| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs5858 | snp | C/T | 0.50003 | 0.0168484 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352920 | GTTGAGGTGTCTTTT[C/T]TTTTTCTTTCTTTAG | 5977 |
| rs540341 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336272 | tgaggcaggcagatt[A/G]cttgaggtcaggagt | 5977 |
| rs610864 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | DPF2 | GRCh38.p7 | 11:65335147 | ACCCCTCCTCCCAAC[A/G]CTATTGTCTTTCTCT | 5977 |
| rs615768 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | DPF2 | GRCh38.p7 | 11:65342275 | ttatttttagtagag[A/G]caaggtcctgctatg | 5977 |
| rs616639 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342101 | ttaatttttttTTTT[G/T]gttgcccaggctgga | 5977 |
| rs620888 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | DPF2 | GRCh38.p7 | 11:65351500 | AAGTCTTCAAATATT[A/G]TGAAATATCATCCTC | 5977 |
| rs629710 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | DPF2 | GRCh38.p7 | 11:65341762 | TGTGATAAAAGTGAA[G/T]GAATGAGAGTCTATA | 5977 |
| rs633673 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350911 | gcttactctaacctc[G/T]gcctcccagattcaa | 5977 |
| rs634016 | snp | G/T | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65350885 | ttcaagcaattctct[G/T]gcctcagcctctata | 5977 |
| rs642848 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336280 | gcagattgcttgagg[C/T]caggagtttgagacc | 5977 |
| rs642860 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336289 | ttgaggtcaggagtt[C/T]gagaccagcctggcc | 5977 |
| rs656964 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336290 | tggccaggctggtct[C/T]aaactcctgacctca | 5977 |
| rs657005 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336271 | ctcctgacctcaagc[A/G]atctgcctgcctcaa | 5977 |
| rs665076 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65352998 | GAAAGGCAGGAGATA[A/G]ACCATCCAGCAGAGG | 5977 |
| rs681440 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | DPF2 | GRCh38.p7 | 11:65349720 | agaatggcgtgaacc[C/T]gggaagcggagcttg | 5977 |
| rs689288 | snp | C/T | 0.214541 | 0.247473 | intron-variant | DPF2 | GRCh38.p7 | 11:65351526 | GACTTAGAGGTTTAT[C/T]CCAGCTCAGGAAACC | 5977 |
| rs1044768 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352795 | GATTCCTCAAGTTTT[C/T]TGCTTAGTGGCACTG | 5977 |
| rs1144926 | snp | A/G | 0.369346 | 0.219673 | intron-variant | DPF2 | GRCh38.p7 | 11:65347414 | ttgagcctgaaggga[A/G]aggttttagtgagct | 5977 |
| rs1152618 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | DPF2 | GRCh38.p7 | 11:65347379 | ctgtcatccaggctg[C/G]agtgcagtgacgcga | 5977 |
| rs1309237 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337854 | ttgcgccattgcact[A/C]cagcctgggcaacaa | 5977 |
| rs1309440 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343106 | ctccatgttggtcag[A/G]ctggtctcgaactgc | 5977 |
| rs1309471 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337883 | tgggaggcggaggtt[G/T]cggtgagccgagatc | 5977 |
| rs1783473 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348608 | TAGAGCTTGGGCTTT[A/T]GGGGaaaaaaaaaaa | 5977 |
| rs1783474 | snp | A/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65348612 | GCTTGGGCTTTAGGG[A/G]AAAAAAAAAAAAAAA | 5977 |
| rs1786671 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335152 | TCCTCCCAACACTAT[G/T]GTCTTTCTCTCTGAT | 5977 |
| rs2269224 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DPF2 | GRCh38.p7 | 11:65335907 | CAACCTCCGCCTCCC[A/G]GGTTCCAGCAATTCT | 5977 |
| rs2307264 | snp | C/T | 0.0252716 | 0.109531 | intron-variant | DPF2 | GRCh38.p7 | 11:65346380 | TATCCCCGCCCCCTC[C/T]TCAGCATGGCTCCTT | 5977 |
| rs2307265 | snp | A/G | 0.031825 | 0.122064 | intron-variant | DPF2 | GRCh38.p7 | 11:65341189 | tcaaatgaatatgat[A/G]tgattctttccttta | 5977 |
| rs2307266 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | DPF2 | GRCh38.p7 | 11:65349020 | TTATGTTATCACTTA[C/T]ATATTCTTCCAAATT | 5977 |
| rs2307267 | snp | A/G | 0.020409 | 0.0989342 | intron-variant | DPF2 | GRCh38.p7 | 11:65341076 | TCTATTAAGCCAGGT[A/G]AGGCACATACTTCCT | 5977 |
| rs2904969 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337504 | atatatatatatata[G/T]agagagagagagaga | 5977 |
| rs3218610 | snp | C/G/T | 0.0140046 | 0.0825028 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333844 | GGCGCCTGCGCGCTG[C/G/T]GGACTGTGGGGCTTC | 5977 |
| rs4647563 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65334675 | ATAGCTGTTGGGGCC[A/G]TGGACGCTGGCCTAT | 5977 |
| rs4647564 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | DPF2 | GRCh38.p7 | 11:65334796 | TGGGCGAATAGAGCT[G/T]CTTTTAATGGGTATG | 5977 |
| rs4647566 | in-del | -/T | 0.022469 | 0.103584 | intron-variant | DPF2 | GRCh38.p7 | 11:65335780 | TGTTATACATTGAGT[-/T]ACATTGAGGTCAGGA | 5977 |
| rs4647567 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | DPF2 | GRCh38.p7 | 11:65338886 | GTTTGCTGTCTCATC[C/T]CCAGGCTGTTTCTTG | 5977 |
| rs4647568 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DPF2 | GRCh38.p7 | 11:65338922 | TCCTGATATGTCAAA[A/G]CTCATTTGGTCCAAC | 5977 |
| rs4647569 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | DPF2 | GRCh38.p7 | 11:65338985 | ACCTGGGCTGACTAA[A/G]TGTCCATGTTCGTGT | 5977 |
| rs4647570 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | DPF2 | GRCh38.p7 | 11:65339018 | CTTGCAGGCAAGCCA[G/T]GTCTTTTTACTCTCA | 5977 |
| rs4647571 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DPF2 | GRCh38.p7 | 11:65339040 | TTACTCTCAAGTCAA[A/G]TCTGACTGTATCTCA | 5977 |
| rs4647572 | snp | A/G | 0.0114282 | 0.0747228 | intron-variant | DPF2 | GRCh38.p7 | 11:65339176 | tacttgggaggctaa[A/G]gcaggaggatcactt | 5977 |
| rs4647573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65339297 | AGTTTGTTAACCTCC[A/G]TTACCAAAGTCCTTG | 5977 |
| rs4647574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65339456 | AGTCTTTTGAGACCA[A/G]GAAGATTTTTTCCTA | 5977 |
| rs4647575 | snp | A/C/T | 0.122515 | 0.215389 | intron-variant | DPF2 | GRCh38.p7 | 11:65339698 | CCCACTTTTTCTCCC[A/C/T]GCTGACCTGCAGTTT | 5977 |
| rs4647576 | snp | C/G | 0.187053 | 0.241946 | intron-variant | DPF2 | GRCh38.p7 | 11:65339983 | atttgggaggtgatt[C/G]taggaaagagggaat | 5977 |
| rs4647577 | snp | C/T | 0.046775 | 0.145601 | intron-variant | DPF2 | GRCh38.p7 | 11:65340308 | TTCTAGAGAAGCAGA[C/T]GGCAGGGGAGAGGAA | 5977 |
| rs4647578 | snp | C/T | 0.00616026 | 0.055156 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340442 | CAATTACAATGCTCG[C/T]CTCTGTGCTGAGCGC | 5977 |
| rs4647579 | in-del | -/ATAAGTTA | 0.0114282 | 0.0747228 | intron-variant | DPF2 | GRCh38.p7 | 11:65341240 | gagacagGTAAACAG[-/ATAAGTTA]TGGTGCCAAGTGAAC | 5977 |
| rs4647580 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | DPF2 | GRCh38.p7 | 11:65341273 | tgaactagggtGTCT[C/T]AATTCCTGGGCGTGC | 5977 |
| rs4647581 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | DPF2 | GRCh38.p7 | 11:65343574 | ATCCCAAAGTATGGA[A/G]GGGAGCAGGAGCAGG | 5977 |
| rs4647582 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DPF2 | GRCh38.p7 | 11:65343646 | GTGTGGGTGGGACCA[C/T]GTCACAGAGGAGGTT | 5977 |
| rs4647583 | snp | A/C/G | 0.00454607 | 0.0474597 | intron-variant | DPF2 | GRCh38.p7 | 11:65343956 | CCTCAGGCCCAGCTA[A/C/G]CAAAATAAGGGTGTC | 5977 |
| rs4647584 | snp | A/G | 0.00824449 | 0.0636732 | intron-variant | DPF2 | GRCh38.p7 | 11:65344093 | CTCACAAGTGGGTGG[A/G]TAGACCTTGCCTTGG | 5977 |
| rs4647585 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DPF2 | GRCh38.p7 | 11:65344314 | GTTGCTTGTGGGGGC[C/T]ACAGCAGGCAGGGTT | 5977 |
| rs4647586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65344409 | CACTGAGTTTTTCAA[C/T]GTCTGTTCTCTTTTT | 5977 |
| rs4647587 | snp | C/T | 0.207559 | 0.246371 | intron-variant | DPF2 | GRCh38.p7 | 11:65344504 | CTCTCTCGTTTGCTC[C/T]GCTTTCCTGCTGCTG | 5977 |
| rs4647588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346126 | GCTTGCTGGCCTCTA[A/G]GGCTGTCATAACCAG | 5977 |
| rs4647589 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | DPF2 | GRCh38.p7 | 11:65346136 | CTCTAGGGCTGTCAT[A/G]ACCAGCCCACCTCGC | 5977 |
| rs4647590 | snp | G/T | 0.00492123 | 0.0493599 | intron-variant | DPF2 | GRCh38.p7 | 11:65346404 | GCTCCTTCTGGGCTT[G/T]TACTGCTGTTTGCAC | 5977 |
| rs4647591 | in-del | -/A | 0.0111728 | 0.0739025 | intron-variant | DPF2 | GRCh38.p7 | 11:65346447 | AGTGAGCTTTCTTTT[-/A]AAAAGGGAGCAGGAT | 5977 |
| rs4647592 | in-del | -/TT | 0.0115144 | 0.0749975 | intron-variant | DPF2 | GRCh38.p7 | 11:65349091 | TCCTAACATTTCAAC[-/TT]TTAAAGGGTTTAGTG | 5977 |
| rs4647593 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | DPF2 | GRCh38.p7 | 11:65351104 | ccGTATTGACCTTTG[A/G]GTTAGAAAGGACTTA | 5977 |
| rs4647594 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | DPF2 | GRCh38.p7 | 11:65351116 | TTGGGTTAGAAAGGA[C/T]TTACATTTTTGAGTC | 5977 |
| rs4647595 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | DPF2 | GRCh38.p7 | 11:65351246 | TCAAAAAAAATTAGA[A/G]GAATTCAGCCATAGT | 5977 |
| rs4647596 | in-del | -/CT | 0.0298439 | 0.118454 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352112 | GAGCAGCTCACTTCT[-/CT]GTGTTCTGCCTCCCC | 5977 |
| rs4647597 | snp | A/G | 0.0132444 | 0.080292 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352427 | CTCACTCTTACGGTC[A/G]GTCTCCAGTGACTGA | 5977 |
| rs4647598 | snp | A/G/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352687 | TCTGCCACCTGCCCC[A/G/T]TGTATCCTGGCTCTC | 5977 |
| rs4647599 | snp | A/T | 0.0999677 | 0.199976 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353107 | TCCCCCCAAATTAAA[A/T]TTTTTTTGTGGAACC | 5977 |
| rs4930290 | snp | A/T | 0.499653 | 0.0131743 | intron-variant | DPF2 | GRCh38.p7 | 11:65336906 | ccagcctggccaagg[A/T]ggtgaaacccgtctc | 5977 |
| rs7105557 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65340650 | TTCCCTACTGCCTTC[C/T]ACCTATGGATGAATA | 5977 |
| rs7117137 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | DPF2 | GRCh38.p7 | 11:65348598 | aaaTATACCATAGAG[C/T]TTGGGCTTTAGGGaa | 5977 |
| rs7947014 | snp | C/G | 0.207253 | 0.246318 | intron-variant | DPF2 | GRCh38.p7 | 11:65343115 | gaccagcctgaccaa[C/G]atgaagaaaccccgt | 5977 |
| rs7950149 | snp | C/T | 0.207253 | 0.246318 | intron-variant | DPF2 | GRCh38.p7 | 11:65347696 | gttttactcttgtca[C/T]ccaggctggagtaca | 5977 |
| rs11227177 | snp | C/T | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65337154 | TGGTTTTGAAACTTT[C/T]TAGGCAAAATCTAGA | 5977 |
| rs11227178 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337421 | TTGCACCACTGCATT[C/T]TAACCTGGGCGGCAA | 5977 |
| rs11395305 | in-del | -/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333120 | TTTTTTTTTTTTTTT[-/T]CTTGAGATGGAGCCT | 5977 |
| rs11553935 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340995 | CAGCTGTACTCCTAC[C/T]CTGCCCGGCGCTGGC | 5977 |
| rs11553936 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352915 | TTGGAGTTGAGGTGT[C/T]TTTTCTTTTTCTTTC | 5977 |
| rs11553937 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352866 | GGAGTAGCCTTCCCC[C/T]TTGGCCGTGGGCAGG | 5977 |
| rs11600253 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337474 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 5977 |
| rs11820951 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347072 | caggctggagtacag[A/T]ggcacaatctcagct | 5977 |
| rs11823234 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340012 | ataaggaggAACTTA[A/G]GAGGGACTATCATCT | 5977 |
| rs12222749 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333033 | catatgtatatatat[A/G]tgtatatatatatat | 5977 |
| rs12222750 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333049 | tgtatatatatatat[A/G]tatatatgtgtatat | 5977 |
| rs12222752 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333057 | tatatatgtatatat[A/G]tgtatatatatatgt | 5977 |
| rs12225450 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333037 | tgtatatatatgtgt[A/G]tatatatatatgtat | 5977 |
| rs12225451 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333051 | tatatatatatatgt[A/G]tatatgtgtatatat | 5977 |
| rs12225452 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333061 | tatgtatatatgtgt[A/G]tatatatatgtgtat | 5977 |
| rs12274694 | snp | G/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332306 | gaggtggaggttgca[G/T]tgagctgagatagtg | 5977 |
| rs12418663 | snp | A/G | 0.258288 | 0.249863 | intron-variant | DPF2 | GRCh38.p7 | 11:65347084 | cagtggcacaatctc[A/G]gctcactgcaacctc | 5977 |
| rs12574891 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333035 | tatgtatatatatgt[A/G]tatatatatatatgt | 5977 |
| rs12574894 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333085 | tgtgtatatatatat[A/G]tatatatattttttt | 5977 |
| rs12577028 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333031 | tacatatgtatatat[A/G]tgtgtatatatatat | 5977 |
| rs12577030 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333045 | tatgtgtatatatat[A/G]tatgtatatatgtgt | 5977 |
| rs12577032 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333081 | tatatgtgtatatat[A/G]tatgtatatatattt | 5977 |
| rs12785597 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333218 | ggctcaagtgatcct[C/T]ccacctcagcctccc | 5977 |
| rs28468644 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337472 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 5977 |
| rs28781278 | snp | C/T | 0.325327 | 0.238382 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332666 | CCATGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 5977 |
| rs34231475 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336969 | GCGTGCACCTGTAGT[-/A]CCCAGCTACTCAGGA | 5977 |
| rs34659148 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331919 | AAAAAAAATTAGTCA[A/G]GCTACATAAGATCTA | 5977 |
| rs34700000 | snp | A/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331949 | ATGTGCTTCTCTTTA[A/T]GTATATTTCAATTAA | 5977 |
| rs34879490 | in-del | -/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344267 | GGACCTGCATGCTCT[-/G]GGGAAAGATTTCTGC | 5977 |
| rs35038130 | in-del | -/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336865 | GAGGCTGAGGCGGGC[-/T]GGATCACAAGGTCAG | 5977 |
| rs35129548 | snp | A/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331911 | AAAAAAAAAAAAAAA[A/T]TTAGTCAAGCTACAT | 5977 |
| rs35324711 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331957 | CTCTTTATGTATATT[C/T]CAATTAAAAGTTTGA | 5977 |
| rs35387404 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351945 | ACCTCTGGCCCCAGG[-/C]CCTCAGGGAGAAAGG | 5977 |
| rs35405661 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348922 | CCGTCCATGTCTGAG[-/C]CCCCTGAAGGTAAGT | 5977 |
| rs35521433 | snp | A/C | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331960 | TTTATGTATATTTCA[A/C]TTAAAAGTTTGAATT | 5977 |
| rs35694028 | snp | A/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331990 | TTAAAAATAGTACTA[A/T]TAATAAATAGGCTAG | 5977 |
| rs35769947 | in-del | -/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339422 | TAAAGATTTACCCTT[-/G]GATTCAGATTTCAAA | 5977 |
| rs35922774 | in-del | -/AC | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333017 | CATATGTATATATAT[-/AC]ATATGTATATATATG | 5977 |
| rs35923641 | in-del | -/CT/T | 0.465052 | 0.127485 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333103 | TATATATTTTTTTCC[-/CT/T]TTTTTTTTTTTTTTT | 5977 |
| rs35947979 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352969 | TAGTAAAAATAAATG[-/T]TTTTACACAGAGCCC | 5977 |
| rs36039888 | in-del | -/TA | 0.282369 | 0.247896 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333036 | ATGTATATATATGTG[-/TA]TATATATATATGTAT | 5977 |
| rs36067492 | in-del | -/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346923 | GGCAAGCACTGCCAG[-/G]ATCTCTGGGGCCTCG | 5977 |
| rs55812677 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333982 | CCTGGGAGTAGGGGG[C/T]GGTGGGGGAAGGGAC | 5977 |
| rs56032535 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348611 | AAAAAAAAAAAAAAA[-/A]GTGGAGGTGATTTGA | 5977 |
| rs56128681 | snp | A/G | 0.311614 | 0.242289 | intron-variant | DPF2 | GRCh38.p7 | 11:65347140 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 5977 |
| rs56217546 | snp | C/T | 0.262159 | 0.249704 | intron-variant | DPF2 | GRCh38.p7 | 11:65347107 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 5977 |
| rs56262440 | snp | A/G | 0.261884 | 0.249717 | intron-variant | DPF2 | GRCh38.p7 | 11:65347108 | CAACCTCTGCCTCCT[A/G]GGTTCAAGTGATTCT | 5977 |
| rs56951778 | in-del | -/AT | 0.5 | 0 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333047 | TGTGTATATATATAT[-/AT]GTATATATGTGTATA | 5977 |
| rs57324882 | snp | C/G | 0.264906 | 0.249555 | intron-variant | DPF2 | GRCh38.p7 | 11:65347096 | CTCAGCTCACTGCAA[C/G]CTCTGCCTCCTGGGT | 5977 |
| rs57579516 | in-del | -/T/TT | 0.264632 | 0.249571 | intron-variant | DPF2 | GRCh38.p7 | 11:65335079 | GTTTTTTTTTTTTTT[-/T/TT]AAGTTGCTTTCTGCT | 5977 |
| rs59557862 | in-del | -/A | 0.0283406 | 0.115616 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333094 | TATATGTATATATAT[-/A]TTTTTTTCCTTTTTT | 5977 |
| rs59621783 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336783 | ACAGCAAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 5977 |
| rs60304778 | in-del | -/TATATATAGA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337498 | ATATATATATATATA[-/TATATATAGA]GAGAGAGAGAGAGAG | 5977 |
| rs60933608 | snp | C/G/T | 0.186737 | 0.241863 | intron-variant | DPF2 | GRCh38.p7 | 11:65350337 | CTTGCAAGCTGTTTT[C/G/T]TTTTCTTTTCTTTTC | 5977 |
| rs61072220 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DPF2 | GRCh38.p7 | 11:65346758 | CTTCTGGGAGGGTGA[C/T]GCTGGTGTTGAAATT | 5977 |
| rs61660366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65338189 | TGGTCTCAAGAGATC[C/T]ACCAGCCTTGGCCTC | 5977 |
| rs61736579 | snp | A/G/T | 0.00728839 | 0.0599256 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345988 | TGACTTCTGCCTGGG[A/G/T]GACTCAAAGATTAAC | 5977 |
| rs61895421 | snp | A/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331914 | AAAAAAAAAAAAATT[A/T]GTCAAGCTACATAAG | 5977 |
| rs61895422 | snp | C/T | 0.422315 | 0.181128 | intron-variant | DPF2 | GRCh38.p7 | 11:65337318 | AGCTGGGCGTGGTGG[C/T]GCATGCCACTCGGGA | 5977 |
| rs61895423 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343560 | CACAGGGGAAAGATA[C/T]CCCAAAGTATGGAAG | 5977 |
| rs61895424 | snp | G/T | 0.331411 | 0.236373 | intron-variant | DPF2 | GRCh38.p7 | 11:65348507 | GATCACTTGGGCCCA[G/T]GAGGTCAAGGCTGCA | 5977 |
| rs61895425 | snp | A/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65348609 | AGAGCTTGGGCTTTA[A/G]GGAAAAAAAAAAAAA | 5977 |
| rs71064878 | in-del | -/TCTATATATATA | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65337496 | CTCTCTCTCTCTCTC[-/TCTATATATATA]TATATATATATATAT | 5977 |
| rs71468699 | snp | C/G | 0.5 | 0 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344046 | CCATCCTGGAGGACC[C/G]GGATAAGCCCTATGC | 5977 |
| rs72934975 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353185 | AAATTCAAGTTTATA[A/G]CAATTCTTTGTTATA | 5977 |
| rs73482254 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334131 | GGCACACTGGAGCCC[C/T]GACGGGCGGCATCCC | 5977 |
| rs73482257 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | DPF2 | GRCh38.p7 | 11:65342677 | TATGGGGTAGGTCCT[A/G]TGTTCCCCATTTCAC | 5977 |
| rs74370342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338997 | TAAGTGTCCATGTTC[A/G]TGTGACTTGCAGGCA | 5977 |
| rs74424217 | snp | A/G | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65349812 | AAGAAAAAAAAAAAA[A/G]AGCCAACAGAAATTC | 5977 |
| rs74563389 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336807 | AAAAAAAAAAAAAAA[A/G]AAGCCGGGCACGGTG | 5977 |
| rs74711281 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341377 | CCTTTTGAGCCTTGC[C/T]TTATCCTGACCTTGC | 5977 |
| rs74950469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65340127 | TTTCACCTCTTTGGG[A/G]GTTAAACTTAAGTCT | 5977 |
| rs75834053 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | DPF2 | GRCh38.p7 | 11:65350182 | TCGAGGTAGTGGAGA[A/G]CTGCAGGCCCGAGTG | 5977 |
| rs76113686 | snp | C/T | 0.0364509 | 0.129988 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331763 | AAATATATACACCTA[C/T]GATGTACCCACAAAA | 5977 |
| rs76278499 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341380 | TTTGAGCCTTGCTTT[A/T]TCCTGACCTTGCTTG | 5977 |
| rs77663475 | snp | A/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65349799 | AGACTCCATCTCAAA[A/G]AAAAAAAAAAAAAAG | 5977 |
| rs78756853 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65351568 | CTGCTGCAGAGCATC[A/C]CTCGTCCTACCTGTA | 5977 |
| rs79697830 | snp | A/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65349800 | GACTCCATCTCAAAG[A/G]AAAAAAAAAAAAAGC | 5977 |
| rs80219065 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331779 | GATGTACCCACAAAA[A/C]TTAAAAAATTGAAAA | 5977 |
| rs80344838 | snp | G/T | 0.375 | 0.216506 | intron-variant | DPF2 | GRCh38.p7 | 11:65337506 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 5977 |
| rs111452455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334315 | GCCGCCCACCCCGCC[A/C]CGTCCCGTCCCGTTC | 5977 |
| rs111538993 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65338656 | AGATTCGTGCCTACC[C/T]CAGATTACAGTCATT | 5977 |
| rs111713619 | snp | A/T | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65346575 | TCTAGTCACTAAAGA[A/T]GCTAAAGACAAACAA | 5977 |
| rs111807312 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DPF2 | GRCh38.p7 | 11:65343065 | AGCACTTTGGGAGGC[C/T]GAGGCAGTTGGATCA | 5977 |
| rs111844146 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353476 | TGGCTTCAGTTGCCT[G/T]CAGCGCTCCCAGGCC | 5977 |
| rs111882060 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | DPF2 | GRCh38.p7 | 11:65337190 | GGCGCGGTGGCTTAC[A/G]CCTGTAATCCCAGAA | 5977 |
| rs111894418 | snp | G/T | 0.444444 | 0.157135 | intron-variant | DPF2 | GRCh38.p7 | 11:65339941 | CTGGAGCAGACCTTG[G/T]GGCAAGGATGTGGGA | 5977 |
| rs111974471 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65351475 | GATGATTATTTCTTT[C/G]ATCTCCATAGAGGAT | 5977 |
| rs111991224 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351716 | TGTGTCTGGACCTGT[C/T]GAAAGAGAAAGCTTC | 5977 |
| rs111995285 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | DPF2 | GRCh38.p7 | 11:65347274 | CTGCCTCAGCCTCCC[A/T]AAGTGCTGGGATTAT | 5977 |
| rs112042410 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | DPF2 | GRCh38.p7 | 11:65338130 | TTTTTAACGTTTTGT[A/G]GAGATGGGATCTCAC | 5977 |
| rs112334384 | snp | C/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65340765 | TGTGTGTCTGGAGAA[C/G]TATGTGTTAGCCAAG | 5977 |
| rs112337755 | snp | G/T | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65349247 | TGGTAGATTATCTGA[G/T]GTGAAACTTCTGCAG | 5977 |
| rs112521603 | snp | A/G | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65338501 | CCAGTGTCCGTATCA[A/G]TTCCCATCAGCAGAA | 5977 |
| rs112708804 | snp | C/G | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65344888 | ATCAGGAGCCCATTA[C/G]AATCAGACCCTTCCG | 5977 |
| rs112857572 | snp | C/T | 0.0225045 | 0.103662 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332286 | GGAGAATCACTTGAA[C/T]CCAGGAGGTGGAGGT | 5977 |
| rs112868332 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65348407 | CAACGTAAGGAGATC[G/T]TGTCTCTCCAAAAAC | 5977 |
| rs112950061 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65343561 | ACAGGGGAAAGATAT[C/G]CCAAAGTATGGAAGG | 5977 |
| rs113033312 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332477 | TTTTGAGACGGAGTC[C/T]CGCTCTGTCACCCAG | 5977 |
| rs113046136 | snp | C/T | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65342209 | ATTTGCCTTATCTGT[C/T]TTTGCTAAACTATTT | 5977 |
| rs113085570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65351367 | CTGAGGTGCTTGACA[A/G]ACTTCTGTCTTCCCA | 5977 |
| rs113230076 | snp | A/G | 0.0178098 | 0.0926698 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333327 | TTTATTTATTGAGAA[A/G]GAGTCTCGCTCTGTC | 5977 |
| rs113319390 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65349638 | GTCTCTACTAAAAAT[A/G]CAAAAAAATTAGCCG | 5977 |
| rs113378926 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65340632 | GAGACAGTTGATAGG[A/G]TTTTCCCTACTGCCT | 5977 |
| rs113441665 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333192 | TGGCTCACTGGAGCC[C/T]CAAACTCCTGGGCTC | 5977 |
| rs113775426 | snp | C/T | 0.5 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65336527 | TTGGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA | 5977 |
| rs113815291 | snp | C/G | 0.0252325 | 0.109451 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332519 | GTGGCGCGATCTTGG[C/G]TCACTGCAAACTCCG | 5977 |
| rs113927625 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332736 | TATTACAAGCGTGAA[C/G]CAATGCTCCTGGCCT | 5977 |
| rs113929582 | snp | G/T | 0.121369 | 0.214369 | intron-variant | DPF2 | GRCh38.p7 | 11:65348290 | ACCTTGTCTCAAAAA[G/T]AAATAGTCACTGGGC | 5977 |
| rs114279317 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DPF2 | GRCh38.p7 | 11:65341807 | TACACATATATAATT[C/T]TCATTAAAAAAATTA | 5977 |
| rs114529921 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | DPF2 | GRCh38.p7 | 11:65348307 | AATAGTCACTGGGCA[C/T]GGCGTCTCACACCTG | 5977 |
| rs114549146 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353190 | CAAGTTTATAACAAT[A/T]CTTTGTTATAAAGAA | 5977 |
| rs114870583 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DPF2 | GRCh38.p7 | 11:65335490 | GCTTTCAAGTTGTGT[C/T]ATAAGTGAGGGGTTG | 5977 |
| rs115002680 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | DPF2 | GRCh38.p7 | 11:65347642 | GTCTGGCCTTGTCTT[A/T]TATTTTATTTTATAT | 5977 |
| rs115807112 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DPF2 | GRCh38.p7 | 11:65350851 | GGGCGTGGTGCTGTG[C/T]GCTTGTAATCTCAGC | 5977 |
| rs116493493 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DPF2 | GRCh38.p7 | 11:65343571 | GATATCCCAAAGTAT[A/G]GAAGGGAGCAGGAGC | 5977 |
| rs116742819 | snp | A/C | 0.199873 | 0.244923 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332422 | AAATATAAACAAATA[A/C]TGTTGTTACGAACAT | 5977 |
| rs116893210 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65348701 | AGTGACTGGATCTGC[A/G]GTGGAGAGGGGCAGC | 5977 |
| rs117642614 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348633 | AAAAAAAAAAAAAAG[G/T]GGAGGTGATTTGATC | 5977 |
| rs117711707 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | DPF2 | GRCh38.p7 | 11:65343256 | GTAAGCCAGTATTGC[A/G]CCATTGCACTCCAGC | 5977 |
| rs117966430 | snp | G/T | 0.0236746 | 0.106192 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332753 | AATGCTCCTGGCCTG[G/T]TTTTTTTTGTTTTTT | 5977 |
| rs118143837 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65350839 | GAGAAATTAGCTGGG[C/T]GTGGTGCTGTGCGCT | 5977 |
| rs137866238 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352916 | TGGAGTTGAGGTGTC[-/T]TTTTTTTTTCTTTCT | 5977 |
| rs137910391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65338179 | CTCTAACTCTTGGTC[C/T]CAAGAGATCCACCAG | 5977 |
| rs137933237 | snp | G/T | 0.000509502 | 0.0159528 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333895 | AGGGAAGATGGCGGC[G/T]GTGGTGGAGAATGTA | 5977 |
| rs137954020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344478 | TGGGAGCACCATCGC[C/T]GCTGGGGTTTCTCTC | 5977 |
| rs137977488 | in-del | -/G | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334381 | ACTGCGGGGCTGGCT[-/G]GTTTCAGTTCCAGGC | 5977 |
| rs138318168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347047 | TGAGATGGAGTCTTG[C/T]TCTGTCGCCCAGGCT | 5977 |
| rs138330073 | in-del | -/TC | 0.0185938 | 0.0946107 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352109 | GGAGAGCAGCTCACT[-/TC]TCTGTGTTCTGCCTC | 5977 |
| rs138433278 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DPF2 | GRCh38.p7 | 11:65341255 | ATAAGTTATGGTGCC[A/G]AGTGAACTAGGGTGT | 5977 |
| rs138582021 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352491 | GCCTCCCTTCCTACT[C/G]CTTTTGGTTTTGTGG | 5977 |
| rs138590272 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65340833 | ACTATTCCACCTAAC[C/G]CCCTAGGCCCTCACT | 5977 |
| rs138617598 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | DPF2 | GRCh38.p7 | 11:65338550 | TCAACCTTGTTTATC[C/G]AATTTTATTCTGTGT | 5977 |
| rs138937960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345427 | CAACATGGAAGAGCA[C/G]TGGTGGCCATGGGGT | 5977 |
| rs139683997 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | DPF2 | GRCh38.p7 | 11:65342869 | TACAAAAAAAATTAG[C/G]CAGGCGTGGTGGTGG | 5977 |
| rs139698375 | snp | A/C/T | 8.24499e-05 | 0.00642023 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340490 | CTTGGACTCACAGAC[A/C/T]GGAGTAGCCCAGAGC | 5977 |
| rs139700249 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DPF2 | GRCh38.p7 | 11:65338981 | GTCCACCTGGGCTGA[C/G]TAAGTGTCCATGTTC | 5977 |
| rs139753616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338940 | CATTTGGTCCAACCT[C/T]CTCAATCTATAGAAG | 5977 |
| rs139774791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65334817 | AATGGGTATGTTGGG[C/T]TTGGTGCAAGGGTGG | 5977 |
| rs139908268 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334627 | TTATACGATACCATT[A/G]TGCTGGTCAGATTTC | 5977 |
| rs139931446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342582 | GAAGATAAGAATACA[C/T]GTAAAAATAACAGCT | 5977 |
| rs139955640 | snp | C/T | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341551 | CCTGTGACCAACAGT[C/T]GAGCGCGAAAGGTAC | 5977 |
| rs140025125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65339261 | AAAAAAAAAAAACAA[C/G]ATTGATTGAATATAA | 5977 |
| rs140259644 | snp | A/G | 0.000362528 | 0.0134585 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346287 | CCCCGTGATGATGGC[A/G]GCAGTGAAGACATAC | 5977 |
| rs140311199 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65340866 | CAGAATTTCTCCCTT[C/G]CTCTAGAACTCAAAG | 5977 |
| rs140362866 | in-del | -/AT | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332991 | TATATTTATATATAT[-/AT]ATATATATATACATA | 5977 |
| rs140692382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340307 | CTTCTAGAGAAGCAG[A/G]TGGCAGGGGAGAGGA | 5977 |
| rs141032113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65344735 | AAATCTCTGGAATGG[C/T]ATGGGGGTAGGAGCA | 5977 |
| rs141391426 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65340079 | CTTAACTAGCACAGG[C/G]GTGGGCTTGTGAGAC | 5977 |
| rs141412058 | snp | G/T | 0.0707826 | 0.174302 | intron-variant | DPF2 | GRCh38.p7 | 11:65342245 | GAAACTTCAAAAACT[G/T]TTCAGTCTAGGCAAC | 5977 |
| rs141478728 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | DPF2 | GRCh38.p7 | 11:65337844 | AGTTTCGCTCTTGTT[A/G]CCCAGGCTGGAGTGC | 5977 |
| rs141563355 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343883 | GGACAGGGTGGCCTA[A/G]GGAATTCCTTATTTT | 5977 |
| rs141688611 | snp | C/T | 0.0244538 | 0.107838 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333000 | ATATATATATATATA[C/T]ACATATGTATATATA | 5977 |
| rs142056934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343591 | GGAGCAGGAGCAGGA[C/T]TATAGCATGCTTGAA | 5977 |
| rs142171251 | snp | C/T | 3.40397e-05 | 0.00412537 | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333897 | GGAAGATGGCGGCTG[C/T]GGTGGAGAATGTAGT | 5977 |
| rs142214940 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | DPF2 | GRCh38.p7 | 11:65334632 | CGATACCATTGTGCT[G/T]GTCAGATTTCAAGCA | 5977 |
| rs142361667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336234 | CAGTGGCTTACGCCT[A/G]TAATCCCAACACTTT | 5977 |
| rs143062296 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65338943 | TTGGTCCAACCTCCT[C/G]AATCTATAGAAGAGT | 5977 |
| rs143089128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338420 | CATTCCCCGCAAAAC[C/T]GTTTCCAGCCTCCTT | 5977 |
| rs143815887 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352506 | CCTTTTGGTTTTGTG[A/G]GGAGAGGGGAAGGAT | 5977 |
| rs143896778 | snp | A/T | 0.257732 | 0.24988 | intron-variant | DPF2 | GRCh38.p7 | 11:65347078 | GGAGTACAGTGGCAC[A/T]ATCTCAGCTCACTGC | 5977 |
| rs144003802 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | DPF2 | GRCh38.p7 | 11:65349750 | GCAGTGAACCGAGAT[C/G]GCACCACTGCACTCC | 5977 |
| rs144201503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65335133 | TGTCTCTTTCAGCCA[C/T]CCCTCCTCCCAACGC | 5977 |
| rs144367702 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | DPF2 | GRCh38.p7 | 11:65342856 | TCTCTACTAAAAATA[C/G]AAAAAAAATTAGCCA | 5977 |
| rs144381715 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DPF2 | GRCh38.p7 | 11:65341879 | CTTTGGGAGGCCAAG[A/G]CAGGAGGATTGCTCA | 5977 |
| rs144397948 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DPF2 | GRCh38.p7 | 11:65339310 | CCATTACCAAAGTCC[C/T]TGTTAAACCCTGCAA | 5977 |
| rs144611863 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340981 | GATTGGCCTCCGGAC[A/G]GCTGTACTCCTACCC | 5977 |
| rs145009790 | snp | C/G | 9.93443e-05 | 0.00704715 | synonymous-codon, intron-variant | DPF2 | GRCh38.p7 | 11:65344047 | CATCCTGGAGGACCG[C/G]GATAAGCCCTATGCC | 5977 |
| rs145217412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335375 | AAAGGAAGATTCTCA[C/T]TGTACTGGGGGAGTA | 5977 |
| rs145264138 | snp | A/G | 8.24029e-05 | 0.00641831 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341556 | GACCAACAGTCGAGC[A/G]CGAAAGGTACAGGAT | 5977 |
| rs145363217 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DPF2 | GRCh38.p7 | 11:65344476 | CCTGGGAGCACCATC[A/G]CCGCTGGGGTTTCTC | 5977 |
| rs145454365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65342710 | AGAGGCTGAAACAAA[A/G]CAGTTTAAAAACTTC | 5977 |
| rs145748592 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339126 | TTTAAGATTGATTGA[C/T]GCCAGGTACTGTGAC | 5977 |
| rs146359123 | snp | C/T | 0.000392723 | 0.0140074 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333907 | GGCTGTGGTGGAGAA[C/T]GTAGTGAAGCTGTGA | 5977 |
| rs146378836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65338816 | CTGTCACATTCTAGA[A/G]CAGGGTTTGTTGGTG | 5977 |
| rs146389394 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | DPF2 | GRCh38.p7 | 11:65334746 | TTATTCCTACAGAAG[A/T]ATCAGAATGAGTTTT | 5977 |
| rs146452900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350211 | TGTCCTCACTGTAGT[A/G]TTAAGGCAGCTGAGG | 5977 |
| rs146460934 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353434 | CATGGGACACACACA[A/G]AAGTTCTTGCAGGAG | 5977 |
| rs146942767 | snp | C/G | 0.0569829 | 0.158885 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332693 | CCTGACCTCGTGATC[C/G]GCCCACCGTGGCCTC | 5977 |
| rs147269065 | snp | C/T | 0.258288 | 0.249863 | intron-variant | DPF2 | GRCh38.p7 | 11:65347083 | ACAGTGGCACAATCT[C/T]AGCTCACTGCAACCT | 5977 |
| rs147467395 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | DPF2 | GRCh38.p7 | 11:65342315 | ATTAGCTGGGCATGG[C/T]GGCACACGCCTGCAG | 5977 |
| rs147826073 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | DPF2 | GRCh38.p7 | 11:65339753 | ATAGTTTTATTTGAC[A/C/G]CTTCTCAGCAGTGTA | 5977 |
| rs147848982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65337603 | CTTAAGTTTTTGTTA[C/T]TGCTTTTTTTTGTTT | 5977 |
| rs147915994 | snp | A/C | 3.30376e-05 | 0.0040642 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341058 | CCACGACTTTCCTTC[A/C]CATCTATTAAGCCAG | 5977 |
| rs148355951 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343133 | GAAGAAACCCCGTCT[C/T]TACTAAAAATCCAAA | 5977 |
| rs148363068 | in-del | -/AG | 0.0185938 | 0.0946107 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352292 | CTGTGTTCCTGCTAC[-/AG]AGTGTTCTTTTCTGG | 5977 |
| rs148383892 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65342043 | AGAATCACTTGAGCC[A/T]ATGAGTTCGAGACTG | 5977 |
| rs148550551 | snp | C/T | 1.71073e-05 | 0.00292461 | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333909 | CTGTGGTGGAGAATG[C/T]AGTGAAGCTGTGAGT | 5977 |
| rs149069343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65351001 | AAAAAAAAATAAAGG[A/G]AGTTAAAAAAAAAAT | 5977 |
| rs149073109 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345936 | TCTCTGTAGCCAAAA[A/C]GGGTCCTGATGGATT | 5977 |
| rs149124566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343381 | AAACTAGGAGGCGAG[C/T]GTCAGGACAGAACCA | 5977 |
| rs149432821 | snp | C/T | 3.29935e-05 | 0.00406149 | intron-variant | DPF2 | GRCh38.p7 | 11:65345922 | ATCAAAACTCTTTCT[C/T]TCTGTAGCCAAAAAG | 5977 |
| rs149746532 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DPF2 | GRCh38.p7 | 11:65347846 | AGAGACGGGGTTTCA[C/T]CATGTTGGCCAAGCT | 5977 |
| rs149755484 | in-del | -/ATATAA | 0.0174175 | 0.0916809 | cds-indel, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353382 | CAGGACCAGAAGTTT[-/ATATAA]ATATAATTAATAAGC | 5977 |
| rs149780932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65339059 | GACTGTATCTCAGAC[A/G]TCGTCATGAGTATTA | 5977 |
| rs149940807 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DPF2 | GRCh38.p7 | 11:65342877 | AAATTAGCCAGGCGT[A/G]GTGGTGGGCACCTGC | 5977 |
| rs150256628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345277 | AAGTTTGGAGTCTTA[C/T]CCACTTTTCCCCCTT | 5977 |
| rs150287049 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DPF2 | GRCh38.p7 | 11:65338159 | ACTATGTTGCCCAAG[C/T]TGGTCTCTAACTCTT | 5977 |
| rs150607308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65338945 | GGTCCAACCTCCTCA[A/G]TCTATAGAAGAGTAA | 5977 |
| rs150655394 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333822 | CCTGGTACCCCGGTG[C/T]GGTCCCGGCGCCTGC | 5977 |
| rs150681380 | snp | C/T | 0.000247148 | 0.0111136 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340445 | TTACAATGCTCGCCT[C/T]TGTGCTGAGCGCAGC | 5977 |
| rs150923096 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65340138 | TGGGGGTTAAACTTA[A/C]GTCTGATTAGACATA | 5977 |
| rs150974833 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336451 | GAGCTGATATCACAC[C/T]ACTGCCCTCCAGCCT | 5977 |
| rs151052113 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | DPF2 | GRCh38.p7 | 11:65335779 | ATGTTATACATTGAG[-/T]TACATTGAGGTCAGG | 5977 |
| rs151219453 | snp | A/G | 0.000131846 | 0.00811822 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346015 | TAACAAGAAGACGGG[A/G]CAACCCGAGGAGCTG | 5977 |
| rs151300662 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351180 | ATAATGTCCAAATGC[A/C/G]CATAGGTATAATTTT | 5977 |
| rs180836536 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65349089 | CCTTCCTAACATTTC[A/T]ACTTAAAGGGTTTAG | 5977 |
| rs180848953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342411 | TGCTTATGCCTCTGC[A/T]CTCCAGCCTGGGTAA | 5977 |
| rs180887245 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332721 | CTCCCAAAGTGCTGG[G/T]ATTACAAGCGTGAAC | 5977 |
| rs180918247 | snp | A/G | 0.257732 | 0.24988 | intron-variant | DPF2 | GRCh38.p7 | 11:65347076 | CTGGAGTACAGTGGC[A/G]CAATCTCAGCTCACT | 5977 |
| rs180958832 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DPF2 | GRCh38.p7 | 11:65336757 | TCGCACCACTGCACT[A/C]CAGCCTGGCAACAGC | 5977 |
| rs181368944 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65337607 | AGTTTTTGTTATTGC[G/T]TTTTTTTGTTTTAAG | 5977 |
| rs181374163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346873 | CAAGCCAGATGACAG[A/G]GCATGGGAGAGTATG | 5977 |
| rs181542187 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DPF2 | GRCh38.p7 | 11:65337541 | GAGAGAGAGAGAGAG[A/G]GAGAGAACAATGTTA | 5977 |
| rs181573025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334456 | ACTACAAATATTCTT[A/G]GGAAGAATTTATCGA | 5977 |
| rs181575392 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350072 | GCTTTGGGGAGAAGT[C/T]GCATGTTTATGTTTT | 5977 |
| rs182012583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342151 | AGTACAATGAAATAC[C/T]ACATACTCTTTACCT | 5977 |
| rs182147424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344974 | ACCTCCTCCTGCCAT[C/T]CTCTCTCCCCACTCC | 5977 |
| rs182239820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333979 | GGGCCTGGGAGTAGG[A/G]GGCGGTGGGGGAAGG | 5977 |
| rs182308282 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337861 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 5977 |
| rs182431661 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65347369 | CAGAGTCTCTCTGTC[A/T]TCCAGGCTGGAGTGC | 5977 |
| rs182492816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65349577 | GAGGTGGGCGGATCA[C/T]GAGGTCAGGACATGG | 5977 |
| rs182517413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351158 | AAGAGCTGATAAAAG[C/T]CCTAGAATAATGTCC | 5977 |
| rs182795369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65334862 | GTCTAGCTGTCCAGT[A/C]AGGGTTTTTGCATTT | 5977 |
| rs182986410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338026 | GGCTGGTCTCGAACT[C/G]CTGACCTCAGGTGAT | 5977 |
| rs183035539 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DPF2 | GRCh38.p7 | 11:65347791 | CTCCCAGGTAGCTGG[G/T]ATTACAGGCGCCCGC | 5977 |
| rs183266844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335270 | TTATCCTTCCTGACT[C/G]AGATGTTCTTTCTTT | 5977 |
| rs183291048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342904 | CTGCAGTCCCAGCTA[C/T]TCAGGCGCAAACCCG | 5977 |
| rs183681710 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65343423 | CTCCCAGGGTGGCCA[A/G]TCAGAGGCAGGAGAG | 5977 |
| rs184006657 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332509 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 5977 |
| rs184014113 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65348497 | GAGGTAGGAGGATCA[A/C]TTGGGCCCAGGAGGT | 5977 |
| rs184259235 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65342081 | TCATGATCATGCCAC[G/T]GCACTCCAGCCTGGG | 5977 |
| rs184263245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65346931 | ACTGCCAGATCTCTG[A/G]GGCCTCGGGTTTTAT | 5977 |
| rs184393950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336416 | AGAATCGCCTGAACC[C/T]AGGCGGCAGAGGTTG | 5977 |
| rs184521601 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333166 | GCTGGAGTGCAGTGA[G/T]GTGGCTCCAGTGGCT | 5977 |
| rs184541437 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65336917 | AAGGTGGTGAAACCC[A/G]TCTCTAGTAAAAATA | 5977 |
| rs184637094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349454 | TTGGTTGCATCTCCA[C/T]AAGTCCCCTTCCAGC | 5977 |
| rs184717038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335844 | TTAGACAGAGTCTCA[C/T]TGTTGTCGGCCCGGG | 5977 |
| rs185091736 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65348160 | GTGTGGTGGCACACA[C/T]GTTAGTCCCAGCTAC | 5977 |
| rs185271980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65334622 | TCCTATTATACGATA[C/G]CATTGTGCTGGTCAG | 5977 |
| rs185419600 | snp | A/G | 4.95045e-05 | 0.00497492 | intron-variant | DPF2 | GRCh38.p7 | 11:65345911 | CCATGGGTGTCATCA[A/G]AACTCTTTCTCTCTG | 5977 |
| rs185455887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346635 | ACAGGAACAACAATA[A/G]GCAAGGATGTAAATG | 5977 |
| rs185456333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342659 | CTTTAGTCTGTACAA[C/T]CTTATGGGGTAGGTC | 5977 |
| rs185459339 | snp | A/C/G | 0.0139044 | 0.0824329 | intron-variant | DPF2 | GRCh38.p7 | 11:65350469 | AACCTCTGCTTCCCC[A/C/G]GGCTCAGGTAATCTG | 5977 |
| rs186019977 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DPF2 | GRCh38.p7 | 11:65337543 | GAGAGAGAGAGAGAG[A/G]GAGAACAATGTTAAT | 5977 |
| rs186166415 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342158 | TGAAATACCACATAC[C/T]CTTTACCTAGATTTA | 5977 |
| rs186433749 | snp | A/G | 0.031825 | 0.122064 | intron-variant | DPF2 | GRCh38.p7 | 11:65337882 | CAATCTCGGCTCACC[A/G]CAACCTCCGCCTCCC | 5977 |
| rs186649762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65337711 | TAGGCTCAAATGATT[C/T]CCCTACCTCATCCGC | 5977 |
| rs186748045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345281 | TTGGAGTCTTATCCA[C/T]TTTTCCCCCTTCCTG | 5977 |
| rs187070218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65347458 | CCCACCTCAGCCTCC[C/T]GGGTAGCTGGGACCA | 5977 |
| rs187107436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347176 | CGTGCCACCACACCC[A/G]GCTAATTTTGTATTT | 5977 |
| rs187427129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348253 | TCACACCACCGCACT[C/G]TAGCCTGGGCAACAA | 5977 |
| rs187609561 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331816 | GTCAAGCTATGAACC[C/G/T]GGAAGGCGGAGGTTG | 5977 |
| rs187714805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65334864 | CTAGCTGTCCAGTCA[G/T]GGTTTTTGCATTTTG | 5977 |
| rs187932330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335353 | ACACAGGTTTCTCCA[A/G]AAATAAAAAGGAAGA | 5977 |
| rs187960931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344460 | ACTTCTGTCCCTCCA[C/T]CCTGGGAGCACCATC | 5977 |
| rs187984335 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352213 | GGCCACGTCCACAAG[C/G]AGCTTTTCATGCCCC | 5977 |
| rs188162087 | snp | C/T | 0.257732 | 0.24988 | intron-variant | DPF2 | GRCh38.p7 | 11:65347075 | GCTGGAGTACAGTGG[C/T]ACAATCTCAGCTCAC | 5977 |
| rs188235212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336350 | TATAAAAATTAGTTA[A/G]GTGTGGTGGCGCACA | 5977 |
| rs188290807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65339937 | CCCTCTGGAGCAGAC[C/T]TTGGGGCAAGGATGT | 5977 |
| rs188495823 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65338044 | GACCTCAGGTGATCC[A/G]TCCACCTCAGTCTCC | 5977 |
| rs188621245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65346872 | ACAAGCCAGATGACA[A/G]GGCATGGGAGAGTAT | 5977 |
| rs188678655 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DPF2 | GRCh38.p7 | 11:65348797 | GTGTCCTGTAGTGGC[A/C]TGAGGCACATCAGTT | 5977 |
| rs188694969 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332597 | GGATTACAGGCGTCC[A/G]CCACCATGCCCGGCT | 5977 |
| rs188742600 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65348071 | GGGAGGATCACTTGA[A/G]CCCAGGAATTCAAGA | 5977 |
| rs189071111 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65336436 | GGCAGAGGTTGAAGT[A/G]AGCTGATATCACACC | 5977 |
| rs189329516 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DPF2 | GRCh38.p7 | 11:65337217 | AGAACTTTGGAAGGC[C/T]GAGGTGGGCGGATCA | 5977 |
| rs189535616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347634 | CCCACCATGTCTGGC[C/T]TTGTCTTATATTTTA | 5977 |
| rs189777570 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337545 | GAGAGAGAGAGAGAG[A/G]GAACAATGTTAATGT | 5977 |
| rs189875381 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DPF2 | GRCh38.p7 | 11:65342132 | AACCAGAAGGTGCAA[A/G]AATAGTACAATGAAA | 5977 |
| rs190035623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342263 | CAGTCTAGGCAACAT[A/G]GCAGGACCTTGTCTC | 5977 |
| rs190268769 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351047 | TGGCTCACACACCCT[A/G]AAATATTTAACACTC | 5977 |
| rs190316559 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65349560 | CAGCACTTTGGGAGG[A/C]CGAGGTGGGCGGATC | 5977 |
| rs190361867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65349775 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 5977 |
| rs190580141 | snp | A/G | 0.000364062 | 0.013487 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333921 | ATGTAGTGAAGCTGT[A/G]AGTGGTCGTTTCTTT | 5977 |
| rs190623710 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DPF2 | GRCh38.p7 | 11:65337724 | TTCCCCTACCTCATC[C/T]GCCCCAGGGGCTACG | 5977 |
| rs190872929 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352224 | CAAGGAGCTTTTCAT[G/T]CCCCTGTGCCGCATA | 5977 |
| rs190952428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342690 | CTGTGTTCCCCATTT[C/G]ACACAGAGGCTGAAA | 5977 |
| rs191092486 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340436 | GTGCCACAATTACAA[C/T]GCTCGCCTCTGTGCT | 5977 |
| rs191199899 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65337890 | GCTCACCGCAACCTC[C/T]GCCTCCCAGGTTCAA | 5977 |
| rs191368000 | snp | C/G | 1.65209e-05 | 0.00287405 | intron-variant | DPF2 | GRCh38.p7 | 11:65345654 | TTTCTCTGCAATCTT[C/G]TTCCCACTCAGTTTG | 5977 |
| rs191407984 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65343378 | TTTAAACTAGGAGGC[G/T]AGTGTCAGGACAGAA | 5977 |
| rs191841498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65344843 | CCTAGAGCTGCTCGG[C/T]CCAGTGCATGGGGTG | 5977 |
| rs191973293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335604 | GCCAGTAATGAGAAA[C/T]CAACTCTCTCCTCCT | 5977 |
| rs192196194 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334872 | CCAGTCAGGGTTTTT[C/G]CATTTTGACTGGATG | 5977 |
| rs192223802 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332005 | ATAATAAATAGGCTA[C/G]CTGCATATAATTGGA | 5977 |
| rs192233973 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65348276 | GGCAACAAAGCAAGA[A/C]CTTGTCTCAAAAAGA | 5977 |
| rs192636470 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65341331 | TGGTAAGCCCCAGCA[G/T]TATGTGGACTCAGAG | 5977 |
| rs192776998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65336365 | GGTGTGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT | 5977 |
| rs192896807 | snp | C/T | 3.33444e-05 | 0.00408303 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346341 | ATGTTGCAATATCTG[C/T]GGCACCTCCGAGAAT | 5977 |
| rs193179286 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338817 | TGTCACATTCTAGAG[C/T]AGGGTTTGTTGGTGT | 5977 |
| rs193288337 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DPF2 | GRCh38.p7 | 11:65348155 | GCCAGGTGTGGTGGC[A/G]CACACGTTAGTCCCA | 5977 |
| rs199512449 | snp | C/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345721 | CCACTATGCCCACTC[C/G]CACTTGGCTGAGGAG | 5977 |
| rs199638754 | in-del | -/CTT | | | cds-indel, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351836 | CATACCCATCTTTCC[-/CTT]CTTCCTCCTCTCCTT | 5977 |
| rs199784907 | snp | A/C/G | 0.000203157 | 0.0100767 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333881 | CGAGGCAGAGGAACA[A/C/G]GGAAGATGGCGGCTG | 5977 |
| rs199801105 | snp | A/G | 6.60578e-05 | 0.0057467 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341020 | GCTGGCGGAAAAAGC[A/G]GCGAGCCCATCCCCC | 5977 |
| rs199960633 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333047 | TGTGTATATATATAT[A/G]TGTATATATGTGTAT | 5977 |
| rs200015058 | snp | C/G/T | 8.24156e-05 | 0.00641887 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346021 | GAAGACGGGACAACC[C/G/T]GAGGAGCTGGTGTCC | 5977 |
| rs200082256 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333002 | ATATATATATATATA[C/T]ATATGTATATATATA | 5977 |
| rs200224680 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333104 | ATATATTTTTTTTCC[C/T]TTTTTTTTTTTTTTT | 5977 |
| rs200300435 | in-del | -/AGGCAGAAGCTGCAGT | 0.0197687 | 0.0974348 | intron-variant | DPF2 | GRCh38.p7 | 11:65337365 | TCGTTGGAACCCGGG[-/AGGCAGAAGCTGCAGT]AGGCAGAAGCTGCAG | 5977 |
| rs200364248 | snp | A/C | 8.24042e-05 | 0.00641836 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346290 | CGTGATGATGGCGGC[A/C]GTGAAGACATACCGC | 5977 |
| rs200387896 | snp | A/G | | | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341490 | CCCCCTGGAGAAGCG[A/G]GGTGCCCCGGATCCC | 5977 |
| rs200480588 | snp | A/G | 0.000296711 | 0.0121765 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346266 | TCCATCTTGCCTCCA[A/G]TTTACCCCCGTGATG | 5977 |
| rs200488945 | in-del | -/TA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333085 | GTGTATATATATATG[-/TA]TATATATATTTTTTT | 5977 |
| rs200523504 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335094 | GTTTTTTTTTTTTTT[A/T]AGTTGCTTTCTGCTC | 5977 |
| rs200674111 | in-del | -/GGCACCC | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349180 | GCTGAGCCGAGATCA[-/GGCACCC]AGAAGGAATGATTTA | 5977 |
| rs200748807 | snp | C/T | 0.000187099 | 0.0096703 | intron-variant | DPF2 | GRCh38.p7 | 11:65343855 | GAGGGGCCAGCGTGC[C/T]GCCTGCATCTTGGGA | 5977 |
| rs200755932 | in-del | -/A | 0.0387552 | 0.1337 | intron-variant | DPF2 | GRCh38.p7 | 11:65342913 | CAGCTACTCAGGCGC[-/A]AACCCGGGAGGCAGA | 5977 |
| rs200766161 | snp | A/G | 0.000169279 | 0.00919842 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333880 | CCGAGGCAGAGGAAC[A/G]GGGAAGATGGCGGCT | 5977 |
| rs200873941 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333903 | TGGCGGCTGTGGTGG[C/T]GAATGTAGTGAAGCT | 5977 |
| rs200885751 | snp | A/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333095 | TATATGTATATATAT[A/T]TTTTTTCCTTTTTTT | 5977 |
| rs201023047 | snp | A/G | 0.000972113 | 0.0220252 | intron-variant | DPF2 | GRCh38.p7 | 11:65341391 | CTTTATCCTGACCTT[A/G]CTTGCAGACACAGAC | 5977 |
| rs201110572 | snp | G/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333429 | CTGCCTCAGCCTCCC[G/T]AGTAGCTGGGACTAC | 5977 |
| rs201162180 | snp | A/C | 1.65318e-05 | 0.002875 | intron-variant | DPF2 | GRCh38.p7 | 11:65346243 | CTCACTTCCCCCACT[A/C]CAGGGCATCCATCTT | 5977 |
| rs201171823 | snp | A/G | 3.31879e-05 | 0.00407343 | intron-variant | DPF2 | GRCh38.p7 | 11:65340359 | CCCGCTCCAACATAC[A/G]CGCCTGATTTCTATC | 5977 |
| rs201280099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343731 | TACCCATGCTAACCC[C/T]CCTGTCCACTCAGCG | 5977 |
| rs201339411 | in-del | -/A | 0.0425829 | 0.139564 | intron-variant | DPF2 | GRCh38.p7 | 11:65348578 | GCAATACCCTGTCTC[-/A]AAAAAAATATACCAT | 5977 |
| rs201395223 | snp | C/T | | | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351705 | GAGCTGCCACCTGTG[C/T]CTGGACCTGTTGAAA | 5977 |
| rs201627562 | snp | A/C/T | 0.000372767 | 0.0136471 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333933 | TGTGAGTGGTCGTTT[A/C/T]TTTCTCTCCTAGGGC | 5977 |
| rs201703619 | snp | A/C | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334383 | CTGCGGGGCTGGCTG[A/C]TTCAGTTCCAGGCAG | 5977 |
| rs201776355 | snp | C/T | 0.000165033 | 0.00908236 | intron-variant | DPF2 | GRCh38.p7 | 11:65345882 | TGCATGGGTGTTGAG[C/T]GGCTCAGGGACCCCC | 5977 |
| rs201807910 | snp | C/T | 4.98169e-05 | 0.00499059 | intron-variant | DPF2 | GRCh38.p7 | 11:65341080 | TTAAGCCAGGTAAGG[C/T]ACATACTTCCTGAGC | 5977 |
| rs201833172 | in-del | -/CTTTCTTTC | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350366 | TCTCTTTTTCTTTTT[-/CTTTCTTTC]TTTTTTTTTTTTTTT | 5977 |
| rs201879348 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333102 | ATATATATTTTTTTT[C/T]CTTTTTTTTTTTTTT | 5977 |
| rs201989932 | snp | C/T | 0.000104284 | 0.0072202 | intron-variant | DPF2 | GRCh38.p7 | 11:65346371 | TGACGTGTGTATCCC[C/T]GCCCCCTCCTCAGCA | 5977 |
| rs202050658 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335079 | CTCCTCTTGTGGTTT[G/T]TTTTTTTTTTTTTTA | 5977 |
| rs202153116 | snp | C/T | 6.59337e-05 | 0.0057413 | intron-variant | DPF2 | GRCh38.p7 | 11:65341392 | TTTATCCTGACCTTG[C/T]TTGCAGACACAGACC | 5977 |
| rs202228737 | snp | A/C/G/T | 0.000185207 | 0.0096217 | intron-variant | DPF2 | GRCh38.p7 | 11:65346205 | CTCCTCTCTTCCCCC[A/C/G/T]GCATTTCCGACTGTC | 5977 |
| rs202235809 | snp | A/G | 0.00075835 | 0.0194576 | intron-variant | DPF2 | GRCh38.p7 | 11:65341567 | GAGCGCGAAAGGTAC[A/G]GGATTATCCCTGTGG | 5977 |
| rs367559374 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346039 | GGAGCTGGTGTCCTG[C/T]TCTGACTGTGGCCGC | 5977 |
| rs367800599 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DPF2 | GRCh38.p7 | 11:65335642 | AGCTGCACAGGGCCT[C/T]AGATCACAATTAATA | 5977 |
| rs367837666 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336452 | AGCTGATATCACACC[A/G]CTGCCCTCCAGCCTG | 5977 |
| rs367850661 | snp | C/G | 0.000248701 | 0.0111485 | intron-variant | DPF2 | GRCh38.p7 | 11:65346110 | CCCCAAGGGGCTCTT[C/G]GCTTGCTGGCCTCTA | 5977 |
| rs367991143 | snp | C/G/T | 8.23735e-05 | 0.00641723 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341472 | GGCTCTGTTGCGCAC[C/G/T]GACCCCCTGGAGAAG | 5977 |
| rs368016884 | snp | C/G/T | 1.69919e-05 | 0.00291473 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333861 | GACTGTGGGGCTTCT[C/G/T]GGCCCGAGGCAGAGG | 5977 |
| rs368023279 | in-del | -/CCCGT | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334328 | CCCGTCCCGTCCCGT[-/CCCGT]TCGCTGCAGCAACAG | 5977 |
| rs368128402 | snp | C/T | 0.000100123 | 0.00707472 | intron-variant | DPF2 | GRCh38.p7 | 11:65340345 | AGCACCCTATGCCCC[C/T]CGCTCCAACATACAC | 5977 |
| rs368203040 | snp | C/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333538 | TCCATGTCCTGACCT[C/G]GTGATCCGCCCGCCT | 5977 |
| rs368370361 | snp | G/T | 7.17386e-05 | 0.00598867 | intron-variant | DPF2 | GRCh38.p7 | 11:65343710 | GCTTTTGGATGCACA[G/T]ATTTCTACCCATGCT | 5977 |
| rs368637192 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347381 | GTCATCCAGGCTGGA[A/G]TGCAGTGACGCGATC | 5977 |
| rs368684909 | snp | G/T | 1.65299e-05 | 0.00287483 | intron-variant | DPF2 | GRCh38.p7 | 11:65341591 | CCTGTGGCTAAGGGA[G/T]CTTTGATGGAAATCA | 5977 |
| rs369045124 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341209 | TCTTTCCTTTAAGGA[C/T]CTCAGTCTAGAAGGG | 5977 |
| rs369325857 | snp | C/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340516 | AGAGCAATTGTTACA[C/T]CTGGATGGAAAAGCG | 5977 |
| rs369343587 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351971 | AAAGGAGCAACACAC[C/T]GCCCCTAGGCGTGCG | 5977 |
| rs369476069 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337178 | ATCTAGAGGCAGGGC[A/G]CGGTGGCTTACACCT | 5977 |
| rs369482110 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353141 | ATATGTAAAGCGAAT[A/T]TAAAATTGGTTATTT | 5977 |
| rs369661687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342951 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 5977 |
| rs369788967 | snp | A/G | 4.97418e-05 | 0.00498682 | intron-variant | DPF2 | GRCh38.p7 | 11:65340361 | CGCTCCAACATACAC[A/G]CCTGATTTCTATCTT | 5977 |
| rs369824078 | snp | A/G | 4.94417e-05 | 0.00497176 | intron-variant | DPF2 | GRCh38.p7 | 11:65348817 | GCACATCAGTTATTC[A/G]GTCCCCATCCTCTTC | 5977 |
| rs369949613 | snp | C/T | 8.28411e-05 | 0.00643535 | intron-variant | DPF2 | GRCh38.p7 | 11:65343973 | AAAATAAGGGTGTCT[C/T]TTTGCTCTTCTTGGC | 5977 |
| rs369987104 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349612 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 5977 |
| rs370081510 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337476 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 5977 |
| rs370101833 | snp | C/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332274 | AAAGCTGAGGCAGGA[C/G]AATCACTTGAACCCA | 5977 |
| rs370206123 | snp | A/C/G | 4.96121e-05 | 0.00498036 | intron-variant | DPF2 | GRCh38.p7 | 11:65346071 | CAGGTACTGCTTCCC[A/C/G]TGAAGGCTGCTGCTT | 5977 |
| rs370360359 | snp | C/G | 0.000115558 | 0.00760038 | intron-variant | DPF2 | GRCh38.p7 | 11:65345887 | GGGTGTTGAGTGGCT[C/G]AGGGACCCCCATGGG | 5977 |
| rs370394340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65348530 | AGGCTGCAGTGAGCC[A/G]TGATTGCACCACTGC | 5977 |
| rs370514099 | snp | A/C/G | 6.59211e-05 | 0.0057408 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341403 | CTTGCTTGCAGACAC[A/C/G]GACCAGACCCTGAAG | 5977 |
| rs370555530 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DPF2 | GRCh38.p7 | 11:65337716 | TCAAATGATTCCCCT[A/G]CCTCATCCGCCCCAG | 5977 |
| rs370927704 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339356 | GGTTCTATATACACG[A/C]TTCTTAGAACCAGAT | 5977 |
| rs370965145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344243 | CTGGGTCCCTGCTAT[A/G]TGACGGGTGGGACCT | 5977 |
| rs371077385 | snp | C/G | 1.74439e-05 | 0.00295325 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333925 | AGTGAAGCTGTGAGT[C/G]GTCGTTTCTTTCTCT | 5977 |
| rs371126081 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345404 | CAAGGGCTAAGCCCC[C/G]CAAAAGTCAACATGG | 5977 |
| rs371135016 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338255 | CCCGGCCTCCCTTAA[A/G]TTCTTAAGAGCTCAC | 5977 |
| rs371135127 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349989 | AATGAGGCCCCTGAC[A/C]ATGTCTAAGAGTCCT | 5977 |
| rs371177361 | snp | A/G | 8.37865e-05 | 0.00647196 | intron-variant | DPF2 | GRCh38.p7 | 11:65341102 | TTCCTGAGCAGAGGC[A/G]TGGCCTGCTGCATGG | 5977 |
| rs371274172 | snp | C/T | 1.69945e-05 | 0.00291496 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333857 | TGCGGACTGTGGGGC[C/T]TCTCGGCCCGAGGCA | 5977 |
| rs371277298 | snp | A/C | 1.6941e-05 | 0.00291036 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333871 | CTTCTCGGCCCGAGG[A/C]AGAGGAACAGGGAAG | 5977 |
| rs371303549 | snp | C/T | 6.63735e-05 | 0.00576041 | intron-variant | DPF2 | GRCh38.p7 | 11:65340360 | CCGCTCCAACATACA[C/T]GCCTGATTTCTATCT | 5977 |
| rs371324783 | snp | C/T | 1.66399e-05 | 0.00288438 | intron-variant | DPF2 | GRCh38.p7 | 11:65345616 | GCAGGGATGGGGACA[C/T]GGCACTCTTGTATCC | 5977 |
| rs371530733 | snp | A/G | 0.000283299 | 0.0118983 | intron-variant | DPF2 | GRCh38.p7 | 11:65343851 | AGGTGAGGGGCCAGC[A/G]TGCTGCCTGCATCTT | 5977 |
| rs371775941 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347091 | ACAATCTCAGCTCAC[A/T]GCAACCTCTGCCTCC | 5977 |
| rs371888353 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346305 | AGTGAAGACATACCG[C/G]TGGCAGTGCATCGAG | 5977 |
| rs371941018 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353194 | TTTATAACAATTCTT[C/T]GTTATAAAGAACAAT | 5977 |
| rs371970023 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340102 | TGTGAGACACGTGGA[A/G]TGAACATTCTTTCAC | 5977 |
| rs371983211 | snp | A/C/G/T | 0.000216939 | 0.0104128 | intron-variant | DPF2 | GRCh38.p7 | 11:65340346 | GCACCCTATGCCCCC[A/C/G/T]GCTCCAACATACACG | 5977 |
| rs372204674 | in-del | C/TT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350379 | TTCTTTCTTTCTTTT[C/TT]TTTTTTTTTTTTGAG | 5977 |
| rs372284211 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352021 | GCTCTCCATTAAGTG[C/G]ATTCACTCTGCTTGC | 5977 |
| rs372407098 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352751 | TTCCCTTGCACGCTC[A/G]CTAGCAGCTGGTAAG | 5977 |
| rs372497624 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337478 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 5977 |
| rs372536184 | snp | A/G | 8.25008e-05 | 0.00642212 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346254 | CACTACAGGGCATCC[A/G]TCTTGCCTCCAATTT | 5977 |
| rs372648631 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | DPF2 | GRCh38.p7 | 11:65341579 | TACAGGATTATCCCT[A/G]TGGCTAAGGGAGCTT | 5977 |
| rs372781721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65335856 | TCACTGTTGTCGGCC[C/T]GGGCTGGAATGCAGT | 5977 |
| rs373091945 | snp | A/G | 1.65362e-05 | 0.00287538 | intron-variant | DPF2 | GRCh38.p7 | 11:65345648 | AACACCTTTCTCTGC[A/G]ATCTTCTTCCCACTC | 5977 |
| rs373181445 | snp | C/T | 0.00047796 | 0.0154516 | intron-variant | DPF2 | GRCh38.p7 | 11:65341388 | TTGCTTTATCCTGAC[C/T]TTGCTTGCAGACACA | 5977 |
| rs373186765 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348877 | TTCTGTGATGACTGC[A/G]ATCGTGGCTACCACA | 5977 |
| rs373233186 | snp | A/G | 1.8478e-05 | 0.00303951 | intron-variant | DPF2 | GRCh38.p7 | 11:65340947 | TAGGGCCTGACTTCT[A/G]TCTTTCTTCCTGCCA | 5977 |
| rs373715640 | snp | A/G | 0.000199402 | 0.00998304 | intron-variant | DPF2 | GRCh38.p7 | 11:65340355 | GCCCCCCGCTCCAAC[A/G]TACACGCCTGATTTC | 5977 |
| rs373761595 | snp | C/T | 1.68912e-05 | 0.00290608 | intron-variant | DPF2 | GRCh38.p7 | 11:65341118 | TGGCCTGCTGCATGG[C/T]GAGAGCCTGCTAATC | 5977 |
| rs373762591 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346018 | CAAGAAGACGGGACA[A/G]CCCGAGGAGCTGGTG | 5977 |
| rs373776965 | snp | C/T | 3.34353e-05 | 0.00408859 | intron-variant | DPF2 | GRCh38.p7 | 11:65344082 | ACAGTGAGTGCCTCA[C/T]AAGTGGGTGGGTAGA | 5977 |
| rs373816969 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336770 | CTCCAGCCTGGCAAC[A/G]GCAAGACTCCATCTC | 5977 |
| rs373954217 | snp | C/G | 0.000437904 | 0.0147905 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333827 | TACCCCGGTGCGGTC[C/G]CGGCGCCTGCGCGCT | 5977 |
| rs374113791 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65350139 | TCTATGTTACAGAAT[A/G]GCTTTCCTATTAAAG | 5977 |
| rs374150853 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | DPF2 | GRCh38.p7 | 11:65343704 | AGGGGAGCTTTTGGA[C/T]GCACATATTTCTACC | 5977 |
| rs374406235 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347058 | CTTGCTCTGTCGCCC[A/T]GGCTGGAGTACAGTG | 5977 |
| rs374488587 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352199 | AGCGAGCAAGCTGAG[A/G]CCACGTCCACAAGGA | 5977 |
| rs374595777 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344972 | CCACCTCCTCCTGCC[A/T]TCCTCTCTCCCCACT | 5977 |
| rs374651671 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65346109 | TCCCCAAGGGGCTCT[A/T]GGCTTGCTGGCCTCT | 5977 |
| rs374973318 | snp | C/G | 6.59055e-05 | 0.00574007 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341427 | CCTGAAGAAGGAGGG[C/G]CTGATCTCTCAGGAT | 5977 |
| rs374991419 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341199 | ATGATGTGATTCTTT[C/T]CTTTAAGGACCTCAG | 5977 |
| rs375192866 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347424 | AACCTTTCCCTTCAG[C/G]CTCAAGCAGTACAAT | 5977 |
| rs375383394 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342740 | CCCATGGGTCGGGCA[C/T]GGTAGCTCACGCCTG | 5977 |
| rs375387282 | snp | A/G | 0.000118386 | 0.0076928 | intron-variant | DPF2 | GRCh38.p7 | 11:65344107 | GGTAGACCTTGCCTT[A/G]GACCCAGCTCCTGCT | 5977 |
| rs375437984 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339062 | TGTATCTCAGACATC[A/G]TCATGAGTATTAGGG | 5977 |
| rs375672962 | snp | A/T | 1.65468e-05 | 0.00287631 | intron-variant | DPF2 | GRCh38.p7 | 11:65346082 | TCCCGTGAAGGCTGC[A/T]GCTTTGCCCAGTCCC | 5977 |
| rs375695620 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345481 | CCCAGAAGCTAGAGA[G/T]CCCCACGGCCTGATG | 5977 |
| rs375718927 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336059 | CCTCAGGAGTTCACC[C/T]GCCTCGGCCTCCCAA | 5977 |
| rs375769428 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332108 | TGGCCAGGCGTGGTA[A/G]CTCATGCCTGTAATC | 5977 |
| rs376100876 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343299 | AGCGAAACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 5977 |
| rs376241523 | snp | C/T | 4.23379e-05 | 0.00460078 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343780 | CTTCCTGGATGACCT[C/T]GATGATGAAGACTAT | 5977 |
| rs376305567 | in-del | -/GCT | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65336390 | CCAGCTACTTGAGAG[-/GCT]GAGGCACAAGAATCG | 5977 |
| rs376349656 | snp | G/T | 1.70194e-05 | 0.00291709 | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333899 | AAGATGGCGGCTGTG[G/T]TGGAGAATGTAGTGA | 5977 |
| rs376357637 | snp | A/G | 3.29804e-05 | 0.00406068 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340491 | TTGGACTCACAGACC[A/G]GAGTAGCCCAGAGCA | 5977 |
| rs376580739 | snp | A/G | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346307 | TGAAGACATACCGCT[A/G]GCAGTGCATCGAGTG | 5977 |
| rs376636599 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353294 | ATTTGGAGAATTCTC[C/T]TAGTCTTGGATACAT | 5977 |
| rs376780986 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335274 | CCTTCCTGACTCAGA[A/T]GTTCTTTCTTTGTTT | 5977 |
| rs376804384 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349669 | GCTGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 5977 |
| rs376807610 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | DPF2 | GRCh38.p7 | 11:65348808 | TGGCCTGAGGCACAT[C/G]AGTTATTCAGTCCCC | 5977 |
| rs376872492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337803 | TGTTTGTTTTGTTTT[G/T]TTTAATTTTATTTTT | 5977 |
| rs376925116 | snp | C/T | 8.34161e-05 | 0.00645764 | intron-variant | DPF2 | GRCh38.p7 | 11:65343941 | CAAAAGAGTCTAACT[C/T]CTCAGGCCCAGCTAC | 5977 |
| rs377282343 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345572 | GAAGGGATGGTTGCC[C/T]TCTGCCTCAGGTGGA | 5977 |
| rs377683764 | snp | A/C | 0.000189157 | 0.00972331 | intron-variant | DPF2 | GRCh38.p7 | 11:65340920 | GTTTGGTATTACTTT[A/C]TAATACTGGGTTAGG | 5977 |
| rs377719049 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345034 | TATTACTTCTCAAGA[C/T]GACAAAATGCCTCAT | 5977 |
| rs377750990 | snp | C/T | 0.000217652 | 0.0104297 | intron-variant | DPF2 | GRCh38.p7 | 11:65341101 | CTTCCTGAGCAGAGG[C/T]GTGGCCTGCTGCATG | 5977 |
| rs386754380 | multinucleotide-polymorphism | CACA/TGCT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347075 | GCTGGAGTACAGTGG[CACA/TGCT]ATCTCAGCTCACTGC | 5977 |
| rs386754381 | multinucleotide-polymorphism | CA/TG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347083 | ACAGTGGCACAATCT[CA/TG]GCTCACTGCAACCTC | 5977 |
| rs397771833 | in-del | -/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335093 | GTTTTTTTTTTTTTT[-/T]AAGTTGCTTTCTGCT | 5977 |
| rs397787336 | in-del | -/A | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65348631 | AAAAAAAAAAAAAAA[-/A]GTGGAGGTGATTTGA | 5977 |
| rs397843675 | in-del | -/TT | 0.0118339 | 0.076006 | intron-variant | DPF2 | GRCh38.p7 | 11:65349093 | CTAACATTTCAACTT[-/TT]AAAGGGTTTAGTGTT | 5977 |
| rs527368098 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333814 | GCAAGGAACCTGGTA[C/G]CCCGGTGCGGTCCCG | 5977 |
| rs527417562 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333373 | CAGTGGCGCGATCTC[C/G]GCTCACTGCAAACTC | 5977 |
| rs527467055 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65347115 | TGCCTCCTGGGTTCA[A/C]GTGATTCTCCTGCCT | 5977 |
| rs527684293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334408 | AGGCAGCCCCGTGAT[A/G]TTTGGGAGGATCTTG | 5977 |
| rs527745743 | snp | A/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341446 | ATCTCTCAGGATGGC[A/T]GTAGTTTAGAGGCTC | 5977 |
| rs527809546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347569 | AAACTCCTGAGCTCA[A/G]GCAGTCCTCCCACCT | 5977 |
| rs527855720 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | DPF2 | GRCh38.p7 | 11:65337378 | GGAGGCAGAAGCTGC[A/T]GTAGGCAGAAGCTGC | 5977 |
| rs528011056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335155 | TCCCAACGCTATTGT[C/G]TTTCTCTCTGATCTG | 5977 |
| rs528272911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336916 | CAAGGTGGTGAAACC[C/T]GTCTCTAGTAAAAAT | 5977 |
| rs528311424 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342662 | TAGTCTGTACAACCT[C/T]ATGGGGTAGGTCCTG | 5977 |
| rs528330425 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DPF2 | GRCh38.p7 | 11:65343323 | AAAAAAAAAAAAAAA[C/G]CTTCCCACAAGGTCA | 5977 |
| rs528339251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336242 | TACGCCTATAATCCC[A/G]ACACTTTGGGAGGTT | 5977 |
| rs528734748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350845 | TTAGCTGGGCGTGGT[C/G]CTGTGCGCTTGTAAT | 5977 |
| rs528931697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338347 | CAGCCCTTTTACCCC[C/T]AAGACTGTTTGCCTG | 5977 |
| rs529212209 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332645 | TTTAGTAGAGATGGG[C/G]TTTCACCATGTTAGC | 5977 |
| rs529225637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346423 | TGCTGTTTGCACAGT[A/T]CCCTCTAAAGTGAGC | 5977 |
| rs529272501 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339846 | TCCTTCTTATGGCTA[A/G]GTAGAATTTCATTGT | 5977 |
| rs529317366 | snp | C/G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342129 | TAAAACCAGAAGGTG[C/G/T]AAGAATAGTACAATG | 5977 |
| rs529331177 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353394 | TTTATATAAATATAA[C/T]TAATAAGCAAACTAA | 5977 |
| rs529375389 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352918 | GAGTTGAGGTGTCTT[G/T]TTTTTTTCTTTCTTT | 5977 |
| rs529479472 | snp | A/G/T | 0.000153267 | 0.00875281 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333842 | CCGGCGCCTGCGCGC[A/G/T]GCGGACTGTGGGGCT | 5977 |
| rs529513876 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333521 | TGTTAGCCAGGATGG[C/T]CTCCATGTCCTGACC | 5977 |
| rs529613180 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343214 | TGAGGCAGGAGGATC[A/G]CTTGAACCCAGGAGA | 5977 |
| rs529886851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65351572 | TGCAGAGCATCCCTC[A/G]TCCTACCTGTAGCTG | 5977 |
| rs529933254 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343312 | TCAAAAAAAAAAAAA[-/A]AAAAAAAAAAGCTTC | 5977 |
| rs529951680 | in-del | -/T | 0.259951 | 0.249802 | intron-variant | DPF2 | GRCh38.p7 | 11:65350375 | CTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 5977 |
| rs530106314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335941 | GCTTCAGCCTCCCGG[A/G]TAGCTGAGATTACAG | 5977 |
| rs530235056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65342154 | ACAATGAAATACCAC[A/G]TACTCTTTACCTAGA | 5977 |
| rs530465126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65349782 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 5977 |
| rs530506483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350672 | CAGGTGTGAACCACT[A/G]CATCTAGCCTGAAGA | 5977 |
| rs530670985 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DPF2 | GRCh38.p7 | 11:65337627 | TTTGTTTTAAGAGAC[A/G]GAGCCTCCCTCTGTC | 5977 |
| rs530692821 | in-del | -/ATATATATAGAGAGAG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337497 | TATATATATATATAT[-/ATATATATAGAGAGAG]AGAGAGAGAGAGAGA | 5977 |
| rs530733019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343928 | TAGCGGCCACTTCCA[A/G]AAGAGTCTAACTCCT | 5977 |
| rs530789684 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348075 | GGATCACTTGAGCCC[A/T]GGAATTCAAGACCAG | 5977 |
| rs530824512 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342950 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 5977 |
| rs531177167 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352529 | GGAAGGATCAGGGGG[C/T]CAGGCCAGCAGCTCG | 5977 |
| rs531326811 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333220 | CTCAAGTGATCCTCC[C/T]ACCTCAGCCTCCCTA | 5977 |
| rs531451913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338951 | ACCTCCTCAATCTAT[A/G]GAAGAGTAACCAAGG | 5977 |
| rs531604606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347448 | GTACAATCCTCCCAC[C/G]TCAGCCTCCCGGGTA | 5977 |
| rs531840645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334336 | CGTCCCGTTCGCTGC[A/T]GCAACAGGCTCGGCG | 5977 |
| rs531869353 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336993 | CTCAGGAGGCTGAGG[C/T]AGAAGAATCGCTTGA | 5977 |
| rs531970869 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351277 | CAATATTAATAAACA[A/G]GGAATGACCCAATTG | 5977 |
| rs531988039 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350835 | AATAGAGAAATTAGC[G/T]GGGCGTGGTGCTGTG | 5977 |
| rs532203819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342756 | GGTAGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 5977 |
| rs532245866 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347907 | CCTGCCTCAGCCTCC[A/C]AAAATGCTGGTATTA | 5977 |
| rs532265156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348939 | CCCTGAAGGTAAGTT[G/T]CCCAGATCTTTTACT | 5977 |
| rs532423803 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333986 | GGAGTAGGGGGCGGT[-/G]GGGGAAGGGACTAGG | 5977 |
| rs532620518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65336864 | GGGAGGCTGAGGCGG[A/G]CGGATCACAAGGTCA | 5977 |
| rs532684891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65336138 | TATGACTTGCATCTT[A/G]TCCTGGGAAAAGAAT | 5977 |
| rs533142276 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352663 | CTGCTCTTAACTGAA[C/T]TGGGAGCCTCTGCCA | 5977 |
| rs533465446 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353242 | TACAAAATTTGGGTT[A/G]AAATCAACTTTAACA | 5977 |
| rs533565138 | in-del | -/A | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352420 | TCCTGGCTCACTCTT[-/A]ACGGTCGGTCTCCAG | 5977 |
| rs533570534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339576 | CTTCAAGGAACTTCA[A/G]GTACTTGTAGACATC | 5977 |
| rs533736262 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353055 | AGATTTCCATGATGG[C/T]GGTTTTTTTTTTTAA | 5977 |
| rs533993941 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333376 | TGGCGCGATCTCGGC[C/T]CACTGCAAACTCCGC | 5977 |
| rs534018538 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65346770 | TGATGCTGGTGTTGA[A/C]ATTTTGGTGATACCA | 5977 |
| rs534056450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340808 | ATATATCTATTTTTC[G/T]TTTCCACAGACTATT | 5977 |
| rs534170291 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344643 | CTCTCAACTTTTCAG[A/C]CTTGTGGTTTTCCTT | 5977 |
| rs534325605 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333659 | CGGAGCTCCGGGATG[C/T]ATGCCAATCTCCGGT | 5977 |
| rs534354930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348322 | CGGCGTCTCACACCT[A/G]TAATCCAAGCACTTT | 5977 |
| rs534414898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347746 | CTGCAACCTCTGCCT[C/T]CCAGGTTCAAGCAAT | 5977 |
| rs534586738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65334804 | TAGAGCTTCTTTTAA[C/T]GGGTATGTTGGGCTT | 5977 |
| rs534626005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335541 | CATCTTGTTTCTCTT[C/T]GAAAAACTGTAGAGA | 5977 |
| rs534801400 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338482 | CCTGCCTTCCATTTG[A/T]CTTCCAGTGTCCGTA | 5977 |
| rs534884369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65337247 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC | 5977 |
| rs535027753 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65337368 | TTGGAACCCGGGAGG[C/G]AGAAGCTGCAGTAGG | 5977 |
| rs535227098 | in-del | -/CT | 0.00478085 | 0.0486577 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332536 | CACTGCAAACTCCGC[-/CT]CCCAGGTTCACGCCA | 5977 |
| rs535335942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65350223 | AGTGTTAAGGCAGCT[A/G]AGGGGCAACCCCTAG | 5977 |
| rs535336063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343087 | GTTGGATCACCTGAG[A/G]TCGGGAGTTCGAGAC | 5977 |
| rs535459170 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332431 | CAAATAATGTTGTTA[C/T]GAACATTCTTGTACA | 5977 |
| rs535551709 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | DPF2 | GRCh38.p7 | 11:65337807 | TGTTTTGTTTTTTTT[A/T]ATTTTATTTTTTTTG | 5977 |
| rs535559097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345148 | GCCCAACTGGCTTCA[C/T]TGATAGGCTATCCCC | 5977 |
| rs535651900 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335664 | CAATTAATACGTACT[C/T]CCACAGAATTATCCC | 5977 |
| rs536161241 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332780 | TTTTTTTTTTAAGAG[A/C]CAGGATCTTGCTATG | 5977 |
| rs536221740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346880 | GATGACAGGGCATGG[G/T]AGAGTATGGTGGGCA | 5977 |
| rs536363675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334461 | AAATATTCTTGGGAA[G/T]AATTTATCGAGGAGC | 5977 |
| rs536411964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348440 | TGAAAAATTAGCTAG[G/T]TGTGGTGGTGTGTGC | 5977 |
| rs536425325 | snp | C/T | 1.76412e-05 | 0.0029699 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333930 | AGCTGTGAGTGGTCG[C/T]TTCTTTCTCTCCTAG | 5977 |
| rs536494688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340882 | CTCTAGAACTCAAAG[G/T]GGGGCCTACTTAATT | 5977 |
| rs536690201 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65335684 | AGAATTATCCCTTTA[A/C]GAAGGGGCTTCTATT | 5977 |
| rs536755125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342427 | CTCCAGCCTGGGTAA[C/T]AGAGGGAGACCCTGT | 5977 |
| rs537017069 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335777 | CTGATGTTATACATT[A/G]AGTACATTGAGGTCA | 5977 |
| rs537096992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350332 | AATAGCTTGCAAGCT[C/G]TTTTGTTTTCTTTTC | 5977 |
| rs537258050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65347173 | ACACGTGCCACCACA[C/T]CCGGCTAATTTTGTA | 5977 |
| rs537437160 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65350997 | GAAAAAAAAAAAATA[A/C]AGGGAGTTAAAAAAA | 5977 |
| rs537621143 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65338421 | ATTCCCCGCAAAACT[C/G]TTTCCAGCCTCCTTG | 5977 |
| rs537689685 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65345274 | AAAAAGTTTGGAGTC[G/T]TATCCACTTTTCCCC | 5977 |
| rs537757006 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352089 | GTGTCCTCCTAGAAA[C/G]AGTGGGAGAGCAGCT | 5977 |
| rs537770075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344373 | CCTGGCCTCAGTTAA[A/G]CCAGGGCCCCAGGGG | 5977 |
| rs537841997 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333612 | CCGGCCCCGGCTCCT[C/G]CTCCTCTAAATATTA | 5977 |
| rs537907600 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332982 | TAGTGATTATATTTA[C/T]ATATATATATATATA | 5977 |
| rs537957751 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332016 | GCTAGCTGCATATAA[C/T]TGGAAAGGCAGCTTA | 5977 |
| rs537971358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339253 | CTCTTAAAAAAAAAA[A/C]AAAACAAGATTGATT | 5977 |
| rs538093494 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352958 | ATTCTAAACATTAGT[A/C]AAAATAAATGTTTTT | 5977 |
| rs538237418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347710 | ATCCAGGCTGGAGTA[C/T]AATGGCGCAATCTCG | 5977 |
| rs538677628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347205 | TTTTAGTAGAGATGG[A/G]GTTTCTCCATGTTTG | 5977 |
| rs538844866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65343021 | AAAACTTCCCATGGC[C/T]GGCCACGGTGGCTGA | 5977 |
| rs538912420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349212 | ATTTATTTTCTTCCA[A/G]CCAGTCCAGAAAACT | 5977 |
| rs539245948 | in-del | -/AAGTTA | 0.00557542 | 0.0525036 | intron-variant | DPF2 | GRCh38.p7 | 11:65341242 | GACAGGTAAACAGAT[-/AAGTTA]TGGTGCCAAGTGAAC | 5977 |
| rs539328905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65348521 | AGGAGGTCAAGGCTG[C/T]AGTGAGCCGTGATTG | 5977 |
| rs539415361 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352872 | GCCTTCCCCCTTGGC[C/T]GTGGGCAGGCCCTAA | 5977 |
| rs539437530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337965 | ATGTACCACCACGCC[C/T]GGCTAATTTTGTATT | 5977 |
| rs539480229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337100 | CTTTAAGCGTTCTTA[A/C]TAGGAAAGTAAAATA | 5977 |
| rs539496082 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351829 | CATATTTCATACCCA[C/T]CTTTCCCTTCTTCCT | 5977 |
| rs539543909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343498 | TATTTGATTTGGCCA[C/T]GTGGCATGGTGGGGA | 5977 |
| rs539805597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344903 | CAATCAGACCCTTCC[A/G]CTCCCTCCCCAGACC | 5977 |
| rs539873389 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344610 | AGCATACCTCGAAAG[C/T]GCCCCAGAGAGGTAG | 5977 |
| rs539990159 | in-del | -/TTTG | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65337782 | CTAGCTGATGGTTTT[-/TTTG]TTTGTTTGTTTTGTT | 5977 |
| rs539992725 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352434 | TTACGGTCGGTCTCC[A/G]GTGACTGAAGCATTC | 5977 |
| rs540028843 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333015 | TACATATGTATATAT[A/G]TACATATGTATATAT | 5977 |
| rs540075024 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332604 | AGGCGTCCGCCACCA[C/T]GCCCGGCTAATTTTG | 5977 |
| rs540100356 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332174 | AGGTCAGGAGTTCGA[C/G]ACCAACCTGGCCAAC | 5977 |
| rs540186196 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353266 | TTTAACATCTATTTT[G/T]ATGTTTCAGTTGATT | 5977 |
| rs540191317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345310 | TGCCACCCCAAAGAT[A/G]TAGGAATATCCTTCC | 5977 |
| rs540390852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347293 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCACC | 5977 |
| rs540522236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338844 | GTGTAGCCCGAGTTA[C/T]GGACAGAAACCACAG | 5977 |
| rs540770158 | snp | A/G | 0.000116818 | 0.00764167 | intron-variant | DPF2 | GRCh38.p7 | 11:65341092 | AGGCACATACTTCCT[A/G]AGCAGAGGCGTGGCC | 5977 |
| rs541157498 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336420 | TCGCCTGAACCCAGG[C/T]GGCAGAGGTTGAAGT | 5977 |
| rs541219667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65339423 | TAAAGATTTACCCTT[A/G]ATTCAGATTTCAAAT | 5977 |
| rs541364663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335887 | GGCACGATCTTGGCT[C/T]ACTGCAACCTCCGCC | 5977 |
| rs541404049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342672 | AACCTTATGGGGTAG[G/T]TCCTGTGTTCCCCAT | 5977 |
| rs541469138 | snp | A/G | 0 | 0 | intron-variant | DPF2 | GRCh38.p7 | 11:65348657 | TTTGATCAATTAGGA[A/G]CTCTGAAAGGACCCA | 5977 |
| rs541592571 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65344475 | CCCTGGGAGCACCAT[A/C/T]GCCGCTGGGGTTTCT | 5977 |
| rs541650096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65336714 | GAATCACTTGAATCC[A/G]GGAGGCAGAGGTTGC | 5977 |
| rs541651732 | snp | C/T | 4.23325e-05 | 0.00460049 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343777 | TGACTTCCTGGATGA[C/T]CTCGATGATGAAGAC | 5977 |
| rs541659441 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331849 | GTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC | 5977 |
| rs542312563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338062 | CACCTCAGTCTCCCA[A/G]AGTGCTGGGATTACA | 5977 |
| rs542347951 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353111 | CCCAAATTAAAATTT[G/T]TTTGTGGAACCCCAA | 5977 |
| rs542446676 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65348758 | TCTGTTCTTACCTGC[C/T]ACCTACCCCTCTTGG | 5977 |
| rs542500912 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333704 | GGGCTCCCGTGGGGT[C/T]CACGCATTTCCTACC | 5977 |
| rs542612213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339327 | GTTAAACCCTGCAAG[A/G]TGAGAACAAGATAGG | 5977 |
| rs542795063 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334296 | GCGGCCCTACGGCTG[G/T]CCCGCCGCCCACCCC | 5977 |
| rs542795119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341927 | CCAGCCTGGGCAACA[A/G]AGTGAGACCCCATCT | 5977 |
| rs543047516 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336686 | CCCAGCTACTCAGGA[C/T]GCTGAGGGAAGGGAA | 5977 |
| rs543058250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346150 | TAACCAGCCCACCTC[A/G]CTTTTCCTAACCAAG | 5977 |
| rs543414666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338593 | GCTGCCTCCTAAAGG[C/T]GAGCCCACAGAGGCA | 5977 |
| rs543588439 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341699 | TCTGTTCTTACTTCA[A/G]TCCCTGATTATTGTC | 5977 |
| rs543823429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65336779 | GGCAACAGCAAGACT[C/T]CATCTCAAAAAAAAA | 5977 |
| rs543881820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343168 | ATCAGGTGTGGTGGC[A/G]CATGCCTGTAATTCC | 5977 |
| rs543883928 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DPF2 | GRCh38.p7 | 11:65336084 | TCCCAAAGTGCTGGG[A/T]TTATAGGCGTGAGCC | 5977 |
| rs543904898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350727 | TGGCTGTGCACTGTG[A/G]CTCGCATCTGTAATC | 5977 |
| rs543985163 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349515 | AGAAATTGAGTAGCA[G/T]CTGGGCGCGGTGGCT | 5977 |
| rs543986973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65338723 | ATTGCCGTCTCTGTG[C/T]GTCGTATGTGTCTTT | 5977 |
| rs543994166 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345048 | ATGACAAAATGCCTC[A/G]TGGGGATCTGCTTTC | 5977 |
| rs544101274 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348100 | GACCAGCCTGAGCAA[C/T]ATAGGGAGATCCTGT | 5977 |
| rs544169212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351267 | CAGCCATAGTCAATA[A/T]TAATAAACAAGGAAT | 5977 |
| rs544502946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344493 | CGCTGGGGTTTCTCT[C/G]TCGTTTGCTCTGCTT | 5977 |
| rs544527633 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65338311 | TGAGATTCTCCCCCC[-/A]ACACTTCAGTGTTTC | 5977 |
| rs544531549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351197 | ATAGGTATAATTTTG[C/T]TTATCATTTCAAGGC | 5977 |
| rs544576285 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352542 | GGCCAGGCCAGCAGC[G/T]CGGGGGCCACAAGGA | 5977 |
| rs544576662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338183 | AACTCTTGGTCTCAA[A/G]AGATCCACCAGCCTT | 5977 |
| rs544643894 | in-del | -/TT | 0.00199481 | 0.0315187 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332978 | GCTTTAGTGATTATA[-/TT]TATATATATATATAT | 5977 |
| rs544727546 | snp | A/G | 1.66763e-05 | 0.00288753 | intron-variant | DPF2 | GRCh38.p7 | 11:65340347 | CACCCTATGCCCCCC[A/G]CTCCAACATACACGC | 5977 |
| rs544915435 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345339 | CCCTTTCCTGACCTG[A/G]AGCGTCCCAGACTGT | 5977 |
| rs545006940 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333784 | GCGCGCGCCCGGACG[A/G]CGCCTGCGCAGAGGG | 5977 |
| rs545047317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347981 | AAGATGACTTTGGGT[A/G]CCGTGTGGAGGGTAG | 5977 |
| rs545071701 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333272 | CACCACCATGCCCAG[C/T]TAATCTTTTTTCTTT | 5977 |
| rs545078039 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341852 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 5977 |
| rs545136945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339471 | AGAAGATTTTTTCCT[A/G]TATAATTTTATTTTG | 5977 |
| rs545345603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333983 | CTGGGAGTAGGGGGC[C/G]GTGGGGGAAGGGACT | 5977 |
| rs545359271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341342 | AGCATTATGTGGACT[C/T]AGAGCAGTCTGCTTT | 5977 |
| rs545379551 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337988 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCTCC | 5977 |
| rs545381016 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347769 | CAAGCAATTCTCCTG[C/T]CTCAGCCTCCCAGGT | 5977 |
| rs545387595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65342061 | GAGTTCGAGACTGCA[A/G]TGAGTCATGATCATG | 5977 |
| rs545423693 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332148 | GAAAGCCTAGGCGGG[C/T]GGAACACATGAGGTC | 5977 |
| rs545566005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65350385 | CTTTCTTTTTTTTTT[C/T]TTTTTTTGAGACAGT | 5977 |
| rs545630495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342624 | AGCATTGGGTTAAGT[G/T]CCTTTTCATGCCCTT | 5977 |
| rs545982523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65336866 | GAGGCTGAGGCGGGC[A/G]GATCACAAGGTCAGG | 5977 |
| rs546164302 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347485 | ACCACAGATGCACAC[C/T]ACCATGTCTGGCTAC | 5977 |
| rs546302512 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343239 | AGGAGACGGAGGTTG[C/T]GGTAAGCCAGTATTG | 5977 |
| rs546583523 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65350732 | GTGCACTGTGGCTCG[C/T]ATCTGTAATCCCAGC | 5977 |
| rs546668385 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351928 | AGGTGGCAGCTCTGA[C/T]CACCTCTGGCCCCAG | 5977 |
| rs546806064 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | DPF2 | GRCh38.p7 | 11:65341240 | GAGACAGGTAAACAG[-/A]TAAGTTATGGTGCCA | 5977 |
| rs546845150 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333374 | AGTGGCGCGATCTCG[A/G]CTCACTGCAAACTCC | 5977 |
| rs546882461 | snp | C/G/T | 3.66752e-05 | 0.00428212 | intron-variant | DPF2 | GRCh38.p7 | 11:65346397 | CAGCATGGCTCCTTC[C/G/T]GGGCTTTTACTGCTG | 5977 |
| rs547060405 | in-del | -/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351977 | GCAACACACTGCCCC[-/T]AGGCGTGCGTGTGGC | 5977 |
| rs547407700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334450 | CCTAAGACTACAAAT[A/G]TTCTTGGGAAGAATT | 5977 |
| rs547516986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337618 | TTGCTTTTTTTTGTT[C/T]TAAGAGACAGAGCCT | 5977 |
| rs547568672 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341499 | GAAGCGAGGTGCCCC[A/G]GATCCCCGAGTTGAT | 5977 |
| rs547569114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347604 | CTCTCAAAGTGCTGG[G/T]ATTACAGGCATGAAC | 5977 |
| rs547630385 | snp | C/T | 0.264632 | 0.249571 | intron-variant | DPF2 | GRCh38.p7 | 11:65347117 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 5977 |
| rs547734978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335230 | TCAATTTAGAAATGA[C/T]ACTGTTGATCTACCA | 5977 |
| rs547798630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65349062 | CACCTTGCCTTGGCT[C/T]AGTTTAGAATGCCTT | 5977 |
| rs548071984 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65343371 | ATTTTAATTTAAACT[A/G]GGAGGCGAGTGTCAG | 5977 |
| rs548180789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336256 | CAACACTTTGGGAGG[C/T]TGAGGCAGGCAGATT | 5977 |
| rs548446151 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333121 | TTTTTTTTTTTTTTT[C/T]TTGAGATGGAGCCTC | 5977 |
| rs548533381 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65351531 | AGAGGTTTATCCCAG[C/G]TCAGGAAACCATGGA | 5977 |
| rs548670320 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332653 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGACGG | 5977 |
| rs548760237 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333858 | GCGGACTGTGGGGCT[C/T]CTCGGCCCGAGGCAG | 5977 |
| rs548770120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344793 | CAAAGTCCTGAAGGC[C/T]GCCTTTACCACTGCT | 5977 |
| rs548999217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346456 | TCTTTTAAAAAGGGA[A/G]CAGGATCCCTCCCAC | 5977 |
| rs549007905 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331998 | AGTACTAATAATAAA[C/T]AGGCTAGCTGCATAT | 5977 |
| rs549107085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338362 | CAAGACTGTTTGCCT[A/G]CCTTATGTAGCTCAC | 5977 |
| rs549208545 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353395 | TTATATAAATATAAT[G/T]AATAAGCAAACTAAT | 5977 |
| rs549275369 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340529 | CATCTGGATGGAAAA[A/G]CGACACCGGGGTCCA | 5977 |
| rs549449562 | in-del | -/A/AA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348612 | CTTGGGCTTTAGGGA[-/A/AA]AAAAAAAAAAAAAAA | 5977 |
| rs549660601 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333526 | GCCAGGATGGTCTCC[A/C]TGTCCTGACCTCGTG | 5977 |
| rs549868810 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65337931 | TGCCTCAGCCTCCCC[C/G/T]GTAGCTGGGATTATG | 5977 |
| rs549971956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342197 | ACATTTTGCCACATT[G/T]GCCTTATCTGTCTTT | 5977 |
| rs550036749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341625 | TCCTCTTCACTGGGG[A/G]CCACCTAGTTTCTAG | 5977 |
| rs550067165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349117 | TAGTGTTTGCACATT[A/G]TCAGCTACATTTACA | 5977 |
| rs550133417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337003 | TGAGGCAGAAGAATC[C/G]CTTGAACCCAGGAGA | 5977 |
| rs550172802 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339751 | TGATAGTTTTATTTG[A/G]CGCTTCTCAGCAGTG | 5977 |
| rs550258282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342918 | ACTCAGGCGCAAACC[C/T]GGGAGGCAGAGCTTG | 5977 |
| rs550471251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337642 | AGAGCCTCCCTCTGT[C/T]CCCCAGGCTGAAGTG | 5977 |
| rs550649812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65350073 | CTTTGGGGAGAAGTC[A/G]CATGTTTATGTTTTG | 5977 |
| rs550928421 | snp | C/T | 0.000197726 | 0.00994102 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345697 | CAAGAACCGACCAGG[C/T]CTCAGTTACCACTAT | 5977 |
| rs551232572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338484 | TGCCTTCCATTTGAC[A/T]TCCAGTGTCCGTATC | 5977 |
| rs551254099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344881 | AAGCATTATCAGGAG[C/G]CCATTACAATCAGAC | 5977 |
| rs551404499 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339083 | AGTATTAGGGATACT[A/G]TGAGAAATAAATCAA | 5977 |
| rs551511142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340651 | TCCCTACTGCCTTCC[A/G]CCTATGGATGAATAT | 5977 |
| rs551512170 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332686 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCACCG | 5977 |
| rs551606819 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65335494 | TCAAGTTGTGTCATA[A/T]GTGAGGGGTTGCCCA | 5977 |
| rs551618467 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353480 | TTCAGTTGCCTGCAG[C/T]GCTCCCAGGCCAGAG | 5977 |
| rs551622535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342875 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCACCT | 5977 |
| rs551669234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334371 | CTGCGGAGTGCACTG[C/T]GGGGCTGGCTGTTTC | 5977 |
| rs551842253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340001 | GGAAAGAGGGAATAA[A/G]GAGGAACTTAGGAGG | 5977 |
| rs551942247 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348010 | AGACTGTAGGGACAA[A/G]GATGGAGGCTCATGC | 5977 |
| rs552043364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65348985 | ATTAGTTACTTGGAA[A/G]ATACTGAGTTCTATG | 5977 |
| rs552110928 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349461 | CATCTCCACAAGTCC[C/T]CTTCCAGCTGGATTT | 5977 |
| rs552164124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347717 | CTGGAGTACAATGGC[A/G]CAATCTCGGCTCACT | 5977 |
| rs552311717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336230 | GGTGCAGTGGCTTAC[A/G]CCTATAATCCCAACA | 5977 |
| rs552376945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342788 | GAGGCCGAGGCAGGC[A/G]GATCTTGAGGTCAGG | 5977 |
| rs552441279 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65343499 | ATTTGATTTGGCCAT[G/T]TGGCATGGTGGGGAA | 5977 |
| rs552519687 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344444 | CTGTCTGCCTTGCCC[C/T]ACTTCTGTCCCTCCA | 5977 |
| rs552752850 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65350439 | GAGTGGAGTGGCATG[A/T]TCTCAGCTCACTGCA | 5977 |
| rs552754516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350751 | TGTAATCCCAGCACT[G/T]TGGGATCTCTTGAGC | 5977 |
| rs552821967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350176 | GGGACATCGAGGTAG[C/T]GGAGAGCTGCAGGCC | 5977 |
| rs552885622 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339256 | TTAAAAAAAAAAAAA[A/C]ACAAGATTGATTGAA | 5977 |
| rs552967781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344932 | CCAGGCAGCTGGTGG[G/T]CAGCTCATGTTCCCC | 5977 |
| rs553046017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338552 | AACCTTGTTTATCCA[A/G]TTTTATTCTGTGTGG | 5977 |
| rs553233951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343683 | GGCCTTGGCCAGTCT[C/T]ATCATAGGGGAGCTT | 5977 |
| rs553548988 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350636 | ATCCACCCACCTCAG[C/T]TTCCCAAAGTGCTGG | 5977 |
| rs553640590 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333688 | GTTGCGCCTGCGCGT[C/T]GGGCTCCCGTGGGGT | 5977 |
| rs553701639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340101 | TTGTGAGACACGTGG[A/C]GTGAACATTCTTTCA | 5977 |
| rs553825718 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353076 | TTTTTTTTAATGTTT[C/T]GAAATACAGCTTTTT | 5977 |
| rs553906104 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65347772 | GCAATTCTCCTGTCT[C/T]AGCCTCCCAGGTAGC | 5977 |
| rs553965692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347302 | TATAGGCGTGAGCCA[C/T]TGCACCCAGCTATTT | 5977 |
| rs554003005 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344803 | AAGGCTGCCTTTACC[A/T]CTGCTTGTTTCCCAC | 5977 |
| rs554177777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65342364 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 5977 |
| rs554300009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65334807 | AGCTTCTTTTAATGG[G/T]TATGTTGGGCTTGGT | 5977 |
| rs554536335 | in-del | -/AAAAAAAAAAAAA | 0.115088 | 0.210473 | intron-variant | DPF2 | GRCh38.p7 | 11:65343300 | GCGAAACTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAGCTTC | 5977 |
| rs554959817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336728 | CAGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATC | 5977 |
| rs555022161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349528 | CAGCTGGGCGCGGTG[C/G]CTCAAGCCTGTAATC | 5977 |
| rs555104504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345184 | ACCCATCCCCTGCTT[A/G]TTTACCCACATTCAG | 5977 |
| rs555179093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337311 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCATGCCA | 5977 |
| rs555275603 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344293 | TCTGCCATCCTCTGG[A/G]GTAGGGTTGCTTGTG | 5977 |
| rs555296733 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351982 | ACACTGCCCCTAGGC[G/T]TGCGTGTGGCCCAGT | 5977 |
| rs555374754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339106 | TAAATCAATTCTGCC[C/G]TTGGTTTAAGATTGA | 5977 |
| rs555447699 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332891 | AGGCATTGCACTCAG[C/T]TTCTTGTACAGCTTT | 5977 |
| rs555485606 | in-del | -/AAAT | 0.00636936 | 0.0560724 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332390 | CAAAACTCCGTCTCA[-/AAAT]AAATAAATAAATAAA | 5977 |
| rs555569295 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336113 | CCACCACGCCCGGCC[A/C]CTCATCTTGTATGAC | 5977 |
| rs555622105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351230 | TAAGGACTAATTTTA[C/T]TCAAAAAAAATTAGA | 5977 |
| rs555684892 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341200 | TGATGTGATTCTTTC[C/T]TTTAAGGACCTCAGT | 5977 |
| rs555767426 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332457 | GTACAGCTTTATTTT[A/T]TTTTTTTTGAGACGG | 5977 |
| rs556075614 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332543 | AACTCCGCCTCCCAG[A/G]TTCACGCCATTCTCC | 5977 |
| rs556269971 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353137 | CCCAATATGTAAAGC[A/G]AATATAAAATTGGTT | 5977 |
| rs556299553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342498 | TACTCTTTTATCACA[A/G]AAGTTTGTGTCACAG | 5977 |
| rs556354022 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349330 | TCTGAACTGGGAAGG[G/T]ACTTGACTTTGGAGC | 5977 |
| rs556362763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341980 | AAAAAATAGCCAGGC[A/G]TAGCAGCATGCGCCT | 5977 |
| rs556459868 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335107 | TTAAGTTGCTTTCTG[A/C]TCTATCCTGCTGTCT | 5977 |
| rs556495648 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333781 | AGTGCGCGCGCCCGG[A/G]CGGCGCCTGCGCAGA | 5977 |
| rs556563980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347926 | ATGCTGGTATTACAG[G/T]TGTGAGCCACCGTGC | 5977 |
| rs556576844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336414 | CAAGAATCGCCTGAA[C/T]CCAGGCGGCAGAGGT | 5977 |
| rs556637465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335704 | GGGCTTCTATTCTTC[C/T]AGTTCATTTGGAGAT | 5977 |
| rs556648975 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338867 | AACCACAGAGACTTA[A/G]TCTGTTTGCTGTCTC | 5977 |
| rs557025395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344380 | TCAGTTAAGCCAGGG[A/C]CCCAGGGGTCTGACA | 5977 |
| rs557212912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349580 | GTGGGCGGATCACGA[C/G]GTCAGGACATGGAGA | 5977 |
| rs557339430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343600 | GCAGGATTATAGCAT[A/G]CTTGAAAGGCGTTGG | 5977 |
| rs557495211 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347288 | CAAAGTGCTGGGATT[A/T]TAGGCGTGAGCCACT | 5977 |
| rs557677001 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65337897 | GCAACCTCCGCCTCC[C/G]AGGTTCAAGCAATTC | 5977 |
| rs557757250 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333613 | CGGCCCCGGCTCCTG[C/T]TCCTCTAAATATTAG | 5977 |
| rs557932544 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338494 | TTGACTTCCAGTGTC[C/G]GTATCAATTCCCATC | 5977 |
| rs557943076 | snp | A/G | 4.9498e-05 | 0.00497459 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340503 | ACCGGAGTAGCCCAG[A/G]GCAATTGTTACATCT | 5977 |
| rs558064045 | snp | A/G | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352978 | TAAATGTTTTTACAC[A/G]GAGCCCTCTGCTGGA | 5977 |
| rs558123128 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352128 | TGTGTTCTGCCTCCC[C/T]TCTGGTCTCCAGAGT | 5977 |
| rs558345216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347238 | AGGCTGGTATCGAAC[C/T]CCTGACCTCCGGTGA | 5977 |
| rs558414807 | in-del | -/CTT | 0.00129534 | 0.0254163 | intron-variant | DPF2 | GRCh38.p7 | 11:65344547 | CAAGTGTATCAAGGC[-/CTT]CTTCTCATGACTTTT | 5977 |
| rs558478719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341719 | TGATTATTGTCAGGT[A/G]CTGACTGGCTTCTCT | 5977 |
| rs558539950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334013 | TAGGCGGAGAGAGGG[A/C]CATCCCCGGGAAAGC | 5977 |
| rs558662084 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65347049 | AGATGGAGTCTTGCT[C/G]TGTCGCCCAGGCTGG | 5977 |
| rs558886191 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350840 | AGAAATTAGCTGGGC[A/G]TGGTGCTGTGCGCTT | 5977 |
| rs558901043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335851 | GAGTCTCACTGTTGT[C/T]GGCCCGGGCTGGAAT | 5977 |
| rs558967417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342642 | TTTTCATGCCCTTTC[C/T]CCTTTAGTCTGTACA | 5977 |
| rs559063343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65336519 | AGAGGCTGTTGGGCG[C/T]GGTGGCTCATGCCTG | 5977 |
| rs559123064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343028 | CCCATGGCCGGCCAC[A/G]GTGGCTGACGCCTGT | 5977 |
| rs559174336 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338080 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 5977 |
| rs559205814 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65349713 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAAGCG | 5977 |
| rs559269423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65348998 | AAAATACTGAGTTCT[A/G]TGTTCTTTATGTTAT | 5977 |
| rs559274280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349311 | ATTTCCTATCCCTTC[A/C]CCTTCTGAACTGGGA | 5977 |
| rs559520326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343261 | CCAGTATTGCGCCAT[C/T]GCACTCCAGCCTGGG | 5977 |
| rs559569168 | snp | C/T | 6.59207e-05 | 0.00574073 | intron-variant | DPF2 | GRCh38.p7 | 11:65348814 | GAGGCACATCAGTTA[C/T]TCAGTCCCCATCCTC | 5977 |
| rs559825035 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352746 | CTTTCTTCCCTTGCA[C/T]GCTCGCTAGCAGCTG | 5977 |
| rs560099666 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350425 | TGTTGCCCATGTTGG[A/G]GTGGAGTGGCATGAT | 5977 |
| rs560112341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338253 | TGCCCGGCCTCCCTT[A/C]AGTTCTTAAGAGCTC | 5977 |
| rs560127324 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353311 | AGTCTTGGATACATA[A/G]ATGGAAGTGATGACA | 5977 |
| rs560181649 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332634 | GTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 5977 |
| rs560211916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345342 | TTTCCTGACCTGGAG[C/T]GTCCCAGACTGTTAG | 5977 |
| rs560272297 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352389 | ACAGTAGCTTCACCT[C/T]GTTATTCCCATTGCT | 5977 |
| rs560273905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344700 | TCCTGCCTTTCTCAT[C/T]TCCTGGGATGCTAGC | 5977 |
| rs560326975 | snp | C/T | 0.0433465 | 0.140692 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333018 | ATATGTATATATATA[C/T]ATATGTATATATATG | 5977 |
| rs560440266 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333828 | ACCCCGGTGCGGTCC[C/G]GGCGCCTGCGCGCTG | 5977 |
| rs560602035 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342320 | CTGGGCATGGTGGCA[C/G]ACGCCTGCAGTCCCA | 5977 |
| rs560766515 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DPF2 | GRCh38.p7 | 11:65350237 | TGAGGGGCAACCCCT[A/G]GAAGTATCAGATGTT | 5977 |
| rs560779236 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348164 | GGTGGCACACACGTT[A/T]GTCCCAGCTACTTGG | 5977 |
| rs561028492 | in-del | -/AA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339243 | AGACCTTGTCTCTTA[-/AA]AAAAAAAAAAAAAAC | 5977 |
| rs561034968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334200 | GGTTTCCAGAGCATG[A/G]CGCCCTGCCTGCACG | 5977 |
| rs561314332 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65351006 | AAAATAAAGGGAGTT[-/A]AAAAAAAAATGCATG | 5977 |
| rs561328542 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333649 | AGCCTCGAACCGGAG[C/T]TCCGGGATGCATGCC | 5977 |
| rs561354638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348700 | CAGTGACTGGATCTG[C/T]GGTGGAGAGGGGCAG | 5977 |
| rs561882397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350510 | CACCTCAGCCTCCTG[A/G]GTACCTGGGACTACA | 5977 |
| rs562026880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339255 | CTTAAAAAAAAAAAA[A/C]AACAAGATTGATTGA | 5977 |
| rs562306398 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333171 | AGTGCAGTGATGTGG[C/G]TCCAGTGGCTCACTG | 5977 |
| rs562372659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351552 | AAACCATGGAACTTT[A/C]CTGCTGCAGAGCATC | 5977 |
| rs562450136 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | DPF2 | GRCh38.p7 | 11:65339222 | GTCCAGCTTGGGCAA[-/C]ATAGTGAGACCTTGT | 5977 |
| rs562527406 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332655 | ATGGGGTTTCACCAT[C/G]TTAGCCAGGACGGTC | 5977 |
| rs562620405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345576 | GGATGGTTGCCCTCT[A/G]CCTCAGGTGGAGCCC | 5977 |
| rs562742095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347088 | GGCACAATCTCAGCT[C/T]ACTGCAACCTCTGCC | 5977 |
| rs562819064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341324 | AGACCTTTGGTAAGC[A/C]CCAGCATTATGTGGA | 5977 |
| rs563030631 | snp | A/C | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332888 | ATGAGGCATTGCACT[A/C]AGCTTCTTGTACAGC | 5977 |
| rs563087146 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65341865 | CTGTAATCCCAGCAC[A/T]TTGGGAGGCCAAGGC | 5977 |
| rs563608944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343230 | CTTGAACCCAGGAGA[C/T]GGAGGTTGCGGTAAG | 5977 |
| rs563633627 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345130 | TTTCTTTGGGGACCA[A/G]CTGCCCAACTGGCTT | 5977 |
| rs563684759 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DPF2 | GRCh38.p7 | 11:65336813 | AAAAAAAAAGAAGCC[A/G]GGCACGGTGGCTCAT | 5977 |
| rs563749978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336106 | GCGTGAGCCACCACG[C/T]CCGGCCCCTCATCTT | 5977 |
| rs563843399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342734 | AAACTTCCCATGGGT[C/T]GGGCACGGTAGCTCA | 5977 |
| rs563890883 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332594 | CTGGGATTACAGGCG[C/T]CCGCCACCATGCCCG | 5977 |
| rs564113928 | snp | C/T | 1.6585e-05 | 0.00287962 | intron-variant | DPF2 | GRCh38.p7 | 11:65343968 | CTACCAAAATAAGGG[C/T]GTCTCTTTGCTCTTC | 5977 |
| rs564176769 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DPF2 | GRCh38.p7 | 11:65350731 | TGTGCACTGTGGCTC[G/T]CATCTGTAATCCCAG | 5977 |
| rs564252460 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339643 | CTAGTTCAAAATTCA[A/G]AAGATATAAAAAGGC | 5977 |
| rs564261730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344496 | TGGGGTTTCTCTCTC[A/G]TTTGCTCTGCTTTCC | 5977 |
| rs564402650 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353233 | TTTGATCAATACAAA[A/G]TTTGGGTTAAAATCA | 5977 |
| rs564468673 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352658 | GCCTCCTGCTCTTAA[A/C]TGAATTGGGAGCCTC | 5977 |
| rs564496467 | in-del | -/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341672 | GGAGTCCAGGAAGCA[-/G]GCCCCTGCAGTTCTG | 5977 |
| rs564873634 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DPF2 | GRCh38.p7 | 11:65339526 | TGGGCCTTAGAGCAA[A/T]CAAGTTTCTTATGAG | 5977 |
| rs564891299 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333809 | AGAGGGCAAGGAACC[C/T]GGTACCCCGGTGCGG | 5977 |
| rs564941400 | in-del | -/TA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332982 | TAGTGATTATATTTA[-/TA]TATATATATATATAT | 5977 |
| rs565098048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345488 | GCTAGAGAGCCCCAC[A/G]GCCTGATGCTCCTGG | 5977 |
| rs565173844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65346556 | ATTTTATGTCAGACA[C/G]TGTTCTAGTCACTAA | 5977 |
| rs565280508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334402 | AGTTCCAGGCAGCCC[C/T]GTGATGTTTGGGAGG | 5977 |
| rs565283580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65348012 | ACTGTAGGGACAAGG[A/G]TGGAGGCTCATGCCT | 5977 |
| rs565344797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65347490 | AGATGCACACCACCA[C/T]GTCTGGCTACTTTTT | 5977 |
| rs565345736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348317 | GGGCACGGCGTCTCA[C/T]ACCTGTAATCCAAGC | 5977 |
| rs565407475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347722 | GTACAATGGCGCAAT[A/C]TCGGCTCACTGCAAC | 5977 |
| rs565612530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342074 | CAATGAGTCATGATC[A/G]TGCCACTGCACTCCA | 5977 |
| rs565918418 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338337 | GTTTCCTTCCCAGCC[C/G]TTTTACCCCCAAGAC | 5977 |
| rs565947135 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65335500 | TGTGTCATAAGTGAG[C/G]GGTTGCCCATTTAAA | 5977 |
| rs565976069 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340024 | TTAGGAGGGACTATC[A/T]TCTGCTTCTTAGCCT | 5977 |
| rs566171336 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350917 | TGGGAGGCAGAGGTT[-/A]AGAGTAAGCTGAGAT | 5977 |
| rs566284901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343550 | TAACGTGAAGCACAG[C/G]GGAAAGATATCCCAA | 5977 |
| rs566601681 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352884 | GGCCGTGGGCAGGCC[C/G]TAACTCACTGTCGCT | 5977 |
| rs566615140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65344135 | GCTCTGGATATGAGA[A/G]GAGGGAGGGTTGTGT | 5977 |
| rs566661095 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351950 | TGGCCCCAGGCCCTC[A/G]GGGAGAAAGGAGCAA | 5977 |
| rs566868256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338555 | CTTGTTTATCCAATT[G/T]TATTCTGTGTGGTGA | 5977 |
| rs567074676 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333491 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACCGT | 5977 |
| rs567348552 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344247 | GTCCCTGCTATATGA[C/T]GGGTGGGACCTGCAT | 5977 |
| rs567480411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347624 | CAGGCATGAACCCAC[C/T]ATGTCTGGCCTTGTC | 5977 |
| rs567539721 | snp | C/G | 0.264632 | 0.249571 | intron-variant | DPF2 | GRCh38.p7 | 11:65347118 | CTCCTGGGTTCAAGT[C/G]ATTCTCCTGCCTCAG | 5977 |
| rs567619689 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | DPF2 | GRCh38.p7 | 11:65339251 | TCTCTTAAAAAAAAA[-/C]AAAAAACAAGATTGA | 5977 |
| rs567703590 | snp | A/C | 1.7565e-05 | 0.00296347 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333928 | GAAGCTGTGAGTGGT[A/C]GTTTCTTTCTCTCCT | 5977 |
| rs567749891 | in-del | -/CCCGT | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334313 | CGCCGCCCACCCCGC[-/CCCGT]CCCGTCCCGTCCCGT | 5977 |
| rs567842234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65348435 | AACATTGAAAAATTA[A/G]CTAGGTGTGGTGGTG | 5977 |
| rs567892117 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349774 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 5977 |
| rs568001192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336955 | TAGCTGGGCATGGTG[A/G]CGTGCACCTGTAGTC | 5977 |
| rs568036040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349074 | GCTCAGTTTAGAATG[C/T]CTTCCTAACATTTCA | 5977 |
| rs568223432 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333360 | CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTCGGC | 5977 |
| rs568431391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350243 | GCAACCCCTAGAAGT[A/G]TCAGATGTTCTAGGT | 5977 |
| rs568672829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344841 | CTCCTAGAGCTGCTC[A/G]GCCCAGTGCATGGGG | 5977 |
| rs568686909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350983 | AAACTCTTGTCTCAG[A/G]AAAAAAAAAAATAAA | 5977 |
| rs568736235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344317 | GCTTGTGGGGGCCAC[A/G]GCAGGCAGGGTTGGC | 5977 |
| rs568862969 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353368 | TCAGACATTTAAAAC[A/G]GGACCAGAAGTTTAT | 5977 |
| rs568975824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65339121 | CTTGGTTTAAGATTG[A/T]TTGACGCCAGGTACT | 5977 |
| rs569183789 | snp | A/C/G/T | 0.000135688 | 0.00823588 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333866 | TGGGGCTTCTCGGCC[A/C/G/T]GAGGCAGAGGAACAG | 5977 |
| rs569249870 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333536 | TCTCCATGTCCTGAC[C/T]TCGTGATCCGCCCGC | 5977 |
| rs569277444 | snp | A/G | 9.94431e-05 | 0.00705065 | intron-variant | DPF2 | GRCh38.p7 | 11:65346103 | GCCCAGTCCCCAAGG[A/G]GCTCTTGGCTTGCTG | 5977 |
| rs569298274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65346532 | TTGCCAGATATATAT[C/T]GAGTGCTGATTTTAT | 5977 |
| rs569363414 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353418 | AAACTAATGACATCA[C/T]CATGGGACACACACA | 5977 |
| rs569713858 | in-del | -/GGCAACA | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334053 | ACTCCTGGTGGGGAG[-/GGCAACA]GGAGACTCCGGAGAA | 5977 |
| rs569751563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65342202 | TTGCCACATTTGCCT[C/T]ATCTGTCTTTGCTAA | 5977 |
| rs569929555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65341675 | GTCCAGGAAGCAGGC[C/G]CCTGCAGTTCTGTTC | 5977 |
| rs569950523 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338081 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCA | 5977 |
| rs570117566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65337047 | CACTCCAGCCCAGGC[A/G]ACAGAGCGAGACTCC | 5977 |
| rs570202857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335421 | TTTTGGGAGTTAAAC[A/G]TAGTGAGGTTCTTCG | 5977 |
| rs570223845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349209 | ATGATTTATTTTCTT[C/T]CAACCAGTCCAGAAA | 5977 |
| rs570419132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343466 | TGTGGCATCAGGGCA[A/G]CCTTTTGGAAGCATG | 5977 |
| rs570483908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350127 | TCAAACAGATGATCT[A/G]TGTTACAGAATGGCT | 5977 |
| rs570504731 | snp | G/T | 1.65272e-05 | 0.0028746 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351804 | CTAAGGCTGTTTCTC[G/T]CCTCCACTTCATATT | 5977 |
| rs570599085 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337648 | TCCCTCTGTCCCCCA[G/T]GCTGAAGTGCAGTGG | 5977 |
| rs570816229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65344387 | AGCCAGGGCCCCAGG[A/G]GTCTGACACTGAGTT | 5977 |
| rs571025532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338495 | TGACTTCCAGTGTCC[A/G]TATCAATTCCCATCA | 5977 |
| rs571061047 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332172 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGGCCA | 5977 |
| rs571085617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65344884 | CATTATCAGGAGCCC[A/G]TTACAATCAGACCCT | 5977 |
| rs571178663 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335751 | TTATAGTGTGCCTAG[C/T]CTTCTGACAGCTGAT | 5977 |
| rs571313265 | snp | A/G | 1.69375e-05 | 0.00291006 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333884 | GGCAGAGGAACAGGG[A/G]AGATGGCGGCTGTGG | 5977 |
| rs571334732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65340885 | TAGAACTCAAAGGGG[A/G]GCCTACTTAATTAGA | 5977 |
| rs571390363 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333652 | CTCGAACCGGAGCTC[C/T]GGGATGCATGCCAAT | 5977 |
| rs571503032 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339127 | TTAAGATTGATTGAC[A/G]CCAGGTACTGTGACA | 5977 |
| rs571603981 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65352983 | GTTTTTACACAGAGC[C/T]CTCTGCTGGATGGTT | 5977 |
| rs571681370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340666 | ACCTATGGATGAATA[C/T]GGTCTTCCTGTGATT | 5977 |
| rs571695174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65340075 | GCATCTTAACTAGCA[C/T]AGGGGTGGGCTTGTG | 5977 |
| rs571862822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DPF2 | GRCh38.p7 | 11:65349521 | TGAGTAGCAGCTGGG[C/T]GCGGTGGCTCAAGCC | 5977 |
| rs572015854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334076 | GAGACTCCGGAGAAG[A/C]CGTTGCGCTTCTTTG | 5977 |
| rs572078771 | snp | C/T | 3.29995e-05 | 0.00406185 | intron-variant | DPF2 | GRCh38.p7 | 11:65340380 | GATTTCTATCTTCCC[C/T]GCAGCCTTGGGGAGC | 5977 |
| rs572194462 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336370 | GGTGGCGCACACCTG[C/T]AGTCCCAGCTACTTG | 5977 |
| rs572431136 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344473 | CACCCTGGGAGCACC[A/G]TCGCCGCTGGGGTTT | 5977 |
| rs572533245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65348026 | GATGGAGGCTCATGC[C/T]TGTAATCCTAACACT | 5977 |
| rs573324691 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350721 | AAAAACTGGCTGTGC[A/G]CTGTGGCTCGCATCT | 5977 |
| rs573587858 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341167 | CAGTACTAGATCCCA[A/G]ATATACTCAAATGAA | 5977 |
| rs573792600 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333691 | GCGCCTGCGCGTCGG[C/G]CTCCCGTGGGGTCCA | 5977 |
| rs573796023 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352482 | TCATCTTCTGCCTCC[C/T]TTCCTACTCCTTTTG | 5977 |
| rs573828022 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333023 | TATATATATACATAT[A/G]TATATATATGTGTAT | 5977 |
| rs574020419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65339324 | CTTGTTAAACCCTGC[A/G]AGATGAGAACAAGAT | 5977 |
| rs574203538 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347362 | TTTGAGACAGAGTCT[C/T]TCTGTCATCCAGGCT | 5977 |
| rs574310931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65336970 | GCGTGCACCTGTAGT[C/T]CCAGCTACTCAGGAG | 5977 |
| rs574438117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65334808 | GCTTCTTTTAATGGG[G/T]ATGTTGGGCTTGGTG | 5977 |
| rs574473761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334231 | CGAGACTCACCGTCC[C/G]GGTCCTCTCCCGAGA | 5977 |
| rs574873527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65343129 | AGATGAAGAAACCCC[A/G]TCTCTACTAAAAATC | 5977 |
| rs575071297 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DPF2 | GRCh38.p7 | 11:65344410 | ACTGAGTTTTTCAAC[A/G]TCTGTTCTCTTTTTC | 5977 |
| rs575087544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338152 | GGATCTCACTATGTT[A/G]CCCAAGCTGGTCTCT | 5977 |
| rs575111266 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349489 | TTTCTGTACATAAAC[A/G]CCTCCTGTACAGAAA | 5977 |
| rs575235353 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332916 | AGCTTTCTTGTGTGT[A/G]TATCCAGGAGTGGAC | 5977 |
| rs575360091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338705 | CCAGGCTATATTTGT[A/G]GCATTGCCGTCTCTG | 5977 |
| rs575385246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65345219 | GATGGGCTCCATGGT[A/G]TGTGGGGTAGCATGA | 5977 |
| rs575446528 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351992 | TAGGCGTGCGTGTGG[C/T]CCAGTTTCTCTCTGC | 5977 |
| rs575869916 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342042 | GAGAATCACTTGAGC[C/T]TATGAGTTCGAGACT | 5977 |
| rs576043489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347005 | TGACATGGTTATTTA[C/T]GTATTTATTTATTTA | 5977 |
| rs576214195 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335236 | TAGAAATGACACTGT[G/T]GATCTACCATTTATC | 5977 |
| rs576217421 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331817 | TCAAGCTATGAACCC[A/G]GAAGGCGGAGGTTGC | 5977 |
| rs576432643 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333782 | GTGCGCGCGCCCGGA[C/G]GGCGCCTGCGCAGAG | 5977 |
| rs576435120 | snp | C/T | 0.000565049 | 0.016799 | intron-variant | DPF2 | GRCh38.p7 | 11:65340921 | TTTGGTATTACTTTC[C/T]AATACTGGGTTAGGG | 5977 |
| rs576548955 | in-del | -/T | 0.0021057 | 0.0323793 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353108 | CCCCCCAAATTAAAA[-/T]TTTTTTGTGGAACCC | 5977 |
| rs576561026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65335842 | TTTTAGACAGAGTCT[C/T]ACTGTTGTCGGCCCG | 5977 |
| rs576689192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65347937 | ACAGGTGTGAGCCAC[C/T]GTGCTTGGCCCTTGT | 5977 |
| rs576963090 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65349609 | GACCATCCTGGCTAA[C/G/T]ACGGTGAAACCCCGT | 5977 |
| rs576984832 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340581 | GAAGGGGACTCAGGA[A/G]CATAAGGAGGAAGAA | 5977 |
| rs577237405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343626 | GTTGGTGAGGAATGA[A/G]GCTGGTGTGGGTGGG | 5977 |
| rs577300757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65350342 | AAGCTGTTTTGTTTT[C/G]TTTTCTTTTCTCTTT | 5977 |
| rs577301325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65343240 | GGAGACGGAGGTTGC[A/G]GTAAGCCAGTATTGC | 5977 |
| rs577318450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65337435 | TCTAACCTGGGCGGC[A/G]AAGCAAGACTCTATC | 5977 |
| rs577574620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DPF2 | GRCh38.p7 | 11:65339746 | ATAAATGATAGTTTT[A/G]TTTGACGCTTCTCAG | 5977 |
| rs577707409 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352204 | GCAAGCTGAGGCCAC[A/G]TCCACAAGGAGCTTT | 5977 |
| rs577754714 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DPF2 | GRCh38.p7 | 11:65336562 | TTTGGGAGTCCGAGG[C/T]GGGCAGATCACAAGG | 5977 |
| rs577760288 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333009 | TATATATACATATGT[A/G]TATATATACATATGT | 5977 |
| rs577769777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65351466 | AGTCCTCTAGATGAT[A/T]ATTTCTTTCATCTCC | 5977 |
| rs577831743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DPF2 | GRCh38.p7 | 11:65338837 | TTTGTTGGTGTAGCC[C/T]GAGTTACGGACAGAA | 5977 |
| rs578108922 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DPF2 | GRCh38.p7 | 11:65341693 | TGCAGTTCTGTTCTT[A/T]CTTCAGTCCCTGATT | 5977 |
| rs578140435 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344902 | ACAATCAGACCCTTC[C/T]GCTCCCTCCCCAGAC | 5977 |
| rs745399161 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345455 | GGTTGGAGTTCAGGA[A/G]GGAAAAGAGCCCCAG | 5977 |
| rs745535715 | snp | A/C | 1.66515e-05 | 0.00288539 | intron-variant | DPF2 | GRCh38.p7 | 11:65341089 | GTAAGGCACATACTT[A/C]CTGAGCAGAGGCGTG | 5977 |
| rs745602444 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340429 | TGGAGCAGTGCCACA[A/G]TTACAATGCTCGCCT | 5977 |
| rs745799949 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345834 | AGAAGTGGTGGGCAA[A/G]CAGAAGTTGGCCTGG | 5977 |
| rs745850709 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347618 | GGATTACAGGCATGA[A/G]CCCACCATGTCTGGC | 5977 |
| rs745853040 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant | DPF2 | GRCh38.p7 | 11:65345644 | TCCTAACACCTTTCT[C/T]TGCAATCTTCTTCCC | 5977 |
| rs745857942 | in-del | -/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333093 | ATATATGTATATATA[-/T]TTTTTTTTCCTTTTT | 5977 |
| rs745874106 | snp | C/T | 1.6543e-05 | 0.00287597 | intron-variant | DPF2 | GRCh38.p7 | 11:65343982 | GTGTCTCTTTGCTCT[C/T]CTTGGCAGGGTAAGG | 5977 |
| rs746037351 | snp | A/G | | | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341492 | CCCTGGAGAAGCGAG[A/G]TGCCCCGGATCCCCG | 5977 |
| rs746123223 | snp | A/G | 1.65201e-05 | 0.00287398 | intron-variant | DPF2 | GRCh38.p7 | 11:65341586 | TTATCCCTGTGGCTA[A/G]GGGAGCTTTGATGGA | 5977 |
| rs746153448 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340262 | TGGAGGCAAATAGAA[C/T]GGAAGAGACAGCCAC | 5977 |
| rs746166076 | snp | A/G | 1.65499e-05 | 0.00287657 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341005 | CCTACCCTGCCCGGC[A/G]CTGGCGGAAAAAGCG | 5977 |
| rs746234689 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351919 | TGCAAGCTGAGGTGG[-/C]AGCTCTGACCACCTC | 5977 |
| rs746279278 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335906 | GCAACCTCCGCCTCC[C/T]GGGTTCCAGCAATTC | 5977 |
| rs746573495 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338412 | CTCTCATTCATTCCC[C/T]GCAAAACTGTTTCCA | 5977 |
| rs746637789 | snp | G/T | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340998 | CTGTACTCCTACCCT[G/T]CCCGGCGCTGGCGGA | 5977 |
| rs746715804 | snp | A/G | 1.66225e-05 | 0.00288287 | intron-variant | DPF2 | GRCh38.p7 | 11:65345628 | ACATGGCACTCTTGT[A/G]TCCTAACACCTTTCT | 5977 |
| rs746759161 | snp | A/G | 1.70142e-05 | 0.00291664 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333898 | GAAGATGGCGGCTGT[A/G]GTGGAGAATGTAGTG | 5977 |
| rs746856930 | snp | A/G/T | 0.000151704 | 0.00870808 | intron-variant | DPF2 | GRCh38.p7 | 11:65346206 | TCCTCTCTTCCCCCC[A/G/T]CATTTCCGACTGTCT | 5977 |
| rs746954424 | snp | C/G/T | 3.30585e-05 | 0.00406551 | synonymous-codon, intron-variant | DPF2 | GRCh38.p7 | 11:65344029 | TAAGAAGCTGGATGC[C/G/T]TCCATCCTGGAGGAC | 5977 |
| rs747023470 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | DPF2 | GRCh38.p7 | 11:65341569 | GCGCGAAAGGTACAG[A/G]ATTATCCCTGTGGCT | 5977 |
| rs747112875 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340060 | GGGTTAAGAGAAATA[G/T]CATCTTAACTAGCAC | 5977 |
| rs747240416 | snp | C/T | 4.94752e-05 | 0.00497344 | intron-variant | DPF2 | GRCh38.p7 | 11:65348953 | TGCCCAGATCTTTTA[C/T]TCAGAACAATTACTT | 5977 |
| rs747298628 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352744 | CCCTTTCTTCCCTTG[C/G]ACGCTCGCTAGCAGC | 5977 |
| rs747337649 | snp | C/G | 4.94425e-05 | 0.0049718 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346012 | GATTAACAAGAAGAC[C/G]GGACAACCCGAGGAG | 5977 |
| rs747351055 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347143 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGA | 5977 |
| rs747363309 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348053 | CACTTGAGAGGCTGA[A/G]GCGGGAGGATCACTT | 5977 |
| rs747492190 | snp | A/G | 4.2372e-05 | 0.00460263 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343781 | TTCCTGGATGACCTC[A/G]ATGATGAAGACTATG | 5977 |
| rs747564541 | in-del | -/TGG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338929 | ATGTCAAAGCTCATT[-/TGG]TCCAACCTCCTCAAT | 5977 |
| rs747568247 | snp | A/C | 3.32292e-05 | 0.00407597 | intron-variant | DPF2 | GRCh38.p7 | 11:65340556 | TCCAGGTGAGGGTCC[A/C]GACTTGGGAGAAGGG | 5977 |
| rs747685812 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335857 | CACTGTTGTCGGCCC[A/G]GGCTGGAATGCAGTG | 5977 |
| rs747745445 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345983 | TACTGTGACTTCTGC[C/T]TGGGGGACTCAAAGA | 5977 |
| rs747794162 | in-del | -/C | 1.672e-05 | 0.00289132 | intron-variant | DPF2 | GRCh38.p7 | 11:65340340 | GCTCAGCACCCTATG[-/C]CCCCCCGCTCCAACA | 5977 |
| rs747810698 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349203 | GAAGGAATGATTTAT[G/T]TTCTTCCAACCAGTC | 5977 |
| rs747879173 | snp | C/G/T | 0.000132021 | 0.00812369 | intron-variant | DPF2 | GRCh38.p7 | 11:65345900 | CTCAGGGACCCCCAT[C/G/T]GGTGTCATCAAAACT | 5977 |
| rs748019412 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342678 | ATGGGGTAGGTCCTG[A/T]GTTCCCCATTTCACA | 5977 |
| rs748076222 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335063 | AAGCTAAGTGCCTTT[A/C]CTCCTCTTGTGGTTT | 5977 |
| rs748206492 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352564 | CCACAAGGAGATGGA[G/T]AATGTGCCTGTTTTT | 5977 |
| rs748548327 | in-del | -/AG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340076 | CATCTTAACTAGCAC[-/AG]GGGTGGGCTTGTGAG | 5977 |
| rs748585126 | in-del | -/CA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342690 | CTGTGTTCCCCATTT[-/CA]CACAGAGGCTGAAAC | 5977 |
| rs748650780 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341555 | TGACCAACAGTCGAG[C/T]GCGAAAGGTACAGGA | 5977 |
| rs748703811 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348927 | CATGTCTGAGCCCCC[C/T]GAAGGTAAGTTGCCC | 5977 |
| rs748705843 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341468 | TAGAGGCTCTGTTGC[A/G]CACTGACCCCCTGGA | 5977 |
| rs748726296 | snp | C/T | 1.65048e-05 | 0.00287265 | intron-variant | DPF2 | GRCh38.p7 | 11:65345886 | TGGGTGTTGAGTGGC[C/T]CAGGGACCCCCATGG | 5977 |
| rs748837942 | snp | C/T | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334235 | ACTCACCGTCCCGGT[C/T]CTCTCCCGAGACGCC | 5977 |
| rs749013769 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346475 | GATCCCTCCCACATG[C/T]CACACGCCCCTCCCT | 5977 |
| rs749048277 | snp | C/T | 1.65433e-05 | 0.002876 | intron-variant | DPF2 | GRCh38.p7 | 11:65348975 | CAATTACTTTATTAG[C/T]TACTTGGAAAATACT | 5977 |
| rs749070374 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341582 | AGGATTATCCCTGTG[A/G]CTAAGGGAGCTTTGA | 5977 |
| rs749111778 | snp | A/G | | | intron-variant, utr-variant-5-prime | DPF2 | GRCh38.p7 | 11:65334526 | CCTTGGCCCCGTCCA[A/G]TAGCAGCCATCAAAA | 5977 |
| rs749186309 | in-del | -/G/GGGGCTTCTCGGCCCGA | 3.40334e-05 | 0.00412502 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333851 | CGCGCTGCGGACTGT[-/G/GGGGCTTCTCGGCCCGA]GGGGCTTCTCGGCCC | 5977 |