SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3701869 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125118633 | AGGAGTAATTGTGGT[A/G]TACAAACTTACATAT | 107932 |
rs3714944 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125114694 | TGTTTATTAATCTTA[C/T]TAGTTCTCCATAAAA | 107932 |
rs3715011 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125114728 | AATTTTTTTTAAAGA[C/T]TTATTTATTATATAT | 107932 |
rs3716297 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Chd4 | Mm_Celera | 6:125114931 | AAACGTAGACGAAAC[A/T]ATACATTAAATAACT | 107932 |
rs6270784 | snp | G/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097337 | CCAGTGAGGCTGCGT[G/T]CGCGCGCTGCTTGTC | 107932 |
rs13463119 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130499 | ttttttttttttttt[C/T]tCAACTTTATTTAGC | 107932 |
rs13463120 | snp | A/G | 0.475309 | 0.108333 | synonymous-codon | Chd4 | Mm_Celera | 6:125113968 | GTTTGTGACCCGTGC[A/G]TCAGTGGAGGAGCGC | 107932 |
rs13463121 | snp | A/T | 0.444444 | 0.157135 | missense | Chd4 | Mm_Celera | 6:125122006 | AAGGAAGTTAAATCT[A/T]CAGCCCCTGAGGCGA | 107932 |
rs13463122 | snp | A/G | 0.5 | 0 | synonymous-codon | Chd4 | Mm_Celera | 6:125110118 | CCTGAAAGAGGGAGG[A/G]CATCGTGTGCTCATC | 107932 |
rs13463123 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Chd4 | Mm_Celera | 6:125113986 | AGTGGAGGAGCGCAT[C/T]ACGCAGGTGGCAAAG | 107932 |
rs29825573 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Chd4 | Mm_Celera | 6:125104795 | CCATAGACACTGATA[C/T]TCATATTCTTTCAGG | 107932 |
rs29833908 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125102771 | TGGGGTGGGGTAACC[C/T]GAGTCTCTGGTTTTA | 107932 |
rs29869109 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Chd4 | Mm_Celera | 6:125121691 | CTGCTGGTACGTCTG[C/T]TGTCATGTCATTTCT | 107932 |
rs29874475 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101292 | GTTCTCAGAGGAGGA[C/T]TACCGGACCCTCACC | 107932 |
rs29914292 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125108516 | GAGGAGACTGTTGAG[C/T]GAGTCACTGCTGTTG | 107932 |
rs29920912 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Chd4 | Mm_Celera | 6:125121496 | GAAGGGAGTCTTGAA[C/T]TTGCTGTTCATTGCT | 107932 |
rs29923991 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Chd4 | Mm_Celera | 6:125106883 | AATGGTGCTCTGTGT[C/T]AGGTCTACCTGAAGC | 107932 |
rs29924516 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125117611 | CCCCACTCCCACCCC[C/T]GGCTTCTTGGGGGCT | 107932 |
rs29967617 | snp | A/G/T | 0.345679 | 0.230967 | intron-variant | Chd4 | GRCm38.p3 | 6:125103314 | CTAGGGCCTGCTGAC[A/G/T]GCATTAGGTTGCTTA | 107932 |
rs29972284 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125107861 | ATAAGTATGGTTGTG[C/T]ACCACCTGTGTGCAG | 107932 |
rs29974106 | snp | C/G | 0.455 | 0.143091 | intron-variant | Chd4 | Mm_Celera | 6:125113052 | GCTAGATAAAAAGCT[C/G]CTTAGCTGACATTTC | 107932 |
rs29984267 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Chd4 | Mm_Celera | 6:125109665 | CGTGGTCGCTGCTTG[A/T]TAGCTTAGCTCCACA | 107932 |
rs30020848 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125100727 | CTCAGGACTGTCCTG[A/G]GTGAGCATGTGTGTA | 107932 |
rs30031775 | snp | A/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125110244 | TAATTAAATTGTTCC[A/G]TTTTACAGATGACCA | 107932 |
rs30072370 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099676 | TACAAAGAAAGCTGC[C/T]TCCCAGCCTTCTCCC | 107932 |
rs30133357 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096209 | GCGGCGAGGAGGAGC[C/T]GGAGCGGGAGTGACA | 107932 |
rs30173456 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130746 | TTTAGCAAACTGTTC[G/T]CAGAGCACTCCTGCA | 107932 |
rs30213549 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Chd4 | Mm_Celera | 6:125104852 | AATTGAGATTAAGTG[A/G]TGTCTTTTTAACAGT | 107932 |
rs30219394 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Chd4 | Mm_Celera | 6:125112587 | AGTTCCTGCGTCTGG[A/G]CGTCACAGTGGAAGA | 107932 |
rs30220306 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Chd4 | Mm_Celera | 6:125109655 | ATGAGGATGGCGTGG[C/T]CGCTGCTTGTTAGCT | 107932 |
rs30220337 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125125677 | AATCTTAGTATTTGC[A/G]TAGTGGAAGCAGGAG | 107932 |
rs30236935 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125119395 | GGGATTAAAGGCGTG[C/T]GCCACCACTGCCGGG | 107932 |
rs30264149 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Chd4 | Mm_Celera | 6:125127203 | GACCAGGCTGGCCTA[A/G]AACTCAGAAATTGCC | 107932 |
rs30264203 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Chd4 | Mm_Celera | 6:125121076 | GGTGTTGCTAGCTGC[G/T]GTTGGCAGGTGATGC | 107932 |
rs30264573 | snp | A/G | 0.33241 | 0.236027 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101055 | TTTCTCCCAGATACC[A/G]CCCTGCCCTGTAGCA | 107932 |
rs30278026 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Chd4 | Mm_Celera | 6:125117501 | GGCTCAAAGCTAGAG[C/T]GCGTCCCATTGGGCC | 107932 |
rs30279940 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Chd4 | Mm_Celera | 6:125109757 | CCTCAGTCCAACCGG[A/T]CCTTGTGTCTTGTTC | 107932 |
rs30314437 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125104144 | TGCCTTTCTAGCGCT[A/G]GCATCAAAAACTTGG | 107932 |
rs30317234 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Chd4 | Mm_Celera | 6:125118314 | CTGTTATGGAGTTAC[A/G]TAATAAGTGGTTTGG | 107932 |
rs30364078 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099625 | GGTGGCTTGGGAAGA[A/G]GGAGAAGGGAACTGG | 107932 |
rs30365166 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Chd4 | Mm_Celera | 6:125126875 | GCCTCTAGCTTGCAG[C/T]TCTCTTTCTTGCCTC | 107932 |
rs30371834 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Chd4 | Mm_Celera | 6:125117527 | GGGCCCGCAGCTGGA[G/T]TGCCCAGGTCACACT | 107932 |
rs30379346 | snp | A/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125112480 | CTCTGACTCTACACG[A/T]ATGTACACACACTTG | 107932 |
rs30407438 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125127321 | TAAAGAAACCCAGAT[A/G]ACCTGATTGATTCCA | 107932 |
rs30414412 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Chd4 | Mm_Celera | 6:125118957 | ACAGCAGTTTTACTC[A/T]GTCATGGTGGGCTTG | 107932 |
rs30420870 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Chd4 | Mm_Celera | 6:125127357 | CAGGTGACTATGCCA[C/T]TATTAAGAAAAAGCT | 107932 |
rs30446800 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125112392 | GGGGCCAGCAGGTGA[A/G]GGTACTTGTCACCCA | 107932 |
rs30456980 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Chd4 | Mm_Celera | 6:125121444 | GCCTGTTTTCATTTT[G/T]AAAGTTGAGAAACTG | 107932 |
rs30463814 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Chd4 | Mm_Celera | 6:125125388 | GTGAGAAAGGTGCTC[A/G]TGTGAGCAGAGAAGC | 107932 |
rs30466515 | snp | C/T | 0.432133 | 0.171253 | synonymous-codon | Chd4 | Mm_Celera | 6:125109454 | GCGCGTGGAGTTGAG[C/T]CCTATGCAGAAGTGA | 107932 |
rs30508241 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125123113 | TGTGTGTGTGTATGT[A/G]TGTGTGTGTGTGTGT | 107932 |
rs30508261 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125110903 | CAGATGGGGAAGTCA[C/T]GGGAAAGCGTACATG | 107932 |
rs30509590 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125102707 | AAACGGGAGCTTTGG[A/G]AAATGTATGTGTAAA | 107932 |
rs30561110 | snp | C/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125110598 | TGCCTAGGTACTCTG[C/G]GACTGGAGTGACAGA | 107932 |
rs30561144 | snp | G/T | 0.493827 | 0.0552116 | synonymous-codon | Chd4 | Mm_Celera | 6:125109803 | CAAGTATATTCTCAC[G/T]CGGAATTTCGAAGCA | 107932 |
rs30565299 | snp | A/G | 0.375 | 0.216506 | intron-variant | Chd4 | Mm_Celera | 6:125108813 | TGAGGTGTGGGAGGA[A/G]ACGGCCTCCAGTTCT | 107932 |
rs30618367 | snp | A/C | 0.5 | 0 | missense | Chd4 | Mm_Celera | 6:125122141 | GCACAGCCCCCTGCC[A/C]CTGCCCCTGCCACTG | 107932 |
rs30661215 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125102755 | CTGACGTGGGGTGGG[A/G]TGGGGTGGGGTAACC | 107932 |
rs30666174 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Chd4 | Mm_Celera | 6:125111795 | TAAAATATATTTAGA[C/T]TTTAAAGGTGTGAAC | 107932 |
rs30668821 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125120806 | TTTGGTGAGGAGAGA[C/T]TTGCTTCCTCTCACA | 107932 |
rs30705315 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099979 | GTGGTTCTGAGCAGT[A/G]ATAGTCCCAAAGGGG | 107932 |
rs30711271 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Chd4 | Mm_Celera | 6:125120586 | ATCTTGCGAGTTGTG[C/T]AGCTGTTGGCATTGT | 107932 |
rs30716592 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101295 | CTCAGAGGAGGACTA[C/T]CGGACCCTCACCAAC | 107932 |
rs30754853 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Chd4 | GRCm38.p3 | 6:125126728 | GTGTGTGTGTGTGTG[A/T]GAGAACCTGTGCTCT | 107932 |
rs30763676 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098556 | ATGCTGTCTGACCAG[C/T]GTTGCTTCCCATCTT | 107932 |
rs30799485 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125109932 | ATGGTATGTGCACCT[C/T]CTTGTCTTCTGTGCC | 107932 |
rs30799569 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Chd4 | Mm_Celera | 6:125119586 | TTCTGAATTGTCAAT[G/T]CGAAAAACTGTAACT | 107932 |
rs30804263 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125112401 | AGGTGAAGGTACTTG[C/T]CACCCAGCAGTTTAT | 107932 |
rs30806225 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Chd4 | Mm_Celera | 6:125121089 | GCGGTTGGCAGGTGA[C/T]GCTGTTGTTCCCGAG | 107932 |
rs30841830 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125120818 | AGACTTGCTTCCTCT[C/T]ACAGAGGTTTTTTTT | 107932 |
rs30847307 | snp | A/G | 0.290657 | 0.246672 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101328 | CAAGGCCTTCAGCCA[A/G]TTTGTTAGGTAAGTC | 107932 |
rs30851837 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125104319 | GCTGTTATAGGAAGA[C/T]GTACCTGAAAAGAAA | 107932 |
rs30863919 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Chd4 | Mm_Celera | 6:125117413 | CAACCGGGCCATGTC[C/T]CCAGCCCCTGTAAGT | 107932 |
rs30900563 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125120800 | TTGGTCTTTGGTGAG[A/G]AGAGACTTGCTTCCT | 107932 |
rs30900624 | snp | C/T | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125112456 | GAGAACCAGTTCCTG[C/T]GAGAAGTCCTCTGAC | 107932 |
rs30908637 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Chd4 | Mm_Celera | 6:125104752 | TGACCTTTGAGTTCA[C/T]GCTCATGCTTGTGCG | 107932 |
rs30934954 | snp | C/G | 0.345679 | 0.230967 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101561 | CTTCAAGGGCAGCTC[C/G]GGAGCATCAGTGGCA | 107932 |
rs30948316 | snp | A/G | 0.375 | 0.216506 | intron-variant | Chd4 | Mm_Celera | 6:125113188 | CTGTACGTGATGTTG[A/G]TATTTGTCCTTTCTA | 107932 |
rs30949066 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Chd4 | Mm_Celera | 6:125107145 | TGATGTCTGTCTGTC[C/G]GTTAGGGCCTGGTGG | 107932 |
rs30952151 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Chd4 | Mm_Celera | 6:125127885 | CTTCGCAGGAATGAT[C/T]ATCTGTGGCGTTATG | 107932 |
rs30962354 | snp | A/G | 0.5 | 0 | intron-variant | Chd4 | Mm_Celera | 6:125127269 | GTGCCACAACTGCCC[A/G]ACAGCGTTGGGTTTT | 107932 |
rs45697545 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125118888 | AGGCTTGTAGTGAGC[A/G]CCTTTACTCTGTGAG | 107932 |
rs45714474 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101160 | GTTTGACTTCCCAGT[C/T]GGTTGTCTTAGCCAG | 107932 |
rs45750912 | snp | A/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125128734 | TGGAGGAAGAGATGA[A/G]TCTGTCAGTGAGAAC | 107932 |
rs45761131 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125118462 | GTAGTCTGGACTGCT[C/T]TTTATTGACGTCCTG | 107932 |
rs45807917 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125121913 | GGGCCTTCCTGATTG[C/G]TTGTCTTTTGGTCTG | 107932 |
rs45808661 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125123711 | ACAGATGTGCCCTCA[G/T]TTGGCTCTGAAGGTC | 107932 |
rs45831706 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117453 | GGCTGGCCTTTAACT[A/T]TTTTTTGATTCTCTT | 107932 |
rs46043935 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094169 | GGTGATGATGGGGAT[A/G]GGAGGGAAGGGACAG | 107932 |
rs46059651 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125118003 | CGTGCACACTTCAGC[A/T]CTGGAACTTCTTCCC | 107932 |
rs46063157 | snp | A/G | 0.21875 | 0.248039 | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094511 | GTTTCTTGAAGGAAG[A/G]CACCTGTGTGTTGGT | 107932 |
rs46074641 | snp | C/T | 0.408163 | 0.193609 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098033 | GCTCCCTGGACTGGC[C/T]AAACCCGTATTATTA | 107932 |
rs46097974 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125113203 | ATATTTGTCCTTTCT[A/G]GTGATTATTGGTCAC | 107932 |
rs46169042 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Chd4 | Mm_Celera | 6:125123380 | AGAGCGGGCAGCCAC[A/C]GTCACTAAGAAGACT | 107932 |
rs46196659 | snp | C/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125106942 | ATCCTAGGCCGCATC[C/G]TGCAGTGAGCAGTGA | 107932 |
rs46236331 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Chd4 | Mm_Celera | 6:125106753 | TGAGTATGGGTGGAA[C/G]AGGAAGGGTGTGTTT | 107932 |
rs46247978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125116526 | GCATCCGTCCTGTCC[C/T]GATTACTGCCTGAGT | 107932 |
rs46283882 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125113114 | AGTTTCTAGCCAGTT[A/G]TTCCAAGTAGTGTCT | 107932 |
rs46309172 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125122781 | GGGCCCACTGGTTTC[A/G]GATCGCAGCTGACGT | 107932 |
rs46313628 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125128419 | TACATAAAATACAGT[A/G]TTAAAAATGTGGACT | 107932 |
rs46359164 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124264 | TGGGAAACTGTAGGT[G/T]GGGTGTTTAGGGGAG | 107932 |
rs46391545 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125129172 | TGAACTCTTAAGTCT[A/T]TTGAGATTTTGAGCA | 107932 |
rs46470935 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125110789 | CCCCTCCCCAGTCCC[A/G]GTCATTTTCTTCTAT | 107932 |
rs46487848 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chd4 | Mm_Celera | 6:125125387 | GGTGAGAAAGGTGCT[C/T]ATGTGAGCAGAGAAG | 107932 |
rs46503625 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Chd4 | Mm_Celera | 6:125110022 | CCAGGAAGCCCCTAA[A/G]ATGCCTAATGGTATG | 107932 |
rs46508161 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125118867 | TTTTGCTCCCTCTTG[G/T]GTATAAGGCTTGTAG | 107932 |
rs46599147 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Chd4 | Mm_Celera | 6:125119422 | CGGGCATAAAGTTGA[C/T]CTAGAAGTGGCTCTA | 107932 |
rs46616564 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125127907 | GGCGTTATGTACTTA[C/G]AGCTGTGAGTCTGAG | 107932 |
rs46647791 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125128213 | GCATCAAATGCAGGT[C/G]CTTAGGCTTTGCTGC | 107932 |
rs46655179 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125124007 | TCATACCTTTGCTTC[C/G]AAGTGACTTAGCTAA | 107932 |
rs46719103 | snp | A/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094414 | CACTGAGTAGCAGAG[A/T]ATGGCCTTGATCCCT | 107932 |
rs46719467 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125119767 | TAAATACCGTGTATG[C/T]GTGTATCTGTGTAAC | 107932 |
rs46793161 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125112519 | CAAGATAAATAAGAA[A/G]GCCAGTGAGATGTTT | 107932 |
rs46798563 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099319 | TTTCTTGTCTGGGAC[A/G]TGAGGGTGACCTCTT | 107932 |
rs46833610 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125116466 | GGAGAGTAGTTGCTG[A/G]GCACAGCCCATGCCA | 107932 |
rs46882202 | snp | A/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125100731 | GGACTGTCCTGGGTG[A/T]GCATGTGTGTAGCAT | 107932 |
rs46894475 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Chd4 | Mm_Celera | 6:125123398 | CACTAAGAAGACTTA[C/T]GAGATCTGGCACCGT | 107932 |
rs46964447 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Chd4 | Mm_Celera | 6:125124193 | TTGAATTTATGAGCT[A/G]TTCAGGAGTTGTGGC | 107932 |
rs47082993 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125126433 | GAAAGAACCTTTAAA[C/T]GATGGGTACTTTGTA | 107932 |
rs47196948 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125122629 | TCATTATCTATTACT[A/G]TAGACATTTTATTCC | 107932 |
rs47219522 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125114200 | ACTCTGGGAAGAAAG[A/G]ACCTTTGATAGCAAG | 107932 |
rs47235666 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Chd4 | Mm_Celera | 6:125103078 | TGGGAGCAGTGTCCT[A/C]ACAGCCCAAGGGTTT | 107932 |
rs47237834 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Chd4 | Mm_Celera | 6:125113361 | TGCAGTATCTATCAG[A/G]GCACCGTGCTGACAA | 107932 |
rs47299998 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098851 | AAGGCTTTGGTGGGT[A/G]CTGTAAGGGCTGTGG | 107932 |
rs47346431 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125113333 | TCTTTTTGTTCATAA[A/G]CTTGGATGTTGATGC | 107932 |
rs47355350 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123899 | GAAGGTTGTGAGCTA[C/T]CCTGTGTATGCTGGT | 107932 |
rs47380233 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098427 | TGAGATAAGGGACTT[A/G]GATCTGTGTCTGATC | 107932 |
rs47403044 | snp | G/T | 0.277778 | 0.248452 | missense, downstream-variant-500B, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097229 | GAGGAGGATATGGAC[G/T]CACTTCTGAACAACA | 107932 |
rs47431622 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125104822 | CAGGGTTTGATGCAT[C/T]TCCCTGTGGTACTGA | 107932 |
rs47457589 | snp | C/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100164 | TGGAGTTAGCTCTTT[C/G]ACTTACTAAGTTCCA | 107932 |
rs47464903 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125111287 | TCGTCTGTTGTTCTT[C/T]AGGGTCTCGGTTGCT | 107932 |
rs47535972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125122669 | GACTGTTTCCAAATG[C/T]AGTTGTTAGGGAGCT | 107932 |
rs47542126 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125109976 | CCTCCTTGTGGGTGT[A/T]CCTTAAATATATCTT | 107932 |
rs47587897 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097824 | TTTTTGAGTGGAGAA[A/G]GATGGAGGGCTAGGA | 107932 |
rs47607084 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125109559 | CCAGGCATCTGGTGA[C/T]GGAAGCAAGCGGGGC | 107932 |
rs47624572 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102222 | CAGTATCAACAGCTA[C/T]TCTGTTTCGGATGGT | 107932 |
rs47675629 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125125866 | AGGCCCGTTCTCAGC[G/T]GTCTAGGGAAGAAAA | 107932 |
rs47736333 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Chd4 | Mm_Celera | 6:125123281 | TTTTTTAATTTATAT[C/T]CTCCCAGATTATTTG | 107932 |
rs47770310 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Chd4 | Mm_Celera | 6:125121978 | TAAAGAAGAAGAGAG[C/T]ACAGAAGGAGAGAAG | 107932 |
rs47854801 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105828 | GGCCACGTCTGCTCC[C/T]GGGCTCACTCACTCC | 107932 |
rs47864679 | snp | A/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125106849 | TGAGATGGTCAGAAA[A/G]CAAACGCTGGGTGTT | 107932 |
rs47865568 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Chd4 | Mm_Celera | 6:125125546 | TCTCTTGAGAAAGTG[C/T]TTTTAAAAACAGCAG | 107932 |
rs47893334 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125109952 | TCTTCTGTGCCTTGC[C/T]GAGTCAGTCCTCCTT | 107932 |
rs47910109 | snp | G/T | 0.336735 | 0.234472 | synonymous-codon | Chd4 | Mm_Celera | 6:125102583 | CATGGAGAAGGCCCC[G/T]GAGGGCAAGTGGAGC | 107932 |
rs47917508 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Chd4 | Mm_Celera | 6:125109779 | GTCTTGTTCATGTAG[A/G]AAGTACTACAAGTAT | 107932 |
rs47942875 | snp | A/C/T | 0.32 | 0.24 | synonymous-codon | Chd4 | GRCm38.p3 | 6:125102948 | CCTGTGCTGTGACAC[A/C/T]TGCCCTTCTTCCTAC | 107932 |
rs47965653 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125112670 | CGCTGACACATAAGT[C/G]TACTCAAAGTCAAAG | 107932 |
rs48098713 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Chd4 | Mm_Celera | 6:125113667 | CTGTCATGTGAAACG[G/T]AGGTGTGAAACAACA | 107932 |
rs48131136 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125121101 | TGACGCTGTTGTTCC[C/T]GAGAGCTGTGTGCCT | 107932 |
rs48151364 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Chd4 | Mm_Celera | 6:125116357 | GGAGGATTTTATATA[A/C]TTTGGTAGTACATTC | 107932 |
rs48301885 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125115281 | CCTGCATCAGTTGCT[A/G]GGATTATAGGCCTGG | 107932 |
rs48317351 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Chd4 | Mm_Celera | 6:125104962 | GCCTCCAGATGCTGA[C/T]CCTAATACCCCGTCG | 107932 |
rs48334656 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106277 | TGGACCTTTGGAAGA[A/G]CAGTCGGGTACTCTT | 107932 |
rs48620540 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Chd4 | Mm_Celera | 6:125107144 | CTGATGTCTGTCTGT[C/T]CGTTAGGGCCTGGTG | 107932 |
rs48640109 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125122073 | CCGTTGGCAGATGGC[A/T]CTGAGATGCCTGCGC | 107932 |
rs48685347 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100018 | GGGTGTTTGTTGTGT[C/T]GTAGGCCCTGAGCCT | 107932 |
rs48724285 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125112589 | TTCCTGCGTCTGGAC[A/G]TCACAGTGGAAGAAG | 107932 |
rs48740260 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125125617 | GAATTTGGTGCAGGT[A/T]TGTAAGAACAGGGCC | 107932 |
rs48772644 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Chd4 | Mm_Celera | 6:125118095 | GAGCTGTACTGAAAC[A/G]TGGTTCAAAACTCAA | 107932 |
rs48799142 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125105967 | AAAGGGACGTTGCCA[A/T]CGACTTACGTTCAAG | 107932 |
rs48809012 | snp | A/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125106982 | CACTCCCTCTGCCAA[A/G]TGTATTGAGGGTCAC | 107932 |
rs48860534 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Chd4 | GRCm38.p3 | 6:125105364 | GTGGATGATGATCCA[C/T]CGCATCCTCAACCAC | 107932 |
rs48921055 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125109522 | ACACCGGCCGTGCTG[C/T]CAGCAGCTTCTTCCA | 107932 |
rs48980619 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125124366 | CGTATGAATAAAAAA[C/T]GGGAAGGCTGGGTGC | 107932 |
rs49037338 | snp | G/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125106336 | TTTGTCGGTTTTTAA[G/T]AGCAAGGCTGACTAG | 107932 |
rs49075703 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102134 | CCTTGGCCTGGACTT[G/T]TAACTTTGTTTTCTG | 107932 |
rs49092003 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125113367 | ATCTATCAGAGCACC[A/G]TGCTGACAATTGCTT | 107932 |
rs49114731 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125103232 | GCAGGTTGGAGCACC[A/G]TTCCAGCTTAGAGTA | 107932 |
rs49127058 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Chd4 | Mm_Celera | 6:125116490 | CATGCCAGGGAGAAA[C/T]CCATGCTAGTGACTG | 107932 |
rs49154736 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117096 | TTTCGAGACAGGGTT[C/T]CTCTGTGTAGCCCTG | 107932 |
rs49175455 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125113069 | TTAGCTGACATTTCA[C/T]CCCTGTCCTTGCATG | 107932 |
rs49187434 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Chd4 | GRCm38.p3 | 6:125105764 | CTGGGCTCACTCACT[A/C]CCTGTTAGGTACCAC | 107932 |
rs49262364 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094349 | AATAAATAAATAAAT[C/T]ATAATTATCCGAGAC | 107932 |
rs49271208 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100412 | CCATCTGCATTGGGC[C/T]CTCACCTGTGCTGTT | 107932 |
rs49273465 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125119987 | TATGTCTCGTCGTAA[C/T]AGTTTCTTTTACTCA | 107932 |
rs49277218 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125124502 | ATCAAGTAGGAAACC[A/G]TGGAAATAGATGCAG | 107932 |
rs49319028 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Chd4 | GRCm38.p3 | 6:125122059 | GACTGAGTGCCATGC[C/G/T]GTTGGCAGATGGCTC | 107932 |
rs49428619 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Chd4 | Mm_Celera | 6:125109197 | GCCTGTCAGTCAGTC[A/G]GTCCCTAGCTCTACT | 107932 |
rs49472323 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Chd4 | Mm_Celera | 6:125117504 | TCAAAGCTAGAGCGC[A/G]TCCCATTGGGCCCGC | 107932 |
rs49534268 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125121480 | CAAGTAACTGTAGCT[A/G]GAAGGGAGTCTTGAA | 107932 |
rs49559507 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112963 | TCGCCAGTTTTTCTC[C/T]TACTCTCCTTTCCTG | 107932 |
rs49590463 | snp | C/G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | GRCm38.p3 | 6:125095249 | TGAAATTATGGGATG[C/G/T]GAGAGTAGATAGAGT | 107932 |
rs49663033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125113604 | GGTGAGTAGAGTATT[C/T]GCTTTGGGAGGTCCT | 107932 |
rs49686157 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102096 | CAGACAGGTGTGACT[A/C]GGCTCCTTCTGGGCA | 107932 |
rs49709460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125107381 | AATATCTAGTGAGGA[C/T]TTGTGTAGGAGGAAG | 107932 |
rs49796324 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125123322 | CACTTTCTAACCTTC[C/T]GCTAAATTCCTCCTC | 107932 |
rs49903475 | snp | C/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125120103 | CAAGTGTTTACAAAT[C/G]GAGCCATGCAAAGGA | 107932 |
rs49969599 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125109600 | CTGATACCTGGGAGG[A/C]GGAGCTTGTAGTTCT | 107932 |
rs50027779 | snp | G/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094534 | GTGTTGGTATCCTCG[G/T]TCTCGGTCGGTAAGT | 107932 |
rs50044153 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098259 | GGTTACTACCCTGTG[A/G]AGCCTGGCTGTCCTG | 107932 |
rs50099667 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113307 | GAGGGAGAAGCTTGA[C/T]TATGCTAATGTCTTT | 107932 |
rs50102190 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Chd4 | Mm_Celera | 6:125129380 | GGAGCACTTGGAGGC[A/C/G]GGAGCACGATGAGAT | 107932 |
rs50116661 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125118074 | TTCACCAAAGACTGG[C/T]TATCCGAGCTGTACT | 107932 |
rs50136944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125125843 | ACTGACTACAAGCCA[A/G]TGAAAACAGGCCCGT | 107932 |
rs50150278 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Chd4 | Mm_Celera | 6:125102691 | GTCTGGGTGGAAATA[A/C]AAACGGGAGCTTTGG | 107932 |
rs50165259 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Chd4 | Mm_Celera | 6:125103158 | TTTGCTTAGTCTTGG[A/G]ACATCATCTCCTGTG | 107932 |
rs50192716 | snp | A/G | 0.375 | 0.216506 | intron-variant | Chd4 | Mm_Celera | 6:125118040 | TCTGAACTCCGTGGA[A/G]CCTCGAAAGCTTTCA | 107932 |
rs50333861 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Chd4 | Mm_Celera | 6:125124201 | ATGAGCTGTTCAGGA[C/G]TTGTGGCTGTACATA | 107932 |
rs50362322 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Chd4 | Mm_Celera | 6:125106552 | ACAGGTCGGTGACTG[C/T]GAGCGAGCAAGGAAG | 107932 |
rs50398153 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Chd4 | Mm_Celera | 6:125118044 | AACTCCGTGGAGCCT[C/T]GAAAGCTTTCAGGTT | 107932 |
rs50401692 | snp | A/G | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125124473 | TACTGAGTATGCCCT[A/G]CAGGAAGGTATCAAT | 107932 |
rs50403871 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094878 | CTGGAGGGAGGTAAG[C/T]ATCTAGAACATACCT | 107932 |
rs50472370 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Chd4 | GRCm38.p3 | 6:125105135 | GCAGGAAGCTGGTTG[A/G]CTGCAGCTCCCGGAG | 107932 |
rs50499794 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125128714 | CTTTACAGATTCTTG[C/T]TAGCTGGAGGAAGAG | 107932 |
rs50547222 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125100487 | TGAGGAAGACCCAGA[C/T]GAGGATTTATCCGAA | 107932 |
rs50591942 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125121901 | GCCTCTGACCCAGGG[C/T]CTTCCTGATTGGTTG | 107932 |
rs50599547 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125118105 | GAAACGTGGTTCAAA[A/G]CTCAAGACACCTATT | 107932 |
rs50664026 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101745 | TGACAAGTCTGACAG[C/T]TAGGAATGCGGCATT | 107932 |
rs50714706 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Chd4 | Mm_Celera | 6:125111745 | TCATTTTTTTTGAGA[C/T]AAGTTCTCTGTGTGA | 107932 |
rs50771504 | snp | A/C | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101120 | TATTATTTCCTCTGT[A/C]CCTCGCTCGCTCTTG | 107932 |
rs50791903 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125122427 | GGAGCTGTGGAACTC[C/T]GTTGCAGCCGTGTGG | 107932 |
rs50812645 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125124307 | ATCCCTGAGGACGTA[C/G]GGCTGGGAATGGGCT | 107932 |
rs50865428 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099275 | AGTACTGCAGTCATT[C/T]CAATAGTTTACTCTG | 107932 |
rs50886603 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125105098 | CAGGCTGCACGTGTG[A/C]GGTGACGCCGCAGAG | 107932 |
rs50912285 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097710 | GGTTGCTTTCTGTCC[C/T]GATCTCTTACGGGTT | 107932 |
rs51034681 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098457 | CACTGAGGTGTAGGC[C/T]TGCGGAGCTCTGCCT | 107932 |
rs51155956 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125125753 | AACCCTTCCTAAAAG[C/G]CAAGGCTAAACCTGT | 107932 |
rs51158358 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Chd4 | Mm_Celera | 6:125104731 | GACCAGCCATCTCTT[C/T]AGAGTTGACCTTTGA | 107932 |
rs51210846 | snp | A/C/G | 0.260355 | 0.249785 | intron-variant | Chd4 | GRCm38.p3 | 6:125105530 | CTGGGCTCACTCACT[A/C/G]CCTGTTAGGTACCAC | 107932 |
rs51362186 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105630 | AGGTACCACGTCTGC[C/T]CCTGGGCTCACTCAC | 107932 |
rs51423607 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101141 | CTCGCTCTTGGAAGC[A/T]GCAGTTTGACTTCCC | 107932 |
rs51504856 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Chd4 | GRCm38.p3 | 6:125109933 | ATGGTATGTGCACCT[C/T]TTGTCTTCTGTGCCT | 107932 |
rs51526816 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Chd4 | Mm_Celera | 6:125117987 | CTTAATCGCTCCGTC[A/G]CGTGCACACTTCAGC | 107932 |
rs51596561 | snp | C/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098677 | ATGACCCAGTTTTTC[C/T]TCTGGCCACACCCAG | 107932 |
rs51666384 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125119007 | CACACATGGTCTCAT[A/G]TATTCTGAGATGGCC | 107932 |
rs51677281 | snp | C/G | 0.32 | 0.24 | synonymous-codon | Chd4 | Mm_Celera | 6:125107509 | GGAGTATCTGGATGC[C/G]ACGGGTGGAACCCTG | 107932 |
rs51678915 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Chd4 | Mm_Celera | 6:125104751 | TTGACCTTTGAGTTC[A/C]TGCTCATGCTTGTGC | 107932 |
rs51686397 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Chd4 | Mm_Celera | 6:125106508 | GGAGATTCAGGACTA[C/T]GACCTGTTCAAGCAG | 107932 |
rs51702382 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125117641 | TGAGATGATAGGCAT[A/G]TGGTGATCAATTTAC | 107932 |
rs51705330 | snp | G/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125106798 | ATGCTGCAGTCATGG[G/T]GAAGCTCCAAGTCAT | 107932 |
rs51819697 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125506 | GGGGTCTAAACCTCA[A/G]TATGTGTGCTTGGTA | 107932 |
rs51820274 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101091 | TCTCCATGTAGGTGT[A/G]CTCATTTCTTCTGTA | 107932 |
rs51885034 | snp | A/C | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101043 | TCCTCTCTGTCCTTT[A/C]TCCCAGATACCACCC | 107932 |
rs51980242 | snp | A/C | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B, nc-transcript-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097555 | GGGTTAGCTTTACCT[A/C]GTGCAGGTTCTTGGA | 107932 |
rs52040952 | snp | C/T | 0.32 | 0.24 | intron-variant | Chd4 | Mm_Celera | 6:125115195 | TTTCTTCAGAGAGCA[C/T]GGTTAGGTTATTCTT | 107932 |
rs52192954 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125123074 | GAGCTAGATCTGGAC[A/C]ATATTGAGATGGATT | 107932 |
rs52204846 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115768 | ATCTATCCTCTATCT[A/T]TCTATCTATCTATCT | 107932 |
rs52238096 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125127935 | GAGGCTTGGGCTGCA[C/T]GAGCCTGTGTAAGAG | 107932 |
rs52238964 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Chd4 | Mm_Celera | 6:125129403 | GATGAGATGTGCTCA[G/T]GCTTGGCTGCATAGG | 107932 |
rs52253056 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106170 | TATTATATGTAAGTA[C/T]ACTATAGCTGTCTTC | 107932 |
rs52275761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chd4 | Mm_Celera | 6:125127944 | GCTGCACGAGCCTGT[A/G]TAAGAGGTCAGAGGA | 107932 |
rs52303456 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106174 | ATATGTAAGTATACT[A/G]TAGCTGTCTTCAGAC | 107932 |
rs52350481 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115846 | ATCTATCTATCTATC[A/T]ATCATCTATCTATTT | 107932 |
rs52458356 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123096 | AGATGGATTGGCGGG[G/T]GTGTGTGTGTGTGTG | 107932 |
rs52537465 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116858 | GAGTACACTGTTGCT[A/G]TCTTCAGACACACCA | 107932 |
rs108115349 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115787 | TCTATCTATCTATCT[A/T]TCTATCTTTCTATCT | 107932 |
rs108119026 | snp | A/G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115795 | TCTATCTATCTATCT[A/G/T]TCTATCTATCTATCT | 107932 |
rs108449202 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115779 | ATCTATCCTCTATCT[A/T]TCTATCTATCTATCT | 107932 |
rs108693408 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125128577 | ACTCTGTCTCAAAAA[A/C]CAAAAAAAAAAAAAA | 107932 |
rs108857492 | snp | C/T | | | missense | Chd4 | Mm_Celera | 6:125122133 | TGCAGTGTGCACAGC[C/T]ccctgcccctgcccc | 107932 |
rs211759251 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125109741 | AGTCATTCAAAAGAC[-/T]CCTCAGTCCAACCGG | 107932 |
rs211777105 | in-del | -/CTTA | | | intron-variant | Chd4 | Mm_Celera | 6:125105932 | ACTACCTGTTAGGGC[-/CTTA]CTTACTGAAGGGCTC | 107932 |
rs211813627 | snp | A/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101364 | GAGCCTGTGCGGTGG[A/G]AAGGGAGGAGTCTTT | 107932 |
rs211820882 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111749 | TTTTTTTGAGACAAG[C/T]TCTCTGTGTGATCCT | 107932 |
rs211854006 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102429 | TCCCTCTTCCTTGCC[C/T]AGGCGAGGAGGAGGT | 107932 |
rs211995555 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118014 | CAGCTCTGGAACTTC[C/T]TCCCAGCAGGTCTGA | 107932 |
rs212006004 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127102 | AGTTCAAGGCCAGCG[A/T]TGGGTTTGTTTGTTG | 107932 |
rs212184451 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126262 | ACCCTGTCTAGAAAA[C/T]AGAAAAACAAACAAA | 107932 |
rs212276300 | in-del | -/CGCC | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130209 | GCAGCAGTAGCGCAG[-/CGCC]CGCCCGCCCGCCATG | 107932 |
rs212302033 | snp | A/C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125104567 | TGTGTGTGTGTGTGT[A/C/G]TGTGTCTGTGTCTGT | 107932 |
rs212320193 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099654 | GGGAGCTGGTGTACA[C/T]GGCTGGTACAAAGAA | 107932 |
rs212368322 | in-del | -/GGGA | | | intron-variant | Chd4 | Mm_Celera | 6:125129199 | GCATAGCTTTATGGG[-/GGGA]GGGGGGGTGAAATGA | 107932 |
rs212438567 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107940 | AGACTATAAGCCATC[A/G]TGTGGGTGCTGGGAT | 107932 |
rs212604328 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116814 | TTATAATCAACTTTT[A/T]AAGTATTATTTATTT | 107932 |
rs212906770 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096230 | GGGAGTGACACCGGC[A/G]AGACCCAGCGCGACC | 107932 |
rs212910410 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117414 | AACCGGGCCATGTCT[C/T]CAGCCCCTGTAAGTT | 107932 |
rs212988618 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125200 | GTATGAATCTTATTT[A/T]TACTTTTCTCATAGC | 107932 |
rs213036341 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125105931 | TTACTACCTGTTAGG[C/G]CCTTACTGAAGGGCT | 107932 |
rs213076287 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094965 | AAATGATGAGCTAGG[A/G]AGTCTGGGGGTCCTG | 107932 |
rs213153937 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114996 | TTTCCCTTTTATATA[G/T]CTCCTTGTTTTTTTT | 107932 |
rs213231923 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122733 | GAGTGTGGAGGCGGA[A/G]GTAGACAGAGAGAGC | 107932 |
rs213367660 | in-del | -/AAAAAG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128596 | AAAAAAAAAAAAAAA[-/AAAAAG]AGAGAGAGAGAGAGA | 107932 |
rs213379619 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130136 | GTAAAGGAACAGCCC[C/T]GCGCAGTGGGGCAGG | 107932 |
rs213442207 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115477 | ACAGGGTCTCATATG[C/T]TCCAGGATGGTCTTG | 107932 |
rs213600552 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112648 | CACTGGCATGCAAAC[C/T]CTGACACGCTGACAC | 107932 |
rs213672690 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122200 | TGACAAGGCTCCTGC[C/T]GAGCCTCCTGAGGGG | 107932 |
rs213765744 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112151 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCA | 107932 |
rs213824370 | in-del | -/TT | | | intron-variant | Chd4 | Mm_Celera | 6:125117703 | GTGGTGCCACATGCC[-/TT]ACATCCCAGCACTTG | 107932 |
rs213913296 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125120752 | GTACCGTATGATCCT[A/C]TAGTGGGAGAAAGGC | 107932 |
rs214016905 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112741 | GTCCCCAGCACCGCG[-/T]TAAGTGGTGATGCAA | 107932 |
rs214038962 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128696 | GTGGAGGGGCCGGCA[C/T]TTCTTTACAGATTCT | 107932 |
rs214122393 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116641 | CGATCTGCCAGCCTC[A/T]ACCTCTAAGAGTTGG | 107932 |
rs214324048 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117994 | GCTCCGTCGCGTGCA[C/T]ACTTCAGCTCTGGAA | 107932 |
rs214368942 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127899 | TTATCTGTGGCGTTA[C/T]GTACTTACAGCTGTG | 107932 |
rs214702522 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125125534 | GTACTGTGGACATCT[A/C]TTGAGAAAGTGTTTT | 107932 |
rs214754700 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125106658 | GTTAATGAGGGGTGA[A/G]GAAGGACGACCCGGC | 107932 |
rs214760886 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116733 | GGTGGTGTTGCTGAG[A/G]ATGGAACCTAGGGCC | 107932 |
rs214763966 | in-del | -/AT | | | intron-variant | Chd4 | Mm_Celera | 6:125110477 | GGCAGAGGCATGCAG[-/AT]ATCTCTGTGAGTTCA | 107932 |
rs214801325 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107085 | TCTTCCCTGGAGCTC[A/G]TGCCCACATTCGTGC | 107932 |
rs214841796 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129163 | ATTTTCTTTGAACTC[-/T]TTAAGTCTATTGAGA | 107932 |
rs214928358 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115675 | TTGATTAGCATGATT[A/G]CAGTGGCGCTATCTA | 107932 |
rs215041880 | in-del | -/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099002 | CTGGCTCCAGCATCA[-/T]TTTAGGGCTACTTCT | 107932 |
rs215110956 | in-del | -/C | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130744 | CTTTAGCAAACTGTT[-/C]CGCAGAGCACTCCTG | 107932 |
rs215125841 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126148 | AACAGTGGTGCAGAC[C/T]TTTAATCCCAGCACT | 107932 |
rs215311662 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119268 | TTTAAACATTTCTTA[-/T]TTTTTTTTGAGATAG | 107932 |
rs215337845 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113616 | ATTCGCTTTGGGAGG[C/T]CCTAGCACTTCATAG | 107932 |
rs215361614 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098676 | CATGACCCAGTTTTT[C/T]CTCTGGCCACACCCA | 107932 |
rs215425183 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123462 | AAGTATCCTTGCCTG[A/T]GTTGAGATTGGGGTC | 107932 |
rs215490810 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122058 | TGACTGAGTGCCATG[C/T]CGTTGGCAGATGGCT | 107932 |
rs215697259 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094833 | TCTAGTCAGCATATT[A/G]TTTGTTTGAGTTTAC | 107932 |
rs215776326 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105448 | GCTCCTGGGCTCACT[C/T]ACTACCTGTTAGGTA | 107932 |
rs215889933 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125119318 | GGCTGTCCTGGAACT[A/C]ACTCTGTAGACCAGG | 107932 |
rs215922717 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111864 | ACATGCCTGGGGGCA[C/T]AGGCATGTATTCTCA | 107932 |
rs216004585 | in-del | -/AGG | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097296 | GGGCCCAGGGCAGGA[-/AGG]AGATGTTTGATCTTT | 107932 |
rs216040519 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118496 | AGACATTTGTGGGGG[G/T]GGGGGGGTGGAGGGC | 107932 |
rs216102917 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127215 | CTAGAACTCAGAAAT[C/T]GCCTGCCTCTCCCTC | 107932 |
rs216181815 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129736 | TATCCTGTGTATGCC[A/G]GCGTGACAACCAGCC | 107932 |
rs216206267 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094110 | GAGAGAGAGAGAGAA[A/G]TAGAGGACTGGAGAG | 107932 |
rs216409545 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125104689 | GCTACAGTGTAGATA[C/T]CAGGAATGAGCTCTG | 107932 |
rs216475774 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117950 | CTGCTCATGGGGCAA[A/G]AGAAGAAGAGCAGAC | 107932 |
rs216510857 | in-del | -/TGTGTGGGA | | | intron-variant | Chd4 | Mm_Celera | 6:125108490 | ATGAAGGTATCTTAG[-/TGTGTGGGA]TGTGTGGGAGGAGGA | 107932 |
rs216559706 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125124460 | CCAGCAGCCTACTTA[A/C]TGAGTATGCCCTACA | 107932 |
rs216596044 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125385 | TCGGTGAGAAAGGTG[C/T]TCATGTGAGCAGAGA | 107932 |
rs216605459 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128762 | AACGTGGCCATCAGT[C/T]CAACCCCTGTCTTCT | 107932 |
rs216632143 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111058 | GTCTGGGTGTTTTGC[C/T]TGCATGTGTGTCTGT | 107932 |
rs216705010 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125105904 | GGGGCCACGTCTGCT[-/C]CCTGGGCTCACTTAC | 107932 |
rs216821307 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096588 | TGGGTGCTCGCTTTC[C/T]TCCGGCGTCCCGACT | 107932 |
rs216850473 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127862 | AAAATTAACAAAATA[C/T]TAACATGCTTCGCAG | 107932 |
rs216856538 | snp | G/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097631 | GTGGGGATTTCTGTT[G/T]CGGGAGCCCTGCCAG | 107932 |
rs217121815 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122809 | CGTTTGCTTTGGTGT[A/T]TCCTGTAGAAGAGAA | 107932 |
rs217198524 | snp | C/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094733 | GAATGTTGAGAAATA[C/G]TTTTGGGATGGGGGT | 107932 |
rs217594238 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099207 | GTTTGGTAACCTCCA[C/T]TGAGCCCTTGTTAAG | 107932 |
rs217682413 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127936 | AGGCTTGGGCTGCAC[A/G]AGCCTGTGTAAGAGG | 107932 |
rs217689008 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108034 | TACAGGATCAGAGCC[C/G]TGGTAGACTCAGTGC | 107932 |
rs217709748 | in-del | -/GTTAC | | | intron-variant | Chd4 | Mm_Celera | 6:125126952 | AGATATAGCTCAGTT[-/GTTAC]AGAGCTTAGCTAGAA | 107932 |
rs217786137 | in-del | -/TGTC | | | intron-variant | Chd4 | Mm_Celera | 6:125104576 | GTGTGTCTGTGTCTG[-/TGTC]TGTGTCTGTGTGTGT | 107932 |
rs217820066 | in-del | -/TC | | | intron-variant | Chd4 | Mm_Celera | 6:125127021 | GGTGCCTGCCTGTAA[-/TC]TCAGCACATAGGATC | 107932 |
rs217859087 | in-del | -/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099596 | CTTCCCTACTCCCCC[-/T]CTTCTTGAGCGGGGG | 107932 |
rs217877319 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126609 | GACAATAGCCTTCAA[A/G]AACATAGTATTGCCT | 107932 |
rs217942040 | in-del | -/AG | | | intron-variant | Chd4 | Mm_Celera | 6:125129616 | GCAGGACCTGAGCTC[-/AG]AAGTCTCAGGCCATC | 107932 |
rs218019734 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125670 | TTCCTGAAATCTTAG[C/T]ATTTGCGTAGTGGAA | 107932 |
rs218070200 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124703 | ACTAAATGTCCCGGG[A/G]AAGTTGTTCAGGGCC | 107932 |
rs218081192 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100408 | TGAACCATCTGCATT[C/G]GGCCCTCACCTGTGC | 107932 |
rs218268652 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098085 | TGCCCTCAAGTGATG[A/G]CTGATGTCATGCTTG | 107932 |
rs218296707 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107053 | GATGACCTTTCCCCT[C/T]CCCTCAGCCGCCCCA | 107932 |
rs218415397 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096864 | GCCAGGCTAGCTTCT[C/T]CCTTCCCCTCCATGC | 107932 |
rs218495533 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106624 | AGAGGCAGCTGTGGT[A/G]TGTTTTCTTTCCTAG | 107932 |
rs218529445 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115089 | GTAATTTCAAAGCAT[C/T]GCTTTCTTTGCTGGT | 107932 |
rs218584213 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115590 | TTACCTGAGATAGCG[C/T]CCGACGCTGCATGCA | 107932 |
rs218945963 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130946 | GTATAAATTTTTTGA[A/G]GGTCTAAGTAACTAC | 107932 |
rs219123262 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104458 | AACAGACGCTCACTA[A/G]ACCTAGAGCTCGGGC | 107932 |
rs219142573 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125104773 | TGCTTGTGCGACCGT[G/T]CTCTGCCCATAGACA | 107932 |
rs219199688 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103815 | CCTCCAGAGCACTGA[A/G]ATTAAAGGTGTGCAT | 107932 |
rs219203742 | in-del | -/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103904 | CGAAAAAAAAAAAAA[-/C]AACAAAAAACAAAAA | 107932 |
rs219240508 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103323 | GCTGACAGCATTAGG[C/T]TGCTTAAGAGAAGGA | 107932 |
rs219304521 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125112710 | TGGTGAGGAGTGCTT[A/C]CCTAACATTTCGTGA | 107932 |
rs219332318 | in-del | -/GTGGCA | | | intron-variant | Chd4 | Mm_Celera | 6:125117683 | GCTGAGCCCATCATT[-/GTGGCA]GTGGTGCCACATGCC | 107932 |
rs219343059 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125102714 | AGCTTTGGGAAATGT[A/G]TGTGTAAAGGAATGG | 107932 |
rs219369898 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125113447 | AGGAGAGAACTCATG[A/G]TGTTTTTTGTTTCTT | 107932 |
rs219477905 | snp | C/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101742 | GCTTGACAAGTCTGA[C/G]AGCTAGGAATGCGGC | 107932 |
rs219488077 | in-del | -/TTGTTGTTG | | | intron-variant | Chd4 | Mm_Celera | 6:125119783 | TGTATCTGTGTAACT[-/TTGTTGTTG]TTGTTGTTGTTGTTG | 107932 |
rs219524829 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111133 | GGATCCACTGGAACT[A/G]GAGGTACAGCTGAGT | 107932 |
rs219690928 | in-del | -/CA | | | intron-variant | Chd4 | Mm_Celera | 6:125107078 | CCCCATTCTTCCCTG[-/CA]GAGCTCGTGCCCACA | 107932 |
rs220044183 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125108198 | CAGCTTCACTGTGGG[G/T]TGGGGCAGGGGTGGG | 107932 |
rs220200382 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094028 | TCTTTCTCTCTTTCG[-/T]TTTTTCTAGTATGGA | 107932 |
rs220206394 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108091 | GTTGGTCTTGGAGGA[A/G]TTTGGTTTTTGTCAC | 107932 |
rs220231938 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125117013 | TTTTTAGTTTTTAAT[A/C]ATGTGTATTCATTAT | 107932 |
rs220266718 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107230 | AGTATTTCCTTCTGG[A/T]TCCAGGACTGGCCTT | 107932 |
rs220330529 | in-del | -/GTCG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125109197 | CCTGTCAGTCAGTCA[-/GTCG]GTCCCTAGCTCTACT | 107932 |
rs220381512 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116449 | TGTTTTTTAGATCTT[G/T]CGGAGAGTAGTTGCT | 107932 |
rs220497128 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117198 | GTGCTGGGACTAAAG[C/G]CGTGTGCCACCACTG | 107932 |
rs220503325 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106120 | GTCGGTTTTTTTTTT[G/T]TTTTTTTTTGTTTTT | 107932 |
rs220556995 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115237 | AAATCTTTCTATTTA[C/T]TTAGCATAGATCTTA | 107932 |
rs220729027 | in-del | -/TTTTTTTTTT | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116405 | TTTAGATCTTGCTTC[-/TTTTTTTTTT]TTTTTTTTTTAGATC | 107932 |
rs220758189 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116116 | GTCTGGAACTCACTA[C/T]ATTGTCAAGAATGAC | 107932 |
rs220957250 | in-del | -/TGTC | | | intron-variant | Chd4 | GRCm38.p3 | 6:125104564 | GTGTGTGTGTGTGTG[-/TGTC]TGTGTCTGTGTCTGT | 107932 |
rs221046209 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113688 | GAAACAACAGACTTC[-/T]TTTTTTTTGAGTGTC | 107932 |
rs221204225 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101776 | GCCCCTAAGTCTGTC[-/CCT]AATGGGCAGGAGTGA | 107932 |
rs221263237 | snp | A/C | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098196 | TTGCAAGGTCGGTAT[A/C]TTCTCTGCGTCCACG | 107932 |
rs221313477 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122885 | AACTCCCAAGGATCT[C/T]AGTGATGAGAAGCAG | 107932 |
rs221317433 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112775 | TAACCTCAGCATCGG[A/G]GAAGGGGAGACAGGA | 107932 |
rs221326085 | in-del | -/AAA | | | intron-variant | Chd4 | Mm_Celera | 6:125129472 | AAAAAAAAAAAAAAG[-/AAA]GAAAGAAAAAGAAAA | 107932 |
rs221331291 | in-del | -/AAA | | | intron-variant | Chd4 | Mm_Celera | 6:125110556 | CTTCTGTCTTAAAAC[-/AAA]AAAAAAAATACTATT | 107932 |
rs221343086 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119648 | TTGTTCCTAATGAGC[C/T]CTAGCCAGCCTGGTC | 107932 |
rs221359514 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115341 | TTTGAATTCTGTATG[C/T]AGCTTAAGCTGATTT | 107932 |
rs221424567 | in-del | -/AAG | | | upstream-variant-2KB, cds-indel | Nop2, Chd4 | Mm_Celera | 6:125130513 | GGAAAAAAAAAAAAA[-/AAG]AAAAAGAACCAAAAG | 107932 |
rs221664811 | in-del | -/CGCG | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095956 | CGGTTGCCCAGGTGA[-/CGCG]CGCGCGCGCGCGCTC | 107932 |
rs221678743 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105684 | CCCTGGGCTCACTCA[C/T]TACCTGTTAGGTACC | 107932 |
rs221691512 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125119816 | TGTTTGTTTTCAAAC[A/C]GTTGCTAATTTCTTC | 107932 |
rs221702411 | in-del | -/CAAT | | | intron-variant | Chd4 | Mm_Celera | 6:125107297 | TATAGGCGGGTCCTA[-/CAAT]CAATGCCTTATTTCC | 107932 |
rs221740897 | in-del | -/TCAAAG | | | intron-variant | Chd4 | Mm_Celera | 6:125112674 | GACACATAAGTGTAC[-/TCAAAG]TCAAAGGGTGTTGTC | 107932 |
rs221776094 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094216 | GAGCAAGAATTACTA[A/G]ATATTTTTATATTGT | 107932 |
rs221820379 | in-del | -/ATG | | | intron-variant | Chd4 | Mm_Celera | 6:125122695 | AGCTGGCTGGTGATG[-/ATG]CCTTGCCCTGGTCTG | 107932 |
rs222117990 | in-del | -/CAA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126300 | ACAACCCCCCCCCCC[-/CAA]AAAAAAAACCCACCT | 107932 |
rs222267526 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129026 | CTGCTCCTTCCACCT[C/G]CCCCTCCACTCTCCC | 107932 |
rs222287482 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125121143 | AGAGACAGACCGTAG[A/G]CCATAGTGTGGATCT | 107932 |
rs222342276 | in-del | -/CCGTCC | | | intron-variant | Chd4 | Mm_Celera | 6:125107410 | AGCAGCTACTGTCTG[-/CCGTCC]CCGTCTCCGGGAAGG | 107932 |
rs222369981 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122370 | AGGAAGTGATCCAGC[C/T]GGGACCCTTGCTTCT | 107932 |
rs222421141 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125121470 | AACTGAGGGCCAAGT[A/T]ACTGTAGCTAGAAGG | 107932 |
rs222435496 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110824 | GGAGTGATCACTTTA[-/T]TTTTTTTTTAAAGTG | 107932 |
rs222465565 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126506 | TACATAGTGAGTTCT[A/T]GGATAGCCAGGATTA | 107932 |
rs222474583 | in-del | -/CTCGTT | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094530 | CTGTGTGTTGGTATC[-/CTCGTT]CTCGGTCGGTAAGTA | 107932 |
rs222548368 | in-del | -/AAAA | | | intron-variant | Chd4 | Mm_Celera | 6:125110555 | CTTCTGTCTTAAAAC[-/AAAA]AAAAAAAAAAATACT | 107932 |
rs222567159 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116896 | GCATCTGATCCCATT[A/G]CAGATGGTTGTGAGC | 107932 |
rs222568599 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129083 | TTCCAAACTGTCTGC[C/T]GAGCCTGTGTGGAAC | 107932 |
rs222617897 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123757 | GTTCTGTGAAGGACC[A/G]TCAGCCACACTTGCA | 107932 |
rs222657534 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116127 | ACTATATTGTCAAGA[A/G]TGACCTTGAACTTGA | 107932 |
rs222786350 | snp | G/T | | | missense | Chd4 | Mm_Celera | 6:125122911 | AGCAGAAGAAAAACA[G/T]CAAACAGCGTTTCAT | 107932 |
rs222840872 | snp | A/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102071 | AGGGGCACATAGGGT[A/G]CTACTGCTTCAGACA | 107932 |
rs222857134 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099222 | TTGAGCCCTTGTTAA[A/G]TCTTAGTTCTAATGT | 107932 |
rs222862863 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127240 | TCCCTCCCAGGTGCT[A/G]GGATTAAAGGCATGT | 107932 |
rs222961772 | in-del | -/GAGAGAGA | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094090 | AGGAGGGAGGAGAGT[-/GAGAGAGA]GAGAGAGAGAGAGAG | 107932 |
rs223012565 | snp | G/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095082 | ACCCTCTCTGCTCTA[G/T]TTGGAAGAGCCTGAC | 107932 |
rs223126035 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101371 | GCGGTGGGAAGGGAG[-/GA]GAGTCTTTCTAGAAT | 107932 |
rs223180625 | in-del | -/A | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130500 | GCTAAATAAAGTTGG[-/A]AAAAAAAAAAAAAAG | 107932 |
rs223261660 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124492 | GAAGGTATCAATCAA[A/G]TAGGAAACCGTGGAA | 107932 |
rs223297725 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098289 | GTTTTTTGTTCCTTA[C/T]GGCATGGCTCTCACT | 107932 |
rs223609129 | in-del | -/TT | | | intron-variant | Chd4 | Mm_Celera | 6:125120825 | TTCCTCTTACAGAGG[-/TT]TTTTTTTTCCTTAGG | 107932 |
rs223635978 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096753 | GAGCGCCCCCCCACT[C/T]CCAAGTGACCTTGTG | 107932 |
rs223866560 | snp | C/T | | | missense | Chd4 | Mm_Celera | 6:125122854 | AGAAAAAGGACGTGA[C/T]GCTTCAGAATGGAGA | 107932 |
rs223894165 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125966 | GCCCTGCCTTAAAAA[C/T]AAAACAACAGGGGCT | 107932 |
rs223951244 | in-del | -/CTTACTAG | | | intron-variant | Chd4 | Mm_Celera | 6:125118422 | AGGTAGATTTACAGA[-/CTTACTAG]CTGAGTATCCATACA | 107932 |
rs223975284 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125270 | GTTATACCAAAATGG[A/G]CCATGAGCAAGATTC | 107932 |
rs224074280 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130830 | CATGGAATACATATG[C/T]GTGAATATGTAATTA | 107932 |
rs224090603 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095724 | AGGGGAGGGAGGGGT[A/G]ATGAGTTATTATGGG | 107932 |
rs224109045 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129197 | TGAGCATAGCTTTAT[G/T]GGGGGGGGGTGAAAT | 107932 |
rs224212626 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104353 | AGCACATGTGTGGGT[A/G]TTGTATGTGCACATG | 107932 |
rs224268531 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129474 | AAAAAAAAAAAAGAA[A/G]GAAAGAAAAAGAAAA | 107932 |
rs224320072 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097587 | GAATGCAGGTGGTTC[C/T]GACTCTGGTGGTGAC | 107932 |
rs224358410 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103555 | ATTTATTTATTATAT[A/G]TAAGTACACTGTAGC | 107932 |
rs224594987 | in-del | -/CCAACTTGTT | | | intron-variant | Chd4 | Mm_Celera | 6:125111250 | CCATCCCTCCAAACC[-/CCAACTTGTT]CTTGTGTGTCTCTCG | 107932 |
rs224600207 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125102852 | GGGTGAGGAGATTCT[A/G]GAAGAAGTCGGGGGG | 107932 |
rs224696011 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128114 | TCAAACTCAGAAATC[C/T]GCCTGTCTCTGCCTC | 107932 |
rs224778151 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127397 | GGTGCATGCCTTTAG[A/T]CCTACCACTCAGGAG | 107932 |
rs224972872 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101582 | ATCAGTGGCAGCTGC[A/G]GCGGCGGCGGCTGTG | 107932 |
rs225021389 | in-del | -/TGT | | | intron-variant | Chd4 | Mm_Celera | 6:125108069 | ATGTGTTTTGAGGGA[-/TGT]ATTACAGTTGGTCTT | 107932 |
rs225025522 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129350 | TCTGTGGGCATTTGC[C/T]GTGCTCCCAACTTGG | 107932 |
rs225157283 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125108739 | CATCTTGGGTTCTAT[C/T]GACTGGGCCTGCCTC | 107932 |
rs225296113 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125102987 | CTGCCTGAACCCCCC[A/G]CTGCCAGAGATCCCA | 107932 |
rs225424818 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111609 | AGAGCAGCAATGATA[C/T]TCTATCTCTATCCCC | 107932 |
rs225452449 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099516 | GGGTGCCCTGGGCTG[C/G]CTTCTGCGGTCAGGA | 107932 |
rs225492765 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125110790 | CCCTCCCCAGTCCCG[A/G]TCATTTTCTTCTATT | 107932 |
rs225518550 | snp | C/G | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097313 | GATGTTTGATCTTTC[C/G]TCGAGACTCCAGTGA | 107932 |
rs225591226 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107870 | GTTGTGCACCACCTG[G/T]GTGCAGTACCTTGGG | 107932 |
rs225628092 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108887 | GAAGAAGGGAAAGTG[C/G]TCTTTATTTCCTTCC | 107932 |
rs225654563 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117403 | AGCACTTTACCAACC[G/T]GGCCATGTCTCCAGC | 107932 |
rs225859787 | in-del | -/TA | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097787 | GATCTGTAGAACTTT[-/TA]GTTAGTCAGATTGTT | 107932 |
rs225874999 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107218 | CACTCCAAAGACAGT[A/T]TTTCCTTCTGGTTCC | 107932 |
rs226148165 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104841 | CTGTGGTACTGAATT[C/G]AGATTAAGTGGTGTC | 107932 |
rs226509443 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125106896 | GTCAGGTCTACCTGA[A/C]GCCTAGATATGTAGC | 107932 |
rs226624545 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094182 | TAGGAGGGAAGGGAC[-/AG]AGCAGGAAGAGAGTT | 107932 |
rs226628708 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115428 | GAATTTTTATTTATT[A/G]TTATCTTTTTTTGTG | 107932 |
rs226643087 | in-del | -/GG | | | intron-variant | Chd4 | Mm_Celera | 6:125123093 | TTGAGATGGATTGGC[-/GG]GGGTGTGTGTGTGTG | 107932 |
rs226643501 | in-del | -/AG | | | intron-variant | Chd4 | Mm_Celera | 6:125110611 | TGGGACTGGAGTGAC[-/AG]AGGGTTGTGAGCTAC | 107932 |
rs226662456 | snp | A/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125106499 | CGAGGACGTGGAGAT[A/T]CAGGACTACGACCTG | 107932 |
rs226682232 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114933 | ACGTAGACGAAACAA[A/T]ACATTAAATAACTAG | 107932 |
rs226722563 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112627 | TGTCCCCCGACTTGA[C/T]GTGTGCACTGGCATG | 107932 |
rs226758500 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113178 | CGATGGGATACTGTA[C/T]GTGATGTTGATATTT | 107932 |
rs226785313 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125120577 | AGCGGGGCCATCTTG[C/G]GAGTTGTGTAGCTGT | 107932 |
rs226867168 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112373 | AAAGGTGGAGGGGCA[G/T]CGAGGGGCCAGCAGG | 107932 |
rs227061314 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119493 | ATGGTTTCATGCATT[A/G]CTGAAGGTCAGATCC | 107932 |
rs227141557 | in-del | -/CTTACGGTGAT | | | intron-variant | Chd4 | Mm_Celera | 6:125118199 | CAGGGTGACCTTGAA[-/CTTACGGTGAT]CTTCCAGCTTCATCC | 107932 |
rs227213114 | in-del | -/AA | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130499 | GCTAAATAAAGTTGG[-/AA]AAAAAAAAAAAAAAA | 107932 |
rs227532297 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111182 | TGGGAATGAACCCAA[A/G]TCTCCTGGAAGAACA | 107932 |
rs227610326 | in-del | -/GTA | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099441 | TACTCTCCGCTCTGT[-/GTA]GTACTTCTGTTGGCT | 107932 |
rs227704901 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111446 | TGAAAGGAAGATGTG[A/G]TTAGTTTTGGTTTAA | 107932 |
rs227752136 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117821 | ACAAGTCATATTGGG[A/G]AGGGCGAGAAAGCTG | 107932 |
rs227776347 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107412 | CAGCTACTGTCTGCC[G/T]TCCCCGTCTCCGGGA | 107932 |
rs227818963 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124823 | CCAAGCCAGAGATTC[A/G]AAAGGTTAAGATAAG | 107932 |
rs227819536 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118266 | AACTATCATGTTATA[C/T]GTGTATCTGTCTGTC | 107932 |
rs227820800 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116547 | CTGCCTGAGTCCACT[A/G]TAGCTCTGATCATTT | 107932 |
rs227849918 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117255 | AAGCTAGACCTGAAT[G/T]TAAACAGTCAAGGAT | 107932 |
rs227850681 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110682 | AGATACAAAATCTCA[C/T]TGTTGTATCCTTGAG | 107932 |
rs227855602 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127130 | TGGTTTTGTTTTTTG[-/T]TTTTTTCAAGACTGG | 107932 |
rs227864863 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124146 | CATAGTCCCTGTATT[C/T]CAACAGAAAAACAAC | 107932 |
rs227870135 | in-del | -/GTA | | | intron-variant | Chd4 | Mm_Celera | 6:125113224 | ATTGGTCACTTGGTT[-/GTA]GTCATGGTGTCTGCT | 107932 |
rs227871153 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117978 | GACTGCTTTCTTAAT[C/T]GCTCCGTCGCGTGCA | 107932 |
rs227896514 | in-del | -/TCTATG | | | intron-variant | Chd4 | Mm_Celera | 6:125127332 | GATAACCTGATTGAT[-/TCTATG]TCCATAGGCCAGGTG | 107932 |
rs227986280 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123256 | TTGCTGTCCACCGCC[C/T]AACTTTTTCTTTTTT | 107932 |
rs228020342 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126134 | TTCTTGAGCCGGACA[A/G]CAGTGGTGCAGACCT | 107932 |
rs228028632 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115505 | TTGACCTTACTTTGT[A/G]GCTGAGGGTAACCTG | 107932 |
rs228077043 | in-del | -/TTTTT | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103419 | TTATAGATCCTTAAC[-/TTTTT]TTTTTTTTTTAGCTC | 107932 |
rs228206284 | in-del | -/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125109932 | ATGGTATGTGCACCT[-/C]TTTGTCTTCTGTGCC | 107932 |
rs228306627 | snp | C/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095822 | GGGGAGCAGGTTTTA[C/G]TTTGTAAAAGATCTG | 107932 |
rs228394028 | snp | C/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094796 | AAAGTTTTTCATCAT[C/G]AAGTTTTATGCAAGT | 107932 |
rs228398793 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125114887 | CTCTCCAGCTCCCAT[-/A]AAAAAAATTTTAATG | 107932 |
rs228587447 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122668 | TGACTGTTTCCAAAT[G/T]TAGTTGTTAGGGAGC | 107932 |
rs228622823 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130986 | CTGCCTCTCAAGTGG[A/G]GGAATTAAGGATGTT | 107932 |
rs228639187 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124111 | CTACATGGTGAGCTT[C/T]ATTCAGGCCAACAAG | 107932 |
rs228713059 | in-del | -/TA | | | intron-variant | Chd4 | Mm_Celera | 6:125116325 | CTTTTAGTCATAGTT[-/TA]TATGTGTGACTGGTT | 107932 |
rs228784912 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129587 | GCCTAGAGTCACAGG[A/G]ACTCAAGAGACACAG | 107932 |
rs228881364 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128009 | TGGTTTTGGTTTTGG[-/T]TTTGGTTTGGTTTTT | 107932 |
rs228967047 | in-del | -/CACCT | | | intron-variant | Chd4 | Mm_Celera | 6:125111229 | CTGAGCCGTGTCCAG[-/CACCT]CACCTCCATCCCTCC | 107932 |
rs228995603 | in-del | -/CAGAG | | | intron-variant | Chd4 | Mm_Celera | 6:125129333 | GGCTGAGAATAAAAA[-/CAGAG]CTCTGTGGGCATTTG | 107932 |
rs229017570 | in-del | -/TGG | | | intron-variant | Chd4 | Mm_Celera | 6:125113381 | GTGCTGACAATTGCT[-/TGG]TGGTTTTCTGAAGCG | 107932 |
rs229075352 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114733 | TTTTTAAAGATTTAT[A/T]TATTATATATGAGTA | 107932 |
rs229118468 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119316 | CTGGCTGTCCTGGAA[C/T]TCACTCTGTAGACCA | 107932 |
rs229147701 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122514 | GGAGGAGAAGTCTGC[A/G]GTAGACCTGACCCCG | 107932 |
rs229181406 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127624 | CTACACAGAGCTACA[A/G]ACTCAGATGCTGCCT | 107932 |
rs229288263 | in-del | -/AAG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128599 | AAAAAAAAAAAAAAA[-/AAG]AGAGAGAGAGAGAGA | 107932 |
rs229293034 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125120763 | TCCTATAGTGGGAGA[A/G]AGGCCTGAGATTGCC | 107932 |
rs229337991 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130534 | AAGAACCAAAAGCAT[-/A]AAAAACCACAGCAAA | 107932 |
rs229522998 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119152 | CATTGGATTCCATTA[C/T]AGATGGTTGTGAGCC | 107932 |
rs229684382 | snp | A/C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098190 | CATTCATTGCAAGGT[A/C/T]GGTATCTTCTCTGCG | 107932 |
rs229734059 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094184 | GGAGGGAAGGGACAG[-/AA]CAGGAAGAGAGTTAG | 107932 |
rs229781641 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127451 | TTAGTTCAAGGCTAA[C/G]CTGGTCTGCAAATCC | 107932 |
rs229797956 | snp | C/G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123755 | AGGTTCTGTGAAGGA[C/G/T]CATCAGCCACACTTG | 107932 |
rs229822920 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124352 | CGGATCATGGAATTC[A/G]TATGAATAAAAAACG | 107932 |
rs229834520 | in-del | -/GCAG | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097545 | GAGCTCTCTGGGTTA[-/GCAG]GCTTTACCTCGTGCA | 107932 |
rs229941484 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096302 | AGACATCTCTCTCAG[C/T]CCGACGTCGTCCCGG | 107932 |
rs229995932 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094970 | ATGAGCTAGGAAGTC[C/T]GGGGGTCCTGAACTT | 107932 |
rs229996296 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106570 | GCGAGCAAGGAAGAG[C/T]AGACGTGCTCTTGCT | 107932 |
rs230036534 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126973 | GAGCTTAGCTAGAAG[A/G]CACAAAGCCAGCACA | 107932 |
rs230080276 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125118385 | GCAACTAATTGTTTC[A/C]GATATGGGAGAAGTT | 107932 |
rs230145134 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125105948 | CTTACTGAAGGGCTC[A/G]AGAAAAGGGACGTTG | 107932 |
rs230327114 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117753 | TTTCTAAGTTTGAGG[A/T]CAGCCAGGCCTACAC | 107932 |
rs230390707 | snp | A/C/G | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130215 | AGTAGCGCAGCGCCC[A/C/G]CCCGCCATGTGCAGG | 107932 |
rs230554351 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129044 | CCTCCACTCTCCCCT[C/T]CCCAACATCCATAAA | 107932 |
rs230647267 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103261 | TAGTAGTTCTTCTGA[A/T]TCCTTCCTTTTTTCA | 107932 |
rs230767886 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112166 | TGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 107932 |
rs230799039 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125015 | CAAGTTCCAATAAAA[C/T]TTGCAGGTGGATTTC | 107932 |
rs230850350 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095861 | GTCTGTAGCCCCGGG[C/T]ACATATATGCATAGA | 107932 |
rs230980250 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102392 | GTTGGGGGGAGGTGG[-/T]TTTTTTCTAATAATT | 107932 |
rs231148549 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131089 | TATATGAGTACACTT[A/C]AGACACACCAGAAGA | 107932 |
rs231153843 | snp | C/G | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097339 | AGTGAGGCTGCGTTC[C/G]CGCGCTGCTTGTCCC | 107932 |
rs231165472 | in-del | -/TGG | | | intron-variant, cds-indel | Chd4, Gm32616 | Mm_Celera | 6:125100123 | GTCTTAGGAGCTGTT[-/TGG]TGGCCACTTTTGGGA | 107932 |
rs231182667 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122715 | GCCCTGGTCTGGGAG[A/G]CTGAGTGTGGAGGCG | 107932 |
rs231222262 | in-del | -/AGC | | | intron-variant | Chd4 | Mm_Celera | 6:125104405 | AGTGCTGGGCCAGAG[-/AGC]AGCAGTGCTGTACTC | 107932 |
rs231348679 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100196 | GCTGCTCAATTCAGC[A/G]GTGCTGGTAGACACA | 107932 |
rs231425324 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104213 | TTTCTGGGCATGATG[A/G]TGCATCCCTTTAATT | 107932 |
rs231474219 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | Chd4 | Mm_Celera | 6:125103418 | TTATAGATCCTTAAC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 107932 |
rs231527327 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108107 | TTTGGTTTTTGTCAC[A/G]GTGGGCCTAAGAGAG | 107932 |
rs231641742 | in-del | -/TTTCT | | | intron-variant | Chd4 | Mm_Celera | 6:125107796 | CTGCAGTGCAAATCC[-/TTTCT]TTTCTTTTTCTTTTT | 107932 |
rs231711855 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107097 | CTCGTGCCCACATTC[A/G]TGCCTTTTGTTCTGT | 107932 |
rs231740115 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128493 | GAGACAGAGGCAGGC[A/G]GATTTCTGAGTTCAA | 107932 |
rs231802145 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094456 | TGTGTTCTCTGAGTG[C/T]TGAGGTTATTGGCAT | 107932 |
rs231825725 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115872 | TATTTAAGGTGGCTT[A/G]TGTGAGGCTTAATCA | 107932 |
rs231862186 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116779 | CATGCTAAAAGAATT[G/T]TGTTGTTTTTTAATT | 107932 |
rs231905562 | in-del | -/TTC | | | intron-variant | Chd4 | Mm_Celera | 6:125119058 | AGTTGATCTTTTTCT[-/TTC]TTTTTTTTTTTTTTA | 107932 |
rs232019122 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103181 | CTCCTGTGTAAACAT[A/G]CAGCTAACTGAATTG | 107932 |
rs232190747 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130908 | CCTCTCAAGTGGGGG[-/A]AATTAAGGATGTGTT | 107932 |
rs232198713 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127866 | TTAACAAAATACTAA[C/T]ATGCTTCGCAGGAAT | 107932 |
rs232371026 | in-del | -/GTGGA | | | intron-variant | Chd4 | Mm_Celera | 6:125118503 | TGTGGGGGTGGGGGG[-/GTGGA]GGGCACTTGGAGGGA | 107932 |
rs232548629 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101280 | CATCGACCATGTGTT[C/T]TCAGAGGAGGATTAT | 107932 |
rs232655622 | in-del | -/TGA | | | intron-variant | Chd4 | Mm_Celera | 6:125122690 | TAGGGAGCTGGCTGG[-/TGA]TGATGCCTTGCCCTG | 107932 |
rs232668491 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107063 | CCCCTTCCCTCAGCC[A/G]CCCCATTCTTCCCTG | 107932 |
rs232794452 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111921 | CAAGAACTCAGTGAG[C/G]CTGGGAAGAGCATTG | 107932 |
rs232901086 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118550 | CTGAGCACTGATTCC[A/G]GAGTTACAAACATCT | 107932 |
rs232930662 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105882 | TGGGCTCACTCACTA[C/T]CTGTTAGGGGCCACG | 107932 |
rs232934457 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111118 | CCAGAAGAGGGCATC[A/G]GATCCACTGGAACTG | 107932 |
rs232939805 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119341 | AGACCAGGCTGGCCT[C/G]GAACTCAGAAGTCAT | 107932 |
rs233066765 | snp | A/C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105413 | CTGGGCTCACTCACT[A/C/G]CCTGTTAGGTGCCAC | 107932 |
rs233175296 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112810 | CAGAGTCATCCTGGC[A/G]ATCTGAAGAGTTCAA | 107932 |
rs233219505 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114862 | TCAGTGCTCTGACCT[G/T]TTGAGCCATCTCTCC | 107932 |
rs233253928 | in-del | -/AAAG | | | intron-variant | Chd4 | Mm_Celera | 6:125112282 | ACATAAAATAAAAAT[-/AAAG]ATATAAAAAAAATTT | 107932 |
rs233284949 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107754 | GGAGGAGGAGGAGGT[A/G]CTGCTGAGGGGTAGG | 107932 |
rs233303983 | in-del | -/AAATA | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094341 | GTGCTGGTAATAAAT[-/AAATA]AATTATAATTATCCG | 107932 |
rs233321286 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098512 | GGAAGACTTACTTTT[C/T]CTTCCTTGTCTTTAT | 107932 |
rs233467679 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125123762 | GTGAAGGACCATCAG[-/C]CACACTTGCACCTCC | 107932 |
rs233604068 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125117532 | GCAGCTGGATTGCCC[-/A]AGGTCACACTCAGTT | 107932 |
rs233627720 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112600 | GGACGTCACAGTGGA[A/T]GAAGACTCCTCTGTC | 107932 |
rs233661607 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103084 | CAGTGTCCTCACAGC[C/T]CAAGGGTTTGCTCTC | 107932 |
rs233721014 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105467 | ACCTGTTAGGTACCA[C/T]GTCTGCTCCTGGGCT | 107932 |
rs233865628 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115595 | TGAGATAGCGCCCGA[C/T]GCTGCATGCATGCTA | 107932 |
rs233979450 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122843 | GGAGGAGGAGGAGAA[A/G]AAGGACGTGATGCTT | 107932 |
rs234011577 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115147 | GCCGGCATCCCAAGC[C/T]TTCACATCCTCCTGA | 107932 |
rs234013689 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115368 | ATTTTGAATTCCCAA[C/T]TCTCCTGCACCTCCC | 107932 |
rs234045648 | in-del | -/G | | | intron-variant, nc-transcript-variant | Chd4, Mir7045, Gm32616 | GRCm38.p3 | 6:125097068 | GTCACTCACTGTTCT[-/G]CCCCCCTCCCCCGCA | 107932 |
rs234121818 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110448 | TATATATACCCTAAT[C/T]CCAGTACTCAGGAGG | 107932 |
rs234323792 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125117418 | GGGCCATGTCTCCAG[A/C]CCCTGTAAGTTGATG | 107932 |
rs234343105 | in-del | -/GTTTTTTAGATCTTGCTTCTTTTTTTTTTAGATCTTTTT | | | intron-variant | Chd4 | Mm_Celera | 6:125116385 | TCAACCAAAAACTTG[lengthTooLong]GTTTTTTAGATCTTG | 107932 |
rs234355508 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108031 | TTTTACAGGATCAGA[C/G]CCCTGGTAGACTCAG | 107932 |
rs234384834 | in-del | -/CC | | | intron-variant | Chd4 | Mm_Celera | 6:125110185 | CCAGTAGCAGGACAA[-/CC]CTAGTGACTGAGAAA | 107932 |
rs234421872 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119057 | AAGTTGATCTTTTTC[-/T]TTTTTTTTTTTTTTT | 107932 |
rs234446993 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106109 | GAATGGTTTTGTCGG[-/T]TTTTTTTTTTGTTTT | 107932 |
rs234531857 | in-del | -/CCAAGGCTAAA | | | intron-variant | Chd4 | Mm_Celera | 6:125125753 | AACCCTTCCTAAAAG[-/CCAAGGCTAAA]CCTGTGGAATACTCA | 107932 |
rs234573434 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116119 | TGGAACTCACTATAT[A/T]GTCAAGAATGACCTT | 107932 |
rs234612402 | in-del | -/TAATTT | | | intron-variant | Chd4 | Mm_Celera | 6:125128263 | CATCTTGCCAGTCCA[-/TAATTT]TAATTCTATATAAAT | 107932 |
rs234628479 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125104058 | ATCCCACTTTATATC[C/T]CTGGCTGGCCTGAAA | 107932 |
rs234637327 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116964 | GGAAGAGCAGTCAGT[A/G]CTCTTAACCACTGAG | 107932 |
rs234672523 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117476 | ATTCTCTTTCCTCAT[C/T]CTCTATAGTGGCTCA | 107932 |
rs234729649 | in-del | -/TC | | | intron-variant | Chd4 | Mm_Celera | 6:125119059 | GTTGATCTTTTTCTT[-/TC]TTTTTTTTTTTTTAA | 107932 |
rs234768630 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125102747 | TGTGGGTTCTGACGT[-/G]GGGTGGGGTGGGGTG | 107932 |
rs235116438 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125121993 | CACAGAAGGAGAGAA[A/G]GAAGTTAAATCTACA | 107932 |
rs235167786 | snp | C/G | | | missense | Chd4 | Mm_Celera | 6:125122276 | CCTATGGAGACAGAG[C/G]CCAAAGGTAAATATG | 107932 |
rs235250036 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126343 | AACAACAAACTAAAA[A/T]TTAATACTTAGTAGA | 107932 |
rs235284467 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127183 | TTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 107932 |
rs235392705 | in-del | -/CCC | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | GRCm38.p3 | 6:125096459 | GAGTCCTGCTCCCCG[-/CCC]CCCCCCCCTCCTGGG | 107932 |
rs235473320 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098958 | TGTGGATGGGAGGCC[C/T]GTGGCACTTTGTCCA | 107932 |
rs235592449 | snp | A/G | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096903 | GCCCTCGGGGGCGTC[A/G]TTCCCTCTTCTTGGG | 107932 |
rs235618497 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119425 | GCATAAAGTTGATCT[A/T]GAAGTGGCTCTATGT | 107932 |
rs235645423 | snp | A/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095794 | AGTGGTTATTATGGG[A/T]TATCTAAGGGAGGGG | 107932 |
rs235673192 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125109255 | TCCTTTCTTCCTTGT[C/T]TCCCCTTCTCTAACA | 107932 |
rs235806846 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128737 | AGGAAGAGATGAATC[C/T]GTCAGTGAGAACGTG | 107932 |
rs235863187 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107203 | ATTCTTTATTGTTAT[C/T]ACTCCAAAGACAGTA | 107932 |
rs235942920 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116837 | ATTTATTTATTTAAT[G/T]TCTTTGAGTACACTG | 107932 |
rs236061834 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117995 | CTCCGTCGCGTGCAC[A/G]CTTCAGCTCTGGAAC | 107932 |
rs236218085 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094447 | ATCATCTCGTGTGTT[-/C]TCTGAGTGCTGAGGT | 107932 |
rs236228295 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126200 | TTTCTGAGTTAGAGG[C/T]TAGCTTGATCTACAG | 107932 |
rs236511456 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096821 | GCCTCCCCACTCGAA[C/T]CCCACTCCCCAGGCA | 107932 |
rs236536838 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127523 | GTCTCTTAAAAAAAA[A/C]AAAACATTTTTCCTT | 107932 |
rs236564377 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115031 | GAAGGCAAAATCTAC[C/T]AAAAGAGAATGTGTG | 107932 |
rs236580024 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128342 | AGTGTGGACCTCCAG[A/G]GCTGGAGAGATGCTC | 107932 |
rs236874133 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122864 | CGTGATGCTTCAGAA[C/T]GGAGAAACTCCCAAG | 107932 |
rs236911146 | in-del | -/AGAG | | | intron-variant | Chd4 | Mm_Celera | 6:125122740 | GAGGCGGAGGTAGAC[-/AGAG]AGAGCAGGCAGTGCT | 107932 |
rs236913483 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111136 | TCCACTGGAACTGGA[A/G]GTACAGCTGAGTGAG | 107932 |
rs236947352 | in-del | -/TC | | | intron-variant | Chd4 | Mm_Celera | 6:125119858 | AAGACCAGAATACTT[-/TC]TGTTCTAAAGATCTC | 107932 |
rs237045043 | in-del | -/ATC | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115708 | TCTATCTATCTATCT[-/ATC]ATCTATCTATCTATC | 107932 |
rs237064051 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094111 | AGAGAGAGAGAGAAG[C/T]AGAGGACTGGAGAGA | 107932 |
rs237220152 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122888 | TCCCAAGGATCTTAG[C/T]GATGAGAAGCAGAAG | 107932 |
rs237243245 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130959 | GAGGGTCTAAGTAAC[A/T]ACTGCCTGCCCCTGC | 107932 |
rs237448069 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125127261 | AAAGGCATGTGCCAC[A/C]ACTGCCCGACAGCGT | 107932 |
rs237473491 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118713 | ATACATTTCTATTTC[A/G]TATTTTTAGATTTTG | 107932 |
rs237554104 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094263 | TTGGTTGTTTAATGT[C/T]TCTTCATTATACATT | 107932 |
rs237558669 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128784 | CTGTCTTCTTTCTCC[A/G]TGTGCAGCTCTTAGA | 107932 |
rs237596545 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125103907 | AAAAAAAAAAAAAAA[A/C]AAAAAACAAAAAAAA | 107932 |
rs237748463 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125102695 | GGGTGGAAATACAAA[C/T]GGGAGCTTTGGGAAA | 107932 |
rs237761099 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125103075 | GGATGGGAGCAGTGT[A/C]CTCACAGCCCAAGGG | 107932 |
rs237798121 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111733 | AATTATTTTTGTTCA[-/T]TTTTTTTGAGACAAG | 107932 |
rs238034421 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106121 | TCGGTTTTTTTTTTG[G/T]TTTTTTTTGTTTTTT | 107932 |
rs238087150 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117502 | GCTCAAAGCTAGAGC[A/G]CGTCCCATTGGGCCC | 107932 |
rs238097249 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127226 | AAATTGCCTGCCTCT[C/G]CCTCCCAGGTGCTAG | 107932 |
rs238203898 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115265 | TTAAATGTTCGATCC[C/T]CCTGCATCAGTTGCT | 107932 |
rs238213310 | in-del | -/AAAA | | | intron-variant | Chd4 | Mm_Celera | 6:125114705 | TTACTAGTTCTCCAT[-/AAAA]AAAAAAAAATTTTTT | 107932 |
rs238259510 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114723 | AAAAAAATTTTTTTT[A/T]AAGATTTATTTATTA | 107932 |
rs238394159 | snp | G/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100019 | GGTGTTTGTTGTGTT[G/T]TAGGCCCTGAGCCTG | 107932 |
rs238419161 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097928 | TTACTAGGGGCTTCC[A/G]CCACTCTGAGGTAGC | 107932 |
rs238708954 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098343 | TGGAGGGTGAGATAT[C/T]CAGAAGAAATCATTT | 107932 |
rs238748450 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099232 | GTTAAGTCTTAGTTC[C/T]AATGTCTTTAAAGAA | 107932 |
rs238875748 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107331 | AGGGCTTTTTTATTT[G/T]GTTTGGTTTTGTTTC | 107932 |
rs238878784 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123469 | CTTGCCTGAGTTGAG[A/T]TTGGGGTCTCTGTGT | 107932 |
rs238966736 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106901 | GTCTACCTGAAGCCT[A/G]GATATGTAGCCCTGT | 107932 |
rs239024598 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106110 | GAATGGTTTTGTCGG[G/T]TTTTTTTTTGTTTTT | 107932 |
rs239110517 | in-del | -/TCTA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115796 | CTATCTATCTATCTT[-/TCTA]TCTATCTATCTATCT | 107932 |
rs239290166 | in-del | -/CTACCTCTAAGA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116640 | ACGATCTGCCAGCCT[-/CTACCTCTAAGA]GTTGGGGTTAAAGGC | 107932 |
rs239371954 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130770 | TCCTGCAGGAAGTAG[C/T]CACTTGCCTGGTACA | 107932 |
rs239447355 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118045 | ACTCCGTGGAGCCTC[G/T]AAAGCTTTCAGGTTT | 107932 |
rs239494996 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125129869 | GAAAGCTGATGTGAC[A/G]CGGCTCCCAGCCACC | 107932 |
rs239509457 | in-del | -/CC | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127523 | TCTCTTAAAAAAAAA[-/CC]AAAACATTTTTCCTT | 107932 |
rs239559761 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103390 | CTATTTCGGTTTATT[A/G]TTTAGAATATAGCTT | 107932 |
rs239630479 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112741 | GGTCCCCAGCACCGC[A/G]TAAGTGGTGATGCAA | 107932 |
rs239715750 | in-del | -/TT | | | intron-variant | Chd4 | Mm_Celera | 6:125110823 | GGAGTGATCACTTTA[-/TT]TTTTTTTTTTAAAGT | 107932 |
rs239736969 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125102751 | GTTCTGACGTGGGGT[-/G]GGGGTGGGGTGGGGT | 107932 |
rs239882922 | snp | G/T | | | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101606 | GGCTGTGGCTGTGGT[G/T]GAGAGCATGGTGACA | 107932 |
rs239899977 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129470 | AAAAAAAAAAAAAAA[A/G]GAAAGAAAGAAAAAG | 107932 |
rs240183968 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125110957 | GAGTCCTGAGGACTG[A/C]ACAGAGATCACCTAG | 107932 |
rs240203923 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111449 | AAGGAAGATGTGGTT[A/G]GTTTTGGTTTAAGTA | 107932 |
rs240247280 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118472 | CTGCTTTTTATTGAC[A/G]TCCTGTTAAGACATT | 107932 |
rs240323532 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126434 | AAAGAACCTTTAAAT[A/G]ATGGGTACTTTGTAA | 107932 |
rs240576457 | snp | G/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099208 | TTTGGTAACCTCCAT[G/T]GAGCCCTTGTTAAGT | 107932 |
rs240583063 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116211 | GTGTGGAGTTGCCTG[-/T]TCCATTCCTGTGGTG | 107932 |
rs240624882 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125117560 | GTTCCTGGGAGTCCC[-/A]GGCTTGCCTCGGGCT | 107932 |
rs240657037 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125108035 | ACAGGATCAGAGCCC[G/T]GGTAGACTCAGTGCC | 107932 |
rs240662411 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122416 | CTGGCAGCAGTGGAG[C/G]TGTGGAACTCTGTTG | 107932 |
rs240685430 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125129120 | ATGTGAGCTGAGGGG[A/C]TTTTCTTTGCAGGCA | 107932 |
rs240843131 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128481 | TCTAGCACTTGGGAG[A/G]CAGAGGCAGGCAGAT | 107932 |
rs240867416 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106816 | AGCTCCAAGTCATGG[C/T]CTGTGGATAGCTCTA | 107932 |
rs240886015 | in-del | -/TTTTTA | | | intron-variant | Chd4 | Mm_Celera | 6:125103433 | TTTTTTTTTTTTTTT[-/TTTTTA]AGCTCTGTGATAATA | 107932 |
rs241141520 | in-del | -/GG | | | intron-variant | Chd4 | Mm_Celera | 6:125129460 | AAAAAAAAAAAAAAA[-/GG]AAAAAAAAAAGAAAG | 107932 |
rs241217944 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114818 | CATGTGGTTGCTGGG[A/T]TTTGAACTCAGGACC | 107932 |
rs241273587 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116160 | TCCTCCCACCTCTAC[C/T]TCCTGAGTGCTGGAA | 107932 |
rs241299660 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122976 | GAATGCGGGTCCTGC[A/G]GGGAGGCTGGGCTTC | 107932 |
rs241338086 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115376 | TTCCCAATTCTCCTG[C/T]ACCTCCCAAGTGCTG | 107932 |
rs241439145 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106627 | GGCAGCTGTGGTGTG[G/T]TTTCTTTCCTAGGGA | 107932 |
rs241488283 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096599 | TTTCCTCCGGCGTCC[C/T]GACTCTTCGGGACCC | 107932 |
rs241567555 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094359 | TAAATTATAATTATC[C/T]GAGACTTGTTTTTAC | 107932 |
rs241773203 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125676 | AAATCTTAGTATTTG[C/G]GTAGTGGAAGCAGGA | 107932 |
rs241792593 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124126 | CATTCAGGCCAACAA[A/G]GCTACATAGTCCCTG | 107932 |
rs241825473 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124720 | AGTTGTTCAGGGCCA[G/T]TGCATGAGAGACTTC | 107932 |
rs241904836 | in-del | -/AAAAAAAAAAAAAAAAAG | | | intron-variant | Chd4 | Mm_Celera | 6:125129454 | ATATAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAG]AAAGAAAGAAAAAGA | 107932 |
rs241987527 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119817 | GTTTGTTTTCAAACA[A/G]TTGCTAATTTCTTCT | 107932 |
rs242178407 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125113550 | TGCGGACACAGTTAT[C/T]ATATATGACTCTGAC | 107932 |
rs242179222 | snp | C/G | | | synonymous-codon | Chd4 | GRCm38.p3 | 6:125105373 | GATCCACCGCATCCT[C/G]AACCACAGGTACCAC | 107932 |
rs242221058 | snp | C/G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125104469 | ACTAGACCTAGAGCT[C/G/T]GGGCTGGCTGGCGGC | 107932 |
rs242270728 | in-del | -/A | | | intron-variant | Chd4 | GRCm38.p3 | 6:125107662 | CCTCTATAAGGAGGT[-/A]AAAGATGCCAGGAGA | 107932 |
rs242329021 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104366 | GTGTTGTATGTGCAC[A/G]TGTATGTTCCAGGAT | 107932 |
rs242332716 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113073 | CTGACATTTCACCCC[-/T]GTCCTTGCATGGCAT | 107932 |
rs242430984 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126649 | GAGACTTGTACAAGA[C/T]TGAATAATAAAAGCA | 107932 |
rs242461610 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118080 | AAAGACTGGCTATCC[A/G]AGCTGTACTGAAACG | 107932 |
rs242469564 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127347 | TTCCATAGGCCAGGT[G/T]ACTATGCCACTATTA | 107932 |
rs242469629 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118168 | TGTTTGTGTGTGTGT[G/T]TGTTTTAGTTATACC | 107932 |
rs242657556 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126550 | TATCTTGAAGAACTA[A/G]AAAGTTCTGTCTCTT | 107932 |
rs242693636 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099281 | GCAGTCATTCCAATA[C/G]TTTACTCTGGTGCTG | 107932 |
rs242720509 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114715 | CTCCATAAAAAAAAA[-/T]TTTTTTTAAAGATTT | 107932 |
rs243080976 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126979 | AGCTAGAAGACACAA[A/G]GCCAGCACACCTCAT | 107932 |
rs243170829 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118030 | TCCCAGCAGGTCTGA[A/G]CTCCGTGGAGCCTCG | 107932 |
rs243235606 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117014 | TTTTAGTTTTTAATC[A/G]TGTGTATTCATTATG | 107932 |
rs243315559 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098822 | GCTCACTTCTGCTCC[A/G]CAGGCAGAGGAAGAA | 107932 |
rs243317204 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125109003 | AGCTTGGCATTCTGT[G/T]GCAATACTCTGGTGC | 107932 |
rs243467562 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107924 | CTTAAACTGGAATTG[C/T]AGACTATAAGCCATC | 107932 |
rs243472577 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125117593 | TCATCCCCATCCTTA[-/C]CCCCCCACTCCCACC | 107932 |
rs243684157 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128727 | TGCTAGCTGGAGGAA[A/G]AGATGAATCTGTCAG | 107932 |
rs243711188 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094465 | TGAGTGCTGAGGTTA[C/T]TGGCATGTGATAATG | 107932 |
rs243833448 | snp | C/G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115365 | CTGATTTTGAATTCC[C/G/T]AATTCTCCTGCACCT | 107932 |
rs243890020 | in-del | -/CTCCCA | | | cds-indel | Chd4 | Mm_Celera | 6:125122141 | CACAGCCCCCTGCCC[-/CTCCCA]CTGCCCCTGCCACTG | 107932 |
rs243959019 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102393 | TTGGGGGGAGGTGGT[C/T]TTTTTCTAATAATTG | 107932 |
rs243990235 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125127264 | GGCATGTGCCACAAC[-/T]GCCCGACAGCGTTGG | 107932 |
rs244084398 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129203 | TAGCTTTATGGGGGG[A/G]GGGTGAAATGAAAAG | 107932 |
rs244104940 | snp | C/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101358 | CAGGAGGAGCCTGTG[C/G]GGTGGGAAGGGAGGA | 107932 |
rs244126243 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125121828 | GGCTGTCCTAAGAAT[A/G]GGGCTGGCTCTTAAA | 107932 |
rs244170109 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110876 | GCATCTGCACACATG[C/T]GCACCATGGCACAGA | 107932 |
rs244241251 | in-del | -/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118497 | ACATTTGTGGGGGTG[-/T]GGGGGGTGGAGGGCA | 107932 |
rs244424307 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103198 | AGCTAACTGAATTGA[A/G]GAGGGGTATTCCTCT | 107932 |
rs244430586 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125102864 | TCTGGAAGAAGTCGG[A/G]GGGGACCCAGAAGAG | 107932 |
rs244461089 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104240 | AATTCCAGCAGAGGC[A/G]AGGGCAAGCAGTTCT | 107932 |
rs244540873 | in-del | -/AAA | | | intron-variant | Chd4 | Mm_Celera | 6:125127514 | GAAACCCTGTCTCTT[-/AAA]AAAAAAAAAAAAACA | 107932 |
rs244564952 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112645 | GTGCACTGGCATGCA[A/T]ACTCTGACACGCTGA | 107932 |
rs244613529 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125121192 | GTGTCATAGGCCTTA[C/T]CTTGAGGTGTAGCCA | 107932 |
rs244789883 | in-del | -/TAGAAG | | | intron-variant | Chd4 | Mm_Celera | 6:125125811 | GGTGAGAAACACACT[-/TAGAAG]TAGATTAGTAAGTTT | 107932 |
rs244947830 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127402 | ATGCCTTTAGTCCTA[C/G]CACTCAGGAGGCAGA | 107932 |
rs244973952 | in-del | -/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099159 | TCCTCAAGCTAAAGC[-/T]TTCTGATTCCTTGTA | 107932 |
rs245059680 | in-del | -/GG | | | intron-variant | Chd4 | Mm_Celera | 6:125104349 | AGAAAGCACATGTGT[-/GG]GTGTTGTATGTGCAC | 107932 |
rs245115513 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107738 | AAGGAGTTGGAGGAA[-/G]GGAGGAGGAGGAGGT | 107932 |
rs245193244 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115470 | TTTTGAGACAGGGTC[G/T]CATATGTTCCAGGAT | 107932 |
rs245193356 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105917 | CTCCCTGGGCTCACT[C/T]ACTACCTGTTAGGGC | 107932 |
rs245268254 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125114971 | TTCAAATGTGAGAGG[A/G]TTCATTCTCTTTCCC | 107932 |
rs245304217 | in-del | -/CTTGTCTC | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098118 | AGTGGATGTCTTTCT[-/CTTGTCTC]CTTATTTAGAGCCCC | 107932 |
rs245369915 | snp | G/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101012 | CCTAGATCTCTGTCT[G/T]TCAAGACCCTGCCCG | 107932 |
rs245488369 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117348 | CACCTGCTTTATATG[A/G]TGGTAGGAATTGGAT | 107932 |
rs245524463 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117785 | GAGAAACCCTGTCTC[A/G]GAAAAAAAGAAAAAA | 107932 |
rs245583494 | in-del | -/GTGA | | | intron-variant | Chd4 | Mm_Celera | 6:125106551 | CACAGGTCGGTGACT[-/GTGA]GCGAGCAAGGAAGAG | 107932 |
rs245597861 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125125880 | CGGTCTAGGGAAGAA[A/C]AATTGGGAACAGAGG | 107932 |
rs245626531 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116677 | AAGGCATCCAGTGCC[A/T]CTCCTGGGTAGTTAT | 107932 |
rs245819629 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115959 | GATTTTTCTTCCTAC[-/T]TTTTATAGTATGTTT | 107932 |
rs245990275 | in-del | -/TG | | | intron-variant | Chd4 | Mm_Celera | 6:125126697 | TGAAACCAAGGACAT[-/TG]TGTGTGTGTGTGTGT | 107932 |
rs246032529 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098268 | CCTGTGAAGCCTGGC[C/T]GTCCTGTTTTTTGTT | 107932 |
rs246128258 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125110775 | ACAGAGTGCGTTTGC[A/C]CCTCCCCAGTCCCGG | 107932 |
rs246195577 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124019 | TTCCAAGTGACTTAG[C/T]TAACAGAGATCGGGA | 107932 |
rs246273996 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125109570 | GTGACGGAAGCAAGC[A/G]GGGCCTGAAGGAACC | 107932 |
rs246274088 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118313 | TCTGTTATGGAGTTA[C/T]ATAATAAGTGGTTTG | 107932 |
rs246280145 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107222 | CCAAAGACAGTATTT[C/T]CTTCTGGTTCCAGGA | 107932 |
rs246513824 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095530 | GGAGACTGATTATTA[C/T]GGGATCCGTGTGGGA | 107932 |
rs246559183 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125120060 | TCTGTTAAATTTCTT[C/T]CAAGTTTTTAGGTCC | 107932 |
rs246668754 | in-del | -/AAAGAG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128598 | AAAAAAAAAAAAAAA[-/AAAGAG]AGAGAGAGAGAGAGA | 107932 |
rs246671400 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118474 | GCTTTTTATTGACGT[C/T]CTGTTAAGACATTTG | 107932 |
rs246673387 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127751 | CCCATGGTTTTGAAG[A/G]ACAAAAGGAATATCT | 107932 |
rs246679312 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122432 | TGTGGAACTCTGTTG[C/T]AGCCGTGTGGGACCA | 107932 |
rs246703238 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119317 | TGGCTGTCCTGGAAC[G/T]CACTCTGTAGACCAG | 107932 |
rs246731593 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095091 | GCTCTAGTTGGAAGA[A/G]CCTGACAACTTCTAG | 107932 |
rs246874347 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130848 | GAATATGTAATTATA[G/T]AAGTATAAATTTTTT | 107932 |
rs246945804 | in-del | -/TCTTC | | | intron-variant | Chd4 | Mm_Celera | 6:125118011 | TTCAGCTCTGGAACT[-/TCTTC]TCTTCCCAGCAGGTC | 107932 |
rs246971838 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104099 | AAAACAACTAGGCTG[A/G]TCTTCAATTAAGAGA | 107932 |
rs247132032 | in-del | -/TGTGTGTGTG | | | intron-variant | Chd4 | Mm_Celera | 6:125118156 | TGGGGACAGTGTGTT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 107932 |
rs247206150 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103563 | ATTATATGTAAGTAC[A/G]CTGTAGCTGTCTTCA | 107932 |
rs247279227 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114894 | GCTCCCATAAAAAAA[A/T]TTTTAATGCTACCTC | 107932 |
rs247372892 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128115 | CAAACTCAGAAATCC[A/G]CCTGTCTCTGCCTCC | 107932 |
rs247402688 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125122045 | GTGAGAGGCAGGGTG[A/C]CTGAGTGCCATGCCG | 107932 |
rs247607500 | in-del | -/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115693 | GTGGCGCTATCTATC[-/T]ATCTATCTATCTATC | 107932 |
rs247788373 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122785 | CCACTGGTTTCGGAT[C/G]GCAGCTGACGTTTGC | 107932 |
rs247837678 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125122365 | TCAGGAGGAAGTGAT[A/C]CAGCTGGGACCCTTG | 107932 |
rs247869538 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099358 | TGTCATCCTAGAGTA[A/G]GTATTAGAGATCACT | 107932 |
rs247945823 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129061 | CCAACATCCATAAAC[A/G]GCTTATTTCCAAACT | 107932 |
rs247981512 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130667 | GGAAGACTGCCTGTG[C/T]TCCTGACAGGGTGAC | 107932 |
rs248208461 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125102769 | GGTGGGGTGGGGTAA[C/T]CTGAGTCTCTGGTTT | 107932 |
rs248398508 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117561 | TTCCTGGGAGTCCCA[A/G]GCTTGCCTCGGGCTC | 107932 |
rs248434366 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128601 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA | 107932 |
rs248437967 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124927 | AGTAAGTCAGTAATC[C/T]TTATTGGGCCTTATG | 107932 |
rs248443166 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117826 | TCATATTGGGGAGGG[C/T]GAGAAAGCTGATTTT | 107932 |
rs248566572 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125373 | CTTCAGTTTGAGTCG[A/G]TGAGAAAGGTGCTCA | 107932 |
rs248604087 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125979 | AACAAAACAACAGGG[A/G]CTGAGAGAGAGAGAA | 107932 |
rs248706172 | in-del | -/TG | | | intron-variant | Chd4 | Mm_Celera | 6:125104573 | GTGTGTGTCTGTGTC[-/TG]TGTGTCTGTGTCTGT | 107932 |
rs248771240 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106858 | CAGAAAGCAAACGCT[A/G]GGTGTTGTAAATGGT | 107932 |
rs248812458 | snp | C/T | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097331 | GAGACTCCAGTGAGG[C/T]TGCGTTCGCGCGCTG | 107932 |
rs248867544 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097611 | TGGTGACATGGTGGG[A/G]TGCGGTGGGGATTTC | 107932 |
rs249018568 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096325 | CGTCCCGGGGGTCAT[C/T]CCTTCACCTGTCCCT | 107932 |
rs249150712 | in-del | -/TGTGTG | | | intron-variant | Chd4 | Mm_Celera | 6:125118157 | TGGGGACAGTGTGTT[-/TGTGTG]TGTGTGTGTTTTAGT | 107932 |
rs249162310 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112678 | CATAAGTGTACTCAA[A/G]GTCAAAGGGTGTTGT | 107932 |
rs249325616 | in-del | -/TTGTTG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119789 | TGTATCTGTGTAACT[-/TTGTTG]TTGTTGTTGTTTGTT | 107932 |
rs249349298 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106761 | GGTGGAACAGGAAGG[C/G]TGTGTTTGTTGTGTG | 107932 |
rs249381677 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096840 | ACTCCCCAGGCACTC[C/T]TGGCTCAGGCCAGGC | 107932 |
rs249621150 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103523 | TTTATTTGAGATGGC[-/T]TTTTTTTTTTTTAAA | 107932 |
rs249729311 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125114331 | CAGCAGTGTTATCCA[C/T]TATGACGATAAGGCC | 107932 |
rs249730558 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119587 | CTGAATTGTCAATTC[-/G]GAAAAACTGTAACTC | 107932 |
rs249740879 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118390 | TAATTGTTTCAGATA[C/T]GGGAGAAGTTGGGAT | 107932 |
rs250066354 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096612 | CCCGACTCTTCGGGA[-/CC]CCGGAGCGCCCGAGC | 107932 |
rs250180256 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125100624 | TTCTGGGGAGTGAGA[-/AG]AGAGAGGAGGAGGAG | 107932 |
rs250279011 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099260 | GAATACAAGTGAGTG[A/G]GTACTGCAGTCATTC | 107932 |
rs250311573 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100287 | CTGGCCTGGCCTGGC[A/G]GCCGATTTTGGGTAT | 107932 |
rs250336250 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125102774 | GGTGGGGTAACCTGA[A/G]TCTCTGGTTTTATTG | 107932 |
rs250348797 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125125121 | AAAAACCAAACAATA[A/T]CAGCAGTAAGAAAAA | 107932 |
rs250444360 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108193 | GGCATCAGCTTCACT[C/G]TGGGGTGGGGCAGGG | 107932 |
rs250452566 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112097 | AGAACATACACAGAA[A/G]CCGGGCGTGGTGGCG | 107932 |
rs250507545 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111123 | AGAGGGCATCGGATC[C/T]ACTGGAACTGGAGGT | 107932 |
rs250645232 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118073 | TTTCACCAAAGACTG[C/G]CTATCCGAGCTGTAC | 107932 |
rs250663354 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118625 | CAGGCACCAGGAGTA[A/T]TTGTGGTATACAAAC | 107932 |
rs250723486 | snp | C/T | | | intron-variant, downstream-variant-500B | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125097340 | GTGAGGCTGCGTTCG[C/T]GCGCTGCTTGTCCCT | 107932 |
rs250725396 | in-del | -/TCC | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095535 | CTGATTATTACGGGA[-/TCC]GTGTGGGAGGAGGCC | 107932 |
rs250868144 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125123217 | ACTGTAGCCCTGGCT[A/G]GCCTGGGATTCAGTA | 107932 |
rs251050241 | in-del | -/TG | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100070 | GGTAAGGGATGAGTC[-/TG]TGTTCAGTGCCTTCT | 107932 |
rs251074862 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130018 | AGACCCAGAGTGATA[G/T]CCACCTCCACCACTC | 107932 |
rs251104698 | in-del | -/TA | | | intron-variant | Chd4 | Mm_Celera | 6:125123107 | GGGGGTGTGTGTGTG[-/TA]TGTGTATGTGTGTGT | 107932 |
rs251387868 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107415 | CTACTGTCTGCCGTC[C/T]CCGTCTCCGGGAAGG | 107932 |
rs251441750 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103737 | TTTATTTATTTTGTT[C/T]TCTGGAATTCTGTAG | 107932 |
rs251442775 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125113718 | CACTATCTTTTAAGC[A/C]TGGGAATTAGAATTG | 107932 |
rs251555833 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115643 | GTTGAATCACATCCT[G/T]ATCCCTCCATCAGAT | 107932 |
rs251675727 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117203 | GGGACTAAAGGCGTG[C/T]GCCACCACTGCTTTG | 107932 |
rs251726351 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116424 | TTTTTTTTTTTTTTT[-/G]AGATCTTTTTGTTTT | 107932 |
rs251728997 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122421 | AGCAGTGGAGCTGTG[G/T]AACTCTGTTGCAGCC | 107932 |
rs251765102 | snp | C/G | | | missense | Chd4 | Mm_Celera | 6:125122849 | GGAGGAGAAAAAGGA[C/G]GTGATGCTTCAGAAT | 107932 |
rs251765252 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114490 | GGGTCCAAGGCAGTG[C/T]TGTTCTTGGTGATTC | 107932 |
rs251924566 | in-del | -/TTTTTTTTC | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103426 | CCTTAACTTTTTTTT[-/TTTTTTTTC]TTTTTTTAGCTCTGT | 107932 |
rs252104020 | in-del | -/CCCA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126298 | AAACAACCCCCCCCC[-/CCCA]AAAAAAAAACCCACC | 107932 |
rs252104331 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126135 | TCTTGAGCCGGACAA[C/T]AGTGGTGCAGACCTT | 107932 |
rs252542733 | in-del | -/ACAT | | | intron-variant | Chd4 | Mm_Celera | 6:125104363 | GGGTGTTGTATGTGC[-/ACAT]ACATGTATGTTCCAG | 107932 |
rs252564907 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107846 | GTCTGTATATTGACC[A/G]TAAGTATGGTTGTGC | 107932 |
rs252584347 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108041 | TCAGAGCCCTGGTAG[A/G]CTCAGTGCCTGGCAT | 107932 |
rs252632288 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107229 | CAGTATTTCCTTCTG[A/G]TTCCAGGACTGGCCT | 107932 |
rs252632400 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125117483 | TTCCTCATCCTCTAT[A/C]GTGGCTCAAAGCTAG | 107932 |
rs252761263 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125126377 | GTAGCTTAGTTCCAC[A/C]ACACTAGCCTGGGCC | 107932 |
rs252763073 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117562 | TCCTGGGAGTCCCAG[G/T]CTTGCCTCGGGCTCA | 107932 |
rs252763782 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125113414 | TCACCTTCCTTCTCT[C/T]CTTATTTATTGGAAT | 107932 |
rs252775069 | in-del | -/CCAA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126299 | AACAACCCCCCCCCC[-/CCAA]AAAAAAAACCCACCT | 107932 |
rs252820871 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116994 | GCCATCTCCCCAGCC[C/T]AACTTTTTAGTTTTT | 107932 |
rs252874309 | in-del | -/TT | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131042 | GTTTATTGTTATCAC[-/TT]TTTTTTTGTTTGAAG | 107932 |
rs252924335 | snp | A/C | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098213 | TCTCTGCGTCCACGT[A/C]GTTTCCTACACCGTG | 107932 |
rs252953961 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098982 | TTGTCCAACCTTGGG[A/G]TCTGACTGGCTCCAG | 107932 |
rs252996052 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125118491 | TGTTAAGACATTTGT[-/G]GGGGTGGGGGGGTGG | 107932 |
rs253015645 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095838 | TTTGTAAAAGATCTG[C/T]ACTATATGTCTGTAG | 107932 |
rs253041646 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116640 | ACGATCTGCCAGCCT[C/G]TACCTCTAAGAGTTG | 107932 |
rs253276225 | in-del | -/AAAAAC | | | intron-variant | Chd4 | Mm_Celera | 6:125112230 | AAACCCTGTCTCGAA[-/AAAAAC]AAAAACAAAAACAAA | 107932 |
rs253313295 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125111571 | GATACAGGCACTGGG[-/C]ACTGAACCTAGAATC | 107932 |
rs253322501 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131055 | ACTTTTTTTTTGTTT[A/G]AAGATTTATTTATTA | 107932 |
rs253326413 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115697 | CGCTATCTATCTATC[-/T]ATCTATCTATCATCT | 107932 |
rs253450018 | in-del | -/TTTTC | | | intron-variant | Chd4 | Mm_Celera | 6:125118809 | TGAAAATTTGTTTTG[-/TTTTC]TTTTTTAGTGTTTAT | 107932 |
rs253489610 | in-del | -/TTTT | | | intron-variant | Chd4 | Mm_Celera | 6:125124631 | AGATTAGCATGGTGG[-/TTTT]TTTTCAGCATTTAGT | 107932 |
rs253775134 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111853 | AATACCACCTTACAT[A/G]CCTGGGGGCATAGGC | 107932 |
rs253808296 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125102601 | GGGCAAGTGGAGCTG[C/T]CCGCACTGTGTGAGT | 107932 |
rs253818930 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125121002 | TGGGTATACTAGTTG[A/G]AGCCAGGGCTTACAG | 107932 |
rs253825918 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128359 | CTGGAGAGATGCTCA[A/G]TAGTTAAGAACACTG | 107932 |
rs253880978 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127527 | CTTAAAAAAAAAAAA[A/C]CATTTTTCCTTTAAT | 107932 |
rs253884785 | in-del | -/GT | | | intron-variant | Chd4 | Mm_Celera | 6:125118493 | TAAGACATTTGTGGG[-/GT]GGTGGGGGGGTGGAG | 107932 |
rs253918219 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111709 | TCCCCCCAATCTTTC[A/G]TATTAATTAATTATT | 107932 |
rs253928170 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128096 | TTGTAGACCAGGCTG[G/T]CCTCAAACTCAGAAA | 107932 |
rs253964575 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119630 | GAGAGCTGTGGTGGC[A/G]CTTTGTTCCTAATGA | 107932 |
rs254035592 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119192 | TTGCTGGGACTTGAA[C/T]GCAGGACCTCAGGAA | 107932 |
rs254086021 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102031 | CCTGGCTCTTGCCAC[C/T]GGAGAAGGGGGAGCT | 107932 |
rs254173981 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126224 | TCTACAGAGTTCCAG[A/G]ACAACCAGGGCTATA | 107932 |
rs254801168 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116784 | TAAAAGAATTGTGTT[A/G]TTTTTTAATTGCTTT | 107932 |
rs254916302 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107039 | TGTCCCCATGCCCCG[A/G]TGACCTTTCCCCTTC | 107932 |
rs254950742 | in-del | -/TG | | | intron-variant | Chd4 | Mm_Celera | 6:125124947 | GGGCCTTATGGCCTC[-/TG]TGCAAATCCACAGCT | 107932 |
rs255006487 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124285 | TTTAGGGGAGGGAAT[G/T]AACTGGATCCCTGAG | 107932 |
rs255038756 | in-del | -/TTG | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131032 | TTTTTCCTTGGTTTA[-/TTG]TTATCACTTTTTTTT | 107932 |
rs255105696 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125125182 | ATTATTAAAAACTAG[-/C]ACGTATGAATCTTAT | 107932 |
rs255148424 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125105399 | ACCACGTCTGCTCCC[-/T]GGGCTCACTCACTAC | 107932 |
rs255151497 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122339 | CTTTATTTACTAGGA[-/T]TTTTGAACCATCAGG | 107932 |
rs255172218 | snp | C/G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106137 | TTTTTTTTGTTTTTT[C/G/T]TTTATAAATGAACAC | 107932 |
rs255207169 | in-del | -/CT | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100093 | TGCCTTCTGGGAAGA[-/CT]CTCCTTATTTCCTGT | 107932 |
rs255262276 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123756 | GGTTCTGTGAAGGAC[C/G]ATCAGCCACACTTGC | 107932 |
rs255338012 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125103915 | AAAAAAACAAAAAAC[-/A]AAAAAAAAAGGTGTG | 107932 |
rs255363248 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117785 | GAGAAACCCTGTCTC[-/G]GAAAAAAAGAAAAAA | 107932 |
rs255497574 | snp | G/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094331 | TTAGAGCACGGTGCT[G/T]GTAATAAATAAATAA | 107932 |
rs255533340 | snp | C/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125095001 | TGAGAGCCCAGAATG[C/G]TCCTATTGCCCAGGA | 107932 |
rs255576165 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122731 | CTGAGTGTGGAGGCG[A/G]AGGTAGACAGAGAGA | 107932 |
rs255657060 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111146 | CTGGAGGTACAGCTG[A/G]GTGAGCCACCATGTG | 107932 |
rs255718198 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118862 | GTTGATTTTGCTCCC[A/T]CTTGGGTATAAGGCT | 107932 |
rs256089209 | in-del | -/CACTT | | | intron-variant | Chd4 | Mm_Celera | 6:125107176 | ATTCTTTGGCTACTC[-/CACTT]CACTTTAATTCTTTA | 107932 |
rs256305622 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128549 | TCCAGGACAGCCAGG[A/G]CTACACAGAGAAACT | 107932 |
rs256363624 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126560 | AACTAAAAAGTTCTG[C/T]CTCTTGGAGTATATT | 107932 |
rs256508839 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125887 | GGGAAGAAAAATTGG[A/G]AACAGAGGCTGGTAG | 107932 |
rs256511849 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125108825 | GGAAACGGCCTCCAG[C/T]TCTAGTCCTTGGGGA | 107932 |
rs256584771 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117658 | GGTGATCAATTTACA[A/G]AAGAGAAAAGCTGAG | 107932 |
rs256702685 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125104253 | CAAGGGCAAGCAGTT[-/C]CTGAGTGTAAGGTCA | 107932 |
rs256764602 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102150 | TAACTTTGTTTTCTG[C/T]TTTTTCTTCCAGAGT | 107932 |
rs256777847 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117380 | CAAGAATTGGTGCAC[A/G]CTAGGCAAGCACTTT | 107932 |
rs256789652 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098418 | CTAGGCTGCTGAGAT[A/G]AGGGACTTAGATCTG | 107932 |
rs256864937 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125123582 | GCAGGACATCCAGAA[C/T]GACCCACGGTATGCC | 107932 |
rs256900343 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115916 | AGTTAGCCCTTTGAA[A/G]GATCCTAAATCAAAC | 107932 |
rs256962402 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125126922 | ATCTTTGCAAAGTCA[A/G]AGAAGTGGGATTGGA | 107932 |
rs257092962 | in-del | -/GCCTCTACCTCC | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103793 | GATTCCCCTGCATCT[-/GCCTCTACCTCC]AGAGCACTGAGATTA | 107932 |
rs257120982 | snp | A/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094911 | ATTTGGTGGGGTTTG[A/T]TGGGGCTCGAGGTTG | 107932 |
rs257215896 | in-del | -/AGGA | | | intron-variant | Chd4 | Mm_Celera | 6:125122558 | CAAAGGTCAGTGTGT[-/AGGA]AGGAAAGCTGGTTGT | 107932 |
rs257250151 | in-del | -/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118498 | CATTTGTGGGGGTGG[-/T]GGGGGTGGAGGGCAC | 107932 |
rs257554486 | in-del | -/CA | | | intron-variant | Chd4 | Mm_Celera | 6:125124420 | CTCTTCTGAGCATTC[-/CA]CAGAGACAGCCTCAT | 107932 |
rs257561825 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125107079 | CCCCATTCTTCCCTG[C/G]AGCTCGTGCCCACAT | 107932 |
rs257602144 | snp | A/C | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097716 | TTTCTGTCCCGATCT[A/C]TTACGGGTTCTCTGT | 107932 |
rs257665748 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125128183 | AGTTGGTGTTCTTGC[A/C]CCATGTGGTTCTGGG | 107932 |
rs257831064 | snp | A/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101704 | GCAAAGGTGCAGTGG[A/G]ATTTAATGAAGAGTC | 107932 |
rs257911523 | snp | A/C | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102159 | TTTCTGTTTTTTCTT[A/C]CAGAGTGAGGACGAC | 107932 |
rs257919542 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112493 | CGAATGTACACACAC[C/T]TGTATACACACAAGA | 107932 |
rs257941410 | in-del | -/GACTCAAACACGTAGAGATG | | | intron-variant | Chd4 | Mm_Celera | 6:125110727 | CTGTAGACCAATCTA[-/GACTCAAACACGTAGAGATG]GACCTGCCTTTAGAC | 107932 |
rs257986459 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111523 | ACAGGTGCCTGAAGC[A/G]GCCAGAAAGTTAGAA | 107932 |
rs258005146 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112619 | GACTCCTCTGTCCCC[C/T]GACTTGATGTGTGCA | 107932 |
rs258033182 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115003 | TTATATAGCTCCTTG[-/T]TTTTTTTTAACAGAA | 107932 |
rs258092751 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126450 | ATGGGTACTTTGTAA[C/T]TTATGAACTAAATAC | 107932 |
rs258270726 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094827 | GTTTCATCTAGTCAG[C/T]ATATTATTTGTTTGA | 107932 |
rs258279743 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118494 | AAGACATTTGTGGGG[-/T]GTGGGGGGGTGGAGG | 107932 |
rs258347766 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105424 | CACTACCTGTTAGGT[A/G]CCACGTCTGCTCCTG | 107932 |
rs258455414 | snp | A/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099218 | TCCATTGAGCCCTTG[A/T]TAAGTCTTAGTTCTA | 107932 |
rs258543692 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129657 | TGTGAGACCAGAGCC[A/G]CTTGCAACTAGAATG | 107932 |
rs258597277 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125124476 | TGAGTATGCCCTACA[G/T]GAAGGTATCAATCAA | 107932 |
rs258769652 | in-del | -/TTC | | | intron-variant | Chd4 | Mm_Celera | 6:125111385 | GGAGTCTTTGGTCTT[-/TTC]TGCTTAAAAGGGGGC | 107932 |
rs258830031 | in-del | -/AGTGCGCCTGTC | | | intron-variant | Chd4 | Mm_Celera | 6:125109177 | TGAGAGGTTCCAGTA[-/AGTGCGCCTGTC]AGTCAGTCAGTCCCT | 107932 |
rs258874765 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129195 | TTGAGCATAGCTTTA[-/T]TGGGGGGGGGGTGAA | 107932 |
rs258881733 | snp | C/G | | | intron-variant, upstream-variant-2KB | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125096738 | TCCCCGGGCGCAGAG[C/G]AGCGCCCCCCCACTC | 107932 |
rs259016597 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103151 | TTCCTTTTTTGCTTA[G/T]TCTTGGGACATCATC | 107932 |
rs259038831 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106636 | GGTGTGTTTTCTTTC[C/T]TAGGGAGTTAATGAG | 107932 |
rs259046432 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116358 | GAGGATTTTATATAA[C/T]TTGGTAGTACATTCA | 107932 |
rs259115359 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112617 | AAGACTCCTCTGTCC[C/T]CCGACTTGATGTGTG | 107932 |
rs259124950 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115412 | TCATGCACAACTACC[A/G]GAATTTTTATTTATT | 107932 |
rs259129336 | in-del | -/GAG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128601 | AAAAAAAAAAAAAAA[-/GAG]AGAGAGAGAGAGAGA | 107932 |
rs259175325 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117204 | GGACTAAAGGCGTGT[G/T]CCACCACTGCTTTGG | 107932 |
rs259281602 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125122701 | GCTGGTGATGCCTTG[C/T]CCTGGTCTGGGAGGC | 107932 |
rs259317978 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125123070 | TAGCGAGCTAGATCT[A/G]GACCATATTGAGATG | 107932 |
rs259370101 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124799 | AGCCAGAGGCCAGGG[C/G]GTGTACCACCAAGCC | 107932 |
rs259432775 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124134 | CCAACAAGGCTACAT[A/G]GTCCCTGTATTCCAA | 107932 |
rs259473980 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101124 | ATTTCCTCTGTACCT[C/T]GCTCGCTCTTGGAAG | 107932 |
rs259505976 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104470 | CTAGACCTAGAGCTC[A/G]GGCTGGCTGGCGGCC | 107932 |
rs259539941 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094027 | TCTCTTTCTCTCTTT[C/T]GTTTTTCTAGTATGG | 107932 |
rs259621796 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125102804 | GCAGGAGAAGGAGGG[A/G]ATCCAGTGGGAAGCT | 107932 |
rs259626696 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095816 | AGGGAGGGGGAGCAG[A/G]TTTTAGTTTGTAAAA | 107932 |
rs259712898 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125110493 | TATCTCTGTGAGTTC[A/C]AGGCCAACCTGGTTG | 107932 |
rs259742445 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125108033 | TTACAGGATCAGAGC[A/C]CTGGTAGACTCAGTG | 107932 |
rs259805635 | in-del | -/GC | | | intron-variant | Chd4 | Mm_Celera | 6:125105931 | TACTACCTGTTAGGG[-/GC]CCTTACTGAAGGGCT | 107932 |
rs259854988 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125128750 | TCTGTCAGTGAGAAC[A/G]TGGCCATCAGTCCAA | 107932 |
rs259936811 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117419 | GGCCATGTCTCCAGC[C/T]CCTGTAAGTTGATGT | 107932 |
rs259976612 | in-del | -/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099062 | GGAGGGAGTCTGCTG[-/T]TTTGGGGGCTTGGGC | 107932 |
rs260136655 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102056 | GAGCTGTGTGGGGGA[-/G]GGGGCACATAGGGTA | 107932 |
rs260268016 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118904 | CCTTTACTCTGTGAG[C/T]CACTCTGGCATCTCG | 107932 |
rs260400024 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125118254 | ATTACAGGTGTGAAC[C/T]ATCATGTTATATGTG | 107932 |
rs260418317 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125990 | AGGGGCTGAGAGAGA[A/G]AGAACTAACTGACTA | 107932 |
rs260437683 | snp | A/C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125115588 | GCTTACCTGAGATAG[A/C/T]GCCCGACGCTGCATG | 107932 |
rs260449003 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126822 | TGTTGGGGTCTGTTT[G/T]TTTTGAGATGGGGTC | 107932 |
rs260477802 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106603 | CTCTTGGAAGGACAG[A/G]GACCAAGAGGCAGCT | 107932 |
rs260591894 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125105997 | GAGACGTTTCTTCTG[-/A]ATTTGGCCCACAGCG | 107932 |
rs260655899 | snp | G/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098475 | CGGAGCTCTGCCTTT[G/T]CGAGGGTGAGGTGGG | 107932 |
rs260734112 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125107217 | TCACTCCAAAGACAG[A/T]ATTTCCTTCTGGTTC | 107932 |
rs260895432 | in-del | -/GA | | | intron-variant | Chd4 | Mm_Celera | 6:125112227 | GAGAAACCCTGTCTC[-/GA]AAAAAACAAAAACAA | 107932 |
rs261029694 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119465 | TAGTATTGTAGCAGG[C/T]ACATGCTACTGCATG | 107932 |
rs261060401 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125112370 | ACAAAAGGTGGAGGG[A/G]CAGCGAGGGGCCAGC | 107932 |
rs261079833 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125105966 | AAAAGGGACGTTGCC[A/G]TCGACTTACGTTCAA | 107932 |
rs261161744 | in-del | -/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097864 | GCAGTAGCCTAGTGA[-/G]GGGCAGAGGGAGGGA | 107932 |
rs261202665 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115049 | AAGAGAATGTGTGGG[C/G]TTTGGTTTATATTTC | 107932 |
rs261233915 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125122906 | TGAGAAGCAGAAGAA[A/G]AACAGCAAACAGCGT | 107932 |
rs261349278 | in-del | -/GGCCT | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100269 | CAGCTGCCCCAGGTG[-/GGCCT]GGCCTGGCCTGGCGG | 107932 |
rs261361425 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122658 | CCAAGATAAATGACT[A/G]TTTCCAAATGTAGTT | 107932 |
rs261407462 | in-del | -/CATG | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094234 | ATTTTTATATTGTAT[-/CATG]CATGGTCTCTTTGGT | 107932 |
rs261408017 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130969 | GTAACTACTGCCTGC[C/T]CCTGCCTCTCAAGTG | 107932 |
rs261412287 | in-del | -/TTGCAAGGTCGGTATC | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098181 | ACTCCCCCACATTCA[-/TTGCAAGGTCGGTATC]TTCTCTGCGTCCACG | 107932 |
rs261437258 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119241 | ACCACTGAGCCATCT[C/T]TTCAGCCCGTTTTTT | 107932 |
rs261481310 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125109930 | CAATGGTATGTGCAC[-/C]CTTTTGTCTTCTGTG | 107932 |
rs261558312 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125103959 | ACTCAGATTGAATGA[A/T]GTTTTTATAAGTCAT | 107932 |
rs261671961 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124684 | ATGTGTTGGGGAGCA[A/G]GCTACTAAATGTCCC | 107932 |
rs261721226 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125117807 | AAGAAAAAAACAAAA[C/G]AAGTCATATTGGGGA | 107932 |
rs261788303 | in-del | -/GTGTGTGTGTGTGTGTGA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126711 | ATTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGA]GAGAACCTGTGCTCT | 107932 |
rs261833175 | in-del | -/ACA | | | intron-variant | Chd4 | Mm_Celera | 6:125129636 | CTCAGGCCATCCTGG[-/ACA]ACATGTGAGACCAGA | 107932 |
rs261921828 | snp | G/T | | | missense | Chd4 | Mm_Celera | 6:125122882 | AGAAACTCCCAAGGA[G/T]CTTAGTGATGAGAAG | 107932 |
rs262023106 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125124031 | TAGCTAACAGAGATC[A/G]GGATATATAGATGTG | 107932 |
rs262043828 | snp | A/C | | | intron-variant | Chd4 | Mm_Celera | 6:125116479 | TGAGCACAGCCCATG[A/C]CAGGGAGAAACCCAT | 107932 |
rs262073377 | in-del | -/C | | | intron-variant | Chd4 | Mm_Celera | 6:125105396 | GGTACCACGTCTGCT[-/C]CCTGGGCTCACTCAC | 107932 |
rs262127269 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094144 | CTGGCCATCATGAAC[A/G]TGGAGAGCAGGTGAT | 107932 |
rs262188951 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095605 | TGACAATCATGGGAT[A/G]TCAAACTGGGGGTGG | 107932 |
rs262213336 | in-del | -/GGTCT | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097948 | TCTGAGGTAGCTTGG[-/GGTCT]GGTCTGGATTGGTGG | 107932 |
rs262246781 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125128863 | CATGTCCGAGGACCC[C/T]TCTCACCCGTCTATG | 107932 |
rs262347715 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130858 | TTATAGAAGTATAAA[A/T]TTTTTGAGGGTCTAA | 107932 |
rs262365583 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125122436 | GAACTCTGTTGCAGC[C/G]GTGTGGGACCAGGGT | 107932 |
rs262431083 | in-del | -/TCCCTG | | | cds-indel | Chd4 | Mm_Celera | 6:125122132 | TGCAGTGTGCACAGC[-/TCCCTG]CCCCTGCCCCTGCCC | 107932 |
rs262504116 | in-del | -/TTG | | | intron-variant | Chd4 | Mm_Celera | 6:125127123 | TGTTTGTTGGTTTTG[-/TTG]TTTTTTGTTTTTTCA | 107932 |
rs262534479 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127234 | TGCCTCTCCCTCCCA[A/G]GTGCTAGGATTAAAG | 107932 |
rs262596378 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119787 | ATCTGTGTAACTTTG[C/T]TGTTGTTGTTGTTTG | 107932 |
rs262696056 | in-del | -/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125097823 | TTTTTGAGTGGAGAA[-/G]GGATGGAGGGCTAGG | 107932 |
rs262698156 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125100158 | GCTGGATGGAGTTAG[C/G]TCTTTCACTTACTAA | 107932 |
rs262739432 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125126961 | TCAGTTGTTACAGAG[C/T]TTAGCTAGAAGACAC | 107932 |
rs262877556 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099418 | AATTTGAGAAGTTTT[C/T]TTTGAGGGTACTCTC | 107932 |
rs262901393 | in-del | -/GGGTCCACT | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123754 | AGGTTCTGTGAAGGA[-/GGGTCCACT]CCATCAGCCACACTT | 107932 |
rs262924686 | in-del | -/A | | | upstream-variant-2KB, synonymous-codon | Nop2, Chd4 | Mm_Celera | 6:125130001 | AGCCCAGCAGCAGTG[-/A]AAGACCCAGAGTGAT | 107932 |
rs262955360 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125014 | ACAAGTTCCAATAAA[A/G]TTTGCAGGTGGATTT | 107932 |
rs263105777 | snp | C/G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106111 | AATGGTTTTGTCGGT[C/G/T]TTTTTTTTGTTTTTT | 107932 |
rs263126712 | snp | A/G | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095157 | GCCAGACCTGTGTGC[A/G]GTGATGGAGTGTAGC | 107932 |
rs263305161 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125130774 | GCAGGAAGTAGCCAC[C/T]TGCCTGGTACAGTTG | 107932 |
rs263379538 | in-del | -/AAAA | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126301 | CAACCCCCCCCCCCC[-/AAAA]AAAAAACCCACCTGC | 107932 |
rs263385212 | snp | A/G | | | synonymous-codon | Chd4 | Mm_Celera | 6:125104923 | GAAGTGGGGCCAGCC[A/G]CCGTCTCCCACACCA | 107932 |
rs263456842 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112752 | CCGCGTAAGTGGTGA[C/T]GCAACTGTAACCTCA | 107932 |
rs263473919 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125103466 | CAGAGACGGGGAGGA[A/G]GTCCTAGTGGGTTTT | 107932 |
rs263678787 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101564 | CAAGGGCAGCTCCGG[A/G]GCATCAGTGGCAGCT | 107932 |
rs263749818 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110986 | AGGCACCTTTTGCTG[C/T]GGAGCCGCCTCACTA | 107932 |
rs263849644 | in-del | -/AA | | | intron-variant | Chd4 | Mm_Celera | 6:125103914 | AAAAAAACAAAAAAC[-/AA]AAAAAAAAAAGGTGT | 107932 |
rs264056467 | in-del | -/TTT | | | intron-variant | Chd4 | Mm_Celera | 6:125123162 | AGACAAGGGTACCCC[-/TTT]TTTTTTTTAATCTTT | 107932 |
rs264084174 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106829 | GGCCTGTGGATAGCT[C/G]TAGCTGAGATGGTCA | 107932 |
rs264121624 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125116126 | CACTATATTGTCAAG[A/G]ATGACCTTGAACTTG | 107932 |
rs264252716 | in-del | -/TGTA | | | intron-variant | Chd4 | Mm_Celera | 6:125115335 | ACCGACTTTGAATTC[-/TGTA]TGTAGCTTAAGCTGA | 107932 |
rs264286098 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125112296 | AAAGATATAAAAAAA[-/T]ATTTAAAAATAATTC | 107932 |
rs264339598 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125106220 | GGCAGATCTTGTTAC[A/G]GATGGTTGTGAGCCA | 107932 |
rs264341981 | in-del | -/TTTTTTTTTTTTAGATCTTTTTG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116413 | TTGCTTCTTTTTTTT[-/TTTTTTTTTTTTAGATCTTTTTG]TTTTTTAGATCTTGC | 107932 |
rs264423437 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125115366 | TGATTTTGAATTCCC[A/G]ATTCTCCTGCACCTC | 107932 |
rs264426079 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125114067 | GACAGGCTCAATGTC[C/T]AAACAGGAGCTTGAT | 107932 |
rs264444576 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125129471 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA | 107932 |
rs264534874 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125119966 | TTGCCAGGAGGAAGG[C/G]CCCGCTATGTCTCGT | 107932 |
rs264713247 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110441 | GGCATGGTATATATA[C/T]CCTAATCCCAGTACT | 107932 |
rs264869772 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125117078 | CACAGGGTCTTTTTG[G/T]TTTTTCGAGACAGGG | 107932 |
rs264944972 | snp | G/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123253 | AAATTGCTGTCCACC[G/T]CCTAACTTTTTCTTT | 107932 |
rs264948360 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125123236 | TGGGATTCAGTATGT[-/A]AAAATTGCTGTCCAC | 107932 |
rs265021837 | snp | A/C | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | Mm_Celera | 6:125094478 | TATTGGCATGTGATA[A/C]TGTTCCCAGCTGTGA | 107932 |
rs265060456 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125121895 | GACATGGCCTCTGAC[C/T]CAGGGCCTTCCTGAT | 107932 |
rs265104134 | snp | A/T | | | intron-variant | Chd4 | Mm_Celera | 6:125129254 | CGGGGACATTGGGGA[A/T]ATAAAAAGGTGTGGA | 107932 |
rs265220970 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125127435 | CAGGTGAATCTCTGA[C/G]TTAGTTCAAGGCTAA | 107932 |
rs265231387 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125119127 | TGGCTTCAGACACCC[C/T]AGAAGAAGGCATTGG | 107932 |
rs265260225 | in-del | -/TA | | | intron-variant | Chd4 | Mm_Celera | 6:125123109 | GGGTGTGTGTGTGTG[-/TA]TGTATGTGTGTGTGT | 107932 |
rs265298877 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125101024 | TCTGTCAAGACCCTG[C/T]CCGTCCTCTCTGTCC | 107932 |
rs265381912 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125111245 | ACCTCCATCCCTCCA[-/G]AACCCCAACTTGTTC | 107932 |
rs265396756 | snp | C/G | | | intron-variant | Chd4 | Mm_Celera | 6:125125856 | CAATGAAAACAGGCC[C/G]GTTCTCAGCGGTCTA | 107932 |
rs265441702 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125098274 | AAGCCTGGCTGTCCT[C/G]TTTTTTGTTCCTTAC | 107932 |
rs265478991 | in-del | -/G | | | intron-variant | Chd4 | Mm_Celera | 6:125104037 | TTAAAAACTTTTTTT[-/G]ATGGGATCCCACTTT | 107932 |
rs265496348 | snp | C/T | | | synonymous-codon | Chd4 | Mm_Celera | 6:125106455 | ATCAAGTGGCGAGAC[C/T]TGCCCTATGACCAGG | 107932 |
rs265506133 | snp | C/T | | | upstream-variant-2KB, intron-variant | Chd4, Mir7045, Gm32616 | Mm_Celera | 6:125095854 | ACTATATGTCTGTAG[C/T]CCCGGGCACATATAT | 107932 |
rs265518695 | in-del | -/TTTTGG | | | intron-variant | Chd4 | Mm_Celera | 6:125127985 | AGTTAGTGTTCTTTT[-/TTTTGG]TTTTGGTTTTGGTTT | 107932 |
rs265533946 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123928 | GTAGCTGAACCTGGG[C/T]TTTCTGTAGGAACAG | 107932 |
rs265589762 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131088 | ATATATGAGTACACT[A/T]CAGACACACCAGAAG | 107932 |
rs265698311 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125128492 | GGAGACAGAGGCAGG[C/T]AGATTTCTGAGTTCA | 107932 |
rs265774427 | snp | G/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | Mm_Celera | 6:125102108 | ACTCGGCTCCTTCTG[G/T]GCAGTTCTCTCCTTG | 107932 |
rs265815257 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125111293 | GTTGTTCTTTAGGGT[C/T]TCGGTTGCTTGACAC | 107932 |