
| rs77780795 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214625 | TCTTTCTTTCTTGTC[C/T]ACACGGTGAAATTTT | 79931 |
| rs77790529 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179173 | TTGTTAAAGGCTTAT[G/T]GGTAGCTAGAACACA | 79931 |
| rs77800522 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178540 | CCCAAAGGTGCTCCT[A/G]AGAGTGGTACAGCAA | 79931 |
| rs77966215 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121152563 | AGCTAATTAAATTCA[C/T]CCATTCACCCATTCA | 79931 |
| rs78047079 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156075 | AAGGAAATGACTGCT[A/C]CATGGCAGAAAGGGA | 79931 |
| rs78263261 | snp | A/C | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188323 | TTAAAAAAAAAAACT[A/C]TCCCCTAAGTTATAT | 79931 |
| rs78312147 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215895 | TAAAAAAAAAAAAAA[A/G]GAAATAACTGAACCA | 79931 |
| rs78329763 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208843 | ACTACACCTAAGTTA[C/T]GCTAATGAAGTCTGT | 79931 |
| rs78433706 | snp | A/C | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194859 | CAATAGAAAAAAAAA[A/C]GTACACACACACACA | 79931 |
| rs78468190 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163046 | TTTTTCTTTAATAAA[A/T]AAAAATTACTGAAAA | 79931 |
| rs78521910 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131773 | CTGAGTAGCTGGGTT[G/T]ATAGGTGTGTGCCAC | 79931 |
| rs78545419 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220685 | AATTGTCATAAATAG[C/T]GTGGGGGAATAAACA | 79931 |
| rs78666746 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141247 | CCTCACTAATTCAGG[C/T]TGACTGTCCAAATCA | 79931 |
| rs78667475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173204 | ACCAATGATGGAAAA[A/G]CATCGCAGGAGCCTA | 79931 |
| rs78670187 | snp | G/T | 0.079617 | 0.182947 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164879 | CATGACTCATTTGAA[G/T]TGAAATCTTCTCATG | 79931 |
| rs78695006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160488 | TCTCAAAAAAAAAAA[A/G]GAAGGAATTACAAAA | 79931 |
| rs78774944 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177721 | CCAAATAGAAATTTT[A/C]TTATATTTTTTCCCT | 79931 |
| rs78809723 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208968 | TCCAGGAAGGGGAGG[A/G]AGCTCCCCAATCTCC | 79931 |
| rs78812165 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121210095 | TTTTAAATGGTGTCA[A/C]TGAGATAGTGGATGC | 79931 |
| rs78845855 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186135 | CACAGTGAGACTGAG[C/T]GTGGTGACTACAGCT | 79931 |
| rs78922708 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138973 | TGAATATCTGCAGAA[A/G]TATAAACACTTGTAA | 79931 |
| rs79035319 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215906 | AAAAAGAAATAACTG[A/G]ACCAACGAATAGAAG | 79931 |
| rs79107683 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151373 | GCAAATGTGTGGTTT[C/T]GAGTATGTGAATAGG | 79931 |
| rs79141973 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154946 | GACCCCAGGAAAAAA[A/C]AAATCAAAATTCCCA | 79931 |
| rs79231273 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121177722 | CAAATAGAAATTTTC[G/T]TATATTTTTTCCCTT | 79931 |
| rs79232849 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211480 | GAAGGAATAAAAACA[A/G]AAAGATTCAAACCAA | 79931 |
| rs79240233 | snp | C/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143861 | CTATAAGGCACATCA[C/G]ATCCTTCATGCTTAG | 79931 |
| rs79240574 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171464 | CATACAATTCTTTCA[A/G]CTTTCCTACATGTTT | 79931 |
| rs79249796 | snp | A/C | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121195051 | CAGGTGGCTGTAATC[A/C]CAGCTACTCAGGAGG | 79931 |
| rs79278695 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180444 | GTAAGATATTTTAAG[A/G]AAATTGAATGACTAA | 79931 |
| rs79319714 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154359 | TAGGGACAAAAATTC[C/T]CTAAAGCCTCCTTAG | 79931 |
| rs79474439 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145011 | AGTACCCTAAGCATC[G/T]TTCACTTTACCACAT | 79931 |
| rs79513876 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121189503 | GATTTACTGTAACTA[C/T]GCTCCTGGTGATTTT | 79931 |
| rs79609016 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175238 | TACTTGCTGAAGTCA[C/T]GCAAGTCTGGAAGAA | 79931 |
| rs79611124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179007 | GAGGGGGCTGAGTAA[C/T]GCCATGTGGGACTAG | 79931 |
| rs79627245 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159274 | AAAAAGAAAAGAAAA[A/G]AAAAGAAAAACCAGT | 79931 |
| rs79705295 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134548 | ATTTAATGCTATACA[A/G]AGAGAAAGCCAAGTC | 79931 |
| rs79721973 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151026 | TAGCTCATGATGGGC[A/G]TATCATTACATTATG | 79931 |
| rs79785996 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163973 | AAACTAGCCATTTCT[G/T]TTCTTATTAATAAGT | 79931 |
| rs79814774 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211431 | TGAAAACTCAACTCA[C/T]TGAGGATATTACATT | 79931 |
| rs79895551 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196088 | TTTAAGGTGGAAACT[C/G]TCTCCCTGTTCTTAG | 79931 |
| rs79957512 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214184 | TTCTTTCCCACTTCC[C/T]TCAGACAAAGACATG | 79931 |
| rs79975458 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142570 | AAGGCCTTGGTGGTG[C/T]CTAAGCACTGTCTAT | 79931 |
| rs79991473 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134254 | AAGCATAACTCTGTA[C/T]CCTATGAAAAATTTG | 79931 |
| rs79995307 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148404 | TCACTGTAACAAATA[C/T]GAACCAAATCATTAT | 79931 |
| rs80057343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134838 | TCCTCACAGTGTGAG[C/T]GACGTTTCCTCCAGA | 79931 |
| rs80112720 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189093 | TAGAAATAACTTGAA[A/C]AATCATTTAATTGAC | 79931 |
| rs80131420 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197106 | GAAAGCAGTGGGCTA[C/T]TTATCAGTGCAATAT | 79931 |
| rs80157672 | snp | C/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220841 | GGATTCGTTCCTGCT[C/G]TGATTTGGCTGAGTA | 79931 |
| rs80162297 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121162037 | TATTGGATGATGAGA[G/T]TAATTCCTACATCTG | 79931 |
| rs80201454 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153765 | GTCCAAAATACAGGG[G/T]TTGAGCACCTGTTTC | 79931 |
| rs80214553 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205422 | AAAGAGAGCCAGTTC[A/G]AGGAGGTTCGTGGGC | 79931 |
| rs80258605 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202862 | GGGAAATGCGAATCA[A/G]AACTATAATGAAATA | 79931 |
| rs80301007 | snp | A/C | 0.0799831 | 0.183287 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163638 | AAAGAAAACTAGAAA[A/C]TATTTGAATTCATTC | 79931 |
| rs80314028 | snp | A/C | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142881 | TGACAGCAGTAATAC[A/C]AACAAAAATAGCCAC | 79931 |
| rs80347417 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180478 | GTGTCAAATGCAAAT[A/T]AAAAGACAAGTGAAA | 79931 |
| rs111340291 | in-del | -/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176366 | ACACAACAATGCAAC[-/T]TTTTTTTTTCTAGCA | 79931 |
| rs111358914 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173270 | GAATTAAGCGTTTTT[G/T]AGGGATAGATATGAG | 79931 |
| rs111376785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203857 | CATTCTTCCATATTT[C/T]TCTCTGTGTTTATAC | 79931 |
| rs111385303 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188845 | ATTTTGTTTGCATGA[A/C]CATCATGTTTTTAAC | 79931 |
| rs111390571 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192913 | GAGCACAATTATTTA[C/T]TCCTTAATGAAGCTG | 79931 |
| rs111402700 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121224379 | AAAAATAAAAAGAAA[A/G]AAGAAAAAAGAAAAA | 79931 |
| rs111412204 | snp | C/T | 0.030665 | 0.119967 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224949 | AGCATACACTGTGTC[C/T]GAGAGTCATCTGGCT | 79931 |
| rs111424774 | snp | A/G | 0.0720575 | 0.175603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141929 | TCTGAGGAGAACAAA[A/G]CTGTGGGGTCACTAC | 79931 |
| rs111461182 | snp | A/G | 0.0460142 | 0.144533 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172177 | TTTCTCCACACCACC[A/G]TGGTACACGGCTGTG | 79931 |
| rs111515500 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133101 | ATCCTATAGAAAGAC[A/T]TGTTGGTGTATCATG | 79931 |
| rs111529188 | snp | A/G | | | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228590 | TTTTCAAAAATTTTA[A/G]AAAATAATCTATTAT | 79931 |
| rs111572391 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178358 | CTAAAACCTGAACAA[A/C]GACAAAGTGAAAGGA | 79931 |
| rs111612508 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156250 | ATATCAGTGATAAGA[G/T]TTCCCCTCAGAGTCT | 79931 |
| rs111627896 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146904 | TCATCTCTTTACAAG[A/T]TTGTTTAAGAATGAC | 79931 |
| rs111661105 | snp | C/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169585 | CCATTTTAGTGCCTG[C/T]GCGTGTTCATGTGGG | 79931 |
| rs111667544 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225500 | TCTAAGGTCTTTATC[C/T]TTCATGAAATAAATA | 79931 |
| rs111686882 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135050 | TCTGCACTCAAGAGT[C/G]CTTATGATGGGAAGG | 79931 |
| rs111726360 | snp | A/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161327 | TCCTGTTGCGATTTA[A/T]AAAATACCTGATTCT | 79931 |
| rs111726498 | snp | C/G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197529 | AGAGCGAGACTCTGT[C/G/T]TCAAAAAAAAAAAAA | 79931 |
| rs111751215 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200540 | GAGACCCCCGAGCAC[A/G]CATACCCTGACCAGT | 79931 |
| rs111863202 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131867 | TAGAACTCCTGGCCT[C/T]AAAGCAATCCACCTG | 79931 |
| rs111865355 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223258 | CCGCTTGAAAGGGAA[A/G]TAAAGGACAGCCTGA | 79931 |
| rs111875054 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121168967 | ATTTTTGCATGACAC[C/G]AACTCACCATCATCT | 79931 |
| rs111910885 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190856 | TCATGGGTAAGGTAA[C/G]CCTGGAAGACCAAGT | 79931 |
| rs111942002 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180003 | TTGAGTAACACTAAT[A/G]TAGCACAAGCAGGTG | 79931 |
| rs111959444 | in-del | -/A | 0.423413 | 0.180077 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168779 | CCACCACAGCTTCTC[-/A]AAAAAAAATGCCTTT | 79931 |
| rs111979253 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175459 | CCCCCACCAAGCCTC[C/G]CAGTGTTGTCGTCTG | 79931 |
| rs111980757 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145751 | TATTTTTTGTTCTAA[A/T]ACTGTTTTACTGGCA | 79931 |
| rs111997395 | snp | A/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177518 | GGGAACTTGACATAT[A/G]TCTCAGGCTCTTTCA | 79931 |
| rs111998733 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172448 | AGGCCAATGAAAAAA[C/T]CCGTAAGAGATAGAC | 79931 |
| rs112032454 | snp | C/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139962 | AACATGAAATATTAT[C/T]TTTAAATTAACTTTG | 79931 |
| rs112071387 | snp | C/T | 0.089084 | 0.191327 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171070 | ATCTGCCCATCTCGG[C/T]CTCCCAAAGTGCTGA | 79931 |
| rs112074787 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169833 | ATTCACTTGTGTCCC[A/G]CCTGGTTGGAACTCT | 79931 |
| rs112145947 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163922 | TGTTACATAATTTTG[C/G]TTAAAAATATAGAGC | 79931 |
| rs112148055 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166827 | CTGAATCTATTTGCA[C/T]GAATTTTTAAGTGTA | 79931 |
| rs112219172 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149708 | GAGGCGGAAGTTGCG[A/G]TGAGCGGAGGTTGTA | 79931 |
| rs112223331 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158501 | TGCTCAAGACAACTC[A/G]CTGACACCGTTCATT | 79931 |
| rs112238157 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196013 | GATGGCAGGATTCAT[A/G]GAGCCAGGCACTGCA | 79931 |
| rs112243280 | snp | G/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165910 | AAAATCTGCTCATCA[G/T]AAAAGAAAAAGAAAA | 79931 |
| rs112249126 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175059 | AGAATATAATGAACA[C/T]ATTTGCTAAACAACT | 79931 |
| rs112261069 | snp | C/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205952 | AGAAAGGCACCTTCT[C/T]CACAGGATGGCAAGA | 79931 |
| rs112266194 | snp | G/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187535 | GTGACCTCAGCCATT[G/T]TTAATAAAGAAGGAC | 79931 |
| rs112267036 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197594 | TTTGAAGTATTTAAA[A/T]TTTTTAGATAAAAAT | 79931 |
| rs112329605 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196421 | AGAAAATAAATCGAC[A/G]AATATAATATTTGGC | 79931 |
| rs112411036 | in-del | -/C | 0 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168525 | CTTTTCTTTGCTTTT[-/C]TTTTTTTTTTTAAGA | 79931 |
| rs112416274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189403 | GATGTTCAAACATCA[A/G]GAATCTGGGTGACCC | 79931 |
| rs112523283 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142847 | CAAGCCACTCTTGAC[A/C]TACTCAAGTGTCAGG | 79931 |
| rs112560682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142081 | CAGGACCAATACAAA[C/T]GAGGCTCACAGGTCA | 79931 |
| rs112599363 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174392 | CCTGAGTGACAGAGC[A/G]AGACCCTGTCTCTAA | 79931 |
| rs112611229 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214219 | GCGGCCCCTGCCTCA[C/T]TGCCTCATCCCTCAT | 79931 |
| rs112624723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186457 | TCAGAACTTGCATAT[A/G]AACCCTCTGAAAGAA | 79931 |
| rs112628702 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191218 | ATTTAGAGAATAGGA[A/C]ACATTGGCTCCTAAT | 79931 |
| rs112641486 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217478 | TTTTGTGTTGTTTTC[A/G]GCTTGTGACAGCTGT | 79931 |
| rs112666986 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151550 | AATAATTTATGTTTT[C/T]TGAGGATTTGTGTTA | 79931 |
| rs112687120 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185172 | GATCTCGTTTCCTTG[C/T]TATCTTTCTAATCTC | 79931 |
| rs112708961 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146526 | TTTTAGTATGCTTAC[A/G]TTTAATATATTCTAT | 79931 |
| rs112711632 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214353 | TTTCAGAAATACAAA[A/T]TTTTAACCACTGTAG | 79931 |
| rs112714805 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223763 | GCATAATTGTAATAC[C/T]AGTTTTTCTACTCCT | 79931 |
| rs112754359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183892 | ATTATGGTGAGTTAT[A/G]TAATTATTTCATTAT | 79931 |
| rs112759253 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148335 | TAGAGGCACTGCAAA[A/T]CTACGGAGATGGATT | 79931 |
| rs112763488 | snp | A/C | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165568 | CACTGAGCTGTCTGG[A/C]ACACAGCAGGCATTC | 79931 |
| rs112771822 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171692 | GGATGTTTCTCAGTT[A/C]TCATGAGGAAATGGA | 79931 |
| rs112783146 | in-del | -/AC/ACAC | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154000 | CTAGTCCATAAAACA[-/AC/ACAC]ACACACACACACACA | 79931 |
| rs112802648 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176801 | ATCTTGTGAAGTGTC[A/G]TAAGTATATATTAAT | 79931 |
| rs112804823 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223836 | TTCTGATTTCCATCA[A/C]ATTTTCAGCAATAGA | 79931 |
| rs112872975 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171255 | CTTTGAATTTCAAGA[A/G]CTAGTGTTTTCAAAA | 79931 |
| rs112879894 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158480 | TTTGCACCTTTCTTT[A/G]GCTATTGCTCAAGAC | 79931 |
| rs112920647 | snp | C/G | 0.109814 | 0.206997 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134820 | CTCCTCCAGCCACAC[C/G]CTTCCTCACAGTGTG | 79931 |
| rs112982168 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180803 | ACTACTACTCTGCAA[A/C]TCATTTTCGTTTTAC | 79931 |
| rs113065135 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187606 | TTTCCATTTTGACAG[C/G]CATTTCTGCTCTAGT | 79931 |
| rs113091011 | snp | C/T | 0.157972 | 0.232445 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135595 | GTAGAGACAGGGTTT[C/T]ACCATGTTGCCCAGG | 79931 |
| rs113096894 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197378 | GCTAAAAATACAAAA[A/G]TTAGCTGGGCGTGGT | 79931 |
| rs113102685 | snp | C/G | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157681 | CAGTAATTTGCAGCA[C/G]TTGACCTCCTACTAG | 79931 |
| rs113103336 | snp | A/G | 0.108402 | 0.206034 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131491 | TCAAATCCAAGGGAA[A/G]GAAAAACACAGATTT | 79931 |
| rs113132130 | snp | C/T | 0.141934 | 0.225437 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196927 | CAGTCATTAAAAAAA[C/T]GTAAGAAATAAAATT | 79931 |
| rs113184206 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138761 | AAATACAATTAGGCT[A/G]TGTGGCTTTTATTAA | 79931 |
| rs113282653 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161484 | ATCTGTATACTATAA[C/T]GGGTAAGTCAGAGAT | 79931 |
| rs113293571 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143417 | CATCATTGTCATTCC[C/T]ACACTCCATGTCCCA | 79931 |
| rs113324314 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163813 | GAACAAAAATCAAGA[A/G]CAAAATAAGGAACCC | 79931 |
| rs113408081 | in-del | -/CTT | 0.0807149 | 0.183963 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162513 | GGCCCGTAATTGGAC[-/CTT]CTTCTTTTGGGGAAG | 79931 |
| rs113437864 | snp | C/T | 0.046775 | 0.145601 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180847 | CTCCCTACCTTCCAA[C/T]AGTCATTTCATATCT | 79931 |
| rs113466430 | snp | A/C | 0.0448719 | 0.142907 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168664 | TAGCTACAGGTGTGT[A/C]CAACCACATCTGGCT | 79931 |
| rs113478329 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206905 | AGCTCCTGAGGGTAC[A/T]GAGCTACCTAATTTT | 79931 |
| rs113499064 | snp | A/G | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164538 | CCAAGTGTTTCCTCA[A/G]TAGCCTAACTGTTAT | 79931 |
| rs113520554 | snp | A/T | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141399 | AAAATGTCAAAATCT[A/T]TTTTGCACATATGTA | 79931 |
| rs113521235 | snp | A/C | 0.108755 | 0.206276 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158001 | GGTAACAAAATGAGG[A/C]AGAAAGGAAAAATGC | 79931 |
| rs113525341 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171352 | ATGAGTTGATGGATT[A/T]AAAGAGGGGTGGATA | 79931 |
| rs113562509 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194127 | CGATGTTCATTTTCC[A/G]ATTTTGATGGTTATC | 79931 |
| rs113566174 | snp | C/T | 0.16028 | 0.233346 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219076 | GTGGTGGTGTGCACC[C/T]GTAATCCCAGCTACT | 79931 |
| rs113622862 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144445 | CCCACTCTGTTGCCC[A/G]GACTGGAATGCAGTG | 79931 |
| rs113676870 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167327 | ATGAATGATAGAGAC[A/T]ATAAAGCCTGTAAGA | 79931 |
| rs113690080 | snp | A/C/T | 0.0287284 | 0.116357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222962 | AGGCGCCCACCACCA[A/C/T]GCCCGCCTAATTTTT | 79931 |
| rs113716689 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198615 | AAAAACAAAAACTAT[A/G]GCATTATTTTGCCTC | 79931 |
| rs113742747 | snp | A/G | 0.5 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180172 | TTGGGAGGCCGAGGC[A/G]GGTGGATCAAGAGGT | 79931 |
| rs113747352 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212623 | GCTGCTGCTTGTTTA[C/G]TGAAAAGAAAAATAC | 79931 |
| rs113801419 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185605 | GAATAAATATGACTC[C/T]AGGAAGAGATTTAAC | 79931 |
| rs113863098 | snp | C/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169480 | TTTTTCTTCTTTTTG[C/T]TGATTGCCTCCCGAC | 79931 |
| rs113863547 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151854 | TTCCTTGAACAAACA[C/T]CTATAACCTATTCTA | 79931 |
| rs113880656 | in-del | -/ACAAACAA | 0.214541 | 0.247473 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219199 | GAATGAAACTCCATT[-/ACAAACAA]ACAAACAAACAAACA | 79931 |
| rs113894873 | snp | C/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185888 | GGTACTGACTTTTCA[C/T]AGAAATAATCACATG | 79931 |
| rs113943102 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203315 | AAAATAATGGCATTC[A/G]CAGCAGCCTGGATAG | 79931 |
| rs114002017 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169133 | CCTTTCAGTGGCTTC[A/C]CATGTCACTCATAGT | 79931 |
| rs114015715 | snp | C/G | 0.00663735 | 0.0572243 | missense | TNIP3 | GRCh38.p7 | 4:121157194 | GGATCCTTCTCCCGC[C/G]TGCTGAGGAATCTTT | 79931 |
| rs114035444 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214204 | ACAAAGACATGGACC[A/G]CGGCCCCTGCCTCAC | 79931 |
| rs114042394 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146448 | ATTTTCCTTCATTAA[C/T]ATCACTATTTACCCA | 79931 |
| rs114052844 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135647 | CAAGCAATCTGCCCA[C/T]GTTGGCCTCACAAAG | 79931 |
| rs114061668 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175378 | TCTAGGAAGACTTAT[A/G]TTCTTCTAATTAACA | 79931 |
| rs114077886 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199937 | GACACCTCGTGTGGG[G/T]CTGCATATGCCCAGA | 79931 |
| rs114081423 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226551 | TGCCACAGGGCATTG[A/G]TCGAGATTCCTAAGA | 79931 |
| rs114085788 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136178 | AATCTTACATAGTAC[C/T]GTGCCTTTTACTTGT | 79931 |
| rs114095206 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145010 | AAGTACCCTAAGCAT[C/T]TTTCACTTTACCACA | 79931 |
| rs114100134 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183446 | TGGCCATTAGCTGAT[A/G]ATGCCAAAATTAAAC | 79931 |
| rs114126276 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215601 | TAGCCTTTCCTTCTA[C/T]TTTTCCATCTTTCTC | 79931 |
| rs114170700 | snp | C/T | 0.100588 | 0.200439 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218756 | GGGCTCAAGCAATTC[C/T]CCTCCCTCAGGATCC | 79931 |
| rs114246996 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187749 | TTTTGACCAAAGTCC[A/G]TGGATGGGATTCAAT | 79931 |
| rs114247097 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121167417 | TGCTGGGCCTTGAAG[A/G]GTAGATAGGATTTTG | 79931 |
| rs114248621 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209484 | ATGGAGAGTTGTGGG[A/G]AAAAAACTACGCATT | 79931 |
| rs114253348 | snp | A/G | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183013 | TACAAAGGAAGATAC[A/G]GACAAGTTTAGGAAT | 79931 |
| rs114253450 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169443 | TCACCTTTCCTGCTT[A/T]ATTTTTCCATAACAC | 79931 |
| rs114307066 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226918 | CCCCTGCAGAGGAAC[A/T]CACTAAATGGATGCT | 79931 |
| rs114328437 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215970 | AATGTGGAAAGCGCC[G/T]AAGTAAGGGATTTTT | 79931 |
| rs114370444 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176363 | CTCACACAACAATGC[A/G]ACTTTTTTTTTTCTA | 79931 |
| rs114411576 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202977 | TTTTACACTGCTGTT[G/T]GGAATGAAAACTACT | 79931 |
| rs114416478 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135191 | TGGTTTTCCATGTAT[C/G]TTTATCAAGGTAGGA | 79931 |
| rs114451453 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158286 | GTGGAAAATAGGTCA[C/T]GCTATCTAATTAAAG | 79931 |
| rs114466110 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174152 | AGCTTGGATACTTCA[G/T]GTGAAAGAGAACTAC | 79931 |
| rs114481941 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164622 | CGGTTTCCCTAAAGG[C/T]GAGATTTTCTGGCAA | 79931 |
| rs114482211 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143914 | ATATACGTGTGGGCC[A/T]TTCTAAACCATGAAA | 79931 |
| rs114485290 | snp | A/C | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121218245 | GTAAACACCCCAAAA[A/C]TGGCATGTGCAAAGG | 79931 |
| rs114501888 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214172 | TTGTCTTTATTCTTC[G/T]TTCCCACTTCCCTCA | 79931 |
| rs114512921 | snp | C/T | 0.0168055 | 0.0901129 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228394 | TGGACAACGATGAGC[C/T]CCTTCTACACTTCCA | 79931 |
| rs114526875 | snp | C/T | 0.366473 | 0.221211 | intron-variant | TNIP3 | GRCh38.p7 | 4:121161848 | TTTCTTTTCAGTTAT[C/T]TTTTTCAGGAGTGAG | 79931 |
| rs114533956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184423 | TTTGGTTATAACTGA[C/T]TGGACCAAGAGTAAA | 79931 |
| rs114554312 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166451 | ATTTTAAGAGTCTGG[C/T]TTTTAGTCAAGCTTT | 79931 |
| rs114561932 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212995 | GAAAAAAAAATGGAG[C/T]TTTAAGGGACTTTTA | 79931 |
| rs114582404 | snp | A/C | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185189 | ATCTTTCTAATCTCA[A/C]CTTCTACTCTCTTCC | 79931 |
| rs114641771 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153366 | TTTGTGTCTACATTT[A/G]GGGAAATTAACTAGA | 79931 |
| rs114649898 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203644 | ACAACTTAGGTCATC[C/T]GATATAATACATAAA | 79931 |
| rs114650233 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205187 | AATGGAGTGATCAAA[G/T]GTGGGACTTATTGAA | 79931 |
| rs114662326 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162836 | CAATATATTCCCATT[C/G]TAGGGAATAAATTAT | 79931 |
| rs114670396 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203482 | GGAAAGAATGGGACA[A/G]GGGTGAGGGATAAAA | 79931 |
| rs114690821 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135935 | ATCAACTGTGGAAGC[C/T]AGTAAAGGAGGCATA | 79931 |
| rs114694883 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191250 | AACTTTATGAACAAG[G/T]CTGAGCCCCTATATT | 79931 |
| rs114736373 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189749 | AAAATTTAAATAGAT[A/G]TCGAAGAATTGTATT | 79931 |
| rs114738606 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149861 | GTGCCCCTCTTTTAA[C/T]TGTGTGATCTTGGGT | 79931 |
| rs114747080 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172765 | GATAATTCTTGCATA[A/C]CACTGCACAGAAAAT | 79931 |
| rs114747244 | snp | C/T | 0.0352966 | 0.128072 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228610 | TAATCTATTATATGA[C/T]GTAGCTTGCATATGC | 79931 |
| rs114751556 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186925 | TATTCTTTAATTAAT[A/G]TAGGAATTTGTACAT | 79931 |
| rs114753583 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156466 | GAGCTTTAGAATCTG[A/G]AGGTTGGGTTCAAGT | 79931 |
| rs114754085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211985 | AGACACACAAATTTT[A/G]TGCTGGTACCAGTAC | 79931 |
| rs114778224 | snp | A/C | 0.000987445 | 0.0221979 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158656 | AGGATAATGGCTTTA[A/C]AGAAAATACCGAATA | 79931 |
| rs114870507 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152008 | CTGGCTTCAGGAGCC[C/T]GATAAAAACAAACTC | 79931 |
| rs114871445 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TNIP3 | GRCh38.p7 | 4:121168996 | CTCTTAGCTGGATTA[C/T]TGCAATAACCTAAGG | 79931 |
| rs114872973 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181334 | CATATTTCCATGAAG[G/T]AATAAATTTCTAGTT | 79931 |
| rs114941185 | snp | C/T | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168031 | TCCAGATCAAAAATC[C/T]TGGAGTCATCCTTGA | 79931 |
| rs114945578 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198187 | TGTAAGAGAAAGTAA[A/G]CAATGACATTTTTAG | 79931 |
| rs114950519 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177608 | CCAATTTCCTGCTCC[C/T]GGAAAGGGAATCTAC | 79931 |
| rs114951645 | snp | A/C/T | 0.00438476 | 0.0466401 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184519 | ATGGGTAGAGAAATG[A/C/T]GGAGCTGAGAGATGG | 79931 |
| rs114959760 | snp | A/G/T | 0.141258 | 0.225111 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194289 | AATATTTTTGTGCAC[A/G/T]TCTTAAAAATTTTTT | 79931 |
| rs114966307 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192947 | TTTAAGTTGCAATCA[A/T]TGTTGGACATTTATA | 79931 |
| rs114980306 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155006 | CTCACACTGTCTCCC[A/G]GCCTGGAGTGCAATG | 79931 |
| rs114999415 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185709 | CAAACTCATAGGACT[A/G]ATAAAGTGGAAACAC | 79931 |
| rs115073931 | snp | A/C | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165819 | GGGTTCTGAAAGTAA[A/C]AAGTTATAACTCACA | 79931 |
| rs115080472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135207 | TTTATCAAGGTAGGA[A/G]GATAGATTATACTTT | 79931 |
| rs115113178 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183092 | GCCAGGTTCTTTCAC[A/G]CATTTTCTTATTCAA | 79931 |
| rs115130336 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156031 | TGAGGGAAAAATTAC[C/T]CAGATTCCTGGCTAG | 79931 |
| rs115139431 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162563 | CTGGGTTAGAACAGA[C/T]TAACTATTAAGCATC | 79931 |
| rs115139859 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186396 | CACTGTCTTTTCTCA[C/T]TGCCAATATGATTGA | 79931 |
| rs115144034 | snp | A/G | 0.030278 | 0.119257 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131186 | GTTATATGTATATAT[A/G]TATATATGTATATAC | 79931 |
| rs115155923 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175470 | CCTCCCAGTGTTGTC[A/G]TCTGCTCCCTTGCCC | 79931 |
| rs115170233 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179227 | AATGTATAGAAGACA[C/T]TAAAACACTACAGGA | 79931 |
| rs115180383 | snp | A/G | 0.0275645 | 0.114116 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183223 | CAAACTGAAACATCG[A/G]CAGGGCCAAGATCAA | 79931 |
| rs115185303 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169452 | CTGCTTTATTTTTCC[A/G]TAACACTAAATTTTT | 79931 |
| rs115192113 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214192 | CACTTCCCTCAGACA[A/G]AGACATGGACCGCGG | 79931 |
| rs115267091 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203770 | CAAGCAAACATTAGA[G/T]AACACAAAAAAGTTA | 79931 |
| rs115287433 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143671 | GAAATGTTGGGTTAA[G/T]TTTCTGCTAGCCTCT | 79931 |
| rs115302449 | snp | G/T | 0 | 0 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173510 | TAATCTGTGTTTGAG[G/T]TTTTTTTTAAAAATT | 79931 |
| rs115375663 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154867 | TCTTTGGATGCACAC[C/T]AGAATTAGGATTGAA | 79931 |
| rs115416600 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143807 | TGGTCAAGAGTACTA[A/T]AACATGTCTTAATGA | 79931 |
| rs115424217 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168668 | TACAGGTGTGTACAA[C/T]CACATCTGGCTATTT | 79931 |
| rs115431125 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188622 | AGGATTCTAAACTTG[G/T]AGAATCCTATCTGGT | 79931 |
| rs115446445 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217916 | CACTGTGGAGAACAC[A/G]CTAAGAATTATAATG | 79931 |
| rs115464536 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193666 | TCCTACCACCAAGTA[C/T]GTAATGAATACTAGG | 79931 |
| rs115488163 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189323 | CCCTGGAGAACAAAG[C/T]TCATCTTCAAATATG | 79931 |
| rs115488966 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211761 | TCAGAGATGTTTTCA[G/T]CATAAACTCTGAAGC | 79931 |
| rs115495534 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174249 | AAGTTATAATTATAA[A/T]AATTAAGAGACTAGG | 79931 |
| rs115515322 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203325 | CATTCGCAGCAGCCT[A/G]GATAGAATTAGAGAC | 79931 |
| rs115558818 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180117 | TAATATTATAGATGT[C/T]GGGCTGGGCGCGGTG | 79931 |
| rs115562936 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152800 | GTTTATTTTTTCTTC[C/T]AATTTTAAGAGAAAT | 79931 |
| rs115577737 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222454 | ACTATATGTCTTTGG[A/G]CATATTATTTAAATA | 79931 |
| rs115585826 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224791 | ATTGTTTTGCCTTTC[A/G]TAATTTAAAAAATGT | 79931 |
| rs115626364 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196492 | TTTGTGTGGTTGACT[A/G]TGTAATAGAAATCAT | 79931 |
| rs115671731 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187275 | TTAGTTCTGTGGGTA[C/T]ATAGTTGTTCCCACC | 79931 |
| rs115704363 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200318 | ATAATCCACTAAGAA[A/G]AGGAATATTTACAGT | 79931 |
| rs115720661 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208352 | ATATTTTACAGACCC[A/T]GAACTCAATGTGTCG | 79931 |
| rs115720962 | snp | A/C | 0.00451547 | 0.0473006 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150226 | CTGAAGAGCCTACGT[A/C]ATAAGATAAGTACAC | 79931 |
| rs115735201 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149706 | GGGAGGCGGAAGTTG[C/T]GGTGAGCGGAGGTTG | 79931 |
| rs115748565 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211973 | TTTCCAGTCTCTAGA[A/C]ACACAAATTTTATGC | 79931 |
| rs115785183 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197970 | CACATGTGAAAGATT[C/T]ACTGATATTACAGGC | 79931 |
| rs115785808 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207397 | TTTAAATCTATTAAA[A/G]TTTCATAGAAACCAG | 79931 |
| rs115789824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188720 | TCTAACACTTCTCCA[A/T]TAAATTGTTTATGAA | 79931 |
| rs115858093 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196995 | AATTCAGTTTAAAGC[A/C]TTCAAGAACAAACAC | 79931 |
| rs115944132 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220821 | TACTGAGCGAATGGA[C/T]AGCAGGATTCGTTCC | 79931 |
| rs115946777 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187796 | TAATATGTGTGCTAT[A/G]TGTTTATCGTCTCTT | 79931 |
| rs115947561 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193974 | ACTGAGAAACTGACC[A/C]AGATTGTAAGAGAAT | 79931 |
| rs115957077 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204055 | GAAAAAATCTCTGAC[C/T]ATTCCTTCAGTTCAT | 79931 |
| rs115960826 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189465 | TCAAGCAGCAATTTT[C/T]AGGTTTTAGTTTTTG | 79931 |
| rs115961927 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211944 | ACATTTCCATGGAAG[C/T]AAAAGCTGAGTGATT | 79931 |
| rs116007809 | snp | A/G/T | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154039 | CCTGCATGCACACAC[A/G/T]CACACTTTTCCTCTC | 79931 |
| rs116011994 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188656 | GAAGATAATCCAAAA[G/T]GTTATGGTTTACTGC | 79931 |
| rs116015576 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181436 | CCTTATTTGACCTCA[A/T]AACCATTAGTACACA | 79931 |
| rs116058917 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121188558 | ATTGTTTAATGAGCT[A/C]ATCTAAAGTTTATTT | 79931 |
| rs116108178 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160951 | CACAGACACTGAGAC[A/C]ACAAGTATGAAACAT | 79931 |
| rs116108534 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185257 | AAACTTTATGGAACA[C/T]GCCAAGCAGTTCCCA | 79931 |
| rs116111846 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203638 | TTCAAAACAACTTAG[G/T]TCATCTGATATAATA | 79931 |
| rs116112385 | snp | A/C | 0.0103295 | 0.0711199 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228967 | AGATCTAACTAATGT[A/C]TTTCTTTCCTGAAAG | 79931 |
| rs116123374 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163692 | TGCTGAACAAAATCT[A/G]TGGTACCAATTGTAA | 79931 |
| rs116126368 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170802 | TGTAGCTAATTCTTT[C/T]TTTGCTCGGTAAGAG | 79931 |
| rs116147568 | snp | A/C/T | 0.00182725 | 0.0301713 | intron-variant | TNIP3 | GRCh38.p7 | 4:121154544 | CCATGCTTGACCTGA[A/C/T]TGATACCTTATTGAG | 79931 |
| rs116152933 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196840 | TTTCTTTCGATTTAT[A/G]TACGTATTTTTAAAA | 79931 |
| rs116179397 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214527 | AAGGAAATGGCTTGT[G/T]AATATGGAGAGGTGG | 79931 |
| rs116207982 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144276 | AAGAACTGAAAGTAC[C/G]ATGCTAATTATAAAC | 79931 |
| rs116228964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225857 | TAAATGGGAACTTTG[C/T]CTGTCTCTTCTACAC | 79931 |
| rs116237885 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | TNIP3 | GRCh38.p7 | 4:121157737 | TGACAGGTCCTCAGA[G/T]TGGCCACAGTCCAGA | 79931 |
| rs116262483 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160575 | AAGAGTAAAGAGGTT[C/T]TAACATTCATTAAGC | 79931 |
| rs116268505 | snp | A/G/T | 0.0189856 | 0.0955633 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179823 | TGTGGTGGCCAGGGT[A/G/T]GGGGAGGGATGACAA | 79931 |
| rs116321615 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190319 | TTAGCCTGCTAATCA[C/T]TGTATTTTTCAGAGC | 79931 |
| rs116321961 | snp | A/G | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165010 | GATACTTGGAGCTGC[A/G]TAAGTGAACTGCGAT | 79931 |
| rs116347195 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174616 | AACATTTGCTAAGTC[A/G]GTTTTAATGACAAAC | 79931 |
| rs116352966 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181703 | TGGTCTCTATAGGTG[A/G]TGAGCCTACTGGTGG | 79931 |
| rs116354707 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155675 | ACCTCTTAATTTTGT[A/G]TAATAGATAGCAAAC | 79931 |
| rs116358276 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219405 | GCTTTCTGTTTCACT[G/T]AGCCGAAAGATGTCC | 79931 |
| rs116360517 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177221 | CTTGGACTATAACTT[A/G]GTTATATATAACTTT | 79931 |
| rs116413209 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196417 | AGTTAGAAAATAAAT[C/T]GACGAATATAATATT | 79931 |
| rs116430428 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207538 | GTTTAAATGCTTTAT[G/T]TAACTACTTTAACAC | 79931 |
| rs116438343 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146464 | ATCACTATTTACCCA[C/T]CGTGGCAACTTCCTG | 79931 |
| rs116550753 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222356 | CCCAAATTACAAATT[C/T]GCTTTTTCAAACGTG | 79931 |
| rs116562131 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166948 | CACTCACTGCTTGTG[C/T]CTTTGGTCATCTAAG | 79931 |
| rs116581149 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144443 | ATCCCACTCTGTTGC[C/T]CAGACTGGAATGCAG | 79931 |
| rs116584225 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178486 | TGGAGTTCTCGAAGA[C/T]ATATTCCACATTGAG | 79931 |
| rs116640612 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169090 | GAGACTTTTAAAATG[A/T]CATTTCATGTCATTC | 79931 |
| rs116645896 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135987 | TTTGAGTGAGGAATT[C/T]TTTGGTGGTGCCCTA | 79931 |
| rs116659035 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206377 | AGGAGCTGTTATTCC[C/T]TGATCCTCGGTTAAG | 79931 |
| rs116663383 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215874 | TGCATGTATTAGGTG[C/T]CACATTAAAAAAAAA | 79931 |
| rs116663720 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180525 | ACCATTGGATTTATC[C/T]AGATAGAGGTTATTA | 79931 |
| rs116665727 | snp | C/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164361 | ATTTTAACTTTTCTT[C/G]TCTTCCAAATAGGGA | 79931 |
| rs116668162 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222222 | AGGACCTAGTTTTCC[A/G]TAGAATGTTCCTTCA | 79931 |
| rs116668287 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150755 | GGCATGCCTCCAACA[A/G]GAGAGAGGGACATCC | 79931 |
| rs116719278 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145783 | CAAGTAAAACAGTTT[C/G]TGCAGAGACAACTTA | 79931 |
| rs116719405 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162722 | TAAGCTTGCTAAACA[C/T]AGAGCATCCTGAACA | 79931 |
| rs116723026 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121166419 | TTCACCTCCATCCCT[C/T]TCACATTGTGCCACA | 79931 |
| rs116723254 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191824 | ATTGTTAAGGCTGAG[A/T]TTCATTGGGACAAAT | 79931 |
| rs116753171 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152940 | AACCAAGATTAGTAG[C/G]TAGAAAACAAATAAA | 79931 |
| rs116769064 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223515 | TCCTATAAGAAAATC[A/C]CTTTTGCTACTTGCT | 79931 |
| rs116776488 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185863 | AACAATTGAGTATCC[A/G]TTATTGCAAGGTACT | 79931 |
| rs116831596 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | TNIP3 | GRCh38.p7 | 4:121175011 | GATGTCCCTAGGAGA[C/G]ATCCACATCCTGTCA | 79931 |
| rs116852946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186465 | TGCATATGAACCCTC[C/T]GAAAGAAGCATTGTG | 79931 |
| rs117001696 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220333 | GGCTCTGTTTTCTAA[C/G]GAGAGATCTATTAGT | 79931 |
| rs117096595 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180524 | GACCATTGGATTTAT[C/G]CAGATAGAGGTTATT | 79931 |
| rs117295880 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195241 | AGTAACCCCCATACA[C/T]CTTCAAAATCAACTG | 79931 |
| rs117636201 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208573 | ACAGATTTGAGTAAG[A/T]ATAAAACTGGTCTCT | 79931 |
| rs117730181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178287 | ATGAAATGAGCTAAT[C/G]AATAGAAATACTTTG | 79931 |
| rs118102210 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224604 | CTTATTGTTTTCACC[C/T]ATATTTAGGCAGGTT | 79931 |
| rs137857546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163182 | GAAAAATAGAAAACA[C/T]AGTGACTAGGAATGG | 79931 |
| rs137878574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195531 | ACTCTTTGTTTATTA[C/T]AACATGTCAAACAAT | 79931 |
| rs137931307 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156490 | TTCAAGTCCTTTTTC[A/G]TCAACGTGGGCAATT | 79931 |
| rs137947176 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146844 | AATGCAATTTCTTGG[A/G]CAATTCCTTAATATA | 79931 |
| rs137950318 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229211 | GGGATAACTCAGCTA[C/T]TTGGGAGGCTGAGGT | 79931 |
| rs137977445 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207573 | TTAAGATATTAGTTA[A/G]TAAAAACAATAAGCC | 79931 |
| rs138037957 | snp | A/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121163045 | ATTTTTCTTTAATAA[A/T]TAAAAATTACTGAAA | 79931 |
| rs138050274 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222995 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCGTGT | 79931 |
| rs138052576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142230 | AAGAAAATCTATTCA[C/T]TGAGTCATAAAATAG | 79931 |
| rs138084684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190395 | TTAAGTATTTGACAA[A/G]AGAGTAAATTGACAA | 79931 |
| rs138169426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180928 | GTAGATGTCTTTACC[C/T]CATACTTCACAAAGA | 79931 |
| rs138189700 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222202 | GAATTTCTTCCCCTG[C/T]GAAGAGGACCTAGTT | 79931 |
| rs138208955 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186292 | CTGTGGGAGGGATAC[A/G]TTTTGAGCACTCAGG | 79931 |
| rs138307078 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137360 | CTTTCTAATAAAACA[A/C]CTCCATTATTGTTGG | 79931 |
| rs138326085 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208883 | ATCCATGGAGAGCTT[C/G]AGGGTGGGGCCGCCA | 79931 |
| rs138329131 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217305 | TTAGGAGTTAGGCCC[A/G]TGGGAAACACGAAGC | 79931 |
| rs138442340 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170624 | ATTTAATAAATAAAT[A/G]ATATAAATAATTAGA | 79931 |
| rs138449868 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170321 | GAATGAGTCCGTTTA[C/T]GTATGAATCTATAGT | 79931 |
| rs138483937 | in-del | -/TA | 0.0861826 | 0.188849 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203907 | TACAATATATGTGTG[-/TA]TATATATATATACTA | 79931 |
| rs138499208 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173341 | CAAATTCCCACCATG[C/G]CATGCCTAGAGATTA | 79931 |
| rs138512822 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121150909 | AGAGAGTGCCCTGCT[C/T]TCTTGACATCCAGTA | 79931 |
| rs138512873 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202966 | AAAGGGAACACTTTT[A/G]CACTGCTGTTGGGAA | 79931 |
| rs138536404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213771 | TTCTTACAATATTAC[C/T]ACAGGAAAGCATCTG | 79931 |
| rs138542837 | snp | A/G | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121155859 | AAATTTAAGAAATCC[A/G]CTTTAGGTAATTCAT | 79931 |
| rs138596392 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198807 | TAACAAAATCATGGA[A/C]TACGTTATGAGAACA | 79931 |
| rs138610170 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121185901 | CACAGAAATAATCAC[A/G/T]TGCAGTCATCACTGT | 79931 |
| rs138649839 | snp | A/C/T | 8.27159e-05 | 0.00643058 | missense | TNIP3 | GRCh38.p7 | 4:121150207 | ACTTGATATTCAAGG[A/C/T]ATCCTGAAGAGCCTA | 79931 |
| rs138720768 | in-del | -/ATG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176515 | CATCCTACTAGCATT[-/ATG]ATGATGATGATGATG | 79931 |
| rs138735153 | in-del | -/A | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121174675 | TATCTTCCTCACTGG[-/A]AAAAAAAAAGGAATA | 79931 |
| rs138735579 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216962 | TTTCTCCAACAGGAG[A/T]TTATGATTATTTCTA | 79931 |
| rs138758827 | in-del | -/TT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222822 | GGTGTTTTTTGTGCG[-/TT]TTTTTTTTTTTTTTT | 79931 |
| rs138779637 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146635 | TCCTCAGTCTCACAT[A/G]TAAATGGCATTTAGA | 79931 |
| rs138788371 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184759 | GTGAAATATCTGTAC[A/C]TCATGTGTCATTTAT | 79931 |
| rs138823119 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136046 | GGCCAGCCATAGTTA[C/G]TTGCAGAGCTGTGTT | 79931 |
| rs138845762 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149533 | ACACTTTGGAAGGCC[A/G]AGGCAGGTGGATCAC | 79931 |
| rs138861896 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181143 | AAGAGGTTTTTACCA[A/T]GTAAAGGAGGACCAA | 79931 |
| rs138937998 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121174695 | AAAAAGGAATAATTG[A/G]TCTTTTTTTTGCTAC | 79931 |
| rs139098507 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139617 | GAGCATTTACAAGGC[C/T]GCCAGACCACTGAAA | 79931 |
| rs139201632 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215401 | CTTTATAAACAGAAA[C/T]ATTGGCCTGTAGAAT | 79931 |
| rs139204516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121132749 | TGACATAAAGTTCCA[A/G]GATGGCAAAAAAAAA | 79931 |
| rs139217831 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208146 | CAGCAGCATGAAAAT[C/G]AACTAATATACAACC | 79931 |
| rs139269346 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121172146 | AGTCCAGGGAAGGTA[C/T]AAGCCTTGAAGAGAA | 79931 |
| rs139311213 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171861 | TCAGCCTCCCAAGTA[A/G]TTGGGACTACAGGCA | 79931 |
| rs139336052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177596 | GTCATAAAGAAACCA[A/G]TTTCCTGCTCCTGGA | 79931 |
| rs139340429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199375 | TTGCACTTAAAAGAA[G/T]TCGGACATGAGGTCT | 79931 |
| rs139359107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121204818 | ATAATTTTCATTTCT[A/G]TCAGCTATGTGTAAG | 79931 |
| rs139383338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121187804 | GTGCTATGTGTTTAT[C/T]GTCTCTTCCTGAAGA | 79931 |
| rs139435681 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179126 | GAAAGAGTAAACAGC[A/G]TGTGAAATGATAGCA | 79931 |
| rs139488535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218793 | GCTGGGACTCCTGGG[C/T]TCAAGCAATTCTCCT | 79931 |
| rs139501144 | snp | C/T | 0.0378779 | 0.132304 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182720 | GCATGGCCTCTGGGG[C/T]GAACCGTTTTGGATG | 79931 |
| rs139556064 | in-del | -/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183517 | ACCAGGGGTCCCCAA[-/C]CCCCCACTGCCAGTC | 79931 |
| rs139628466 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178183 | TATTTGAGTTTAGGT[A/C]CAGAATCTAAATCCC | 79931 |
| rs139637864 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135030 | CAGCTGGGCTGTCTT[-/C]CAAGTCTGCACTCAA | 79931 |
| rs139659031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148212 | CCAACTCAGTTTCTT[C/T]GTGCATTTAAACCCT | 79931 |
| rs139673141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121166045 | AGGGATGTGGTAACA[C/T]TGACCTAGAAAAGTG | 79931 |
| rs139683295 | in-del | -/GG | | | intron-variant, splice-acceptor-variant | TNIP3 | GRCh38.p7 | 4:121182515 | TAACAGGAAGTGGCT[-/GG]GTGTGAGAGAAGTTT | 79931 |
| rs139683580 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197326 | TGACGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 79931 |
| rs139720327 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151893 | ACGATTAGTATGGAT[A/G]TCCTAAACAGATCTA | 79931 |
| rs139742727 | in-del | -/T | 0.102014 | 0.201495 | intron-variant | TNIP3 | GRCh38.p7 | 4:121177792 | GTTTTAAATATAGGG[-/T]TTTCTTTCTGCAGAA | 79931 |
| rs139776467 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121209170 | TGTGACAGCATCCCC[A/G]TGCCTCACCCTTTGG | 79931 |
| rs139835279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153751 | ATCATGGGCATGTGG[C/T]CCAAAATACAGGGTT | 79931 |
| rs139835461 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205922 | ACTTACAATCATGGC[A/G]GAAGGCGAAGGGGAA | 79931 |
| rs139853574 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158032 | TGCTATATTACAATA[C/T]TCATGGTCAAGTTTC | 79931 |
| rs139901436 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158319 | TTAGGGCTAACCTGG[A/C]GTAAACAGTATGGAC | 79931 |
| rs139909722 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211850 | AATTCATTCAGCTGG[C/T]TGCAGGTTGTCTGTG | 79931 |
| rs139913843 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144471 | CAGTGGCCCAATCTC[A/G]GCTCACTGCAACCTC | 79931 |
| rs139932469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225535 | AAAGATCCAAACTGT[C/G]ACAACTCCAAACAGA | 79931 |
| rs139937958 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131849 | ATGCTGGCCAGGCTG[A/G]TCTAGAACTCCTGGC | 79931 |
| rs139943252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214677 | CCAAAGGAGGATGGG[C/T]ATCATCTTTCCTAGA | 79931 |
| rs139983424 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121200470 | CGTTTTTCATCTTTA[C/T]GCAGAGCTTTGACAG | 79931 |
| rs140098549 | in-del | -/GTGTGTGT | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121181625 | AAGTTAATAAGACAG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 79931 |
| rs140112799 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192130 | ATGATTACAAGTCTT[A/G]ATTCTACCTCACCAG | 79931 |
| rs140121953 | in-del | -/TGTGTGTGTGTGTG/TGTGTGTGTGTGTGTG/TGTGTGTGTGTGTGTGTG | 0.40867 | 0.248736 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206538 | TACATTTGTATATAT[lengthTooLong]TGTGTGTGTGTTTTA | 79931 |
| rs140145551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196186 | TACTTAGGAATAAAT[A/G]ATCCATTTTCTGTAC | 79931 |
| rs140183816 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121164892 | AAGTGAAATCTTCTC[A/G]TGGAGAATCATTTTC | 79931 |
| rs140222366 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207380 | AAGAAAATTCCATTA[A/C]GTTTAAATCTATTAA | 79931 |
| rs140256501 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121162255 | TTTTCTATCTTTTCT[C/G]TGTTTGTTTATGTTT | 79931 |
| rs140261199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186753 | CAAGTTTGGAAAGTA[A/G]GAGCCATAAATTTAG | 79931 |
| rs140282131 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121201308 | TTCTATGCAAGATGG[C/T]GTGTGGTCAATGGCT | 79931 |
| rs140323540 | in-del | -/TTGC | 0.41141 | 0.19091 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226945 | TGCTGGCTCTGCTCA[-/TTGC]TTAATCAAGATTGTT | 79931 |
| rs140324439 | snp | A/C/T | 0.00637159 | 0.0561118 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139095 | GGAAAAAAAGTTTAA[A/C/T]ACAAGTTTTCTAATG | 79931 |
| rs140365461 | in-del | -/ATTCATAAGTAAT | 0.163892 | 0.234703 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163121 | GTACTAGTTTTTGAA[-/ATTCATAAGTAAT]ATTCAGTTATAGGTG | 79931 |
| rs140404042 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183062 | GGCAAGAATTGAATC[A/G]AACACTCACGGTGAG | 79931 |
| rs140406952 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168853 | TTTTATTCATAGGAA[C/T]ATTTTTAAGAGCGTG | 79931 |
| rs140465712 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121193748 | TAATCAAATGATCAA[A/G]GTTAAAATCACCTGT | 79931 |
| rs140472666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121227347 | CCCTGGTAAGTAAGC[A/G]AAATGAAAGTAAAGG | 79931 |
| rs140600022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143079 | ACATTGGAATTGTCA[A/G]CCTGACATTCAAAGG | 79931 |
| rs140622848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180495 | AAAGACAAGTGAAAA[C/G]TAAAATGCAAAATGA | 79931 |
| rs140692041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170120 | AGCTACTTCCTTCTT[C/T]ATGATCTCATGGTGC | 79931 |
| rs140695580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121221820 | GACTTTCATCACCTA[C/T]TTCCTTCTAAGAAGT | 79931 |
| rs140717670 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145001 | CATATTTCTAAGTAC[C/G]CTAAGCATCTTTCAC | 79931 |
| rs140725714 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226333 | TGTTTTTCTCTTCTA[C/G]ACTTTAAAAATTCAT | 79931 |
| rs140760594 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121199522 | GGGAGGAGGAAGTGA[C/T]ACCTGGGAACCATTG | 79931 |
| rs140788815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213185 | GCTCCTTAAGTGCAT[A/C]TGAAATCCACCATAT | 79931 |
| rs140819114 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121160277 | TGAGGATAGGAGTTC[C/T]AGACCAGGCTGGCCA | 79931 |
| rs140828736 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159104 | AAAACTTAGCCGGAC[A/G]TGGTGGCATGCACCT | 79931 |
| rs140861780 | snp | A/G | 1.65176e-05 | 0.00287376 | missense | TNIP3 | GRCh38.p7 | 4:121147165 | TGAAGTCTTCTTCGT[A/G]TATTTGCACCTAAGA | 79931 |
| rs140901988 | snp | A/G | 1.6577e-05 | 0.00287893 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121158701 | CCTTTCTTTCATATA[A/G]CTCTTTCATACTTCT | 79931 |
| rs140961808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148409 | GTAACAAATATGAAC[A/C]AAATCATTATTATAA | 79931 |
| rs140967369 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189957 | TGTGCCCAGGAGGAC[C/T]GTGCAGGCAGAGGAG | 79931 |
| rs141057002 | in-del | -/AC | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121154001 | CTAGTCCATAAAACA[-/AC]ACACACACACACACA | 79931 |
| rs141068996 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121202504 | TAGACATTGGCAAAA[C/T]CTTTCTAGACATTGG | 79931 |
| rs141104985 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121216944 | GACCGCTCATGCCAG[A/C]TTTTTCTCCAACAGG | 79931 |
| rs141132976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207035 | AAAAATGTGATCAGG[C/T]AGACGAAAATGTTTT | 79931 |
| rs141200926 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226804 | TGTTTAAATAAAACA[A/G]TCCAGTAACTTTATA | 79931 |
| rs141233531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173288 | GGATAGATATGAGGT[A/G]GCTTGACCTTTGACG | 79931 |
| rs141306580 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222423 | TGTATTCAAATCTGT[C/G]TCTCACGTTTAACAG | 79931 |
| rs141306807 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194905 | GGGTAGAGTGGCTCA[C/T]GCCTGTAATACTAGC | 79931 |
| rs141317689 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149646 | TGGTGCATGCCTGTA[A/C]TCCCAGCTACTCGGG | 79931 |
| rs141367237 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121182218 | CAAATACCCTGAAAC[A/G]AGTGGAAGTTCAAAG | 79931 |
| rs141411997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171443 | ATGGTGGGTATATGT[C/G]TATACCATACAATTC | 79931 |
| rs141433180 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189240 | ATGCCACATTTCTTC[C/T]CAGTCCATTGCCAAG | 79931 |
| rs141481636 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121185485 | GTTTACTTTTCTCCT[C/T]CCTTGCCCCATCTAT | 79931 |
| rs141485476 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214456 | CTGGCTGTGGAGAAG[A/T]GGCAAGAGAATGGGA | 79931 |
| rs141505133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156235 | TGCCATTGCCTCACG[A/G]TATCAGTGATAAGAT | 79931 |
| rs141510088 | snp | C/T | 0.000181538 | 0.00952554 | missense | TNIP3 | GRCh38.p7 | 4:121164080 | TATGCTCCGTAGAAC[C/T]TTCTGCGGCAATCAT | 79931 |
| rs141583491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199014 | GGCCAGAGTCACAAA[A/G]TTGTAAACAATTAAG | 79931 |
| rs141600845 | snp | C/G | 4.95086e-05 | 0.00497512 | missense | TNIP3 | GRCh38.p7 | 4:121164110 | TTCTAGATGTGCCCT[C/G]TACAAAATGTGCCAT | 79931 |
| rs141643385 | in-del | -/A/AA/AAA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121160476 | GAGCAACACTGTCTC[-/A/AA/AAA]CAAAAAAAAAAAAGA | 79931 |
| rs141650583 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149229 | CTGTCCACTTGGCAA[C/T]AGCGCGTGAGGTTAG | 79931 |
| rs141651562 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150957 | CATGACATGAGGAGA[A/G]GAAAGAAAGAAGTAA | 79931 |
| rs141651976 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TNIP3 | GRCh38.p7 | 4:121150319 | GCACCCACAAATATG[C/T]ATTTCATGTTTAACG | 79931 |
| rs141660160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156917 | TCCTTCTTATTCTAG[A/G]GAAGTGACCCTTGTT | 79931 |
| rs141729948 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TNIP3 | GRCh38.p7 | 4:121213721 | GACAGAGTAAGACTC[C/T]GTCTCAAAAAAAAAA | 79931 |
| rs141735185 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214689 | GGGTATCATCTTTCC[C/T]AGAAGTTGTTCAACA | 79931 |
| rs141795368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121138241 | TCTGTCTGCCAGTGA[C/T]ATTTAAAACATCTGT | 79931 |
| rs141797475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215984 | CTAAGTAAGGGATTT[C/T]TTTTCATAAGGAACT | 79931 |
| rs141839585 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208966 | TCTCCAGGAAGGGGA[A/G]GGAGCTCCCCAATCT | 79931 |
| rs141902132 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121141721 | AAAACAGAGGCTCTT[G/T]CTGTAGATAATATAA | 79931 |
| rs141942219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | TNIP3 | GRCh38.p7 | 4:121136635 | GGATCACTTGAGGCC[A/G]GGAGTTCGAGACCAG | 79931 |
| rs141943688 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121203592 | ATAACCAAACACCAC[C/G]TGTTCCCCAAAAACC | 79931 |
| rs142000585 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181184 | GAACAGAATTGCAAA[A/G]AAGGTCAGTCATGAG | 79931 |
| rs142057289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173262 | TTTTATGGGAATTAA[A/G]CGTTTTTGAGGGATA | 79931 |
| rs142063761 | snp | A/G | 0.0142736 | 0.0832652 | downstream-variant-500B, utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131116 | CATTTTCAGCTTTGC[A/G]GTTGCTTTAGGTTTA | 79931 |
| rs142131725 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186757 | TTTGGAAAGTAGGAG[C/T]CATAAATTTAGTATA | 79931 |
| rs142207948 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146299 | TAAATTTTTTTATGA[C/T]GAAGAATCTTGAAGC | 79931 |
| rs142233338 | in-del | -/T | 0.104149 | 0.203046 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121184125 | GCATTAATTGTGTGA[-/T]TTTTTTTTTCTTTCT | 79931 |
| rs142312875 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121159688 | AGAAATTATAGTTTC[A/G]TCATAGGACAATATT | 79931 |
| rs142331666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198334 | AGAAGAAAATAACCC[A/G]AAACATATGGATTTG | 79931 |
| rs142353775 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | TNIP3 | GRCh38.p7 | 4:121157108 | CCTCCTCCCGCTGCA[A/G]CCGGTCCCGGGTCAG | 79931 |
| rs142433168 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153041 | ACCAGTAGTATAGTA[C/G/T]GTAATTTTAATTAGG | 79931 |
| rs142456270 | snp | A/G/T | 8.26267e-05 | 0.00642708 | utr-variant-3-prime, missense | TNIP3 | GRCh38.p7 | 4:121132635 | AGTGTGTACTTCTAC[A/G/T]GATGGACTTTCTTTA | 79931 |
| rs142475397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195898 | AGGATGAATGGGAAA[C/T]AGTAGCATTCTGCTA | 79931 |
| rs142481362 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121220531 | ATCCAATTCAAATTT[G/T]GTAACTTAACCTTTA | 79931 |
| rs142513096 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173794 | TCACCATGCCCAGCT[A/G]ATTTTTTTGTAATTT | 79931 |
| rs142539406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191673 | TCTAGGAATATGAGA[A/G]GACTAAATTTTGAGT | 79931 |
| rs142572822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144304 | AACTAAATGAAACTA[C/T]TAAACATGCCCCCTC | 79931 |
| rs142576752 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179752 | GAATCCAGGATTCCC[C/G/T]CAAGTTTGGATGATT | 79931 |
| rs142613505 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206183 | ATCAGACAGGGAAGA[C/T]CAAAAGAAGAGCAAA | 79931 |
| rs142742494 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181078 | AAATTTCAGTGAAGT[C/T]CCAAAAGGAGACATA | 79931 |
| rs142846998 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TNIP3 | GRCh38.p7 | 4:121224153 | AGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 79931 |
| rs142851176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121143433 | ACACTCCATGTCCCA[C/T]ATTCCCATAAGGGAT | 79931 |
| rs142868450 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176485 | ACCATTAAAGAAAAT[G/T]TTGAGGCTCAAGCTC | 79931 |
| rs142916925 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146640 | AGTCTCACATATAAA[C/T]GGCATTTAGAAATAC | 79931 |
| rs142925318 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121228756 | AAAGCATTTTGAATA[C/T]GTCTTTTAAAAAGCC | 79931 |
| rs142959561 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197232 | GAATGCTCTCTTTAA[A/G]AACACCTAAGTCCTG | 79931 |
| rs143061800 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163746 | TACTCTATTGTTACA[A/G]TATGTTCTATTTCTA | 79931 |
| rs143165548 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121155621 | CTGAAGGTTAGCTGC[A/G]TAAACATCAACAGGC | 79931 |
| rs143220478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147890 | TTTATCAATTTTATT[A/G]TTCTAAGTCGACAGC | 79931 |
| rs143247724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214049 | ACCATAATATCAATA[C/T]GTAGGACCGAAAGCA | 79931 |
| rs143267862 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121205019 | TCTTGACTGATTTTT[C/T]ATTATGGGTGTCTTT | 79931 |
| rs143304045 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145686 | AAATTAAAGTTGTTT[A/T]ACTTGCTGTTTTACT | 79931 |
| rs143310157 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226917 | TCCCCTGCAGAGGAA[C/T]ACACTAAATGGATGC | 79931 |
| rs143333925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121208374 | AATGTGTCGGCTGGA[A/G]CCACCCAGATCAATA | 79931 |
| rs143343686 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121207992 | TCTCCTGAAATCTGA[C/T]GGTTTTATCAGGGGT | 79931 |
| rs143346486 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121180143 | CGGTGGCTCACGCCT[A/G]TAATCCCAACACTTT | 79931 |
| rs143365273 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168445 | ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 79931 |
| rs143416104 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229329 | GGTGCGGTGGCTCAC[C/G]CCTGTAATCCCAGTA | 79931 |
| rs143445364 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121207066 | CATTGGAAAAAAACA[C/G]TCATGGAAGATCATA | 79931 |
| rs143510467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212121 | TTCTACATTGAATCC[A/T]AGAGTTTATGCAAGC | 79931 |
| rs143521869 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152206 | ATTCCATGCTGTGAT[-/G]GGATGGTGTGCAAAA | 79931 |
| rs143586633 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197790 | TGAAAGAGAAATGAA[A/G]ATTGTTGGTATTATT | 79931 |
| rs143600728 | in-del | -/CTT | 0.102014 | 0.201495 | intron-variant, cds-indel | TNIP3 | GRCh38.p7 | 4:121166803 | GAGCTGAAAAACCTT[-/CTT]TGTTTCCTGAATCTA | 79931 |
| rs143605751 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121142569 | AAAGGCCTTGGTGGT[G/T]CCTAAGCACTGTCTA | 79931 |
| rs143618889 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121149785 | ACAAAAACAAAAACC[A/T]TGTCTACGTGAAACT | 79931 |
| rs143682240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186409 | CATTGCCAATATGAT[C/T]GACATTGTCACTGTC | 79931 |
| rs143727022 | snp | C/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121222513 | AGTAAGGATAACACT[C/T]CCCTTCTTCAAGGAA | 79931 |
| rs143734148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189686 | AGTAACATTTTCCTC[A/G]GACAAGAAGGAACAT | 79931 |
| rs143744033 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121190590 | TAACAGTTGAGTTGC[A/G]TAACAGGGGACACAC | 79931 |
| rs143759576 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TNIP3 | GRCh38.p7 | 4:121134737 | GTACTCAGCACCTAC[C/T]ACCCTCAGTCCCTAG | 79931 |
| rs143796970 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121144692 | CAGGCATGAGTCACC[A/G/T]CACCCGGCCTGTTTT | 79931 |
| rs143833986 | snp | A/T | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121183774 | TAGGCTGCCTGCTCC[A/T]TATGAGAATCTAATG | 79931 |
| rs143848483 | snp | A/G | 0.0433465 | 0.140692 | upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121229499 | CAGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 79931 |
| rs143849858 | snp | G/T | | | missense | TNIP3 | GRCh38.p7 | 4:121157129 | CCCGGGTCAGGTCGC[G/T]CTGCCTGTCGTCCTC | 79931 |
| rs143875211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121189666 | TTTGCTGAGAGAATT[C/T]TGAAAGTAACATTTT | 79931 |
| rs143938699 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121192545 | AACTGCTCCTGAAAA[A/G]CTTCTATCGAGCTTT | 79931 |
| rs143984142 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147686 | TGACTTACTGTTGAC[G/T]GAAGGTTAGCAGACT | 79931 |
| rs144055687 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121165408 | CTCCATCCAACCTTA[C/T]GACGGGGAAAACCTA | 79931 |
| rs144111626 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TNIP3 | GRCh38.p7 | 4:121170754 | AAGTATTAACTGATG[A/G]TCCCCCAAAACACAC | 79931 |
| rs144134024 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169392 | CTTTACTTGGCCTCC[C/T]AATTTAAAATTGCTC | 79931 |
| rs144168482 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172617 | ATACAATATTCTGCC[A/G]TTTATCTGAAATTTA | 79931 |
| rs144189403 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121223633 | AAAAATGCCTCATTA[A/T]CACACGTGCATTTCA | 79931 |
| rs144194660 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121218928 | GAAGTGGCCAGCCAT[A/G]GTGGCTCACGCCTGT | 79931 |
| rs144196895 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139402 | TCTCCAAGGCCAGCA[C/T]CTCTGTATTTAACGC | 79931 |
| rs144241693 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | TNIP3 | GRCh38.p7 | 4:121171887 | AGGCATGAACCACCA[C/G]GCCTGGCTAATTTTT | 79931 |
| rs144275915 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121206010 | TCCCCTTGTAAAATC[A/G]TCAGATCTCTTGAGA | 79931 |
| rs144338009 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215657 | TTAAAGCACTTCTTC[A/G]TGTATTTCTATCCCA | 79931 |
| rs144340516 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | TNIP3 | GRCh38.p7 | 4:121133371 | AAGCAAATAGGAAGA[A/T]AATAAGTTACTTTTC | 79931 |
| rs144378465 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199433 | AGCCCAGAAATACTC[A/C/T]TTTCTGGCAGAGGTA | 79931 |
| rs144411826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121152066 | TGCAAATAAATTGAA[C/T]AGAGTACACATAATT | 79931 |
| rs144474593 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145042 | TACTTATTTTCACTG[A/G]CTTAACGCATCCTCA | 79931 |
| rs144476718 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226505 | AGGTCTGTGCATGCA[G/T]TGCCACTTGAAAGGA | 79931 |
| rs144496210 | in-del | -/AG | 0.0174175 | 0.0916809 | intron-variant | TNIP3 | GRCh38.p7 | 4:121212814 | AATAGTTTAATTTAG[-/AG]TCAGGTAAGAAGGGG | 79931 |
| rs144516454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191353 | AGTGGAAATACACTC[A/G]GGTGGGTTTATTGAT | 79931 |
| rs144541250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148265 | GTGATGTAATGATTG[A/C]GGGTGCCTGATTAGA | 79931 |
| rs144548559 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121137640 | AGACTTGTAAAGTTC[A/T]CAACCTGCAAAACTA | 79931 |
| rs144609635 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121199735 | CAATGCCCAGAATAG[A/T]GGCATCATTCTTTTG | 79931 |
| rs144645941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121186263 | ATGGAGAGAGTGGGC[A/G]TCAGTGTTGACCGCT | 79931 |
| rs144680254 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176205 | TGGCTCATTTAAATA[A/T]CTTCACCCATGTTGC | 79931 |
| rs144698172 | snp | C/G | 4.95733e-05 | 0.00497837 | utr-variant-3-prime, missense | TNIP3 | GRCh38.p7 | 4:121132636 | GTGTGTACTTCTACG[C/G]ATGGACTTTCTTTAC | 79931 |
| rs144719759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TNIP3 | GRCh38.p7 | 4:121168121 | AATATATCCAGACAG[A/G]GGAGGAGCACATTGC | 79931 |
| rs144724457 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121198503 | TGAGCACCTATTATG[A/G]GCCAGATGCATTTCT | 79931 |
| rs144750053 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197355 | CAACATGGTGAAACA[C/T]CTTCTCTGCTAAAAA | 79931 |
| rs144762502 | snp | A/G | 0.000247584 | 0.0111234 | missense | TNIP3 | GRCh38.p7 | 4:121164073 | ACCTCTTTATGCTCC[A/G]TAGAACTTTCTGCGG | 79931 |
| rs144833183 | in-del | -/ACAC | | | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121132214 | TTTTTACCCCAGGAA[-/ACAC]ACACACACACACACA | 79931 |
| rs144901760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215548 | ACGTGACTTTCCTAC[C/T]ACCACGTCTTTGTAC | 79931 |
| rs145016167 | snp | A/G | 0.00194552 | 0.0311284 | missense, utr-variant-5-prime | TNIP3 | GRCh38.p7 | 4:121182732 | GGGTGAACCGTTTTG[A/G]ATGAGGAGACGCATT | 79931 |
| rs145070383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121173115 | CTTCCTGGTTTACTT[A/C]CCCCAAAGAACCTTT | 79931 |
| rs145081004 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TNIP3 | GRCh38.p7 | 4:121181087 | TGAAGTCCCAAAAGG[A/C]GACATAACCTGTAGC | 79931 |
| rs145092916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219149 | AGGTTGCAGTGAGCC[A/G]AGATCACACCATTGC | 79931 |
| rs145098714 | snp | G/T | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121212555 | AATTTATGAAAAAAA[G/T]TATGATTGGTCTATG | 79931 |
| rs145145190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194093 | GAATGGAGTTTGAGG[A/C]TTAGATGTAGTAGTG | 79931 |
| rs145148910 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121135697 | AGCCACCACTCCTGG[C/T]CTTAAACTAGTGATT | 79931 |
| rs145158544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121179127 | AAAGAGTAAACAGCA[C/T]GTGAAATGATAGCAC | 79931 |
| rs145170452 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TNIP3 | GRCh38.p7 | 4:121225460 | AGACTTGTGGATGTA[C/G]ACGTGAAAAGTGATT | 79931 |
| rs145201564 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TNIP3 | GRCh38.p7 | 4:121145109 | CAGAATGCCAGAATG[A/T]TTTGACCTAAATATT | 79931 |
| rs145251349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121163143 | AGTAATATTCAGTTA[C/T]AGGTGGGGGAGGATA | 79931 |
| rs145349922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TNIP3 | GRCh38.p7 | 4:121158336 | TAAACAGTATGGACT[C/T]TAAACCATATCTCAC | 79931 |
| rs145364665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121139896 | TAAATATCCTGTAAT[A/G]TTACCAACACTATAG | 79931 |
| rs145369854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121219672 | AGTTTACTCACATAG[C/G]TTTTACAGACCTTGA | 79931 |
| rs145395009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121156328 | AGAGTTTAAGGTTTC[A/C]TCCCATTTTCTACAA | 79931 |
| rs145473595 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121178481 | GCATTTGGAGTTCTC[A/G]AAGACATATTCCACA | 79931 |
| rs145485288 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TNIP3 | GRCh38.p7 | 4:121153854 | ATCTAGTTGAGAGAG[A/G]CATATCTCAACTCAA | 79931 |
| rs145541982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121197638 | GAGTAATGAGAAAGA[A/G]ATTATCTTTAACATG | 79931 |
| rs145639810 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121222168 | TTGATGCATCTTAGA[A/G]GCTTAGTGAAATATT | 79931 |
| rs145642012 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121141481 | ATTTTTCTTGTTTTG[C/T]CATATCCACTTTCCT | 79931 |
| rs145684857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TNIP3 | GRCh38.p7 | 4:121148589 | GAGCTTTAAGACTGT[A/G]CATATTACCCTTATT | 79931 |
| rs145723557 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TNIP3 | GRCh38.p7 | 4:121136688 | AGCAAGACACCATCT[A/G]AACAAAAAATAAAAA | 79931 |
| rs145809864 | in-del | -/TCTCTGCCTGTCGTCCTT | 0.0740909 | 0.17764 | cds-indel | TNIP3 | GRCh38.p7 | 4:121157145 | CTGCCTGTCGTCCTC[-/TCTCTGCCTGTCGTCCTT]TCTCTGCCTCTGATG | 79931 |
| rs145965399 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TNIP3 | GRCh38.p7 | 4:121195935 | TGACATTTACACTCA[C/T]GTTGCTGATGCTTGT | 79931 |
| rs145978022 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TNIP3 | GRCh38.p7 | 4:121146390 | TTACAAATAAAAATG[A/G]TGCAGTTTGTTTTAT | 79931 |
| rs146003793 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121211302 | ATGATATAAAATACT[A/G]AAAAGAGGAATAAAA | 79931 |
| rs146087498 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TNIP3 | GRCh38.p7 | 4:121176904 | CAGCCACTGGGAGTT[C/T]CTCCCTTAACTTGTA | 79931 |
| rs146130017 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TNIP3 | GRCh38.p7 | 4:121191937 | GTGATAAGGACATAA[C/T]TTTTATGAGTATATC | 79931 |
| rs146207211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121151354 | TAAAGGTAGGAAAAG[A/G]AAAGCAAATGTGTGG | 79931 |
| rs146209465 | snp | A/G | 0.000194996 | 0.00987219 | missense | TNIP3 | GRCh38.p7 | 4:121154667 | ATTCTTCATTTAGGC[A/G]TTCCTTTTCCTTCTG | 79931 |
| rs146217631 | in-del | -/GATA | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121203224 | ATGTGATATAGATAG[-/GATA]ATAGATAGATAGATA | 79931 |
| rs146231151 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TNIP3 | GRCh38.p7 | 4:121215241 | TCTTTTAATGAAAAC[A/G]TTCTCATAGAGAATC | 79931 |
| rs146249447 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TNIP3 | GRCh38.p7 | 4:121172052 | TTCCCCTACTTCTAG[A/G]TACTCATCTGTCATC | 79931 |
| rs146249785 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | TNIP3 | GRCh38.p7 | 4:121217643 | TTGTTTATATGGAAC[A/G]CTGGAGATATTACAC | 79931 |
| rs146263175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TNIP3 | GRCh38.p7 | 4:121194349 | AAAAAGCAATTAAAA[G/T]ATTAAACCTAAAAGA | 79931 |
| rs146322352 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | TNIP3 | GRCh38.p7 | 4:121131575 | TAGCCATATAGCCAT[C/T]ATCATCCCATCAGGA | 79931 |
| rs146326002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121214676 | ACCAAAGGAGGATGG[A/G]TATCATCTTTCCTAG | 79931 |
| rs146349820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121196943 | GTAAGAAATAAAATT[A/C]TCCTTCTTTTACTCA | 79931 |
| rs146370473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121147972 | ATGCAGATACACATA[C/T]TACATTTTTAAGGCT | 79931 |
| rs146418961 | in-del | -/ATG | | | intron-variant | TNIP3 | GRCh38.p7 | 4:121176533 | TGATGATGATGATGA[-/ATG]TGATGATGATGATGA | 79931 |
| rs146428348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121169590 | TTAGTGCCTGTGCGT[G/T]TTCATGTGGGACTCA | 79931 |
| rs146554891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TNIP3 | GRCh38.p7 | 4:121226719 | ACCTTCCTTGCAGGA[G/T]AGTTTAACTGCTCAC | 79931 |