| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs370617415 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038246 | TTGTCTATCTTGTTT[A/T]TAGTTAGATTCCCAG | 6596 |
| rs370639641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149061879 | AAAAAGAATTGGCTC[C/T]TATCAAAGAAAATAC | 6596 |
| rs370658214 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149044365 | CTTTACTAACACTAA[C/T]TATTCCCTGGCATGG | 6596 |
| rs370687576 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047875 | TTTCCAAACAAGCAT[C/G]ACTAGGTTCTGAAAG | 6596 |
| rs370768229 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065871 | GAGATACGTAACTAG[A/T]AGAGTTACTTTAGAC | 6596 |
| rs370806697 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030790 | AAAGGGACCAGGAAG[A/G]TTCTAGCTGGCTAAT | 6596 |
| rs370864114 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149082665 | TTATCATACGTAAAC[A/C]ACATCTCAATAAAGT | 6596 |
| rs370880281 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149079881 | CAGGCGTGAGCCACC[A/G]TGCCCCATGCCCAGC | 6596 |
| rs371010358 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149035683 | AAAAAAAAAAAAAAA[A/G]GGGGGTTTTAAGAGT | 6596 |
| rs371028097 | snp | C/G/T | 3.31281e-05 | 0.00406978 | missense | HLTF | GRCh38.p7 | 3:149041509 | TCATTCTGAATGACT[C/G/T]GGCAAATACAGGGTT | 6596 |
| rs371048166 | snp | A/T | 1.65111e-05 | 0.0028732 | intron-variant | HLTF | GRCh38.p7 | 3:149064786 | ATTTCAAAATTAGCA[A/T]TTACCTTTGCTTAGT | 6596 |
| rs371152141 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068844 | TTCAATATTTACTGC[A/T]GCTTAATTCATAGTT | 6596 |
| rs371152352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047408 | GCACTTTGGGAGGTC[A/G]AGGCAAGAGGATAAC | 6596 |
| rs371175977 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061234 | GCCACTACACCCAGC[A/G]AATTTCACTATTATT | 6596 |
| rs371233960 | snp | A/G | 0.000277431 | 0.0117745 | missense | HLTF | GRCh38.p7 | 3:149046258 | TTAGGGACTGTAAAC[A/G]CCTAATCAGAATAAA | 6596 |
| rs371458543 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066837 | GCTCAGGGTGAGGAA[C/T]TGAACCTGAGACTTC | 6596 |
| rs371518741 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044950 | TCCTATTCAAATAAC[C/G]TAAATCTGAGCACAG | 6596 |
| rs371556194 | in-del | -/TA | | | intron-variant | HLTF | GRCh38.p7 | 3:149062647 | TTCAAATTCTCCCTC[-/TA]GTCTATGTTAATATA | 6596 |
| rs371572759 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081351 | TACTACATAACAAAA[C/T]GTGGTGGCTAAAGGC | 6596 |
| rs371583563 | snp | C/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085026 | ATTAATAGTTACTCT[C/G]GTTAAAGCAGGAATT | 6596 |
| rs371638358 | in-del | -/GTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149055686 | TTAAGACGAACATTT[-/GTT]TTATGCAGTTTTCTG | 6596 |
| rs371662252 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149069472 | GAAACTCCATCTCAA[A/G]AAAAAAAAAAAAAAA | 6596 |
| rs371668196 | snp | A/T | 0.000153988 | 0.00877327 | missense | HLTF | GRCh38.p7 | 3:149050281 | AAAACAATATCCTGT[A/T]TTGAAAGTAAGGCCG | 6596 |
| rs371673284 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041013 | CACAATAGCCAATAA[G/T]CACATGGGGCAATTA | 6596 |
| rs371701673 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087506 | CCAGATAATACTTGC[A/G]CGTCACAGAGAGGTC | 6596 |
| rs371726117 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055998 | TATGGAAGGATGCAC[A/G]TAGTGAGGATCTGAA | 6596 |
| rs371728757 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149056269 | TGTTACACAGTAATA[G/T]GTAACTAATATATTA | 6596 |
| rs371760430 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149057434 | CCGTCTCAAAACAAA[C/G]AAACAAACAAACAAA | 6596 |
| rs371788406 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086873 | TCTACCGTATCCTTC[C/T]TCTTATTTTCTTCTC | 6596 |
| rs371833923 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061847 | GTCTCAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 6596 |
| rs371921090 | snp | A/G | 1.65353e-05 | 0.00287531 | missense | HLTF | GRCh38.p7 | 3:149042262 | GGACATCTGCATAAT[A/G]TGCCAGGACAGTCCC | 6596 |
| rs371927446 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon | HLTF | GRCh38.p7 | 3:149068285 | AATAGGAAGAGGTCT[A/G]CCATCATGGAAGTTG | 6596 |
| rs372031516 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049234 | GCTAAGTAAGTATGT[C/T]ACCCAAAGCACCACA | 6596 |
| rs372033544 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149072159 | TACTCACTGAAGAGC[A/G]AATGAACAGGTGCTT | 6596 |
| rs372062942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149063204 | AACTGGGACTACAGG[C/T]GCCCACGACCACGCC | 6596 |
| rs372129397 | snp | C/T | 0.000325767 | 0.0127584 | missense | HLTF | GRCh38.p7 | 3:149039675 | TTAAGTCAGTCAATG[C/T]GTGCATTAGCGCATT | 6596 |
| rs372195591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149044569 | CCACACATAGCTGAC[C/T]TTGAACTCGACTCTC | 6596 |
| rs372238111 | snp | A/C/G | 3.34857e-05 | 0.00409167 | missense | HLTF | GRCh38.p7 | 3:149040078 | TTTTCTCACTGTCAC[A/C/G]TGCTAATTCTTCTGG | 6596 |
| rs372248167 | snp | C/T | 4.9675e-05 | 0.00498348 | missense | HLTF | GRCh38.p7 | 3:149050294 | GTTTTGAAAGTAAGG[C/T]CGGTTCTCTAATACG | 6596 |
| rs372275635 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073532 | GATTCTGTCTCTACA[A/T]AAAATACAAAAATTA | 6596 |
| rs372334720 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149063251 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 6596 |
| rs372403608 | snp | A/T | 1.68035e-05 | 0.00289853 | intron-variant | HLTF | GRCh38.p7 | 3:149059833 | AACAAAGAATCTTAA[A/T]TTTTTTTCAAATTAT | 6596 |
| rs372410832 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149046810 | GTTCCACAATCTTTA[C/G]ATTTCTTTCTCAGTA | 6596 |
| rs372432234 | snp | C/T | 3.42789e-05 | 0.00413984 | missense | HLTF | GRCh38.p7 | 3:149048998 | ATGGACTATCTCCTT[C/T]AGTCTGAAATAAATG | 6596 |
| rs372453274 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057157 | AATGGGCCAGGCATG[G/T]TGGCTCATGCCTGTA | 6596 |
| rs372645862 | in-del | -/TTTTTTGTTTT/TTTTTTTTTTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149036297 | ATTAAAACTATGAGG[-/TTTTTTGTTTT/TTTTTTTTTTT]TTTTTTTTTTGAGAT | 6596 |
| rs372661850 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | HLTF | GRCh38.p7 | 3:149071456 | AGCCTATAAATAAAA[A/T]GTCATAAAGCGAAAT | 6596 |
| rs372744307 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045574 | TCCCACTCTCTCTAA[G/T]TCCTATCAAACCTGC | 6596 |
| rs372751079 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087585 | TTTTTCTTTTTTTTG[-/TTT]TTTTTTCTTTTTTAT | 6596 |
| rs372765693 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149055144 | AAAATTTCTTCAATT[A/C]AGCAAACATAATCCA | 6596 |
| rs372798587 | snp | A/G | 0.000113928 | 0.00754658 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086338 | AACATCCAGGACATG[A/G]CGCTGAGTGGGATGA | 6596 |
| rs372819037 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149052612 | AGTTTCTGTAGTGAG[G/T]GGAAGCAAAAACCAG | 6596 |
| rs372830148 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HLTF | GRCh38.p7 | 3:149080407 | GCTTCAAACCTCTCC[C/T]AGCATGTCTACTGAC | 6596 |
| rs372885074 | snp | A/G | 5.25104e-05 | 0.00512372 | intron-variant | HLTF | GRCh38.p7 | 3:149050194 | ATATTTCTTACATTC[A/G]ATCTTTAAAAGATCT | 6596 |
| rs372909267 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067672 | TATGCCCAGCCTTTA[A/T]AACAATGTTGAGGGA | 6596 |
| rs372936393 | snp | A/C | 5.15238e-05 | 0.00507536 | intron-variant | HLTF | GRCh38.p7 | 3:149048174 | AGTACCTAGAAATAA[A/C]AGGAAACTGTTATAA | 6596 |
| rs372942090 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149036028 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 6596 |
| rs372946042 | snp | A/C | 1.64944e-05 | 0.00287175 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084728 | TGACCTCTCAAACTT[A/C]CAAATAAAACGGAAT | 6596 |
| rs373003496 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070542 | AAGCAAAAGCTCTTT[C/G]AAATCAGTAATTTTT | 6596 |
| rs373026916 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053511 | TGTGGCCTCACCAGA[A/G]GCAGATGCCAGCACG | 6596 |
| rs373244543 | snp | A/G | 5.57336e-05 | 0.00527861 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086370 | AAGAGGAGCGCCTCG[A/G]CTCCCCTGGATCGTT | 6596 |
| rs373300038 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149065656 | CCAACACAGCAAAAC[A/C]CTGTCTCTACTAAAT | 6596 |
| rs373371361 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082184 | ACTTGTGTGGCCGGG[C/T]GCAGTGGCTCACACC | 6596 |
| rs373389596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060029 | ATGGTAAGACTTGAG[A/G]AGAAGAAATGAAAGT | 6596 |
| rs373399276 | snp | A/G | 0.000122621 | 0.00782914 | intron-variant | HLTF | GRCh38.p7 | 3:149041449 | AAAGACAGGTACACT[A/G]CTCTATCAAACACTG | 6596 |
| rs373405860 | snp | A/G | 0.000153988 | 0.00877328 | missense | HLTF | GRCh38.p7 | 3:149060847 | TCTATGTACTGGACA[A/G]CAGTTTTTCTTCTAA | 6596 |
| rs373407601 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | HLTF | GRCh38.p7 | 3:149074322 | AGAGGCATGGTAAAA[A/G]CATTGTTTGCACCAA | 6596 |
| rs373470873 | snp | A/T | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029823 | GTACAATGATTGATT[A/T]AGAGTGCTATCTGTG | 6596 |
| rs373474753 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048754 | ATTTATATGATTAAT[C/T]TTGGGGCAGAATTTA | 6596 |
| rs373502586 | snp | C/T | 3.83796e-05 | 0.00438045 | intron-variant | HLTF | GRCh38.p7 | 3:149049035 | ATGAATTAAAAAACA[C/T]AGGAAAGTAAAATAG | 6596 |
| rs373509596 | snp | A/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030938 | TTCTATCAAATGACT[A/T]CCAACACTCTTAAGT | 6596 |
| rs373510868 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075332 | GGCGGGCAGATCACC[C/T]GAGGTCAGGAGTTCG | 6596 |
| rs373511315 | snp | C/T | 0.000153988 | 0.00877328 | missense | HLTF | GRCh38.p7 | 3:149075989 | TTTACTTTAATTGCA[C/T]TCTTATCATAAGGGT | 6596 |
| rs373623847 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149050146 | AAAAAAAGTATAAAG[A/C]CTGAATTTTGGAACA | 6596 |
| rs373688591 | snp | C/G/T | 0.000214418 | 0.0103524 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032169 | TCTGTATTTTTCTCA[C/G/T]TTCTAAAACTTAAGT | 6596 |
| rs373696155 | snp | C/T | 5.45301e-05 | 0.00522131 | intron-variant | HLTF | GRCh38.p7 | 3:149071248 | TAAAGAAAAAAATAA[C/T]TACCAAACCCATATC | 6596 |
| rs373736550 | snp | A/C | 0.000132334 | 0.00813324 | intron-variant | HLTF | GRCh38.p7 | 3:149055426 | GAACCACTGATAGAA[A/C]CTTTAGCTGTTTTTC | 6596 |
| rs373807149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149060071 | TATGCAAAGTAATTC[A/G]GCTCTCAGGTGGAAG | 6596 |
| rs373813481 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149061410 | AGCGACACTCCATCT[A/C]AAAAAAATAAAATAA | 6596 |
| rs373823328 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149039503 | GCAAAACAAATTAAG[-/T]TTTTTTTTTTTGCTA | 6596 |
| rs373853705 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149057606 | AAATACTGAGGGATG[A/G]CTGTACTGTAATAAA | 6596 |
| rs373859449 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082783 | CAACAAGGAAATTAT[A/G]AGTCCAATATAGATG | 6596 |
| rs373873572 | snp | C/T | 6.70399e-05 | 0.00578925 | intron-variant | HLTF | GRCh38.p7 | 3:149059707 | ACTAGAAAACAAGGA[C/T]ATTTACTGACCCTTT | 6596 |
| rs373873604 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149059268 | GTTCAATCTCTTCCC[A/T]TCTCAAATATTTAGT | 6596 |
| rs373985413 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | HLTF | GRCh38.p7 | 3:149055327 | GCTTAACACAGAAAG[C/T]GGACAGATGATCAGT | 6596 |
| rs373997005 | snp | A/G | 3.92927e-05 | 0.00443225 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039211 | ACCATCCAAACGAGT[A/G]AACACAAATCCAGAG | 6596 |
| rs374007638 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084812 | TCAAAACGTGGAAAG[A/G]AAGTTGGATATGAGA | 6596 |
| rs374012927 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149064343 | TATCTTTAGAAATAA[A/G]CTTTATGAGGGTCAT | 6596 |
| rs374063988 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079587 | GAGCAAAGGTTTTTT[-/T]GGGGTTTTCTTTGTT | 6596 |
| rs374096846 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082898 | AAACAAGTGTAGAAG[A/G]TAAGTTATGGTTCTG | 6596 |
| rs374156872 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041520 | GACTTGGCAAATACA[C/G]GGTTTACAAAATACA | 6596 |
| rs374188045 | snp | A/G | 1.68653e-05 | 0.00290385 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071441 | CAGTGGTGTTTCAAT[A/G]GCCTATAAATAAAAA | 6596 |
| rs374498620 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038273 | CCAGTGCCTATAAAA[A/G]CTGACGCAAAGCAGG | 6596 |
| rs374500727 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061559 | ATTGGCTCGTGGCCA[C/G]GCACGGTGGCTCATG | 6596 |
| rs374502917 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149039023 | AGAAGTACTAAGATT[C/G]TGAAAAAATTTACAG | 6596 |
| rs374512437 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149047541 | CAGCTACTTGGGAGG[A/C]TGAGACAGGAGAATC | 6596 |
| rs374569601 | in-del | -/AGA | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073860 | TTTTCATTCGCTATC[-/AGA]AGATTATTTTTGCCT | 6596 |
| rs374583115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149043841 | CTCAGTTCTAACAGT[A/G]GCATTGTAAAAGTAC | 6596 |
| rs374590360 | snp | A/G | | | stop-gained | HLTF | GRCh38.p7 | 3:149041492 | GCAAAAAACTAACCT[A/G]CTCATTCTGAATGAC | 6596 |
| rs374609722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149032912 | AGCTTGCAGTAAGCC[A/G]ACATTGCGCCACTGC | 6596 |
| rs374634358 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054221 | GGAATTAGTAAGTAA[A/G]AGCACAAAGTAGAAA | 6596 |
| rs374678894 | snp | C/G | 1.65622e-05 | 0.00287764 | missense | HLTF | GRCh38.p7 | 3:149050288 | TATCCTGTTTTGAAA[C/G]TAAGGCCGGTTCTCT | 6596 |
| rs374686211 | snp | A/G | 3.50036e-05 | 0.00418337 | intron-variant | HLTF | GRCh38.p7 | 3:149050195 | TATTTCTTACATTCA[A/G]TCTTTAAAAGATCTG | 6596 |
| rs374765283 | snp | A/C | 0.000173974 | 0.00932505 | intron-variant | HLTF | GRCh38.p7 | 3:149039546 | TGATTATATAAAATC[A/C]TTTTACTGAAAGTGA | 6596 |
| rs374794722 | snp | A/T | | | missense | HLTF | GRCh38.p7 | 3:149074258 | ATGTTTCTTCAACTG[A/T]TCTGAAACCGCTTTT | 6596 |
| rs374815591 | snp | C/G/T | 0.000188175 | 0.0096982 | intron-variant | HLTF | GRCh38.p7 | 3:149039704 | TTAATCTGCAAAAAA[C/G/T]ATTAAGATGTCCATT | 6596 |
| rs374837360 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149048635 | CTACTCCATTTCCAA[C/G]GTTCAAGAATAAGTC | 6596 |
| rs374876594 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149056698 | GTGCAGTAAGAGATT[C/T]GTAACAACAAAGAAT | 6596 |
| rs374881413 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | HLTF | GRCh38.p7 | 3:149035298 | TTTCATTTTTAAAAG[A/T]ATCTATGTGTGCTTA | 6596 |
| rs374883330 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051055 | ATGATGAAGTCCTAA[A/G]CCAGCAAGGTAGAAG | 6596 |
| rs374888571 | snp | G/T | 1.65685e-05 | 0.00287819 | intron-variant | HLTF | GRCh38.p7 | 3:149042120 | ATCACTCTTATTTAA[G/T]TATCTCTGACAAATA | 6596 |
| rs374917288 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149080955 | GTTGTTCCACAAGAT[C/T]ATAATGGGGCTGCCC | 6596 |
| rs374923316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149080875 | ATGAGAATTAATCAT[A/G]ACAGTATAGTCATAC | 6596 |
| rs374957345 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149040293 | TTTAATGGATTTCAT[A/C]CATTTAAGAGACATC | 6596 |
| rs375040421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149063306 | ACCTCATGATCCGCC[C/T]GCCTCGGCCTCCCAA | 6596 |
| rs375097234 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149077241 | GACAGAGCGAGACTT[A/C]ATCTCAAAATAAATA | 6596 |
| rs375154890 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031909 | CCTTATTTGAAATAC[A/G]AAAAAGCTGAGTACT | 6596 |
| rs375216462 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149054213 | TGAATTAAGGAATTA[C/G]TAAGTAAAAGCACAA | 6596 |
| rs375241005 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070999 | GCAGTGAGCCAAGAT[C/T]GCGTCACTGCACTCC | 6596 |
| rs375275554 | snp | A/G | 8.75572e-05 | 0.00661596 | intron-variant | HLTF | GRCh38.p7 | 3:149055273 | TAAAATATAAATTAT[A/G]TTACATTTTTAAAGG | 6596 |
| rs375281125 | in-del | -/TG | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032156 | TCATTTCTAAAACTC[-/TG]TATTTTTCTCATTTC | 6596 |
| rs375282981 | in-del | -/A | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029717 | AAAACAAAGCACACA[-/A]CTGCCGAAGATCATT | 6596 |
| rs375291700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073919 | GTCAGGGGTTTCCAG[A/G]TGTTACCATTAGGGA | 6596 |
| rs375449441 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149037467 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 6596 |
| rs375452014 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037865 | GCCAAACAGCCCCTT[-/T]GTACACGTAGAAAAA | 6596 |
| rs375503267 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149084139 | ACAAGTATGAAAATA[A/T]AAAAACTTAGGAAAT | 6596 |
| rs375559128 | snp | A/C | 0.00034862 | 0.013198 | intron-variant | HLTF | GRCh38.p7 | 3:149073220 | AAAATAAAAGAGAAG[A/C]ACACCTGTTCAGTTG | 6596 |
| rs375590675 | in-del | -/ATAAG | | | intron-variant | HLTF | GRCh38.p7 | 3:149082898 | AAACAAGTGTAGAAG[-/ATAAG]TTATGGTTCTGGATG | 6596 |
| rs375619984 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149056105 | CCAATGTTCAGATGA[C/G]GGCGGCCCCTGAAGA | 6596 |
| rs375620558 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084978 | CATGCTTTACTTCAG[C/T]AAATGAAATCTTACA | 6596 |
| rs375689071 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HLTF | GRCh38.p7 | 3:149055474 | TAAGGAGATGGCAAT[A/G]ATGTGCCTCCATGAA | 6596 |
| rs375712165 | snp | C/T | 1.67525e-05 | 0.00289413 | intron-variant | HLTF | GRCh38.p7 | 3:149048818 | ACTTACATAATGATA[C/T]ATTTTAGAGATTTAA | 6596 |
| rs375734180 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062814 | TCTAAAATCTCAAAA[A/T]AAAGCAAAAATCCCA | 6596 |
| rs375760082 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149051156 | ATGAAATATGAAATA[C/T]GAATAATAATAATAA | 6596 |
| rs375819372 | in-del | -/CTTTTGGTAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149052212 | AGCACATGTGTCAGA[-/CTTTTGGTAA]TTTTTGAATCTTGAT | 6596 |
| rs375929269 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087618 | TGAGATGGAGTCTTG[C/T]TCTGTCCCCCAGGCT | 6596 |
| rs375970563 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149041048 | CTTGAAATGTGGCTA[A/G]GCCAAATTGAGGTGT | 6596 |
| rs376018792 | snp | C/T | 5.06633e-05 | 0.0050328 | intron-variant | HLTF | GRCh38.p7 | 3:149034898 | AACCTAGTCTTAAAA[C/T]AGTTTGTTTAAAAAC | 6596 |
| rs376099936 | snp | A/G | 0.000115413 | 0.00759562 | intron-variant | HLTF | GRCh38.p7 | 3:149060696 | AGTTTGCCTAAAAAT[A/G]AAACAAAAATAAACA | 6596 |
| rs376167663 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051340 | TACCTAACTGAAGAC[A/G]TATACTAGGAAAATG | 6596 |
| rs376175005 | snp | C/T | 4.2594e-05 | 0.00461467 | intron-variant | HLTF | GRCh38.p7 | 3:149049048 | CACAGGAAAGTAAAA[C/T]AGTACTTAATATGAT | 6596 |
| rs376261471 | snp | C/T | 4.95626e-05 | 0.00497784 | intron-variant | HLTF | GRCh38.p7 | 3:149064876 | ATATTCCTGGGTAAA[C/T]AGGCATATTTCTTAA | 6596 |
| rs376263937 | snp | A/C | 3.34986e-05 | 0.00409245 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048030 | TGAAAGTACTTACCT[A/C]AGTCCTCCTTCATCT | 6596 |
| rs376385570 | in-del | -/CTTA | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030424 | TGCCAAACTTACTTA[-/CTTA]TGAGTGTGTTTTAAA | 6596 |
| rs376394865 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149074666 | GTAGAGTTTGGCTAA[C/T]GGAACCACTGAGGGT | 6596 |
| rs376459436 | in-del | -/GATAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149068739 | AAAATTTGACTTAAA[-/GATAA]TACCAAGCTTAAAAG | 6596 |
| rs376542154 | snp | A/C | 1.64972e-05 | 0.00287199 | missense | HLTF | GRCh38.p7 | 3:149075927 | TATAGGCCAAAGCAC[A/C]TGCAAGCTCTTTCTT | 6596 |
| rs376548302 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031539 | CTCAGACACAGCAAG[C/T]TACATTTAAACAATG | 6596 |
| rs376569882 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149074130 | TGAGCACAAATTAGC[C/T]AACAAACTCCAAGAG | 6596 |
| rs376602779 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079846 | TCCACTCACCTTGGC[C/T]TCCCAAAGCGCTGGG | 6596 |
| rs376642217 | snp | A/C/T | 0.00676609 | 0.0577691 | intron-variant | HLTF | GRCh38.p7 | 3:149072971 | GATACAAAAATATGC[A/C/T]GTGCATAAACAGGAA | 6596 |
| rs376706640 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088519 | GCCTGAGCAACAGAG[C/T]GAGACTCCATCTCAA | 6596 |
| rs376746077 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057420 | GACAGAGTGAGACTC[C/T]GTCTCAAAACAAACA | 6596 |
| rs376818593 | snp | C/T | 0.000365006 | 0.0135044 | intron-variant | HLTF | GRCh38.p7 | 3:149040160 | TTTAGCATGTGGCTA[C/T]ATAAGAAAGAACGAA | 6596 |
| rs376827516 | snp | C/T | 0.000149015 | 0.00863049 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050295 | TTTTGAAAGTAAGGC[C/T]GGTTCTCTAATACGA | 6596 |
| rs376884709 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037902 | CCTATGTGAATGCAC[A/G]TCCAGGTCACACAGC | 6596 |
| rs377004804 | snp | A/G | 0.000174642 | 0.00934294 | missense | HLTF | GRCh38.p7 | 3:149046177 | ATACTTTACGTTCTG[A/G]TAACTCCAAAACAGG | 6596 |
| rs377015794 | snp | A/C/T | 0.00034122 | 0.0130581 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086361 | TGGGATGACAAGAGG[A/C/T]GCGCCTCGGCTCCCC | 6596 |
| rs377087341 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | HLTF | GRCh38.p7 | 3:149040206 | AACAGAAGAACAAAT[A/G]TAAATATGCCTAAAA | 6596 |
| rs377117817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149052672 | ATGAAATAAAGGCAA[A/G]AATGCAGAGAGGATA | 6596 |
| rs377123730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067390 | CTAAAAAGAATCATG[A/G]AAGTGATTATTCATC | 6596 |
| rs377199943 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063929 | TGTTCGGCTCCCCTA[C/T]CCATTTATCAGAATG | 6596 |
| rs377221291 | snp | A/T | 5.0336e-05 | 0.00501652 | intron-variant | HLTF | GRCh38.p7 | 3:149071563 | TGAGTAGTCTTAAAT[A/T]AAAAATATTGGTTCA | 6596 |
| rs377234012 | snp | C/G/T | 0.000277004 | 0.0117654 | intron-variant | HLTF | GRCh38.p7 | 3:149042323 | AAATATTATTAAGTC[C/G/T]GCTAAACAATAATAA | 6596 |
| rs377254385 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067183 | TTATATACATATATA[A/T]ATGTATATATATACA | 6596 |
| rs377373776 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084844 | GCGTGGAAAATTTCC[A/G]TGAACTCCATACTGG | 6596 |
| rs377392204 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HLTF | GRCh38.p7 | 3:149047634 | ACGACAGAGCAAGAC[C/T]CCATCTCAAATAAAT | 6596 |
| rs377423098 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149075626 | TTGGAGAAATGGAAT[A/G]TACTTCCTAATATTT | 6596 |
| rs377477594 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149082987 | CTGGGCGCGGTGGCT[A/C]ATGCCTGTAATCCCA | 6596 |
| rs377482213 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149059600 | GGTTATATACTTTAA[A/C]AAATAGTCTCTATTT | 6596 |
| rs377600214 | snp | C/T | 1.77212e-05 | 0.00297663 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032191 | AACTTAAGTATCCAA[C/T]CAAACTGACCTTACT | 6596 |
| rs377640663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149064373 | TTTAAGTAAAATCCA[C/T]AGATCTCTTTCCATT | 6596 |
| rs377667549 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037558 | GTATGATGACCCTAG[C/T]TATAATCTTACTGAG | 6596 |
| rs377670999 | snp | C/T | 6.88192e-05 | 0.00586557 | intron-variant | HLTF | GRCh38.p7 | 3:149032413 | GTAGTTTTTAAGGCA[C/T]AGTATTTAAAATCTT | 6596 |
| rs377676729 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057987 | CTCCTTGGTAATTGG[C/T]GCTCCCATCAACAAT | 6596 |
| rs386398206 | in-del | -/AA | | | intron-variant | HLTF | GRCh38.p7 | 3:149083760 | ATACAAAAAAAAAAA[-/AA]ATACAAAAATTAGCT | 6596 |
| rs386666936 | multinucleotide-polymorphism | CA/TG | | | intron-variant | HLTF | GRCh38.p7 | 3:149077204 | AGTGAGCCAAGATAG[CA/TG]CCCCTGCACTCCAGC | 6596 |
| rs386666937 | multinucleotide-polymorphism | AAT/GAC | | | intron-variant | HLTF | GRCh38.p7 | 3:149078936 | GTCTAAAAGCATGGA[AAT/GAC]GATGTCTCACCAAAC | 6596 |
| rs397723758 | in-del | -/C | 0 | 0 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087735 | GGGATTGCAGGAGCC[-/C]GCCACCACGCCCAGC | 6596 |
| rs397770416 | in-del | -/A | 0 | 0 | intron-variant | HLTF | GRCh38.p7 | 3:149069487 | AAAAAAAAAAAAAAA[-/A]GAAGAAGAATGTTCT | 6596 |
| rs397826036 | in-del | -/A | 0 | 0 | intron-variant | HLTF | GRCh38.p7 | 3:149051250 | TAAAAAAAAAAAAAA[-/A]GAAGGGAAAAGTGGG | 6596 |
| rs397874683 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149078871 | CAAAAAAAAAAAAAA[-/A]TAAGTTCAAAGACCT | 6596 |
| rs398106571 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149040445 | AGTTTAAAAAAAAAA[-/A]TCTATGAATAACAAT | 6596 |
| rs398106572 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149069168 | CAGTTAAAAAAAAAA[-/A]GTTTTCCTTAAGAAT | 6596 |
| rs527255477 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087055 | GAGACACAACGAGTT[C/T]GGAAAATCTTAAATG | 6596 |
| rs527281743 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149035576 | GGCAGGAGAATGGCC[G/T]GAACCCCGGGAGGCG | 6596 |
| rs527292738 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149078905 | GCAAATCATTTCTTT[C/T]GACATGAAAACGCAT | 6596 |
| rs527309757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149036233 | GACCCCTGGTAAGTG[A/G]TTTTTAAATAGTATC | 6596 |
| rs527352579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042497 | GGCTGCCAATTGCAG[A/T]CTAAGTCAGATAGGA | 6596 |
| rs527397954 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149042998 | GGGACACATGGCAGT[C/G]AAAGAAAACTCAGCA | 6596 |
| rs527512422 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149069471 | GAAACTCCATCTCAA[-/G]GAAAAAAAAAAAAAA | 6596 |
| rs527570919 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149073069 | ATAAAATGTTAACAT[A/T]TATATATTCTATTTA | 6596 |
| rs527575398 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061602 | GCACTTTGGGAGGCG[A/G]AGGTGGGCAGATCAC | 6596 |
| rs527608752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073566 | GAGCGTGATGGTGTG[C/T]GCCTGTAGTCCCAGC | 6596 |
| rs527655369 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HLTF | GRCh38.p7 | 3:149057047 | CCCAGGGGGCGGAGC[C/T]TGCAGTGAGCCGAGA | 6596 |
| rs527690470 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149052819 | TGGGTGGCCTTGAAA[C/T]GGGACAGTGCATTAT | 6596 |
| rs527772857 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082117 | TACATACTGTAGAAT[G/T]CAATGTATATGAAGT | 6596 |
| rs527811545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078260 | TTTTAAATATGTTCA[A/T]AGGGGCTGGGCATGG | 6596 |
| rs527812739 | snp | C/T | 8.25048e-05 | 0.00642228 | missense | HLTF | GRCh38.p7 | 3:149071346 | TAGTATAAGTCATTT[C/T]GCTGTTCCCAGAATG | 6596 |
| rs527872973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149058079 | CTGAAAATATGAAGG[A/G]TAAGAGCATCCCCCT | 6596 |
| rs527936981 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149043719 | AATATAGCCTAACGG[-/C]TAAGAGTACAAATTT | 6596 |
| rs528027820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057375 | AGGTTGCAGTGCGCC[A/G]TGATCGCACCACTGC | 6596 |
| rs528229003 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149067462 | CTATATCGTTTAACT[G/T]TTCCCTTGTCAAAAG | 6596 |
| rs528235381 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077809 | GTCAGGGGCCTTAGA[C/G]TGTTGAAGGAATGCC | 6596 |
| rs528349239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061193 | TCCCGCCTTAGCCTC[C/G]GGAGTACCTAGGACT | 6596 |
| rs528359251 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072040 | CCTGGGCAAGAAAGT[A/G]AGACCCTGTCCCAAA | 6596 |
| rs528479276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149051696 | CGAAACCCTGCCTCT[A/G]CTAAAAATACAAAAA | 6596 |
| rs528537787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058877 | AGTGGTTTCTAATGT[A/G]TAATTTAATTCTATC | 6596 |
| rs528547020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066321 | AAAGTGCTGGGATTA[C/T]AGGAATGAGTCACTA | 6596 |
| rs528566304 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042803 | CTGTTTATGTGTACT[A/G]ATAAAACCTAAAGTA | 6596 |
| rs528627139 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149083116 | ATTAGCTGGGCATGA[-/T]GGCGCATGCCTGTAA | 6596 |
| rs528635632 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149059597 | ATGGGTTATATACTT[G/T]AAAAAATAGTCTCTA | 6596 |
| rs528643468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149080711 | CAATTAGTTAACTGT[C/T]GTTACAAATAAGTAA | 6596 |
| rs528681238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149037785 | CAGAAACAGCAGAGG[A/G]TTGCCTTTAGCCCAC | 6596 |
| rs528689206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149081814 | CTTGGAAAGAGTAAC[A/T]AGAACCAAGGCATAA | 6596 |
| rs528717780 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029617 | TTATATTTTTAATGA[A/C]TCTCATCCAAATGCT | 6596 |
| rs528724528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149082350 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 6596 |
| rs528761408 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055544 | TTTAACAGGGAATAA[A/G]TTTTACCTCATCACT | 6596 |
| rs528761659 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087917 | AAGACACATTTGTTC[A/C]TTATCGTAAATAAAC | 6596 |
| rs528806064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045054 | TGTCATAAAAAGTAA[A/G]AGCCAAAGTCCTTGA | 6596 |
| rs528894826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066749 | GTCTTATGTGCTTCT[A/G]TCAAATCTGGTAACC | 6596 |
| rs529017081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074563 | GAGTGCCAGAAAAAA[A/T]TGAGAAAATGGAATA | 6596 |
| rs529137529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067449 | GTAAGTTTTATGGCT[A/G]TATCGTTTAACTGTT | 6596 |
| rs529189283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149060570 | AACATTCCAACCTAG[C/T]GAGATACAAATCAAT | 6596 |
| rs529257972 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031300 | TTTAAGAGTTGAAAC[A/G]ACTTTGGAGATCATC | 6596 |
| rs529281506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058773 | TTCTCTTTCAAAGAT[A/G]TACTTAGTTTGGTTA | 6596 |
| rs529347997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073554 | CAAAAATTAGCAGAG[C/T]GTGATGGTGTGCGCC | 6596 |
| rs529402173 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061272 | ATTTGATAGCCGGGC[A/G]TGGTGGTGGGTGCCT | 6596 |
| rs529428264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065647 | CTAGCCTGGCCAACA[C/G]AGCAAAACCCTGTCT | 6596 |
| rs529440176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149036536 | TCATGATCCGCCCAC[A/C]TCGGCCTCCCACAAA | 6596 |
| rs529448507 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149058310 | GAACTCATGGGCCTC[C/G]GCCTCCCAAAGTGCT | 6596 |
| rs529474150 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087434 | GCTGGCCTTTTAATC[C/G]CACAGGGCAGGAAGC | 6596 |
| rs529520758 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087830 | GACCTCAGGTGATCC[A/G]CCCGCCTCGGCCTCC | 6596 |
| rs529618580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051648 | GGTGGATCACTTGAG[A/G]TCAGGAGTTCGAGAC | 6596 |
| rs529622057 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043609 | TATACAAAATACAGT[A/G]GTACAATGACAACAT | 6596 |
| rs529662483 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078423 | GGTATGGTGGTACAT[A/G]CCTGTAGTCCCAGCT | 6596 |
| rs529680703 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080509 | CTATGAGGCAGAGCT[A/G]TGTTCTCTCCCAGTC | 6596 |
| rs529690965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149055711 | GTTTTCTGAATTTGT[A/G]TTATATTTAATTTGG | 6596 |
| rs529705789 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149070074 | ATGAGCAAGATACAC[A/T]AATAGATTTTAACAA | 6596 |
| rs529744705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062125 | CATAAGAAAAATAGA[A/C]ATAAAAATATAATCC | 6596 |
| rs529789629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062817 | AAAATCTCAAAAAAA[A/G]GCAAAAATCCCAAGA | 6596 |
| rs529855153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054999 | TCAATCTGTAAATGT[A/G]GAGGAGTCAAACTAT | 6596 |
| rs529868358 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088404 | CAGACGTGGTGGCAC[A/G]CACCTGTAGTCCTAG | 6596 |
| rs529880001 | snp | C/T | 5.51577e-05 | 0.00525127 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084648 | TTAACGCCAGAAATA[C/T]AATCAAAATTTAATT | 6596 |
| rs529889615 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HLTF | GRCh38.p7 | 3:149032734 | TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT | 6596 |
| rs529920422 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058302 | CTGATCTTGAACTCA[C/T]GGGCCTCGGCCTCCC | 6596 |
| rs529957234 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085880 | GCGATGCGTTTTCCT[C/T]GCAAGTGGCGCATAT | 6596 |
| rs530034459 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149035276 | GATTAATCAATTTGG[-/T]TTTTTTTTTCATTTT | 6596 |
| rs530036922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082636 | TAGGATCATACATTT[A/G]AAATATGTACATTTT | 6596 |
| rs530098402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053557 | CCTGCAGTATCATGA[A/G]CCAATTAAAACTCTT | 6596 |
| rs530128394 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078787 | ATGTGAACCTGGGAG[A/G]CAGAGCTTGCAGTGA | 6596 |
| rs530147156 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030681 | GCTCCTAATGCTAGC[A/C/G]GGCTAATCCCACATT | 6596 |
| rs530317570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075764 | ATTTAACACGTACCA[A/G]AAGTACAGTGATAGA | 6596 |
| rs530321985 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085382 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 6596 |
| rs530326412 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149052273 | AAATTTTTTAAAATA[A/C]TCTTTTTAAAAAATT | 6596 |
| rs530342206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069394 | GAGAATCACTTGAAC[C/T]TGGGAGGCGGAGGGT | 6596 |
| rs530352857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149076379 | TGAGCGCTTACTATG[C/T]GCCAAGCATTGGTCT | 6596 |
| rs530435201 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031822 | CACTGCATCACAAAT[C/T]GGAGGCTTTGGTAAA | 6596 |
| rs530480281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076317 | AGCAAATTCAAATTA[C/T]CTAAAATTTTCAACA | 6596 |
| rs530498875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062083 | ATTTTAAGTAAATTA[C/T]CTAATATTCTTCAAT | 6596 |
| rs530518486 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149042019 | AAAAAAATTATTGGA[C/T]GTATTCCTAGCTGAG | 6596 |
| rs530609093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149039473 | GAATATCTTTCAGAT[A/C]AAATGACTAAAACTG | 6596 |
| rs530609517 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149047876 | TTCCAAACAAGCATC[A/T]CTAGGTTCTGAAAGA | 6596 |
| rs530718960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055622 | CTATGACAGAGAGTA[A/G]GTCACAAGGAGGAAG | 6596 |
| rs530839339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047102 | CTCTTCTCTATTTCA[C/T]TGTCTTTTTAAATGC | 6596 |
| rs530876205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051753 | TGCGCACCTATAATT[C/T]CAGCTACTCGGGAGG | 6596 |
| rs530945099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149038351 | CAGTTAATATTTATT[A/G]TAGAAGAAAAGTAGA | 6596 |
| rs531080539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149052570 | TTGTACATGGCAATA[C/T]TGAAGTCTGAAGATC | 6596 |
| rs531155833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075587 | TAAACACTTCCAAAT[G/T]CCTAAACCTAGGTAC | 6596 |
| rs531200850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042347 | ATAATAACTTCCTAT[C/T]CTAAAACAGCAGAGT | 6596 |
| rs531202075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037840 | CTGAATTAGTCCAAG[C/G]TCCTCTCAGGCCAAA | 6596 |
| rs531215772 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086394 | GATCGTTTTCGAGCC[G/T]CCTCGATACGCCTCC | 6596 |
| rs531220204 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053995 | CTTCTGGTCCTAAGA[C/G]GAAAAATGATACACT | 6596 |
| rs531241282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149038436 | CCTATTACTAACTGT[A/G]TGATACTGGGCACAT | 6596 |
| rs531243352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085639 | ATCACTGTAACTCCC[C/T]GCGAGCAGAACACCT | 6596 |
| rs531313492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049978 | GCCTGGGCAACAAGA[A/G]CAAAACTCCATCGAG | 6596 |
| rs531366467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042901 | ACCTTTCCCTTTTGT[A/G]TATCTGGACTAGCAA | 6596 |
| rs531405087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049150 | TAATTATTGAATACT[C/T]ACAAGTTTATAAAAT | 6596 |
| rs531411913 | in-del | -/ATAAAATAAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149061437 | ATAAAATAAAATAAA[-/ATAAAATAAA]TTTGAAAAACTAAGT | 6596 |
| rs531430043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149072972 | ATACAAAAATATGCC[A/G]TGCATAAACAGGAAC | 6596 |
| rs531501719 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086990 | ATTCCCTGTGGTGAA[C/G]CGTGGGGACTTTCGC | 6596 |
| rs531535037 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149078850 | CGACAAAGCAAGACT[A/C]CGTCTCAAAAAAAAA | 6596 |
| rs531547162 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149035530 | GGGAGAGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 6596 |
| rs531549392 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | HLTF | GRCh38.p7 | 3:149035780 | CTTTAAAGCTGAGCT[-/A]AAAAAAAGTACCATT | 6596 |
| rs531629837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149077505 | GTTTGTCAAAACAAT[G/T]TTACAGGAAAGTGTT | 6596 |
| rs531673362 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065137 | GAAAGCAAATCTCAA[G/T]TATAAATGACACATT | 6596 |
| rs531680825 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057668 | CAAAATACCTTATTG[C/T]ATATAATATTTTAGA | 6596 |
| rs531706662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032689 | CCATTCTGGCCGGGC[A/G]CGGTGGCTCACACCT | 6596 |
| rs531738278 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085017 | ACGGTAAAGATTAAT[A/G]GTTACTCTCGTTAAA | 6596 |
| rs531747372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149070644 | AATACTCTGCATAAC[A/C]CAATATTTGTGATGG | 6596 |
| rs531769896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056655 | TTTCCCTATATATAC[C/G]TACAATAAAGTTTAA | 6596 |
| rs531840846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084535 | GTGGGAGGGTCACTT[A/G]AGGTATTTGTTATTT | 6596 |
| rs531867697 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149077120 | GGGTGTGGTGGCACG[C/T]GCCTGTAGTCCTAGC | 6596 |
| rs532066005 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149059496 | AGGAGTAAGGGCCCC[C/T]ATCACATTTTGGCCC | 6596 |
| rs532126777 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048936 | ATTTGGATTTCGTAT[A/G]GCATGTCCTTCATCC | 6596 |
| rs532144366 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149045116 | TCTCTGATATCATGA[A/C]TATTTTCTCTCGTTC | 6596 |
| rs532165142 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149032458 | ATGAAAGATTTGCCT[-/A]AATGGCAAAAACCGC | 6596 |
| rs532174483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086266 | TCAGGTTCATTTGGG[A/G]ACGCCTCCAGGCCGT | 6596 |
| rs532189577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149055781 | ATATTCACAATCTTG[A/T]GTAATCTCCTCCCAT | 6596 |
| rs532212101 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149078363 | CCAGCCTGGGAAACA[C/T]AGCAAGACCCCATTT | 6596 |
| rs532289897 | snp | A/G | 0 | 0 | intron-variant | HLTF | GRCh38.p7 | 3:149048251 | GAGAAGACAACAATT[A/G]AAAATGGGCACTCTG | 6596 |
| rs532360841 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082355 | TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA | 6596 |
| rs532376425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076444 | ACAGCTCTATTGGGA[A/G]GTACTATCATTATTC | 6596 |
| rs532404846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084376 | GAAGATTCCACAAAA[C/T]GATCTCCTTTTTGCA | 6596 |
| rs532506217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149083294 | ACATGCATTAATTAT[A/G]AAATAAATGATATCT | 6596 |
| rs532662181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069511 | ATGTTCTTGACGAAG[C/G]AGTACACATTAATTT | 6596 |
| rs532756156 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149049069 | TTAATATGATTTGCT[A/G]ACTAGTTGTTATCAT | 6596 |
| rs532762092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062879 | AAAAGTAGTAGAAAG[A/G]TGAGTGATTATTAAA | 6596 |
| rs532809844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073726 | ATAAATAAATAAAAC[G/T]TGCATAACAAACTGC | 6596 |
| rs532843787 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149078713 | ATACAAAAAATTAGC[C/T]GGGCGAGGTGGCGGG | 6596 |
| rs532875279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149036391 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 6596 |
| rs532894447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149052398 | CTGGGATCCAAAGAA[C/T]ATAAAAGTTTCAAGA | 6596 |
| rs532963635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149080292 | TTGCACAACCTTGTG[A/G]GTATTCTAAAAACTA | 6596 |
| rs532979524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067377 | TGTCATTTTTTAACT[A/G]AAAAGAATCATGAAA | 6596 |
| rs533101503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066424 | TAAACTTTTTATCAA[A/G]TCCAAGCTGGATGAA | 6596 |
| rs533210260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074438 | TTTTAAGTGTATCAT[A/T]TACATTTTACATTGA | 6596 |
| rs533333123 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149043094 | CAATAAAACAATTCC[C/T]CCAAAAAAAAAAAAT | 6596 |
| rs533335765 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149035212 | TACTACTTCTAATAC[A/C]TAATACAGGCCCCGA | 6596 |
| rs533416071 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HLTF | GRCh38.p7 | 3:149058224 | CTACAGGCATGTGCT[A/G]CCATGCCTGGCTAAT | 6596 |
| rs533447528 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149035318 | ATGTGTGCTTAACAG[C/T]AGAAAAAGGTTATAC | 6596 |
| rs533447876 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086541 | AACAATCTGGGAGAC[C/G]AGCGTCGCTCTGTGA | 6596 |
| rs533460015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078774 | ACACAGGAGAATGAT[A/G]TGAACCTGGGAGGCA | 6596 |
| rs533495804 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149072830 | TCATCCTAAATTACA[A/C]ATTAGACAATGTGAA | 6596 |
| rs533497602 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149064248 | TATTTCTTTCCTGTT[A/C]CAAACTTAAGTAATA | 6596 |
| rs533501430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050444 | ATAGATGTATAAAAA[A/C]GTAACTGCCCTGGCA | 6596 |
| rs533552725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051134 | GACTGATAGGACTTG[C/G]GGACTAATGAAATAT | 6596 |
| rs533620909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149077983 | CACTAACAAACACAC[A/G]CTAATTACAAAACTC | 6596 |
| rs533727392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058736 | TTCTGTCTCCATTCA[C/T]AGAGTTTTGTTTCTA | 6596 |
| rs533825124 | in-del | -/GAGGT | | | intron-variant | HLTF | GRCh38.p7 | 3:149083018 | GCACTTTGGAAGGCC[-/GAGGT]GAGTGGATCACCTGA | 6596 |
| rs533866025 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086470 | GGATCAGGAGCGCAC[A/G]ACTGAAAGGTAAGTC | 6596 |
| rs533885197 | in-del | -/TG | 0.00795532 | 0.062565 | intron-variant | HLTF | GRCh38.p7 | 3:149037421 | GCAGTGAGCCAAGAT[-/TG]TGTGCCACCACACTC | 6596 |
| rs533955609 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085885 | GCGTTTTCCTTGCAA[A/G]TGGCGCATATCTCTA | 6596 |
| rs533955813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055885 | ACAAAAGAAGTTTCC[A/G]TATTGGGTGTGCAAG | 6596 |
| rs534015805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058391 | GCATCTCCCCAATAA[C/T]TCTGAATCAGCATAT | 6596 |
| rs534026507 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149050079 | TTTCACGCAAAAAGT[A/C]AAAAAAAAAAACCAT | 6596 |
| rs534068003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063049 | AAGGGTCATGGTCAT[A/C]TCTATCTCTCTCTTT | 6596 |
| rs534107090 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149058679 | CTTTTGTGTCTTACT[A/G]AAGAGATCACTATCT | 6596 |
| rs534332068 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149047073 | ATGTATCATGCACTC[C/T]GATATTTACTAATCT | 6596 |
| rs534562339 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149044727 | TAAACAGCAATTCCA[G/T]CCTTCCACTTATGCA | 6596 |
| rs534598345 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088320 | TGGATCACCTGAGGT[C/T]AGGAGTTCGAGACCA | 6596 |
| rs534603605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033078 | CATTCCTGATAAAAA[C/T]TTGATTTTAAAATAC | 6596 |
| rs534659694 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149037585 | TGAGAAGGATACCGT[A/C]AGTTGAGGGAGGAAA | 6596 |
| rs534664102 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087164 | ATGTTTATTACAGCT[A/G]TGGGGGCGTTTGCCT | 6596 |
| rs534710575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066833 | GGTTGCTCAGGGTGA[A/G]GAATTGAACCTGAGA | 6596 |
| rs534725965 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149068510 | AAATGCTTTCCCCCA[C/T]TGCATTATTAGGGAA | 6596 |
| rs534749653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149059908 | ATATCATTTTCACCC[C/T]CTATTGTAAGAGCTT | 6596 |
| rs534802908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149038061 | TTTCTCAAATTGTGA[C/T]CCTAGACCACCTGTA | 6596 |
| rs534912883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066115 | GCAACGGCACAATCT[C/T]GGCTCATTGAAACCT | 6596 |
| rs534927059 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149072098 | TTAAAAACCACAAAC[-/TA]TAGTCAAACGCCAAA | 6596 |
| rs535009144 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031677 | GTAGCTGTAGGAAAA[A/G]TAAAAACCTGTGCTA | 6596 |
| rs535035378 | in-del | -/TC | | | intron-variant | HLTF | GRCh38.p7 | 3:149037720 | ACATGTTAAAAATCT[-/TC]TGAGTTTCAGGTAAC | 6596 |
| rs535058408 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087459 | GGAAGCTGGTGGTGG[C/T]GCCCAGCTGCACAGG | 6596 |
| rs535082312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149050687 | AGAAGGCCCTTTAAT[A/G]CTGCATTAGTTAGCA | 6596 |
| rs535109581 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085583 | AACTATTAATGTACC[-/AGA]AGTTGTTTATAATTT | 6596 |
| rs535255421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149076679 | ATTCTGATTCTACTT[C/T]ATTAAAAACTGTATG | 6596 |
| rs535302823 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088269 | GGCGCAATGGCTCAC[A/G]CCTATAATCCCAGCA | 6596 |
| rs535316277 | snp | A/C | 1.66192e-05 | 0.00288259 | synonymous-codon | HLTF | GRCh38.p7 | 3:149059800 | TTCTATAACCTTAGA[A/C]GATCCTGCTGATAAA | 6596 |
| rs535317180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079781 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 6596 |
| rs535318241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051466 | CCTAAAGAGAGCATG[C/T]ACAGTGAGCAAACGT | 6596 |
| rs535340588 | snp | C/T | 0.000511412 | 0.0159826 | missense | HLTF | GRCh38.p7 | 3:149063522 | CACTACATCTAGATG[C/T]GTCTATTTCAAAGAA | 6596 |
| rs535399390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051923 | CCAACACTGGGAGGC[C/T]GAGGTGGGCGGAACG | 6596 |
| rs535436165 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149064195 | AACAAAATCAAAAAC[-/A]AAAAAAAACCTCATC | 6596 |
| rs535457143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042640 | GAACAGGGTGCATGC[C/T]TGGTGACTTGAGCTT | 6596 |
| rs535490582 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065489 | CCCCTTAGAGTTAAG[C/T]CTTACTAAAAATGTG | 6596 |
| rs535536023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073917 | AAGTCAGGGGTTTCC[A/G]GATGTTACCATTAGG | 6596 |
| rs535561905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066089 | TTCACTCTTGTTGCC[C/G]AGGCTGGAGTGCAAC | 6596 |
| rs535591337 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149059677 | TTCATTCAAAAACAG[-/A]AAAAAAAACCAAAAA | 6596 |
| rs535613306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050081 | TCACGCAAAAAGTCA[A/G]AAAAAAAAACCATTT | 6596 |
| rs535616199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044640 | ACGGGCATCCTATGA[C/T]CAATGTGTCCAAAAC | 6596 |
| rs535706357 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087394 | GGGCTGGTCGCTTTG[C/T]GTTGAGGAGGCTGCT | 6596 |
| rs535818524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149050636 | AAAACCAAAGTTATT[A/G]AAAACAATAATGAGT | 6596 |
| rs535892574 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086721 | CCCAAGGCGGGCGCG[C/T]GGGAAAGCCACGAGG | 6596 |
| rs535904849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057515 | TCATATATACTCGTC[A/C]TGCAGGGCAGACTGT | 6596 |
| rs535953497 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037532 | CATGATATTCACCCA[C/T]GAAGGCCTAAGTATG | 6596 |
| rs535973700 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149056239 | GATTTTAAATGGCTA[A/C]GTTTTAGGATAATTT | 6596 |
| rs535994047 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072569 | TTGAAAATTAACACA[C/T]GAACACAGCAGCAGC | 6596 |
| rs536109463 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149043143 | AGCTTTGAAAAAATA[C/T]GGCAAGAGAACAGGA | 6596 |
| rs536112225 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031165 | CAAAAAAGTAAAAAA[A/G]AAAGAAAAGAAAAAA | 6596 |
| rs536133375 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087123 | TTAAGGAAAATTTTC[C/G]TTTCTTGGTGCAGGA | 6596 |
| rs536208156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082085 | ATGCTGAGTGAAAAA[C/T]GCCAGACTTAAAATA | 6596 |
| rs536248302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075279 | CCAGGCTGGGCACGG[G/T]GGCTCACGCCTGTAA | 6596 |
| rs536294982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149082804 | AATATAGATGATATT[C/T]CTAATCACATTAGGC | 6596 |
| rs536308612 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077482 | AAAAAAACCTCCCTT[A/G]GGCGGATGTTTGTCA | 6596 |
| rs536313312 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149054345 | TGAGTATGTATCAGG[A/C]AGAGCCAGTGGGAAG | 6596 |
| rs536353143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037922 | GGTCACACAGCTTGG[C/T]GAGTAAAGTTCAAAG | 6596 |
| rs536451991 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HLTF | GRCh38.p7 | 3:149077233 | AGCCTGGTGACAGAG[C/T]GAGACTTCATCTCAA | 6596 |
| rs536457282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069724 | GACAACTATCAATCA[C/T]GACTGAGTGTCTGAA | 6596 |
| rs536573084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149082408 | AGCTTGCAATGAGCC[A/G]AGATCCCGCCACTGC | 6596 |
| rs536624314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149054198 | CAAGCCAGATTACAA[C/T]GAATTAAGGAATTAG | 6596 |
| rs536641402 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029817 | CAAAATGTACAATGA[C/T]TGATTAAGAGTGCTA | 6596 |
| rs536786299 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038983 | AAGGTATTTACCAAA[A/T]AGTTTTTTGTCTTAT | 6596 |
| rs536799665 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075028 | GAGAGTTCCAGTCAA[C/T]TATTGTCATATGGAA | 6596 |
| rs536860144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053274 | ATGAGGGGCCTGGAG[G/T]TGGAAGGTGTATGGC | 6596 |
| rs537022033 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088142 | AATTCTTGGAAAATA[A/T]GCCAGAAATTGCTCA | 6596 |
| rs537023745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079855 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 6596 |
| rs537031112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045631 | ATGTTTTGAAGATTC[C/T]CCTTTCACAGTCCTA | 6596 |
| rs537060445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074093 | AAAAAGACTCCTGAA[A/G]AAAAGTTGTACCTTG | 6596 |
| rs537134949 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087607 | TTCTTTTTTATTGAG[A/T]TGGAGTCTTGCTCTG | 6596 |
| rs537193278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053157 | GAGAGCCAGGAAGAC[A/G]GTATCTTGTTCAGAT | 6596 |
| rs537261644 | snp | G/T | 1.66026e-05 | 0.00288115 | synonymous-codon | HLTF | GRCh38.p7 | 3:149075961 | ATGGCCAACTTGATT[G/T]CCATTCACATTGTTT | 6596 |
| rs537378284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075225 | CCTACATCATATCAC[A/T]GAATACCAGTTTATA | 6596 |
| rs537390506 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149066021 | AAATGTTTATTCAAA[C/G]ATAAAGGATGTCCTT | 6596 |
| rs537422028 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085797 | CCAATTTGGACAATG[A/C]AAAGTGAAGGGGAGT | 6596 |
| rs537455128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149077892 | AATCATCAGCTGACC[A/G]CTAAGCTAACCAAGT | 6596 |
| rs537490976 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HLTF | GRCh38.p7 | 3:149059130 | TGACTTGCTTATTGT[A/G]TATTTCTCTCATCAT | 6596 |
| rs537527887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033696 | GTGACAGAACAAATC[G/T]TTCTTCATCTGATAA | 6596 |
| rs537533640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084994 | AAATGAAATCTTACA[C/T]GGGAATCACGGTAAA | 6596 |
| rs537591375 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087235 | TGCTCCAGCCAAGAG[C/G]GGGAGGCCCTTGTTT | 6596 |
| rs537657849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149067581 | AATCATAGCTGACCA[C/T]AGGCTCAAACTCCTG | 6596 |
| rs537748836 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | HLTF | GRCh38.p7 | 3:149071750 | CATTTAATTAACTGG[A/C/T]GTTAATGTCAAACGG | 6596 |
| rs537789124 | in-del | -/AAATAAAT | 0.0362389 | 0.129639 | intron-variant | HLTF | GRCh38.p7 | 3:149075545 | TGAGACTTCGTCTCA[-/AAATAAAT]AAATAAATAAATAAA | 6596 |
| rs537950851 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149076576 | TCCTGAGCCTCAATT[A/C]TCCAGAATATAAAAG | 6596 |
| rs537981849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069684 | ACTAGTCACTTTTTT[A/C]ATGCGACACCATTTT | 6596 |
| rs538036310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149048371 | TGCTCTAATTTTTAG[C/G]TCTCACATGACACAC | 6596 |
| rs538053074 | in-del | -/TTCT | 0.0134861 | 0.0810011 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031086 | TGCTAAATTTCTAGC[-/TTCT]TTGTTTTAAATATGC | 6596 |
| rs538092577 | in-del | -/AAAC | 0.0532157 | 0.154195 | intron-variant | HLTF | GRCh38.p7 | 3:149057426 | TGAGACTCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 6596 |
| rs538101507 | snp | A/G | 0.00316543 | 0.0396572 | intron-variant | HLTF | GRCh38.p7 | 3:149063032 | AACTACTTAACAAAT[A/G]TAAGGGTCATGGTCA | 6596 |
| rs538168378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149063812 | GCTAAGAGCTATTGG[A/G]AAAAAAAATCAACAG | 6596 |
| rs538325808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068625 | CATTTAATCCTGAAC[A/T]CTTGATTTTTATCAT | 6596 |
| rs538469854 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050892 | CCCTGACTTTCTTGA[A/G]GACATGATCAGTTTT | 6596 |
| rs538532024 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149032873 | GAGGCTGAGGCAGGA[C/G]AATGGTGTGAACCCG | 6596 |
| rs538617722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075809 | CTTTATAGGCTCTAA[C/G]AAGAAGCCCTAACAA | 6596 |
| rs538624655 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040633 | ACATCTGTTGTACCC[A/C/G]TTTGAACCTGTTAAT | 6596 |
| rs538654371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068514 | GCTTTCCCCCACTGC[A/C]TTATTAGGGAATTAT | 6596 |
| rs538738482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082673 | CGTAAACCACATCTC[A/G]ATAAAGTAGAAAAAA | 6596 |
| rs538741607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075315 | GCATTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 6596 |
| rs538764210 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030768 | TCCTTACCTGCTACT[G/T]CCTCAAAAAGGGACC | 6596 |
| rs538778921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067828 | AACAATTTTAAGACT[A/C]CTGATACAAATTATC | 6596 |
| rs538786290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149039856 | AGAACACTCTAATAA[G/T]CTGAACCCATTCCAT | 6596 |
| rs538855902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063174 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCTGGGTA | 6596 |
| rs538883051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055220 | GTATATTTACCCCAA[C/T]GAATGACTCTTTAAC | 6596 |
| rs538995982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149062208 | CACAATAACATAACT[A/G]TTAGCTATAACATGT | 6596 |
| rs539047696 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149074798 | AAAGTGAGACATTAT[A/G]AGCATTTATTTTCTC | 6596 |
| rs539049538 | in-del | -/A | 0.428484 | 0.175052 | intron-variant | HLTF | GRCh38.p7 | 3:149040435 | ATTGTAAGCAAGTTT[-/A]AAAAAAAAAATCTAT | 6596 |
| rs539062696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065348 | CCTCTCTTCTTACTC[C/G]ATGGGGTATTTTCCT | 6596 |
| rs539095973 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030107 | ATAAAGTCAAAATTA[C/T]GGCACCGAGGAAGGT | 6596 |
| rs539097297 | in-del | -/TC | | | intron-variant | HLTF | GRCh38.p7 | 3:149071546 | AGTATATTTAAACAT[-/TC]TGAGTAGTCTTAAAT | 6596 |
| rs539119818 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149035614 | CAGTGAGCCGAGATC[C/G]CGCCACTGCACTCCA | 6596 |
| rs539142409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072561 | AGATATTTTTGAAAA[A/T]TAACACATGAACACA | 6596 |
| rs539176917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064670 | CCTAAATTTTTGTAC[A/C]GTACAAAGCCAAAAC | 6596 |
| rs539181356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073141 | CACAAATACCCACAC[A/G]TACATATTCATCCTG | 6596 |
| rs539471075 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149058288 | CATGTTGCCCACCCC[-/T]GATCTTGAACTCATG | 6596 |
| rs539554684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149061505 | CAGGTTTAATATTTG[A/G]TAGTTCAATTAAAGC | 6596 |
| rs539590777 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HLTF | GRCh38.p7 | 3:149056891 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGCTCG | 6596 |
| rs539598499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051370 | GTAAATAATTACCTA[C/T]AGATAGAAGTGAGAG | 6596 |
| rs539615855 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086507 | AGTCCAGTCAGACGT[A/C]GACGCCGTCTCCTTC | 6596 |
| rs539652839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149078596 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 6596 |
| rs539662546 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149036294 | TTAAATTAAAACTAT[A/G]AGGTTTTTTTTTTGA | 6596 |
| rs539692277 | in-del | -/AAAC | 0.00126949 | 0.0251621 | intron-variant | HLTF | GRCh38.p7 | 3:149071678 | ATAAACAGCAACAAG[-/AAAC]AATGTAAAACAAACT | 6596 |
| rs539703864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149041799 | CCATAGGCAAAAAGC[A/G]TAATTTAAATTTGAA | 6596 |
| rs539818027 | snp | C/T | 4.94703e-05 | 0.0049732 | intron-variant | HLTF | GRCh38.p7 | 3:149063423 | ATAATCAAACCATAA[C/T]AGTTTACCTTTTGGG | 6596 |
| rs539845157 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149034772 | CTTAAACAGCATATA[-/T]TAAATTATTGATGAA | 6596 |
| rs539876037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149056054 | AGGTCTGCTGACAAC[C/T]ATGTGAGTGAACTTG | 6596 |
| rs540108567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086048 | GTTTTGTTAAATAAA[A/G]CACTGGCCGAGATGC | 6596 |
| rs540328680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054781 | TCCATCATTTATTAG[A/C]TGGATGACCTTAGGC | 6596 |
| rs540364106 | snp | C/T | 5.00563e-05 | 0.00500256 | intron-variant | HLTF | GRCh38.p7 | 3:149055451 | TTTTTCTGAAATATA[C/T]ATGTCAATAAGGAGA | 6596 |
| rs540364177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149046968 | CTTGAAGCTTTCTCA[C/T]TATAACTCACAGTAA | 6596 |
| rs540369484 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080682 | AATTTATCATAATAA[A/G]CTATCATTAATTACA | 6596 |
| rs540382483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077008 | GCCCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGA | 6596 |
| rs540457887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042014 | TTGGTAAAAAAATTA[C/T]TGGATGTATTCCTAG | 6596 |
| rs540468709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077314 | ATAGCTTGTTGGGAT[C/T]CTAGGTAAAGCCTGG | 6596 |
| rs540542533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084336 | AACATAAGAAACATA[C/T]GGAGAAATGAAAGAA | 6596 |
| rs540566304 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049878 | ATGCCTGTAATCCCA[A/C/G]CTACTTGGGAGGCTG | 6596 |
| rs540614383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149032563 | TTATATAAAGAATAT[A/G]GCTGTACGAATAGAA | 6596 |
| rs540645645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044167 | ATGTGGATAATTATA[C/T]TGACCTAATAGGATT | 6596 |
| rs540693655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149036250 | TTTTAAATAGTATCA[C/T]GAATTGTTTGGATAA | 6596 |
| rs540723996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051061 | AAGTCCTAAACCAGC[A/G]AGGTAGAAGTAGGAA | 6596 |
| rs540760666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149051533 | GAAGACTTGTTTTTA[C/T]TGGGAGAAAACACAT | 6596 |
| rs540777855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085229 | GATGCGGTGGCTCAC[A/G]CCTGGAATCCCAGCA | 6596 |
| rs540805982 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149078531 | CTCCAGCCTGGGTAA[C/T]AGAGCAAGAACCTAT | 6596 |
| rs540832248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066325 | TGCTGGGATTACAGG[A/C]ATGAGTCACTATGCC | 6596 |
| rs540837945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149081274 | ACACACTAAAAAAAA[A/T]AAAACAAAAAATAAA | 6596 |
| rs540866035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149070125 | CTGATATGATTTAGC[A/G]TTCCATATTACAACA | 6596 |
| rs541068141 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087759 | GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 6596 |
| rs541166104 | in-del | -/AGG | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085893 | TTGCAAGTGGCGCAT[-/AGG]ATCTCTACTAGCGCC | 6596 |
| rs541208214 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063924 | AACACTGTTCGGCTC[C/T]CCTACCCATTTATCA | 6596 |
| rs541236296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149058090 | AAGGGTAAGAGCATC[C/T]CCCTATTCCTTTATT | 6596 |
| rs541272918 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149041071 | TGAGGTGTGCTGTAA[A/G]TATACACCACCACCA | 6596 |
| rs541281389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149036886 | ATGTTCAATGAAGAA[C/T]ACTCAACTTACTATA | 6596 |
| rs541344278 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149065074 | GTTATCTCAAAAAAA[A/T]AAAAATAAATAAAAC | 6596 |
| rs541431675 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149035253 | AGCACCCAAAATAAG[C/T]ATTTGTTGATTAATC | 6596 |
| rs541447487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050864 | TAACTAAAAATGAAG[A/G]ACAAATAATCATCCC | 6596 |
| rs541481544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149072761 | AATGTTATTTTTAAA[C/T]TGATCTGCATTAATT | 6596 |
| rs541483222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042942 | CAAGAAGAACTCAAG[A/G]TATTCAAATATAAGT | 6596 |
| rs541498769 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086785 | GGTGTTTTGTTTGAT[C/T]CCCTGCCTCAAACGG | 6596 |
| rs541520463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078285 | GCATGGTGGCTCACA[C/T]TTGTAATCCCAGCAC | 6596 |
| rs541560488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058526 | AGTTCTTACATAGTC[C/T]AGAATTGAACCTTTT | 6596 |
| rs541575942 | snp | C/T | 0.0566069 | 0.158427 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087733 | CCGGGATTGCAGGAG[C/T]CCGCCACCACGCCCA | 6596 |
| rs541584622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149065564 | TAAAAATCTGCCGGG[C/T]GCAGTGGCTCATGCC | 6596 |
| rs541589304 | in-del | -/TAAAGA | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149068735 | TATTAAAATTTGACT[-/TAAAGA]TAATACCAAGCTTAA | 6596 |
| rs541619689 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149058649 | GTGGCATTTAATCAA[C/T]CTTTTCCTTATGACC | 6596 |
| rs541665122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037899 | GCTCCTATGTGAATG[C/T]ACGTCCAGGTCACAC | 6596 |
| rs541734739 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149043474 | AAGGGGGGAAAAGCC[C/T]GGAATCTAAAGATTT | 6596 |
| rs541738801 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087289 | GCTCTGAGGCCCTCC[A/G]TGGCTCTCTTTCCAG | 6596 |
| rs541911968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041342 | TGCATTAGAAGAAAT[A/T]TATCACCTATTAAAA | 6596 |
| rs542020702 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149042801 | CTCTGTTTATGTGTA[-/C]TAATAAAACCTAAAG | 6596 |
| rs542112109 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149056925 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 6596 |
| rs542135234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149071897 | CTACAAAAAAATTTT[A/T]AAAAAATTAGCCAGG | 6596 |
| rs542185180 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149083650 | AATTAGAGGCCGGGT[A/G]CAGCATCCCAGCACT | 6596 |
| rs542186625 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149081583 | CAATAAAAAAGACAC[A/G]AATGTGTAACACAAA | 6596 |
| rs542195471 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086100 | AGTCGGTGACAGAGA[C/T]TTCCCAAGTCCCTAA | 6596 |
| rs542261290 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149049745 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAGGCCAA | 6596 |
| rs542276127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047655 | TCAAATAAATAAATA[A/C]ATAAATAAATAAATA | 6596 |
| rs542351330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041961 | AAGGGTATCTATCAC[C/T]GGAATTCCTGGAAAG | 6596 |
| rs542356517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085435 | CGTAGGTTGCAGCGA[A/G]CCGAGATTGTGCCAC | 6596 |
| rs542373628 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149072608 | AATCAGGCCAGGTCT[A/G]AAAAATCAGAAGTAA | 6596 |
| rs542427123 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149059155 | CATCATTACATCATA[C/T]GCTATATGAAAACAG | 6596 |
| rs542429504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068942 | TCCACAGGCCACTGG[A/G]GATGGGGAGGGTTTC | 6596 |
| rs542466141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061786 | GGTTGCAGTGAGCCG[A/C]GATCATGCCATTGCA | 6596 |
| rs542538316 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149083284 | AAATAAAAGAACATG[C/T]ATTAATTATAAAATA | 6596 |
| rs542598267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149082336 | TGGTGGCAGGCGCCT[A/G]TAGTCCCAGCTACTT | 6596 |
| rs542686199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075458 | TAAGGCAGGGAGAGT[A/T]GCTTGAACCCTGGAG | 6596 |
| rs542750324 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076992 | AGGCACAGTAGCTCA[C/T]GCCCCCAGCACTTTG | 6596 |
| rs542759759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149081582 | TCAATAAAAAAGACA[C/T]GAATGTGTAACACAA | 6596 |
| rs542922968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076107 | ACAATAACTTTGTTA[C/T]ACTTTATCTGGGATT | 6596 |
| rs542979564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066227 | AATTTTGTATTTTCA[G/T]TAGAGACAGGGCTTC | 6596 |
| rs542981797 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044417 | CATTTCAATTTAAGA[C/G]ATCTCTTTTGAGTGC | 6596 |
| rs543054023 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149059494 | AGAGGAGTAAGGGCC[A/C]CCATCACATTTTGGC | 6596 |
| rs543063791 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149057799 | CATAGCATCATACTG[A/C]AAAGTAGATTACAAT | 6596 |
| rs543179196 | in-del | -/GGGA | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088289 | TAATCCCAGCACTTT[-/GGGA]GGCCGAGTTGGGTGG | 6596 |
| rs543187816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040920 | AAAAATTCTACCCCA[C/G]CTGAATGACTGCTTA | 6596 |
| rs543196594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044795 | ACATGCCATAACATA[C/T]CAACCAGCAAGTTCT | 6596 |
| rs543214079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060402 | GGTAGTAGAAAATTG[C/T]TTTAAGTATAGTTTA | 6596 |
| rs543214127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149067924 | TGAGGCAGGTAGATG[A/G]CTTGAGCTCATGAGT | 6596 |
| rs543225365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149075432 | CAGGCACCTGTAGCT[A/G]CTCAGGAGGCTAAGG | 6596 |
| rs543229701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044927 | GGTCTCCCTACTTCT[A/G]ACCTTATTCCTATTC | 6596 |
| rs543298556 | in-del | -/A | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087076 | TCTTAAATGGAACTT[-/A]AGAGTCCCCTCCCCA | 6596 |
| rs543313484 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030329 | TTAGGAAGGACAAAT[G/T]AAATTTTTTAAATTA | 6596 |
| rs543339458 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082230 | TTGGGAGGCCGAGGC[A/C/G]GGCGGATCACGAGGT | 6596 |
| rs543455579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149044384 | TCCCTGGCATGGTCA[C/T]ATCTTACTGATACTC | 6596 |
| rs543537577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072862 | AATTTGGAGTTAAAT[C/T]TTTAGCACTGCATTT | 6596 |
| rs543559868 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087819 | CTTGAACTCCTGACC[G/T]CAGGTGATCCGCCCG | 6596 |
| rs543666676 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034718 | ATGTTTTTAAGGAGA[G/T]GTACACATAACTATA | 6596 |
| rs543689576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074967 | TTTAGAAAAAGAAAA[A/C]AGAAACAGGTGATAA | 6596 |
| rs543751711 | snp | C/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030912 | ACACAACATTGTCTC[C/T]GATCTCATCTTTCTA | 6596 |
| rs543765172 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HLTF | GRCh38.p7 | 3:149075613 | GGTACCAAAAGGTTT[A/G]GAGAAATGGAATGTA | 6596 |
| rs543772592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073472 | GCCAAGGCAGGTGGT[C/T]TGCCTGAGTCCAGTA | 6596 |
| rs543839545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149065605 | GAGACCGAGGCGGGC[A/G]GATCACCTAAGATCA | 6596 |
| rs543898128 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149050434 | GTCAGACTTAATAGA[C/T]GTATAAAAAAGTAAC | 6596 |
| rs543901060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149036089 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 6596 |
| rs543947752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076914 | AAAAGAATAAACAGC[C/T]GAATATCAGTACTTC | 6596 |
| rs544091294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149048793 | TTAAGTTTACAAAGT[C/T]ACTTTACTAACTTAC | 6596 |
| rs544118796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066135 | CATTGAAACCTCTAC[C/T]TCCTGAGTTCAAGTG | 6596 |
| rs544195606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149071006 | GCCAAGATCGCGTCA[C/T]TGCACTCCAGCCTGG | 6596 |
| rs544238395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062789 | TCCCCTTAAATCCAT[A/G]AAGAAAACTTCTAAA | 6596 |
| rs544288830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061033 | AGCATTCTGCTTTCA[A/T]AACCAGATAGATGCA | 6596 |
| rs544292553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032475 | ATGGCAAAAACCGCA[A/G]TTACTTTTGCACCAA | 6596 |
| rs544293521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054644 | ATAAACAATTAATCA[A/G]GAGGTTCCATTCCAA | 6596 |
| rs544327764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061761 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 6596 |
| rs544371125 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149055884 | TACAAAAGAAGTTTC[C/T]GTATTGGGTGTGCAA | 6596 |
| rs544406146 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149048791 | CTTTAAGTTTACAAA[A/G]TTACTTTACTAACTT | 6596 |
| rs544442621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149084049 | AAGATATATTACAAA[A/G]ATTTTAAATTCAGCC | 6596 |
| rs544507576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149063241 | ATTTTTGTCTATTTT[C/T]AGTAGAGACGGGGTT | 6596 |
| rs544516120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055701 | GTTTTATGCAGTTTT[C/T]TGAATTTGTGTTATA | 6596 |
| rs544544652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056204 | CAGCCCTGTCAAAGT[G/T]TGTGAGATAATAAAT | 6596 |
| rs544590167 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076627 | AAGTCAGGATGGAAC[G/T]AGGTAAGAAAAATAT | 6596 |
| rs544609277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045961 | ACTGTAATTCATAGA[A/T]GCAAATTATCTTTCA | 6596 |
| rs544675928 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149073817 | AAGTAATTCCACATT[A/C]TTTGAACAAACTCTT | 6596 |
| rs544676791 | in-del | -/C | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149030021 | TTCTGTTACAGTAAT[-/C]TTCATGTACTCTCAA | 6596 |
| rs544719995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053477 | AGAGTGTAAGCTTCC[A/T]GAGGCTGTGTAAGCT | 6596 |
| rs544761589 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149083082 | CATGGCAAAACCTCA[A/T]CTCTCCTAAATACAA | 6596 |
| rs544800191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149039973 | TTTGATATACTGTGT[A/G]TATTTCCTTATATAA | 6596 |
| rs544803961 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149051944 | GGGCGGAACGAGGTC[A/C]GGAGTTCGAGACCAG | 6596 |
| rs544824339 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031532 | TTTATACCTCAGACA[C/T]AGCAAGTTACATTTA | 6596 |
| rs544949342 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149044642 | GGGCATCCTATGATC[A/C]ATGTGTCCAAAACTG | 6596 |
| rs545048451 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030536 | TAAGCAGAAAGAGTA[A/G]ACTGTGTTGTTTTTT | 6596 |
| rs545373356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053328 | GTGGCTTAGTGCTAT[A/C]CCCTTGGTGATGAGT | 6596 |
| rs545402856 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149052503 | TTACAAAATAAGACA[A/T]AACAAATAATAAATG | 6596 |
| rs545480531 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037887 | GTAGAAAAACACGCT[C/T]CTATGTGAATGCACG | 6596 |
| rs545484419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063989 | GACCCCTTTGCCTAG[A/G]TTATAACTCCTTTTA | 6596 |
| rs545514072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149060318 | AGTATTGCCAGGAAG[A/G]CATTCTCAACCTAAT | 6596 |
| rs545670851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149045068 | AAAGCCAAAGTCCTT[A/G]ACATATGCGTTACAT | 6596 |
| rs545729073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078816 | GAGCCGAGATCGTGC[C/T]ACTGCACTCCAGCCT | 6596 |
| rs545750399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149045822 | TAGAAGCAAGCAAAA[C/T]CTTCTGGCTAGCAAT | 6596 |
| rs545770346 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149041248 | GTGTCTCACATTATC[A/T]ATCCATTTATTGAAC | 6596 |
| rs545825493 | in-del | -/AAAAT | 0.15692 | 0.232026 | intron-variant | HLTF | GRCh38.p7 | 3:149061423 | TCAAAAAAATAAAAT[-/AAAAT]AAAATAAAATAAAAT | 6596 |
| rs545846744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047757 | TGTTAATGCTGGTTT[G/T]GGGGCTTTGGGGCTT | 6596 |
| rs545855154 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149083842 | GAGAATTGCTTGAGT[C/G]TGGGAGGCAGAGATT | 6596 |
| rs545863739 | in-del | -/AT | 0.999923 | 0.000821873 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031420 | ACATAAATAAAAATT[-/AT]CTATTTATAGAAATA | 6596 |
| rs545867089 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084426 | AAGGCGCTGGGGTGT[-/G]GGGGTGGGGTGCTAC | 6596 |
| rs545927088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085352 | AAATTAGCCAGGCGT[A/G]GTGGCGCCCATATGT | 6596 |
| rs545997210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149035455 | AAAAGTATAAAAAAA[A/G]GGTTTCTCCTGGCTA | 6596 |
| rs546007443 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066588 | TTCAGCTGCCATTTC[A/T]ATTAATGTAGCAACC | 6596 |
| rs546076312 | snp | A/G | 4.9507e-05 | 0.00497504 | missense | HLTF | GRCh38.p7 | 3:149042226 | GGCAACAAATTTGCC[A/G]CAGTCTAAGCAAAAG | 6596 |
| rs546082503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149057413 | CCTGGGCGACAGAGT[A/G]AGACTCCGTCTCAAA | 6596 |
| rs546127026 | in-del | -/TTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149059659 | ACTTAAAATTTTAAA[-/TTT]TTTCATTCAAAAACA | 6596 |
| rs546138814 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084457 | CCATAATAACCAAAC[A/G]TAACGCACTGAGGCC | 6596 |
| rs546144574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033148 | GTGAAACAATAAAAG[G/T]ATTCTACAACAAAAC | 6596 |
| rs546161857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042871 | TATTTCCTGCTGGTC[A/G]GGGACATGATTGTGA | 6596 |
| rs546326507 | in-del | -/AAAGTC | 0.00159617 | 0.0282053 | downstream-variant-500B, cds-indel | HLTF | GRCh38.p7 | 3:149030094 | ATTTTATTTGAAGAT[-/AAAGTC]AAAATTATGGCACCG | 6596 |
| rs546388144 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079662 | CAGTCGCACAATCTC[A/G/T]GCTCACTGCAACCTC | 6596 |
| rs546575505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040358 | TAGAACGGATAAAGG[A/C]GGGAGCAAAAGTATG | 6596 |
| rs546591020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055712 | TTTTCTGAATTTGTG[C/T]TATATTTAATTTGGT | 6596 |
| rs546612276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032778 | CCATCCTGGCTAACA[C/T]GGTGAAATGCCATCT | 6596 |
| rs546619260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149083274 | AAACAAAAACAAATA[A/C]AAGAACATGCATTAA | 6596 |
| rs546633631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149075770 | CACGTACCAAAAGTA[C/T]AGTGATAGAAATTGT | 6596 |
| rs546701574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055032 | ATCTTTCCCACTTTG[A/G]GGGACAAAAATAGCA | 6596 |
| rs546732812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085550 | GGATTGAGCTATATA[A/T]AAGACTTATAAAAAT | 6596 |
| rs546776438 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HLTF | GRCh38.p7 | 3:149077251 | GACTTCATCTCAAAA[C/T]AAATAAATAAATAAA | 6596 |
| rs546804440 | snp | A/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087013 | ACTTTCGCTCCAAAT[A/T]TTCATGTTAAGCCTC | 6596 |
| rs546855192 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045509 | TTGTTGAAAGAATAT[G/T]AAAAGAAAGAAGATT | 6596 |
| rs546907075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149076402 | ATTGGTCTAAGTACA[C/T]TGCACAGACTGACTT | 6596 |
| rs547085942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043029 | GAAAAATGTTGCCAC[A/G]GAGCAAATAAAAATT | 6596 |
| rs547157040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149065727 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 6596 |
| rs547245785 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149043175 | GAGATGAAAGATGAG[A/C]TGGTATGGCTCAAGA | 6596 |
| rs547253830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068433 | ATCGAATATCAAATA[C/T]CATTCAAGGTCACAA | 6596 |
| rs547408967 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042108 | TAAAAAAAATTTATC[A/G]CTCTTATTTAAGTAT | 6596 |
| rs547442134 | snp | A/G | 0.000940245 | 0.0216619 | synonymous-codon | HLTF | GRCh38.p7 | 3:149063523 | ACTACATCTAGATGC[A/G]TCTATTTCAAAGAAA | 6596 |
| rs547478240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149056836 | CAGAATGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 6596 |
| rs547489374 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087072 | GAAAATCTTAAATGG[A/G]ACTTAGAGTCCCCTC | 6596 |
| rs547543951 | in-del | -/TCAC | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149069642 | TTAGCTAGAGAAAAA[-/TCAC]TCAAGATGGGAGTTA | 6596 |
| rs547594018 | snp | C/T | 3.44976e-05 | 0.00415303 | intron-variant | HLTF | GRCh38.p7 | 3:149050415 | TAACAATGAGCAGAT[C/T]TGTGTCAGACTTAAT | 6596 |
| rs547713638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149050056 | AGCATCTAAATAAAA[C/T]GCAACCCTTTCACGC | 6596 |
| rs547775250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064162 | CCTAACTCATCTAGG[C/T]AGATGAGTTAGACCA | 6596 |
| rs547776637 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086403 | CGAGCCGCCTCGATA[A/C]GCCTCCTTCCAGGCC | 6596 |
| rs547894937 | snp | A/G | 3.30115e-05 | 0.00406259 | missense | HLTF | GRCh38.p7 | 3:149071386 | CTTTGCTATTTTCCC[A/G]TGACACCATCCAAGC | 6596 |
| rs547975694 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041648 | TTAACTTCTTTCTCA[A/G]TTCTTCAGGTGTATC | 6596 |
| rs548061441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057381 | CAGTGCGCCGTGATC[A/G]CACCACTGCACTCTA | 6596 |
| rs548204070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072185 | TGCTTTAGTTGTTAG[C/G]AGGTAAAAGAATATA | 6596 |
| rs548217223 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149040509 | TTAGTACTATTCTTT[-/A]AAAAAAAATCCATCT | 6596 |
| rs548225385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063042 | CAAATATAAGGGTCA[C/T]GGTCATCTCTATCTC | 6596 |
| rs548231408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149032690 | CATTCTGGCCGGGCA[C/T]GGTGGCTCACACCTG | 6596 |
| rs548260895 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149054052 | ATAAATAAATAAACC[-/A]AAAACTTATATAAAA | 6596 |
| rs548318887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149073021 | GGGTACAAATGTTCA[C/T]GTATGGATTTATTCC | 6596 |
| rs548360448 | in-del | -/ACA | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149036159 | CAAAAAACAAAAAAC[-/ACA]ACAACAGCAATAAAA | 6596 |
| rs548386748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057329 | TACTTGGGAGGCTGA[A/G]ACAGGAGAATTGCTT | 6596 |
| rs548408619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077121 | GGTGTGGTGGCACGC[C/G]CCTGTAGTCCTAGCT | 6596 |
| rs548447495 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088025 | ATGAGGAAGATAAAG[A/G]CAATGGCATTTCAAA | 6596 |
| rs548457763 | snp | C/T | 0.000399281 | 0.0141238 | missense | HLTF | GRCh38.p7 | 3:149063477 | TGCGAAACTTACTCT[C/T]CTCCTTGATATCTGA | 6596 |
| rs548469240 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088541 | CCATCTCAAAAAAAT[-/AA]AAAGACTTAAGATCT | 6596 |
| rs548576604 | snp | A/G | 0.000255953 | 0.0113098 | synonymous-codon | HLTF | GRCh38.p7 | 3:149032271 | GGCTTGTTTCATTTC[A/G]TCAGCATTTGGTTTT | 6596 |
| rs548612090 | snp | A/G | 1.70481e-05 | 0.00291955 | intron-variant | HLTF | GRCh38.p7 | 3:149059859 | ATTATCTCCTGTGCT[A/G]GAGTACAGGTACTTT | 6596 |
| rs548920407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149066775 | TAACCTAAAACTTCA[A/G]TTTCAATAACCAAAT | 6596 |
| rs548935447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057686 | ATAATATTTTAGAAC[G/T]GAAACTGTAGAACGT | 6596 |
| rs549117421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074645 | TAAAATAAGTTAAAT[C/T]AAAGGGTAGAGTTTG | 6596 |
| rs549139407 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149071722 | ATACTTGCATTTAAG[C/T]CAGATTTGAAATCAT | 6596 |
| rs549292058 | snp | C/T | 3.31279e-05 | 0.00406975 | missense | HLTF | GRCh38.p7 | 3:149074325 | GGCATGGTAAAAGCA[C/T]TGTTTGCACCAAAAG | 6596 |
| rs549302459 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087834 | TCAGGTGATCCGCCC[A/G]CCTCGGCCTCCCAGA | 6596 |
| rs549331233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037241 | TTTGGGAGGCTGAGG[C/G]AGGTGGATCATGAGG | 6596 |
| rs549368683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050685 | TTAGAAGGCCCTTTA[A/C]TGCTGCATTAGTTAG | 6596 |
| rs549415842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065862 | ATATTTTTAGAGATA[C/T]GTAACTAGAAGAGTT | 6596 |
| rs549420154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149036392 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 6596 |
| rs549447264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044451 | CCATGTGCTAAATAT[C/T]AGAAGCTTCCTTCCT | 6596 |
| rs549482297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058333 | AAAGTGCTGCAATTT[C/T]AGGCATGTGCCACCA | 6596 |
| rs549528445 | snp | C/T | 0 | 0 | synonymous-codon | HLTF | GRCh38.p7 | 3:149059770 | TGAAGTTAATGCACA[C/T]GCAAATGCCACATCT | 6596 |
| rs549579868 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062225 | TAGCTATAACATGTG[C/T]GTCAGCTGTTGTTAA | 6596 |
| rs549652264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149043863 | TAAAAGTACCTACCT[C/T]ATACAACTACTGTTA | 6596 |
| rs549653517 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050947 | TCATGAAAAAAACCA[A/G]ACCTAGAAGATTTTC | 6596 |
| rs549683038 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149036569 | GCTGGGATTACAGGC[A/C]TGAGCCTCCGCGCCA | 6596 |
| rs549797774 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054063 | AACCAAAAACTTATA[C/T]AAAAAAAGATAATTC | 6596 |
| rs549828201 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058248 | GGCTAATTTTGTGTA[-/T]TTTTTTGTAGAAACA | 6596 |
| rs549850293 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149067036 | GCATACATCTTTTTG[C/T]TATTTCCTTCTATTT | 6596 |
| rs549909770 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149050076 | CCCTTTCACGCAAAA[A/G]GTCAAAAAAAAAAAC | 6596 |
| rs550069693 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149035741 | TTGATGCTATTTTCT[C/G]TATCAGTATTTGACG | 6596 |
| rs550162887 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149065087 | AAAAAAAATAAATAA[A/T]ACTACTTGGCCTTCA | 6596 |
| rs550356098 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053892 | CATTCAAGTACCCAT[A/G]TACTATCCTTCCCAT | 6596 |
| rs550380918 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032160 | TTCTAAAACTCTGTA[A/T]TTTTCTCATTTCTAA | 6596 |
| rs550424338 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087407 | TGCGTTGAGGAGGCT[A/G]CTGTCCCCGAAGCTG | 6596 |
| rs550439455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050498 | AAAATTGTATGAAAT[C/T]AAGTTTCCTTCAGTC | 6596 |
| rs550589525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082018 | TAAATAAAATGGATG[C/T]TTTTCTTCAAAAATG | 6596 |
| rs550637635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149069271 | GAGGTAGGAGTTCAA[C/G]ACCAGCCTGGACCAA | 6596 |
| rs550653080 | snp | C/T | | | synonymous-codon | HLTF | GRCh38.p7 | 3:149048930 | CTGAGCATTTGGATT[C/T]CGTATGGCATGTCCT | 6596 |
| rs550661394 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088176 | TGATGTTTTGTAAGA[A/G]TAAGAAAGTCATGCT | 6596 |
| rs550780251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149076621 | ATTTATAAGTCAGGA[C/T]GGAACTAGGTAAGAA | 6596 |
| rs550871031 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084530 | CTGAGGTGGGAGGGT[C/T]ACTTAAGGTATTTGT | 6596 |
| rs550907461 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085818 | GAAGGGGAGTCTACT[G/T]GAGCATTGCAAAAAG | 6596 |
| rs550942580 | snp | A/G | 8.2763e-05 | 0.00643231 | synonymous-codon | HLTF | GRCh38.p7 | 3:149068252 | TACCTTCTTCAGTAG[A/G]TTCTTTTTAACTCTT | 6596 |
| rs551011402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037873 | GCCCCTTTGTACACG[C/T]AGAAAAACACGCTCC | 6596 |
| rs551044437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044586 | TGAACTCGACTCTCC[C/T]ATCCAACTAATTATT | 6596 |
| rs551088675 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | HLTF | GRCh38.p7 | 3:149059511 | CATCACATTTTGGCC[A/C]TAACTAAAACAAATA | 6596 |
| rs551123725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037382 | GCTGAGGCAGTGAAC[C/T]GCTTGAACCCAGGAG | 6596 |
| rs551179110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047074 | TGTATCATGCACTCC[A/G]ATATTTACTAATCTC | 6596 |
| rs551249051 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029759 | GTAACAAACTACATA[A/G]GGTTAGTTTGTATTT | 6596 |
| rs551250753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149038445 | AACTGTATGATACTG[A/G]GCACATTATTTACTT | 6596 |
| rs551270445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149075237 | CACAGAATACCAGTT[C/T]ATAACCTCTGATATA | 6596 |
| rs551321462 | snp | A/C | 3.29761e-05 | 0.00406041 | missense | HLTF | GRCh38.p7 | 3:149060674 | AGTTTCAGACTGTAC[A/C]TTTTTCAGTTTGCCT | 6596 |
| rs551361517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068170 | CTTGGTAGTTTTTTT[A/T]AATGATGAAATTTAA | 6596 |
| rs551577445 | snp | A/C | 0.000363545 | 0.0134774 | intron-variant | HLTF | GRCh38.p7 | 3:149059685 | AAAAACAGAAAAAAA[A/C]CCAAAAACTAGAAAA | 6596 |
| rs551612243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051732 | TGGGCATGGTGGTGA[C/T]GGTGATGCGCACCTA | 6596 |
| rs551643865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149081824 | GTAACTAGAACCAAG[A/G]CATAAAAGGGAGTTT | 6596 |
| rs551660139 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029653 | ATAAACCTTGACAAG[A/T]AGTATAAATAAAACA | 6596 |
| rs551893609 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067610 | TGGGCTCCAGCAATC[C/T]TCCTGCTTCAGCCTC | 6596 |
| rs551898794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051337 | GAATACCTAACTGAA[A/G]ACGTATACTAGGAAA | 6596 |
| rs551902979 | in-del | -/AA/AAA | 0.440746 | 0.161604 | intron-variant | HLTF | GRCh38.p7 | 3:149083749 | CCTAAAAAAAAATAC[-/AA/AAA]AAAAAAAAAAAATAC | 6596 |
| rs551911880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085722 | ACCCGCCTTCCGTCG[C/T]CGGTTTAAGCATAAC | 6596 |
| rs551935479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043989 | TGGCAACAAACATTT[C/G]TGAATATTCAAGAAT | 6596 |
| rs552051919 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149075193 | GTCTAAAACACTGCA[C/G]GGCAAAATGAAATTC | 6596 |
| rs552056080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037336 | TAGCCACGCGTGGTG[C/G]CAGGTGCCTGTAATC | 6596 |
| rs552142265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037802 | TGCCTTTAGCCCACA[C/T]AGTACCCAGTGCAAA | 6596 |
| rs552212168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077748 | GCTCACCTTTGCCTG[A/C]ACTTGAGCATTTAAA | 6596 |
| rs552228774 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149053231 | ATCTCCTCCAAATCT[C/T]ATGTTGAAATGTAAT | 6596 |
| rs552237901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056571 | CTCCTTATCCACTGG[A/G]GGTATGTTCCAAGAC | 6596 |
| rs552250843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076462 | ACTATCATTATTCCC[A/G]TTTTACAAATGAAGA | 6596 |
| rs552263644 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050510 | AATCAAGTTTCCTTC[A/G]GTCTAGACCAAAATA | 6596 |
| rs552276505 | in-del | -/GA | 0.00835141 | 0.0640778 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030860 | AAGGACTTATCTGGT[-/GA]GAGATTTGGCATATA | 6596 |
| rs552331690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040696 | AAAACACCATTACAA[G/T]TAAATAATTCTGAAG | 6596 |
| rs552364147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149071502 | TTTTTCACATGCAGA[C/T]CCTGTGATTAAACAA | 6596 |
| rs552449257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149072143 | AACTCTAGAATTACA[C/T]TACTCACTGAAGAGC | 6596 |
| rs552451206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149033517 | TTACTTTAGGAAACC[A/G]TAGTTGTTATAAGAG | 6596 |
| rs552491332 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055171 | TCCAATTCACCTGAT[A/G]ATTATTTGAACTTAG | 6596 |
| rs552584672 | snp | G/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030473 | TGGGCAAAGAAGCAA[G/T]CTGTCCTCCCTTTAC | 6596 |
| rs552588410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077077 | CATGGTGAGACCCCC[A/G]TCTCTACTAAAAATA | 6596 |
| rs552614788 | in-del | -/AA | | | intron-variant | HLTF | GRCh38.p7 | 3:149050079 | TTCACGCAAAAAGTC[-/AA]AAAAAAAAAAACCAT | 6596 |
| rs552691265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053096 | GACAAAAAAGGGAAT[A/G]TAAGTCAGTTCTAGC | 6596 |
| rs552704676 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031273 | ATTGTTTACATTCAG[A/G]ATTAAGATGTCTTTA | 6596 |
| rs552871817 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076363 | AATAGCCAACCCTTA[C/T]TGAGCGCTTACTATG | 6596 |
| rs552903048 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149036619 | TTATACAATGTTCAA[C/T]GAAAAGGTAAAAGAA | 6596 |
| rs552933427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149062498 | CTAGCAGAGACAAAT[C/T]TGCGATGACTTGTGT | 6596 |
| rs552999647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082905 | TGTAGAAGATAAGTT[A/C]TGGTTCTGGATGATA | 6596 |
| rs553038323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076111 | TAACTTTGTTATACT[G/T]TATCTGGGATTTCCA | 6596 |
| rs553070128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082104 | AGACTTAAAATAGTA[C/T]ATACTGTAGAATTCA | 6596 |
| rs553070212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074819 | TTATTTTCTCTTCAA[A/G]CTCACCTAGGATTAT | 6596 |
| rs553095527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149046550 | ATTTTTGTTCCAATC[A/G]CTAACTCTTTTACTT | 6596 |
| rs553106370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061663 | TAACATGGTGAAACC[C/T]CGTTTCTACTAAAAA | 6596 |
| rs553135794 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149067762 | GTAACTCCTTTCAGA[G/T]AGTTTCTTAGAAATG | 6596 |
| rs553158794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069748 | GTCTGAAAGATACTT[C/T]CTAGAAAATGAACAA | 6596 |
| rs553167872 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044512 | GTTAGATCTCTTTCA[C/G]TTTACTCACTCCCTT | 6596 |
| rs553324479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076726 | ATGATGTATATTTTT[A/T]AAAACTGAAGGAGGG | 6596 |
| rs553331353 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037737 | TGAGTTTCAGGTAAC[A/G]AGTTACAACCACAAA | 6596 |
| rs553371369 | snp | A/G | 3.31873e-05 | 0.0040734 | missense | HLTF | GRCh38.p7 | 3:149060793 | CCTTTCATTTTCTGC[A/G]GCAATTCACTTGTTT | 6596 |
| rs553440514 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068711 | ATTCCAGTATGCATA[C/T]AATCATTTTATTAAA | 6596 |
| rs553442961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063910 | AACTCTTTTTACTAA[A/T]CACTGTTCGGCTCCC | 6596 |
| rs553472868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149071784 | AGGAGTGGTGGCTCA[C/T]GCCAATAATCTCAGC | 6596 |
| rs553551203 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149034121 | AGGTTTTAGGTAAAT[A/G]CAAATTAGAACAGCA | 6596 |
| rs553571309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053293 | AAGGTGTATGGCTCA[C/T]AGCGGTGGATCCCTC | 6596 |
| rs553608079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045733 | AGAATTTCATACCTT[C/T]TACCAATCCTTAATC | 6596 |
| rs553608340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054413 | ATGTGGGAAAAGAGA[G/T]AATCCAATGTAGAGA | 6596 |
| rs553652617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058415 | AGCATATTTTTTCCA[C/G]TGTTAACTGGTTATT | 6596 |
| rs553753484 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | HLTF | GRCh38.p7 | 3:149048636 | TACTCCATTTCCAAG[G/T]TTCAAGAATAAGTCT | 6596 |
| rs553772075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064612 | ATCTCCTTCATGAAA[C/G]CTTTCCTATCAGTAC | 6596 |
| rs553977086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149050129 | TAAGTATCTAAAGAG[A/G]AAAAAAAAGTATAAA | 6596 |
| rs554015787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149042731 | TGCACTGTATTTTCA[A/G]AAAAAGACTATGGGC | 6596 |
| rs554015850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050741 | CAGTAAAAGAACAAC[A/C]ACCAATATTTCCAAG | 6596 |
| rs554035145 | in-del | -/A | 0.359152 | 0.224913 | intron-variant | HLTF | GRCh38.p7 | 3:149037467 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6596 |
| rs554036722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049245 | ATGTTACCCAAAGCA[A/C]CACAGGTGGCAGAAC | 6596 |
| rs554102597 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149056038 | TAGCCAGCAAGTAAT[G/T]AGGTCTGCTGACAAC | 6596 |
| rs554179300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085253 | CCCAGCACTTTGGGA[C/G]GCAGAGGCAGGTGGA | 6596 |
| rs554212504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085010 | GGGAATCACGGTAAA[A/G]ATTAATAGTTACTCT | 6596 |
| rs554263088 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149071017 | GTCACTGCACTCCAG[C/T]CTGGGTGACAGAGCA | 6596 |
| rs554319859 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061273 | TTTGATAGCCGGGCG[C/T]GGTGGTGGGTGCCTG | 6596 |
| rs554331787 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062625 | CAGAGGGGAATTACA[A/T]CTTTTATTCAAATTC | 6596 |
| rs554357628 | snp | C/T | 1.66156e-05 | 0.00288228 | missense | HLTF | GRCh38.p7 | 3:149059793 | CCACATCTTCTATAA[C/T]CTTAGAAGATCCTGC | 6596 |
| rs554426675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064396 | TTTCCATTTCTCCTA[A/T]GACTTCAGAATTTGG | 6596 |
| rs554588734 | snp | A/G | 0.000399281 | 0.0141238 | missense | HLTF | GRCh38.p7 | 3:149055364 | CTTGGTCTCTCCTCA[A/G]CATCAGTTTTCTTTG | 6596 |
| rs554593831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149082797 | TAAGTCCAATATAGA[C/T]GATATTCCTAATCAC | 6596 |
| rs554664605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061771 | AACCCGGGAGGCAGA[A/G]GTTGCAGTGAGCCGA | 6596 |
| rs554700556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149032950 | CCTGGGTGACAGAGC[A/G]ACGTCTCAAAAAAAA | 6596 |
| rs554716883 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076335 | AAAATTTTCAACATC[A/T]TAACTTCTGAAAAAT | 6596 |
| rs554737290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033737 | TTAGACTCATGTCAC[A/G]AATCATAAAACAAAA | 6596 |
| rs554829722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055859 | ATAGTATGTCACTTC[C/T]GAGATAGATTACAAA | 6596 |
| rs554839264 | snp | C/T | 1.73159e-05 | 0.00294239 | missense | HLTF | GRCh38.p7 | 3:149040038 | TACTTTACCTTTGAA[C/T]TGGATGTCCATTCCA | 6596 |
| rs554849643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149049812 | AGCCTGACCAAGATG[A/G]TGAAACCTCATCTCT | 6596 |
| rs554850062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057588 | TGGAACCAAATCCCT[A/G]ACAAATACTGAGGGA | 6596 |
| rs554869090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063830 | AAAAAATCAACAGAA[C/T]CACAAATAGGTGCTG | 6596 |
| rs554901248 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149059043 | AGCTTCATAAACAAG[A/C]CCCTTCAGGTCAATC | 6596 |
| rs554945679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047599 | GTGAGCCAAGATCGC[A/G]CCACTGCCCTCCAGC | 6596 |
| rs554990236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051477 | CATGTACAGTGAGCA[A/G]ACGTTAGGGACAGAG | 6596 |
| rs555012749 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149046826 | ATTTCTTTCTCAGTA[C/T]TGGAAAAAAAGAGAT | 6596 |
| rs555066750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149069708 | CCATTTTTACTTGAA[C/T]GACAACTATCAATCA | 6596 |
| rs555194906 | in-del | -/T | 0.0147168 | 0.0845092 | intron-variant | HLTF | GRCh38.p7 | 3:149079581 | AGCTGTGAGCAAAGG[-/T]TTTTTTGGGGTTTTC | 6596 |
| rs555208236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032494 | CTTTTGCACCAAACT[A/G]TAATAACTATTTAAT | 6596 |
| rs555226804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051952 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGATCA | 6596 |
| rs555256037 | snp | C/G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149032758 | ATGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 6596 |
| rs555262100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149075538 | AACAGAGTGAGACTT[C/T]GTCTCAAAATAAATA | 6596 |
| rs555286176 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149073041 | GGATTTATTCCTTAT[A/C]AGTACTTTTTATATA | 6596 |
| rs555484410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043146 | TTTGAAAAAATATGG[C/T]AAGAGAACAGGAAGA | 6596 |
| rs555511633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149036857 | AAGTTAGAAACAACA[C/T]TGGAAAGCTTGATAT | 6596 |
| rs555566119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041999 | TATAATTCCATTTCA[C/T]TGGTAAAAAAATTAT | 6596 |
| rs555606876 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149037583 | ACTGAGAAGGATACC[A/G]TCAGTTGAGGGAGGA | 6596 |
| rs555639828 | in-del | -/AAAA | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149043330 | AAATCAAAATTAAAC[-/AAAA]AAATGTAAAAGATCA | 6596 |
| rs555702347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042663 | TTGAGCTTCCATGGA[A/G]AAATTTATATCAAAA | 6596 |
| rs555743116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149035067 | TGCATTTGTCCTTTC[A/G]TTTCACTAGTATTCA | 6596 |
| rs555788642 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068420 | TTAAAATCAAGTAAT[C/T]GAATATCAAATATCA | 6596 |
| rs555789240 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149058499 | GGGTGGTCTTTTTCC[A/C]ATTGTTTGGAAAGTT | 6596 |
| rs555830537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149078726 | GCCGGGCGAGGTGGC[A/G]GGTGCCTGTAGTCCC | 6596 |
| rs555879498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050106 | CCATTTATTTTTCTA[C/T]ATATCGTTAAGTATC | 6596 |
| rs555970415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065560 | AAACTAAAAATCTGC[C/T]GGGCGCAGTGGCTCA | 6596 |
| rs556057988 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149051436 | TATTTACAGCTGTAA[C/G]AATGAATGAAATTTC | 6596 |
| rs556094783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149044032 | CAAAATAATACAAAG[A/G]TTAAACTTACAAGCT | 6596 |
| rs556114856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149079046 | ATAAGAAAAATCAGC[A/G]AAGCTGAAGATAGGT | 6596 |
| rs556142248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041880 | CTCATAGAGAAGCAT[C/T]ATTATAACATGACAA | 6596 |
| rs556173963 | in-del | -/AGTT | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029981 | AATTGAGCAAAATAA[-/AGTT]AGTTAGGATATGAGG | 6596 |
| rs556228329 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058898 | TAATTCTATCTCAAC[C/T]GAAATTTCCACATTT | 6596 |
| rs556391131 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051937 | CCGAGGTGGGCGGAA[C/T]GAGGTCAGGAGTTCG | 6596 |
| rs556401581 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149036122 | CCTGGGCGACAGAGC[A/G]AGACTACATCTCAAA | 6596 |
| rs556431713 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149034079 | ACAGAAAAAATGTTA[A/C]TAAACAAGATATGTG | 6596 |
| rs556486610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149049424 | AAAAGGTAATATTTT[C/T]ACTAGAAGACTGAAA | 6596 |
| rs556519864 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036914 | ATAAAACTGCTAAAA[C/T]GTTCTGTAAATTTTT | 6596 |
| rs556675775 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149078100 | ACATTATTTAAAATG[A/T]CAATTTTTCAAGAAA | 6596 |
| rs556743385 | snp | C/T | 0 | 0 | intron-variant | HLTF | GRCh38.p7 | 3:149072373 | TAAAATTCTGTGATG[C/T]TATCAGTTGTATTCA | 6596 |
| rs556744033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072570 | TGAAAATTAACACAT[G/T]AACACAGCAGCAGCT | 6596 |
| rs556787625 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149056335 | TTTAAAAATAGTGAT[A/T]ATAAAGTGTTTTTAC | 6596 |
| rs556805089 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149050920 | TTTAAAAACTTATTA[C/T]TATTTTTTTAATCAT | 6596 |
| rs556843724 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047365 | AGCTATGTAAGGCCA[C/G]GTGTGGTAGCTCATG | 6596 |
| rs556896089 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086515 | CAGACGTCGACGCCG[C/T]CTCCTTCTGCAACAA | 6596 |
| rs557104346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074767 | AAAAACCTGATAAAC[C/T]GAAAAAGGAGAAAAC | 6596 |
| rs557227455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149075436 | CACCTGTAGCTACTC[A/G]GGAGGCTAAGGCAGG | 6596 |
| rs557227569 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079913 | ACAAAGTTTTTTATA[C/T]ACTGTTAAGTTGGCA | 6596 |
| rs557261306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082233 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 6596 |
| rs557296241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082739 | ATTTTTATTATTTTT[A/G]TAATAGTGATTAACT | 6596 |
| rs557314941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149074139 | ATTAGCCAACAAACT[C/T]CAAGAGAGAATAAAT | 6596 |
| rs557431961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149079912 | CACAAAGTTTTTTAT[A/G]TACTGTTAAGTTGGC | 6596 |
| rs557433336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149052119 | AGATCGCGCCATTGC[A/G]CTCCAGCCTGGGCGA | 6596 |
| rs557470286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077644 | CCAGTGTATTTCTGG[A/G]TATCTAGAAGGCCGT | 6596 |
| rs557550409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060234 | GAATTACAGGAAAAT[A/G]AAACATATTTTAAAG | 6596 |
| rs557580780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149052291 | TTTTTAAAAAATTAT[A/G]TGTTGTATGGAAATA | 6596 |
| rs557624447 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149045598 | AACCTGCTTTGTACC[G/T]ACCTCACTGAAGTTT | 6596 |
| rs557624546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037623 | CCTGAGTAAACATAT[A/G]TGCATCAACAAGGTA | 6596 |
| rs557634438 | snp | C/T | 6.59783e-05 | 0.00574324 | intron-variant | HLTF | GRCh38.p7 | 3:149060742 | CAGGACATTAGAATA[C/T]AGGACACATTATCAA | 6596 |
| rs557666794 | in-del | -/AAAT | 0.0931687 | 0.194689 | intron-variant | HLTF | GRCh38.p7 | 3:149075549 | ACTTCGTCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 6596 |
| rs557682228 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030173 | TAAAATCCAGTTTTA[A/G]CCACAAAATTGTTTG | 6596 |
| rs557705764 | in-del | -/T | 0.00353705 | 0.0419048 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084892 | CAAACTGGATCCCTA[-/T]TTTTTTTTTAAAGGC | 6596 |
| rs557708155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149067135 | TAAACTAATTTTTAA[C/T]TCTTAGAAACCAAAT | 6596 |
| rs557783249 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149071897 | TACAAAAAAATTTTT[-/A]AAAAAATTAGCCAGG | 6596 |
| rs557809287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051553 | AGAAAACACATGATG[C/T]CTGGGGTATAATTAA | 6596 |
| rs557901034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079817 | AGGATGGTCTCAATC[A/T]CCTAACCTCGTGATC | 6596 |
| rs557926242 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034420 | GGTAGTTGCCAGGGG[C/T]TGGGGGGAGAGGAAT | 6596 |
| rs557977640 | in-del | -/A | 0.430285 | 0.173197 | intron-variant | HLTF | GRCh38.p7 | 3:149069158 | CTGCCACATACAGTT[-/A]AAAAAAAAAAGTTTT | 6596 |
| rs557995766 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088362 | ATGGTGAAAGCCTGA[C/G]TCTACTAAGAAAATA | 6596 |
| rs558034770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149081384 | CGCAATACTTAACAC[A/G]TTTAAAGATTAAAAG | 6596 |
| rs558047564 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061706 | CCAGGTGTGGTGGTG[C/T]GTGCCTGTAGTTCTA | 6596 |
| rs558050182 | in-del | -/T | 0.0576439 | 0.159685 | intron-variant | HLTF | GRCh38.p7 | 3:149063067 | ATCTCTCTCTTTTTC[-/T]TTTTTTTTTTGAGAC | 6596 |
| rs558219547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073398 | TAAGTAGCTTTTAAA[A/G]TATGCATTAACAGGG | 6596 |
| rs558241563 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087207 | GGGACCATTTTCCCC[A/G]TGGGCACTTGGCTGC | 6596 |
| rs558257120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076880 | TTGCAGAAATCTGGG[A/T]AACATTTATTCAAGA | 6596 |
| rs558276530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043224 | AATCATCAGAGAAAT[C/G]AAAGTCACACTGAAA | 6596 |
| rs558335513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149066116 | CAACGGCACAATCTC[A/G]GCTCATTGAAACCTC | 6596 |
| rs558369661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149084031 | TACAAAGATTTTATT[A/G]CAAAGATATATTACA | 6596 |
| rs558370704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149059184 | AGATAGCCTGCTATA[G/T]CCCCAACATGTAAAA | 6596 |
| rs558474812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068614 | CTACAATTCTACATT[C/T]AATCCTGAACTCTTG | 6596 |
| rs558511737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073953 | TTAGGGGAGGGTATA[C/T]ATGAGACTTCATTGC | 6596 |
| rs558512869 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084782 | AAGTCATCTGGAGGG[A/G]TAACATCTTGGAATT | 6596 |
| rs558619801 | snp | C/G/T | 1.82573e-05 | 0.00302131 | intron-variant | HLTF | GRCh38.p7 | 3:149055252 | GAATACTTTCTACCT[C/G/T]GTAGATAAAATATAA | 6596 |
| rs558707797 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149083264 | TTCAAAAAAAAAACA[A/G]AAACAAATAAAAGAA | 6596 |
| rs558716205 | snp | A/C | 0.000586315 | 0.0171118 | intron-variant | HLTF | GRCh38.p7 | 3:149032396 | AGAAAAAAAAAAGTT[A/C]AGTAGTTTTTAAGGC | 6596 |
| rs558826253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063691 | CTAATCTAGTATTTC[C/T]TCATTTCTAATTAGA | 6596 |
| rs558963574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054522 | ACTTGGAAGTGGCAA[A/G]AACGGTGAGTGGTCC | 6596 |
| rs558969063 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149070182 | TGAATTTTGATGCAG[-/TA]TATATCAAAGAAATC | 6596 |
| rs559074072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053913 | TCCTTCCCATAACAA[A/T]CAACAAATTAAAGAA | 6596 |
| rs559108353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047516 | GCATGCTGGCGCAGA[A/C]CTGTAATCTCAGCTA | 6596 |
| rs559113656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068133 | AGAGAGACCATTCAT[C/T]GCATTTCTGAAAACA | 6596 |
| rs559164906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054791 | ATTAGCTGGATGACC[C/T]TAGGCAACTTAACCT | 6596 |
| rs559260416 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | HLTF | GRCh38.p7 | 3:149038620 | CAATCAATCTTTCCG[-/A]CTTAGCCCTGCAAGT | 6596 |
| rs559387256 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149075486 | GAGGCGGAGGTTGCA[C/G]TCAGCCGAGATCACA | 6596 |
| rs559402853 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149061180 | GCTCAAGTGATCATC[C/G]CGCCTTAGCCTCGGG | 6596 |
| rs559426193 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030453 | AAAACAACTTTGTAA[A/C]TGTCTGGGCAAAGAA | 6596 |
| rs559501404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082346 | CGCCTGTAGTCCCAG[A/C]TACTTGGGAGGCTGA | 6596 |
| rs559501517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149075130 | ATAAATTAATATGTA[C/T]AAAATGCGGACTTAG | 6596 |
| rs559614646 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149068970 | TTCCCAGGAGCCCTT[A/C]ACGAAAATGCAAAGT | 6596 |
| rs559717740 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149055156 | ATTCAGCAAACATAA[C/T]CCAATTCACCTGATG | 6596 |
| rs559820062 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032025 | CAGTATATAACGGAA[C/T]TTATTGCTATTTGAA | 6596 |
| rs559883661 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149080382 | TTCCTTGAAAATATA[A/C]AAGAAAGCTGCTTCA | 6596 |
| rs559931921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149057059 | AGCCTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 6596 |
| rs560041667 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087877 | CAGGCATGAGCCACC[C/G]TGCCAGGCCGGTAGT | 6596 |
| rs560045581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056478 | CAAAATTAAACTGGA[A/C]GGTGAGCAAAGTATC | 6596 |
| rs560067987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149052417 | AAAGTTTCAAGAAAA[A/G]AAACCAAGGTGGACT | 6596 |
| rs560068218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044470 | AGCTTCCTTCCTCCT[A/T]TTTCACCAGCCATTG | 6596 |
| rs560076826 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149083831 | GGCTGAATTGGGAGA[A/C]TTGCTTGAGTCTGGG | 6596 |
| rs560121334 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043609 | TATACAAAATACAGT[-/G]GTACAATGACAACAT | 6596 |
| rs560162219 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081668 | GGAGCCAATAAGGCA[C/T]ATAAAATTATGTTCT | 6596 |
| rs560195406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149046984 | TATAACTCACAGTAA[A/G]AAACACATTCTATCC | 6596 |
| rs560250697 | snp | C/T | 1.78902e-05 | 0.00299078 | missense | HLTF | GRCh38.p7 | 3:149039180 | TTGATTCAACTCTTT[C/T]CTTTTGGGCCATGGA | 6596 |
| rs560271593 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086232 | ATCGCCCAGGGAACG[C/T]AGAGGAACGCGGGGA | 6596 |
| rs560287026 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031900 | AAGGTCTGACCTTAT[C/T]TGAAATACGAAAAAG | 6596 |
| rs560424971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077017 | ACTTTGGGAGGCCGA[A/G]GTGGGAAGATCACGA | 6596 |
| rs560459798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149049884 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 6596 |
| rs560460855 | snp | C/G | 5.10738e-05 | 0.00505315 | intron-variant | HLTF | GRCh38.p7 | 3:149041477 | CTGAACCTGTACTGA[C/G]CAAAAAACTAACCTG | 6596 |
| rs560540290 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon | HLTF | GRCh38.p7 | 3:149040079 | TTTCTCACTGTCACG[A/T]GCTAATTCTTCTGGA | 6596 |
| rs560549088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062874 | AGAAAAAAAGTAGTA[A/G]AAAGATGAGTGATTA | 6596 |
| rs560666257 | in-del | -/TAAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149077291 | AAATAAATAAATAAA[-/TAAA]AATAATAGCTTGTTG | 6596 |
| rs560828421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032570 | AAGAATATGGCTGTA[C/T]GAATAGAAGTTACAG | 6596 |
| rs560843701 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045293 | CTCAGTGAGGTCTTC[C/T]TTAATACCCTACTAA | 6596 |
| rs560878903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040211 | AAGAACAAATATAAA[C/T]ATGCCTAAAAATTTT | 6596 |
| rs560965394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149048346 | ATATACACATCTCAA[G/T]ATACAGTTTTGCTCT | 6596 |
| rs560983399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062121 | TCCTCATAAGAAAAA[C/T]AGAAATAAAAATATA | 6596 |
| rs561047035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047957 | GTTAAAATAGTAAAG[A/T]AAGTGCCAACTGGTT | 6596 |
| rs561083562 | snp | A/T | 0.000399281 | 0.0141238 | missense | HLTF | GRCh38.p7 | 3:149046107 | GCTCTGCCTTCATTT[A/T]TCACAGACTGATAAA | 6596 |
| rs561254023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149083217 | GATTGCACCATTGCA[C/T]TCCAGCCTGGGCAAT | 6596 |
| rs561287858 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149077099 | CTAAAAATACAAAAA[C/T]TAGCTGGGTGTGGTG | 6596 |
| rs561318100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149076369 | CAACCCTTATTGAGC[A/G]CTTACTATGTGCCAA | 6596 |
| rs561331180 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HLTF | GRCh38.p7 | 3:149049953 | GCTGAGATCACACCA[C/T]TATATTCCAGCCTGG | 6596 |
| rs561377514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149046930 | GAATCAAGTGGATAG[C/T]ACTGCCAACTAGGTT | 6596 |
| rs561426745 | snp | A/G | 1.66319e-05 | 0.00288369 | missense | HLTF | GRCh38.p7 | 3:149050260 | GTTAAAATATTATAC[A/G]TAGTCAAAACAATAT | 6596 |
| rs561441164 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031756 | GTTTTTGAAAGCCCA[A/G]TAAAATTAATTCTTG | 6596 |
| rs561552109 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030663 | CCAGGTAACTTCCCA[A/G]CTGCTCCTAATGCTA | 6596 |
| rs561574362 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149043530 | AAGTCAACAAAGAAG[C/T]TGCTGAACTTCAGAG | 6596 |
| rs561577590 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149074528 | ACCATAAACAATCAG[A/C]AGGGTGATTTTTAGA | 6596 |
| rs561656055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079364 | GGGCAAAAGGGTAAC[A/G]ACAGTTTCTAAAAAA | 6596 |
| rs561737023 | snp | C/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031029 | TAATCTTTCTTTGGA[C/T]TAAAGTTTCCCTTTG | 6596 |
| rs561755263 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058327 | CCTCCCAAAGTGCTG[C/T]AATTTCAGGCATGTG | 6596 |
| rs561783360 | in-del | -/TTG | 0.00636936 | 0.0560724 | intron-variant | HLTF | GRCh38.p7 | 3:149055684 | CATTAAGACGAACAT[-/TTG]TTTTATGCAGTTTTC | 6596 |
| rs561805446 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087298 | CCCTCCATGGCTCTC[C/T]TTCCAGAGTCTGAGG | 6596 |
| rs561819857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149036230 | ATAGACCCCTGGTAA[A/G]TGGTTTTTAAATAGT | 6596 |
| rs561831612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033277 | GAAATACATATAAGA[G/T]CTACATAAATGGAGA | 6596 |
| rs561833530 | in-del | -/AT | | | intron-variant | HLTF | GRCh38.p7 | 3:149071892 | CATCTCTACAAAAAA[-/AT]TTTTAAAAAATTAGC | 6596 |
| rs561848674 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149069940 | ATGAATGTAAGTTTT[A/G]GATATTGCATATGAA | 6596 |
| rs561905648 | in-del | -/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031895 | ATAAAAGGTCTGACC[-/T]TTATTTGAAATACGA | 6596 |
| rs561909390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149034351 | GGTTAAATATATTAC[A/G]ATATATCTATATGGT | 6596 |
| rs561947228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065693 | AGATTAGCCAGGCAT[A/G]GTGGCGGGCACCTGT | 6596 |
| rs561976341 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036334 | TCGCTCTGTCACCAG[G/T]CTGGAGTGCAGTGGC | 6596 |
| rs561985933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149050022 | GGAGGAGTGGAGAAA[A/C]GAAAAATACTCCTAA | 6596 |
| rs561987931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149058017 | TGCACGAATTCCTAT[C/T]GCTGCACAACTTTGT | 6596 |
| rs562097900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064965 | TTTGCATAATAAAAA[C/T]GACTTAAATTGCTAC | 6596 |
| rs562145402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072058 | ACCCTGTCCCAAAAA[A/C]TTAAGAAATTGAAAT | 6596 |
| rs562172951 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149077592 | GCTTATAAAGAAGAG[C/T]TAGGGAATGAGATGT | 6596 |
| rs562173006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086130 | ACACGGGACTCGCCC[C/T]AGGAGCCCCTACTCG | 6596 |
| rs562227001 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149060730 | AAATGGGCAAAACAG[C/G]ACATTAGAATATAGG | 6596 |
| rs562265583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057283 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 6596 |
| rs562394189 | snp | C/T | 8.75128e-05 | 0.00661428 | intron-variant | HLTF | GRCh38.p7 | 3:149050197 | TTTCTTACATTCAAT[C/T]TTTAAAAGATCTGTT | 6596 |
| rs562396833 | snp | C/T | 0.000288198 | 0.0120007 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086298 | AGACCGAGCGCCCCA[C/T]CCCCTCCGCCCCCTT | 6596 |
| rs562412438 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085535 | CCAAAATTTCAATAG[C/G]GATTGAGCTATATAA | 6596 |
| rs562422104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064125 | CAACCTTACTTCTTT[C/G]CTTCTACTGCTAACT | 6596 |
| rs562550391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033212 | TATTTAACATTGTTT[A/C]AGAAGACCCAATTAC | 6596 |
| rs562591993 | in-del | -/GAGA | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149051033 | CTGGGAAGCTATGAG[-/GAGA]GAGATGATGAAGTCC | 6596 |
| rs562670009 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | HLTF | GRCh38.p7 | 3:149033894 | TAAAAATTTTAAAGC[-/T]TTTTCATGACCAAAA | 6596 |
| rs562681934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078847 | GGGCGACAAAGCAAG[A/G]CTCCGTCTCAAAAAA | 6596 |
| rs562717883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077118 | CTGGGTGTGGTGGCA[C/T]GCGCCTGTAGTCCTA | 6596 |
| rs562737305 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149083411 | ACACTAGAGTTTACC[A/G]AAGTCATAGAGATTA | 6596 |
| rs562752669 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149034620 | TTCATCTAAATGTAC[A/T]TATGAGGTAGTCTCC | 6596 |
| rs562775707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064028 | TGACCTATTTCACTT[C/T]ACAAAGAAAATGAGA | 6596 |
| rs562849717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085421 | TTGAACCCGGGAGGC[A/G]TAGGTTGCAGCGAGC | 6596 |
| rs562852118 | snp | G/T | 3.30726e-05 | 0.00406635 | missense | HLTF | GRCh38.p7 | 3:149071304 | TTTTCTGGTCGGTCC[G/T]TCTCAGAAAAATTTG | 6596 |
| rs562913201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037701 | GTATCTCAGTAGAAT[C/T]CCTACATGTTAAAAA | 6596 |
| rs562930037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149071849 | CTCAGGAGTTTGAGA[A/C]CAGCCTGGATAACAT | 6596 |
| rs562976746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056590 | ATGTTCCAAGACCCT[C/T]AATAGATACTTAAAA | 6596 |
| rs563137546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060453 | TTTAATTTGCAACTA[C/T]TTATTCACTTTTCCT | 6596 |
| rs563163375 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149077496 | TGGGCGGATGTTTGT[C/G]AAAACAATTTTACAG | 6596 |
| rs563176729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149061070 | ATACAAAATGGAGTA[A/C]CACCGTTATTGTTTT | 6596 |
| rs563324882 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149076628 | AGTCAGGATGGAACT[A/C]GGTAAGAAAAATATA | 6596 |
| rs563416040 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088490 | GTGAGCCGAGATCAA[G/T]CCACTGCACTCCAGC | 6596 |
| rs563416280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149080466 | AGTATTAGACAGATA[C/T]TCATCTCTAGACTTT | 6596 |
| rs563670105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149065619 | CGGATCACCTAAGAT[C/T]AGGAGCTCGAGACTA | 6596 |
| rs563692379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149051624 | CCGGCACTTTGGGAG[A/G]CCAAGGCGGGTGGAT | 6596 |
| rs563706907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058771 | GCTTCTCTTTCAAAG[A/G]TATACTTAGTTTGGT | 6596 |
| rs563781079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065107 | CTTGGCCTTCACCTT[C/T]TCGAAAGGAATACCG | 6596 |
| rs563903875 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087761 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACG | 6596 |
| rs563928127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074900 | GATACTTAAATTGAG[A/G]TCACAAGTACAAATG | 6596 |
| rs563938397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149066353 | GCCCAGCTTTGCATT[A/C]TTCTTTATATTAAAA | 6596 |
| rs563977716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149067286 | TGGTACAGATAGTGT[A/G]GTGAATGGACTTAAA | 6596 |
| rs564045136 | in-del | -/GA | 0.00557542 | 0.0525036 | intron-variant | HLTF | GRCh38.p7 | 3:149069817 | TCAATGATAAAATGT[-/GA]GTTTTCAATAGAAAA | 6596 |
| rs564096673 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060100 | AGGAGAATTTTTCAA[G/T]GAAACAAACAGTTTG | 6596 |
| rs564184364 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057528 | TCCTGCAGGGCAGAC[C/T]GTGGGACTTGAGTAT | 6596 |
| rs564188035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149080289 | TGGTTGCACAACCTT[C/G]TGAGTATTCTAAAAA | 6596 |
| rs564246738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051327 | GGTCACTATAGAATA[C/G]CTAACTGAAGACGTA | 6596 |
| rs564302966 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149066678 | GAAAAATAAGAGAAA[A/T]CCTTATTGTTAATTG | 6596 |
| rs564397528 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086827 | CTTCCTTTATCCTAC[C/G]AGTCCTAAGACTGAA | 6596 |
| rs564411407 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149035275 | TGATTAATCAATTTG[G/T]TTTTTTTTTTCATTT | 6596 |
| rs564497171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065075 | TTATCTCAAAAAAAA[A/T]AAAATAAATAAAACT | 6596 |
| rs564572037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149072120 | AACGCCAAAAAGGCA[C/T]ATAAATCAACTCTAG | 6596 |
| rs564725620 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149042900 | GACCTTTCCCTTTTG[C/T]ATATCTGGACTAGCA | 6596 |
| rs564792946 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HLTF | GRCh38.p7 | 3:149075568 | AAATAAATAAATAAA[C/T]AAATAAACACTTCCA | 6596 |
| rs564872912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069114 | GCAGTTGGCACTAAG[G/T]TATATTAGTACTAGT | 6596 |
| rs564908133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149061983 | GTGTAGAAAGTTTAA[C/T]AGTGATTAAGTGCCT | 6596 |
| rs564958948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149083108 | TACAAAAAATTAGCT[A/G]GGCATGATGGCGCAT | 6596 |
| rs564994309 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051762 | ATAATTCCAGCTACT[C/T]GGGAGGCTAAGGCAT | 6596 |
| rs565050688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055484 | GCAATAATGTGCCTC[C/T]ATGAAAAGATAAATT | 6596 |
| rs565135790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047863 | GAAATCTTTGTCTTT[C/G]CAAACAAGCATCACT | 6596 |
| rs565203560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149062722 | TGTGAAGAACTGAAA[C/T]GATCAAGAATGCTTT | 6596 |
| rs565259379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060342 | ACCTAATTTTGTAAT[G/T]ACTATTCATACTACA | 6596 |
| rs565319880 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149053405 | GTAGCACCTCTCCAC[A/T]CTCTCTCTTACTCCC | 6596 |
| rs565341467 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030550 | AGACTGTGTTGTTTT[A/T]TGCCAAAAACTGTTT | 6596 |
| rs565362270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149052032 | GGTGGCATGTGCCTG[C/T]AATTCCACCTACTCA | 6596 |
| rs565529802 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149059893 | AGGGTAAGAAATAGA[A/T]TATCATTTTCACCCT | 6596 |
| rs565556524 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149037821 | ACCCAGTGCAAATTA[A/G]AAACTGAATTAGTCC | 6596 |
| rs565660475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067459 | TGGCTATATCGTTTA[A/T]CTGTTCCCTTGTCAA | 6596 |
| rs565697418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060621 | TTGAAGTCTAGATTA[G/T]GGGTATATAGTATAC | 6596 |
| rs565754638 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149074674 | TGGCTAACGGAACCA[C/G]TGAGGGTAGTAACTC | 6596 |
| rs565779761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149038033 | CTCAGAACATTCCAT[C/T]AATGATAATTTGTTT | 6596 |
| rs566021324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043164 | GAGAACAGGAAGAGA[C/T]GAAAGATGAGCTGGT | 6596 |
| rs566034209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051280 | GCATCCAAGTAAGAA[A/G]GAGATGAATATTTTA | 6596 |
| rs566068810 | snp | C/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030772 | TACCTGCTACTGCCT[C/T]AAAAAGGGACCAGGA | 6596 |
| rs566088670 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087141 | TCTTGGTGCAGGAAA[C/T]CCATCACATGTTTAT | 6596 |
| rs566103296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149035902 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 6596 |
| rs566129792 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149071885 | AGATCCCATCTCTAC[-/A]AAAAAAATTTTTAAA | 6596 |
| rs566195753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050686 | TAGAAGGCCCTTTAA[G/T]GCTGCATTAGTTAGC | 6596 |
| rs566202862 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087451 | ACAGGGCAGGAAGCT[A/G]GTGGTGGCGCCCAGC | 6596 |
| rs566219018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149036578 | ACAGGCATGAGCCTC[C/T]GCGCCAGGCCATATT | 6596 |
| rs566227880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037298 | ACATGGTAAAACCCC[A/G]TCTCTACTAAAAATG | 6596 |
| rs566262780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149073927 | TTTCCAGATGTTACC[A/C]TTAGGGAAAATTAGG | 6596 |
| rs566320526 | snp | C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030814 | GGCTAATTCACTGTT[C/G]CCTTTGAGCAAGAAA | 6596 |
| rs566425911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079711 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 6596 |
| rs566426235 | snp | A/G | 0.000399281 | 0.0141238 | missense | HLTF | GRCh38.p7 | 3:149048157 | AAAGAATTCTGGATT[A/G]GAGTACCTAGAAATA | 6596 |
| rs566446624 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085924 | TCTGCAAATACTTAT[C/T]TGCACGTCTGTGCAT | 6596 |
| rs566460240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149055776 | TCCTGATATTCACAA[C/T]CTTGTGTAATCTCCT | 6596 |
| rs566482386 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082963 | GCCATTTAAAAATAA[G/T]GAACGTGGCTGGGCG | 6596 |
| rs566483828 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085697 | GGGAAATTGGCCCCA[A/G]GCCACCCGTACCCGC | 6596 |
| rs566515916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149040364 | GGATAAAGGAGGGAG[C/T]AAAAGTATGTGATCT | 6596 |
| rs566586798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149047435 | TAACCTGAGGTCAGA[A/G]GTTTGAGACTAGCCT | 6596 |
| rs566596159 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061545 | TGGAACAAAAAAGAA[C/T]TGGCTCGTGGCCAGG | 6596 |
| rs566709250 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084691 | ACTCACTACTCCCGT[A/G]TAATAGCGTAGTCCA | 6596 |
| rs566739813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032835 | GGGCATGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 6596 |
| rs566811705 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | HLTF | GRCh38.p7 | 3:149077264 | AATAAATAAATAAAT[A/T]AATAAATAAATAAAT | 6596 |
| rs566823839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149069411 | GGGAGGCGGAGGGTG[C/T]AGTGAGCCAAGACTG | 6596 |
| rs566837698 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149051364 | GAAAATGTAAATAAT[C/T]ACCTATAGATAGAAG | 6596 |
| rs566906213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049931 | CAGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGATC | 6596 |
| rs566937334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149038593 | CTGAAACTTCAACCT[C/T]CTGGGCCCAAGCAAT | 6596 |
| rs567041962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062148 | TATAATCCTCATAGA[A/T]TAAAATGTTACTACA | 6596 |
| rs567053074 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149061367 | AGTGAGCGGAGATTG[C/T]GCCACTGCACACCAG | 6596 |
| rs567095498 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149077553 | TGAGGCAGTGGATAA[A/C]AGCTGAAGCAAAAAA | 6596 |
| rs567171207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032691 | ATTCTGGCCGGGCAC[A/G]GTGGCTCACACCTGT | 6596 |
| rs567190950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149038790 | AGTGCTGGGATTACA[A/G]GCATGTGCCACAGCA | 6596 |
| rs567225028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054998 | GTCAATCTGTAAATG[C/T]AGAGGAGTCAAACTA | 6596 |
| rs567306070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082032 | GCTTTTCTTCAAAAA[C/T]GTAACTAACCAAAAT | 6596 |
| rs567451329 | snp | C/T | 7.44837e-05 | 0.00610216 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084637 | TATTTTCTAGGTTAA[C/T]GCCAGAAATATAATC | 6596 |
| rs567624455 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149068421 | TAAAATCAAGTAATC[A/G]AATATCAAATATCAT | 6596 |
| rs567767139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045234 | TCTGGCTGAAACACC[C/T]CTTAATCCCAATCTC | 6596 |
| rs567778692 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085839 | TTGCAAAAAGTTTCC[A/G]TTCTCCTAAGAACAG | 6596 |
| rs567890009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149061342 | CGTGAAGCCAGGAGA[C/T]GGAGTTTCCAGTGAG | 6596 |
| rs567928705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149034726 | AAGGAGATGTACACA[C/T]AACTATAAATGTAGG | 6596 |
| rs568042284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149042491 | AGAAATGGCTGCCAA[A/T]TGCAGTCTAAGTCAG | 6596 |
| rs568109524 | in-del | -/AAAG | 0.00119737 | 0.0244387 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030387 | AGAACTGTACAAAAC[-/AAAG]AGACATTTTTTAAAC | 6596 |
| rs568125160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033814 | AAAATGTGAAAATAA[A/G]GCCTTCTGTCCTAGG | 6596 |
| rs568146604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055873 | CTGAGATAGATTACA[A/T]AAGAAGTTTCCGTAT | 6596 |
| rs568152233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065158 | ATGACACATTATTGT[A/G]AGAAAAATTCAAGAA | 6596 |
| rs568270309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049176 | AAAATAAGTACTTAT[C/T]AGCACACCTAATTTT | 6596 |
| rs568273428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073022 | GGTACAAATGTTCAC[A/G]TATGGATTTATTCCT | 6596 |
| rs568288270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058379 | TTCCTTTAATTTGCA[A/T]CTCCCCAATAATTCT | 6596 |
| rs568347382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064432 | AAGCTAGCTTTCTAG[C/T]ATTATCTGCTGTTAT | 6596 |
| rs568432451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149056788 | GATGCACTTACATGC[A/C]AATTTTTGTTAACCA | 6596 |
| rs568435088 | snp | C/G | 0.00130366 | 0.0254976 | intron-variant | HLTF | GRCh38.p7 | 3:149063044 | AATATAAGGGTCATG[C/G]TCATCTCTATCTCTC | 6596 |
| rs568442229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149059112 | CATTATTTAAAATTA[C/T]ATTGACTTGCTTATT | 6596 |
| rs568481525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033413 | TTATAACTAAAATCT[A/G]AAGTTCAATTCAAGA | 6596 |
| rs568543912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149070672 | TGGAATACAATTTCA[C/T]ATAACATTGTTTTGT | 6596 |
| rs568715610 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149039754 | TAAAATTAGTCTAAA[A/C/T]GTTTTTATCATAAAG | 6596 |
| rs568808604 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076229 | TATGACTCCTTAATA[A/T]TATTTTTCTAATCTA | 6596 |
| rs568832071 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HLTF | GRCh38.p7 | 3:149032909 | CGGAGCTTGCAGTAA[A/G]CCGACATTGCGCCAC | 6596 |
| rs568883908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049076 | GATTTGCTAACTAGT[C/T]GTTATCATTATTTAA | 6596 |
| rs568894720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149069642 | TTAGCTAGAGAAAAA[C/T]CACTCAAGATGGGAG | 6596 |
| rs568910450 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149057930 | ATTTACAGAGTTACA[A/G]ATGGTCTATATTCAG | 6596 |
| rs568994187 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032058 | TTCATTAAAAATAGG[C/T]TCATATATAGAAGAA | 6596 |
| rs569054454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063752 | TTTCTTTGTACTCAT[A/C]CAGCCCATCCCCACA | 6596 |
| rs569099838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078442 | GTAGTCCCAGCTATT[A/C]AGGAGTCTGAGGTGG | 6596 |
| rs569152405 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043424 | AAAATAATGGAACAG[A/G]AAACAATATTTAAAG | 6596 |
| rs569179871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062251 | GTTAAGTTTTTCTCA[G/T]GTCCTCACCATTATT | 6596 |
| rs569216951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063002 | TAGTTTCAAATAAAA[G/T]AATGTATTTGAAAGA | 6596 |
| rs569273934 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149077464 | TCTGAGCTCACCAAG[C/T]ACAAAAAAACCTCCC | 6596 |
| rs569375536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076538 | AGGTAGCAGAGCTAG[C/G]ATCTGAACCCACACA | 6596 |
| rs569395934 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051089 | GAACAGGGTGGAAAG[A/G]ACAGGTGTGAAAAAC | 6596 |
| rs569399615 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149046707 | ATTAAAATCAAAAGT[A/G]TATAAATAAGTAATT | 6596 |
| rs569428758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149055798 | TAATCTCCTCCCATA[C/G]TCCACCAGGACTGGT | 6596 |
| rs569467301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149048364 | ACAGTTTTGCTCTAA[C/T]TTTTAGCTCTCACAT | 6596 |
| rs569619963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079638 | TCTTGCTGTCACCAG[A/G]CTGGAGTACAGTCGC | 6596 |
| rs569657219 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HLTF | GRCh38.p7 | 3:149073854 | CAATCCTTTTCATTC[A/G]CTATCAGAAGATTAT | 6596 |
| rs569702797 | snp | C/T | 3.38662e-05 | 0.00411484 | intron-variant | HLTF | GRCh38.p7 | 3:149073197 | TTTAAAATTCACTTT[C/T]AGATTACAAAATAAA | 6596 |
| rs569745671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051832 | CTGAGACTGTGCCAC[C/T]GCACTCCAGCCTGGG | 6596 |
| rs569758966 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149070642 | TTAATACTCTGCATA[-/AC]ACAATATTTGTGATG | 6596 |
| rs569784765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044593 | GACTCTCCTATCCAA[C/T]TAATTATTTGATATC | 6596 |
| rs569867130 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037286 | CCAGCCTGGCCAACA[A/T]GGTAAAACCCCGTCT | 6596 |
| rs569877150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149035827 | CATGATCATGAGAAC[C/T]GTTTTAAGCTAAAAA | 6596 |
| rs569950316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051437 | ATTTACAGCTGTAAG[A/C]ATGAATGAAATTTCC | 6596 |
| rs569964837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149036529 | CTTGACCTCATGATC[C/T]GCCCACCTCGGCCTC | 6596 |
| rs570091828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149073105 | TAACATGTTTCATTA[C/T]AACTTAATATATTTG | 6596 |
| rs570185208 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149070909 | AATTAGCTGGGCATG[C/G]TGGCACATGCCTGTA | 6596 |
| rs570273263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043105 | TTCCTCCAAAAAAAA[A/G]AAATCTTAAAGCAAA | 6596 |
| rs570403173 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087075 | AATCTTAAATGGAAC[G/T]TAGAGTCCCCTCCCC | 6596 |
| rs570408385 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087112 | TTTTGTTATTTTTAA[G/T]GAAAATTTTCCTTTC | 6596 |
| rs570425623 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HLTF | GRCh38.p7 | 3:149065779 | AGGTTGTAGTGAGCC[A/G]AGGTTGCGCCACTGC | 6596 |
| rs570432886 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149035613 | GCAGTGAGCCGAGAT[C/G]GCGCCACTGCACTCC | 6596 |
| rs570494079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078917 | TTTCGACATGAAAAC[A/G]CATGTCTAAAAGCAT | 6596 |
| rs570505574 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086756 | AGGAGTGCGACTGCG[A/G]TGCCTGCGGTGCCGG | 6596 |
| rs570554404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149058894 | AATTTAATTCTATCT[C/T]AACCGAAATTTCCAC | 6596 |
| rs570621111 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149034424 | TTGCCAGGGGCTGGG[-/TC]GGGAGAGGAATGGGA | 6596 |
| rs570690510 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149032638 | AAACTATATAGGCAA[C/T]TCTGGCAAAATGACT | 6596 |
| rs570693973 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149057437 | CTCAAAACAAACAAA[-/C]CAAACAAACAAAAAA | 6596 |
| rs570745471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064223 | ATCTTACCCTAACTC[A/G]CCACCTTTCTATTTC | 6596 |
| rs570777857 | snp | A/G | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029642 | AATGCTAATGCATAA[A/G]CCTTGACAAGTAGTA | 6596 |
| rs570780530 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086034 | GGTATCTAATGGATG[C/T]TTTGTTAAATAAAGC | 6596 |
| rs570786191 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149037863 | AGGCCAAACAGCCCC[-/T]TTGTACACGTAGAAA | 6596 |
| rs570822440 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149056862 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 6596 |
| rs570823928 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149050061 | CTAAATAAAATGCAA[A/C]CCTTTCACGCAAAAA | 6596 |
| rs570887055 | snp | A/C | 0.000467626 | 0.0152838 | intron-variant | HLTF | GRCh38.p7 | 3:149059686 | AAAACAGAAAAAAAA[A/C]CAAAAACTAGAAAAC | 6596 |
| rs570947553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045618 | CACTGAAGTTTTTAT[G/T]TTTTGAAGATTCCCC | 6596 |
| rs570989081 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149056436 | AATTTCTGAGTTTTT[-/A]AAAAAATTGTATTTT | 6596 |
| rs571038431 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086506 | GAGTCCAGTCAGACG[A/T]CGACGCCGTCTCCTT | 6596 |
| rs571064677 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050684 | ATTAGAAGGCCCTTT[A/G]ATGCTGCATTAGTTA | 6596 |
| rs571065744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149082172 | TAGTGATAGAAGACT[C/T]GTGTGGCCGGGCGCA | 6596 |
| rs571151730 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079674 | CTCGGCTCACTGCAA[C/T]CTCTGACTCCCTAGT | 6596 |
| rs571154020 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149039317 | AAATCTCTTCAATAA[A/G]TTCTTTCACTCATTT | 6596 |
| rs571154429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053146 | ATCCTTTACTTGAGA[G/T]CCAGGAAGACGGTAT | 6596 |
| rs571220442 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075376 | AACATGGCAAATCTC[C/T]GTCTCTACTAAAAAA | 6596 |
| rs571375167 | snp | A/C/T | 4.94616e-05 | 0.0049728 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149060689 | ATTTTTCAGTTTGCC[A/C/T]AAAAATAAAACAAAA | 6596 |
| rs571541685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149046450 | AATAAAATTATTAAA[A/C]CAAATGTATGGAAAT | 6596 |
| rs571626964 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149036597 | CCAGGCCATATTACC[C/G]CAATACTTATACAAT | 6596 |
| rs571697973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043536 | ACAAAGAAGTTGCTG[A/G]ACTTCAGAGGGAAAA | 6596 |
| rs571713230 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149071486 | ACATTAAGCCATTCC[-/T]TTTTTCACATGCAGA | 6596 |
| rs571715579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037354 | GGTGCCTGTAATCCC[A/T]GCTACTCAGGAGGCT | 6596 |
| rs571743935 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087539 | TGTTACACGCCTGTC[A/T]GCACAATAATATTAG | 6596 |
| rs571764469 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081429 | ATTAAGTGCTCAAAT[C/T]GCAAGTCCAACAGAA | 6596 |
| rs571810798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050995 | TGATTAAACTGAAAA[C/G]AGAAGATACCAGGGA | 6596 |
| rs571830518 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149043344 | CAAAAAAATGTAAAA[G/T]ATCAGAAATAAAATG | 6596 |
| rs571853426 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149066986 | AAAAACTAGGAAGAA[A/T]GGTAATTCAGAAGAG | 6596 |
| rs571898000 | in-del | -/A | 0.426813 | 0.17674 | intron-variant | HLTF | GRCh38.p7 | 3:149083928 | GTCTCAAAAAAAAAG[-/A]AAAAAAAAAAAAATC | 6596 |
| rs571935971 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085667 | CCTATTCTGGTATCC[-/A]AACCACGCCACCGTG | 6596 |
| rs572009280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149058626 | GATGCATGGAAATTT[A/G]AAATGTAGTGGCATT | 6596 |
| rs572012256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074735 | CTTGTGATTCACTAA[A/G]TTATTCTCAATAACT | 6596 |
| rs572034981 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087080 | TAAATGGAACTTAGA[C/G]TCCCCTCCCCACCTC | 6596 |
| rs572062413 | in-del | -/T | 0.00681628 | 0.05798 | intron-variant | HLTF | GRCh38.p7 | 3:149079581 | GCTGTGAGCAAAGGT[-/T]TTTTTTGGGGTTTTC | 6596 |
| rs572073663 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | HLTF | GRCh38.p7 | 3:149065681 | CTAAATAGACACAGA[-/T]TAGCCAGGCATGGTG | 6596 |
| rs572077537 | snp | C/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087568 | AGGTGGTCAGCTTTT[C/G]TTTTTTCTTTTTTTT | 6596 |
| rs572259697 | snp | C/T | | | synonymous-codon | HLTF | GRCh38.p7 | 3:149046181 | TTTACGTTCTGGTAA[C/T]TCCAAAACAGGTTTT | 6596 |
| rs572266911 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HLTF | GRCh38.p7 | 3:149036883 | GATATGTTCAATGAA[A/G]AACACTCAACTTACT | 6596 |
| rs572313299 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149062723 | GTGAAGAACTGAAAC[A/G]ATCAAGAATGCTTTT | 6596 |
| rs572491820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086176 | CATTTATTTCTCCGG[C/T]GGCCACATATGCGAC | 6596 |
| rs572520510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149034354 | TAAATATATTACGAT[A/G]TATCTATATGGTTTT | 6596 |
| rs572523645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149065561 | AACTAAAAATCTGCC[A/G]GGCGCAGTGGCTCAT | 6596 |
| rs572580855 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149060412 | AATTGTTTTAAGTAT[-/A]GTTTAAATATTATTA | 6596 |
| rs572589877 | in-del | -/GGAA | 0.00557542 | 0.0525036 | intron-variant | HLTF | GRCh38.p7 | 3:149043367 | TAAAATGATACCTAT[-/GGAA]GGAACACAGATAAAA | 6596 |
| rs572728190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149072675 | TCTAACAATAAGCAG[A/G]GTAAATATGGTAACT | 6596 |
| rs572738662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149079063 | AGCTGAAGATAGGTC[A/G]ATTGAGATTATACAA | 6596 |
| rs572747804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149064988 | ATTGCTACCCAATTC[C/T]GGAGCAACTGAAGGG | 6596 |
| rs572804133 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051677 | ACCAGCCTAGCCAAC[A/G]TGGCGAAACCCTGCC | 6596 |
| rs572825998 | snp | A/T | 1.64991e-05 | 0.00287215 | synonymous-codon | HLTF | GRCh38.p7 | 3:149073279 | ACTATAGCTTGGTCC[A/T]GCTCTTCCAGAGCCC | 6596 |
| rs572846012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149048779 | AATTTACACCCACTT[C/T]AAGTTTACAAAGTTA | 6596 |
| rs572891340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149076183 | AATATATTTTCTAGA[C/G]ACAAACTACAGAAAT | 6596 |
| rs572911138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149038929 | TGTTATTTATTTCTA[A/C]AGTTTGCCTAAGAAT | 6596 |
| rs572977604 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149079634 | AGAGTCTTGCTGTCA[C/T]CAGGCTGGAGTACAG | 6596 |
| rs572978658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062501 | GCAGAGACAAATTTG[C/T]GATGACTTGTGTAGA | 6596 |
| rs572985793 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061834 | GGAGCAAAACTCTGT[C/T]TCAAAAAAAAAAAAA | 6596 |
| rs573048454 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149042760 | GCACAGCACTCTACA[A/C]TCCAAGCACCCCTAA | 6596 |
| rs573126471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149076762 | CAATAAAGAATGGTA[A/G]AATGAGGACTTTCAA | 6596 |
| rs573142964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060309 | AACAATAATAGTATT[G/T]CCAGGAAGACATTCT | 6596 |
| rs573177090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067798 | ATTGACTGGCAAAAT[C/T]GTTCAAAGATTATAA | 6596 |
| rs573346892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054473 | CTCTTCCTCCTCTGA[C/T]ATAAGAAGAATGGCG | 6596 |
| rs573472792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045809 | ACGATTTTGGAAATA[A/G]AAGCAAGCAAAATCT | 6596 |
| rs573504908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149046628 | CTAAGTATCTATTAA[C/G]TGCCAGGCACTGAAT | 6596 |
| rs573550328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149052484 | AAGAAGGTTTAGAGA[C/T]AGCTTACAAAATAAG | 6596 |
| rs573575601 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030905 | CCCTATAACACAACA[C/T]TGTCTCCGATCTCAT | 6596 |
| rs573590205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053296 | GTGTATGGCTCATAG[A/C]GGTGGATCCCTCCTG | 6596 |
| rs573667143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149037725 | TTAAAAATCTTCTGA[A/G]TTTCAGGTAACAAGT | 6596 |
| rs573696747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149045703 | GCTCACATTAAACCT[A/G]ATCTTGCTTGGACCA | 6596 |
| rs573701235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149082300 | CGTCTCTACCAAAAA[C/T]ACAAAAAAATTAGCC | 6596 |
| rs573751566 | in-del | -/TT | | | intron-variant | HLTF | GRCh38.p7 | 3:149044289 | TACTTTAAAAATAAC[-/TT]ATTTTCTGAGAACAG | 6596 |
| rs573755481 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149079975 | TGTTAATTGTAATCC[C/G]TAAAGCAATCATAAG | 6596 |
| rs573777634 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088518 | AGCCTGAGCAACAGA[A/G]CGAGACTCCATCTCA | 6596 |
| rs573813732 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149075457 | CTAAGGCAGGGAGAG[A/T]TGCTTGAACCCTGGA | 6596 |
| rs574096859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149074146 | AACAAACTCCAAGAG[A/G]GAATAAATGTTTCAT | 6596 |
| rs574241486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149067145 | TTTAATTCTTAGAAA[C/T]CAAATATAAATGTAT | 6596 |
| rs574313193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149053253 | AAATGTAATCTCCAG[A/G]GTTGGATGAGGGGCC | 6596 |
| rs574325844 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149073130 | TATTTGAAGACCACA[A/G]ATACCCACACGTACA | 6596 |
| rs574349860 | snp | A/C | 1.65113e-05 | 0.00287322 | intron-variant | HLTF | GRCh38.p7 | 3:149063401 | AGAGTCTAAATAAAC[A/C]TATGACATAATCAAA | 6596 |
| rs574354495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149059473 | GAAGAAATATCTCTG[C/G]TATTCAGAGGAGTAA | 6596 |
| rs574368519 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149070700 | TGTCTTTACTTTTTA[A/C]AAGAAAACCTATGAA | 6596 |
| rs574390072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149060246 | AATAAAACATATTTT[A/C]AAGAAAAAGAAAAAA | 6596 |
| rs574484682 | snp | C/G/T | 0.000181716 | 0.00953032 | intron-variant | HLTF | GRCh38.p7 | 3:149055421 | AAAATGAACCACTGA[C/G/T]AGAACCTTTAGCTGT | 6596 |
| rs574514163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149071084 | GAACACATCTTTATA[C/T]CACTATTTTAACTAA | 6596 |
| rs574546985 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149052014 | CAAAAATTAGCCGGG[C/T]ATGGTGGCATGTGCC | 6596 |
| rs574556252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149061785 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCATTGC | 6596 |
| rs574586214 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149049164 | TCACAAGTTTATAAA[A/G]TAAGTACTTATTAGC | 6596 |
| rs574593031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149054673 | AATGTCAATGTTTCA[A/G]AACAGAAAAGCAATC | 6596 |
| rs574673282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149049828 | TGAAACCTCATCTCT[A/G]CTGAATAACAAAAAT | 6596 |
| rs574693475 | snp | A/C | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086233 | TCGCCCAGGGAACGC[A/C]GAGGAACGCGGGGAA | 6596 |
| rs574730137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149046962 | GTGGCTCTTGAAGCT[C/T]TCTCACTATAACTCA | 6596 |
| rs574784654 | in-del | -/AA | 0.00318978 | 0.0398085 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031158 | TATTAACAAAAAAGT[-/AA]AAAAAAAAAAGAAAA | 6596 |
| rs574786788 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HLTF | GRCh38.p7 | 3:149057041 | GTGAACCCCAGGGGG[C/T]GGAGCCTGCAGTGAG | 6596 |
| rs574829577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149084309 | GCTTCAGACACCCTA[C/T]TGAGAAGCTTAAACA | 6596 |
| rs574841107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149062376 | TAAATCTGAAGCAAT[G/T]AGATTTAGATAACAC | 6596 |
| rs574868094 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149047596 | GCAGTGAGCCAAGAT[C/T]GCGCCACTGCCCTCC | 6596 |
| rs574884499 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149074509 | AAAAAGGAAAAGAAA[C/T]AGAACCATAAACAAT | 6596 |
| rs574910496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149059004 | CTTGGACCAAAAGTC[A/G]GCTCTTTCTCATGAG | 6596 |
| rs574919278 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149050116 | TTCTATATATCGTTA[A/T]GTATCTAAAGAGAAA | 6596 |
| rs574950737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149084033 | CAAAGATTTTATTAC[A/G]AAGATATATTACAAA | 6596 |
| rs574971920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032955 | GTGACAGAGCGACGT[C/T]TCAAAAAAAAAAAAA | 6596 |
| rs574981802 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149033930 | CAGTTTAAAGACAAG[A/G]AAGAGTATGGGATAA | 6596 |
| rs575290930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149067912 | ACTTTGGGAGGCTGA[C/G]GCAGGTAGATGGCTT | 6596 |
| rs575341473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149076885 | GAAATCTGGGTAACA[C/T]TTATTCAAGAATAAA | 6596 |
| rs575378396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149068622 | CTACATTTAATCCTG[A/T]ACTCTTGATTTTTAT | 6596 |
| rs575417629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149070976 | CTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG | 6596 |
| rs575435656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149032467 | TTTGCCTAATGGCAA[A/C]AACCGCAATTACTTT | 6596 |
| rs575577597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149062732 | TGAAACGATCAAGAA[C/T]GCTTTTGTCAAGTTA | 6596 |
| rs575625546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149058501 | GTGGTCTTTTTCCAA[C/T]TGTTTGGAAAGTTCT | 6596 |
| rs575737116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149065472 | AAGCACTTAAAAAAT[C/T]CCCCCTTAGAGTTAA | 6596 |
| rs575738934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149057953 | ATATTCAGCTTCATT[A/G]TATTTTTGTCCAGTT | 6596 |
| rs575768099 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149083111 | AAAAAATTAGCTGGG[C/T]ATGATGGCGCATGCC | 6596 |
| rs575865869 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HLTF | GRCh38.p7 | 3:149054526 | GGAAGTGGCAAGAAC[A/G]GTGAGTGGTCCTTAT | 6596 |
| rs575881894 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149044399 | TATCTTACTGATACT[A/C]AGCATTTCAATTTAA | 6596 |
| rs575946972 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031587 | CTAAAATGGAAAAAA[C/T]AGTACTCTTAACATA | 6596 |
| rs575993834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063182 | CTCCTGCCTCAGCCT[C/T]CTGGGTAACTGGGAC | 6596 |
| rs576062975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149034186 | TCATATAAATCCTAT[A/T]TTGAAACCAACTCGA | 6596 |
| rs576100382 | in-del | -/CTT | 0.00120361 | 0.0245022 | cds-indel, intron-variant | HLTF | GRCh38.p7 | 3:149031567 | ATGAGTGTAGTACTA[-/CTT]AACTAAAATGGAAAA | 6596 |
| rs576138980 | in-del | -/TTTAAGAGACAGA | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149035702 | GTTTTAAGAGTCAGT[-/TTTAAGAGACAGA]AAGTCCTAAAAATTA | 6596 |
| rs576163641 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073040 | TGGATTTATTCCTTA[-/T]CAGTACTTTTTATAT | 6596 |
| rs576182205 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149044042 | CAAAGATTAAACTTA[A/C]AAGCTCTAAACCAAA | 6596 |
| rs576257676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149036166 | CAAAAAACACAACAA[C/T]AGCAATAAAATGGTG | 6596 |
| rs576268048 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038107 | ATATATGCTAAAAAT[A/G]CAGCTTCCTGGGTCT | 6596 |
| rs576275004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149043413 | CAGAGAGAAATAAAA[C/T]AATGGAACAGAAAAC | 6596 |
| rs576304486 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030861 | AGGACTTATCTGGTG[A/G]GAGATTTGGCATATA | 6596 |
| rs576304866 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065786 | AGTGAGCCAAGGTTG[C/T]GCCACTGCACTCCCT | 6596 |
| rs576351600 | snp | C/T | 1.65018e-05 | 0.00287239 | missense | HLTF | GRCh38.p7 | 3:149034929 | TCACTTTTGTGATGA[C/T]AACTTCTTGCTTCTG | 6596 |
| rs576356448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041939 | ATCCAATATGAATCT[C/T]TCATCAAAGGGTATC | 6596 |
| rs576414744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HLTF | GRCh38.p7 | 3:149064654 | CTTTTAAAAAAGAGA[C/T]CCTAAATTTTTGTAC | 6596 |
| rs576483503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149071798 | ATGCCAATAATCTCA[A/G]CACTTTGGGAGACCA | 6596 |
| rs576529757 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070221 | TCTAAAAAGCTATTA[C/T]AATACTCCTCTCTTT | 6596 |
| rs576543274 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HLTF | GRCh38.p7 | 3:149072604 | AAGAAATCAGGCCAG[G/T]TCTAAAAAATCAGAA | 6596 |
| rs576587147 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149066465 | GTTAGAATCTAGGGG[A/G]ATTTAAATCAATATT | 6596 |
| rs576635006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078191 | AATCAATGTCAACTG[G/T]CCCCAAGAAAGTATA | 6596 |
| rs576708485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149078684 | AACACAGTGAAACCC[A/C]GTCTCTACTAAAAAT | 6596 |
| rs576719526 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HLTF | GRCh38.p7 | 3:149071875 | AACATAGTGAGAGAT[C/T]CCATCTCTACAAAAA | 6596 |
| rs576766252 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086707 | GGTTCTTCCCCGCCC[A/C]CAAGGCGGGCGCGCG | 6596 |
| rs576824970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149048659 | ATAAGTCTAGTGACT[A/G]TTCCATAAATTATCA | 6596 |
| rs576859762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149041134 | CATTAATACTTTTTA[C/T]ATTTTAGATATATTG | 6596 |
| rs576946831 | in-del | -/AA | 0.0115144 | 0.0749975 | intron-variant | HLTF | GRCh38.p7 | 3:149045108 | CAATAAATCTCTGAT[-/AA]ATCATGACTATTTTC | 6596 |
| rs576963660 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149035278 | TTAATCAATTTGGTT[A/T]TTTTTTTCATTTTTA | 6596 |
| rs576967040 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149050820 | ATTATTGGCCTACTA[A/T]TTGCCAGGTATCAAC | 6596 |
| rs576971168 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086840 | ACGAGTCCTAAGACT[A/G]AACCCCATTCTAAAG | 6596 |
| rs577074315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149050158 | AAGCCTGAATTTTGG[A/C]ACACTCTAGAAACCT | 6596 |
| rs577111520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149042827 | TAAAGTAACTCAACA[C/T]GTAACCCTGAGTCTT | 6596 |
| rs577171545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033238 | ATTACTGCAATAACT[A/G]AAGCTATATAATAAA | 6596 |
| rs577183755 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076461 | TACTATCATTATTCC[C/T]ATTTTACAAATGAAG | 6596 |
| rs577213175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149044747 | CCACTTATGCAGGTA[A/G]AAAGGCTTGAAGTTA | 6596 |
| rs577241327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149063150 | CTGCAAGCTCTGCCT[C/G]CCGGGTTCACGCCAT | 6596 |
| rs577325133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149033903 | TAAAGCTTTTTCATG[A/C]CCAAAAAAATGCAGT | 6596 |
| rs577326052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149044375 | ACTAATTATTCCCTG[A/G]CATGGTCATATCTTA | 6596 |
| rs577478779 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051932 | GGAGGCCGAGGTGGG[C/T]GGAACGAGGTCAGGA | 6596 |
| rs577494484 | in-del | -/CAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149078052 | AATTACAAAACTCAG[-/CAA]CAACAAACCACCCTG | 6596 |
| rs577496692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149077412 | TCTCCTGAAGTTCCC[C/T]GGAAGACCCCACTTG | 6596 |
| rs577634517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149051579 | ATTAAAAATATTCCA[C/G]GCCAGGTGCAGTAGC | 6596 |
| rs577637656 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HLTF | GRCh38.p7 | 3:149078851 | GACAAAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 6596 |
| rs577723896 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030208 | ACAAGTGGTAATACA[A/G]TGTCTTCAATATTTT | 6596 |
| rs577732662 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088403 | GCAGACGTGGTGGCA[C/T]GCACCTGTAGTCCTA | 6596 |
| rs577852183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HLTF | GRCh38.p7 | 3:149081430 | TTAAGTGCTCAAATC[A/G]CAAGTCCAACAGAAA | 6596 |
| rs577890731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HLTF | GRCh38.p7 | 3:149074943 | AAGGTAACTGAAAGA[C/T]TGAAAGAGTTTAGAA | 6596 |
| rs577899381 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HLTF | GRCh38.p7 | 3:149082209 | CACACCTGTAATCCC[A/T]GCACTTTGGGAGGCC | 6596 |
| rs577931611 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HLTF | GRCh38.p7 | 3:149073559 | ATTAGCAGAGCGTGA[C/T]GGTGTGCGCCTGTAG | 6596 |
| rs578026933 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087224 | GGGCACTTGGCTGCT[C/G]CAGCCAAGAGGGGGA | 6596 |
| rs578083216 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149073454 | ACCCAAGCACTTTGG[G/T]AGGCCAAGGCAGGTG | 6596 |
| rs578098857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149059200 | CCCCAACATGTAAAA[C/T]AATGGAGACCAAGGG | 6596 |
| rs578129458 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068889 | AAATCTCTGGCAATT[C/T]TAAAGCAGTGTAAAT | 6596 |
| rs578157776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149036048 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCAGGA | 6596 |
| rs578211639 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HLTF | GRCh38.p7 | 3:149074556 | GAAACAGAGTGCCAG[-/A]AAAAAATTGAGAAAA | 6596 |
| rs578239473 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HLTF | GRCh38.p7 | 3:149065599 | CTTTGGGAGACCGAG[A/G]CGGGCGGATCACCTA | 6596 |
| rs745425815 | snp | A/G | 1.6552e-05 | 0.00287676 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050313 | TTCTCTAATACGATC[A/G]GGACCATAATAAACA | 6596 |
| rs745426954 | snp | C/T | 0.000115413 | 0.00759562 | missense | HLTF | GRCh38.p7 | 3:149064824 | CCTTTTCACTGGTAT[C/T]GTTTCCTCCAAGTTT | 6596 |
| rs745466555 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | HLTF | GRCh38.p7 | 3:149041602 | CATTCCTCATCTGAA[C/T]CTGAGCTCAGAATTA | 6596 |
| rs745559081 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149064471 | ATTACATTTTAAATA[A/C]AACAAAATTCACTGA | 6596 |
| rs745597897 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072431 | ATGACATTCCATTTA[C/T]TATTACTGCAATAAG | 6596 |
| rs745607109 | snp | A/C | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087031 | CATGTTAAGCCTCAG[A/C]GTATGCATGAGACAC | 6596 |
| rs745653604 | in-del | -/TTG | 1.71187e-05 | 0.00292559 | cds-indel | HLTF | GRCh38.p7 | 3:149032323 | GCAAGTTCTCTCTTT[-/TTG]TTTTGTATTTTCAGC | 6596 |
| rs745662926 | snp | A/T | 3.33595e-05 | 0.00408395 | missense | HLTF | GRCh38.p7 | 3:149039061 | TACTGGATCCATTAA[A/T]AACACTCGAGAAGCT | 6596 |
| rs745669136 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149053569 | TGAGCCAATTAAAAC[A/T]CTTAAATTATCCAGC | 6596 |
| rs745695249 | snp | C/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086105 | GTGACAGAGATTTCC[C/G]AAGTCCCTAACACGG | 6596 |
| rs745741464 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149036974 | CAACTTTTTCATACT[A/C]ATTATTTTGGTATTA | 6596 |
| rs745750885 | snp | C/T | | | missense | HLTF | GRCh38.p7 | 3:149039176 | TGAATTGATTCAACT[C/T]TTTTCTTTTGGGCCA | 6596 |
| rs745786676 | snp | G/T | 1.65291e-05 | 0.00287476 | intron-variant | HLTF | GRCh38.p7 | 3:149063535 | TGCGTCTATTTCAAA[G/T]AAAAATGCAAATATA | 6596 |
| rs745816115 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066807 | TAGGAAGAACAAGAC[A/T]TAAAACATTAGGTTG | 6596 |
| rs745827729 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050703 | CTGCATTAGTTAGCA[A/G]ACTTAATAATATAAA | 6596 |
| rs745839598 | snp | C/T | 1.66735e-05 | 0.00288729 | intron-variant | HLTF | GRCh38.p7 | 3:149074353 | AAGGAACTACCCTAT[C/T]ATATTTGGGAGAAAA | 6596 |
| rs745888588 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082983 | GTGGCTGGGCGCGGT[A/G]GCTCATGCCTGTAAT | 6596 |
| rs745920274 | in-del | -/GT | 1.64904e-05 | 0.00287139 | intron-variant | HLTF | GRCh38.p7 | 3:149063425 | AATCAAACCATAATA[-/GT]TTACCTTTTGGGGCG | 6596 |
| rs745922433 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032662 | AATGACTTCAGCATT[A/G]TATTAAAAAGGCCAT | 6596 |
| rs745950400 | in-del | -/AC | | | intron-variant | HLTF | GRCh38.p7 | 3:149032976 | AAAAAAAAAAAAAAA[-/AC]ACAAAAAACTATTCC | 6596 |
| rs746011923 | snp | C/T | 4.78606e-05 | 0.00489163 | intron-variant | HLTF | GRCh38.p7 | 3:149071218 | ATCATAATCACAAAA[C/T]TAGATTTTATTAACT | 6596 |
| rs746039113 | snp | A/C | 1.66247e-05 | 0.00288307 | missense | HLTF | GRCh38.p7 | 3:149059804 | ATAACCTTAGAAGAT[A/C]CTGCTGATAAAACAA | 6596 |
| rs746059934 | snp | C/G | 3.36905e-05 | 0.00410416 | missense | HLTF | GRCh38.p7 | 3:149046115 | TTCATTTTTCACAGA[C/G]TGATAAATCTTTCTC | 6596 |
| rs746077278 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072936 | CTTAAAATTACTACT[C/T]GAACATTTAAAACAT | 6596 |
| rs746090690 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149040453 | AAAAAAAATCTATGA[A/C]TAACAATTTATTGAA | 6596 |
| rs746102088 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | HLTF | GRCh38.p7 | 3:149071331 | TTTGTTATTGTGTTA[C/T]AGTATAAGTCATTTC | 6596 |
| rs746113824 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062667 | TATGTTAATATAATA[C/T]TGTCCACAAATAACT | 6596 |
| rs746113839 | snp | A/C | 1.67019e-05 | 0.00288975 | splice-donor-variant | HLTF | GRCh38.p7 | 3:149059717 | AAGGATATTTACTGA[A/C]CCTTTTTCAACATTT | 6596 |
| rs746200995 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057745 | TGGGATTTACACTTA[C/T]TAGTATTTGTAGCTC | 6596 |
| rs746203195 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041148 | ATATTTTAGATATAT[C/T]GGGTTAAATACAAAT | 6596 |
| rs746245268 | in-del | -/AA | | | intron-variant | HLTF | GRCh38.p7 | 3:149080425 | CATGTCTACTGACTC[-/AA]GAGATTACAGCCAGA | 6596 |
| rs746288848 | snp | G/T | | | missense | HLTF | GRCh38.p7 | 3:149055371 | TCTCCTCAACATCAG[G/T]TTTCTTTGACCCCTC | 6596 |
| rs746291988 | snp | A/G | 2.37527e-05 | 0.00344613 | intron-variant | HLTF | GRCh38.p7 | 3:149060900 | TTTTGGACCAACCCA[A/G]AGCAAAATAAGATAT | 6596 |
| rs746328993 | snp | C/G/T | 9.67771e-05 | 0.0069556 | intron-variant | HLTF | GRCh38.p7 | 3:149049037 | GAATTAAAAAACACA[C/G/T]GAAAGTAAAATAGTA | 6596 |
| rs746348235 | snp | A/G | 1.65302e-05 | 0.00287486 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084699 | CTCCCGTGTAATAGC[A/G]TAGTCCAACCACATG | 6596 |
| rs746381891 | snp | A/T | 3.29679e-05 | 0.00405991 | missense | HLTF | GRCh38.p7 | 3:149048895 | CTTTCTGATTCTAAG[A/T]CAAGTACAGCTTTTG | 6596 |
| rs746401140 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084831 | TTGGATATGAGAGGC[A/G]TGGAAAATTTCCATG | 6596 |
| rs746444461 | in-del | -/T | 0.000118895 | 0.0077093 | intron-variant | HLTF | GRCh38.p7 | 3:149050394 | AAGAAAAATTAGGAA[-/T]ATTTTTAACAATGAG | 6596 |
| rs746514029 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon | HLTF | GRCh38.p7 | 3:149042176 | CCTACCTGAGGGGCC[A/G]TTGGAAGACACTGCA | 6596 |
| rs746516015 | snp | C/T | 3.51952e-05 | 0.0041948 | utr-variant-3-prime, splice-donor-variant | HLTF | GRCh38.p7 | 3:149032200 | ATCCAATCAAACTGA[C/T]CTTACTAAAATCCCA | 6596 |
| rs746554134 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon | HLTF | GRCh38.p7 | 3:149055390 | CTTTGACCCCTCCAC[C/T]GCACAAGCTCCTAAA | 6596 |
| rs746571034 | snp | C/T | 1.64857e-05 | 0.00287099 | missense | HLTF | GRCh38.p7 | 3:149041631 | TAACTTCATCTTCCT[C/T]ATTAACTTCTTTCTC | 6596 |
| rs746603930 | snp | A/G | 3.43212e-05 | 0.00414239 | stop-gained | HLTF | GRCh38.p7 | 3:149032330 | CTCTCTTTTTGTTTT[A/G]TATTTTCAGCATATT | 6596 |
| rs746631449 | snp | C/G | 1.64988e-05 | 0.00287213 | intron-variant | HLTF | GRCh38.p7 | 3:149060744 | GGACATTAGAATATA[C/G]GACACATTATCAAAT | 6596 |
| rs746633740 | in-del | -/AC | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149030046 | TCTCAAAAAAATGTA[-/AC]ACTTGCATAGAAATG | 6596 |
| rs746643096 | snp | C/T | 1.65059e-05 | 0.00287275 | missense | HLTF | GRCh38.p7 | 3:149073292 | CCAGCTCTTCCAGAG[C/T]CCCAACCACTTTCCA | 6596 |
| rs746706194 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149058434 | TAACTGGTTATTTGG[A/G]TTTTCTTTCTATGGA | 6596 |
| rs746738253 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061358 | GGAGTTTCCAGTGAG[C/T]GGAGATTGCGCCACT | 6596 |
| rs746769623 | snp | C/G | | | stop-gained | HLTF | GRCh38.p7 | 3:149050284 | ACAATATCCTGTTTT[C/G]AAAGTAAGGCCGGTT | 6596 |
| rs746770547 | in-del | -/AA | 3.49284e-05 | 0.00417887 | intron-variant | HLTF | GRCh38.p7 | 3:149048188 | ACAGGAAACTGTTAT[-/AA]CTCTTTAACCAGAGT | 6596 |
| rs746821765 | snp | C/T | 1.79355e-05 | 0.00299456 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039181 | TGATTCAACTCTTTT[C/T]TTTTGGGCCATGGAA | 6596 |
| rs746848421 | snp | C/T | 1.6729e-05 | 0.00289209 | intron-variant | HLTF | GRCh38.p7 | 3:149063570 | ATTAGTAAGGTGTCT[C/T]AGAAACTAGTATTAT | 6596 |
| rs746851033 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088221 | AAAATTCCAAATATG[A/G]GAACATAGCTCTTTC | 6596 |
| rs746852945 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073749 | CAAACTGCATTAAAA[G/T]CCTTGTATTTTAGAG | 6596 |
| rs746925328 | snp | C/T | 1.64898e-05 | 0.00287135 | missense | HLTF | GRCh38.p7 | 3:149055305 | CTTAAAGACTTACAA[C/T]CCAGTTGCTTAACAC | 6596 |
| rs746982688 | snp | C/G | 1.64912e-05 | 0.00287147 | missense | HLTF | GRCh38.p7 | 3:149064844 | CCTCCAAGTTTCATA[C/G]AGTCATCGTTAACAT | 6596 |
| rs746986828 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038170 | GCAAAGGAAATTGCA[G/T]TTTACCTAATTCTTA | 6596 |
| rs747050082 | snp | C/T | 0.000132301 | 0.00813223 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071303 | ATTTTCTGGTCGGTC[C/T]TTCTCAGAAAAATTT | 6596 |
| rs747115749 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038098 | TCACCTATGATATAT[G/T]CTAAAAATGCAGCTT | 6596 |
| rs747143495 | snp | A/C | 1.66829e-05 | 0.00288811 | intron-variant | HLTF | GRCh38.p7 | 3:149059817 | ATCCTGCTGATAAAA[A/C]AACAAAGAATCTTAA | 6596 |
| rs747160732 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070187 | TTTTGATGCAGTATA[A/T]CAAAGAAATCTGCAA | 6596 |
| rs747162464 | in-del | -/AAAAAAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149032957 | ACAGAGCGACGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 6596 |
| rs747180073 | snp | A/T | 1.70737e-05 | 0.00292174 | intron-variant | HLTF | GRCh38.p7 | 3:149048007 | TGTAACTAATATTAA[A/T]CACTGTCTGAAAGTA | 6596 |
| rs747207862 | snp | C/T | 0.000149861 | 0.00865495 | missense | HLTF | GRCh38.p7 | 3:149039068 | TCCATTAAAAACACT[C/T]GAGAAGCTGCAGACA | 6596 |
| rs747211092 | snp | A/G | 1.6793e-05 | 0.00289763 | intron-variant | HLTF | GRCh38.p7 | 3:149074376 | GGAGAAAAAGAAAGG[A/G]AAATCAGAAGCATTA | 6596 |
| rs747243485 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | HLTF | GRCh38.p7 | 3:149060637 | GGGTATATAGTATAC[A/G]CATACCTTTCGCCCT | 6596 |
| rs747249635 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049108 | ATCAAATTTACTATG[C/T]GCTAGGTACTGCTTT | 6596 |
| rs747321956 | snp | A/G | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031520 | CCACAGACTATATTT[A/G]TACCTCAGACACAGC | 6596 |
| rs747339531 | in-del | -/TTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149074057 | CAATAGAGGCAAAAG[-/TTT]GAAAAATCAGAGATT | 6596 |
| rs747370512 | snp | C/T | 1.66394e-05 | 0.00288434 | missense | HLTF | GRCh38.p7 | 3:149040098 | AATTCTTCTGGAGGA[C/T]ATTCTAATAAATTAT | 6596 |
| rs747406622 | in-del | -/T | 1.65363e-05 | 0.00287539 | frameshift-variant | HLTF | GRCh38.p7 | 3:149071410 | CCAAGCTAGAGCTTG[-/T]TTTTTGATGTGGAAG | 6596 |
| rs747451071 | snp | C/T | 2.00914e-05 | 0.00316943 | intron-variant | HLTF | GRCh38.p7 | 3:149049043 | AAAAACACAGGAAAG[C/T]AAAATAGTACTTAAT | 6596 |
| rs747464947 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149059309 | GTGTTGTTTTCCTAT[A/G]AATTACAAAATATAA | 6596 |
| rs747472980 | snp | C/T | 1.64879e-05 | 0.00287118 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084851 | AAATTTCCATGAACT[C/T]CATACTGGACAGTCT | 6596 |
| rs747488845 | snp | A/G | 1.65034e-05 | 0.00287253 | missense | HLTF | GRCh38.p7 | 3:149071335 | TTATTGTGTTATAGT[A/G]TAAGTCATTTCGCTG | 6596 |
| rs747517103 | in-del | -/AAC | | | intron-variant | HLTF | GRCh38.p7 | 3:149081774 | AGAGCACCAACTTAA[-/AAC]AACCAAAAAAATGGT | 6596 |
| rs747542593 | in-del | -/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088426 | TAGTCCTAGCTACTT[-/G]GGAGGCTGAGGCAGG | 6596 |
| rs747606043 | in-del | -/ATC | 1.69407e-05 | 0.00291034 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086379 | CCTCGGCTCCCCTGG[-/ATC]ATCGTTTTCGAGCCG | 6596 |
| rs747606780 | snp | A/G | 1.6591e-05 | 0.00288015 | intron-variant | HLTF | GRCh38.p7 | 3:149034912 | ATAGTTTGTTTAAAA[A/G]CTCACTTTTGTGATG | 6596 |
| rs747659820 | snp | A/C | 1.92569e-05 | 0.00310291 | intron-variant | HLTF | GRCh38.p7 | 3:149046045 | AAACAAAGTAAACAA[A/C]AACTAATTTTTAACA | 6596 |
| rs747667063 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054940 | TTATTGTTATAAAAA[C/T]AAGTTATTGTTGGTA | 6596 |
| rs747695381 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149058041 | ACTTTGTCAATACTT[A/G]GCATTGTGAGATTTT | 6596 |
| rs747714841 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048903 | TTCTAAGTCAAGTAC[A/G]GCTTTTGTCTGCTGA | 6596 |
| rs747734230 | snp | C/T | 1.82754e-05 | 0.0030228 | intron-variant | HLTF | GRCh38.p7 | 3:149032376 | CTTTACAATGAACTT[C/T]AAAAAGAAAAAAAAA | 6596 |
| rs747745467 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054667 | CATTCCAATGTCAAT[A/G]TTTCAGAACAGAAAA | 6596 |
| rs747761775 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149068102 | CTTTCATTCTTATCA[A/G]CAACACATAAAAGAC | 6596 |
| rs747792933 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086678 | GGTCCGGGCTGCAAG[A/G]GTGGTTCCATCCGGG | 6596 |
| rs747819424 | snp | C/T | 5.03233e-05 | 0.00501589 | intron-variant | HLTF | GRCh38.p7 | 3:149074193 | AATATCAGAATAATA[C/T]TAAGTGAAACCCTAA | 6596 |
| rs747913227 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063965 | TACCAGAATGATCCA[C/T]ACTACATTGACCCCT | 6596 |
| rs747941949 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076947 | TCCCATCCCCAGCAA[G/T]CCTGTAGCCTTTAAA | 6596 |
| rs748013913 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149062864 | TTGACAAAATAGAAA[A/G]AAAGTAGTAGAAAGA | 6596 |
| rs748071776 | snp | A/G | 1.64936e-05 | 0.00287168 | synonymous-codon | HLTF | GRCh38.p7 | 3:149042191 | ATTGGAAGACACTGC[A/G]TTTGTAAGAAGGTAA | 6596 |
| rs748084757 | snp | C/T | 1.64846e-05 | 0.0028709 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149055401 | CCACTGCACAAGCTC[C/T]TAAAAAAATGAACCA | 6596 |
| rs748132481 | in-del | -/AAAAAAAAAAAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149079374 | GTAACGACAGTTTCT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 6596 |
| rs748187028 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149059538 | AATACAGTAGGAAAA[C/T]GCACCAAAAGGAAAA | 6596 |
| rs748294284 | snp | A/T | 1.69404e-05 | 0.00291031 | intron-variant | HLTF | GRCh38.p7 | 3:149048017 | ATTAATCACTGTCTG[A/T]AAGTACTTACCTAAG | 6596 |
| rs748315105 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | HLTF | GRCh38.p7 | 3:149060712 | AAACAAAAATAAACA[C/T]AAAAATGGGCAAAAC | 6596 |
| rs748331055 | snp | A/C | 7.59734e-05 | 0.00616287 | intron-variant | HLTF | GRCh38.p7 | 3:149039281 | TATTATTATAAAAAT[A/C]AAACAAAGTTAAGTA | 6596 |
| rs748366675 | snp | C/T | 3.5113e-05 | 0.0041899 | intron-variant | HLTF | GRCh38.p7 | 3:149071471 | AGTCATAAAGCGAAA[C/T]ACATTAAGCCATTCC | 6596 |
| rs748385990 | snp | C/G | 1.83195e-05 | 0.00302646 | missense | HLTF | GRCh38.p7 | 3:149039190 | TCTTTTCTTTTGGGC[C/G]ATGGAACCATCCAAA | 6596 |
| rs748423904 | in-del | -/T | 1.69385e-05 | 0.00291015 | frameshift-variant | HLTF | GRCh38.p7 | 3:149040062 | CATTCCATATCAGAC[-/T]TTTTCTCACTGTCAC | 6596 |
| rs748522021 | snp | C/T | | | synonymous-codon | HLTF | GRCh38.p7 | 3:149039184 | TTCAACTCTTTTCTT[C/T]TGGGCCATGGAACCA | 6596 |
| rs748562089 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149080223 | GACTACAAATGGGAA[A/T]GAGGTTTCTTTTTGG | 6596 |
| rs748593119 | snp | A/G | 5.20693e-05 | 0.00510215 | intron-variant | HLTF | GRCh38.p7 | 3:149041459 | ACACTACTCTATCAA[A/G]CACTGAACCTGTACT | 6596 |
| rs748617381 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045051 | TCCTGTCATAAAAAG[G/T]AAAAGCCAAAGTCCT | 6596 |
| rs748700002 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066892 | TAGAAAGTAGGAAGT[A/T]AAACTAAGTGCAGAC | 6596 |
| rs748780959 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077007 | CGCCCCCAGCACTTT[A/G]GGAGGCCGAGGTGGG | 6596 |
| rs748788131 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149075451 | AGGAGGCTAAGGCAG[A/G]GAGAGTTGCTTGAAC | 6596 |
| rs748818724 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040926 | TCTACCCCAGCTGAA[A/T]GACTGCTTAACAGAC | 6596 |
| rs748835430 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149080518 | AGAGCTATGTTCTCT[A/C]CCAGTCGCCACCCCT | 6596 |
| rs748851681 | snp | C/T | 1.65619e-05 | 0.00287762 | missense | HLTF | GRCh38.p7 | 3:149040129 | CTTCATGTATATCAT[C/T]TCTGCATAAAGGGCA | 6596 |
| rs748863072 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149083081 | ACATGGCAAAACCTC[A/C]TCTCTCCTAAATACA | 6596 |
| rs748872340 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | HLTF | GRCh38.p7 | 3:149063443 | TACCTTTTGGGGCGG[A/G]AGCTAGACAATTCTG | 6596 |
| rs748957525 | snp | C/T | 3.35452e-05 | 0.0040953 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086320 | CGCCCCCTTCACCTC[C/T]TGAACATCCAGGACA | 6596 |
| rs748978305 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085240 | TCACGCCTGGAATCC[C/T]AGCACTTTGGGAGGC | 6596 |
| rs749198473 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | HLTF | GRCh38.p7 | 3:149034926 | AACTCACTTTTGTGA[C/T]GATAACTTCTTGCTT | 6596 |
| rs749212225 | snp | C/T | 4.97855e-05 | 0.00498902 | intron-variant | HLTF | GRCh38.p7 | 3:149074210 | AAGTGAAACCCTAAA[C/T]TTACTTTTTGGTGCA | 6596 |
| rs749228029 | snp | A/G | 1.8266e-05 | 0.00302203 | intron-variant | HLTF | GRCh38.p7 | 3:149046060 | AAACTAATTTTTAAC[A/G]TGGTTTTCTTTCTCC | 6596 |
| rs749242198 | in-del | -/A | 1.72892e-05 | 0.00294012 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149032217 | TTACTAAAATCCCAC[-/A]AATTATAAGTCAATT | 6596 |
| rs749255954 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149064149 | GCTAACTCATCTACC[G/T]AACTCATCTAGGTAG | 6596 |
| rs749300741 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054256 | CCTCCAAGAGTATGA[C/T]AGTGAAGGAAAGCAG | 6596 |
| rs749365602 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149048699 | ATGTTGTTATATCAC[A/G]GGCAATTATGAAGAA | 6596 |
| rs749373972 | snp | C/T | 4.63757e-05 | 0.00481516 | intron-variant | HLTF | GRCh38.p7 | 3:149039569 | GAAAGTGAAAAACAC[C/T]GTGGAACTTACTTAA | 6596 |
| rs749377680 | snp | A/G | 9.58727e-05 | 0.00692294 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039676 | TAAGTCAGTCAATGC[A/G]TGCATTAGCGCATTA | 6596 |
| rs749406730 | in-del | -/TC | 1.74148e-05 | 0.00295078 | intron-variant | HLTF | GRCh38.p7 | 3:149050207 | TCAATCTTTAAAAGA[-/TC]TGTTAAGTATCAACA | 6596 |
| rs749412155 | in-del | -/GGCCGGGCGCGGTGGCTCACGCTTGTAATCCC | 1.66194e-05 | 0.00288261 | intron-variant | HLTF | GRCh38.p7 | 3:149040174 | TATAAGAAAGAACGA[lengthTooLong]AGTATGAGCAACACT | 6596 |
| rs749437227 | snp | C/T | 1.72525e-05 | 0.002937 | intron-variant | HLTF | GRCh38.p7 | 3:149068382 | GATTGTGAAACCCAG[C/T]TCACCAGAAAAACGT | 6596 |
| rs749439022 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061058 | GATGCATTAACTATA[C/T]AAAATGGAGTACCAC | 6596 |
| rs749451509 | snp | A/G | 4.94393e-05 | 0.00497164 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084814 | AAAACGTGGAAAGAA[A/G]GTTGGATATGAGAGG | 6596 |
| rs749455102 | snp | C/T | 1.66871e-05 | 0.00288847 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084679 | ATCTACTATTATACT[C/T]ACTACTCCCGTGTAA | 6596 |
| rs749477236 | snp | A/C | 1.65037e-05 | 0.00287256 | intron-variant | HLTF | GRCh38.p7 | 3:149055415 | CCTAAAAAAATGAAC[A/C]ACTGATAGAACCTTT | 6596 |
| rs749480296 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149059987 | CTAAGGATATCTTTT[C/G]AACTCAGAGAAACGA | 6596 |
| rs749606859 | snp | C/T | 1.70746e-05 | 0.00292182 | missense | HLTF | GRCh38.p7 | 3:149032300 | TTTTAGTTCCAAAGG[C/T]TCCTGCTGCAAGTTC | 6596 |
| rs749634860 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149069687 | AGTCACTTTTTTCAT[A/G]CGACACCATTTTTAC | 6596 |
| rs749670940 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034773 | TTAAACAGCATATAT[G/T]AAATTATTGATGAAG | 6596 |
| rs749718157 | snp | C/T | 4.44771e-05 | 0.00471556 | intron-variant | HLTF | GRCh38.p7 | 3:149071708 | AACTAATTAAAATAA[C/T]ACTTGCATTTAAGTC | 6596 |
| rs749728504 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149032561 | TCTTATATAAAGAAT[A/C]TGGCTGTACGAATAG | 6596 |
| rs749806475 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081920 | ATCATACCACCAAAC[C/T]CCAATTCCAGAAAAT | 6596 |
| rs749808291 | snp | C/T | 3.29799e-05 | 0.00406065 | intron-variant | HLTF | GRCh38.p7 | 3:149060727 | TAAAAATGGGCAAAA[C/T]AGGACATTAGAATAT | 6596 |
| rs749914229 | snp | G/T | 0.000123076 | 0.00784365 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039610 | TATTAAAGACAGGAA[G/T]GTTGTAAACTGAGAA | 6596 |
| rs749916690 | snp | A/T | | | missense | HLTF | GRCh38.p7 | 3:149068271 | TTTTTAACTCTTTCA[A/T]TAGGAAGAGGTCTGC | 6596 |
| rs749926480 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149055415 | CTAAAAAAATGAACC[-/T]ACTGATAGAACCTTT | 6596 |
| rs749969307 | in-del | -/AAAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149077255 | CATCTCAAAATAAAT[-/AAAT]AAATAAATAAATAAA | 6596 |
| rs749969364 | snp | C/G/T | 6.8989e-05 | 0.00587287 | intron-variant | HLTF | GRCh38.p7 | 3:149039236 | CCAGAGGCTCTAAAG[C/G/T]GGGGAAGAAAAGAGA | 6596 |
| rs749970392 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037002 | TTAACCTCTTTGGTA[C/G]TAAGATTATAAGCAA | 6596 |
| rs749996471 | snp | C/T | 1.6743e-05 | 0.0028933 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149068336 | CGTAAGAGTTTTACC[C/T]TTAAAAATGTTTTAA | 6596 |
| rs750029419 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060411 | AAATTGTTTTAAGTA[C/T]AGTTTAAATATTATT | 6596 |
| rs750049721 | snp | A/C | 1.64781e-05 | 0.00287033 | missense | HLTF | GRCh38.p7 | 3:149055380 | CATCAGTTTTCTTTG[A/C]CCCCTCCACTGCACA | 6596 |
| rs750095469 | snp | C/T | 1.6945e-05 | 0.00291071 | intron-variant | HLTF | GRCh38.p7 | 3:149068190 | ATGAAATTTAAAGAT[C/T]TCACAATAAACTGGA | 6596 |
| rs750113771 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072910 | AGTTAAGTCTCAGCT[G/T]CAATTTTTTTCTTAA | 6596 |
| rs750121326 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149059173 | TATATGAAAACAGAT[A/G]GCCTGCTATATCCCC | 6596 |
| rs750152545 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149073553 | ACAAAAATTAGCAGA[A/G]CGTGATGGTGTGCGC | 6596 |
| rs750170119 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149056542 | TTTTCTCTCAGTGCT[A/G]TCTACAGTAGTCCCT | 6596 |
| rs750194803 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068774 | TCATAACTTCTCCAT[A/T]AAGCATAAAAGATAT | 6596 |
| rs750209857 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053110 | TATAAGTCAGTTCTA[C/G]CCTGCTCTGTAGAAT | 6596 |
| rs750225118 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085890 | TTCCTTGCAAGTGGC[A/G/T]CATATCTCTACTAGC | 6596 |
| rs750232301 | snp | C/T | 3.42847e-05 | 0.00414019 | intron-variant | HLTF | GRCh38.p7 | 3:149047997 | AACAGTTATTTGTAA[C/T]TAATATTAATCACTG | 6596 |
| rs750273899 | snp | A/C | 1.66189e-05 | 0.00288256 | missense | HLTF | GRCh38.p7 | 3:149048132 | GGAAAGAAGAGACCA[A/C]AAGTCCTTTAAAGAA | 6596 |
| rs750283415 | snp | C/T | 3.30825e-05 | 0.00406696 | intron-variant | HLTF | GRCh38.p7 | 3:149060629 | TAGATTATGGGTATA[C/T]AGTATACACATACCT | 6596 |
| rs750284302 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067706 | AAAAATAATAATAAT[A/T]AAAAAAAACCTGTAT | 6596 |
| rs750295082 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | HLTF | GRCh38.p7 | 3:149071597 | CCTCAGCTGGTTCCA[C/T]TTCATGGGTTTTATC | 6596 |
| rs750347818 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082243 | GCGGGCGGATCACGA[A/G]GTCAGGAGATACAGA | 6596 |
| rs750359619 | snp | A/T | 9.90115e-05 | 0.00703534 | missense | HLTF | GRCh38.p7 | 3:149075915 | TGTTGTCCATGATAT[A/T]GGCCAAAGCACCTGC | 6596 |
| rs750372143 | in-del | -/AACA | 0.000103098 | 0.00717903 | intron-variant | HLTF | GRCh38.p7 | 3:149047982 | CTGGTTCAAGCTACT[-/AACA]GTTATTTGTAACTAA | 6596 |
| rs750374631 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081180 | AACTGTATTTTAAAA[C/T]AGAAAAAGAAATAAA | 6596 |
| rs750457735 | snp | C/T | 1.66871e-05 | 0.00288847 | intron-variant | HLTF | GRCh38.p7 | 3:149040193 | ATGAGCAACACTTAA[C/T]AGAAGAACAAATATA | 6596 |
| rs750485431 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149045717 | TGATCTTGCTTGGAC[C/G]AGAATTTCATACCTT | 6596 |
| rs750490325 | snp | A/G | 1.69691e-05 | 0.00291278 | intron-variant | HLTF | GRCh38.p7 | 3:149050390 | CCTAAAGAAAAATTA[A/G]GAATATTTTTAACAA | 6596 |
| rs750534897 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063890 | GTCACCTTGTGTCAC[C/T]TGGTAACTCTTTTTA | 6596 |
| rs750592920 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | HLTF | GRCh38.p7 | 3:149041537 | GTTTACAAAATACAT[A/G]TGCACAATGTGTTAT | 6596 |
| rs750597887 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149077734 | AGAAGGCCCTAAACG[C/T]TCACCTTTGCCTGAA | 6596 |
| rs750634432 | snp | C/T | 1.66471e-05 | 0.00288501 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071429 | TTGATGTGGAAGCAG[C/T]GGTGTTTCAATAGCC | 6596 |
| rs750723952 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072039 | GCCTGGGCAAGAAAG[C/T]GAGACCCTGTCCCAA | 6596 |
| rs750742519 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037567 | CCCTAGTTATAATCT[C/T]ACTGAGAAGGATACC | 6596 |
| rs750747702 | in-del | -/A | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088275 | ATGGCTCACACCTAT[-/A]ATCCCAGCACTTTGG | 6596 |
| rs750785353 | snp | A/G | 1.70292e-05 | 0.00291793 | synonymous-codon | HLTF | GRCh38.p7 | 3:149046148 | TTCATCTGAAAGTGT[A/G]ATGTGCTGAATAAAT | 6596 |
| rs750795776 | snp | C/T | 1.65282e-05 | 0.00287469 | intron-variant | HLTF | GRCh38.p7 | 3:149035036 | ACTTTACTACTGCCC[C/T]GATCTTTCAGTGTTT | 6596 |
| rs750811828 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085824 | GAGTCTACTGGAGCA[C/T]TGCAAAAAGTTTCCA | 6596 |
| rs750813639 | snp | C/G | 1.69269e-05 | 0.00290915 | intron-variant | HLTF | GRCh38.p7 | 3:149074169 | TGTTTCATAATCCCT[C/G]CATCTTACAATATCA | 6596 |
| rs750830364 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051042 | TATGAGGAGAGAGAT[C/G]ATGAAGTCCTAAACC | 6596 |
| rs750851030 | snp | A/C | 1.69789e-05 | 0.00291362 | intron-variant | HLTF | GRCh38.p7 | 3:149034895 | ATCAACCTAGTCTTA[A/C]AATAGTTTGTTTAAA | 6596 |
| rs750884394 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon | HLTF | GRCh38.p7 | 3:149063517 | TTGTTCACTACATCT[A/G]GATGCGTCTATTTCA | 6596 |
| rs750934809 | snp | A/G | 1.65029e-05 | 0.00287248 | intron-variant | HLTF | GRCh38.p7 | 3:149063408 | AAATAAACATATGAC[A/G]TAATCAAACCATAAT | 6596 |
| rs750948157 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149084280 | AAACTCCTAAGGAAT[C/G]TCCTGTCGAACATGC | 6596 |
| rs750964533 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149049970 | ATATTCCAGCCTGGG[A/C]AACAAGAGCAAAACT | 6596 |
| rs750991610 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078257 | TATTTTAAATATGTT[-/G]CAAAGGGGCTGGGCA | 6596 |
| rs750993617 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082446 | CCTGAGAAACAGAGC[A/G]AGACTCCGTCTCAAA | 6596 |
| rs751066192 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066099 | TTGCCCAGGCTGGAG[G/T]GCAACGGCACAATCT | 6596 |
| rs751105039 | snp | A/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032049 | ATTTGAAGTTTCATT[A/T]AAAATAGGTTCATAT | 6596 |
| rs751112077 | snp | G/T | 1.74974e-05 | 0.00295776 | missense | HLTF | GRCh38.p7 | 3:149040032 | CATGAGTACTTTACC[G/T]TTGAACTGGATGTCC | 6596 |
| rs751117048 | snp | C/T | 1.66123e-05 | 0.00288199 | missense | HLTF | GRCh38.p7 | 3:149059784 | ATGCAAATGCCACAT[C/T]TTCTATAACCTTAGA | 6596 |
| rs751121906 | snp | C/T | 5.04953e-05 | 0.00502445 | intron-variant | HLTF | GRCh38.p7 | 3:149068344 | TTTTACCCTTAAAAA[C/T]GTTTTAAAAAGATAA | 6596 |
| rs751127587 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149064016 | TTTATTCCAAGATGA[A/C]CTATTTCACTTTACA | 6596 |
| rs751165617 | snp | C/T | 3.52516e-05 | 0.00419816 | intron-variant | HLTF | GRCh38.p7 | 3:149042336 | TCCGCTAAACAATAA[C/T]AACTTCCTATTCTAA | 6596 |
| rs751336597 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040676 | TATCTTAAATAACTA[C/T]ATATAAAACACCATT | 6596 |
| rs751358981 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079163 | TACATAAGAGTACCA[C/T]AAGGAGAAAAGAGAA | 6596 |
| rs751394762 | snp | A/T | 3.45226e-05 | 0.00415453 | missense | HLTF | GRCh38.p7 | 3:149039633 | ACTGAGAAACAACCA[A/T]ACTTTTTATGTTGGG | 6596 |
| rs751424577 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054825 | TGTGTTTCAATGTGG[C/G]CACCTGGAAAATCAG | 6596 |
| rs751446434 | snp | A/G | 1.72636e-05 | 0.00293794 | missense | HLTF | GRCh38.p7 | 3:149060835 | GAATCACTGCTTTCT[A/G]TGTACTGGACAGCAG | 6596 |
| rs751466212 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149069260 | GTGGATCACCTGAGG[C/T]AGGAGTTCAAGACCA | 6596 |
| rs751483667 | snp | C/T | 2.30646e-05 | 0.00339585 | intron-variant | HLTF | GRCh38.p7 | 3:149076089 | TTACATTATAAATAA[C/T]AGACAATAACTTTGT | 6596 |
| rs751512147 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036607 | TTACCCCAATACTTA[C/T]ACAATGTTCAATGAA | 6596 |
| rs751514545 | in-del | -/T | 1.6504e-05 | 0.00287258 | frameshift-variant | HLTF | GRCh38.p7 | 3:149073289 | GTCCAGCTCTTCCAG[-/T]AGCCCCAACCACTTT | 6596 |
| rs751588036 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149033010 | AAATTCAAGAATGAA[C/T]CTTTAGTATAATTCA | 6596 |
| rs751671627 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051149 | GGGACTAATGAAATA[A/T]GAAATATGAATAATA | 6596 |
| rs751712990 | snp | C/T | 3.41087e-05 | 0.00412955 | missense | HLTF | GRCh38.p7 | 3:149032270 | TGGCTTGTTTCATTT[C/T]GTCAGCATTTGGTTT | 6596 |
| rs751740845 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149078978 | AGAGTCAAAAGGTAC[A/C]ATAACTGAAGAAAAA | 6596 |
| rs751760699 | snp | C/T | 6.61419e-05 | 0.00575036 | missense | HLTF | GRCh38.p7 | 3:149073233 | AGCACACCTGTTCAG[C/T]TGTCATCTGTACTGC | 6596 |
| rs751784523 | snp | A/T | 3.29755e-05 | 0.00406038 | intron-variant | HLTF | GRCh38.p7 | 3:149060706 | AAAATAAAACAAAAA[A/T]AAACATAAAAATGGG | 6596 |
| rs751841073 | snp | A/C | 1.64977e-05 | 0.00287203 | missense | HLTF | GRCh38.p7 | 3:149060649 | TACACATACCTTTCG[A/C]CCTGCCTTTAGTTTC | 6596 |
| rs751868018 | snp | C/T | 1.65754e-05 | 0.00287879 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050277 | AGTCAAAACAATATC[C/T]TGTTTTGAAAGTAAG | 6596 |
| rs751884631 | in-del | -/AAG | | | intron-variant | HLTF | GRCh38.p7 | 3:149045501 | ATAAATTTTTGTTGA[-/AAG]AATATGAAAAGAAAG | 6596 |
| rs751898526 | snp | C/T | 1.66707e-05 | 0.00288705 | missense | HLTF | GRCh38.p7 | 3:149039129 | ACAGAAGCATTATAG[C/T]TGGAGATCCTGCTTC | 6596 |
| rs751954085 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038589 | CTCACTGAAACTTCA[A/G]CCTCCTGGGCCCAAG | 6596 |
| rs751965976 | in-del | -/TGA | 3.30415e-05 | 0.00406444 | cds-indel | HLTF | GRCh38.p7 | 3:149034923 | AAAAACTCACTTTTG[-/TGA]TGATAACTTCTTGCT | 6596 |
| rs751977158 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073053 | TATCAGTACTTTTTA[C/T]ATAAAATGTTAACAT | 6596 |
| rs752054588 | snp | A/G | 1.74075e-05 | 0.00295016 | intron-variant | HLTF | GRCh38.p7 | 3:149050423 | AGCAGATTTGTGTCA[A/G]ACTTAATAGATGTAT | 6596 |
| rs752063388 | snp | C/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086739 | GAAAGCCACGAGGCC[C/G]CAGGAGTGCGACTGC | 6596 |
| rs752097092 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149060936 | CATGTTTAATAAATG[C/G]AATAAAAAACTTTTG | 6596 |
| rs752107703 | snp | C/T | 1.65031e-05 | 0.00287251 | missense | HLTF | GRCh38.p7 | 3:149064791 | AAAATTAGCATTTAC[C/T]TTTGCTTAGTCCATC | 6596 |
| rs752121296 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149070737 | GTCACCCTGAATTTC[A/C]AAGAGCAAAGAAAAT | 6596 |
| rs752138560 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037611 | GGAAAAAGGAAGCCT[A/G]AGTAAACATATATGC | 6596 |
| rs752233699 | snp | C/T | 3.33467e-05 | 0.00408316 | intron-variant | HLTF | GRCh38.p7 | 3:149046282 | GAATAAAACAAATAA[C/T]TATGTAACTTTTAAT | 6596 |
| rs752246801 | snp | G/T | 1.73168e-05 | 0.00294246 | missense | HLTF | GRCh38.p7 | 3:149046168 | GCTGAATAAATACTT[G/T]ACGTTCTGGTAACTC | 6596 |
| rs752262281 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088049 | TTTCAAATTATTTTA[A/G]TTGTTGTATGTTCTT | 6596 |
| rs752312192 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149069534 | ATTAATTTTATTAAG[G/T]CTCATTACTTCAGTA | 6596 |
| rs752325702 | snp | G/T | | | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149032374 | TCCTTTACAATGAAC[G/T]TTAAAAAGAAAAAAA | 6596 |
| rs752334805 | snp | A/C | 1.80435e-05 | 0.00300357 | intron-variant | HLTF | GRCh38.p7 | 3:149039026 | AGTACTAAGATTCTG[A/C]AAAAATTTACAGAAC | 6596 |
| rs752334813 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149033286 | ATAAGATCTACATAA[A/T]TGGAGAAAGGATACT | 6596 |
| rs752366943 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149036261 | ATCATGAATTGTTTG[A/G]ATAAGGATCATTAAA | 6596 |
| rs752413246 | in-del | -/TT | 1.77497e-05 | 0.00297902 | frameshift-variant | HLTF | GRCh38.p7 | 3:149039177 | GAATTGATTCAACTC[-/TT]TTCTTTTGGGCCATG | 6596 |
| rs752422542 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048658 | AATAAGTCTAGTGAC[G/T]GTTCCATAAATTATC | 6596 |
| rs752473743 | snp | A/G | 4.94482e-05 | 0.00497209 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084760 | TACTTCTTCATCACT[A/G]GTTAGAAAGTCATCT | 6596 |
| rs752496033 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077873 | GATTTATTAGTTCCA[A/G]CACAATCATCAGCTG | 6596 |
| rs752525526 | snp | A/C | 1.70577e-05 | 0.00292037 | stop-gained | HLTF | GRCh38.p7 | 3:149040051 | AACTGGATGTCCATT[A/C]CATATCAGACTTTTT | 6596 |
| rs752565849 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041828 | AAATTTAAGAAACAT[G/T]CAGAAGCCAAAATAG | 6596 |
| rs752567218 | snp | A/G | 1.75299e-05 | 0.00296051 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084906 | TATTTTTTTTTAAAG[A/G]CAAAGAAAAACAATA | 6596 |
| rs752586644 | snp | C/T | 3.30879e-05 | 0.00406729 | missense | HLTF | GRCh38.p7 | 3:149071301 | ACATTTTCTGGTCGG[C/T]CCTTCTCAGAAAAAT | 6596 |
| rs752596045 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149033933 | TTTAAAGACAAGGAA[A/G]AGTATGGGATAAACC | 6596 |
| rs752603721 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149056550 | CAGTGCTATCTACAG[C/T]AGTCCCTCCTTATCC | 6596 |
| rs752641503 | snp | C/T | 1.69502e-05 | 0.00291115 | intron-variant | HLTF | GRCh38.p7 | 3:149068357 | AATGTTTTAAAAAGA[C/T]AAATGGTCAGATTGT | 6596 |
| rs752647478 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063821 | TATTGGAAAAAAAAA[C/T]CAACAGAACCACAAA | 6596 |
| rs752731578 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073378 | AGTAGGTTTTTATCT[G/T]TTATTAAGTAGCTTT | 6596 |
| rs752765331 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086788 | GTTTTGTTTGATTCC[C/T]TGCCTCAAACGGAGG | 6596 |
| rs752775424 | snp | A/G | 1.64993e-05 | 0.00287218 | missense | HLTF | GRCh38.p7 | 3:149073259 | ACTGCAGCATGCACT[A/G]GCATACTATAGCTTG | 6596 |
| rs752793811 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149052921 | ACTCCATCTCTAGAC[A/G]GTGTTAGGCTCTACT | 6596 |
| rs752828882 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149053213 | GAAATCGTTTGGATG[C/T]TCATCTCCTCCAAAT | 6596 |
| rs752863490 | snp | A/C/T | 6.07827e-05 | 0.00551255 | intron-variant | HLTF | GRCh38.p7 | 3:149060870 | TCTTCTAAAATTAAG[A/C/T]ATACACAAAGAAATT | 6596 |
| rs752878406 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055930 | CATTCTCTCTCTCCA[A/G]TCTTTCACTCTGGTG | 6596 |
| rs752881814 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067560 | GAAGGTGGAGTGCAA[C/T]AGTGCAATCATAGCT | 6596 |
| rs752899087 | in-del | -/AAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149054692 | AGAAAAGCAATCTGG[-/AAA]AAAAAAATTTCTGAT | 6596 |
| rs752915015 | snp | A/T | 1.65274e-05 | 0.00287462 | intron-variant | HLTF | GRCh38.p7 | 3:149063392 | TAAGAAAACAGAGTC[A/T]AAATAAACATATGAC | 6596 |
| rs752984332 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149046589 | TCCTGTCAACTCCAT[C/T]ACCGAATAGTCAACA | 6596 |
| rs752996393 | snp | A/T | 1.64789e-05 | 0.0028704 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041556 | ACAATGTGTTATCAC[A/T]GGAACTGTTAAAGAA | 6596 |
| rs753016558 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072112 | ACTAGTCAAACGCCA[A/G]AAAGGCACATAAATC | 6596 |
| rs753051679 | snp | C/T | 1.79774e-05 | 0.00299806 | intron-variant | HLTF | GRCh38.p7 | 3:149055263 | ACCTTGTAGATAAAA[C/T]ATAAATTATGTTACA | 6596 |
| rs753106222 | snp | A/C | 1.6476e-05 | 0.00287014 | missense | HLTF | GRCh38.p7 | 3:149055368 | GTCTCTCCTCAACAT[A/C]AGTTTTCTTTGACCC | 6596 |
| rs753159370 | snp | C/T | 6.6313e-05 | 0.00575779 | intron-variant | HLTF | GRCh38.p7 | 3:149064904 | TAAACAGTACTGCTA[C/T]CAGTTTTAAATAACT | 6596 |
| rs753187186 | snp | A/G | 1.656e-05 | 0.00287745 | intron-variant | HLTF | GRCh38.p7 | 3:149042128 | TATTTAAGTATCTCT[A/G]ACAAATACAATGATA | 6596 |
| rs753335244 | snp | A/C | 1.65187e-05 | 0.00287386 | missense | HLTF | GRCh38.p7 | 3:149048098 | ATTCTCTATCAATAA[A/C]TGGTTTAAGTTTTAA | 6596 |
| rs753356856 | in-del | -/A | 4.4824e-05 | 0.00473392 | intron-variant | HLTF | GRCh38.p7 | 3:149039697 | AGCGCATTAATCTGC[-/A]AAAAAATATTAAGAT | 6596 |
| rs753373605 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058948 | GGGTAAAGAATAATC[C/T]ACCCAACATGCCTAT | 6596 |
| rs753382705 | in-del | -/GA | 1.69372e-05 | 0.00291004 | frameshift-variant | HLTF | GRCh38.p7 | 3:149046139 | TTTCTCTCTTCATCT[-/GA]GAAAGTGTAATGTGC | 6596 |
| rs753384192 | snp | C/T | 3.41804e-05 | 0.00413389 | intron-variant | HLTF | GRCh38.p7 | 3:149046309 | TAATTTCTACATAAA[C/T]TGATCCAAGAAGAAC | 6596 |
| rs753425236 | snp | A/T | 2.06703e-05 | 0.00321477 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039220 | ACGAGTAAACACAAA[A/T]CCAGAGGCTCTAAAG | 6596 |
| rs753463193 | snp | G/T | 4.98509e-05 | 0.00499229 | missense | HLTF | GRCh38.p7 | 3:149074341 | TGTTTGCACCAAAAG[G/T]AACTACCCTATTATA | 6596 |
| rs753469368 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149071963 | GATGCTGAGATGGGA[G/T]GATCACTTCAGCCTA | 6596 |
| rs753474795 | snp | A/G | 2.54417e-05 | 0.00356654 | synonymous-codon | HLTF | GRCh38.p7 | 3:149076036 | TAATGCAACCATTTC[A/G]TTATTATTAACCTAA | 6596 |
| rs753530650 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon | HLTF | GRCh38.p7 | 3:149075910 | CAATTTGTTGTCCAT[A/G]ATATAGGCCAAAGCA | 6596 |
| rs753544573 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085629 | TCCAGCATCCATCAC[C/T]GTAACTCCCTGCGAG | 6596 |
| rs753551053 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070967 | GGAGAACTGCTTGAA[C/G]CTGGGAGGCGGAGGC | 6596 |
| rs753659148 | snp | A/G | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029800 | AGCTGTAATTTTAAG[A/G]ACAAAATGTACAATG | 6596 |
| rs753668334 | snp | A/T | 1.66043e-05 | 0.00288129 | intron-variant | HLTF | GRCh38.p7 | 3:149060597 | CAATGGAGCTGTACT[A/T]TAATAATCTTGAAGT | 6596 |
| rs753717314 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057651 | GGTCATTCTCTGTCT[C/T]TCAAAATACCTTATT | 6596 |
| rs753721362 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078050 | CTAATTACAAAACTC[A/G]GCAACAACAAACCAC | 6596 |
| rs753751150 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149044353 | AAATAGAATAACCTT[C/T]ACTAACACTAATTAT | 6596 |
| rs753805401 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087833 | CTCAGGTGATCCGCC[C/T]GCCTCGGCCTCCCAG | 6596 |
| rs753856656 | snp | A/G | 1.79053e-05 | 0.00299204 | intron-variant | HLTF | GRCh38.p7 | 3:149049013 | TAGTCTGAAATAAAT[A/G]TTTTATATGAATTAA | 6596 |
| rs753887646 | snp | C/G | 4.94817e-05 | 0.00497377 | intron-variant | HLTF | GRCh38.p7 | 3:149035006 | TTCCAGGCCTAACAA[C/G]AACATGGATGAGTTA | 6596 |
| rs753928186 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075018 | TAGCTAAAGGGAGAG[C/T]TCCAGTCAACTATTG | 6596 |
| rs753945365 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040548 | TATAAAGCTATTAAG[C/T]TTATAAAGCTTATAA | 6596 |
| rs753953247 | snp | C/T | 1.68035e-05 | 0.00289853 | missense | HLTF | GRCh38.p7 | 3:149040074 | GACTTTTTCTCACTG[C/T]CACGTGCTAATTCTT | 6596 |
| rs753963086 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081320 | AGAAAACACCAGAGT[C/T]AAAAATAAAGAATGC | 6596 |
| rs753966730 | snp | A/G | 1.65228e-05 | 0.00287422 | intron-variant | HLTF | GRCh38.p7 | 3:149063395 | GAAAACAGAGTCTAA[A/G]TAAACATATGACATA | 6596 |
| rs754115498 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149084079 | CCAACTGTCATTAAG[C/T]CCTTCATAACTTTCA | 6596 |
| rs754146671 | snp | A/G | 7.69512e-05 | 0.00620239 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084924 | AAGAAAAACAATATA[A/G]TATTTAAGTATTTCC | 6596 |
| rs754149678 | in-del | -/AAAAC | 0.000115439 | 0.00759646 | intron-variant | HLTF | GRCh38.p7 | 3:149060696 | AGTTTGCCTAAAAAT[-/AAAAC]AAAAATAAACATAAA | 6596 |
| rs754188017 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149033526 | GAAACCATAGTTGTT[A/C]TAAGAGTAATACTGC | 6596 |
| rs754246572 | snp | G/T | 3.32546e-05 | 0.00407752 | missense | HLTF | GRCh38.p7 | 3:149042278 | TGCCAGGACAGTCCC[G/T]TCATTAAAATACCTA | 6596 |
| rs754295851 | snp | A/G | 1.66341e-05 | 0.00288388 | intron-variant | HLTF | GRCh38.p7 | 3:149055446 | AGCTGTTTTTCTGAA[A/G]TATATATGTCAATAA | 6596 |
| rs754300673 | snp | C/T | 2.05691e-05 | 0.00320689 | intron-variant | HLTF | GRCh38.p7 | 3:149060874 | CTAAAATTAAGTATA[C/T]ACAAAGAAATTTTTG | 6596 |
| rs754322379 | in-del | -/CC | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030813 | GGCTAATTCACTGTT[-/CC]CCCTTTGAGCAAGAA | 6596 |
| rs754355631 | snp | A/C | 1.65015e-05 | 0.00287237 | missense | HLTF | GRCh38.p7 | 3:149073283 | TAGCTTGGTCCAGCT[A/C]TTCCAGAGCCCCAAC | 6596 |
| rs754357401 | in-del | -/AAGAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149082894 | CAGAAACAAGTGTAG[-/AAGAT]AAGATAAGTTATGGT | 6596 |
| rs754388752 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063808 | GGCAGCTAAGAGCTA[C/T]TGGAAAAAAAAATCA | 6596 |
| rs754419112 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149053746 | ACATTACTTGAACTT[G/T]CCTAAATATAAAATT | 6596 |
| rs754445863 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149069283 | CAAGACCAGCCTGGA[A/C]CAACACGGTGAAACC | 6596 |
| rs754483107 | snp | A/C | | | utr-variant-5-prime, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086487 | CTGAAAGGTAAGTCG[A/C]CGCGAGTCCAGTCAG | 6596 |
| rs754554950 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081647 | AAAGTTTTTAAAAAG[C/T]TTAATGGAGCCAATA | 6596 |
| rs754587369 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149046492 | ACCTAACATAGTTTA[A/T]TCTTTTTATATCCTG | 6596 |
| rs754611917 | snp | A/C | 1.97701e-05 | 0.00314399 | intron-variant | HLTF | GRCh38.p7 | 3:149046033 | TCAGTGAATGGGAAA[A/C]AAAGTAAACAAAAAC | 6596 |
| rs754635603 | snp | C/T | 1.70662e-05 | 0.00292109 | synonymous-codon | HLTF | GRCh38.p7 | 3:149046154 | TGAAAGTGTAATGTG[C/T]TGAATAAATACTTTA | 6596 |
| rs754636847 | snp | A/C | 1.6513e-05 | 0.00287336 | missense | HLTF | GRCh38.p7 | 3:149073298 | CTTCCAGAGCCCCAA[A/C]CACTTTCCAAATTGA | 6596 |
| rs754656281 | snp | A/C | 3.37297e-05 | 0.00410654 | intron-variant | HLTF | GRCh38.p7 | 3:149074183 | TGCATCTTACAATAT[A/C]AGAATAATATTAAGT | 6596 |
| rs754683928 | in-del | -/TC | 3.52591e-05 | 0.00419861 | intron-variant | HLTF | GRCh38.p7 | 3:149048194 | ACTGTTATAACTCTT[-/TC]TAACCAGAGTATCCA | 6596 |
| rs754751780 | snp | A/T | 1.66208e-05 | 0.00288273 | intron-variant | HLTF | GRCh38.p7 | 3:149048844 | TTTAAGGTTTTAGTA[A/T]GTTTAATGCTATGAT | 6596 |
| rs754753679 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076408 | CTAAGTACATTGCAC[A/T]GACTGACTTTTTAAA | 6596 |
| rs754787389 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031342 | CCATCCAGATATCAC[A/G]CCTCTCACATATAGT | 6596 |
| rs754809472 | in-del | -/AAAA | 0.000125112 | 0.00790824 | intron-variant | HLTF | GRCh38.p7 | 3:149059678 | TTCATTCAAAAACAG[-/AAAA]AAAACCAAAAACTAG | 6596 |
| rs754811744 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040700 | CACCATTACAATTAA[A/T]TAATTCTGAAGCTAA | 6596 |
| rs754843757 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075169 | ATAATTAGTACTGAA[C/T]GAAAAAATGTCTAAA | 6596 |
| rs754895989 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054853 | CAGGGTAACAGTTAT[A/G]AGAATTAAATGAGAA | 6596 |
| rs754901630 | snp | A/G | 1.68912e-05 | 0.00290608 | intron-variant | HLTF | GRCh38.p7 | 3:149068350 | CCTTAAAAATGTTTT[A/G]AAAAGATAAATGGTC | 6596 |
| rs754933188 | snp | G/T | 1.64844e-05 | 0.00287087 | missense | HLTF | GRCh38.p7 | 3:149055397 | CCCTCCACTGCACAA[G/T]CTCCTAAAAAAATGA | 6596 |
| rs754933819 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087909 | AGCTTTTCAAGACAC[A/G]TTTGTTCATTATCGT | 6596 |
| rs754965743 | snp | G/T | 3.46753e-05 | 0.0041637 | missense | HLTF | GRCh38.p7 | 3:149039642 | CAACCAAACTTTTTA[G/T]GTTGGGATTCTTCTT | 6596 |
| rs755031313 | snp | C/T | 5.50055e-05 | 0.00524402 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071646 | AAACAATTTGTCAAA[C/T]TCTGTTTTAAGCTAC | 6596 |
| rs755034208 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053126 | CCTGCTCTGTAGAAT[A/G]CTAGATCCTTTACTT | 6596 |
| rs755061114 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037632 | ACATATATGCATCAA[C/T]AAGGTAGCCTCACCC | 6596 |
| rs755062310 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085908 | TATCTCTACTAGCGC[C/T]TCTGCAAATACTTAT | 6596 |
| rs755153215 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051181 | TAATAAGACTAAGAT[A/G]CTCTGATACTTGAAT | 6596 |
| rs755157727 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049485 | TTAACTTTTGAACAA[C/T]TGGAATTATAAAGGT | 6596 |
| rs755230904 | snp | A/C | 1.70124e-05 | 0.00291649 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149048164 | TCTGGATTGGAGTAC[A/C]TAGAAATAACAGGAA | 6596 |
| rs755238421 | snp | A/C | 1.6498e-05 | 0.00287206 | missense | HLTF | GRCh38.p7 | 3:149064796 | TAGCATTTACCTTTG[A/C]TTAGTCCATCTGCCT | 6596 |
| rs755285970 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | HLTF | GRCh38.p7 | 3:149060707 | AAATAAAACAAAAAT[A/G]AACATAAAAATGGGC | 6596 |
| rs755309629 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149068636 | GAACTCTTGATTTTT[A/G]TCATGCAACTATTTA | 6596 |
| rs755313059 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149044832 | TCTACGTTCACAATT[C/T]AACAGAATCTAATCA | 6596 |
| rs755345751 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037582 | TACTGAGAAGGATAC[C/G]GTCAGTTGAGGGAGG | 6596 |
| rs755360171 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149048855 | AGTAAGTTTAATGCT[A/G]TGATTACCTGTCAAA | 6596 |
| rs755418420 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149059419 | ACCAAAATTAAATTA[A/G]GCTTTAAAGCAGCCA | 6596 |
| rs755434351 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066865 | TTCAACAGGTTTAAC[C/T]CTCAATAAAAGTAGA | 6596 |
| rs755435293 | in-del | -/AAAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149075544 | TGAGACTTCGTCTCA[-/AAAT]AAATAAATAAATAAA | 6596 |
| rs755454529 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | HLTF | GRCh38.p7 | 3:149041546 | ATACATGTGCACAAT[A/G]TGTTATCACAGGAAC | 6596 |
| rs755509581 | snp | C/T | 1.75724e-05 | 0.0029641 | intron-variant | HLTF | GRCh38.p7 | 3:149041445 | TATTAAAGACAGGTA[C/T]ACTACTCTATCAAAC | 6596 |
| rs755554282 | snp | A/G | 1.7336e-05 | 0.00294409 | missense | HLTF | GRCh38.p7 | 3:149046171 | GAATAAATACTTTAC[A/G]TTCTGGTAACTCCAA | 6596 |
| rs755595700 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057268 | CGTCTCTATTAAAAA[C/T]ACAAAAAATTAGCCG | 6596 |
| rs755639943 | snp | A/T | 0.000150395 | 0.00867034 | intron-variant | HLTF | GRCh38.p7 | 3:149074198 | CAGAATAATATTAAG[A/T]GAAACCCTAAACTTA | 6596 |
| rs755719704 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070820 | GAGGCCAAGGCGGGC[A/G]GATCACTTGAAGTCA | 6596 |
| rs755725000 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149033427 | TAAAGTTCAATTCAA[G/T]AGCAATAATAATAAC | 6596 |
| rs755743345 | snp | A/G | 7.07439e-05 | 0.00594701 | intron-variant | HLTF | GRCh38.p7 | 3:149039037 | TCTGAAAAAATTTAC[A/G]GAACTACTTACTGGA | 6596 |
| rs755757366 | snp | C/T | 1.67801e-05 | 0.00289651 | missense | HLTF | GRCh38.p7 | 3:149039138 | TTATAGTTGGAGATC[C/T]TGCTTCAGTGTTTTG | 6596 |
| rs755783896 | snp | C/T | 1.65034e-05 | 0.00287253 | missense | HLTF | GRCh38.p7 | 3:149063524 | CTACATCTAGATGCG[C/T]CTATTTCAAAGAAAA | 6596 |
| rs755815666 | in-del | -/A | 0.000331913 | 0.0128781 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149039231 | AAATCCAGAGGCTCT[-/A]AAAGGGGGGAAGAAA | 6596 |
| rs755837584 | in-del | -/CTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149044858 | ATCATTTCTCACTCC[-/CTT]CTTTATCACTACTAT | 6596 |
| rs755849445 | snp | A/C | 1.70449e-05 | 0.00291928 | intron-variant | HLTF | GRCh38.p7 | 3:149068368 | AAGATAAATGGTCAG[A/C]TTGTGAAACCCAGTT | 6596 |
| rs755860159 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084781 | AAAGTCATCTGGAGG[C/G]ATAACATCTTGGAAT | 6596 |
| rs755882072 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057253 | TAACATGGTGAAACC[C/T]GTCTCTATTAAAAAT | 6596 |
| rs755908278 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065395 | TTCTTTTCCAATGTA[C/T]CTTTGTTTCCAAAGG | 6596 |
| rs756028921 | snp | C/T | 1.66164e-05 | 0.00288235 | missense | HLTF | GRCh38.p7 | 3:149059796 | CATCTTCTATAACCT[C/T]AGAAGATCCTGCTGA | 6596 |
| rs756036645 | snp | A/G | 1.70168e-05 | 0.00291687 | missense | HLTF | GRCh38.p7 | 3:149040053 | CTGGATGTCCATTCC[A/G]TATCAGACTTTTTCT | 6596 |
| rs756046045 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149076965 | TGTAGCCTTTAAAAA[C/T]AGCTCACGGCCAGGC | 6596 |
| rs756062602 | snp | A/G | 1.90729e-05 | 0.00308805 | intron-variant | HLTF | GRCh38.p7 | 3:149046050 | AAGTAAACAAAAACT[A/G]ATTTTTAACATGGTT | 6596 |
| rs756076490 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149041891 | GCATCATTATAACAT[A/G]ACAATAACATACCAC | 6596 |
| rs756113953 | snp | C/T | 0.000132323 | 0.0081329 | missense | HLTF | GRCh38.p7 | 3:149071302 | CATTTTCTGGTCGGT[C/T]CTTCTCAGAAAAATT | 6596 |
| rs756125020 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149060975 | ATTTATTTTTTGAAA[A/C]ATTTTTTAAAGATTT | 6596 |
| rs756236730 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073458 | AAGCACTTTGGGAGG[C/T]CAAGGCAGGTGGTTT | 6596 |
| rs756263932 | snp | A/G | 1.71408e-05 | 0.00292747 | missense | HLTF | GRCh38.p7 | 3:149049000 | GGACTATCTCCTTTA[A/G]TCTGAAATAAATGTT | 6596 |
| rs756379202 | snp | C/T | 1.84137e-05 | 0.00303422 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039670 | CTTTCTTAAGTCAGT[C/T]AATGCGTGCATTAGC | 6596 |
| rs756385930 | snp | A/G/T | 3.304e-05 | 0.00406437 | splice-donor-variant | HLTF | GRCh38.p7 | 3:149048861 | TTTAATGCTATGATT[A/G/T]CCTGTCAAAACCCAT | 6596 |
| rs756417745 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048665 | CTAGTGACTGTTCCA[C/T]AAATTATCAATAAGT | 6596 |
| rs756420238 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149073016 | ATGTTGGGTACAAAT[A/G]TTCACGTATGGATTT | 6596 |
| rs756479170 | snp | G/T | 1.64776e-05 | 0.00287028 | missense | HLTF | GRCh38.p7 | 3:149055374 | CCTCAACATCAGTTT[G/T]CTTTGACCCCTCCAC | 6596 |
| rs756513561 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149046593 | GTCAACTCCATCACC[A/G]AATAGTCAACACTCA | 6596 |
| rs756570321 | snp | A/T | 1.64874e-05 | 0.00287113 | intron-variant | HLTF | GRCh38.p7 | 3:149060716 | AAAAATAAACATAAA[A/T]ATGGGCAAAACAGGA | 6596 |
| rs756598832 | snp | A/T | 1.65578e-05 | 0.00287726 | intron-variant | HLTF | GRCh38.p7 | 3:149042131 | TTAAGTATCTCTGAC[A/T]AATACAATGATATGA | 6596 |
| rs756603568 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149062452 | AGAACAATTAACATA[C/G]CCAGTTTCAAAACCT | 6596 |
| rs756768119 | snp | C/T | 3.30109e-05 | 0.00406256 | missense | HLTF | GRCh38.p7 | 3:149075912 | ATTTGTTGTCCATGA[C/T]ATAGGCCAAAGCACC | 6596 |
| rs756793557 | snp | C/T | 1.66463e-05 | 0.00288494 | missense | HLTF | GRCh38.p7 | 3:149074347 | CACCAAAAGGAACTA[C/T]CCTATTATATTTGGG | 6596 |
| rs756822122 | in-del | -/T | 1.97791e-05 | 0.0031447 | frameshift-variant | HLTF | GRCh38.p7 | 3:149046230 | TTGTTCTTCTAAGTG[-/T]TAATATTTTTAATTA | 6596 |
| rs756831793 | snp | A/G | 1.70635e-05 | 0.00292087 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039154 | TGCTTCAGTGTTTTG[A/G]AAACACTGAATTGAT | 6596 |
| rs756920042 | snp | C/T | 2.07157e-05 | 0.0032183 | missense | HLTF | GRCh38.p7 | 3:149039221 | CGAGTAAACACAAAT[C/T]CAGAGGCTCTAAAGG | 6596 |
| rs756943593 | snp | A/T | 4.98658e-05 | 0.00499304 | missense | HLTF | GRCh38.p7 | 3:149059802 | CTATAACCTTAGAAG[A/T]TCCTGCTGATAAAAC | 6596 |
| rs756953790 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149057634 | AAAACTTATGTGAAT[C/G]TGGTCATTCTCTGTC | 6596 |
| rs756955738 | snp | A/G | 5.41062e-05 | 0.00520098 | intron-variant | HLTF | GRCh38.p7 | 3:149055264 | CCTTGTAGATAAAAT[A/G]TAAATTATGTTACAT | 6596 |
| rs756959646 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149071990 | CCTAGTAGGTAGAGG[A/G]TAGAGTGAACCATGA | 6596 |
| rs757018453 | snp | C/G | 1.65363e-05 | 0.00287539 | missense | HLTF | GRCh38.p7 | 3:149071410 | TCCAAGCTAGAGCTT[C/G]TTTTTGATGTGGAAG | 6596 |
| rs757023936 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082016 | TCTAAATAAAATGGA[C/T]GCTTTTCTTCAAAAA | 6596 |
| rs757086826 | in-del | -/AAAC | | | intron-variant | HLTF | GRCh38.p7 | 3:149057427 | TGAGACTCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 6596 |
| rs757167208 | snp | C/G | 3.43867e-05 | 0.00414634 | intron-variant | HLTF | GRCh38.p7 | 3:149047984 | GGTTCAAGCTACTAA[C/G]AGTTATTTGTAACTA | 6596 |
| rs757167364 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149079321 | TCACATCATAATCAA[A/C]CTGTCAAAAGAAGTT | 6596 |
| rs757189362 | in-del | -/TATA | 1.93697e-05 | 0.00311199 | intron-variant | HLTF | GRCh38.p7 | 3:149039982 | CTGTGTATATTTCCT[-/TATA]TAAAGGTAAAACAAA | 6596 |
| rs757214237 | snp | A/G/T | 0.000122849 | 0.00783658 | missense, synonymous-codon | HLTF | GRCh38.p7 | 3:149046180 | CTTTACGTTCTGGTA[A/G/T]CTCCAAAACAGGTTT | 6596 |
| rs757247931 | snp | A/G | 1.6591e-05 | 0.00288015 | intron-variant | HLTF | GRCh38.p7 | 3:149060611 | TTTAATAATCTTGAA[A/G]TCTAGATTATGGGTA | 6596 |
| rs757288507 | in-del | -/AAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149046621 | CAAATTCTAAGTATC[-/AAT]TATTAAGTGCCAGGC | 6596 |
| rs757297184 | snp | C/T | 1.82354e-05 | 0.00301949 | intron-variant | HLTF | GRCh38.p7 | 3:149049019 | GAAATAAATGTTTTA[C/T]ATGAATTAAAAAACA | 6596 |
| rs757386946 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062620 | AAGATCAGAGGGGAA[C/T]TACATCTTTTATTCA | 6596 |
| rs757416768 | snp | C/T | 1.65111e-05 | 0.0028732 | missense | HLTF | GRCh38.p7 | 3:149071321 | CTCAGAAAAATTTGT[C/T]ATTGTGTTATAGTAT | 6596 |
| rs757455150 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084821 | GGAAAGAAAGTTGGA[C/T]ATGAGAGGCGTGGAA | 6596 |
| rs757503352 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040568 | AAAGCTTATAATAGC[C/T]TATAAAGCTACTAGG | 6596 |
| rs757506600 | snp | A/T | 3.13908e-05 | 0.00396162 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086283 | CGCCTCCAGGCCGTT[A/T]GACCGAGCGCCCCAC | 6596 |
| rs757526301 | snp | C/T | 1.67984e-05 | 0.00289809 | missense | HLTF | GRCh38.p7 | 3:149040075 | ACTTTTTCTCACTGT[C/T]ACGTGCTAATTCTTC | 6596 |
| rs757549039 | in-del | -/A | 1.64803e-05 | 0.00287052 | frameshift-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084811 | TCAAAACGTGGAAAG[-/A]AAAGTTGGATATGAG | 6596 |
| rs757567941 | snp | C/T | 1.65018e-05 | 0.00287239 | synonymous-codon | HLTF | GRCh38.p7 | 3:149073285 | GCTTGGTCCAGCTCT[C/T]CCAGAGCCCCAACCA | 6596 |
| rs757663949 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034028 | AAACTATTTGTACCA[C/T]AACTATGAGAACTGG | 6596 |
| rs757764901 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042971 | GTAATAATCAGCAGA[A/G]AGCAAAGGTAGGGGA | 6596 |
| rs757789443 | snp | A/T | 1.69169e-05 | 0.00290829 | intron-variant | HLTF | GRCh38.p7 | 3:149068205 | TTCACAATAAACTGG[A/T]GGTTTCACATAAAGC | 6596 |
| rs757800653 | snp | A/G | 2.07592e-05 | 0.00322167 | intron-variant | HLTF | GRCh38.p7 | 3:149060877 | AAATTAAGTATACAC[A/G]AAGAAATTTTTGGAC | 6596 |
| rs757854627 | snp | A/T | 1.72907e-05 | 0.00294025 | intron-variant | HLTF | GRCh38.p7 | 3:149034883 | TGTAAAAATCGTATC[A/T]ACCTAGTCTTAAAAT | 6596 |
| rs757859783 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081215 | ATTATAAAATAAAGC[C/T]TTTGATGGGTCAAAA | 6596 |
| rs757956601 | in-del | -/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149061176 | CTGGGCTCAAGTGAT[-/C]ATCCCGCCTTAGCCT | 6596 |
| rs757975440 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149060527 | AGTTCAAATGTAAAC[A/G]TCAGCCAAGTTTAAG | 6596 |
| rs758065489 | snp | C/T | 3.4229e-05 | 0.00413683 | intron-variant | HLTF | GRCh38.p7 | 3:149048001 | GTTATTTGTAACTAA[C/T]ATTAATCACTGTCTG | 6596 |
| rs758094000 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077173 | GAACCACTTGAACCC[A/G]GCAGGCAGAGGTTGC | 6596 |
| rs758118066 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149043655 | TGGGTGATCCAAAAA[G/T]TATATAACCAGGCCA | 6596 |
| rs758138292 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054676 | GTCAATGTTTCAGAA[C/T]AGAAAAGCAATCTGG | 6596 |
| rs758140684 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086747 | CGAGGCCCCAGGAGT[A/G]CGACTGCGGTGCCTG | 6596 |
| rs758156939 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | HLTF | GRCh38.p7 | 3:149055382 | TCAGTTTTCTTTGAC[C/T]CCTCCACTGCACAAG | 6596 |
| rs758191302 | in-del | -/TACTT | 1.79168e-05 | 0.00299301 | intron-variant | HLTF | GRCh38.p7 | 3:149040023 | ATATTTGCACATGAG[-/TACTT]TACCTTTGAACTGGA | 6596 |
| rs758204100 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | HLTF | GRCh38.p7 | 3:149060699 | TTGCCTAAAAATAAA[A/G]CAAAAATAAACATAA | 6596 |
| rs758229841 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149053125 | GCCTGCTCTGTAGAA[G/T]GCTAGATCCTTTACT | 6596 |
| rs758292477 | snp | C/T | 1.78248e-05 | 0.00298531 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039178 | AATTGATTCAACTCT[C/T]TTCTTTTGGGCCATG | 6596 |
| rs758315818 | in-del | -/CTGT | 8.52479e-05 | 0.00652814 | intron-variant | HLTF | GRCh38.p7 | 3:149048010 | AACTAATATTAATCA[-/CTGT]CTGAAAGTACTTACC | 6596 |
| rs758336149 | snp | G/T | 4.1295e-05 | 0.00454376 | intron-variant | HLTF | GRCh38.p7 | 3:149076072 | ATGATAAACAGATAA[G/T]ATTACATTATAAATA | 6596 |
| rs758353621 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049999 | CTCCATCGAGAGGGA[G/T]GGGGAGGGGAGGAGT | 6596 |
| rs758377662 | in-del | -/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031088 | TAAATTTCTAGCTTC[-/T]TTTGTTTTAAATATG | 6596 |
| rs758383299 | snp | A/G | 1.66366e-05 | 0.0028841 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048135 | AAGAAGAGACCACAA[A/G]TCCTTTAAAGAATTC | 6596 |
| rs758472323 | in-del | -/AATT | | | intron-variant | HLTF | GRCh38.p7 | 3:149068524 | ACTGCATTATTAGGG[-/AATT]ATTAAATGATTTACA | 6596 |
| rs758503058 | snp | A/G | 4.95127e-05 | 0.00497533 | missense | HLTF | GRCh38.p7 | 3:149071332 | TTGTTATTGTGTTAT[A/G]GTATAAGTCATTTCG | 6596 |
| rs758543037 | snp | A/G | 1.67203e-05 | 0.00289134 | intron-variant | HLTF | GRCh38.p7 | 3:149040198 | CAACACTTAACAGAA[A/G]AACAAATATAAATAT | 6596 |
| rs758554213 | in-del | -/AGAC | 6.27333e-05 | 0.00560024 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086283 | CGCCTCCAGGCCGTT[-/AGAC]CGAGCGCCCCACCCC | 6596 |
| rs758583550 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065149 | CAATTATAAATGACA[C/T]ATTATTGTGAGAAAA | 6596 |
| rs758635626 | snp | C/G | 1.65395e-05 | 0.00287567 | missense | HLTF | GRCh38.p7 | 3:149074310 | AAAGTCATATGCAGA[C/G]GCATGGTAAAAGCAT | 6596 |
| rs758679659 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063918 | TTACTAAACACTGTT[C/T]GGCTCCCCTACCCAT | 6596 |
| rs758681664 | snp | C/T | 1.65288e-05 | 0.00287474 | intron-variant | HLTF | GRCh38.p7 | 3:149060634 | TATGGGTATATAGTA[C/T]ACACATACCTTTCGC | 6596 |
| rs758731371 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149059242 | ATTTGTCTCAGATCT[C/T]CTCAACCTTAGTTCA | 6596 |
| rs758733185 | snp | A/G | 3.29984e-05 | 0.00406179 | intron-variant | HLTF | GRCh38.p7 | 3:149063411 | TAAACATATGACATA[A/G]TCAAACCATAATAGT | 6596 |
| rs758736711 | snp | A/G | 1.67094e-05 | 0.0028904 | missense | HLTF | GRCh38.p7 | 3:149071433 | TGTGGAAGCAGTGGT[A/G]TTTCAATAGCCTATA | 6596 |
| rs758783282 | in-del | -/AG | | | intron-variant | HLTF | GRCh38.p7 | 3:149042546 | CTGCAGATCTCAAAC[-/AG]AGCTGCCAAAACACA | 6596 |
| rs758799142 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077178 | ACTTGAACCCGGCAG[A/G]CAGAGGTTGCAGTGA | 6596 |
| rs758823272 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072106 | CCACAAACTAGTCAA[A/T]CGCCAAAAAGGCACA | 6596 |
| rs758828757 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036216 | ATAACCAAAAAGATA[C/T]AGACCCCTGGTAAGT | 6596 |
| rs758864585 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | HLTF | GRCh38.p7 | 3:149063521 | TCACTACATCTAGAT[C/G]CGTCTATTTCAAAGA | 6596 |
| rs758881607 | snp | C/T | 1.66743e-05 | 0.00288736 | synonymous-codon | HLTF | GRCh38.p7 | 3:149040091 | ACGTGCTAATTCTTC[C/T]GGAGGACATTCTAAT | 6596 |
| rs758902429 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149083444 | CTCAGATCAAAAATA[A/C]TGATTGTTCTAAGAT | 6596 |
| rs758931644 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049378 | GGCAGTTGTAAGAAT[C/T]ACTTGAATTCAACAT | 6596 |
| rs758971713 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149084283 | CTCCTAAGGAATCTC[C/T]TGTCGAACATGCTTC | 6596 |
| rs758983730 | snp | A/G | 3.31055e-05 | 0.00406837 | stop-gained | HLTF | GRCh38.p7 | 3:149071299 | GGACATTTTCTGGTC[A/G]GTCCTTCTCAGAAAA | 6596 |
| rs759000757 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080007 | AACTCAAAATATATA[A/G]TAAAAGAAACAAGGG | 6596 |
| rs759077576 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149044758 | GGTAAAAAGGCTTGA[A/C]GTTATCTTTGATTCC | 6596 |
| rs759085122 | snp | C/G | 1.69714e-05 | 0.00291298 | intron-variant | HLTF | GRCh38.p7 | 3:149059851 | TTTTTCAAATTATCT[C/G]CTGTGCTAGAGTACA | 6596 |
| rs759149743 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149065066 | TTCACGGGTTATCTC[-/A]AAAAAAAAAAAAATA | 6596 |
| rs759171506 | snp | A/G | 1.65932e-05 | 0.00288034 | intron-variant | HLTF | GRCh38.p7 | 3:149040159 | ATTTAGCATGTGGCT[A/G]TATAAGAAAGAACGA | 6596 |
| rs759214479 | snp | G/T | 1.64977e-05 | 0.00287203 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071360 | TCGCTGTTCCCAGAA[G/T]GGTGGAAGTTCTTTG | 6596 |
| rs759260915 | snp | C/T | 1.66114e-05 | 0.00288192 | missense | HLTF | GRCh38.p7 | 3:149059787 | CAAATGCCACATCTT[C/T]TATAACCTTAGAAGA | 6596 |
| rs759333857 | snp | A/T | 1.65282e-05 | 0.00287469 | intron-variant | HLTF | GRCh38.p7 | 3:149063388 | CACATAAGAAAACAG[A/T]GTCTAAATAAACATA | 6596 |
| rs759371992 | snp | G/T | 3.29843e-05 | 0.00406092 | missense | HLTF | GRCh38.p7 | 3:149034936 | TGTGATGATAACTTC[G/T]TGCTTCTGACCAAGT | 6596 |
| rs759380311 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149084095 | CCTTCATAACTTTCA[-/T]TTTATGAAACTGTCA | 6596 |
| rs759381674 | in-del | -/AGT | 1.75795e-05 | 0.0029647 | intron-variant | HLTF | GRCh38.p7 | 3:149073363 | AAAGCCATCAAATAA[-/AGT]AGGTTTTTATCTTTT | 6596 |
| rs759395566 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149063187 | GCCTCAGCCTCCTGG[A/G]TAACTGGGACTACAG | 6596 |
| rs759478589 | snp | C/T | 1.67489e-05 | 0.00289381 | splice-acceptor-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084890 | TTCCAAACTGGATCC[C/T]TATTTTTTTTTAAAG | 6596 |
| rs759500064 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085438 | AGGTTGCAGCGAGCC[A/G]AGATTGTGCCACTGC | 6596 |
| rs759511469 | snp | C/T | 1.74011e-05 | 0.00294962 | intron-variant | HLTF | GRCh38.p7 | 3:149050207 | TCAATCTTTAAAAGA[C/T]CTGTTAAGTATCAAC | 6596 |
| rs759517251 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047840 | GGAAGGGTAGTTATC[A/G]ACAATTAGAAATCTT | 6596 |
| rs759567008 | snp | A/G | 1.66596e-05 | 0.00288609 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048987 | TATGCTATGTAATGG[A/G]CTATCTCCTTTAGTC | 6596 |
| rs759608594 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149081330 | AGAGTTAAAAATAAA[C/G]AATGCTACTACATAA | 6596 |
| rs759681955 | snp | A/C | | | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084813 | CAAAACGTGGAAAGA[A/C]AGTTGGATATGAGAG | 6596 |
| rs759686415 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149045410 | AAATATAAATTCCTC[A/G]AGTGCAGGCATTTTT | 6596 |
| rs759686520 | snp | A/C | 9.90524e-05 | 0.00703679 | missense | HLTF | GRCh38.p7 | 3:149042243 | AGTCTAAGCAAAAGA[A/C]CCAGGACATCTGCAT | 6596 |
| rs759719125 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038387 | ATAGCATAATAGTAC[G/T]TAAATATTTACATGG | 6596 |
| rs759726476 | snp | A/T | 1.84361e-05 | 0.00303607 | intron-variant | HLTF | GRCh38.p7 | 3:149041730 | TGACAAGTTAATCTA[A/T]CTTATAAGGAAAAGT | 6596 |
| rs759787583 | snp | A/G/T | 3.49371e-05 | 0.00417942 | intron-variant | HLTF | GRCh38.p7 | 3:149073359 | GAATAAAGCCATCAA[A/G/T]TAAAGTAGGTTTTTA | 6596 |
| rs759817076 | snp | C/G | 3.61716e-05 | 0.00425259 | missense | HLTF | GRCh38.p7 | 3:149060845 | TTTCTATGTACTGGA[C/G]AGCAGTTTTTCTTCT | 6596 |
| rs759833974 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149075541 | AGAGTGAGACTTCGT[C/G]TCAAAATAAATAAAT | 6596 |
| rs759872382 | snp | G/T | 1.96446e-05 | 0.003134 | missense | HLTF | GRCh38.p7 | 3:149039210 | AACCATCCAAACGAG[G/T]AAACACAAATCCAGA | 6596 |
| rs759948672 | snp | C/T | 1.78455e-05 | 0.00298704 | intron-variant | HLTF | GRCh38.p7 | 3:149048198 | GTTATAACTCTTTAA[C/T]CAGAGTATCCAGTAA | 6596 |
| rs760012898 | in-del | -/T | 3.31614e-05 | 0.00407181 | intron-variant | HLTF | GRCh38.p7 | 3:149035048 | CCTGATCTTTCAGTG[-/T]TTTTGCATTTGTCCT | 6596 |
| rs760061545 | snp | A/C/T | 0.00016474 | 0.00907441 | missense, stop-gained | HLTF | GRCh38.p7 | 3:149055359 | TTGTTCTTGGTCTCT[A/C/T]CTCAACATCAGTTTT | 6596 |
| rs760064091 | in-del | -/T | 1.66743e-05 | 0.00288736 | frameshift-variant | HLTF | GRCh38.p7 | 3:149041497 | AAACTAACCTGCTCA[-/T]TCTGAATGACTTGGC | 6596 |
| rs760096395 | snp | A/G | 3.84312e-05 | 0.00438339 | missense | HLTF | GRCh38.p7 | 3:149039587 | GGAACTTACTTAAGT[A/G]GTATTTCTATTAAAG | 6596 |
| rs760096548 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | HLTF | GRCh38.p7 | 3:149068317 | TAAGGATTACTGCAA[C/T]GGCCGTAAGAGTTTT | 6596 |
| rs760111829 | snp | A/G | 1.66136e-05 | 0.00288211 | intron-variant | HLTF | GRCh38.p7 | 3:149060592 | CAAATCAATGGAGCT[A/G]TACTTTAATAATCTT | 6596 |
| rs760121386 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054249 | AAATTAACCTCCAAG[A/T]GTATGACAGTGAAGG | 6596 |
| rs760147934 | snp | C/T | 3.31516e-05 | 0.0040712 | intron-variant | HLTF | GRCh38.p7 | 3:149064901 | TCTTAAACAGTACTG[C/T]TATCAGTTTTAAATA | 6596 |
| rs760163852 | snp | C/T | 2.49007e-05 | 0.00352842 | intron-variant | HLTF | GRCh38.p7 | 3:149071538 | AGATTCTAAGTATAT[C/T]TAAACATTCTGAGTA | 6596 |
| rs760209244 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149071856 | GTTTGAGACCAGCCT[A/G]GATAACATAGTGAGA | 6596 |
| rs760286020 | snp | C/T | 1.65132e-05 | 0.00287339 | missense | HLTF | GRCh38.p7 | 3:149048091 | TGCCACCATTCTCTA[C/T]CAATAAATGGTTTAA | 6596 |
| rs760289095 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085573 | ATAAAAATACAACTA[C/T]TAATGTACCAGAAGT | 6596 |
| rs760322330 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049647 | TCATTTACAAATTGC[A/T]TCATATACTTACAAT | 6596 |
| rs760340950 | snp | A/T | 1.64876e-05 | 0.00287116 | missense | HLTF | GRCh38.p7 | 3:149060681 | GACTGTACATTTTTC[A/T]GTTTGCCTAAAAATA | 6596 |
| rs760376880 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149083790 | TGGGTATGGTGGTGA[A/G]CGCCAGCAGTCCCAG | 6596 |
| rs760411573 | snp | C/T | 1.68105e-05 | 0.00289914 | intron-variant | HLTF | GRCh38.p7 | 3:149075875 | TAAATTCTGAAAGTA[C/T]ATTACCCTTCAATTT | 6596 |
| rs760434444 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043092 | CTCAATAAAACAATT[C/G]CTCCAAAAAAAAAAA | 6596 |
| rs760444280 | in-del | -/TAT | 1.70758e-05 | 0.00292192 | intron-variant | HLTF | GRCh38.p7 | 3:149042311 | GATTAAAATGTCAAA[-/TAT]TATTAAGTCCGCTAA | 6596 |
| rs760476126 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044343 | CAACTTTTTCAAATA[A/G]AATAACCTTTACTAA | 6596 |
| rs760515982 | snp | C/G | 1.65124e-05 | 0.00287331 | missense | HLTF | GRCh38.p7 | 3:149071397 | TCCCGTGACACCATC[C/G]AAGCTAGAGCTTGTT | 6596 |
| rs760546650 | snp | A/T | 1.65743e-05 | 0.00287869 | missense | HLTF | GRCh38.p7 | 3:149050339 | AAACATAAAAATTCA[A/T]GTGTACATCTGATTT | 6596 |
| rs760570439 | snp | A/C | 1.83616e-05 | 0.00302993 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084917 | AAAGGCAAAGAAAAA[A/C]AATATAATATTTAAG | 6596 |
| rs760582674 | snp | C/T | 1.70825e-05 | 0.00292249 | intron-variant | HLTF | GRCh38.p7 | 3:149050227 | TAAGTATCAACAATA[C/T]TTACTCCATAGTCAT | 6596 |
| rs760645921 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044627 | ACTTGGAAAATTCAC[A/G]GGCATCCTATGATCA | 6596 |
| rs760688597 | snp | A/C/G | 5.34786e-05 | 0.00517078 | intron-variant | HLTF | GRCh38.p7 | 3:149073367 | CCATCAAATAAAGTA[A/C/G]GTTTTTATCTTTTAT | 6596 |
| rs760689387 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072624 | AAAAATCAGAAGTAA[C/G]CGGGGGCTTATCTAC | 6596 |
| rs760727991 | snp | C/T | 1.68955e-05 | 0.00290645 | synonymous-codon | HLTF | GRCh38.p7 | 3:149046127 | AGACTGATAAATCTT[C/T]CTCTCTTCATCTGAA | 6596 |
| rs760767730 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149055661 | ATTTTCTGATAGTCA[C/T]AGTCATTCATTAAGA | 6596 |
| rs760790990 | in-del | -/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149036056 | GGAGAATGGCGTGAA[-/C]CCCAGGAGGCGGAGC | 6596 |
| rs760793644 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040370 | AGGAGGGAGCAAAAG[C/T]ATGTGATCTGGACTA | 6596 |
| rs760801264 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149068619 | ATTCTACATTTAATC[A/C]TGAACTCTTGATTTT | 6596 |
| rs760815478 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | HLTF | GRCh38.p7 | 3:149034965 | GTCTATGGCATCTGT[C/T]AAAGCACTGATCTTC | 6596 |
| rs760838222 | snp | A/G/T | 4.9567e-05 | 0.0049781 | intron-variant | HLTF | GRCh38.p7 | 3:149063393 | AAGAAAACAGAGTCT[A/G/T]AATAAACATATGACA | 6596 |
| rs760844271 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149065590 | ATGCCAGCACTTTGG[C/G]AGACCGAGGCGGGCG | 6596 |
| rs760871654 | snp | A/G | 2.34491e-05 | 0.00342404 | intron-variant | HLTF | GRCh38.p7 | 3:149032414 | TAGTTTTTAAGGCAT[A/G]GTATTTAAAATCTTT | 6596 |
| rs760917479 | snp | G/T | 3.30136e-05 | 0.00406273 | stop-gained | HLTF | GRCh38.p7 | 3:149074262 | TTCTTCAACTGATCT[G/T]AAACCGCTTTTCTAT | 6596 |
| rs760927241 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | HLTF | GRCh38.p7 | 3:149063469 | TTCTGACATGCGAAA[C/T]TTACTCTTCTCCTTG | 6596 |
| rs760977669 | snp | A/G | 4.94817e-05 | 0.00497377 | synonymous-codon | HLTF | GRCh38.p7 | 3:149064852 | TTTCATAGAGTCATC[A/G]TTAACATTATATTCC | 6596 |
| rs761055691 | snp | A/G | 1.65968e-05 | 0.00288065 | missense | HLTF | GRCh38.p7 | 3:149068325 | ACTGCAATGGCCGTA[A/G]GAGTTTTACCCTTAA | 6596 |
| rs761078714 | snp | C/T | 7.61136e-05 | 0.00616855 | intron-variant | HLTF | GRCh38.p7 | 3:149040001 | TAAAGGTAAAACAAA[C/T]ACTCAAATATTTGCA | 6596 |
| rs761122417 | in-del | -/C | 1.64762e-05 | 0.00287016 | frameshift-variant | HLTF | GRCh38.p7 | 3:149055339 | AAGCGGACAGATGAT[-/C]AGTGTTGTTCTTGGT | 6596 |
| rs761180166 | snp | A/C/T | 3.39117e-05 | 0.00411763 | intron-variant | HLTF | GRCh38.p7 | 3:149074165 | TAAATGTTTCATAAT[A/C/T]CCTGCATCTTACAAT | 6596 |
| rs761203147 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149052108 | GCAGTGAGCTGAGAT[C/T]GCGCCATTGCACTCC | 6596 |
| rs761216314 | snp | C/T | 1.6537e-05 | 0.00287545 | synonymous-codon | HLTF | GRCh38.p7 | 3:149042263 | GACATCTGCATAATG[C/T]GCCAGGACAGTCCCT | 6596 |
| rs761233854 | snp | C/G | 4.98666e-05 | 0.00499308 | missense | HLTF | GRCh38.p7 | 3:149059747 | TTCTTTTTTGTTGTA[C/G]GAACAGATGAAGTTA | 6596 |
| rs761274500 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041274 | TGAACAGCAATGATA[C/T]AAACAGCGGAATTAA | 6596 |
| rs761311037 | in-del | -/ATAATTTATATTTTAT/CC | | | intron-variant | HLTF | GRCh38.p7 | 3:149055414 | CCTAAAAAAATGAAC[-/ATAATTTATATTTTAT/CC]CACTGATAGAACCTT | 6596 |
| rs761373385 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038370 | AAGAAAAGTAGAATA[A/G]CATAGCATAATAGTA | 6596 |
| rs761383244 | snp | C/T | 1.65302e-05 | 0.00287486 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048108 | AATAAATGGTTTAAG[C/T]TTTAAAAAGGAAAGA | 6596 |
| rs761384636 | snp | C/T | 1.65072e-05 | 0.00287286 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084713 | CGTAGTCCAACCACA[C/T]GACCTCTCAAACTTC | 6596 |
| rs761450921 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072778 | GATCTGCATTAATTA[C/T]TTTATATACTTTTTT | 6596 |
| rs761472812 | snp | C/T | 1.78624e-05 | 0.00298846 | intron-variant | HLTF | GRCh38.p7 | 3:149048204 | ACTCTTTAACCAGAG[C/T]ATCCAGTAAGAGTAT | 6596 |
| rs761488009 | snp | C/T | 2.5443e-05 | 0.00356663 | missense | HLTF | GRCh38.p7 | 3:149076037 | AATGCAACCATTTCA[C/T]TATTATTAACCTAAT | 6596 |
| rs761514615 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086346 | GGACATGGCGCTGAG[C/T]GGGATGACAAGAGGA | 6596 |
| rs761544271 | snp | A/C | 0.000265305 | 0.0115144 | intron-variant | HLTF | GRCh38.p7 | 3:149064906 | AACAGTACTGCTATC[A/C]GTTTTAAATAACTTT | 6596 |
| rs761590419 | in-del | -/TCT | 4.9894e-05 | 0.00499445 | cds-indel | HLTF | GRCh38.p7 | 3:149071614 | TCATGGGTTTTATCA[-/TCT]TCTTTTAAATCTTCA | 6596 |
| rs761607385 | snp | G/T | 1.70394e-05 | 0.0029188 | missense | HLTF | GRCh38.p7 | 3:149032236 | TATAAGTCAATTAAT[G/T]TTCTGATTTCATTAA | 6596 |
| rs761635389 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031599 | AAATAGTACTCTTAA[C/T]ATAATCCCTAATTTT | 6596 |
| rs761637225 | in-del | -/GTACA | | | intron-variant | HLTF | GRCh38.p7 | 3:149064666 | AGATCCTAAATTTTT[-/GTACA]GTACAAAGCCAAAAC | 6596 |
| rs761660272 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149044464 | ATTAGAAGCTTCCTT[C/T]CTCCTATTTCACCAG | 6596 |
| rs761660478 | snp | C/T | 1.65132e-05 | 0.00287339 | missense | HLTF | GRCh38.p7 | 3:149041651 | ACTTCTTTCTCAGTT[C/T]TTCAGGTGTATCATT | 6596 |
| rs761723970 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067935 | GATGGCTTGAGCTCA[G/T]GAGTTCGAGACCAGC | 6596 |
| rs761727214 | snp | C/T | 1.6495e-05 | 0.0028718 | missense | HLTF | GRCh38.p7 | 3:149041534 | AGGGTTTACAAAATA[C/T]ATGTGCACAATGTGT | 6596 |
| rs761734107 | snp | G/T | 1.69766e-05 | 0.00291342 | intron-variant | HLTF | GRCh38.p7 | 3:149074399 | AAGCATTACTTTTTA[G/T]CCCCACTAAGAATTA | 6596 |
| rs761814742 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | HLTF | GRCh38.p7 | 3:149063495 | CCTTGATATCTGAAA[C/T]ACTGGGTTGTTCACT | 6596 |
| rs761914922 | in-del | -/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149033114 | TAGGAATGAATGTCT[-/C]CAACCTTACATATTT | 6596 |
| rs761917151 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149042576 | CAATTCTTTAAAATG[G/T]ATGGCATGCCCTGAG | 6596 |
| rs761928482 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149077502 | GATGTTTGTCAAAAC[A/C]ATTTTACAGGAAAGT | 6596 |
| rs761929355 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058107 | CCTATTCCTTTATTT[C/T]ATGTTTTTGAGACAT | 6596 |
| rs761953733 | in-del | -/A | 0.0267107 | 0.112436 | intron-variant | HLTF | GRCh38.p7 | 3:149032383 | ATGAACTTTAAAAAG[-/A]AAAAAAAAAGTTAAG | 6596 |
| rs761992391 | snp | A/G | 1.66021e-05 | 0.0028811 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050346 | AAAATTCAAGTGTAC[A/G]TCTGATTTTATATGT | 6596 |
| rs762019305 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149056010 | CACATAGTGAGGATC[C/T]GAAGACTACAGTTAG | 6596 |
| rs762020302 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085710 | CAAGCCACCCGTACC[C/T]GCCTTCCGTCGCCGG | 6596 |
| rs762034774 | snp | C/G | 1.65701e-05 | 0.00287833 | missense | HLTF | GRCh38.p7 | 3:149039080 | ACTCGAGAAGCTGCA[C/G]ACAGATTCAAACCAA | 6596 |
| rs762042519 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050996 | GATTAAACTGAAAAG[A/G]GAAGATACCAGGGAG | 6596 |
| rs762045765 | snp | A/T | 1.65603e-05 | 0.00287747 | intron-variant | HLTF | GRCh38.p7 | 3:149064769 | AGATCAAATATTGGA[A/T]CATTTCAAAATTAGC | 6596 |
| rs762131019 | snp | C/T | 5.73312e-05 | 0.00535372 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086373 | AGGAGCGCCTCGGCT[C/T]CCCTGGATCGTTTTC | 6596 |
| rs762154956 | snp | A/G | 1.66062e-05 | 0.00288146 | missense | HLTF | GRCh38.p7 | 3:149059769 | ATGAAGTTAATGCAC[A/G]TGCAAATGCCACATC | 6596 |
| rs762284991 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149049886 | AATCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA | 6596 |
| rs762294418 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080818 | AAGAAAAAACAGGAC[A/G]TATAAAAAAACAAAA | 6596 |
| rs762322616 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149063217 | GGCGCCCACGACCAC[A/G]CCTGGCTAATTTTTG | 6596 |
| rs762370379 | snp | C/G | 3.30033e-05 | 0.00406209 | intron-variant | HLTF | GRCh38.p7 | 3:149035016 | AACAAGAACATGGAT[C/G]AGTTACTTTACTACT | 6596 |
| rs762370405 | snp | A/G | 8.25362e-05 | 0.00642349 | missense | HLTF | GRCh38.p7 | 3:149074268 | AACTGATCTGAAACC[A/G]CTTTTCTATTTTCTT | 6596 |
| rs762372116 | snp | C/T | 2.1944e-05 | 0.00331233 | missense | HLTF | GRCh38.p7 | 3:149046251 | TTTTTAATTAGGGAC[C/T]GTAAACGCCTAATCA | 6596 |
| rs762399183 | snp | C/T | 3.37832e-05 | 0.0041098 | intron-variant | HLTF | GRCh38.p7 | 3:149059846 | AAATTTTTTTCAAAT[C/T]ATCTCCTGTGCTAGA | 6596 |
| rs762423430 | snp | A/T | 1.69304e-05 | 0.00290945 | missense | HLTF | GRCh38.p7 | 3:149046137 | ATCTTTCTCTCTTCA[A/T]CTGAAAGTGTAATGT | 6596 |
| rs762428846 | snp | A/C | 1.72546e-05 | 0.00293718 | missense | HLTF | GRCh38.p7 | 3:149039630 | TAAACTGAGAAACAA[A/C]CAAACTTTTTATGTT | 6596 |
| rs762485670 | in-del | -/T | 1.64985e-05 | 0.0028721 | frameshift-variant | HLTF | GRCh38.p7 | 3:149073282 | ATAGCTTGGTCCAGC[-/T]CTTCCAGAGCCCCAA | 6596 |
| rs762506034 | snp | A/C | 1.64999e-05 | 0.00287222 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084721 | AACCACATGACCTCT[A/C]AAACTTCCAAATAAA | 6596 |
| rs762559351 | snp | A/T | 1.65806e-05 | 0.00287924 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084880 | CTGCAAGTACTTCCA[A/T]ACTGGATCCCTATTT | 6596 |
| rs762672929 | snp | C/T | 1.86659e-05 | 0.00305493 | intron-variant | HLTF | GRCh38.p7 | 3:149040009 | AAACAAATACTCAAA[C/T]ATTTGCACATGAGTA | 6596 |
| rs762678726 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070274 | ACAAATTTTCTTCAT[A/G]TACTTCAACCAAAAC | 6596 |
| rs762699678 | snp | A/C | 5.04834e-05 | 0.00502386 | intron-variant | HLTF | GRCh38.p7 | 3:149068341 | GAGTTTTACCCTTAA[A/C]AATGTTTTAAAAAGA | 6596 |
| rs762769825 | snp | A/G | 1.66868e-05 | 0.00288845 | intron-variant | HLTF | GRCh38.p7 | 3:149048835 | TTTTAGAGATTTAAG[A/G]TTTTAGTAAGTTTAA | 6596 |
| rs762772477 | snp | C/T | 1.6571e-05 | 0.0028784 | splice-donor-variant | HLTF | GRCh38.p7 | 3:149073224 | TAAAAGAGAAGCACA[C/T]CTGTTCAGTTGTCAT | 6596 |
| rs762786306 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149082413 | GCAATGAGCCGAGAT[A/C]CCGCCACTGCGCTCC | 6596 |
| rs762795085 | snp | G/T | 1.65004e-05 | 0.00287227 | missense | HLTF | GRCh38.p7 | 3:149042221 | AGTATGGCAACAAAT[G/T]TGCCGCAGTCTAAGC | 6596 |
| rs762802534 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032391 | TAAAAAGAAAAAAAA[A/G]AGTTAAGTAGTTTTT | 6596 |
| rs762863740 | snp | A/T | 1.70316e-05 | 0.00291813 | missense | HLTF | GRCh38.p7 | 3:149032267 | TTTTGGCTTGTTTCA[A/T]TTCGTCAGCATTTGG | 6596 |
| rs762870563 | snp | C/G | 1.65236e-05 | 0.00287429 | intron-variant | HLTF | GRCh38.p7 | 3:149064878 | ATTCCTGGGTAAATA[C/G]GCATATTTCTTAAAC | 6596 |
| rs762903392 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032820 | TAGAAAAAGTTAGCC[A/G]GGCATGGTGGTGGGC | 6596 |
| rs762914327 | in-del | -/ATAATTTATATT | 1.65162e-05 | 0.00287365 | intron-variant | HLTF | GRCh38.p7 | 3:149055417 | AAAAAAATGAACCAC[-/ATAATTTATATT]TGATAGAACCTTTAG | 6596 |
| rs762988909 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047768 | GTTTTGGGGCTTTGG[A/G]GCTTAGCAACACACA | 6596 |
| rs762991033 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031934 | AGTACTTGGAAGATA[C/T]GTGAAAATACTCAGC | 6596 |
| rs763011294 | snp | A/G | 1.67203e-05 | 0.00289134 | missense | HLTF | GRCh38.p7 | 3:149060811 | AATTCACTTGTTTCA[A/G]TTTCCTCTGAATCAC | 6596 |
| rs763066870 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149080379 | AAATTCCTTGAAAAT[A/C]TACAAGAAAGCTGCT | 6596 |
| rs763089896 | snp | A/T | 1.71463e-05 | 0.00292795 | intron-variant | HLTF | GRCh38.p7 | 3:149050406 | GAATATTTTTAACAA[A/T]GAGCAGATTTGTGTC | 6596 |
| rs763129433 | snp | A/T | 1.6582e-05 | 0.00287936 | missense | HLTF | GRCh38.p7 | 3:149041665 | TCTTCAGGTGTATCA[A/T]TTCCTAGAGAAAAGG | 6596 |
| rs763168134 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042630 | GCAGAAACAGGAACA[C/G]GGTGCATGCTTGGTG | 6596 |
| rs763182508 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | HLTF | GRCh38.p7 | 3:149055334 | ACAGAAAGCGGACAG[A/G]TGATCAGTGTTGTTC | 6596 |
| rs763234822 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087454 | GGGCAGGAAGCTGGT[A/G]GTGGCGCCCAGCTGC | 6596 |
| rs763257592 | snp | A/C | 2.46024e-05 | 0.00350722 | missense | HLTF | GRCh38.p7 | 3:149071601 | AGCTGGTTCCATTTC[A/C]TGGGTTTTATCATCT | 6596 |
| rs763293274 | snp | A/C | 3.31153e-05 | 0.00406898 | intron-variant | HLTF | GRCh38.p7 | 3:149046272 | CGCCTAATCAGAATA[A/C]AACAAATAATTATGT | 6596 |
| rs763340489 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086642 | GCAACTCCGCCCCGC[C/T]GCCATTCAAAGACGG | 6596 |
| rs763388341 | snp | A/C | 1.75551e-05 | 0.00296264 | missense | HLTF | GRCh38.p7 | 3:149075994 | TTTAATTGCATTCTT[A/C]TCATAAGGGTTATTA | 6596 |
| rs763433345 | in-del | -/T | 1.74072e-05 | 0.00295013 | intron-variant | HLTF | GRCh38.p7 | 3:149034878 | TAATTGTAAAAATCG[-/T]TATCAACCTAGTCTT | 6596 |
| rs763482062 | snp | A/C/G | 3.45466e-05 | 0.004156 | intron-variant | HLTF | GRCh38.p7 | 3:149075852 | CTATAATTCACAATT[A/C/G]TTAAAACTAAATTCT | 6596 |
| rs763496643 | snp | A/T | 4.95577e-05 | 0.00497759 | intron-variant | HLTF | GRCh38.p7 | 3:149064782 | GATCATTTCAAAATT[A/T]GCATTTACCTTTGCT | 6596 |
| rs763512201 | snp | C/T | 3.6702e-05 | 0.00428365 | missense | HLTF | GRCh38.p7 | 3:149039192 | TTTTCTTTTGGGCCA[C/T]GGAACCATCCAAACG | 6596 |
| rs763528995 | snp | C/T | 1.66333e-05 | 0.00288381 | missense | HLTF | GRCh38.p7 | 3:149048040 | TACCTAAGTCCTCCT[C/T]CATCTCCCATTGTGA | 6596 |
| rs763554421 | snp | A/C | 1.64876e-05 | 0.00287116 | missense | HLTF | GRCh38.p7 | 3:149060687 | ACATTTTTCAGTTTG[A/C]CTAAAAATAAAACAA | 6596 |
| rs763555905 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030522 | AGGCTTTGTCTTTGT[A/G]AGCAGAAAGAGTAGA | 6596 |
| rs763567216 | snp | C/G | 1.65825e-05 | 0.00287941 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039115 | ACCTGCTTTTAAGGA[C/G]AGAAGCATTATAGTT | 6596 |
| rs763578358 | in-del | -/TATA | 5.64127e-05 | 0.00531067 | intron-variant | HLTF | GRCh38.p7 | 3:149039272 | AACAAACACTATTAT[-/TATA]AAAATAAAACAAAGT | 6596 |
| rs763607239 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | HLTF | GRCh38.p7 | 3:149060596 | TCAATGGAGCTGTAC[C/T]TTAATAATCTTGAAG | 6596 |
| rs763621556 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037197 | ACAGACCGGCTGGGC[A/G]CGGTGGCTCATGCCT | 6596 |
| rs763659301 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048451 | CTGCTTATTTAGTTT[C/T]TAAAGCAGCAGCACT | 6596 |
| rs763700041 | snp | C/T | 3.37399e-05 | 0.00410717 | missense | HLTF | GRCh38.p7 | 3:149039144 | TTGGAGATCCTGCTT[C/T]AGTGTTTTGAAAACA | 6596 |
| rs763705831 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149071960 | AGGGATGCTGAGATG[G/T]GAGGATCACTTCAGC | 6596 |
| rs763767912 | snp | C/T | 3.76343e-05 | 0.00433771 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084922 | CAAAGAAAAACAATA[C/T]AATATTTAAGTATTT | 6596 |
| rs763780376 | in-del | -/AAT | 5.23674e-05 | 0.00511674 | intron-variant | HLTF | GRCh38.p7 | 3:149042331 | TTAAGTCCGCTAAAC[-/AAT]AATAACTTCCTATTC | 6596 |
| rs763782961 | snp | A/T | 1.65187e-05 | 0.00287386 | missense | HLTF | GRCh38.p7 | 3:149048095 | ACCATTCTCTATCAA[A/T]AAATGGTTTAAGTTT | 6596 |
| rs763792435 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149056160 | AGACCATAAGCCATT[-/A]AACCATCCAGCTAAG | 6596 |
| rs763793756 | snp | C/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085581 | ACAACTATTAATGTA[C/G]CAGAAGTTGTTTATA | 6596 |
| rs763803270 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149049672 | TACAATCCAAATTTA[A/C]AATCTTAACTTAAAA | 6596 |
| rs763804314 | snp | C/T | 8.49538e-05 | 0.00651688 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050232 | ATCAACAATACTTAC[C/T]CCATAGTCATGAGTT | 6596 |
| rs763813347 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149044352 | CAAATAGAATAACCT[C/T]TACTAACACTAATTA | 6596 |
| rs763875975 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149083859 | GGGAGGCAGAGATTG[C/T]AGTGAGGCCAGATCA | 6596 |
| rs763904960 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149060162 | ATCAGTCAAGATGAT[C/G]AGTTATTTTCCAAAT | 6596 |
| rs763908817 | snp | A/C | 1.66277e-05 | 0.00288333 | missense | HLTF | GRCh38.p7 | 3:149075887 | GTACATTACCCTTCA[A/C]TTTGTGCCAATTTGT | 6596 |
| rs763973596 | snp | A/G | 5.57057e-05 | 0.00527728 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086369 | CAAGAGGAGCGCCTC[A/G]GCTCCCCTGGATCGT | 6596 |
| rs764011305 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041305 | GATATTGACTGTGAA[C/T]ATCTTTTTATGTTGC | 6596 |
| rs764134229 | snp | G/T | 1.65176e-05 | 0.00287376 | missense | HLTF | GRCh38.p7 | 3:149041522 | CTTGGCAAATACAGG[G/T]TTTACAAAATACATG | 6596 |
| rs764148281 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058848 | TGTATCACAGCTATG[C/T]ATCTGCAACTGAAAG | 6596 |
| rs764156766 | snp | A/G/T | 6.60833e-05 | 0.00574786 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071405 | CACCATCCAAGCTAG[A/G/T]GCTTGTTTTTGATGT | 6596 |
| rs764252807 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040496 | ACAGCTACACTATTT[A/T]GTACTATTCTTTAAA | 6596 |
| rs764277677 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053084 | GGATTATTTGAAGAC[A/G]AAAAAGGGAATATAA | 6596 |
| rs764324692 | in-del | -/T/TAACATAATTTATATTTT | 1.64963e-05 | 0.00287192 | intron-variant | HLTF | GRCh38.p7 | 3:149055411 | GCTCCTAAAAAAATG[-/T/TAACATAATTTATATTTT]AACCACTGATAGAAC | 6596 |
| rs764344814 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054573 | AGAGAGTCATTATTT[C/T]ATCATAACAAGAAGT | 6596 |
| rs764355968 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149068685 | GAAGTTCGGAGCTAA[A/G]GTGATTAGTAATTCC | 6596 |
| rs764359762 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | HLTF | GRCh38.p7 | 3:149063476 | ATGCGAAACTTACTC[G/T]TCTCCTTGATATCTG | 6596 |
| rs764391793 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149064229 | CCCTAACTCGCCACC[-/T]TTCTATTTCTTTCCT | 6596 |
| rs764432368 | snp | A/G | 5.3313e-05 | 0.00516272 | intron-variant | HLTF | GRCh38.p7 | 3:149049010 | CTTTAGTCTGAAATA[A/G]ATGTTTTATATGAAT | 6596 |
| rs764451984 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048669 | TGACTGTTCCATAAA[C/T]TATCAATAAGTCAAA | 6596 |
| rs764506102 | in-del | -/GGTTTTAAGAGTCA | | | intron-variant | HLTF | GRCh38.p7 | 3:149035687 | AAAAAAAAAAAGGGG[-/GGTTTTAAGAGTCA]GTTTTAAGAGTCAGT | 6596 |
| rs764515735 | snp | C/G | 1.65605e-05 | 0.0028775 | intron-variant | HLTF | GRCh38.p7 | 3:149055432 | CTGATAGAACCTTTA[C/G]CTGTTTTTCTGAAAT | 6596 |
| rs764530519 | snp | G/T | 8.28246e-05 | 0.00643471 | intron-variant | HLTF | GRCh38.p7 | 3:149064899 | TTTCTTAAACAGTAC[G/T]GCTATCAGTTTTAAA | 6596 |
| rs764541984 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149063805 | CAAGGCAGCTAAGAG[C/G]TATTGGAAAAAAAAA | 6596 |
| rs764542356 | in-del | -/A | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030653 | CTTGATCTACCAGGT[-/A]AACTTCCCAACTGCT | 6596 |
| rs764559410 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075151 | GCGGACTTAGCTATT[A/T]CAATAATTAGTACTG | 6596 |
| rs764564890 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | HLTF | GRCh38.p7 | 3:149055376 | TCAACATCAGTTTTC[C/T]TTGACCCCTCCACTG | 6596 |
| rs764582461 | in-del | -/A | 2.53309e-05 | 0.00355876 | intron-variant | HLTF | GRCh38.p7 | 3:149046268 | TAAACGCCTAATCAG[-/A]ATAAAACAAATAATT | 6596 |
| rs764604518 | snp | C/G | 1.81283e-05 | 0.00301061 | intron-variant | HLTF | GRCh38.p7 | 3:149048214 | CAGAGTATCCAGTAA[C/G]AGTATCTATTTGGCC | 6596 |
| rs764697623 | snp | C/G | 1.6896e-05 | 0.0029065 | missense | HLTF | GRCh38.p7 | 3:149046128 | GACTGATAAATCTTT[C/G]TCTCTTCATCTGAAA | 6596 |
| rs764748974 | snp | A/G | 1.6554e-05 | 0.00287693 | synonymous-codon | HLTF | GRCh38.p7 | 3:149042268 | CTGCATAATGTGCCA[A/G]GACAGTCCCTTCATT | 6596 |
| rs764764394 | in-del | -/AAAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149075548 | ACTTCGTCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 6596 |
| rs764811304 | snp | A/C | 1.65908e-05 | 0.00288012 | missense | HLTF | GRCh38.p7 | 3:149048129 | AAAGGAAAGAAGAGA[A/C]CACAAGTCCTTTAAA | 6596 |
| rs764820039 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044780 | TTTGATTCCTCTTTC[A/G]CATGCCATAACATAT | 6596 |
| rs764863958 | snp | C/T | 1.66532e-05 | 0.00288554 | intron-variant | HLTF | GRCh38.p7 | 3:149064911 | TACTGCTATCAGTTT[C/T]AAATAACTTTAAATG | 6596 |
| rs764873252 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149042457 | AAGAGAGATCTATAA[A/C]AATAAGGCACAATAT | 6596 |
| rs764876584 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084716 | AGTCCAACCACATGA[C/T]CTCTCAAACTTCCAA | 6596 |
| rs764911735 | snp | C/T | 1.78436e-05 | 0.00298688 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039604 | TATTTCTATTAAAGA[C/T]AGGAATGTTGTAAAC | 6596 |
| rs764912700 | snp | A/G | 1.65573e-05 | 0.00287721 | intron-variant | HLTF | GRCh38.p7 | 3:149060624 | AAGTCTAGATTATGG[A/G]TATATAGTATACACA | 6596 |
| rs764933189 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149033905 | AAGCTTTTTCATGAC[A/C]AAAAAAATGCAGTTT | 6596 |
| rs764938465 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149037383 | CTGAGGCAGTGAACC[A/G]CTTGAACCCAGGAGG | 6596 |
| rs764970134 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031787 | TATAGTCTGTATATA[C/T]TGTTTACAAGGACTA | 6596 |
| rs764991552 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072025 | GCCACTGCACTCCAG[C/G]CTGGGCAAGAAAGTG | 6596 |
| rs765019065 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067702 | AAAAAAAAATAATAA[C/T]AATAAAAAAAAACCT | 6596 |
| rs765094486 | snp | G/T | 2.49461e-05 | 0.00353163 | intron-variant | HLTF | GRCh38.p7 | 3:149071572 | TTAAATAAAAAATAT[G/T]GGTTCAATACCTCAG | 6596 |
| rs765113301 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081172 | CAACACATAACTGTA[G/T]TTTAAAATAGAAAAA | 6596 |
| rs765147389 | snp | A/G | 1.65897e-05 | 0.00288003 | missense | HLTF | GRCh38.p7 | 3:149071422 | CTTGTTTTTGATGTG[A/G]AAGCAGTGGTGTTTC | 6596 |
| rs765171978 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149065949 | TTTCATCAAACATCC[-/T]ATCAAGTCTACAATA | 6596 |
| rs765251306 | snp | C/T | 1.70098e-05 | 0.00291627 | missense | HLTF | GRCh38.p7 | 3:149032249 | ATGTTCTGATTTCAT[C/T]AATTTTGGCTTGTTT | 6596 |
| rs765264559 | snp | C/T | 1.65622e-05 | 0.00287764 | intron-variant | HLTF | GRCh38.p7 | 3:149064770 | GATCAAATATTGGAT[C/T]ATTTCAAAATTAGCA | 6596 |
| rs765264673 | snp | A/G | 5.00964e-05 | 0.00500457 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050250 | ATAGTCATGAGTTAA[A/G]ATATTATACGTAGTC | 6596 |
| rs765277664 | snp | A/C | 1.64866e-05 | 0.00287106 | intron-variant | HLTF | GRCh38.p7 | 3:149060694 | TCAGTTTGCCTAAAA[A/C]TAAAACAAAAATAAA | 6596 |
| rs765375275 | snp | C/T | 3.2981e-05 | 0.00406071 | missense | HLTF | GRCh38.p7 | 3:149041536 | GGTTTACAAAATACA[C/T]GTGCACAATGTGTTA | 6596 |
| rs765412728 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077710 | GTGCACATTCTCAAG[A/G]AAGACCTGAGAAGGC | 6596 |
| rs765428464 | in-del | -/TC | | | intron-variant | HLTF | GRCh38.p7 | 3:149069027 | ACAGACCTTACTCTG[-/TC]TTAACATCTGCACTA | 6596 |
| rs765493645 | snp | C/T | 1.68539e-05 | 0.00290287 | splice-acceptor-variant | HLTF | GRCh38.p7 | 3:149050376 | TTGTCCAAACTGGTC[C/T]TAAAGAAAAATTAGG | 6596 |
| rs765547714 | snp | A/G | 3.32801e-05 | 0.00407908 | intron-variant | HLTF | GRCh38.p7 | 3:149040182 | AAGAACGAAGTATGA[A/G]CAACACTTAACAGAA | 6596 |
| rs765604479 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149035808 | ATTAGCTAATTAACA[C/G]AGACATGATCATGAG | 6596 |
| rs765621296 | snp | G/T | 0.000212127 | 0.0102965 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086387 | TCCCCTGGATCGTTT[G/T]CGAGCCGCCTCGATA | 6596 |
| rs765642061 | snp | A/T | 1.66081e-05 | 0.00288163 | missense | HLTF | GRCh38.p7 | 3:149059783 | CATGCAAATGCCACA[A/T]CTTCTATAACCTTAG | 6596 |
| rs765648439 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051004 | TGAAAAGAGAAGATA[C/T]CAGGGAGACACAGCT | 6596 |
| rs765649881 | snp | G/T | 1.69476e-05 | 0.00291093 | stop-gained | HLTF | GRCh38.p7 | 3:149046140 | TTTCTCTCTTCATCT[G/T]AAAGTGTAATGTGCT | 6596 |
| rs765674617 | in-del | -/TTCT | | | frameshift-variant | HLTF | GRCh38.p7 | 3:149039653 | TTTATGTTGGGATTC[-/TTCT]TTCTTAAGTCAGTCA | 6596 |
| rs765732600 | snp | C/T | 1.65312e-05 | 0.00287495 | missense | HLTF | GRCh38.p7 | 3:149074302 | TTCCCCAAAAAGTCA[C/T]ATGCAGAGGCATGGT | 6596 |
| rs765757055 | snp | C/G | 1.77846e-05 | 0.00298194 | intron-variant | HLTF | GRCh38.p7 | 3:149040025 | ATTTGCACATGAGTA[C/G]TTTACCTTTGAACTG | 6596 |
| rs765779320 | snp | A/G | 1.68284e-05 | 0.00290067 | intron-variant | HLTF | GRCh38.p7 | 3:149068343 | GTTTTACCCTTAAAA[A/G]TGTTTTAAAAAGATA | 6596 |
| rs765788337 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149043548 | CTGAACTTCAGAGGG[-/A]AAAAAAAAAAAAAAA | 6596 |
| rs765803825 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149081477 | CTAAGTAGAAAAACC[A/G]AATGTAAGAGTAATT | 6596 |
| rs765812726 | in-del | -/TCC | 1.6501e-05 | 0.00287232 | cds-indel | HLTF | GRCh38.p7 | 3:149073285 | GCTTGGTCCAGCTCT[-/TCC]AGAGCCCCAACCACT | 6596 |
| rs765851385 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084725 | ACATGACCTCTCAAA[C/T]TTCCAAATAAAACGG | 6596 |
| rs765886230 | snp | A/C | 9.90802e-05 | 0.00703778 | intron-variant | HLTF | GRCh38.p7 | 3:149035027 | GGATGAGTTACTTTA[A/C]TACTGCCCTGATCTT | 6596 |
| rs765905700 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149041915 | ATACCACCACACAAT[A/G]AAAGGCAGATCCAAT | 6596 |
| rs765910238 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061924 | AATAAGCAGCCAAAA[A/G]GCAAAAATGTAATTC | 6596 |
| rs766002591 | snp | C/T | | | missense | HLTF | GRCh38.p7 | 3:149046138 | TCTTTCTCTCTTCAT[C/T]TGAAAGTGTAATGTG | 6596 |
| rs766115454 | snp | C/T | 1.65666e-05 | 0.00287802 | synonymous-codon | HLTF | GRCh38.p7 | 3:149071297 | ATGGACATTTTCTGG[C/T]CGGTCCTTCTCAGAA | 6596 |
| rs766152740 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060070 | ATATGCAAAGTAATT[C/T]GGCTCTCAGGTGGAA | 6596 |
| rs766168167 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070386 | ATGTGACAATGCCAG[C/T]TGTTGCAACAAAAAT | 6596 |
| rs766168322 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054804 | CCTTAGGCAACTTAA[C/T]CTCTCTGTGTTTCAA | 6596 |
| rs766239958 | snp | A/G | 1.68286e-05 | 0.0029007 | missense | HLTF | GRCh38.p7 | 3:149060820 | GTTTCAATTTCCTCT[A/G]AATCACTGCTTTCTA | 6596 |
| rs766263589 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149069135 | TAGTACTAGTCATCA[C/T]ATTCTTAACTGCCAC | 6596 |
| rs766274921 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATT | | | intron-variant | HLTF | GRCh38.p7 | 3:149079377 | ACGACAGTTTCTAAA[lengthTooLong]ATTTAAAAAAATAAA | 6596 |
| rs766293346 | snp | A/G | 1.65416e-05 | 0.00287586 | synonymous-codon | HLTF | GRCh38.p7 | 3:149073231 | GAAGCACACCTGTTC[A/G]GTTGTCATCTGTACT | 6596 |
| rs766295055 | snp | A/C | 4.94629e-05 | 0.00497283 | intron-variant | HLTF | GRCh38.p7 | 3:149060700 | TGCCTAAAAATAAAA[A/C]AAAAATAAACATAAA | 6596 |
| rs766330766 | in-del | -/AT | 1.66172e-05 | 0.00288242 | intron-variant | HLTF | GRCh38.p7 | 3:149055446 | AGCTGTTTTTCTGAA[-/AT]ATATATGTCAATAAG | 6596 |
| rs766336556 | snp | C/G | 5.17647e-05 | 0.00508721 | missense | HLTF | GRCh38.p7 | 3:149039631 | AAACTGAGAAACAAC[C/G]AAACTTTTTATGTTG | 6596 |
| rs766361834 | in-del | -/AA | | | intron-variant | HLTF | GRCh38.p7 | 3:149041197 | TGTTTCTTTTTACTT[-/AA]GAGTATGACTACTAG | 6596 |
| rs766365106 | snp | C/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085941 | GCACGTCTGTGCATA[C/G]AGATAAGCTGTGAGC | 6596 |
| rs766369593 | snp | A/C | 0.000155848 | 0.00882609 | intron-variant | HLTF | GRCh38.p7 | 3:149076084 | TAATATTACATTATA[A/C]ATAATAGACAATAAC | 6596 |
| rs766397408 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032836 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 6596 |
| rs766410203 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149047821 | TCAGTTTAGCCACAA[C/T]AGGGGAAGGGTAGTT | 6596 |
| rs766438860 | snp | C/G | 6.59044e-05 | 0.00574002 | missense | HLTF | GRCh38.p7 | 3:149055336 | AGAAAGCGGACAGAT[C/G]ATCAGTGTTGTTCTT | 6596 |
| rs766494632 | snp | C/G | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031935 | GTACTTGGAAGATAC[C/G]TGAAAATACTCAGCA | 6596 |
| rs766526481 | in-del | -/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031741 | GGAATGCAAATATGG[-/T]TTTTTGAAAGCCCAA | 6596 |
| rs766573963 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149066165 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAACTG | 6596 |
| rs766582722 | snp | G/T | 1.7042e-05 | 0.00291903 | missense | HLTF | GRCh38.p7 | 3:149032268 | TTTGGCTTGTTTCAT[G/T]TCGTCAGCATTTGGT | 6596 |
| rs766637045 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149036090 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 6596 |
| rs766656294 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149042680 | AATTTATATCAAAAA[A/C]AGAGGGAAGGTAAAC | 6596 |
| rs766714795 | snp | A/G | 1.66477e-05 | 0.00288506 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039127 | GGACAGAAGCATTAT[A/G]GTTGGAGATCCTGCT | 6596 |
| rs766771675 | snp | A/G | 0.00037928 | 0.0137658 | intron-variant | HLTF | GRCh38.p7 | 3:149046273 | GCCTAATCAGAATAA[A/G]ACAAATAATTATGTA | 6596 |
| rs766778303 | snp | C/T | 2.4933e-05 | 0.0035307 | missense | HLTF | GRCh38.p7 | 3:149071614 | TCATGGGTTTTATCA[C/T]CTTCTTTTAAATCTT | 6596 |
| rs766792375 | snp | C/T | 1.65436e-05 | 0.00287602 | missense | HLTF | GRCh38.p7 | 3:149074314 | TCATATGCAGAGGCA[C/T]GGTAAAAGCATTGTT | 6596 |
| rs766811905 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086646 | CTCCGCCCCGCTGCC[A/G]TTCAAAGACGGCGGG | 6596 |
| rs766828338 | snp | C/T | | | missense | HLTF | GRCh38.p7 | 3:149048076 | CGCTGTATTGTTCTA[C/T]GCCACCATTCTCTAT | 6596 |
| rs766833541 | snp | C/T | 5.79637e-05 | 0.00538317 | missense | HLTF | GRCh38.p7 | 3:149039206 | ATGGAACCATCCAAA[C/T]GAGTAAACACAAATC | 6596 |
| rs766890703 | in-del | -/GTTT | 1.68596e-05 | 0.00290336 | intron-variant | HLTF | GRCh38.p7 | 3:149034900 | CCTAGTCTTAAAATA[-/GTTT]GTTTAAAAACTCACT | 6596 |
| rs766920999 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053015 | TTGTCTAAATATCCA[-/G]GAACAAATATGTGGT | 6596 |
| rs766981183 | snp | A/C/T | 6.60186e-05 | 0.00574499 | missense | HLTF | GRCh38.p7 | 3:149071385 | TCTTTGCTATTTTCC[A/C/T]GTGACACCATCCAAG | 6596 |
| rs766988898 | in-del | -/GC | | | intron-variant | HLTF | GRCh38.p7 | 3:149078814 | GTGAGCCGAGATCGT[-/GC]CACTGCACTCCAGCC | 6596 |
| rs767048362 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048433 | TCTCCTTATCAAGTA[C/T]ATCTGCTTATTTAGT | 6596 |
| rs767087362 | snp | G/T | | | missense | HLTF | GRCh38.p7 | 3:149041659 | CTCAGTTCTTCAGGT[G/T]TATCATTTCCTAGAG | 6596 |
| rs767089450 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149074026 | TACTGTGTATATTTT[C/T]ATGTGTGAATCTATT | 6596 |
| rs767122886 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036820 | TTTTATTGAATCATT[A/T]TGTTTCTCGGACCTG | 6596 |
| rs767212196 | snp | G/T | 1.69879e-05 | 0.00291439 | intron-variant | HLTF | GRCh38.p7 | 3:149059855 | TCAAATTATCTCCTG[G/T]GCTAGAGTACAGGTA | 6596 |
| rs767226199 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | HLTF | GRCh38.p7 | 3:149063390 | CATAAGAAAACAGAG[C/T]CTAAATAAACATATG | 6596 |
| rs767234268 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084741 | TTCCAAATAAAACGG[A/G]ATCTACTTCTTCATC | 6596 |
| rs767380569 | snp | C/T | 1.66815e-05 | 0.00288799 | missense | HLTF | GRCh38.p7 | 3:149048988 | ATGCTATGTAATGGA[C/T]TATCTCCTTTAGTCT | 6596 |
| rs767413892 | in-del | -/G | 6.9587e-05 | 0.00589819 | intron-variant | HLTF | GRCh38.p7 | 3:149075835 | AACAAGTTCAAAGAT[-/G]ACTATAATTCACAAT | 6596 |
| rs767433508 | snp | A/C/T | 3.30498e-05 | 0.00406497 | intron-variant | HLTF | GRCh38.p7 | 3:149048860 | GTTTAATGCTATGAT[A/C/T]ACCTGTCAAAACCCA | 6596 |
| rs767533371 | snp | A/G | 1.70499e-05 | 0.0029197 | missense | HLTF | GRCh38.p7 | 3:149032275 | TGTTTCATTTCGTCA[A/G]CATTTGGTTTTTTAG | 6596 |
| rs767562758 | snp | C/T | 3.43755e-05 | 0.00414567 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084901 | ATCCCTATTTTTTTT[C/T]AAAGGCAAAGAAAAA | 6596 |
| rs767570785 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149038607 | TCCTGGGCCCAAGCA[A/C]TCAATCTTTCCGACT | 6596 |
| rs767608090 | snp | C/T | 8.25076e-05 | 0.00642238 | synonymous-codon | HLTF | GRCh38.p7 | 3:149073255 | CTGTACTGCAGCATG[C/T]ACTGGCATACTATAG | 6596 |
| rs767609362 | snp | C/T | 1.71205e-05 | 0.00292574 | stop-gained | HLTF | GRCh38.p7 | 3:149040047 | TTTGAACTGGATGTC[C/T]ATTCCATATCAGACT | 6596 |
| rs767627501 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054454 | GTCTTAAAAAGAGTA[-/G]GATCTCTTCCTCCTC | 6596 |
| rs767715784 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149052791 | AGAATCCAATATGAG[A/C]AAACTGAATCAATGG | 6596 |
| rs767762385 | snp | A/G | 2.05717e-05 | 0.00320709 | intron-variant | HLTF | GRCh38.p7 | 3:149032400 | AAAAAAAAGTTAAGT[A/G]GTTTTTAAGGCATAG | 6596 |
| rs767843353 | snp | A/G | 2.01986e-05 | 0.00317787 | intron-variant | HLTF | GRCh38.p7 | 3:149060869 | TTCTTCTAAAATTAA[A/G]TATACACAAAGAAAT | 6596 |
| rs767868886 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075564 | AAATAAATAAATAAA[C/T]AAACAAATAAACACT | 6596 |
| rs767901361 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051233 | AAAATATAAGGAAGT[-/T]TTAAAAAAAAAAAAA | 6596 |
| rs767928832 | in-del | -/T | 1.78998e-05 | 0.00299159 | intron-variant | HLTF | GRCh38.p7 | 3:149039032 | AAGATTCTGAAAAAA[-/T]TTACAGAACTACTTA | 6596 |
| rs767945972 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087679 | GCAACCTCCGCCTCC[C/T]GGATTCAAGCGATTC | 6596 |
| rs767961467 | snp | A/T | 3.31581e-05 | 0.00407161 | intron-variant | HLTF | GRCh38.p7 | 3:149064903 | TTAAACAGTACTGCT[A/T]TCAGTTTTAAATAAC | 6596 |
| rs767973763 | snp | A/C | 8.485e-05 | 0.0065129 | missense | HLTF | GRCh38.p7 | 3:149076023 | TAGGATCTCGTTGTA[A/C]TGCAACCATTTCATT | 6596 |
| rs768012806 | snp | C/G/T | 3.29828e-05 | 0.00406085 | missense | HLTF | GRCh38.p7 | 3:149064806 | CTTTGCTTAGTCCAT[C/G/T]TGCCTTTTCACTGGT | 6596 |
| rs768024073 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054436 | TGTAGAGACTAAATA[C/T]TGGTCTTAAAAAGAG | 6596 |
| rs768053493 | in-del | -/AAG | 1.64953e-05 | 0.00287182 | cds-indel | HLTF | GRCh38.p7 | 3:149042197 | AGACACTGCATTTGT[-/AAG]AAGGTAAGTATGGCA | 6596 |
| rs768064749 | snp | C/T | 2.52541e-05 | 0.00355337 | intron-variant | HLTF | GRCh38.p7 | 3:149071556 | AACATTCTGAGTAGT[C/T]TTAAATAAAAAATAT | 6596 |
| rs768172508 | snp | C/T | 1.70156e-05 | 0.00291677 | intron-variant | HLTF | GRCh38.p7 | 3:149073193 | AACATTTAAAATTCA[C/T]TTTTAGATTACAAAA | 6596 |
| rs768202785 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149054361 | AGAGCCAGTGGGAAG[A/C]GACTAAATAAACAAG | 6596 |
| rs768217018 | snp | A/G | 1.71858e-05 | 0.00293132 | stop-lost | HLTF | GRCh38.p7 | 3:149032222 | AAAATCCCACAAATT[A/G]TAAGTCAATTAATGT | 6596 |
| rs768221517 | snp | C/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086250 | AGGAACGCGGGGAAG[C/G]TCAGGTTCATTTGGG | 6596 |
| rs768296263 | snp | A/G | 1.78688e-05 | 0.00298899 | intron-variant | HLTF | GRCh38.p7 | 3:149048202 | TAACTCTTTAACCAG[A/G]GTATCCAGTAAGAGT | 6596 |
| rs768309478 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051561 | CATGATGCCTGGGGT[A/G]TAATTAAAAATATTC | 6596 |
| rs768331879 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067180 | ATATTATATACATAT[A/T]TATATGTATATATAT | 6596 |
| rs768347437 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | HLTF | GRCh38.p7 | 3:149060758 | AGGACACATTATCAA[A/G]TCAAATCTATTACAT | 6596 |
| rs768421968 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149080092 | GAGGCCAGACCCAAA[A/T]GCCACATATTGTATC | 6596 |
| rs768433348 | snp | A/C | 1.65419e-05 | 0.00287588 | synonymous-codon | HLTF | GRCh38.p7 | 3:149075952 | TTTCTTTAAATGGCC[A/C]ACTTGATTTCCATTC | 6596 |
| rs768447234 | snp | G/T | 1.66142e-05 | 0.00288216 | intron-variant | HLTF | GRCh38.p7 | 3:149064743 | GGGTCATATTCAAAT[G/T]AAAGTTTACCAGATC | 6596 |
| rs768467606 | snp | C/T | 6.59979e-05 | 0.00574409 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041643 | CCTTATTAACTTCTT[C/T]CTCAGTTCTTCAGGT | 6596 |
| rs768516413 | snp | C/T | 1.64876e-05 | 0.00287116 | stop-gained | HLTF | GRCh38.p7 | 3:149055306 | TTAAAGACTTACAAT[C/T]CAGTTGCTTAACACA | 6596 |
| rs768570504 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149039396 | TCAGTCATTTTCTGA[G/T]AAATTCAGGACTTAA | 6596 |
| rs768639084 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055678 | GTCATTCATTAAGAC[A/G]AACATTTGTTTTATG | 6596 |
| rs768657274 | in-del | -/AA | | | intron-variant | HLTF | GRCh38.p7 | 3:149074078 | ATCAGAGATTTCCTC[-/AA]AAAGACTCCTGAAAA | 6596 |
| rs768677366 | in-del | -/AAA | | | intron-variant | HLTF | GRCh38.p7 | 3:149035657 | GCGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 6596 |
| rs768686416 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149073761 | AAAGCCTTGTATTTT[A/G]GAGGTATTTTAAAAG | 6596 |
| rs768721708 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149062438 | CAGCTATTAATGACA[A/G]AACAATTAACATAGC | 6596 |
| rs768788560 | snp | G/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032121 | AATATGCCCCTTTTA[G/T]AAGACGTGTTCTCTA | 6596 |
| rs768794352 | snp | A/G | 1.66333e-05 | 0.00288381 | stop-gained | HLTF | GRCh38.p7 | 3:149039069 | CCATTAAAAACACTC[A/G]AGAAGCTGCAGACAG | 6596 |
| rs768799200 | snp | C/T | 1.89181e-05 | 0.0030755 | synonymous-codon | HLTF | GRCh38.p7 | 3:149046217 | AATTTTGCTTGTCTT[C/T]GTTCTTCTAAGTGTA | 6596 |
| rs768836321 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085004 | TTACATGGGAATCAC[A/G]GTAAAGATTAATAGT | 6596 |
| rs768864078 | snp | C/T | 1.67514e-05 | 0.00289403 | missense | HLTF | GRCh38.p7 | 3:149071277 | TCATCAGCTAAAATT[C/T]CTCCATGGACATTTT | 6596 |
| rs768888358 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084862 | AACTCCATACTGGAC[A/G]GTCTGCAAGTACTTC | 6596 |
| rs768902155 | snp | C/T | 3.61343e-05 | 0.0042504 | missense | HLTF | GRCh38.p7 | 3:149039185 | TCAACTCTTTTCTTT[C/T]GGGCCATGGAACCAT | 6596 |
| rs768924236 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149083246 | ATGCAAGCAAGACTC[C/T]GTTTCAAAAAAAAAA | 6596 |
| rs768924460 | snp | A/G | 1.6855e-05 | 0.00290297 | intron-variant | HLTF | GRCh38.p7 | 3:149074386 | AAAGGGAAATCAGAA[A/G]CATTACTTTTTATCC | 6596 |
| rs768935235 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043730 | ACGGCTAAGAGTACA[A/G]ATTTTTAGAGCTAGC | 6596 |
| rs769032257 | snp | A/C | 1.70801e-05 | 0.00292229 | intron-variant | HLTF | GRCh38.p7 | 3:149048008 | GTAACTAATATTAAT[A/C]ACTGTCTGAAAGTAC | 6596 |
| rs769076149 | in-del | -/TATT | 4.95025e-05 | 0.00497482 | intron-variant | HLTF | GRCh38.p7 | 3:149071535 | AGTAGATTCTAAGTA[-/TATT]TAAACATTCTGAGTA | 6596 |
| rs769102487 | snp | C/T | 6.44891e-05 | 0.00567806 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086308 | CCCCACCCCCTCCGC[C/T]CCCTTCACCTCTTGA | 6596 |
| rs769169330 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149065211 | GAATTCTCAGACTTC[A/C]AACTTTTCAAACCAA | 6596 |
| rs769223266 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149033053 | AGAGAAAAATAAAAC[A/G]TGATCATCTCATTCC | 6596 |
| rs769261535 | snp | G/T | 0.000165153 | 0.00908565 | missense | HLTF | GRCh38.p7 | 3:149048070 | ACAGGACGCTGTATT[G/T]TTCTATGCCACCATT | 6596 |
| rs769274147 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057939 | GTTACAGATGGTCTA[C/T]ATTCAGCTTCATTAT | 6596 |
| rs769280307 | snp | A/C | 4.96956e-05 | 0.00498451 | intron-variant | HLTF | GRCh38.p7 | 3:149034915 | GTTTGTTTAAAAACT[A/C]ACTTTTGTGATGATA | 6596 |
| rs769285610 | snp | C/T | 1.67685e-05 | 0.00289551 | intron-variant | HLTF | GRCh38.p7 | 3:149059828 | AAAACAACAAAGAAT[C/T]TTAAATTTTTTTCAA | 6596 |
| rs769302957 | snp | C/T | 0.000186237 | 0.009648 | intron-variant | HLTF | GRCh38.p7 | 3:149063052 | GGTCATGGTCATCTC[C/T]ATCTCTCTCTTTTTC | 6596 |
| rs769329031 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149039708 | TCTGCAAAAAATATT[A/G]AGATGTCCATTAGAT | 6596 |
| rs769336676 | snp | C/T | 1.66087e-05 | 0.00288168 | synonymous-codon | HLTF | GRCh38.p7 | 3:149059764 | AACAGATGAAGTTAA[C/T]GCACATGCAAATGCC | 6596 |
| rs769388068 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077834 | AATGCCCTAACATAC[A/G]GAAGTTCTCAGCAAA | 6596 |
| rs769424998 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | HLTF | GRCh38.p7 | 3:149040003 | AAGGTAAAACAAATA[C/T]TCAAATATTTGCACA | 6596 |
| rs769436707 | snp | A/C | 1.65993e-05 | 0.00288086 | stop-gained | HLTF | GRCh38.p7 | 3:149073317 | TTTCCAAATTGAATC[A/C]TAAAGCTATAATTTA | 6596 |
| rs769527252 | snp | A/T | 1.65012e-05 | 0.00287234 | intron-variant | HLTF | GRCh38.p7 | 3:149055412 | GCTCCTAAAAAAATG[A/T]ACCACTGATAGAACC | 6596 |
| rs769576597 | snp | C/T | 1.65168e-05 | 0.00287369 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041652 | CTTCTTTCTCAGTTC[C/T]TCAGGTGTATCATTT | 6596 |
| rs769657734 | snp | G/T | 1.64958e-05 | 0.00287187 | missense | HLTF | GRCh38.p7 | 3:149042195 | GAAGACACTGCATTT[G/T]TAAGAAGGTAAGTAT | 6596 |
| rs769704376 | snp | A/G | 3.43974e-05 | 0.00414699 | intron-variant | HLTF | GRCh38.p7 | 3:149048176 | TACCTAGAAATAACA[A/G]GAAACTGTTATAACT | 6596 |
| rs769736559 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149064113 | TATACTTTCCTTCAA[C/G]CTTACTTCTTTCCTT | 6596 |
| rs769801840 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149043913 | AGTATTTAAAATAGT[G/T]CCTGGACTATATTAA | 6596 |
| rs769824400 | snp | C/T | 0.00297785 | 0.0384715 | intron-variant | HLTF | GRCh38.p7 | 3:149063082 | CTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 6596 |
| rs769873051 | in-del | -/AAGTT | 0.000157763 | 0.00888012 | intron-variant | HLTF | GRCh38.p7 | 3:149032391 | TAAAAAGAAAAAAAA[-/AAGTT]AAGTAGTTTTTAAGG | 6596 |
| rs769912386 | snp | A/G | 1.66172e-05 | 0.00288242 | intron-variant | HLTF | GRCh38.p7 | 3:149073218 | ACAAAATAAAAGAGA[A/G]GCACACCTGTTCAGT | 6596 |
| rs769933430 | snp | C/T | 6.80504e-05 | 0.00583271 | intron-variant | HLTF | GRCh38.p7 | 3:149074400 | AGCATTACTTTTTAT[C/T]CCCACTAAGAATTAG | 6596 |
| rs769936829 | snp | A/C/G | 0.000128205 | 0.00800547 | missense | HLTF | GRCh38.p7 | 3:149039191 | CTTTTCTTTTGGGCC[A/C/G]TGGAACCATCCAAAC | 6596 |
| rs769964938 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086079 | TTTAAGCCCCAGGCC[C/T]CCCACAGTCGGTGAC | 6596 |
| rs770003320 | snp | A/C | 1.65097e-05 | 0.00287308 | stop-gained | HLTF | GRCh38.p7 | 3:149068269 | TCTTTTTAACTCTTT[A/C]AATAGGAAGAGGTCT | 6596 |
| rs770007905 | snp | A/G/T | 3.38033e-05 | 0.00411105 | intron-variant | HLTF | GRCh38.p7 | 3:149059847 | AATTTTTTTCAAATT[A/G/T]TCTCCTGTGCTAGAG | 6596 |
| rs770024459 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032953 | GGGTGACAGAGCGAC[A/G]TCTCAAAAAAAAAAA | 6596 |
| rs770038481 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051233 | AAAAATATAAGGAAG[-/T]TTAAAAAAAAAAAAA | 6596 |
| rs770048221 | in-del | -/AC | 1.66477e-05 | 0.00288506 | frameshift-variant | HLTF | GRCh38.p7 | 3:149040096 | TAATTCTTCTGGAGG[-/AC]ACATTCTAATAAATT | 6596 |
| rs770055050 | snp | A/T | 1.65179e-05 | 0.00287379 | intron-variant | HLTF | GRCh38.p7 | 3:149064875 | TATATTCCTGGGTAA[A/T]TAGGCATATTTCTTA | 6596 |
| rs770061207 | snp | C/T | | | missense | HLTF | GRCh38.p7 | 3:149071618 | GGGTTTTATCATCTT[C/T]TTTTAAATCTTCAAA | 6596 |
| rs770061848 | snp | A/G/T | 4.94975e-05 | 0.0049746 | synonymous-codon, stop-gained | HLTF | GRCh38.p7 | 3:149071347 | AGTATAAGTCATTTC[A/G/T]CTGTTCCCAGAATGG | 6596 |
| rs770068057 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149067324 | TGAATATATTATTTA[C/G]AAAGTGAGGAACCAA | 6596 |
| rs770383881 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080224 | ACTACAAATGGGAAT[A/G]AGGTTTCTTTTTGGA | 6596 |
| rs770455904 | snp | A/C | 1.65976e-05 | 0.00288072 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084882 | GCAAGTACTTCCAAA[A/C]TGGATCCCTATTTTT | 6596 |
| rs770491514 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149063376 | CTATCTCTTTTACAC[A/G]TAAGAAAACAGAGTC | 6596 |
| rs770508801 | snp | A/G | 7.58351e-05 | 0.00615726 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086337 | GAACATCCAGGACAT[A/G]GCGCTGAGTGGGATG | 6596 |
| rs770529259 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149075491 | GGAGGTTGCAGTCAG[C/T]CGAGATCACACAACT | 6596 |
| rs770602053 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149040994 | CTAGACCTACCTTAT[C/T]CAACACAATAGCCAA | 6596 |
| rs770639227 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149032728 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 6596 |
| rs770651808 | snp | C/T | 3.39351e-05 | 0.00411903 | missense | HLTF | GRCh38.p7 | 3:149046093 | ACCTTCCAATAGTGG[C/T]TCTGCCTTCATTTTT | 6596 |
| rs770653719 | snp | A/C | 8.036e-05 | 0.00633826 | intron-variant | HLTF | GRCh38.p7 | 3:149032392 | AAAAAGAAAAAAAAA[A/C]GTTAAGTAGTTTTTA | 6596 |
| rs770654993 | snp | A/G | 3.31159e-05 | 0.00406901 | missense | HLTF | GRCh38.p7 | 3:149040135 | GTATATCATTTCTGC[A/G]TAAAGGGCATTTAGC | 6596 |
| rs770669148 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149061837 | GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 6596 |
| rs770724389 | snp | A/G | 3.44311e-05 | 0.00414902 | intron-variant | HLTF | GRCh38.p7 | 3:149073348 | CAAAATAAAAAGAAT[A/G]AAGCCATCAAATAAA | 6596 |
| rs770747485 | snp | A/G | 3.31137e-05 | 0.00406887 | missense | HLTF | GRCh38.p7 | 3:149050296 | TTTGAAAGTAAGGCC[A/G]GTTCTCTAATACGAT | 6596 |
| rs770761754 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030105 | AGATAAAGTCAAAAT[C/T]ATGGCACCGAGGAAG | 6596 |
| rs770794252 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149036900 | ACACTCAACTTACTA[A/T]AAAACTGCTAAAACG | 6596 |
| rs770828196 | snp | A/C | 1.65756e-05 | 0.00287881 | splice-donor-variant | HLTF | GRCh38.p7 | 3:149074213 | TGAAACCCTAAACTT[A/C]CTTTTTGGTGCAGGA | 6596 |
| rs770829829 | snp | A/T | 1.67265e-05 | 0.00289188 | intron-variant | HLTF | GRCh38.p7 | 3:149039046 | ATTTACAGAACTACT[A/T]ACTGGATCCATTAAA | 6596 |
| rs770846399 | snp | C/T | 0.00067123 | 0.0183075 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039685 | CAATGCGTGCATTAG[C/T]GCATTAATCTGCAAA | 6596 |
| rs770877601 | in-del | -/CCTGGGTTCAAG | | | intron-variant | HLTF | GRCh38.p7 | 3:149036378 | GTGCAACCTCCACCT[-/CCTGGGTTCAAG]CCTGGGTTCAAGCGA | 6596 |
| rs770879371 | in-del | -/CACTT | 1.6623e-05 | 0.00288292 | intron-variant | HLTF | GRCh38.p7 | 3:149040176 | TAAGAAAGAACGAAG[-/CACTT]TATGAGCAACACTTA | 6596 |
| rs770882459 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149034799 | TGAAGGAGGAAAAAG[A/G]TGACTTATATTTTGC | 6596 |
| rs770898013 | in-del | -/TCTC | 3.41807e-05 | 0.00413391 | frameshift-variant | HLTF | GRCh38.p7 | 3:149032314 | GCTCCTGCTGCAAGT[-/TCTC]TCTTTTTGTTTTGTA | 6596 |
| rs770938050 | snp | A/G | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030913 | CACAACATTGTCTCC[A/G]ATCTCATCTTTCTAT | 6596 |
| rs771027805 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045269 | AGATCTTTACCTATA[C/T]ATCATCTTCTCAGTG | 6596 |
| rs771046148 | snp | C/G | 9.57992e-05 | 0.00692029 | intron-variant | HLTF | GRCh38.p7 | 3:149063109 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTGCGA | 6596 |
| rs771051727 | snp | C/T | 0.000529757 | 0.0162665 | intron-variant | HLTF | GRCh38.p7 | 3:149064896 | ATATTTCTTAAACAG[C/T]ACTGCTATCAGTTTT | 6596 |
| rs771057787 | in-del | -/A | 1.71889e-05 | 0.00293158 | intron-variant | HLTF | GRCh38.p7 | 3:149050223 | CTGTTAAGTATCAAC[-/A]ATACTTACTCCATAG | 6596 |
| rs771071475 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067235 | GAAAAGTCACCCTTA[C/T]TCTCATCACTAGGAC | 6596 |
| rs771103987 | snp | A/T | 4.95503e-05 | 0.00497722 | intron-variant | HLTF | GRCh38.p7 | 3:149055418 | AAAAAAATGAACCAC[A/T]GATAGAACCTTTAGC | 6596 |
| rs771135031 | snp | G/T | | | missense | HLTF | GRCh38.p7 | 3:149040088 | GTCACGTGCTAATTC[G/T]TCTGGAGGACATTCT | 6596 |
| rs771148946 | snp | C/T | 1.65597e-05 | 0.00287743 | missense | HLTF | GRCh38.p7 | 3:149048050 | CTCCTTCATCTCCCA[C/T]TGTGACAGGACGCTG | 6596 |
| rs771180210 | snp | G/T | 1.67379e-05 | 0.00289287 | intron-variant | HLTF | GRCh38.p7 | 3:149059710 | AGAAAACAAGGATAT[G/T]TACTGACCCTTTTTC | 6596 |
| rs771233265 | snp | A/T | 3.4525e-05 | 0.00415467 | intron-variant | HLTF | GRCh38.p7 | 3:149068383 | ATTGTGAAACCCAGT[A/T]CACCAGAAAAACGTT | 6596 |
| rs771255683 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149060078 | AGTAATTCGGCTCTC[A/G]GGTGGAAGGAGAATT | 6596 |
| rs771287794 | snp | C/G | 1.7277e-05 | 0.00293908 | intron-variant | HLTF | GRCh38.p7 | 3:149073174 | CTTTTAAATACAAAC[C/G]TGCAACATTTAAAAT | 6596 |
| rs771412999 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050744 | TAAAAGAACAACAAC[C/G]AATATTTCCAAGGAT | 6596 |
| rs771422616 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032611 | AAGCAAAGCAATAAA[C/G]AAAAAAAAAGCAAAC | 6596 |
| rs771440451 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149069731 | ATCAATCACGACTGA[A/G]TGTCTGAAAGATACT | 6596 |
| rs771452091 | snp | C/T | 4.50999e-05 | 0.00474846 | intron-variant | HLTF | GRCh38.p7 | 3:149039571 | AAGTGAAAAACACTG[C/T]GGAACTTACTTAAGT | 6596 |
| rs771470721 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084399 | TTTTTGCAACAAATC[A/G]ATGACATGAACAAGG | 6596 |
| rs771501750 | snp | C/G | 1.92821e-05 | 0.00310495 | missense | HLTF | GRCh38.p7 | 3:149076010 | TCATAAGGGTTATTA[C/G]GATCTCGTTGTAATG | 6596 |
| rs771505287 | snp | C/T | 1.75582e-05 | 0.0029629 | intron-variant | HLTF | GRCh38.p7 | 3:149048192 | GAAACTGTTATAACT[C/T]TTTAACCAGAGTATC | 6596 |
| rs771521769 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082008 | TTTGAATATCTAAAT[A/G]AAATGGATGCTTTTC | 6596 |
| rs771626551 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149067428 | ATACTTAATGGTTAC[A/G]TAATAGTAAGTTTTA | 6596 |
| rs771723551 | snp | C/T | 1.66815e-05 | 0.00288799 | intron-variant | HLTF | GRCh38.p7 | 3:149074355 | GGAACTACCCTATTA[C/T]ATTTGGGAGAAAAAG | 6596 |
| rs771768046 | snp | A/G | 1.76036e-05 | 0.00296673 | intron-variant | HLTF | GRCh38.p7 | 3:149071472 | GTCATAAAGCGAAAT[A/G]CATTAAGCCATTCCT | 6596 |
| rs771792275 | snp | A/G | 1.66774e-05 | 0.00288763 | missense | HLTF | GRCh38.p7 | 3:149039062 | ACTGGATCCATTAAA[A/G]ACACTCGAGAAGCTG | 6596 |
| rs771804528 | in-del | -/G | 1.71322e-05 | 0.00292674 | frameshift-variant | HLTF | GRCh38.p7 | 3:149032325 | AAGTTCTCTCTTTTT[-/G]TTTTGTATTTTCAGC | 6596 |
| rs771806209 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149058151 | CACCCAGGCTGGAAT[C/G]CAGTGGCGCTATTAT | 6596 |
| rs771810108 | in-del | -/TCT | | | intron-variant | HLTF | GRCh38.p7 | 3:149047269 | CTCAACTTTTATCTA[-/TCT]CCACCAGAAACAACC | 6596 |
| rs771811427 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084661 | TATAATCAAAATTTA[A/G]TTATCTACTATTATA | 6596 |
| rs771857247 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038090 | TACCTCAATCACCTA[-/T]GATATATGCTAAAAA | 6596 |
| rs771885791 | snp | C/G/T | 0.000115341 | 0.00759336 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041604 | TTCCTCATCTGAACC[C/G/T]GAGCTCAGAATTAAC | 6596 |
| rs771890901 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037030 | CAAGAAAAATAAAAT[C/T]TGGGATTTGTTCTAA | 6596 |
| rs771910038 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072497 | ATGCTAACTTAATTG[A/G]CTATTTAAACTAGGT | 6596 |
| rs771911399 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070978 | TGAACCTGGGAGGCG[A/G]AGGCTGCAGTGAGCC | 6596 |
| rs771912152 | snp | G/T | 1.65094e-05 | 0.00287305 | missense | HLTF | GRCh38.p7 | 3:149074244 | CCCAATTTAAATCCA[G/T]GTTTCTTCAACTGAT | 6596 |
| rs771950428 | snp | C/T | 1.6582e-05 | 0.00287936 | intron-variant | HLTF | GRCh38.p7 | 3:149063549 | AGAAAAATGCAAATA[C/T]AAAGTATTAGTAAGG | 6596 |
| rs771995196 | snp | G/T | 6.67557e-05 | 0.00577697 | missense | HLTF | GRCh38.p7 | 3:149059721 | ATATTTACTGACCCT[G/T]TTTCAACATTTTCTT | 6596 |
| rs772054660 | snp | C/G | 1.66062e-05 | 0.00288146 | missense | HLTF | GRCh38.p7 | 3:149068326 | CTGCAATGGCCGTAA[C/G]AGTTTTACCCTTAAA | 6596 |
| rs772092362 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086173 | ATGCATTTATTTCTC[C/T]GGCGGCCACATATGC | 6596 |
| rs772128982 | snp | A/G | 1.65534e-05 | 0.00287688 | synonymous-codon | HLTF | GRCh38.p7 | 3:149050319 | AATACGATCAGGACC[A/G]TAATAAACATAAAAA | 6596 |
| rs772129813 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149062570 | ACCTACTTCAGAAGA[-/T]TAAATGAAGTTTGTA | 6596 |
| rs772157209 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149066965 | GTACTGCCTTCTCTG[-/A]AAACTAAAAACTAGG | 6596 |
| rs772180466 | snp | A/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085518 | AAAAATGAAATCATA[A/T]GCCAAAATTTCAATA | 6596 |
| rs772182130 | snp | A/G | 1.7221e-05 | 0.00293432 | intron-variant | HLTF | GRCh38.p7 | 3:149050220 | GATCTGTTAAGTATC[A/G]ACAATACTTACTCCA | 6596 |
| rs772199811 | in-del | -/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149032971 | CAAAAAAAAAAAAAA[-/C]AAAAAACAAAAAACT | 6596 |
| rs772226314 | snp | A/C | 1.68513e-05 | 0.00290265 | missense | HLTF | GRCh38.p7 | 3:149046121 | TTTCACAGACTGATA[A/C]ATCTTTCTCTCTTCA | 6596 |
| rs772271334 | snp | C/T | 3.6974e-05 | 0.00429949 | missense | HLTF | GRCh38.p7 | 3:149039595 | CTTAAGTGGTATTTC[C/T]ATTAAAGACAGGAAT | 6596 |
| rs772272818 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon | HLTF | GRCh38.p7 | 3:149034939 | GATGATAACTTCTTG[C/T]TTCTGACCAAGTCTA | 6596 |
| rs772282479 | snp | A/C | 2.00934e-05 | 0.00316959 | intron-variant | HLTF | GRCh38.p7 | 3:149071235 | AGATTTTATTAACTA[A/C]AGAAAAAAATAATTA | 6596 |
| rs772320983 | snp | C/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149031354 | CACGCCTCTCACATA[C/T]AGTAGTCTTCTGAAT | 6596 |
| rs772327180 | snp | G/T | 1.78944e-05 | 0.00299113 | missense | HLTF | GRCh38.p7 | 3:149046193 | TAACTCCAAAACAGG[G/T]TTTCCTTTAATTTTG | 6596 |
| rs772368736 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | HLTF | GRCh38.p7 | 3:149048900 | TGATTCTAAGTCAAG[C/T]ACAGCTTTTGTCTGC | 6596 |
| rs772378778 | snp | A/G | 1.6643e-05 | 0.00288465 | intron-variant | HLTF | GRCh38.p7 | 3:149059810 | TTAGAAGATCCTGCT[A/G]ATAAAACAACAAAGA | 6596 |
| rs772556798 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149084102 | AACTTTCATTTTATG[A/T]AACTGTCATTCATAA | 6596 |
| rs772574174 | in-del | -/AAATT | | | intron-variant | HLTF | GRCh38.p7 | 3:149072070 | AAAATTAAGAAATTG[-/AAATT]AAATTAAATTTAAAA | 6596 |
| rs772575050 | snp | A/G | 3.29755e-05 | 0.00406038 | stop-gained | HLTF | GRCh38.p7 | 3:149048932 | GAGCATTTGGATTTC[A/G]TATGGCATGTCCTTC | 6596 |
| rs772595844 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149041210 | TTAAGAGTATGACTA[A/C]TAGAAAACTGAAAAT | 6596 |
| rs772597752 | snp | C/G | 1.65206e-05 | 0.00287403 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084704 | GTGTAATAGCGTAGT[C/G]CAACCACATGACCTC | 6596 |
| rs772649048 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084843 | GGCGTGGAAAATTTC[C/T]ATGAACTCCATACTG | 6596 |
| rs772675628 | in-del | -/A | 1.81813e-05 | 0.00301502 | intron-variant | HLTF | GRCh38.p7 | 3:149055258 | TTCTACCTTGTAGAT[-/A]AAAATATAAATTATG | 6596 |
| rs772691405 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149039761 | AGTCTAAAAGTTTTT[A/G]TCATAAAGAAAAGGT | 6596 |
| rs772700433 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070057 | GGTAAAATATTCATT[C/T]AATGAGCAAGATACA | 6596 |
| rs772734235 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084720 | CAACCACATGACCTC[C/T]CAAACTTCCAAATAA | 6596 |
| rs772754144 | in-del | -/TAAAA | 3.42056e-05 | 0.00413541 | intron-variant | HLTF | GRCh38.p7 | 3:149073184 | CAAACCTGCAACATT[-/TAAAA]TTCACTTTTAGATTA | 6596 |
| rs772755798 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149075406 | ATACAAAAATTAATT[A/G]GGCATGGTGGCAGGC | 6596 |
| rs772851965 | snp | C/T | 1.75108e-05 | 0.0029589 | intron-variant | HLTF | GRCh38.p7 | 3:149050192 | GCATATTTCTTACAT[C/T]CAATCTTTAAAAGAT | 6596 |
| rs772860937 | snp | G/T | 0.00018714 | 0.00967135 | synonymous-codon | HLTF | GRCh38.p7 | 3:149032256 | GATTTCATTAATTTT[G/T]GCTTGTTTCATTTCG | 6596 |
| rs772882145 | snp | C/T | 0.000186168 | 0.0096462 | intron-variant | HLTF | GRCh38.p7 | 3:149063072 | CTCTCTTTTTCTTTT[C/T]TTTTTGAGACGGAGT | 6596 |
| rs772940950 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087736 | GGATTGCAGGAGCCC[A/G]CCACCACGCCCAGCT | 6596 |
| rs772962922 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038400 | ACTTAAATATTTACA[G/T]GGACTATGATTCTGG | 6596 |
| rs772965159 | snp | C/T | 8.27506e-05 | 0.00643183 | stop-gained, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084877 | AGTCTGCAAGTACTT[C/T]CAAACTGGATCCCTA | 6596 |
| rs772967707 | snp | A/C | 1.64988e-05 | 0.00287213 | missense | HLTF | GRCh38.p7 | 3:149042218 | GTAAGTATGGCAACA[A/C]ATTTGCCGCAGTCTA | 6596 |
| rs772969804 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149083247 | TGCAAGCAAGACTCC[A/G]TTTCAAAAAAAAAAC | 6596 |
| rs773014724 | snp | A/T | 1.65721e-05 | 0.0028785 | missense | HLTF | GRCh38.p7 | 3:149041664 | TTCTTCAGGTGTATC[A/T]TTTCCTAGAGAAAAG | 6596 |
| rs773018962 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149055414 | TCCTAAAAAAATGAA[A/C]CACTGATAGAACCTT | 6596 |
| rs773059885 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082391 | ATGAACTTGGGAGGC[A/G]GAGCTTGCAATGAGC | 6596 |
| rs773137772 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149049175 | TAAAATAAGTACTTA[C/T]TAGCACACCTAATTT | 6596 |
| rs773209892 | snp | C/T | 1.65449e-05 | 0.00287614 | intron-variant | HLTF | GRCh38.p7 | 3:149064772 | TCAAATATTGGATCA[C/T]TTCAAAATTAGCATT | 6596 |
| rs773217390 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038097 | ATCACCTATGATATA[C/T]GCTAAAAATGCAGCT | 6596 |
| rs773218214 | in-del | -/GAAC | 4.98227e-05 | 0.00499088 | intron-variant | HLTF | GRCh38.p7 | 3:149040169 | TGGCTATATAAGAAA[-/GAAC]GAAGTATGAGCAACA | 6596 |
| rs773227622 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047486 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCGGGG | 6596 |
| rs773266678 | snp | A/G | 1.95842e-05 | 0.00312917 | intron-variant | HLTF | GRCh38.p7 | 3:149032389 | TTTAAAAAGAAAAAA[A/G]AAAGTTAAGTAGTTT | 6596 |
| rs773316070 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045779 | TTTCATCAGTTCCTA[C/T]TTCCAGATTTCCATA | 6596 |
| rs773325253 | in-del | -/AGTT | 3.9452e-05 | 0.00444122 | intron-variant | HLTF | GRCh38.p7 | 3:149032392 | AAAAAGAAAAAAAAA[-/AGTT]AAGTAGTTTTTAAGG | 6596 |
| rs773364974 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042624 | TCATGTGCAGAAACA[A/G]GAACAGGGTGCATGC | 6596 |
| rs773367079 | snp | A/C | | | missense | HLTF | GRCh38.p7 | 3:149059757 | TTGTAGGAACAGATG[A/C]AGTTAATGCACATGC | 6596 |
| rs773394169 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149078925 | TGAAAACGCATGTCT[A/T]AAAGCATGGAGACGA | 6596 |
| rs773431408 | snp | A/G | 4.9467e-05 | 0.00497303 | stop-gained | HLTF | GRCh38.p7 | 3:149060670 | CTTTAGTTTCAGACT[A/G]TACATTTTTCAGTTT | 6596 |
| rs773457013 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058471 | ATGTACATCCTTTGA[C/T]TATTCTCCTATTGGG | 6596 |
| rs773458440 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149065579 | CGCAGTGGCTCATGC[A/C]AGCACTTTGGGAGAC | 6596 |
| rs773545878 | snp | A/G | 1.74151e-05 | 0.0029508 | intron-variant | HLTF | GRCh38.p7 | 3:149075833 | CTAACAAGTTCAAAG[A/G]TGACTATAATTCACA | 6596 |
| rs773613750 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149052250 | ATGAGTAGATGGAGA[C/T]CTCATTAAAATTTTT | 6596 |
| rs773643061 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149054826 | GTGTTTCAATGTGGG[A/C]ACCTGGAAAATCAGG | 6596 |
| rs773689393 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149052281 | TAAAATACTCTTTTT[-/A]AAAAATTATATGTTG | 6596 |
| rs773709485 | snp | A/G | 3.31285e-05 | 0.00406978 | missense | HLTF | GRCh38.p7 | 3:149040141 | CATTTCTGCATAAAG[A/G]GCATTTAGCATGTGG | 6596 |
| rs773723726 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048341 | TAAAAATATACACAT[C/T]TCAAGATACAGTTTT | 6596 |
| rs773790511 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149067334 | ATTTACAAAGTGAGG[A/G]ACCAAACTCCACACA | 6596 |
| rs773798235 | snp | C/T | 1.67013e-05 | 0.0028897 | missense, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084887 | TACTTCCAAACTGGA[C/T]CCCTATTTTTTTTTA | 6596 |
| rs773811328 | snp | C/T | 1.64814e-05 | 0.00287061 | missense | HLTF | GRCh38.p7 | 3:149063440 | GTTTACCTTTTGGGG[C/T]GGGAGCTAGACAATT | 6596 |
| rs773844361 | in-del | -/TGTT | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030560 | TTTTTTGCCAAAAAC[-/TGTT]TGTTTATACTTAATC | 6596 |
| rs773903698 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149064330 | GTCTGCTCTAATCTA[C/T]CTTTAGAAATAAGCT | 6596 |
| rs773997380 | snp | A/G | 2.91049e-05 | 0.00381465 | intron-variant | HLTF | GRCh38.p7 | 3:149071663 | CTGTTTTAAGCTACA[A/G]TAAACAGCAACAAGA | 6596 |
| rs774058917 | snp | C/G | 1.74124e-05 | 0.00295057 | intron-variant | HLTF | GRCh38.p7 | 3:149073356 | AAAGAATAAAGCCAT[C/G]AAATAAAGTAGGTTT | 6596 |
| rs774149457 | snp | C/T | 1.68957e-05 | 0.00290647 | missense | HLTF | GRCh38.p7 | 3:149046099 | CAATAGTGGCTCTGC[C/T]TTCATTTTTCACAGA | 6596 |
| rs774151303 | snp | G/T | 2.03089e-05 | 0.00318654 | intron-variant | HLTF | GRCh38.p7 | 3:149032393 | AAAAGAAAAAAAAAA[G/T]TTAAGTAGTTTTTAA | 6596 |
| rs774189031 | snp | A/C | 3.30262e-05 | 0.0040635 | missense | HLTF | GRCh38.p7 | 3:149074239 | CAGGACCCAATTTAA[A/C]TCCATGTTTCTTCAA | 6596 |
| rs774232380 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149033061 | ATAAAACGTGATCAT[C/T]TCATTCCTGATAAAA | 6596 |
| rs774269216 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082102 | CCAGACTTAAAATAG[C/T]ACATACTGTAGAATT | 6596 |
| rs774270354 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070591 | TGAGACTGAAAAATA[C/T]AAAAACTGCTAGTGT | 6596 |
| rs774281001 | snp | A/G | 0.000192105 | 0.00979874 | intron-variant | HLTF | GRCh38.p7 | 3:149063123 | GCAGTGCAGTGGTGC[A/G]ATCTTAACTCACTGC | 6596 |
| rs774330706 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | HLTF | GRCh38.p7 | 3:149055347 | AGATGATCAGTGTTG[C/T]TCTTGGTCTCTCCTC | 6596 |
| rs774351521 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149065351 | CTCTTCTTACTCCAT[-/G]GGGTATTTTCCTGCT | 6596 |
| rs774356402 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149083351 | AAATTTAAAGTATAT[A/C]TATTTGGCAAAATAA | 6596 |
| rs774368030 | in-del | -/AAAT | | | intron-variant | HLTF | GRCh38.p7 | 3:149054035 | AAGGTGTAATTTAAA[-/AAAT]AAATAAATAAACCAA | 6596 |
| rs774401590 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067890 | GGCTCACACCTATAG[C/T]CCCAGCACTTTGGGA | 6596 |
| rs774418904 | snp | C/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030994 | TCAAACATGAAGCTT[C/T]TCTTGTTTGTTAGAG | 6596 |
| rs774476637 | snp | G/T | 1.65176e-05 | 0.00287376 | intron-variant | HLTF | GRCh38.p7 | 3:149055419 | AAAAAATGAACCACT[G/T]ATAGAACCTTTAGCT | 6596 |
| rs774486076 | snp | A/C | 1.65042e-05 | 0.0028726 | missense | HLTF | GRCh38.p7 | 3:149042234 | ATTTGCCGCAGTCTA[A/C]GCAAAAGACCCAGGA | 6596 |
| rs774506276 | snp | A/G | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029693 | TACAGCAATGTCTTT[A/G]CCATTCCCCAAAACA | 6596 |
| rs774529192 | snp | G/T | 1.64923e-05 | 0.00287156 | synonymous-codon | HLTF | GRCh38.p7 | 3:149068306 | ATGGAAGTTGGTAAG[G/T]ATTACTGCAATGGCC | 6596 |
| rs774561056 | in-del | -/TACTCCA | 1.70598e-05 | 0.00292055 | intron-variant | HLTF | GRCh38.p7 | 3:149050229 | AGTATCAACAATACT[-/TACTCCA]TAGTCATGAGTTAAA | 6596 |
| rs774646610 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034758 | GCAGAGAAAGGCCCC[C/T]TAAACAGCATATATT | 6596 |
| rs774672173 | snp | C/T | 1.75625e-05 | 0.00296327 | intron-variant | HLTF | GRCh38.p7 | 3:149048193 | AAACTGTTATAACTC[C/T]TTAACCAGAGTATCC | 6596 |
| rs774727117 | snp | A/C | 1.64966e-05 | 0.00287194 | intron-variant | HLTF | GRCh38.p7 | 3:149060743 | AGGACATTAGAATAT[A/C]GGACACATTATCAAA | 6596 |
| rs774738011 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048756 | TTATATGATTAATTT[G/T]GGGGCAGAATTTACA | 6596 |
| rs774783492 | snp | A/T | 1.93313e-05 | 0.00310891 | synonymous-codon | HLTF | GRCh38.p7 | 3:149039586 | TGGAACTTACTTAAG[A/T]GGTATTTCTATTAAA | 6596 |
| rs774793287 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078322 | AGGCTGAAGTGTGAG[A/G]ATCTCTTGAGGCCAG | 6596 |
| rs774857150 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149035494 | AAACCCCGTCTCTAC[A/T]AAAAATAGAAAAAAT | 6596 |
| rs774916990 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149051193 | GATGCTCTGATACTT[C/G]AATGACTACCTAGAA | 6596 |
| rs774929780 | in-del | -/AACAG | 1.66726e-05 | 0.00288722 | intron-variant | HLTF | GRCh38.p7 | 3:149040191 | GTATGAGCAACACTT[-/AACAG]AAGAACAAATATAAA | 6596 |
| rs774945089 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054207 | TTACAATGAATTAAG[A/G]AATTAGTAAGTAAAA | 6596 |
| rs774974723 | snp | C/T | 2.45607e-05 | 0.00350424 | intron-variant | HLTF | GRCh38.p7 | 3:149071533 | AAAGTAGATTCTAAG[C/T]ATATTTAAACATTCT | 6596 |
| rs774998250 | snp | A/G | 3.91481e-05 | 0.00442409 | synonymous-codon | HLTF | GRCh38.p7 | 3:149076012 | ATAAGGGTTATTAGG[A/G]TCTCGTTGTAATGCA | 6596 |
| rs775040107 | snp | A/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149048330 | TAATCATTTATTAAA[A/T]ATATACACATCTCAA | 6596 |
| rs775049640 | snp | A/G | 1.6537e-05 | 0.00287545 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084697 | TACTCCCGTGTAATA[A/G]CGTAGTCCAACCACA | 6596 |
| rs775062484 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149049590 | AATCAAATCATTGTG[A/G]TAGAAAACAATTTTC | 6596 |
| rs775106716 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085532 | ATGCCAAAATTTCAA[C/T]AGGGATTGAGCTATA | 6596 |
| rs775130766 | snp | A/C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060124 | CAGTTTGATTCCTAA[A/C/T]GATAAGGCTGCCAAA | 6596 |
| rs775165370 | snp | C/T | 1.6661e-05 | 0.00288621 | missense | HLTF | GRCh38.p7 | 3:149039066 | GATCCATTAAAAACA[C/T]TCGAGAAGCTGCAGA | 6596 |
| rs775213807 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149046829 | CTTTCTCAGTACTGG[-/A]AAAAAAAGAGATGTA | 6596 |
| rs775251908 | in-del | -/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149047924 | AAACACTTTTTAGAA[-/G]GAAAAGTTAAGAGTC | 6596 |
| rs775341259 | snp | G/T | 1.66468e-05 | 0.00288498 | intron-variant | HLTF | GRCh38.p7 | 3:149063565 | AAAGTATTAGTAAGG[G/T]GTCTTAGAAACTAGT | 6596 |
| rs775356839 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149067432 | TTAATGGTTACATAA[C/T]AGTAAGTTTTATGGC | 6596 |
| rs775417390 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149070114 | TAAAAAGCTCACTGA[C/T]ATGATTTAGCGTTCC | 6596 |
| rs775429236 | snp | C/G | 9.9397e-05 | 0.00704902 | missense | HLTF | GRCh38.p7 | 3:149050337 | ATAAACATAAAAATT[C/G]AAGTGTACATCTGAT | 6596 |
| rs775523469 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149071832 | TGGGAGGATCACTTG[A/G]GCTCAGGAGTTTGAG | 6596 |
| rs775539806 | snp | C/G/T | 0.000101359 | 0.00711838 | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086363 | GGATGACAAGAGGAG[C/G/T]GCCTCGGCTCCCCTG | 6596 |
| rs775559732 | snp | C/T | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087703 | GCGATTCTCCTGCCT[C/T]AGCCTCCGGAGTAGC | 6596 |
| rs775614755 | in-del | -/AGTA | 0.000132888 | 0.00815024 | intron-variant | HLTF | GRCh38.p7 | 3:149063558 | CAAATATAAAGTATT[-/AGTA]AGGTGTCTTAGAAAC | 6596 |
| rs775619855 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031562 | AAACAATGAGTGTAG[C/T]ACTACTTAACTAAAA | 6596 |
| rs775621609 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054362 | GAGCCAGTGGGAAGA[C/G]ACTAAATAAACAAGG | 6596 |
| rs775624819 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149083196 | GCGGAGGTTGCAGTG[A/G]GCCAAGATTGCACCA | 6596 |
| rs775639447 | snp | C/T | 1.65064e-05 | 0.00287279 | synonymous-codon | HLTF | GRCh38.p7 | 3:149074261 | TTTCTTCAACTGATC[C/T]GAAACCGCTTTTCTA | 6596 |
| rs775646317 | snp | C/T | 1.79952e-05 | 0.00299954 | missense | HLTF | GRCh38.p7 | 3:149046194 | AACTCCAAAACAGGT[C/T]TTCCTTTAATTTTGC | 6596 |
| rs775657881 | snp | A/G | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085242 | ACGCCTGGAATCCCA[A/G]CACTTTGGGAGGCAG | 6596 |
| rs775738082 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149032729 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAT | 6596 |
| rs775745147 | snp | G/T | 1.66468e-05 | 0.00288498 | missense | HLTF | GRCh38.p7 | 3:149059735 | TTTTTCAACATTTTC[G/T]TTTTTGTTGTAGGAA | 6596 |
| rs775782962 | snp | A/C | 1.76179e-05 | 0.00296793 | intron-variant | HLTF | GRCh38.p7 | 3:149073363 | AAAGCCATCAAATAA[A/C]GTAGGTTTTTATCTT | 6596 |
| rs775789409 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149075589 | AACACTTCCAAATTC[C/G]TAAACCTAGGTACCA | 6596 |
| rs775804646 | snp | A/G | 9.60864e-05 | 0.00693065 | intron-variant | HLTF | GRCh38.p7 | 3:149039993 | TCCTTATATAAAGGT[A/G]AAACAAATACTCAAA | 6596 |
| rs775852301 | snp | C/T | 3.29696e-05 | 0.00406001 | synonymous-codon | HLTF | GRCh38.p7 | 3:149034942 | GATAACTTCTTGCTT[C/T]TGACCAAGTCTATGG | 6596 |
| rs775857943 | snp | A/C/G | 3.68021e-05 | 0.00428952 | missense | HLTF | GRCh38.p7 | 3:149039596 | TTAAGTGGTATTTCT[A/C/G]TTAAAGACAGGAATG | 6596 |
| rs775858234 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | HLTF | GRCh38.p7 | 3:149048902 | ATTCTAAGTCAAGTA[C/T]AGCTTTTGTCTGCTG | 6596 |
| rs775876671 | snp | C/G | 1.65132e-05 | 0.00287339 | synonymous-codon, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084709 | ATAGCGTAGTCCAAC[C/G]ACATGACCTCTCAAA | 6596 |
| rs775905420 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149077343 | GGCAGTCACCAGAAA[A/G]AAAGAGAATGGAGTT | 6596 |
| rs775984967 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066529 | TTGAAAGAGTGACAA[-/T]TTTTTTTTTTTTTTT | 6596 |
| rs775992341 | snp | A/G | 1.65767e-05 | 0.00287891 | missense | HLTF | GRCh38.p7 | 3:149068322 | ATTACTGCAATGGCC[A/G]TAAGAGTTTTACCCT | 6596 |
| rs775994183 | in-del | -/TGT | 1.65312e-05 | 0.00287495 | cds-indel | HLTF | GRCh38.p7 | 3:149042261 | AGGACATCTGCATAA[-/TGT]GCCAGGACAGTCCCT | 6596 |
| rs775998526 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042529 | GATGCTGAGAGGGAT[A/G]ACTGCAGATCTCAAA | 6596 |
| rs776031593 | in-del | -/AAAC | | | intron-variant | HLTF | GRCh38.p7 | 3:149057430 | ACTCCGTCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 6596 |
| rs776045204 | snp | C/T | 1.69853e-05 | 0.00291416 | intron-variant | HLTF | GRCh38.p7 | 3:149073194 | ACATTTAAAATTCAC[C/T]TTTAGATTACAAAAT | 6596 |
| rs776045652 | in-del | -/TA | 1.78803e-05 | 0.00298995 | intron-variant | HLTF | GRCh38.p7 | 3:149055270 | AGATAAAATATAAAT[-/TA]TGTTACATTTTTAAA | 6596 |
| rs776075566 | snp | A/C | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086273 | CATTTGGGGACGCCT[A/C]CAGGCCGTTAGACCG | 6596 |
| rs776080384 | snp | A/G | 1.65302e-05 | 0.00287486 | intron-variant | HLTF | GRCh38.p7 | 3:149055422 | AAATGAACCACTGAT[A/G]GAACCTTTAGCTGTT | 6596 |
| rs776084139 | snp | A/T | 1.86301e-05 | 0.003052 | intron-variant | HLTF | GRCh38.p7 | 3:149071244 | TAACTAAAGAAAAAA[A/T]TAATTACCAAACCCA | 6596 |
| rs776088211 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149041243 | TCTTTGTGTCTCACA[C/T]TATCAATCCATTTAT | 6596 |
| rs776117457 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038286 | AAACTGACGCAAAGC[A/G]GGATCTCATTATTTG | 6596 |
| rs776183901 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087362 | AACCTTGGACCAGCT[A/G]CAGCCGACGCCTGGC | 6596 |
| rs776202638 | snp | G/T | 0.00105065 | 0.0228959 | intron-variant | HLTF | GRCh38.p7 | 3:149048203 | AACTCTTTAACCAGA[G/T]TATCCAGTAAGAGTA | 6596 |
| rs776210465 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149052011 | AAACAAAAATTAGCC[A/G]GGCATGGTGGCATGT | 6596 |
| rs776255360 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086383 | CGGCTCCCCTGGATC[G/T]TTTTCGAGCCGCCTC | 6596 |
| rs776270484 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041532 | ACAGGGTTTACAAAA[C/T]ACATGTGCACAATGT | 6596 |
| rs776295631 | snp | A/C | 1.71185e-05 | 0.00292557 | missense | HLTF | GRCh38.p7 | 3:149032228 | CCACAAATTATAAGT[A/C]AATTAATGTTCTGAT | 6596 |
| rs776302804 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149050958 | ACCAGACCTAGAAGA[C/T]TTTCAGCAGAAAAAA | 6596 |
| rs776444706 | snp | C/T | 1.65004e-05 | 0.00287227 | missense | HLTF | GRCh38.p7 | 3:149064859 | GAGTCATCGTTAACA[C/T]TATATTCCTGGGTAA | 6596 |
| rs776468657 | snp | C/T | 1.64863e-05 | 0.00287104 | stop-gained | HLTF | GRCh38.p7 | 3:149055307 | TAAAGACTTACAATC[C/T]AGTTGCTTAACACAG | 6596 |
| rs776582285 | snp | C/T | 2.52e-05 | 0.00354956 | intron-variant | HLTF | GRCh38.p7 | 3:149071562 | CTGAGTAGTCTTAAA[C/T]AAAAAATATTGGTTC | 6596 |
| rs776650200 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149061487 | AATTAAAAATTTCAA[C/T]ACCAGGTTTAATATT | 6596 |
| rs776689400 | snp | C/T | 1.69596e-05 | 0.00291196 | intron-variant | HLTF | GRCh38.p7 | 3:149074397 | AGAAGCATTACTTTT[C/T]ATCCCCACTAAGAAT | 6596 |
| rs776689450 | snp | G/T | 1.64827e-05 | 0.00287073 | synonymous-codon | HLTF | GRCh38.p7 | 3:149063490 | CTTCTCCTTGATATC[G/T]GAAATACTGGGTTGT | 6596 |
| rs776737512 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149060190 | AATGCAATACAATTT[A/C]TCAACGAATGAGAAA | 6596 |
| rs776741745 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149074005 | TTTTTAATATCCCCT[C/T]ACTCTTACTGTGTAT | 6596 |
| rs776742173 | snp | C/T | 6.64066e-05 | 0.00576185 | missense | HLTF | GRCh38.p7 | 3:149039075 | AAAACACTCGAGAAG[C/T]TGCAGACAGATTCAA | 6596 |
| rs776775910 | snp | A/G | 5.46025e-05 | 0.00522478 | missense | HLTF | GRCh38.p7 | 3:149039188 | ACTCTTTTCTTTTGG[A/G]CCATGGAACCATCCA | 6596 |
| rs776777121 | snp | G/T | 1.65712e-05 | 0.00287843 | intron-variant | HLTF | GRCh38.p7 | 3:149064766 | ACCAGATCAAATATT[G/T]GATCATTTCAAAATT | 6596 |
| rs776843860 | in-del | -/AAATA | 2.5193e-05 | 0.00354907 | intron-variant | HLTF | GRCh38.p7 | 3:149071558 | ATTCTGAGTAGTCTT[-/AAATA]AAATAAAAAATATTG | 6596 |
| rs776853106 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149055800 | ATCTCCTCCCATACT[C/G]CACCAGGACTGGTCT | 6596 |
| rs776867698 | in-del | -/A | 0.0267107 | 0.112436 | intron-variant | HLTF | GRCh38.p7 | 3:149032382 | ATGAACTTTAAAAAG[-/A]AAAAAAAAAAGTTAA | 6596 |
| rs776869626 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149070250 | TTACAGCAACATACC[A/G]TCGTAAGGACAAATT | 6596 |
| rs776873058 | snp | A/C | 1.91801e-05 | 0.00309672 | missense | HLTF | GRCh38.p7 | 3:149046221 | TTGCTTGTCTTTGTT[A/C]TTCTAAGTGTAATAT | 6596 |
| rs776932528 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149038325 | ATGAACCACTACCCT[A/G]AAAAGCATTACAGTT | 6596 |
| rs777047950 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149042563 | AGCTGCCAAAACACA[A/G]TTCTTTAAAATGGAT | 6596 |
| rs777075156 | in-del | -/TATT | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030302 | AGTGGCTTTTTTATA[-/TATT]TATCCTTCTTAGGAA | 6596 |
| rs777075595 | snp | C/T | 8.28356e-05 | 0.00643513 | missense | HLTF | GRCh38.p7 | 3:149040123 | AATTATCTTCATGTA[C/T]ATCATTTCTGCATAA | 6596 |
| rs777095963 | snp | G/T | 3.32209e-05 | 0.00407546 | missense | HLTF | GRCh38.p7 | 3:149071289 | ATTCCTCCATGGACA[G/T]TTTCTGGTCGGTCCT | 6596 |
| rs777122403 | snp | C/T | 1.66073e-05 | 0.00288156 | missense | HLTF | GRCh38.p7 | 3:149059768 | GATGAAGTTAATGCA[C/T]ATGCAAATGCCACAT | 6596 |
| rs777160310 | snp | A/T | 1.65108e-05 | 0.00287317 | missense | HLTF | GRCh38.p7 | 3:149034925 | AAACTCACTTTTGTG[A/T]TGATAACTTCTTGCT | 6596 |
| rs777202145 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149058531 | TTACATAGTCTAGAA[C/T]TGAACCTTTTGTCAG | 6596 |
| rs777212216 | snp | C/T | 1.6894e-05 | 0.00290633 | missense | HLTF | GRCh38.p7 | 3:149046129 | ACTGATAAATCTTTC[C/T]CTCTTCATCTGAAAG | 6596 |
| rs777255078 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149055249 | ACAGAATACTTTCTA[C/T]CTTGTAGATAAAATA | 6596 |
| rs777274567 | snp | C/T | 1.74096e-05 | 0.00295034 | synonymous-codon | HLTF | GRCh38.p7 | 3:149046175 | AAATACTTTACGTTC[C/T]GGTAACTCCAAAACA | 6596 |
| rs777281897 | in-del | -/T | 1.73972e-05 | 0.00294929 | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149032210 | CTGACCTTACTAAAA[-/T]TCCCACAAATTATAA | 6596 |
| rs777404879 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon | HLTF | GRCh38.p7 | 3:149074327 | CATGGTAAAAGCATT[A/G]TTTGCACCAAAAGGA | 6596 |
| rs777436782 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054965 | TTGGTATAGCTCTTA[C/G]AAAAGACAGTTCCAA | 6596 |
| rs777498395 | snp | C/T | 1.65108e-05 | 0.00287317 | intron-variant | HLTF | GRCh38.p7 | 3:149063528 | ATCTAGATGCGTCTA[C/T]TTCAAAGAAAAATGC | 6596 |
| rs777517446 | snp | A/G | 5.04003e-05 | 0.00501972 | intron-variant | HLTF | GRCh38.p7 | 3:149059704 | AAAACTAGAAAACAA[A/G]GATATTTACTGACCC | 6596 |
| rs777607486 | in-del | -/AAAC | | | intron-variant | HLTF | GRCh38.p7 | 3:149034081 | AGAAAAAATGTTAAT[-/AAAC]AAGATATGTGAAATA | 6596 |
| rs777612627 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149069591 | GAAATGGAAACTACA[C/T]ATTAACTACTTCTGT | 6596 |
| rs777622439 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149065416 | TTTCCAAAGGCACCA[A/C]TGTACATGAATTGAA | 6596 |
| rs777632037 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149041971 | ATCACCGGAATTCCT[A/G]GAAAGACCTCATTAT | 6596 |
| rs777653001 | snp | C/T | 1.7056e-05 | 0.00292022 | intron-variant | HLTF | GRCh38.p7 | 3:149068369 | AGATAAATGGTCAGA[C/T]TGTGAAACCCAGTTC | 6596 |
| rs777687831 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149077387 | AGATTCATTCCCAAA[G/T]AACTGTTATTCTCCT | 6596 |
| rs777724079 | snp | C/T | 3.34711e-05 | 0.00409078 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084677 | TTATCTACTATTATA[C/T]TCACTACTCCCGTGT | 6596 |
| rs777736606 | snp | A/T | 4.07922e-05 | 0.00451602 | intron-variant | HLTF | GRCh38.p7 | 3:149060872 | TTCTAAAATTAAGTA[A/T]ACACAAAGAAATTTT | 6596 |
| rs777754345 | snp | C/T | 3.78731e-05 | 0.00435145 | intron-variant | HLTF | GRCh38.p7 | 3:149046053 | TAAACAAAAACTAAT[C/T]TTTAACATGGTTTTC | 6596 |
| rs777754346 | snp | A/G | 1.66194e-05 | 0.00288261 | missense | HLTF | GRCh38.p7 | 3:149059798 | TCTTCTATAACCTTA[A/G]AAGATCCTGCTGATA | 6596 |
| rs777769646 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034174 | AATTAACAATTTTCA[G/T]ATAAATCCTATTTTG | 6596 |
| rs777829878 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061044 | TTCATAACCAGATAG[A/G]TGCATTAACTATACA | 6596 |
| rs777849456 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149069636 | TGAGGGTTAGCTAGA[G/T]AAAAATCACTCAAGA | 6596 |
| rs777887028 | snp | A/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087030 | TCATGTTAAGCCTCA[A/G]CGTATGCATGAGACA | 6596 |
| rs777930185 | snp | C/T | 3.49981e-05 | 0.00418304 | intron-variant | HLTF | GRCh38.p7 | 3:149048190 | AGGAAACTGTTATAA[C/T]TCTTTAACCAGAGTA | 6596 |
| rs777939228 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060987 | AAAATTTTTTAAAGA[-/T]TTTTGACAAATGAAA | 6596 |
| rs778009036 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | HLTF | GRCh38.p7 | 3:149041596 | ATTGCACATTCCTCA[C/T]CTGAACCTGAGCTCA | 6596 |
| rs778011668 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149032484 | ACCGCAATTACTTTT[G/T]CACCAAACTATAATA | 6596 |
| rs778075876 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149073450 | TGTAACCCAAGCACT[G/T]TGGGAGGCCAAGGCA | 6596 |
| rs778085213 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149072311 | TATTCCTATAAAATG[A/G]AAGGGATGAACTAAA | 6596 |
| rs778091493 | in-del | -/AAGTC | 3.29679e-05 | 0.00405991 | frameshift-variant | HLTF | GRCh38.p7 | 3:149048892 | CTTCTTTCTGATTCT[-/AAGTC]AAGTACAGCTTTTGT | 6596 |
| rs778094820 | snp | A/G | 3.50933e-05 | 0.00418872 | intron-variant | HLTF | GRCh38.p7 | 3:149071688 | ACAAGAAACAATGTA[A/G]AACAAACTAATTAAA | 6596 |
| rs778163079 | snp | A/C | 1.65241e-05 | 0.00287433 | intron-variant | HLTF | GRCh38.p7 | 3:149042150 | ACAATGATATGAAGC[A/C]ATCAAATTTACCTAC | 6596 |
| rs778198352 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149037897 | ACGCTCCTATGTGAA[C/T]GCACGTCCAGGTCAC | 6596 |
| rs778225782 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057876 | TTCCATTAAAATAAT[G/T]CTGCAATGAAAACCA | 6596 |
| rs778273299 | snp | C/T | 3.29826e-05 | 0.00406082 | intron-variant | HLTF | GRCh38.p7 | 3:149060722 | AAACATAAAAATGGG[C/T]AAAACAGGACATTAG | 6596 |
| rs778304214 | snp | G/T | | | utr-variant-3-prime | HLTF | GRCh38.p7 | 3:149030756 | AAATCAGCCCTTTCC[G/T]TACCTGCTACTGCCT | 6596 |
| rs778304921 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149045087 | TATGCGTTACATACC[C/T]CCATTCCAATAAATC | 6596 |
| rs778355604 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081848 | GGAGTTTAAGTATGT[G/T]TTCCTCCAATTCAAA | 6596 |
| rs778397992 | snp | G/T | 3.41495e-05 | 0.00413202 | missense | HLTF | GRCh38.p7 | 3:149032299 | TTTTTAGTTCCAAAG[G/T]CTCCTGCTGCAAGTT | 6596 |
| rs778457207 | snp | G/T | 1.65037e-05 | 0.00287256 | missense | HLTF | GRCh38.p7 | 3:149075914 | TTGTTGTCCATGATA[G/T]AGGCCAAAGCACCTG | 6596 |
| rs778543884 | snp | C/T | 6.59533e-05 | 0.00574215 | missense | HLTF | GRCh38.p7 | 3:149064815 | GTCCATCTGCCTTTT[C/T]ACTGGTATTGTTTCC | 6596 |
| rs778576284 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149043548 | CTGAACTTCAGAGGG[A/G]AAAAAAAAAAAAAAA | 6596 |
| rs778596876 | snp | C/T | 1.65168e-05 | 0.00287369 | intron-variant | HLTF | GRCh38.p7 | 3:149063531 | TAGATGCGTCTATTT[C/T]AAAGAAAAATGCAAA | 6596 |
| rs778612440 | in-del | -/TC | 0.444444 | 0.157135 | frameshift-variant | HLTF | GRCh38.p7 | 3:149032314 | GCTCCTGCTGCAAGT[-/TC]TCTCTTTTTGTTTTG | 6596 |
| rs778637715 | snp | C/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086668 | GACGGCGGGGGGTCC[C/G]GGCTGCAAGGGTGGT | 6596 |
| rs778655393 | snp | C/T | 1.66518e-05 | 0.00288542 | synonymous-codon | HLTF | GRCh38.p7 | 3:149074348 | ACCAAAAGGAACTAC[C/T]CTATTATATTTGGGA | 6596 |
| rs778751499 | snp | C/G | | | | | GRCh38.p7 | 3:149065548 | ACCAATCAAAAAAAA[C/G]TAAAAATCTGCCGGG | 6596 |
| rs778769353 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149066741 | AGTAAGTAGTCTTAT[A/G]TGCTTCTATCAAATC | 6596 |
| rs778770385 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149051551 | GGAGAAAACACATGA[C/T]GCCTGGGGTATAATT | 6596 |
| rs778788754 | snp | G/T | 1.66228e-05 | 0.0028829 | synonymous-codon | HLTF | GRCh38.p7 | 3:149059803 | TATAACCTTAGAAGA[G/T]CCTGCTGATAAAACA | 6596 |
| rs778843346 | snp | A/G | 2.44221e-05 | 0.00349435 | intron-variant | HLTF | GRCh38.p7 | 3:149071206 | ACTTTCTAGAAAATC[A/G]TAATCACAAAATTAG | 6596 |
| rs778863582 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149046981 | CACTATAACTCACAG[C/T]AAGAAACACATTCTA | 6596 |
| rs778875566 | snp | A/T | 1.66877e-05 | 0.00288852 | missense | HLTF | GRCh38.p7 | 3:149039060 | TTACTGGATCCATTA[A/T]AAACACTCGAGAAGC | 6596 |
| rs778935196 | snp | C/T | 3.34336e-05 | 0.00408848 | intron-variant | HLTF | GRCh38.p7 | 3:149059714 | AACAAGGATATTTAC[C/T]GACCCTTTTTCAACA | 6596 |
| rs778935954 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149060752 | GAATATAGGACACAT[G/T]ATCAAATCAAATCTA | 6596 |
| rs779031264 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149049917 | GAATCATCTGAAACC[A/G]GGAGGCAGAGGTTGC | 6596 |
| rs779047044 | snp | C/T | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149031972 | TTATGAAAAGCTGAA[C/T]AACAAAGTAACCTTT | 6596 |
| rs779066647 | snp | A/G | 2.31715e-05 | 0.0034037 | intron-variant | HLTF | GRCh38.p7 | 3:149039703 | ATTAATCTGCAAAAA[A/G]TATTAAGATGTCCAT | 6596 |
| rs779138042 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149071123 | GGAAAAACTGTGTTC[C/T]ACAAAGATAGTAAGA | 6596 |
| rs779148751 | snp | A/T | 3.14362e-05 | 0.00396448 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086289 | CAGGCCGTTAGACCG[A/T]GCGCCCCACCCCCTC | 6596 |
| rs779175324 | in-del | -/T | 0.0576439 | 0.159685 | intron-variant | HLTF | GRCh38.p7 | 3:149063068 | ATCTCTCTCTTTTTC[-/T]TTTTTTTTTGAGACG | 6596 |
| rs779176918 | snp | A/G | 1.65048e-05 | 0.00287265 | missense | HLTF | GRCh38.p7 | 3:149073290 | GTCCAGCTCTTCCAG[A/G]GCCCCAACCACTTTC | 6596 |
| rs779209951 | snp | A/G | 1.65075e-05 | 0.00287289 | missense | HLTF | GRCh38.p7 | 3:149071325 | GAAAAATTTGTTATT[A/G]TGTTATAGTATAAGT | 6596 |
| rs779229334 | snp | C/G | 8.73916e-05 | 0.0066097 | intron-variant | HLTF | GRCh38.p7 | 3:149060890 | ACAAAGAAATTTTTG[C/G]ACCAACCCAAAGCAA | 6596 |
| rs779232317 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149084207 | TCAGACAATCAAAAA[A/G]CAATTTGAAACGTTC | 6596 |
| rs779299960 | in-del | -/T | 0.00353705 | 0.0419048 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084893 | CAAACTGGATCCCTA[-/T]TTTTTTTTAAAGGCA | 6596 |
| rs779311514 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149070671 | ATGGAATACAATTTC[-/A]CATAACATTGTTTTG | 6596 |
| rs779366897 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149082802 | CCAATATAGATGATA[C/T]TCCTAATCACATTAG | 6596 |
| rs779411331 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149066884 | AATAAAAGTAGAAAG[C/T]AGGAAGTAAAACTAA | 6596 |
| rs779427720 | snp | C/T | 3.42425e-05 | 0.00413764 | missense | HLTF | GRCh38.p7 | 3:149032321 | CTGCAAGTTCTCTCT[C/T]TTTGTTTTGTATTTT | 6596 |
| rs779453571 | snp | A/C | 1.64969e-05 | 0.00287196 | splice-donor-variant | HLTF | GRCh38.p7 | 3:149055302 | GGGCTTAAAGACTTA[A/C]AATCCAGTTGCTTAA | 6596 |
| rs779465991 | snp | A/G | 1.65083e-05 | 0.00287296 | intron-variant | HLTF | GRCh38.p7 | 3:149063406 | CTAAATAAACATATG[A/G]CATAATCAAACCATA | 6596 |
| rs779466153 | snp | G/T | 1.64846e-05 | 0.0028709 | missense | HLTF | GRCh38.p7 | 3:149048888 | CCATCTTCTTTCTGA[G/T]TCTAAGTCAAGTACA | 6596 |
| rs779509974 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149082980 | AACGTGGCTGGGCGC[A/G]GTGGCTCATGCCTGT | 6596 |
| rs779533497 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149066956 | GAAACTGATGTACTG[A/C]CTTCTCTGAAAACTA | 6596 |
| rs779585789 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | HLTF | GRCh38.p7 | 3:149055383 | CAGTTTTCTTTGACC[C/T]CTCCACTGCACAAGC | 6596 |
| rs779606910 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149078465 | TGAGGTGGGAGGACT[C/G]CTTGAATGCAGGAGT | 6596 |
| rs779636177 | in-del | -/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149068770 | AAAGTCATAACTTCT[-/C]CATAAAGCATAAAAG | 6596 |
| rs779640825 | snp | A/C | 1.68576e-05 | 0.00290319 | intron-variant | HLTF | GRCh38.p7 | 3:149068220 | AGGTTTCACATAAAG[A/C]GCACTTACTACTACT | 6596 |
| rs779674100 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149080510 | TATGAGGCAGAGCTA[C/T]GTTCTCTCCCAGTCG | 6596 |
| rs779674644 | snp | A/G | 1.69149e-05 | 0.00290812 | missense | HLTF | GRCh38.p7 | 3:149048158 | AAGAATTCTGGATTG[A/G]AGTACCTAGAAATAA | 6596 |
| rs779698623 | snp | A/T | 1.70892e-05 | 0.00292306 | intron-variant | HLTF | GRCh38.p7 | 3:149073187 | ACCTGCAACATTTAA[A/T]ATTCACTTTTAGATT | 6596 |
| rs779700662 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149079902 | CATGCCCAGCCACAA[A/G]GTTTTTTATATACTG | 6596 |
| rs779763241 | in-del | -/A | 1.69824e-05 | 0.00291392 | frameshift-variant | HLTF | GRCh38.p7 | 3:149040057 | TGTCCATTCCATATC[-/A]AGACTTTTTCTCACT | 6596 |
| rs779865021 | snp | C/G | 3.34146e-05 | 0.00408732 | intron-variant | HLTF | GRCh38.p7 | 3:149074360 | TACCCTATTATATTT[C/G]GGAGAAAAAGAAAGG | 6596 |
| rs779867510 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149057372 | TGGAGGTTGCAGTGC[A/G]CCGTGATCGCACCAC | 6596 |
| rs779887716 | in-del | -/ATTGGAGT | 1.6825e-05 | 0.00290038 | frameshift-variant | HLTF | GRCh38.p7 | 3:149048154 | TTTAAAGAATTCTGG[-/ATTGGAGT]ACCTAGAAATAACAG | 6596 |
| rs779907442 | snp | A/G | 2.42233e-05 | 0.0034801 | intron-variant | HLTF | GRCh38.p7 | 3:149039240 | AGGCTCTAAAGGGGG[A/G]AAGAAAAGAGACAAG | 6596 |
| rs779909164 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149038993 | CCAAATAGTTTTTTG[C/T]CTTATTTTTTTGAAA | 6596 |
| rs779913230 | snp | A/G | 1.70863e-05 | 0.00292281 | intron-variant | HLTF | GRCh38.p7 | 3:149048006 | TTGTAACTAATATTA[A/G]TCACTGTCTGAAAGT | 6596 |
| rs779989896 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149054141 | TGACAATTAAACTAT[C/T]ACAAGTAGTCTTTTC | 6596 |
| rs780112217 | snp | C/T | 1.68335e-05 | 0.00290111 | intron-variant | HLTF | GRCh38.p7 | 3:149040207 | ACAGAAGAACAAATA[C/T]AAATATGCCTAAAAA | 6596 |
| rs780188033 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149050013 | AGGGGGAGGGGAGGA[A/G]TGGAGAAAAGAAAAA | 6596 |
| rs780223585 | in-del | -/GAG | 1.66043e-05 | 0.00288129 | cds-indel, nc-transcript-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086357 | TGAGTGGGATGACAA[-/GAG]GAGCGCCTCGGCTCC | 6596 |
| rs780260595 | snp | A/T | 9.99117e-05 | 0.00706724 | intron-variant | HLTF | GRCh38.p7 | 3:149059812 | AGAAGATCCTGCTGA[A/T]AAAACAACAAAGAAT | 6596 |
| rs780260800 | snp | C/T | 1.67652e-05 | 0.00289522 | missense | HLTF | GRCh38.p7 | 3:149071436 | GGAAGCAGTGGTGTT[C/T]CAATAGCCTATAAAT | 6596 |
| rs780285777 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149059292 | ATTTAGTCTCTTAAG[A/C]AGTGTTGTTTTCCTA | 6596 |
| rs780366523 | snp | A/G | 1.96265e-05 | 0.00313255 | intron-variant | HLTF | GRCh38.p7 | 3:149049040 | TTAAAAAACACAGGA[A/G]AGTAAAATAGTACTT | 6596 |
| rs780450641 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149044000 | ATTTCTGAATATTCA[A/G]GAATGCAAGGAATAG | 6596 |
| rs780464976 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149063933 | CGGCTCCCCTACCCA[C/T]TTATCAGAATGATCC | 6596 |
| rs780491583 | snp | A/G | 9.91506e-05 | 0.00704028 | intron-variant | HLTF | GRCh38.p7 | 3:149060635 | ATGGGTATATAGTAT[A/G]CACATACCTTTCGCC | 6596 |
| rs780562063 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149057852 | ACAACATGTACATTA[C/T]TTCTAATATTCCATT | 6596 |
| rs780563994 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149069285 | AGACCAGCCTGGACC[A/G]ACACGGTGAAACCCC | 6596 |
| rs780582388 | snp | C/T | 3.29875e-05 | 0.00406112 | missense | HLTF | GRCh38.p7 | 3:149042187 | GGCCATTGGAAGACA[C/T]TGCATTTGTAAGAAG | 6596 |
| rs780645513 | snp | C/T | 1.68134e-05 | 0.00289938 | intron-variant | HLTF | GRCh38.p7 | 3:149074188 | CTTACAATATCAGAA[C/T]AATATTAAGTGAAAC | 6596 |
| rs780650076 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149071243 | TTAACTAAAGAAAAA[A/G]ATAATTACCAAACCC | 6596 |
| rs780677433 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149053940 | AGAAAGAACAGTTTC[A/G]TTGGAATAAAAAAAT | 6596 |
| rs780695765 | snp | A/G | 5.25399e-05 | 0.00512515 | intron-variant | HLTF | GRCh38.p7 | 3:149059674 | TTTTTTCATTCAAAA[A/G]CAGAAAAAAAACCAA | 6596 |
| rs780715352 | snp | C/T | 1.95189e-05 | 0.00312395 | intron-variant | HLTF | GRCh38.p7 | 3:149046042 | GGGAAACAAAGTAAA[C/T]AAAAACTAATTTTTA | 6596 |
| rs780737036 | in-del | -/G | 3.29989e-05 | 0.00406182 | frameshift-variant | HLTF | GRCh38.p7 | 3:149064795 | TTAGCATTTACCTTT[-/G]CTTAGTCCATCTGCC | 6596 |
| rs780742235 | snp | A/G | 1.65427e-05 | 0.00287595 | synonymous-codon | HLTF | GRCh38.p7 | 3:149073309 | CCAACCACTTTCCAA[A/G]TTGAATCCTAAAGCT | 6596 |
| rs780794801 | in-del | -/T | 4.99813e-05 | 0.00499881 | frameshift-variant | HLTF | GRCh38.p7 | 3:149059730 | GACCCTTTTTCAACA[-/T]TTTCTTTTTTGTTGT | 6596 |
| rs780840350 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149068084 | AAAAGAATGTGACAC[A/G]AACTTTCATTCTTAT | 6596 |
| rs780890450 | snp | G/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149034642 | GTAGTCTCCAATGTA[G/T]AGTTTTAAGGGAAAC | 6596 |
| rs780920069 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149064281 | ACCAATTGTTATTTA[C/T]AATTTTTCACCTACT | 6596 |
| rs780930735 | snp | A/G | 3.72731e-05 | 0.00431685 | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149084638 | ATTTTCTAGGTTAAC[A/G]CCAGAAATATAATCA | 6596 |
| rs781018676 | in-del | -/ATA | | | cds-indel | HLTF | GRCh38.p7 | 3:149030243 | AAGTTATTTTTCTAT[-/ATA]ATAATAAGACAACAG | 6596 |
| rs781023116 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149081749 | TAAAGGGTACTGAAA[C/T]TTAAGGTTCAGAGCA | 6596 |
| rs781025551 | snp | C/G | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149088329 | TGAGGTCAGGAGTTC[C/G]AGACCAGCCTGGCCA | 6596 |
| rs781041878 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149054933 | ACTGTTGTTATTGTT[A/C]TAAAAATAAGTTATT | 6596 |
| rs781060662 | snp | C/T | 1.64841e-05 | 0.00287085 | missense | HLTF | GRCh38.p7 | 3:149055398 | CCTCCACTGCACAAG[C/T]TCCTAAAAAAATGAA | 6596 |
| rs781071752 | snp | C/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149040814 | AGGCAGCAGATACAG[C/G]AATATGTTTACCTCA | 6596 |
| rs781092650 | snp | C/T | 1.75409e-05 | 0.00296145 | missense | HLTF | GRCh38.p7 | 3:149039651 | TTTTTATGTTGGGAT[C/T]CTTCTTTCTTAAGTC | 6596 |
| rs781107362 | snp | A/G | 4.94605e-05 | 0.0049727 | intron-variant | HLTF | GRCh38.p7 | 3:149060708 | AATAAAACAAAAATA[A/G]ACATAAAAATGGGCA | 6596 |
| rs781147669 | snp | A/G | 1.67276e-05 | 0.00289197 | intron-variant | HLTF | GRCh38.p7 | 3:149039264 | AGACAAGTAACAAAC[A/G]CTATTATTATAAAAA | 6596 |
| rs781158620 | snp | C/T | 1.65026e-05 | 0.00287246 | missense | HLTF | GRCh38.p7 | 3:149071654 | TGTCAAATTCTGTTT[C/T]AAGCTACAATAAACA | 6596 |
| rs781176614 | snp | C/G | 3.38564e-05 | 0.00411425 | intron-variant | HLTF | GRCh38.p7 | 3:149068355 | AAAATGTTTTAAAAA[C/G]ATAAATGGTCAGATT | 6596 |
| rs781356927 | snp | C/T | 1.65018e-05 | 0.00287239 | synonymous-codon | HLTF | GRCh38.p7 | 3:149060647 | TATACACATACCTTT[C/T]GCCCTGCCTTTAGTT | 6596 |
| rs781368125 | snp | A/G | 3.31757e-05 | 0.00407269 | splice-donor-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149086315 | CCCTCCGCCCCCTTC[A/G]CCTCTTGAACATCCA | 6596 |
| rs781391092 | snp | A/G | 1.702e-05 | 0.00291714 | intron-variant | HLTF | GRCh38.p7 | 3:149048012 | CTAATATTAATCACT[A/G]TCTGAAAGTACTTAC | 6596 |
| rs781398596 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149080208 | AGAGATAATGGGAGT[A/G]ACTACAAATGGGAAT | 6596 |
| rs781420266 | snp | A/G | | | utr-variant-3-prime, intron-variant | HLTF | GRCh38.p7 | 3:149032152 | GATCTCATTTCTAAA[A/G]CTCTGTATTTTTCTC | 6596 |
| rs781449206 | snp | A/G | 1.65477e-05 | 0.00287638 | missense | HLTF | GRCh38.p7 | 3:149075953 | TTCTTTAAATGGCCA[A/G]CTTGATTTCCATTCA | 6596 |
| rs781498106 | snp | C/T | | | intron-variant, upstream-variant-2KB | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149085144 | CTAGTCAGAGTTCAC[C/T]AACCTCTTTCCCAGT | 6596 |
| rs781522301 | in-del | -/CTT | | | intron-variant | HLTF | GRCh38.p7 | 3:149056524 | ATCATTCACAACTTG[-/CTT]TTTTCTCTCAGTGCT | 6596 |
| rs781589636 | snp | C/T | 3.65263e-05 | 0.00427339 | intron-variant | HLTF | GRCh38.p7 | 3:149055254 | ATACTTTCTACCTTG[C/T]AGATAAAATATAAAT | 6596 |
| rs781631030 | snp | C/T | | | missense | HLTF | GRCh38.p7 | 3:149060834 | TGAATCACTGCTTTC[C/T]ATGTACTGGACAGCA | 6596 |
| rs781751201 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | HLTF | GRCh38.p7 | 3:149041547 | TACATGTGCACAATG[C/T]GTTATCACAGGAACT | 6596 |
| rs796131708 | in-del | -/CA | | | intron-variant | HLTF | GRCh38.p7 | 3:149032978 | AAAAAAAAAAAAAAA[-/CA]AAAAACTATTCCCAG | 6596 |
| rs796231475 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149039890 | CCCTCAAATTCACCA[A/C]TAAAAATAAAAAGCC | 6596 |
| rs796281325 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149079591 | AAGGTTTTTTTGGGG[-/T]TTTTCTTTGTTGTTG | 6596 |
| rs796316100 | in-del | -/A | | | intron-variant | HLTF | GRCh38.p7 | 3:149071045 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 6596 |
| rs796321982 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149061155 | AGTCACTGCAACCTC[A/G]TACTCCTGGGCTCAA | 6596 |
| rs796377360 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149048774 | GGCAGAATTTACACC[A/C]ACTTTAAGTTTACAA | 6596 |
| rs796441316 | in-del | -/CC | | | intron-variant | HLTF | GRCh38.p7 | 3:149055414 | TCCTAAAAAAATGAA[-/CC]ACTGATAGAACCTTT | 6596 |
| rs796441666 | snp | A/C | | | missense | HLTF | GRCh38.p7 | 3:149064817 | CCATCTGCCTTTTCA[A/C]TGGTATTGTTTCCTC | 6596 |
| rs796451582 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149054819 | CCTCTCTGTGTTTCA[A/G]TGTGGGCACCTGGAA | 6596 |
| rs796499358 | in-del | -/AT | | | intron-variant | HLTF | GRCh38.p7 | 3:149040018 | CTCAAATATTTGCAC[-/AT]GAGTACTTTACCTTT | 6596 |
| rs796530128 | in-del | -/GAG | | | intron-variant | HLTF | GRCh38.p7 | 3:149060026 | TTCATGGTAAGACTT[-/GAG]GAGAAGAAATGAAAG | 6596 |
| rs796544461 | snp | A/C | | | intron-variant | HLTF | GRCh38.p7 | 3:149074817 | ATTTATTTTCTCTTC[A/C]AACTCACCTAGGATT | 6596 |
| rs796614493 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | HLTF, HLTF-AS1 | GRCh38.p7 | 3:149087584 | TTTTTTCTTTTTTTT[-/GT]TTTTTTTTCTTTTTT | 6596 |
| rs796664615 | in-del | -/A | | | downstream-variant-500B | HLTF | GRCh38.p7 | 3:149029716 | CAAAACAAAGCACAC[-/A]ACTGCCGAAGATCAT | 6596 |
| rs796690144 | in-del | -/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149068162 | ACAATTTCTTGGTAG[-/T]TTTTTTTTAATGATG | 6596 |
| rs796792554 | snp | A/G | | | intron-variant | HLTF | GRCh38.p7 | 3:149033751 | CAAATCATAAAACAA[A/G]AAATAAAATCTTCCA | 6596 |
| rs796844154 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149033755 | TCATAAAACAAAAAA[C/T]AAAATCTTCCAAAAG | 6596 |
| rs796898811 | snp | C/T | | | intron-variant | HLTF | GRCh38.p7 | 3:149072217 | AAGAATTTTAAGTCC[C/T]GAGTTTCAGTCACAG | 6596 |