| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs265915035 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | Mm_Celera | 6:125099299 | TACTCTGGTGCTGTC[C/T]TGGCTTTCTTGTCTG | 107932 |
| rs265932671 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125108563 | ACCTGGTCTCTAAGT[A/G]AGGCAGAAAGAGAAC | 107932 |
| rs266007699 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125116542 | GATTACTGCCTGAGT[C/T]CACTGTAGCTCTGAT | 107932 |
| rs266126926 | snp | C/T | | | intron-variant | Chd4 | Mm_Celera | 6:125114832 | GATTTGAACTCAGGA[C/T]CTCTGGAAGAGCAGT | 107932 |
| rs266136004 | snp | A/G | | | intron-variant | Chd4 | Mm_Celera | 6:125105384 | TCCTCAACCACAGGT[A/G]CCACGTCTGCTCCCT | 107932 |
| rs386951544 | in-del | -/TCT | | | intron-variant | Chd4 | Mm_Celera | 6:125111386 | GAGTCTTTGGTCTTT[-/TCT]GCTTAAAAGGGGGCA | 107932 |
| rs386998774 | in-del | -/TG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126727 | GTGTGTGTGTGTGTG[-/TG]AGAGAACCTGTGCTC | 107932 |
| rs387022182 | in-del | -/ACA | | | intron-variant | Chd4 | Mm_Celera | 6:125129639 | AGGCCATCCTGGACA[-/ACA]TGTGAGACCAGAGCC | 107932 |
| rs387175309 | in-del | -/TGCAAGGTCGGTATCT | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098182 | CTCCCCCACATTCAT[-/TGCAAGGTCGGTATCT]TCTCTGCGTCCACGT | 107932 |
| rs387216106 | in-del | -/AGT | | | intron-variant | Chd4 | Mm_Celera | 6:125113226 | TGGTCACTTGGTTGT[-/AGT]CATGGTGTCTGCTGA | 107932 |
| rs387246332 | in-del | -/A | | | intron-variant | Chd4 | Mm_Celera | 6:125107665 | CTATAAGGAGGTAAA[-/A]GATGCCAGGAGATGC | 107932 |
| rs387318426 | in-del | -/AGGG | | | intron-variant | Chd4 | Mm_Celera | 6:125129202 | TAGCTTTATGGGGGG[-/AGGG]GGGGTGAAATGAAAA | 107932 |
| rs387342896 | in-del | -/CTATCTATCTAT | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115684 | ATGATTACAGTGGCG[-/CTATCTATCTAT]CTATCTATCTATCAT | 107932 |
| rs387348782 | in-del | -/GG | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123096 | AGATGGATTGGCGGG[-/GG]TGTGTGTGTGTGTGT | 107932 |
| rs387450422 | in-del | -/AA | | | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | Nop2, Chd4 | Mm_Celera | 6:125130514 | AAAAAAAAAAAAAAA[-/AA]GAAAAAGAACCAAAA | 107932 |
| rs387543643 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125110833 | CTTTATTTTTTTTTT[-/T]AAAGTGTGCATGTAT | 107932 |
| rs387549822 | in-del | -/TT | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131043 | TTTATTGTTATCACT[-/TT]TTTTTTGTTTGAAGA | 107932 |
| rs387574310 | in-del | -/TTTTTTTTTT | | | intron-variant | Chd4 | Mm_Celera | 6:125116415 | GCTTCTTTTTTTTTT[-/TTTTTTTTTT]AGATCTTTTTGTTTT | 107932 |
| rs387629797 | in-del | -/AGAGC | | | intron-variant | Chd4 | Mm_Celera | 6:125129334 | GCTGAGAATAAAAAC[-/AGAGC]TCTGTGGGCATTTGC | 107932 |
| rs387731964 | in-del | -/GCAAGGTCGGTATCTT | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098183 | TCCCCCACATTCATT[-/GCAAGGTCGGTATCTT]CTCTGCGTCCACGTA | 107932 |
| rs387813949 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125123170 | GTACCCCTTTTTTTT[-/T]AATCTTTGGGGATTT | 107932 |
| rs387859164 | in-del | -/T | | | intron-variant | Chd4 | Mm_Celera | 6:125106119 | GTCGGTTTTTTTTTT[-/T]GTTTTTTTTTGTTTT | 107932 |
| rs387871794 | in-del | -/TT | | | upstream-variant-2KB, downstream-variant-500B | Nop2, Chd4 | Mm_Celera | 6:125131049 | GTTATCACTTTTTTT[-/TT]GTTTGAAGATTTATT | 107932 |
| rs578394620 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115684 | ATGATTACAGTGGCG[A/C]TATCTATCTATCTAT | 107932 |
| rs578422617 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106182 | GTATACTATAGCTGT[C/T]TTCAGACACTCCAGA | 107932 |
| rs578425298 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119281 | TTATTTTTTTTGAGA[C/T]AGGGTTTCTCTGTGT | 107932 |
| rs578603680 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105904 | GGGGCCACGTCTGCT[C/G]CCTGGGCTCACTTAC | 107932 |
| rs578930550 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119864 | AGAATACTTTCTGTT[C/T]TAAAGATCTCTTGCA | 107932 |
| rs578954278 | snp | C/G | | | upstream-variant-2KB, intron-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125094521 | GGAAGGCACCTGTGT[C/G]TTGGTATCCTCGTTC | 107932 |
| rs579044863 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115320 | TTAGCAGAAACCTAG[A/C]CCGACTTTGAATTCT | 107932 |
| rs579179019 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127270 | TGCCACAACTGCCCG[A/G]CAGCGTTGGGTTTTT | 107932 |
| rs579179505 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115717 | ATCTATCATCTATCT[A/G]TCTATCTATCTATCT | 107932 |
| rs579367165 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103859 | AGAGTGAGTTCCAGG[A/T]CAGCCAGGGCTATAC | 107932 |
| rs579526273 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115840 | CTATCTATCTATCTA[C/T]CTATCTATCATCTAT | 107932 |
| rs579697331 | snp | A/C | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098998 | TCTGACTGGCTCCAG[A/C]ATCATTTAGGGCTAC | 107932 |
| rs579699204 | snp | A/C | | | missense | Chd4 | GRCm38.p3 | 6:125122153 | GCCCCTGCCCCTGCC[A/C]CTGCCCCTGCCACTG | 107932 |
| rs579703761 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123090 | ATATTGAGATGGATT[A/G]GCGGGGGTGTGTGTG | 107932 |
| rs579742043 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125097941 | CCGCCACTCTGAGGT[A/G]GCTTGGGGTCTGGTC | 107932 |
| rs579820665 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125111396 | GTCTTTGCTTAAAAG[A/G]GGGCATTTTCTCTAA | 107932 |
| rs580089333 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106549 | ACCACAGGTCGGTGA[C/T]TGTGAGCGAGCAAGG | 107932 |
| rs580102993 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125099149 | GACACTTGGTTCCTC[A/G]AGCTAAAGCTTTCTG | 107932 |
| rs580120125 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123241 | TTCAGTATGTAAAAA[C/T]TGCTGTCCACCGCCT | 107932 |
| rs580365293 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115799 | TCTATCTATCTTTCT[A/G]TCTATCTATCTATCT | 107932 |
| rs580377240 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105477 | TACCACGTCTGCTCC[C/T]GGGCTCACTCACTAC | 107932 |
| rs580756621 | snp | A/C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105608 | CTGGGCTCACTCACT[A/C/G]CCTGTTAGGTACCAC | 107932 |
| rs580768203 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125112738 | TGAGGTCCCCAGCAC[C/T]GCGTAAGTGGTGATG | 107932 |
| rs580806429 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125126313 | CCCAAAAAAAAAACC[C/T]ACCTGCTTGGCAGTA | 107932 |
| rs580899933 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | GRCm38.p3 | 6:125101772 | CATTGCCCCTAAGTC[A/G/T]GTCCCTAATGGGCAG | 107932 |
| rs580918714 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127033 | GTAATCAGCACATAG[C/G]ATCTCACAGGCAGGA | 107932 |
| rs580928512 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115322 | AGCAGAAACCTAGAC[C/T]GACTTTGAATTCTGT | 107932 |
| rs581073155 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118494 | TAAGACATTTGTGGG[G/T]GTGGGGGGGTGGAGG | 107932 |
| rs581316423 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105902 | TAGGGGCCACGTCTG[A/C]TCCCTGGGCTCACTT | 107932 |
| rs581397496 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115860 | CTATCATCTATCTAT[C/T]TAAGGTGGCTTGTGT | 107932 |
| rs581455737 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105803 | CTGGGCTCACTCACT[A/C]CCTGTTAGGGGCCAC | 107932 |
| rs581484779 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125117519 | GTCCCATTGGGCCCG[C/G]AGCTGGATTGCCCAG | 107932 |
| rs581653997 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125114873 | ACCTGTTGAGCCATC[C/T]CTCCAGCTCCCATAA | 107932 |
| rs581882121 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115706 | TCTATCTATCTATCT[A/G]TCATCTATCTATCTA | 107932 |
| rs582182424 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125104617 | TGTGTGTGTGTGTGT[A/G]TGTGTGATGTGCAGT | 107932 |
| rs582217170 | snp | C/T | | | missense | Chd4 | GRCm38.p3 | 6:125122177 | GCCACTGCCACTGCC[C/T]CTGAGGATGACAAGG | 107932 |
| rs582312261 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105905 | GGGCCACGTCTGCTC[C/G]CTGGGCTCACTTACT | 107932 |
| rs582779269 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106266 | GATTTGAACTCTGGA[C/T]CTTTGGAAGAACAGT | 107932 |
| rs582809754 | snp | A/G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115737 | TCTATCTATCTATCT[A/G/T]TCTATCTATCTATCT | 107932 |
| rs582828553 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115850 | ATCTATCTATCTATC[A/T]TCTATCTATTTAAGG | 107932 |
| rs582862515 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119373 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 107932 |
| rs582906409 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128541 | AAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA | 107932 |
| rs582914662 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103912 | AAAAAAAAAACAAAA[A/C]ACAAAAAAAAAAGGT | 107932 |
| rs583345743 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105569 | CTGGGCTCACTCACT[C/G]CCTGTTAGGTACCAC | 107932 |
| rs583409174 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115803 | TCTATCTTTCTATCT[A/G]TCTATCTATCTATCT | 107932 |
| rs583444635 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125112247 | AAACAAAAACAAAAA[C/T]AAAAACAAAACACCC | 107932 |
| rs583562343 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106550 | CCACAGGTCGGTGAC[G/T]GTGAGCGAGCAAGGA | 107932 |
| rs583595134 | snp | C/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125099166 | GCTAAAGCTTTCTGA[C/T]TCCTTGTAGGGATGA | 107932 |
| rs583672771 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123249 | GTAAAAATTGCTGTC[C/T]ACCGCCTAACTTTTT | 107932 |
| rs583787558 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105491 | CTGGGCTCACTCACT[A/G]CCTGTTAGGTACCAC | 107932 |
| rs583828349 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125128009 | TTGGTTTTGGTTTTG[G/T]TTTGGTTTGGTTTTT | 107932 |
| rs583905623 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125112739 | GAGGTCCCCAGCACC[A/G]CGTAAGTGGTGATGC | 107932 |
| rs583948977 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118507 | GGGGTGGGGGGGTGG[A/G]GGGCACTTGGAGGGA | 107932 |
| rs584024503 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125099057 | TTAAAGGGAGGGAGT[C/G]TGCTGTTTGGGGGCT | 107932 |
| rs584036713 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123154 | GTGTGTGACAGACAA[A/G]GGTACCCCTTTTTTT | 107932 |
| rs584072488 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116340 | TATATGTGTGACTGG[C/T]TGGAGGATTTTATAT | 107932 |
| rs584236468 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105670 | GGTACCACGTCTGCC[C/T]CTGGGCTCACTCATT | 107932 |
| rs584338511 | snp | C/T | | | intron-variant, upstream-variant-2KB | Chd4, Gm32616 | GRCm38.p3 | 6:125101781 | TAAGTCTGTCCCTAA[C/T]GGGCAGGAGTGAGCC | 107932 |
| rs584465925 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105903 | AGGGGCCACGTCTGC[A/T]CCCTGGGCTCACTTA | 107932 |
| rs584603996 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118430 | TTTACAGACTGAGTA[C/T]CCATACACCAAGGTC | 107932 |
| rs584676780 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127018 | ATGTGGTGCCTGCCT[A/G]TAATCAGCACATAGG | 107932 |
| rs584711090 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125104541 | GTAGGCTGCAGGTGT[G/T]TGTGTGTGTGTGTGT | 107932 |
| rs584837078 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115263 | TCTTAAATGTTCGAT[C/T]CTCCTGCATCAGTTG | 107932 |
| rs584999687 | snp | C/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105842 | CCGGGCTCACTCACT[C/G]CCTGTTAGGTACCAC | 107932 |
| rs585029558 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125122729 | GGCTGAGTGTGGAGG[C/T]GGAGGTAGACAGAGA | 107932 |
| rs585137645 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127142 | TTTGTTTTTTCAAGA[A/C]TGGGTTTCTCTGTGC | 107932 |
| rs585168757 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125103688 | TCGGGTGCTCTTACC[A/C]ACTGAGCCATCTCAC | 107932 |
| rs585290442 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125098269 | CTGTGAAGCCTGGCT[A/G]TCCTGTTTTTTGTTC | 107932 |
| rs585336444 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125119375 | GCCTCTGCCTCCCGA[A/G]TGCTGGGATTAAAGG | 107932 |
| rs585525886 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125104631 | TGTGTGTGATGTGCA[G/T]TGACAGAAGAGGGTG | 107932 |
| rs585620020 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105452 | CTGGGCTCACTTACT[A/G]CCTGTTAGGTACCAC | 107932 |
| rs585758098 | snp | G/T | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125097807 | GTCAGATTGTTGGGA[G/T]TTTTTTGAGTGGAGA | 107932 |
| rs585884129 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115823 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 107932 |
| rs586090595 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125106543 | ACTGGAACCACAGGT[C/T]GGTGACTGTGAGCGA | 107932 |
| rs586154645 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125110544 | CAGCCTCAGCTGCTT[C/T]TGTCTTAAAACAAAA | 107932 |
| rs586226774 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125127026 | CCTGCCTGTAATCAG[A/C]ACATAGGATCTCACA | 107932 |
| rs586267130 | snp | A/G | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115713 | ATCTATCTATCATCT[A/G]TCTATCTATCTATCT | 107932 |
| rs586632035 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125118492 | GTTAAGACATTTGTG[G/T]GGGTGGGGGGGTGGA | 107932 |
| rs586634696 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125112671 | GCTGACACATAAGTG[C/T]ACTCAAAGTCAAAGG | 107932 |
| rs586665873 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105711 | TACCACGTCTGCTCC[C/T]GGGCTCACTCACTCC | 107932 |
| rs586682748 | snp | A/C | | | intron-variant | Chd4 | GRCm38.p3 | 6:125115852 | CTATCTATCTATCAT[A/C]TATCTATTTAAGGTG | 107932 |
| rs586871634 | snp | C/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125099600 | CCTACTCCCCCTCTT[C/G]TTGAGCGGGGGTGGC | 107932 |
| rs587033793 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105591 | AGGTACCACGTCTGC[C/T]CCTGGGCTCACTCAC | 107932 |
| rs587102205 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125105516 | TACCACGTCTGCTCC[C/T]GGGCTCACTCACTCC | 107932 |
| rs587278790 | snp | C/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125124931 | AGTCAGTAATCTTTA[C/T]TGGGCCTTATGGCCT | 107932 |
| rs587336743 | snp | G/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116931 | ATGTGGTTGCTGGGA[G/T]TTGAACTTAGGACCT | 107932 |
| rs587580381 | snp | A/G | | | intron-variant, nc-transcript-variant | Chd4, Gm32616 | GRCm38.p3 | 6:125099076 | TGTTTGGGGGCTTGG[A/G]CATGGTTTCTGCAGG | 107932 |
| rs587582868 | snp | A/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125123240 | ATTCAGTATGTAAAA[A/T]TTGCTGTCCACCGCC | 107932 |
| rs864279800 | in-del | -/T | | | intron-variant | Chd4 | GRCm38.p3 | 6:125116064 | ATGAACCACAATGTG[-/T]TTTTTTTTGAGACAG | 107932 |
| rs864291370 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | GRCm38.p3 | 6:125130487 | CAGCCACTGAGCAGC[A/T]AAATAAAGTTGGAAA | 107932 |